The Protonephridia of the Arctic Kinorhynch Echinoderes aquilonius (Cyclorhagida,Echinoderidae)

The cyclorhagid kinorhynch Echinoderes aquilonius Higgins & Kristensen, 1988 possesses a single pair of protonephridia located in segments 10 and 11. The protonephridia consist of: (1) three terminal cells T-1, T-2. T-3, each with two cilia; (2) a single non-ciliated canal cell; (3) a nephridiopore cell with many microvilli and a cuticular sieve plate. The protonephridia of Echinoderes are presumed to develop from the ectoderm near the area of the sieve plate on the eleventh segment, and are suspended in the dorso-lateral pseudocoelomic cavity where they are surrounded by a basal lamina. One of the terminal cells (T-1) secondarily penetrates the basal lamina of the tenth segment and a part of the cell attaches to the cuticle. The kinorhynch protonephridia are compared with the excretory organs of other Bilateria. expecially the ‘aschelminths’, and apomorphic characters of the kinorhynch protonephridia are defined.     

First account on kinorhynchs from Portugal,with the description of two new species: Echinoderes lusitanicus sp. nov. and E. reicherti sp. nov.

The first exploration of the kinorhynch meiofauna in Portuguese marine waters has revealed the existence of two undescribed species of the cyclorhagid genus Echinoderes. In the present contribution we describe Echinoderes lusitanicus sp. nov. and Echinoderes reicherti sp. nov., both collected from subtidal regions of the coast of Algarve in the southernmost region of Portugal. Echinoderes lusitanicus sp. nov. is recognized by the presence of tubes on segment 2 in subdorsal and ventrolateral positions, on segment 5 in lateroventral positions, on segment 8 in lateral accessory positions, and on segment 10 in laterodorsal positions. Spines are present in middorsal position on segments 4 to 8, and in lateroventral positions on segments 8 and 9. The females have minute lateral terminal accessory spines. The second species, E. reicherti sp. nov., is characterized by tubes on segment 2 in subdorsal and ventrolateral positions, on segment 5 in lateroventral positions, and segment 8 in sublateral positions. In addition, the species possesses acicular spines in the middorsal position on segment 4, and in lateroventral positions on segments 6 to 9. Morphological aspects such as tube/spine pattern of the trunk or sexually dimorphic traits are discussed and compared with other Echinoderes species showing close resemblance.

http://zoobank.org/urn:lsid:zoobank.org:pub:79C25EEE-9064-46F8-95E2-EE493DC82185     

Two new species in the Echinoderes coulli group (Echinoderidae,Cyclorhagida, Kinorhyncha) from the Ryukyu Islands,Japan

Two new species belonging to the Echinoderes coulli group are described with their external morphologies and sequences of nuclear 18S rRNA and 28S rRNA genes, and mitochondrial COI gene. The first species, Echinoderes komatsui sp. n., is characterized by absence of acicular spines, and presence of lateroventral tubules on segments 5 and 8, laterodorsal tubules on segment 10, inverted triangle or wide oval shaped large sieve plates, lateral terminal accessory spines in female, and short tips of ventral pectinate fringe on segment 10. The second species, Echinoderes hwiizaa sp. n., is characterized by absence of acicular spines, and presence of lateroventral tubules on segments 5 and 7–9, midlateral tubules on segment 8, laterodorsal tubules on segment 10, large narrow oval shaped sieve plates on segment 9, and thick, short and blunt lateral terminal spines about 10–15% of trunk length. The diagnostic characters and key to species of E. coulli group are provided as well.     

New species of Echinoderes (Kinorhyncha: Cyclorhagida) from Spitsbergen,with additional information about known Arctic species

The kinorhynch fauna in two Arctic fjords at Spitsbergen was explored and eight species of Echinoderes were recorded, of which three are new to science and described herein. Echinoderes daenerysae sp. nov. is recognized by middorsal spines on segments 6 and 8 only, lateroventral spines on segments 6–9, laterodorsal and ventrolateral tubes on segment 2, lateroventral tubes on segment 5, lateral accessory tubes on segment 8, laterodorsal tubes on segment 9 and small laterodorsal tubes on segment 10. Echinoderes rhaegali sp. nov. has middorsal spines on segments 4, 6 and 8, lateroventral spines on segments 6–9, sublateral and ventrolateral tubes on segment 2, lateroventral tubes on segment 5, lateral accessory tubes on segment 8 and laterodorsal tubes on segment 10 in males. Echinoderes drogoni sp. nov. has middorsal spines on segments 4–8, lateroventral spines on segments 6–9, lateral accessory tubes on segment 5, glandular cell outlets type 2 in subdorsal, laterodorsal, sublateral and ventromedial positions on segments 2, in midlateral positions on segment 5, in sublateral positions on segment 8 and in subdorsal positions on segment 10; segment 11 has divided tergal plates. Moreover, types of other Arctic Echinoderes, including E. angustus, E. aquilonius, E. eximus, E. peterseni, E. svetlanae and E. tubilak, were re-examined and new information on glandular cell outlets type 2 is provided. Our results suggest that Arctic Echinoderes species have a circum-Artic distribution. Morphological analysis indicates that the occurrence of tubes may show intraspecific variation.

