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The subgenus Hystricochaetonotus Schwank, 1990 is one of the most species-rich subgenera of Chaetonotus Ehrenberg, 1830. It has a worldwide distribution and encompasses 37 species predominantly living in the benthos and periphyton of limnetic habitats. We have discovered further nine new species in running and stagnant waters in Slovakia (Central Europe): Ch. (H.) arcanus sp. nov., Ch. (H.) avarus sp. nov., Ch. (H.) gulosus sp. nov., Ch. (H.) iratus sp. nov., Ch. (H.) luxus sp. nov., Ch. (H.) mirabilis sp. nov., Ch. (H.) optabilis sp. nov., Ch. (H.) slavicus sp. nov., and Ch. (H.) superbus sp. nov. Their morphology was studied using differential interference contrast microscopy and subsequent morphometric analyses were carried out. In addition, the primary and secondary structures of their 18S, ITS2, and 28S rRNA molecules as well as their barcoding mitochondrial gene encoding for cytochrome c oxidase (COI) were analyzed. Species boundaries were tested also using the compensatory base change analysis. The new species could be well separated both morphologically and molecularly. The present barcoding analyses revealed that the nuclear ITS2 sequences represent a powerful DNA barcode in addition to the mitochondrial COI gene. According to the multi-gene phylogenetic analyses, the lineage leading to the last common ancestor of the ‘Hystricochaetonotus’ clade is the longest internal branch within the family Chaetonotidae Gosse, 1864. Since members of the subgenus Hystricochaetonotus are morphologically highly heterogeneous, parallel evolution of Chaetonotus-like and/or Hystricochaetonotus-like characters of scales and spines occurred during its radiation.
Five species of Batillipes Richters, 1909 were collected from subtidal sediments of the Portuguese coast. Two of them, B. algharbensis sp. nov. and B. lusitanus sp. nov., are new to science. Batillipes algharbensis sp. nov. differs from all the other Batillipes species in having the middle toes 3 on the fourth feet longer than middle toes 4 and by the presence of rounded lateral body projections between legs III and IV. Batillipes lusitanus sp. nov. has the middle toes of the fourth feet equal in length, but it exhibits a dorsal cuticular ornamentation, constituted by large pillars, similar to the cuticle of B. adriaticus Grimaldi de Zio, Morone De Lucia, D’Addabbo Gallo & Grimaldi, 1979 and B. roscoffensis Kristensen, 1978. However, contrary to B. adriaticus, the caudal apparatus of B. lusitanus sp. nov. is a roundish cuticular expansion and B. roscoffensis lacks caudal apparatus. Batillipes adriaticus and B. phreaticus Renaud-Debyser, 1959 are new records for Portugal. Based on the examination of specimens of B. phreaticus collected at the Portuguese coast and their comparison with type material of this species and also of B. littoralis Renaud-Debyser, 1959, the toe arrangement patterns in species of Batillipes are clarified and a new identification key to species of this genus is provided.
The bathyal kinorhynch fauna along the Northwest American continental rise is explored, with emphasis on species of Echinoderidae Zelinka, 1894. Seven species of Echinoderes Claparède, 1863 are described as new to science: E. anniae sp. nov., E. dubiosus sp. nov., E. hamiltonorum sp. nov., E. hviidarum sp. nov., E. juliae sp. nov., E. lupherorum sp. nov. and E. yamasakii sp. nov. Three known species, Echinoderes hakaiensis Herranz, Yangel & Leander, 2017, E. cf. unispinosus Yamasaki, Neuhaus & George, 2018 and Fissuroderes higginsi Neuhaus & Blasche, 2006, are reported. The numerous new species indicate that the deep-sea still holds a great, undiscovered diversity of kinorhynchs, and that Echinoderes, as is also the case in more shallow, coastal waters, represents an important component of the deep-sea kinorhynch fauna. The presence of E. hakaiensis in the deepsea sediments demonstrates that the species may occur at a great depth range, and suggests that depth may play a less important role for the distribution of some kinorhynch species. The finding of the Northeast Atlantic species E. cf. unispinosus and the Southwest Pacific species Fissuroderes higginsi could indicate that kinorhynch species in the deep-sea may cover considerably larger distributional ranges than is assumed for coastal species of Echinoderidae.
