{"id":870,"date":"2015-12-17T15:42:09","date_gmt":"2015-12-17T14:42:09","guid":{"rendered":"http:\/\/www.paleurafrica.be\/?page_id=870"},"modified":"2021-04-27T09:45:03","modified_gmt":"2021-04-27T07:45:03","slug":"results","status":"publish","type":"page","link":"https:\/\/www.paleurafrica.be\/","title":{"rendered":"<span data-icon=\"\ue02b\"><\/span>  Results"},"content":{"rendered":"<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A reassessment of the Oligocene hyracoids from Malembo, Cabinda, Angola<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Oligocene Malembo locality, Cabinda exclave, Angola has yielded a rich vertebrate fauna represented by fragmentary remains. This fossiliferous locality is the only definite occurrence of Oligocene terrestrial mammals in sub-Saharan West Africa. The hyracoids from Malembo have only been very succinctly described and compared thus far, so that their systematic attribution is not consensual among specialists. A revision now allows the identification of three (or four) medium to large-sized species represented by <em>Geniohyus dartevellei<\/em>, <em>Pachyhyrax<\/em> cf. <em>crassidentatus<\/em>, and two undetermined taxa. The species <em>G. dartevellei<\/em> is revived for the holotype of <em>Palaeochoerus dartevellei<\/em> Hooijer, 1963; this species is unique to Malembo but appears close to <em>Geniohyus mirus<\/em>, a species only known from the early Oligocene of the Fayum, Egypt. Other species of <em>Geniohyus<\/em> and <em>Pachyhyrax crassidentatus<\/em> are also only known from the early Oligocene of the Fayum. The presence of <em>Geniohyus<\/em> and <em>Pachyhyrax<\/em> cf. <em>crassidentatus<\/em> at Malembo supports thus an early Oligocene age for the fauna.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (Tabuce et al., in press).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Hyracoides.jpg\" title=\"Hyracoids from Malembo, Angola: &lt;em&gt;Geniohyus dartevellei&lt;\/em&gt;, RMCA-RG6412, right m3 in occlusal (A), lingual (B), and labial (C) views; &lt;em&gt;Pachyhyrax&lt;\/em&gt; cf. &lt;em&gt;crassidentatus&lt;\/em&gt;, RMCA-RG6423, left m3 on a mandible fragment in occlusal (D), lingual (E), and labial (F) views (the arrow indicates the mandibular depression, see text for details); Hyracoidea, genus and species indet., RMCA-RG6416, fragment of a right m1 or m2 in occlusal (G), lingual (H), and labial (I) views; Hyracoidea, genus and species indet., RMCA-RG6425, a proximal phalanx in dorsal (J), plantar (K), and lateral (L, M), distal (N), and proximal (O) views. Scale bar = 1cm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Hyracoides-656x486.jpg\" alt=\"Hyracoids from Malembo, Angola: &lt;em&gt;Geniohyus dartevellei&lt;\/em&gt;, RMCA-RG6412, right m3 in occlusal (A), lingual (B), and labial (C) views; &lt;em&gt;Pachyhyrax&lt;\/em&gt; cf. &lt;em&gt;crassidentatus&lt;\/em&gt;, RMCA-RG6423, left m3 on a mandible fragment in occlusal (D), lingual (E), and labial (F) views (the arrow indicates the mandibular depression, see text for details); Hyracoidea, genus and species indet., RMCA-RG6416, fragment of a right m1 or m2 in occlusal (G), lingual (H), and labial (I) views; Hyracoidea, genus and species indet., RMCA-RG6425, a proximal phalanx in dorsal (J), plantar (K), and lateral (L, M), distal (N), and proximal (O) views. Scale bar = 1cm.\" width=\"656\" height=\"486\" \/><span class=\"su-custom-gallery-title\">Hyracoids from Malembo, Angola: <em>Geniohyus dartevellei<\/em>, RMCA-RG6412, right m3 in occlusal (A), lingual (B), and labial (C) views; <em>Pachyhyrax<\/em> cf. <em>crassidentatus<\/em>, RMCA-RG6423, left m3 on a mandible fragment in occlusal (D), lingual (E), and labial (F) views (the arrow indicates the mandibular depression, see text for details); Hyracoidea, genus and species indet., RMCA-RG6416, fragment of a right m1 or m2 in occlusal (G), lingual (H), and labial (I) views; Hyracoidea, genus and species indet., RMCA-RG6425, a proximal phalanx in dorsal (J), plantar (K), and lateral (L, M), distal (N), and proximal (O) views. Scale bar = 1cm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New specimens of the mesonychid <em>Dissacus praenuntius<\/em> from the early Eocene of Wyoming and evaluation of body size through the PETM in North America<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"> The Mesonychia is a group of archaic carnivorous mammals of uncertain phylogenetic affinities with a Holarctic distribution during the Paleogene. Intensive fossil collecting efforts in the Bighorn Basin, Wyoming, have resulted in recovery of the largest sample and most complete specimens yet known of the mesonychid <em>Dissacus praenuntius<\/em> from the second biozone of the Wasatchian North American Land Mammal Age (Wa-0). The Wa-0 biozone corresponds to the body of the Paleocene-Eocene Thermal Maximum (PETM), a brief but intense global warming event that occurred ~56 Ma ago that significantly impacted terrestrial mammal faunas, including dwarfing in many mammal lineages. To evaluate the potential response of this lineage to climate change, we compared the PETM sample of <em>D. praenuntius<\/em> with those recovered from just before the PETM in the last biozone of the Clarkforkian North American Land Mammal Age (Cf-3) and just after the PETM in the Wa-1 biozone. While the sample size is still too small to say with certainty, tooth size (as a proxy for body weight) of <em>D. praenuntius<\/em> appears to be smaller during the late PETM than during either the pre-PETM Cf-3, or post-PETM Wa-1 biozones, suggesting the possibility of a muted dwarfing response to the PETM. However, the pattern observed for <em>D. praenuntius<\/em> differs from that of many other PETM mammals, as the shift to smaller body size is less pronounced and may have only occurred in late Wa-0.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (Sol\u00e9 et al., in press).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Dissacus.jpg\" title=\"Sizes [ln (L \u00d7 W) in millimeters] of lower premolars and molars of North American &lt;em&gt;Dissacus&lt;\/em&gt; species from the Torrejonian, middle Paleocene, through Wasatchian, early Eocene, strata. The range of variation expected in each sample is 0.40 units on a natural-log (ln) scale (mean \u00b1 two standard deviations, where s = 0.10; e.g., Gingerich, 1989, p. 25; Gingerich, 2019). Abbreviations: Cf = Clarkforkian; m = meter level in the Cabin Fork master section; PB = Polecat Bench; Ti = Tiffanian; To = Torrejonian; Wa = Wasatchian.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Dissacus-656x784.jpg\" alt=\"Sizes [ln (L \u00d7 W) in millimeters] of lower premolars and molars of North American &lt;em&gt;Dissacus&lt;\/em&gt; species from the Torrejonian, middle Paleocene, through Wasatchian, early Eocene, strata. The range of variation expected in each sample is 0.40 units on a natural-log (ln) scale (mean \u00b1 two standard deviations, where s = 0.10; e.g., Gingerich, 1989, p. 25; Gingerich, 2019). Abbreviations: Cf = Clarkforkian; m = meter level in the Cabin Fork master section; PB = Polecat Bench; Ti = Tiffanian; To = Torrejonian; Wa = Wasatchian.\" width=\"656\" height=\"784\" \/><span class=\"su-custom-gallery-title\">Sizes [ln (L \u00d7 W) in millimeters] of lower premolars and molars of North American <em>Dissacus<\/em> species from the Torrejonian, middle Paleocene, through Wasatchian, early Eocene, strata. The range of variation expected in each sample is 0.40 units on a natural-log (ln) scale (mean \u00b1 two standard deviations, where s = 0.10; e.g., Gingerich, 1989, p. 25; Gingerich, 2019). Abbreviations: Cf = Clarkforkian; m = meter level in the Cabin Fork master section; PB = Polecat Bench; Ti = Tiffanian; To = Torrejonian; Wa = Wasatchian.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New hyaenodonts (Mammalia) from the late Ypresian locality of Pr\u00e9montr\u00e9 (France) support a radiation of the hyaenodonts in Europe already at the end of the early Eocene<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We describe three new hyaenodonts from the late Ypresian locality of Pr\u00e9montr\u00e9 (Aisne, France; close to MP 10 reference level). The new species \u2013 <em>Lesmesodon gunnelli<\/em> nov. sp., <em>Cynohyaenodon smithae<\/em> nov. sp., and <em>Eurotherium mapplethorpei<\/em> nov. sp. \u2013 represent the oldest occurrences of these three European genera. <em>Lesmesodon gunnelli<\/em> is also reported from the locality of Cuis (Marne, France; Ypresian, \u2248MP 10). We further present the dentition of two specimens of <em>Lesmesodon edingeri<\/em> from Messel (Hessia, Germany; type locality of the genus) based on \u03bcCT scans. <em>Cynohyaenodon smithae<\/em> and <em>Lesmesodon gunnelli<\/em> support the presence of small (300-400 g) hyaenodonts in the late Ypresian of the Paris Basin. Estimation of dental indices indicates that these hyaenodonts had an insectivorous diet. The third species \u2013 referred to <em>Eurotherium<\/em> \u2013 may have weighed 4-5 kg and, based on dental indices, likely incorporated more vertebrate prey into its diet. We also performed a phylogenetic analysis in order to test the relationships of these new taxa. These newly discovered species imply that the <em>Proviverra\/Allopterodon<\/em>, <em>Cynohyaenodon<\/em>, and <em>Eurotherium<\/em> clades appeared in Europe earlier than previously known (i.e., Lutetian, MP 11). They reinforce the hypothesis that the hyaenodonts radiated during the middle-late Ypresian (MP 8\/9-10) in Europe and adapted at that time to diverse ecological niches that they still occupied in the Priabonian (MP 13-14).<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (Sol\u00e9 et al., in press).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Hyaenodontes-scaled.jpg\" title=\"&lt;em&gt;Lesmesodon edingeri&lt;\/em&gt; (Springhorn, 1982), HLMD-Be 155. A, Original specimen in 1378 lateral view (right). B, Digitized specimen. C-E, right upper dentition; C, occlusal view; D, 1379 lingual view; E, labial view. F-H, right lower dentition; F, occlusal view; G, lingual view; H, 1380 labial view. Reversed views: D, G. Upper scale bar: A-B; lower scale bar: C-H.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Hyaenodontes-scaled.jpg\" alt=\"&lt;em&gt;Lesmesodon edingeri&lt;\/em&gt; (Springhorn, 1982), HLMD-Be 155. A, Original specimen in 1378 lateral view (right). B, Digitized specimen. C-E, right upper dentition; C, occlusal view; D, 1379 lingual view; E, labial view. F-H, right lower dentition; F, occlusal view; G, lingual view; H, 1380 labial view. Reversed views: D, G. Upper scale bar: A-B; lower scale bar: C-H.\" width=\"656\" height=\"839\" \/><span class=\"su-custom-gallery-title\"><em>Lesmesodon edingeri<\/em> (Springhorn, 1982), HLMD-Be 155. A, Original specimen in 1378 lateral view (right). B, Digitized specimen. C-E, right upper dentition; C, occlusal view; D, 1379 lingual view; E, labial view. F-H, right lower dentition; F, occlusal view; G, lingual view; H, 1380 labial view. Reversed views: D, G. Upper scale bar: A-B; lower scale bar: C-H.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A new basal raoellid artiodactyl (Mammalia) from the middle Eocene Subathu Group of Rajouri District, Jammu and Kashmir, northwest Himalaya, India<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A new artiodactyl of moderate size, <em>Rajouria gunnelli<\/em> gen. et sp. nov., is described based on several dentaries, maxillae and isolated teeth from the middle Eocene Subathu Group of the Kalakot area, Rajouri District, Jammu and Kashmir, India. Despite its general resemblance with the family Dichobunidae by the retention of a paraconid on m1-2 and a simple P4 where endocristids do not form an anterior loph, this taxon shares with Raoellidae two unambiguous characters: the presence of a hypoconid on p4, and an asymmetrical P4. The phylogenetic position of the new taxon within the Cetacea \/ Raoellidae clade is strongly supported by eight seven non ambiguous synapomorphies, among which a cristid obliqua on lower molars anteriorly pointing towards the postectoprotocristid, and a P3 with only two roots. The presence of a new basal raoellid in the middle Eocene Subathu Group sheds new light on the phylogeny and paleobiogeography of raoellid artiodactyls.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (Rana et al., in press).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Rajouria.jpg\" title=\"Lower dentition of &lt;em&gt;Rajouria gunnelli&lt;\/em&gt; gen. nov. sp. nov. A-C. GU\/RJ\/362, left dentary and holotype with i3 erupting, dp3, m1-2, trigonid part of m3 and alveoli of i1-2, c, p1-2, and p4 in occlusal (A), labial (B), lingual (C) views. D-F. GU\/RJ\/303, right dentary fragment with m1-2 in occlusal (D), labial (E), lingual (F) views. G-I. GU\/RJ\/144, left dentary fragment with p2-4 in occlusal (G), labial (H), lingual (I) views. Scale bar: 10 mm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Rajouria-656x630.jpg\" alt=\"Lower dentition of &lt;em&gt;Rajouria gunnelli&lt;\/em&gt; gen. nov. sp. nov. A-C. GU\/RJ\/362, left dentary and holotype with i3 erupting, dp3, m1-2, trigonid part of m3 and alveoli of i1-2, c, p1-2, and p4 in occlusal (A), labial (B), lingual (C) views. D-F. GU\/RJ\/303, right dentary fragment with m1-2 in occlusal (D), labial (E), lingual (F) views. G-I. GU\/RJ\/144, left dentary fragment with p2-4 in occlusal (G), labial (H), lingual (I) views. Scale bar: 10 mm.\" width=\"656\" height=\"630\" \/><span class=\"su-custom-gallery-title\">Lower dentition of <em>Rajouria gunnelli<\/em> gen. nov. sp. nov. A-C. GU\/RJ\/362, left dentary and holotype with i3 erupting, dp3, m1-2, trigonid part of m3 and alveoli of i1-2, c, p1-2, and p4 in occlusal (A), labial (B), lingual (C) views. D-F. GU\/RJ\/303, right dentary fragment with m1-2 in occlusal (D), labial (E), lingual (F) views. G-I. GU\/RJ\/144, left dentary fragment with p2-4 in occlusal (G), labial (H), lingual (I) views. Scale bar: 10 mm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Presence of the large aquatic snake <em>Palaeophis africanus<\/em> in the middle Eocene marine margin of the Congo Basin, Cabinda, Angola<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Ten isolated snake vertebrae from Landana and Sassa-Zao, Cabinda Exclave, Angola, present a \u201cprimitive\u201d grade morphology with a weak lateral compression and do not belong to <em>Palaeophis<\/em> aff. <em>typhaeus<\/em> as originally referred to. They well belong to a single taxon and are here attributed to <em>Palaeophis africanus<\/em> for which the intracolumnar variation is described and illustrated. This species is Lutetian (middle Eocene) in age and originates from a marine coastal environment confirming again the aquatic capabilities of palaeophiid snakes. It represents the third largest species of <em>Palaeophis<\/em> with <em>P. colossaeus<\/em> and <em>P. maghrebianus<\/em> to which it is closely related in our tentative phylogenetic analysis, indicating that these three taxa could belong to an African clade. This study also contributes to the debate on the existence of primitive and advanced grades among palaeophiid snakes. <em>Palaeophis<\/em> presents laterally compressed anterior trunk vertebrae that could have been often erroneously considered as representing advanced grade species and potential parataxonomy.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (Folie et al., in press).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Palaeophis.jpg\" title=\"Comparison between the &lt;em&gt;Palaeophis africanus&lt;\/em&gt; vertebrae from Cabinda and Nigeria. A\u2013C. NHMUK PV R 4964, trunk vertebra, holotype, in anterior (A), lateral (B) and dorsal (C) views. D\u2013F. Drawings of NHMUK PV R 4964, trunk vertebra, holotype, in anterior (D), lateral (E) and dorsal (F) views. G\u2013I. RMCA-RGP 16031a, anterior trunk vertebra in anterior (G), (reversed) lateral (H) and dorsal (I) views. Scale bar: 1 cm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Palaeophis-656x788.jpg\" alt=\"Comparison between the &lt;em&gt;Palaeophis africanus&lt;\/em&gt; vertebrae from Cabinda and Nigeria. A\u2013C. NHMUK PV R 4964, trunk vertebra, holotype, in anterior (A), lateral (B) and dorsal (C) views. D\u2013F. Drawings of NHMUK PV R 4964, trunk vertebra, holotype, in anterior (D), lateral (E) and dorsal (F) views. G\u2013I. RMCA-RGP 16031a, anterior trunk vertebra in anterior (G), (reversed) lateral (H) and dorsal (I) views. Scale bar: 1 cm.\" width=\"656\" height=\"788\" \/><span class=\"su-custom-gallery-title\">Comparison between the <em>Palaeophis africanus<\/em> vertebrae from Cabinda and Nigeria. A\u2013C. NHMUK PV R 4964, trunk vertebra, holotype, in anterior (A), lateral (B) and dorsal (C) views. D\u2013F. Drawings of NHMUK PV R 4964, trunk vertebra, holotype, in anterior (D), lateral (E) and dorsal (F) views. G\u2013I. RMCA-RGP 16031a, anterior trunk vertebra in anterior (G), (reversed) lateral (H) and dorsal (I) views. Scale bar: 1 cm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Systematics and diversity of the giant soft-shelled turtles (Cryptodira, Trionychidae) from the earliest Eocene of Belgium<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">In 1909, the famous paleontologist Louis Dollo identified two putative new species of giant soft-shelled turtles from the lowest Eocene record of Belgium, \u2018<em>Trionyx erquelinnensis<\/em>\u2019 and \u2018<em>Trionyx levalensis<\/em>\u2019, from Erquelinnes and Leval, respectively. However, these proposals did not meet the requirements of The International Code of Zoological Nomenclature, so they were considered as nomina nuda. The information on these specimens or about any other specimen of this lineage of giant turtles from the Belgian record is currently extremely limited. Relatively scarce material from giant trionychids has been described for the lower Eocene record of other European regions. Considering the available information, all the European material has recently been recognized as belonging to the genus <em>Axestemys<\/em>, which has a North American origin, and possibly attributable to a single species, <em>Axestemys vittata<\/em>, which currently lacks a diagnosis. Numerous and well-preserved Belgian specimens are deposited in the Royal Belgian Institute of Natural Sciences. In addition to the cited individuals from Erquelinnes and Leval, additional specimens from both localities, as well as others from Orp-le-Grand, are part of this collection. These specimens, found between the decades of 1910 and 1930, have been recently restored, and their study is carried out here.<br \/>\nThe presence of <em>Axestemys vittata<\/em> in Belgium (in Leval and Orp-le-Grand) is confirmed Knowledge about this species is significantly improved, and a diagnosis is proposed.<br \/>\nHowever, the hypothesis proposed by Dollo is here confirmed, this species being not the only identified in the Belgian record. So, <em>Axestemys erquelinnensis<\/em> nov. sp. is defined based on the carapace from Erquelinnes known by Dollo, suggesting that the genus probably reached Europe during the Paleocene Eocene Thermal Maximum.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (P\u00e9rez-Garc\u00eda and Smith, in press).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Perez-Garcia-Smith-2021-Axestemys.jpg\" title=\"Shells of &lt;em&gt;Axestemys&lt;\/em&gt; (Cryptodira, Trionychidae), from the Tienen Formation (basal Ypresian, earliest Eocene) of several Belgian localities. A\u2013D. Shell of the specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt; IRSNB R423, from Leval (Hainaut). A, B: carapace, in dorsal (A) and ventral (B) views; C, D: partial plastron, in ventral (C) and dorsal (D) views. E\u2013I. Comparison of the length of the carapace of five Belgian specimens of &lt;em&gt;Axestemys&lt;\/em&gt;, using the profile of the individual of Erquelinnes IRSNB R86. E: IRSNB R423, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, from Leval; F: IRSNB R86, holotype of &lt;em&gt;Axestemys erquelinnensis&lt;\/em&gt; nov. sp., from Erquelinnes (Hainaut); G: IRSNB R421, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, from Leval; H: IRSNB R420, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, holotype of \u2018&lt;em&gt;Trionyx levalensis&lt;\/em&gt;\u2019, from Leval; I: IRSNB R428, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, from Orp-le-Grand (Walloon Brabant). Scale bar: 20 cm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Perez-Garcia-Smith-2021-Axestemys-656x794.jpg\" alt=\"Shells of &lt;em&gt;Axestemys&lt;\/em&gt; (Cryptodira, Trionychidae), from the Tienen Formation (basal Ypresian, earliest Eocene) of several Belgian localities. A\u2013D. Shell of the specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt; IRSNB R423, from Leval (Hainaut). A, B: carapace, in dorsal (A) and ventral (B) views; C, D: partial plastron, in ventral (C) and dorsal (D) views. E\u2013I. Comparison of the length of the carapace of five Belgian specimens of &lt;em&gt;Axestemys&lt;\/em&gt;, using the profile of the individual of Erquelinnes IRSNB R86. E: IRSNB R423, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, from Leval; F: IRSNB R86, holotype of &lt;em&gt;Axestemys erquelinnensis&lt;\/em&gt; nov. sp., from Erquelinnes (Hainaut); G: IRSNB R421, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, from Leval; H: IRSNB R420, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, holotype of \u2018&lt;em&gt;Trionyx levalensis&lt;\/em&gt;\u2019, from Leval; I: IRSNB R428, specimen of &lt;em&gt;Axestemys vittata&lt;\/em&gt;, from Orp-le-Grand (Walloon Brabant). Scale bar: 20 cm.\" width=\"656\" height=\"794\" \/><span class=\"su-custom-gallery-title\">Shells of <em>Axestemys<\/em> (Cryptodira, Trionychidae), from the Tienen Formation (basal Ypresian, earliest Eocene) of several Belgian localities. A\u2013D. Shell of the specimen of <em>Axestemys vittata<\/em> IRSNB R423, from Leval (Hainaut). A, B: carapace, in dorsal (A) and ventral (B) views; C, D: partial plastron, in ventral (C) and dorsal (D) views. E\u2013I. Comparison of the length of the carapace of five Belgian specimens of <em>Axestemys<\/em>, using the profile of the individual of Erquelinnes IRSNB R86. E: IRSNB R423, specimen of <em>Axestemys vittata<\/em>, from Leval; F: IRSNB R86, holotype of <em>Axestemys erquelinnensis<\/em> nov. sp., from Erquelinnes (Hainaut); G: IRSNB R421, specimen of <em>Axestemys vittata<\/em>, from Leval; H: IRSNB R420, specimen of <em>Axestemys vittata<\/em>, holotype of \u2018<em>Trionyx levalensis<\/em>\u2019, from Leval; I: IRSNB R428, specimen of <em>Axestemys vittata<\/em>, from Orp-le-Grand (Walloon Brabant). Scale bar: 20 cm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Additional vertebral material of <em>Thaumastophis<\/em> (Serpentes: Caenophidia) from the early Eocene of India provides new insights on the early diversification of colubroidean snakes<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Ypresian Cambay Shale Formation at Vastan, Mangrol, and Tadkeshwar lignite mines in Gujarat, western India, has yielded a rich vertebrate fauna including madtsoiid, palaeophiid, booid, and colubroidean-like snakes. The latter are particularly abundant, but their systematic affinities are difficult to resolve. Here we describe new specimens of the colubroidean-like snake <em>Thaumastophis missiaeni<\/em>, including anterior, middle, and posterior trunk vertebrae, as well as caudal vertebrae. The combination of primitive and derived caenophidian and colubroidean vertebral characters confirms <em>Thaumastophis<\/em> as the earliest known stem-colubriform snake while <em>Procerophis<\/em>, from the same beds, is more derived and considered to represent a crown-Colubriformes. Additionally, <em>Thaumastophis<\/em> shares with <em>Renenutet enmerwer<\/em> from the late Eocene of Egypt a unique combination of vertebral characters that suggests an exchange with North Africa was possible along the southern margin of the Neotethys. We erect the new family Thaumastophiidae for <em>Thaumastophis<\/em> and <em>Renenutet<\/em> on the basis of their shared derived vertebral morphology.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (Zaher et al., in press).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Zaher-et-al-2021-Thaumastophis.jpg\" title=\"Distribution maps of colubroidean records in the Eocene and Oligocene. Early Eocene: &lt;em&gt;Thaumastophis missiaeni&lt;\/em&gt; and &lt;em&gt;Procerophis sahnii&lt;\/em&gt; (Ypresian of India; Rage et al., 2008); Colubroidea indet. (Ypresian of India; Rage et al., 2003). Middle Eocene: Colubroidea incertae sedis (Lutetian of Namibia; Rage et al., 2013). Late Eocene: &lt;em&gt;Renenutet enmerwer&lt;\/em&gt; (Priabonian of Egypt; McCartney and Seiffert, 2015); Colubroidea indet. (Bartonian of Myanmar; Head et al., 2005); Colubroidea indet. (Priabonian of Thailand; Rage et al., 1992); Colubroidea indet. (Priabonian of U.S.A.; Smith, 2013); &lt;em&gt;Vectophis wardi&lt;\/em&gt; (Priabonian of England; Rage and Ford 1980); &lt;em&gt;Nebraskophis&lt;\/em&gt; sp. (Priabonian of U.S.A.; Parmley and Holman, 2003). Oligocene: Elapidae indet. (Chattian of Tanzania; McCartney et al., 2014); &lt;em&gt;Coluber cadurci&lt;\/em&gt; (Rupelian of France; Rage, 1974); &lt;em&gt;Texasophis galbreathi&lt;\/em&gt; (Rupelian of U.S.A.; Holman, 1984).