Behavioural responses of a south-east Australian floodplain fish community to gradual hypoxia

1. Hypoxic conditions occur frequently during hot, dry summers in the small lentic waterbodies (billabongs) that occur on the floodplains of the Murray‐Darling River system of Australia. Behavioural responses to progressive hypoxia were examined for the native and introduced floodplain fish of the Ovens River, an unregulated tributary of the Murray River in south‐east Australia. 2. Given the high frequency of hypoxic episodes in billabongs on the Ovens River floodplain, it was hypothesised that all species would exhibit behaviours that would confer a degree of hypoxia‐tolerance. Specifically, it was hypothesised that as hypoxia progressed, gill ventilation rates (GVRs) would increase and aquatic surface respiration (ASR) would become increasingly frequent. Fish were subjected to rapid, progressive hypoxia from normoxia to anoxia in open tanks. 3. All tested species exhibited behaviours consistent with their use of potentially hypoxic habitats. As hypoxia progressed, GVRs increased and all species, with the exception of oriental weatherloach, began to switch increasingly to ASR with 90% of individuals using ASR at various oxygen concentrations below 1.0 mg O₂ L⁻¹. Australian smelt, redfin perch and flat‐headed galaxias were the first three species to rise to ASR, with 10% of individuals using ASR by 2.55, 2.29 and 2.21 mg O₂ L⁻¹ respectively. Goldfish and common carp were the last two species to rise to ASR, with 10% of individuals using ASR by 0.84 and 0.75 mg O₂ L⁻¹ respectively. In contrast to other species, oriental weatherloach largely ceased gill ventilation and used air‐gulping as their primary means of respiration during severe hypoxia and anoxia. 4. Australian smelt, redfin perch and flat‐headed galaxias were unable to maintain ASR under severe hypoxia, and began exhibiting erratic movements, termed terminal avoidance behaviour, and loss of equilibrium. All other species continued to use ASR through severe hypoxia and into anoxia. Following a rise to ASR, GVRs either remained steady or decreased slightly indicating partial or significant relief from hypoxic stress for these hypoxia‐tolerant species. 5. Behavioural responses to progressive hypoxia amongst the fish species of the Ovens River floodplain indicate a generally high level of tolerance to periodic hypoxia. However, species‐specific variation in hypoxia‐tolerance may have implications for community structure of billabong fish communities following hypoxic events.     

烟台牟平海洋牧场季节性低氧对大型底栖动物群落的生态效应

由于气候变化和人类活动的影响, 世界许多海区尤其是近岸海区发生了不同程度的低氧现象, 导致海洋动物大量死亡, 对海洋生态系统产生了不同程度的影响。为明确烟台牟平海洋牧场低氧对大型底栖动物的生态效应, 我们于2016年夏季(6月、8月、9月共3个航次)在该海域进行现场调查, 分析低氧对大型底栖动物群落时空变化的影响。结果表明: 牟平海洋牧场8月低氧事件发生时, 大型底栖动物群落的优势种为短叶索沙蚕(Lumbrinereis latreilli)、不倒翁虫(Sternaspis scutata)和内肋蛤(Endopleura lubrica)。低氧在一定程度上改变了大型底栖动物的群落结构, 表现为物种组成和优势种变化上。例如, 耐受低氧的机会种数量增加, 如短叶索沙蚕; 敏感种数量减少, 如微小海螂(Leptomya minuta)、长吻沙蚕(Glycera chirori)、大蝼蛄虾(Upogebia major)、极地蚤钩虾(Pontocrates altamarimus)、塞切尔泥钩虾(Eriopisella sechellensis)等。同时, 低氧也导致了物种多样性的降低, 但丰度和生物量受其影响不明显, 这主要是由于机会种短叶索沙蚕丰度和生物量的剧增所致。大型底栖动物不同物种耐受低氧的阈值不同。例如, 短叶索沙蚕在溶解氧(DO) < 1.0 mg/L受影响最大, 在DO = 2.0 mg/L时受到的影响不明显, 而其他敏感种如微小海螂、大蝼蛄虾、极地蚤钩虾、塞切尔泥钩虾等在DO < 2.5 mg/L时, 已表现出明显的不适。低氧事件之后, 大型底栖动物群落得到一定程度的恢复, 其恢复程度和需要的时间长短与低氧发生的程度有关。     

