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Parallel Evolution (parallel + evolution)
Selected AbstractsHistorical Parallel Evolution of Injury Prevention and Control Science and Emergency MedicineACADEMIC EMERGENCY MEDICINE, Issue 11 2009Federico E. Vaca MD First page of article [source] Parallel evolution of larval morphology and habitat in the snail-killing fly genus TetanoceraJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2006E. G. CHAPMAN Abstract In this study, we sequenced one nuclear and three mitochondrial DNA loci to construct a robust estimate of phylogeny for all available species of Tetanocera. Character optimizations suggested that aquatic habitat was the ancestral condition for Tetanocera larvae, and that there were at least three parallel transitions to terrestrial habitat, with one reversal. Maximum likelihood analyses of character state transformations showed significant correlations between habitat transitions and changes in four larval morphological characteristics (cuticular pigmentation and three characters associated with the posterior spiracular disc). We provide evidence that phylogenetic niche conservatism has been responsible for the maintenance of aquatic-associated larval morphological character states, and that concerted convergence and/or gene linkage was responsible for parallel morphological changes that were derived in conjunction with habitat transitions. These habitat,morphology associations were consistent with the action of natural selection in facilitating the morphological changes that occurred during parallel aquatic to terrestrial habitat transitions in Tetanocera. [source] New Phylogenetic Analysis of the Family Elephantidae Based on Cranial-Dental Morphology,THE ANATOMICAL RECORD : ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY, Issue 1 2010Nancy E. Todd Abstract In 1973, Vincent Maglio published a seminal monograph on the evolution of the Elephantidae, in which he revised and condensed the 100+ species named by Henry Fairfield Osborn in 1931. Michel Beden further revised the African Elephantidae in 1979, but little systematic work has been done on the family since this publication. With addition of new specimens and species and revisions of chronology, a new analysis of the phylogeny and systematics of this family is warranted. A new, descriptive character dataset was generated from studies of modern elephants for use with fossil species. Parallel evolution in cranial and dental characters in all three lineages of elephants creates homoplastic noise in cladistic analysis, but new inferences about evolutionary relationships are possible. In this analysis, early Loxodonta and early African Mammuthus are virtually indistinguishable in dental morphology. The Elephas lineage is not monophyletic, and results from this analysis suggest multiple migration events out of Africa into Eurasia, and possibly back into Africa. New insight into the origin of the three lineages is also proposed, with Stegotetrabelodon leading to the Mammuthus lineage, and Primelephas as the ancestor of Loxodonta and Elephas. These new results suggest a much more complex picture of elephantid origins, evolution, and paleogeography. Anat Rec, 2010. © 2009 Wiley-Liss, Inc. [source] Morphological divergence of North-European nine-spined sticklebacks (Pungitius pungitius): signatures of parallel evolutionBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 2 2010GÁBOR HERCZEG Parallel evolution is characterised by repeated, independent occurrences of similar phenotypes in a given habitat type, in different parts of the species distribution area. We studied body shape and body armour divergence between five marine, four lake, and ten pond populations of nine-spined sticklebacks [Pungitius pungitius (Linnaeus, 1758)] in Fennoscandia. We hypothesized that marine and lake populations (large water bodies, diverse fish fauna) would be similar, whereas sticklebacks in isolated ponds (small water bodies, simple fish fauna) would be divergent. We found that pond fish had deeper bodies, shorter caudal peduncles, and less body armour (viz. shorter/absent pelvic spines, reduced/absent pelvic girdle, and reduced number of lateral plates) than marine fish. Lake fish were intermediate, but more similar to marine than to pond fish. Results of our common garden experiment concurred with these patterns, suggesting a genetic basis for the observed divergence. We also found large variation among populations within habitat types, indicating that environmental variables other than those related to gross habitat characteristics might also influence nine-spined stickleback morphology. Apart from suggesting parallel evolution of morphological characteristics of nine-spined sticklebacks in different habitats, the results also show a number of similarities to the evolution of three-spined stickleback (Gasterosteus aculeatus Linnaeus, 1758) morphology. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 101, 403,416. [source] Parallel evolution of termite-egg mimicry by sclerotium-forming fungi in distant termite groupsBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2010KENJI MATSUURA Among the great diversity of insect,fungus associations, fungal mimicry of termite eggs is a particularly fascinating consequence of evolution. Along with their eggs, Reticulitermes termites often harbour sclerotia of the fungus Fibularhizoctonia sp., called ,termite balls', giving the fungus competitor-free habitat within termite nests. The fungus has evolved sophisticated morphological and chemical camouflage to mimic termite eggs. To date, this striking insect,fungus association has been found in eight temperate termite species, but is restricted to the lower termite genera Reticulitermes and Coptotermes. Here, we report the discovery of a novel type of termite ball (,Z-type') in the subtropical termite, Nasutitermes takasagoensis. Phylogenetic analysis indicated that the Z-type termite ball is an undescribed Trechisporoid fungus, Trechispora sp., that is phylogenetically distant from Fibularhizoctonia, indicating two independent origins of termite-egg mimicry in sclerotium-forming fungi. Egg protection bioassays using dummy eggs revealed that Reticulitermes speratus and N. takasagoensis differ in egg-size preference. A comparative study of termite ball size and egg-size preference of host termites showed that both fungi evolved a termite ball size that optimized the acceptance of termite balls as a unit investment. Termite-egg mimicry by these fungi offers a model case of parallel evolution. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 531,537. [source] Parallel evolution of lichen growth forms in the family Roccellaceae (Arthoniales, Ascomycota)CLADISTICS, Issue 5 2007Anders Tehler The phylogenetic relationships within the family Roccellaceae (lichen fungi) were investigated. Seventy-two nucleotide sequences of the nuclear large subunit ribosomal RNA gene (LSU) and the second largest RNA polymerase subunit (RPB2) were newly obtained from 48 taxa. The family Roccellaceae was highly supported as monophyletic. The fruticose growth habit has evolved or been lost multiple times in the family and several times even within genera. In Roccellina with 31 species it has evolved three times and in Pentagenella with three species it has been lost once. The genera Roccella and Roccellina were found paraphyletic as two Roccella species nested with Roccellina. The non-fruticose genus Roccellina was emended to include these two fruticose species as well as the monotypic, fruticose genus Roccellaria. As a result of the phylogenetic analyses six new nomenclatural combinations were made: Pentagenella corallina (Follm. and Peine) Tehler, Pentagenella ligulata (Peine and Follm.) Tehler, Roccellina cumingiana (Gay) Tehler, Roccellina hypomecha (Ach.) Tehler, Roccellina mollis (Hampe) Tehler, Roccellina portentosa (Mont. ex Gay) Tehler. Roccella is mainly distributed on the northern hemisphere while Roccellina is mainly distributed on the southern hemisphere. The Roccella species present on the Galapagos Islands are related to those in California and the northern hemisphere not, as was generally believed, to those in Chile and the southern hemisphere. The present data set may indicate that Bayesian analysis can give misleading topologies and overestimated posterior support values when insufficiently sampled taxa are included in an otherwise well sampled data set. © The Willi Hennig Society 2007. [source] Human and livestock genetics: parallel evolution and horizontal exchangeJOURNAL OF ANIMAL BREEDING AND GENETICS, Issue 6 2009Chris Haley No abstract is available for this article. [source] Biogeography of Plagiochila (Hepaticae): natural species groups span several floristic kingdomsJOURNAL OF BIOGEOGRAPHY, Issue 7 2003Henk Groth Abstract Aim This paper presents a synthesis of our recent results regarding the biogeography of Plagiochila using a molecular approach, and documents intercontinental ranges within this largest genus of the hepatics. Methods A maximum likelihood analysis of sixty-one nrITS sequences of Plagiochila was performed and the molecular topology obtained was compared with morphological, phytochemical and geographical data. Results Our molecular data set allowed the identification of eleven Plagiochila sections, the majority of which cover