New species in the rheophilous genus Nicsmirnovius Chiambeng & Dumont, 1999 (Branchiopoda: Anomopoda: Chydoridae) and reassignment of Alona eximia Kiser, 1948 and Alonella fitzpatricki Chien, 1970

A morphological comparison of specimens previously assigned to Alona eximia Kiser, 1948 from tropical Africa, Eastern Asia and the Americas shows that this species-group shares a number of morphological characters on the postabdomen, head pores, first antenna and second and fourth limb that separate them from Alona Baird, 1843 but unite them with Nicsmirnovius Chiambeng & Dumont, 1999. Alonella fitzpatricki Chien, 1970, formerly believed to be a junior synonym of A. eximia, is separated from the latter and assigned to the genus Nicsmirnovius. Two new taxa, from Africa and the Island of Socotra (Yemen) are added to the genus. The relationship between the specialised habitat of these chydorids and their morphology is discussed. The geographic range of all known populations is figured and a key to species is presented.     

A revision of the genus Camptocercus (Anomopoda, Chydoridae, Aloninae)

The genus Camptocercus is revised. Camptocercus streletskayae sp. n. is described from East Siberia. The status of other species is discussed on the basis of a standard set of morphological features, including the structure of the cephalic region, the post-abdomen and post-abdominal claw, the dorsal keel, denticles at the ventro-posterior angle of valve, and setae on the inner distal lobe of limb I. Geographical distribution of species of this genus is discussed. A key to the species of this genus is composed. This revised version was published online in July 2006 with corrections to the Cover Date.     

Species richness of the Cladocera (Branchiopoda: Anomopoda and Ctenopoda) in southern Thailand, and its complementarity with neighboring regions

Seventy-two cladoceran species from southern Thailand include eleven first records. Species accumulation curves were used to estimate the total number of species present, and Chaos estimator was used to extrapolate the species number observed in 212 samples to the total number present. This S*max amounted to 76.06 species, with a low ratio of variance/estimator. Cladoceran faunas were compared by a complementarity index at three levels: between habitat types, between different zones of Thailand, and between Thailand and other countries. The geographical gradient was quite strong, but because not all areas have been studied to the same degree and with the same taxonomic accuracy, some comparisons are robust while others are not.     

Redescription of Ilyocryptus brevidentatus Ekman, 1905 (Anomopoda,Cladocera, Branchiopoda)

During the wet season of 1999–2000, we studied the effects of the hydroperiod and other physical and chemical variables on planktonic copepod communities from six stations in Everglades National Park. Two stations were located in a slough (Taylor Slough 1, Taylor Slough 2) and four stations in the marl prairies of the Rocky Glades (Long Pine Key 7, Long Pine Key 8, Pa-hay-okee, Chekika). During the period of investigation, Taylor Slough sites had the longest hydroperiods, together with Pa-hay-okee, which is located near the eastern edge of Shark River Slough. Long Pine Key 7 and Long Pine Key 8 had the shortest hydroperiods, and Chekika had an intermediate hydroperiod. The pineland edge sites in the southern Rocky Glades (Long Pine Key) had higher numbers of individuals, and high percentages of larval stages, especially at the end of the wet season. The pineland ecotone is morphologically very heterogeneous, with solution holes in the limestone bedrock that provide below-ground refugia when there is no water on the marsh surface. The slough stations had the lowest numbers of individuals, as well as Chekika in the Rocky Glades, probably as a consequence of the altered water quality and hydropatterns caused by water management structures and operations We collected two species of calanoids, 18 cyclopoids, and three harpacticoids. The most abundant species were Acanthocyclops robustus, Tropocyclops prasinus mexicanus, Arctodiaptomus floridanus, Mesocyclops americanus, Macrocyclops albidus, Osphranticum labronectum, Microcyclops varicans, Microcyclops rubellus, Eucyclops conrowae, and Mesocyclops edax. Of these species, T. prasinus mexicanus and A. floridanus seemed to be adapted to short-hydroperiod habitats, M. rubellus and M. varicans to longer hydroperiod habitats, and E. conrowae to high conductivity habitats. Acanthocyclops robustus, M. albidus, and O. labronectum were dominant regardless of hydroperiod. As regards the temporal distribution, A. robustus was abundant throughout the entire wet season, M. edax, M. rubellus, M. americanus and M. varicans were most abundant in mid-wet season, in September–October, and T. prasinus mexicanus, M. albidus, and E. conrowae were abundant late in the wet season, in winter. The two calanoids only slightly overlapped in time: A. floridanus was abundant at the beginning of the wet season, in July–August, and O. labronectum was abundant at the end of the wet season, in December.     

