Global diversity of ostracods (Ostracoda,Crustacea) in freshwater

There are close to 2,000 subjective species and about 200 genera of Recent non-marine Ostracoda. Together, Cyprididae (1,000 spp.) and Candonidae (c. 550 spp.) represent more than 75% of the extant specific diversity; the remaining 11 families comprise the other 25% of the species. The Palaearctic region has the highest absolute non-marine ostracod diversity, followed by the Afrotropical. The Australian region has the highest relative endemicity. About 90% of the species and 60% of the genera occur in one zoogeographical region only. This means that all the biological mechanisms which lead up to efficient dispersal and which are present in at least part of the non-marine Ostracoda (e.g. brooding, drought-resistant eggs, parthenogenesis) have not induced common cosmopolitan distributions in ostracods. Several habitats are hotspots for ostracod diversity and endemicity. For example, it appears that the ancient lakes hold up to 25% of the total ostracod diversity. Other speciation-prone habitats are groundwater, temporary pools and Australian salt lakes; in the latter two instances, cladogenesis has often been paralleled by gigantism. The present ostracod diversity results from 9 to 12 separate invasions of the non-marine habitat, starting about 400 Myr ago. Genetic diversity can be very different in different species, mostly, but not always, related to reproductive mode. Guest editors: E. V. Balian, C. Lévêque, H. Segers & K. Martens Freshwater Animal Diversity Assessment     

Taxonomy, morphology and speciation of the Semicytherura henryhowei group (Crustacea, Ostracoda)

The genus Semicytherura belongs to the family Cytheruridae, and was distinguished from Cytherura on the basis of carapace features. Species of Semicytherura from Japan and adjacent seas can be divided into two groups. One is represented by Semicytherura miurensis Hanai, 1957, characterized by a thin, oval carapace covered with fine reticulation. The other is represented by Semicytherura henryhowei Hanai & Ikeya, 1977, characterized by a thick sub-rectangular carapace in lateral view. Semicytherura henryhowei, which is distributed from Hokkaido to Okinawa in Japan, has been regarded as having several morphotypes distinguishable on outline and reticulation of carapace. However, as a result of detailed observations on the copulatory organ, carapace outline and distributional pattern of pore systems, remarkable differences are shown to exist between the two most frequently occurring morphotypes. In order to recognize S. henryhowei sensu stricto, the carapace of the holotype was re-examined. Consequently, neither of the two morphotypes are considered to belong to S. henryhowei due to differences of carapace outline and distribution of pore systems. The two morphotypes are here regarded as independent taxa, described as new: S. kazahanan. sp. and S. sasameyukin. sp. The geographical distributions of the two new species overlap, but their micro-habitats differ from each other; the former lives on calcareous algae on rocky shores, the latter lives on silty sand bottom within the inner bay. A third new species, S. slipperi sp. nov., is also described. In view of their present geographical distributions and fossil records, the origin of this group of species would appear to be the Japanese islands or adjacent areas in and after the Miocene. This group then migrated to the Arctic Ocean and East Pacific Ocean during or before the middle Pliocene.     

A taxonomic reevaluation of freshwater ostracods (Crustacea,Ostracoda) referred to the genus Cypridopsis Brady, 1868 from Southeast Asia

A taxonomic reevaluation of five species of Southeast Asian freshwater ostracods formerly assigned to the genus Cypridopsis Brady, 1868 has resulted in the retention of Cypridopsis adusta Sars, 1903, Cypridopsis exigua Sars, 1903 and Cypridopsis dubia Sars, 1903 in Cypridopsis and transfer of Cypridopsis albida (Vavra) 1898 and Cypridopsis arsenia Tressler, 1937 to the genus Plesiocypridopsis Rome, 1965.     

Pleistocene and Recent species of the family Darwinulidae Brady & Norman, 1889 (Crustacea, Ostracoda) in Europe

Six species in two genera of Darwinulidae are herereported from Europe; two of these are known fromfossils only.Microdarwinula zimmeri (Menzel) is, in Europe,an interstitial species. Darwinula stevensoni(Brady & Robertson), the type species of thegenus, is also the most common darwinulid. Althoughit abounds in the shallow littoral of lakes, it canalso occur in rivers, bogs and springs, both infresh and saline waters. Darwinula boteaiDanielopol is found in interstitial habitats inRumania. Darwinula pagliolii Pinto & Kotzian,originally described from Recent South Americanpopulations, is reported from fossil, Germanlocalities. Darwinula brasiliensis Pinto &Kotzian, originally described as D. africanabrasiliensis, also from South America, is hereelevated to specific rank. It has been found extantin a bog in southern France and is reported from amuseum collection from a Scottish lake. The latterspecies is here reported from Europe for the firsttime. Finally, Darwinula danielopoli n.sp. isalso described from German Holocene (Subrecent)fossils. This species represents the first nominaltaxon of a distinctly separate lineage within Darwinula s.l.Global and European distribution, history,ecological tolerance ranges, brooding and clonaltaxonomy in this group are discussed.     

