Como resultado do seu passado evolutivo, a família dos camarões Palaemonidae reúne representantes de ambientes osmóticos dos mais variados. Sejam de ambientes marinhos, estuarinos ou dulcícolas, estáveis ou variáveis, as espécies destes camarões mantêm a concentração osmo-iônica da hemolinfa independente da concentração do meio. Essas espécies hiper-regulam a osmolalidade e íons da hemolinfa em meio diluído e água doce e hipo-regulam em meio concentrado ou água do mar. Um importante local de transporte iônico envolvido na regulação osmo-iônica é o epitélio brânquial, pois nas membranas de seus ionócitos constituintes encontra-se um conjunto de transportadores que efetuam o movimento transepitelial de íons. Dentre estes transportadores, o simportador Na+, K+, 2Cl- (NKCC) é considerado ter um papel na secreção de sal, objetivo primário dessa investigação. Espécies representativas de habitat marinho do gênero Palaemon foram coletadas em regiões de estuário e de poça de maré, e de habitat dulcícola do gênero Macrobrachium foram coletadas em rios que desembocam no mar e também em riachos continentais sem influência do aporte salobro. Avaliou-se os limites letais de salinidade superior (LSS50) das espécies marinhas P. northropi e P. pandaliformis e dulcícolas diádromas M. acanthurus, M. olfersi, M. amazonicum que dependem de água salobra para completo desenvolvimento larval, e hololimnéticas M. potiuna e M. brasiliense com ciclo reprodutivo completo em água doce. Objetivou-se aqui (i) caracterizar os mecanismos de hiperregulação (condição controle de 18 S P. northropi, 17 S P. pandaliformis, água doce <0,5 S nas espécies de Macrobrachium) e hiporegulação [a curto (24 h) e longo prazo (120 h) em salinidade correspondente a 80% da LSS50] da osmolalidade e [Cl-] da hemolinfa, da expressão gênica e proteica e a localização por imunofluorescência do NKCC nos ionócitos branquiais; (ii) da existência de um padrão filogenético nesses parâmetros; e (iii) testar as hipóteses de um efeito da salinidade na evolução da expressão gênica e proteica desse simportador. As espécies de Palaemon apresentaram os maiores limites de tolerância ao aumento da salinidade, assim como exibiram uma maior capacidade hiporegulatória a longo prazo (120 h) comparada aos representantes de Macrobrachium. Dentre as espécies de Macrobrachium, os limites de tolerância foram maiores nas espécies diádromas do que nas hololimnéticas. Os parâmetros LSS50, osmolalidade e [Cl-] da hemolinfa demonstraram-se estruturados na filogenia, sendo as semelhanças compartilhadas justificadas pela estreita proximidade entre as espécies. As análises filogenéticas revelaram que a capacidade hiper-regulatória da [Cl-] da hemolinfa foi correlacionada com a expressão gênica do simportador NKCC nas brânquias, enquanto que a síntese proteica do NKCC parece estar associada à hiper-regulação da osmolalidade da hemolinfa. A avaliação da localização do NKCC por imunofluorescência demonstrou que o simportador está distribuído em ambas as células que compõem o epitélio das brânquias, as células pilares e células do septo intralamelar. A localização na porção inferior das franjas e no corpo da célula pilar e por toda célula do septo não diferiu entre as espécies, e também não difereiu entre as condições controle e a curto e longo prazo em salinidade elevada. Esses resultados em conjunto sugerem a importância do NKCC também na captação de sal pelas brânquias. Houve um aumento da síntese proteica do NKCC nas brânquias dos representantes de Macrobrachium, exceto M. potiuna, quando em salinidade elevada. Observou-se que este aumento é explicado pela proximidade filogenética entre as espécies. Não houve mudança na transcrição de RNAm para o NKCC apesar do aumento na síntese proteica, o que sugere uma possível regulação pós-transcricional. A reconstrução da história evolutiva da osmorregulação, incorporando o conceito de filofisiologia, revelou a existência de mecanismos em nível molecular, celular e sistêmico que evoluíram acompanhando os eventos cladogenéticos dos Palaemonidae durante a irradiação e ocupação de diferentes nichos osmóticos. / Owing to their evolutionary history, the shrimp family Palaemonidae includes species from widely distinct osmotic environments. Whether from marine, estuarine, or fresh waters, inhabiting stable or variable osmotic niches, these shrimps maintain the osmotic-ionic concentration of their hemolymph independently of the concentration of the external