Evaluating trans-tethys migration: an example using acrodont lizard phylogenetics

A phylogenetic tree for acrodont lizards (Chamaeleonidae and Agamidae) is established based on 1434 bases (1041 informative) of aligned DNA positions from a 1685-1778 base pair region of the mitochondrial genome. Sequences from three protein-coding genes (ND1, ND2, and COI) are combined with sequences from eight intervening tRNA genes for samples of 70 acrodont taxa and two outgroups. Parsimony analysis of nucleotide sequences identifies eight major clades in the Acrodonta. Most agamid lizards are placed into three distinct clades. One clade is composed of all taxa occurring in Australia and New Guinea; Physignathus cocincinus from Southeast Asia is the sister taxon to the Australia-New Guinea clade. A second clade is composed of taxa occurring from Tibet and the Indian Subcontinent east through South and East Asia. A third clade is composed of taxa occurring from Africa east through Arabia and West Asia to Tibet and the Indian Subcontinent. These three clades contain all agamid lizards except Uromastyx, Leiolepis, and Hydrosaurus, which represent three additional clades of the Agamidae. The Chamaeleonidae forms another clade weakly supported as the sister taxon to the Agamidae. All eight clades of the Acrodonta contain members occurring on land masses derived from Gondwanaland. A hypothesis of agamid lizards rafting with Gondwanan plates is examined statistically. This hypothesis suggests that the African/West Asian clade is of African or Indian origin, and the South Asian clade is either of Indian or Southeast Asian origin. The shortest tree suggests a possible African origin for the former and an Indian origin for the latter, but this result is not statistically robust. The Australia-New Guinea clade rafted with the Australia-New Guinea plate and forms the sister group to a Southeast Asian taxon that occurs on plates that broke from northern Australia-New Guinea. Other acrodont taxa are inferred to be associated with the plates of Afro-Arabia and Madagascar (Chameleonidae), India (Uromastyx), or southeast Asia (Hydrosaurus and Leiolepis). Introduction of different biotic elements to Asia by way of separate Gondwanan plates may be a major theme of Asian biogeography. Three historical events may be responsible for the sharp faunal barrier between Southeast Asia and Australia-New Guinea, known as Wallace's line: (1) primary vicariance caused by plate separations; (2) secondary contact of Southeast Asian plates with Eurasia, leading to dispersal from Eurasia into Southeast Asia, and (3) dispersal of the Indian fauna (after collision of that subcontinent) to Southeast Asia. Acrodont lizards show the first and third of these biogeographic patterns and anguid lizards exhibit the second pattern. Modern faunal diversity may be influenced primarily by historical events such as tectonic collisions and land bridge connections, which are expected to promote episodic turnover of continental faunas by introducing new faunal elements into an area. Repeated tectonic collisions may be one of the most important phenomena promoting continental biodiversity. Phylogenetics is a powerful method for investigating these processes.     

Molecular probes of phylogeny and biogeography in toads of the widespread genus Bufo

Genetic relationships among 25 species of Central and South American Bufo and among representative North, Central, and South American, Asian, and African Bufo were probed, using the quantitative immunological technique of microcomplement fixation (MC'F) which indicated a clear separation of North, Central, and South American lineages of Bufo. The South American lineage likely diverged from the Central and North American lineages in the Eocene; the latter two lineages diverged later, probably in the mid-Oligocene. Some species groups of South American toads, defined on the basis of traditional morphological studies, are genetically quite similar within groups, whereas others are genetically divergent. The amount of albumin evolution does not appear to parallel the amount of karyotypic, morphological, ecological, or behavioral evolution documented. Comparisons suggest that the African lineages separated from the American and Asian lineages in the late Cretaceous, corresponding to the time of the final separation of Gondwanaland, the southern supercontinent including the modern continents of South America, Africa, Australia, Antarctica, and India. The Asian lineages diverged from the lineage giving rise to all of the American species in the early Paleocene.      

Correlation of eustatic and biotic events in the Ordovician paleobasins of the Siberian and Russian platforms

Nine sedimentary sequences are recognized in the Ordovician of the Siberian Platform. These sequences correspond to sea level fluctuations of the 3rd order, from 1 to 6 My. Correlation with the sequences recognized in the Ordovician of the Russian Platform suggest their possible eustatic nature. Cold water nontropical carbonates are suggested in the Ordovician of the Tungus Syneclise, which may be explained by the upwelling of cold oceanic waters. The upwelling was caused by re-distribution of oceanic currents due to largescale tectonic events in the mid-Ordovician. The Ordovician evolution of the Siberian Platform was much more similar to that of the North American Platform than of the Russian Platform.     