at least two floristic kingdoms. Seven sections have species in Europe (sect. Arrectae, Carringtoniae, Fuscoluteae, Glaucescentes, Plagiochila, Rutilantes, Vagae). Plagiochila species from Atlantic Europe are usually close to or conspecific with neotropical taxa, whereas species widespread in Europe are closely related to Asian ones and not to those in the Neotropics. Plagiochila sect. Arrectae represents a neotropical , Atlantic European clade. The section is not closely related , as has often been suggested , to the morphologically similar sect. Zonatae from Asia and western North America. Sequence data show that the African P. integerrima and the neotropical P. subplana are members of the Asian sect. Cucullatae (sect. Ciliatae, syn. nov.), which becomes pantropical in distribution. An ITS sequence of P. boryana from Uganda confirms the Afro-American range of the primarily neotropical sect. Hylacoetes. Similarities in sporophyte morphology between the sect. Cucullatae and sect. Hylacoetes are the result of parallel evolution. Main conclusions Our results indicate that intercontinental ranges at section and species level are common in Plagiochila. Carl's (1931) subdivision of Plagiochila into sections restricted to one floristic kingdom is outdated. Biogeographical patterns in Plagiochila are not dissimilar to those of other groups of bryophytes but elucidation of the geographical ranges of the taxa requires a molecular approach. Contrary to earlier belief, most Plagiochila species from Atlantic Europe do not have close relatives in Asia but are conspecific with or closely related to species from tropical America. [source] Rapid evolution towards heavy metal resistance by mountain birch around two subarctic copper,nickel smeltersJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 2 2008J. K. ERÄNEN Abstract Adaptations to pollution among long-lived trees have rarely been documented, possibly because of their long reproductive cycles and the evolutionarily short timescales of anthropogenic pollution. Here, I present the results of a greenhouse experiment that suggest rapid evolutionary adaptation of mountain birch [Betula pubescens subsp. czerepanovii (Orlova) Hämet-Ahti] to heavy metal (HM) stress around two copper,nickel smelters in NW Russia. The adaptation incurs a cost with reduced performance of adapted seedlings in pristine conditions. The industrial barrens around the studied smelters are extremely high-stress sites with low seed germination and survival. It is likely that strong natural selection has eliminated all sensitive genotypes within one or two generations, with only the most tolerant individuals persisting and producing adapted seeds in the individual barrens. The results were similar from around both smelters, suggesting parallel evolution towards HM resistance. [source] This is not déjà vu all over again: male guppy colour in a new experimental introductionJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2007N. KARIM Abstract We use an experimental introduction in nature to examine factors that influence parallel evolution. In 1996, 200 high-predation guppies (Poecilia reticulata) from the Yarra River were introduced into the Damier River, which previously lacked guppies. Eight years later, we quantified the colour of wild-caught guppies (,phenotypic' divergence) and lab-reared guppies (,genetic' divergence) from low- and high-predation environments in both rivers. Phenotypic and genetic divergence between predation environments within the Yarra was evident for black and for orange. Phenotypic divergence within the Damier was parallel to the Yarra for black but not for orange. Genetic divergence was absent between predation environments within the Damier, but was evident when comparing both Damier populations to their Yarra ancestors. The evolution of male colour thus depends on factors other than the simple contrast between ,high' and ,low' predation. We suggest that the parallel evolution of male signalling traits may sometimes first require the parallel evolution of female preferences. [source] Comparative innervation of cephalic photophores of the loosejaw dragonfishes (Teleostei: Stomiiformes: Stomiidae): Evidence for parallel evolution of long-wave bioluminescenceJOURNAL OF MORPHOLOGY, Issue 4 2010Christopher P. Kenaley Abstract Four genera of the teleost family Stomiidae, the loosejaw dragonfishes, possess accessory cephalic photophores (AOs). Species of three genera, Aristostomias, Malacosteus, and Pachystomias, are capable of producing far-red, long-wave emissions (>650nm) from their AOs, a character unique among vertebrates. Aristostomias and Malacosteus posses a single far-red AO, while