Amphibian chytridiomycosis, an emerging infectious disease caused by the fungus Batrachochytrium dendrobatidis (Bd), has been a significant driver of amphibian declines. While globally widespread, Bd had not yet been reported from within Madagascar. We document surveys conducted across the country between 2005 and 2014, showing Bd's first record in 2010. Subsequently, Bd was detected in multiple areas, with prevalence reaching up to 100%. Detection of Bd appears to be associated with mid to high elevation sites and to have a seasonal pattern, with greater detectability during the dry season. Lineage-based PCR was performed on a subset of samples. While some did not amplify with any lineage probe, when a positive signal was observed, samples were most similar to the Global Panzootic Lineage (BdGPL). These results may suggest that Bd arrived recently, but do not exclude the existence of a previously undetected endemic Bd genotype. Representatives of all native anuran families have tested Bd-positive, and exposure trials confirm infection by Bd is possible. Bd's presence could pose significant threats to Madagascar's unique “megadiverse” amphibians.

The diurnal, brightly colored, and toxic frogs of the genus Mantella are among the most prominent representatives of the endemic anuran fauna of Madagascar. Especially three closely related species, M. aurantiaca, M. crocea, and M. milotympanum, are intensively collected for the pet trade, although basic data on their natural history and genetic diversity are still lacking. Our phylogenetic analyses based on 2.8 kbp of partial 16S rRNA, 12S rRNA, cytochrome b, and rhodopsin DNA sequences confirmed that these species belong to one of the five major clades in Mantella, the M. madagascariensis group. A haplotype network constructed using 830 bp of cytochrome b in 49 individuals from seven populations revealed that M. milotympanum and M. crocea have largely similar haplotypes sharing, confirming doubts about the species validity of M. milotympanum and indicating independent evolution of bright orange pattern in M. milotympanum and M. aurantiaca. Further, clustering of four individuals of M. aurantiaca from Andranomena with M. crocea suggests incomplete lineage sorting or introgression resulting from secondary contact of refugial populations. AMOVA confirmed significant intrapopulation nucleotide diversity (>20%). These diversity patterns and our field observations indicate relatively large population sizes. Hence, overcollecting is probably a minor problem and conservation efforts should rather focus on saving some large populations from habitat destruction through logging and forest fires.

Polystomatid flatworms are parasites of high host specificity, which mainly infect amphibian hosts. Only one polystome species has so far been recorded from Madagascar despite the high species richness and endemicity of amphibians on this island. Out of the 86 screened Malagasy frog species, we recovered polystomes from 25 in the families Ptychadenidae and Mantellidae. Molecular phylogenetic analysis uncovered an unexpected diversity of polystome species belonging to two separate clades: one forming a lineage within the genus Metapolystoma, with one species in Ptychadena and several species in the mantellid host genera Aglyptodactylus and Boophis; and the second corresponding to an undescribed genus that was found in the species of the subfamily Mantellinae in the family Mantellidae. The phylogenetic position of the undescribed genus along with molecular dating suggests that it may have colonized Madagascar in the Late Mesozoic or Early Cainozoic. By contrast, the more recent origin of Metapolystoma in Madagascar at ca 14-2 Myr ago strongly suggests that the ancestors of Ptychadena mascareniensis colonized Madagascar naturally by overseas dispersal, carrying their Metapolystoma parasites. Our findings provide a striking example of how parasite data can supply novel insights into the biogeographic history of their hosts.

Based on specimens identified by DNA barcoding, we describe the tadpoles of 11 species of treefrogs (Boophis) in the Malagasy family Mantellidae. All tadpoles belong to species of the stream-breeding clade within Boophis. Based on these and other published descriptions of Boophis tadpoles which develop in running water bodies, we tentatively distinguish three ecomorphological guilds for these larvae. Guild A, in which we describe the larvae of B. boehmei, B. reticulatus, B. pyrrhus, B. tasymena, and B. viridis which have few lotic adaptations, their oral disc width being 31-43% of body width, with a single row of 48-81 marginal papillae, and the first upper keratodont row having 58-144 keratodonts. Guild B, in which we describe the tadpoles of B. albilabris, B. madagascariensis, B. luteus, and of an undescribed species here named B. sp. aff. elenae, is intermediate, with an enlarged oral disc, an increasing number of keratodont rows and a lower height of the caudal fin. In these tadpoles, oral disc width is 43-63% of body width, they have one or two rows of 69-164 marginal papillae, and the first upper keratodont row has 164-238 keratodonts. Guild C contains tadpoles with a very large oral disc, living on submerged rocks and stones in stream sections of strong current. In this guild we describe the tadpoles of B. marojezensis and B. sibilans. Their oral disc width is 63-89% of body width, there are multiple rows of many marginal papillae, and the first upper keratodont row has many small keratodonts which are difficult to count, but consistently amount to over 200. In B. marojezensis, the dorsal gap in the marginal papillae rows, apparent in all other species, is closed. These larval morphologies show a rather good fit with recently published molecular phylogenetic data: species groups that were confirmed to be monophyletic in most cases have similar larval morphologies, and, in contrast, where species of the same group have disparate larval morphologies the monophyly of the group is questionable (e.g. the B. majori group). Nevertheless, some cases of convergent evolution are apparent, such as the highly specialized Guild C morphology, which may have evolved separately in the B. albipunctatus group, B. mandraka group, and in some species of the B. majori group.

No abstract