medium. These species hyper-regulate hemolymph osmolality and ions in dilute medium and fresh water and hypo-regulate this fluid in concentrated medium or seawater. The gill epithelium constitutes an important interface of ion transport, and its constituent ionocytes express an ensemble of ion transporters that enable active transepithelial ion movements. The Na+, K+, 2Cl- cotransporter (NKCC) is thought to play a significant role in compensatory salt secretion. Species representative of the marine habitat (Palaemon) were collected from estuaries and tidal pools; diadromous species from the fresh water habitat (Macrobrachium) were collected near the mouths of rivers that flow into the sea, while hololimnetic species were collected in continental streams lacking the influence of brackish waters. The critical upper salinity limits (LSS50) of the marine species P. northropi and P. pandaliformis and the diadromous freshwater species M. acanthurus, M. olfersi, M. amazonicum that depend on brackish water for complete larval development, and the hololimnetic M. potiuna and M. brasiliense that complete their reproductive cycle entirely in fresh water were established. Our objectives were to characterize the mechanisms of hyper-regulation (control condition 18 S P. northropi, 17 S P. pandaliformis, fresh water <0.5 S for Macrobrachium) and hypo-regulation [short-term (24 h) and long-term 120 h) at salinities corresponding to 80% of LSS50] of hemolymph osmolality and [Cl-], gene and protein expression, and NKCC localization for immunofluorescence in the gill ionocytes; (ii) the existence of a phylogenetic pattern in these parameters; and (iii) to test hypotheses for a salinity effect on the evolution of the gene and protein expression of this symporter. The species of Palaemon had the highest tolerance limits to increased salinity, and also exhibited a greater hypo-regulatory capacity for long-term acclimation compared to the species of Macrobrachium. Among the Macrobrachium species, the LSS50 were higher in the diadromous species than in the hololimnetic species. The parameters LSS50 and osmolality and [Cl-] of the hemolymph were phylogenetically structured, similarities being shared by closely related species. The hyper-regulatory capacity of hemolymph [Cl-] correlated with NKCC gene expression in the gills, while NKCC protein synthesis appears to be associated with hyper-regulation of hemolymph osmolality. Immunofluorescence analysis showed that the NKCC was located in both cell types that constitute the gill epithelium, the pillar cells and the septal cells. The location of the NKCC in the lower flanges and perikarya of the pillar cells and throughout the septal cells, did not differ among species, and also did not differ among control conditions or short and long-term exposure at high salinity. These results together also suggest the importance of the NKCC in salt uptake by the gills. When in high salinity there was an increase in NKCC protein synthesis in the gills of the Macrobrachium species, except for M. potiuna. This increase can be explained by the phylogenetic proximity among those species, which excludes adaptive inferences. There was no change in NKCC mRNA transcription, which suggests possible post-transcriptional regulation. The reconstruction of the evolutionary history of osmoregulation, incorporating the concept of phylophysiology, revealed the existence of mechanisms at the molecular, cellular and systemic levels that have evolved accompanying the cladogenetic events of the Palaemonidae during their radiation and occupation of different osmotic niches.

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / In aquatic organisms, changes in salinity in water provoke a variety of physiological responses, so this study aimed to evaluate the effect of water salinity on weight gain, survival and expression of the genes Catalase (CAT), Glutathione Reductase (GSR), Glutathione Synthase (GSS), Glutaione peroxidase (GPX), and heat shock protein (HSP70) in the liver of Nile Tilapia (Oreochromis niloticus). For the conduction of the experiment, 160 tilapias with a mean weight of 20.8 g ( ± 4.02) were used. The experiment was conducted in a completely randomized design (DIC) composed of four treatments and four replicates, being: T1 = Treatment 1 (salinity 0 + basal diet); T2 = Treatment 2 (salinity 7 + basal diet); T3 = Treatment 3 (salinity 21 + basal diet); T4 = treatment 4 (salinity 21 + diet with 1500 mg of