Pachystomias possesses anterior and posterior far-red AOs, each with smaller separate photophores positioned in their ventral margins. The purpose of this study was to establish the primary homology of the loosejaw AOs based on topological similarity of cranial nerve innervation, and subject these homology conjectures to tests of congruence under a phylogenetic hypothesis for the loosejaw dragonfishes. On the basis of whole-mount, triple-stained specimens, innervation of the loosejaw AOs is described. The AO of Aristostomias and the anterior AO of Pachystomias are innervated by the profundal ramus of the trigeminal (Tpr), while the far-red AO of Malacosteus and a small ventral AO of Pachystomias are innervated by the maxillary ramus of the trigeminal (Tmx). The largest far-red AO of Pachystomias, positioned directly below the orbit, and the short-wave AO of Photostomias are innervated by a branch of the mandibular ramus of the trigeminal nerve. Conjectures of primary homology drawn from these neuroanatomical similarities were subjected to tests of congruence on a phylogeny of the loosejaws inferred from a reanalysis of a previously published morphological dataset. Optimized for accelerated transformation, the AO innervated by the Tpr appears as a single transformation on the new topology, thereby establishing secondary homology. The AOs innervated by the Tmd found in Pachystomias and Photostomias appear as two transformations in a reconstruction on the new topology, a result that rejects secondary homology of this structure. The secondary homology of AOs innervated by the Tmx found in Malacosteus and Pachystomias is rejected on the same grounds. Two short-wave cephalic photophores present in all four genera, the suborbital (SO) and the postorbital (PO), positioned in the posteroventral margin of the orbit and directly posterior to the orbit, respectively, are innervated by separate divisions of the Tmd. The primary homologies of the loosejaw PO and SO across loosejaw taxa are proposed on the basis of similar innervation patterns. Because of dissimilar innervation of the loosejaw SO and SO of basal stomiiforms, primary homology of these photophores cannot be established. Because of similar function and position, the PO of all other stomiid taxa is likely homologous with the loosejaw PO. Nonhomology of loosejaw long-wave photophores is corroborated by previously published histological evidence. The totality of evidence suggests that the only known far-red bioluminescent system in vertebrates has evolved as many as three times in a closely related group of deep-sea fishes. J. Morphol., 2010. © 2009 Wiley-Liss, Inc. [source] A NEW PARADIGM FOR FRESHWATER FRAGILARIOID DIATOM CLASSIFICATION?JOURNAL OF PHYCOLOGY, Issue 2001A CRITIQUE OF LANGE-BERTALOT'S NEW SYSTEM Morales, E. A.1 & Trainor, F. R.2 1Phycology Section, Patrick Center for Environmental Research, The Academy of Natural Sciences of Philadelphia, PA 19103-1195 USA; 2Department of Ecology & Evolutionary Biology, University of Connecticut, Storrs, CT 06269-3043 USA In a recent study of freshwater diatoms from South America (Rumrich et al. 2000), Lange-Bertalot introduced a new paradigm for the classification of fragilarioid diatoms. This new system is antagonistic to that presented by Williams and Round (1987) because Lange-Bertalot recognizes a marked variability in the characters chosen and a supposed overall continuity of morphological features among the genera created by his English counterparts. Lange-Bertalot then proposes a partitioning of Fragilaria into two genera: Fragilaria and Staurosira mainly based on the presence/absence of rimoportulae and areolate girdle bands. The newly defined Fragilaria includes relatively large phytoplankters such as F. capucina and F. crotonensis. In turn, Staurosira includes, for the most part, small periphytic organisms, and contains several new species that were based on varieties of old Fragilaria taxa. This fragmentation of species and their varieties is based on a supposed morphological discontinuity. As a consequence an apparent increase in species diversity has occurred within the fragilarioid group. The present work analyzes Lange-Bertalot's new paradigm and confronts it with recent LM and SEM evidence. The incorporation of concepts such as plasticity, polymorphism, and parallel evolution in current classification systems is also discussed. It is concluded that Lange-Bertalot's system represents a step backward from that of Williams and Round. Some adjustments in the latter scheme could be sufficient to accommodate the diversity of fragilarioids known at present. [source] Phylogeny of Thalassinidea (Crustacea, Decapoda) inferred