On two reports associated with James Wood-Mason and Alfred William Alcock published by the Indian Museum and the Indian Marine Survey between 1890 and 1891: implications for malacostracan nomenclature.

Two rare documents associated with the Indian Museum and the Indian Marine Survey for the administrative year April 1890 to March 1891 have been examined and found to have nomenclatural consequences for malacostracan crustaceans. Even though they constitute available published works according to the International Code for Zoological Nomenclature, these reports have rarely been cited. Dating these two publications is of importance as they make decapod scientific names available and, in a few instances, describe the same taxa. After searching the collections deposited in the Asian and African Room, British Library, the Administration Report of the Indian Marine for the year April 1890 to March 1891 could be dated with some degree of certainty as 25 August 1891. In contrast, dating the Indian Museum Annual Report proved more difficult because after examination of copies held by the General Library in the Natural History Museum, London, it was evident that not all of these reports were consistently published on time to meet an end of year deadline. However, the publication of volume XXII of the Indian Museum Annual Report for the year April 1890 to March 1891 appeared to be contemporary with the year printed at the bottom of the title page. As no exact date could be established with confidence, the publication date for this volume was fixed as 31 December 1891 in accordance with ICZN Art. 21.3.2. Therefore the Administration Report of the Indian Marine (published 25 August 1891) is considered to take precedence over the Indian Museum Annual Report (published 31 December 1891) and as such the names made available in the former take priority. As original copies of the Administration Report of the Indian Marine are not readily available in most libraries and few scientists have actually had access to these publications, the relevant Appendix No. XIII, in which the names of several malacostracan taxa are made available, is reproduced here. Since the appendix is not conclusively attributable to a specific author, it is considered to be written anonymously and should therefore be cited as Anonymous (1891). A number of names in Appendix No. XIII are available since they are accompanied by a brief description of the taxa they denote, and are either attributable to James Wood-Mason or remain with anonymous authorship; others are nomina nuda without a diagnosis or indication, or have been diagnosed previously in the "Natural History Notes from H.M. Indian Marine Survey Steamer Investigator". The nomenclatural implications for eight names made available in Anonymous (1891) are discussed: Glyphocrangon caeca, Glyphocrangon sculptus var. coecescens, Psalidopodidae, Psalidopus, Psalidopus mirabilis, Psathyrocaris, Psathyrocaris fragilis and Psopheticus crepitans. The nomenclatural history of various other taxa, initially denoted by unavailable names in Anonymous (1891), is also documented. The authorships of the various crustacean taxa collected by the Indian Marine Survey Steamer Investigator during the seasons 1889-1890 and 1890-1891, and published in two series of connected parts in the Annals and Magazine of Natural History, are also re-assessed and summarised. A rare document containing the list of R.I.M.S. Investigator stations for the period 1884-1913 is reproduced for the future benefit of the scientific community. 

A new genus and species of oceanic planktonic Tisbidae (Crustacea, Copepoda, Harpacticoida) with enlarged modified eyes.

Both sexes of a new monotypic genus of Tisbidae (Copepoda, Harpacticoida) are described from the epi- or mesopelagic zone in the Kuroshio region, Japan. Gyoromeguttatumgen. et sp. nov. belongs to a monophyletic lineage of deepwater holoplanktonic genera defined by a suite of characters. Within this clade, Gyoromegen. nov. appears most closely related to Neotisbella Boxshall, 1979. The most distinguishable feature of G.guttatumgen. et sp. nov. is the presence of large, paired, frontal modified eyes, each consisting of a baculiform ocellus, a globular (Gicklhorn's?) organ, and a semi-parabolic plate. The taxonomic position of Tisbespinulosa Bradford & Wells, 1983 is discussed and a key to the six meso- and bathypelagic tisbid species is provided. Confusion surrounding earlier literature reports of supernumerary elements on the caudal ramus in some harpacticoid taxa is clarified. Secondary modifications of ocellar components of the typical naupliar eye in the Harpacticoida are reviewed. It is suggested that the development of specialized eyes in G.guttatumgen. et sp. nov. may provide a means for detecting bioluminescent food particles in oligotrophic pelagic environments. The large, vaulted prosome indicates the species is an opportunistic macrophage that has adopted gorging as a feeding strategy.