A revised classification of the higher taxa of the Ostracoda (Crustacea)

Focusing on palaeontological data from the literature of the last four decades, a new classification of the Ostracoda is outlined. The superorder Podocopomorpha is accepted as a mantle term for the ‘P-orders’ Palaeocopida, Punciocopida, Platycopida and Podocopida; its counterpart are the Myodocopomorpha (Cypridinida, Halocypridida and ? Leperditicopida). The Podocopida comprise the suborders Bairdiocopina, Cytherocopina, Sigilliocopina, Cypridocopina, Darwinulocopina and Healdiocopina (n.;=Metacopina s.s.). The non-calcifying ostracodomorph arthropods (Archaeocopida and Phosphatocopida) of the Early Palaeozoic, now excluded from the Ostracoda by many authors, are also considered briefly.     

On the origin of the putative furca of the Ostracoda (Crustacea)

The posterior end of body of the extant ostracods exhibits a pair of variously shaped appendages, commonly designated as furca(e), uropods or caudal rami, used for feeding and/or locomotion. It is here shown that the so-called furca of all extant ostracods has evolved from the (probably epipodal) vibratory plates of a pair of uropods. The transformation comprised the following steps: (a) complete reduction of the uropodal protopodite and endopodite; (b) sclerotisation of the lateral walls of the vibratory plates; (c) transformation of the branchial filaments into spines and/or claws; (d) re-orientation of the plates from posterodorsal to posteroventral. These modifications are suggested to have evolved in parallel with a change in function, from respiratory to locomotory and/or feeding. The most primitive condition, reminiscent of the ancestral state of character, is seen in the Platycopida: the ‘furca’ still appears similar in shape to the vibratory plates of the pair of sixth limbs. In the Podocopida the uropodal plates have been modified into plate-like, more often into rod-shaped rami mainly used for locomotion. In both the Platycopida and Podocopida the anus has remained in its original place, posterior to the ‘furcal’ plates or rami. In the Myodocopida and Halocyprida the uropodal vibratory plates are transformed into heavily developed lamellae bearing sturdy spines. They are activated by a complex apparatus of muscles and sclerites, the development of which necessitated the displacement of the anus from the end of the body towards its present place, anterior to the ‘furca’. The furca of the Ostracoda being not a ‘true’ furca, a change in terminology is proposed: uropodal plates or lamellae in the Platycopida, Palaeocopida and Myodocopida/Halocyprida; uropodal rami in the Podocopida. The so-called furcae of the Ostracoda being homologous structures, it is concluded that all extant ostracods belong to a monophyletic lineage.     

Two new species of Pseudocythere Sars (Crustacea,Ostracoda) from Britain and Norway

Two new species of the genus Pseudocythere Sars are described, one each from British and Norwegian waters respectively.     

The ontogeny of appendages of Heterocypris salina (Brady, 1868) Ostracoda (Crustacea)

The post-embryonic development of the appendages of the Cyprididae ostracod Heterocypris salina (Brady, 1868) are described in detail and compared with those of other podocope species documented in previous studies. Generally, the appearence of limbs during onotgeny of H. salina is similar to that of other species, but small differences in limb morphologies were identified between H. salina and other Cyprididae species, including other Heterocypris species. Some features appear either earlier or later in the development of H. salina compared with other species, even species of the same genus. These features may be useful characters for phylogenetic analyses at the genus and family levels.     

The Ontogeny of Neonesidea oligodentata (Bairdioidea, Ostracoda, Crustacea)

This is the first detailed ontogenetic study of the appendages and carapace of a bairdioidean ostracod. This paper uses the development of the appendages and changes in the pore systems of the carapace through ontogeny to help determine the relationship between the Bairdioidea and other podocope groups. Neonesidea oligodentata has eight post-embryonic stages: one fewer than the Cypridoidea, Cytheroidea and Darwinuloidea. The first instar of N. oligodentata resembles that of the second instar of the Cypridoidea and Cytheroidea in terms of appendages, and it is postulated that there is an additional instar stage of N. oligodentata that molts within the egg. The general sequence of appearance of the limbs from instar A-7 onwards is similar to that of the Cypridoidea and Cytheroidea, but different from that of the Darwinuloidea. Like the Cypridoidea and Cytheroidea, N. oligodentata has a gap in its ontogenetic development during instar A-6, where no new Anlage is added. Pore system analysis of A-7 instars suggests that the Bairdioidea may be more closely related to the Cypridoidea than to the Cytheroidea.     

