FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1541632015> ?p ?o ?g. }

• W1541632015 endingPage "213" @default.
• W1541632015 startingPage "195" @default.
• W1541632015 abstract "In this paper, we describe four fossil rodent taxa from two new localities situated in the Idam Unit (‘Bioturbated Unit’) of the Dur At-Talah escarpment in central Libya. These rodents belong to the family Phiomyidae (Hystricognathi) and are distributed amongst three genera (Phiomys, Protophiomys, and Talahphiomys gen. nov.) that include three new species (Phiomys hammudai sp. nov., Protophiomys durattalahensis sp. nov., and Talahphiomys libycus sp. nov.). Although some of these new species are morphologically close to certain phiomyids from the latest Eocene and Oligocene of the Jebel el-Qatrani Formation of the Fayum in Egypt, the Idam rodent faunas lack the abundant and somewhat morphologically derived Fayum phiomyids (such as: Metaphiomys, Gaudeamus, Paraphiomys, Phiocricetomys), thereby excluding a similar age for the Dur At-Talah rodent assemblages. More resemblance is shared with the phiomyid (Protophiomys algeriensis) of the Nementcha locality in Algeria, for which a late middle Eocene age is presently admitted. Protophiomys is a primitive representative of the phiomyid African radiation and it is represented at Dur At-Talah by a slightly more derived species (Pr. durattalahensis) than that of Nementcha, thereby suggesting a younger age for Dur At-Talah. As a result, the new rodent assemblages suggest a late middle Eocene age for the Idam (‘Bioturbated') deposits of the Dur At-Talah escarpment. This age hypothesis is substantiated by other mammals (especially Proboscidea), which occur in the same sedimentological unit. Interestingly, the dental pattern of Protophiomys and that of Talahphiomys have somewhat stronger affinities with South Asian hystricognath baluchimyines than with Fayum phiomyids. It is clear that baluchimyines and phiomyids have a common ancestry, and that dispersal occurred between Asia and Africa during the middle of the Palaeogene. However, it is not clear if both groups can be strictly separated in two distinct natural groups inasmuch as some baluchimyines (e.g. Lophibaluchia, Bugtimys, Hodsahibia) appear to be phiomyid-like, and some early members of phiomyids (e.g. Protophiomys, Talahphiomys) are baluchimyine-like. South Asia and North Africa represent two centres of adaptive radiation of early hystricognathous rodents. The strong dental resemblances between early Asian and African forms are perhaps the result of subsequent convergent evolution after an initial dispersal from Asia. Otherwise, the systematics of these rodents has to be entirely revised, or we must consider that their historical biogeography is much more complex." @default.
• W1541632015 created "2016-06-24" @default.
• W1541632015 creator A5012585249 @default.
• W1541632015 creator A5020691888 @default.
• W1541632015 creator A5022843716 @default.
• W1541632015 creator A5025594488 @default.
• W1541632015 creator A5040296933 @default.
• W1541632015 creator A5070168001 @default.
• W1541632015 creator A5072447931 @default.
• W1541632015 creator A5073901907 @default.
• W1541632015 creator A5081448473 @default.
• W1541632015 creator A5089728650 @default.
• W1541632015 creator A5090457217 @default.
• W1541632015 creator A5091485602 @default.
• W1541632015 date "2010-08-18" @default.
• W1541632015 modified "2023-10-14" @default.
• W1541632015 title "New rodent assemblages from the Eocene Dur At-Talah escarpment (Sahara of central Libya): systematic, biochronological, and palaeobiogeographical implications" @default.
• W1541632015 cites W1964787489 @default.
• W1541632015 cites W1966722059 @default.
• W1541632015 cites W1982708613 @default.
• W1541632015 cites W1983750617 @default.
• W1541632015 cites W1999568277 @default.
• W1541632015 cites W2007083706 @default.
• W1541632015 cites W2014955006 @default.
• W1541632015 cites W2016217705 @default.
• W1541632015 cites W2027297844 @default.
• W1541632015 cites W2045632101 @default.
• W1541632015 cites W2050265902 @default.
• W1541632015 cites W2056066293 @default.
