We show that the distributions of both exploited and nonexploited North Sea fishes have responded markedly to recent increases in sea temperature, with nearly two-thirds of species shifting in mean latitude or depth or both over 25 years. For species with northerly or southerly range margins in the North Sea, half have shown boundary shifts with warming, and all but one shifted northward. Species with shifting distributions have faster life cycles and smaller body sizes than nonshifting species. Further temperature rises are likely to have profound impacts on commercial fisheries through continued shifts in distribution and alterations in community interactions.

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Climate Change and Distribution Shifts in Marine Fishes

The fish gill is a multipurpose organ that, in addition to providing for aquatic gas exchange, plays dominant roles in osmotic and ionic regulation, acid-base regulation, and excretion of nitrogenous wastes Thus, despite the fact that all fish groups have functional kidneys, the gill epithelium is the site of many processes that are mediated by renal epithelia in terrestrial vertebrates Indeed, many of the pathways that mediate these processes in mammalian renal epithelial are expressed in the gill, and many of the extrinsic and intrinsic modulators of these processes are also found in fish endocrine tissues and the gill itself The basic patterns of gill physiology were outlined over a half century ago, but modern immunological and molecular techniques are bringing new insights into this complicated system Nevertheless, substantial questions about the evolution of these mechanisms and control remain

https://people.clas.ufl.edu/devans/files/PRVGill.pdf

The Multifunctional Fish Gill: Dominant Site of Gas Exchange, Osmoregulation, Acid-Base Regulation, and Excretion of Nitrogenous Waste

 – Among the species in the family Salmonidae, those represented by the genera Salmo, Salvelinus, and Oncorhynchus (subfamily Salmoninae) are the most studied. Here, various aspects of phenotypic and life-history variation of Atlantic salmon Salmo salar L., brown trout Salmo trutta L., and Arctic charr Salvelinus alpinus (L.) are reviewed. While many strategies and tactics are commonly used by these species, there are also differences in their ecology and population dynamics that result in a variety of interesting and diverse topics that are challenging for future research. Atlantic salmon display considerable phenotypic plasticity and variability in life-history characters ranging from fully freshwater resident forms, where females can mature at approximately 10 cm in length, to anadromous populations characterised by 3–5 sea-winter (5SW) salmon. Even within simple 1SW populations, 20 or more spawning life-history types can be identified. Juveniles in freshwater can use both fluvial and lacustrine habitats for rearing, and while most smolts migrate to sea during the spring, fall migrations occur in some populations. At sea, some salmon undertake extensive oceanic migrations while other populations stay within the geographical confines of areas such as the Baltic Sea. At the other extreme are those that reside in estuaries and return to freshwater to spawn after spending only a few months at sea. The review of information on the diversity of life-history forms is related to conservation aspects associated with Atlantic salmon populations and current trends in abundance and survival. Brown trout is indigenous to Europe, North Africa and western Asia, but was introduced into at least 24 countries outside Europe and now has a world-wide distribution. It exploits both fresh and salt waters for feeding and spawning (brackish), and populations are often partially migratory. One part of the population leaves and feeds elsewhere, while another part stays as residents. In large, complex systems, the species is polymorphic with different size morphs in the various parts of the habitat. Brown trout feed close to the surface and near shore, but large individuals may move far offshore. The species exhibits ontogenetic niche shifts partly related to size and partly to developmental rate. They switch when the amount of surplus energy available for growth becomes small with fast growers being younger and smaller fish than slow growers. Brown trout is an opportunistic carnivore, but individuals specialise at least temporarily on particular food items; insect larvae are important for the young in streams, while littoral epibenthos in lakes and fish are most important for large trout. The sexes differ in resource use and size. Females are more inclined than males to become migratory and feed in pelagic waters. Males exploit running water, near-shore and surface waters more than females. Therefore, females feed more on zooplankton and exhibit a more uniform phenotype than males. The Arctic charr is the northernmost freshwater fish on earth, with a circumpolar distribution in the Holarctic that matches the last glaciation. Recent mtDNA studies indicate that there are five phylogeographic lineages (Atlantic, Arctic, Bering, Siberian and Acadian) that may be of Pleistocene origin. Phenotypic expression and ecology are more variable in charr than in most fish. Weights at maturation range from 3 g to 12 kg. Population differences in morphology and coloration are large and can have some genetic basis. Charr live in streams, at sea and in all habitats of oligotrophic lakes, including very deep areas. Ontogenetic habitat shifts between lacustrine habitats are common. The charr feed on all major prey types of streams, lakes and near-shore marine habitats, but has high niche flexibility in competition. Cannibalism is expressed in several cases, and can be important for developing and maintaining bimodal size distributions. Anadromy is found in the northern part of its range and involves about 40, but sometimes more days in the sea. All charr overwinter in freshwater. Partial migration is common, but the degree of anadromy varies greatly among populations. The food at sea includes zooplankton and pelagic fish, but also epibenthos. Polymorphism and sympatric morphs are much studied. As a prominent fish of glaciated lakes, charr is an important species for studying ecological speciation by the combination of field studies and experiments, particularly in the fields of morphometric heterochrony and comparative behaviour.

