Behavioural thermoregulation and critical thermal limits of Macrobrachium acanthurus (Wiegman)

• (1)The preferred temperatures of Macrobrachium acanthurus were determined for prawns acclimated to 20°C, 23°C, 26°C, 29°C and 32°C, and the final preferendum estimate was (29.5°C).
• (2)The critical thermal minima (CTMin) and maxima (CTMax) were 11.0°C, 12.1°C, 13.0°C and 14.8°C, and 34.2°C, 35.0°C, 36.1°C and 39.8°C, respectively.
• (3)The zone of thermal tolerance assessed using the CTMin and CTMax boundaries was 644°C².
• (4)The acclimation response ratio was between 0.33 and 0.62.
• (5)To cultivate this species in the southeastern region of México it should be done in not <15°C (CTMin) during the winter and below 38°C in summer (CTMax).

     

Effects of acclimation temperature,season, and time of day on the critical thermal maxima and minima of the crayfish Orconectes rusticus

• 1.1. The critical thermal minima (CTMin) and maxima (CTMax) were determined for field-acclimatized and laboratory-acclimated crayfish (Orconectes rusticus) throughout 1984.
• 2.2. The CTMin and CTMax of field-acclimatized crayfish were seasonally adjusted by 9.7 C and 14.7 C respectively.
• 3.3. Seasonal variation in both tolerance regimes persisted in crayfish acclimated in the laboratory at 5 and 25°C for one week; however, no diel variation existed in either the CTMin or CTMax of laboratory-acclimated crayfish.
• 4.4. Integration of thermal acclimation of the CTMin and CTMax with seasonal conditioning may influence the functional capacities of this species when considered in relation to the seasonal ranges in stream temperature.

     

Entomopathogenic fungal infection (Deuteromycotina: Hyphomycetes) affects water relations of the german cockroach,Blattella germanica (L.) (Dictyoptera: Blattellidae)

• 1.1. The total body water, lipid content, and cuticular permeability of fungus infected and uninfected German cockroaches, Blattella germanica, were examined.
• 2.2. Infected adult cockroaches weighed less and had significantly more body water than did uninfected specimens of the same size.
• 3.3. Uninfected medium-size nymphs weighed significantly more than infected nymphs, but there was no difference in body size between infected and uninfected small nymphs.
• 4.4. Cuticular permeability and lipid content of infected and uninfected cockroaches was not significantly different.
• 5.5. Sequestering of water by the fungal cells is discussed as a possible factor in the pathology of this fungal parasite.

     

Temperature acclimation in respiratory and cytochrome c oxidase activity in common carp (Cyprinus carpio)

• 1.1. Common carp (Cyprinus carpio) exposed to experimental temperatures of 12, 18, 24, 30 or 36°C for a 4-week period were used to investigate the effect of temperature acclimation on the frequency of opercular movement (FOM), growth and cytochrome c oxidase (CCO) activity in heart, liver and muscle.
• 2.2. An exponential relationship between FOM and temperature after the first week (10₁₀ =1.76) disappeared after the second week.
• 3.3. The initially high FOM at temperatures of 30 or 36°C and the low FOM at 18 or 12°C changed over 4 weeks to approach the FOM of fish at 24°C.
• 4.4. This change in the relationship of FOM to temperature from highly dependent to independent appeared to be thermal compensation.
• 5.5. Heart and liver CCO activities were significantly affected by temperature, with the lowest activity at the approximate optimum temperature for growth, 24°C.
• 6.6. Highest CCO activities for heart and liver occurred at both the highest and lowest temperatures.
• 7.7. Among the three tissues, heart CCO activity was generally the highest and most affected by acclimation temperature.
• 8.8. Muscle tissue had the lowest CCO activity and was unaffected by temperature.
• 9.9. The high CCO activity at a cold acclimation of temperature 12°C was probably due to thermal compensation and the high activity at 36°C may have been a result of thermal stress.