from three rDNA sequences: implications for morphological evolution and superfamily classificationJOURNAL OF ZOOLOGICAL SYSTEMATICS AND EVOLUTIONARY RESEARCH, Issue 3 2008L. M. Tsang Abstract The infraorder Thalassinidea is a group of cryptic marine burrowing decapods of which the higher taxonomy is often contentious. The present analysis attempts to reconstruct phylogenetic relationship among 12 of the 13 currently recognized families using partial nuclear 18S, 28S rDNA and mitochondrial 16S rDNA sequences. The infraorder is divided into two distinct clades, with the first clade consisting of Thalassinidae, Laomediidae, Axianassidae and Upogebiidae, and the second clade including Axiidae, Calocarididae, Eiconaxiidae, Callianassidae, Ctenochelidae, Micheleidae, Strahlaxiidae and Callianideidae. Within the first clade, the Upogebiidae is the basal family. The Axianassidae shows low affinity to other laomediid genera indicating that it is a valid family. The interfamilial relationships are less well resolved in the second clade. The Axiidae is paraphyletic with respect to Calocarididae and Eiconaxiidae. Thus, the status of these two latter families is not supported if the currently defined Axiidae is maintained. All three families appear to be basal in the thalassinidean clade. The Micheleidae is closely related to the Callianideidae and they form a sister group to the Strahlaxiidae. The monophyletic Callianassidae aligns with the Micheleidae + Callianideidae + Strahlaxiidae clade. The relationship among the Axiidae + Calocarididae + Eiconaxiidae clade, Callianassidae + Micheleidae + Callianideidae + Strahlaxiidae clade and the Ctenochelidae cannot be resolved which might be due to a rapid radiation of the three lineages. Our results do not support the generally used classification scheme of Thalassinidea and suggest that the infraorder might be divided into two superfamilies instead of three as suggested based on larval morphology, second pereiopod morphology in adults and gastric mill structure. The two superfamilies are Thalassinoidea (i.e. Thalassinidae, Laomediidae, Upogebiidae and Axianassidae) and Callianassoidea (i.e. Axioidea + Callianassoidea, as defined in Martin and Davis (2001) but excluding Laomediidae and Upogebiidae). It also appears that gill-cleaning adaptations are important in thalassinidean evolution while the presence of linea thalassinica is a result of parallel evolution. Résumé L'infraordre des Thalassinidea est un groupe de décapodes marins fouisseurs cryptiques dont la taxonomie au niveau supérieur est souvent controversée. Cette analyse tente de reconstruire les relations phylogénétiques entre 12 familles sur les 13 actuellement reconnues en utilisant les séquences partielles de rDNA nucléaire 18S, 28S et de rDNA mitochondrial 16S. L'infraordre est divisé en deux clades distincts, le premier comprenant les Thalassinidae, Laomediidae, Axianassidae et Upogebiidae, et le deuxième comprenant les Axiidae, Calocarididae, Eiconaxiidae, Callianassidae, Ctenochelidae, Micheleidae, Strahlaxiidae et Callianideidae. Dans le premier clade, les Upogebiidae est la famille basale. Les Axianassidae montre peu d'affinité avec les autres genres de laomedidés, ce qui indique que la famille est valide. Les relations interfamiliales sont moins bien résolues dans le second clade. La famille des Axiidae est paraphylétique par rapport aux Calocarididae et Eiconaxiidae. Ainsi le statut de ces deux dernières familles n'est pas supporté si la famille des Axiidae est maintenue dans sa définition actuelle. Toutes les trois familles apparaissent basales dans le clade thalassinidéen. La famille des Micheleidae est très proche des Callianideidae et elles forment un groupe frère des Strahlaxiidae. La famille monophylétique des Callianassidae s'aligne avec le clade Micheleidae + Callianideidae + Strahlaxiidae. La relation entre le clade Axiidae + Calocarididae + Eiconaxiidae, le clade des Callianassidae + Micheleidae + Callianideidae + Strahlaxiidae et la famille des Ctenochelidae ne peut être résolue, ce qui pourrait être dûà une radiation rapide des trois lignées Nos résultats ne supportent pas le schéma de classification généralement utilisé pour les Thalassinidea et suggèrent que l'infraordre pourrait être divisé en deux superfamilles au lieu de trois comme suggéré sur la base de la morphologie larvaire, de la morphologie du deuxième péréiopode de l'adulte et de la structure du moulin gastrique. Les deux superfamilles sont: les Thalassinoidea (c'est-à-dire Thalassinidae, Laomediidae, Upogebiidae et Axianassidae) et Callianassoidea (c'est-à-dire Axioidea + Callianassoidea, comme définis dans Martin et Davis 2001 mais