A new deep water catshark species Apnstui us exsanguis , is described based on twenty‐nine specimens collected from the waters around New Zealand It has strong similarities with Apristurus sp B (Paulin et al, 1989) fiom New Zealand Apristurus sp A (Last & Stevens 1994) from Australia and Apristurus japonicus Nakaya, 1975, from Japan, but oan be separated from species ‘A and B by colouration, relative dorsal fin sizes and position, and spiral valve count, and from A japonicus by counts of spiral valves, tooth rows and monospondylus vertebrae
1 December 2001 in New Zealand Journal of Marine and Freshwater Research
Commercial tuna longline fishing targeting bigeye tuna, Thunnus obesus (Lowe 1839), on the Three Kings Rise, northern New Zealand, resulted in the bycatch of a single specimen of a mature male crocodile shark, Pseudocarcharias kamoharai (Matsubara 1936). This is the first record for the New Zealand Exclusive Economic Zone, and a major southern range extension of the species in the Indo‐Pacific.
The genus Dichichthys was resurrected for five species previously allocated to the genus Parmaturus in the family Pentanchidae. Supraorbital crests on the chondrocranium distinguish Dichichthys from Parmaturus and other members of the family Pentanchidae. A new family, Dichichthyidae, has been proposed to contain Dichichthys. The sequence of the NADH2 mitochondrial gene confirms the placement of Dichichthys outside of the Pentanchidae family, as well as separate from the Atelomycteridae and Scyliorhinidae families. Dichichthys albimarginatus was described using a holotype collected off the coast of New Caledonia. A second juvenile specimen collected off the coast of Papua New Guinea was tentatively assigned as D. cf. albimarginatus. Dichichthys bigus is known from the holotype collected in the Coral Sea off the coast of Queensland, Australia. A new, parasite-afflicted underwater observation was reported further north of Queensland. The type species Dichichthys melanobranchus, previously only known from juvenile specimens, was redescribed based on adult specimens. Dichichthys nigripalatum is known from the holotype collected off Sumbawa, Indonesia, and a tentatively identified photo record from West Java. Dichichthys satoi n. sp. is described from the West Norfolk Ridge and off the North Island of New Zealand. Members of the genus Dichichthys have unique curved egg cases which have pliable ridges made up of numerous fibres and long coiled tendrils on the posterior end.
A single specimen of a new Bathyraja skate was collected by the authors in 2003 during a survey of the deepwater biota of the northern Tasman Sea by the New Zealand FRV Tangaroa. This skate, labelled the ‘blonde skate’ by voyage participants, is uniformly white on all surfaces of the body and the skin is partly translucent. It belongs to a subgroup of Bathyraja with a large, almost smooth, quadrangular disc and well-developed and equally spaced median tail thorns. Other similar and probably closely related Bathyraja specimens have been caught in seas to the south of New Zealand since the discovery of this species, but their identity is yet to be confirmed.
The high intraspecific variation among and the conservative external morphology of Merluccius spp. have resulted in serious identification difficulties. Four hundred and twenty fresh and preserved specimens of Merluccius were analyzed, including the type series of Merluccius australis, M. tasmanicus and M. hubbsi; specimens of M. hubbsi from Argentina, Brazil and Uruguay, and individuals of M. australis from Argentina and New Zealand were examined. The nomenclatural status of the type specimens of M. australis is discussed and the designation of a lectotype and a paralectotype is proposed. The comparative study of morphology, meristic, traditional and landmark-based morphometry, both external and internal, and through DNA-based Barcoding molecular tools demonstrates that Merluccius tasmanicus is a junior synonym of Merluccius australis. Meristic and morphometric characters of types of M. tasmanicus completely overlap those of M. australis, whereas M. hubbsi show fewer scales along the lateral line, total vertebrae, second dorsal and anal-fin rays. A trend of a longer snout and wider head in M. australis and M. tasmanicus, and larger eyes and longer pelvic fins, in M. hubbsi was observed. While discriminant characters were found in the internal elements (hyomandibula, urohyal and sagitta otolith) between M. hubbsi and M. australis, none were observed between M. australis and those reported for M. tasmanicus. DNA barcoding analyses found no evidence of the existence of other species of Merluccius besides M. hubbsi and M. australis.