Hatschekia longiabdominalis Uyeno & Nagasawa, 2013

Soler-Jimenez, Lilia C., Morales-Serna, F. Neptali, Aguirre-Macedo, Ma. Leopoldina, McLaughlin, John P., Jaramillo, Alejandra G., Shaw, Jenny C., James, Anna K., Hechinger, Ryan F., Kuris, Armand M., Lafferty, Kevin D. & Vidal-Martinez, Victor M., 2019, Parasitic copepods (Crustacea, Hexanauplia) on fishes from the lagoon flats of Palmyra Atoll, Central Pacific, ZooKeys 833, pp. 85-106 : 85

publication ID

https://dx.doi.org/10.3897/zookeys.833.30835

publication LSID

lsid:zoobank.org:pub:6F31349B-BF7D-434D-8C06-4128FDD76A56

persistent identifier

https://treatment.plazi.org/id/CC1B8A68-CECE-59A6-5171-7CF76CF9F4F6

treatment provided by

ZooKeys by Pensoft

scientific name

Hatschekia longiabdominalis Uyeno & Nagasawa, 2013
status

 

Hatschekia longiabdominalis Uyeno & Nagasawa, 2013 View in CoL

Type host.

Arothron hispidus ( Tetraodontidae ).

Other host and localities.

Arothron hispidus ( Tetraodontidae ) from Japan ( Uyeno and Nagasawa 2013). To date, H. longiabdominalis has not been recorded from others host and locality.

Current host.

Arothron hispidus ( Tetraodontidae ).

Site of infection.

Gills.

Prevalence and mean intensity.

53.3 and 100 ± 329.2 (n = 15).

Specimens deposited.

CHCM No. 576 (voucher) (1 vial, 1 specimen ♀). USNM

No. 1550605 (voucher) (1 vial, 1 specimen ♀).

Remarks.

Of the nine genera included in the Hatschekiidae , the most speciose genus is Hatschekia , with approximately 140 valid species so far. According to Uyeno and Nagasawa (2013), H. longiabdominalis may be separated from other congeners by having a fusiform trunk with posterior lobes, the urosome markedly projecting beyond posterior lobes of the trunk, and unique intercoxal sclerites of legs 1 and 2, which strongly project from the middle of the anterior margin and bear four blunt processes on the posterior margin. We observed all of these characters in our specimens.