vitamin C / kg of feed). The parameters of water quality were monitored daily and were kept within the range of comfort for the species. For the analysis of gene expression samples of liver of tilapia were collected in two distinct periods, 24 hours and 14 days after the beginning of the experiment. Gene expression quantification was performed by qRT-PCR. There was a significant effect of the treatments on weight gain, treatment 1 (4.10 g) and treatment 2 (6.42 g) had the highest weight improve. Animals from T4 had greater weight gain than animals from T3. Higher survival was observed in treatment 2 followed by control (T1). HSP 70 and GSS were more expressed in the 24 h period and GSRR was more expressed in the 14 day period, whereas CAT and GPX did not differ from one period to the other (P <0.05). The salinity variation had an effect under the expression of the genes evaluated in the liver of O. niloticus with the exception of catalase for the 24 hour period. After 14 days of evaluation, animals raised in salinity 21 and fed with vitamin C supplementation presented greater expression of GPX, GSR and GSS, suggesting that animals raised at this level of salinity had greater need of action of glutathione system, and that the supplementation of vitamin C under these conditions allowed greater expression of these genes. It was concluded that salinity had an effect on the expression of the antioxidant defense system genes evaluated, which varied considerably over the 24-hour period and presented a more defined pattern in the 14-day period. Supplementation of vitamin C contributed, in parts, for better development of tilapia created in salinity 21, which can be observed, through the results of weight gain and gene expression. / Em organismos aquáticos, mudanças de salinidade na água provocam uma variedade de respostas fisiológicas, assim, este estudo objetivou avaliar o efeito da salinidade da água sobre o ganho de peso, a sobrevivência e a expressão dos genes Catalase (CAT), Glutatona Redutase (GSR), Glutationa Sintetase (GSS), Glutationa peroxidase (GPX) e o da proteína de choque térmico (HSP70) no fígado de Tilápias do Nilo (Oreocrhomis niloticus). Para a condução do experimento foram utilizadas 160 tilápias com peso médio 20,8 g (± 4,02). O experimento foi conduzido em delineamento inteiramente casualizado (DIC) compostos por quatro tratamentos e quatro repetições, sendo: T1 = Tratamento 1 (salinidade 0 + dieta basal); T2= Tratamento 2 (salinidade 7 + dieta basal); T3= Tratamento 3 (salinidade 21 + dieta basal ); T4 = tratamento 4 (salinidade 21 + dieta com 1500 mg de vitamina C/ kg de ração). Os parâmetros de qualidade de água foram monitorados diariamente e se mantiveram dentro da faixa de conforto para a espécie. Para as análises de expressão gênica foram coletadas amostras do fígado de tilápias em dois períodos distintos, 24 horas e 14 dias após o início do experimento. A quantificação da expressão gênica foi realizada por qRT-PCR. Houve efeito significativo dos tratamentos sobre o ganho de peso, tilápias do tratamento 1 (4,10g) e tratamento 2 (6,42 g) obtiveram os maiores ganhos de peso. Animais do tratamento 4 (salinidade 21 + acréscimo de vitamina C na ração) tiveram maior ganho de peso que os animais do tratamento 3 (salinidade 21 + dieta basal). Maior sobrevivência foi observada no tratamento 2 seguido pelo controle. HSP 70 e GSS foram mais expressos no período de 24 h e GSR sendo mais expressa no período de 14 dias, enquanto que CAT e GPX não diferiram de um período para o outro. A variação de salinidade teve efeito sob a expressão dos genes avaliados no fígado de O.niloticus com exceção da catalase para o período de 24 horas. Após 14 dias de avaliação animais criados em salinidade 21 e alimentados com suplementação de vitamina C apresentaram maior expressão de GPX, GSR e GSS, sugerindo que animais criados nesse nível de salinidade, tiveram maior necessidade de ação do sistema glutationa, e que a suplementação de vitamina C nessas condições permitiu maior expressão desses genes. Conclui-se que a salinidade apresentou efeito sobre a expressão dos genes do sistema de defesa antioxidantes avaliados, os quais variaram bastante no período de 24 horas e apresentaram um padrão mais definido no período de 14 dias. A suplementação de vitamina C contribuiu em partes, para melhor desenvolvimento das tilápias criadas em salinidade 21, o que pode ser observado, pelos resultados de ganho de peso e expressão gênica.

