Bryocyclops maholarnensis, Watiroyram & Brancelj & Sanoamuang, 2015
publication ID |
https://doi.org/ 10.5281/zenodo.5385497 |
publication LSID |
lsid:zoobank.org:pub:D3C1BD2A-1A08-4AFA-A649-706FD0DEBCC0 |
persistent identifier |
https://treatment.plazi.org/id/B2EA4D88-040A-4AF7-8B5B-AD43EE465674 |
taxon LSID |
lsid:zoobank.org:act:B2EA4D88-040A-4AF7-8B5B-AD43EE465674 |
treatment provided by |
Valdenar |
scientific name |
Bryocyclops maholarnensis |
status |
sp. nov. |
Bryocyclops maholarnensis , new species
( Figs. 2–6 View Fig View Fig View Fig View Fig View Fig )
Type locality. It is located in Wat Tham Maholarn (Wat = temple, Tham = cave, Maholarn = local name of the cave) in Nonghin District , Loei Province, northeastern Thailand. The coordinates of the entrance are: 17°06’23.04” N, 101°52’48.54” E; altitude 315 m a.s.l. ( Fig. 1 View Fig ). The cave is about 220 m long, with several pools filled exclusively with dripping water. A pool on a stalagmite at the entrance zone filled exclusively with water dripping from the ceiling was selected as the locality type. It is in a semi-illuminated zone. The water temperature during sampling was 23.0°C, pH 8.1, and conductivity 405 μS cm−1 GoogleMaps .
Material examined. Holotype: an adult female was dissected and mounted on a slide in glycerol and sealed with nail polish, NHMUK 2015.2782 About NHMUK , coll. S. Watiroyram, 21 August 2014 . Allotype: an adult male was dissected and mounted on a slide in glycerol and sealed with nail polish, NHMUK 2015.2783 About NHMUK , coll. S. Watiroyram, 21 August 2014 . Paratypes: four females and three males were stored in 70 % alcohol, NHMUK 2015.2784 About NHMUK – 2790 About NHMUK ; two females and two males were stored in 70 % alcohol, NPU 2015.001, all specimens were collected at the same place and on the same date as the holotype.
Additional material: 10 females and five males were stored in 70% alcohol, NPU 2015.002, Phra cave, Chiang Kan District , Loei Province, 17°43’38.22” N, 101°45’53.34” E GoogleMaps ; 10 females and five males were stored in 70% alcohol, NPU 2015.003, Erawan cave, Nawang District , Nong Bua Lamphu Province, 17°20’54.74” N, 102°01’05.59” E GoogleMaps ; five females and two males were stored in 70% alcohol, NPU 2015.004, Phar Kham cave, Na Duang District , Loei Province, 17°06’23.04” N, 101°52’48.54” E GoogleMaps . All specimens were collected between October 2013 and August 2014, coll. S. Watiroyram.
Description. Female ( Figs. 2–4 View Fig View Fig View Fig ): body length: 410–480 μm (mean: 430 μm; n = 10), color of preserved specimens colorless. Cephalosome wider than rest of body, compressed dorsoventrally ( Fig. 2A View Fig ). Naupliar eye not discernible. Cephalosome (incl. rostrum), pedigers 2–5, genital double-somite, urosomites and anal somite (incl. anal operculum) covered with fine refractile points. Posterior dorsal margins of cephalosome, pedigers 2–5, genital doublesomite and urosomite with smooth hyaline frills. Genital double-somite ( Fig. 2B–D View Fig ) symmetrical, with a slightly expanded anterior part, about 1.4× as wide as long; with a pair of dorsal sclerotised and rounded structures accompanied by three minute spinules of P6 on inner margin; copulatory pore ventrally, single, large, circular, situated at 1/2 of genital segment; copulatory duct narrow, sclerotised. Anal somite ( Fig. 2B, C View Fig ) with a transverse row of spinules along the posterior margin on the ventral surface. Base of anal operculum with small sensillum at each side.
