Carapace movements associated with ventilation and irrigation of the branchial chambers in the semaphore crab,Heloecius cordiformis (Decapoda: Brachyura: Ocypodidae)

Summary Carapace movements in crabs are briefly reviewed. While on land and recirculating branchial water, the Australian semaphore crab Heloecius cordiformis (Decapoda: Ocypodidae), a semi-terrestrial air-breathing mangrove crab, sequentially depresses and elevates its carapace relative to its thorax (0.5–1 mm excursion) in a regular pump-like manner. In quiescent crabs each carapace-pumping cycle lasts about 4 s; carapace depression takes 3 s and elevation 1 s. Carapace movements are brought about by pressures generated within the branchial chambers by the scaphognathites, probably in combination with carapace muscles. Carapace movements are associated with bilaterally synchronised scaphognathite activity. Unilateral scaphognathite activity was not observed. During normal forward recirculation of branchial water the scaphognathites beat at about 1.5 Hz (slow-forward pumping) and the lungs (epibranchial chambers) are not ventilated. In Heloecius, the lungs are not physically separated from the gills below by an anatomical barrier. Lung ventilation is accomplished during the following sequence of events: the carapace is lowered and the scaphognathites pump in a fast-forward mode at about 2.8 Hz. This activity preferentially pumps air out of the lungs and generates suction within the branchial chambers (4–10 cm H₂O below ambient) which draws water from external body surfaces into the hypobranchial space below and around the gills. At the end of the carapace's downward travel the scaphognathites switch from fast-forward to fastreverse beating at about 4 Hz. This pumps air into the lungs and the carapace elevates. As a result, during carapace elevation the water which had previously been drawn into the branchial chambers by fast-forward pumping activity is released and flows out between the legs and into the abdominosternal cavity. When the carapace reaches its original resting or up position the scaphognathites switch from fast-reverse to slowforward beating to re-establish water recirculation through the branchial chambers. This cycle is subsequently repeated. In stationary crabs, there are 2 carapace-pumping cycles per minute, increasing to 14 per minute in active crabs (walking). When water is absent, the lungs are preferentially ventilated by slow-reverse scaphognathite pumping activity. Carapace movements do not occur in the absence of branchial water. Carapace pumping is thought to provide a mechanism which permits the scaphognathites to ventilate the lungs in the presence of recirculating branchial water, without this water interfering with lung ventilation or being lost to the environment.Abbreviations FF, FR, SF, SR fast-forward, fast-reverse, slowforward, slow-reverse scaphognathite pumping - MEA Milne Edwards aperture     

Carapace movements aid air breathing in the semaphore crab,Heloecius cordiformis (Decapoda: Brachyura: Ocypodidae)

Summary While on land and recirculating branchial water the Australian semaphore crab Heloecius cordiformis (Decapoda: Ocypodidae), a semi-terrestrial airbreathing mangrove crab, sequentially depresses and elevates its carapace in a regular pump-like manner. The functional role of these carapace movements in aerial oxygen consumption is investigated. Carapace immobilisation (reversible and non-injurious) did not appear to affect branchial water circulation. In dry crabs (branchial water removed) carapace immobilisation had no effect on the rate of oxygen consumption (VO₂), heart rate or whole-body lactate (WBL) levels. In wet crabs (with branchial water) carapace immobilisation caused VO₂ to drop by 38% from 81 to 46 l O₂ · g^-1 · h^-1, heart rate to decline by 32%, from 2.5 to 1.7 Hz, and WBL levels to increase over 2.5-fold, from 0.27 to 0.67 mg · g^-1, after 3 h of carapace immobilisation. The (VO₂) of carapace-immobilised crabs with branchial water was similar to lung-occluded crabs with branchial water. Severe hypoxia induced physiological responses similar to those of carapace-immobilised crabs with branchial water. After 3 h of severe hypoxia, heart rate had declined by 80%, from 2.2 to 0.43 Hz, and the incidence of carapace pumping slowed by 85%, from 2.4 to 0.37 cycles · min^-1. It is concluded that in the absence of carapace movements branchial water in some way inteferes with lung ventilation. Under normal circumstances water circulation and lung ventilation are mutually exclusive processes (due to their singular dependence on the scaphognathites), yet in Heloecius these processes must be carried out simultaneously. Carapace movements may alleviate this conflict.Abbreviations FF, FR, SF, SR fast-forward, fast-reverse, slow-forward, slow-reverse scaphognathite pumping - MEA Milne Edwards aperture - VO₂ rate of oxygen consumption - WBL whole-body lactate     

