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A new species of the alpheid shrimp genus Athanas Leach, 1814 is described based on a holotype from Wakasa Bay, Sea of Japan side of Honshu, Japan, at a depth of 90 m. Athanas exilis n. sp. appears close to A. sydnyensis Anker & Ahyong, 2007, but is distinguished from the latter by some morphological features, including the different shape of the telson, the shorter antennular stylocerite, more strongly produced distal lamella of the antennal scaphocerite, and less developed armature of the merus of the major cheliped. Preliminary genetic analysis using the mitochondrial 16S rRNA gene was performed to compare interspecific genetic divergence within the genus.

Three species of nannosquillid mantis shrimps, including two new species, Acanthosquilla ryukyuensis n. sp. and Acanthosquilla shoheii n. sp., are described based on specimens collected from the Ryukyu Islands, Japan. The two new species resemble A. derijardi Manning, 1970, but can be distinguished from A. derijardi by the following features: 1) rostral plate anterolateral corner forms almost a right angle; 2) the distal tip of the antennular somite dorsal process reaches or slightly falls short of proximal half of rostral plate; and 3) eighth thoracic somite (= TS8) posterior margin is black medially. Furthermore, A. ryukyuensis n. sp. and A. shoheii n. sp. are easy to identify by the bifurcated lateral tooth of the telson, and by the posterodorsal pattern of the telson, respectively. In this study, molecular analyses based on partial sequences of mitochondrial 12S and 16S ribosomal DNA, cytochrome oxidase subunit I (COI), and the partial nuclear gene of 28S ribosomal DNA recovers these three species of Acanthosquilla and A. multifasciata (Wood-Mason, 1895) (the type species of the genus) in a single clade. The resulting trees also suggest the polyphyly of Nannosquillidae but with low nodal support. Detailed examinations of the morphological and color features and DNA barcoding results allowed us to delineate intraspecific variations and interspecific differences. The number and shape of setae under the dorsal spine of raptorial claw carpus was found to be useful in distinguishing A. shoheii n. sp. from A. derijardi and A. ryukyuensis n. sp., while combinations of the coloration of the rostral plate, posterior margin of TS8 and posterodorsal surface of telson are useful to distinguish the three species.

Estimating stomatopod species diversity using morphology alone has long been difficult; though over 450 species have been described, new species are still being discovered regularly despite the cryptic behaviors of adults. However, the larvae of stomatopods are more easily obtained due to their pelagic habitat, and have been the focus of recent studies of diversity. Studies of morphological diversity describe both conserved and divergent traits in larval stomatopods, but generally cannot be linked to a particular species. Conversely, genetic studies of stomatopod larvae using DNA barcoding can be used to estimate species diversity, but are generally not linked to known species by analyses of morphological characters. Here we combine these two approaches, larval morphology and genetics, to estimate stomatopod species diversity in the Hawaiian Islands. Over 22 operational taxonomic units (OTUs) were identified genetically, corresponding to 20 characterized morphological types. Species from three major superfamilies of stomatopod were identified: Squilloidea (4 OTUs, 3 morphotypes), Gonodactyloidea (9, 8), and Lysiosquilloidea (6, 7). Among these, lysiosquilloids were more diverse based on larval morphotypes and OTUs as compared to previously documented Hawaiian species (3), while squilloids had a lower diversity of species represented by collected larvae as compared to the seven species previously documented. Two OTUs / morphotypes could not be identified to superfamily as their molecular and morphological features did not closely match any available information, suggesting they belong to poorly sampled superfamilies. The pseudosquillid, Pseudosquillana richeri, was discovered for the first time from Hawai'i. This study contributes an updated estimate for Hawaiian stomatopod diversity for a total of 24 documented species, provides references for identification of larval stomatopods across the three major superfamilies, and emphasizes the lack of knowledge of species diversity in more cryptic stomatopod superfamilies, such as Lysiosquilloidea.