\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Zaher-et-al-2021-Thaumastophis-656x498.jpg\" alt=\"Distribution maps of colubroidean records in the Eocene and Oligocene. Early Eocene: &lt;em&gt;Thaumastophis missiaeni&lt;\/em&gt; and &lt;em&gt;Procerophis sahnii&lt;\/em&gt; (Ypresian of India; Rage et al., 2008); Colubroidea indet. (Ypresian of India; Rage et al., 2003). Middle Eocene: Colubroidea incertae sedis (Lutetian of Namibia; Rage et al., 2013). Late Eocene: &lt;em&gt;Renenutet enmerwer&lt;\/em&gt; (Priabonian of Egypt; McCartney and Seiffert, 2015); Colubroidea indet. (Bartonian of Myanmar; Head et al., 2005); Colubroidea indet. (Priabonian of Thailand; Rage et al., 1992); Colubroidea indet. (Priabonian of U.S.A.; Smith, 2013); &lt;em&gt;Vectophis wardi&lt;\/em&gt; (Priabonian of England; Rage and Ford 1980); &lt;em&gt;Nebraskophis&lt;\/em&gt; sp. (Priabonian of U.S.A.; Parmley and Holman, 2003). Oligocene: Elapidae indet. (Chattian of Tanzania; McCartney et al., 2014); &lt;em&gt;Coluber cadurci&lt;\/em&gt; (Rupelian of France; Rage, 1974); &lt;em&gt;Texasophis galbreathi&lt;\/em&gt; (Rupelian of U.S.A.; Holman, 1984).\" width=\"656\" height=\"498\" \/><span class=\"su-custom-gallery-title\">Distribution maps of colubroidean records in the Eocene and Oligocene. Early Eocene: <em>Thaumastophis missiaeni<\/em> and <em>Procerophis sahnii<\/em> (Ypresian of India; Rage et al., 2008); Colubroidea indet. (Ypresian of India; Rage et al., 2003). Middle Eocene: Colubroidea incertae sedis (Lutetian of Namibia; Rage et al., 2013). Late Eocene: <em>Renenutet enmerwer<\/em> (Priabonian of Egypt; McCartney and Seiffert, 2015); Colubroidea indet. (Bartonian of Myanmar; Head et al., 2005); Colubroidea indet. (Priabonian of Thailand; Rage et al., 1992); Colubroidea indet. (Priabonian of U.S.A.; Smith, 2013); <em>Vectophis wardi<\/em> (Priabonian of England; Rage and Ford 1980); <em>Nebraskophis<\/em> sp. (Priabonian of U.S.A.; Parmley and Holman, 2003). Oligocene: Elapidae indet. (Chattian of Tanzania; McCartney et al., 2014); <em>Coluber cadurci<\/em> (Rupelian of France; Rage, 1974); <em>Texasophis galbreathi<\/em> (Rupelian of U.S.A.; Holman, 1984).<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">(U-Th)\/He Dating of Supergene Iron (Oxyhydr-)Oxides of the Nefza-Sejnane District (Tunisia): New Insights into Mineralization and Mammalian Biostratigraphy<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The mining district of Nefza-Sejnane (Tunisia) encloses numerous ores and raw material deposits, all formed in relation with successive Fe-rich fluids of meteoric and\/or hydrothermal origins. Here, for the first time in Tunisia, (U-Th)\/He ages were obtained on supergene goethite from various localities\/deposits of the district highlight direct dating of significant weathering episodes during late Tortonian and late Pleistocene. These weathering events are most likely associated with favorable conditions that combine (i) wet climate displaying sufficient meteoric water\/fluid; and (ii) regional exhumation, due to large-scale vertical lithospheric movements enhancing the percolation of fluids. Matched with previous works, these results refine the stratigraphic frame for the polymetallic mineralization and clay deposits in the district, confirming the influence of meteoric fluids circulation during the late Cenozoic.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Yans-et-al-2021-Minerals.jpg\" title=\"Stratigraphic frame of the Nefza-Sejnane district (Tunisia), including the new (U-Th)\/He data on Fe (oxyhydr-)oxides. In red: data on supergene goethite; in red purple: data on mixed hydrothermal-meteoric hematite-goethite. Olig. = Oligocene. Questions marks (?) refer to potential larger stratigraphic extension.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Yans-et-al-2021-Minerals-656x355.jpg\" alt=\"Stratigraphic frame of the Nefza-Sejnane district (Tunisia), including the new (U-Th)\/He data on Fe (oxyhydr-)oxides. In red: data on supergene goethite; in red purple: data on mixed hydrothermal-meteoric hematite-goethite. Olig. = Oligocene. Questions marks (?) refer to potential larger stratigraphic extension.\" width=\"656\" height=\"355\" \/><span class=\"su-custom-gallery-title\">Stratigraphic frame of the Nefza-Sejnane district (Tunisia), including the new (U-Th)\/He data on Fe (oxyhydr-)oxides. In red: data on supergene goethite; in red purple: data on mixed hydrothermal-meteoric hematite-goethite. Olig. = Oligocene. Questions marks (?) refer to potential larger stratigraphic extension.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">As a consequence of the new (U-Th)\/He data, we moreover propose a taxonomic and stratigraphic revision of the well-known mammalian fauna from the Fe-rich Douahria locality, suggesting an early Tortonian age for the fossils, i.e., prior to the first episode of meteoric event in the area.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Minerals<\/em> (Yans et al., in press).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New Specimens of <em>Frugivastodon<\/em> (Mammalia: Apatotheria) from the Early Eocene of India Confirm Its Apatemyid Status and Elucidate Dispersal of Apatemyidae<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We here describe 18 new specimens of the sole apatemyid mammal known outside North America and Europe: <em>Frugivastodon cristatus<\/em> from the early Eocene Cambay Shale Formation of Vastan Lignite Mine, Gujarat, India. This mammal was previously represented by a single isolated lower molar, which hindered the establishment of its relationships among Apatemyidae. The new fossils show that the Indian apatemyid is unique and represents a new morphotype among this family.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Apatemyidae-scaled.jpg\" title=\"Schematic map showing the hypothetical geographic dispersion of apatemyids. Apatemyidae dispersed between North America and Europe via the Greenland Bridge and Thulean route; they dispersed from Europe to India probably through the Turgai Strait and\/or along the Tethyan shore. Oldest apatemyids are recorded in the Paleocene of North America (Torrejonian) (Simpson 1940; McKenna 1963a; Szalay 1968; West 1973b). See text for explanations of the dispersal events. The exact timing of the dispersals of Apatemyidae in India is unknown but probably occurred in the Ypresian. Paleogeographic map adapted from Ron Blakey, Eocene (http:\/\/www2.nau.edu\/rcb7\/050Marect.jpg)\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Apatemyidae-scaled.jpg\" alt=\"Schematic map showing the hypothetical geographic dispersion of apatemyids. Apatemyidae dispersed between North America and Europe via the Greenland Bridge and Thulean route; they dispersed from Europe to India probably through the Turgai Strait and\/or along the Tethyan shore. Oldest apatemyids are recorded in the Paleocene of North America (Torrejonian) (Simpson 1940; McKenna 1963a; Szalay 1968; West 1973b). See text for explanations of the dispersal events. The exact timing of the dispersals of Apatemyidae in India is unknown but probably occurred in the Ypresian. Paleogeographic map adapted from Ron Blakey, Eocene (http:\/\/www2.nau.edu\/rcb7\/050Marect.jpg)\" width=\"656\" height=\"258\" \/><span class=\"su-custom-gallery-title\">Schematic map showing the hypothetical geographic dispersion of apatemyids. Apatemyidae dispersed between North America and Europe via the Greenland Bridge and Thulean route; they dispersed from Europe to India probably through the Turgai Strait and\/or along the Tethyan shore. Oldest apatemyids are recorded in the Paleocene of North America (Torrejonian) (Simpson 1940; McKenna 1963a; Szalay 1968; West 1973b). See text for explanations of the dispersal events. The exact timing of the dispersals of Apatemyidae in India is unknown but probably occurred in the Ypresian. Paleogeographic map adapted from Ron Blakey, Eocene (http:\/\/www2.nau.edu\/rcb7\/050Marect.jpg)<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">It is notably characterized by mesiodistally elongated lower molars with a reduced m3, a small hypocone on the upper molars, and a transversely wider M1 than in other apatemyids. The new data supports the inclusion of the enigmatic Uintan <em>Aethomylos<\/em> within Apatemyidae. The Indian <em>Frugivastodon<\/em> and the North American <em>Aethomylos<\/em> might represent a distinct clade of Apatemyidae that originated around the Paleocene-Eocene boundary. A paleobiogeographic analysis suggests that <em>Frugivastodon<\/em> dispersed from Europe into India during the early Ypresian. We also review the dispersal events that characterized the history of Apatemyidae.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Vertebrate Paleobiology and Paleoanthropology Series<\/em> (Sol\u00e9 et al., in press).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Anatomy, Relationships, and Paleobiology of <em>Cambaytherium<\/em> (Mammalia, Perissodactylamorpha, Anthracobunia) from the lower Eocene of western India<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The anatomy of <em>Cambaytherium<\/em>, a primitive, perissodactyl-like mammal from the lower Eocene Cambay Shale Formation of Gujarat, India, is described in detail on the basis of more than 350 specimens that represent almost the entire dentition and the skeleton. <em>Cambaytherium<\/em> combines plesiomorphic traits typical of archaic ungulates such as phenacodontids with derived traits characteristic of early perissodactyls. <em>Cambaytherium<\/em> was a subcursorial animal better adapted for running than phenacodontids but less specialized than early perissodactyls. The cheek teeth are bunodont with large upper molar conules, not lophodont as in early perissodactyls; like perissodactyls, however, the lower molars have twinned metaconids and m3 has an extended hypoconulid lobe.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Rose-et-al-2020-Cambaytherium.jpg\" title=\"Skeletal reconstruction of &lt;em&gt;Cambaytherium thewissi&lt;\/em&gt;, with preserved elements shown in grey. Although much of the skeleton is represented, proportions should be regarded as approximate because elements were found isolated and represent multiple individuals. Because phalanges cannot be assigned definitively to digit or limb, representative phalanges are shown only in one manus but likely represent both manus and pes.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Rose-et-al-2020-Cambaytherium-656x314.jpg\" alt=\"Skeletal reconstruction of &lt;em&gt;Cambaytherium thewissi&lt;\/em&gt;, with preserved elements shown in grey. Although much of the skeleton is represented, proportions should be regarded as approximate because elements were found isolated and represent multiple individuals. Because phalanges cannot be assigned definitively to digit or limb, representative phalanges are shown only in one manus but likely represent both manus and pes.\" width=\"656\" height=\"314\" \/><span class=\"su-custom-gallery-title\">Skeletal reconstruction of <em>Cambaytherium thewissi<\/em>, with preserved elements shown in grey. Although much of the skeleton is represented, proportions should be regarded as approximate because elements were found isolated and represent multiple individuals. Because phalanges cannot be assigned definitively to digit or limb, representative phalanges are shown only in one manus but likely represent both manus and pes.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">A steep wear gradient with heavy wear in the middle of the tooth row suggests an abrasive herbivorous diet. Three species of <em>Cambaytherium<\/em> are recognized: <em>C. thewissi<\/em> (\u223c23 kg), <em>C. gracilis<\/em> (\u223c10 kg), and <em>C. marinus<\/em> (\u223c99 kg). Body masses were estimated from tooth size and long bone dimensions. Biostratigraphic and isotopic evidence indicates an age of ca. 54.5 Ma for the Cambay Shale vertebrate fauna, the oldest Cenozoic continental vertebrate assemblage from India, near or prior to the initial collision with Asia. Cambaytheriidae (also including <em>Nakusia<\/em> and <em>Perissobune<\/em>) and Anthracobunidae are sister taxa, constituting the clade Anthracobunia, which is sister to Perissodactyla. We unite them in a new higher taxon, Perissodactylamorpha. The antiquity and occurrence of <em>Cambaytherium<\/em>\u2014the most primitive known perissodactylamorph\u2014in India near or before its collision with Asia suggest that Perissodactyla evolved during the Paleocene on the Indian Plate or in peripheral areas of southern or southwestern Asia.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Vertebrate Paleontology<\/em> (Rose et al., 2020).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">The upper Eocene-Oligocene carnivorous mammals from the Quercy Phosphorites (France) housed in Belgian collections<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Quercy Phosphorites Formation in France is world famous for its Eocene to Miocene faunas, especially those from the upper Eocene to lower Oligocene, the richest of all. The latter particularly helped to understand the \u2018Grande Coupure\u2019, a dramatic faunal turnover event that occurred in Europe during the Eocene-Oligocene transition. Fossils from the Quercy Phosphorites were excavated from the middle 19th century until the early 20th century in a series of sites and became subsequently dispersed over several research institutions, while often losing the temporal and geographical information in the process. In this contribution, we provide an overview and reassess the taxonomy of these barely known collections housed in three Belgian institutions: the Universit\u00e9 de Li\u00e8ge, KU Leuven, and the Royal Belgian Institute of Natural Sciences. We focus our efforts on the carnivorous mammals (Hyaenodonta and Carnivoramorpha) and assess the stratigraphic intervals covered by each collection.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Sol\u00e9-et-al-2021-Quercy-collections.jpg\" title=\"Carnivorous mammals from Pech du Fraysse (MP28) housed at the RBINS. A, &lt;em&gt;Hyaenodon leptorhynchus&lt;\/em&gt;, RBINS M 2326 (in labial view); B, &lt;em&gt;Cyonarctos dessei&lt;\/em&gt;, RBINS M 2327 (in occlusal view); C, &lt;em&gt;Phoberogale minor&lt;\/em&gt;, RBINS M 2328 (in labial view).\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Sol\u00e9-et-al-2021-Quercy-collections-656x374.jpg\" alt=\"Carnivorous mammals from Pech du Fraysse (MP28) housed at the RBINS. A, &lt;em&gt;Hyaenodon leptorhynchus&lt;\/em&gt;, RBINS M 2326 (in labial view); B, &lt;em&gt;Cyonarctos dessei&lt;\/em&gt;, RBINS M 2327 (in occlusal view); C, &lt;em&gt;Phoberogale minor&lt;\/em&gt;, RBINS M 2328 (in labial view).\" width=\"656\" height=\"374\" \/><span class=\"su-custom-gallery-title\">Carnivorous mammals from Pech du Fraysse (MP28) housed at the RBINS. A, <em>Hyaenodon leptorhynchus<\/em>, RBINS M 2326 (in labial view); B, <em>Cyonarctos dessei<\/em>, RBINS M 2327 (in occlusal view); C, <em>Phoberogale minor<\/em>, RBINS M 2328 (in labial view).<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">These fossils are derived from upper Eocene (Priabonian), lower Oligocene (Rupelian), and upper Oligocene (Chattian) deposits in the Quercy area. The richness of the three collections (e.g., the presence of numerous postcranial elements in the Li\u00e8ge collection), the presence of types and figured specimens in the Leuven collection, and some identified localities in the RBINS collection make these collections of great interest for further studies on systematics and the evolution of mammals around the \u2018Grande Coupure\u2019.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geologica Belgica<\/em> (Sol\u00e9 et al., 2021).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2021<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Skeleton of a new owl from the early Eocene of North America (Aves, Strigiformes) with an accipitrid-like foot morphology<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We describe a partial skeleton of a large-sized owl from Wasatchian strata of the Willwood Formation (Wyoming, U.S.A.). The holotype of <em>Primoptynx poliotauros<\/em>, gen. et sp. nov., includes all major postcranial bones and is one of the most substantial Paleogene records of the Strigiformes. The fossil shows that owls exhibited a considerable morphological diversity in the early Eocene of North America and occupied disparate ecological niches. As in the protostrigid taxon Minerva from the late early to early middle Eocene of North America, but unlike in extant owls, the ungual phalanges of the hallux and the second toe of the new species are distinctly larger than those of the other toes. <em>Primoptynx poliotauros<\/em> gen. et sp. nov., however, does not exhibit the derived tibiotarsus morphology of the Protostrigidae. Even though the new species may well be a stem group representative of protostrigid owls, current data do not allow an unambiguous phylogenetic placement. Concerning the size of the ungual phalanges, the feet of <em>P. poliotauros<\/em> correspond to those of extant hawks and allies (Accipitridae). We therefore hypothesize that it used its feet to dispatch prey items in a hawk-like manner, whereas extant owls kill prey with their beak. <em>Primoptynx<\/em> and protostrigid owls were possibly specialized in foraging on prey items that required an accipitrid-like killing strategy, such as larger-sized or more defensive mammals. The extinction of these peculiar owls may have been related to the radiation of accipitrid diurnal birds of prey, which appear to have diversified in the late Eocene and early Oligocene.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Vertebrate Paleontology<\/em> (Mayr et al., 2020).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Mayr-et-al-2020-Primoptynx.jpg\" title=\"&lt;em&gt;Primoptynx poliotauros&lt;\/em&gt;, gen. et sp. nov., UMMP 96195, holotype, from the Willwood Formation of the northern Bighorn Basin, Wyoming, U.S.A., pedal phalanges in comparison with those of extant owls. Note the large ungual phalanges of the first and second toes of the fossil species. A, B, &lt;em&gt;P. poliotauros&lt;\/em&gt;, A, right and B, left feet. C, D, pedal phalanges of the right foot of C, &lt;em&gt;Tyto alba&lt;\/em&gt; (Tytonidae) and D, &lt;em&gt;Bubo scandiacus&lt;\/em&gt; (Strigidae); in C, the ungual phalanges bear the keratinous sheaths. The phalanges are numbered; the dotted lines indicate missing phalanges or parts thereof. All fossil bones were coated with ammonium chloride. Abbreviations: mtI, os metatarsale I; rdg, ridge on medial surface of ungual phalanx of third toe. Scale bars equal 5 mm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2021\/04\/Mayr-et-al-2020-Primoptynx-656x761.jpg\" alt=\"&lt;em&gt;Primoptynx poliotauros&lt;\/em&gt;, gen. et sp. nov., UMMP 96195, holotype, from the Willwood Formation of the northern Bighorn Basin, Wyoming, U.S.A., pedal phalanges in comparison with those of extant owls. Note the large ungual phalanges of the first and second toes of the fossil species. A, B, &lt;em&gt;P. poliotauros&lt;\/em&gt;, A, right and B, left feet. C, D, pedal phalanges of the right foot of C, &lt;em&gt;Tyto alba&lt;\/em&gt; (Tytonidae) and D, &lt;em&gt;Bubo scandiacus&lt;\/em&gt; (Strigidae); in C, the ungual phalanges bear the keratinous sheaths. The phalanges are numbered; the dotted lines indicate missing phalanges or parts thereof. All fossil bones were coated with ammonium chloride. Abbreviations: mtI, os metatarsale I; rdg, ridge on medial surface of ungual phalanx of third toe. Scale bars equal 5 mm.\" width=\"656\" height=\"761\" \/><span class=\"su-custom-gallery-title\"><em>Primoptynx poliotauros<\/em>, gen. et sp. nov., UMMP 96195, holotype, from the Willwood Formation of the northern Bighorn Basin, Wyoming, U.S.A., pedal phalanges in comparison with those of extant owls. Note the large ungual phalanges of the first and second toes of the fossil species. A, B, <em>P. poliotauros<\/em>, A, right and B, left feet. C, D, pedal phalanges of the right foot of C, <em>Tyto alba<\/em> (Tytonidae) and D, <em>Bubo scandiacus<\/em> (Strigidae); in C, the ungual phalanges bear the keratinous sheaths. The phalanges are numbered; the dotted lines indicate missing phalanges or parts thereof. All fossil bones were coated with ammonium chloride. Abbreviations: mtI, os metatarsale I; rdg, ridge on medial surface of ungual phalanx of third toe. Scale bars equal 5 mm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2020<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"> Supergene manganese ore records 75 Myr-long Campanian to Pleistocene geodynamic evolution and weathering history of the Central African Great Lakes Region \u2013 Tectonics drives, climate assists<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"> The southeastern part of the Democratic Republic of the Congo locally hosts Proterozoic manganese deposits. The deposits of Kisenge-Kamata are the most significant, but manganese ores are also known to occur at Kasekelesa (former Katanga Province) and Mwene-Ditu (former Kasai Province). For the present study, cryptomelane-rich samples from these two localities were dated, using the 40Ar\/39Ar step-heating method with a CO2 laser probe. The ages obtained are within a range of c. 77 Myr to c. 2 Myr. Cryptomelane formation took place at c. 76.4 Ma, c. 59.6 Ma, c. 45 Ma, c. 35 Ma, c. 23.8 Ma, c. 15.4 Ma, and c. 13.3 Ma at Kasekelesa, and it occurred at c. 35 Ma, c. 22.4 Ma, c. 15 Ma, c. 5.5\u20137.2 Ma, c. 3.6 Ma, and c. 2.1\u20132.3 Ma at Mwene-Ditu. The Campanian age (c. 76.4 Ma) recorded at Kasekelesa is the oldest 40Ar\/39Ar age that has up to now been recorded for Mn ores from Africa. It documents the formation of oxidized ore along a Campanian or older erosion surface, which could be part of the \u2018African Erosion Surface\u2019. The complete age record suggests that continent-wide tectonics accounts for most of the recognized supergene ore formation episodes, controlled by vertical lithospheric movements that are ultimately responsible for alternating stages of landscape stability and erosion. Tectonics is thus regarded as the first-order control for secondary ore formation in Central Africa, over the last 80 Myr. Climate is a second-order control, because sufficient water supply is needed for supergene enrichment, whereby climatic conditions are recognized to have been favourable during some relatively cold Late Mesozoic and Paleogene periods, as well as during some humid and warm Neogene stages.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Gondwana Research<\/em> (De Putter &amp; Ruffet, 2020).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2020\/03\/Fig13\u00e9cras\u00e9e3.jpg\" title=\"Validated ages and frequency diagrams of apparent ages (Kasekelesa (blue), Mwene-Ditu (green) and Kisenge (yellow)) vs. \u03b418O benthic.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2020\/03\/Fig13\u00e9cras\u00e9e3-656x944.jpg\" alt=\"Validated ages and frequency diagrams of apparent ages (Kasekelesa (blue), Mwene-Ditu (green) and Kisenge (yellow)) vs. \u03b418O benthic.\" width=\"656\" height=\"944\" \/><span class=\"su-custom-gallery-title\">Validated ages and frequency diagrams of apparent ages (Kasekelesa (blue), Mwene-Ditu (green) and Kisenge (yellow)) vs. \u03b418O benthic.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2020<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"> An enigmatic new ungulate-like mammal from the early Eocene of India<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"> We report a new genus and species of herbivorous mammal, <em>Pahelia mysteriosa<\/em>, from the early Eocene Cambay Shale Formation, Tadkeshwar Lignite Mine, Gujarat, India. The new taxon, approximately the size of a small phenacodontid (e.g. <em>Ectocion parvus<\/em>), is represented by three mandibular fragments, the most complete of which documents nearly the entire symphysis and mandibular body plus P3\u2013M3. <em>Pahelia<\/em> has incipiently selenolophodont molars with strong exodaenodonty, absent paraconids, weak but distinct entolophids, and prominent ectostylids. Molar size increases distally, but M3 does not develop a prominent third lobe. Premolars are simple, with prominent protoconids and short talonids but little development of other trigonid cusps. The mandibular symphysis is strongly fused, and there is an enlarged alveolus for an anterior tooth. The combination of features present in the new taxon does not closely match that of any known mammal, but there are some similarities to a diversity of ungulates from Africa, Asia, Europe and North America. Preserved morphology is insufficient to assess the affinities of the new taxon with confidence, but a link to Quettacyonidae, also endemic to the Indian subcontinent, is morphologically and biogeographically plausible. If this scenario is correct, it suggests that <em>P. mysteriosa<\/em> could be a part of the endemic mammalian fauna of India prior to its initial faunal contact with Asia.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Papers in Palaeontology<\/em> (Zack et al, 2019).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2020\/03\/Zack-et-al-2019-Pahelia.jpg\" title=\"GU\/RSR\/TAD 9201, mandible with left dentary and P3\u2013M3, holotype of &lt;em&gt;Pahelia mysteriosa&lt;\/em&gt; gen. et sp. nov. Scale bars represent 10 mm (A\u2013E); 5 mm (F\u2013H).\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2020\/03\/Zack-et-al-2019-Pahelia-656x621.jpg\" alt=\"GU\/RSR\/TAD 9201, mandible with left dentary and P3\u2013M3, holotype of &lt;em&gt;Pahelia mysteriosa&lt;\/em&gt; gen. et sp. nov. Scale bars represent 10 mm (A\u2013E); 5 mm (F\u2013H).\" width=\"656\" height=\"621\" \/><span class=\"su-custom-gallery-title\">GU\/RSR\/TAD 9201, mandible with left dentary and P3\u2013M3, holotype of <em>Pahelia mysteriosa<\/em> gen. et sp. nov. Scale bars represent 10 mm (A\u2013E); 5 mm (F\u2013H).