Respiratory rate,haemolymph oxygen tension and haemocyanin level in the shrimp Palaemon adspersus: Rathke

The marine shrimp Palaemon adspersus Rathke, frequenting Zostera meadows, shows an oxygen consumption rate (MO₂) that is independent of water oxygen tension (P_wO₂) as PO₂ decreases to a critical point (P_cr) near 70 mm Hg. This respiratory independence is associated with maintenance of a relatively constant “arterial” (post-branchial) haemolymph tension (P_aO₂) at 70–80 mm Hg. At lower P_wO₂ values, both MO₂ and P_aO₂ fall, reflecting, in contrast to the above independence, a direct dependence of MO₂ on internal PO₂.Haemolymph copper measurements demonstrate relatively high haemocyanin concentrations and oxygen-carrying capacities, but MO₂ levels reflect an insignificant rôle for the pigment as an oxygen store.The data are discussed as regards adaptations for aerobic metabolism.     

Effects of evisceration on oxygen consumption by Stichopus parvimensis Clark (Echinodermata: Holothuroidea)

Near Santa Barbara, California, autotomy of the principal viscera (evisceration) by the holothurian Stichopus parvimensis Clark occurs during October and November, but not during the remainder of the year. The loss of both respiratory trees significantly affects neither the pattern nor magnitude of oxygen consumption relative to that of intact animals. Intact S. parvimensis regulate oxygen consumption over the range of oxygen tensions from P₀₂ = 50 mm Hg to air saturation, while animals without viscera are independent of oxygen tension above a P₀₂ of 75 mm Hg.     

The oxygen consumption of mayfly (Ephemeroptera) and stonefly (Plecoptera) larvae at different oxygen concentration

1. The aim of this investigation was to elucidate how four acquatic insect larvae, from different habitats and having different respiratory organs or types of respiratory regulation, react to a lowered oxygen concentration, and how their oxygen consumption is affected. The species investigated were the stoneflies Taeniopteryx nebulosa, Diura nanseni and Nemoura cincerea and the mayfly Cloëon dipterum.
2. The measurements were performed in a respiratory apparatus of open, flowing-water type. Its design is shown in Fig. 1. Water of known oxygen concentration was allowed to flow past the experimental larvae. The oxygen consumption of the larvae was calculated from the lowering of the oxygen concentration in which ensued.
3. The water used in the experiments was standardized, so that the electrode had the necessary stability (conductivity 470 micromhos/cm). The calcium ion was excluded in order to prevent the precipitation of CaCO₃ in the electrode capillary.
4. A large variation in the values of oxygen consumption was found as seen in Fig. 2–5. The reason for that is a corresponding variation in the motor activity of the experimental animals.
5. The physiological reasons for the general form of the curves A and C in Fig. 2–5 are discussed. The curves A and C represent oxygen consumption of the larvae at different degrees of stimulation, entailing different levels of motor activity. Curve A represents intentinally activated animals, curve C non-activated, motionless animals. The curves A and C are boundary curves corresponding to a sort of scope for activity of the animals. Over this scope area a series of curves of the same form could in principal be construed, representing different degrees of stimulation.
6. Within a certain oxygen concentration interval a motor activation was observed caused by a reduced oxygen concentration. The result of that activation can be seen in Fig. 2–5 as a zone with no or very few oxygen consumption values between curve C and D. The more easily activated the species is, the broader the zone will be. Cloën has the most narrow zone and was observed to be less activated than the other species.
7. Small larvae of Cloën (2–4 mm and 42–6 mm) and Nemoura (2–4 mm) showed clearly a greater ability to take up oxygen at low oxygen concentrations than full-grown larvae (see Fig. 8 and 9).
8. The critical point on the curve representing mean oxygen consumption as a function of oxygen concentrations was found to be at 2–5 mg O₂/1 for Taeniopteryx and Diura, at 2.2–2.5 mg O₂/1 for Cloëon, and at about 2–7 mg O₂/1 for Nemoura. The values refer to 8°. Cloëon is the species which is exposed to the greatest variations in oxygen concentration in its natural environment.
9. No influence on the oxygen consumption of starvation for 4 to 5 days was found. No difference between the oxygen consumption values obtained in the presence or in the absence of calcium ions could be observed during the experiments (Fig. 10, 11).
10. The basic picture obtained in this investigation is a set of oxygen consumption values scattered between a curve connecting highest values obtained and a curve of the standard metabolism together with a zone in which the larvae are activated by reduced oxygen concentrations. This picture is presumed to be general in aquatic animals with a well developed motor activity.

