Clades Of Snakes Research Articles

Genetic variability and differentiation among the populations of Dice snake, Natrix tessellata (Sepentes, Colubridae) in the Iranian Plateau

The Dice snake, Natrix tessellate, is one of the widely distributed but poorly studied reptiles of the Iranian plateau. Here, we sequenced a partial fragment of Cyt b for 14 samples of Natrix tessellata from Iran. The data were added to the previously published data from GenBank. The phylogenetic analyses indicated that the Iranian populations of N. tessellata are well divided into two major clades. The north, eastern and NE populations of Dice snake in Iran in an association with the Central Asian populations constitute the first clade which is in turn a sister clade to the European populations. The other clade that is placed in the base of the whole Dice snake clade, is formed by the southern and western Iranian populations. These are separated from the first group with high bootstrap and posterior probability values. Position of the western and southern Iranian populations in the phylogenetic tree and its close relation to the N. natrix samples, included in the analyses, imply that the group is most ancient among all populations of Dice snake in the Palearctic region with a long history in the area.

Toxin-resistant isoforms of Na+/K+-ATPase in snakes do not closely track dietary specialization on toads

Toads are chemically defended by bufadienolides, a class of cardiotonic steroids that exert toxic effects by binding to and disabling the Na+/K+-ATPases of cell membranes. Some predators, including a number of snakes, have evolved resistance to the toxic effects of bufadienolides and prey regularly on toads. Resistance in snakes to the acute effects of these toxins is conferred by at least two amino acid substitutions in the cardiotonic steroid binding pocket of the Na+/K+-ATPase. We surveyed 100 species of snakes from a broad phylogenetic range for the presence or absence of resistance-conferring mutations. We found that such mutations occur in a much wider range of taxa than previously believed. Although all sequenced species known to consume toads exhibited the resistance mutations, many of the species possessing the mutations do not feed on toads, much less specialize on that food source. This suggests that either there is little performance cost associated with these mutations or they provide an unknown benefit. Furthermore, the distribution of the mutation among major clades of advanced snakes suggests that the origin of the mutation reflects evolutionary retention more than dietary constraint.

Full-Length Venom Protein cDNA Sequences from Venom-Derived mRNA: Exploring Compositional Variation and Adaptive Multigene Evolution.

Envenomation of humans by snakes is a complex and continuously evolving medical emergency, and treatment is made that much more difficult by the diverse biochemical composition of many venoms. Venomous snakes and their venoms also provide models for the study of molecular evolutionary processes leading to adaptation and genotype-phenotype relationships. To compare venom complexity and protein sequences, venom gland transcriptomes are assembled, which usually requires the sacrifice of snakes for tissue. However, toxin transcripts are also present in venoms, offering the possibility of obtaining cDNA sequences directly from venom. This study provides evidence that unknown full-length venom protein transcripts can be obtained from the venoms of multiple species from all major venomous snake families. These unknown venom protein cDNAs are obtained by the use of primers designed from conserved signal peptide sequences within each venom protein superfamily. This technique was used to assemble a partial venom gland transcriptome for the Middle American Rattlesnake (Crotalus simus tzabcan) by amplifying sequences for phospholipases A2, serine proteases, C-lectins, and metalloproteinases from within venom. Phospholipase A2 sequences were also recovered from the venoms of several rattlesnakes and an elapid snake (Pseudechis porphyriacus), and three-finger toxin sequences were recovered from multiple rear-fanged snake species, demonstrating that the three major clades of advanced snakes (Elapidae, Viperidae, Colubridae) have stable mRNA present in their venoms. These cDNA sequences from venom were then used to explore potential activities derived from protein sequence similarities and evolutionary histories within these large multigene superfamilies. Venom-derived sequences can also be used to aid in characterizing venoms that lack proteomic profiles and identify sequence characteristics indicating specific envenomation profiles. This approach, requiring only venom, provides access to cDNA sequences in the absence of living specimens, even from commercial venom sources, to evaluate important regional differences in venom composition and to study snake venom protein evolution.

Are Diet Preferences Associated to Skulls Shape Diversification in Xenodontine Snakes?