Interaction of a biotic factor (predator presence) and an abiotic factor (low oxygen) as an influence on benthic invertebrate communities

We examined the response of benthic invertebrates to hypoxia and predation risk in bioassay and behavioral experiments. In the bioassay, four invertebrate species differed widely in their tolerance of hypoxia. The mayfly, Callibaetis montanus, and the beetle larva, Hydaticus modestus, exhibited a low tolerance of hypoxia, the amphipod, Gammarus lacustris, was intermediate in its response and the caddisfly, Hesperophylax occidentalis, showed high tolerance of hypoxia. In the behavioral experiments, we observed the response of these benthic invertebrates, which differ in locomotor abilities, to vertical oxygen and temperature gradients similar to those in an ice-covered pond. With adequate oxygen, invertebrates typically remained on the bottom substrate. As benthic oxygen declined in the absence of fish, all taxa moved above the benthic refuge to areas with higher oxygen concentrations. In the presence of fish mayflies increased activity whereas all other taxa decreased activity in response to hypoxia. Mayflies and amphipods remained in the benthic refuge longer and endured lower oxygen concentrations whereas the vertical distribution of caddisflies and beetle larvae was not influenced by the presence of fish. As benthic oxygen declined in the presence of fish, all but the beetle larva reduced activity over all oxygen concentrations compared to when fish were absent. As benthic oxygen continued to decline, mayflies and amphipods moved above the benthic refuge and were preyed upon by fish. Thus, highly mobile taxa unable to tolerate hypoxia (mayflies and amphipods) responded behaviorally to declining oxygen concentrations by migrating upward in the water column. Taxa that were less mobile (beetle larvae) or hypoxia-tolerant (caddisflies) showed less of a response. Taxa most vulnerable to fish predation (mayflies and amphipods) showed a stronger behavioral response to predator presence than those less vulnerable (caddisflies and beetle larvae). Because invertebrates differ in their ability to withstand hypoxia, episodes of winter hypoxia could have long-lasting effects on benthic invertebrate communities either by direct mortality or selective predation on less tolerant taxa.     

Quantifying Hypoxia Impacts on an Estuarine Demersal Community Using a Hierarchical Ensemble Approach

In coastal marine ecosystems, hypoxia and anoxia are emerging as growing threats whose ecological impacts are difficult to ascertain because of the frequent lack of adequate references for comparison. We applied conventional and hierarchical ensemble analyses to evaluate the weight of evidence in support of hypoxia impacts on local densities of individual and groups of demersal fish and invertebrate species in Hood Canal, WA, which is subject to seasonal hypoxia in its southern reaches. Central to our approach was a sample design and analysis scheme that was designed specifically to consider multiple alternative hypotheses regarding factors that dictate local species’ densities. We anticipated persistent effects of hypoxia (felt even when seasonal hypoxia was absent) on species densities would be most pronounced for sessile species, but that immediate effects (felt only when seasonal hypoxia was present) would dominate for mobile species. Conventional analysis provided strong evidence that densities of sessile species were persistently reduced in the hypoxic-impacted site, but did not indicate widespread immediate density responses during hypoxic events among mobile species. The absence of strong weights of evidence for hypoxia effects was partly a consequence of alternative hypotheses that better explained spatial-temporal variation in species’ densities. The hierarchical ensemble analysis improved the precision of species-specific effect sizes, and also allowed us to make inferences about the response of aggregated groups of species. The estimated mean density reductions during hypoxic events (dissolved oxygen ~2 mg/l) ranged from 73 to 98% among mobile invertebrates, benthic, and benthopelagic fishes. The large reduction in benthic and benthopelagic species suggests substantial effects of hypoxia in Hood Canal even at oxygen levels that were marginally hypoxic. Understanding the full ecological consequence of hypoxia will require a greater knowledge on the spatial extent of distributional shifts and their effects on competitive and predator–prey interactions.     