     

Temperature and salinity tolerance of the mole crab,Emerita talpoida (Say) (Crustacea,Anomura)

• 1.1. Adult Emerita talpoida were subjected to 25 temperature-salinity combinations within the range of 5–35°C and 15–65‰.
• 2.2. E. talpoida tolerated 15–65‰ salinity at 20°C and below.
• 3.3. Optimum salinity for survival at stressful temperatures was 40‰.
• 4.4. Crabs transferred directly from one salinity to another experienced changes in osmoconcentration toward that of the new salinity.
• 5.5. Temperature modified the rate of change toward the experimental salinity. Q values averaged 1.2.

     

Identification and characterization of a third form (D3) of cyclic 3'5'-nucleotide phosphodiesterase from rhizobwm fredii

• 1.1. A third form (D3) of cyclic nucleotide phosphodiesterase from Rhizobiumfrediiv/as detected and characterized for the first time.
• 2.2. The enzyme could hydrolyse both cyclic AMP and cyclic GMP with apparent K_m for cyclic AMP of approx. 0.2 μM.
• 3.3. D3 cyclic nucleotide phosphodiesterase had a pH optimum of about 6.0 when hydrolysing cyclic AMP.
• 4.4. The enzyme lost almost all its activity when heated to 60°C for 20 min.
• 5.5. Gel filtration with Sephadex G-100 gave a mol. wt of approx. 42.5 kD for the native enzyme.

     

Effects of temperature and acid stress on hatching,survival capacity,metabolism and postural reflexes in caenid mayflies (ephemeroptera)

• 1.1. Mortality was 100% at pH 3.5 over a temperature range of 10–30°C for embryos and nymphs of Caenis diminuta and C. hilaris.
• 2.2. Hatching success for both species was highest at pH values above 4.5.
• 3.3. Survival capacities were significantly higher at 20°C over a pH range of 4.0-7.2.
• 4.4. Oxygen consumption rates increase as a function of increasing temperature and reduced acidity.
• 5.5. Loss of the nymphal righting response was observed at pH 3.5. This response can be used as a behavioral assay for acid stress.

     

Effect of starvation and experimental feeding on the proximate composition and caloric content of an antarctic teleost,Notothenia coriiceps neglecta

• 1.1. Starving Notothenia coriiceps nn/lecta at 1°C for 20 days resulted in a loss of 4.22 gcal/kcal per day.
• 2.2. During starvation energy was obtained from lipid and carbohydrate stores of the liver and red muscle.
• 3.3. Feeding N. coriiceps neglecta low lipid, high protein shrimp meat at 18.9 gcal/kcal per day at 1°C for 20 days resulted in a gain of 8.5 gcal/kcal per day.
• 4.4. The level of carbohydrate in the liver and red muscle increased five times.
• 5.5. Gross growth efficiency (K₁) equalled 0.52.
• 6.6. Net growth efficiency (K₂) equalled 0.67.

     

Characterization of two distinct latent proteinases associated with myofibrils of crucian carp (Carassius auratus cuvieri)

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• 1.1. Enzymatic properties of two distinct proteinases tightly associated with crucian carp myofibrils were characterized.
• 2.2. These proteinases were latent but activated at 50 and 60°C, respectively.
• 3.3. The optimum pH of 50°C-proteinase was neutral-alkaline, while that of 60°C-proteinase was weak acid-neutral pH.
• 4.4. Both proteinases required more than 1% NaCl for the activity, but 50°C-proteinase was partially inhibited at higher concentrations of NaCl.
• 5.5. Both proteinases were regarded as trypsin-like proteinases belonging to a serine proteinase family, but only 60°C-proteinase was sensitive to urea, n-butanol and iso-propanol.

     

Metabolic rate and body temperature of adult and juvenile hyrax (Procavia capensis)

• 1.1. Resting metabolic rates (RMR) below thermoneutrality in adult hyrax acclimated to 26, 15 and 10°C remained unchanged, i.e. thermal conductance (K) remained constant.
• 2.2. Conductance in juveniles decreased with acclimation to lower ambient temperatures (T_a).
• 3.3. Body temperature (T_b) dropped by 3.8°C in adults exposed to T_a of 30 – 5°C. The decrease was constant.
• 4.4. Body temperature fell by 1.5°C in juveniles exposed to T_a of 30 – 20°C but stabilized between 20 and 5°C.
• 5.5. The labile T_b, associated with behavioural strategies and lower than predicted RMR, can be seen as an energy-conserving mechanism of particular importance during winter conditions.