https://onlinelibrary.wiley.com/doi/pdf/10.1034/j.1600-0633.2003.00010.x

Atlantic salmon Salmo salar L., brown trout Salmo trutta L. and Arctic charr Salvelinus alpinus (L.): a review of aspects of their life histories

The physiological mechanisms limiting and adjusting cold and heat tolerance have regained interest in the light of global warming and associated shifts in the geographical distribution of ectothermic animals. Recent comparative studies, largely carried out on marine ectotherms, indicate that the processes and limits of thermal tolerance are linked with the adjustment of aerobic scope and capacity of the whole animal as a crucial step in thermal adaptation on top of parallel adjustments at the molecular or membrane level. In accordance with Shelford's law of tolerance decreasing whole animal aerobic scope characterises the onset of thermal limitation at low and high pejus thresholds (pejus=getting worse). The drop in aerobic scope of an animal indicated by falling oxygen levels in the body fluids and or the progressively limited capacity of circulatory and ventilatory mechanisms. At high temperatures, excessive oxygen demand causes insufficient oxygen levels in the body fluids, whereas at low temperatures the aerobic capacity of mitochondria may become limiting for ventilation and circulation. Further cooling or warming beyond these limits leads to low or high critical threshold temperatures (T(c)) where aerobic scope disappears and transition to an anaerobic mode of mitochondrial metabolism and progressive insufficiency of cellular energy levels occurs. The adjustments of mitochondrial densities and their functional properties appear as a critical process in defining and shifting thermal tolerance windows. The finding of an oxygen limited thermal tolerance owing to loss of aerobic scope is in line with Taylor's and Weibel's concept of symmorphosis, which implies that excess capacity of any component of the oxygen delivery system is avoided. The present study suggests that the capacity of oxygen delivery is set to a level just sufficient to meet maximum oxygen demand between the average highs and lows of environmental temperatures. At more extreme temperatures only time limited passive survival is supported by anaerobic metabolism or the protection of molecular functions by heat shock proteins and antioxidative defence. As a corollary, the first line of thermal sensitivity is due to capacity limitations at a high level of organisational complexity, i.e. the integrated function of the oxygen delivery system, before individual, molecular or membrane functions become disturbed. These interpretations are in line with the more general consideration that, as a result of the high level of complexity of metazoan organisms compared with simple eukaryotes and then prokaryotes, thermal tolerance is reduced in metazoans. A similar sequence of sensitivities prevails within the metazoan organism, with the highest sensitivity at the organismic level and wider tolerance windows at lower levels of complexity. However, the situation is different in that loss in aerobic scope and progressive hypoxia at the organismic level define the onset of thermal limitation which then transfers to lower hierarchical levels and causes cellular and molecular disturbances. Oxygen limitation contributes to oxidative stress and, finally, denaturation or malfunction of molecular repair, e.g. during suspension of protein synthesis. The sequence of thermal tolerance limits turns into a hierarchy, ranging from systemic to cellular to molecular levels.

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Climate variations and the physiological basis of temperature dependent biogeography: systemic to molecular hierarchy of thermal tolerance in animals.

Global climate change is frequently considered a major conservation threat. The Earth's climate has already warmed by 0.5 8 C over the past century, and recent studies show that it is possible to detect the ef- fects of a changing climate on ecological systems. This suggests that global change may be a current and fu- ture conservation threat. Changes in recent decades are apparent at all levels of ecological organization: pop- ulation and life-history changes, shifts in geographic range, changes in species composition of communities, and changes in the structure and functioning of ecosystems. These ecological effects can be linked to recent population declines and to both local and global extinctions of species. Although it is impossible to prove that climate change is the cause of these ecological effects, these findings have important implications for conser- vation biology. It is no longer safe to assume that all of a species' historic range remains suitable. In drawing attention to the importance of climate change as a current threat to species, these studies emphasize the need for current conservation efforts to consider climate change in both in situ conservation and reintroduction efforts. Additional threats will emerge as climate continues to change, especially as climate interacts with other stressors such as habitat fragmentation. These studies can contribute to preparations for future chal- lenges by providing valuable input to models and direct examples of how species respond to climate change.

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Ecological Consequences of Recent Climate Change