Diversity, habitat endemicity and trophic ecology of the fauna of Loki's Castle vent field on the Arctic Mid-Ocean Ridge.

Loki's Castle Vent Field (LCVF, 2300 m) was discovered in 2008 and represents the first black-smoker vent field discovered on the Arctic Mid-Ocean Ridge (AMOR). However, a comprehensive faunal inventory of the LCVF has not yet been published, hindering the inclusion of the Arctic in biogeographic analyses of vent fauna. There is an urgent need to understand the diversity, spatial distribution and ecosystem function of the biological communities along the AMOR, which will inform environmental impact assesments of future deep-sea mining activities in the region. Therefore, our aim with this paper is to provide a comprehensive inventory of the fauna at LCVF and present a first insight into the food web of the vent community. The fauna of LCVF has a high degree of novelty, with five new species previously described and another ten new species awaiting formal description. Most of the new species from LCVF are either hydrothermal vent specialists or have been reported from other chemosynthesis-based ecosystems. The highest taxon richness is found in the diffuse venting areas and may be promoted by the biogenic habitat generated by the foundation species Sclerolinum contortum. The isotopic signatures of the vent community of LCVF show a clear influence of chemosynthetic primary production on the foodweb. Considering the novel and specialised fauna documented in this paper, hydrothermal vents on the AMOR should be regarded as vulnerable marine ecosystems and protective measures must therefore be implemented, especially considering the potential threat from resource exploration and exploitation activities in the near future.

Sabelliphilidae (Copepoda: Cyclopoida) associated with the tube anemone Pachycerianthus maua (Carlgren) and the horseshoe worm Phoronis australis Haswell off New Caledonia.

Examination of washings of the ceriantharian Pachycerianthus maua (Carlgren) and its phoronid symbiont Phoronis australis Haswell in New Caledonian waters revealed two species of symbiotic copepods belonging to the family Sabelliphilidae (Cyclopoida). Phoronicola spinulatus Boxshall & Humes, 1988, the only other copepod known to be associated with a phoronid and originally described from Hong Kong, was found on both the lophophore of Phoronis australis and the tentacular crown of Pachycerianthus maua. Both sexes of Phoronicola spinulatus are redescribed based on the New Caledonian material and re-examination of the type-material revealed some observational errors in the original description. Myxomolgus hoi n. sp. was exclusively found on the ceriantharian host and appears most closely related to its only known Pacific congener, M. invulgus Kim, 2001, in lacking the strong spines on antennulary segments 1-2, the presence of closely set, fine teeth along the convex margin of the mandibular blade, and the absence of a proximal bulbous protrusion along the inner margin of leg 5 exopod. Differences between both species are found in the rostrum, antennule, antenna, maxillule, leg 4, caudal rami and body size. The relatively low number of specimens of P. spinulatus recovered from washings of the lophophores (and its presence on Pachycerianthus maua) suggests that its real host is a ceriantharian rather than a phoronid. It is conceivable that both Phoronicola spinulatus and M. hoi n. sp. live and feed on/inside the mucilaginous ceriantharian tube rather than on the lophophore or tentacular crown of their respective hosts.

John Berkeley James WellsAn appreciation of his contributions to harpacticoid diversity and systematics.

John Wells was born in Hammersmith, a district in west London, where he spent most of his childhood and teenage life. It was a surprise to find out only recently that he had received a scholarship to Latymer Upper School on King Street which is literally one block away from where I used to live when I started working at the Natural History Museum in the early 1990s. The site has a long history and can be traced to a charity school founded in 1624 by the English merchant Edward Latymer, a wealthy lawyer and puritan, who left part of his wealth for the clothing and education of eight poore boyes from Hammersmith.