Three new species of the genus Heteromysis S.I. Smith, 1873 (tribus Heteromysini), are described from a rich stock of mysids obtained on request from the international community of professional aquarium keepers. The 18S rDNA and COI sequences of the three species were distinct from each other and also from other sequences published in DNA databases. Heteromysis (Olivemysis) schoenbrunnensis sp. nov. is morphologically characterized within the subgenus Olivemysis based on the structure of the first and second antennae, male pleopods, uropods, and telson. Heteromysis (Heteromysis) gulfarii sp. nov. is outstanding within the subgenus Heteromysis by sexually dimorphic modified setae on the antennular trunk. These setae are non-dimorphic in the very similar Heteromysis (Heteromysis) korntalensis sp. nov. Both species H. gulfarii and to a lesser degree also H. korntalensis show modified eyes, subquadrate in dorsal view, eyestalks anteriorly tapering in lateral view; small, well-developed cornea implanted laterally on modified eyestalk. Apart from eye structure H. gulfarii and H. korntalensis clearly fall morphologically within the nominotypical subgenus Heteromysis.

Two new planktonic ostracods of the genus Proceroecia Kock, 1992, P. hwanghaensis sp. nov. and P. joseondonghaensis sp. nov., collected from neritic waters off the south coast of South Korea are described. Morphologically, they are similar to P. microprocera (Angel, 1971), the type species of the genus, but show several clear morphological differences, most prominent being the shape of the male endopodite on the second antenna and the presence of a sensilla on the coxale of the fifth limb. The two new species have subtle differences, such as the length of the frontal organ, number of spines on the comb-like e-seta on the first antenna in males, number of spinules on the b-seta on the second antenna in females, etc. Sequences derived from partial mitochondrial cytochrome oxidase c subunit 1 (mtCOI) for these novel species have been compared with sequences available for other Proceroecia species on GenBank, including P. microprocera. These comparisons suggest that both new species are distinct taxa. They also indicate that one set of sequences on GeneBank previously attributed to P. microprocera and derived from material collected from Chinese waters, belong to P. hwanghaensis, and that another set of sequences of an unidentified Proceroecia species from the South China Sea can be attributable to P. joseondonghaensis. Hence, these new species occur widely in the neritic waters of East Asia. The present study increases the number of the known Proceroecia species to nine, and the numbers of halocyprid ostracod species recorded from Korean waters to six.

We investigated the phylogenetic position of Triops granarius populations from four localities in the Western Ghats using partial sequences of three mitochondrial genes (COI, 12S rRNA and 16S rRNA) publicly available on the GenBank database. One of these localities, Panchgani, is particularly important since it is the type locality of the former Apus orientalis which is currently treated as a junior synonym of T. granarius. Phylogenetic analyses reveal that populations from all the four localities (Kolhapur, Chalkewadi, Panchgani, and Dighi) form a single lineage, which is here named 'Maharashtra lineage'. One of the two previously published samples from India, treated as lineage 'Triops granarius 4' is nested within this clade. The 'Maharashtra lineage' is separated from other lineages by mean maximum likelihood distance ≥ 11.9% in the COI gene. This distance is suggestive of a separation on species level from other lineages of T. granarius. This interpretation is further supported by a conservative genus-wide species delimitation analysis performed in the present study upon application of the Automatic Barcode Gap Discovery method. The 'Maharashtra lineage' branches out in two sub-lineages of Panchgani+Kolhapur and Dighi+L4+Chalkewadi samples, separated by 5.9% mean ML distance (uncorrected p-distance = 5.4%) in COI. The application of a 5% threshold to the COI dataset would thus even suggest a possible differentiation of both sub-lineages on species level. Comparative morphological data is presently not available because most vouchers associated with the sequences were depleted for DNA extraction. Further studies are needed in order to prepare a sound taxonomic revision. Thus, in the current study we refrain from re-instating Apus orientalis to full species status (likewise, for other names of Asian taxa in this morphogroup, including Apus sinensis Uéno, we retain the status as junior synonym of T. granarius). Nonetheless, our study highlights the fact that still there may be undescribed cryptic species associated with the specific name in this part of Western Ghats (Linnean Shortfall) and paves the way for future taxonomic investigations and conservation strategies for the genus Triops in India.