<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2019<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"> Dinoflagellate cyst biostratigraphy and palaeoecology of the early Paleogene Landana reference section, Cabinda Province, Angola<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"> Forty-four rock samples from the Landana section, belonging to the historical Dartevelle collection of the Royal Museum for Central Africa (RMCA) at Tervuren, Belgium, were palynologically processed and analysed. Systematic analysis of the samples from the Landana sea cliff locality has revealed 90 dinoflagellate cyst taxa spanning an interval that ranges at least from the middle Paleocene to the late Eocene\/early Oligocene. This locality represents the first extensive sub-equatorial African Paleogene dinoflagellate cyst record. Dinoflagellate cyst occurrences were calibrated and evaluated against newly revised foraminiferal ranges. This novel dinoflagellate cyst biostratigraphic record was compared and correlated with contemporaneous records relatively close by in the Gulf of Guinea, as well as with records from more distant locations such as Antarctica, Australia and New Zealand.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/11\/Steeman-et-al-2019-Palyno-Landana.jpg\" title=\"Landana stratigraphy, selected important dinoflagellate cyst bioevents and overall dinoflagellate cyst assemblage shifts next to total organic carbon (TOC) and %TP value changes\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/11\/Steeman-et-al-2019-Palyno-Landana-656x516.jpg\" alt=\"Landana stratigraphy, selected important dinoflagellate cyst bioevents and overall dinoflagellate cyst assemblage shifts next to total organic carbon (TOC) and %TP value changes\" width=\"656\" height=\"516\" \/><span class=\"su-custom-gallery-title\">Landana stratigraphy, selected important dinoflagellate cyst bioevents and overall dinoflagellate cyst assemblage shifts next to total organic carbon (TOC) and %TP value changes<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">A preliminary dinoflagellate cyst zonation is here proposed comprising three zones and five unzoned yet otherwise distinct intervals. The lower part of the Landana section records a large portion of the early to middle\/late Selandian, which is made apparent by the presence of taxa such as Isabelidinium cingulatum, Isabelidinium? viborgense, and Spinidinium densispinatum. The Thanetian through Lutetian part of the section is more fragmentary and is devoid of any significant marker taxa normally typical for this time interval elsewhere. The upper part of the record is largely devoid of dinoflagellate cysts, with the few dinoflagellate cyst-bearing samples pointing to an Eocene to early Oligocene age. Dinoflagellate cyst assemblages are relatively variable and often largely dominated by a single particular taxon or complex. We record remarkably abundant peridinioid cysts signalling high palaeoproductivity for protracted periods of time, resulting from either heightened terrestrial influence or enhanced upwelling.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Palynology <\/em> (Steeman et al, 2019).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2019<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"> New Paleocene bird fossils from the North Sea Basin in Belgium and France<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"> We describe new avian remains from Paleocene localities of Belgium and France. Four bones from the early to middle Selandian of Maret (Belgium) are among the earliest Cenozoic avian remains known from Europe and include the oldest temporally well constrained European records of the Gastornithidae, as well as tentative records of the palaeognathous Lithornithidae and the Ralloidea. A more comprehensive fossil assemblage from the middle Thanetian of Templeuve (France) contains multiple bones of the Lithornithidae as well as a record of the Pelagornithidae. Specimens from the latest Thanetian of Rivecourt-Petit P\u00e2tis (France) are tentatively assigned to the Ralloidea and Leptosomiformes (cf. Plesiocathartes). Because of the fragmentary nature of the fossils, the taxonomic identity of a number of other specimens remains uncertain. We note, however, that Paleocene avifaunas of Europe and North America appear to have had different compositions and only a few taxa, such as the palaeognathous Lithornithidae, are known from both continents. This suggests that the very similar early Eocene avifaunas of Europe and North America are the result of early Cenozoic dispersal events.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geologica Belgica<\/em> (Mayr &amp; Smith, 2019).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/10\/Lithornithidae-Templeuve.jpg\" title=\"Palaeognathous lithornithid bird from the late Paleocene of Templeuve (France). A-B, coracoid. C-F, proximal and distal extremities of humerus from the same individual. G, radius lacking distal tip. H-I, carpometacarpus in two pieces. J-K, proximal end of carpometacarpus. L-M, distal portion of carpometacarpus. N-P, distal end of tibiotarsus. Scale bar = 5 mm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/10\/Lithornithidae-Templeuve-656x826.jpg\" alt=\"Palaeognathous lithornithid bird from the late Paleocene of Templeuve (France). A-B, coracoid. C-F, proximal and distal extremities of humerus from the same individual. G, radius lacking distal tip. H-I, carpometacarpus in two pieces. J-K, proximal end of carpometacarpus. L-M, distal portion of carpometacarpus. N-P, distal end of tibiotarsus. Scale bar = 5 mm.\" width=\"656\" height=\"826\" \/><span class=\"su-custom-gallery-title\">Palaeognathous lithornithid bird from the late Paleocene of Templeuve (France). A-B, coracoid. C-F, proximal and distal extremities of humerus from the same individual. G, radius lacking distal tip. H-I, carpometacarpus in two pieces. J-K, proximal end of carpometacarpus. L-M, distal portion of carpometacarpus. N-P, distal end of tibiotarsus. Scale bar = 5 mm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2019<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A diverse bird assemblage from the Ypresian of Belgium furthers knowledge of early Eocene avifaunas of the North Sea Basin<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We describe an assemblage of 54 avian bones from early Eocene marine sediments of the Ampe quarry near Egem in Belgium. The fossils belong to at least 20 species in more than 11 higher-level taxa. Well-identifiable specimens are assigned to the Odontopterygiformes, Galliformes, Messelornithidae, Apodiformes, Halcyornithidae, Leptosomiformes (cf. Plesiocathartes), and Coraciiformes (cf. Septencoracias). Further specimens are tentatively referred to the phaethontiform Prophaethontidae and to the Accipitridae, Masillaraptoridae, and Alcediniformes. The three-dimensionally preserved fossils from Egem provide new data on the osteology of taxa that are otherwise mainly known from compression fossils with crushed bones. The material also includes specimens that further knowledge of the composition of early Eocene avifaunas of the North Sea Basin. The comparatively well-represented small galliform species is clearly distinguished from the early Eocene Gallinuloididae and most closely resembles Argillipes aurorum, a largely ignored galliform species from the London Clay.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/10\/Messelornithidae-Egem.jpg\" title=\"Fossil bones of a leg (tarsometatarsus) and a wing (carpometacarpus) of a Messelornithidae from the early Eocene of Egem (Belgium) compared to those of &lt;em&gt;Messelornis cristata&lt;\/em&gt; from the middle Eocene of Messel, Germany. Scale bar = 5 mm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/10\/Messelornithidae-Egem-656x480.jpg\" alt=\"Fossil bones of a leg (tarsometatarsus) and a wing (carpometacarpus) of a Messelornithidae from the early Eocene of Egem (Belgium) compared to those of &lt;em&gt;Messelornis cristata&lt;\/em&gt; from the middle Eocene of Messel, Germany. Scale bar = 5 mm.\" width=\"656\" height=\"480\" \/><span class=\"su-custom-gallery-title\">Fossil bones of a leg (tarsometatarsus) and a wing (carpometacarpus) of a Messelornithidae from the early Eocene of Egem (Belgium) compared to those of <em>Messelornis cristata<\/em> from the middle Eocene of Messel, Germany. Scale bar = 5 mm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The tentatively identified fossils of Accipitridae and Alcediniformes would represent the earliest fossil records of these clades. The bird assemblage from Egem includes relatively few seabirds (Odontopterygiformes, cf. Prophaethontidae) and is dominated by remains of terrestrial species (Galliformes, Messelornithidae). Arboreal birds (Halcyornithidae, Leptosomiformes, cf. Alcediniformes, Coraciiformes) are less abundant and aerial insectivores (Apodiformes) very scarce, which either indicates a taphonomic bias in the composition of the avifauna or particular paleoenvironmental characteristics of the nearshore habitats in that area of the southern North Sea Basin.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Neues Jahrbuch f\u00fcr Geologie und Pal\u00e4ontologie, Abhandlungen<\/em> (Mayr &amp; Smith, 2019).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2019<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New paroxyclaenid mammals from the early Eocene of the Paris Basin (France) shed light on the origin and evolution of these endemic European cimolestans<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We describe four new species of an enigmatic family of mammals, which is endemic to Europe, the Paroxyclaenidae. The fossils described come from six localities of the Ypresian of the Paris Basin (France): Pourcy, Mutigny, Avenay, Cond\u00e9-en-Brie, Grauves and Pr\u00e9montr\u00e9. They allow the description of three new genera and four new species belonging to the subfamilies Merialinae and Paroxyclaeninae. Two of these new species represent the earliest occurrence of each subfamily. Fossils from Mutigny, Avenay and Cond\u00e9-en-Brie indicate that merialines were more abundant than paroxyclaenines during the Ypresian. Surprisingly, merialines disappeared from the fossil record at the end of the Ypresian \u2013 the youngest records are close to the Ypresian\/Lutetian boundary \u2013 while the paroxyclaenines were present in Europe until the end of the middle Eocene.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/03\/Sol\u00e9-et-al-2019-New-paroxyclaenids-Europe-Ypresian-3.jpg\" title=\"Temporal distribution and the evolution of body mass in paroxyclaenids. The four new paroxyclaenids described in the present paper are in bold.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/03\/Sol\u00e9-et-al-2019-New-paroxyclaenids-Europe-Ypresian-3-656x392.jpg\" alt=\"Temporal distribution and the evolution of body mass in paroxyclaenids. The four new paroxyclaenids described in the present paper are in bold.\" width=\"656\" height=\"392\" \/><span class=\"su-custom-gallery-title\">Temporal distribution and the evolution of body mass in paroxyclaenids. The four new paroxyclaenids described in the present paper are in bold.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Based on comparison with the data presently available for European mammals during the Ypresian, we suggest the existence of two periods of faunal turnover that must be more extensively studied in the future in order to be fully characterized: the \u2018Intra-Ypresian Mammal Turnover\u2019 and the \u2018Ypresian\u2013Lutetian Mammal Turnover\u2019. Finally, because the oldest paroxyclaenids appear morphologically closer to cimolestids such as Procerberus than to pantolestans, it is suggested that similarities between paroxyclaenids and pantolestans could be due to convergence.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Systematic Palaeontology<\/em> (Sol\u00e9 et al, 2019).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on February 2019<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"><em>Cabindachanos dartevellei<\/em> gen. and sp. nov., a new chanid fish (Ostariophysi, Gonorynchiformes) from the marine Paleocene of Cabinda (Central Africa)<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The osteology of <em>Cabindachanos dartevellei<\/em> gen. and sp. nov., a fossil fish from the marine Danian or early Selandian deposits of Landana (Cabinda Territory, Central Africa), is here studied in detail. This fish is known by only one partially preserved specimen that shows typical characters. The opercle is greatly hypertrophied. The preopercle has a very broad dorsal limb and a long narrower ventral limb. There is a wide plate\u2010like suprapreopercle. The lower jaw is deep, with a well\u2010marked coronoid process formed by the dentary. The articulation between the quadrate and the<br \/>\nmandible is located before the orbit. The first supraneurals are enlarged. These characters indicate that <em>C. dartevellei<\/em> belongs to the family Chanidae (Teleostei, Gonorynchiformes). <em>Cabindachanos dartevellei<\/em> differs from all the other known fossil or recent chanid fishes by the gigantic development of its opercle and by the loss of the subopercle. <\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/02\/Cabindachanos.jpg\" title=\"&lt;em&gt;Cabindachanos dartevellei&lt;\/em&gt; gen. and sp. nov. Holotype MRAC RG 4629; head, pectoral fin and beginning of the body (right side)\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2019\/02\/Cabindachanos-656x400.jpg\" alt=\"&lt;em&gt;Cabindachanos dartevellei&lt;\/em&gt; gen. and sp. nov. Holotype MRAC RG 4629; head, pectoral fin and beginning of the body (right side)\" width=\"656\" height=\"400\" \/><span class=\"su-custom-gallery-title\"><em>Cabindachanos dartevellei<\/em> gen. and sp. nov. Holotype MRAC RG 4629; head, pectoral fin and beginning of the body (right side)<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The straight angle formed by the two limbs of the preopercle and the well\u2010developed posterior median crest of the supraoccipital indicate that <em>C. dartevellei<\/em> belongs to the subfamily Chaninae and the tribe Chanini.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geologica Belgica<\/em> (Taverne et al, 2019).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on January 2019<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"><em>Calcardea junnei<\/em> Gingerich, 1987 from the late Paleocene of North America is not a heron, but resembles the early Eocene Indian taxon <em>Vastanavis<\/em> Mayr et al., 2007<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We revisit the holotype of <em>Calcardea junnei<\/em> Gingerich, 1987 from the latest Paleocene (Clarkforkian) of the Willwood Formation (Wyoming, USA). The species is based on a partial skeleton and was originally assigned to the Ardeidae (herons). As we show, this classification cannot be upheld and <em>Calcardea<\/em> Gingerich, 1987 more closely resembles the taxon <em>Vastanavis<\/em> Mayr et al., 2007 (Vastanavidae), a parrot-like bird from the early Eocene of India. Even though <em>C. junnei<\/em> is a large bird, its long wings and short tarsometatarsus argue against a predominantly terrestrial way of living, and the morphology of the tarsometatarsus and pedal phalanges instead suggest strong grasping feet. We conclude that an assignment of <em>Calcardea<\/em> to the landbird clade (Telluraves) is better supported than its classification into the waterbird clade (Aequornithes), which includes Ardeidae and other \u2018ciconiiform\u2019 and \u2018pelecaniform\u2019 taxa. <em>Calcardea junnei<\/em> is one of the oldest known representatives of Telluraves and its morphology shows plesiomorphic features, which contributed to its previous misidentification as a heron. <em>Calcardea<\/em> exhibits a distinctive osteology and affords a glimpse of a previously unknown late Paleocene avian morphotype.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Paleontology<\/em> (Mayr et al., 2018).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/12\/Mayr-et-al-Calcardea.jpg\" title=\"Coracoid (above) and tarsometatarsus (below) of &lt;em&gt;Calcardea&lt;\/em&gt; from the late Paleocene of Wyoming (USA) compared to those of &lt;em&gt;Vastanavis&lt;\/em&gt; from the early Eocene of Gujarat (India) and &lt;em&gt;Berruornis&lt;\/em&gt; from the late Paleocene of France. Scale bars = 10 mm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/12\/Mayr-et-al-Calcardea-656x708.jpg\" alt=\"Coracoid (above) and tarsometatarsus (below) of &lt;em&gt;Calcardea&lt;\/em&gt; from the late Paleocene of Wyoming (USA) compared to those of &lt;em&gt;Vastanavis&lt;\/em&gt; from the early Eocene of Gujarat (India) and &lt;em&gt;Berruornis&lt;\/em&gt; from the late Paleocene of France. Scale bars = 10 mm.\" width=\"656\" height=\"708\" \/><span class=\"su-custom-gallery-title\">Coracoid (above) and tarsometatarsus (below) of <em>Calcardea<\/em> from the late Paleocene of Wyoming (USA) compared to those of <em>Vastanavis<\/em> from the early Eocene of Gujarat (India) and <em>Berruornis<\/em> from the late Paleocene of France. Scale bars = 10 mm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on December 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New fossils, systematics, and biogeography of the oldest known crown primate <em>Teilhardina<\/em> from the earliest Eocene of Asia, Europe, and North America<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Omomyiform primates are among the most basal fossil haplorhines, with the oldest classified in the genus <em>Teilhardina<\/em> and known contemporaneously from Asia, Europe, and North America during the Paleocene Eocene Thermal Maximum (PETM) 56 million years ago. Characterization of morphology in this genus has been limited by small sample sizes and fragmentary fossils. A new dental sample (n = 163) of the North American species <em>Teilhardina brandti<\/em> from PETM strata of the Bighorn Basin, Wyoming, documents previously unknown morphology and variation, prompting the need for a systematic revision of the genus. The p4 of <em>T. brandti<\/em> expresses a range of variation that encompasses that of the recently named, slightly younger North American species \u2018<em>Teilhardina gingerichi<\/em>\u2019, which is here synonymized with <em>T. brandti<\/em>. A new partial dentary preserving the alveoli for p1-2 demonstrates that <em>T. brandti<\/em> variably expresses an unreduced, centrally-located p1, and in this regard is similar to that of <em>T. asiatica<\/em> from China.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/12\/Morse-et-al-2018-Teilhardina-spp.jpg\" title=\"Comparative size of the p1 alveolus in &lt;em&gt;Teilhardina&lt;\/em&gt; and &lt;em&gt;Bownomomys&lt;\/em&gt;. n = sample size of specimens. (Rev) indicates = specimens reversed. Scale bars = 1 mm\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/12\/Morse-et-al-2018-Teilhardina-spp-656x422.jpg\" alt=\"Comparative size of the p1 alveolus in &lt;em&gt;Teilhardina&lt;\/em&gt; and &lt;em&gt;Bownomomys&lt;\/em&gt;. n = sample size of specimens. (Rev) indicates = specimens reversed. Scale bars = 1 mm\" width=\"656\" height=\"422\" \/><span class=\"su-custom-gallery-title\">Comparative size of the p1 alveolus in <em>Teilhardina<\/em> and <em>Bownomomys<\/em>. n = sample size of specimens. (Rev) indicates = specimens reversed. Scale bars = 1 mm<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">This observation, coupled with further documentation of variability in p1 alveolar size, position, and presence in the European type species <em>T. belgica<\/em>, indicates that the original diagnosis of <em>T. asiatica<\/em> is insufficient at distinguishing this species from either <em>T. belgica<\/em> or <em>T. brandti<\/em>. Likewise, the basal omomyiform \u2018<em>Archicebus achilles<\/em>\u2019 requires revision to be distinguished from <em>Teilhardina<\/em>. Results from a phylogenetic analysis of 1890 characters scored for omomyiforms, adapiforms, and other euarchontan mammals produces a novel clade including <em>T. magnoliana<\/em>, <em>T. brandti<\/em>, <em>T. asiatica<\/em>, and <em>T. belgica<\/em> to the exclusion of two species previously referred to <em>Teilhardina<\/em>, which are here classified in a new genus (<em>Bownomomys americanus<\/em> and <em>Bownomomys crassidens<\/em>). While hypotheses of relationships and inferred biogeographic patterns among species of <em>Teilhardina<\/em> could change with the discovery of more complete fossils, the results of these analyses indicate a similar probability that the genus originated in either Asia or North America.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal Human Evolution<\/em> (Morse et al., 2018).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on November 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Reassessment of historical sections from the Paleogene marine margin of the Congo Basin reveals an almost complete absence of Danian deposits<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The early Paleogene is critical for understanding global biodiversity patterns in modern ecosystems. During this interval, Southern Hemisphere continents were largely characterized by isolation and faunal endemism following the breakup of Gondwana (Africa, Antarctica, India, Madagascar, South America, and Australia. Africa has been proposed as an important source area for the origin of several marine vertebrate groups but its Paleogene record is poorly sampled, especially from sub-Saharan Africa. To document the early Paleogene marine ecosystems of Central Africa, we revised the stratigraphic context of sedimentary deposits from three fossil-rich vertebrate localities: the Landana section in the Cabinda exclave (Angola), and the Manzadi and Bololo localities in western Democratic Republic of Congo. We provide more refined age constraints based on invertebrate and vertebrate faunas, foraminiferal and dinoflagellate cyst assemblages, and carbon isotope records. We find an almost complete absence of Danian-aged rocks in the Landana section, contrary to prevailing interpretations over the last half a century.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Refining the age of these Paleocene layers is indeed crucial for analyzing fish evolution in a global framework, with implications for the early appearance of Scombridae (tunas and mackerels) and Tetraodontiformes (puffer fishes). The combination of vertebrate fossil records from Manzadi and Landana sections suggests important environmental changes around the Cretaceous\/Paleogene transition characterized by an important modification of the ichthyofauna. A dramatic faunal shift is the decrease in overall richness that lasts from the Selandian (middle Paleocene) to the Ypresian (early Eocene). The Lutetian (middle Eocene) of West Central Africa is characterized by the first appearance of numerous cartilaginous and bony fishes. Our analysis of the ichthyofauna moreover indicates two periods of faunal exchanges: one during the Paleocene, where Central Africa appears to have been a source for the European marine fauna, and another during the Eocene when Europe was the source of the Central Africa fauna. These data indicate that Central Africa has had connections with the Tethyian realm.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geoscience Frontiers<\/em> (Sol\u00e9 et al., 2018).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Sol\u00e9-et-al.jpg\" title=\"Stratigraphic log of the Landana section with ages estimated based on the identified sub-tropical zones of planktonic foraminiferans\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Sol\u00e9-et-al-656x1121.jpg\" alt=\"Stratigraphic log of the Landana section with ages estimated based on the identified sub-tropical zones of planktonic foraminiferans\" width=\"656\" height=\"1121\" \/><span class=\"su-custom-gallery-title\">Stratigraphic log of the Landana section with ages estimated based on the identified sub-tropical zones of planktonic foraminiferans<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Shell anatomy of the African Paleocene bothremydid turtle <em>Taphrosphys congolensis<\/em> and systematic implications within Taphrosphyini<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The bothremydid pleurodiran turtle <em>Taphrosphys congolensis<\/em> is a member of Taphrosphyina from the Paleocene of the Cabinda Province (Congo Basin, Angola). Very few specimens corresponding to elements of its shell have been so far figured. Abundant unpublished remains are analyzed in this paper. As a consequence, several regions of the shell are figured and characterized here for the first time, and intraspecific variability is recognized for several characters. Previous authors proposed some putative differences between the shells of <em>Taphrosphys congolensis<\/em> and the North American Paleocene <em>Taphrosphys sulcatus<\/em>. The increase in the knowledge about the shell of this African form allows us to refute most of them, the shell of both forms being recognized as more similar than previously identified. Thus, the identification of the genus <em>Taphrosphys<\/em> as restricted to three forms (i.e. the skull taxon <em>Taphrosphys ippolitoi<\/em>, and the skull and shell forms <em>T. congolensis<\/em> and <em>T. sulcatus<\/em>) is supported, and the record unquestionably attributable to this genus is modified from the Upper Cretaceous\u2013Eocene lapse of time to the Paleocene exclusively.