excluant les Laomediidae et les Upogebiidae). Il apparaît aussi que les adaptations pour le nettoyage des branchies sont importantes dans l'évolution thalassinidéenne alors que la présence de la linea thalassinica est le résultat d'une évolution parallèle. [source] Diversification on an ecologically constrained adaptive landscapeMOLECULAR ECOLOGY, Issue 12 2008GARY A. WELLBORN Abstract We used phylogenetic analysis of body-size ecomorphs in a crustacean species complex to gain insight into how spatial complexity of ecological processes generates and maintains biological diversity. Studies of geographically widespread species of Hyalella amphipods show that phenotypic evolution is tightly constrained in a manner consistent with adaptive responses to alternative predation regimes. A molecular phylogeny indicates that evolution of Hyalella ecomorphs is characterized by parallel evolution and by phenotypic stasis despite substantial levels of underlying molecular change. The phylogeny suggests that species diversification sometimes occurs by niche shifts, and sometimes occurs without a change in niche. Moreover, diversification in the Hyalella ecomorphs has involved the repeated evolution of similar phenotypic forms that exist in similar ecological settings, a hallmark of adaptive evolution. The evolutionary stasis observed in clades separated by substantial genetic divergence, but existing in similar habitats, is also suggestive of stabilizing natural selection acting to constrain phenotypic evolution within narrow bounds. We interpret the observed decoupling of genetic and phenotypic diversification in terms of adaptive radiation on an ecologically constrained adaptive landscape, and suggest that ecological constraints, perhaps acting together with genetic and functional constraints, may explain the parallel evolution and evolutionary stasis inferred by the phylogeny. [source] The origins of weedy riceMOLECULAR ECOLOGY, Issue 21 2007NOLAN C. KANE Abstract Where do weeds come from? How do they evolve from nonweedy ancestors? In this issue of Molecular Ecology, Londo and Schaal examine the origin of weedy rice (Oryza sativa) populations in the USA. Analysing nuclear DNA sequence and microsatellite data, they show the importance of parallel evolution, hybridization, gene flow, and migration in the evolution of these weeds. [source] Structure of the cerebral cortex of the humpback whale, Megaptera novaeangliae (Cetacea, Mysticeti, Balaenopteridae)THE ANATOMICAL RECORD : ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY, Issue 1 2007Patrick R. Hof Abstract Cetaceans diverged from terrestrial mammals between 50 and 60 million years ago and acquired, during their adaptation to a fully aquatic milieu, many derived features, including echolocation (in odontocetes), remarkable auditory and communicative abilities, as well as a complex social organization. Whereas brain structure has been documented in detail in some odontocetes, few reports exist on its organization in mysticetes. We studied the cerebral cortex of the humpback whale (Megaptera novaeangliae) in comparison to another balaenopterid, the fin whale, and representative odontocetes. We observed several differences between Megaptera and odontocetes, such as a highly clustered organization of layer II over the occipital and inferotemporal neocortex, whereas such pattern is restricted to the ventral insula in odontocetes. A striking observation in Megaptera was the presence in layer V of the anterior cingulate, anterior insular, and frontopolar cortices of large spindle cells, similar in morphology and distribution to those described in hominids, suggesting a case of parallel evolution. They were also observed in the fin whale and the largest odontocetes, but not in species with smaller brains or body size. The hippocampal formation, unremarkable in odontocetes, is further diminutive in Megaptera, contrasting with terrestrial mammals. As in odontocetes, clear cytoarchitectural patterns exist in the neocortex of Megaptera, making it possible to define many cortical domains. These observations demonstrate that Megaptera differs from Odontoceti in certain aspects of cortical cytoarchitecture and may provide a neuromorphologic basis for functional and behavioral differences between the suborders as well as a reflection of their divergent evolution. Anat Rec, 290:1,31, 2007. © 2006 Wiley-Liss, Inc. [source] Origin and evolution of chromosomal sperm proteinsBIOESSAYS, Issue 10 2009José M. Eirín-López Abstract In the eukaryotic cell, DNA compaction is achieved through its interaction with histones, constituting a nucleoprotein complex called chromatin. During metazoan evolution, the