The relation of Late Ordovician glaciation to the Ordovician-Silurian changeover in North American brachiopod faunas

Sheehan, P. M.: The relation of Late Ordovician glaciation to the Ordovician-Silurian changeover in North American brachiopod faunas.
The Ordovician-Silurian changeover of brachiopod faunas in North American epicontinental seas involved the abrupt extinction of endemic Late Ordovician stocks and subsequent repopulation of North American seas by Old World taxa. The Late Ordovician Gondwanaland glaciation may have lowered sea levels sufficiently to place severe stress on the widespread shallow marine faunas in North America, resulting in their eventual extinction. The Late Ordovician depositional history in North America is not well enough known to establish the presence of a latest Ordovician regression, but the earliest Silurian was an interval of off-lap in North America. Therefore, the glacial lowering of sea level is considered to be the most likely cause of the faunal changeover.     

Mesozoic palaeogeography of the Southern Cape,South Africa

Four palaeogeographical reconstructions are presented for the southern Cape covering the period Late Permian to Late Cretaceous. This time spans the commencement to an advanced stage of breakup of Gondwanaland, during which the area moved from a mid-continental, high latitude, to an ocean-dominated, middle latitude position. These movements can be traced in facies changes and erosional cycles associated with the rift between West Gondwana and Antarctica (proto southwest Indian Ocean) and the later rift between South America and Africa (proto southeast Atlantic Ocean).     

Historical biogeography of scarabaeine dung beetles

Abstract Aim (1) To review briefly global biogeographical patterns in dung beetles (Coleoptera: Scarabaeidae: Scarabaeinae), a group whose evolutionary history has been dominated by ecological specialization to vertebrate dung in warmer climates. (2) To develop hypotheses accounting for the evolution of these patterns. Location Six principal biogeographical regions: Palaearctic, Oriental, Afrotropical, Australasia, Neotropical, Nearctic and five outlying islands or island groups harbouring endemic genera: Caribbean, Madagascar, Mauritius, New Caledonia, New Zealand. Methods Major patterns of tribal, generic and species distribution are investigated using cluster analysis, ordination, parsimony analysis of endemism and track analysis. Attempts are made to resolve biogeographical patterns with findings in the fields of plate tectonics, fossil and evolutionary history, plus phylogeny of both mammals and dung beetles. Results Because of conflict between published findings, it is uncertain at what point in time density of dinosaur dung, mammal dung or both became sufficiently great to select for specialized habits in dung beetles. However, biogeographical evidence would suggest a Mesozoic origin followed by further taxonomic radiation during the Cenozoic, possibly in response to the increasing size and diversity of mammalian dung types in South America and Afro‐Eurasia. Proportional generic distribution in fourteen tribes and subtribes showed four principal biogeographical patterns: (1) southerly biased Gondwanaland distribution, (2) Americas or (3) Madagascar endemism, and (4) northerly biased, Afro‐Eurasian‐centred distribution with limited numbers of genera also widespread in other regions. Proportional composition of faunas in eleven geographical regions indicated three principal distributional centres, East Gondwanaland fragments, Afro‐Eurasia and the Americas. These patterns probably result from three principal long‐term range expansion and vicariance events (Mesozoic: Gondwanaland interchange and fragmentation, Cenozoic: Afro‐Eurasian/Nearctic interchange and the Great American interchange). It is suggested that old vicariance caused by the Mesozoic fragmentation of Gondwanaland leads to a high degree of regional endemism at generic or tribal level across one or more Gondwanaland tracks. In contrast, it is suggested that the more recent Cenozoic range expansions occurred primarily towards northern regions leading to endemism primarily at species level. These Cenozoic radiations were facilitated by the re‐linking of continents, either because of tectonic plate movements (Africa to Eurasia in Miocene), climatically induced sea‐level change (Afro‐Eurasia to Nearctic in Miocene and Pleistocene), or similar coupled with orogenics (Nearctic to Neotropical in Pliocene). Speciation has followed vicariance either because of climatic change or physical barrier development. These recent range expansions probably occurred principally along an Afro‐Eurasian land track to the Nearctic and Neotropical and an Americas land track northwards from the Neotropics to the Nearctic, with limited dispersal from Eurasia to Australia, probably across a sea barrier. This accounts for the overall, spatially constrained, biogeographical pattern comprising large numbers of species‐poor genera endemic to a single biogeographical region and fewer more species‐rich genera, many of which show wider biogeographical distributions. In most southerly regions (Australasia, Madagascar, Neotropical), faunal composition and generic endemism is primarily dominated by elements with Gondwanaland ancestry, which is consistent with the Gondwanaland origin claimed for Scarabaeinae. In Afro‐Eurasia (Palaearctic, Oriental, Afrotropical), generic endemism of monophyletically derived Afro‐Eurasian and widespread lineages is centred in the Afrotropical region and faunal composition is numerically dominated by Afro‐Eurasian and widespread elements. In the Nearctic region, the fauna is jointly dominated by widespread elements, derived from Afro‐Eurasia, and Gondwanaland and Americas elements derived from the Neotropical region. Main conclusions Global biogeographical patterns in scarabaeine dung beetles primarily result from Mesozoic and Cenozoic range expansion events followed by vicariance, although recent dispersal to Australia may have occurred across sea barriers. Detailed phylogenetics research is required to provide data to support dispersal/vicariance hypotheses.     