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Perez-Garcia-et-al.jpg\" title=\"&lt;em&gt;Taphrosphys congolensis&lt;\/em&gt;, from Landana (Cabinda Province, Angola). Anterior (A) and posterior (B) regions of the carapace, and partial plastron (C). Reconstruction of the carapace in dorsal view and plastron in ventral view\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Perez-Garcia-et-al-656x468.jpg\" alt=\"&lt;em&gt;Taphrosphys congolensis&lt;\/em&gt;, from Landana (Cabinda Province, Angola). Anterior (A) and posterior (B) regions of the carapace, and partial plastron (C). Reconstruction of the carapace in dorsal view and plastron in ventral view\" width=\"656\" height=\"468\" \/><span class=\"su-custom-gallery-title\"><em>Taphrosphys congolensis<\/em>, from Landana (Cabinda Province, Angola). Anterior (A) and posterior (B) regions of the carapace, and partial plastron (C). Reconstruction of the carapace in dorsal view and plastron in ventral view<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Historical Biology<\/em> (P\u00e9rez Garc\u00eda et al., 2018). <\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Mastication and enamel microstructure in <em>Cambaytherium<\/em>, a perissodactyl like ungulate from the early Eocene of India<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The dentition of <em>Cambaytherium<\/em> was investigated in terms of dental wear, tooth replacement and enamel microstructure. The postcanine tooth row shows a significant wear gradient, with flattened premolars and anterior molars at a time when the last molars are only little worn. This wear gradient, which is more intensive in <em>Cambaytherium thewissi<\/em> than in <em>Cambaytherium gracilis<\/em>, and the resulting flattened occlusal surfaces, may indicate a preference for a durophagous diet. The tooth replacement (known only in <em>C. thewissi<\/em>) shows an early eruption of the permanent premolars. They are in function before the third molars are fully erupted. During the dominant phase I of the chewing cycle the jaw movement is very steep, almost orthal, with a slight mesiolingual direction and changes into a horizontal movement during phase II. The enamel microstructure shows Hunter-Schreger-bands (HSB) in the inner zone of the enamel. In some teeth the transverse orientation of the HSB is modified into a zig-zag pattern, possibly an additional indicator of a durophagous diet.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Koenigswald-et-al.jpg\" title=\"Hunter-Schreger bands in the enamel of &lt;em&gt;Cambaytherium thewissi&lt;\/em&gt; shown by different techniques\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Koenigswald-et-al-656x450.jpg\" alt=\"Hunter-Schreger bands in the enamel of &lt;em&gt;Cambaytherium thewissi&lt;\/em&gt; shown by different techniques\" width=\"656\" height=\"450\" \/><span class=\"su-custom-gallery-title\">Hunter-Schreger bands in the enamel of <em>Cambaytherium thewissi<\/em> shown by different techniques<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Pal\u00e4ontologische Zeitschrift<\/em> (Koenigswald et al., 2018). <\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New fossils from Tadkeshwar Mine (Gujarat, India) increase primate diversity from the early Eocene Cambay Shale<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Several new fossil specimens from the Cambay Shale Formation at Tadkeshwar Lignite Mine in Gujarat document the presence of two previously unknown early Eocene primate species from India. A new species of <em>Asiadapis<\/em> is named based on a jaw fragment preserving premolars similar in morphology to those of <em>A. cambayensis<\/em> but substantially larger. Also described is an exceptionally preserved edentulous dentary (designated cf. <em>Asiadapis<\/em>, unnamed sp. nov.) that is slightly larger and much more robust than previously known Cambay Shale primates. Its anatomy most closely resembles that of Eocene adapoids, and the dental formula is the same as in <em>A. cambayensis<\/em>. A femur and calcaneus are tentatively allocated to the same taxon. Although the dentition is unknown, exquisite preservation of the dentary of cf. <em>Asiadapis<\/em> sp. nov. enables an assessment of masticatory musculature, function, and gape adaptations, as well as comparison with an equally well-preserved dentary of the asiadapid <em>Marcgodinotius indicus<\/em>, also from Tadkeshwar. The new <em>M. indicus<\/em> specimen shows significant gape adaptations but was probably capable of only weak bite force, whereas cf. <em>Asiadapis<\/em> sp. nov. probably used relatively smaller gapes but could generate relatively greater bite forces.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Human Evolution<\/em> (Rose et al., 2018).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Rose-et-al-primates.jpg\" title=\"Lateral (buccal) views of lower jaws of primates from Tadkeshwar Lignite Mine, India. A, &lt;em&gt;Asiadapis tapiensis&lt;\/em&gt; sp. nov. B, cf. &lt;em&gt;Asiadapis&lt;\/em&gt; sp. nov. C, &lt;em&gt;Marcgodinotius indicus&lt;\/em&gt;\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/11\/Rose-et-al-primates-656x820.jpg\" alt=\"Lateral (buccal) views of lower jaws of primates from Tadkeshwar Lignite Mine, India. A, &lt;em&gt;Asiadapis tapiensis&lt;\/em&gt; sp. nov. B, cf. &lt;em&gt;Asiadapis&lt;\/em&gt; sp. nov. C, &lt;em&gt;Marcgodinotius indicus&lt;\/em&gt;\" width=\"656\" height=\"820\" \/><span class=\"su-custom-gallery-title\">Lateral (buccal) views of lower jaws of primates from Tadkeshwar Lignite Mine, India. A, <em>Asiadapis tapiensis<\/em> sp. nov. B, cf. <em>Asiadapis<\/em> sp. nov. C, <em>Marcgodinotius indicus<\/em><\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on July 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Plesiadapid mammals from the latest Paleocene of France offer new insights on the evolution of Plesiadapis during the Paleocene-Eocene transition<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Plesiadapidae are among the most successful mammal families of the Paleocene, but in North America they disappear abruptly around the Paleocene-Eocene boundary. In contrast, in Europe, they survive a few million years into the Eocene, although only as the genus <em>Platychoerops<\/em>. The latest Paleocene deposits of Petit-Patis (Paris Basin, France) have produced three new plesiadapid species, one of each genus known in Europe: <em>Plesiadapis ploegi<\/em>, sp. nov., <em>Platychoerops boyeri<\/em>, sp. nov., and <em>Chiromyoides mauberti<\/em>, sp. nov. Each of these new species is represented by the very characteristic upper incisor, thus ascertaining their concomitant presence and in particular the spatial and temporal coexistence of <em>Plesiadapis<\/em> and <em>Platychoerops<\/em>. <em>Plesiadapis ploegi<\/em>, sp. nov., is morphologically intermediate between <em>Plesiadapis tricuspidens<\/em> and <em>Platychoerops russelli<\/em>, with a tricuspid I1 typical of <em>Plesiadapis<\/em> and a semimolariform p4 closer to <em>Platychoerops<\/em>. Its relatively high morphological variability is illustrated. <em>Platychoerops boyeri<\/em>, sp. nov., has the simple derived I1 of all <em>Platychoerops<\/em> and a p4 slightly more molariform than that of <em>Ples. ploegi<\/em>.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Plesiadapids.jpg\" title=\"Phylogeny of plesiadapids, including the three new species and their dentition. Skeleton of &lt;em&gt;Plesiadapis&lt;\/em&gt;\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Plesiadapids-656x500.jpg\" alt=\"Phylogeny of plesiadapids, including the three new species and their dentition. Skeleton of &lt;em&gt;Plesiadapis&lt;\/em&gt;\" width=\"656\" height=\"500\" \/><span class=\"su-custom-gallery-title\">Phylogeny of plesiadapids, including the three new species and their dentition. Skeleton of <em>Plesiadapis<\/em><\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\"><em>Chiromyoides mauberti<\/em>, sp. nov., is closest to <em>Chiromyoides campanicus<\/em>, but it is smaller and has a particular I1 with multiple posterocones. The systematic position of \u2018<em>Platychoerops<\/em>\u2019 <em>georgei<\/em> is discussed; this taxon is considered a chimera, and its type I1 belongs to either <em>Chiromyoides<\/em> or <em>Plesiadapis<\/em>. Cladistic analysis highlights the paraphyly or polyphyly of all genera of Plesiadapidae. Finally, there is some indication of morphological convergences between European and North American plesiadapids, which may be the result of similar environmental changes on both continents just before the Paleocene-Eocene boundary.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Vertebrate Paleontology<\/em> (De Bast et al., 2018).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on July 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A Fossil Gekkotan (Squamata) from the Late Oligocene Nsungwe Formation, Rukwa Rift Basin, Tanzania<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We describe the first record of a fossil gekkotan from the Late Oligocene Nsungwe Formation in the Rukwa Rift Basin, Tanzania. The specimen consists of an almost complete maxilla containing 23 tooth positions, with 10 teeth still in place. Typical gekkotan features include the tall facial process along with a posteriorly sloping angle, and the presence of unicuspid, pleurodont teeth with large resorption pits. Limited preservation does not allow for a more specific systematic assignment, which is why we refer the specimen to Gekkota incertae sedis. The material represents the second record of a Paleogene gekkotan from Africa and the first one from the central part of the continent.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Herpetology<\/em> (M\u00fcller et al., 2018).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Gekkota-incertae-sedis.jpg\" title=\"Specimen photograph and locality map. (A) RRBP 13002, gekkotan right maxilla in lateral view and (B) in medial view (scale bar = 1 mm); (C) map showing the Nsungwe Formation within the Rukwa Rift Basin (Tanzania) and the collection locality, including its relative position within Tanzania\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Gekkota-incertae-sedis-656x799.jpg\" alt=\"Specimen photograph and locality map. (A) RRBP 13002, gekkotan right maxilla in lateral view and (B) in medial view (scale bar = 1 mm); (C) map showing the Nsungwe Formation within the Rukwa Rift Basin (Tanzania) and the collection locality, including its relative position within Tanzania\" width=\"656\" height=\"799\" \/><span class=\"su-custom-gallery-title\">Specimen photograph and locality map. (A) RRBP 13002, gekkotan right maxilla in lateral view and (B) in medial view (scale bar = 1 mm); (C) map showing the Nsungwe Formation within the Rukwa Rift Basin (Tanzania) and the collection locality, including its relative position within Tanzania<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on June 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Morphological diversification of ampullariid gastropods (Nsungwe Formation, Late Oligocene, Rukwa Rift Basin, Tanzania) is coincident with onset of East African Rifting<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A new freshwater gastropod fauna is described from the late Oligocene Nsungwe Formation of the Rukwa Rift Basin, Tanzania. Six new species of ampullariids are established including five species of <em>Lanistes<\/em> (<em>L. microovum<\/em>, <em>L. nsungwensis<\/em>, <em>L. rukwaensis<\/em>, <em>L. songwellipticus<\/em> and <em>L. songweovum<\/em>) and one species of <em>Carnevalea<\/em> (<em>C. santiapillaii<\/em>). These taxa occupy a morphospace region comparable to nearly half of extant <em>Lanistes<\/em>, a common and widespread genus in Africa and Madagascar. Palaeoecological evidence indicates that Nsungwe ampullariids inhabited fluvial, pond and paludal environments. Among these species are the oldest high-spired and fluvially adapated <em>Lanistes<\/em> taxa. We suggest that Nsungwe <em>Lanistes<\/em> rapidly diversified in concert with habitat heterogeneity associated with the initiation of rifting along the western branch of the East African Rift System (EARS). Taxonomy, evolution and the biogeographical affinities of Nsungwe Formation freshwater gastropods contributes significantly to expanding the undersampled Palaeogene<br \/>\ninvertebrate fossil record of continental Africa.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Papers in Palaeontology<\/em> (Epa et al., 2018).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Lanistes-nsungwensis.jpg\" title=\"Depressed &lt;em&gt;Lanistes&lt;\/em&gt; morphotypes. A\u2013D, &lt;em&gt;L. nsungwensis&lt;\/em&gt; sp. nov.; E, &lt;em&gt;L. carinatus&lt;\/em&gt; (Olivier, 1804), ANSP 367298-11; F\u2013Q, &lt;em&gt;L. rukwaensis&lt;\/em&gt; sp. nov. Scale bars represent 10 mm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Lanistes-nsungwensis-656x842.jpg\" alt=\"Depressed &lt;em&gt;Lanistes&lt;\/em&gt; morphotypes. A\u2013D, &lt;em&gt;L. nsungwensis&lt;\/em&gt; sp. nov.; E, &lt;em&gt;L. carinatus&lt;\/em&gt; (Olivier, 1804), ANSP 367298-11; F\u2013Q, &lt;em&gt;L. rukwaensis&lt;\/em&gt; sp. nov. Scale bars represent 10 mm.\" width=\"656\" height=\"842\" \/><span class=\"su-custom-gallery-title\">Depressed <em>Lanistes<\/em> morphotypes. A\u2013D, <em>L. nsungwensis<\/em> sp. nov.; E, <em>L. carinatus<\/em> (Olivier, 1804), ANSP 367298-11; F\u2013Q, <em>L. rukwaensis<\/em> sp. nov. Scale bars represent 10 mm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on June 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Geology, biostratigraphy and carbon isotope chemostratigraphy of the Palaeogene fossil-bearing Dakhla sections, southwestern Moroccan Sahara<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">New Palaeogene vertebrate localities were recently reported in the southern Dakhla area (southwestern Morocco). The Eocene sediment strata crops out on cliffs along the Atlantic Ocean coast. Vertebrate remains come from five conglomeratic sandstone beds and are principally represented by isolated teeth belonging to micromammals, selachians and bony fishes, a proboscidean assigned to ?<em>Numidotherium<\/em> sp. and many remains of archaeocete whales (Basilosauridae). From fieldwork five lithostratigraphic sections were described, essentially based on the lithological characteristic of sediments.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Geology-Morocco.jpg\" title=\"Carbon isotope values (\u2030 VPDB) of the Porto Rico and El Argoub sections, compared to \u03b413C curves around the Eocene\u2013Oligocene transition at ODP Site 1218 (Erhardt, P\u00e4like &#038; Paytan, 2013) and reference \u03b413C composite curve (Cramer et al. 2009; modified by Vandenberghe, Hilgen &#038; Speijer, 2012). EOT \u2013 Eocene\u2013Oligocene Transition; U1\u2013U5 \u2013 lithological units defined in the text; B1, B2, C1, C2 \u2013 fossil-bearing levels\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Geology-Morocco-656x261.jpg\" alt=\"Carbon isotope values (\u2030 VPDB) of the Porto Rico and El Argoub sections, compared to \u03b413C curves around the Eocene\u2013Oligocene transition at ODP Site 1218 (Erhardt, P\u00e4like &#038; Paytan, 2013) and reference \u03b413C composite curve (Cramer et al. 2009; modified by Vandenberghe, Hilgen &#038; Speijer, 2012). EOT \u2013 Eocene\u2013Oligocene Transition; U1\u2013U5 \u2013 lithological units defined in the text; B1, B2, C1, C2 \u2013 fossil-bearing levels\" width=\"656\" height=\"261\" \/><span class=\"su-custom-gallery-title\">Carbon isotope values (\u2030 VPDB) of the Porto Rico and El Argoub sections, compared to \u03b413C curves around the Eocene\u2013Oligocene transition at ODP Site 1218 (Erhardt, P\u00e4like &#038; Paytan, 2013) and reference \u03b413C composite curve (Cramer et al. 2009; modified by Vandenberghe, Hilgen &#038; Speijer, 2012). EOT \u2013 Eocene\u2013Oligocene Transition; U1\u2013U5 \u2013 lithological units defined in the text; B1, B2, C1, C2 \u2013 fossil-bearing levels<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Despite the lateral variations of facies, correlations between these five sections were possible on the basis of fossil-bearing beds (A1, B1, B2, C1 and C2) and five lithological units were identified. The lower part of the section consists of rhythmically bedded, chert-rich marine siltstones and marls with thin black phosphorite with organic matter at the base. The overlying units include coarse-grained to microconglomeratic sandstones interbedded with silts, indicating deposition in a shallow-marine environment with fluvial influence. The natural remanence magnetization of a total of 50 samples was measured; the intensity of most of the samples is too weak however, before or after the first step of demagnetization. The palaeomagnetic data from the samples are very unstable, except for eight from three similar sandstone levels which show a normal polarity. Matched with biostratigraphic data on rodents, primates, the selachian, sirenian and cetacean faunas, the new carbon isotope chemostratigraphy on organics (1) refines the age of the uppermost C2 fossil-bearing bed to earliest Oligocene time and (2) confirms the Priabonian age of the B1 to C1 levels.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geological Magazine<\/em> (Benammi et al., 2017).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on June 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">The first hyaenodont from the late Oligocene Nsungwe Formation of Tanzania: Paleoecological insights into the Paleogene-Neogene carnivore transition<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Throughout the Paleogene, most terrestrial carnivore niches in Afro-Arabia were occupied by Hyaenodonta, an extinct lineage of placental mammals. By the end of the Miocene, terrestrial carnivore niches had shifted to members of Carnivora, a clade with Eurasian origins. The transition from a hyaenodont-carnivore fauna to a carnivoran-carnivore fauna coincides with other ecological changes in Afro-Arabia as tectonic conditions in the African Rift System altered climatic conditions and facilitated faunal exchange with Eurasia. Fossil bearing deposits in the Nsungwe Formation in southwestern Tanzania are precisely dated to ~25.2 Ma (late Oligocene), preserving a late Paleogene Afro-Arabian fauna on the brink of environmental transition, including the earliest fossil evidence of the split between Old World monkeys and apes. Here we describe a new hyaenodont from the Nsungwe Formation, <em>Pakakali rukwaensis<\/em> gen. et sp. nov., a bobcat-sized taxon known from a portion of the maxilla that preserves a deciduous third premolar and alveoli of dP4 and M1. The crown of dP3 bears an elongate parastyle and metastyle and a small, blade-like metacone. Based on alveolar morphology, the two more distal teeth successively increased in size and had relatively large protocones.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Pakali-rukwaensis-jpg.jpg\" title=\"Phylogeny and biogeography of Afro-Arabian Hyaenodonta with &lt;em&gt;Pakakali&lt;\/em&gt; is nested within Hyainailouroidea and Teratodontinae\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/06\/Pakali-rukwaensis-jpg-656x494.jpg\" alt=\"Phylogeny and biogeography of Afro-Arabian Hyaenodonta with &lt;em&gt;Pakakali&lt;\/em&gt; is nested within Hyainailouroidea and Teratodontinae\" width=\"656\" height=\"494\" \/><span class=\"su-custom-gallery-title\">Phylogeny and biogeography of Afro-Arabian Hyaenodonta with <em>Pakakali<\/em> is nested within Hyainailouroidea and Teratodontinae<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Using a hyaenodont character-taxon matrix that includes deciduous dental characters, Bayesian phylogenetic methods resolve <em>Pakakali<\/em> within the clade Hyainailouroidea. A Bayesian biogeographic analysis of phylogenetic results resolve the Pakakali clade as Afro-Arabian in origin, demonstrating that this small carnivorous mammal was part of an endemic Afro-Arabian lineage that persisted into the Miocene. Notably, <em>Pakakali<\/em> is in the size range of carnivoran forms that arrived and began to diversify in the region by the early Miocene. The description of <em>Pakakali<\/em> is important for exploring hyaenodont ontogeny and potential influences of Afro-Arabian tectonic events upon mammalian evolution, providing a deep time perspective on the stability of terrestrial carnivore niches through time.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>PLOS ONE<\/em> (Borths &amp; Stevens, 2017).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on May 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Incus facet morphology in carnivorous mammals from different ecosystems: Taxonomy vs. habitat<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study is prompted by the discovery of an incus of Hyaenodon, the first known auditory ossicle of this genus and thus of any hyaenodont mammal so far. The Hyaenodon incus is small, delicate and possesses an incudo-mallear facet of a general saddle-shape with two articulation facets, a large superior articulation area and a circular, inferior articulation area. Its general morphology and facet shape is most similar to the felid incus morphology. A large set of incus of recent Carnivora (felids, hyaenids, viverrids, herpestids, nandiniid and canids) of different ecosystems has been analysed. This study especially focuses on the incudo-mallear facet. The incudo-mallear facet is composed of: (1) three articular surfaces in felids, (2) a U-shaped surface in hyaenids and (3) four sur-faces in canids. Both taxonomy (on family level) and habitat (open, closed or mixed habitat preference) might have an impact on the morphology of the incus facets, the former having a major impact in our sample.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Geobios<\/em> (Bastl, Nagel &amp; Sol\u00e9, 2017)<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/05\/Bastl-et-al-2017.jpg\" title=\"Simplified phylogenetic tree illustrating the relationships between the carnivorous mammals studied, with indication of their morphological incus types.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/05\/Bastl-et-al-2017-656x487.jpg\" alt=\"Simplified phylogenetic tree illustrating the relationships between the carnivorous mammals studied, with indication of their morphological incus types.\" width=\"656\" height=\"487\" \/><span class=\"su-custom-gallery-title\">Simplified phylogenetic tree illustrating the relationships between the carnivorous mammals studied, with indication of their morphological incus types.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on May 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Evolution of the hypercarnivorous dentition in mammals (Metatheria, Eutheria) and its bearing on the development of tribosphenic molars<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">One major innovation of mammals is the tribosphenic molar, characterized by the evolution of the protocone and the talonid that occlude and provide shearing and crushing functions. This type of molar is an evolutionarily flexible structure that enabled mammals to achieve complex dental adaptations. Among carnivorous mammals, hypercarnivory is a common trend that evolved several times among therians (marsupials, placentals, and stem relatives). Hypercarnivory involves an important simplification of the carnassial molar pattern from the ancestral tribosphenic molar pattern, with the modification of the triangular tooth crown, and the loss of several cusps and cuspids typical of the tribosphenic molar. These losses confer to the molars of the hypercarnivorous mammals a plesiomorphic \/paedomorphic morphology that resembles more the earliest mammaliaforms than the earliest therians. Here, we demonstrate that the modification of the molar morphology is fully explained by a patterning cascade mode of cusp development. Contrary to what was previously proposed, our study concludes that the metaconid (mesiolingual cusp of lower molars, associated with a puncturing function) does not influence cusp development of the talonid (distal crushing heel of lower molars). Moreover, it provides a new example of how heterochronic changes were crucial to the evolution of mammal dentition.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Evolution &amp; Development<\/em> (Sol\u00e9 &amp; Ladev\u00e8ze, 2017)<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/05\/Sole-Ladeveze-2016.jpg\" title=\"Modes of tooth crown morphogenesis of lower and upper tribosphenic molars. (a) Illustration of the cascade development model proposed by Polly (1998) (left) and hypothesis of cascade development proposed. (b) Directions of propagation of the cusp development. In black: first cusps to develop. (c) Directions of propagation mapped on a diagrammatic drawing in occlusal view of lower and upper molars.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/05\/Sole-Ladeveze-2016-656x1047.jpg\" alt=\"Modes of tooth crown morphogenesis of lower and upper tribosphenic molars. (a) Illustration of the cascade development model proposed by Polly (1998) (left) and hypothesis of cascade development proposed. (b) Directions of propagation of the cusp development. In black: first cusps to develop. (c) Directions of propagation mapped on a diagrammatic drawing in occlusal view of lower and upper molars.\" width=\"656\" height=\"1047\" \/><span class=\"su-custom-gallery-title\">Modes of tooth crown morphogenesis of lower and upper tribosphenic molars. (a) Illustration of the cascade development model proposed by Polly (1998) (left) and hypothesis of cascade development proposed. (b) Directions of propagation of the cusp development. In black: first cusps to develop. (c) Directions of propagation mapped on a diagrammatic drawing in occlusal view of lower and upper molars.