Open Access
19 July 2017 A new species of the genus Halectinosoma (Copepoda, Harpacticoida, Ectinosomatidae) from Korea
Jong Guk Kim, Tae Won Jung, Seong Myeong Yoon
Author Affiliations +

A new species of harpacticoid copepod, Halectinosoma foveolata, was described from sandy sediments on several intertidal areas of Korea. This new species is mostly similar to H. dimorphum Coull, 1970, but differs from the latter by the following characteristics combined: (1) the third segment of antennule is longest; (2) the first exopodal segment of antenna has a row of spinules; (3) the mandibular gnathobase is composed of chitinous teeth without dorsal seta; (4) the female P5 has an incomplete boundary between the exopod and the baseoendopod; (5) the female P5 baseoendopod has two rows of spinules. We also discuss the state of H. arenicola sensu Itô (1973), reported from the Japanese coast, which is considered here a synonym with the new species.

The genus Halectinosoma Vervoort, 1962 is a large group composed of about 70 nominal species within the family Ectinosomatidae (Soyer 1972, Huys & Bodin 1997, Clément & Moore 2000, Karanovic & Pesce 2001, Wells 2007, Huys 2009, Boxshall et al. 2010, Suárez-Morales & Fuentes-Reinés 2015). The name of this genus was first proposed as a subgenus of the genus Ectinosoma Boeck, 1865 by Lang (1944), and Vervoort's (1962) consequently designated Ectinosoma (Halectinosoma) sarsi Boeck, 1873 as the type species of the subgenus (Suárez-Morales & Fuentes-Reinés 2015). Lang (1965) lately upgraded it to the genus level without an awareness on Vervoort's (1962) fixation. It is presently accepted that Vervoort's designation of the type species for the genus Halectinosoma is available (Huys 2009). Halectinosoma shows high abundance and diversity in the harpacticoid copepod assemblage from marine sediments (Clément & Moore 2000, 2007). The study of this genus is taxonomically confusing due to insufficient descriptions, lack of type materials, and small differences between species (Clément & Moore 2007, Kihara & Huys 2009). Recently, Halectinosoma was revised by Clément & Moore (1995, 2000, 2007) and the mouthpart features and body ornamentation patterns, which had long been ignored in previous records, are presently regarded as important characteristics to distinguish the Halectinosoma species (Kihara & Huys 2009).

In East Asia, the Halectinosoma species are poorly known despite being one of the largest groups in the family Ectinosomatidae. Known species have been recorded in Japan [H. arenicola (Rouch 1962), H. japonicum (Miura 1964) (but, present in the species inquirendae by Karanovic & Pesce 2001), and H. perforatum Itô, 1981 (Miura 1964, Itô 1973, 1981, Karanovic & Pesce 2001); and Korea [H. perforatum (Kim et al. 2015)]. According to some ecological studies on benthic harpacticoids in this region (Mu et al. 2002, Back et al. 2009), however, many species belonging to this genus are still awaiting description.

During a taxonomic study of harpacticoid copepods along Korean coasts, we collected a new species of Halectinosoma from sandy beaches. In the present study, we describe the new species, and the taxonomic state of H. arenicola sensu Itô, 1973 reported from Japanese coast, which is closely related to the new species, is discussed.

Materials and Methods

Sediment samples were collected from sandy beaches on Korean and Japanese coasts (Fig. 1). Samples were washed over a standard 212 μm sieve and fixed with 5% formaldehyde-seawater solution. Harpacticoid copepods were sorted in the laboratory and preserved in vials with 99.9% ethyl alcohol. Three specimens of the new Halectinosoma species were dissected under a stereo microscope (Discovery, V8; Carl Zeiss, Germany), mounted on slides in lactophenol solution, and sealed with Canada balsam. Drawings were made using a drawing tube mounted on a light microscope (ECLIPSE 80i; Nikon, Japan). Several specimens were prepared for scanning electron microscopy (SEM) study. Prior to SEM each specimen was submitted to ultrasonic cleaner (3 sec; one time; Power sonic 405) to remove attached debris, prefixed with 4% glutaraldehyde, postfixed with 2% OsO4, dehydrated through graded ethanol series (60%, 70%, 80%, 90%, 100%; 30 min per change), air-dried, and sputter coated with gold for 90 sec (OM-SC7620) and examined under the SEM (VEGA 3 LM; Tescan, Czech Rebublic). All materials examined were deposited in Chosun University and the National Institute of Biological Resources (NIBR), Korea.

Fig. 1. 

Localities of the sampling stations of the present study. Korea: St. 1, Baekbawi beach, Yeonggwang-gun; St. 2, Myeongsasipri beach, Wando-gun (type locality); St. 3, Haedanghwa beach, Wando-gun; St. 4, Sangju beach, Namhae-gun; St. 5, Daejin beach, Gosung-gun; St. 6, Hyeopjae beach, Jeju-si. Japan: St. 7, Siki beach, Amakusa.