     

Hypothermia and blood of crabs

• 1.1. The effect of acclimation to 10° and 30°C on the blood volume, clotting time, total blood protein and numbers of cells was determined in Uca pugilator.
• 2.2. There was no significant difference between blood volume in the 10° and 30° animals but there were significantly more cells and a higher blood protein in the 30° crabs.
• 3.3. The clotting time is significantly longer for the 10° crabs.
• 4.4. These changes associated with the blood parameters can be associated with the ecology of the animal.

     

Oxygen consumption in the tortoise,Testudo hermanni G., subjected to sudden temperature changes in summer and autumn

• 1.1. A respirometer for long-term measurements of oxygen consumption in terrestrial vertebrates is described.
• 2.2. The tortoise, Testudo hermanni Gmelin, investigated in summer and autumn, presents a day-night rhythm of oxygen consumption at 28 and 18°C but not at 8°C.
• 3.3. The standard metabolic rate presents an important and constant thermal dependence in the range 8-18-28°C.

     

Effect of low rearing temperature on development of Galleria mellonella larvae and their sensitivity to juvenilizing treatment

• 1.1. The development of Gallena mellonella is strongly affected by a low temperature of 18°C (the last instar persists for more than one year, instead of about 9 days at 30°C). At 18°C the last instar Galleria mellonella larvae respond to juvenilizing treatment—chilling stress or juvenile hormone analogue—with a very low percentage or no supernumerary moults, respectively.
• 2.3. Experiments in which larvae subjected to such treatments were transferred from 18°C to 30°C and vice versa showed that for the realization of the larval programme after chilling stress application the higher (30°C) temperature is needed.
• 3.4. In last instar larvae reared at 18°C there coexist very high juvenile hormone titre and high juvenile hormone esterase activity.
• 4.5. This phenomenon which is found in both, chilled and unchilled larvae, is discussed.

     

Effects of temperature and metabolic inhibitors on contraction of anterior byssus retractor muscle of Mytilus

• 1.1. Anterior byssus retractor muscle of Mytilus (ABRM) was stimulated to contract by ACh (acetylcholine) and effects of temperature (5–30°C), FDNB (1-fluoro 2,4 dinitro-benzene) and IAA (iodoacetic acid) on tension response were examined.
• 2.2. Isometric tension was highest at the temperature range of 10–20°C and decreased at higher and lower temperature than that range.
• 3.3. The rate of tension decay after washing of ACh was accelerated by the increase of temperature.
• 4.4. Tension redevelopment after release of 1 % during contraction was much smaller at 5°C than at 20°C.
• 5.5. Tension development by ACh and the rate of tension decay after washing of ACh were remarkably decreased by the treatment of FDNB or IAA.
• 6.6. The above results were discussed from the viewpoint that energy metabolism might be related to catch.

     

The effect of temperature on the acid-base status of the blood of the hatching quail (Coturnix c. japonica)

• 1.1. The ambient temperature of embryos of pipped eggs was reduced from 38 to 28°C for a period of 45 min.
• 2.2. The blood P_CO2 was lower and the blood more alkaline at 28°C than at 38°C.
• 3.3. At 28°C plasma [HCO₃⁻] ] was lower than predicted from the blood buffer line determined in vitro.
• 4.4. The plasma concentrations of strong ions and lactate were the same at both temperatures.
• 5.5. After the ambient temperature had been returned to 38°C for a period of 45 min, blood pH was more acidic than before cooling, but there was no difference in blood P_CO2.
• 6.6. The plasma [HCO₃⁻] was the same as that at 28°C and plasma [K⁺] was higher than before cooling.
• 7.7. The results arc discussed in relation to the factors affecting blood pH in embryos at this stage of development.