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A fossil heron from the early Oligocene of Belgium: the earliest temporally well-constrained record of the Ardeidae<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We describe the earliest temporally well-constrained fossil that can be assigned to the Ardeidae (herons), from the lowermost Oligocene (32.0\u201333.0 million years ago) of Belgium. The specimen, a partial tarsometatarsus, belongs to a small species and is described as <em>Proardea<\/em>? <em>deschutteri <\/em>n. sp. It exhibits the characteristic tarsometatarsus morphology found in extant heron species, but a confident assignment to one of the ardeid subclades is not possible and even the assignment of the new fossil species to the crown group (the clade including the extant species) cannot be established. The fossil indicates a divergence of herons from their sister taxon by at least the earliest Oligocene, and current paleontological data suggest that herons arrived in Europe shortly after a major faunal turnover at the Eocene\/Oligocene boundary. We consider that dispersal is the likely reason for the sudden appearance of herons in the earliest Oligocene of Europe but it is uncertain from where exactly this took place, with Asia and Africa being among the candidate areas. <\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in the journal <em>IBIS <\/em>(Mayr et al., 2018).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/04\/Proardea-deschutteri.jpg\" title=\"Distal end (plantar and distal view) of the tarsometatarsus of &lt;em&gt;Proardea&lt;\/em&gt;? &lt;em&gt;deschutteri&lt;\/em&gt; n. sp. from the earliest Oligocene of Belgium (IRSNB Av 129) in comparison with selected extant Ardeidae. Scale bars: 5 mm. Strict consensus tree of the analysis of the emended data matrices of Worthy et al. (2013) with &lt;em&gt;Proardea&lt;\/em&gt;? &lt;em&gt;deschutteri&lt;\/em&gt; n. sp. added.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/04\/Proardea-deschutteri-656x422.jpg\" alt=\"Distal end (plantar and distal view) of the tarsometatarsus of &lt;em&gt;Proardea&lt;\/em&gt;? &lt;em&gt;deschutteri&lt;\/em&gt; n. sp. from the earliest Oligocene of Belgium (IRSNB Av 129) in comparison with selected extant Ardeidae. Scale bars: 5 mm. Strict consensus tree of the analysis of the emended data matrices of Worthy et al. (2013) with &lt;em&gt;Proardea&lt;\/em&gt;? &lt;em&gt;deschutteri&lt;\/em&gt; n. sp. added.\" width=\"656\" height=\"422\" \/><span class=\"su-custom-gallery-title\">Distal end (plantar and distal view) of the tarsometatarsus of <em>Proardea<\/em>? <em>deschutteri<\/em> n. sp. from the earliest Oligocene of Belgium (IRSNB Av 129) in comparison with selected extant Ardeidae. Scale bars: 5 mm. Strict consensus tree of the analysis of the emended data matrices of Worthy et al. (2013) with <em>Proardea<\/em>? <em>deschutteri<\/em> n. sp. added.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">First Old World record of the poorly known, swan-sized anseriform bird <em>Paranyroca <\/em>from the late Oligocene\/early Miocene of France<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A tarsometatarsus of a large anseriform bird from the late Oligocene\/early Miocene of the Saint-G\u00e9rand-le-Puy area in France is assigned to the distinctive taxon <em>Paranyroca<\/em>, which was before only known from the early Miocene of North America. <em>Paranyroca<\/em> may be a stem group representative of Anatidae and its tarsometatarsus exhibits a peculiar character mosaic, with an Anhimidaelike hypotarsus and an Anatidae-like distal end. With regard to these features, the bone resembles the tarsometatarsus of another anseriform bird from Saint-G\u00e9rand-le-Puy, which was described as <em>Cygnopterus alphonsi<\/em> but has not yet been compared with <em>Paranyroca<\/em> in the original description. <em>C. alphonsi<\/em> was originally identified as a swan, but this classification has subsequently been contested and here it is proposed that the species is more closely related to <em>Paranyroca<\/em>. <\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Neues Jahrbuch f\u00fcr Geologie und Pal\u00e4ontologie<\/em> (Mayr &amp; Smith, 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/04\/Anseriform-Paranyroca.jpg\" title=\"Tarsometatarsus of &lt;em&gt;Paranyroca&lt;\/em&gt; sp. from Saint-G\u00e9rand-le-Puy (PLV 1988\/17-1, A-D, M-N) compared to &lt;em&gt;Paranyroca magna&lt;\/em&gt; from South Dakota, USA (E-F, O-P), &lt;em&gt;Cygnopterus alphonsi&lt;\/em&gt; (G-H, Q), &lt;em&gt;Chauna torquata&lt;\/em&gt; (Anhimidae, I, R), &lt;em&gt;Anseranas semipalmata&lt;\/em&gt; (Anseranatidae, J, S), &lt;em&gt;Cygnus olor&lt;\/em&gt; (Anatidae, K, T), &lt;em&gt;Dendrocygna viduata&lt;\/em&gt; (Anatidae, Dendrocygninae, L, U), and &lt;em&gt;Saintandrea chenoides&lt;\/em&gt; from the late Oligocene of France (V). Scale bars equal 10 mm.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/04\/Anseriform-Paranyroca-656x640.jpg\" alt=\"Tarsometatarsus of &lt;em&gt;Paranyroca&lt;\/em&gt; sp. from Saint-G\u00e9rand-le-Puy (PLV 1988\/17-1, A-D, M-N) compared to &lt;em&gt;Paranyroca magna&lt;\/em&gt; from South Dakota, USA (E-F, O-P), &lt;em&gt;Cygnopterus alphonsi&lt;\/em&gt; (G-H, Q), &lt;em&gt;Chauna torquata&lt;\/em&gt; (Anhimidae, I, R), &lt;em&gt;Anseranas semipalmata&lt;\/em&gt; (Anseranatidae, J, S), &lt;em&gt;Cygnus olor&lt;\/em&gt; (Anatidae, K, T), &lt;em&gt;Dendrocygna viduata&lt;\/em&gt; (Anatidae, Dendrocygninae, L, U), and &lt;em&gt;Saintandrea chenoides&lt;\/em&gt; from the late Oligocene of France (V). Scale bars equal 10 mm.\" width=\"656\" height=\"640\" \/><span class=\"su-custom-gallery-title\">Tarsometatarsus of <em>Paranyroca<\/em> sp. from Saint-G\u00e9rand-le-Puy (PLV 1988\/17-1, A-D, M-N) compared to <em>Paranyroca magna<\/em> from South Dakota, USA (E-F, O-P), <em>Cygnopterus alphonsi<\/em> (G-H, Q), <em>Chauna torquata<\/em> (Anhimidae, I, R), <em>Anseranas semipalmata<\/em> (Anseranatidae, J, S), <em>Cygnus olor<\/em> (Anatidae, K, T), <em>Dendrocygna viduata<\/em> (Anatidae, Dendrocygninae, L, U), and <em>Saintandrea chenoides<\/em> from the late Oligocene of France (V). Scale bars equal 10 mm.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on February 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A gymnodont fish jaw with remarkable molariform teeth from the early Eocene of Gujarat, India (Teleostei, Tetraodontiformes)<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The lower jaw of a gymnodont fish collected from the lower Eocene Cambay Shale Formation in Gujarat Province, western India, has fused dentaries without a beak and a remarkable series of teeth that are unique among all known fossil and living Tetraodontiformes. The teeth are molariform, with raised spokes radiating inward from the emarginated peripheral edge of the crown. Tooth development is intraosseous, with new teeth developing in spongy bone before they erupt and attach to the dentary by pedicels. Although many of the 110 tooth loci in the fossil have lost their teeth, in life the teeth would have grown to fit tightly together to form a broad and continuous crushing surface. The estimated age of the Cambay Shale vertebrate fauna is ca. 54.5 Ma, making the jaw the second oldest confirmed gymnodont fossil. Preliminary comparisons with extant taxa of gymnodonts with fused dentaries (e.g., <em>Diodon<\/em>, <em>Chilomycterus<\/em>, and <em>Mola<\/em>) show detailed similarities in jaw structure, but further study of the dentition is needed to better understand the evolutionary position of the new fossil. We describe the new gymnodont as <em>Avitoplectus molaris<\/em>, gen. et sp. nov., in Avitoplectidae, fam. nov., and place the family as incertae sedis within Gymnodontes.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study is published in <em>Journal of Vertebrate Paleontology<\/em> (Bemis et al., 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/04\/Avitoplectus.jpg\" title=\"Left: the jaw of &lt;em&gt;Avitoplectus molaris&lt;\/em&gt; (WIF\/A 2340) in anterior labial (A), ventral view (B), and dorsal views. Right: micro-CT reconstructions to show aspects of tooth replacement (A-B)\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/04\/Avitoplectus-656x516.jpg\" alt=\"Left: the jaw of &lt;em&gt;Avitoplectus molaris&lt;\/em&gt; (WIF\/A 2340) in anterior labial (A), ventral view (B), and dorsal views. Right: micro-CT reconstructions to show aspects of tooth replacement (A-B)\" width=\"656\" height=\"516\" \/><span class=\"su-custom-gallery-title\">Left: the jaw of <em>Avitoplectus molaris<\/em> (WIF\/A 2340) in anterior labial (A), ventral view (B), and dorsal views. Right: micro-CT reconstructions to show aspects of tooth replacement (A-B)<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on January 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Dispersal of the earliest European crocodyloids before the Paleocene-Eocene Thermal Maximum<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Crocodyloid remains from the late Paleocene of Mont de Berru (France) hosted in the collections of the Mus\u00e9um National d\u2019Histoire Naturelle (Paris, France) and in the Institut royal des Sciences naturelles de Belgique (Brussels, Belgium) are described for the first time. This material, although fragmentary, can be clearly referred on a morphological basis to <em>Asiatosuchus depressifrons<\/em> (Blainville, 1855), a species previously reported from several Eocene Belgian localities thanks to abundant material including a nearly complete skeleton. The Paleocene material shares with A. depressifrons the number of alveoli involved in the dentary symphysis, the exclusion of the splenials from the symphysis, and the presence of a distinct depression on the jugal. The fossil remains from Berru represent the oldest European crocodyloid. Along with the alligatoroid <em>Diplocynodon remensis<\/em> Martin, Smith, de Lapparent de Broin, Escuilli\u00e9 and Delfino, 2014, previously reported from the same locality, the crocodyloid <em>A. depressifrons<\/em> indicates that these genera reached Europe before the Paleocene-Eocene Thermal Maximum. Although more complete remains from outside Europe are needed to refine phylogenetic hypotheses, according to the currently established fossil record the forerunners of diplocynodontids likely dispersed from North America, whereas those related to <em>Asiatosuchus <\/em>likely dispersed from Asia.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Historical Biology<\/em> (Delfino et al., 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/02\/depressifrons-berru.jpg\" title=\"Right dentary of &lt;em&gt;Asiatosuchus depressifrons&lt;\/em&gt; (Blainville, 1855) from the late Paleocene of Berru (specimen IRSNB R358 in lateral view).\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/02\/depressifrons-berru-656x433.jpg\" alt=\"Right dentary of &lt;em&gt;Asiatosuchus depressifrons&lt;\/em&gt; (Blainville, 1855) from the late Paleocene of Berru (specimen IRSNB R358 in lateral view).\" width=\"656\" height=\"433\" \/><span class=\"su-custom-gallery-title\">Right dentary of <em>Asiatosuchus depressifrons<\/em> (Blainville, 1855) from the late Paleocene of Berru (specimen IRSNB R358 in lateral view).<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on January 2018<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A turtle of the African\u2013European Erymnochelys group (Pleurodira, Podocnemididae) in the Belgian fossil record<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">An almost complete plastron, as well as several peripherals and a costal plate of a turtle from the middle Eocene of Saint-Gilles (Brussels), is presented here. Although this turtle specimen was donated to the Institut royal des Sciences naturelles de Belgique (Brussels, Belgium) more than a century ago, it remained undescribed. Its study allows us to recognize the second pleurodiran in the Belgian fossil record, where, until now, the Eocene <em>Neochelys <\/em>was the only one known. The Belgian material of <em>Neochelys <\/em>is known in lower Eocene (early Ypresian) levels, but the new pleurodiran specimen comes from the middle Eocene (early Lutetian, NP14 biozone, 46 to 48 Ma). It is the first partial articulate shell of a pleurodiran turtle recognized in Belgium, and the only member of this clade recognized in this country at specific level. The new specimen is a representative of the so-called <em>Erymnochelys <\/em>group, this lineage being known in Africa from the Upper Cretaceous to the present but in Europe only during the Eocene. It represents the first specimen of <em>Eocenochelus eremberti<\/em> identified outside its type locality, the French region of Saint-Germain-en-Laye (Yvelines, \u00cele-de-France), where only one specimen was found. The plastron of the Belgian individual corresponds to the most complete for this species. Its analysis allows us not only to broaden the range of paleobiogeographical distribution of <em>Eocenochelus eremberti<\/em> but also to improve the knowledge about the anatomy and variability of this taxon.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Fossil Record<\/em> (Perez-Garcia &amp; Smith, 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/02\/Podocnemid-turtle-from-the-middle-Eocene-of-Brussels.jpg\" title=\"Location of Aqueduc Street in Saint-Gilles (Brussels municipality, Belgium) where the specimen IRSNB R356 of &lt;em&gt;Eocenochelus eremberti&lt;\/em&gt; was discovered (a plastron and articulated right bridge peripherals in dorsal view), in the lower Lutetian Brussels Sand Formation (middle Eocene).\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2018\/02\/Podocnemid-turtle-from-the-middle-Eocene-of-Brussels-656x745.jpg\" alt=\"Location of Aqueduc Street in Saint-Gilles (Brussels municipality, Belgium) where the specimen IRSNB R356 of &lt;em&gt;Eocenochelus eremberti&lt;\/em&gt; was discovered (a plastron and articulated right bridge peripherals in dorsal view), in the lower Lutetian Brussels Sand Formation (middle Eocene).\" width=\"656\" height=\"745\" \/><span class=\"su-custom-gallery-title\">Location of Aqueduc Street in Saint-Gilles (Brussels municipality, Belgium) where the specimen IRSNB R356 of <em>Eocenochelus eremberti<\/em> was discovered (a plastron and articulated right bridge peripherals in dorsal view), in the lower Lutetian Brussels Sand Formation (middle Eocene).<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on June 2017<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Estimating body size in early primates: The case of Archicebus and Teilhardina<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Obtaining accurate estimations of the body mass of fossil primates has always been a subject of interest in paleoanthropology because mass is an important determinant for so many other aspects of biology, ecology, and life history. This paper focuses on the issues involved in attempting to reconstruct the mass of two early Eocene haplorhine primates, <\/span><em><span style=\"color: #000000;\">Teilhardina<\/span><\/em><span style=\"color: #000000;\"> and <\/span><em><span style=\"color: #000000;\">Archicebus<\/span><\/em><span style=\"color: #000000;\">, which pose particular problems due to their small size and temporal and phylogenetic distance from extant primates. In addition to a ranking of variables from more to less useful, the effect of using models of varying taxonomic and size compositions is examined. Phylogenetic correction is also applied to the primate database. Our results indicate that the choice of variable is more critical than the choice of model. The more reliable variables are the mediolateral breadth across the femoral condyles and the area of the calcaneocuboid facet of the calcaneus.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">These variables suggest a body mass of 39 g (range 33-46 g) for <\/span><em><span style=\"color: #000000;\">Archicebus<\/span><\/em><span style=\"color: #000000;\"> and 48 g (range 44-56 g) for <\/span><em><span style=\"color: #000000;\">Teilhardina<\/span><\/em><span style=\"color: #000000;\">. The width of the distal femur is found to be the most consistent estimator across models of various composition and techniques. The effect of phylogenetic correction is small but the choice of branch length assumption affects point estimates for the fossils. The majority of variables and models predict the body mass of <\/span><em><span style=\"color: #000000;\">Archicebus<\/span><\/em><span style=\"color: #000000;\"> and <\/span><em><span style=\"color: #000000;\">Teilhardina<\/span><\/em><span style=\"color: #000000;\"> to be in the range of the smaller extant mouse lemurs, as expected.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This research was published in <em>Journal of Human Evolution<\/em> (Dagosto et al., 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/06\/Teilhardina-belgica.jpg\" title=\"Body mass (in natural log) of early Eocene Chinese Archicebus and Belgian Teilhardina from conventional ordinary least squares regression models. The drawing illustrates the reconstruction of Teilhardina from Dormaal, Belgium (done by Pascale Golinvaux, RBINS)\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/06\/Teilhardina-belgica-656x542.jpg\" alt=\"Body mass (in natural log) of early Eocene Chinese Archicebus and Belgian Teilhardina from conventional ordinary least squares regression models. The drawing illustrates the reconstruction of Teilhardina from Dormaal, Belgium (done by Pascale Golinvaux, RBINS)\" width=\"656\" height=\"542\" \/><span class=\"su-custom-gallery-title\">Body mass (in natural log) of early Eocene Chinese Archicebus and Belgian Teilhardina from conventional ordinary least squares regression models. The drawing illustrates the reconstruction of Teilhardina from Dormaal, Belgium (done by Pascale Golinvaux, RBINS)<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2017<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">33 million year old Myotis (Chiroptera, Vespertilionidae) and the rapid global radiation of modern bats <\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The bat genus Myotis is represented by 120+ living species and 40+ extinct species and is found on every continent except Antarctica. The time of divergence of Myotis has been contentious as has the time and place of origin of its encompassing group the Vespertilionidae, the most diverse (450+ species) and widely distributed extant bat family. Fossil Myotis species are common, especially in Europe, beginning in the Miocene but earlier records are poor. Recent study of new specimens from the Belgian early Oligocene locality of Boutersem reveals the presence of a relatively large vespertilionid. Morphological comparison and phylogenetic analysis confirms that the new, large form can be confidently assigned to the genus Myotis, making this record the earliest known for that taxon and extending the temporal range of this extant genus to over 33 million years. This suggests that previously published molecular divergence dates for crown myotines (Myotis) are too young by at least 7 million years.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Additionally, examination of first fossil appearance data of 1,011 extant placental mammal genera indicates that only 13 first occurred in the middle to late Paleogene (48 to 33 million years ago) and of these, six represent bats, including Myotis. Paleogene members of both major suborders of Chiroptera (<em>Yangochiroptera<\/em> and <em>Yinpterochiroptera<\/em>) include extant genera indicating early establishment of successful and long-term adaptive strategies as bats underwent an explosive radiation near the beginning of the Early Eocene Climatic Optimum in the Old World. A second bat adaptive radiation in the New World began coincident with the Mid-Miocene Climatic Optimum. <\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This research was published in <em>PLOS ONE<\/em> (Gunnell et al., 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/04\/Boutersem-bats.jpg\" title=\"Proposed trajectory of bat evolutionary history\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/04\/Boutersem-bats-656x596.jpg\" alt=\"Proposed trajectory of bat evolutionary history\" width=\"656\" height=\"596\" \/><span class=\"su-custom-gallery-title\">Proposed trajectory of bat evolutionary history<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2017<br \/>\n<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">The evolution of the European mesonychids (Mammal, Mesonychia), and their bearings on the European paleoecosystems and biostratigraphy <\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Mesonychids are an extinct group of primitive hoofed mammals, which possibly have had a scavenger-like diet similar to extant hyenas. Two years ago, the authors started a revision of the fossils of mesonychids that have been found in Europe in order to order their evolution on this landmass. The mesonychids are known from Thanetian and Ypresian localities (from MP6 to MP10 reference-levels). Only the genera <em>Dissacus<\/em> and <em>Pachyaena<\/em> were present in this continent. We can describe two new species, respectively from Palette (Ypresian, MP7) \u2013 <em>Dissacus rougierae<\/em> \u2013, and from La Borie and S\u00e9zanne-Broyes (Ypresian, MP8+9) \u2013 <em>Dissacus raslanloubatieri<\/em>. The evolution of the geographic distribution of the European mesonychids is characterized by three phases: (1) the mesonychid <em>Dissacus<\/em> appeared in Europe during the Thanetian (\u2248 57-58 Mya), probably due to dispersal from North America; <em>D. europaeus<\/em> survived the PETM event (\u2248 56 Mya) and possibly experienced a dwarfism; (2) the large mesonychid <em>Pachyaena<\/em> migrated into Europe shortly after the Paleocene-Eocene boundary (\u2248 55 Mya), but it was restricted to Northwestern Europe, while <em>Dissacus<\/em> is recorded at this time only in southwestern Europe (Palette); and (3) <em>Pachyaena<\/em> rapidly disappeared from European environments, while <em>Dissacus<\/em> subsequently dispersed into Northwestern Europe (\u2248 54-52 Myr ago). <em>Dissacus<\/em>, which has probably evolved endemically in Europe, reached very large size (close to 60-40 kg), especially in the Southern France and Northern Spain.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"> The long presence in Europe of the mesonychids is possibly due to the few competitors in the European ecosystems. Finally; It seems that the mesonychids went through two radiative events: the first during the Paleocene, the second mostly during the early Eocene. The first one corresponds to the diversification of <em>Dissacus<\/em>, while the latter resulted in the appearance of the most specialized mesonychids, such as <em>Pachyaena<\/em> and <em>Mesonyx<\/em>.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This research was published in <em>Journal of Mammalian Evolution<\/em> (Sol\u00e9 et al., 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/03\/Dissacus-raslanloubatieri-small.jpg\" title=\"Specimens referred to the new species Dissacus raslanloubatieri\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/03\/Dissacus-raslanloubatieri-small-656x826.jpg\" alt=\"Specimens referred to the new species Dissacus raslanloubatieri\" width=\"656\" height=\"826\" \/><span class=\"su-custom-gallery-title\">Specimens referred to the new species Dissacus raslanloubatieri<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2017<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"> New data on the osteoglossid fishes (Teleostei, Osteoglossiformes) from the marine Danian (Paleocene) of Landana (Cabinda Enclave, Angola) <\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A caudal skeleton of a fish from the layer 3 of the marine Danian of Landana (Cabinda Enclave, Angola, Central Africa) is studied in details. Its general characters and its autogenous hypurals show that it is a primitive member of the family Osteoglossidae. The shape and the size of its two ventral hypurals strongly differ from what is known in other Osteoglossidae and even in other Osteoglossomorpha. That justifies the attribution of a peculiar generic status for this fish. Some chronological, stratigraphical and faunal criterions lead to think that it must be reported to the species <em>Ridewoodichthys caheni<\/em> of which the type material comes from the layers 4 and 5. The caudal skeleton of osteoglossid pattern from the layer 10 of the Danian of Landana previously ranged in <em>R. caheni<\/em> belongs to a younger and more evolved osteoglossid fish that has not yet received a scientific name. <\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This research was published in <em>Geo-Eco-Trop<\/em> (Taverne, 2017).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/03\/Ridewoodichthys-caheni.jpg\" title=\"Ridewoodichthys caheni. Caudal skeleton of specimen MRAC RG 1275\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/03\/Ridewoodichthys-caheni-656x499.jpg\" alt=\"Ridewoodichthys caheni. Caudal skeleton of specimen MRAC RG 1275\" width=\"656\" height=\"499\" \/><span class=\"su-custom-gallery-title\">Ridewoodichthys caheni. Caudal skeleton of specimen MRAC RG 1275<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on February 2017<br \/>\n<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\"> Patterns of dental emergence in early anthropoid primates from the Fayum Depression, Egypt<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Fayum Depression of Egypt has produced a remarkable diversity of fossil anthropoids, and this, combined with advances in genetic analyses of living anthropoids, has led to establishment of a temporal and phylogenetic framework for anthropoids that is achieving some degree of consensus. Less well understood are the evolutionary mechanisms and selective factors behind the origin and early diversification of anthropoids. One area that has remained under explored is investigation into the life history patterns of early anthropoids, a major omission given that understanding patterns of growth and development is essential for interpreting the paleobiology of fossil species. Here we detail dental emergence sequences for five species in four families of early anthropoid primates from the Fayum, and use these data to test Schultz\u2019s Rule concerning the timing of emergence of molars versus premolars in mammals. Two important results are generated: (1) only the species <em>Aegyptopithecus zeuxis<\/em> had a dental eruption sequence identical to that observed among crown catarrhine primates; and (2) in all cases, the permanent canine was the last post-incisor dental element to fully erupt, a finding that may be significant for interpreting early anthropoid behavioral strategies. <\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This research was published in <em>Historical Biology<\/em> (Miller et al., 2017). <\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/02\/Aegyptopithecus-zeuxis.jpg\" title=\"Juvenile Aegyptopithecus zeuxis from Fayum Quarry I. DPC 9866, left dentary dp4-m1fully erupted, m2 in crypt near alveolar margin, in occlusal (A) and lateral cutaway (B) views, arrows in B indicate positions of permanent canine, p3-4, and m2 embedded in the mandible. DPC 13599, right dentary p4-m2, m3 in crypt near alveolar margin, in occlusal (C) and lateral cutaway (D) views, arrow in D indicates m3 enamel cap still entombed in mandible while p4 is fully erupted.