Snakes are a highly successful group of vertebrates, within great diversity in habitat, diet, and morphology. The unique adaptations for the snake skull for ingesting large prey in more primitive macrostomatan snakes have been well documented. However, subsequent diversification in snake cranial shape in relation to dietary specializations has rarely been studied (e.g. piscivory in natricine snakes). Here we examine a large clade of snakes with a broad spectrum of diet preferences to test if diet preferences are correlated to shape variation in snake skulls. Specifically, we studied the Xenodontinae snakes, a speciose clade of South American snakes, which show a broad range of diets including invertebrates, amphibians, snakes, lizards, and small mammals. We characterized the skull morphology of 19 species of xenodontine snakes using geometric morphometric techniques, and used phylogenetic comparative methods to test the association between diet and skull morphology. Using phylogenetic partial least squares analysis (PPLS) we show that skull morphology is highly associated with diet preferences in xenodontine snakes.

Postovipositional development of the sand snake Psammophis sibilans (Serpentes:Lamprophiidae) in comparison with other snake species

AbstractCharacterizing and comparing developmental progress across different species helps to interpret how different or similar body forms evolved. We present an embryonic table for the oviparous African Sand Snake Psammophis sibilans from the Lamprophidae family, describing its postovipositional in ovo development. Psammophis is a good model of a genus that is widely distributed in Africa and Asia and includes 22 species. We describe ten embryonic stages based on the development of externally visible morphological characteristics such as; pharyngeal arches, facial processes, eyes, scales, body pigmentation and body colour pattern development. This study discusses the development of this snake and compares it with that of the closely related brown house snake Lamprophis fulliginosus (Lamprophidae) and the medically important venomous cobras Naja haje haje and Naja kaouthia from the sister lineage Elapidae. The distantly related basal snake Python sebae, which displays different morphology and behaviour, was chosen for deeper insight into the evolution of body structures within the snake clade. We found interspecific differences in the relative stage of development of embryonic structures at the time of oviposition and during postovipositional embryonic development. One of the outcomes of this study is that embryonic structures such as the pharyngeal processes, eye pigmentation and scales are interspecifically conservative in regard to timing of morphodifferentiation, while body pigmentation, colour and colour pattern are interspecifically plastic in their temporospatial development.

Diversification rates and phenotypic evolution in venomous snakes (Elapidae)

The relationship between rates of diversification and of body size change (a common proxy for phenotypic evolution) was investigated across Elapidae, the largest radiation of highly venomous snakes. Time-calibrated phylogenetic trees for 175 species of elapids (more than 50% of known taxa) were constructed using seven mitochondrial and nuclear genes. Analyses using these trees revealed no evidence for a link between speciation rates and changes in body size. Two clades (Hydrophis, Micrurus) show anomalously high rates of diversification within Elapidae, yet exhibit rates of body size evolution almost identical to the general elapid ‘background’ rate. Although correlations between speciation rates and rates of body size change exist in certain groups (e.g. ray-finned fishes, passerine birds), the two processes appear to be uncoupled in elapid snakes. There is also no detectable shift in diversification dynamics associated with the colonization of Australasia, which is surprising given that elapids appear to be the first clade of venomous snakes to reach the continent.

The origin of snakes: revealing the ecology, behavior, and evolutionary history of early snakes using genomics, phenomics, and the fossil record.