The terminology used to describe the body and appendages morphology follows Huys & Boxshall (1991). The setal formula of thoracic legs is after that of Huys & Boxshall (1991) and Huys et al. (1996). Abbreviations used in the text are: ae, aesthetasc; exp, exopod; enp, endopod; P1–P6, first to sixth thoracic legs; exp (enp)-1 (2, 3) to denote the proximal (middle, distal) segment of a three-segmented ramus. Abbreviations used in the table are: A1, antennule; A2, antenna; exp, exopod; enp, endopod; L:W, length to width; Md, mandible; P1, first thoracic leg; P4, fourth thoracic leg; P5, fifth leg; seg., segments.

This work has been registered in ZooBank with the registration number LSID-E9B45EBA-D15B-43D2-86D0-C4B2932D2007.


Family Ectinosomatidae Sars, 1903
Genus Halectinosoma Vervoort, 1962
Halectinosoma foveolata, new species
Figs. 210.

  • Synonym. Halectinosoma arenicola (Rouch 1962): Itô, 1973, p. 524, figs. 5–7.

  • Fig. 2. 

    Halectinosoma foveolata, female (paratype, NIBRIV0000326511). A, habitus, dorsal; B, habitus, lateral. Scale bar: 100 μm.


    Fig. 3. 

    Halectinosoma foveolata, female (paratype, NIBRIV0000326511). A, urosome, ventral; B, anal somite, dorsal (right) and ventral (left); C, rostrum; D, antennule; E, antenna; F, P5. Scale bars: 50 μm.


    Fig. 4. 

    Halectinosoma foveolata, female (paratype, NIBRIV0000326511). A, mandible; B, maxillule; C, maxilla; D, distal endite on syncoxa of maxilla; E, middle endite on syncoxa of maxilla; F, proximal endite on syncoxa of maxillar; G, maxilliped. Scale bar: 50 μm. Arrowheads indicate the unique feature on the mandibular gnathobase.


    Fig. 5. 

    Halectinosoma foveolata, female (paratype, NIBRIV0000326511). A, P1; B, P2. Scale bar: 50 μm.


    Fig. 6. 

    Halectinosoma foveolata, female (paratype, NIBRIV0000326511). A, P3; B, P4. Scale bar: 50 μm.


    Fig. 7. 

    Halectinosoma foveolata, male (A–D, paratype, NIBRIV0000326513), female (E, NIBRIV0000470363). A, habitus; B, antennule; C, P5, D, urosomite 2, ventral; E, P5. Scale bars: 50 μm.


    Fig. 8. 

    Scanning electron microscope photographs. Halectinosoma foveolata, female: A, habitus, lateral (rostrum hidden); B, cephalothorax, lateral (rostrum hidden); C, thoracic somites 2-4, lateral; D, P5 bearing-somite and genital double somite, lateral; E, genital double somites, lateral; F, urosomite 4, lateral.


    Fig. 9. 

    Scanning electron microscope photographs. Halectinosoma foveolata, female: A, urosome, dorsal; B, postgenital somites, ventral; C, urosomite 5, anal somite and caudal ramus, lateral; D-F, anal smite and caudal rami, lateral (D), dorsal (E), ventral (F).


    Fig. 10. 

    Scanning electron microscope photographs. Halectinosoma foveolata, female: A, caudal setae; B, surface of cephalosome; C, D, P5. Arrowheads indicate the vestiges of spinules.


    Type locality.—Myeongsasipri beach (34°19′35.87"N, 126°48′34.67"E), Sin-ri, Sinji-myeon, Wando-gun, Jeollanam-do, Korea.

    Type materials examined.—Holotype ♀ (NIBRIV0000326509), allotype ♂ (NIBRIV0000326510), both undissected and preserved in 99.9% ethyl alcohol. Paratypes: 1 ♀ (NIBRIV0000326511) dissected and mounted on nine slides; 1 ♀ (NIBRIV0000326512) dissected and mounted on two slides; 1 ♂ (NIBRIV0000326513) dissected and mounted on three slides; 26♀♀, 11 ♂♂ (NIBRIV0000470359) preserved in 99.9% ethyl alcohol. All specimens were collected from the type locality (St. 2) on 25 Jun 2013 (Fig. 1).

    Additional materials examined.— Korea: 2♀♀ (NIBRIV0000470363, NIBRIV0000470364), Baekbawi beach (St. 1; 35°14′43.20"N, 126°18′18.80"E), Duu-ri, Yeomsan-myeon, Yeonggwang-gun, Jeollanam-do on 20 Apr 2015; 17 ♀♀, 3 ♂♂ (NIBRIV0000470360), Haedanghwa beach (St. 3; 34°19′35.51.07"N, 127°3′31.40"E), Wolsong-ri, Geumil-eup, Wando-gun, Jeollanam-do on 30 Jun 2014; 9 ♀♀, 2 ♂♂ (NIBRIV0000470362), Sangju beach (St. 4; 34°43′14.90"N, 127°59′19.90"E), Sangju-ri, Snagju-myeon, Namhae-gun, Gyeongsangnam-do on 15 Mar 2014; 4 ♀♀, Daejin beach (St. 5 in Fig. 1; 38°30′16.00"N, 128°25′32.90"E), Daejin-ri, Hyeonnea-myeon, Goseong-gun, Gangwon-do on 19 Jul 2016; 8 ♀♀, 2 ♂♂, (NIBRIV0000470361), Hyeopjae beach (St. 6; 33°23′41.05"N, 126°14′25.10"E) , Hyeopjae-ri, Hallim-eup, Jeju-si, Jeju-do on 25 Jun 2014 (Fig. 1). Japan: 1 ♀, 5 ♂♂, Siki beach (St. 7 in Fig. 1; 32°31′15.70"N, 130°01′53.20"E), Amakusa, Kumamoto, Kyushu on 13 Aug 2016 (Fig. 1).

