Review of naupliar development among Miraciidae (Copepoda,Harpacticoida) with a naupliar description of <Emphasis Type="Italic">Paramphiascella</Emphasis><Emphasis Type="Italic">choi</Emphasis> sp. nov. from Thailand

Both genders of Paramphiascella choi sp. nov. were collected from the green alga Enteromorpha clathrata in Rayong province, Thailand. P. choi shares with other species of the genus: cylindrical body shape, rostrum not bifid, eight-segmented antennules, three-segmented exopodal antenna, and female P5 exopod with five setae. The new species distinguished from other conspecific species by: three-segmented exopodal antenna, inner edge of basis of male P1 and P2 bear a bare ovate-knob each. Enp-1 very elongate, Enp-2 of male P2 transformed into a large, strong, slightly curved and tapering attenuation with two central chitinous ridges, and bearing one medially directed knob close to enp-1. At the base of this knob arise three plumose setae of unequal length. These characters are suggested to be autapomorphies of the new species. Six naupliar stages are obtained and described a key for the identification of stages is provided. Nauplius I has one pair of caudal setae; three-segmented antennules; antenna consists of a coxa, basis, endopod and exopod; mandible has a coxa, basis, endopod and exopod; hindbody bears two caudal setae. Nauplius II develops one aesthetasc on the antennule; antenna has added an arthrite arising from the coxa; mandible has a row of tiny spinulose setae. Nauplius III has added two pairs of caudal setae. Nauplius IV bears bilobed bud of the maxillule armed with two setae and four pairs of caudal setae. Nauplius V bears a multilobed bud of the maxillule with three setae and five pairs of caudal setae. At Nauplius VI, the buds of swimming legs 1 and 2 are added.     

Description of Eucyclops tziscao sp. n., E. angeli sp. n., and a new record of E. festivus Lindberg, 1955 (Cyclopoida,Cyclopidae, Eucyclopinae) in Chiapas,Mexico

Two new species of the freshwater cyclopoid genera Eucyclops are described, Eucyclops tziscao sp. n. and E. angeli sp. n. Both species belong to the serrulatus-group defined by morphological features such as: the presence of distal spinules or hair-like setae (groups N1 and N2) on frontal surface of antennal basis; the fourth leg coxa with a strong inner spine that bears dense setules on inner side, yet proximally naked (large gap) on outer side; and a 12-segmented antennule with smooth hyaline membrane on the three distalmost segments. Eucyclops tziscao sp. n. is morphologically similar to E. bondi and E. conrowae but differs from these species in having a unique combination of characters, including a caudal ramus 4.05±0.25 times as long as wide, lateral seta of Enp3P4 modified as a strong, sclerotized blunt seta, coxal spine of fourth leg with inner spinule-like setules distally, and sixth leg of males bearing a strong and long inner spine 2.3 times longer than median seta. Eucyclops angeli sp. n. can be distinguished by an unique combination of morphological features: the short caudal ramus; the long spine on the sixth antennular segment of A1; the presence of one additional group of spinules (N12’) on the caudal surface of A2; the presence of long setae in females, or short spinules in males on the lateral margin of fourth prosomite; the strong ornamentation of the intercoxal sclerite of P4, specially group I modified as long denticles; the distal modified setae of Exp3P3 and Exp3P4 in females and males; and the short lateral seta of P5. Finally, we report on a new record of E. festivus in México, and add data on morphology of the species.     

Larval development of Octomeris sulcata Nilsson-Cantell (Cirripedia: Thoracica: Chthamalidae) from Japan and Korea

Embryos obtained from gravid adults of the chthamalid barnacle Octomeris sulcata Nilsson-Cantell from Japan and Korea were cultured through six naupliar stages to the cyprid and juvenile barnacle stage in laboratory conditions, fed either the diatom Skeletonema costatum (Grev.) Cleve or the dinoflagellate Prorocentrum minimum (Pavillard) Schiller. The nauplii were planktotrophic and, depending on diet, reached the cyprid stage 9 or 17 days after hatching in individual cultures at 22 °C with 24 h illumination. The survival rate was higher and the duration of the naupliar stages was shorter when fed P. minimum rather than S. costatum. This is probably due to the presence of feathered setae on the antennae. Feathered or plumose setae in nauplii of different cirripede taxa are apparently linked to the type of phytoplankton in the seas when these taxa first evolved.The larval stages of O. sulcata are described, and morphological differences between larvae reared from Japanese andKorean adults are compared. The polygonal cephalic shield and unilobed labrum, a pair of posterior shield spines after naupliar stage IV, feathered setae and a hispid seta on the coxa of the antenna, a cuspidate seta on the mandible, and the gnathobase of the antenna are important in distinguishing the nauplii of this species from other species, including Chthamalidae.     