     

Quantitative aspects of oxygen and carbon dioxide exchange through the lungs in Ocypode ceratophthalmus (Crustacea: Decapoda) during rest and exercise in water and air

Ghost crabs Ocypode ceratophthalmus were exercised in air and water to measure CO₂ and O₂ exchange rates using the method of instantaneous measurements of oxygen consumption rate (MO₂) where applicable. Average heart rate increased from 100 to nearly 400 pulses per minute after five minutes of exercise on a treadmill at a run rate of 0.133 m s^?1. It took less than a minute for oxygen taken up through the lung epithelium from the air inside the branchial cavity to reach the maximal oxygen consumption rate of 26.1 mmol O₂ kg^?1 h^?1. Resting MO₂ was 4.06 mmol O₂ kg^?1 h^?1 in air, but decreased to 3.37 mmol O₂ kg^?1 h^?1 in seawater. Radioactive CO₂ from injected l-lactate is released linearly by the lung. The percent accumulated 14-CO₂ in exhaled air, plotted against time, intersects zero time on the x -axis, indicating rapid gas exchange at the lung surface. The P ₅₀ values for native haemocyanin of 4.89 mm Hg before exercise, and 8.99 mm Hg after exercise, are typical of a high-affinity haemocyanin usually associated with terrestrial crabs. The current notion that Ocypode ceratophthalmus drown when submerged in seawater was not substantiated by our experiments. MO₂ in seawater increased from 3.37 mmol O₂ kg^?1 h^?1 for resting crabs to 5.72 mmol O₂ kg^?1 h^?1 during exercise. When submerged by wave-seawater in the natural environment and during exercise in respirometer-seawater O. ceratophthalmus do not swim but, having a specific density of 1.044, float nearly weightless with a minimum of body movements.     

Contribution of the polychaete,Neanthes japonica (Izuka), to the oxygen uptake and carbon dioxide production of an intertidal mud-flat of the Nanakita River estuary,Japan

The benthic oxygen consumption and carbon dioxide production of undisturbed and sieved sediment cores with various values for the biomass of polychaetes collected from the intertidal mud-flat of Nanakita River estuary of Japan were measured simultaneously. The benthic oxygen consumption and carbon dioxide production increased in proportion to the biomass of a dominant polychaete species Neanthes japonica (Izuka). This increase was not explained by the respiration of the animals alone. The residual increase in benthic O₂ and CO₂ fluxes may be due to mineralization processes in the burrow wall and enhanced diffusion caused by the pumping activity of the worms. From the average biomass of polychaetes at the study site, total benthic O₂ and CO₂ fluxes were estimated to be 5.2 mmol·m⁻²·h⁻¹ and 7.3 mmol·m⁻²·h⁻¹, respectively, at 20 ° C. The worms were responsible for 79% of the total O₂ flux and 73% of the total CO₂ flux but the respiration of the worms accounted for only 53% of the total O₂ flux and 36% of the total CO₂ flux. The residual enhanced fluxes were 26% and 37% for the total O₂ and CO₂ fluxes, respectively.     