Historical biogeography and distribution of the freshwater calanoid copepods (Crustacea: Copepoda) of the Yucatan Peninsula, Mexico

Aim To determine and analyse the distribution of the freshwater calanoid copepod (Diaptomidae and Pseudodiaptomidae) fauna of the Yucatan Peninsula (YP) and its relation to the geological history of this Neotropical karstic plain. Location The Yucatan Peninsula, Mexico. Methods Plotting of geo‐referenced sites, analysis of local and regional geological history, analysis and comparison of regional and local records. Results The current composition and distribution of Diaptomidae and Pseudodiaptomidae in the YP mainly reflects recent, post‐Pliocene colonization events. This invasion did not reach America, but only parts of Central America (CA). The presence of diaptomids in the continent since the pre‐Cretaceous and the presumed post‐Cretaceous (Palaeocene–Oligocene) radiation of Diaptomidae in Middle America suggest earlier colonizations of the YP. The marine transgressions kept most of the YP submerged in different geological periods, thus eliminating any original primary freshwater colonizers, such as the diaptomids. The periods of marine regression probably represented opportunities for new waves of diaptomid colonization of the YP. The latest dispersal of diaptomids in the YP during the Holocene (8000 yr bp ) was probably an intermittent process because of the alternative dry and wet periods and interglacial transgressions. The presence of the Nearctic Leptodiaptomus and Arctodiaptomus in the YP and the current distribution of Mastigodiaptomus might represent remnants of earlier invasions of Diaptomidae in Middle America. The Neotropical Mastigodiaptomus probably originated in the Late Cretacic CA/proto‐Antilles complex. Forms derived from a M. albuquerquensis type ancestor radiated into the YP leaving relatively isolated populations of three species in the northern half of the peninsula. The distribution of the brackish water Pseudodiaptomus marshi well inside the coastline might have resulted from stranding and subsequent adaptation of this species during a marine regression in the Bacalar formation; this agrees with the vision of this taxon as being in process of invasion of freshwater environments. Main conclusions It is not probable that the South American (SA) diaptomid fauna originated from an invasion of upper Neotropical/Nearctic forms. The current distribution of freshwater calanoid copepods reflects relatively recent, post‐Pliocene biogeographical patterns, but probably older patterns are involved as well. The northern and eastern coasts of the Yucatan are the most recently colonized by diaptomids. Differing from other freshwater groups surveyed in the Yucatan that have marine relatives (i.e. fishes, amphipods, isopods, mysids, macrocrustaceans), there is no evidence of local vicariant events involving cave‐dwelling forms or marine relicts in the diaptomid fauna of the YP.     

Ecological strategies in the ancient asexual animal group Darwinulidae (Crustacea, Ostracoda)

• 1 We investigated the relationship between geographical distribution and ecological tolerance within the ancient asexual family Darwinulidae. Distribution maps were compiled based on data from the literature, the Non‐marine Ostracod Distribution in Europe database and personal collections. Ecological tolerance was assessed experimentally by exposing individual ostracods to a combination of eight different salinities (range from 0 to 30 g L^?1) and three different temperatures (10, 20 and 30 °C).
• 2 The type species of the family, Darwinula stevensoni, is ubiquitous and cosmopolitan; the two species Penthesilenula brasiliensis and Microdarwinula zimmeri also have an intercontinental distribution. Two other darwinulid species tested here (Vestalenula molopoensis and P. aotearoa) are known only from their type localities. The latter is also true for most extant darwinulids.
• 3 Darwinula stevensoni and P. brasiliensis had a broad salinity tolerance, tolerating distilled water and also salinity up to 25–30 g L^?1, whereas the maximum salinity tolerance of V. molopoensis was 12 g L^?1 and of P. aotearoa, 20 g L^?1.
• 4 The results indicate that both ecological specialists and generalists, as well as intermediate forms, exist in the Darwinulidae and that taxa with the broadest ecological tolerance also have the widest distribution.