A new species of Peltidium Philippi, 1839 (Crustacea,Copepoda, Harpacticoida) from the Pacific coast of Mexico

During the analysis of phytal meiobenthic samples collected from a rocky-sandy beach in the state of Nayarit, in the Mexican Pacific, several specimens of harpacticoid copepods were obtained and taxonomically examined. These specimens were found to represent an undescribed species of the peltidiid genus Peltidium Philippi, 1839. The new species, Peltidium nayarit sp. n. is described herein. It resembles Peltidium nichollsi Geddes and Peltidium lerneri Geddes from Bahamas but also the widespread Peltidium speciosum Thompson & Scott and Peltidium purpureum Philippi. The new species from the Mexican Pacific differs from its known congeners by its possession of a unique combination of characters, including a modified pectinate seta on the antennary exopod, three terminal setae on the second endopodal segment of leg 1, third exopodal segment of leg 1 with three elements, inner terminal claw twice as long as outer claw, female fifth leg with 5 exopodal setae, exopodal setae I-III stout, spinulose and seta IV being as long as seta V. This is the second species of the family known to be distributed in the Eastern Tropical Pacific and in Mexico. Pending additional data, the distribution of this species appears to be restricted to this area of the Mexican Pacific.     

Cannibalistic behaviour of rock-pool copepods: An experimental approach for space, food and kinship

Studies on cannibalism in harpacticoid copepods are restricted to predation on naupliar larvae in rock-pool harpacticoids of the genus Tigriopus. An earlier experimental study on the Mediterranean copepod Tigriopus fulvus indicated that females recognized their own larvae and preferentially preyed on nauplii other than their own. In a series of laboratory experiments, we tested if there were differences in naupliar predation as a function of crowding, food level and sex in Tigriopus brevicornis and T. fulvus. Results show that cannibalism was restricted to the first larval stages (N1 and N2). Both food availability and adult density significantly affected the predation rate. Contrary to earlier suggestions, adult males also preyed on the nauplii. We found no evidence that adults spare their own offspring, for neither T. fulvus nor T. brevicornis.This is in accordance with what one would expect for species having the life history characteristics of Tigriopus, i.e.: multiple broods and large number of offspring. Earlier results indicating parental care in Tigriopus must be taken with caution.     

Larval development of Japanese 'conchostracans': part 2, larval development of Caenestheriella gifuensis (Crustacea, Branchiopoda, Spinicaudata, Cyzicidae), with notes on homologies and evolution of certain naupliar appendages within the Branchiopoda

As part of a larger project examining and comparing the ontogeny of all major taxa of the Branchiopoda in a phylogenetic context, the larval development of Caenestheriella gifuensis (Ishikawa, 1895), a Japanese spinicaudatan ‘conchostracan’, is described by scanning electron microscopy. Seven different larval stages are recognised, in most cases based on significant morphological differences. They range in length from about 200 to 850 μm. Nauplius 1 has a plumb and lecithotrophic appearance with a rounded hind body and a labrum with an incipient medial spine. Limb segmentation is mostly unclear but the second antennae have more putative segments delineated than are expressed in the later stages. Feeding structures such as the mandibular coxal process and antennal coxal spine are only weakly developed. Nauplius 2 is very different from nauplius 1 and has three large spines on the labral margin and two long caudal spines. Feeding structures such as the mandibular coxal process and various spines and setae are developed, but whether feeding begins at this stage was not determined. The mandible has developed an ‘extra’ seta on endopod segment 1, absent in Nauplius 1. The segmentation of the second antenna has changed significantly due to fusions of various early segments. Nauplius 3 is like nauplius 2 in morphological detail, but larger and more elongate. Nauplius 4 has developed a pair of small anlagen of the carapace and rudiments of the first five pairs of trunk limbs, and the coxal spine of the antenna has become distally bifid. Nauplius 5 has a larger carapace anlage, externally visible enditic portions of the elongate trunk limbs, and a pair of primordial dorsal telson setae. Nauplius 6 has a larger and partly free carapace and better-developed, partly free trunk limbs with incipient enditic, endopodal, and exopodal setation. A pair of caudal spines, dorsal to the large caudal spines, has appeared. Nauplius 7 is quite similar to nauplius 6 but is larger and has slightly longer caudal and labral spines; also, the setation of the most anterior trunks limbs is better developed. The larval development is largely similar to that of other spinicaudatans. The larval mandible, which is evolutionarily conservative within the Branchiopoda, reveals a setation pattern similar to that of the Anostraca and Notostraca (two setae on mandibular endopod segment 1). Most other spinicaudatans and all examined laevicaudatans share another setal pattern (one seta on mandibular endopod segment 1), which could indicate a close relationship among these taxa. The second antenna undergoes a special development, which provides an insight into the evolution of this limb within the Branchiopoda. In nauplius 1 the basipod, endopod, and exopod are all superficially divided into a relatively high number of segments. In later nauplii some of these have fused, forming fewer but larger segments. We suggest that this ontogeny reflects the evolution of antennae in the conchostracans. Various aspects of the morphology of the antennae are discussed as possible synapormorphies for either the Diplostraca or subgroups of the Conchostraca.     