Exposure to hypoxia primes the respiratory and metabolic responses of the epaulette shark to progressive hypoxia

The majority of vertebrates are not tolerant to hypoxia but epaulette sharks (Hemiscyllium ocellatum) living on shallow reef platforms appear to tolerate hypoxic periods during tidal fluctuations. The effects of progressive hypoxia on the metabolic and ventilatory responses of these elasmobranchs were examined in a closed respirometer. In order to determine whether repeated exposure to hypoxia primes these sharks to alter their metabolism, one group of sharks was exposed to repeated sub-lethal hypoxia, at 5% of air saturation, prior to respirometry. In response to falling oxygen concentration [O(2)], the epaulette shark increased its ventilatory rate and maintained its O(2) consumption rate (VO(2)) down to 2.2 mg O(2) l(-1) at 25 degrees C. This is the lowest critical [O(2)] ([O(2)](crit)) ever measured for any elasmobranch. After reaching the [O(2)](crit), the shark remained in the respirometer for a further 4-5 h of progressive hypoxia. Only after the [O(2)] fell to 1.0 mg l(-1) was there a decrease in the ventilatory rate followed by a rise in blood lactate levels, indicating that the epaulette shark responds to severe hypoxia by entering a phase of metabolic and ventilatory depression. Interestingly, hypoxia tolerance was dynamic because hypoxic pre-conditioning lowered the VO(2) of the epaulette shark by 29%, which resulted in a significantly reduced [O(2)](crit) (1.7 mg O(2) l(-1)), revealing that hypoxic pre-conditioning elicits an enhanced physiological response to hypoxia.     

Seasonal structuring of a benthic community exposed to regular hypoxic events

The Western Trough of the Lough Hyne Marine Reserve in southern Ireland features annual episodes of profound hypoxia beneath an oxy-thermocline that develops each summer. Previous work had indicated that the hypoxia caused mass mortality of the sessile benthic fauna, but information about the winter fauna, or about mobile species was lacking. Here we report on a combined remote-operated vehicle, SCUBA and baited trap study, backed by regular oxygen-temperature-depth monitoring of the Trough. Our results show that there is community of resident benthic and mobile species during the oxic winter months that disappears in the summer. Mobile fish and crustaceans avoid the hypoxic areas of the Trough, though the prawn Palaemon serratus will venture into the hypoxic zone to scavenge on baits. At the oxy-thermocline itself, burrows of benthic fauna remain evident in summer, but their inhabitants show much reduced activity or death. Regular hypoxic episodes clearly structure the benthic community of the Trough, but this is not a simple matter of alternating mass mortality and recolonization; mobile species are clearly capable of avoiding the hypoxic zone in summer, but benefit from its productivity in winter and spring.     

Direct and indirect effects of hypoxia on benthos in Corpus Christi Bay, Texas, U.S.A.

Hypoxia (low oxygen conditions) has been found in the southeastern region of Corpus Christi Bay, Texas, U.S.A. every summer since 1988. The objectives of the current study were to determine direct and indirect effects of hypoxia on macrofauna. Direct physiological effects of hypoxia include reduction of benthic abundance, biomass, diversity, species richness and species evenness because of physiological intolerance. Indirect ecological effects of hypoxia include predation of emerging benthic fauna from the sediment. Macrofaunal community characteristics were compared vertically within sediments in caged and uncaged sediment samples in hypoxic and normoxic areas. Cage effects were determined with partial cages, which had reduced flow and no predator exclusion. Dissolved oxygen concentrations during the experiment was monitored in water column profiles and continuous measurement of bottom water in the hypoxic and normoxic areas. Hypoxia in Corpus Christi Bay in 1999 occurred as transient events, many of which were of short duration (less than 1 h) and moderate intensity (around 2 mg l^− 1). The macrobenthic community characteristics (i.e., abundance, biomass, species richness, diversity, and evenness) were directly affected by hypoxia as indicated by depressed levels and few deeper-dwelling organisms in the hypoxic area. Community structure was also different between the hypoxic and normoxic areas because of loss of species (presumably due to intolerance to low oxygen) in the hypoxic areas. Benthic invertebrates were found primarily in the surface in the hypoxic area, but there was no significant indication of indirect effects, i.e., increased predation pressure in the hypoxic area. The increased exposure to predation risk may be mitigated by predator avoidance of hypoxic areas. In conclusion, hypoxia in Corpus Christi Bay has negative direct effects on benthic organisms, but no indirect effects, such as increased predation pressure. The most significant finding is the interaction between hypoxia and vertical distributions of infauna, which drive hypoxia intolerant organisms to the surface and out of sediments.     

