... , 22 . 10.1186/1741-7007-6-22 Carleton , K. L. , Escobar-Camacho , D. , Stieb , S. M. , Cortesi , F. and Marshall , N. J. ( 2020 ). Seeing the rainbow: mechanisms underlying spectral sensitivity in teleost fishes . J. Exp. Biol. 223 , jeb193334 . 10.1242/jeb...

... , F. and Marshall , N. J. ( 2020 ). Seeing the rainbow: mechanisms underlying spectral sensitivity in teleost fishes . J. Exp. Biol. 223 , jeb193334 . 10.1242/jeb.193334 Carlson , B. A. and Bass , A. H. ( 2000 ). Sonic/vocal motor pathways in squirrelfish (Teleostei...

...Günther K. H. Zupanc ABSTRACT Adult neurogenesis, the generation of functional neurons from adult neural stem cells in the central nervous system (CNS), is widespread, and perhaps universal, among vertebrates. This phenomenon is more pronounced in teleost fish than in any other vertebrate taxon...

... nuclear power plant. Relative to the temperature of the surrounding Baltic Sea archipelago, this elevates the average water temperature by ∼5°C (summer) to ∼10°C (winter) ( Huss et al., 2019 ) (see Fig. S1 ). The semi-natural ecosystem in the Biotest enclosure holds several species of teleost fish...

...Fanny de Busserolles; Fabio Cortesi; Lily Fogg; Sara M. Stieb; Martin Luehrmann; N. Justin Marshall ABSTRACT The visual systems of teleost fishes usually match their habitats and lifestyles. Since coral reefs are bright and colourful environments, the visual systems of their diurnal inhabitants...

... deprivation on three behavioural traits – risk taking, exploratory activity and solitariness – as well as the relationships between them, in juvenile sea bass. Behaviour Teleost fish Exploratory activity Sociability Risk taking Behavioural interaction Food availability and accessibility...

... digestive function and metabolic rate during food deprivation, but regain digestive capacity during refeeding, potentially at the cost of decreased swimming performance. Energy budget Metabolic rate Aerobic scope Teleost fish Plasticity Metabolic rate reflects the energetic cost of fueling...

...William S. Marshall; Jason P. Breves; Ellen M. Doohan; Christian K. Tipsmark; Scott P. Kelly; George N. Robertson; Patricia M. Schulte ABSTRACT To provide insight into claudin (Cldn) tight junction (TJ) protein contributions to branchial salt secretion in marine teleost fishes, this study examined...

.... ( 1999 ). Scaling of metabolic rate with body mass and temperature in teleost fish . J. Anim. Ecol.   68 , 893 - 905 . 10.1046/j.1365-2656.1999.00337.x Collins , D. , Woods , A. , Herd , R. , Blake , G. , Fogelman , I. , Wheeler , M. and Swaminathan , R. ( 1998...

... + -permeable paracellular pathway and an increase in conductance of the epithelium. Tight junction CFTR Immunocytochemistry Electrophysiology Fundulus heteroclitus Euryhaline Teleost fish Gill epithelium Ionocyte Chloride cell The mummichog (or common killifish) Fundulus heteroclitus...

... Summary: Muting experiments show that fish sounds are efficient territorial ‘keep-out’ signals, similar to bird song. Batrachoididae Halobatrachus didactylus ‘Keep-out’ signal Muting experiments Sound production Teleost fish Territorial behaviour An individual fish's probability...

.... Competing interests The authors declare no competing financial interests. 3 10 2013 11 11 2013 © 2014. Published by The Company of Biologists Ltd 2014 Foraging Trade-offs Ecophysiology Teleost fish Food deprivation Locomotion Compensatory growth Extended periods...

... 2013 © 2013. Published by The Company of Biologists Ltd 2013 paternal care mate choice male size sound production playback experiments teleost fish Mate choice plays a major role in sexual selection and can influence the genetic structure of a population ( Andersson, 1994...

... and acellular fish bone may perform similarly from a mechanical standpoint, there are previously unappreciated differences in the structure and composition of these bone types. * Author for correspondence ( [email protected] ) 13 2 2012 © 2012. 2012 acellular bone teleost fish...

... ( [email protected] ) 7 4 2010 © 2010. 2010 specific dynamic action SDA heat increment of feeding HIF oxygen consumption rates teleost fish digestion caloric intake feeding respirometry metabolic rate energy expenditure Bluefin tunas ( Thunnus maccoyii, Thunnus...

...,North Haugh, St Andrews, Fife KY16 9ST, UK 29 9 2008 © The Company of Biologists Limited 2008 2008 IGF-I IGF-I receptor IGF binding proteins teleost fish growth skeletal muscle myogenesis rainbow trout coho salmon feeding nutrition The insulin-like growth factor...

... later use. MyoD in the rainbow trout was shown to occur as two paralogues,which was thought to reflect the tetraploidization of the salmonid genome( Rescan and Gauvry, 1996 ). Subsequently two myoD paralogues of lower percentage identity were identified in five Percomorpic teleost fish...

... The Company of Biologists Limited 2006 2006 Na + /H + -exchanger 2 (NHE2) Na + /K + -ATPase V-H + -ATPase acid-base regulation Myoxocephalus octodecemspinosus longhorn sculpin teleost fish Long-term compensation of pH changes due to the breakdown of carbohydrates,fats and proteins...

... Limited 2006 2006 posterior lateral line particle image velocimetry teleost fish Carassius auratus Fishes and aquatic amphibians use the mechanosensory lateral line to detect weak water motions such as those generated by conspecifics, predators or prey( Bleckmann, 1994 ). The smallest...

... and Holmgren,1997 ; Funakoshi et al.,1999 ), suggest that NOS is a highly conserved enzyme amongst vertebrates. Several studies have established the presence of n-type NOS and i-type NOS, but not eNOS, in teleost fish (e.g. Laing et al., 1999 ;Øjan et al., 2000; Cox et al.,2001 ; Jennings, 2004...