A new species of Helmutkunzia Wells amp; Rao, 1976 from an intertidal sandy beach in Xiamen, China and proposal of Pseudobalucopsylla gen. nov. (Copepoda, Harpacticoida, Miraciidae).

A new species of the genus Helmutkunzia Wells Rao, 1976 (Miraciidae) is described from specimens collected from an intertidal sandy beach in Xiamen, Fujian Province, China. Helmutkunzia xiamenensis sp. nov. differs from its two congeners by the length/width ratio of the female P5 exopod, the number or length of the setae on the sexually dimorphic P2 endopod in the male and the relative length of the spines on the endopodal lobe of the male P5. The Chinese species is morphologically closest to H. variabilis Wells Rao, 1987 from the Andaman and Nicobar island chain. Females of both species can readily be differentiated by the relative length of the P5 exopod while males can be differentiated by the length of the armature elements on P2 enp-2 and the endopodal lobe of P5. The genus Balucopsylla Rao, 1972 is reviewed, resulting in the proposal of Pseudobalucopsylla gen. nov. to accommodate the type species Balucopsylla triarticulata Wells Rao, 1987 and three new Indo-Pacific species previously identified with it: P. obscura sp. nov. from the Andaman Islands, P. costaricensis sp. nov. from the Pacific coast of Costa Rica and P. mielkei sp. nov. from the Galpagos archipelago. A key to species of Pseudobalucopsylla sp. nov. is provided.

Johnwellsia, a new intertidal genus of Parastenheliidae (Copepoda, Harpacticoida) from the Taiwan Strait, China, including a review of the family and key to genera.

A new genus of Parastenheliidae, Johnwellsia gen. nov., is proposed for its type and only species, J. bipartita sp. nov., collected from Dadeji Beach in Xiamen, Taiwan Strait, China. The intricate taxonomic history of the family is reviewed with special emphasis on its type genus Parastenhelia Thompson Scott, 1903. It is concluded that P. hornelli Thompson Scott, 1903 is the type of the genus and that the widely adopted previous designation of Harpacticus spinosus Fischer, 1860 as type species of Parastenhelia is invalid. The taxonomic concept of Parastenhelia is restricted to the hornelli-group which includes four valid species: P. hornelli, P. similis Thompson Scott, 1903, P. oligochaeta Wells Rao, 1987, and P. willemvervoorti sp. nov. The currently accepted concept of Parastenhelia spinosa as a highly variable cosmopolitan species is rejected. The genus Microthalestris Sars, 1905 (type: Thalestris forficula Claus, 1863) is resurrected to accommodate most Parastenhelia species that were previously placed in the spinosa-group. Two species, Thalestris forficuloides Scott Scott, 1894 and Parastenhelia antarctica Scott, 1912, are reinstated as valid members of the genus which further includes Parastenhelia gracilis Brady, 1910, Microthalestris littoralis Sars, 1911, P. costata Pallares, 1982, P. minuta Pallares, 1982, P. bulbosa Gee, 2006 and five new species: M. campbelliensis sp. nov.; M. polaris sp. nov.; M. santacruzensis sp. nov.; M. sarsi sp. nov. and M. variabilis sp. nov. Both the type species, Thalestris forficula, and Harpacticus spinosus are considered species inquirendae in Microthalestris. Three new genera are proposed to accommodate the remaining Parastenhelia species. Porirualia gen. nov. contains P. megarostrum Wells, Hicks Coull, 1982 (type) and P. pyriformis Song, Kim Chang, 2003, and is the sistergroup of Johnwellsia gen. nov. Parastenhelia aydini Kuru Karaytu, 2015 is placed in the monotypic genus Karaytugia gen. nov. while all species with penicillate elements on the antenna and P1 are transferred to Penicillicaris gen. nov., including Thalestris pectinimana Car, 1884, which is removed from the synonyms of the Parastenhelia spinosa (Fischer, 1860) complex, and three new species: P. maldivensis sp. nov., P. penicillata sp. nov., and P. sewelli sp. nov. The genus Karllangia Noodt, 1964 (type: K. arenicola Noodt, 1964) is relegated to a junior subjective synonym of Thalestrella Monard, 1935a (type: T. ornatissima Monard, 1935a). New or updated diagnoses for each genus, and differential diagnoses for species where appropriate, are provided. A key to the ten currently recognized genera in the Parastenheliidae is presented as well as keys to species for Parastenhelia, Microthalestris, Thalestrella and Penicillicaris gen. nov.

