Historical biogeography of Southeast Asia and the West Pacific,or the generality of unrooted area networks as historical biogeographic hypotheses

Aim Unrooted area networks are perhaps a general way in which different historical biogeographical patterns may be combined. Location Southeast Asia up to the West Pacific, Australia, South America. Methods Unrooted area networks based on Primary Brooks Parsimony Analysis of different data sets of Southeast Asian–West Pacific, Australian and South American clades. Results A large Brooks Parsimony historical (cladistic) biogeographic analysis of Southeast Asia and the West Pacific gave a meaningful result when all clades (representing different historical biogeographic patterns) were united into one matrix and an unrooted area network was produced. This network showed geographically adjacent areas as neighbours, which is interpreted as clades dispersing and speciating as soon as areas rafted towards each other. This pseudo‐vicariance mechanism, together with the very limited, mainly linear dispersal possibilities, a few large, widespread clades with many endemic species, and the large overlap in distributions displayed by different patterns, may explain the peculiar result. When applied to examples from other areas (bird data from Australia and South America), unrooted area networks for all data perform very poorly. Main conclusions Unrooted historical general area networks are not universally applicable. In general, it is better to split historical patterns a priori and analyse them separately.     

一种改进的PAE方法及其在锦鸡儿组(锦鸡儿属)特有性分析中的应用

针对特有性简约性分析（PAE）不足之处,提出一个新的改进分析方法。主要区别是,新方法对分布区内分类群区分了原始和演化,相应地编码为0／1;为了获取分类群原始和演化的特性,分析以分类群分支图为基础。新方法是系统发育与地理分布相统一原理的一个具体的定量化探讨。用新方法分析了豆科锦鸡儿属锦鸡儿组15种,结果表明新方法优于以前的PAE方法。用新的改进方法分析得到的可能的祖先分布区是原始类群树锦鸡儿和一大类属内原始类群的分布区。与目前属的起源问题的一般观点相一致。     

Distribution patterns and biogeographic analysis of Austral Polychaeta (Annelida)

Aim We investigate the biogeography of Austral Polychaeta (Annelida) using members of the families Eunicidae, Lumbrineridae, Oenonidae, Onuphidae, Serpulidae and Spionidae and Parsimony Analysis of Endemicity (PAE). We determine whether observed polychaete distribution patterns correspond to traditional shallow-water marine areas of endemism, estimate patterns of endemism and relationships between areas of endemism, and infer the biological processes that have caused these patterns. Location The study is concerned with extant polychaete taxa occupying shallow-water areas derived from the breakup of the Gondwana landmass (i.e. Austral areas). Methods Similarity was assessed using a significance test with Jaccard's indices. Areas not significantly different at 0.99 were combined prior to the PAE. Widespread species and genera (155 taxa) were scored for presence/absence for each area of endemism. PAE was used to derive hypotheses of area relationships. Hierarchical patterns in the PAE trees were identified by testing for congruence with patterns derived from cladistic biogeographic studies of other Gondwanan taxa and with geological evidence. Results The polychaete faunas of four area-pairs were not significantly different and the areas amalgamated: South-west Africa and South Africa, New Zealand South Island and Chatham Islands, Macquarie Island and Antipodean Islands, and West Antarctica and South Georgia. Areas with the highest levels of species endemism were southern Australia (67.0%), South-east South America (53.2%) and South Africa (40.4%). About 60% of species and 7.5% of genera occupied a single area of endemism. The remainder were informative in the PAE. Under a no long-distance dispersal assumption a single minimal-length PAE tree resulted (l=367; ci=0.42); under dispersal allowed, three minimal-length trees resulted (l=278; ci=0.56). In relation to the sister grouping of the New Zealand areas and Australia we find congruence between our minimal-length trees and those derived from a biogeographic study of land plants, and with area relationships predicted by the Expanding Earth Model. Main conclusions The polychaete distribution patterns in this study differ slightly from the classical areas of endemism, most notably in being broader, thereby bringing into question the value of using single provincial system for marine biogeographic studies. The Greater New Zealand region is found to be ‘monophyletic’ with respect to polychaetes, that is comprising a genuine biogeographical entity, and most closely related to the polychaete fauna of southern Australia. This finding is consistent with studies of land plants and with the Expanding Earth model, but disagrees with conventional geology and biogeographic hypothesis involving a ‘polyphyletic’ New Zealand. Both vicariance and concerted range expansion (=biotic dispersion) appear to have played important roles in shaping present-day distribution patterns of Austral polychaetes. Shallow-water ridge systems between the Australian and Greater New Zealand continental landmasses during the Tertiary are thought to have facilitated biotic dispersion.     