http://zoobank.org/urn:lsid:zoobank.org:pub:CBE29FE8-9233-4E3C-9757-FF9576B06C74     

New Harpacticoida (Crustacea, Copepoda) from the North Atlantic Ocean. VIII. The description of Eurycletodes (Oligocletodes) quadrispinosa sp.n. and the male of E. (O.) monardi Smirnov (Cletodidae)

Eurycletodes (O.) quadrispinosa Sp.n. and the male of Eurycletodes (O.) monardi are described. E. quadrispinosa differs from the closely related species E. echinatus Lang, E. parasimilis Por and E. arcticus Lang in the setation of segment 1 and 2 Exp P2–P4, of segment 2 Exp p24 and of the Exp P5. Because of the same setation of the A2, Pl-P4 Exp and Exp as the female of E. monardi Smirnov the described male is regarded as that of E. monardi Smirnov. The species were collected at the Iceland Faroe Ridge from depths of 500. 1540 and 2500 m.     

Localized euchromatinization of the X chromosome during spermatogenesis in the grasshopper Melanoplus femur-rubrum

In grasshoppers, as well as in most other animals, the X chromosome is heteropycnotic (heterochromatic) during prophase I and metaphase I of spermatogenesis. During the same stages, in some of the cells of three Melanoplus femur-rubrum males (out of several hundred males examined) part of the X appeared euchromatic (E). In one male, the E segment was observed in 90% of the cells of a single cyst in which all the cells lacked one of the smallest autosomes. In another cyst of the same follicle all the cells contained one additional small autosome, and none of the Xs exhibited an E segment. The size of the E segment suggested that it resulted from the failure of part of the X to become heteropycnotic prior to the formation of the cyst. In the other two males, many of the cells contained chromosome fragments and translocations. In many cells in which the X exhibited an E segment, however, there was no evidence of chromosome breakage. The E segments were sometimes terminal and sometimes interstitial in the same cyst. This variation suggested that they resulted from the euchromatinization of part of the X immediately prior to prophase I of meiosis. Because fragmentation and the presence of Xs with an E segment were each very rare, it was concluded that they were in some way causally related. It was also concluded that in this species the heterochromatinization of the X is not controlled by a single inactivation center.     

Differences in the formation of poles of Enterococcus and Bacillus.

The pole of Enterococcus hirae (Streptococcus faecium) is more pointed than that of Bacillus subtilis; i.e. the pole of the former is prolate and the latter is oblate. Both species form their poles by constructing annular additions on the inside surface. In both cases, the thick septum starts to split from the outside before the septum is complete. Physiochemical considerations dictate that the peptidoglycan must be unstretched as laid down. However, it later becomes stressed and may stretch to increase its surface area or to change its shape. Our earlier analysis for B. subtilis demonstrated that, without the addition of new peptidoglycan, the nascent wall is stretched after it is externalized to 1.51 times the original area. The wall of partially formed poles that is already exteriorized continues to deform with further development. For E. hirae, Higgins & Shockman's measurements showed that the completed pole has a surface area 2.18 times larger than a completed septal disk and the wall changes shape very little after exteriorization. A model is presented here for the streptococcus in which the septal wall does not increase its surface area on exteriorization either by expansion or by murein insertion. Instead, the septal wall as it is split and exteriorized twists to become oblique, increasing the inner radius of the incomplete septum. In consequence of this rotation, extra layers of peptidoglycan are added to the inside face of the developing septum. This additional murein forms the more pointed pole shape for E. hirae. This "split-and-splay" model thus refines and extends the surface stress theory of E. hirae developed a decade ago by proposing a source of the extra wall needed for the formation of its prolate, more pointed, pole.     