As propriedades bioquímicas da (Na+,K+)-ATPase branquial do siri eurialino Callinectes danae aclimatado à salinidade de 15 o/oo foram estudadas. A análise do gradiente de centrifugação em sacarose revelou a presença de um único pico entre 30-35% de sacarose, com uma boa correlação entre as atividades PNFFase a ATPase totais e (Na+,K+)-ATPase. A atividade residual observada na presença de ouabaína 3 mM sugere a presença de outros sistemas de enzimas atuantes. A eletroforese em condições desnaturantes nos microsomas de brânquias de C. danae em animais recém-coletados em salinidade de 33 o/oo (não aclimatados) e de aclimatados a salinidades de 15 e 33 o/oo por um período de 10 dias mostrou a presença de pequenas diferenças nos padrões eletroforéticos das diferentes amostras. A análise por Western blot mostrou um aumento significativo da proporção relativa da subunidade alfa da (Na+,K+)-ATPase em relação à proteína total na fração microsomal do tecido branquial de animais aclimatados à salinidade de 15 o/oo quando comparados aos animais aclimatados a 33 o/oo. Entretanto, proporções similares de subunidade alfa foram observadas para amostras de animais recém-coletados a salinidade de 33 o/oo e aclimatados a 15 o/oo. A estimulação da atividade (Na+,K+)-ATPase pelo ATP ocorreu através de uma curva de saturação monofásica apresentando interações sítio-sítio (nH=1,2), com V= 298,8 ± 16,7 U/mg, com K0,5 de 174,2 ± 9,8 uM. A estimulação da atividade ATPase da (Na+,K+)-ATPase por íons Mg2+ (V= 299,16 ± 14,06 U/mg; K0,5= 767,31 ± 36,06 uM), íons Na+ (V= 309,0 ± 15,8 U/mg; K0,5= 7,8 ± 0,4 mM), íons K+ (V= 300,6 ± 15,3 U/mg; K0,5= 1,63 ± 0,08 mM) e íons NH4+ (V= 345,1 ± 19,0 U/mg; K0,5= 6,0 ± 0,3 mM) ocorreu através de interações sítio-sítio. A atividade da enzima foi modulada sinergisticamente pelos íons K+ com atividade máxima variando de 300,6 ± 15,3 U/mg para 514,6 ± 26,2 U/mg, na ausência e na presença 50 mM de íons NH4+, respectivamente. Além disso, foi observado um significativo aumento na afinidade aparente da enzima pelo íon K+ da ordem de 10 vezes (diminuiu de 1,6 ± 0,08 mM para 0,157 ± 0,008 mM). Similarmente ao observado para os íons K+, o íon NH4+ estimulou sinergisticamente a atividade da enzima na presença de diferentes concentrações de íons K+. A estimulação da atividade da enzima pelo íon NH4+ também ocorreu através de interações cooperativas entre os sítios. Embora tenha sido observado um aumento da atividade específica da enzima de 345,1 ± 19,0 U/mg para 516,8 ± 27,9 U/mg, não foram observadas variações significativas nos valores de nH e K0,5 com o aumento da concentração de íons K+. A ouabaína inibiu cerca de 90% da atividade ATPase total. A inibição pela ouabaína apresentou valor de KI de 45,09 ± 2,51 uM. O ortovanadato também inibiu atividade (Na+,K+)-ATPase na mesma faixa (90%) através de uma curva de inibição monofásica, com valor de KI da ordem de 1,31 ± 0,06 uM. O emprego de bafilomicina A1, tapsigargina e teofilina, juntamente com a ouabaína, na atividade ATPase total descartam a presença de V-ATPase, Ca2+-ATPase ou fosfatase, respectivamente. Apesar da inibição por oligomicina corresponder a menos de 3,7%, esse valor aparentemente sugere a presença de uma F0F1-ATPase. Além disso, a inibição por ácido etacrínico, em conjunto com os experimentos de estimulação por da atividade ATPase da enzima por íons Na+ sugere fortemente a presença de uma K+-ATPase. A (Na+,K+)-ATPase hidrolisou o substrato PNFF obedecendo à cinética Michaeliana com velocidade de V= 102,9 ± 4,3 U/mg e KM= 1,7 ± 0,1 mM. Já a estimulação da atividade K+-fosfatase da enzima por íons Mg2+ (V= 93,7 ± 2,3 U/mg; K0,5= 1,40 ± 0,03 mM), K+ (V= 94,9 ± 3,5 U/mg; K0,5= 2,9 ± 0,1 mM) e NH4+ (V= 106,2 ± 2,2 U/mg; K0,5= 9,8 ± 0,2 mM) seguiu uma cinética cooperativa, sugerindo a presença de múltiplos sítios de ligação. Entretanto, a atividade K+-fosfatase não foi estimulada sinergísticamente na presença de íons K+ mais NH4+. Os íons sódio (KI= 22,7 ± 1,7 mM) e ortovanadato (KI= 28,1 ± 1,4 nM) inibiram completamente a atividade fosfatase total através de uma única curva de inibição. / The biochemical properties of the (Na+,K+)-ATPase from the gill microsomal tissue of the euryhaline, marine, swimming crab Callinectes danae, acclimated to 15 0/00 salinity, were investigated. Sucrose gradient centrifugation analyses revealed a unique peak, between 30-35% sucrose, coincident with the total PNPPase, ATPase, and (Na+,K+)-ATPase activities. The residual activity observed in the presence of 3 mM ouabain suggests the existence of other enzyme systems. Electrophoresis under denaturing conditions, using material from fresh-caught crabs (33 o/oo salinity, not acclimated), and from crabs acclimated to 15 or 33 o/oo salinity, for 10 days, revealed differences in migration pattern. Western blot analyses