When simplicity is not parsimonious: a priori and a posteriori methods in historical biogeography

Despite using the same null hypothesis, a priori and a posteriori approaches in historical biogeography differ fundamentally. Methods such as Component Analysis (CA) and Reconciled Tree Analysis (RTA) may eliminate or modify input data in order to maximize fit to the null hypothesis, by invoking assumptions 1 and 2. Methods such as Brooks Parsimony Analysis (BPA) modify the null hypothesis, if necessary, to maintain the integrity of the input data, as required by assumption 0. Two exemplars illustrate critical empirical differences between CA/RTA and BPA: (1) CA rather than BPA may select the incorrect general area cladogram for a set of data (2) BPA, not RTA, provides the most parsimonious interpretation of all available data and (3) secondary BPA, proposed in 1990, applied to data sets for which dispersal producing areas with reticulate histories is most parsimonious, provides biologically realistic interpretations of area cladograms. These observations lead to the conclusion that BPA and CA/RTA are designed to implement different research programmes based on different conceptual frameworks. BPA is designed to assess the biogeographic context of speciation events, whereas CA/RTA are designed to find the best fitting pattern of relationships among areas based on the taxa that inhabit them. Unique distributional elements and reticulate (hybrid) histories of areas are essential for explaining complex histories of speciation. The conceptual framework for BPA, thus, assumes biogeographical complexity, relying on parsimony as an explanatory tool to summarize complex results, whereas CA/RTA assumes biogeographical simplicity, assuming conceptual parsimony a priori .     

The phylogeny of varanoid lizards and the affinities of snakes

Evidence that platynotan squamates (living varanoid lizards, snakes and their fossil relatives) are monophyletic is presented. Evolutionary relationships within this group are then ascertained through a cladistic analysis of 144 osteological characters. Mosasauroids (aigialosaurs and mosasaurs), a group of large marine lizards, are identified as the nearest relatives of snakes, thus resolving the long-standing problem of snake affinities. The mosasauroid–snake clade (Pythonomorpha) is corroborated by 40 derived characters, including recumbent replacement teeth, thecodonty, four or fewer premaxillary teeth, supratemporal–prootic contact, free mandibular tips, crista circumfenestralis, straight vertical splenio-angular joint, loss of posterior ramus of the coronoid, reduced basipterygoid processes, reduced interpterygoid vacuity, zygosphene–zygantral articulations, and absence of epiphyses on the axial skeleton and skull. After mosasauroids, the next closest relatives of snakes are varanids (Varanus, Saniwa and Saniwides) and lanthanotids (Lanthanotus and Cherminotus). Derived features uniting varanids and lanthanotids include nine cervical vertebrae and three or fewer pairs of sternal ribs. The varanid–lanthanotid–pythonomorph clade, here termed Thecoglossa, is supported by features such as the anteriorly positioned basal tubera, and the loss of the second epibranchial. Successive outgroups to thecoglossans are Telmasaurus, an unresolved polytomy (Estesia, Gobidermatidae and Helodermatidae), Paravaranus and Proplatynota. The ''necrosaurs'' are demonstrated to be an artificial (polyphyletic) assemblage of primitive platynotans that are not particularly closely related to each other.Snakes are presumed to have evolved from small, limbless, burrowing lizards and the inability of previous analyses to resolve the affinities of snakes has been attributed to extensive convergence among the numerous lineages of such lizards. The present study contradicts this claim, demonstrating that the problem is due instead to omission of critical fossil taxa. No modern phylogenetic analysis of squamate relationships has simultaneously included both mosasauroids and snakes: previous studies have therefore failed to identify the mosasauroid–snake association and the suite of derived characters supporting it. Mosasauroids are large aquatic animals with well-developed appendages, and none of the derived characters uniting mosasauroids and snakes is obviously correlated with miniaturization, limb reduction or fossoriality. Recognition that mosasauroids, followed by varanids and lanthanotids, are the nearest relatives of snakes will also facilitate studies of relationships within snakes, which until now have been hampered by uncertainty over the most appropriate (closely-related) lizard outgroups.     