    Description of female.—Based on paratype (NIBRIV0000326511). Body (Figs. 2A, B, 8A) fusiform; total length including tip of rostrum and caudal rami about 798 μm in lateral view (range from 662.4 to 872.8 μm, mean = 752.5 μm, n = 62); surface sculptured with longitudinal furrows (Fig. 10B). Rostrum (Fig. 3C) well-developed, subrectangular in shape, separated from cephalothorax at its base, twice as long as wide, and with 1 pair of lateral sensilla subdistally.

    Prosome (Figs. 2A, B, 8A–D) 4-segmented, comprising cephalothorax and 3 free pedigerous somites. Cephalothorax slightly shorter than 3 succeeding somites combined; surface (Fig. 10B) ornamented with small foveae, with 13 pairs of sensilla. P2-bearing somite with row of fine spinules and 5 pairs of sensilla on surface. P3- and P4-bearing somites with row of fine spinules and 4 pairs of sensilla, respectively. Each surfaces of 3 free pedigerous somites ornamented with small foveae.

    Urosome (Figs. 2A, B, 3A, 8D–F, 9A–C) 5-segmented, comprising P5-bearing, genital double-, and 3 postgenital somites. P5-bearing somite with row of fine spinules and 2 pairs of sensilla on dorsal surface; posterior margin serrate minutely. Genital double-somite (Fig. 3A) subdivided by cuticular suture ventrally and laterally, while fused dorsally; anterior somite with 2 rows of fine spinules and 2 pairs of sensilla on dorsal surface; each posterior somite with rows of dorsal, lateral and ventral fine spinules, and 2 pairs of sensilla on surface; posterior margin of posterior somite serrate minutely. Genital field with copulatory pore medially and vestigial P6 represented by seta. Urosomite 4, dorsal surface with 1 row of fine spinules and 3 sensilla; lateral surface with 2 rows of fine spinules; ventral surface with 2 rows of fine spinules and 1 pair of sensilla. Urosomite 5, dorsal surface with 1 row of fine spinules; lateral surface with 2 rows of fine sinules; ventral surface with 1 row of fine spinues and 1 pair of sensilla. Anal somite (Figs. 3B, 9D–F), dorsal surface deeply cleft medially, with several rows of delicate setules, 1 row of spinules, 2 small pores, and 2 sensillia; ventral surface with pair of large and small pores on each side; lateral surface with small pore; posterior border ornamented with spinules; operculum obscure, with row of delicate setules.

    Caudal rami (Figs. 3B, 9D–F) as long as anal somite in dorsal view, with dorsal and ventral transparent lappets, and furnished with 7 setae: seta I short and stout; seta II short and slender; seta III about 3.6 times of seta I in length and slender; setae IV and V (Fig. 10A) well-developed, each side ornamented with spinules; seta VI stout, shorter than seta III, and furnished with outer setules proximally; seta VII short, slender, and articulated.

    Antennule (Fig. 3D) 6-segmented, short, and slender; segment 1 short; segment 2 shorter than preceding one; segment 3 longest, with 1 peduncle at distal corner; peduncle on segment 3 with aesthetasc; segment 6 incompletely separated from preceding one, with long peduncle-like process bearing long seta and aesthetasc; each aesthetasc fused with seta basally. Setal formula as follows: 1-[1], 2-[10], 3-[7 + ae], 4-[1], 5-[1], 6-[8 + ae].

    Antenna (Fig. 3E): Coxa small. Basis with 1 group of long setules on anterior margin and 1 group of small spinules on inner margin. Exopod 3-segmented; proximal segment elongate, fused to basis, with 1 row of spinules medially; middle segment shortest, with 1 spinulose seta; distal segment longest, with 2 long spinulose setae. Endopod 2-segmented; proximal segment elongate, longer than basis, without ornamentation; distal segment with 2 groups of spinules and 1 row of small spinules on surface, 2 spinulose setae on abexopodal margin, and 6 spinulose and 1 slender plumose setae on distal margin.

    Mandible (Fig. 4A): Gnathobase well-developed, with 5 unicuspid teeth on cutting edge, 3 sclerite protrusions (see arrowheads in Fig. 4A) on dorsal margin, and 2 rows of small spinules on surface; ventrodistal corner with 1 group of spinules. Basis elongate, 3.5 times as long as greatest width, and with 1 row of long setules proximally on lateral margin and 3 setae on distal corner. Exopod 1-segmented, small, with 1 spinulose, 1 plumose, and 1 small naked setae. Endopod 1- segmented, elongate, and with 10 naked and 1 plumose setae; lateral margin ornamented with 1 row of long hairs.