Physiological biomarkers of hypoxic stress in red swamp crayfish Procambarus clarkii from field and laboratory experiments

The crayfish industry in Louisiana is the largest in the United States, with crayfish frequently harvested from waters that experience episodic or chronic hypoxia (dissolved oxygen [DO]≤ 2 mg/l). We examined physiological biomarkers (hemolymph lactate, glucose, and protein concentrations) of hypoxic stress in the red swamp crayfish Procambarus clarkii from chronically hypoxic natural habitats and laboratory hypoxia experiments. P. clarkii from normoxic and hypoxic areas in the Atchafalaya River Basin were sampled monthly from April to July 2010. Laboratory experiments subjected P. clarkii to severe hypoxia (1 mg/l DO), moderate hypoxia (2 mg/l DO), or normoxic conditions (control: DO>7.5 mg/l) for 12, 24, and 48 h. P. clarkii from normoxic and hypoxic natural habitats did not display significantly different hemolymph lactate or glucose concentrations; however, mean hemolymph protein concentration was significantly lower in crayfish from hypoxic areas. P. clarkii exposed to severe hypoxia in laboratory experiments had significantly higher hemolymph lactate and glucose concentrations for all three exposure times, whereas large differences in protein concentrations were not observed. These results suggest that elevated hemolymph lactate and glucose concentrations are responses to acute hypoxia in P. clarkii, while differences in protein concentrations are the result of chronic hypoxic exposure.     

Hypoxia,Blackwater and Fish Kills: Experimental Lethal Oxygen Thresholds in Juvenile Predatory Lowland River Fishes

Hypoxia represents a growing threat to biodiversity in freshwater ecosystems. Here, aquatic surface respiration (ASR) and oxygen thresholds required for survival in freshwater and simulated blackwater are evaluated for four lowland river fishes native to the Murray-Darling Basin (MDB), Australia. Juvenile stages of predatory species including golden perch Macquaria ambigua, silver perch Bidyanus bidyanus, Murray cod Maccullochella peelii, and eel-tailed catfish Tandanus tandanus were exposed to experimental conditions of nitrogen-induced hypoxia in freshwater and hypoxic blackwater simulations using dried river red gum Eucalyptus camaldulensis leaf litter. Australia''s largest freshwater fish, M. peelii, was the most sensitive to hypoxia but given that we evaluated tolerances of juveniles (0.99±0.04 g; mean mass ±SE), the low tolerance of this species could not be attributed to its large maximum attainable body mass (>100,000 g). Concentrations of dissolved oxygen causing 50% mortality (LC₅₀) in freshwater ranged from 0.25±0.06 mg l⁻¹ in T. tandanus to 1.58±0.01 mg l⁻¹ in M. peelii over 48 h at 25–26°C. Logistic models predicted that first mortalities may start at oxygen concentrations ranging from 2.4 mg l⁻¹ to 3.1 mg l⁻¹ in T. tandanus and M. peelii respectively within blackwater simulations. Aquatic surface respiration preceded mortality and this behaviour is documented here for the first time in juveniles of all four species. Despite the natural occurrence of hypoxia and blackwater events in lowland rivers of the MDB, juvenile stages of these large-bodied predators are vulnerable to mortality induced by low oxygen concentration and water chemistry changes associated with the decomposition of organic material. Given the extent of natural flow regime alteration and climate change predictions of rising temperatures and more severe drought and flooding, acute episodes of hypoxia may represent an underappreciated risk to riverine fish communities.     

Difference in the hypoxia tolerance of the round crucian carp and largemouth bass: implications for physiological refugia in the macrophyte zone

The hypoxia tolerance of larval and juvenile round crucian carp, Carassius auratus grandoculis, and largemouth bass, Micropterus salmoides, was determined using respirometry to examine the potential of hypoxic areas in the macrophyte zone as physiological refugia for round crucian carp. The tolerance, which was measured as the critical oxygen concentration (Pc), was 1.32 mg O₂/l in the round crucian carp and 1.93 mg O₂/l in the largemouth bass. As the round crucian carp tolerated hypoxia better than the largemouth bass, hypoxic areas in the macrophyte zone might function as physiological refugia for round crucian carp.     