Biogeography of the Limacoidea sensu lato (Gastropoda: Stylommatophora): vicariance events and long-distance dispersal

Aim Reconstruction of the historical biogeography of the Limacoidea sensu lato (including the Staffordiidae, Dyakiidae, Gastrodontoidea, Parmacelloidea, Zonitidae, Helicarionoidea and Limacoidea). Evaluation of the relative importance of dispersal and its consequences. Location World‐wide. Methods Weighted ancestral area analysis. Results The ancestral areas of the individual clades have been delimited using weighted ancestral area analysis and a sequence of possible vicariance and dispersal events has been suggested. The results of the ancestral area analysis have tentatively been correlated with Cretaceous and Tertiary palaeogeography. The widely overlapping distribution patterns of several families of the Limacoidea testify to extensive dispersal events. Dispersal capacity of land snails is correlated with body size. The significant negative correlation between body size and distribution area size corroborates the importance of passive dispersal for the evolution of the distribution patterns. Main conclusions The existence of extensive dispersal events of poor active dispersers like land snails diminishes the importance of recent distribution patterns for the reconstruction of palaeogeography. On the other hand, dispersal ensures that biogeographical data reflect the geographical configurations at a given time and renders the use of palaeobiogeographic data for the reconstruction of palaeogeographic configurations of the respective age possible.     

A Posteriori and a Priori Methodologies for Testing Hypotheses of Causal Processes in Vicariance Biogeography

Methods used in vicariance biogeography fall into the categories of a posteriori methods (e.g., Component Compatibility Analysis and Brooks Parsimony Analysis) and a priori methods (e.g., Component Analysis, Reconciled Tree Analysis, and Three Area Statement Analysis). Each category corresponds to a particular methodology that arrives at general area cladograms by testing null hypotheses in a particular way. A posteriori methods assume the process of vicariance only (A0) as a common cause of the distribution of different monophyletic groups of taxa under the null hypothesis. Whenever a parsimony analysis of combined data from these monophyletic groups results in a general area cladogram with homoplasy, the null hypothesis is rejected and extinction and dispersal are invoked a posteriori as ad hoc process explanations. A priori methods assume not only vicariance (A0) but also combinations of vicariance with the processes of extinction (A1) and dispersal (A2) as possible causes of the distribution of the taxa of different monophyletic groups. Each assumed set of processes corresponds to a different null hypothesis. Under the assumption of independence and thus additivity of the processes involved, the sets of area cladograms obtained under A0, A1, and A2 from data of each monophyletic group must be inclusive (requirement I). Whenever no congruent area cladograms are found in the intersection of sets of area cladograms derived under the same assumption for different monophyletic groups (II), the corresponding null hypothesis is rejected.     

Does vicariance shape biotas? Biogeographical tests of the vicariance model in the north‐west European land snail fauna

Aim To investigate the importance of vicariance in shaping the north‐west European land snail fauna. Location North‐west Europe. Methods We tested whether there is a non‐random congruence, i.e. a clustering of species ranges, using a Monte Carlo procedure with a null model that generates range data sets such that their range size distribution, the species richness distribution of the geographic cells and the spatial autocorrelation of the occurrences of a taxon approach the parameters in the real data set. Biotic elements, groups of species with similar ranges, were delimited with Model based Gaussian clustering. The prediction that closely related species belong to different biotic elements, has been tested with a chi‐square test. Results The distribution areas of the north‐west European land snail species are significantly clustered as predicted by the vicariance model. One widespread and seven regional biotic elements were identified. Contrary to the predictions of the vicariance model, closely related north‐west European land snail species belong significantly more often to the same biotic element than should be expected by chance. Main conclusions The clustering of closely related north‐west European land snail species within the same biotic element indicates that speciation modes other than vicariance were frequent or that the imprint of vicariance on the ranges was obscured by extensive post‐speciational dispersal. Extensive dispersal may have been caused by Pleistocene climatic fluctuations. The core areas of the regionally restricted biotic elements might indicate the positions of glacial refugia of land snails.     