different structural and functional constraints imposed on the somatic and germinal cell lines led to a unique process of specialization of the sperm nuclear basic proteins (SNBPs) associated with chromatin in male germ cells. SNBPs encompass a heterogeneous group of proteins which, since their discovery in the nineteenth century, have been studied extensively in different organisms. However, the origin and controversial mechanisms driving the evolution of this group of proteins has only recently started to be understood. Here, we analyze in detail the histone hypothesis for the vertical parallel evolution of SNBPs, involving a "vertical" transition from a histone to a protamine-like and finally protamine types (H,,,PL,,,P), the last one of which is present in the sperm of organisms at the uppermost tips of the phylogenetic tree. In particular, the common ancestry shared by the protamine-like (PL)- and protamine (P)-types with histone H1 is discussed within the context of the diverse structural and functional constraints acting upon these proteins during bilaterian evolution. [source] Morphological divergence of North-European nine-spined sticklebacks (Pungitius pungitius): signatures of parallel evolutionBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 2 2010GÁBOR HERCZEG Parallel evolution is characterised by repeated, independent occurrences of similar phenotypes in a given habitat type, in different parts of the species distribution area. We studied body shape and body armour divergence between five marine, four lake, and ten pond populations of nine-spined sticklebacks [Pungitius pungitius (Linnaeus, 1758)] in Fennoscandia. We hypothesized that marine and lake populations (large water bodies, diverse fish fauna) would be similar, whereas sticklebacks in isolated ponds (small water bodies, simple fish fauna) would be divergent. We found that pond fish had deeper bodies, shorter caudal peduncles, and less body armour (viz. shorter/absent pelvic spines, reduced/absent pelvic girdle, and reduced number of lateral plates) than marine fish. Lake fish were intermediate, but more similar to marine than to pond fish. Results of our common garden experiment concurred with these patterns, suggesting a genetic basis for the observed divergence. We also found large variation among populations within habitat types, indicating that environmental variables other than those related to gross habitat characteristics might also influence nine-spined stickleback morphology. Apart from suggesting parallel evolution of morphological characteristics of nine-spined sticklebacks in different habitats, the results also show a number of similarities to the evolution of three-spined stickleback (Gasterosteus aculeatus Linnaeus, 1758) morphology. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 101, 403,416. [source] Tracking island colonization history and phenotypic shifts in Indian Ocean bulbuls (Hypsipetes: Pycnonotidae)BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2005BEN H. WARREN Molecular phylogenies of island organisms provide useful systems for testing hypotheses of convergent or parallel evolution, since selectively neutral molecular characters are likely to be independent of phenotype, and the existence of similar environments on multiple isolated islands provides numerous opportunities for populations to evolve independently under the same constraints. Here we construct a phylogenetic hypothesis for Hypsipetes bulbuls of the western Indian Ocean, and use this to test hypotheses of colonization pattern and phenotypic change among islands of the region. Mitochondrial sequence data were collected from all extant taxa of the region, combined with sequence data from relevant lineages in Asia. Data are consistent with a single Hypsipetes colonization of the western Indian Ocean from Asia within the last 2.6 Myr. The expansion of Hypsipetes appears to have occurred rapidly, with descendants found across the breadth of its western Indian Ocean range. The data suggest that a more recent expansion of Hypsipetes madagascariensis from Madagascar led to the colonization of Aldabra and a secondary colonization of the Comoros. Groupings of western Indian Ocean Hypsipetes according to phenotypic similarities do not correspond to mtDNA lineages, suggesting that these similarities have evolved by convergence or parallelism. The direction of phenotypic change cannot be inferred with confidence, since the primary expansion occurred rapidly relative to the rate of mtDNA substitution, and the colonization sequence remains uncertain. However, evidence from biogeography and comparison of independent colonization events are consistent