Seasonal Differences in Hypoxia Tolerance in Gulf Killifish, Fundulus Grandis (Fundulidae)

Many estuarine habitats are characterized by episodes of hypoxia, the frequency and severity of which may vary seasonally. Accordingly, resident fish species may show seasonal differences in their capacity to tolerate hypoxia. We have tested this hypothesis in the gulf killifish, Fundulus grandis, sampled from the Lake Pontchartrain estuary (Louisiana) at different times of the year. We measured 2 indicators of hypoxia tolerance, the frequency of aquatic surface respiration (ASR) during gradual reduction in dissolved oxygen (D.O.) and survival time during severe hypoxic stress, and found both to be significantly affected by season. Fish collected during the summer did not engage in ASR until the D.O. concentration dropped to values lower than that required to elicit ASR by fish collected during other seasons. Laboratory acclimation of fish to low oxygen did not change the relationship between ASR behavior and D.O., suggesting that the observed seasonal effect on ASR was not simply due to previous exposure of summer fish to environmental hypoxia. Furthermore, fish collected during the summer and winter had significantly longer survival times during exposure to severe hypoxia than fish collected during the fall. Survival analysis indicated that the condition of fish was positively associated with survival time, and seasonal variation in condition accounted for about half of the observed difference between survival times of fish collected during the summer and fall. Seasonal variation in ASR and survival, when taken together, demonstrate that hypoxia tolerance in F. grandis may be subject to acclimatization. An increase in hypoxia tolerance during the summer could increase survivorship of fish when exposed to elevated temperatures and low oxygen concentrations which prevail during the summer months.     

Respiratory responses and tolerance to hypoxia in two marine teleosts,Epinephelus akaara (Temminck & Schlegel) and Mylio macrocephalus (Basilewsky)

The respiratory responses and tolerance of hypoxia were studied in two marine teleosts, the red grouper (Epinephelus akaara, a sluggish species) and the black sea bream (Mylio macrocephalus, an active species). Neither species showed abnormal behaviour or mortality when exposed to 2 mg O₂ l^–1 for 7 h. The black sea bream was, however, comparatively more tolerant when exposed to 1 mg O₂ l^–1, but tolerance of both species became similar under extremely hypoxic conditions (i.e. 0.5 mg O₂ l^–1). In contrast to most other teleosts, both species showed a reduction in opercular beating rate during hypoxia, and oxygen conformity was found in the range of 0.5 to 7.0 mg O₂l ^–1. O₂ dissociation curves were constructed, and the P₅₀ value of the black sea breams (27 ± 5.6 mm Hg) was found to be much lower than that of the red groupers (50 ± 2.5 mm Hg). For both species, the general levels of venous PO₂ showed a direct relationship to ambient PO₂, and were markedly reduced after 1 h exposure to various levels of hypoxia. Compared with the red groupers, the black sea breams appeared to be more able to maintain its venous PO₂ levels during prolonged hypoxic exposure.     