Effects of the brackish deposit-feeding polychaetes Notomastus sp. (Capitellidae) and Neanthes japonica (Izuka) (Nereidae) on sedimentary O2 consumption and CO2 production rates

The benthic O₂ consumption and CO₂ production of sieved sediment cores containing a varied biomass of two polychaete species, Notomastus sp. (deep deposit-feeder) and Neanthes japonica (Izuka) (surface deposit-feeder), were measured simultaneously. Each species increased the benthic O₂ consumption and CO₂ production in proportion to its biomass. This increase was not explained by the respiration of the animals alone. The residual O₂ and CO₂ fluxes increased markedly in the presence of polychaetes. In the presence of Notomastus (the deeper burrowing species with low irrigation activity), the enhanced CO₂ flux was much higher than that in the presence of Neanthes, whereas the enhanced O₂ flux was lower in the presence of Notomastus.     

Walking performance and aerobic and anaerobic metabolism of Carcinus maenas (L.) in sea water at 15°C

Walking performance of the shore crab Carcinus maenas (L.) in sea water at 15 °C was assessed. In large crabs there was an inverse relationship between fatigue time and speed; crabs ran for $\text{\$}\text{?}$10 min at 3.2 m·min^?1 and for only 2 min at 14 m·min^?1. There were linear relationships between oxygen consumption and walking speeds for small and large animals walking at up to 4 m·min^?1 Estimates of maximum oxygen consumption were proportional to W^0.13 whereas inactive consumption is proportional to W^0.44 this resulted in aerobic scope (i.e. the difference between inactive and maximal rates of oxygen consumption) remaining almost constant across a weight range of animals whereas the aerobic expansibility (maximal rates/inactive rates) declined from 7- to 4-fold with increasing size. After a 12-h period without handling (settled animals) the animals could immediately become active and reach maximal rates of oxygen consumption similar to those of animals handled 1 h before the experiment. The aerobic expansibility of these settled animals could range from 21 to 8 times their inactive rates of oxygen consumption in small and large animals respectively. After 10 min of exercise oxygen consumption and whole body lactate levels returned to pre-exercise values within 5 to 25 min. The net oxygen debts range from 16 to 64% of the net oxygen consumption increase during exercise in small and large animals respectively.Calculations of the energy gained from lactate accumulation indicated that the net aerobic energy production during walking was supplemented from 4 to 71 % by anaerobic metabolism in small and large animals respectively. With increasing animal size the decline in aerobic expansibility was offset by an increased capacity for lactate production so that the overall maximum energy production during sustained activity remained almost constant at around seven times the inactive rate. The cost of transport (the net increase in oxygen consumption per g per m) falls with increased walking speed and increased animal size.     

The influence of hypoxia on the blood regulation of the brackish water shrimp Palaemonetes varians Leach

During periods of hypoxia in hypotonic media, Palaemonetes varians Leach showed an unimpaired regulation of blood chloride until some minutes before death. Heart rate showed no clear dependence on the water oxygen tension (P_wO₂) and postbranchial haemolymph oxygen tensions slowly decreased during progressive hypopoxia from a normoxic level of ≈ 30 mm Hg until the animals turned opaque some minutes before they died. Blood pH increased in hypoxia, from 7.6 in normoxia to > 8 in P_wO₂ 10 mm Hg. Taken together, these data have been taken to indicate that the oxygen consumption rate at the critical point (MO₂ P_cr) of this species is very low (P_wO₂ = < 10 mm Hg) compared with other brackish water natantians studied. The ecological significance of this to the species is considered.     

Haemocyanin oxygen binding and the physiological ecology of a range of talitroidean amphipods (Crustacea)

Summary Haemolymph PO₂ and pH of two amphipod species, Apohyale pugettensis (aquatic) and Megalorchestia californiana (semi-terrestrial) in vivo were examined during immersion and emersion at 15 and 25°C, and also after activity in air at 15°C. For M. californiana arterial O₂ tensions were higher in air than in water. This situation was reversed in A. pugettensis, although all O₂ tensions measured for both species were comparatively high. No arterial-venous PO₂ difference was apparent in the haemolymph of quiescent M. californiana. Haemocyanin (Hc) was 100% saturated in vivo only in the following; A. pugettensis in water (15 and 25°C) and air (15°C), and M. californiana in air (15°C). The Hc of both species becomes important in O₂ transport during activity; under such circumstances the haemolymph of M. californiana delivered more O₂ to the tissues than did that of A. pugettensis, despite the greater O₂ content of the latter. The animals studied here may exhibit a stage (size class?) where cutaneous gas exchange is sufficient for resting aerobic metabolism while specialized respiratory carriers (and respiratory structures) are important in meeting the increased aerobic demands of activity or environmental stress.Abbreviations Hc haemocyanin - PO₂ partial pressure of oxygen     