     

Evolution of distribution and habitat patterns in endemic millipedes of the genus Dolichoiulus (Diplopoda: Julidae) on the Canary Islands, with notes on distribution patterns of other Ganarian species swarms

Forty-six species of the genus Dolichoiulus , all endemic, occur on the Canary Islands The highest number of species occur on the largest, highest island (Tenerife); fewest occur on Lanzarote, Fuerteventura (low, xeric), El Hierro and La Palma (small, remote). Most of the Dolichoiulus species live on one island only, as in other endemic Canarian species swarms. The scarcity of pluri-insular Dolichoiulus species, in connection with information on phylogeny, suggests that speciation has mainly taken place within individual islands. Distribution patterns are partly governed by habitat differences between species, but vicariance patterns between species living in the same kind of habitat are evident on La Gomera and Tenerife. Dolichoiulus species occur in all kinds of natural habitats. Laurisilva and cave species are generally paler than other species. In the laurisilva of eastern Tenerife, microhabitat differentiation between species is pronounced. In some, but far from all, cases, species coexisting in the same microhabitat are of different sizes. The ancestral colonizing species of Dolichoiulus is/are hypothesized to have been small and to have lived in coastal habitats. Colonization of higher altitudes was usually accompanied by an increase in body size. Invasion of the laurisilva was usually accompanied by a habitat shift from the ground layer to logs.     

Phylogeny and evolution of Loxoconcha (Ostracoda, Crustacea) species around Japan

The pore-systems of 17 extant species of Loxoconcha around Japan were studied in order to understand their phylogeny and evolution. The phylogeny was estimated by two steps. First, the 17 species were divided into two groups, Group A (12 species) and Group B (five species) by Pore pattern Below Eye tubercle (PBE) analysis. Then, intragroup relationships were estimated by Differentiation of Distributional pattern of Pore-system (DDP) analysis. PBE analysis reveals that species of Groups A and B have on average different ecological preferences. Species of Group A, which appeared in the late Pliocene, are more diverse, have both phytal and bottom-dwelling modes of life, possess fewer pore-systems in the ventral area, and inhabit normal marine environments. Species of Group B, whose oldest fossil record is the lower Miocene, are less diverse, have only bottom-dwelling species, possess more pore-systems in the ventral area, and tend to inhabit brackish water environments. The results of this study suggest that the differences in ecology may have had an impact on the late Cenozoic diversification around Japan. The primary invasion of Group B occurred before the lower Miocene,with no subsequent diversification. Group A invaded after the late Pliocene and immediately diversified, which created the present abundance of Loxoconcha species around Japan in both species diversity and variety of modes of life.     

A revision of the genus Paradoxostoma Fischer (Crustacea; Ostracoda) in British waters

Species of the genus Paradoxostoma Fischer are an important component of marine and estuarine ostracod faunas throughout the world. This revision of the genus in British waters deals with 17 species of which six are described as new. Each species is diagnosed and illustrated in detail, and comments are made on their ecology and distribution. The specialized mouthparts which characterize the genus are illustrated by means of the scanning electron microscope for the first time. A key to the genus is given.     

The ontogeny of Loxoconcha japonica Ishizaki, 1968 (Cytheroidea, Ostracoda, Crustacea)

The ontogeny of the cytheroidean species Loxoconcha japonica is documented from the earliest instar to the adult. The first instar (instar A-8) of L. japonica is different from that of cypridoidean species in that it has an additional appendage, the furca, present. From instar A-7 onwards, the appearance of the appendages is similar to that of cypridoidean and bairdioidean species. The furca is well developed in instars A-8 to A-5, and is probably an important appendage in these early instars, despite its reduced form in the adults. Some appendages of L. japonica (e.g. the antennae) gain very few setae and claws through ontogeny, compared with species from other superfamilies. This possibly reflects paedomorphic evolution of this species.     

Marine Ostracoda of the Galapagos Islands and Ecuador

Marine algae collected from rock pools on Hood, Fernandina and Mosquera, in the Galapagos Islands, have provided a fauna of 26 ostracod species of which 14 are new. One genus, belonging to the Hemicytheridae, is also new and appears to be endemic to the Islands. From two littoral algal samples collected from Punta Canoa and San Pedro beach, Ecuador, an assemblage of some nine species, four of which are new, is also described. Two ostracods: Touroconcha lapidiscola and Loxoconcha (Lox-ocorniculum) lenticuloides , are the only species so far known to be present both in the Galapagos Islands and off the coast of Central and South America. One species: Cytherelloidea praecipua recorded from off Tobago and Clipperton Islands may be present in the Galapagos but this has not definitely been confirmed. The evolution in the Gulf Coast/Caribbean region of several ostracods and their subsequent dispersal westwards is discussed.     

