60 research outputs found
Observations and re-description of Zonosaurus boettgeri Steindachner 1891 and description of a second new species of long-tailed Zonosaurus from western Madagascar
http://deepblue.lib.umich.edu/bitstream/2027.42/57175/1/OP739.pd
An integrative taxonomic revision and redefinition of Gephyromantis (Laurentomantis) malagasius based on archival DNA analysis reveals four new mantellid frog species from Madagascar
The subgenus Laurentomantis in the genus Gephyromantis contains some of the least known amphibian species of Madagascar. The six currently valid nominal species are rainforest frogs known from few individuals, hampering a full understanding of the species diversity of the clade. We assembled data on specimens collected during field surveys over the past 30 years and integrated analysis of mitochondrial and nuclear-encoded genes of 88 individuals, a comprehensive bioacoustic analysis, and morphological comparisons to delimit a minimum of nine species-level lineages in the subgenus. To clarify the identity of the species Gephyromantis malagasius, we applied a target-enrichment approach to a sample of the 110 year-old holotype of Microphryne malagasia Methuen and Hewitt, 1913 to assign this specimen to a lineage based on a mitochondrial DNA barcode. The holotype clustered unambiguously with specimens previously named G. ventrimaculatus. Consequently we propose to consider Trachymantis malagasia ventrimaculatus Angel, 1935 as a junior synonym of Gephyromantis malagasius. Due to this redefinition of G. malagasius, no scientific name is available for any of the four deep lineages of frogs previously subsumed under this name, all characterized by red color ventrally on the hindlimbs. These are here formally named as Gephyromantis fiharimpe sp. nov., G. matsilo sp. nov., G. oelkrugi sp. nov., and G. portonae sp. nov. The new species are distinguishable from each other by genetic divergences of >4% uncorrected pairwise distance in a fragment of the 16S rRNA marker and a combination of morphological and bioacoustic characters. Gephyromantis fiharimpe and G. matsilo occur, respectively, at mid-elevations and lower elevations along a wide stretch of Madagascar’s eastern rainforest band, while G. oelkrugi and G. portonae appear to be more range-restricted in parts of Madagascar’s North East and Northern Central East regions. Open taxonomic questions surround G. horridus, to which we here assign specimens from Montagne d’Ambre and the type locality Nosy Be; and G. ranjomavo, which contains genetically divergent populations from Marojejy, Tsaratanana, and Ampotsidy.info:eu-repo/semantics/publishedVersio
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Methods for prioritizing protected areas using individual and aggregate rankings
Despite their legal protection status, protected areas (PAs) can benefit from priority ranks when ongoing threats to their biodiversity and habitats outpace the financial resources available for their conservation. It is essential to develop methods to prioritize PAs that are not computationally demanding in order to suit stakeholders in developing countries where technical and financial resources are limited. We used expert knowledge-derived biodiversity measures to generate individual and aggregate priority ranks of 98 mostly terrestrial PAs on Madagascar. The five variables used were state of knowledge (SoK), forest loss, forest loss acceleration, PA size and relative species diversity, estimated by using standardized residuals from negative binomial models of SoK regressed onto species diversity. We compared our aggregate ranks generated using unweighted averages and principal component analysis (PCA) applied to each individual variable with those generated via Markov chain (MC) and PageRank algorithms. SoK significantly affected the measure of species diversity and highlighted areas where more research effort was needed. The unweighted- and PCA-derived ranks were strongly correlated, as were the MC and PageRank ranks. However, the former two were weakly correlated with the latter two. We recommend using these methods simultaneously in order to provide decision-makers with the flexibility to prioritize those PAs in need of additional research and conservation efforts
Ultraconserved elements-based phylogenomic systematics of the snake superfamily Elapoidea, with the description of a new Afro-Asian family
The highly diverse snake superfamily Elapoidea is considered to be a classic example of ancient, rapid radiation. Such radiations are challenging to fully resolve phylogenetically, with the highly diverse Elapoidea a case in point. Previous attempts at inferring a phylogeny of elapoids produced highly incongruent estimates of their evolutionary relationships, often with very low statistical support. We sought to resolve this situation by sequencing over 4,500 ultraconserved element loci from multiple representatives of every elapoid family/sub-family level taxon and inferring their phylogenetic relationships with multiple methods. Concatenation and multispecies coalescent based species trees yielded largely congruent and well-supported topologies. Hypotheses of a hard polytomy were not retained for any deep branches. Our phylogenies recovered Cyclocoridae and Elapidae as diverging early within Elapoidea. The Afro-Malagasy radiation of elapoid snakes, classified as multiple subfamilies of an inclusive Lamprophiidae by some earlier authors, was found to be monophyletic in all analyses. The genus Micrelaps was consistently recovered as sister to Lamprophiidae. We establish a new family, Micrelapidae fam. nov., for Micrelaps and assign Brachyophis to this family based on cranial osteological syn-apomorphy. We estimate that Elapoidea originated in the early Eocene and rapidly diversified into all the major lineages during this epoch. Ecological opportunities presented by the post-Cretaceous-Paleogene mass extinction event may have promoted the explosive radiation of elapoid snakes.Peer reviewe
Protected area surface extension in Madagascar: Do endemism and threatened species remain useful criteria for site selection?