The respiratory responses of the dog cockle Glycymerisglycymeris (L.) to declining environmental oxygen tension

The subtidal bivalve Glycymeris glycymeris (L.) exhibits a high degree of respiratory independence in conditions of declining environmental oxygen tension. In contrast to other bivalves previously studied, the index of respiratory independence, $\text{K}{}_1\text{K}{}_2$ decreases with increasing weight specific oxygen consumption indicating that small Glycymeris are better regulators of oxygen consumption than large Glycymeris.The respiratory responses of Glycymeris to hypoxia include a small initial increase in ventilation, brought about by increasing the percentage of time spent pumping and a large increase in oxygen utilization. Heart activity is elevated, principally through a large increase in the amplitude of heart beat, which suggests increased perfusion of the respiratory surfaces. The ventilation : relative perfusion ratio, therefore, declines over the range of oxygen tension that respiratory independence is maintained.The respiratory mechanism of Glycymeris is compared with that previously described for other bivalves and it is concluded that there are no clearcut differences between the respiratory responses to hypoxia of intertidal and subtidal species.     

Photosynthesis and Activation of Ribulose Bisphosphate Carboxylase in Wheat Seedlings : Regulation by CO(2) and O(2)

Photosynthetic carbon assimilation in plants is regulated by activity of the ribulose 1,5-bisphosphate (RuBP) carboxylase/oxygenase. Although the carboxylase requires CO₂ to activate the enzyme, changes in CO₂ between 100 and 1,400 microliters per liter did not cause changes in activation of the leaf carboxylase in light. With these CO₂ levels and 21% O₂ or 1% or less O₂, the levels of ribulose bisphosphate were high and not limiting for CO₂ fixation. With high leaf ribulose bisphosphate, the K_act(CO₂) of the carboxylase must be lower than in dark, where RuBP is quite low in leaves. When leaves were illuminated in the absence of CO₂ and O₂, activation of the carboxylase dropped to zero while RuBP levels approached the binding site concentration of the carboxylase, probably by forming the inactive enzyme-RuBP complex.

The mechanism for changing activation of the RuBP carboxylase in the light involves not only Mg²⁺ and pH changes in the chloroplast stroma, but also the effects of binding RuBP to the enzyme. In light when RuBP is greater than the binding site concentration of the carboxylase, Mg²⁺ and pH most likely determine the ratio of inactive enzyme-RuBP to active enzyme-CO₂-Mg²⁺-RuBP forms. Higher irradiances favor more optimal Mg²⁺ and pH, with greater activation of the carboxylase and increased photosynthesis.

     

The Dependence of the Oxygen-Concentrating Mechanism of the Teleost Eye (Salmo gairdneri) on the Enzyme Carbonic Anhydrase

Microoxygen polarographic electrodes were constructed and used to measure oxygen tension (P_OO2) in the eyes of rainbow trout (Salmo gairdneri). The values obtained are compared with arterial blood and environmental water P_OO2 and indicate that there is an oxygen-concentrating mechanism in the eye supplying oxygen to the avascular retina. Anatomically similar retes suggest that the mechanism is similar to the one which exists in the swim bladder. Elimination of the arterial blood supply to the choroidal gland rete mirabile of the eye (through pseudobranchectomy) and the consequent lowering of ocular oxygen tensions implicate the choroidal gland as one of the major components of the oxygen-concentrating mechanism. After pseudobranchectomy the presence of ocular P_OO2 above that of arterial blood is indicative of a secondary structure in the eye capable of concentrating oxygen. Inhibition of carbonic anhydrase, using acetazolamide, is shown to result in complete suppression of the oxygen-concentrating mechanism. A hypothesis is advanced for the participation of retinal-choroidal and erythrocyte carbonic anhydrase in the oxygen-concentrating mechanism.     

