Dendromonocotyle species (Monogenea: Monocotylidae) are the only monocotylids to parasitize the skin of chondrichthyan hosts. Currently 11 species are recorded from the skin of ray species in the Dasyatidae, Myliobatidae and Urolophidae. There have been increasing reports of Dendromonocotyle outbreaks on rays kept in public aquaria. This paper provides a broad review of Dendromonocotyle that should assist taxonomists and aquarists with species identification and help decisions on potential control methods for Dendromonocotyle infections. The taxonomy and host-specificity of Dendromonocotyle are discussed and a key to current species is provided. We summarise what little is known about the biology of Dendromonocotyle including egg embryonation and hatching, feeding, camouflage and reproduction. The efficacy of freshwater baths, chemical treatments and biological control measures such as the use of cleaner fish for Dendromonocotyle is also discussed. We demonstrate that effective control of Dendromonocotyle on captive rays is hampered by the lack of basic biological data on the life cycle of the parasites. A case history is provided outlining the success of a public aquarium (Underwater World, Mooloolaba, Queensland, Australia) in managing D. pipinna infections on captive Taeniura meyeni without chemical intervention simply by taking measures to reduce host stress.
Two new species of entobdelline (capsalid) monogeneans are described from the skin of Australian dasyatid stingrays, namely Neoentobdella cribbi sp. n., a small parasite from the estuarine stingray, Dasyatis fluviorum Ogilby (Elasmobranchii: Dasyatidae) and Neoentobdella baggioi sp. n., a relatively large parasite from the porcupine ray, Urogymnus asperrimus (Bloch et Schneider) (Elasmobranchii: Dasyatidae). A striking feature of both of these new parasite species is a pad, possibly located within the genital atrium, armed with rows of closely spaced, rod-shaped microsclerites. Both species also possess a muscular papilla in the genital tract and a club-shaped structure near the common genital opening on the left lateral margin of the body. In N. cribbi, the latter feature is large and located anterior to the genital pad and in N. baggioi, it is small and located in a more posterior position. Similar embellishments in the genital area occur in N. natans Kearn et Whittington, 2005 and in N. parvitesticulata Kearn et Whittington, 2005, while other species (e.g. N. garneri Whittington et Kearn, 2009 and N. taiwanensis Whittington et Kearn, 2009) lack these features and differ also in functional aspects of the male copulatory apparatus and the haptor. Separate generic status for these two groupings is indicated, but must await a comparative and comprehensive review of all Neoentobdella spp.