showed a significant increase in the amount of (Na+,K+)-ATPase alpha-subunit relative to total protein, for crabs acclimated to 15 o/oo compared to those acclimated to 33 o/oo salinity. However, the proportion of alpha-subunit in samples from fresh-caught crabs acclimated to 33 o/oo and those acclimated to 15 o/oo salinity was similar. (Na+,K+)-ATPase activity was stimulated by ATP and showed a single saturation curve, exhibiting site-site interactions (nH=1.2), with V= 298.8 ± 16.7 U/mg, and K0.5= 174.2 ± 9.8 uM. Stimulation of the ATPase activity by Mg2+ (V= 299.16 ± 14.06 U/mg; K0.5= 767.31 ± 36.06 uM), Na+ (V= 309.0 ± 15.8 U/mg; K0.5= 7.8 ± 0.4 mM), K+ (V= 300.6 ± 15.3 U/mg; K0.5= 1.63 ± 0.08 mM) and NH4+ ions (V= 345.1 ± 19.0 U/mg; K0.5= 6.0 ± 0.3 mM) occurred through site-site interactions. (Na+,K+)-ATPase activity was synergistically modulated by K+ ions, maximum activity varying from 300.6 ± 15.3 U/mg to 514.6 ± 26.2 U/mg, in the absence and presence of 50 mM NH4+ ions, respectively. K+ ions induced a 10-fold increase in enzyme apparent affinity (from 1.6 ± 0.08 mM to 0.157 ± 0.008 mM). As for K+ ions, NH4+ synergistically stimulated enzyme activity in the presence of variable K+ concentrations. The stimulation by NH4+ ions exhibited cooperative, site-site interactions. Although an increase in specific activity from 345.1 ± 19.0 U/mg to 516.8 ± 27.9 U/mg was seen, no significant changes in nH and K0.5 were observed. Ouabain inhibited total ATPase activity by about 90%, showing a KI= 45.09 ± 2.51 uM. Orthovanadate also inhibited the (Na+,K+)-ATPase with a KI of 1.31 ± 0.06 uM. Although the inhibitory effect of oligomycin was minimal (3.7%), this inhibition may suggest F0F1-ATPase activity. The inhibition by ethacrynic acid, in association with Na+ ion stimulation of the ATPase activity, suggests the presence of a K+-ATPase. The (Na+,K+)-ATPase hydrolyzed PNPP (K+-phosphatase activity) obeying Michaelian kinetics, with V= 102.9 ± 4.3 U/mg and KM= 1.7 ± 0.1 mM. The stimulation of K+-phosphatase activity by Mg2+ (V= 93.7 ± 2.3 U/mg; K0.5= 1.4 ± 0.03 mM), K+ (V= 94.9 ± 3.5 U/mg; K0.5= 2.9 ± 0.1 mM), and NH4+ ions (V= 106.2 ± 2.2 U/mg; K0.5= 9.8 ± 0.2 mM) following cooperative kinetics, suggests multiple binding sites. K+-phosphatase activity, however, was not synergistically stimulated by K+ and NH4+. Sodium ions (KI= 22.7 ± 1.7 mM), and orthovanadate (KI= 28.1 ± 1.4 nM) totally inhibited the total phosphatase activity.

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Seawater teleost fish are hyposmotic to their environment and as a consequence must deal with a constant diffusive loss of water and a net gain of salts. In contrast to living in seawater, teleosts fish in a freshwater environment are faced with the opposite dilemma, a constant osmotic influx of water and depletion of salts. Between these environments there are estuarine regions, which are habitats of several species. The purpose of this study was to investigate Na+, Cl-, K+, Ca2+, and Mg2+ levels in the fluid phase and total amount of the contents of the segments of the gastrointestinal tract and plasma of freshwater and estuarine teleosts collected in different salinities (0 to 34 ) in the São Gonçalo channel in Pelotas, southern Brazil. Moreover, a possible relationship between the ion levels and salinity was investigated. After capture of the fishes, blood was collected and specimens were sacrificed for removal gastrointestinal tract segments: stomach, pyloric ceca/anterior intestine, mid- and posterior intestine. The results showed that there was no relationship between ion levels in the plasma, in the fluid phase and in the total amount of the segments of the gastrointestinal tract with salinity when considering all species together, but species (Micropogonias furnieri and Netuma barba) collected in three or more salinities demonstrated significant relationship of these parameters with salinity. The ion levels in the fluid phase and total amount of the most species showed significantly higher values in the anterior intestine than stomach. Moreover, ion levels showed a variation throughout the gastrointestinal tract suggesting possible ion absorption. These results suggest that the change of salinity affected ion levels in the plasma and in the content of the gastrointestinal tract of Micropogonias furnieri and Netuma barba, indicating that this system might be related with osmoregulation of these species. / Peixes teleósteos adaptados à água do mar são hiposmóticos em relação ao meio em que vivem e como conseqüência disso convivem com uma constante perda de água por osmose e ganho de sais por difusão. Ao contrário dos teleósteos que vivem na água salgada, peixes teleósteos adaptados à água doce convivem com o dilema oposto, uma constante entrada de água por osmose e perda de