Two sides of a coin: the phylum Kinorhyncha in Panama. II) Pacific Panama

Pardos, Fernando; Herranz, María; Sánchez, Nuria

doi:10.1016/j.jcz.2016.06.006

Cited by 28 publications

(20 citation statements)

References 42 publications

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“…Glandular cell outlets type 2: the presence and positions of glandular cell outlets type 2 has become an important character in modern echinoderid taxonomy (see e.g., Neuhaus & Blasche 2006;Sørensen et al 2012Sørensen et al , 2018Pardos et al 2016aPardos et al , 2016bCepeda et al 2019a;. Among species of the E. dujardinii group we consistently find minute glandular cell outlets type 2 in laterodorsal or midlateral positions of segment 8, and in those with short middorsal spines (except for E. songae Sørensen & Chang sp.…”

Section: Notes On Diagnostic Characters For the E Dujardinii Species Groupmentioning

confidence: 75%

Description, redescription and revision of sixteen putatively closely related species of Echinoderes (Kinorhyncha: Cyclorhagida), with the proposition of a new species group – the Echinoderes dujardinii group

Sørensen

Goetz

Herranz

et al. 2020

EJT

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1,546

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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)

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Section: Notes On Diagnostic Characters For the E Dujardinii Species Groupmentioning

confidence: 75%

Description, redescription and revision of sixteen putatively closely related species of Echinoderes (Kinorhyncha: Cyclorhagida), with the proposition of a new species group – the Echinoderes dujardinii group

Sørensen

Goetz

Herranz

et al. 2020

EJT

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1,546

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“…Unfortunately, kinorhynchs found in these studies were not identified beyond the group level, except for Echinoderes bengalensis collected at Kakinada Bay (east coast of India) (Annapurna et al 2015). Eight additional kinorhynch species have been identified in mangroves worldwide, including: Sphenoderes indicus in India (Higgins 1969); Pycnophyes alexandroi, Echinoderes belenae and Echinoderes strii in Panama (Pardos et al 2016); Echinoderes caribiensis in Venezuela (Kirsteuer 1964); Echinoderes teretis in Australia (Nicholas and Sørenson 2009); Echinoderes komatsui in Japan (Yamasaki and Fujimoto 2014); and Echinoderes applicitus in Indonesia. These kinorhynch species were surprisingly abundant, ranking the second or third most abundant taxon in some samples (Ostmann et al 2012).…”

Section: Mangrove Meiofaunamentioning

confidence: 99%

Characteristics of meiofauna in extreme marine ecosystems: a review

et al. 2017

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Extreme marine environments cover more than 50% of the Earth's surface and offer many opportunities for investigating the biological responses and adaptations of organisms to stressful life conditions. Extreme marine environments are sometimes associated with ephemeral and unstable ecosystems, but can host abundant, often endemic and welladapted meiofaunal species. In this review, we present an integrated view of the biodiversity, ecology and physiological responses of marine meiofauna inhabiting several extreme marine environments (mangroves, submarine caves, Polar ecosystems, hypersaline areas, hypoxic/anoxic environments, hydrothermal vents, cold seeps, carcasses/sunken woods, deep-sea canyons, deep hypersaline anoxic basins [DHABs] and hadal zones). Foraminiferans, nematodes and copepods are abundant in almost all of these habitats and are dominant in deep-sea ecosystems. The presence and dominance of some other taxa that are normally less common may be typical of certain extreme conditions. Kinorhynchs are particularly well adapted to cold seeps and other environments that experience drastic changes in salinity, rotifers are well represented in polar ecosystems and loriciferans seem to be the only metazoan able to survive multiple stressors in DHABs. As well as natural processes, human activities may generate stressful conditions, including deoxygenation, acidification and rises in temperature. The behaviour and physiology of different meiofaunal taxa, such as some foraminiferans, nematode and copepod species, can provide vital information on how organisms may respond to these challenges and can provide a warning signal of anthropogenic impacts. From an evolutionary perspective, the discovery of new meiofauna taxa from extreme environments very often sheds light on phylogenetic relationships, while understanding how meiofaunal organisms are able to survive or even flourish in these conditions can explain evolutionary pathways. Finally, there are multiple potential economic benefits to be gained from ecological, biological, physiological and evolutionary studies of meiofauna in extreme environments. Despite all the advantages offered by meiofauna studies from extreme environments, there is still an urgent need to foster meiofauna research in terms of composition, ecology, biology and physiology focusing on extreme environments.

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“…This phenomenon is referred to the “meiofauna paradox” or “everything is everywhere hypothesis” (Giere 2009; Fontaneto 2011). Such wide distribution patterns have been explained or hypothesized by the stepping stone hypothesis (George 2013; Packmor and Riedl 2016), artificial dispersal (artificial invasion) (Herranz and Leander 2016; Pardos et al 2016; Cvitković et al 2017), or long range dispersal using currents and/or drifting (Walters and Bell 1994; Neuhaus and Sørensen 2013; Neuhaus et al 2014; Yamasaki et al 2014). Some are even regarded as a pseudo-wide distribution via the detection of cryptic species (Jörger et al 2012; Leasi et al 2016).…”

Section: Introductionmentioning

confidence: 99%

Echinoderes pterus sp. n. showing a geographically and bathymetrically wide distribution pattern on seamounts and on the deep-sea floor in the Arctic Ocean, Atlantic Ocean, and the Mediterranean Sea (Kinorhyncha, Cyclorhagida)

Yamasaki

Grzelak

Sørensen

et al. 2018

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Kinorhynchs rarely show a wide distribution pattern, due to their putatively low dispersal capabilities and/or limited sampling efforts. In this study, a new kinorhynch species is described, Echinoderes pterus sp. n., which shows a geographically and bathymetrically wide distribution, occurring on the Karasik Seamount and off the Svalbard Islands (Arctic Ocean), on the Sedlo Seamount (northeast Atlantic Ocean), and on the deep-sea floor off Crete and on the Anaximenes Seamount (Mediterranean Sea), at a depth range of 675–4,403 m. The new species is characterized by a combination of middorsal acicular spines on segments 4–8, laterodorsal tubes on segment 10, lateroventral tubes on segment 5, lateroventral acicular spines on segments 6–9, tufts of long hairs rising from slits in a laterodorsal position on segment 9, truncated tergal extensions on segment 11, and the absence of any type-2 gland cell outlet. The specimens belonging to the populations from the Arctic Ocean, the Sedlo Seamount, and the Mediterranean Sea show morphological variation in the thickness and length of the spines as well as in the presence/absence of ventromedial sensory spots on segment 7. The different populations are regarded as belonging to a single species because of their overlapping variable characters.

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Two sides of a coin: the phylum Kinorhyncha in Panama. II) Pacific Panama

Cited by 28 publications

References 42 publications

Description, redescription and revision of sixteen putatively closely related species of Echinoderes (Kinorhyncha: Cyclorhagida), with the proposition of a new species group – the Echinoderes dujardinii group

Description, redescription and revision of sixteen putatively closely related species of Echinoderes (Kinorhyncha: Cyclorhagida), with the proposition of a new species group – the Echinoderes dujardinii group

Characteristics of meiofauna in extreme marine ecosystems: a review

Echinoderes pterus sp. n. showing a geographically and bathymetrically wide distribution pattern on seamounts and on the deep-sea floor in the Arctic Ocean, Atlantic Ocean, and the Mediterranean Sea (Kinorhyncha, Cyclorhagida)

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