Thirteen species of Echinoderes with nearly identical spine/tube patterns, and apparently similar tergal extensions were re-examined and compared. Based on this, redescriptions and/or emended species diagnoses are provided for Echinoderes aureus, E. dujardinii, E. gerardi, E. imperforatus, E. pacificus, E. pilosus, E. sensibilis, E. sublicarum and E. worthingi, and new details about cuticular structures are added for E. kozloffi and E. gizoensis. The new information derived from the redescriptions, and the subsequent comparative studies revealed that: 1) the holotype of Echinoderes lanceolatus is identical with the types of Echinoderes aureus, and E. lanceolatus is thus a junior synonym of E. aureus; other potentially synonymous species that should be addressed further in the future include: E. dujardinii + E. gerardi; E. imperforatus + E. sensibilis, and E. pacificus + E. sublicarum; 2) the paratypes of E. lanceolatus represented a different yet undescribed species, here described as E. songae Sørensen & Chang sp. nov.; 3) a comparison with literature information about E. ehlersi showed that the species is so insufficiently described that a redescription of topotype material is required before the species should be considered for taxonomic comparison; 4) specimens from the Andaman Islands, India, that previously have been reported as Echinoderes cf. ehlersi represent two different undescribed species, of which one is described as E. chandrasekharai Sørensen & Chatterjee sp. nov. and the other is left undescribed due to the limited material available; 5) out of a total of fifteen addressed species, it is proposed that eleven represent a putatively monophyletic group that is named the Echinoderes dujardinii group. The group includes following species: E. dujardinii, E. ehlersi, E. gerardi, E. imperforatus, E. kozloffi, E. sensibilis, E. pacificus, E. sublicarum, E. songae Sørensen & Chang sp. nov., E. chandrasekharai Sørensen & Chatterjee sp. nov., and Echinoderes sp. from the Andaman Islands, and is supported by a similar spine/tube pattern (except for variation regarding the presence of lateral accessory tubes on segment 8); generally short middorsal spines, especially on segments 4 to 6; glandular cell outlets type 1 always present in middorsal positions on segments 1 to 3, and in subdorsal positions on segments 4 to 9; glandular cell outlets type 2 always present in laterodorsal or midlateral positions on segment 8, and sometimes in same positions on segment 9 but never at any other segments or positions; female papillae always present on sternal plates of segments 7 and 8, and occasionally also on segment 6; tergal extensions well-spaced, triangular, gradually tapered cones, and pectinate fringes of sternal extensions are differentiated into seta-like tufts. The comparisons furthermore showed potential taxonomic significance of two echinoderid character traits that previously have been slightly neglected as diagnostic traits, namely the presence and appearance of female papillae, and the dorsal pattern of glandular cell outlets type 1. Female papillae may occur on the sternal plates of segments 6 to 8, but the positions may differ from ventrolateral to ventromedial, and the morphology of the intracuticular substructure also differ at species level. Information about position and morphology of female papillae proved helpful for species recognition, but it might also provide information of phylogenetic importance. Analyses of glandular cell outlet type 1 patterns on the dorsal sides of segments 1 to 9 in species of Echinoderidae, revealed several apparently unique or rare patterns, but also three distinct patterns that applied to larger groups of species. One pattern is the one present in all species of the E. dujardinii group, whereas the other two common patterns included 1) middorsal outlets on segments 1 to 3, and paradorsal outlets on segments 4 to 9 (found in 27 species), and 2) middorsal outlets on segments 1 to 3, 5 and 7, and paradorsal outlets on segments 4, 6 and 8 to 9 (found in 27 species).
Limited data are available for the kinorhynch fauna from the Southern Hemisphere, with little or no data from New Zealand. Here, we provide a first comprehensive overview of the diversity of mud dragons, with an emphasis on species of Echinoderes from the continental slope of New Zealand, from a variety of habitats such as slopes, canyons and seamounts located in the Hikurangi Margin region. The study revealed fifteen species of Echinoderes. Of these, ten are described as new to science: E. aragorni sp. nov., E. blazeji sp. nov., E. dalzottoi sp. nov., E. frodoi sp. nov., E. galadrielae sp. nov., E. gandalfi sp. nov., E. landersi sp. nov., E. leduci sp. nov., E. legolasi sp. nov. and E. samwisei sp. nov. Moreover, Echinoderes juliae Sørensen et al., 2018, Echinoderes sp. aff. E. balerioni, Echinoderes sp. aff. E. galadrielae/beringiensis, Echinoderes sp. aff. E. lupherorum and Echinoderes sp. aff. E. unispinosus are reported in the investigated region. The most abundant among all was E. gandalfi sp. nov., but it was found only in canyons. Interestingly, the second most common species was E. juliae that was found at several stations in canyons, seamount and on the slope. This species is one of the deep-sea species originally found on the abyssal plain off Oregon and along the continental rise off California, Northeast Pacific, recorded in polymetallic nodules in the tropical eastern Pacific, and recently found on the abyssal plains off Chile, east of the Atacama Trench. These findings, together with records of Echinoderes sp. aff. E. lupherorum and Echinoderes sp. aff. E. unispinosus indicate that, despite their low dispersal abilities, kinorhynchs, similar to other meiofaunal species, may exhibit a wider distribution pattern than previously assumed. The number of recorded species and numerous new species show that New Zealand sediments not only are inhabited by a diverse kinorhynch fauna, but Echinoderes, the most speciose genus, still holds much to discover.