Preface 1. Temperature thresholds for protein adaptation: when does temperature start to 'hurt'? G. N. Somero, and G. E. Hofmann 2. Membrane constraints to physiological function at different temperatures: does cholesterol stabilize membranes at elevated temperatures? J. C. Robertson, and J. R. Hazel 3. The effect of temperature on protein metabolism in fish: the possible consequences for wild Atlantic salmon (Salmo salar L.) stocks in Europe as a result of global warming I. D. McCarthy, and D. F. Houlihan 4. Thermal stress and muscle function in fish I. A. Johnston, and D. Ball 5. Factors which may limit swimming performance at different temperatures E. W. Taylor, S. Egginton, S. E. Taylor and P. J. Butler 6. Effects of temperature on cardiovascular performance A. P. Farrell 7. Temperature effects on the reproductive performance of fish G. Van Der Kraak, and N. W. Pankhurst 8. The effects of temperature on embryonic and larval development P. J. Rombough 9. Temperature and growth: modulation of growth rate via temperature change M. Jobling 10. Effects of climate change on cod (Gadus morhua) stocks K. Brander 11. Temperature effects on osmoregulatory physiology of juvenile anadromous fish S. D. McCormick, J. M. Shrimpton, and J. D. Zydlewski 12. Effects of temperature on xenobiotic metabolism C. J. Kennedy, and P. J. Walsh 13. Interactive effects of temperature and pollutant stress S. D. Reid, D. G. McDonald, and C. M. Wood 14. Behavioural compensation for long-term thermal change L. I. Crawshaw, and C. S. O'Connor 15. Thermal niche of fishes and global warming J. J. Magnuson, and B. T. DeStasio Index.

http://www.gbv.de/dms/sub-hamburg/563328592.pdf

Global Warming: Implications for Freshwater and Marine Fish

Adult brook trout (Salvelinus fontinalis) were exposed for up to 11 d to one of a matrix of 18 Al, low pH, and Ca2+ combinations, chosen as representive of acidified softwater environments in the w...

Effects of Aluminum and Low pH on Net Ion Fluxes and Ion Balance in the Brook Trout (Salvelinus fontinalis)

Exhausting activity results in a marked and immediate drop in blood pH which gradually returns to normal over the following 6h. The acidosis is caused largely by elevated Pco2 levels, which vary inversely with pH. Blood lactate concentration increases slowly, reaching a maximum at 2--4h post-exercise, and contributes significantly to the acidosis only late in the recovery period. The slow time course of lactic acid release into the blood permits temporal separation of the peak metabolic acidosis from the peak respiratory acidosis. Evidence is presented that a metabolic acid other than lactic also makes a modest contribution to the pH depression during the recovery period.

An analysis of changes in blood pH following exhausting activity in the starry flounder, Platichthys stellatus.

Gill samples from juvenile brook trout (Salvelinus fontinalis) acclimated to low-level aluminum at pH 5.2 showed severe damage by day 4, with necrosis and fusion of secondary lamellae and hyperplasia and hypertrophy of mucous cells. Over the following 20 d, there was a continual process of repair with proliferation and hypertrophy of mucous cells. Qualitative analysis of gill samples plus physiology and mortality data collected in a companion study indicated progressive development (by day 10 onward) of increasing acclimation to Al. Quantitative analysis of gill samples on day 13 showed that mucous cell volume density had tripled and mucous cell area had doubled in Al-exposed fish compared with control fish. A lamellar fusion index showed evidence of fusion in Al-exposed fish by day 4 with recovery to nearly control levels by day 13. Physiological disturbances appear to be directly related to the histological changes observed in the gill epithelium. At the cellular level, changes in either mucous cell pro...

Nature and time course of acclimation to aluminum in juvenile brook trout (Salvelinus fontinalis). II : Gill histology

Scaphognathite and heart-pumping frequencies, ventilation volume, cardiac output, oxygen uptake and oxygen transport by haemolymph have been studied in unrestrained Dungeness crabs ( Cancer magister ) before, immediately after, and during recovery from 20 min of enforced exhausting activity. Exercise increased oxygen uptake 4-fold. This increase was achieved by more than 2-fold elevation of both ventilation volume and cardiac output and by greater participation of haemocyanin in oxygen delivery. The elevated ventilation volume resulted entirely from an increase in scaphognathite pumping frequency, while the rise in cardiac output resulted largely from increase in stroke volume. Prior to exercise haemocyanin accounts for less than 50% of the oxygen delivered to the tissues. Following exercise this increases to over 80%, the additional oxygen release being mediated by a depression of prebranchial oxygen tension and a substantial Bohr effect resulting from build up of lactate ion in the haemolymph and subsequent fall in pH. These changes allowed % oxygen extraction from branchial water to be maintained at 28% despite a 2-fold increase in ventilation volume, and allowed an increase in %. oxygen extraction by the tissues. Despite these changes oxygen supply fell below demand during exercise, and considerable anaerobic metabolism resulted, as evidenced by a 9-fold increase in haemolymph lactate concentration. The resulting oxygen debt required 8–24 h for repayment. Aerobic metabolic scope, and mechanisms of increasing oxygen uptake and transport in this crab are compared with those of a range of fish species.

/pdf/ventilation-oxygen-uptake-and-haemolymph-oxygen-transport-31borzoxx3.pdf

D. G. McDonald

Papers

Global Warming: Implications for Freshwater and Marine Fish

Effects of Aluminum and Low pH on Net Ion Fluxes and Ion Balance in the Brook Trout (Salvelinus fontinalis)

An analysis of changes in blood pH following exhausting activity in the starry flounder, Platichthys stellatus.

Nature and time course of acclimation to aluminum in juvenile brook trout (Salvelinus fontinalis). II : Gill histology

Ventilation, Oxygen Uptake and Haemolymph Oxygen Transport, Following Enforced Exhausting Activity in the Dungeness Crab Cancer Magister