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2017\/02\/Aegyptopithecus-zeuxis-656x1026.jpg\" alt=\"Juvenile Aegyptopithecus zeuxis from Fayum Quarry I. DPC 9866, left dentary dp4-m1fully erupted, m2 in crypt near alveolar margin, in occlusal (A) and lateral cutaway (B) views, arrows in B indicate positions of permanent canine, p3-4, and m2 embedded in the mandible. DPC 13599, right dentary p4-m2, m3 in crypt near alveolar margin, in occlusal (C) and lateral cutaway (D) views, arrow in D indicates m3 enamel cap still entombed in mandible while p4 is fully erupted.\" width=\"656\" height=\"1026\" \/><span class=\"su-custom-gallery-title\">Juvenile Aegyptopithecus zeuxis from Fayum Quarry I. DPC 9866, left dentary dp4-m1fully erupted, m2 in crypt near alveolar margin, in occlusal (A) and lateral cutaway (B) views, arrows in B indicate positions of permanent canine, p3-4, and m2 embedded in the mandible. DPC 13599, right dentary p4-m2, m3 in crypt near alveolar margin, in occlusal (C) and lateral cutaway (D) views, arrow in D indicates m3 enamel cap still entombed in mandible while p4 is fully erupted.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2016<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Deciduous dentition and dental eruption sequence of <em>Bothriogenys fraasi<\/em> (Anthracotheriidae, Artiodactyla) from the Fayum Depression, Egypt<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Paleogene anthracotheres are poorly documented from Afro-Arabian localities. This is due, in large part, to the fragmentary nature of the specimens that have been described. However, sediments in the Jebel Qatrani Formation, Fayum Depression, Egypt, preserve the richest anthracothere assemblage in all of Afro-Arabia. Unlike other samples, the Fayum collection includes many complete dentitions, skulls, and partial skeletons. Based on these extensive collections, this study provides the first description of the complete deciduous dentition and dental eruption sequence for the early Oligocene anthracothere <em>Bothriogenys fraasi<\/em>. A detailed discussion concerning the pattern and timing of dental growth in <em>B. fraasi<\/em> is provided, and the ontogenetic sequence documented for B. fraasi is compared with those available for suoids and hippos, the two extant groups currently considered as possible sister taxa to anthracotheres. Results show that anthracotheres and suoids share a more similar dental emergence pattern, and one that may be close to the primitive condition for artiodactyls, while hippos have a very different dental eruption sequence as a consequence of their highly divergent life history pattern. As a growing body of life history research indicates that taxa in close phylogenetic proximity may be expected to share features of their dental developmental pattern, this finding suggests a useful test of competing hypotheses of a relationship between Anthracotheriidae and either Hippopotamidae or Suiformes can potentially be developed based on eruption patterns. <\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"> This research was published in <em>Palaeontologia Electronica<\/em> (Sallam et al., 2016).<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/10\/Figure-3-july-23lowres-e1476537564719.jpg\" title=\"Bothriogenys fraasi : 1-4, right partial maxilla of DPC 5167 with dP2-M1, in (1) lateral, (2) medial, (3) anterior, and (4) occlusal views; 5, right partial maxilla of DPC 20439 (http:\/\/doi.org\/10.17602\/M2\/M12647) with dP3- dP4, in occlusal view; 6-8, right dP4 of DPC 3224 (http:\/\/doi.org\/10.17602\/M2\/M12690), in (6) occlusal, (7) lingual, (8) ventral views; 9, DPC 11416 (http:\/\/doi.org\/10.17602\/M2\/M12641) with dP1- dP4, in occlusal view.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/10\/Figure-3-july-23lowres-e1476537564719.jpg\" alt=\"Bothriogenys fraasi : 1-4, right partial maxilla of DPC 5167 with dP2-M1, in (1) lateral, (2) medial, (3) anterior, and (4) occlusal views; 5, right partial maxilla of DPC 20439 (http:\/\/doi.org\/10.17602\/M2\/M12647) with dP3- dP4, in occlusal view; 6-8, right dP4 of DPC 3224 (http:\/\/doi.org\/10.17602\/M2\/M12690), in (6) occlusal, (7) lingual, (8) ventral views; 9, DPC 11416 (http:\/\/doi.org\/10.17602\/M2\/M12641) with dP1- dP4, in occlusal view.\" width=\"656\" height=\"780\" \/><span class=\"su-custom-gallery-title\">Bothriogenys fraasi : 1-4, right partial maxilla of DPC 5167 with dP2-M1, in (1) lateral, (2) medial, (3) anterior, and (4) occlusal views; 5, right partial maxilla of DPC 20439 (http:\/\/doi.org\/10.17602\/M2\/M12647) with dP3- dP4, in occlusal view; 6-8, right dP4 of DPC 3224 (http:\/\/doi.org\/10.17602\/M2\/M12690), in (6) occlusal, (7) lingual, (8) ventral views; 9, DPC 11416 (http:\/\/doi.org\/10.17602\/M2\/M12641) with dP1- dP4, in occlusal view.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<p style=\"text-align: justify;\"><em><span style=\"color: #000000;\">Posted on September 2016<\/span><\/em><\/p>\n<p style=\"text-align: justify;\"><strong><span style=\"color: #000000;\">The oldest Cenozoic mammal fauna of Europe: implication of the Hainin reference fauna for mammalian evolution and dispersals during the Palaeocene<\/span><\/strong><\/p>\n<p style=\"text-align: justify;\"><span style=\"color: #000000;\">The mammal fauna of Hainin is particularly interesting in that it is the oldest of the Cenozoic of Europe. For this reason, it has been chosen as the earliest reference-level (MP1-5) of the mammalian biochronological scale for the European Palaeogene. <\/span><span style=\"color: #000000;\">This paper summarizes the mammal taxa discovered in the fauna, describes four new placental genera and species (<em>Belgoryctes thaleri, Eurolestes dupuisi, Quadratodon sigei, <\/em>and<em> Cingulodon magioncaldai<\/em>), and presents an analysis of the fauna as a whole (relative abundance and species richness). The assemblage is relatively small (about 400 dental specimens), characterized by a high diversity and abundance of small insectivorous species and very low abundance of \u2018plesiadapiforms\u2019 and \u2018condylarths\u2019. By comparison with younger European Palaeocene faunas, \u2018condylarths\u2019 and \u2018plesiadapiforms\u2019 get more and more abundant and diverse through the Palaeocene but collapse at the Palaeocene-Eocene Boundary. \u2018Proteutherians\u2019 decline steadily, while multituberculates remain diverse, although the early Palaeocene is populated mainly by <em>Kogaionidae<\/em> whereas the late Palaeocene is dominated by <em>Neoplagiaulacidae<\/em>. The palaeoecology of Hainin is deduced from the mammal assemblage: the local environment was likely a forested area. Stratigraphically, the Hainin deposits are most likely late Danian, and biochronologically its fauna represents a partial equivalent of the North American Torrejonian Land Mammal Age. Finally, when compared to younger Palaeocene faunas of Europe, the composition of the fauna of Hainin reveals that a relatively important intercontinental dispersal of mammals occurred around the Danian-Selandian boundary, roughly corresponding to the Torrejonian-Tiffanian boundary. This dispersal is marked by the arrival in Europe of typically North American taxa such as arctocyonids, plesiadapids and neoplagiaulacid multituberculates. Additional exchanges of lesser magnitude probably also occurred around the Selandian-Thanetian boundary (i.e. during the Tiffanian), although the evidence is less compelling and mainly concern the plesiadapids Chiromyoides and Plesiadapis, and possibly also the mesonychid <em>Dissacus<\/em>.<\/span><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-1-bis.jpg\" title=\"Hypothetical mammal dispersals involving Europe during the Palaeocene. The main dispersal episode likely happened at or around the Danian-Selandian boundary, more or less corresponding to the Torrejonian-Tiffanian boundary. Possible dispersals, involving mainly Plesiadapidae, could have occurred around the Selandian-Thanetian boundary.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-1-bis-1200x416.jpg\" alt=\"Hypothetical mammal dispersals involving Europe during the Palaeocene. The main dispersal episode likely happened at or around the Danian-Selandian boundary, more or less corresponding to the Torrejonian-Tiffanian boundary. Possible dispersals, involving mainly Plesiadapidae, could have occurred around the Selandian-Thanetian boundary.\" width=\"1200px\" height=\"416px\" \/><span class=\"su-custom-gallery-title\">Hypothetical mammal dispersals involving Europe during the Palaeocene. The main dispersal episode likely happened at or around the Danian-Selandian boundary, more or less corresponding to the Torrejonian-Tiffanian boundary. Possible dispersals, involving mainly Plesiadapidae, could have occurred around the Selandian-Thanetian boundary.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\"> This research was published in <em>Journal of Systematic Paleontology<\/em> (De Bast &amp; Smith, 2017).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on September 2016<br \/>\n<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New fossils of <em>Hyaenodonta<\/em> (Mammalia) from the Eocene localities of Chambi (Tunisia) and Bir el Ater (Algeria), and the evolution of the earliest African hyaenodonts<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study presents the description of new fossils from the Eocene North African localities of Chambi (Tunisia; late Ypresian or early Lutetian) and Bir el Ater (Algeria; latest Bartonian or earliest Priabonian). The specimens from Chambi allow recognizing two recently described hyainailourines: <em>Furodon crocheti <\/em>and<em> Parvavorodon gheerbranti<\/em>; these taxa were previously known from the Gour Lazib area (Algeria; late Ypresian or early Lutetian).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-3.jpg\" title=\"(1) Geographic distribution of the faunal assemblages. (2) Stratigraphic distribution of Tinerhodon and hyaenodont subfamilies in Africa during Paleocene and Eocene, and of the faunal assemblages regarding the main climatic events and mammal appearances.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-3-656x368.jpg\" alt=\"(1) Geographic distribution of the faunal assemblages. (2) Stratigraphic distribution of Tinerhodon and hyaenodont subfamilies in Africa during Paleocene and Eocene, and of the faunal assemblages regarding the main climatic events and mammal appearances.\" width=\"656\" height=\"368\" \/><span class=\"su-custom-gallery-title\">(1) Geographic distribution of the faunal assemblages. (2) Stratigraphic distribution of Tinerhodon and hyaenodont subfamilies in Africa during Paleocene and Eocene, and of the faunal assemblages regarding the main climatic events and mammal appearances.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The new material from Tunisia includes a fragmentary dentary of <em>Parvavorodon<\/em> that substantially supports the hyainailourine status of this genus and represents the oldest dentary fragment presently known for a juvenile of <em>Hyaenodonta<\/em> in Africa. The presence of <em>Furodon<\/em> and <em>Parvavorodon<\/em> in Chambi strengthens support for the hypothesis of contemporaneity of the Eocene Gour Lazib and Chambi mammal-bearing localities. In addition, the find of a typical teratodontine fourth premolar in Chambi testifies to the presence of a small representative of this group. The fossil record in Bir el Ater is scarcer than in Chambi. However, we recognize specimens attributable to a hyainailourine and a teratodontine. The latter is referred as Masrasector cf. ligabuei, and is the oldest record for this genus. Based on faunal assemblages, we tentatively identify a modification of the hyaenodont fauna in the Maghreb after the \u201cEarly Eocene Climatic Optimum\u201d (EECO). This faunal change might be related to the decrease of the global temperature after the EECO event. It appears contemporaneous of a drastic replacement in the composition of the mammal faunas in Africa. Finally, the end of the Eocene (Priabonian) shows an increase in the subfamilial richness amongst hyaenodonts.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Palaeontologia Electronica<\/em> (Sol\u00e9 et al., 2016).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on August 2016<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New euprimate postcrania from the early Eocene of Gujarat, India, and the strepsirrhine-haplorhine divergence<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The oldest primates of modern aspect (euprimates) appear abruptly on the Holarctic continents during a brief episode of global warming known as the Paleocene-Eocene Thermal Maximum, at the beginning of the Eocene (~56 Ma). When they first appear in the fossil record, they are already divided into two distinct clades, Adapoidea (basal members of Strepsirrhini, which includes extant lemurs, lorises, and bushbabies) and Omomyidae (basal Haplorhini, which comprises living tarsiers, monkeys, and apes). Both groups have recently been discovered in the early Eocene Cambay Shale Formation of Vastan lignite mine, Gujarat, India, where they are known mainly from teeth and jaws<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Here, we describe new, exquisitely preserved limb bones of these Indian primates that reveal more primitive postcranial characteristics than have been previously documented for either clade, and differences between them are so minor that in many cases we cannot be certain to which group they belong. Nevertheless, the small distinctions observed in some elements foreshadow postcranial traits that distinguish the groups by the middle Eocene, suggesting that the Vastan primates though slightly younger than the oldest known euprimates may represent the most primitive known remnants of the divergence between the two great primate clades.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-4.jpg\" title=\"Euprimate astragali from Vastan Mine and comparative specimens. Box contains astragali of Pondaungia sp., Adapis parisiensis, Notharctus sp., Eosimias sinensis, and Teilhardina belgica.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-4-656x458.jpg\" alt=\"Euprimate astragali from Vastan Mine and comparative specimens. Box contains astragali of Pondaungia sp., Adapis parisiensis, Notharctus sp., Eosimias sinensis, and Teilhardina belgica.\" width=\"656\" height=\"458\" \/><span class=\"su-custom-gallery-title\">Euprimate astragali from Vastan Mine and comparative specimens. Box contains astragali of Pondaungia sp., Adapis parisiensis, Notharctus sp., Eosimias sinensis, and Teilhardina belgica.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">A paper describing these exciting postcranial bones has been published in <em>Journal of Human Evolution<\/em> (Dunn et al., 2016).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on August 2016<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Anatomy and variability of <em>Cuvierichelys parisiensis<\/em>, a geoemydid turtle that crosses the Eocene-Oligocene boundary in Belgium<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Abundant material of turtles from the early Oligocene site of Boutersem-TGV (Boutersem, Belgium) is presented here. No information on the turtles found there was previously available. All the turtle specimens presented here are attributable to a single freshwater taxon that is identified as a member of Geoemydidae, Cuvierichelys. It is the first representative of the \u2018<em>Palaeochelys<\/em> s. l.\u2013<em>Mauremys<\/em>\u2019 group recognized in the Belgian Paleogene record. This material, which documents all the elements of both the carapace and the plastron of the taxon, cannot be attributed to the only species of the genus <em>Cuvierichelys<\/em> so far identified in the Oligocene, the Spanish form <em>Cuvierichelys iberica<\/em>. Rather, the taxon from Boutersem is recognized as <em>Cuvierichelys parisiensis<\/em>. Thus, both the paleobiogeographic and the biostratigraphic distributions of <em>Cuvierichelys parisiensis<\/em> are extended, its presence being confirmed for the first time outside the French Eocene record. The validity of some European forms is refuted, and several characters previously proposed as different between <em>Cuvierichelys iberica <\/em>and<em> Cuvierichelys parisiensis<\/em> are recognized as subjected to intraspecific variability.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em> Journal of Iberian Geology<\/em> (Perez-Garcia et al., 2016).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-6.jpg\" title=\"Specimens of Cuvierichelys parisiensis, from the early Oligocene of Boutersem (Belgium), corresponding to the carapace. Abbreviations for the plates (in bold): C, costal; N, neural. Abbreviations for the scutes (in normal font): Pl, pleural; V, vertebral. The solid lines represent the edges of the plates. The dashed lines indicate the broken margins. Those composed of a succession of points correspond to unsutured contacts. The scute margins are represented by thicker gray lines.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-6-656x592.jpg\" alt=\"Specimens of Cuvierichelys parisiensis, from the early Oligocene of Boutersem (Belgium), corresponding to the carapace. Abbreviations for the plates (in bold): C, costal; N, neural. Abbreviations for the scutes (in normal font): Pl, pleural; V, vertebral. The solid lines represent the edges of the plates. The dashed lines indicate the broken margins. Those composed of a succession of points correspond to unsutured contacts. The scute margins are represented by thicker gray lines.\" width=\"656\" height=\"592\" \/><span class=\"su-custom-gallery-title\">Specimens of Cuvierichelys parisiensis, from the early Oligocene of Boutersem (Belgium), corresponding to the carapace. Abbreviations for the plates (in bold): C, costal; N, neural. Abbreviations for the scutes (in normal font): Pl, pleural; V, vertebral. The solid lines represent the edges of the plates. The dashed lines indicate the broken margins. Those composed of a succession of points correspond to unsutured contacts. The scute margins are represented by thicker gray lines.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on July 2016<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New bio-chemostratigraphic dating of a unique early Eocene sequence from southern Europe results in precise mammalian biochronological tie-points<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">European early Eocene (Ypresian) mammalian biochronology, covering a timespan of about 8 myr, includes three distinct MP (Mammal Paleogene) reference levels MP7, MP8+9 and MP10. These are represented in the unique succession of the Minervois (Southern France) by the localities of Fournes (close to MP7), Sainte-Eulalie (close to MP8+9) and Azillanet (close to MP10). Considering homogenous terrestrial organic matter contribution as suggested by palynofacies and Rock-Eval pyrolysis, we here demonstrate that the organic carbon isotope curve of the predominantly continental Ypresian of the Minervois closely matches the marine standard carbonate carbon isotope curve.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-5.jpg\" title=\"Correlation of the organic carbon (\u03b413Corg) isotope curve of the Minervois  with the standard marine composite bulk carbonate (\u03b413Ccarb) isotope curve of the Ypresian and with the calcareous nannofossil and larger benthic foraminiferal zones. Black bone indicates mammalian localities; Nannofossils: biostratigraphic control (calcareous nannofossil dating); Pal. = Paleocene; p. = pars.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-5-656x334.jpg\" alt=\"Correlation of the organic carbon (\u03b413Corg) isotope curve of the Minervois  with the standard marine composite bulk carbonate (\u03b413Ccarb) isotope curve of the Ypresian and with the calcareous nannofossil and larger benthic foraminiferal zones. Black bone indicates mammalian localities; Nannofossils: biostratigraphic control (calcareous nannofossil dating); Pal. = Paleocene; p. = pars.\" width=\"656\" height=\"334\" \/><span class=\"su-custom-gallery-title\">Correlation of the organic carbon (\u03b413Corg) isotope curve of the Minervois  with the standard marine composite bulk carbonate (\u03b413Ccarb) isotope curve of the Ypresian and with the calcareous nannofossil and larger benthic foraminiferal zones. Black bone indicates mammalian localities; Nannofossils: biostratigraphic control (calcareous nannofossil dating); Pal. = Paleocene; p. = pars.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The here studied mammalian faunas and their supposed corresponding MP levels can thus be accurately dated and correlated on a global scale. The endemic Fournes mammal fauna, located just above the ETM 2, is assigned to mid-Biochron NP11 Calcareous Nannoplankton Zone. Accordingly, the Fournes mammal site is about 2.5 myr younger than the MP7 reference level of Dormaal (Belgium, latest Biochron NP9), about 1 myr younger than the MP7 mammalian locality of Le Clot in the Corbi\u00e8res (Southern France, late Biochron NP10 or early Biochron NP11) and very close to the Wasatchian Wa-5 mammalian biozone of Wyoming. A mid-Biochron NP12 age is inferred for the endemic Sainte-Eulalie fauna because of its position at the very top of (or just above) the isotopically negative \u201cETM3 interval\u201d, whereas the Azillanet fauna, recorded at the top of a \u03b4<sup>13<\/sup>C<sub>carb<\/sub><sub>org<\/sub>org positive trend above the \u201cETM3 interval\u201d, ranges from late Biochron NP12 to early Biochron NP13. Our results indicate that the shortterm hyperthermals ETM2 and ETM3 did not affect the endemic character of the mammalian faunas in Southern and Northern Europe during the MP7 to MP8+9 interval. The end of this mammalian endemism likely occurred during the early phases of the EECO (Early Eocene Climatic Optimum) in early late Biochron NP12.<br \/>\n<\/span><\/p>\n<p><span style=\"color: #000000;\">This analysis was published in <em>Newsletters on Stratigraphy<\/em> (Noiret et al., 2016).<br \/>\n<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on June 2016<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New early Eocene vertebrate assemblage from western India reveals a mixed fauna of European and Gondwana affinities <\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Ypresian Cambay Shale Formation at Vastan and Mangrol lignite mines in Gujarat, western India, has yielded a rich vertebrate fauna with numerous taxa of European affinities. Here we report a new, approximately contemporary vertebrate assemblage from two fossiliferous layers in the nearby mine of Tadkeshwar. These layers have yielded a similar mammal fauna (perissodactyl-like cambaytheriid <em>Cambaytherium thewissi<\/em>, the adapoid primates Marcgodinotius indicus, and the hyaenodontid <em>Indohyaenodon raoi<\/em>). The presence of these species in both Vastan and Tadkeshwar mines and at different levels suggests that the deposits between the two major lignite seams represent a single land mammal age. There is also a new, smaller species of <em>Cambaytherium<\/em>, and a new genus and species of esthonychid tillodont. This fauna also contains the first large early Eocene vertebrates from India, including an unidentified <em>Coryphodon<\/em>-like pantodont, a dyrosaurid crocodyliform and a new giant madtsoiid snake.<br \/>\nAmong the Tadkeshwar vertebrates several taxa are of Gondwana affinities, such as <em>Pelomedusoides<\/em> turtles, dyrosaurids, and large madtsoiids, attesting that the early Eocene was a crucial period in India during which Laurasian taxa of European affinities co-existed with taxa from Gondwana before the India-Asia collision. <\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-2.jpg\" title=\"Schematic paleogeographic map showing the hypothetical dispersal routes of vertebrates around 54 My ago. 1, Dispersal of taxa with European affinities between the Indian subcontinent and Europe across the Neotethys via the Kohistane-Ladakh island-arc system. 2A-B, Dispersal of taxa with Gondwanan affinities to the Indian subcontinent (2A) from Africa along the southern margins of the Neotethys or (2B) from Madagascar.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-2-656x528.jpg\" alt=\"Schematic paleogeographic map showing the hypothetical dispersal routes of vertebrates around 54 My ago. 1, Dispersal of taxa with European affinities between the Indian subcontinent and Europe across the Neotethys via the Kohistane-Ladakh island-arc system. 2A-B, Dispersal of taxa with Gondwanan affinities to the Indian subcontinent (2A) from Africa along the southern margins of the Neotethys or (2B) from Madagascar.