Rugiloricus bacatus sp. nov. (Loricifera ‐Pliciloricidae) and a ghost‐larva with paedogenetic reproduction

Abstract

A new species of Loricifera, Rugiloricus bacatus sp. nov. is described together with the diagnoses of two other Rugiloricus species, Rugiloricus sp. nov. A and B, from the Faroe Bank (North Atlantic). Characteristic for all three species is the presence of a new type of reduced larva, a ghost‐larva. This type of reduced larva was discovered in 1986 by Jeanne Renaud‐Mornant, but it was with the Faroe Bank material that it was first discovered that the ghost‐larvae belonged to the phylum Loricifera. The ghost‐larvae are eitherfound inside late instar Higgins‐larvae, called penultimate Higgins‐larvae, or in the sediment. The three types of Higgins‐larvae from the Faroe Bank can be distinguished by characters such as anterior setae, posterior setae and toes. The adults of Rugiloricus bacatus sp. nov. are characterised by a prominent ruff resembling a pearl necklace; two of the eight clavoscalids are modified in the 1st row; the 2nd row of leg‐shaped scalids are very large and robust, and the 9th row with 30 beak‐like scalids alternating with 30 alternating plates. The postlarvae are free‐living and their scalids on the introvert are reduced to protoscalids. Postlarvae and adult stages have not been found for Rugiloricus sp. nov. A and B and therefore only diagnoses of these two species are presented here.     

Fissuroderes, a new genus of Kinorhyncha (Cyclorhagida) from the deep sea and continental shelf of New Zealand and from the continental shelf of Costa Rica

Specimens of Kinorhyncha collected by RV Sonne from the continental shelf off the coast of Costa Rica and from the deep sea East of New Zealand as well as by RV Kaharoa in the Firth of Thames are identified as five new species of a new genus Fissuroderes gen. nov. which is distinguished from all other kinorhynch genera by a ring-like cuticle in the first trunk segment and a cuticle with midventral and lateral articulations resulting in two sternal plates and one tergal plate in segments 2-10. Fissuroderes higginsi sp. nov. can be distinguished from all other species of Fissuroderes by a laterodorsal spine in segment 2 and the lack of a lateroventral spine in segment 8. Fissuroderes rangi sp. nov. is recognized from all other species by the lack of a ventrolateral spine in segment 2, the lack of a lateroventral spine in segment 5, an extremely elongate spinose tergal extension of segment 11 and a prominent midventral spinose process of the sternal plates in segment 11. Fissuroderes papai sp. nov. is identified by the short spinose process of the sternal plate of segment 11. Only Fissuroderes thermoi sp. nov. possesses bilobed sternal plates in segment 11 and a short conical tergal extension. Fissuroderes novaezealandia sp. nov. differs from F. higginsi sp. nov. in the lack of a laterodorsal spine in segment 2, the lack of an accessory spine in a lateral position in segment 8, the lack of a sublateral spine in segment 10, the existence of a lateroventral spine in segment 8 and in the lack of a subdorsal type 2-gland cell outlet in segment 2. The former species differs from F. papai sp. nov. in the lack of a lateroventral spine in segment 8, the lack of longitudinal indentations in the posterior part of the trunk cuticle of each segment and in the existence of an elongate spinose tergal extension of segment 11 and of many fine hairs on the surface of the cuticle. Fissuroderes is included into the Echinoderidae which is suggested to enclose also the genera Echinoderes and Cephalorhyncha. Echinoderes nybakkeni Higgins, 1988 is now combined as Cephalorhyncha nybakkeni (Higgins, 1988) comb. nov.     

A review of the genus Eodiaptomus Kiefer, 1932, with the description of E. sanuamuangae n.sp. from Thailand, and a redescription of E. lumholtzi (Sars, 1889) from Australia (Copepoda, Calanoida)

The genus Eodiaptomus Kiefer contains six species, five of which are distributed in Asia, and one in Australia and New Guinea. A seventh species, E. sanuamuangae n.sp., is now added from Thailand. It has hitherto been misidentified as E. sinensis (Burckhardt), but can be recognized by various morphologic criteria. In the female, both spines on either wing of the fifth pediger are laterally placed. The third endopodite-segment of P2–P4 has seven, instead of six, setae. The sensory seta on the basis of P5 is extraordinarily long. On the male right antennule, the spine on segment 8 is much reduced, whereas that on segment 15 is relatively strong; the spinous process on the antepenultimate segment is slender, straight, with a hooked tip and as long as the next segment. Morphologically and geographically, E. sanuamuangae n.sp. links the Asian to the Australian forms. The Australian E. lumholtzi (Sars) is redescribed. A detailed morphological comparison is made of all Eodiaptomus spp. Their taxonomic characters, interspecies relationship, and biogeography are discussed.     