Doridicola indistinctus n. sp. (Copepoda: Poecilostomatoida: Rhynchomolgidae) associated with the soft coral Gersemia fruticosa Sars (Octocorallia: Alcyonacea: Nephtheidae) from the White Sea

A new species of poecilostomatoid copepod, Doridicola indistinctus n. sp. (Rhynchomolgidae), is described from specimens found in association with the soft coral Gersemia fruticosa Sars (Alcyonacea: Nephtheidae), collected from the White Sea. The new species is distinguished from its congeners by the combination of the following features in the female: (i) antenna tipped, with two subequal large claws which are about as long as the segment bearing them; (ii) two naked, extremely unequal setae on the middle segment of the maxilliped, the short, medial seta less than half-length of the outer seta; and (iii) free segment of leg 5 bears the basal swelling and is ornamented with spinules on the outer surface. This is the first report of a copepod occurring in symbiosis with nephtheid corals from the Arctic Zone. It also constitutes the northernmost record for a species of Doridicola Leydig, 1853, which is the largest genus of the Rhynchomolgidae Burmeister, 1835 comprising 52 species, including the present new species.     

Antennular sensilla of the brine shrimp, Artemia salina.

1. Scanning electron microscopy was used to characterize the external morphology of setae found on the antennules of adults and nauplii of the brine shrimp, Artemia salina (L.). The permeability of the antennular setae was studied by means of Slifer's crystal violet method. 2. Each antennule of an adult brine shrimp possessed a terminal cluster of sensory setae. Within a cluster there were two morphologically distinct kinds of sensilla, here designated type 1 and type 2. Three type 1 sensilla were observed on every antennule examined. The number of type 2 sensilla per antennule was usually four or five. 3. Type 1 sensilla of adults were 43 to 80 micrometer long and simple in external morphology. They were widest at the base, decreased in diameter gradually, and terminated as a finely tapered tip. No pores were resolved by scanning electron microscopy. 4. Type 2 sensilla of adults were shorter (shaft length, 12 to 23 micrometer) and displayed a single pore at the tip (average pore diameter, 0.4 micrometer). In thin section they were seen to possess a distinctive articular specialization of the cuticle at the base of the seta. 5. Dye penetration experiments indicated that type 2 sensilla were permeable to aqueous crystal violet, whereas type 1 sensilla were not. 6. The antennular setae of nauplii resembled type 1 sensilla in general shape, in being impermeable to crystal violet, and in lacking a terminal pore and basal articular specialization. Moreover, a total of three setae was normally present on each naupliar antennule, and the same number of type 1 sensilla was found on each adult antennule examined. If the three naupliar setae represent a developmental stage in the formation of three adult sensilla, available observations suggest that the larval setae are developmentally related to type 1, rather than to type 2 adult sensilla.     

A new species of Procolobomatus Castro Romero, 1994 (Copepoda: Philichthyidae) endoparasitic in a deepwater longtail red snapper (Actinopterygii: Lutjanidae) off Ishigaki Island, Japan, with records of philichthyid copepods reported from Asian waters

A new species of the Philichthyidae Vogt, 1877 (Copepoda: Poecilostomatoida), Procolobomatus hoi n. sp., is described based on adult female specimens recovered from the cephalic sensory canals of Etelis coruscans Valenciennes (Actinopterygii: Lutjanidae) caught off Ishigaki Island, the Ryukyu Islands, southern Japan. The new species differs from its congeners by having the following combination of characters: a long medial cephalic lobe about one-third the length of the body; an armature of five spines on the distal exopodal segment of leg 2; one long apical seta on the papillose leg 4; a caudal ramus armed with one medial and four terminal setae (two middle setae are inflated); and spinulose ornamentation covering the body. Procolobomatus hoi n. sp. is the first member of the genus reported from the western Pacific Ocean and from a host of the family Lutjanidae. Previous records of philichthyid copepods from Asian waters are also reported.     