    Maxillule (Fig. 4B): Praecoxal arthrite with 4 stout spinulose claws on distal margin and 2 naked setae on surface. Coxa small, with 1 seta. Basis with 4 spinulose setae distally and subdistally; surface with 2 bare setae. Exopod 1-segmented, small, and with 2 apical plumose setae. Endopod 1-segmented, bilobate; small lobe with 2 setae and large lobe with 4 setae; each seta on lobes fused with neighboring one at its base.

    Maxilla (Fig. 4C): Syncoxa with 3 spinules on outer margin and 2 rows of spinules on surface, and bearing 3 endites (Fig. 4D–F); proximal endite with 1 slender, 1 spinulose, and 2 plumose setae; middle endite slender, with 1 spinulose and 1 bare setae; distal endite with 2 spinulose and 1 plumose setae. Allobasis with 4 bare and 1 spinulose setae, and 1 spinulose spine fused with lateral margin basally; surface with 1 row of long setules. Endopod composed of 3 setae; proximal and middle setae spinulose and geniculated; distal seta divided into 4 small setae.

    Maxilliped (Fig. 4G): Syncoxa small, with 1 long seta. Basis elongate, furnished with setules along each lateral margin. Endopod small, about 3 times as long as greatest width, and with 1 long and 1 short bare setae on apical margin and 1 subdistally and 1 medially inserted spinulose setae on lateral margin.

    P1 (Fig. 5A): Intercoxal sclerite small, without ornamentation. Coxa large, subrectangular, and with 1 row of spinules along distal corner. Basis smaller than coxa, with 1 outer seta and 1 inner spine; outer margin with 1 row of stout spinules; anterior surface with 1 row of stout spinules and 1 row of minute spinules; distal margin behind endopod with hyaline frill. Both rami 3-segmented; each segment ornamented with outer spinules; exp-1 without inner seta; distal margins of exp-1 and exp-2 with hyaline frill; enp-1, anterior margin with 1 row of horizontal spinules, distal margin partially protruded and with hyaline frill; enp-2, posterior surface with several stout spinules, and distal margin with small hyaline frill.

    P2–P4 (Figs. 5B, 6A, B): Intercoxal sclerite larger than that of P1. Coxa subrectangular, with row of spinules along distal corner. Basis smaller than coxa, with 1 row of stout spinules along outer margin and 1 (P4) or 2 (P2 and P3) rows of minute spinules on anterior margin; distal margin midway produced, with small hyaline frill and notch. Both rami 3-segmented; each segment ornamented with outer spinules; distal margins of exp-1 and exp-2 with hyaline frill; enp-1 with 1 row of horizontal spinules on anterior surface; distal margins of enp-1 and enp-2 midway concave, with small hyaline frill; enp-2 except for P4 with several stout spinules on posterior margin.

    Setal formula of P1–P4 as follows:


    P5 (Figs. 3F, 10C, D): Baseoendopod shorter than width, with 2 rows of spinules on anterior surface and 1 plumose outer seta; endopodal lobe reaching to approximately 1/3 of exopod, with 1 row of spinules along inner margin and 2 stout pinnate setae on distal margin; outer seta on distal margin partially fused with endopodal lobe. Exopod slightly longer than wide, fused to baseoendopod anteriorly, with incomplete posterior separation; inner margin ornamented with spinules; distal margin with 3 pinnate setae bearing row of spinules basally; anterior surface with small peduncle bearing 1 seta near outermost distal seta.

    Description of male.—Based on paratype (NIBRIV0000326513). Body (Fig. 7A) smaller than female; total length about 546 μm (range from 502.1 to 623.8 μm, mean = 550.8 μm, n = 18).

    Urosome (Fig. 7A): 6-segmented.

    Antennule (Fig. 7B): 7-segmented, subchirocer. Segment 1 as long as width. Segment 2 smallest. Segment 3 narrower than preceding one. Segment 4 slightly shorter than segment 1, gradually broad towards distal margin. Segment 5 longest, slightly swollen proximally; surface with 1 spine-like process, 1 tube-like seta, 1 row of minute spinules, and 1 aesthetasc. Segment 6 fused with preceding one. Segment 7 elongate, with peduncle bearing aesthetasc fused with seta basally. Setal formula as follows: 1-[1], 2-[1], 3-[8], 4-[3], 5-[6 + ae], 6-[1], 7-[6 + ae].

    P5 (Fig. 7C): Baseoendopod small, with 1 finely bipinnate outer seta; endopodal lobe small, reaching to approximately 1/3 of exopod, and with 2 subequal pinnate setae on distal margin. Exopod separated from baseoendopod, slightly longer than wide, and with 3 terminal and 1 surface setae.

    P6 (Fig. 7D) represented by 1 bare and 1 spinulose stout setae.

    Variability.—Most morphological features are conservative except for the female P5. Ovigerous females lack a row of spinules on the P5 exopod (Fig. 3F), and some ovigerous specimens have small spinules or the vestiges of spinules positioned near the surface seta (arrowhead in Fig. 10D). Among seven populations examined in the present study (Fig. 1), the non-ovigerous form with a distinct spinular row (Fig. 7E) was observed from two specimens collected from Baekbawi beach, Yeonggwang-gun (St. 1). Especially, these two specimens of the non-ovigerous form display additional variability in the detailed characteristics of the female P5 as follows: the outer peduncle has a tube pore (vs. a small pore in the ovigerous form); two spinular rows on the baseoendopod are in a line (vs. two distinguishable rows in the ovigerous form); the boundary between the distal margin of the baseoendopodal lobe and its inner seta is completely separated (vs. partially fused in the ovigerous form); both setae on the baseoendopodal lobe are longer than the length of the baseoendopodal lobe (vs. as long as the baseoendopodal lobe in the ovigerous form); the baseoendopodal lobe has a pore near the outer margin (vs. absent in the ovigerous form).