Description of a new species of Nannopus Brady, 1880 (Copepoda: Harpacticoida: Nannopodidae) from Argentinean waters, including an updated key to species.

Both sexes of a new brackish-water species, Nannopus sinusalbi sp. nov. (Nannopodidae) are described from the Baha Blanca estuary (3853S, 6207W) in Buenos Aires Province, Argentina. The only previous record of the genus in the study area was identified as the type species, Nannopus palustris Brady, 1880, with no description or illustrations, hence its authenticity cannot be confirmed. Nannopus brasiliensis Jakobi, 1956 is relegated to species inquirenda in the genus rather than being considered a junior synonym of the type species. Nomenclatural issues related to the usage of the alternative spellings Iliophilus Lilljeborg, 1902 and Ilyophilus sensu Sars (1909) and the unavailability of Ilyophilus canui Kim, Choi Yoon, 2017 are discussed. An updated key to the 18 identifiable species of Nannopus (excluding the type species N. palustris) is presented. The harpacticoid assemblage at the type locality showed a distinct seasonality with N. sinusalbi sp. nov. representing about 8% of the community. The new species showed densities below 5ind.cm­2 during most of the year, reaching an abrupt peak of 40.17ind.cm­2 towards the end of the summer, when the maximum proportion of ovigerous females was recorded.

New records of Pseudotachidiidae from South Korea, including a key to species of the Pseudomesochrinae (Copepoda: Harpacticoida).

Two species of the marine harpacticoid family Pseudotachidiidae (Copepoda) are reported from subtidal sediments in the Southern Sea of Korea. Psammis wellsi sp. nov. (Danielsseniinae) is most closely related to P. longisetosa Sars, 1910 but differs from its European congener in the ventral ornamentation of the female genital double-somite, the dorsal ornamentation of the second abdominal somite in the male, the armature of the proximal endite of the maxillary syncoxa, the relative setal lengths and general shape of the female P5, and the relative length of the inner seta of the male P5 endopodal lobe and P6. The female of Pseudomesochra tatianae Drzycimski, 1968 is redescribed in detail, constituting the only other record of the species since its discovery at the type locality in western Norway. East Asian records of members of the four subfamilies currently recognized in the Pseudotachidiidae are summarized. Published and other records of the 23 described species in the Pseudomesochrinae are collated and their armature patterns of P1P5 are tabulated and corrected where necessary. Pseudomesochra affinis (Sars, 1920) is removed from its synonymy with P. longifurcata T. Scott, 1902 and formally reinstated as a valid species. An updated female-based key to the 19 valid species of Pseudomesochra T. Scott, 1902 and four species of Keraia Willen Dittmar, 2009 is presented.

A new species of Stylicletodes Lang, 1936 (Copepoda: Harpacticoida: Cletodidae) from the East China Sea, including an updated key to species and synopsis of distribution records.

Both sexes of a new species, Stylicletodes wellsi sp. nov. (Harpacticoida: Cletodidae), are described from material collected from sediments in the East China Sea. The new species belongs to a species group whose members are characterized by an anal operculum that has a backwardly directed, median linguiform process and fifth legs that display naked or sparsely pinnate armature elements in both sexes. Within this group, S. wellsi sp. nov. is morphologically closest to S. reductus Wells, 1965 but differs primarily from its European congener in the armature pattern of P4 (both rami) and the female P5. Distribution records of all species are summarized and an updated identification key to the seven valid species in the genus is presented. Taxonomic issues related to the type species S. longicaudatus (Brady, 1880) are briefly discussed.

Parasites, pathogens, and other symbionts of copepods.