Naupliar and Metanaupliar Development of Thysanoessa raschii (Malacostraca,Euphausiacea) from Godth?bsfjord,Greenland, with a Reinstatement of the Ancestral Status of the Free-Living Nauplius in Malacostracan Evolution

The presence of a characteristic crustacean larval type, the nauplius, in many crustacean taxa has often been considered one of the few uniting characters of the Crustacea. Within Malacostraca, the largest crustacean group, nauplii are only present in two taxa, Euphauciacea (krill) and Decapoda Dendrobranchiata. The presence of nauplii in these two taxa has traditionally been considered a retained primitive characteristic, but free-living nauplii have also been suggested to have reappeared a couple of times from direct developing ancestors during malacostracan evolution. Based on a re-study of Thysanoessa raschii (Euphausiacea) using preserved material collected in Greenland, we readdress this important controversy in crustacean evolution, and, in the process, redescribe the naupliar and metanaupliar development of T. raschii. In contrast to most previous studies of euphausiid development, we recognize three (not two) naupliar (= ortho-naupliar) stages (N1-N3) followed by a metanauplius (MN). While there are many morphological changes between nauplius 1 and 2 (e.g., appearance of long caudal setae), the changes between nauplius 2 and 3 are few but distinct. They involve the size of some caudal spines (largest in N3) and the setation of the antennal endopod (an extra seta in N3). A wider comparison between free-living nauplii of both Malacostraca and non-Malacostraca revealed similarities between nauplii in many taxa both at the general level (e.g., the gradual development and number of appendages) and at the more detailed level (e.g., unclear segmentation of naupliar appendages, caudal setation, presence of frontal filaments). We recognize these similarities as homologies and therefore suggest that free-living nauplii were part of the ancestral malacostracan type of development. The derived morphology (e.g., lack of feeding structures, no fully formed gut, high content of yolk) of both euphausiid and dendrobranchiate nauplii is evidently related to their non-feeding (lecithotrophic) status.     

Pseudocyclops schminkei (Copepoda, Calanoida, Pseudocyclopidae): a new species from Okinawa

Both genders of Pseudocyclops schminkei n. sp. are described from a pearl fishery aquarium on Zamami Island, Okinawa, Japan; it is the 37th species of the genus. Pseudocyclops schminkei sp. nov. differs from other species of the magnus species group in the shape of the lobes of distal exopodal segment of the male left leg 5, and the morphology of setae on middle and distal exopodal segment of male right swimming leg 2. Aspects of the morphology of P. xiphophorus and P. bilobatus are redescribed, and an unnamed Pseudocyclops sp. from the Shedd Aquarium in Chicago, IL, is briefly noted. Females of P. schminkei sp. nov., P. xiphophorus and Pseudocyclops sp. could not be separated from each other with the small number of specimens available in this study for the former two species.     

A new species of Pseudomacrochiron Reddiah, 1969 (Crustacea: Copepoda: Macrochironidae) associated with scyphistomae of the moon jellyfish Aurelia sp. (Cnidaria: Scyphozoa) off Japan

A new species of the Macrochironidae Humes & Boxshall, 1996 (Copepoda: Cyclopoida), Pseudomacrochiron aureliae n. sp., is described based on adult specimens extracted from the gastrovacular cavity of the scyphistomae of Aurelia sp. (Cnidaria: Scyphozoa) collected in the Seto Inland Sea and Ise Bay off the coast of Japan. The new species differs from its congeners by having the following combination of characters: a caudal ramus with a length to width ratio of 3.1; an accessory flagellum on caudal setae II, III and VI; three apical setae on the maxillule; only setae I and II on the maxillary basis; two short spines on the female maxilliped claw (endopod); an armature of III, I, 4 on the terminal exopodal segment of leg 3; an armature of I, II, 2 on the terminal endopodal segment of leg 3; an armature of II, I, 4 on the terminal exopodal segment of leg 4; and a short free exopodal segment of leg 5 (length to width ratio of 1.4) armed with a long seta and short spine. P. aureliae n. sp. is the first member of the genus reported from off Japan and from the scyphistomae of its scyphozoan host.     

