FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1996765330> ?p ?o ?g. }

• W1996765330 endingPage "972" @default.
• W1996765330 startingPage "958" @default.
• W1996765330 abstract "Nitrogen excretion by the gulf toadfish (Opsanus beta) is of interest because of its high proportion of urea excretion compared with that of other teleosts. To better understand the factors influencing the timing of nitrogen excretion, the ratio of excreted urea∶ammonia, and the effector molecules regulating these processes, gulf toadfish were subjected to a series of experiments that moved them progressively from internal laboratory to outdoor mesocosm settings while assessing their behavior, nitrogen excretion patterns, levels of plasma hormones/effectors, and other parameters. In confined flux chambers in both laboratory and outdoor settings, toadfish nitrogen excretion was largely observed as urea pulses, with no apparent diel patterns to the pulses. Unrestrained toadfish in mesocosms exhibited distinctly nocturnal behavior, remaining exclusively in shelters during the day but taking several forays out into the mesocosm at night. In contrast to nitrogen excretion patterns in chambers, urea and ammonia were coexcreted in mesocosms and ratios for urea∶ammonia were very close to 1∶1 for both fed and fasted toadfish. The majority of measured excretion (and corresponding declines in plasma urea levels) occurred during two distinct periods of pulsing during daylight hours (0600-1000 and 1600-1800 hours). The declines in plasma urea associated with excretion were preceded by/coincided with declines in plasma cortisol. No day/night or hourly patterns in plasma serotonin (5-hydroxytryptamine [5-HT]) were observed, but there was a strong positive correlation among all samples between plasma urea and 5-HT. There was also a negative correlation between plasma cortisol and 5-HT. As expected for a nocturnally active species, plasma melatonin was significantly lower in daylight hours. A variety of enzyme activities (glutamine synthetase, glutaminase) and mRNA levels (glutamine synthetase, urea transporter, and Rhesus proteins) showed no significant variation over a diel cycle. Unlike prior laboratory studies, our results show that gulf toadfish in a natural setting have a distinctly diurnal pattern of nitrogen excretion and that ammonia and urea are coexcreted. The decline in plasma cortisol associated with urea pulses noted in prior laboratory studies was not as evident in the natural setting." @default.
• W1996765330 created "2016-06-24" @default.
• W1996765330 creator A5020893508 @default.
• W1996765330 creator A5058719679 @default.
• W1996765330 creator A5062219798 @default.
• W1996765330 date "2010-11-01" @default.
• W1996765330 modified "2023-09-26" @default.
• W1996765330 title "Diel Patterns of Nitrogen Excretion, Plasma Constituents, and Behavior in the Gulf Toadfish (<i>Opsanus beta</i>) in Laboratory versus Outdoor Mesocosm Settings" @default.
• W1996765330 cites W1572100925 @default.
• W1996765330 cites W191160705 @default.
• W1996765330 cites W1974216370 @default.
• W1996765330 cites W1982708854 @default.
• W1996765330 cites W1990792704 @default.
• W1996765330 cites W1990862613 @default.
• W1996765330 cites W1996892583 @default.
• W1996765330 cites W1998048479 @default.
• W1996765330 cites W2007647405 @default.
• W1996765330 cites W2009997462 @default.
• W1996765330 cites W2019570803 @default.
• W1996765330 cites W2022879966 @default.
• W1996765330 cites W2030981637 @default.
• W1996765330 cites W2036955430 @default.
• W1996765330 cites W2039784899 @default.
• W1996765330 cites W2059434108 @default.
• W1996765330 cites W2060421905 @default.
• W1996765330 cites W2070540975 @default.
• W1996765330 cites W2081366882 @default.
• W1996765330 cites W2081789089 @default.
• W1996765330 cites W2091395037 @default.
• W1996765330 cites W2096113253 @default.
• W1996765330 cites W2104060958 @default.
• W1996765330 cites W2105413102 @default.
• W1996765330 cites W2120330903 @default.
• W1996765330 cites W2126660837 @default.
• W1996765330 cites W2138584315 @default.
• W1996765330 cites W2141158257 @default.
• W1996765330 cites W2150081094 @default.
• W1996765330 cites W2153765708 @default.
• W1996765330 cites W2154205247 @default.
• W1996765330 cites W2157706656 @default.
• W1996765330 cites W2165534807 @default.
• W1996765330 cites W2183427423 @default.
• W1996765330 cites W2244096739 @default.
• W1996765330 cites W2257643235 @default.
• W1996765330 cites W2286702231 @default.
• W1996765330 cites W2302082719 @default.
• W1996765330 cites W2345329966 @default.
• W1996765330 doi "https://doi.org/10.1086/656427" @default.
• W1996765330 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20979496" @default.
• W1996765330 hasPublicationYear "2010" @default.
• W1996765330 type Work @default.
• W1996765330 sameAs 1996765330 @default.
• W1996765330 citedByCount "8" @default.
• W1996765330 countsByYear W19967653302012 @default.
• W1996765330 countsByYear W19967653302013 @default.
• W1996765330 countsByYear W19967653302015 @default.
• W1996765330 countsByYear W19967653302017 @default.
• W1996765330 countsByYear W19967653302019 @default.
• W1996765330 countsByYear W19967653302020 @default.
• W1996765330 countsByYear W19967653302023 @default.
• W1996765330 crossrefType "journal-article" @default.
• W1996765330 hasAuthorship W1996765330A5020893508 @default.
• W1996765330 hasAuthorship W1996765330A5058719679 @default.
• W1996765330 hasAuthorship W1996765330A5062219798 @default.
• W1996765330 hasConcept C10146269 @default.
• W1996765330 hasConcept C126322002 @default.
• W1996765330 hasConcept C134018914 @default.
• W1996765330 hasConcept C140793950 @default.
• W1996765330 hasConcept C142796444 @default.
• W1996765330 hasConcept C153102810 @default.
• W1996765330 hasConcept C178790620 @default.
• W1996765330 hasConcept C180553826 @default.
• W1996765330 hasConcept C185592680 @default.
• W1996765330 hasConcept C18903297 @default.
• W1996765330 hasConcept C2779215331 @default.
• W1996765330 hasConcept C2780365088 @default.
• W1996765330 hasConcept C2909208804 @default.
• W1996765330 hasConcept C505870484 @default.
• W1996765330 hasConcept C55493867 @default.
• W1996765330 hasConcept C71924100 @default.
• W1996765330 hasConcept C86803240 @default.
• W1996765330 hasConceptScore W1996765330C10146269 @default.
• W1996765330 hasConceptScore W1996765330C126322002 @default.
• W1996765330 hasConceptScore W1996765330C134018914 @default.
• W1996765330 hasConceptScore W1996765330C140793950 @default.
• W1996765330 hasConceptScore W1996765330C142796444 @default.
• W1996765330 hasConceptScore W1996765330C153102810 @default.
• W1996765330 hasConceptScore W1996765330C178790620 @default.
• W1996765330 hasConceptScore W1996765330C180553826 @default.
• W1996765330 hasConceptScore W1996765330C185592680 @default.
• W1996765330 hasConceptScore W1996765330C18903297 @default.
• W1996765330 hasConceptScore W1996765330C2779215331 @default.
• W1996765330 hasConceptScore W1996765330C2780365088 @default.
• W1996765330 hasConceptScore W1996765330C2909208804 @default.
• W1996765330 hasConceptScore W1996765330C505870484 @default.
• W1996765330 hasConceptScore W1996765330C55493867 @default.
• W1996765330 hasConceptScore W1996765330C71924100 @default.
• W1996765330 hasConceptScore W1996765330C86803240 @default.

• next