Evolutionary Origins of Viviparity in the Reptilia. II. Serpentes, Amphisbaenia, and Ichthyosauria

1985 ◽  
Vol 6 (3) ◽  
pp. 259-291 ◽  
Author(s):  
Daniel G. Blackburn

AbstractSuperimposition of reproductive mode data from the literature over phylogenetic classification systems reveals that viviparity (live-bearing reproduction) has evolved on at least 35 independent occasions among the Serpentes, once in the Amphisbaenia, and once in the Ichthyosauria. Of the ophidian origins of the live-bearing mode, at least fourteen have occurred in the Colubridae, twelve in the Viperidae, three in the Hydrophiidae (used in the sense of Smith et al., 1977), and one in each of the following groups: Boidae, Acrochordidae, Tropidophiidae, Uropeltidae, Typhlopidae, and Elapidae. Previous analysis has distinguished and defined 45 origins of viviparity among the lizards. Here, ten additional saurian origins are recognized on the basis of unpublished and recently published evidence, three in the Iguanidae, two in the Scincidae, and one in each of the following groups: Agamidae, Chamaeleontidae, Anguidae, Xenosauridae, and Anniellidae. As phylogenetic relationships are clarified, further origins seem likely to be detected, particularly in the Colubridae, Hydrophiidae, Scincidae, and Iguanidae. At present, however, at least 92 origins of viviparity can be recognized within the class Reptilia. Reptilian viviparity has arisen on multiple occasions in each of the six major biogeographic regions, with a majority of the origins having occurred in the Old World. Nearly 19% of the extant reptile species are probably live-bearers, including more than 20% of the snakes and over 19% of the lizards. About 71 % of the viviparous species belong to either the Scincidae, Colubridae, Viperidae, or Iguanidae. The discontinuous distribution of the origins of viviparity among the reptilian families supports the hypothesis that selective pressures, preadaptations, and constraints vary at high taxonomic levels.

1982 ◽  
Vol 3 (2) ◽  
pp. 185-205 ◽  
Author(s):  
Daniel G. Blackburn

AbstractReproductive mode data were extracted piecemeal from the literature and superimposed over currently accepted phylogenies to permit estimation of the minimum frequencies with which viviparity (live-bearing) has evolved in lizards, aswell as to facilitateanalysisoffactors hypothesizedto inlluencethis evolution. Viviparity has arisen on at least 45 separate occasions in the Sauria. Each ofthese origins is pinpointed phylogeneticallyas far as is now possible. Ofthese origins, 22 have occurred in the Scincidae, ten in the Iguanidae, five in the Anguidae, two each in the Lacertidae and Gekkonidae, and one each in the Chamaeleontidae, Xantusiidae, Agamidae, and Cordylidae. Further origins may be detected in the Scincidae, Iguanidae, and Diploglossa as phylogenetic relationships are elucidated. Over 19 % of the saurian species are live-bearing, and about 2/3 of the viviparous species are skinks. Most of the sub-generic saurian origins ofviviparity have occurred in cold climates, possibly as an adaptation to facilitate maternal thermoregulation of the developing embryos. Phylogenetic distributions of these origins are consistent with hypotheses that genetic sex-determination of the male-heterogametic type as weil as a tendency towards egg'retention preadapt a lineage for viviparity. Evolution of the live-bearing mode may be constrained by temperature-dependent sex determination, female heterogamety, and formation of highly calcified eggshells.


Taxon ◽  
2010 ◽  
Vol 59 (4) ◽  
pp. 1044-1052 ◽  
Author(s):  
Yin-Zheng Wang ◽  
Rong-Hua Liang ◽  
Bo-Han Wang ◽  
Jia-Mei Li ◽  
Zhi-Jing Qiu ◽  
...  

2012 ◽  
Vol 1 (1) ◽  
Author(s):  
Ming Liu ◽  
Hongjun Liu ◽  
Qixiang Wang ◽  
Shuguang Guan ◽  
Shanshan Ge

1988 ◽  
Vol 34 (4) ◽  
pp. 552-556 ◽  
Author(s):  
Erko Stackebrandt

To establish a hierarchic classification system, ranks cannot be defined by the exclusive and inflexible application of phylogenetic parameters. Because both stability and practicality are prerequisites for a successful system, decisions about the delineation of genera must be made by combining phylogenetic coherency with unifying phenotypic properties of taxonomic value consistent with the needs of a hierarchic system. The phylogenetic depth (age) of a genus has no influence on the decision as long as the members of the genus can be reliably identified as such. The description of those higher taxa that are not easily definable today because of the lack of common phenotypic properties must be postponed until new insights are available. In the end this approach will be both phylogenetic and practical, thus avoiding the use of two classification systems.