    Etymology.—The epithet of the specific name, foveolata, is derived from Latin foveola, meaning ‘small pit' or ‘fovea'. This name refers to the foveate ornamentation on the surface of prosome of the new species.


    Lang (1948) proposed the division of Halectinosoma into the sarsi- (where the P3–P4 exp-3 have three outer spines) and curticone-groups (where the P4 exp-3 has two outer spines) on the basis of the number of outer spines on the P1–P4 exp-3. However, Lang (1965) subsequently declared that it was impracticable because of the uncertainty of these characteristics. Later, Clément & Moore (2000) proposed the herdmani-group in the genus based on the body shape, the setal formula of P1–P4, and the structures of the antennule, antennary exopod, mandibular exopod, and maxillipedal syncoxa. Among these three groups, only the herdmani-group is currently acknowledged in the genus, but additional groups could be recognized with further studies as previously observed in the revision for the species related with H. sarsi (Boeck, 1873) (present in the species inquirendae; see Huys 2009) by Clément & Moore (1995).

    Within the genus, H. foveolata sp. nov. is close to the species belonging to the herdmani-group in the following characteristics: (1) the rostrum is elongate; (2) the body surface is sculptured with longitudinal furrows; (3) the female antennule is composed of six segments; (4) the first exopodal segment of antenna has a row of spinules; (5) the outer distal seta on the mandibular exopod is smaller than the other two setae; (6) the maxillipedal syncoxa has only one seta; (7) the surface seta on the P5 exopod clearly extend beyond its distal margin; (8) the setal formula of P1–P4 coincides with those of species belonging to the herdmani-group (Clément & Moore 2000). However, H. foveolata differs from the herdmani-group by the absence of chitinous patches near the posterior margin of the cephalothorax and the first exopodal segment of antenna has no seta.

    Most Halectinosoma species not dealt in the revisions by Clément & Moore (1995, 2000, 2007) have more or less incomplete and inaccurate descriptions. This presently causes a problem in the taxonomy of the genus (Clément & Moore 1995, 2000, 2007, Kihara & Huys 2009, Suárez-Morales & Fuentes-Reinés 2015). Nevertheless, we believe that previous descriptions for antenna, antennary exopod, mandibular gnathobase, setal formula of P1–P4, and female P5 were relatively exact because of their simple structures. The morphological features of these characters in 70 nominal Halectinosoma species (Soyer 1972, Huys & Bodin 1997, Clément & Moore 2000, Karanovic & Pesce 2001, Wells 2007, Huys 2009, Boxshall et al. 2010, Suárez-Morales & Fuentes-Reinés 2015) are provided in Table 1.

    Table 1.—

    Morphological characteristics of Halectinosoma species.


    Table 1.—



    In most Halectinosoma species, the armature formula of the antennary exopod is a typical “1.1.2”, but the seta on the first segment is known to be absent in several species as well as H. foveolata (see Table 1). However, this new species differs from other species by the presence of a row of spinules on the first exopodal segment of antenna. As far as we know, the combination of the absence of seta and the presence of a row of spinules on the proximal segment is first recognizved in H. foveolata. However, we assume that the latter characteristic was possibly unnoticed or overlooked by previous authors before Clément & Moore (1995, 2000, 2007).

    In ectinosomatid copepods, the mandibular gnathobase is armed with a dorsal seta, a character considered to be present in the ground pattern, which is considered an autapomorphy of the family (Seifried 2003, Seifried et al. 2007). Halectinosoma species typically possess one or two dorsal setae on the gnathobase and its cutting edge is composed of a unidentate pars incisiva and a multidentate lacinia. However, this structure of H. foveolata is composed of five chitinous teeth without dorsal seta. This type of mandibular gnathobase is a unique characteristic of the new species among Halectinosoma species except for H. paraspinicauda Bodin, 1979 (see Bodin 1979, fig. 3Md) and H. arenicola sensu Itô, 1973 (see Itô 1973, fig. 6-3). The new species represents another remarkable characteristic in having three protrusions on the mandibular gnathobase dorsally, which has not yet been reported in Halectinosoma species.

    The structure of female P5 has been considered as a useful diagnostic character to distinguish Halectinosoma species (Lang 1965, Clément & Moore 1995, 2000, Wells 2007). The general shape of the female P5 for H. foveolata is similar to those of H. arenicola (Rouch 1962), H. dimorphum Coull, 1970 (in the ovigerous female), H. pterinum Moore, 1974, H. britannicum Clément & Moore, 2000, and H. itoi Clément & Moore, 2000 (Rouch 1962, Coull 1970, Moore 1974, Clément & Moore 2000). However, H. foveolata clearly differs from these five species by the position of the surface seta inserted near the distal margin on the exopod, the presence of spinular rows on the baseoendopod, and the incomplete boundary between the baseoendopod and the exopod. Especially, H. foveolata shows variability in detailed features of the distal setae on the baseoendopodal lobe, the row of spinules on the exopod, and the tube pore on the outer peduncle. This kind of variability has been reported only from H. dimorphum, which represents a difference in the female P5 between ovigerous and non-ovigerous individuals (Coull 1970).