Phylogeographical and speciation patterns in subterranean worm lizards of the genus Blanus (Amphisbaenia: Blanidae)

The peculiar lifestyle of subterranean reptiles must determine their modes of speciation and diversification. To further understand the evolutionary biology of subterranean reptiles, we studied the phylogeny of worm lizards of the genus Blanus and the phylogeography of its Iberian representatives. We used mitochondrial (ND4 and 16S rRNA) and nuclear (anonymous) partial gene sequences to resolve phylogenetic relationships within Blanus. The Eastern Mediterranean Blanus strauchi was recovered as sister group of Western Mediterranean species. Iberian and North African Blanus were recovered as reciprocally monophyletic groups. The same genes were used to determine phylogeography of 47 populations of Blanus cinereus. Mitochondrial and nuclear sequence data recovered two highly supported Iberian clades. Parapatry and high sequence divergences between them suggest that these clades may represent independent taxonomic units. A molecular clock was calibrated considering that the split between Iberian and North African Blanus was due to the re-opening of the Betic Strait in the Upper Tortonian (8-9 million years ago). Differentiation between the two Iberian clades was estimated to date back to 5.2 million years ago. The Central Iberian clade included five mitochondrial haplotype lineages (A-E). Geographical ranges of two of them broadly overlap in the central Iberian plateau. After testing alternative hypotheses, the most likely explanation for this striking phylogeographical pattern involves recent dispersal of one of the lineages (C) over the geographical range of the other (B). The inferred recent dispersal of this fossorial reptile is explained in terms of demographic advantages associated to underground lifestyle.     

Methods in Vicariance Biogeography: Assessment of the Implementations of Assumptions 0, 1, and 2

As we have argued previously, for the valid derivation of general area cladograms in vicariance biogeography, two requirements should be met. First, sets of area cladograms derived under assumptions 0, 1 and 2 should be inclusive (requirement I). Second, general area cladograms should be based on area cladograms, for different monophyletic groups, derived under the same assumption (requirement II). We now assess for their actual implementation of assumptions A0, A1, and A2 and for the extent to which they meet requirements I and II, the following methods (and correlated computer programs): Component Compatibility Analysis (CAFCA), Brooks Parsimony Analysis (PAUP), Component Analysis (Component 1.5), Reconciled Tree Analysis (Component 2.0), and Three Area Statement Analysis (TAS). For this purpose we use empirical ( Heterandria, Xiphophorus, Cyttaria, Eriococcus/Madarococcus ) and theoretical data sets. All programs appear to violate, to a different degree, requirement I (deriving inclusive sets of area cladograms under assumptions) when dealing with sympatric taxa under A1 or A2. Dealing with sympatric taxa a posteriori only prevents this violation. All programs examined appear to meet requirement II (deriving general area cladograms under a single assumption).     

Evolution of glutamate dehydrogenase genes: Evidence for two paralogous protein families and unusual branching patterns of the archaebacteria in the universal tree of life

Summary The existence of two families of genes coding for hexameric glutamate dehydrogenases has been deduced from the alignment of 21 primary sequences and the determination of the percentages of similarity between each pair of proteins. Each family could also be characterized by specific motifs. One family (Family 1) was composed of gdh genes from six eubacteria and six lower eukaryotes (the primitive protozoan Giardia lamblia, the green alga Chlorella sorokiniana, and several fungi and yeasts). The other one (Family 11) was composed of gdh genes from two eubacteria, two archaebacteria, and five higher eukaryotes (vertebrates). Reconstruction of phylogenetic trees using several parsimony and distance methods confirmed the existence of these two families. Therefore, these results reinforced our previously proposed hypothesis that two close but already different gdh genes were present in the last common ancestor to the three Ur-kingdoms (eubacteria, archaebacteria, and eukaryotes). The branching order of the different species of Family I was found to be the same whatever the method of tree reconstruction although it varied slightly according the region analyzed. Similarly, the topological positions of eubacteria and eukaryotes of Family II were independent of the method used. However, the branching of the two archaebacteria in Family II appeared to be unexpected: (1) the thermoacidophilic Sulfolobus solfataricus was found clustered with the two eubacteria of this family both in parsimony and distance trees, a situation not predicted by either one of the contradictory trees recently proposed; and (2) the branching of the halophilic Halobacterium salinarium varied according to the method of tree construction: it was closer to the eubacteria in the maximum parsimony tree and to eukaryotesin distance trees. Therefore, whatever the actual position of the halophilic species, archaebacteria did not appear to be monophyletic in these gdh gene trees. This result questions the firmness of the presently accepted interpretation of previous protein trees which were supposed to root unambiguously the universal tree of life and place the archaebacteria in this tree. Offprint requests to: B. Labedan     