Author(s):  
Kevin S. Shah ◽  
Kalyanam Shivkumar ◽  
Mehdi Nojoumi ◽  
Barbara Natterson-Horowitz

Cardiovascular (CV) disease is the leading killer of our species. Various evolutionary lenses can be applied to better understand human vulnerability to CV disorders. The evolutionary origins of a healthy human heart—its myocardial, electrophysiologic, valvular and vascular systems—offers a history of the selective pressures, trade-offs and adaptations leading to the normal mammalian CV systems. Beyond these evolutionary-developmental perspectives, the application of a framework based on Tinbergen’s four questions offers a novel evolutionary lens for understanding our species’ vulnerability to CV pathology. This is done by a consideration of comparative information about non-human animals who spontaneously develop the same CV diseases. This phylogenetic information can then be used to develop trade-off-based adaptive hypotheses to explain the nature and origins of vulnerability to a range of CV pathologies including atherosclerosis, heart failure, valvular heart disease and arrhythmias.


2018 ◽  
Author(s):  
Robert Vander Velde ◽  
Nara Yoon ◽  
Viktoriya Marusyk ◽  
Arda Durmaz ◽  
Andrew Dhawan ◽  
...  

ABSTRACTDespite high initial efficacy, therapies that target oncogenic kinases eventually fail in advanced, metastatic cancers. This failure in initially responsive tumors is the direct result of the evolution of drug resistance under therapy-imposed selective pressures. In contrast to the massive body of experimental research on the molecular mechanisms of resistance, understanding of its evolutionary origins and dynamics remains fragmented. Using a combination of experimental studies and mathematical modeling, we sought to dissect the evolution of resistance to different clinical ALK inhibitors in an experimental model of ALK positive NSCLC. We found that resistance can originate from heterogeneous, weakly resistant, sub-populations with variable sensitivity to different ALK inhibitors. Instead of the commonly assumed stochastic single hit (epi) mutational transition, or drug-induced reprogramming, we found evidence of a hybrid scenario, of gradual, multifactorial development through acquisition of multiple cooperating genetic and epigenetic adaptive changes, amplified by selection. Additionally, we found that intermediate resistance phenotypes might present unique, temporally restricted collateral sensitivities, absent in therapy naïve or fully resistant cells, suggesting new opportunities for therapeutic interference.


2018 ◽  
Author(s):  
Erin I. Garcia ◽  
Michael Emerman

AbstractGenes in the APOBEC3 family encode cytidine deaminases that provide a barrier against viral infection and retrotransposition. Of all APOBEC3 genes in humans, APOBEC3H (A3H) is the most polymorphic: some haplotypes encode stable and active A3H proteins, while others are unstable and inactive. Such variation in human A3H affects interactions with the lentiviral antagonist Vif, which counteracts A3H via proteasomal degradation. In order to broaden our understanding of A3H-Vif interactions as well as its evolution in Old World monkeys, we characterized A3H variation within four African green monkey (AGM) subspecies. We found that A3H is highly polymorphic in AGMs and has lost antiviral activity in multiple Old World monkeys. This loss of function was partially related to protein expression levels but was also influenced by amino acid mutations in the N-terminus. Moreover, we demonstrate that the evolution of A3H in the primate lineages leading to AGMs was not driven by Vif. Our work suggests that activity of A3H is evolutionarily dynamic and may have a negative effect on host fitness, resulting in its recurrent loss in primates.ImportanceAdaptation of viruses to their hosts is critical for transmission of viruses between different species. Previous studies had identified changes in a protein from the APOBEC3 family that influenced species-specificity of simian immunodeficiency viruses (SIVs) in African green monkeys. We studied the evolution of a related protein in the same system, APOBEC3H, which has experienced a loss of function in humans. This evolutionary approach revealed that recurrent loss of APOBEC3H activity has taken place during primate evolution suggesting that APOBEC3H places a fitness cost on hosts. The variability of APOBEC3H activity between different primates highlights the differential selective pressures on the APOBEC3 gene family.


Abiotic variables and biotic interactions can act on variation in life history traits, ultimately leading to divergence in reproductive mode. Marine invertebrates have a remarkable diversity in such strategies, sometimes even between closely related species. It is this natural diversity that lends itself to employing a powerful comparative approach, both for particular morphological characteristics as well as molecular signatures from developmental genes. For example, complex life histories, where a larval stage is interposed between the embryo and juvenile, likely represent the product of numerous selection pressures, historical and current, that have shaped the diversity of larval stages in extant marine species. In fact, the very question about “what is a larva?” has to be addressed, as it is so intimately connected to bentho-planktonic life cycle and metamorphosis. Furthermore, novel larval types have evolved in particular lineages and larvae have been secondarily lost in others. This in itself creates an interesting and exciting playground to test evolutionary developmental hypotheses....


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