A problem with variable selection in a comparison of correlative and process‐based species distribution models: Comments on Higgins et al., 2020

Comments are presented on an article published in October 2020 in Ecology and Evolution (“Predictive ability of a process‐based versus a correlative species distribution model”) by Higgins et al. This analyzed natural distributions of Australian eucalypt and acacia species and assessed the adventive range of selected species outside Australia. Unfortunately, inappropriate variables were used with the MaxEnt species distribution model outside Australia, so that large climatically suitable areas in the Northern Hemisphere were not identified. Examples from a previous analysis and from the use of the freely available spatial portal of the Atlas of Living Australia are provided to illustrate how the problem can be overcome. The comparison of methods described in the Higgins et al. paper is worthwhile, and it is hoped that the authors will be able to repeat their analyses using appropriate variables with the correlative model.     

Missense mutations in exon 5 of the human lipoprotein lipase gene. Inactivation correlates with loss of dimerization.

Most missense mutations of the lipoprotein lipase (LPL) gene identified among LPL-deficient subjects cluster in a segment of the sequence that encodes the catalytic triad as well as functional elements involved in the activation of the lipase at lipid-water interfaces. Consequently, loss of activity may result either from direct alterations of such functional elements or from less specific effects on protein folding and stability. This issue was addressed by examining biochemical properties of four such variants (A176T, G188E, G195E, and S244T) in a heterologous expression system (COS-1 cells). Variant G195E (GGA----GAA) was previously unreported. In all instances, inactive enzyme was recovered in medium, albeit at reduced levels. Cellular synthesis and extracellular degradation were similar to those for wild type, suggesting that reduced secretion resulted from increased intracellular degradation. When cell extracts were subjected to heparin-Superose affinity chromatography followed by elution on a linear salt gradient, all variants exhibited a single, inactive, low affinity immunoreactive peak. By contrast, wild-type enzyme presented an additional, high affinity, active species, which we interpret as homodimeric enzyme. Substitution of the active-site serine (S132A) led to loss of activity but maintenance of the high affinity species. When large amounts of the G188E variant were applied to the column, small but significant amounts of high affinity, active enzyme were recovered. Systematic substitutions at residue 188 showed that only glycine could accommodate structural constraints at this position. We conclude that the mutations examined did not impart lipase deficiency by affecting specific functional elements of the enzyme. Rather, they appear to affect protein folding and stability, and thereby formation and maintenance of subunit assembly.     

Morphology and life cycle of a new loriciferan from the Atlantic coast of Florida with an emended diagnosis and life cycle of Nanaloricidae (Loricifera)

Abstract. A new interstitial loriciferan, Nanaloricus gwenae sp. nov., is described from coarse-sand and shell-hash habitats ( Amphioxus sand), at 15–17 m depth, 6–7 miles off the coast of Fort Pierce, FL, USA. The new species is very closely related to the type species Nanaloricus mysticus found off the coast of Roscoff, France in nearly the same kind of sediment ( Dentalium sand). All life stages (Higgins larva, postlarva, and adult) in the life cycle of the new species were found through the 10-year investigation, leading to the conclusion that all species of Nanaloricidae have only a sexual reproductive cycle. The adult of the new species can be distinguished by the different body shape, the lorical spikes and sculpture, and the shape of the scalids. The postlarva has stronger longitudinal ridges on the lorical plates and the Higgins larva has toes with smaller mucrones than those of N. mysticus . An emended definition of the Nanaloricidae is provided based on the new formula of the number of rows and shape of the scalids on the introvert. The associated meiofauna found in the subtidal sand or shell hash is both abundant and diverse. Tardigrades, gastrotrichs, and kinorhynchs are among the most common associates. N . gwenae sp. nov. is represented by only eight specimens collected during a 10-year period of sampling this habitat.     

Eudiaptomus anatolicus n.sp. (Copepoda: Calanoida) from Turkey

Eudiaptomus anatolicus n.sp. displays similarity to E. transylvanicus (Daday, 1890) by possessing an outer marginal spine located proximally on the second exopodite segment of the male right P₅, but it differs from this closest species in the presence of a chitinous projection on the second exopodite segment of the male right P₅, and in the typical shape of the female's thoracic wings. E. transylvanicus (Daday, 1890) has three chitinous processes located on the basipodite segment of the male right P₅, whereas Eudiaptomus anatolicus n.sp. has only one small process on this part. This new species is living in lake Poyraz, which is small and shallow. Some cladoceran species, namely, Pleuroxus truncatus (O.F. Müller, 1785), Pleuroxus laevis (Sars, 1862), Pleuroxus trigonellus (O.F. Müller, 1785), Simocephalus exspinosus (Koch, 1841), Eurycercus lamellatus (O.F. Müller, 1785), Alonella excisa (Fischer, 1854), Lathonura rectirostris (O.F. Müller, 1785), Pseudochydorus globosus (Baird, 1843) and two cyclopoid copepods, Megacyclops viridis (Jurine, 1820) and Eucyclops serrulatus (Fischer, 1851) share the same habitat. This revised version was published online in July 2006 with corrections to the Cover Date.     