Anal operculum ( Fig. 2A, B, D View Fig ) prominent, semi-circular, irregularly serrated along the distal margin; well overreaching distal margin of anal somite. Caudal rami ( Fig. 2B, C View Fig ) asymmetrically conical, about 1.3× as long as wide, with dorsal longitudinal keel. Lateral seta (II) bare, slightly shorter than the caudal ramus, inserted at 1/2 of its length. Dorsal seta (VII) pinnate, about 2× as long as the caudal ramus, inserted at distal inner margin of the caudal ramus. Outermost terminal seta (III) bipinnate, slightly shorter than dorsal seta, with spinules at insertion point on the ventral side. Outer terminal seta (IV) bipinnate, about 4× as long as the caudal ramus; with fracture plane. Inner terminal seta (V) bipinnate, approximately 6× as long as the caudal ramus, with fracture plane. Innermost terminal seta (VI) bare; very short, spiniform.
Rostrum ( Fig. 3A View Fig ) fused to cephalosome, as long as wide in frontal view, rounded anteriorly.
Antennule ( Fig. 3B View Fig ) were relatively short, 11-segmented, not reaching the posterior margin of the cephalosome; with refractile points on the external surface (as on somites). Setal formula as follows: 6.2.5.2.0.2.3.1+A.2.1+A.7+A.
Antenna ( Fig. 3C View Fig ) 4-segmented, comprising coxobasis and three-segmented Endp. Exp absent. Coxobasis with bare seta on distal inner margin. Endp-1 with row of spinules on outer margin; seta on the inner margin at 2/3 of its length. Endp-2 with five smooth setae on the outer distal margin (one laterally and four terminally); row of spinules on the outer margin. Endp-3 with seven terminal setae.
Mandible ( Fig. 3D View Fig ) was short, robust, with six strongly chitinised teeth on gnathobase; short, smooth dorsal seta. Mandibular palp were reduced and represented by one bare seta.
Maxillule ( Fig. 3E View Fig ) with robust praecoxa, coxobasis and onesegmented Endp. Praecoxal arthrite with two strong apical spines fused to arthrite base; with six armature elements along inner margin, proximally one pinnate, others smooth. Coxobasis with three setae distally: one pinnate and two bare. Exp represented by one and Endp with three smooth setae.
Maxilla ( Fig. 3F View Fig ) five-segmented, with praecoxa, coxa, basis, and two-segmented Endp. Praecoxal endite with two spiniform setae. Proximal coxal endite with smooth seta; distal coxal endite with two setae, one smooth and one spiniform. Basis with two claw-shaped expansions; smooth seta at the base of distal claw. Endp-1 with smooth seta. Endp-2 with one spiniform and two smooth setae.
Maxilliped ( Fig. 3G View Fig ) four-segmented, composed of syncoxa, basis and two-segmented Endp. Syncoxa and basis with a row of spinules. Syncoxa with one spiniform and one smooth seta. Basis with spiniform seta. Endp-1 with spiniform seta, Endp-2 with two smooth setae.
P1 ( Fig. 4A View Fig ) two-segmented Exp and two-segmented Endp. Endp shorter than Exp. Intercoxal sclerite with acute projections on distal margin. Coxa without inner seta; with row of spinules and pointed process on outer margin. Basis with bare, slender outer seta and robust inner spine with a cluster of spinules at insertion point; setules on inner distal corner. Exp-1 with outer spine. Exp-2 twice as long as wide, with two spines on outer margin; spine and two apical setae; blunt seta and two normal setae along inner margin. Endp- 1 with seta on inner margin. Endp-2 with apical seta and spine; additional seta on outer margin.
P2 ( Fig. 4B View Fig ) coxa, basis and intercoxal sclerite similar to P1, but basis without inner spine. Exp-1 with outer spine. Exp-2 with two outer lateral spines, apical spine and seta, two inner blunt setae and two normal setae. Endp-1 with inner seta. Endp-2 with inner seta, apical seta and spine; additional seta on the outer margin.
P3 ( Fig. 4C View Fig ) coxa without inner seta, basis with slender outer seta. Intercoxal sclerite with acute projections on the distal margin. Exp similar to those in P2. Endp-1 with inner seta. Endp-2 with apical seta and spine.