    Taking into account the characteristic features mentioned above with those provided in Table 1, H. foveolata mostly resembles H. dimorphum described from Barbados in sharing the 6-segmented and elongate antennule, the first exopodal segment of antenna without seta, the position of surface seta (inserted distally) on the female P5 exopod, and the setal formula of P1–P4. However, the new species shows clear differences from H. dimorphum by the following characteristics: (1) the third segment of antennule is longest (vs. the fourth segment is longest in H. dimorphum); (2) the first segment exopod of antenna has a row of spinules (vs. with only one seta in H. dimorphum); (3) the cutting edge of mandibular gnathobase is composed of chitinous teeth (vs. a typical cutting edge comprising pars incisiva and lacinia in H. dimorphum); (4) the female P5 has an incomplete boundary (separated in the posterior part only) between the exopod and baseoendopod (vs. completely separated in H. dimorphum); (5) the female P5 baseoendopod has two rows of spinules (vs. absent in H. dimorphum). Furthermore, the new species shows distinct features not known from Halectinosoma species such as the foveate ornamentation on the body surface of the prosome (see Figs. 2A, B, 8B, C) and the presence of three protrusions on the mandibular gnathobase (see Fig. 4A).

    Among Halectinosoma species, H. arenicola have been reported only from Brazilian and Japanese coasts (Rouch 1962, Itô 1973). However, Clément & Moore (2000) suggested that H. arenicola sensu Itô (1973) from Japan might not be conspecific with Brazilian species of the original description on the basis of the discrepancy in the first exopodal segment of antenna. They realized that the morphological characteristics of the body surface and cephalosomic appendages are important characters to distinguish Halectinosoma species through the series of their revisions (Clément & Moore 1995, 2000, 2007). In this respect, H. arenicola was poorly and incompletely described in the original description by Rouch (1962). This author did not describe the habitus, antennary endopod, mandible, and maxillule of this species. Additionally, the structures of other appendages were also described and figured with some errors in the original description of the species. Itô (1973) subsequently reported H. arenicola from Japanese coast although he was aware that the Japanese specimens differ from Brazilian species in the structures of the maxillule and maxilliped, which were not considered to be key characteristics at that time. In modern view of Halectinosoma taxonomy, H. arenicola sensu Itô (1973) clearly differs from H. arenicola in the following features: (1) the female P5 baseoendopod has spinules, but it is naked in H. arenicola; (2) the female P5 exopod is fused to the baseoendopod anteriorly, but they are discrete in H. arenicola; (3) the surface seta on the female P5 exopod is inserted near the distal margin, while it is located near the proximal margin of the exopod in H. arenicola; (4) the first exopodal segment of antenna has only a spinular row without seta, while it has a delicate seta without spinules in H. arenicola; (5) the third exopodal segment of antenna is at least three times of second one in length, but it is about twice in H. arenicola.

    Halectinosoma foveolata is very similar to H. arenicola sensu Itô (1973) reported from Japanese beach, but several minor differences exist between them in the structures of maxillule, maxilla, and body surface. To clarify whether this Korean species is conspecific with H. arenicola sensu Itô (1973), we tried to obtain Itô's (1973) materials. However, Itô's materials of H. arenicola does not exist any longer. So, we collected Japanese materials of H. arenicola sensu Itô (1973) from the beach on Siki, Amakusa in Japan, the sampling station of Itô (1973), and compared them with the Korean specimens of H. foveolata. The result revealed that H. foveolata and Japanese specimens of H. arenicola sensu Itô (1973) are similar in almost aspects including the characteristic features of body surface and cephalosomatic appendages.


    This study was supported by the National Institute of Biological Resources of Korea as part of the ‘Survey of indigenous biological resources of Korea (NIBR NO. 2014-02-001)' and the Korea Institute of Ocean Science and Technology, Republic of Korea (contract no. PE99513).

    Literature Cited


    Akatova, N. 1935. Drei neue Copepoden-Arten aus dem Kaspi See. Zoologischer Anzeiger 111(11–12):319–326. Google Scholar


    Apostolov, A. 2007. Marine harpacticoids (Copepoda, Harpacticoida) of Iceland, 1. Genus Halectinosoma Lang, 1944 and genus Leptocaris T. Scott, 1899. Crustaceana 80(10):1153–1169. Google Scholar


    Back, J., K. Kim, S. Lee, K. Lee, D. J. Lee, J. Chae, & W. Lee. 2009. Meiofauna community from sandy sediments near Taean in the Yellow Sea, Korea. Ocean and Polar Research, 31:119–212. Google Scholar


    Bodin, P. 1968. Copépodes harpacticoïdes des étages bathyal et abyssal du Golfe de Gascogne. Mémoires du Muséum national d'Histoire Naturelle, Paris, Série A, Zoologie 55(1):1–107. Google Scholar