Plate tectonics, seaways and climate in the historical biogeography of mammals

The marsupial and placental mammals originated at a time when the pattern of geographical barriers (oceans, shallow seas and mountains) was very different from that of today, and climates were warmer. The sequence of changes in these barriers, and their effects on the dispersal of the mammal families and on the faunas of mammals in the different continents, are reviewed. The mammal fauna of South America changed greatly in the Pliocene/Pleistocene, when the newly-complete Panama Isthmus allowed the North American fauna to enter the continent and replace most of the former South American mammal families. Marsupial, but not placental, mammals reached Australia via Antarctica before Australia became isolated, while rats and bats are the only placentals that dispersed naturally from Asia to Australia in the late Cenozoic. Little is known of the early history of the mammal fauna of India. A few mammal families reached Madagascar from Africa in the early Cenozoic over a chain of islands. Africa was isolated for much of the early Cenozoic, though some groups did succeed in entering from Europe. Before the climate cooled in the mid-Cenozoic, the mammal faunas of the Northern Hemisphere were much richer than those of today.     

Biogeographical and geological evidence for a smaller, completely-enclosed Pacific Basin in the Late Cretaceous

Aim To use biogeographical, palaeomagnetic, palaeosedimentary, and plate circuit data from Late Cretaceous regions in and around the Pacific to test the plate tectonic hypothesis of a pre‐Pacific superocean. Location East Asia, Australia, Antarctica, the western Americas, and the Pacific. Methods Literature surveys of the distributions of Cretaceous, circum‐Pacific taxa were compared with palaeomagnetic and palaeosedimentary data. Uncontroversial plate motions based on seafloor spreading data were also used to test the results of the biogeographical and palaeomagnetic analyses. Results The distributions of Cretaceous terrestrial taxa, mostly dinosaurs, imply direct, continental connections between Australia and East Asia, East Asia and North America, North America and South America, South America and Antarctica, and Antarctica and Australia. Palaeomagnetic, palaeosedimentary, and basic plate circuit analyses require little to no latitudinal motion of the Pacific plate with respect to the surrounding continents. Specifically, the data implies that western North America, East Asia, and the Pacific plate all increased in latitude by roughly the same amount (c. 11 ± 5°) since the Campanian – and that the Pacific Ocean Basin has increased in length north‐to‐south. Main conclusions Each of the analyses provides independent corroboration for the same conclusion: the Late Cretaceous Pacific plate was completely enclosed by the surrounding continents and has not experienced significant latitudinal motion with respect to North America, East Asia, or the Bering land bridge. This contrasts significantly with the plate tectonic history of the Pacific, implying instead that the Pacific plate formed in situ, pushing the continents apart as the plate and basin expanded. These results also substantiate recent biogeographical analyses that have concluded that a narrower Pacific Ocean Basin in the Mesozoic and early Tertiary provides the most reasonable explanation for the great number of trans‐Pacific disjunctions of poor dispersing taxa.     