     

Comparative analysis of cuticular hydrocarbons in the Drosophila virilis species group

• 1.1. Chemical structures were determined for the cuticular alkanes, alkenes, and certain of the alkadienes for 11 D. virilis group species.
• 2.2. Male-specific hydrocarbons occurred in five species: these were 9-heneicosene in D. americana and D. novamexicana, 10-heneicosene in D. virilis, 5,13- and 5,15-pentacosadienes in D. kanekoi, and 9-pentacosene in one strain of D. lummei.
• 3.3. Hydrocarbon profiles of newly emerged flies always differed from mature files.
• 4.4. Relationships among the species, with respect to hydrocarbon profiles, were investigated by cluster analysis.

     

The influence of aerial exposure on gas exchange and cardiac activity in the shore crab,Carcinus maenas (L.)

• 1.1. The cardiovascular physiology of adult Carcinus maenas (L.) emerging into air has been investigated at three different air temperatures.
• 2.2. Transition from seawater to air or vice versa triggered transient increases in cardiac and locomotor activity.
• 3.3. However, crabs became inactive 5–10 min after emerging from seawater (15°C) into air at the same temperature (15°C) or at lower temperatures (12–13°C) and heart rate fell.
• 4.4. At higher air temperatures (18–20°C) heart rate rose but to a lesser extent than predicted from aquatic Q₁₀ heart-rate values.
• 5.5. Crabs were again quiescent in aerial conditions.
• 6.6. Mean arterial oxygen tension (Pa_o2) was ~ 74 mmHg in submerged crabs but fell to ~ 38 mmHg in air while mean arterial carbon dioxide tension (Pa_o2) increased from 1 to 4 mmHg resulting in respiratory acidosis.
• 7.7. A model of gill function is proposed to explain the development of internal hypoxia in air.
• 8.8. The results are discussed in relation to the distribution of adult and juvenile C. maenas in situ.

     

Ventilatory rate in the butterfish (Pholis gunnellus) as a consequence of temperature and previous emersion

• 1.1. Observation of ventilation in immersed Pholis gunnellus showed a linear relationship between ventilatory rate and temperature between 8 and 20°C.
• 2.2. At 13°C and after 30 min emersion, ventilatory rate was initially lower than prior to emersion, providing evidence of adequate uptake of O₂ for standard metabolism during the emersion period.
• 3.3. This species has a laterally elongate body form with reduced scales and extensive mucus secretion.
• 4.4. During emersion, gaping behaviour probably exposes the gills and extensively vascularised oesophageal regions to air.
• 5.5. These are considered to be morphological and behavioural adaptations by P. gunnellus, to aerial respiration in the intertidal habitats occupied by this species.

     

Bacterial endotoxin and infection cause behavioural hypothermia in infant mice

• 1.1. When placed in a temperature gradient, 3–10 day old mice injected with living Escherichia coli or with E. coli endotoxin, select 2–3°C lower temperatures than their litter-mate controls injected with saline.
• 2.2. At the lower selected temperature (32°C) young mouse pups resist bacterial infection for longer and tolerate higher doses of endotoxin than at the temperature selected by the controls (35°C).
• 3.3. It is possible that a controlled hypothermic state, here called cryexia, is in small mammals an alternative strategy to fever for coping with infections.

     

The response of brown adipose tissue mitochondrial glycerolphosphate acyltransferase to cold-exposure in hypothyroidism,after adrenalectomy and after treatment with cycloheximide

• 1.1. Exposure to cold has previously been shown to considerably increase the activity of the mitochondrial form of glycerolphosphate acyltransferase (GPAT) in brown adipose tissue (A.C. Darnley C.A. Carpenter and E. D Saggerson, Biochem.J.253, 351–355, 1988; J.R.D. Mitchell and E.D. Saggerson. PBiochem.J.277, 665–669, 1991).
• 2.2. Both adrenalectomy and chemically-induced hypothyroidism increased mitochondrial GPAT activity in rats maintained at 21°C. This increase was similar to that caused by exposing rats to the cold (4°C) for three days. Whereas exposure of hypothyroid rats to cold (4°C) resulted in a further increase in GPAT activity, no further increase in activity was observed after exposure of adrenalectomized rats to the cold.
• 3.3. Administration of triiodothyronine (T₃) to rats maintained at 21°C had no effect on mitochondrial GPAT activity.
• 4.4. Prior treatment with cycloheximide abolished 60–70% of the increase in GPAT activity caused by cold-exposure.