    Bodin, P. 1979. Copépodes harpacticoïdes marins des environs de La Rochelle. 5 – Espèces nouvelles ou incertaines. Vie et Milieu, series A 27(3):311–357. Google Scholar


    Bodin, P., J. Y. Bodiou, & J. Soyer. 1971. Description d'Halectinosoma cooperatum n. sp. (Copepoda Harpacticoida) récoltée sur le littoral Charentais (Atlantique) et sur la côte des Albères (Méditerranée occidentale). Vie et Milieu, series A 22(1):113–120. Google Scholar


    Boeck, A. 1873. Nye Slægter og Arter af Saltvands-Copepoder. Forhandlinger i Videnskabs-Selskabet i Christiania 1872:35–60. Google Scholar


    Borutsky, E. V. 1952. Fauna of USSR, Crustacea, vol. III, no. 4. Freshwater Harpacticoida. Izdaniya Akademia Nauk SSSR, 50, 426 pp. [original in Russian but consulted for this work in the English translation by A. Mercado published in 1964 by the Israel Program for Scientific Translations, Jerusalem]. Google Scholar


    Boxshall, G., T. C. Walter, & R. Huys. 2010. Halectinosoma Vervoort, 1962 in T. C. Walter & G. Boxshall. 2016. World of Copepods database. (last accessed on 5 May 2016) Google Scholar


    Chislenko, L. L. 1967. Garpaktitsidy (Copepoda Harpacticoida) Karelskogo poberezh'ya Belogo morya [Copepoda Harpacticoida of the Karelian coast of the White Sea]. Pp. 48–196 in Gidrobiontov Issledovaniya na Karel'skom poberezh'e Belogo morya.—Issledovaniya Fauny Morei 7. Google Scholar


    Clément, M., & C. G. Moore. 1995. A revision of the genus Halectinosoma (Harpacticoida: Ectinosomatidae): a reappraisal of H. sarsi (Boeck) and related species. Zoological Journal of the Linnean Society 114(3):247–306. Google Scholar


    Clément, M., & C. G. Moore. 2000. A revision of the genus Halectinosoma (Copepoda: Harpacticoida: Ectinosomatidae): the H. herdmani (Scott & Scott) group of species. Zoological Journal of the Linnean Society 128(3):237–267. Google Scholar


    Clément, M., & C. G. Moore. 2007. Towards a revision of the genus Halectinosoma (Copepoda, Harpacticoida, Ectinosomatidae): new species from the North Atlantic and Arctic regions. Zoological Journal of the Linnean Society 149(3):453–475. Google Scholar


    Coull, B. C. 1970. Harpacticoids copepods from Barbados and Jamaica, W. I., with descriptions of two new species. Caribbean Journal of Science 10(3–4):129–135. Google Scholar


    Coull, B. C. 1975. Three new harpacticoid copepods from the North Inlet estuary, Georgetown, South Carolina, U.S.A. Crustaceana 29(2):113–126. Google Scholar


    Huys, R. 2009. Unresolved cases of type fixation, synonymy and homonymy in harpacticoid copepod nomenclature (Crustacea: Copepoda). Zootaxa 2183:1–99. Google Scholar


    Huys, R., & G. A. Boxshall. 1991. Copepod evolution. The Ray Society, London, United Kingdom, 468 pp. Google Scholar


    Huys, R., & P. Bodin. 1997. First record of Acanthocephala in marine copepods. Ophelia 46(3):217–231. Google Scholar


    Huys, R., J. M. Gee, C. G. Moore, & R. Hamond. 1996. Marine and Brackish Water Harpacticoid Copepods, part 1. In R. S. K. Barnes & J. H. Crothers, eds., Synopses of the British Fauna (new series), no. 51. Field Studies Council, Shrewsbury, United Kingdom, 352 pp. Google Scholar


    Itô, T. 1973. Three species of marine harpacticoid copepods from Amakusa, Kyushu. Journal of the Faculty of Science, Hokkaido University, Series 6, Zoology 18(4):516–531. Google Scholar


    Itô, T. 1981. Descriptions and Records of Marine Harpacticoid Copepods from Hokkaido, VIII. Journal of the Faculty of Science, Hokkaido University, Series 6, Zoology 22(4):422–450. Google Scholar


    Karanovic, T., & G. L. Pesce. 2001. A new genus and species of the family Ectinosomatidae (Crustacea: Copepoda: Harpacticoida) from the groundwaters of India. Annales de Limnologie 37(4):281–292. Google Scholar


    Kihara, T., & R. Huys. 2009. A new genus of Ectinosomatidae (Copepoda, Harpacticoida) from sublittoral sediments in Ubatuba, São Paulo State (Brazil), an updated key to genera and notes on Noodtiella Wells, 1965. ZooKeys 17:57–88. Google Scholar


    Kunz, H. 1949. Die sandbewohnenden Copepoden von Helgoland. II. Kieler Meeresforschungen 6:51–58. Google Scholar


    Kim, J. G., T. W. Jung, & S. M. Yoon. 2015. First record of the genus Halectinosoma (Copepoda: Harpacticoida: Ectinosomatidae) with redescription of H. perforatum from Korea. Korean Journal of Environmental Biology 33(2):132–139. Google Scholar