íons por difusão. Além disso, entre esses ambientes existem as regiões estuarinas, as quais são habitats de várias espécies. A proposta desse estudo foi investigar os níveis de Na+, Cl-, K+, Ca2+ e Mg2+ na fase fluida e quantidade total do conteúdo dos segmentos do trato gastrintestinal e do plasma de teleósteos estuarinos e de água doce coletados em diferentes salinidades (0-34 ) no Canal São Gonçalo em Pelotas, sul do Brasil. Além disso, uma possível relação entre os níveis iônicos e a salinidade foi investigada. Após a captura dos peixes, coletou-se sangue e os espécimes foram submetidos a eutanásia para remoção dos segmentos do trato gastrintestinal: estômago, cecos pilóricos/intestino anterior, intestino médio e posterior. Os resultados mostraram que não houve relação entre os íons no plasma, na fase fluida e na quantidade total dos segmentos do trato gastrintestinal com a salinidade quando se considerou todas as espécies juntas, porém duas espécies (Micropogonias furnieri e Netuma barba) coletadas em três ou mais salinidades demonstraram relação significativa entre esses parâmetros e a salinidade. Os níveis iônicos na fase fluida e quantidade total da maioria das espécies mostraram valores significativamente maiores no intestino anterior em relação ao estômago. Além disso, os níveis iônicos mostraram variação ao longo do trato gastrintestinal sugerindo uma possível absorção de íons. Estes resultados sugerem que a mudança de salinidade afetou os níveis iônicos do plasma e dos conteúdos do trato gastrintestinal de Micropogonias furnieri e Netuma barba, indicando que este sistema pode estar relacionado com a osmorregulação destas espécies.

Many of the habitats occupied by fish are highly dynamic, naturally demonstrating substantial abiotic fluctuations over diurnal, tidal or seasonal cycles. It is also the case that throughout their 545 million year evolutionary history, fish have existed in aquatic environments very different to those of the present day. However, the past several decades have seen unprecedented rates of environmental change, at local and global scales, arising from human activities. The two major themes of the present thesis are: 1) Respiratory responses of fish to changes in environmental oxygen and temperature in the context of exploring intra- and inter-specific trait variation and its ecological implications 2) The effects of environmental factors (oxygen, carbon dioxide, temperature and seawater chemistry) on the intestinal precipitation and excretion of calcium carbonate by marine teleosts. In the first study (chapter two) a comprehensive database of fish critical PO2 (Pcrit) data compiled from the published literature is presented. The systematic review of this literature provided the opportunity to critically examine methodologies for determining Pcrit as well as its usefulness as an indicator of hypoxia tolerance in fish. The second study (chapter three) examines whether inter- and intra-specific variation in thermal and hypoxia tolerance in two reef snapper species (Lutjanus carponotatus and Lutjanus adetii) reflects their distributions across the contrasting biophysical environments of the reef flat and reef slope surrounding Heron Island on the Great Barrier Reef. L. carponotatus was clearly the most thermally and hypoxia tolerant of the two species, demonstrating a ~3.5 °C wider thermal tolerance zone (higher CTmax, lower CTmin) and ~26% lower Pcrit than L. adetii. These results suggest that the contrasting distribution of these species between flat and slope reef zones is reflected in their physiological tolerances. However, there was no evidence of intra-species variation in tolerance between flat and slope caught L. carponotatus individuals, indicating that this species does not form physiologically distinct subpopulations between these reef zones. The third study (chapter four) experimentally quantified the effect of hypercarbia (3000 μatm) and hypoxia (50% air saturation) on gut carbonate production by the European flounder (Platichthys flesus). Both hypercarbia and hypoxia resulted in a significant increase in carbonate excretion rate (1.5-fold and 2.4-fold, respectively) and acted synergistically when combined. In the final study (chapter five), gut carbonate production was measured in the European flounder undergoing conditions simulating the ‘calcite seas’ of the Cretaceous. The results of this study support the hypothesis that ocean conditions prevalent during the Cretaceous period resulted in piscine carbonate production rates substantially higher (~14-fold) than the present day. Ultimately, this thesis directly links the environmental physiology of fish at the individual level to wider scale implications (past, present and future), ranging from local ecological patterns all the way up to global carbon cycles.