A new species of echinoderid kinorhynchs, Echinoderes xiphophorus sp. nov. collected from oxidized brown silt at the deepest depression in the Sea of Japan, North-West Pacific, is described and illustrated using light and electron microscopy. This new representative of the most speciose kinorhynch genus is characterized by the unique set of spines and tubes and can easily be distinguished from most of its congeners. The second trunk segment bears three pairs of tubes in subdorsal, midlateral and ventrolateral position in both sexes; one pair of tubes on trunk segment 5 in lateroventral position and on trunk segment 8 in sublateral position; aciculate lateroventral spines on trunk segments 6–9; aciculate middorsal spines on trunk segments 4, 6, 8. This species is well recognized by very long tergal extensions of the posteriormost segment, some of the longest within the family Echinoderidae. Males of Echinoderes xiphophorus sp. nov. are well distinguished from all the congeners by extremely long sword-like appendages dorsally to three pairs of penile spines. The species constitutes the first deep-sea representative of the Echinoderidae in the Sea of Japan and the deepest representative of the Kinorhyncha in this sea.
In the framework of an ongoing extensive phylogenetic evaluation of the Ceratonotus group (Copepoda, Harpacticoida, Cletodidae), Poropsyllus menzelae gen. et sp. nov. from the sublittoral of south-western Cyprus (eastern Mediterranean Sea) and Paratouphapleura aaroni gen. et sp. nov. from the western Weddell Sea (Antarctica) are described. Both new species fit the autapomorphies of the Ceratonotus group but cannot be assigned to any of the genera so far known. Instead, each new species presents a set of derived characters that justify their placement in new genera, Poropsyllus gen. nov. and Paratouphapleura gen. nov., respectively. Furthermore, a comparison of the species placed in Ceratonotus Sars revealed that because of exclusive morphological deviations, Ceratonotus concavus Conroy-Dalton, C. steiningeri George, C. tauroides George, and C. vareschii George should be excluded from Ceratonotus and transferred to a new monophylum, Tauroceratus gen. nov. Likewise, Polyascophorus monoceratus George, Wandeness & Santos is characterized by several apomorphies that justify its transfer from Polyascophorus to a new taxon, Pseudopolyascophorus gen. nov. The Ceratonotus group is therefore increased to 31 species assigned to 13 genera. The systematic modifications conducted and resulting phylogenetic consequences are discussed in detail.
It appeared necessary to undertake a redescription of Laophontodes typicus T. Scott, 1894, but with the absence of the type specimen, several additional individuals collected from a number of regions were studied. The specimens chosen were from the western coast of Sussex and the Scottish Firth of Forth (UK), the Skjerstad fjord (Norway), the Patagonian continental slope (Chile) and the Great Meteor Seamount (subtropical north-eastern Atlantic Ocean). All specimens examined had been previously determined as L. typicus and deposited in the collections of renowned research institutions.
However, detailed morphological comparison revealed that only the Sussex material can be assigned to L. typicus; the remaining specimens represent distinct species whose original assignment to L. typicus was erroneous, due to a morphological ambiguity. Thus, the current status of L. typicus must be regarded as a species complex. The Sussex material enabled a detailed redescription of L. typicus. Additionally, five new species are described, namely L. scottorum sp. nov., L. sarsi sp. nov., L. gertraudae sp. nov., L. monsmaris sp. nov. and L. norvegicus sp. nov. They exhibit some morphological similarity, but equally present discrete characters justifying their establishment as distinct taxa. The descriptions are
accompanied by a detailed discussion that explains the justification of the splitting of L. typicus.
The fauna of Loricifera along a north-south longitudinal transect following the Atacama Trench was explored. Whereas no loriciferans were collected from the actual trench, the continental slope and surrounding abyssal plains yielded two species of Rugiloricus and two of Pliciloricus. All four species are considered as new to science, but only one of them could be formally described. The new species, Pliciloricus ukupachaensis sp. nov., is closely related with the North Atlantic Pliciloricus leocaudatus, and the two species share different morphological traits, including an enlarged anal field with conspicuous pentagonal and hexagonal fields formed by strong, cuticular ridges. Among other peculiar traits, the new species is characterised by having strongly reduced trichoscalid plates and no double trichoscalids. Comparison with previously published, unidentified specimens suggests that the new species’ distributional range might reach as far as Oregon off the US west coast.
Two new species of marine Platyhelminthes, Microstomum laurae sp. nov. and Microstomum edmondi sp. nov. (Macrostomida: Microstomidae) are described from the west coast of Sweden. Microstomum laurae sp. nov. is distinguished by the following combination of characters: rounded anterior and posterior ends; presence of approximately 20 adhesive papillae on the posterior rim; paired lateral red eyespots located level with the brain; preoral gut extending anterior to brain and and very small sensory pits. Microstomum edmondi sp. nov. is a protandrous hermaphrodite with a single ovary, single testis and male copulatory organ with stylet. It is characterized by a conical pointed anterior end, a blunt posterior end with numerous adhesive papillae along the rim, and large ciliary pits. The stylet is shaped as a narrow funnel with a short, arched tip. In addition, the first records of fully mature specimens of Microstomum rubromaculatum von Graff, 1882 from Fiskebäckskil and a phylogenetic analysis of Microstomum Schmidt, 1848 based on the mitochondrial cytochrome oxidase I (COI) gene are presented.