Altitudinal distribution patterns of bryophytes in the Canary Islands and vulnerability to climate change

We report the pattern of bryophyte distribution through the elevation gradient of three Canary Islands (Fuerteventura, Tenerife and Gomera) assessing their vulnerability risk to climate change. We considered a conservative scenario of upslope climatic shift of 200–400 m and a drop in the upper limit of the cloud belt from 1500 to 1000 m. Climate change vulnerability was analyzed from the overlap between the predicted shift in isotherms or cloud-belt edges and the current species range, following the Colwell and colleagues's model.Liverworts show narrower ranges and tend to live at lower elevations than mosses. Perennials and long-lived shuttle species establish in the upper localities. Many perennials and most of the long-lived shuttle species grow in cloud forests. Many annual shuttle species and colonists establish in the lowest localities. Colonists also occupy the harsh summit in the highest islands.In accordance with the Colwell model, most elements of this bryoflora appears vulnerable to rapid climatic change. Upland extinction and contraction challenges the bryoflora on the driest, lowest island Fuerteventura; range-shift gaps do this on the highest island Tenerife. Liverworts tend to be more vulnerable to range-shift gaps; mosses are more vulnerable to upland extinction. On the lowest island, perennials and long-lived shuttle species are more vulnerable to upland extinction; perennials are also vulnerable to range-shift gaps. Colonists are most vulnerable to upland contraction or extinction on the high islands Gomera and Tenerife. Annual shuttle species tend to be more vulnerable to lowland attrition on these high, most humid islands. Many elements of the bryoflora of the upper limit of the cloud forests appear to be vulnerable, while most of the flora of other cloud forest areas presumably will not be so affected, with the exception of the most restricted species.A simple model illustrates the feasibility of preliminary assessments of climate change on organisms which show a lack of published detailed information on their distribution and biology. This assessment gains by incorporating estimates of biological attributes.     

The life history and culturing of Xestoleberis hanaii (Crustacea,Ostracoda)

Xestoleberis hanaii Ishizaki, 1968 is one of the most abundant species on the Japanese coast and can be collected in all seasons from intertidal calcareous algae on rocky shores. Several characteristics make this species a suitable `experimental animal' in the laboratory: (1) adaptability to artificial environments (room temperature, petri dish, artificial seawater, single cultured food-type), (2) high fertility (active copulatory behaviour, egg brooding within the carapace, high egg productivity) and (3) rapid growth rate. Females mate after the final moult (when the reach sexual maturity); oviposition of fertilized eggs takes place over a period of four days after the final moult. Eggs (about 40 in total) are laid a few at a time in the postero-dorsal brood space of the carapace; they hatch in about 9 d as A-7 instars which are then discharged from the brood space within a day or two. Seven moults take place within the next approx. 33 (female) or 39 (male) days to reach adulthood. Adult females live for about 18 weeks and may repeat the reproductive cycle three times; adult males live for about 14 weeks.     

Comparative ecology of Ostracoda (Crustacea) in two rheocrene springs (Bolu,Turkey)

A total of ten taxa belonging to the class Ostracoda of the Crustacea (Darwinula stevensoni, Candona neglecta, Cypria ophthalmica, Ilyocypris bradyi, Prionocypris zenkeri, Herpetocypris chevreuxi, Psychrodromus olivaceus, Heterocypris incongruens, Scottia pseudobrowniana, Eucypris sp.) were collected from two rheocrene Darwinula stevensoni springs (Çetin Bey and Çaygökp?nar springs) on 15 separate occasions between November 2002 and November 2004. Almost all of the species identified exhibit cosmopolitan distributions – at least in the Holarctic region. The presence of Scottia pseudobrowniana represents the second recording of this species in the ostracod fauna of Turkey. The dominant taxa in both springs was Cy. ophthalmica, I. bradyi, Pr. zenkeri and Ca. neglecta. Correlation analyses suggested a significant positive relationship in relative abundance between I. bradyi, Pr. zenkeri and Cy. ophthalmica. Species composition differed significantly between the upper and lower study sites for each spring, but differences could not be detected between sites at the same elevation across sites. Environmental tolerance index (ETI) values suggest that species with high optima and tolerance ranges show cosmopolitan characteristics.