BackgroundThe highly derived morphology and astounding diversity of snakes has long inspired debate regarding the ecological and evolutionary origin of both the snake total-group (Pan-Serpentes) and crown snakes (Serpentes). Although speculation abounds on the ecology, behavior, and provenance of the earliest snakes, a rigorous, clade-wide analysis of snake origins has yet to be attempted, in part due to a dearth of adequate paleontological data on early stem snakes. Here, we present the first comprehensive analytical reconstruction of the ancestor of crown snakes and the ancestor of the snake total-group, as inferred using multiple methods of ancestral state reconstruction. We use a combined-data approach that includes new information from the fossil record on extinct crown snakes, new data on the anatomy of the stem snakes Najash rionegrina, Dinilysia patagonica, and Coniophis precedens, and a deeper understanding of the distribution of phenotypic apomorphies among the major clades of fossil and Recent snakes. Additionally, we infer time-calibrated phylogenies using both new ‘tip-dating’ and traditional node-based approaches, providing new insights on temporal patterns in the early evolutionary history of snakes.ResultsComprehensive ancestral state reconstructions reveal that both the ancestor of crown snakes and the ancestor of total-group snakes were nocturnal, widely foraging, non-constricting stealth hunters. They likely consumed soft-bodied vertebrate and invertebrate prey that was subequal to head size, and occupied terrestrial settings in warm, well-watered, and well-vegetated environments. The snake total-group – approximated by the Coniophis node – is inferred to have originated on land during the middle Early Cretaceous (~128.5 Ma), with the crown-group following about 20 million years later, during the Albian stage. Our inferred divergence dates provide strong evidence for a major radiation of henophidian snake diversity in the wake of the Cretaceous-Paleogene (K-Pg) mass extinction, clarifying the pattern and timing of the extant snake radiation. Although the snake crown-group most likely arose on the supercontinent of Gondwana, our results suggest the possibility that the snake total-group originated on Laurasia.ConclusionsOur study provides new insights into when, where, and how snakes originated, and presents the most complete picture of the early evolution of snakes to date. More broadly, we demonstrate the striking influence of including fossils and phenotypic data in combined analyses aimed at both phylogenetic topology inference and ancestral state reconstruction.Electronic supplementary materialThe online version of this article (doi:10.1186/s12862-015-0358-5) contains supplementary material, which is available to authorized users.

Trophic divergence despite morphological convergence in a continental radiation of snakes.

Ecological and phenotypic convergence is a potential outcome of adaptive radiation in response to ecological opportunity. However, a number of factors may limit convergence during evolutionary radiations, including interregional differences in biogeographic history and clade-specific constraints on form and function. Here, we demonstrate that a single clade of terrestrial snakes from Australia--the oxyuranine elapids--exhibits widespread morphological convergence with a phylogenetically diverse and distantly related assemblage of snakes from North America. Australian elapids have evolved nearly the full spectrum of phenotypic modalities that occurs among North American snakes. Much of the convergence appears to involve the recurrent evolution of stereotyped morphologies associated with foraging mode, locomotion and habitat use. By contrast, analysis of snake diets indicates striking divergence in feeding ecology between these faunas, partially reflecting regional differences in ecological allometry between Australia and North America. Widespread phenotypic convergence with the North American snake fauna coupled with divergence in feeding ecology are clear examples of how independent continental radiations may converge along some ecological axes yet differ profoundly along others.

Reevaluation of the anatomy of the Cenomanian (Upper Cretaceous) hind-limbed marine fossil snakes Pachyrhachis, Haasiophis, and Eupodophis

ABSTRACT New anatomical observations and reinterpretations of previously identified structures have resulted in new taxonomic diagnoses for the fossil hind-limbed marine snakes Pachyrhachis problematicus, Eupodophis descouensi, and Haasiophis terrasanctus. Among the most important conclusions of our study are the following: Haasiophis and Eupodophis show no evidence of possessing a laterosphenoid; Pachyrhachis and Eupodophis do retain a jugal; Haasiophis, like Eupodophis, has chevron bones in the caudal region; Haasiophis has a large number of unfused intercentra along the anterior portion of the precloacal column; the dentary of Pachyrhachis has numerous mental foramina (at least four); Pachyrhachis has at least one sacral vertebra with unfused sacral ribs. To test the effect of our new observations on the phylogenetic relationships of snakes, we ran three phylogenetic analyses using alternative outgroups to polarize the character transformations. The ingroup consisted of all well-preserved fossil snakes from the Cretaceous, the madtsoiids, and taxa that are representative of all major groups of extant snakes. The analyses yielded a series of most parsimonious trees that placed Pachyrhachis, Eupodophis, and Haasiophis either as a series of stem taxa at the base of the radiation of snakes (two analysis), or as members of a clade of fossil snakes that are the sister group of all living alethinopidians (one analysis). SUPPLEMENTAL DATA—Supplemental materials are available for this article for free at www.tandfonline.com/UJVP

Scolecophidia (Serpentes) of the Late Oligocene and Early Miocene, North America, and a fossil history overview

