Gill morphology during hypercapnia in brown bullhead (Ictalurus nebulosus): role of chloride cells and pavement cells in acid‐base regulation,Time of start of spawning in Atlantic cod (Gadus morhua) females in relation to vitellogenic oocyte diameter, temperature, fish length and condition,Taxonomy, biology and abundance of icefishes, or noodlefishes (Salangidae), in the Yellow River estuary of the Bohai Sea, China,Abundance, reproductive period, and feeding habits of eleotrid fishes in estuarine habitats of north‐east Brazil,Effects of salinity on distribution, growth and survival of three neotropical armoured catfishes (Siluriformes—Callichthyidae),The fate of a roach Rutilus rutilus stock under an extremely strong fishing pressure and its predicted development after the cessation of mass removal,Vertical segregation and seasonal changes in fish depth distributions between lakes of contrasting trophic status,Proteinase inhibitor(s) in seminal plasma of teleost fish,A comparison of the movements of two species of gadoid in the vicinity of an underwater reef,Breeding ecology and nest aggregations in a population of Salaria pavo (Pisces: Blenniidae) in an area where nest sites are very scarce,Genetic variation among Atlantic salmon in six Spanish rivers,Non‐specific cellular responses of rainbow trout to Vibrio anguillarum and its extracellular products (ECPs),The analysis of metabolites in rainbow trout white muscle: a comparison of different sampling and processing methods,Factors affecting the distribution of genetic variability in the guppy, Poecilia reticulata,The growth of grey mullet in a rural and urbanized Irish estuary, Occurrence of Atlantic salmon parr in redds at spawning time, A study on teleost phylogeny using specific antisera,Field observations on a mating attempt of a spawning grayling, Thymallus thymallus with a feeding barbel, Barbus barbus