Achorovermis testisinuosus gen. et sp. n. (Digenea: Aporocotylidae) infects the heart of the smalltooth sawfish, Pristis pectinata Latham (Rhinopristiformes: Pristidae), in the eastern Gulf of Mexico. Specimens of the new genus, along with the other blood flukes that infect batoids are similar by having an inverse U-shaped intestine and a curving testis as well as by lacking tegumental spines. The new genus differs from all of the other blood flukes infecting batoids by having an elongate body (>50 × longer than wide), a testis having >100 curves, and an ovary wholly anterior to the uterus. It differs from Ogawaia glaucostegi Cutmore, Cribb et Yong, 2018, the only other blood fluke infecting a rhinopristiform, by having a body that is >50 × (vs <30 ×) longer than wide, a testis that is >75 × (vs <40 ×) longer than wide and has >100 (vs <70) curves, an ovary wholly anterior to (vs lateral and dorsal to) the seminal vesicle, a uterus wholly posterior to (vs overlapping and lateral to both) the testis and ovary, and a sinuous (vs convoluted) uterus. The new species joins a small group of chondrichthyan blood flukes that lack tegumental spines: O. glaucostegi, Orchispirium heterovitellatum Madhavi et Rao, 1970, Myliobaticola richardheardi Bullard et Jensen, 2008, Electrovermis zappum Warren et Bullard, 2019. Blood flukes infecting batoids are further unique by having a curving testis. That is, the blood flukes infecting species within Selachii are morphologically distinct from those infecting species within the Batoidea (excluding Gymnurahemecus bulbosus Warren et Bullard, 2019). Based on the morphological similarity, we suspect that the new species shares a recent common ancestor with O. glaucostegi. The discovery of the new species brings the total number of chondrichthyan blood flukes to 11 species assigned to nine genera., Micah B. Warren, Micah D. Bakenhaster, Rachel M. Scharer, Gregg R. Poulakis and Stephen A. Bullard., and Obsahuje bibliografii
Copepods of the genus Achtheinus Wilson, 1908 (Pandaridae) are parasites of elasmobranchs that attach to their fins, gill slits and around the nostrils. Specimens of Achtheinus pinguis Wilson, 1912 were collected and examined using histology and scanning electron microscopy to determine their way of attachment to the host and the possible effect on the host. They insert their antennae deep into the dermis of the shark's skin, which causes the most damage due to possible tissue compression and/or fibrosis as well as rupture of the connective tissue. Additionally, the presence of the copepod on the skin causes cell erosion of the epidermal cells and thus reduces the number of epidermal layers. The maxillipeds are used to attach to the placoid scales that cover the shark's skin and probably serve to keep the copepod and inserted antennae in position. This is accomplished by the insertion of the placoid scales into the flaccid corpus of the maxillipeds. Observed damage seems to be negligible to the shark apart from the possibility of secondary infection., Susan M. Dippenaar, Anine Jordaan., and Obsahuje bibliografii
In November of 2013, a specimen of Japanese sleeper ray, Narke japonica (Temminck et Schlegel), caught off Nanfang-ao, Taiwan was found to be parasitised by the cestode Anteropora japonica (Yamaguti, 1934). Specimens comprised whole worms and free proglottids, both of varying degrees of maturity. This material allowed for the opportunity to examine in detail the developmental progression of this hyperapolytic lecanicephalidean species with regard to overall size, scolex dimensions, and microthrix pattern. Complete immature worms ranged in size from 2.4 mm to 14 mm. The smallest scoleces were half as wide as larger scoleces and exhibited a much smaller ratio of apical organ width to bothridial width. Proglottids more than quadrupled in length during maturation from terminal attached immature to detached proglottids. In addition, a change in microthrix pattern was observed on the anterior region of the proglottids from immature to gravid proglottids; the anterior region of attached immature proglottids is covered with gladiate to coniform spinitriches with capilliform filitriches only rarely visible, whereas this region in detached proglottids is covered with gladiate to coniform spinitriches and conspicuous capilliform filitriches. This is the first report of A. japonica from outside Japan expanding its distribution south to Taiwan. In addition, a preliminary phylogenetic analysis of the genus is presented that suggests congeners from the same host species are not each other's closest relatives, nor is there an apparent phylogenetic signal for apical organ type or reproductive strategy (apolysis). However, reproductive strategy does seem to be correlated with host group such that euapolytic species parasitise dasyatid stingrays while hyperapolytic species parasitise either torpediniform rays or orectolobiform sharks., Rachel R. Guyer and Kirsten Jensen., and Obsahuje bibliografii
Southern Africa is considered one of the world's 'hotspots' for the diversity of cartilaginous fishes (Chondrichthyes), with currently 204 reported species. Although numerous literature records and treatises on chondrichthyan fishes are available, a paucity of information exists on the biodiversity of their parasites. Chondrichthyan fishes are parasitised by several groups of protozoan and metazoan organisms that live either permanently or temporarily on and within their hosts. Reports of parasites infecting elasmobranchs and holocephalans in South Africa are sparse and information on most parasitic groups is fragmentary or entirely lacking. Parasitic copepods constitute the best-studied group with currently 70 described species (excluding undescribed species or nomina nuda) from chondrichthyans. Given the large number of chondrichthyan species present in southern Africa, it is expected that only a mere fraction of the parasite diversity has been discovered to date and numerous species await discovery and description. This review summarises information on all groups of parasites of chondrichthyan hosts and demonstrates the current knowledge of chondrichthyan parasites in South Africa. Checklists are provided displaying the host-parasite and parasite-host data known to date., Bjoern C. Schaeffner, Nico J. Smit., and Obsahuje bibliografii