Pacific lamprey is a culturally valuable species to indigenous people, and has significant ecological importance in freshwater and marine ecosystems. Over the past several decades, constrictions in range and reductions in Pacific lamprey abundance have been observed in Western North America, and may be indicators of range-wide declines. In the face of declining populations, the U.S. Fish and Wildlife Service has partnered with tribal, state, federal, and local entities to implement a regional Pacific lamprey conservation agreement aimed at reducing threats to Pacific lamprey and improving their habitats and population status. Research needs identified in the conservation agreement include assessing larval Pacific lamprey occupancy and distribution, habitat requirements, and the limiting factors of larval distribution in the freshwater ecosystem. As part of the effort to address these knowledge gaps, we investigated the potential for larval lampreys to occur in tidally-influenced estuarine environments. Research of this type may be valuable for future conservation, management or recovery efforts of Pacific lamprey throughout its range. We employed a two-phased approach, consisting of laboratory and field components to address our aims. We first conducted a series of controlled laboratory experiments to evaluate osmotic stress tolerance and osmoregulatory status of larval Pacific lamprey exposed to a range of (1) fixed salinity in various dilutions of saltwater and (2) oscillating salinity treatments designed to simulate tidal activity. Tolerance was assessed by monitoring and comparing survival of larvae in various treatments through 96 h. Osmoregulatory status was assessed by quantifying and comparing total body water content, plasma osmolality, and plasma cation (i.e., sodium) concentrations among larvae surviving various treatments. In fixed salinity experiments, 100% survival was observed in 0‰, 6‰, 8‰ and 10‰ through 96 h, while 0% survival was observed through 48 h in 12‰, 30 h in 15‰, and 12 h in 25‰ and 35‰. In oscillating salinity experiments, on the other hand, a significant increase in survival (100%) was observed through 96 h in treatments that oscillated between 12‰ and 0‰ (freshwater) at about 6 h intervals versus fixed 12‰ salinity experiments. A significant increase in survival also occurred in oscillating 15‰ treatments (60%) versus fixed 15‰ through 96 h. Linear regression analysis indicated higher environmental salinity in laboratory experiments was significantly related to increases in plasma osmolality and plasma sodium (the most abundant osmotically active plasma cation) concentrations, and concurrent decreases in total body water content among larvae that survived various treatments. Tidal oscillations in salinity appeared to temper the desiccating effects of salinity, as changes in body water content and sodium ion concentration were less abrupt than fixed salinity treatments. These results suggest larvae cannot osmoregulate in hyperosmotic environments, but are able to tolerate some fixed and oscillating hyperosmotic salinity exposure. Consequently, larvae may be able to occur in certain areas of estuaries, such as oligohaline habitats that are characterized by low levels of salinity. Experimental results were used, in part, to guide larval sampling in a tidally-influenced habitat. Occurrence of larval Pacific lamprey and Lampetra spp. (western brook and river lampreys) was subsequently investigated across a gradient of salinity in Ellsworth Creek (Pacific County, Washington) by electrofishing. Larval Pacific and Lampetra spp. were detected within an approximately 300 m long tidally-influenced segment of the study area. Salinity monitoring was conducted in six tidally-influenced reaches where larvae were detected for up to 14 d following electrofishing. Maximum tidal cycle salinity exceeded 15 ppt during 52% to 80% of tidal cycles within tidally-influenced reaches where larvae were detected. These results suggest potential for larval lamprey to occur in certain portions of tidal estuaries. However, long-term residence of larvae in tidally-influenced habitats and whether larvae are able to subsequently survive, grow, transform, and out-migrate is not known and requires further study. Given the potential for tidally-influenced habitats to be occupied by larvae, assessments of larval occurrence in other areas, such as the lower Columbia River, may be warranted. Knowledge of larval lamprey distribution in estuarine environments may be valuable for habitat restoration, and mitigating potential impacts from dredging and other human disturbances.

No description available.

