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Friday, July 2nd, 2021

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    2:47a
    [PaleoMammalogy • 2021] The Rise and Fall of Proboscidean Ecological Diversity


    Dusk falls on East Africa's Turkana Basin 4 million years ago, where our early upright-walking ape ancestors, Australopithecus anamensis (foreground), shared their habitat with several coexisting proboscidean species, as part of a spectacular herbivore community containing some progenitors of today's charismatic East African animals.
    Background (left to right): Anancus ultimus, last of the African mastodonts; Deinotherium bozasi, colossal herbivore as tall as a giraffe; Loxodonta adaurora, gigantic extinct cousin of modern African elephants, alongside the closely-related, smaller L. exoptata. Middle ground (left to right): Eurygnathohippus turkanense, zebra-sized three-hoofed horse; Tragelaphus kyaloae, a forerunner of the nyala and kudu antelopes; Diceros praecox - ancestor of the modern black rhino.

    in Cantalapiedra, Sanisidro, Zhang, ... et Saarinen, 2021. 
    Illustration: Julius Csotonyi
     
    Abstract
    Proboscideans were keystone Cenozoic megaherbivores and present a highly relevant case study to frame the timing and magnitude of recent megafauna extinctions against long-term macroevolutionary patterns. By surveying the entire proboscidean fossil history using model-based approaches, we show that the dramatic Miocene explosion of proboscidean functional diversity was triggered by their biogeographical expansion beyond Africa. Ecomorphological innovations drove niche differentiation; communities that accommodated several disparate proboscidean species in sympatry became commonplace. The first burst of extinctions took place in the late Miocene, approximately 7 million years ago (Ma). Importantly, this and subsequent extinction trends showed high ecomorphological selectivity and went hand in hand with palaeoclimate dynamics. The global extirpation of proboscideans began escalating from 3 Ma with further extinctions in Eurasia and then a dramatic increase in African extinctions at 2.4 Ma. Overhunting by humans may have served as a final double jeopardy in the late Pleistocene after climate-triggered extinction trends that began long before hominins evolved suitable hunting capabilities.


    Juan L. Cantalapiedra, Óscar Sanisidro, Hanwen Zhang, María T. Alberdi, José L. Prado, Fernando Blanco and Juha Saarinen. 2021. The Rise and Fall of Proboscidean Ecological Diversity. Nature Ecology & Evolution. DOI: 10.1038/s41559-021-01498-w


    1:45p
    [Herpetology • 2021] Leptopelis palmatus • New Evidence for Distinctiveness of the Island-endemic Príncipe Giant Tree Frog (Arthroleptidae)


     Leptopelis palmatus (Peters, 1868)

    in Jaynes, Myers, Drewes et Bell, 2021. 
    Photo: Rayna Bell.

    Abstract
     The Príncipe giant tree frog Leptopelis palmatus is endemic to the small oceanic island of Príncipe in the Gulf of Guinea. For several decades, this charismatic but poorly known species was confused with another large tree frog species from continental Africa, L. rufus. Phylogenetic relationships within the African genus Leptopelis are poorly understood and consequently the evolutionary history of L. palmatus and its affinity to L. rufus remain unclear. In this study, we combined mitochondrial DNA (mtDNA), morphological, and acoustic data for L. palmatus and L. rufus to assess different axes of divergence between the species. Our mtDNA gene tree for the genus Leptopelis indicated that L. palmatus is not closely related to L. rufus or other large species of Leptopelis. Additionally, we found low mtDNA diversity in L. palmatus across its range on Príncipe. We found significant morphological differences between females of L. rufus and L. palmatus, but not between males. We characterised the advertisement call of L. palmatus for the first time, which is markedly distinct from L. rufus. Finally, we summarised our observations of L. palmatus habitats and additional notes on phenotypic variation and behaviour. Our study reinforces the distinctiveness of L. palmatus and provides information important for the conservation of this endangered species.

    Keywords: bioacoustic, morphology, endemic, mitochondrial DNA, island, São Tomé and Príncipe

    colour variation in Leptopelis palmatus 
    (CAS 258958, CAS 258910,
    USNM 591753, USNM 591758)
    Photos A. Stanbridge and R. Bell.


    Leptopelis palmatus (Peters, 1868)

    . (a) Violin plots of adjusted Snout-Vent Length (SVL), Tympanum size (TMP), Tympanum-Eye ratio (TMP:EYE), and Disc-Tympanum ratio (DSC:TMP) in L. palmatus and L. rufus. Comparisons significant at an adjusted P < 0.05 with a Tukey Honest Significant Difference test are indicated with an asterisk.
     (b) Call parameter definitions and representative audio spectrograms of L. palmatus and L. rufus male advertisement calls.
     (c) colour variation in Leptopelis palmatus (from left to right: CAS 258958, CAS 258910, USNM 591753, USNM 591758)
    Photos A. Stanbridge and R. Bell.


     
      Kyle E. Jaynes, Edward A. Myers, Robert C. Drewes and Rayna C. Bell. 2021. New Evidence for Distinctiveness of the Island-endemic Príncipe Giant Tree Frog (Arthroleptidae: Leptopelis palmatus). Herpetological Journal. 31; 162-169. DOI: 10.33256/31.3.162169

    A rã gigante de Príncipe, Leptopelis palmatus, é endêmica da pequena ilha oceânica de Príncipe no Golfo da Guiné. Por várias décadas, esta espécie carismática mas pouco conhecida foi confundida com outra espécie grande de rã da África continental, L. rufus. As relações filogenéticas dentro do gênero africano Leptopelis são mal compreendidas e, conseqüentemente, a história evolutiva de L. palmatus e sua afinidade com L. rufus permanecem obscuras. Neste estudo, combinamos dados de DNA mitocondrial (mtDNA), morfológicos e acústicos de L. palmatus e L. rufus para avaliar diferentes eixos de divergência entre as espécies. Nossa árvore de genes de mtDNA para o gênero Leptopelis indicou que L. palmatus não está proximamente relacionada a L. rufus ou outras espécies grandes de Leptopelis, e encontramos baixa diversidade de mtDNA em L. palmatus em toda a sua distribuição em Príncipe. Encontramos diferenças morfológicas significativas entre as fêmeas de L. rufus e L. palmatus, mas não entre os machos. Caracterizamos o canto reprodutor de L. palmatus pela primeira vez, que é marcadamente distinto do de L. rufus. Finalmente, resumimos nossas observações dos habitats de L. palmatus e notas adicionais sobre variação fenotípica e comportamento. Nosso estudo fornece informações importantes para a conservação dessa espécie ameaçada de extinção

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