Late Ordovician extinctions of bryozoans

An analysis of the final stratigraphic appearances of byrozoan species and genera, compiled in a world-wide bryozoan data base, revealed three discrete Late Ordovician extinctions. A Late Carddoc (Onnian) extinction was most pronounced on the plates of Baltica and Siberia. Endemic species and genera, confined to one plate and one lithotope were most affected and the extinction was coincident with increased migrations of bryozoan genera to Baltica and Siberia. The Late Caradoc extinction may be related to decreasing provinciality and competition between migrant and stenotopic taxa. Two major extinctions occurred in the Late Ashgill. The greatest of the two is recognized at the end of the Rawtheyan. and affected primarily taxa on the North American plate. The extinction at the end of the Hirnantian affected primarily Baltic taxa. The exact timing of the end-Rawtheyan extinction in North America cannot be established owing to incompleteness of the stratigraphic record. The Rawtheyan extinction occurred during a major glaciation centered in North Africa and a regression of epeiric seas. The large majority of North American survivors of the extinction are represented by Faunas preserved on Anticosti Island. which remained submerged during the regression. This evidence supports regression as a cause of the Rawtheyan extinctions in North America. The end-Hirnantian extinctions may be related to the ensuing transgression or to a wave of faunal migrations associated with the transgression. * Bryozoa, extinctions, Ordovician, Rawtheyan, Hirnantian, North America, Baltica .     

Determining biogeographical patterns of dispersal and diversification in oscine passerine birds in Australia, Southeast Asia and Africa

Aim  Several independent studies suggest that oscine passerine birds originated in Eastern Gondwana/Australia and from there spread to Southeast Asia and then to Africa. A recently constructed supertree including 1724 oscine taxa forms the basis for this study, in which we present a more detailed hypothesis of this out-of-Australia scenario.
Location  Australia, Africa, Southeast Asia, western Pacific, Indian Ocean.
Methods  We used the computer program DIVA to identify putative ancestral areas for each node. We also applied a molecular clock calibrated with three recently conducted studies of passerines to estimate the ages of basal nodes. Although these time estimates are rough they give some indication that, together with the putative ancestral areas, they can be compared with known events of plate tectonic movements in the Australian, Southeast Asian and western Pacific regions.
Results  The DIVA analysis shows that Basal Corvida and Crown Corvida originated in Australia. Ancestral nodes for Picathartes / Chaetops and Passerida originated in Africa, and the basal nodes of Sylvioidea also originated in Africa. For Muscicapoidea and Passeroidea we were unable to establish ancestral patterns. The molecular clock showed that Crown Corvida radiated between 20 and 30 Ma whereas Basal Corvida and the Passerida clade radiated from c . 45 to 50 Ma.
Main conclusions  Both approaches agree that: (1) Crown Corvida spread from Australia to Southeast Asia, with several dispersal events around the time when the terranes of Australian and Indomalayan origin came close together some 15 Ma, and (2) a single dispersal event went from Australia across the Indian Ocean to Africa c . 45–50 Ma, leading to the very large radiation of the parvorder Passerida. The latter hypothesis is novel, and contrary to the general view that oscines spread exclusively via Southeast Asia.     

Influence of the Late Ordovician glaciation on basin configuration of the Yangtze Platform in China

The Late Ordovician paleogeographic changes in the Yangtze Platform indicate a widespread regression and consequent subaerial exposure probably caused by the 'locking up' of substantial amounts of marine waters during the Late Ordovician glaciation. The subsequent rapid paleogeographic changes on the Yangtze Platform during the earliest Silurian suggest a rapid melting of the ice. The relatively cool waters in the partially closed Yangtze basin during the latest Ordovician were replaced by open and warm waters during the earliest Silurian. Sedimentation rates and composition of faunal assemblages underwent marked changes during latest Ordovician and Early Silurian. Glaciation, Ordovician, Silurian, Paleogeography, sedimentary rate, faunal change.     