Adaptations of Anomopoda crustaceans (Cladocera) to the benthic mode of life

Crustaceans of the order Anomopoda inhabit both pelagic and littoral zones of fresh water bodies. Different adaptations to the benthic mode of life in representatives of different families and genera of this order are described. They include incomplete molting, the presence of a mucous film on the body surface, protection of the head from frontal damage, large lateral projections on the valves and additional sculpture on the head and valves, well-developed lateral armature of the postabdomen, the presence of projections on the postabdomen preanal margin, specialization of setae and spines of the second antenna, especially large exopodites on limbs IV and V, a reduced compound eye, and a large, well-developed ocellus. Similar adaptations to the benthic mode of life in the Anomopoda and Ostracoda are discussed.     

A taxonomic reappraisal of the European Daphnia longispina complex (Crustacea, Cladocera, Anomopoda)

The Daphnia longispina complex contains some of the most common water flea species in the northern hemisphere, and has been a model organism for many ecological and evolutionary studies. Nevertheless, the systematics and nomenclature of this group, in particular its Palaearctic members, have been in flux for the past 150 years; this hinders the correct interpretation of scientific results and promotes the erroneous use of species names. We revise the systematics of this species complex based on mitochondrial sequence variation (12S rDNA and COI) of representative populations across Europe, with a special focus on samples from type localities of the respective taxa. Combining genetic evidence and morphological assignments of analysed individuals, we propose a comprehensive revision of the European members of the D. longispina complex. We show that D. hyalina and D. rosea morphotypes have evolved several times independently, and we find no evidence to maintain these morphotypes as distinct biological species. Alpine individuals described as D. zschokkei are conspecific with the above-mentioned lineage. We suggest that this morphologically and ecologically plastic but genetically uniform hyalina–rosea–zschokkei clade should be identified as D. longispina (O. F. Müller, 1776). The valid name of Fennoscandian individuals labelled D. longispina sensu stricto in the recent literature is D. lacustris G. O. Sars, 1862. Additionally, we discovered another divergent lineage of this group, likely an undescribed species, in southern Norway. Our results present a solution for several prevailing taxonomic problems in the genus Daphnia , and have broad implications for interpretation of biogeographical patterns, and ecological and evolutionary studies.     

Morphological Radiation with Reference to the Carapace Valves of the Anomopoda (Crustacea: Cladocera)

Diversity of the carapace valve structure in the Anomopoda (Crustacea: Branchiopoda) is described. We found that transformations of shape, modifications of the surface and valve margins, and thickening or thinning of the valves, take place independently in different families, sometimes resulting in a convergent similarity. The limits of morphological diversity in these features determine the range of adaptive radiation in general form of the group. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Study of the late embryogenesis of Daphnia (Anomopoda, ‘Cladocera’, Branchiopoda) and a comparison of development in Anomopoda and Ctenopoda

The embryonic development of Daphnia galeata and D. hyalina (`Cladocera', Anomopoda, Daphniidae) has been investigated by observing living embryos removed from female brood pouches. The sequence of morphological changes was analysed, as was the time at which the activity of certain organs began. The timing of these events at 22 °C is documented for both species.These data were compared with similar information, previously obtained for two representatives of the Ctenopoda (Kotov & Boikova, 1998). The sequence of events is basically similar in the two groups during early and late phases of their development, but the time of shedding of the embryonic membranes is different in the Anomopoda and Ctenopoda. The ctenopod embryo hatching from the second egg membrane is covered by the third membrane, which will be cast some hours later. The anomopod embryo hatches from the second egg membrane approximately simultaneously with the shedding of the third membrane, and it is covered already by the fourth membrane after the shedding of the second egg membrane.Earlier (Kotov & Boikova, 1998), we determined four embryonic instars in the course of the development of the Ctenopoda. Two of them are passed within the egg membranes, the next two instars occur after the shedding the egg membranes within the mother's brood pouch. However, in anomopods, one of the latter (the third) occurs within the second egg membrane, one is incorporated into the egg. Thus, the development of the Anomopoda is more embryonized in comparison with that of the Ctenopoda.     