We used three molecular markers to investigate populations of Triops granarius from a study area in western Morocco that had a north-south span of approx. 434 km, the most distant populations situated at more than 470 km distance from each other. Previous studies had already investigated two Triops granarius populations from this region and revealed their affiliation to the major phylogenetic lineage that includes Triops cancriformis. By contrast, based on the geographic position of the type locality and the morphology of the type, Triops granarius s.s. likely belongs to a clade that forms the sister group to American and Australian Triops, i.e. including Triops longicaudatus and Triops australiensis. In the present study a second, hitherto unknown phylogenetic lineage was discovered among Moroccan populations of Triops granarius s.l. Our phylogenetic analyses show that both Moroccan lineages of Triops granarius s.l. represent a pair of genetically and morphologically well differentiated sister species that should be separated from Triops granarius. We therefore formally describe them as two new species, Triops maximus sp. nov. and Triops multifidus sp. nov. The early larval stages of both species show a peculiar morphology with 10 to 15 setae on the exopodite of the 2 nd antenna. The number of these setae was generally thought to span five to seven in Notostraca. Despite the fact that the antennal setae form a central part of the main locomotory organ in early instars, we found their number to vary by up to two between body-sides of single individuals.

We describe three new species of brackish-water ostracods representing two genera in the ostracod tribe Thalassocypridini from mangrove forests in the Ryukyu Islands, subtropical southwestern Japan, and provide their barcoding sequences for the mitochondrial cytochrome c oxidase subunit I (COI) gene. Mangalocypria ryukyuensis sp. nov. was found on Okinawa Island. We also found a Mangalocypria population on Ishigaki Island that was morphologically identical to M. ryukyuensis on Okinawa, but an individual differed by 4.7% in COI sequence (K2P distance) from an individual from Okinawa. This is the first record for Japan of a species in Mangalocypria. Paracypria longiseta sp. nov., obtained from Okinawa Island, is similar to Pontoparta hartmanni. Paracypria plumosa sp. nov. from Ishigaki Island is similar to Pa. adnata described from Yakushima Island, Japan. The COI genetic distance between individuals of Pa. longiseta and Pa. plumosa was roughly as large as that between either of these species and individuals in the Mangalocypria populations. Our study underscores that genera in Thalassocypridini may not represent natural groups, and that this tribe needs taxonomic revision.

Samples collected from the Antarctic (ANDEEP/2002) and Mid-Pacific (BIONOD/2012) Oceans allowed analyses of several specimens of the family Neotanaidae. From these surveys two new species are described: Neotanais bicornutus and Venusticrus thor. The new material led to a re-diagnosis of Venusticrus, and N. rotermundiae is now assigned to this genus. The male of N. bicornutus shares a number of characters with the "robustus" species group, but differs by having a pleotelson about 1.5 times as wide as long, cheliped carpus about 1.5 times as long as cephalothorax, cheliped propodus with two long dorsal projections, and uropod endopod article 1 with 8-10 fine setae proximal to mid-length on outer margin. The N. bicornutus preparatory female differs from all species by a combination of characters including the number of setae on dorsal margin of cheliped carpus (about 15 setae), the uropod attachment slightly posterior to mid-length, uropod basal article about 2.7 times as long as endopod article 1. The female of V. thor differs from those of V. insolitus, V. glandurus and V. rotermundiae by the body proportions, the pleon having three lateral setae on epimera, pleon with a blunt ventral keel, pereopodal setation, number of setae on maxilliped endite and basis as well as other characters. Total genomic DNA was extracted from two specimens of V. thor and sequences of two genes, i.e., cytochrome oxidase 1 (COI) and ribosomal (28S) were obtained.