The ‘hotspot approach’ considers that endemism and threatened species are key factors in protected area designation. Three wetland and forest sites have been proposed to be included into Madagascar’s system of protected areas (SAPM – Système des Aires Protégées de Madagascar). These sites are Manambolomaty (14,701 ha) and Mandrozo (15,145 ha) in the west and Bemanevika (37,041 ha) in the north. Biodiversity inventories of these three sites recorded 243 endemic species comprised of 44 reptiles, 54 amphibians, 104 birds, 23 small mammals, 17 lemurs and one fish. Of these 243 species, 30 are threatened taxa comprising two Critically Endangered (CR), 11 Endangered (EN) and 17 Vulnerable (VU) species. The long term ecological viability of these sites has been shown by population stability of the two Critically Endangered flagship species, the Madagascar fish eagle (Haliaeetus vociferoides) in Manambolomaty and Mandrozo and the recently rediscovered Madagascar pochard (Aythya innotata) in Bemanevika. Other threatened species and high biological diversity also justifies their inclusion into Madagascar’s SAPM.RÉSUMÉL’endémisme et les espèces menacées constituent les éléments clef pour la création des aires protégées. Trois zones humides de Madagascar ainsi que leurs forêts avoisinantes sont proposées pour la protection sous le nouveau système des aires protégées malgaches connu sous le sigle SAPM (Système d’Aires Protégées de Madagascar) : Manambolomaty (14.701 ha) et Mandrozo (15.145 ha) à l’Ouest et Bemanevika (37.041 ha) dans le Nord. Les inventaires biologiques entrepris dans ces trois sites ont montré que 243 espèces y sont endémiques, avec 44 reptiles, 54 amphibiens, 104 oiseaux, 23 petits mammifères, 17 lémuriens et un poisson. Parmi ces 243 espèces, 30 sont menacées d’extinction avec deux qui sont en danger critique d’extinction (CR), 11 en danger (EN) et 17 vulnérables (VU). La survie écologique à long terme de ces sites a été avérée avec la découverte de la stabilité des populations des deux espèces indicatrices en danger critique d’extinction que sont le Pygargue de Madagascar (Haliaeetus vociferoides) à Manambolomaty et Mandrozo et une espèce récemment redécouverte, le Fuligule de Madagascar (Aythya innotata) à Bemanevika. La stabilité de plusieurs autres espèces menacées ainsi que la diversité biologique de ces sites justifient leur inclusion dans le SAPM. Les sept associations locales, deux à Manambolomaty, deux à Bemanevika et trois à Mandrozo, ont supporté le programme de suivi de ces sites ainsi que de ces espèces indicatrices en montrant ainsi leur engagement dans le processus de création des aires protégées. Le Peregrine Fund a travaillé dans ces sites en vue de mettre en synergie ses objectifs de conservation avec le développement socio-économique local
Tracing a toad invasion: lack of mitochondrial DNA variation, haplotype origins, and potential distribution of introduced Duttaphrynus melanostictus in Madagascar
The black-spined toad, Duttaphrynus melanostictus, is widespread in South and South-East (SE) Asia, although recent molecular analyses have revealed that it represents a species complex (here called the D. melanostictus complex). Invasive populations of this toad have been detected in Madagascar since, at least, 2014. We here trace the origin of this introduction based on mitochondrial DNA sequences of 340 samples. All 102 specimens from Madagascar have identical sequences pointing to a single introduction event. Their haplotype corresponds to a lineage occurring in Cambodia, China, Laos, Thailand, Vietnam, and some locations of eastern Myanmar and northern Malaysia, here named the SE Asian lineage. Within this lineage, specimens from one location in Cambodia and three locations in Vietnam have the same haplotype as found in Madagascar. This includes Ho Chi Minh City, which has a major seaport and might have been the source for the introduction. Species distribution models suggest that the current range of the Madagascan invasive population is within the bioclimatic space occupied by the SE Asian lineage in its native range. The potential invasion zone in Madagascar is narrower than suggested by models from localities representing the full range of the D. melanostictus complex. Thus, an accurate taxonomy is essential for such inferences, but it remains uncertain if the toad might be able to spread beyond the potential suitable range because (1) knowledge on species-delimitation of the complex is insufficient, and (2) the native range in SE Asia might be influenced by historical biogeography or competition
FIGURE 1 in Rediscovery and redescription of the Malagasy dwarf gecko Lygodactylus klemmeri
FIGURE 1. Dorsal and ventral views of a preserved male specimen of Lygodactylus klemmeri (UADBA 17821).Published as part of <i>Puente, Marta, Raselimanana, Achille P. & Vences, Miguel, 2005, Rediscovery and redescription of the Malagasy dwarf gecko Lygodactylus klemmeri, pp. 31-35 in Zootaxa 1073 (1)</i> on page 34, DOI: 10.11646/zootaxa.1073.1.2, <a href="http://zenodo.org/record/10087042">http://zenodo.org/record/10087042</a>
BEAST infile for Oplurus cuvieri, constant pop size
XML formated infile for estimation of Oplurus cuvieri gene tree and divergence times in BEAST 1.6.2. Includes sequence data for ND1 and ND1 flanking regions and assumes constant population size model
BEAST infile for Oplurus cuvieri, exponential growth
XML formated infile for estimation of Oplurus cuvieri gene tree and divergence times in BEAST 1.6.2. Includes sequence data for ND1 and ND1 flanking regions and assumes exponential growth model
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