Behavioral effects of low dissolved oxygen on the bivalve Macoma balthica

Hypoxia, a dissolved oxygen concentration (DO) below 2 mg l^– 1, is a significant stressor in many estuarine ecosystems. Many sedentary organisms, unable to move to avoid hypoxic areas, have metabolic and behavioral adaptations to hypoxic stress. We tested the effects of hypoxia on the behavior and mortality of the clam Macoma balthica, using four levels of dissolved oxygen in flow-through tanks. We used five replicates of each of four treatments: (1) Hypoxic (DO mean ± SE = 1.1 ± 0.06 mg O₂ l^– 1), (2) Moderately hypoxic (DO 2.6 ± 0.05 mg O₂ l^– 1), (3) Nearly normoxic (DO 3.2 ± 0.04 mg O₂ l^– 1), (4) Normoxic (DO = 4.9 ± 0.13 mg O₂ l^– 1). We lowered the dissolved oxygen with a novel fluidized mud-bed, designed to mimic field conditions more closely than the common practice of solely bubbling nitrogen or other gasses. This method for lowering the DO concentrations for a laboratory setup was effective, producing 1.4 l min^–1 of water with a DO of 0.8 mg O₂ l^– 1 throughout the experiment. The setup greatly reduced the use of compressed nitrogen and could easily be scaled up to produce more low-DO water if necessary. The lethal concentration for 50% of the M. balthica population (LC₅₀) was 1.7 mg O₂ l^– 1 for the 28-day experimental period. M. balthica decreased its burial depth under hypoxic and moderately hypoxic (~2.5 mg O₂ l^– 1) conditions within 72 hours of the onset of hypoxia. By the sixth day of hypoxia the burial depth had been reduced by 26 mm in the hypoxic tanks and 10 mm in the moderately hypoxic tanks. Because reduced burial depth makes the clams more vulnerable to predators, these results indicate that the sub-lethal effects of hypoxia could change the rate of predation on M. balthica in the field.     

Characterization of three IGFBP mRNAs in Atlantic croaker and their regulation during hypoxic stress: potential mechanisms of their upregulation by hypoxia

Insulin-like growth factor-binding proteins (IGFBPs) play important roles in downregulating IGF activity and growth and development in vertebrates under hypoxic stress. However, the mechanisms of hypoxia regulation of IGFBPs in teleost fishes are unknown. The involvement of reactive oxygen species (ROS) and hypoxia-inducible factors (HIFs) in hypoxia upregulation of IGFBPs in Atlantic croaker were investigated. Three croaker IGFBPs, IGFBP-1, IGFBP-2, and IGFBP-5, were cloned and characterized. Chronic hypoxia exposure [dissolved oxygen (DO): 1.7 mg/l for 2-4 wk] caused significant increases in hepatic and neural IGFBP-1 mRNA expression compared with tissue mRNA levels in fish held under normoxic conditions (6.5 mg DO/l). Moreover, longer-term chronic hypoxia exposure (2-2.7 mg DO/l for 15-20 wk) caused significant increases in mRNA levels of all three IGFBPs in both liver and brain tissues. Hypoxia exposure also markedly increased superoxide radical (O(2)(·-), an index of ROS) production and HIF-1α mRNA and HIF-2α protein expression in croaker livers. Pharmacological treatment with an antioxidant attenuated the hypoxia-induced increases in O(2)(·-) production and HIFα mRNA and protein expression as well as the elevation of IGFBP-1 mRNA levels. These results suggest that the upregulation of IGFBP expression under hypoxia stress is due, in part, to alterations in the antioxidant status, which may involve ROS and HIFs.     

Intermittent hypoxic training and L-arginine as corrective agents for myocardial energy supply under acute hypoxia

It NO has been shown play to the primary role in several mitochondrial functions. Our aim for this study was to investigate whether exogenous NO (L-arginine) or NO blocker L-NNA modulated the adaptive reactions of rat myocardial tissue respiration on intermittent hypoxic training (IHT). In the control rats an acute hypoxic test (inhalation of 7% O2, 30 min) provoked sharp augmentation of ADP-stimulated tissue respiration with the increase of respiratory coefficient and phosphorylation rate, the decrease of O2 uptake efficacy and switching the energy supply to succinate oxidation pathway. The same hypoxic test but following 14 days of IHT (11% O2, 15-min sessions with 15 min rest intervals, 5 times daily) produced a stimulation of oxidative phosphorylation with primary activation of NAD-dependent pathway, the marked increase of ADP/O ratio. The combination of IHT with L-arginine treatment (600 mg/kg intraperitoneally, daily before IHT sessions) provoked the decrease of tissue oxygen consumption in comparison with untrained animals. L-arginine effects abolished by the NO-synthase blocker L-NNA. Its effects on mitochondrial function deals with succinic acid inhibition utilizatin (increasing level ADP/O) and activation NADH-dependent oxidation. We conclude that the combination of IHT with NO-precursor treatment was capable to increase significantly the tolerance to episodes of acute hypoxia.     