P4 ( Fig. 4D View Fig ) coxa without inner seta; basis with slender outer seta. Intercoxal sclerite with acute projections on distal margin. Two-segmented Exp; Exp-1 with outer spine. Exp- 2 with two outer spines, short apical spine and long seta; three normal setae along inner margin. Endp reduced to stout segment; ancestral division between endopodal segments indicated by transverse ridge; with two pinnate setae: inner and apical ones.
P5 ( Figs. 2D View Fig , 3H View Fig ) completely fused to fifth thoracic somite; with three slender setae. Proximal segment represented by longest seta on prominence. Distal segment with two setae; inner seta longer than outer one.
P6 ( Fig. 2D View Fig ) reduced, fused, forming simple cuticular plate; inserted laterodorsally on genital double-somite, with two minute spines and short seta, increasing in length ventrally.
Adult females with a pair of egg sacs, each with two large eggs.
Male ( Figs. 5 View Fig , 6 View Fig ): slightly smaller than female; body length, excluding caudal setae, 380–460 μm (mean: 410 μm; n = 10). Body shape similar to female, except in genital section ( Fig. 5A View Fig ). Antenna, mouthparts, P1 ( Fig. 6A View Fig ), P2 ( Fig. 6B View Fig ), P3–P4 exopods ( Fig. 6C, D View Fig ) similar to those in female. Anal operculum ( Fig. 5C, D View Fig ) slightly longer than in female. Caudal rami similar to female.
Antennule ( Fig. 5E View Fig ) 15-segments. Setal formula as follows: 7+2A.4.2.2+A.1.3.2.1+A.3.1.1.1+A.0.1.8+A. Seta on segment 11 stout. All setae smooth.
P3 ( Fig. 6C View Fig ) Endp 2-segmented; proximal segment smaller than apical one. Endp-1 with inner seta. Endp-2 with apical spine and seta, equal in length; outer lateral seta slightly shorter than apical one.
P4 ( Fig. 6D View Fig ) Endp two-segmented; proximal segment as long as wide. Endp-1 with inner seta. Endp-2 small, as long as wide, with two apical setae; inner seta about twice as long as outer seta.
P5 ( Fig. 5D View Fig ) as in female.
P6 ( Fig. 5B, D View Fig ) reduced to simple plate, represented by three plumose setae, sub-equal in length.
Variability. P4 Endp-2 of male with one distal seta in two specimens; two setae in 13 specimens.
Etymology. The new species is named after Maholarn cave, the place where it was first found. The name is an adjective having gender agreement (feminine) with the generic name.
Differential diagnosis and remarks. Bryocyclops maholarnensis , new species, is characteristic in 1) the P5 that is equipped with three setae and fused to the fifth thoracic somite, and 2) an intercoxal plate on the P4 has acute protuberances. These condition clearly indicates that the new species is a member of the genus Bryocyclops Kiefer, 1927 , s. str. Among six species groups proposed by Lindberg (1954), the new species is similar to members of the Group II in their sexual dimorphism occurring on P3 Endp-2 and P4 Endp-2, P1 basis with an inner spine, intercoxal plate of P1– P4 with an acute protuberances, the setal and spine formula of P1–P4 Exp-2 (5.5.5.4. and 3.3.3.3, respectively), and an articulation pattern on P4. Group II includes five species: B. muscicola ( Menzel, 1926) , B. bogoriensis ( Menzel, 1926) , B. fidjiensis Lindberg, 1954 , B. caroli Bjornberg, 1985 and B. campaneri Rocha & Bjornberg, 1987 . The new species, however, does not fit into Group II completely, as it differs in the absence of a modified spine on P3 Endp-2 of male (present in Group II, but not confirmed in B. fidjiensis ), the absence of inner seta from P1 coxa (present in Group II), and the number of setae on distal Endp P4 is reduced to two (three and four setae plus one spine in males and females, respectively, except B. fidjiensis which has three setae in females) ( Table 2). Since B. maholarnensis differs significantly from the members of Group II as well as the other five groups proposed by Lindberg (1954), a new group (Group VII) is proposed here. Groups II and VII are, according to observed characters, an intermediate group in terms of evolution toward oligomerization, as they show reductions in armature elements on the swimming legs and number of segment of Endp in females. Group I, with plesiomorphic characteristics by having two-segmented Exp and Endp in both sexes and the primitively spine and seta formula of Exp-2, can be assumed the most primitive group ( Huys & Boxshall, 1991). The new species shows the highest reduction in setation on P4 Endp in both sexes ( Table 1), thus formation of a new group is justified.