with the persistence of a small grey continental bulbul in India and Madagascar, and multiple independent origins of large size and green plumage in insular island populations of the Comoros, Mascarenes and Seychelles. © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 85, 271,287. [source] Climatic variability and the evolution of insect freeze toleranceBIOLOGICAL REVIEWS, Issue 2 2003BRENT J. SINCLAIR ABSTRACT Insects may survive subzero temperatures by two general strategies: Freeze-tolerant insects withstand the formation of internal ice, while freeze-avoiding insects die upon freezing. While it is widely recognized that these represent alternative strategies to survive low temperatures, and mechanistic understanding of the physical and molecular process of cold tolerance are becoming well elucidated, the reasons why one strategy or the other is adopted remain unclear. Freeze avoidance is clearly basal within the arthropod lineages, and it seems that freeze tolerance has evolved convergently at least six times among the insects (in the Blattaria, Orthoptera, Coleoptera, Hymenoptera, Diptera and Lepidoptera). Of the pterygote insect species whose cold-tolerance strategy has been reported in the literature, 29% (69 of 241 species studied) of those in the Northern Hemisphere, whereas 85%(11 of 13 species) in the Southern Hemisphere exhibit freeze tolerance. A randomization test indicates that this predominance of freeze tolerance in the Southern Hemisphere is too great to be due to chance, and there is no evidence of a recent publication bias in favour of new reports of freeze-tolerant species. We conclude from this that the specific nature of cold insect habitats in the Southern Hemisphere, which are characterized by oceanic influence and climate variability must lead to strong selection in favour of freeze tolerance in this hemisphere. We envisage two main scenarios where it would prove advantageous for insects to be freeze tolerant. In the first, characteristic of cold continental habitats of the Northern Hemisphere, freeze tolerance allows insects to survive very low temperatures for long periods of time, and to avoid desiccation. These responses tend to be strongly seasonal, and insects in these habitats are only freeze tolerant for the overwintering period. By contrast, in mild and unpredictable environments, characteristic of habitats influenced by the Southern Ocean, freeze tolerance allows insects which habitually have ice nucleators in their guts to survive summer cold snaps, and to take advantage of mild winter periods without the need for extensive seasonal cold hardening. Thus, we conclude that the climates of the two hemispheres have led to the parallel evolution of freeze tolerance for very different reasons, and that this hemispheric difference is symptomatic of many wide-scale disparities in Northern and Southern ecological processes. [source] Phylogenetic reconstruction of carnivore social organizationsJOURNAL OF ZOOLOGY, Issue 1 2007F. Dalerum Abstract It is generally assumed that carnivore social organizations evolved directionally from a solitary ancestor into progressively more advanced forms of group living. Although alternative explanations exist, this evolutionary hypothesis has never been tested. Here, I used literature data and maximum likelihood reconstruction on a complete carnivore phylogeny to test this hypothesis against two others: one assuming directional evolution from a non-solitary ancestor, and one assuming parallel evolutions from a socially flexible ancestor, that is, an ancestor with abilities to live in a variety of social organizations. The phylogenetic reconstructions did not support any of the three hypotheses of social evolution at the root of Carnivora. At the family level, however, there was support for a non-solitary and socially flexible ancestor to Canidae, a socially flexible or solitary ancestor to Mustelidae, a solitary or socially flexible ancestor to Mephitidae, a solitary or group living ancestor to Phocidae, a group living ancestor to Otariidae and a solitary ancestor to Ursidae, Felidae, Herpestidae and Viverridae. There was equivocal support for the ancestral state of Procyonidae and Hyaenidae. It is unclear whether the common occurrence of a solitary ancestry at the family level was caused by a solitary ancestor at the root of Carnivora or by multiple transitions into a solitary state. The failure to support a solitary ancestor to Carnivora calls for caution when using this hypothesis in an evolutionary framework, and I suggest continued investigations of the pathways of the evolution of carnivore social organizations. [source] | ||||||||||||||||||||||||||||