\" width=\"656\" height=\"528\" \/><span class=\"su-custom-gallery-title\">Schematic paleogeographic map showing the hypothetical dispersal routes of vertebrates around 54 My ago. 1, Dispersal of taxa with European affinities between the Indian subcontinent and Europe across the Neotethys via the Kohistane-Ladakh island-arc system. 2A-B, Dispersal of taxa with Gondwanan affinities to the Indian subcontinent (2A) from Africa along the southern margins of the Neotethys or (2B) from Madagascar.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Our results suggest that terrestrial faunas could have dispersed to or from Europe during episodes of contact between the Indian subcontinent and different island blocks along the northern margin of the Neotethys, such as the Kohistane-Ladakh island-arc system. Gondwana taxa might represent remnants of ghost lineages shared with Madagascar, which reached the Indian subcontinent during the late Cretaceous; alternatively they might have come from North Africa and passed along the southern margin of the Neotethys to reach the Indian subcontinent.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This research was published in <em>Geoscience Frontiers<\/em> (Smith et al., 2016).<br \/>\n<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2016<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New carnivoraforms from the latest Paleocene of Europe and their bearing on the origin and radiation of Carnivoraformes (Carnivoramorpha, Mammalia)<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We recently reported the discovery of the earliest European carnivoraforms, based on two new taxa from the latest Paleocene of France and Romania. A new species of <em>Vassacyon<\/em>, <em>V. prieuri<\/em>, from the locality of Rivecourt (MP6b; Oise, France) is described based on a dentary fragment and isolated teeth. This species displays several primitive features compared with species of <em>Vassacyon<\/em> known from the early Eocene of North America and Europe. A second Paleocene carnivoraform, cf. <em>Gracilocyon<\/em> sp., is described based on fragmentary specimens from the locality of Jibou (MP6b; Transylvania, Romania). Carnivoraformes were previously unknown in Europe before the Eocene, and <em>Vassacyon prieuri <\/em>and cf.<em> Gracilocyon<\/em> sp. are their oldest records in Europe. These discoveries favor the hypothesis of a dispersal of these two genera from Europe to North America during the Paleocene-Eocene Thermal Maximum. <em>Vassacyon prieuri<\/em> and cf. <em>Gracilocyon<\/em> sp. strengthen support for the level MP6b and its correlation with the Clarkforkian. The geographic origin of the Carnivoraformes remains unknown. However, based on the observed biochronological and geographic distributions of the carnivoraforms, we infer a possible Asian origin for this group. In this scenario, <em>Gracilocyon<\/em> and <em>Vassacyon<\/em> dispersed to Europe during the Clarkforkian MP6b time, probably together with rodent taxa, whereas Uintacyon dispersed from Asia to North America shortly after rodents and tillodonts.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A paper describing the new specimens and presenting this paleogeographic scenario has been published in the worldwide distributed <em>Journal of Vertebrate Paleontology<\/em> (Sol\u00e9 et al., 2016).<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-7.jpg\" title=\"Phylogeny of the earliest carnivoraforms showing temporal distributions. Time ranges indicated by thicker lines. Unfilled lines indicate uncertainty as to occurrence. Plio. = Pliocene, P. = Pleistocene.\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2016\/09\/Figure-7-656x804.jpg\" alt=\"Phylogeny of the earliest carnivoraforms showing temporal distributions. Time ranges indicated by thicker lines. Unfilled lines indicate uncertainty as to occurrence. Plio. = Pliocene, P. = Pleistocene.\" width=\"656\" height=\"804\" \/><span class=\"su-custom-gallery-title\">Phylogeny of the earliest carnivoraforms showing temporal distributions. Time ranges indicated by thicker lines. Unfilled lines indicate uncertainty as to occurrence. Plio. = Pliocene, P. = Pleistocene.<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on December 2015<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">The age of supergene manganese deposits in Katanga and its implications for the Neogene evolution of the African Great Lakes Region<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Supergene manganese ores record weathering episodes affecting exposed paleosurfaces; hence, they help identifying and characterizing plateau areas, along the margins of major river basins. Supergene Mn ore deposits commonly contain K-rich Mn oxides with tunnel structure, such as cryptomelane, which are suitable for radiometric dating using the 39Ar\u201340Ar method. In Africa, Mn deposits have been dated by this method for localities in western and southern parts of the continent, whereas only some preliminary data are available for Central Africa. Extending these initial results, we obtained new 39Ar\u201340Ar ages for Mn oxide samples of the Kisenge deposit, in southwestern Katanga, Democratic Republic of the Congo.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-1.jpg\" title=\"Backscattered electron images and SEM-EDS maps for selected samples\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-1-656x342.jpg\" alt=\"Backscattered electron images and SEM-EDS maps for selected samples\" width=\"656\" height=\"342\" \/><span class=\"su-custom-gallery-title\">Backscattered electron images and SEM-EDS maps for selected samples<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The samples represent supergene Mn oxide deposits that formed at the expense of primary Paleoproterozoic rhodochrosite-dominated carbonate ores. Main phases of Mn oxide formation are dated at c. 10.5 Ma, 3.6 Myr and 2.6 Myr for a core that crosses a mineralized interval. The latter shows a decrease in age with increasing depth, recording downward penetration of a weathering front. Surface samples of the Kisenge deposits also record a \u2265c.19.2 Myr phase, as well as c. 15.7 Ma, 14.2 Myr and 13.6 Myr phases. The obtained ages correspond to distinct periods of paleosurface development and stability during the Mio-Pliocene in Katanga. Because Katanga is a key area bordered to the North by the Congo Basin and to the East by the East African Rift System, these ages also provide constraints for the geodynamic evolution of the entire region. For the Mio-Pliocene, the Kisenge deposits record ages that are not systematically found elsewhere in Africa, although the 10.5\u201311 Myr event corresponds to a roughly simultaneous event in the Kalahari Manganese Field, South Africa.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"><br \/>\nA paper describing these results has been published in <em>Ore Geology Reviews<\/em> (De Putter et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on October 2015<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New fossil of hyaenodonts from the Ypresian and Lutetian of France and the evolution of the Proviverrinae in Europe<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Proviverrinae are the most numerous and diversified carnivorous mammals from the Eocene of Europe. This hyaenodont subfamily, which is endemic to Europe, is recorded from the Ypresian of France to the Priabonian of Switzerland. The proviverrines from the Ypresian (MP7\u2013MP10) and Lutetian (MP11\u2013MP14) are represented mainly by species recorded in the northern and central parts of Europe (Paris Basin, Belgian Basin, Germany, Switzerland). In this article, we described fossils from southern France: Saint-Papoul (MP8+9; Aude) and Aigues-Vives 2 (?MP13; Aude). One dentary with secant molars from Saint-Papoul represents a new genus and species, <em>Preregidens langebadrae.<\/em><\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-5.jpg\" title=\"Phylogeny of the Proviverrinae calibrated with stratigraphy and with eustatic and climatic variations\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-5-656x365.jpg\" alt=\"Phylogeny of the Proviverrinae calibrated with stratigraphy and with eustatic and climatic variations\" width=\"656\" height=\"365\" \/><span class=\"su-custom-gallery-title\">Phylogeny of the Proviverrinae calibrated with stratigraphy and with eustatic and climatic variations<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">One of the three dentaries discovered in Aigues-Vives 2 belongs to the hypercarnivorous <em>Oxyaenoides schlosseri<\/em>, previously represented by only two isolated lower molars. This dentary appears to be the most derived of the proviverrines. The two other dentaries from Aigues-Vives 2 support the presence of <em>Eurotherium theriodis<\/em> and provide the first possible evidence of sexual dimorphism in a proviverrine species. A phylogenetic analysis of the proviverrines has been performed to resolve the phylogenetic position of the three taxa. This identifies a close relationship between the new genus (<em>Preregidens<\/em>) and <em>Oxyaenoides<\/em>. The new fossils allow the age of Saint-Papoul and Aigues-Vives 2 to be refined: the first locality is considered to be close in age to Avenay (Ypresian; France), while the second one seems to be close to Egerkingen \u03b3 (Lutetian; Switzerland), which is considered to be possibly close in age to the MP13 reference level. Finally, the presence of <em>O. schlosseri <\/em>and<em> E. theriodis<\/em> in the southern part of France supports the hypothesis that the mammals involved in the first intra-Eocene turnover migrated northwards.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Palaeontology<\/em> (Sol\u00e9 et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on September 2015<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">The oldest tapiroid from India and its implication for the paleobiogeographic origin of perissodactyls<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The presence of cambaytheres, the sister group of perissodactyls, in western India near or before the time of collision with Asia suggests that Perissodactyla may have originated on the Indian Plate during its final drift towards Asia. With this study, we reinforced this hypothesis by reporting two teeth of the first early Eocene tapiromorph Perissodactyla from the Cambay Shale Formation of Vastan Lignite Mine, which we allocate to a new genus and species, <em>Vastanolophus holbrooki<\/em>. The latter presents plesiomorphic characters typical of the paraphyletic \u201cIsectolophidae,\u201d such as small size and weak lophodonty. However, the weaker hypoconulid and low paralophid, higher cusps, lower cristid obliqua, and the lingual opening of the talonid are found in Helaletidae, the most primitive tapiroid family.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-7.jpg\" title=\"Schematic map showing the geographic dispersal of the early perissodactyls. 1: dispersal via the Bering land bridge; 2: dispersal via land connections across the Turgai Strait and\/or along the Tethysian shore; 3: dispersal via the Greenland land bridge\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-7-656x316.jpg\" alt=\"Schematic map showing the geographic dispersal of the early perissodactyls. 1: dispersal via the Bering land bridge; 2: dispersal via land connections across the Turgai Strait and\/or along the Tethysian shore; 3: dispersal via the Greenland land bridge\" width=\"656\" height=\"316\" \/><span class=\"su-custom-gallery-title\">Schematic map showing the geographic dispersal of the early perissodactyls. 1: dispersal via the Bering land bridge; 2: dispersal via land connections across the Turgai Strait and\/or along the Tethysian shore; 3: dispersal via the Greenland land bridge<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Consequently,<em> V. holbrooki<\/em> may be the oldest and the most primitive tapiroid, suggesting that at least tapiroid perissodactyls originated on India. Its discovery is moreover interesting for reconstructing the early history (i.e. dispersals) of the perissodactyls.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in the specialized journal <em>Palaeovertebrata<\/em> (Smith et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on September 2015<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">A new large hyainailourine from the Bartonian of Europe the evolution and ecology of massive hyaenodonts<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The hyainailourines are very large and hypercarnivorous hyaenodonts that originated in Africa. The appearance of this subfamily in Europe is poorly understood but is interesting because it traduces a profound modification of the European ecosystems. In this paper, we presented described a new large-sized species \u2013 <em>Kerberos langebadreae<\/em> \u2013 from the Bartonian locality of Montespieu (Tarn, France). The specimens consist of a skull, two hemimandibles and several hind limb elements (fibula, astragalus, calcaneum, metatarsals, and phalanges). Size estimates suggest <em>K. langebadreae<\/em> may have weighed up to 140 kg, revealing this species as the largest carnivorous mammal in Europe at that time. Moreover, the distinctive skull morphology of the new species reflects a powerful bite force; this hyaenodont was indeed possibly a scavenger. The postcranial elements, which are rarely associated with hyainailourine specimens, indicate an animal capable of a plantigrade stance and adapted for terrestrial locomotion. Based on the first phylogenetic analysis of hyainailourines, we demonstrated that <em>Hemipsalodon<\/em>, a North American taxon, is a hyainailourine and is closely related to European Paroxyaena.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">We reconstructed the biogeographic history of the Hyainailourinae: the first migration to Laurasia occurred during the Bartonian that likely included the ancestors of <em>Kerberos<\/em>, <em>Paroxyaena<\/em> and <em>Hemipsalodon<\/em>, which further dispersed into North America at this time. These migrants have no ecological equivalent in Europe and North America during these intervals and likely did not conflict with the endemic hyaenodonts.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-9.jpg\" title=\"Skull of Kerberos langebadreae gen. &#038; sp. nov. A, dorsal view; B, ventral view\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-9-656x543.jpg\" alt=\"Skull of Kerberos langebadreae gen. &#038; sp. nov. A, dorsal view; B, ventral view\" width=\"656\" height=\"543\" \/><span class=\"su-custom-gallery-title\">Skull of Kerberos langebadreae gen. &#038; sp. nov. A, dorsal view; B, ventral view<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The discovery of <em>K. langebadreae<\/em> shows that large body size appears early in the evolution of hyainailourine but the ancestors of these large hyaenodonts are still unknown in Africa, where this subfamily originated.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A long paper describing this impressive mammal was published in <em>PLOS ONE<\/em> (Sol\u00e9 et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on July 2015<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">First cranial and postcranial elements of <em>Indohyaenodon<\/em>, the oldest hyaenodont from India and their implications for ecology, phylogeny, and biogeography of hyaenodont mammals<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The reconstruction of the biogeographic history of the earliest hyaenodonts have been importantly affected by the discovery of fossils in the early Eocene of India. We recently reported new remains of the hyaenodont Indohyaenodon raoi from the Vastan Lignite Mine in Gujarat, western India, including the first known rostrum, upper dentition, and postcrania, substantially expanding our knowledge of the species and providing insights into its functional morphology and relationships. Craniodental morphology indeed suggests that <em>I. raoi<\/em> had a broad diet, including non-vertebrate material as well as flesh of a diversity of prey species. Postcranial morphology is broadly similar to that of other early hyaenodonts and suggests a scansorial locomotor repertoire.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-8.jpg\" title=\"Skull of Indohyaenodon raoi. Photographs (left) and interpretive drawings (right) of the partial skull with complete right P2\u2013M3, C and P1 alveoli, and left P1; dorsal view\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-8-656x355.jpg\" alt=\"Skull of Indohyaenodon raoi. Photographs (left) and interpretive drawings (right) of the partial skull with complete right P2\u2013M3, C and P1 alveoli, and left P1; dorsal view\" width=\"656\" height=\"355\" \/><span class=\"su-custom-gallery-title\">Skull of Indohyaenodon raoi. Photographs (left) and interpretive drawings (right) of the partial skull with complete right P2\u2013M3, C and P1 alveoli, and left P1; dorsal view<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Dental morphology indicates that<em> I. raoi<\/em> is closely related to other South Asian hyaenodonts. We also presented the most comprehensive phylogenetic analysis of Hyaenodonta to date, which corroborates this relationship but finds South Asian hyaenodonts to be the stem of a group that includes most African hyaenodonts. This and other higher-level relationships within Hyaenodonta are, however, weakly supported, and substantially different alternative hypotheses of relationships are not significantly less parsimonious, reflecting strong character conflict. Factors contributing to this conflict include the isolation of hyaenodont faunas on different continents during much of the Eocene, canalization and simplification of carnivorous dentitions, and a lack of non-dental material for critical hyaenodont groups. The new phylogeny is finally consistent with either an African or an Asian origin for the group.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Journal of Vertebrate Paleontology<\/em> (Rana et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2015<br \/>\n<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New dental elements of the oldest proviverrine mammal from the early Eocene of Southern France support possible African origin of the subfamily<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Paleocene-Eocene Thermal Maximum (PETM), c. 56 Myr ago, is correlated with the first occurrences of modern mammals in Europe (primates, artiodactyls, perissodactyls, carnivoraforms). The carnivorous hyaenodonts are also involved in this faunal event (usually termed Mammal Dispersal Event, MDE). In order to reconstruct the appearance of this group in Europe we studied specimens of hyaenodont mammals from two early Eocene localities of Southern France: Fournes (Minervois) and Fordones (Corbi\u00e8res). Some of these specimens were previously described as cf. <em>Hyracolestes<\/em> sp. (Cimolesta, Sarcodontidae), a taxon only known from Asia, but new arguments allow their referring to the small proviverrine hyaenodont <em>Parvagula palulae<\/em> which was previously only recorded in Palette (Provence).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-3.jpg\" title=\"Comparison of phylogenetic trees and of the three hypotheses of hyaenodont origin and dispersals with focus on the Sinopinae and Proviverrinae. A. African origin with subsequent dispersals of the Sinopinae and Proviverrinae into Europe, and of the Sinopinae from Europe to North America. B. Asian origin with subsequent dispersals of Sinopinae and Proviverrinae into Europe, and of Tinerhodon from Europe to Africa\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-3-656x366.jpg\" alt=\"Comparison of phylogenetic trees and of the three hypotheses of hyaenodont origin and dispersals with focus on the Sinopinae and Proviverrinae. A. African origin with subsequent dispersals of the Sinopinae and Proviverrinae into Europe, and of the Sinopinae from Europe to North America. B. Asian origin with subsequent dispersals of Sinopinae and Proviverrinae into Europe, and of Tinerhodon from Europe to Africa\" width=\"656\" height=\"366\" \/><span class=\"su-custom-gallery-title\">Comparison of phylogenetic trees and of the three hypotheses of hyaenodont origin and dispersals with focus on the Sinopinae and Proviverrinae. A. African origin with subsequent dispersals of the Sinopinae and Proviverrinae into Europe, and of the Sinopinae from Europe to North America. B. Asian origin with subsequent dispersals of Sinopinae and Proviverrinae into Europe, and of Tinerhodon from Europe to Africa<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">This new material shows that, by the beginning of the early Eocene, proviverrines already displayed their typical combination of dental features. The comparison between the earliest European proviverrines and sinopines (a mostly North American radiation) supports the divergence of the two subfamilies by this time \u2013 a separation that could have taken place in Europe. Moreover, the early proviverrines are morphologically similar to the African hyaenodont <em>Tinerhodon<\/em> (late Paleocene). Consequently, we hypothesized that the history of the European proviverrines is likely rooted in Africa.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A paper describing the new specimens and presenting these paleogeographic scenarios has been recently published in <em>Acta Palaeontologica Polonica<\/em> (Sol\u00e9 et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2015<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">The earliest record of the endemic African frog family <em>Ptychadenidae<\/em> from the Oligocene Nsungwe Formation of Tanzania<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Ranoidea is a cosmopolitan radiation of frogs comprising 19 families and more than 2400 extant species (nearly 40% of all anurans). Studies using time-calibrated molecular phylogenies suggest a Cretaceous origin for the Ranoidea, but the Mesozoic and early Cenozoic fossil record of this diverse clade remains poor. Although many fossils have been attributed to the Ranoidea, typically few diagnostic characteristics are provided to assign fossils to specific taxa within the clade. The Ranoidea is thought to have initially diversified in Africa, but the African fossil record of anurans in the Mesozoic and Paleogene is generally poor, with the Afro-Arabian record limited primarily to pipoid frogs or taxonomically enigmatic fossils.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-10.jpg\" title=\"A block-like partial anuran (Ptychadenidae indet.) composite sacral element; A, dorsal view; B, ventral view; C, left lateral view; D, anterior view; E, posterior view\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-10-656x314.jpg\" alt=\"A block-like partial anuran (Ptychadenidae indet.) composite sacral element; A, dorsal view; B, ventral view; C, left lateral view; D, anterior view; E, posterior view\" width=\"656\" height=\"314\" \/><span class=\"su-custom-gallery-title\">A block-like partial anuran (Ptychadenidae indet.) composite sacral element; A, dorsal view; B, ventral view; C, left lateral view; D, anterior view; E, posterior view<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">These fossils constitute the earliest record of the endemic African ranoid frog family <em>Ptychadenidae<\/em> from the late Oligocene Nsungwe Formation in the Rukwa Rift Basin of southwestern Tanzania. Paleogene anuran fossils are typically rare, but they constitute approximately 13% of materials collected from localities in the Nsungwe Formation. Radiometrically dated at \u2248 25 Ma, Nsungwe Formation localities preserve a diverse vertebrate fauna and a number of novel invertebrate taxa. Nsungwe Formation anuran fossils include vertebrae preserving a unique sacral morphology that provides the earliest record of the Ptychadenidae, the earliest definitive record of any family within the diverse ranoid clade Natatanura, and the first late Oligocene record of anurans from Africa below the equator.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A paper describing this endemic African frog has been published in <em>Journal of Vertebrate Paleontology<\/em> (Blackburn et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on November 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New postcranial bones of the earliest Eocene primate <em>Teilhardina belgica <\/em><\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\"><em>Teilhardina belgica<\/em> is the oldest primate from Europe \u2013 it dispersed probably from Asia during the Mammal Dispersal Event. This earliest fossil primate has often been hypothesized as a basal tarsiiform on the basis of its primitive dental formula with four premolars and a simplified molar cusp pattern. Until recently, little was known concerning its postcranial anatomy with the exception of its well-known tarsals. In this paper we describe additional postcranial elements for <em>Teilhardina belgica<\/em> and compare these to other tarsiiforms and to primitive adapiforms. The forelimb of <em>T. belgica<\/em> indicates an arboreal primate with prominent forearm musculature, good elbow rotational mobility and a horizontal, rather than a vertical body posture. The lateral hand positions imply grasps adaptive for relatively large diameter supports given its small body size. The hand is long with very long fingers, especially the middle phalanges. The hindlimb indicates foot inversion capabilities, frequent leaping, arboreal quadrupedalism, climbing, and grasping. The long and well-muscled hallux can be coupled with long lateral phalanges to reconstruct a foot with long grasping digits.