An abundant fossil record of the snake clade Scolecophidia exists in Europe; however, the minute snake is noticeably absent in reports about the North American Paleogene and Neogene. Presented here are four localities from Florida, USA, that contain scolecophidian remains older than the Pleistocene: Thomas Farm (late Early Miocene, Hemingfordian Land Mammal Age, LMA), Live Oak (Oligocene-Miocene transition, latest Arikareean LMA), White Springs 3B (late Arikareean LMA), and Brooksville 2 (Late Oligocene, middle Arikareean LMA). These remains extend their known existence by about 26m.y. and are now the oldest reported scolecophidian remains in North America. Molecular evidence on extant scolecophidians concludes that these tiny snakes have a Gondwanan origin. Interestingly, the oldest record of a scolecophidian is from Europe (Belgium) and dates back to the middle Paleocene (MP 1–5). The earliest African record of the snake clade comes from the Paleocene-Eocene boundary in Morocco. The clade is apparently absent from Europe and Middle East deposits dating from the latest Eocene through to the latest Oligocene (MP 19–30) and to the Early Miocene (MN 4). A portion of this time is known as the booid ‘Dark Period’ which represents an apparent response to global aridization and cooling. Scolecophidians appear to re-emerge into the southern Eurasian record in the Early Miocene (MN 4) and become widely dispersed throughout Europe and Middle East. The fossil record of these minute snakes is largely absent in southern Asia and South America. It is possible that the current lack of a decent fossil scolecophidian record outside of Europe and Middle East is due mainly to a bias in the methodology to recover fossils; wet sieving sediments through<1.0mm mesh is needed to recover the minuscule vertebrae.

Emended diagnosis and phylogenetic relationships of the Upper Cretaceous fossil snake Najash rionegrina Apesteguía and Zaher, 2006

ABSTRACT—The fossil snake Najash rionegrina, from the Cenomanian–Turonian (Upper Cretaceous) of Argentina, is reinterpreted after examination of the type and referred material. The current diagnosis is emended in the light of important considerations that cast doubt on the attribution of type and referred specimens (a braincase, a quadrate, and two dentary/lower jaw fragments) used to systematize this taxon. Alternative interpretations of the anatomy of the sacrum and hind limbs are proposed. Following the reevaluation of the anatomy of the type specimen and the removal from this taxon of the above-mentioned referred material, the phylogenetic position of N. rionegrina was tested in a series of maximum parsimony analyses that included all groups of extant snakes, all best-known fossil snakes (i.e., Pachyrhachis, Haasiophis, Eupodophis, Madtsoiidae, and Dinilysia), and alternative outgroups. Regardless of the outgroup used to polarize the character-state transformations, our phylogenetic analyses found no support for the hypothesis that Najash rionegrina occupies a position as the most basal snake. Depending on the outgroup, Najash is placed (1) in a position basal to all living snakes, but more derived than other fossil forms (most notably Pachyrhachis, Eupodophis, and Haasiophis); or (2) as the most basal representative of a clade of fossil snakes that is the sister group of living snakes; or (3) as the most basal representative of a clade of fossil snakes that is located between the Scolecophidia and the Alethinophidia. SUPPLEMENTAL DATA—Supplemental materials are available for this article for free at www.tandfonline.com/UJVP

New constraints on the evolution of the snake clades Ungaliophiinae, Loxocemidae and Colubridae (Serpentes), with comments on the fossil history of erycine boids in North America

The Medicine Pole Hills of North Dakota, USA, afford an excellent view of an Eocene fauna in the Rocky Mountain interior prior to the climatic deterioration of the earliest Oligocene. I describe the snakes of this locality using 179 isolated vertebrae from all parts of the vertebral column as well as cranial elements. The assemblage comprises four species: (1) a primitive burrowing snake (“anilioid”); (2) a small boid related to Ungaliophiinae (dwarf boas); (3) a mid-sized booid related to Loxocemus (Mexican Burrowing Python); and (4) a colubrid. The dwarf boa, Calamagras weigeli, is conservatively regarded as the earliest secure representative of the total clade of Ungaliophiinae, but the history of this clade may stretch considerably further back. The loxocemid, Ogmophis compactus, is only the second reported fossil of that clade. The colubrid is one of the earliest known and could represent the first appearance of colubrine “racers” in North America; it may have had an elongate tail, but this is not yet statistically clear. Full-column analysis and cranial elements prove crucial for the accurate higher-level identification of snake clades from which these isolated elements derive. The past assignment of most North American Paleogene taxa to Erycinae (sand boas) is further undone in this work; there is no well-founded record of an erycine in North America prior to the Miocene.