Alona iheringula Sinev & Kotov, 2004 (Crustacea,Anomopoda, Chydoridae,Aloninae): Life Cycle and DNA Barcode with Implications for the Taxonomy of the Aloninae Subfamily

Knowledge of reproductive rates and life cycle of the Cladocera species is essential for population dynamic studies, secondary production and food webs, as well as the management and preservation of aquatic ecosystems. The present study aimed to understand the life cycle and growth of Alona iheringula Kotov & Sinev, 2004 (Crustacea, Anomopoda, Chydoridae), a Neotropical species, as well as its DNA barcoding, providing new information on the Aloninae taxonomy. The specimens were collected in the dammed portion of the Cabo Verde River (21°26′05″ S and 46°10′57″ W), in the Furnas Reservoir, Minas Gerais State, Brazil. Forty neonates were observed individually two or three times a day under controlled temperature (25±1°C), photoperiod (12 h light/12 h dark) and feeding (Pseudokirchneriella subcapitata at a concentration of 10⁵ cells.mL⁻¹ and a mixed suspension of yeast and fish feed in equal proportion). Individual body growth was measured daily under optical microscope using a micrometric grid and 40× magnification. The species had a mean size of 413(±29) µm, a maximum size of 510 µm and reached maturity at 3.24(±0.69) days of age. Mean fecundity was 2 eggs per female per brood and the mean number of eggs produced per female during the entire life cycle was 47.6(±6.3) eggs per female. The embryonic development time was 1.79(±0.23) days and the maximum longevity was 54 days. The species had eight instars throughout its life cycle and four instars between neonate and primipara stage. The present study using molecular data (a 461 bp smaller COI fragment) demonstrated a deep divergence in the Aloninae subfamily.     

Separation of Leydigia louisi Jenkin, 1934 from L. leydigi (Schoedler, 1863) (Chydoridae, Anomopoda, Cladocera)

The aim of the present article was to contribute to the systematics of the leydigi-like species of Leydigia consisting of a few (probably 3) formal species with: (1) a large basal spine on the postabdominal claw (as long as claw thickness at the base); (2) a short setulation at anterior margin of labral keel; (3) no longitudinal striation on the female valves; (4) at least three lateral setae in each fascicle on the postabdomen; (5) three large lateral setae on exopodite III. The morphology of L. leydigi (Schoedler, 1863) and L. louisi Jenkin, 1934 are redescribed, and type material of L. macrodonta Sars, 1916 is studied. In contrast to previous suggestions (Jenkin, 1934; Smirnov, 1971), I found that: (1) L. louisi is a valid species, not a subspecies of L. macrodonta; (2) L. macrodonta is not a member of the L. leydigi-group. The third member of leydigi-group, Leydigia macrodonta longiseta Chen Shou-zhong, 1992, was described from China. It is not a subspecies of L. macrodonta, but a relative of L. leydigi; most probably, it is a valid species, but this opinion must to be confirmed by examination of original Asian material. In this article, the presence of L. leydigi in Palearctic only, and that of L. louisi in only Africa was confirmed. A new subspecies of L. louisi, found in Mexico, will be reported separately.     

External morphology of the male of Cyclestheria hislopi (Baird, 1859) (Crustacea, Branchiopoda, Spinicaudata), with a comparison of male claspers among the Conchostraca and Cladocera and its bearing on phylogeny of the 'bivalved' Branchiopoda

The adult male of Cyclestheria hislopi, sole member of the spinicaudate conchostracan clam shrimp family Cyclestheriidae and a species of potential phylogenetic importance, is described for the first time. Several previously unknown features are revealed. Among these are (1) the morphology of the dorsal organ, which is roughly similar in shape to the supposedly homologous structure in other clam shrimps but bears a relatively large, centrally located pore unique to the species; (2) an anterior cuticular pore presumably leading to the ‘internal’ space surrounding the compound eyes, and thereby homologous to the same pore in other clam shrimps and in the Notostraca; (3) the spination and setation of the antennae and thoracopods, and (4) the mature male first thoracopods (claspers). The male claspers are paired and essentially equal in size and shape on right and left sides of the body. The second pair of thoracopods are not modified as claspers, a situation different from all other spinicaudate families but shared (plesiomorphic we propose) with the laevicaudatans and most cladocerans. The claspers bear a field of special spine-like setae on the extremity of the ‘palm’; this setal type, previously unrecognized, is unique to Cyclestheria. The palm of the clasper also bears two palps (one very small), as in other conchostracan species (both laevicaudatans and spinicaudatans). The movable finger of the clasper, modified from the thoracopod endopod, bears a row of long setae along its outer extremity, also unique. Cyclestheria exhibits a mixture of characters, some unique and others typical of the Spinicaudata (Conchostraca). Cladoceran clasper types are briefly reviewed. as are the claspers in the Spinicaudata and Laevicaudata (Conchostraca). Morphology of the clasper of Cyclestheria shows typical spinicaudate characters. It is suggested that claspers on the first thoracopods may be a synapomorphy for the Conchostraca and the Cladocera. The possible role of Cyclestheria or a Cyclestheria-like ancestor in cladoceran phylogeny is briefly discussed in light of recent suggestions (Martin and Cash-Clark, 1995) of cladoceran monophyly and possible ancestral relationships with this genus. Some possibilities concerning the phylogenetic position of Cyclestheria–either as a sister group to the rest of the Spinicaudata or as a sister group to the Cladocera—are discussed.     

