The identity of the Chilean Amphibians collected by the United States exploring expedition.

Between mid-May and early June of 1839, members of the United States Exploring Expedition collected diverse anurans in the environs of Valparaíso, Chile, later described by Girard in 1853. Of this set of species, Metaeus timidus, described there as a new genus and species, attracts attention because is a name that practically disappeared from the herpetological literature. Its identification, along with that of the other Chilean taxa collected by the USEE (Cystignathus nebulosus Girard, 1853, Pleurodema bibroni Tschudi, 1838, Pleurodema elegans Bell, 1843, Bufo lugubrosus Girard, 1853, Bufo thaul Lesson, 1826 and Metaeus timidus Girard, 1853) are the main objectives of this contribution.

Anuran forelimb muscle tendinous structures and their relationship with locomotor modes and habitat use.

The interaction between organisms and their environment is central in functional morphology. Differences in habitat usage may imply divergent morphology of locomotor systems; thus, detecting which morphological traits are conservative across lineages and which ones vary under environmental pressure is important in evolutionary studies. We studied internal and external morphology in 28 species of Neotropical anurans. Our aim was to determine if internal morphology (muscle and tendons) shows lower phylogenetic signal than external morphology. In addition, we wanted to know if morphology varies in relation to the habitat use and if there are different functional groups. We found differences in the degree of phylogenetic signal on the groups of traits. Interestingly, postaxial regions of the forelimb are evolutionarily more labile than the preaxial regions. Phylomorphospace plots show that arboreal (jumpers and graspers) and swimmer frogs cluster based on length of fingers and the lack of sesamoid, also reflected by the use of habitat. These functional clusters are also related to phylogeny. Sesamoid and flexor plate dimensions together with digit tendons showed to be important to discriminate functional groups as well as use of habitat classification. Our results allow us to identify a "grasping syndrome" in the hand of these frogs, where palmar sesamoid and flexor plate are absent and a third metacarpal with a bony knob are typical. Thus, a lighter skeleton, long fingers and a prensile hand may be key for arboreality.

On the identity of Bufo diptychus Cope, 1862 (Anura: Bufonidae).

The enigmatic toad Bufo diptychus was described by Cope (1862) based on a single individual (USNM 5841, now lost) of about 25 mm of SVL, collected during the expedition to La Plata River and tributaries, conducted by Captain Page between 1853 and 1856. As no dwarf species of toad was ever recorded in the surveyed area, and based on some tips that arise from Page's narrative, we postulate that the description was based on a toadlet. With this hypothesis in mind, we compared Cope's characterization of B. diptychus with juveniles of all species of Rhinella present in the region, finding an exact match in almost all characters shown by the juveniles of the common "cururú" or "rococo" toad, Rhinella schneideri (Werner 1894). Henceforth, we postulate that R. schneideri is a junior synonym of B. diptychus, under the combination Rhinella diptycha (Cope 1862).

The Skull of Phyllomedusa sauvagii (Anura, Hylidae).

The hylid genus Phyllomedusa comprises charismatic frogs commonly known as monkey, leaf or green frogs, and is the most diverse genus of the subfamily Phyllomedusinae, including about 31 species. Although there is some information about the anatomy of these frogs, little is known about the osteology. Here the adult skull of Phyllomedusa sauvagii, both articulated and disarticulated, is described and the intraspecific variation is reported. Additionally, cartilage associated with the adult skull, such as the nasal capsules, auditory apparatus, and hyobranchial apparatus, are included in the analysis. Further examination of disarticulated bones reveals their remarkable complexity, specifically in the sphenethmoid and of the oocipital region. The description of disarticulated bones is useful for the identification of fossil remains as well as providing morphological characteristics that are phylogenetically informative. When comparing the skull morphology with the available information of other species of the genus, Phyllomesusa sauvagii skull resembles more that of P. vaillantii and P. venusta than P. atelopoides.

Comments on the type locality, type series, and geographic distribution of Pseudopaludicola falcipes (Hensel, 1867) (Amphibia, Anura).