There is a large diversity of eukaryotic symbionts of copepods, dominated by epizootic protists such as ciliates, and metazoan parasites. Eukaryotic endoparasites, copepod-associated bacteria, and viruses are less well known, partly due to technical limitations. However, new molecular techniques, combined with a range of other approaches, provide a complementary toolkit for understanding the complete symbiome of copepods and how the symbiome relates to their ecological roles, relationships with other biota, and responses to environmental change. In this review we provide the most complete overview of the copepod symbiome to date, including microeukaryotes, metazoan parasites, bacteria, and viruses, and provide extensive literature databases to inform future studies.

A new species of the genus Tegastes (Copepoda: Harpacticoida: Tegastidae) from hydrothermal vents in the Okinawa Trough.

We describe a new species, Tegastes okinawaensis, from 583-711 meter-deep hydrothermal vents in the Okinawa Trough, Japan. This species is clearly distinguishable from its congeners by four combined characters, namely 1) the last three abdominal somites are depressed inwardly towards the body, 2) there is sexual dimorphism in the number of setae of P3 and P4, 3) the male antennule is 9-segmented, with the 7th segment formed by incomplete fusion of two segments, and 4) the caudal rami are small with a distorted quadrangular shape. Additionally, the species is easily distinguishable from its congeners by the distal endopodal segment of P4, which is armed with six setae - this character has never been reported in previous descriptions of congeners. This report is the first of a species in the genus Tegastes living at ocean depths of greater than 580 m in the northwestern Pacific.

Cancrincolidae (Copepoda, Harpacticoida) associated with land crabs: a semiterrestrial leaf of the ameirid tree.

Morphological evidence suggests harpacticoid copepods have recurrently entered into symbiosis with other crustaceans but only members of the family Cancrincolidae have successfully made the transition from marine habitats to semiterrestrial hosts. Cancrincolids are primarily amphi-Atlantic in distribution (with one outlier in the western Pacific) and typically inhabit the gill chambers of grapsoidean land crabs belonging to the families Grapsidae, Sesarmidae, Varunidae and Gecarcinidae. Morphologically, they are difficult to place because they exhibit unusual autapomorphies and the shared derived characters claimed to unite them with the primitively marine Ameiridae are equivocal. Both maximum parsimony and Bayesian inference solutions based on SSU rDNA gene sequences show topological congruence in placing the Cancrincolidae within the Ameiridae and in firmly resolving it as the sistergroup of taxa that have been reported as obligate or commensal associates of crayfish. This relationship is further supported by swimming leg sexual dimorphism and mandibular palp morphology. Morphological comparison with ameirid copepods revealed the majority of synapomorphies previously proposed in support of cancrincolid monophyly and familial distinctiveness can be attributed to heterochrony. The progressive evolution of cancrincolid associates appears to be largely concordant with the sequential adaptation to terrestriality by their grapsoidean hosts. The current amphi-Atlantic distribution of Cancrincola may suggest its possibly free-living ancestor had already assumed a virtually continuous distribution along the northern seaboard of Gondwana prior to the opening of the South Atlantic during the early Cretaceous, implying symbiotic relationships were established only much later when grapsoidean crabs started to emerge, radiate and diversify in the mid-Tertiary (15-35 mya). The adoption of semi-terrestriality in cancrincolid copepods can be viewed as yet another independent attempt (incursion) to colonize low-salinity environments by members of the family Ameiridae. The possible sistergroup relationships of the Ameiridae and the position of the genus Argestigens Willey are discussed.

New Mesopsyllus species from the Bohai Sea, China, re-evaluation of the validity of Vibriopsyllus Kornev & Chertoprud, 2008 and proposal of Sympodella gen. n. (Copepoda, Harpacticoida, Canthocamptidae).