The East China Sea is part of the Warm Temperate Northwest Pacific zoogeographic province and, as such, has a high biodiversity and many tropical and subtropical biotic elements. Nevertheless, many invertebrate groups from this area remain poorly studied. Ostracods are one of them, especially those belonging to the subclass Myodocopa. In this paper we provide the first data on a diverse myodocopid family, Sarsiellidae, not only for the East China Sea, but also for Korea. Five species are reported in this paper from three Korean islands (Jeju, Chuja, and Maemul), and they are only a part of the ostracods collected during this study, indicating a high diversity of the group in this region. Three new species, Eurypylus koreanus sp. nov., Eusarsiella hanguk sp. nov., and Sarsiella nereis sp. nov., clearly stand apart from their respective congeners, mostly by prominent shell characters but also by details of the soft part morphology. Their affinity though clearly indicates a close connection of the region with the more southern zoogeographical realms, especially Central Indo Pacific and partly Temperate Australasia. Two species previously known from Japan (north part of the Sea of Japan and southeastern part of the Pacific Coast of Japan), Sarsiella japonica Hiruta, 1977 and S. misakiensis Kajiyama, 1912, are redescribed. Based on 11 newly obtained COI sequences we construct a preliminary phylogenetic tree, which supports previous hypotheses based on the morphological data, that Eusarsiella Cohen & Kornicker, 1975 is a polyphyletic taxon. With the maps of species distribution provided for each of the three genera, we give an overview of their current zoogeography, and clearly indicate areas that have no data, mostly due to the lack of investigation.

Following recent revelations regarding males with subchelate chelipeds in the tanaidacean genus Parakonarus, a number of Australian leptocheliid taxa are re-assessed, and their males and females variously re-allocated. To assist the interpretation of taxa with subchelate males, Heterotanais anomalus Sars is redescribed based on material from the Balearic Islands. The males of Konarus are now known to have a subchelate cheliped. The male (only) of Pseudoleptochelia bulbus from Melanesia is reassigned to Konarus cheiris, while Pseudoleptochelia bulbus sensu stricto is reassigned to Leptochelia together with its "minuta"-type male, as Leptochelia bulbus. Pseudoleptochelia straddi is rassigned to Konarus, together with its females from Queensland, Australia, which were previously assigned to Konarus cheiris. Pseudoleptocheliafairgo is confirmed as a member of Parakonarus, but material from Queensland is re-described as a new species. Other species previously assigned to Pseudoleptochelia are re-assessed: P. inermis, P. mercantilis and P. mortenseni sensu stricto are transferred to Leptochelia. The "small females" and males of P. mortenseni are transferred to Parakonarus as a new species. P. antarctica is provisionally reverted to Heterotanais, P. mergellinae to Leptochelia, and P. filum is tentatively transferred to Pseudonototanais. Pseudoleptochelia magna is synonymized with P. anomala. Pseudoleptochelia provincialis is tentatively transferred to Parakonarus. Pseudoleptochelia occiporta (females only) is reassigned to Leptochelia; the male of P. occiporta is considered to represent a species of Parakonarus. Pseudoleptocheliajuliae is reassigned to Parakonarus. Konarus, Makraleptochelia, Bassoleptochelia, Parakonarus and Pseudoleptochelia are placed in the new subfamily Konariinae. Generic relationships in this subfamily were confirmed by Principle Components Analysis. Catenarius is placed in the new subfamily Catenariinae.

Three new species of the genus Cypretta Vivra, 1985 are described from Southern Mexico, representing the first record of the genus in the country. Cypretta campechensis n. sp. is closely related to Florida and North Carolina species such as C. nigra Furtos, 1936, C. brevisaepta Furtos, 1934 and C. bilicis Furtos, 1936. Cypretta spinosa n. sp. is related to the North and South American species C. intonsa Furtos, 1936 and C. vivacis Würdig & Pinto, 1993, but also to some Australian and South-East Asian Islands ones, such as C. obfuscata Victor & Fernando, 1981 and C. raciborskii (Grochmalicki, 1915). The last species described herein, Cypretta maya n. sp., is closely related to the South-East Asia islands, Australian and north Indian species, in particular to C. hirsuta Henry, 1923, C. longidactyla Victor & Fernando, 1981, and C. patialensis Battish, 1982.

Alima pacifica and A. orientalis are stomatopods commonly found at Lizard Island, Great Barrier Reef, Australia. There are currently no descriptions that link the larvae to the adult morphotype despite the frequent occurrence of the last larval stage of these two species. We used DNA barcoding of the cytochrome oxidase I (COI) gene to link the last stage larvae of A. pacifica and A. orientalis to the respective adult morphotype. Detailed morphological descriptions of the late larva of each species are provided and compared to other described last-stage Alima larvae. These data support previous studies that suggest paraphyly of the genus Alima.