    Lang, K. 1948. Monographie der Harpacticiden. Two volume set. Hakan Ohlssons, Lund, 1682 pp. Google Scholar


    Lang, K. 1965. Copepoda Harpacticoidea from the Californian Pacific Coast. Kungliga Svenska Vetenskapsakademiens Handlingar, 4th series, vol. 10. Almqvist & Wiksell, Stockholm, 560 pp. Google Scholar


    Miura, Y. 1964. Subterranean harpacticoid copepods from a driven well in Japan. Japanese Journal of Zoology 14:133–141. Google Scholar


    Moore, C. G. 1974. A new species of Halectinosoma (Copepoda, Harpacticoida) from the Isle of Man. Journal of Natural History 8(4):469–476. Google Scholar


    Mu, F.-H., P. J. Somerfield, R. M. Warwick, & Z.-N. Zhang. 2002. Large-scale spatial patterns in the community structure of benthic harpacticoid copepods in the Bohai Sea, China. The Raffles Bulletin of Zoology 50(1):17–26. Google Scholar


    Nicholls, A. G. 1939. Marine harpacticoids and cyclopoids from the shores of the St. Lawrence. Naturaliste Canadien 66:241–316. Google Scholar


    Por, F. D. 1964. A study of Levantine and Pontic Harpacticoida (Crustacea, Copepoda). Zoölogische Verhandelingen, Leiden 64:1–128. Google Scholar


    Rouch, R. 1962. Harpacticoides (Crustacés, Copépodes) d'Amérique du Sud. Pp. 237–280 in Delamare Deboutteville, C. & E. Rapoport, eds., Biologie de l'Amérique Australe, vol. 1. Etudes sur la Faune du Sol. Editions Du Centre National De La Recherche Scientifique, Paris, 657 pp. Google Scholar


    Sars, G. O. 1904. Copepoda Harpacticoida. Parts III & IV. Ectinosomidae, Harpacticidae (part). Pp. 29–56, pls. XVII–XXXII in Sars, G. O. 1903–1911. An Account of the Crustacea of Norway, with short descriptions and figures of all the species, vol. 5. Bergen Museum, Bergen, 449 pp. Google Scholar


    Sars, G. O. 1920. Copepoda Supplement. Parts III & IV. Harpacticoida (continued). Pp. 73–92 + pl. XVII–XXXII in Sars, G. O. 1919–1921. An Account of the Crustacea of Norway, with short descriptions and figures of all the species, vol. 7. Bergen Museum, Bergen, 121 pp. Google Scholar


    Scott, T., & A. Scott. 1896. A revision of the British Copepoda belonging to the genera Bradya Boeck, and Ectinosoma, Boeck. Transactions of the Linnean Society of London, 2nd series, Zoology 6(5):419–446. Google Scholar


    Seifried, S. 2003. Phylogeny of Harpacticoida (Copepoda): Revision of ‘Maxillipedasphalea' and Exanechentera. Cuvillier Verlag, Göttingen, 259 pp. Google Scholar


    Seifried, S., C. Plum, & M. Schulz. 2007. A new species of Parabradya Lang, 1944 (Copepoda: Harpacticoida: Ectinosomatidae) from the abyssal plain of the Angola Basin. Zootaxa 1432:1–21. Google Scholar


    Soyer, J. 1972. Contribution a l'étude des Copépodes Harpacticoïdes de Méditerranée occidentale. 6. Le genre Halectinosoma Lang (Ectinosomidae Sars, Olofsson). Vie et Milieu, series A 23(1):101–126. Google Scholar


    Suárez-Morales, E., & J. M. Fuentes-Reinés. 2015. Two new species of ectinosomatid copepods (Harpacticoida: Ectinosomatidae) from the Caribbean coast of Colombia. Revista Mexicana de Biodiversidad 86:14–27. Google Scholar


    Vervoort, W. 1962. Report on some Copepoda collected during the Melanesia Expedition of the Osaka Museum of Natural history. Publications of the Seto Marine Biological Laboratory 10(2):393–470. Google Scholar


    Wells, J. B. J. 1961. Interstitial copepods from the Isles of Scilly. Crustaceana 2(4):262–274. Google Scholar


    Wells, J. B. J. 1967. The littoral Copepoda (Crustacea) of Inhaca Island, Mozambique. Transactions of the Royal Society of Edinburgh 67(7):189–358. Google Scholar


    Wells, J. B. J. 2007. An annotated checklist and keys to the species of Copepoda Harpacticoida (Crustacea). Zootaxa 1568:1–872. Google Scholar


    Wells, J. B. J., G. R. F. Hicks, & B. C. Coull. 1982. Common harpacticoid copepods from New Zealand harbours and estuaries. New Zealand Journal of Zoology 9(2):151–184. Google Scholar
    Jong Guk Kim, Tae Won Jung, and Seong Myeong Yoon "A new species of the genus Halectinosoma (Copepoda, Harpacticoida, Ectinosomatidae) from Korea," Proceedings of the Biological Society of Washington 130(1), 52-74, (19 July 2017).
    Published: 19 July 2017
    East Asia
    new species
    Back to Top