A new divergent lineage of Daphnia (Cladocera: Anomopoda) and its morphological and genetical differentiation from Daphnia curvirostris Eylmann, 1887

The systematic biology of the subgenus Daphnia s . s . remains confused. Prior attempts at resolution used chiefly postabdominal claw morphology, chromosome numbers and rRNA gene sequences as characters for higher-level relations. Still, several taxa, such as Daphnia curvirostris Eylmann, 1878, have unclear affiliations. We addressed the position of D. curvirostris in this genus by estimating phylogenetic trees from a rapidly evolving protein coding gene (ND2), conducting broad geographical comparisons and carrying out detailed morphological comparisons. The Japanese ' curvirostris' was found to be a new divergent lineage in the subgenus Daphnia , and to possess distinctive morphological characteristics from D. curvirostris . We described this new species as Daphnia tanakai sp. nov. , and redescribed D. curvirostris . The polymorphic postabdominal claw morphology and the distinctive chromosome number of D. tanakai sp. nov. provided evidence for rapid evolution of these traits. Our new morphological, chromosomal and genetic assessment of Daphnia weakened the argument for division of the subgenus Daphnia ( Daphnia ) O. F. Müller, 1785 sensu Johnson, 1952, into two further subgenera.  © 2006 The Linnean Society of London, Zoological Journal of the Linnean Society , 2006, 146 , 385–405.     

A hidden species becoming visible: biogeography and ecology of Rhynchotalona latens (Cladocera,Anomopoda, Chydoridae)

Hydrobiologia - A long hidden chydorid (Chydoridae, Cladocera) taxon, first found as fossil specimens and recently redefined as Rhynchotalona latens (Sarmaja-Korjonen et al., Hydrobiologia 436:...     

Morphological basics of systematics of Eurycercidae Kurz, 1875 sensu Dumont et Silva-Briano, 1998 (Cladocera: Anomopoda) family

We analyzed data from the literature and our own results to discover common principles underlying the systematics of the Eucercidae Kurz, 1875 sensu Dumont et Silva-Briano, 1998 (Cladocera: Anomopoda) family, which is represented only by the genus Eurycercus Baird, 1983. The appropriateness of using various diagnostic features for identification of species was evaluated. We estimated the accuracy of using age variability of different morphometric parameters for determination of species. It was demonstrated that using oligomerous structures is more effective for differentiation of species than counting the structures the number of which can vary considerably. The independence of the Bullatifrons Frey, 1975 subgenus was found to be questionable.     

A new species of Tigriopus (Copepoda, Harpacticoida, Harpacticidae) from Thailand with the description of its naupliar development

Both genders of Tigriopus thailandensis sp. nov. are described from a laboratory stock raised from individuals collected from the seaweed Enteromorpha clathrata in Thailand (Bangsaen Beach, Chonburi Province). Tigriopus thailandensis sp. nov. shares with its closest relative T. japonicus Mori, 1932 two setae on the third exopodal segment of leg 4 while other congeners bear 3 inner setae. However, allobasis and exopod of antenna in both genders are much more slender and elongate than in T. japonicus. All six naupliar stages of T. thailandensis are described from the offspring of isolated females. In comparison with nauplii of T. japonicus, T. thailandensis nauplii are characterized by the following: a smaller body size throughout the naupliar phase; first antennular segment without seta, second antennular segment with only one small seta plus two longer setae; third antennular segment with additional spinules from naupliar stage II onwards; antenna bears three small spinules on the terminal exopodal segment; one additional seta on the anterior surface of the antennary basis, tubular endopod of antenna with one tiny seta midlength at naupliar stage III that increases in size; mandibular basis with several spinules on anterior surface; mandibular coxa with one spinulose seta that is smooth in T. japonicus.     