Antennulary sensory organs in cyprids of Octolasmis and Lepas (Crustacea: Thecostraca: Cirripedia: Thoracica): a scanning electron microscopic study

Cypris larvae of the pedunculate barnacles Octolasmis angulata (Poecilasmatidae), Lepas australis, L. pectinata, and Dosima fascicularis (Lepadidae) were studied with scanning electron microscopy, focusing on the sensory setae and the attachment disc on the antennules. The antennules of O. angulata did not exhibit any remarkable trait, but carry the same number of setae as seen in most other thoracicans. The third segment is bell-shaped and quite distinct from the second and its attachment disc is surrounded by a skirt. We found several potential synapomorphies in antennulary morphology between cyprids of the lepadid species but none of them were shared with the cyprids of Octolasmis; the list of unique lepadid characters includes: one additional, preaxial seta on the second segment; multiple similar (up to eight) postaxial setae (PS3) on the third segment, unlike all other thoracicans, where there is only a single PS3; the third segment consists almost entirely of the attachment disc, which is distended and surrounded by two parallel rows of radial setae; on the fourth segment the terminal seta E is diminutive. We found no traits in cyprids of Octolasmis that seem to be adaptations to their attachment site within the branchial chamber of swimming crabs and, in particular, no similarities with cyprids of rhizocephalan barnacles, many of which also attach in the gill chamber. The synapomorphies between cyprids of the lepadid species may be adaptations to their life in the neuston.     

洪泽湖鱼类寄生甲壳动物区系调查及一新种的记述

1979年秋对江苏省洪泽湖鱼类寄生甲壳动物的调查研究结果,共得18种寄生甲壳动物,其中包括一个新种。分析了该湖寄生甲壳动物的区系组成、繁殖季节及种类分布的情况,同时还根据虫体感染率和感染强度,提出了对鱼类危害性较大的中华鳋和多态锚头鳋,在洪泽湖中不可能出现严重感染的见解。       

Ergasilus thatcheri n. sp. (Copepoda, Poecilostomatoida, Ergasilidae) from the gills of Rhamdia quelen (Teleostei, Siluriformes, Pimelodidae) from southern Brazil

The female of Ergasilus thatcheri n. sp. (Copepoda, Poecilostomatoida, Ergasilidae) is described from the gills of the "jundiá," Rhamdia quelen (Teleostei, Siluriformes, Pimelodidae), from fish ponds in the State of Rio Grande do Sul, Brazil. The new species has a falciform semipinnate terminal seta on the first exopod, which suggests phylogenetic affinity to 10 other congeners, all from fishes of the Amazon Basin. Based on general morphology, the new species shows great similarity to E. callophysus Thatcher and Boeger, 1984, a parasite of another pimelodid fish Callophysus macropterus. Ergasilus thatcheri n. sp., however, can be easily differentiated from E. callophysus in its possession of a more distal sensillum not located on a cuticular elevation, and a row of spinules on the inner margin of the second antennal segment (first endopodal segment).     

Recombination in Escherichia coli and the definition of biological species.

The DNA sequence of part of the gnd (6-phosphogluconate dehydrogenase) gene was determined for eight wild strains of Escherichia coli and for Salmonella typhimurium. Since a region of the trp (tryptophan) operon and the phoA (alkaline phosphatase) gene have been sequenced from the same strains, the gene trees for these three regions were determined and compared. Gene trees are different from species or strain trees in that a gene tree is derived from a particular segment of DNA, whereas a species or strain tree should be derived from many such segments and is the tree that best represents the phylogenetic relationship of the species or strains. If there were no recombination in E. coli, the gene trees for different genes would not be statistically different from the strain tree or from each other. But, if the gene trees are significantly different, there must have been recombination. Methods are proposed that show these gene trees to be statistically different. Since the gene trees are different, we conclude that recombination is important in natural populations of E. coli. Finally, we suggest that gene trees can be used to create an operational means of defining bacterial species by using the biological species definition.