棕榈科植物的地理分布

棕榈科是一个泛热带分布的科,共有１９８属,约２６７０种,下分６亚科,１４族。贝叶棕族是最原始的族,低地榈族则最进化。本科植物在世界上的分布可划分为１３个区,其中以印度－马来西区和新热带区的属、种最多。中国只有１６属和８５种,没有特有属。这些种大部分属热带亚洲分布,与热带亚洲植物区系关系非常密切。关于棕榈科起源地问题,有西冈瓦纳起源和劳亚起源之说。根据化石记录和形态特征的分析,棕榈科很可能于早白垩纪     

Vicariant origin of malagasy reptiles supports late cretaceous antarctic land bridge

Since the acceptance of Wegener's theory of plate tectonics in the 1960s, continental drift vicariance has been proposed as an explanation for pan-Gondwanan faunal distributions. Given the recognition of historical connections among continents, it no longer was necessary to invoke hypotheses of dispersal across nearly insurmountable barriers. The application of continental drift vicariance theory to Gondwanan floral and faunal distributions provided reasonable explanations for such unusual distributions as that of the southern beech (Nothofagus) and chameleons. However, recent studies have demonstrated a significant, if not dominant, role for dispersal in the present-day distributions of these and numerous other "Gondwanan" taxa. The evolutionary histories of three Malagasy groups (boid snakes, podocnemid turtles, and iguanid lizards) commonly have been interpreted as reflecting vicariance because of continental drift associated with the breakup of Gondwana. Bayesian analyses of divergence ages suggest that this pattern is the result of vicariance coincident with the isolation of Madagascar in the Late Cretaceous (approximately 80 million years ago). This represents the first temporal evidence linking the vicariant origin of extant Malagasy vertebrates to a single geologic event. Specifically, our data provide strong, independently corroborated evidence for a contiguous Late Cretaceous Gondwana, exclusive of Africa and connected via Antarctica.     

Geochemistry and palaeogeography of upper Ordovician glaciogenic sedimentary rocks in the Table Mountain Group, South Africa

Evidence for a late Ordovician glaciation is best known from northern Africa and locally in South Africa, and western South America. The South African glacial deposits (Pakhuis Formation of the Table Mountain Group) are present in the western part of the Cape Fold Belt. Two thin diamictites are succeeded by a coarsening upward shale-siltstone unit known as the Cedarberg Formation. These glaciogenic rocks are associated with one of the world's greatest accumulations of mature sandstones. The diamictites are under- and overlain by shales and sandstones that have undergone extensive alteration, presumably as a result of chemical weathering. Some diamictite samples have low values for a Chemical Index of Alteration (CIA), in keeping with their inferred glacial origin. Immediately above the glaciogenic diamictites, black shales, comprising the basal Soom Member of the Cedarberg Formation preserve an unusual soft bodied fauna and are enriched in Mo, U and other trace elements. The unusual chemical composition of these shales is attributed to starved basin conditions and a reducing environment during a rapid sea level rise that accompanied demise of the late Ordovician glaciers. The late Ordovician glacial deposits of western South Africa are widely regarded as the distal deposits of a large continental ice sheet centred on North Africa but they may have been partly derived from piedmont glaciers that descended from highlands formed as a result of late Ordovician orogeny.     

ITS sequence data support a single origin for North American Astereae (Asteraceae) and reflect deep geographic divisions in Aster s.l

The Astereae is the largest tribe of Asteraceae in North America. Morphological diversity suggests that the North American assemblage is polyphyletic as 12 endemic genera, as well as lineages of the genus Erigeron and Conyza (Conyzinae), have been hypothesized to represent at least five separate invasions of North America from Africa, Australia, Eurasia, and South America. This hypothesis was tested with a phylogenetic analysis of nucleotide sequence data from the internal transcribed spacers (ITS) of nuclear ribosomal DNA. Sequences for 62 taxa represent seven outgroup taxa and all major Northern and Southern Hemisphere groups of Astereae, including broad taxonomic and geographic sampling of Conyzinae and Aster s.l. (sensu lato). Parsimony analyses indicate that all North American Astereae are members of a strongly supported clade, and that a diverse group of predominantly woody taxa from Africa, Australia, and South America, are basal Astereae. Furthermore, Aster s.l. is deeply polyphyletic as Eurasian taxa, including Aster s.s. (sensu stricto), appear more closely related to Southern Hemisphere taxa than to North American Aster segregates. There is only low to moderate agreement between proposed higher level Astereae relationships based on ITS and those based either on morphology or chloroplast restriction site data.     