A re-evaluation of the Macrothrix rosea-triserialis group, with the description of two new species (Crustacea Anomopoda: Macrothricidae)

We redescribe Macrothrix rosea (females and males) based on material collected in Belgium. We also compare seven populations of Macrothrix `triserialis' from different parts of the world, including a topotypical population of M. triserialis s. str. from Sri Lanka, and males from South India (here first described), relying heavily on the structure of the trunk limbs, beside classical features of morphology. M. rosea and M. triserialis are extremely closely related: males are easily separated, but the identification of females requires micro-characters such as the relative length of the apical segment of the setae natatoriae and the adornment of the first antenna and of the longest swimming seta of the antenna. M. rosea and triserialis together constitute a sub-group of the rosea-group. Macrothrix triserialis-like animals occur in the tropical–subtropical belts of four continents. We compare populations from Asia, South America and Africa, and find differences in microcharacters of the trunk limbs, but cannot decide whether these represent random variation or sound taxonomical differences. One of the basic characters of the Macrothrix rosea-triserialis subgroup is that the setae natatoriae of the postabdomen are implanted on a prominence, the `heel'. Other characters include the fact that the Fryer' forks are adorned with one or two big teeth only, and that the scrapers of trunk limb two form a row of eight without any doublings. Possibly, scraper five, and scraper four to a lesser degree has an enlarged subapical tooth. The exopodite of trunk limb three has four plumose setae, the back and front row of the endopodite six setae and/or receptors, the exopodite of trunk limb four has two setae, and the back row of the endopodite six setae, plus one on the gnathobase. The pre-epipodite of trunk limb five consists of three lobes, the `endopodite' is small, and the `exopodite' is reduced to a single seta. The male postabdomen has a tubular ending, without true end-claws, although a rudiment of an end-claw is seen in M. triserialis. Two new species are described: M. tabrizensis and M. agsensis. A comparison, including the males of Macrothrix triserialis, M. rosea, M. smirnovi and M. tabrizensis confirms the relationship of all these taxa, but also reveals a morphological series in the shape of the postabdomen, from a complete absence of end-claws, over rudiments of a pair of end-claws, to complete endclaws. Absence of end-claws is here considered to represent an evolved character state. Macrothrix smirnovi Ciros & Elías (1987) is less closely related to the rosea-triserialis group, and is considered to form a sub-group in its own right. It shows a short `heel' on the postabdomen, but carries a supplementary seta behind scraper 4 of the endopodite of trunk limb two, and has a male with a postabdomen that closely resembles that of the female. These are primitive characters, which are also found in Wlassicsia, Bunops and Onchobunops and provide a possible phylogenetic link between Macrothrix and these three genera, although the genetic distance between them is considered to be quite large.     

Separation of two Neotropical species: Macrothrix superaculeata (Smirnov, 1982) versus M. elegans Sars, 1901 (Macrothricidae, Anomopoda, Cladocera)

The morphology of two Neotropical taxa, Macrothrix elegans Sars, 1901 and M. superaculeata (Smirnov, 1982) (Macrothricidae, Anomopoda, Cladocera) was redescribed, based on type materials (a lectotype of M. elegans was selected here), and additional samples from the Americas. Previous conclusion about synonymy of both species was erroneous, because it was based on limited material from South America. M. superaculeata differs from M. elegans in the presence of a sharp spine at postero-dorsal angle of valves; a more fine ring around dorsal head pore; thinner hexagonal reticulation of valves; the presence of setules on basal segment of postabdominal seta; armature of exopod on antenna II, and some features of thoracic limbs. Previously, the discriminative features of the two species were not formulated accurately, and it was a reason of several misidentifications. Actually, M. superaculeata is found only in a limited set of localities from the Amazon basin, while M. elegans is one of the most common anomopod species in all Neotropics, from Argentina to Mexico.     

Description of the male of Pleuroxus wittsteini Studer, 1878 (Anomopoda,Chydoridae) from Heard Island

The male of Pleuroxus wittsteini is described and illustrated.     

Analysis of the Ilyocryptus spinifer-species group (Anomopoda,Branchiopoda), with description of a new species

We studied the morphology and variability of Ilyocryptus spinifer Herrick, 1882 from different parts of the world using optical microscopy and SEM, re-examining type material wherever possible. Morphometric analysis failed to reveal significant regional differences between populations. The following species names for members of Ilyocryptus spinifer group, I. halyi Brady, 1886; I. longiremis Sars, 1888; I. immundus F. Mueller in Ihering, 1895; I. verrucosus Daday, 1905; and I. tetraspinatus Berganim, 1939, are junior synonyms of I. spinifer. A new species from this group is described from Queensland, Australia. Ilyocryptus timmsi n. sp. shows unique morphological characters in the armature of the lateral swimming setae of the antennal endopod, its apical segment and the postabdominal claws.