Bis(oxalato)dioxovanadate(V) and Bis(oxalato)oxoperoxo-vanadate(V) Complexes: Spectroscopic Characterization and Biological Activity

Two structurally related vanadium(V) complexes, K₃[VO₂(C₂O₄)₂]·3H₂O and K₃[VO(O₂)(C₂O₄)₂]·1/2H₂O, were thoroughly characterized by infrared, Raman, and electronic spectroscopies. The effect of both complexes on the viability of the human MG-63 osteosarcoma cells was tested using the MTT assay. The monoperoxo complex shows a very strong antiproliferative activity (at 100-μM concentration, this complex diminished the cell viability ca. 80 %), whereas the dioxo complex was inactive.     

Gas exchange and blood gases of Puna teal (Anas versicolor puna) embryos in the Peruvian Andes

Oxygen consumption, air cell gases, hematology, blood gases and pH of Puna teal (Anas versicolor puna) embryos were measured at the altitude at which the eggs were laid (4150 m) in the Peruvian Andes. In contrast to the metabolic depression described by other studies on avian embryos incubated above 3700 m, O₂ consumption of Puna teal embryos was higher than even that of some lowland avian embryos at equivalent body masses. Air cell O₂ tensions dropped from about 80 toor in eggs with small embryos to about 45 toor in eggs containing a 14-g embryo; simultaneously air cell CO₂ tension rose from virtually negligible amounts to around 26 torr. Arterial and venous O₂ tensions (32–38 and 10–12 toor, respectively, in 12- to 14-g embryos) were lower than described previously in similarly-sized lowland wild avian embryos or chicken embryos incubated in shells with restricted gas exchange. The difference between air cell and arterial O₂ tensions dropped significantly during incubation to a minimum of 11 torr, the lowest value recorded in any avian egg. Blood pH (mean 7.49) did not vary significantly during incubation. Hemoglobin concentration and hematocrits rose steadily throughout incubation to 11.5 g · 100 ml^-1 and 39.9%, respectively, in 14-g embryos.Abbreviations PO₂ partial pressure gradient of O₂ - BM body mass - D diffusion coefficient - G gas conductance (cm³·s^-1·torr^-1) - conductance to water vapor - IP internal pipping of embryos - P _ACO₂ partial pressure of carbon dioxide in air cell - P _AO₂ partial pressure of oxygen in air cell - P _aCO₂ partial pressure of carbon dioxide in arterial blood - P _aCO₂ partial pressure of oxygen in arteries - P _H barometric pressure (torr) - PCO₂ partial pressure of carbon dioxide - P _IO₂ partial pressure in ambiant air - PO₂ partial pressure of oxygen - P _VCO₂ venous carbon dioxide partial pressure - P _VO₂ mixed venous oxygen partial pressure - SE standard error - VO ₂ oxygen consumption     

Oxygen consumption by the bivalve Donax vittatus (da Costa)

The acute oxygen consumption of Donax vittatus (da Costa) freshly collected at different times from a beach at Barrassie, Ayrshire, Scotland, has been measured at different temperatures. The logarithmic relationship between oxygen consumption and body weight showed a significant difference on only one occasion, and a common regression coefficient (b) of 0.865 could be used for regressions of oxygen consumption on weight. Over the temperature range 2.9–20 °C oxygen consumption rose with temperature. There was a linear decline of Q₁₀ with temperature in the range 2.9 –20 °C. Differences in values of the constant (a) in the regression equation suggest that there is some acclimation to temperature, resulting in rotation of the rate/temperature curve counterclockwise for warm-acclimated animals, and a reduction of Q₁₀ in cold-acclimated animals. The differences in oxygen consumption which result are small and appear to have little practical significance. High levels of metabolically-inactive materials such as stored glycogen reserves lead to a reduction in the weight-specific oxygen consumption. Spawning animals show an increased oxygen consumption.     