Facies distribution patterns of some marine benthic faunas in early paleozoic platform environments

Worldwide Late Cambrian—Silurian lithofacies patterns indicate that the platforms of that time were sites of accumulation of two essentially different rocks suites: the platform carbonate rocks and the platform terrigenous rocks. Most of the platform rocks accumulated as sediments in shallow marine environments similar to those of the present but far more widely spread.Present-day marine benthic faunas are distributed in depth zones which are primarily controlled by temperature. Faunas tend to occur in substrate-related discrete clusters (communities) within each life zone; similar substrates in different depth zones commonly have different faunal associations. Individual phyletic stocks may encounter environmental optimum or near-optimum conditions in certain areas, that commonly are revealed by an abundance of species and individuals within species in each stock. Environmental optimum conditions depend upon availability of food that may be utilized, modes of feeding of the animals present, water motion, and substrate, among other factors. Organisms in past seas were distributed in patterns similar to those of the present.Carbonate platforms were particularly widespread during the latest Cambrian—Early Ordovician. Intertidal environments spread widely across those platforms during that time and characteristic faunal associations developed in them. Saukiid and related tribolites dominated latest Cambrian carbonate platform intertidal faunas. The Early Ordovician carbonate platform intertidal was dominated by archeogastropod-nautiloid cephalopod faunas. These animals were joined by tabulate corals and certain brachiopods during the latter part of the Ordovician and Silurian as prominent faunal elements in the carbonate platform intertidal—shallow subtidal. Cruziana and related trace fossils, bivalves, and certain tribolites (notably homalonotids and dalmanitids) dominated most terrigenous platform intertidal—shallow subtidal faunas of the Ordovician and Silurian.Articulate brachiopods (primarily orthoids, strophomenoids, and rhynchonelloids) appear to have been relatively prominent during the Early Ordovician in shallow subtidal environments on both carbonate and terrigenous platforms and to have spread down the bathymetric gradient into increasingly deeper subtidal areas of both platforms during the latter part of the Ordovician. Tribolites dominated faunas in relatively moderate to deep subtidal environments on both platforms during the early part of the Ordovician. They were gradually replaced by brachiopods in first the shallower, and later the deeper subtidal as dominant members of the faunas. Brachiopods (primarily pentameroids and spiriferoids) dominated nearly all Silurian warm-water subtidal environments from the shallow subtidal to the edges of the platforms.Platform uplifts in the Middle Ordovician and glacio-eustatic sea-level fluctuations in the Late Ordovician caused environmental changes across the platforms that were accompanied by marked replacements among marine benthic faunas in all environments. The distribution of Ordovician carbonate platforms and glacial deposits suggests that an Ordovician polar region may have been close to present-day equatorial Africa and that Ordovician warm temperate-tropical regions lay close to the present-day North Pole.     

Relative importance of temperature and other factors in determining geographic boundaries of seaweeds: Experimental and phenological evidence