Night-time lighting alters the composition of marine epifaunal communities

Marine benthic communities face multiple anthropogenic pressures that compromise the future of some of the most biodiverse and functionally important ecosystems in the world. Yet one of the pressures these ecosystems face, night-time lighting, remains unstudied. Light is an important cue in guiding the settlement of invertebrate larvae, and altering natural regimes of nocturnal illumination could modify patterns of recruitment among sessile epifauna. We present the first evidence of night-time lighting changing the composition of temperate epifaunal marine invertebrate communities. Illuminating settlement surfaces with white light-emitting diode lighting at night, to levels experienced by these communities locally, both inhibited and encouraged the colonization of 39% of the taxa analysed, including three sessile and two mobile species. Our results indicate that ecological light pollution from coastal development, shipping and offshore infrastructure could be changing the composition of marine epifaunal communities.     

Interactive effects of episodic hypoxia and cannibalism on juvenile blue crab mortality

We hypothesized that as the spatial extent of hypoxic bottom water increased, (1) adult blue crab predator densities would increase in shallow habitats as they avoided hypoxia, and that (2) juvenile blue crabs, which use shallow unvegetated habitat as a predation refuge from adult conspecifics, would experience increased mortality rates during crowding by cannibalistic adult blue crabs. These hypotheses were tested along a depth gradient of sandy-mud shoreline in the Neuse River Estuary (NRE), North Carolina, USA using a combination of (1) hydrographic measurements to characterize the spatial extent of hypoxia, (2) beach seines to quantify the density of adult blue crab predators in relatively shallow water as a function of 1, and (3) tethering experiments to quantify relative rates of predation on juvenile blue crabs as a function of 1 and 2. During our seven tethering experiments, the NRE study site experienced a range of DO scenarios including normoxia, chronic hypoxia, and hypoxic upwelling. No known predators of juvenile blue crabs, other than adult conspecifics, were collected in any of our shallow-water seines. During the transition from normoxia to chronic hypoxia, blue crab predator densities in shallow refuge habitats increased 4-fold, and relative mortality rates of juvenile blue crabs in shallow habitats increased exponentially with the density of adult conspecifics. Conversely, during hypoxic upwelling events, the density of adult blue crabs in shallow water declined, which may explain why the relative mortality of juvenile crabs did not increase significantly with the increasing spatial extent of hypoxia. Thus, juvenile blue crabs may be relatively safe from adult conspecifics during hypoxic upwelling events, but not during chronic hypoxia. These experimental results highlight the need to consider the effects of dynamic water quality on mobile consumers emigrating from degraded habitats when considering indirect trophic impacts beyond the immediate area of impact.     

Metabolic adjustments in two Amazonian cichlids exposed to hypoxia and anoxia

The effects of graded hypoxia on the physiological and biochemical responses were examined in two closely related species of cichlids of the Amazon: Astronotus crassipinnis and Symphysodon aequifasciatus. Ten fish of each species were exposed to graded hypoxia for 8 h in seven oxygen concentrations (5.92, 3.15, 1.54, 0.79, 0.60, 0.34, and 0.06 mg O(2) L(-)(1)), with the aim to evaluate hypoxia tolerance and metabolic adjustments, where plasma glucose and lactate levels, hepatic and muscle glycogen contents, and maximum enzyme activities (PK, LDH, MDH and CS) in skeletal and cardiac muscles were measured. Another experimental set was done to quantify oxygen consumption (MO(2)) and opercular movements in two oxygen concentrations. Hypoxia tolerance differed between the two species. Astronotus crassipinnis was able to tolerate anoxia for 178 min while S. aequifasciatus was able to withstand 222 min exposure in deep hypoxia (0.75 mg O(2) L(-)(1)). Suppressed MO(2) was observed during exposure to 0.34 (A. crassipinnis) and 0.79 mg O(2) L(-)(1) (S. aequifasciatus), while opercular movements increased in both species exposed to hypoxia. Higher levels of muscle and liver glycogen and larger hypoxia-induced increases in plasma glucose and lactate were observed in A. crassipinnis, which showed a higher degree of hypoxia tolerance. Changes in enzyme levels were tissue-specific and differed between species suggesting differential abilities in down-regulating oxidative pathways and increasing anaerobic metabolism. Based on the present data, we conclude that these animals are good anaerobes and highly adapted to their environment, which is allowed by their abilities to regulate metabolic pathways and adjust their enzyme levels.     