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Our phyletic analysis indicates that we can identify several postcranial characteristics shared in common for stem primates as well as note several derived postcranial characters for Tarsiiformes.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-4.jpg\" title=\"Tibiae. A\u2013E, right tibia; A, anterior view; B, posterior view, C, lateral view; D, medial view; E, distal view. F\u2013J, right tibia; F, anterior view; G, posterior view; lateral view; I, medial view; J, distal view\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-4-656x479.jpg\" alt=\"Tibiae. A\u2013E, right tibia; A, anterior view; B, posterior view, C, lateral view; D, medial view; E, distal view. F\u2013J, right tibia; F, anterior view; G, posterior view; lateral view; I, medial view; J, distal view\" width=\"656\" height=\"479\" \/><span class=\"su-custom-gallery-title\">Tibiae. A\u2013E, right tibia; A, anterior view; B, posterior view, C, lateral view; D, medial view; E, distal view. F\u2013J, right tibia; F, anterior view; G, posterior view; lateral view; I, medial view; J, distal view<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">This research was published in <em>American Journal of Physical Anthropology<\/em> (Gebo et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on November 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New Late Paleocene crocodiliform remains from Berru, France, and the origin of the alligatoroid <em>Diplocynodon<\/em><\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The fossil record of the extinct alligatoroid crocodilian <em>Diplocynodon<\/em>, is very abundant but limited to Europe. However, when and how <em>Diplocynodon<\/em> dispersed to Europe is still unresolved. Crocodilian remains from the late Palaeocene continental locality of Mont de Berru (Marne, France) offer the opportunity to reassess the taxonomic identity of the oldest diplocynodontid from Europe. Owing to significant morphological differences from previously described species of <em>Diplocynodon<\/em>, a new species, <em>Diplocynodon<\/em> <em>remensis<\/em>, has been erected in this article.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-2.jpg\" title=\"Photographs and line drawings of the skull of Diplocynodon remensis from the Late Paleocene of Mont de Berru; A, C, dorsal view; B, D, ventral view\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-2-656x281.jpg\" alt=\"Photographs and line drawings of the skull of Diplocynodon remensis from the Late Paleocene of Mont de Berru; A, C, dorsal view; B, D, ventral view\" width=\"656\" height=\"281\" \/><span class=\"su-custom-gallery-title\">Photographs and line drawings of the skull of Diplocynodon remensis from the Late Paleocene of Mont de Berru; A, C, dorsal view; B, D, ventral view<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Its inclusion in a phylogenetic framework for Eusuchia leads to its positioning as a derived member of diplocynodontids. Diplocynodontidae are viewed as a basal alligatoroid taxon, and, because morphological affinities with the Late Cretaceous\u2212early Eocene North American genus Borealosuchus were mentioned in earlier studies, a comparison amongst <em>D. remensis, Leidyosuchus, <\/em>and<em> Borealosuchus<\/em> is presented. Although <em>D. remensis<\/em> is the geologically oldest diplocynodontid, according to our results, it is not the phylogenetically most primitive. Other morphological discrepancies are highlighted, indicating that the topology recovered here is only tentative. From a biogeographical point of view, the appearance of <em>Diplocynodon<\/em> in Europe prior to the Palaeocene\/Eocene boundary indicates that it did not disperse with North American taxa that reached Europe around the time of the PETM. Therefore, a pre-PETM dispersal from North America at the same times as other vertebrates with clear North American affinities also occurring in the Palaeocene of Europe cannot be excluded.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A manuscript detailing this study has been published in <em> Zoological Journal of the Linnean Society<\/em> (Martins et al., 2014).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on November 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">New fossils suggest the mammalian order Perissodactyla originated in India <\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Perissodactyla is an order of ungulate mammals that includes the extant hippomorphs (equoids) and ceratomorphs (tapiroids and rhinocerotoids) and their extinct relatives, and other extinct groups (chalicotherioids, \u201cisectolophids,\u201d and brontotherioids). It was during the PETM, that perissodactyls first appeared across the Laurasian continents. Since perissodactyls appeared almost simultaneously in Europe, Asia and North America, the place of their origin has long been disputed and numerous authors have tentatively reconstructed the biogeographic history of the earliest perissodactyls from North America, Central America, Africa, India, or Asia. Cambaytheres are recently discovered early Eocene placental mammals from the Indo\u2013Pakistan region. They have been assigned to either Perissodactyla (the clade including horses, tapirs and rhinos, which is a member of the superorder Laurasiatheria) or Anthracobunidae, an obscure family that has been variously considered artiodactyls or perissodactyls, but most recently placed at the base of Proboscidea or of Tethytheria (superorder Afrotheria). We reported new dental, cranial and postcranial fossils of Cambaytherium, from the Cambay Shale Formation, Gujarat, India (c. 54.5 Myr ago). These fossils demonstrate that cambaytheres occupy a pivotal position as the sister taxon of Perissodactyla, thereby providing insight on the phylogenetic and biogeographic origin of Perissodactyla.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The presence of the sister group of perissodactyls in western India near or before the time of collision suggests that Perissodactyla may have originated on the Indian Plate during its final drift toward Asia.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-6.jpg\" title=\"Skull and mandible of Cambaytherium thewissi\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-6-656x590.jpg\" alt=\"Skull and mandible of Cambaytherium thewissi\" width=\"656\" height=\"590\" \/><span class=\"su-custom-gallery-title\">Skull and mandible of Cambaytherium thewissi<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">This discovery was published in <em>Nature Communications<\/em> (Rose et al., 2014) and well covered by the international press. <\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on September 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Reference carbon isotopes on organics of the Late Danian\/Early Selandian, to provide isotopic framework for chemostratigraphic correlations.<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Global Boundary Stratotype Section and Point for the base of the Selandian Stage is defined in the Zumaia section (Spain) at an abrupt change in lithology (base of Itzurun Formation), which coincides with the onset of a negative carbonate carbon isotope shift. However, this lithological change is not always very well expressed in other sections. In order to document the stratigraphic position of the Danian\/Selandian boundary (DSB) on a more global scale, we have investigated three sections across the DSB, the Zumaia reference section (GSSP), the Loubieng section (auxiliary DSB reference section, France) and the Sidi Nasseur section (Tunisia). The Danian\/Selandian boundary interval is subdivided and correlated throughout low latitudes, from the Altlantic Bay of Biscay to the Southern Tethys, on the basis of seven calcareous nannofossil and planktonic foraminiferal events (E-events).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-15.jpg\" title=\"High-resolution geochemistry, carbon isotope, oxygen isotope, \u039413C and biostratigraphy across the Danian\u2013Selandian boundary in the Loubieng section\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-15-656x418.jpg\" alt=\"High-resolution geochemistry, carbon isotope, oxygen isotope, \u039413C and biostratigraphy across the Danian\u2013Selandian boundary in the Loubieng section\" width=\"656\" height=\"418\" \/><span class=\"su-custom-gallery-title\">High-resolution geochemistry, carbon isotope, oxygen isotope, \u039413C and biostratigraphy across the Danian\u2013Selandian boundary in the Loubieng section<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The base of the Selandian is proved to coincide with the end of the Braarudosphaera acme, which correlates with the lowest consistent occurrence (LCsO) of <em>Lithoptychius <\/em>aff<em>. bitectus<\/em> (=<em>Fasciculithus<\/em> <em>janii<\/em> sensu Steurbaut and Sztr\u00e1kos, 2008) (event E4), but which is slightly posterior to the second radiation of the fasciculiths, up to now considered to represent the primary correlation tool of the DSB. A short-term <sup>13<\/sup>C<sub>org<\/sub> negative excursion, associated with an increase in pCO<sub>2<\/sub> is recorded at the very base of the Selandian. It is interpreted as a short period of global warming (hyperthermal), the duration of which is estimated at ~30 kyr. It is followed in all the three studied sections by a long-term decoupled carbon isotope event, marked by increasing <sup>13<\/sup>C<sub>org<\/sub> and decreasing <sup>13<\/sup>C<sub>carb<\/sub> values. It may reflect a period of climatic cooling of a few 100 kyr, interpreted as a possible precursor of the global cooling event, marking the late Paleocene in the North Atlantic realm.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">This study was published in <em>Palaeogeography, Palaeoclimatology, Palaeoecology<\/em> (Storme et al., 2014).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"60%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on April 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Refined dating of the European early placental mammals in the Corbi\u00e8res area, located between reference localities of Northern Europe and Africa.<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Utilizing bio- and chemostratigraphy, we published an integrated dating of the upper part of the continental \u201cSparnacien des Corbi\u00e8res\u201d and the overlying marine \u201clower-middle Ilerdian\u201d succession of Albas-Le Clot (Corbi\u00e8res, France), in order to refine the position and age of the Le Clot mammalian locality. Our data show that this locality, which has yielded a mammal fauna early Ypresian in age (close to MP7, Mammal Paleogene level), is located above the end of the carbon isotope excursion (CIE) the base of which defines the Paleocene-Eocene boundary. The Le Clot mammalian locality is therefore younger than the Paleocene-Eocene Thermal Maximum (PETM), and also younger than the Dormaal MP7 reference fauna in Belgium, which is correlated with the onset of the CIE (nannoplankton Zone NP9b). Moreover, we demonstrate that the Le Clot mammalian locality is older than the Eocene Thermal Maximum 2 (ETM2) event, located in the lower part of NP11 Zone. Associated with the ages of benthic foraminifera and dinocysts observed in the succession, our <sup>13<\/sup>C<sub>org<\/sub> chemostratigraphy suggests that the Le Clot locality is correlated to the upper NP10\u2013lower NP11 Zones. The refined location of the CIE in the Albas-Le Clot section is discussed because two carbon isotope excursions are potentially recorded in the upper \u201cSparnacien des Corbi\u00e8res\u201d, here recognized as mainly Thanetian in age.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A paper describing these results has been published in <em>Newsletters on Stratigraphy<\/em> (Yans et al., 2014).<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-14.jpg\" title=\"\u03b413Corg (\u2030 VPDB). TOC and CaCO3 contents of the Albas-Le Clot section (Corbi\u00e8res)\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-14-486x700.jpg\" alt=\"\u03b413Corg (\u2030 VPDB). TOC and CaCO3 contents of the Albas-Le Clot section (Corbi\u00e8res)\" width=\"486\" height=\"700\" \/><span class=\"su-custom-gallery-title\">\u03b413Corg (\u2030 VPDB). TOC and CaCO3 contents of the Albas-Le Clot section (Corbi\u00e8res)<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on March 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Earliest Colubroid-Dominated Snake Fauna from Africa<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The extant snake fauna has its roots in faunal upheaval occurring across the Paleogene &#8211; Neogene transition. On northern continents, this turnover is well established by the late early Miocene. However, this transition is poorly documented on southern landmasses, particularly on continental Africa, where no late Paleogene terrestrial snake assemblages are documented south of the equator. Here we describe a newly discovered snake fauna from the Late Oligocene Nsungwe Formation in the Rukwa Rift Basin of Tanzania. The fauna is small but diverse with eight identifiable morphotypes, comprised of three booids and five colubroids. This fauna includes <em>Rukwanyoka holmani<\/em> gen. et sp. nov., the oldest boid known from mainland Africa. It also provides the oldest fossil evidence for the African colubroid clade Elapidae. Colubroids dominate the fauna, comprising more than 75% of the recovered material. This is likely tied to local aridification and\/or seasonality and mirrors the pattern of overturn in later snake faunas inhabiting the emerging grassland environments of Europe and North America.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-13.jpg\" title=\"Elapid snakes from late Oligocene of Tanzania (A, B) with comparison to extant Naja nigricollis (c)\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-13-656x434.jpg\" alt=\"Elapid snakes from late Oligocene of Tanzania (A, B) with comparison to extant Naja nigricollis (c)\" width=\"656\" height=\"434\" \/><span class=\"su-custom-gallery-title\">Elapid snakes from late Oligocene of Tanzania (A, B) with comparison to extant Naja nigricollis (c)<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">The early emergence of colubroid dominance in the Rukwa Rift Basin relative to northern continents suggests that the pattern of overturn that resulted in extant faunas happened in a more complex fashion on continental Africa than was previously realized, with African colubroids becoming at least locally important in the late Paleogene, either ahead of or as a consequence of the invasion of colubrids. The early occurrence of elapid snakes in the latest Oligocene of Africa suggests the clade rapidly spread from Asia to Africa, or arose in Africa, before invading Europe.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A paper describing these snakes has been published in <em>PLOS ONE<\/em> (McCartney et al., 2014).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on February 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Endocranial morphology of Paleocene <em>Plesiadapis tricuspidens<\/em> and evolution of the early primate brain<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Expansion of the brain is a key feature of primate evolution. The fossil record, although incomplete, allows a partial reconstruction of changes in primate brain size and morphology through time. Palaeogene plesiadapoids, closest relatives of Euprimates (or crown-group primates), are crucial for understanding early evolution of the primate brain. However, brain morphology of this group remains poorly documented, and major questions remain regarding the initial phase of euprimate brain evolution. Micro-CT investigation of the endocranial morphology of <em>Plesiadapis tricuspidens<\/em> from the Late Paleocene of Europe, the most complete plesiadapoid cranium known, shows that plesiadapoids retained a very small and simple brain.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-12.jpg\" title=\"Endocast of Plesiadapis tricuspidens (a, b) and comparison with the location and extent of the braincase in plesiadapiformes Microsyops annectens (c), Ignacius graybullianus (d), P. tricuspidens (e), and euprimate Tetonius homunculus (f)\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-12-656x282.jpg\" alt=\"Endocast of Plesiadapis tricuspidens (a, b) and comparison with the location and extent of the braincase in plesiadapiformes Microsyops annectens (c), Ignacius graybullianus (d), P. tricuspidens (e), and euprimate Tetonius homunculus (f)\" width=\"656\" height=\"282\" \/><span class=\"su-custom-gallery-title\">Endocast of Plesiadapis tricuspidens (a, b) and comparison with the location and extent of the braincase in plesiadapiformes Microsyops annectens (c), Ignacius graybullianus (d), P. tricuspidens (e), and euprimate Tetonius homunculus (f)<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Plesiadapis has midbrain exposure, and minimal encephalization and neocorticalization, making it comparable with that of stem rodents and lagomorphs. However, <em>Plesiadapis<\/em> shares a domed neocortex and downwardly shifted olfactory-bulb axis with Euprimates. If accepted phylogenetic relationships are correct, then this implies that the euprimate brain underwent drastic reorganization during the Palaeocene, and some changes in brain structure preceded brain size increase and neocortex expansion during evolution of the primate brain.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">These important results have been published in <em>Proceedings of the Royal Society B, London<\/em> (Orliac et al., 2015).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on January 2014<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">First Clarkforkian Equivalent Land Mammal Age in the Latest Paleocene Basal Sparnacian Facies of Europe: Fauna, Flora, Paleoenvironment and (Bio)stratigraphy<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">The Paleocene-Eocene Thermal Maximum (PETM) is correlated with the first occurrences of earliest modern mammals in the Northern Hemisphere. The latest Paleocene Clarkforkian North American Land Mammal Age, that has yielded rodents and carnivorans, is the only exception to this rule. However, until now no pre-PETM localities have yielded modern mammals in Europe or Asia. The new terrestrial vertebrate and macroflora assemblages found at Rivecourt, in the north-central part of the Paris Basin, were analyzed through a multidisciplinary study including sedimentologic, stratigraphic, isotopic, and palynological aspects in order to reconstruct the paleoenvironment and to evaluate biochronologic and paleogeographic implications. The mammals are moderately diverse and not abundant, contrary to turtles and champsosaurs. The macroflora is exceptional in preservation and diversity with numerous angiosperms represented by flowers, fruits, seeds and wood preserved as lignite material, revealing an abundance of <em>Arecaceae, Betulaceae, Icacinaceae, Menispermaceae, Vitaceae <\/em>and probably<em> Cornaceae<\/em>. Results indicate a Late Paleocene age based on Carbon isotope data, palynology and vertebrate occurrences such as the choristoderan <em>Champsosaurus<\/em>, the arctocyonid <em>Arctocyon<\/em>, and the plesiadapid <em>Plesiadapis tricuspidens<\/em>. However, several mammal species compare better with the earliest Eocene. Among these, the particular louisinid <em>Teilhardimys musculus<\/em> suggests a younger age than the typical MP6 reference level.<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Nevertheless, the most important aspect of the Rivecourt fauna is the presence of dental remains of a rodent and a \u201cmiacid\u201d carnivoran, attesting to the presence of two modern mammalian orders in the latest Paleocene of Europe. Therefore, Rivecourt represent the first Clarkforkian equivalent Land Mammal Age in Europe.<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-11.jpg\" title=\"Illustration of several mammals from the late Paleocene locality of Rivecourt\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Figure-11-656x678.jpg\" alt=\"Illustration of several mammals from the late Paleocene locality of Rivecourt\" width=\"656\" height=\"678\" \/><span class=\"su-custom-gallery-title\">Illustration of several mammals from the late Paleocene locality of Rivecourt<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">A long paper describing this new locality was published in <em>PLOS ONE<\/em> (Smith et al., 2014).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n<table width=\"100%\" cellspacing=\"0\" cellpadding=\"4\">\n<tbody>\n<tr valign=\"top\">\n<td style=\"border: none; padding: 0cm;\" width=\"50%\">\n<p align=\"justify\"><em><span style=\"color: #000000;\">Posted on November 2013<\/span><\/em><\/p>\n<p align=\"justify\"><strong><span style=\"color: #000000;\">Refined dating of the early placental mammals in Morocco, using carbon isotopes on various materials<br \/>\n<\/span><\/strong><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">Fossil biogenic apatites were studied for their geochemical composition across the late Cretaceous\u2013early Eocene Moroccan phosphate series in the Ouled Abdoun and Ganntour basins in Morocco in order to characterize paleoenvironmental conditions and to improve stratigraphy. The vertebrate remains show particularly good structural, mineralogical and chemical preservations, which relate to the favorable depositional environment of the phosphorite. The main studied fossils show large range in <sup>13<\/sup>C<sub>carb<\/sub><sub>org<\/sub> values from\u221214 to +6\u2030, which can be coupled to different carbon sources. Enameloid yielded mostly positive <sup>13<\/sup>C isotopic compositions that are comparable with values reported from modern teeth. Coprolites have the lowest <sup>13<\/sup>C values that reflect burial conditions with intensive organic matter recycling. The large variation in <sup>18<\/sup>O<sub>PO4<\/sub> values of the shark teeth can be related to ecological differences. However, the mean 18OPO4 data reflect important temporal variation along the series, together with the corresponding average <sup>13<\/sup>C values.<br \/>\n<\/span><\/p>\n<\/td>\n<td style=\"border: none; padding: 0cm;\" width=\"50%\"><div class=\"su-custom-gallery su-custom-gallery-title-on mouse over\"><div class=\"su-custom-gallery-slide\"><a href=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Fiigure-16-new.jpg\" title=\"Integrated phosphate oxygen (\u03b418OPO4) and carbon \u03b413C (dentine) isotope data from the Ouled Abdoun and Ganntour basins and their comparison to the global record\"><img src=\"https:\/\/www.paleurafrica.be\/wp-content\/uploads\/2015\/12\/Fiigure-16-new-656x410.jpg\" alt=\"Integrated phosphate oxygen (\u03b418OPO4) and carbon \u03b413C (dentine) isotope data from the Ouled Abdoun and Ganntour basins and their comparison to the global record\" width=\"656\" height=\"410\" \/><span class=\"su-custom-gallery-title\">Integrated phosphate oxygen (\u03b418OPO4) and carbon \u03b413C (dentine) isotope data from the Ouled Abdoun and Ganntour basins and their comparison to the global record<\/span><\/a><\/div><div class=\"su-clear\"><\/div><\/div><\/td>\n<\/tr>\n<tr>\n<td style=\"border: none; padding: 0cm;\" colspan=\"2\" valign=\"top\" width=\"100%\">\n<p align=\"justify\"><span style=\"color: #000000;\">Comparisons with the global isotope records allow identifying the Early Eocene Climatic Optimum in the top of the Ouled Abdoun series (above Bed 0). The isotope data further suggest a sedimentary gap during the latest Thanetian and the Paleocene Eocene Thermal Maximum. The top of the Paleocene series (Bed IIa) can be dated to late Selandian\u2013early Thanetian, with the recognition of the Early Late Paleocene Event (ELPE). The Eritherium Bone Bed, that yielded the earliest known placental mammals from Africa, would be located below the ELPE and therefore, cannot be younger than late Selandian. The isotope data from the older Paleocene (Bed IIb) and Cretaceous (upper Bed III) beds in the Ouled Abdoun Basin can be correlated with the latest Danian \u2013 early Selandian and the latest Maastrichtian global isotope record, respectively. Based on the <sup>18<\/sup>O<sub>PO4<\/sub> data, the Cretaceous layers of the Ganntour Basin cover most of the Maastrichtian period except the very early part.<br \/>\n<\/span><\/p>\n<p align=\"justify\"><span style=\"color: #000000;\">A paper describing these results has been published in <em> Palaeogeography, Palaeoclimatology, Palaeoecology<\/em> (Kocsis et al., 2014).<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><span style=\"color: #000000;\"><div class=\"su-divider su-divider-style-default\" style=\"margin:40px 0;border-width:2px;border-color:#000000\"><a href=\"#\" style=\"color:#000000\">Go to top<\/a><\/div><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Posted on April 2021 A reassessment of the Oligocene hyracoids from Malembo, Cabinda, Angola The Oligocene Malembo locality, Cabinda exclave, Angola has yielded a rich vertebrate fauna represented by fragmentary remains. This fossiliferous locality is the only definite occurrence of<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"open","ping_status":"open","template":"page-templates\/contact.php","meta":[],"_links":{"self":[{"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=\/wp\/v2\/pages\/870"}],"collection":[{"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=870"}],"version-history":[{"count":265,"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=\/wp\/v2\/pages\/870\/revisions"}],"predecessor-version":[{"id":2883,"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=\/wp\/v2\/pages\/870\/revisions\/2883"}],"wp:attachment":[{"href":"https:\/\/www.paleurafrica.be\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=870"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}