The European eel, Anguilla anguilla, has a complex life-cycle involving migrations between the Sargasso Sea and the river systems of Europe and North Africa. The requirement to move across large salinity gradients presents a significant physiological challenge and the developmental stages of the eel are closely linked to these migrations. Microarrays were created to elucidate gene expression changes occurring during; i. The transition from juvenile yellow to the adult sexually maturing, migrating silver eel and; ii. Salinity adaptation during the migration from freshwater to seawater. Groups (n = 6) of freshwater-acclimated yellow or silver eels were transferred to seawater for between 6 hours and 5 months and complementary control groups were transferred to freshwater. Brain, kidney, intestine and gill cDNA libraries were constructed using suppression subtractive hybridisation (SSH) techniques and a novel protocol based on Invitrogen's Gateway cloning system. The latter technique produced a low redundancy (~4 %) EST bank with a wide range of insert sizes (0.5 – 10 kb). Two microarray types were produced; one comprised 5760 clones from the two brain libraries whilst the other was a multi-tissue microarray incorporating 6144 clones from the SSH libraries. Pooled RNA samples were probed against the microarrays to highlight differentially expressed genes. Real-time quantitative PCR (QPCR) was used to validate the observed expression changes of selected genes in the tissues of individual fish. Following yellow to silver transformation of freshwater-adapted eels, the expression of tyrosine 3-mono-oxygenase/tryptophan 5-mono-oxygenase activation protein (14-3-3) and vaccinia related kinase 3 was shown to be consistently elevated. Prolactin expression increased in the brains of silver eels following two-day seawater-acclimation but QPCR analysis revealed high variation amongst freshwater-adapted eels. This is the first eel microarray study and the expression profiles highlighted herein will provide new avenues for research into the sexual development and salinity acclimation of A. anguilla.

Fisheries management regulations for dusky kob Argyrosomus japonicus, an important commercial and recreational fisheries species, have failed and the stock is considered collapsed. It is important to take an ecosystems approach to management which includes understanding the effect of environmental factors on recruitment, abundance and distribution. The distribution of early juveniles (20-150 mm TL) in the wild appears to be restricted to the upper reaches of estuaries at salinities below 5 psu. Food availability could not explain the distribution of early juveniles. The aim of this study was to investigate the role of salinity on the distribution of early juvenile dusky kob (<150 mm TL) by examining physiological responses of juveniles exposed to a range of salinities under laboratory conditions. The hypothesis was that the physiological functioning of early juveniles would be optimised at the reduced salinities which they naturally occur at. The objectives of this study were to investigate the effect of salinity on: i) plasma osmolality; ii) growth, food conversion ratio and condition factor; and iii) gill histology with emphasis on chloride cell size and number. A preliminary study was undertaken to determine whether the use of 2-phenoxyethanol had an effect on plasma osmolality. Juveniles pithed prior to blood sampling were used as the control. Plasma osmolality was not affected by exposure or duration of exposure (2, 4, 6, 8, 10 min) to 2-phenoxyethanol. The ability of teleosts to regulate plasma osmolality over a wide range of salinities indicates their degree of ‘physiological euryhalinity’. Plasma osmolality of juveniles exposed to 5, 12 and 35 psu was measured every two weeks over a total of six weeks. Although juveniles were able to regulate plasma osmolality over the duration of the experiment, plasma osmolality at 5 and 12 psu was significantly lower than in fish maintained at 35 psu. Growth is used as an indicator of the relative energy used for osmoregulation at different salinities, as the energy used for osmoregulation becomes unavailable for growth. A nineweek growth experiment was conducted on juveniles exposed to 5, 12 and 35 psu. Juveniles grew and survived at all three salinities. However, growth of juveniles at 5 psu was significantly lower than at 12 and 35 psu. Other than a significantly greater weight gain at 35 psu relative to 12 psu, there was no significant difference in specific growth and length gain between juveniles at 12 and 35 psu. Food conversion ratio and condition factor at 12 and 35 psu were not significantly different, but food conversion ratio and condition factor at 5 psu was significantly greater and lower than at 35 psu respectively. In fish, gills are considered the major organ involved in osmoregulation. Within the gills, chloride cells are the predominant site of ion exchange which is driven by the Na⁺, K⁺- ATPase enzyme. Gill samples of juveniles exposed to 5, 12 and 35 psu for six weeks were examined histologically using light microscopy. Chloride cells of juveniles maintained at 5 psu were significantly more abundant than in juveniles at 12 and 35 psu. Chloride cells of juveniles at 5 psu were significantly larger than in juveniles kept at 12 psu, but not significantly different to those of juveniles kept at 35 psu. The ability of the juvenile fish to regulate plasma osmolality indicates that they are 'physiologically euryhaline', but the reduced growth and proliferation of chloride cells at 5 psu suggests that energy expenditure for osmoregulation is increased at hypoosmotic salinities. Salinity induced physiological responses could therefore not explain the natural distribution of early juvenile dusky kob and it is proposed that other environmental factors (e.g. temperature) are also important. It is also hypothesised that the high conductivity of an estuary in South Africa, to which our understanding is limited, may negate the effect of reduced salinity. Although freshwater input into estuaries is an important factor, further investigations to explain the distribution and abundance of early juveniles is required to make management recommendations. Dusky kob is also becoming an increasingly popular aquaculture species in South Africa. In this regard, early juvenile dusky kob can be grown at salinities as low as 12 psu without negatively affecting growth and production.

No description available.