Mitochondrial DNA sequences suggest unexpected phylogenetic position of Corso-Sardinian grass snakes (Natrix cetti) and do not support their species status, with notes on phylogeography and subspecies delineation of grass snakes

We supplement a previously published mitochondrial DNA data set of grass snake sequences (ND1, ND2, ND4, cyt b, in total 3,806 bp) with sequences of Corso-Sardinian and Tuscan specimens and infer their phylogeny using Bayesian, maximum likelihood and maximum parsimony methods. In addition, we estimate divergence times of grass snake clades using a relaxed molecular clock calibrated with fossil evidence, and, in a second approach, the post-Messinian reopening of the Strait of Gibraltar. Recently it was suggested that Corso-Sardinian grass snakes represent a distinct species: Natrix cetti. All tree-building methods revealed well-supported branching patterns and deep divergences among grass snakes. However, sequences of N. natrix were consistently paraphyletic with respect to Corso-Sardinian sequences. The sister group of Corso-Sardinian grass snakes is a clade embracing N. n. helvetica and N. n. lanzai. Extensive gene flow between N. n. helvetica and a more distantly related subspecies (N. n. natrix) is well known, which is why we conclude that the status of Corso-Sardinian grass snakes as subspecies of N. natrix should be reinstated. Many currently recognized grass snake subspecies conflict with mitochondrial clades, suggestive of inappropriate morphological taxon delineation and mitochondrial introgression. Divergences among grass snakes are old, and the results of the two independent dating approaches are largely congruent. Accordingly, the Alpine orogenesis seems to have caused the origin of the oldest clade, corresponding to Iberian N. n. astreptophora. The formation of Corso-Sardinian grass snakes was dated to the Early Pliocene and could result from post-Messinian flooding of the Mediterranean Basin. Another deeply divergent clade of approximately the same age, endemic in central and northern Europe, suggests the Pleistocene survival of grass snakes north of the Alps. At least one glacial refuge in which old lineages survived Pleistocene cold periods was located on each of the three major southern European peninsulas and in Anatolia. Due to pronounced sequence divergences among Italian and southern Swiss grass snakes, we hypothesize multiple refugia south of the Alps and in the Apennine Peninsula, and there is evidence for two refuges on the Balkan Peninsula.

Phylogenetic relationships among the Stiletto Snakes (genus Atractaspis) based on external morphology

Stiletto Snakes (genus Atractaspis) are the most poorly studied of the three clades of snakes with front-fanged venom-delivery systems. Fossorial and endemic to Africa and the Middle East, Atractaspis possess uniquely derived mobile fangs that allow them to perform a ‘side-stabbing’ method of envenomation, rather than the frontal strike of most other venomous snakes. While many studies have examined the functional anatomy of these unique fangs, the evolutionary history of Atractaspis has been comparatively neglected by researchers. While several evolutionary hypotheses exist for relationships within the Atractaspididae, no study has focused on the phylogenetic relationships within the genus Atractaspis itself. This study presents the first attempt to reconstruct the phylogenetic history of 14 species within this genus, using external morphological data. Using Macrelaps and Homoroselaps as alternate outgroups, We compare the results of two phylogenies and provide a starting point for an investigation of the evolutionary history of this remarkable yet relatively little-known genus.