• W1541632015 cites W2069449804 @default.
• W1541632015 cites W2081352764 @default.
• W1541632015 cites W2095293118 @default.
• W1541632015 cites W2095800081 @default.
• W1541632015 cites W2098142474 @default.
• W1541632015 cites W2118204502 @default.
• W1541632015 cites W2133828233 @default.
• W1541632015 cites W2154744021 @default.
• W1541632015 cites W2158453634 @default.
• W1541632015 cites W2177641888 @default.
• W1541632015 cites W2179237927 @default.
• W1541632015 cites W2221411513 @default.
• W1541632015 cites W2490597215 @default.
• W1541632015 cites W4232328127 @default.
• W1541632015 doi "https://doi.org/10.1111/j.1096-3642.2009.00600.x" @default.
• W1541632015 hasPublicationYear "2010" @default.
• W1541632015 type Work @default.
• W1541632015 sameAs 1541632015 @default.
• W1541632015 citedByCount "57" @default.
• W1541632015 countsByYear W15416320152012 @default.
• W1541632015 countsByYear W15416320152013 @default.
• W1541632015 countsByYear W15416320152014 @default.
• W1541632015 countsByYear W15416320152015 @default.
• W1541632015 countsByYear W15416320152016 @default.
• W1541632015 countsByYear W15416320152017 @default.
• W1541632015 countsByYear W15416320152018 @default.
• W1541632015 countsByYear W15416320152019 @default.
• W1541632015 countsByYear W15416320152020 @default.
• W1541632015 countsByYear W15416320152021 @default.
• W1541632015 countsByYear W15416320152022 @default.
• W1541632015 crossrefType "journal-article" @default.
• W1541632015 hasAuthorship W1541632015A5012585249 @default.
• W1541632015 hasAuthorship W1541632015A5020691888 @default.
• W1541632015 hasAuthorship W1541632015A5022843716 @default.
• W1541632015 hasAuthorship W1541632015A5025594488 @default.
• W1541632015 hasAuthorship W1541632015A5040296933 @default.
• W1541632015 hasAuthorship W1541632015A5070168001 @default.
• W1541632015 hasAuthorship W1541632015A5072447931 @default.
• W1541632015 hasAuthorship W1541632015A5073901907 @default.
• W1541632015 hasAuthorship W1541632015A5081448473 @default.
• W1541632015 hasAuthorship W1541632015A5089728650 @default.
• W1541632015 hasAuthorship W1541632015A5090457217 @default.
• W1541632015 hasAuthorship W1541632015A5091485602 @default.
• W1541632015 hasBestOaLocation W15416320151 @default.
• W1541632015 hasConcept C109007969 @default.
• W1541632015 hasConcept C123575903 @default.
• W1541632015 hasConcept C125471540 @default.
• W1541632015 hasConcept C151730666 @default.
• W1541632015 hasConcept C167570900 @default.
• W1541632015 hasConcept C179226041 @default.
• W1541632015 hasConcept C18903297 @default.
• W1541632015 hasConcept C2776325015 @default.
• W1541632015 hasConcept C2777808111 @default.
• W1541632015 hasConcept C2778768285 @default.
• W1541632015 hasConcept C2778914748 @default.
• W1541632015 hasConcept C71640776 @default.
• W1541632015 hasConcept C73707237 @default.
• W1541632015 hasConcept C86803240 @default.
• W1541632015 hasConcept C90856448 @default.
• W1541632015 hasConceptScore W1541632015C109007969 @default.
• W1541632015 hasConceptScore W1541632015C123575903 @default.
• W1541632015 hasConceptScore W1541632015C125471540 @default.
• W1541632015 hasConceptScore W1541632015C151730666 @default.
• W1541632015 hasConceptScore W1541632015C167570900 @default.
• W1541632015 hasConceptScore W1541632015C179226041 @default.
• W1541632015 hasConceptScore W1541632015C18903297 @default.
• W1541632015 hasConceptScore W1541632015C2776325015 @default.
• W1541632015 hasConceptScore W1541632015C2777808111 @default.
• W1541632015 hasConceptScore W1541632015C2778768285 @default.

• next