Developmental Patterns and Hypotheses of Homology in the Antennules of Thecostracan Nauplius Larvae (Crustacea)

Abstract Antennular development is summarized for non–brooded nauplius larvae of the Ascothoracida (families Lauridae and Petrarcidae) and for selected nauplii of the Facetotecta. In the Cirripedia Thoracica, nauplii of the Lepadomorpha and Scalpellomorpha/Sessilia are shown to differ in their patterns of antennular setal addition and division into articles, and one or two possible apomorphies for each group are identified. Several variations of the scalpellomorphan/sessilian pattern are outlined. These data on the Ascothoracida, Facetotecta, and Cirripedia provide the basis for modifying an earlier proposal of structural homologies among the naupliar antennules of thecostracan maxillopodans. ‘Virtual’ articles (ones that are never completely free) are invoked to account for setae that ‘jump’ across article boundaries at molts and for supposedly homologous setae found on adjacent articles in different taxa. The identities of the preaxial setae in the Cirripedia are ambiguous and force consideration of two models for that group and for the thecostracan antennular Bauplan; the latter may have included up to 11 or 12 articles, more than the previously supposed 8 or 9. The scoring of characters used in an earlier cladistic study of thecostracan and other maxillopodan taxa is not seriously affected. A comparison with the Cambrian maxillopodan Bredocarissuggests that division of the antennule into discrete articles in extant thecostracans is an apomorphic state and that yet one more apical article once existed in the maxillopodan antennule.     

Giselinidae fam. nov., a new monophyletic group of cyclopoid copepods (Copepoda, Crustacea) from the Atlantic deep sea

Four new species of Cyclopoida from deep-sea waters are described and placed in two new genera: Giselina gen. n. and Sensogiselina gen. n. The new genera and species belong to a new monophyletic group within the cyclopinid cyclopoids. A new name, Giselinidae, is proposed for this monophylum. The new family is characterised by the combination of the following characters: (1) tergite of leg 1 fused to cephalosome dorsally, but incompletely fused laterally, (2) absence of aesthetascs on ancestral antennulary segments XVI, XXI and XXV, (3) absence of antennary exopodal setae, (4) presence of only three spines on distal exopodal segment of leg 1, (5) absence of inner setae on first endopodal segments of legs 1–4, (6) outer terminal and distal inner elements of distal endopodal segment of leg 4 transformed into spines, (7) distal outer element of leg 5 exopod transformed into a spine, (8) leg 6 with only one seta, and (9) furcal setae I and III located on dorsal margin. Received in revised form: 16 June 2000 Electronic Publication     

Toxicity of the dinoflagellate Gambierdiscus sp. toward the marine copepod Tigriopus japonicus

The toxic dinoflagellate Gambierdiscus sp. has recently been observed in temperate areas in the Southern Sea of the Republic of Korea. The purpose of this study was to examine the toxicity of Gambierdiscus sp. toward the marine copepod Tigriopus japonicus. T. japonicus adult females and nauplii were exposed to various concentrations of algae or culture medium to assess toxicity and analyze gene expression patterns in the copepod. Based on the toxicity tests, Gambierdiscus sp. increased the mortality of nauplii and the immobility of adult females. The survival and mobility of T. japonicus were not affected by culture medium lacking Gambierdiscus sp. cells in the toxicity test. However, based on the analysis of gene expression in the copepod, exposure of the copepod to culture medium affected the expression of stress or detoxification-related genes. Further studies to identify toxins in Gambierdiscus sp. are required to increase our understanding of dinoflagellate toxicity.     

A new marine cyclopoid copepod of the genus Neocyclops (Cyclopidae,Halicyclopinae) from Korea

A new cyclopoid species of the genus Neocyclops Gurney, 1927 is described. Type specimens were collected from a beach on south-western coast of the Korean Peninsula by rinsing intertidal coarse sandy sediments. Neocyclops hoonsooi sp. n. is most characteristic in showing the conspicuous chitinized transverse ridges originating from the medial margins of the coxae of all swimming legs. The new species is most similar to Neocyclops vicinus, described from the Brazilian coast, and Neocyclops petkovskii, from Australia. All three species share a large body size (more than 750 µm long), the presence of an exopodal seta on the antenna, two setae on the mandibular palp, the same seta/spine armature on the third endopodal segment of leg 3 (3 setae + 3 spines), and the fairly long inner distal spine on the third endopodal segment of the female leg 4. However, Neocyclops hoonsooi sp. n. differs from both species by the much shorter caudal rami (less than 1.7 times as long as wide) and the shorter dorsal caudal seta VII. Furthermore, Neocyclops hoonsooi is clearly distinguished from Neocyclops vicinus by the 10-segmented antennule (vs 12 segments in Neocyclops vicinus), and from Neocyclops petkovskii by the elongate inner distal spine on leg 5 exopod and the 3-segmented leg 5 in male (vs 4-segmented in Neocyclops petkovskii). A tabular comparison of characters separating Neocyclops hoonsooi from its closest allies and a key to Neocyclops species from the Indo-Pacific Ocean are provided. This is the first record of the genus Neocyclops from the northern Pacific.