Phylogenetic relationships within laticaudine sea snakes (Elapidae)

The sea snake subfamily Laticaudinae consists of a single genus with eight named species, based on morphological characters. We used microsatellite and mitochondrial DNA (mtDNA) data to clarify the adaptive radiation of these oviparous sea snakes in the South Pacific, with special reference to New Caledonia and Vanuatu. A mitochondrial DNA data set (ND4 gene 793bp) was obtained from 345 individuals of the five species of Laticauda sp. sea snakes endemic to the region. Maximum likelihood and Bayesian approaches yielded the same optimal tree topology, identifying two major clades (yellow-banded and blue-banded sea snakes). Although all laticaudine sea snakes rely on small islands as oviposition sites, the two lineages differ in their use of marine vs. terrestrial habitats. A highly aquatic species (Laticauda laticaudata) shows a strong pattern of genetic isolation by distance, implying that the patchy distribution of terrestrial habitats has had little impact on gene flow. The more terrestrial clade (Laticauda colubrina, Laticauda frontalis, Laticauda guineai, Laticauda saintgironsi) shows stronger geographic differentiation in allelic frequencies, associated with island groups rather than with geographic distance. Microsatellites and mtDNA suggest that L. frontalis (restricted to Vanuatu) represents a recent founder-induced speciation event, from allopatric migrants of the New Caledonian taxon L. saintgironsi. A major divergence in speciation patterns between the two major clades of laticaudine snakes thus correlates with (and perhaps, is driven by) differences in the importance of terrestrial habitats in the species’ ecology.

Ventral and sub-caudal scale counts are associated with macrohabitat use and tail specialization in viperid snakes

Viperids are a species rich clade of snakes that vary greatly in both morphology and ecology. Many species in the family express tail specializations used for defensive warnings, prey lures, and stability during locomotion and striking. To examine the relationships among ecology, behavior, and vertebral number in the family Viperidae, morphological data (maximum total length and the number of pre-cloacal and caudal vertebrae), macrohabitat use, and tail specialization for 157 viperids were gleaned from published sources. A composite tree topology was constructed from multiple published viperid phylogenies for independent contrasts analysis. The number of vertebrae was strongly correlated with the total length of the snake. Results of both non-phylogenetic and phylogenetically corrected analysis showed that macrohabitat use did not strongly influence total snake length. However, the number of vertebrae per unit length did vary among species according to macrohabitat. Specifically, vertebral density increased with increasing arboreality. Overall, viperids showed a positive correlation between the number of caudal and pre-cloacal vertebrae, but separately rattlesnakes had a significant negative correlation. Species with prehensile tails and those that caudal lure had the most caudal vertebrae. The increased caudal segments of prehensile and luring tails likely improve performance when grasping small vegetation for support or imitating invertebrate prey. These results illustrate that vertebral number is a primary characteristic involved in the diversification of viper species and ecology.

Using regional comparative phylogeographic data from snake lineages to infer historical processes in Middle America

Understanding how historical processes have either similarly, or differentially, shaped the evolution of lineages or biotic assemblages is important for a broad spectrum of fields. Gaining such understanding can be particularly challenging, however, especially for regions that have a complex geologic and biological history. In this study we apply a broad comparative approach to distill such regional biogeographic perspectives, by characterizing sets of divergence times for major biogeographic boundaries estimated from multiple codistributed lineages of snakes. We use a large combined (mitochondrial gene sequence) phylogeographic/phylogenetic dataset containing several clades of snakes that range across Middle America – the tropical region between Mexico and northwestern South America. This region is known for its complex tectonic history, and poorly understood historical biogeography. Based on our results, we highlight how phylogeographic transition zones between Middle and South America and the Nicaragua Depression appear to have undergone multiple episodes of diversification in different lineages. This is in contrast to other examples we find where apparently a single vicariant period is shared across multiple lineages. We specifically evaluate the distributions of divergence time estimates across multiple lineages and estimate the number of temporal periods of lineage diversification per biogeographic break. Overall, our results highlight a great deal of shared temporal divergence, and provide important hypotheses for yet unstudied lineages. These multi‐lineage comparisons across multiple spatial and temporal scales provide excellent predictive power for identifying the roles of geology, climate, ecology and natural history in shaping regional biodiversity.