Metabolic and cardiorespiratory responses of summer flounder Paralichthys dentatus to hypoxia at two temperatures

To quantify the tolerance of summer flounder Paralichthys dentatus to episodic hypoxia, resting metabolic rate, oxygen extraction, gill ventilation and heart rate were measured during acute progressive hypoxia at the fish's acclimation temperature (22° C) and after an acute temperature increase (to 30° C). Mean ±s.e. critical oxygen levels (i.e. the oxygen levels below which fish could not maintain aerobic metabolism) increased significantly from 27 ± 2% saturation (2·0 ± 0·1 mg O(2) l(-1) ) at 22° C to 39 ± 2% saturation (2·4 ± 0·1 mg O(2) l(-1) ) at 30° C. Gill ventilation and oxygen extraction changed immediately with the onset of hypoxia at both temperatures. The fractional increase in gill ventilation (from normoxia to the lowest oxygen level tested) was much larger at 22° C (6·4-fold) than at 30° C (2·7-fold). In contrast, the fractional decrease in oxygen extraction (from normoxia to the lowest oxygen levels tested) was similar at 22° C (1·7-fold) and 30° C (1·5-fold), and clearly smaller than the fractional changes in gill ventilation. In contrast to the almost immediate effects of hypoxia on respiration, bradycardia was not observed until 20 and 30% oxygen saturation at 22 and 30° C, respectively. Bradycardia was, therefore, not observed until below critical oxygen levels. The critical oxygen levels at both temperatures were near or immediately below the accepted 2·3 mg O(2) l(-1) hypoxia threshold for survival, but the increase in the critical oxygen level at 30° C suggests a lower tolerance to hypoxia after an acute increase in temperature.     

Hypoxia tolerance in two juvenile estuary-dependent fishes

Hypoxia events, or low dissolved oxygen (DO) conditions, occur frequently in North Carolina estuaries during the summer. These events may have harmful effects on important fish stocks, including spot (Leiostomus xanthurus) and Atlantic menhaden (Brevoortia tyrannus), but their consequences are not well understood. We investigated direct mortality due to hypoxia in juvenile spot and Atlantic menhaden to determine how the extent of mortality varies with the severity of hypoxia and the duration of exposure, and to explore how vulnerability to hypoxia changes across species, fish size, and temperature.Atlantic menhaden and spot were tested at two temperatures, 25 and 30 °C, and three dissolved oxygen concentrations, 0.6, 0.9, and 1.2 ppm. Survival analyses were performed on the data relating survival rate of each species to dissolved oxygen concentration, duration of exposure, fish size, and temperature. The data were analyzed using an LC₅₀ approach for comparative purposes, and 12-h LC₅₀ estimates ranged from 0.9 to 1.1 ppm O₂. Spot and menhaden exposed to 1.2 ppm O₂ showed no mortality in 24 h at 25 °C, and only 30-40% mortality at 30 °C. In contrast, both species experienced 100% mortality in 2-6 h at 0.6 ppm O₂. There was an effect of size on hypoxia tolerance, with small spot being less tolerant than large spot, while the converse size effect was observed for menhaden. Spot were consistently less tolerant to hypoxia than menhaden and both species were less tolerant to hypoxia at 30 °C than at 25 °C. Preliminary experiments showed a 24-h acclimation to sublethal levels of hypoxia significantly reduced mortality upon subsequent exposure to lethal hypoxia concentrations.Our results indicate that direct mortality due to hypoxia will vary with species, size, and temperature, but will likely only be substantial when these species are exposed to oxygen concentrations less than about 1 ppm O₂. Given the severity of hypoxia necessary to cause mortality and the ability of fish to behaviorally avoid hypoxia, direct mortality due to hypoxia may have limited impacts on fish population dynamics. Therefore, the greatest effects due to hypoxia may be caused by the stress imposed by sublethal hypoxic conditions alone or in concert with other stressors, or by indirect effects incurred by avoiding hypoxic areas.