Two new species of the genus Mesopsyllus Por, 1960 (Canthocamptidae) are described from the Bohai Sea, eastern China. Mesopsyllus dimorphussp. n. and M. spiniferussp. n. differ from their congeners by the presence of two instead of three outer spines on P2-P3 exp-3. They can be differentiated from each other by (1) number of inner setae on P3-P4 enp-2; (2) anterior margin of antennulary segment 7 of male; (3) ornamentation of male abdomen; (4) sexual dimorphism on P2 endopod and P3-P4 exp-3; and (5) differences in length of setae on male P5. Some observations in the original description of M. atargatis Por, 1960 are reinterpreted and the type material of M. secundus (Wells, 1965) is re-examined. Comparison between the type species of Vibriopsyllus Kornev & Chertoprud, 2008 and the four known species of Mesopsyllus shows the former as a junior subjective synonym of the latter. Consequently, Vibriopsyllus curviseta Kornev & Chertoprud, 2008 is formally transferred to Mesopsyllus as M. curvisetus (Kornev & Chertoprud, 2008), comb. n. A key to species and an updated generic diagnosis of Mesopsyllus are presented. The taxonomic status of the genus Carolinicola Huys & Thistle, 1989 is re-evaluated. The characters of its type species, C. trisetosa (Coull, 1973), indicate that the latter (and - by inference - the genus Carolinicola) should remain in the Danielsseniinae. Carolinicola galapagoensis Mielke, 1997 is fixed as the type species of a new genus Sympodellagen. n. and placed in the Hemimesochrinae (Canthocamptidae) as the putative sistertaxon of Pusillargillus Huys & Thistle, 1989. The relationships and potential synonymy of the genera Pyrocletodes Coull, 1973, Perucamptus Huys & Thistle, 1989 and Isthmiocaris George & Schminke, 2003 are briefly discussed.

Preface: Recent Developments in Taxonomy and Biodiversity of Symbiotic Copepoda (Crustacea)-A Volume in Celebration of the Career of Prof. Il-Hoi Kim.

Symbiosis is one of the most successful modes of life displayed by aquatic organisms, as measured by the number of times it evolved and how many symbiotic species are presently in existence. Among the Crustacea copepods utilize an extraordinary range of hosts, occurring on virtually every phylum of marine macroinvertebrates and, jointly with the monogeneans, are the most speciose group of metazoan ectoparasites of marine fishes (Rhode 2005). Several species have a major impact on global finfish and shellfish aquaculture, causing significant effects on farm production, economic viability and sustainability (Shinn et al. 2015). Parasitism by copepods on other metazoans has evolved independently numerous times in the evolutionary history of animal life on Earth and has led to an exceptional diversity in morphologies, physiologies, life-strategies and habitat preferences of its members. Reflecting the diversity of hosts, copepods show an amazing variety of adaptations which secure infection of and survival on the hosts. Since the first descriptions of parasitic copepods occurring on fish by Linnaeus (1758) and the first report of a copepod utilizing an invertebrate host by Say (1818) (Clausidium caudatum (Say, 1818)) the number of described symbiotic copepods has seen a steady increase over a 200-yr period, culminating in a total of 5,306 valid species recognized today. About 38% of all described copepod species utilize either vertebrate (2,450 spp.) or invertebrate hosts (2,856 spp.), however, many host groups have not been thoroughly examined, and for this reason even approximate estimates of true species numbers are futile. Plotting the proposal of new species by decade (Fig. 1) shows a sharp rise since 1950 with 67% of the species having been described in the preceding 65 years. This period of exceptionally rapid progress can be attributed to a number of highly prolific investigators such as Arthur Humes, Il-Hoi Kim, Ju-shey Ho and Jan Stock who, single-handedly or in collaboration with other authors, described 698, 356, 290 and 246 species, respectively. Historically, the number of described copepod species parasitizing fish typically outnumbered those known to be associated with invertebrates. Only during the mid-1970s the species curves of both categories converged and during the last 30 years the discovery of new species associated with invertebrate hosts appears to progress more rapidly. Despite a significant drop in the number of specialists working on symbiotic copepods the steady addition of new taxa shows that the dynamism of their taxonomy is clearly set to continue.

Prof. Il-Hoi Kim: a tribute.