The new species closely resembles B. muscicola in the following combination of morphological characteristics: (a) identical segmentation of swimming legs; two-segmented Endp of P1–P 3 in both sexes but one-segmented Endp of P 4 in females and two segmented in males; (b) identical armature of allobasis, Endp-2 and 3 of antenna; there are one, five and seven setae, respectively on those segments; (c) the absence of inner seta on bases of swimming legs P2–P4; (d) identical setal and spine formula of P1–P4 Exp-2; 5.5.5.4 and 3.3.3.3, respectively; and (e) serrated free margin of anal operculum. The new species, however, differs from B. muscicola in the following characteristics: (a) the absence of inner seta on coxa of P 1 in the new species; (b) the number of setae on P1 and P3 Endp-2; the female of the new species has two and one seta, respectively, but there are three and five setae in B. muscicola ; P3 Endp- 2 in the male of the new species has two setae, but there are four in B. muscicola ; (c) the armature on distal Endp P4; the new species has two setae in both sexes, but B. muscicola has four and three setae plus one spine in females and males, respectively; and (d) the length of anal operculum and innermost seta (VI) is shorter in the new species compared to those in B. muscicola .
The new species also differs from B. bogoriensis , another closely related species, in the following characteristics: a) the female of new species has the setal formula on P1–P4 Endp-2, as 2.3.1.2 but it is 3.5. 5.4 in B. bogoriensis ; b) the anal operculum of the new species is well below the distance of half of the caudal rami length but its tip only reaches the middle of the caudal rami length in B. bogoriensis ; c) the new species has a very short innermost seta (VI) whereas B. bogoriensis has one that is much longer ( Table 2).
There are also differentiating features between the new species and B. campaneri , another member of Group II. The setation on allobasis and Endp-2 and 3 of antenna in the new species is one, five and seven setae, whereas B. campaneri has one, five and six setae, in the original paper, or two, six and six setae in Reid (1999). Coxa of P1 of the new species is without inner seta which is present in B. campaneri . Setal and the spine formula on terminal segments of P1–P4 Endp in the new species is 2.3.1.2 and 1.1.1.0, respectively, whereas 3.3.5.4 and 1.1. 1.1 in B. campaneri . The setal formula on P1–P4 Exp- 2 in the new species is also different from B. campaneri : 5.5. 5.4 in the new species, whereas 4.5. 5.4 in B. campaneri . The new species has the shortest anal operculum and innermost seta on the caudal rami compared to species within Group II, whereas B. campaneri has the longest anal operculum which extends beyond the tip of the caudal rami and it also has a relatively long innermost seta ( Table 2).
The new species, can be distinguished from B. fidjiensis by the articulation pattern on P4: the female of the new species has two-segmented Exp and one-segmented Endp, but there are one-segmented Exp and one/two-segmented Endp in B. fidjiensis . The new species has no inner coxal seta on P1–P3 but they are present in B. fidjiensis . Setal and spine formula on P1–P4 Endp- 2 in the new species are different from those in B. fidjiensis Lindberg, 1954 : 3.4.3.3 and 1.1.1.1. The anal operculum of the new species is serrated and semi-circle shaped but smooth and triangular in B. fidjiensis . The new species has shorter innermost seta (VI) compared to that in B. fidjiensis Lindberg, 1954 ( Table 2).
Additionally, the new species differs from B. caroli in following characteristics: the number of setae on the allobasis, Endp-2 and Endp-3 of antenna (one, five and seven setae, respectively in the new species but there are one, four and six setae in B. caroli Bjornberg, 1985 ); the new species has no inner coxal seta on P1 but it is present in B. caroli . Setal and spine formula on P1–P4 Endp- 2 in the new species is 2.3.1.2 and 1.1.1.0, respectively, whereas in it is 3.3.5.4 and 1.1. 1.1 in B. caroli . The new species has a smaller anal operculum and innermost seta on the caudal rami than those of B. caroli ( Table 2).
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