Ecological and evolutionary components of body size: geographic variation of venomous snakes at the global scale

Biogeographical patterns of animal body size and the environmental and evolutionary mechanisms that may be driving them have been broadly investigated in macroecology, although just barely in ectotherms. We separately studied two snake clades, Viperidae and Elapidae, and used phylogenetic eigenvector regression and ordinary least squares multiple regression methods to perform a global grid-based analysis of the extent at which the patterns of body size (measured for each species as its log10-transformed maximum body length) of these groups are phylogenetically structured or driven by current environment trends. Phylogenetic relatedness explained 20% of the across-species size variation in Viperidae, and 59% of that of Elapidae, which is a more recent clade. Conversely, when we analysed spatial trends in mean body size values (calculated for each grid-cell as the average size of its extant species), an environmental model including temperature, precipitation, primary productivity (as indicated by the global vegetation index) and topography (range in elevation) explained 37.6% of the variation of Viperidae, but only 4.5% of that of Elapidae. These contrasted responses of body size patterns to current environment gradients are discussed, taking into consideration the dissimilar evolutionary histories of these closely-related groups. Additionally, the results obtained emphasize the importance of the need to start adopting deconstructive approaches in macroecology. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 98, 94-109. ADDITIONAL KEYWORDS: Bergmann's rule - ectotherms - interspecific variation - model selection - niche conservatism - phylogenetic eigenvector regression - snakes.

Global conservation strategies for two clades of snakes: combining taxon‐specific goals with general prioritization schemes

AbstractAim We present the first attempt of mapping global conservation priorities for two snake clades, Viperidae and Elapidae. We compared the global conservation priorities of each clade with the nine global conservation schemes defined by Brooks et al. to evaluate how effective these schemes are in ensuring the preservation of viperid and elapid biodiversity.Location Global.Methods Based on range maps of 228 species of Viperidae and 224 species of Elapidae, we used systematic conservation planning methods of complementarity and irreplaceability to generate a set of conservation networks under two cost scenarios: (1) minimizing conservation‐human development conflicts and (2) maximizing environmental suitability for high snake richness. Analysis of variance was used to investigate whether the mean irreplaceability of cells matching the areas covered by each of the nine global prioritization schemes in Brooks et al. was higher than the mean irreplaceability of cells located outside these areas.Results Overall, few areas showed irreplaceability higher than 0.5 based on a goal of representing 25% of the species’ ranges. The conservation networks generated in expectation of low conflicts between human development and conservation were quite different from the networks of high environmental suitability. Areas with higher irreplaceability coincided with the regions covered by global schemes of Endemic Bird Areas (for Viperidae and Elapidae) and High‐Biodiversity Wilderness (for Elapidae).Main conclusions Our findings indicated the existence of viable conservation opportunities for these two snake groups. This study can be viewed as a way to overcome, at least in part, the recent criticism concerning the independent development of several global conservation priorities by evaluating which groups of organisms are better represented in each of them. More than simply determining priorities for snakes’ conservation, our analyses showed that the development of parallel priority‐setting initiatives can be reconciled with those strategies for which financial resources are already being designed.

Global richness patterns of venomous snakes reveal contrasting influences of ecology and history in two different clades

Recent studies addressing broad-scale species richness gradients have proposed two main primary drivers: contemporary climate and evolutionary processes (differential balance between speciation and extinction). Here, we analyze the global richness patterns of two venomous snake clades, Viperidae and Elapidae. We used ordinary least squares multiple regression (OLS) and partial regression analysis to investigate to what extent actual evapotranspiration (AET; summarizing current environmental conditions) and biogeographical regions (representing evolutionary effects) were associated with species richness. For viperids, AET explained 45.6% of the variance in richness whereas the effect of this variable for elapids was almost null (0.5%). On the other hand, biogeographic regions were the best predictors of elapid richness (56.5%), against its relatively small effect (25.9%) in viperid richness. Partial regressions also revealed similar patterns for independent effects of climate and history in both clades. However, the independent historical effect in Elapidae decreased from 45.2 to 17.8% when we excluded Australia from the analyses, indicating that the strong historical effect that had emerged for the global richness pattern was reflecting the historical process of elapid radiation into Australia. Even after excluding Australia, the historical signal in elapid richness in the rest of the globe was still significant and much higher than that observed in viperid richness at a global scale (2.7% after controlling for AET effects). Differences in the evolutionary age of these two clades can be invoked to explain these contrasting results, in that viperids probably had more time for diversification, generating richness responses to environmental gradients, whereas the pattern of distribution of elapid richness can be more directly interpreted in an evolutionary context. Moreover, these results show the importance of starting to adopt deconstructive approaches to species richness, since the driving factors of these patterns may vary from group to group according to their evolutionary history.