Prof. Il-Hoi Kim was born during the Korean War on 28 February 1952 in Buan, North Jeolla Province (South Korea), near the coast of the Yellow Sea whose tidal flats would become one of his favourite sampling grounds during his scientific career. From an early age he developed an intense interest in natural history in general and marine biology in particular. He obtained his B.Sc. in 1974 at the Department of Biology Education, Gongju National College of Education. Between 1974 and 1976 he was conscripted into the South Korean military during which he progressed to the rank of lieutenant of artillery in the Reserve Officers' Training Corps (ROTC). After his graduation in 1980 at the Department of Zoology, Seoul National University, Il-Hoi Kim moved to the Department of Biology, Gangneung-Wonju National University on the East Sea coast where he was first appointed lecturer (1981) before taking up the position of assistant professor (1983), associate professor (1987) and full professor (1993). In 1985 he had previously completed his Ph.D. dissertation on Korean barnacles at Seoul National University under the supervision of the late Prof. Hoon Soo Kim, a pioneer in marine invertebrate taxonomy and renowned as the father of carcinology in Korea.

Enigmas from the past: M'Intosh's (1885) annelidicolous copepods from the voyage of H.M.S. Challenger.

The type material of four monotypic genera, Leaniricola, Oestrella, Praxillinicola and Trophoniphila (Copepoda, Cyclopoida), described by M'Intosh (1885) from deep water polychaete hosts collected during the H.M.S. Challenger expedition, is re-examined. Leaniricola rotundata M'Intosh (1885) is removed from its floating status as species inquirenda in the Nereicolidae and fixed as the type of a new family, Leaniricolidae fam. nov., based on the presence of an oral cone and massive, three-dimensionally expanded, mandibular gnathobases which are used to anchor the parasite in the parapodial integument of its host. The ectoparasitic Praxillinicola kroyeri (M'Intosh, 1885), previously treated as a species inquirenda in the Clausiidae, cannot be placed in any of the currently recognized poecilostome families and is here fixed as the type of a new family, Praxillinicolidae fam. nov. Females are characterized by unique bilobate antennules, contained within anterior sockets shared with the reduced antennae, and by paired labral hooks, both of which probably serve as auxiliary attachment organs. Despite its highly transformed body P. kroyeri has retained the plesiomorphic condition of the female genital system, with the gonopores positioned dorsolaterally and the paired copulatory pores lying close together on the midventral surface. The position of the mesoparasitic Trophoniphila bradyi M'Intosh, 1885 in the Bradophilidae is confirmed based on the presence of a median copulatory pore in the female, the disproportionately large egg sacs, the shape of the ectosoma and host utilization. Both sexes of Bradophila pygmaea Levinsen, 1878 are re-examined and the male is redescribed in detail. Flabellicola Gravier, 1918a is treated as a genus incertae sedis in the Bradophilidae. The anal prominence, previously reported in the female of Oestrella (= Melinnacheres) levinseni M'Intosh, 1885 (Saccopsidae), proved upon re-examination to be one of the paired genital apertures. The third and fourth pairs of appendages reported in male saccopsids are here interpreted as the maxillae and maxillipeds, respectively.

Harpacticoid copepods-their symbiotic associations and biogenic substrata: a review.