Hypoxia impairs visual acuity in snapper (Pagrus auratus)

We investigated the effect of environmental hypoxia on vision in snapper (Pagrus auratus). Juvenile snapper inhabit estuarine environments where oxygen conditions fluctuate on a seasonal basis. Optomotor experiments demonstrated that visual acuity is impaired by environmental hypoxia, but not until levels approach the critical oxygen tension (P _crit) of this species (around 25 % air-saturated seawater). In 100, 80, and 60 % air-saturated seawater, a positive optomotor response was present at a minimum separable angle (M _SA) of 1°. In 40 % air-saturated seawater, vision was partially impaired with positive responses at M _SAs of 2° and above. However, in 25 % air-saturated seawater, visual acuity was seriously impaired, with positive responses only present at M _SAs of 6° and above. Snapper were found to possess a choroid rete, facilitating the maintenance of high ocular oxygen partial pressures (PO₂) during normoxia and moderate hypoxia (PO₂, between 269 and 290 mmHg). However, at 40 and 25 % water oxygen saturation, ocular PO₂ was reduced to below 175 mmHg, which is perhaps linked to impairment of visual acuity in these conditions. The ability to preserve visual function during moderate hypoxia is beneficial for the maintenance of a visual lifestyle in the fluctuating oxygen environments of estuaries.     

The influence of environmental factors and nutrient concentrations in tissues of the seaweed Ahnfeltia tobuchiensis (Rhodophyta: Ahnfeltiales) on the primary production and dark respiration of its population

Complex investigations of the influence of environmental factors, viz., the temperature, photosynthetically active radiation (PAR), ambient seawater concentrations of ammonium (NH₄), and orthophosphate (PO₄), as well as the contents of organic carbon (C), nitrogen, phosphorus, and a-chlorophyll (Ch) on the rate of photosynthesis (P_n) and dark respiration (R_d) in the tissues of the unattached red seaweed Ahnfeltia tobuchiensis (Rhodophyta: Ahnfeltiales) population, were performed in the summers of 2000 and 2008 in Izmeny Bay (Kunashir Island) under in situ conditions. The dependence of photosynthesis on PAR intensity (P-I dependence) is described by the equation of a hyperbolic tangent. The population of A. tobuchiensis forms a layer up to 50 cm thick with an area of 23.3 km₂ and a biomass of 125 000 tons. The P_n rate of seaweed population during daylight hours varies within a wide range, with an average of 1.04 mg O₂ O₂/(g _{dry weight} h) and largely depends on PAR intensity and availability (r = 0.70–0.98). The maximum photosynthesis rate (P_max) is substantially defined by the ambient concentration of NH₄ (r ² = 0.91, p < 0.01). The rate of R_d during the night is on average 0.1 mg O₂/(g _{dry weight} h) and mainly depends on the content of Ch in seaweed tissues (r ² = 0.83, p < 0.01), which, in its turn, is regulated by the ambient concentration of PO₄ (r ² = 0.86, p < 0.01). With average biomass values of 5.4 kg/m² or 1.8 kg_{dry weight}/m², the net primary production (P_n) of seaweed population is estimated to be on average 22.5 g O₂/(m² day) or 8.4 g C/(m² day). Based on these indices, the investigated population is one of the most productive ecosystems of the World Ocean. It is supposed that such indices of the A. tobuchiensis population are attained due to the highly efficient use of weak light and a low light-saturation level of photosynthesis, compared to other seaweeds.     

Antioxidant defenses and oxidative stress parameters in tissues of mud crab (Scylla serrata) with reference to changing salinity

The effects of salinity (10, 17 and 35 ppt) on O₂ consumption, CO₂ release and NH₃ excretion by crabs and oxidative stress parameters and antioxidant defenses of its tissues were reported. An increase in salinity caused a decrease in O₂ consumption and CO₂ release and an increase in ammonia excretion by crabs. Lipid peroxidation, protein carbonyl, H₂O₂ levels and total antioxidant capacity of the tissues elevated significantly at 35 ppt salinity except in abdominal muscle where H₂O₂ content was low. Ascorbic acid content of tissues was higher at 17 ppt salinity than at 10 and 35 ppt salinities. With increasing salinity, a gradual decrease in SOD, an increase in catalase, no change in GPx and a decrease followed by an increase in GR activities were recorded for abdominal muscle. While for hepatopancreas, an increase followed by a decrease in SOD and catalase, decrease in GPx and GR activities were noticed with increasing salinity. In the case of gills, a decrease followed by an increase in SOD, a decrease in catalase and GPx and an increase in GR activities were noted when the salinity increased from 10 ppt to 35 ppt. These results suggest that salinity modulation of oxidative stress and antioxidant defenses in Scylla serrata is tissue specific.