Intact antigen uptake in intestinal epithelial cells of marine fish larvae,Evidence of protandry in a subantarctic notothenid, Eleginops maclovinus (Cuv. & Val., 1830) from the Beagle Channel, Argentina,A biotelemetry system recording fish activity,The crystalline ultrastructure of otoliths of the eel (A. anguilla L. 1758),Acoustic measurement of trout distributions in Spada Lake, Washington, using stationary transducers,Constraints on prey size selection by the three‐spined stickleback: energy requirements and the capacity and fullness of the gut,Mitochondrial DNA analysis of Scottish populations of Arctic charr, Salvelinus alpinus (L.),Closure of the micropyle during embryonic development of some pelagic fish eggs,Territoriality and microhabitat selection in two intertidal New Zealand fish,Selection of prey from a seagrass/mangrove environment by golden lined whiting, Sillago analis (Whitley),Ascorbate concentration in fish ontogeny,Effects of sexual maturation, castration, and androgen implants on growth in one‐ and two‐year‐old parr in a Baltic Atlantic salmon (Salmo salar L.) stock,The effects of mass removal on the roach Rutilus rutilus (L.) stock of Lake Vesijärvi estimated with VPA within one season,Effect of hypoxia on in vivo thromboxane and prostacyclin levels in arterial blood of rainbow trout, Oncorhynchus mykiss (Walbaum),Abundant males in populations of a selfing hermaphrodite fish, Rivulus marmoratus, from some Belize cays,Mugil cephalus L.—a first British record and a further 5°N