Members of the order Harpacticoida are primarily free-living and benthic but some lineages have adopted alternative modes of life which involve a major habitat shift or dependence on a host. Since the first discovery of a harpacticoid associated with an invertebrate host about 150 years ago, a total of 172 species, representing 84 genera and 17 families, have been shown to live in symbiotic partnership with other organisms. The steady addition of new taxa during the last 35 years testifies to the widespread and previously underestimated occurrence of symbiosis in the group. Harpacticoids have entered into associations with Cyanobacteria, Protozoa, macroalgae, grasses, fish hosts, marine tetrapods (including whales, sea turtles and manatees) and at least eleven invertebrate phyla. At present, 86 independent colonizations of marine and freshwater host organisms can be identified but this number is a minimum estimate and is expected to increase as certain host groups will be more properly sampled. In contrast to the Cyclopoida and Siphonostomatoida, which have been extremely successful in developing associations with cnidarians, sponges, echinoderms and ascidiaceans, members of the Harpacticoida have a marked predilection for crustacean hosts. Except for a few species that can be classified as genuine parasites, the precise nature of the relationship between most associated harpacticoids and their hosts has yet to be elucidated but can probably be defined as commensalistic, where the benefit to the copepod may be nutritional or protective. Most are ectosymbiotic but some live as endocommensals in microhabitats which provide considerable protection from predation. The success of symbiotic harpacticoids in freshwater is limited with the few species known to be associated with freshwater hosts typically representing isolated forays into a symbiotic lifestyle from an otherwise free-living lineage. The scattered literature on symbiotic harpacticoids is compiled and presented by host group. Dichotomous keys are provided for the identification of most species while accidental and doubtful records are discussed where appropriate.The genus Idomenella T. Scott, 1906a (Pseudotachidiidae), previously a junior subjective synonym of Dactylopodella Sars, 1905a, is reinstated to accommodate Dactylopodella rostrata (T. Scott, 1893), D. janetae Hicks, 1989, Xouthous coronatus (T. Scott, 1894b), X. antarcticus (Giesbrecht, 1902), X. intermedius (Lang, 1934) and Idomenella paracoronata sp. nov. Kioloaria Harris, 1994 (Porcellidiidae) is adopted as the valid replacement name for the preoccupied Acutiramus Harris, 2014a. The name of a second porcellidiid genus, Murramia Harris, 1994, lacks the mandatory type fixation and is made available here by adopting the original name but taking the present authorship and date. The generic name Ellucana Sewell, 1940 is currently unavailable and must instead be attributed to Coull (1971b). Laophonte commensalis Raibaut, 1962a is fixed as the type of Raibautius gen. nov. in the family Laophontidae, Tegastes cnidicus Humes, 1981b as the type of Aglaogastes gen. nov. in the Tegastidae, and Canuella (Canuella) indica Krishnaswamy, 1957 as the type of Indicanuella gen. nov.A number of new names are proposed for species that had previously been misidentified: Diarthrodes septemtrionalis sp. nov. for D. roscoffensis (Monard, 1935b) sensu Kornev & Chertoprud (2008), Kioloaria jejuensis sp. nov. for Porcellidium brevicaudatum Thompson & Scott, 1903 sensu Kim & Kim (1996), Xouthous andamanensis sp. nov. for X. maldivae [sic] Sewell, 1940 sensu Wells & Rao (1987), X. wellsi sp. nov. for X. laticaudatus (Thompson & Scott, 1903) sensu Wells (1967), X. namibiensis sp. nov. for X. pectinatus (Scott & Scott, 1898) sensu Kunz (1963), and Idomenella paracoronata sp. nov. for Idomene coronata (T. Scott, 1894b) sensu Sars (1909a). The inadequately described Amenophia ovalis Brady, 1910 is relegated to a species inquirenda in Amenophia Boeck, 1865. Idomene australis Brady, 1910, I. pusilla Brady, 1910, Dactylopusia ferrieri T. Scott, 1912 and I. kabylica Monard, 1936 are ranked species incertae sedis in the Pseudotachidiidae. Dactylopus bahamensis Edwards, 1891 is tentatively considered as species incertae sedis in the Dactylopusiidae. Canuellina onchophora Por, 1967 and C. nicobaris Wells & Rao, 1987 are transferred to the genus Ellucana Coull, 1971b while Ellucana secunda Coull, 1971b is assigned to the genus Canuellina Gurney, 1927. Xylora calyptogenae Willen, 2006 is sunk as a junior subjective synonym of X. bathyalis Hicks, 1988a. The incorrect original spellings of Parathalestris pacificus Chislenko, 1971, P. infestus Ho & Hong, 1988, Tripartisoma ovalis Avdeev, 1983, T. trapezoidalis Avdeev, 1983, Amplipedicola pectinatus Avdeev, 2010 and Sunaristes japonicus Ho, 1986a are amended to reflect agreement in gender with their respective generic names.