Experimentally determined ranges of thermal tolerance and requirements for completion of the life history of some 60 seaweed species from the North Atlantic Ocean were compared with annual temperature regimes at their geographic boundaries. In all but a few species, thermal responses accounted for the location of boundaries. Distribution was restricted by: (a) lethal effects of high or low temperatures preventing survival of the hardiest life history stage (often microthalli), (b) temperature requirements for completion of the life history operating on any one process (i.e. [sexual] reproduction, formation of macrothalli or blades), (c) temperature requirements for the increase of population size (through growth or the formation of asexual propagules). Optimum growth/reproduction temperatures or lethal limits of the non-hardiest stage (often macrothalli) were irrelevant in explaining distribution. In some species, ecotypic differentiation in thermal responses over the distribution range influenced the location of geographic boundaries, but in many other species no such ecotypic differences were evident. Specific daylength requirements affected the location of boundaries only when interacting with temperature. The following types of thermal responses could be recognised, resulting in characteristic distribution patterns: (A) Species endemic to the (warm) temperate eastern Atlantic had narrow survival ranges (between ca 5 and ca 25°C) preventing occurrence in NE America. In species with isomorphic life histories without very specific temperature requirements for reproduction, northern and southern boundaries in Eur/Africa are set by lethal limits. Species with heteromorphic life histories often required high and/or low temperatures to induce reproduction in one or both life history phases which further restricted distribution. (B) Species endemic to the tropical western Atlantic also had narrow survival ranges (between ca 10 and ca 35°C). Northern boundaries are set by low, lethal winter temperatures. Thermal properties would potentially allow occurrence in the (sub) tropical eastern Atlantic, but the ocean must have formed a barrier to dispersal. No experimental evidence is so far available for tropical species with an amphi-Atlantic distribution. (C) Tropical to temperate species endemic to the western Atlantic had broad survival ranges (<0 to ca 35°C). Northern boundaries are set by low summer temperatures preventing (growth and) reproduction. Thermal properties would permit occurrence in the (sub)tropical eastern Atlantic, but along potential “stepping stones” for dispersal in the northern Atlantic (Greenland, Iceland, NW Europe) summer temperatures would be too low for growth. (D) In most amphi-Atlantic (tropical-) temperate species, northern boundaries are set by low summer temperatures preventing reproduction or the increase of population size. On European shores, species generally extended into regions with slightly lower summer temperatures than in America, probably because milder winters allow survival of a larger part of the population. (E) Amphi-Atlantic (Arctic-) temperate species survived at subzero temperatures. In species with isomorphic life histories not specifically requiring low temperatures for reproduction, southern boundaries are set by lethally high summer temperatures on both sides of the Atlantic. None of the species survived temperatures over 30°C which prevents tropical occurrence. Species with these thermal responses are characterized by distribution patterns in which southern boundaries in Eur/Africa lie further south than those in eastern N America because of cooler summers. In most species with heteromorphic life histories (or crustose and erect growth forms), low temperatures were required for formation of the macrothalli (either directly or through the induction of sexual reproduction). These species have composite southern boundaries in the north Atlantic Ocean. On American coasts, boundaries are set by lethally high summer temperatures, on European coasts by winter temperatures too high for the induction of macrothalli. Species with this type of thermal responses are characterized by distribution patterns in which the boundaries in Eur/Africa lie further north than those in eastern N America because of warmer winters. Paper presented at the XIV International Botanical Congress (Berlin, 24 July–1 August, 1987), Symposium 6-15, “Biogeography of marine benthic algae”.     

EARLY ORDOVICIAN (ARENIG) TRILOBITE PALAEOECOLOGY AND PALAEOBIOGEOGRAPHY OF THE SOUTH CHINA PLATE

Abstract:  Faunal composition of South Chinese Arenig benthic trilobite associations is investigated using the multivariate techniques of TWINSPAN, DCA and seriation. Eight fairly distinct benthic associations can be differentiated, organized primarily along a palaeobathymetrical gradient across the Yangtze Platform in southern Shaanxi and western Hubei and the Jiangnan Transitional Belt in northern Hunan: the Taihungshania , Neseuretus , Trinucleid and Asaphid- Pseudocalymene associations (shallow shelf), the Asaphid-Raphiophorid and Nileid-Asaphid associations (< 100 m outer shelf), the Nileid-Illaenid Association (deep outer shelf carbonates) and the Pseudopetigurus Association (deep outer shelf clastics). The highest levels of diversity are displayed by the Asaphid-Raphiophorid Association of western Hubei. Investigation of the biogeographical affinities of this fauna indicates that South China is biogeographically closest to the other Chinese geotectonic units, and displays strong faunal connections to other central and eastern Asian regions as well as to Tethyan and South American regions. Subdivision of the South Chinese trilobite fauna into different depth zones shows a statistically significant correlation between increasing water depth and increasing faunal cosmopolitanism, although taxa endemic to China or Gondwana also occur even in slope faunas. The results of this biogeographical analysis are consistent with a tropical or subtropical peri-Gondwanan association of South China with other Asian terranes.     

Historical biogeography of Hexabathynella , a cosmopolitan genus of groundwater Syncarida (Crustacea, Bathynellacea, Parabathynellidae)

Hexabathynella is the only cosmopolitan genus of the order Bathynellacea (Crustacea). The known species number 18, found in Europe (9), Africa (1), South America (2), North America (3) and Australia and New Zealand (3). Phylogenetic analysis suggests that the least derived species are those from South America and the most derived those from the Iberian Peninsula, North America and Australia. The five species with the most plesiomorphic characters occur in salt or brackish water, which supports a marine origin for the genus. Phylogenetic and biogeographical analyses suggest that the distribution of the genus can be explained by dispersion and a double vicariant biogeographical model based on plate tectonics and the evolution of the Tethys during the Mesozoic and Cenozoic.  © 2003 The Linnean Society of London . Biological Journal of the Linnean Society , 2003, 78 , 457–466.