Biogeographic patterns of the East African coastal forest vertebrate fauna

The archipelago-like coastal forest of East Africa is one of the highest priority ecosystems for biodiversity conservation worldwide. Here we investigate patterns of species richness and biogeographic distribution among birds, mammals and reptiles of these forests, using distribution data obtained from recently published reviews and information collated by the WWF Eastern Africa Coastal Forest Ecoregion Programme. Birds and mammals species were divided into forest specialists and generalists, and forest specialist reptiles into ‘coastal’ and ‘forest’ endemics. The species richness of birds and generalist mammals increased with area, and is probably a result of area-dependent extinction. Only in birds, however, species richness increased with decreasing isolation, suggesting possible isolation-dependent colonization. Forest diversity, associated to altitudinal range, is important for specialist birds and mammals, whose species richness increased with wider altitudinal range. The number of relict coastal endemic and forest endemic reptiles was higher in forests with wider altitudinal ranges and on relatively higher altitude, respectively. Such forests have probably provided a suitable (and perhaps stable) environment for these species through time, thus increasing their persistence. Parsimony analysis of distributions (PAD) and cluster analyses showed geographical distance and general ecological similarity among forests as a determinant factor in bird distribution patterns, with compositional similarity decreasing with increasing inter-forest distance. Compositional similarity patterns of mammals among the forests did not show a strong geographical correspondence or a significant correlation with inter-forest distance, and those of reptiles were not resolved, with very low similarity levels among forest faunas. Our results suggest that the relative importance (and causal relationship) of forest attributes affecting the distribution of the East African coastal forest vertebrate fauna varies depending on life history traits such as dispersal ability and forest specialization. The groupings in PAD are partly congruent with some of the previous classifications of areas of endemism for this region, supporting the ‘naturalness’ of these regions.     

A fossil record of the Eastern clade of Blanus (Amphisbaenia: Blanidae) from the late Miocene of Ukraine

The fossil history of worm lizards in Eastern Europe is very patchy because of the small number of localities and the fragmentary vertebral material available. A new record of the genus Blanus from the late Miocene of the Egorovka 1 and 2 localities in Ukraine is reported here. Based on its dental morphology, Blanus from Egorovka differs from all extinct species of the genus and from the extant B. cinereus complex. It is most closely related to the Eastern clade of Blanus (B. strauchi complex) in having enlarged second and small third dentary teeth. Blanus from Egorovka is the second fossil record of the B. strauchi complex and the first record of the Eastern clade outside of its current geographical range. It indicates a wider past range of the Eastern European Blanus, including the northern Black Sea coastal area.     

Latitudinal, habitat and substrate distribution patterns of freshwater ascomycetes in the Florida Peninsula

Freshwater ascomycetes are important decomposers of dead woody and herbaceous debris in aquatic habitats. Despite evidence of their ecological importance, latitudinal, habitat and substrate distributional patterns of freshwater ascomycetes are poorly understood. In this study, we examined the latitudinal and habitat distributional patterns, and substrate recurrences of freshwater ascomycetes by collecting dead submerged woody and herbaceous debris in lentic and lotic habitats at five selected sites along a north-central-south, temperate–subtropical latitudinal ecotone in Florida. One hundred and thirty-two fungal taxa were collected during the study. Seventy-four were meiosporic and 56 were mitosporic ascomycetes, while two species were basidiomycetes. Canonical analyses of principal coordinates (CAP) and Sørenson’s similarity index of species based on presence/absence data revealed a high turnover in species composition between the northern and southern sites, indicating a change in species composition along the temperate–subtropical latitudinal ecotone of the Florida Peninsula. Results from the ordination analysis indicated that freshwater ascomycete community composition is not significantly different between lentic and lotic habitats in Florida. The geographically broadly distributed species and species commonly found in Florida occurred in both habitats, whereas a number of new or rare species occurred in either lentic or lotic habitats, but not both. The same freshwater ascomycete species did not necessarily occur on both woody and herbaceous debris; of the 132 taxa collected, 100 were reported only on woody debris; 14 species occurred exclusively on herbaceous debris; and 18 species were found on both woody and herbaceous debris in lentic or lotic habitats. Implications of data from this study to the conservation and knowledge of biodiversity for freshwater ascomycetes is discussed.     

Distribution patterns and dispersal strategies of Galiciales

In Caliciales both passive and active spore dispersal occurs. A review of the distribution of 162 species is given. Species with small spores have wider distribution than species with large spores, irrespective of dispersal strategy. In antitropical species there is only rarely a differentiation between Northern and Southern Hemisphere populations. It is concluded that in several small-spored genera long-distance dispersal has been instrumental in dispersing the species and range extensions have been much more frequent than in large-spored species for which vicariance explanations are more appropriate. Comparisons with bryophyte distributions show differences in dispersal strategies and distribution patterns.