The genus Pseudopaludicola was erected by Miranda-Ribeiro, 1926 to accommodate Liuperus falcipes Hensel, 1867a. Currently, there are 18 recognized species of Pseudopaludicola, with 45% of the species described since 2003. Although Pseudopaludicola falcipes is the type species, Hensel's description lacked designation of type specimens for that species; furthermore, it was based on a series of 30 individuals (without collection numbers or indication of where were they deposited) from "Provinz S[ão]. Pedro do Rio Grande do Sul" (today Rio Grande do Sul State, Brazil).

The identity of Rana margaritifera Laurenti, 1768 (Anura, Bufonidae).

Rana margaritifera was described by Laurenti in 1768 and currently is associated to the genus Rhinella, under the combination Rhinella margaritifera. Currently, the R. margaritifera species group consists of 16 recognized species. Furthermore, many additional species have been suggested to exist in this group which highlights the ambiguity surrounding the identity of Rhinella margaritifera and impend further description of the species in this group. After an exhaustive bibliographic review, we concluded that the recent designation of a lectotype for R. margaritifera is invalid according with Art. 73, ICZN, 1999. Herein, we designate and provide the description of a neotype for Rana margaritifera Laurenti, 1768.

The identity of Rana lutea Molina, 1782 (Amphibia, Anura).

Rana lutea is one of the two anuran species described in 1782 by the Chilean born priest and naturalist Juan Ignacio Molina, and its nomenclatural history is confusing. After a detailed revision of the pertinent literature, we demonstrate that Bufo thaul Schneider, 1799, is a junior objective synonym of Rana lutea Molina, 1782, but based on the usage of both nomina, we revert the precedence and consider Rana lutea Molina, 1782 as a nomen oblitum whereas Bufo thaul Schneider, 1799 is a nomen protectum. Thus, the authorship of the species currently known as Pleurodema thaul (Lesson, 1826) changes to Pleurodema thaul (Schneider, 1799).

Nomenclatural and taxonomic problems related to the electronic publication of new nomina and nomenclatural acts in zoology, with brief comments on optical discs and on the situation in botany.

In zoological nomenclature, to be potentially valid, nomenclatural novelties (i.e., new nomina and nomenclatural acts) need first to be made available, that is, published in works qualifying as publications as defined by the International Code of zoological Nomenclature ("the Code"). In September 2012, the Code was amended in order to allow the recognition of works electronically published online after 2011 as publications available for the purpose of zoological nomenclature, provided they meet several conditions, notably a preregistration of the work in ZooBank. Despite these new Rules, several of the long-discussed problems concerning the electronic publication of new nomina and nomenclatural acts have not been resolved. The publication of this amendment provides an opportunity to discuss some of these in detail. It is important to note that: (1) all works published only online before 2012 are nomenclaturally unavailable; (2) printed copies of the PDFs of works which do not have their own ISSN or ISBN, and which are not obtainable free of charge or by purchase, do not qualify as publications but must be seen as facsimiles of unavailable works and are unable to provide nomenclatural availability to any nomenclatural novelties they may contain; (3) prepublications online of later released online publications are unavailable, i.e., they do not advance the date of publication; (4) the publication dates of works for which online prepublications had been released are not those of these prepublications and it is critical that the real release date of such works appear on the actual final electronic publication, but this is not currently the case in electronic periodicals that distribute such online prepublications and which still indicate on their websites and PDFs the date of release of prepublication as that of publication of the work; (5) supplementary online materials and subsequent formal corrections of either paper or electronic publications distributed only online are nomenclaturally unavailable; (6) nomenclatural information provided on online websites that do not have a fixed content and format, with ISSN or ISBN, is unavailable. We give precise examples of many of these nomenclatural problems. Several of them, when they arise, are due to the fact that the availability of nomenclatural novelties now depends on information that will have to be sought not from the work itself but from extrinsic evidence. As shown by several examples discussed here, an electronic document can be modified while keeping the same DOI and publication date, which is not compatible with the requirements of zoological nomenclature. Therefore, another system of registration of electronic documents as permanent and inalterable will have to be devised. ZooBank also clearly needs to be improved in several respects. Mention in a work of its registration number (LSID) in ZooBank would seem to be possible only if this registration has occurred previously, but some works that have purportedly been registered in ZooBank are in fact missing on this web application. In conclusion, we offer recommendations to authors, referees, editors, publishers, libraries and the International Commission on Zoological Nomenclature, in the hope that such problems can be limited along with the potential chaos in zoological nomenclature that could result, if careful attention is not paid to the problems we highlight here, from a somewhat misplaced, and perhaps now widespread, understanding that electronic publication of nomenclatural novelties is now allowed and straightforward. We suggest that, as long as the problematic points linked to the new amendment and to electronic publication as a whole are not resolved, nomenclatural novelties continue to be published in paper-printed journals that have so far shown editorial competence regarding taxonomy and nomenclature, which is not the case of several recent electronic-only published journals.

