Transversotrema damsella,

Hunter, Janet A. & Cribb, Thomas H., 2012, A cryptic complex of species related to Transversotrema licinum Manter, 1970 from fishes of the Indo-West Pacific, including descriptions of ten new species of Transversotrema Witenberg, 1944 , Zootaxa 3176, pp. 1-44: 27-28

publication ID

http://doi.org/ 10.5281/zenodo.211252

publication LSID

lsid:zoobank.org:pub:F02B2600-61D3-4024-AB7C-4ECDF6E2489A

persistent identifier

http://treatment.plazi.org/id/74747F77-2262-FF95-FF44-FB0F15E7FF6A

treatment provided by

Plazi

scientific name

Transversotrema damsella
status

 

Transversotrema damsella  n. sp

( Fig. 8View FIGURE 8)

Type-host: Abudefduf bengalensis (Bloch)  ( Pomacentridae  ), Bengal Sergeant

Type-locality: Lizard Island, northern GBR, Queensland, Australia, (14 ° 40 ’S 145 ° 28 ’E)

Other hosts: Pomacentridae  : Abudefduf septemfasciatus (Cuvier)  , banded sergeant; Abudefduf sexfasciatus (Lacepède)  , Scissortail Sergeant; Amblyglyphidodon curacao (Bloch)  , Staghorn damselfish; Pomacentrus moluccensis Bleeker Lemon  damsel. Labridae  : Thalassoma hardwicke (Bennett)  , Six-bar Wrasse. Mugilidae  : Crenemugil crenilabis (Forsskål), Fringelip  mullet.

Site: Beneath the scales

Material examined: Table 3 & 4. Neither Thalassoma hardwicke  nor Pomacentrus moluccensis  appear in the table because these specimens were given to us by Dr. G. Muñoz without associated prevalence data.

Molecular sequence data: ITS 2 rDNA

GenBank accession numbers: Table 2

Deposited specimens: Holotype QMG 231854 (ex A. sexfasciatus  LI coll. Cribb et al. 4 Apr 2006) and paratypes QMG 231855 (ex A. sexfasciatus  LI coll. Cribb et al. 4 Apr 2006), QMG 231856 (ex A. septemfasciatus  LI coll. Cribb et al. 4 Apr 2006), QMG 231857 (ex A. bengalensis  LI coll. Cribb et al. Jun 2007), QMG 231858 (ex A. bengalensis  LI coll. Cribb et al. Jun 2007).

Etymology: As the common name for pomacentrids is damsel fish the species name damsella  was chosen for this species.

Description: Based on measurements of 6 specimens from pomacentrids from Lizard Island. Body D-shaped, strongly dorsoventrally flattened, 685–964 (808) long, 1503–2410 (2001) wide; average width/length range 2.5: 1. Pharynx to anterior margin 203–375 (266); cyclocoel to posterior margin 107–141 (116). Tegumental spines prominent. Eyespots prominent 193–244 (214) apart, 9.7–12.8 (11.75 %) of body width; no pigment evident other than in eyespots. Ventral sucker well posterior to eyespots, 3,022–6,878 (4,512) μm 2. Mouth mid-ventral, inconspicuous. Pharynx slightly posterior to eyespots, 84–101 (93.7) long, 48–65 (53.25) wide. Oesophagus curved 79–236 (131). Caecal bifurcation dorsal to ventral sucker. Caeca-form cyclocoel reaching laterally to envelop testes, ovary and some vitelline follicles. Testes opposite, deeply lobed, left, 10,222–14,084 (12,444) μm 2; right 10,863–13,653 (12,118) μm 2. Seminal vesicle formed of lobed, saccular enclosed portion and winding, tubular extracaecal portion. Enclosed portion distinctly lobed or entire, antero-dextral to right of testis, constricts distally to form narrow duct that passes ventral to cyclocoel to join tubular portion. Tubular portion of seminal vesicle passes mediad along cyclocoel then turns anteriorly and passes between eyespots dextral to pharynx and passes to common genital pore where it unites with uterus without any specialisation. Common genital pore precisely in midline on anterior margin of worm. Ovary sinistral to left testis, prominent extended lobes, 9,051–18,342 (14,204) μm 2, an average of 28.4 % larger than testes. Oviduct passes medio-posteriorly, unites with Laurer’s canal and duct from oviduct passes vitelline reservoir, Laurer’s canal then passes posteriorly to open dorsally close to left testis; median portion dilated, contains sperm or vitelline remnants. Vitelline reservoir immediately anterior to left testis. Extracaecal vitelline follicles large, confluent, lateral and posterior to cyclocoel, loosely assembled anterior to cyclocoel from midway between excretory vesicle and lateral margins and extending to anterior margin. Enclosed follicles (av. 55) in two loosely assembled masses at each lateral extremity scattered posteriorly to testes along inner margins of cyclocoel. Uterus passes medially between anterior half of cyclocoel and testes then between right testis and saccular portion of seminal vesicle. Proximal portions of uterus act as seminal receptacle. Eggs tanned, 65–110 (85.3) long and 36–75 (49) wide, average number in utero 15. Excretory bladder opens posteriorly at small notch in middle of posterior margin, extends anteriorly in initially narrow tube which then expands into large sac which passes ventral to cyclocoel anterior to which it becomes laterally directed.

Remarks: Transversotrema damsella  n. sp. is the most distinctive species from this complex. The body is Dshaped rather than crescent - shaped as in T. licinum  and body proportions are different. T. damsella  n. sp. has an ovary which is larger than the testes and this distinguishes it from all other species in the complex. The oesophagus is also much longer than those found in T. licinum  , T. atkinsoni  n. sp., T. borboleta  n. sp. and T. carmenae  n. sp. The vitelline follicles are large, scattered randomly to the lateral margins and in the anterior margin to approximately half way from the lateral margins to the genital pore. The enclosed follicles are also large and numerous and scattered posterior to the testes along the posterior edge of the cyclocoel. The small testes and large ovary, combined with the distribution of the follicles, both external to and enclosed by the cyclocoel, separates this species from all others. Although we have two clear specimens of this species from the labrid Thalassoma hardwicke  donated by G. Munoz, we found no specimens of this species ourselves from examination of 73 labrids at Lizard Island. These fishes did not include T. hardwicke  but eight individuals of two other species of Thalassoma  were not infected.