A phylogenetic analysis of Pleurodema (Anura: Leptodactylidae: Leiuperinae) based on mitochondrial and nuclear gene sequences, with comments on the evolution of anuran foam nests.

Species of the genus Pleurodema are relatively small, plump frogs that mostly occur in strong-seasonal and dry environments. The genus currently comprises 14 species distributed from Panama to southern Patagonia. Here we present a phylogenetic analysis of Pleurodema, including all described species and several outgroups. Our goals include testing its monophyly and the monophyly of the species groups that were historically proposed, and studying the evolution of some character systems, particularly macroglands and egg-clutch structure; this last point also provided the chance for a discussion of foam nest evolution in anurans. Our dataset includes portions of the mitochondrial genes cytochromeb, 12S, 16S, and the intervening tRNAVal ; the nuclear gene sequences include portions of rhodopsin exon 1 and seven in absentia homolog I. Our results support a clade composed of Pleurodema and including the monotypic SomuncuriaLynch, 1978 nested within it. The latter genus is therefore considered a junior synonym of Pleurodema and its sole species is added to this genus. Furthermore, our results indicate the non-monophyly of several species groups proposed previously. We recognize four clades in Pleurodema: the P. bibroni clade (P. bibroni, P. cordobae and P. kriegi), the P. thaul clade (P. bufoninum, P. marmoratum, P. somuncurensis and P. thaul), the P. brachyops clade (P. alium, P. borellii, P. brachyops, P. cinereum, P. diplolister and P. tucumanum) and the P. nebulosum clade (P. guayapae and P. nebulosum). Our results further indicate the need for a taxonomic reassessment of P. borellii and P. cinereum (as did previous studies), P. guayapae and P. nebulosum, and the three species in the P. bibroni clade. Pleurodema shows a striking pattern of variation in presence/absence of lumbar glands. Our results indicate multiple losses or independent gains of this character associated with defensive displays. The reproductive modes of Pleurodema include four different egg-clutch structures. The optimization of these indicates that there are at least two independent transformations from the plesiomorphic mode of foam nests to egg-clutch structures involving gelatinous masses of different sorts (ovoid plates, masses, or strings). We hypothesize that these independent transformations could involve changes at the behavioural (the loss of foam beating behaviour by the parent) and/or structural level (transformations involving the pars convoluta dilata, the section of the oviduct where the foam-making substance is secreted). Finally, our study of foam nest evolution in Pleurodema is extended to the other groups of anurans where foam-nesting occurs, on the basis of available data and recent phylogenetic hypotheses. In the different hyloid groups where it occurs, foam-nesting evolved from clutches laid in water. However, in all ranoids in which foam-nesting occurs, it evolved from terrestrial clutches, with eggs laid hanging in vegetation, or, if the clutches are laid on a restricted volume of water, involving endotrophic development. © The Willi Hennig Society 2012.

First record of chytridiomycosis in Bolivia (Rhinella quechua; Anura: Bufonidae).

The finding of tadpoles of Rhinella quechua (Huayramayu River, Carrasco National Park, Cochabamba, Bolivia) with oral abnormalities caused by Batrachochytrium dendrobatidis constitutes the first record of this fungal infection reported for Bolivian amphibians.