The effects of temperature and moisture on survival capacity,cuticular permeability,hemolymph osmoregulation and metabolism in the scorpion,Centruroides hentzi (banks) (scorpiones,buthidae)

• 1.1. The temperature and water relations of Centruroides hentzi females were investigated. At 12 and 72% relative humidity (RH), the lower and upper Lt₅₀ were -4.5 and 43.7°C, and -4.7 and 45.1°C, respectively. When exposed to high temperature stress, survivorship was significantly greater under mesic conditions.
• 2.2. Cuticular water loss was higher under xeric conditions (12% RH), ranging from 0.061 mg/cm²/hr at 30°C to 0.211 at 41°C.
• 3.3. Exposure to dry air (0–5% RH) resulted in a significant increase in hemolymph osmolality: from 441 to 688 mOsm over a 5 day period.
• 4.4. Mean oxygen consumption rates increased from 161.7 mm³/g/hr at 34°C to 541.6 at 44°C. ATPase activity was significantly higher in animals acclimated and tested at 35°C.

     

Oxygen consumption rates of adults and chicks during brooding in king quail (Coturnix chinensis)

Oxygen consumption rates were measured in chicks (0–7 days of age), and in non-brooding and brooding adults. Brooded chicks maintained a constant oxygen consumption rate at a chamber ambient temperature of 10–35°C (0–5 days of age: 2.95ml O₂·g^-1·h^-1 and 6–17 days of age: 5.80 ml O₂·g^-1·h^-1) while unbrooded chicks increased oxygen consumption rate at ambient temperature below 30°C to double the brooded oxygen consumption rate at 25 and 15°C for chicks < 5 days of age and>5 days of age, respectively. The massspecific oxygen consumption rate of breeding male and females (non-brooding) were significantly elevated within the thermoneutral zone thermal neutral zone (28–35°C) in comparison to non-breeding adults. Below the thermal neutral zone, oxygen consumption rate was not significantly different. The elevation in oxygen consumption rate of breeding quail was not correlated with the presence of broodpatches, which developed only in females, but is a seasonal adjustment in metabolism. Male and females that actively brooded one to five chicks had significantly higher oxygen consumption rate than non-brooding quail at ambient temperature below 30°C. Brooding oxygen consumption rate was constant during day and night, indicating a temporary suppression of the circadian rhythm of metabolism. Brooding oxygen consumption rate increased significantly with brood number, but neither adult body mass nor adult sex were significant factors in the relationship between brooding oxygen consumption rate and ambient temperature. The proportion of daylight hours that chicks were brooded by parents was negatively correlated with ambient temperature. After chicks were 5 days old brooding time was reduced but brooding oxygen consumption rate was unchanged. Heat from the brooding parent appeared to originate mainly from the apteria under the wings and legs rather than the broodpatch. The parental heat contribution to chick temperature regulation below the chicks' thermal neutral zone is achieved by increasing parental thermal conductance by a feedback control similar to that suggested for the control of egg temperature via the brood-patch. It is concluded that the brooding period is an energetic burden to parent quail, and the magnitude of the cost increases directly with brood number and inversely with ambient temperature during this period. The oxygen consumption rate of brooding parents was 5.80–6.90 ml O₂·g^-1·h^-1 (ambient temperature 10–15°C) at night and up to 5.10 ml O₂·g^-1·h^-1 (ambient temperature 18°C) during the day, which are 100 and 40% higher than non-brooding birds, respectively.Abbreviations bm body mass - SMR standard metabolic rate - T _a ambient temperature - T _b body temperature - I/O₂ oxygen consumption rate - C _wet wet thermal conductance - TNZ thermal neutral zone - ANOVA analysis of variance - ANCOVA analysis of covariance     

Ecdysteroids and diapause in pupae of Heliothis punctiger

Most pupae of H. punctiger enter diapause when reared at 19°C, 12L:12D. When pharate pupae were treated for only 12 hr at 28°C about 50% developed at 19°C. The proportion of non-diapausing pupae increased as the temperature at which the pharate pupal stage was spent increased.The quantity of injected 20-hydroxyecdysone necessary to promote development in diapausing pupae varied from about 1 μg g^?1 soon after pupation to about 4 μg g^?1 after 50 days. It fell somewhat after 150 days.Removing brains from non-diapausing pupae showed that the brain secreted its hormone at the time of pupation (or just before). However, if the pupae were kept at 19°C development did not occur unless the brain remained in situ for at least 20 hr at 28°C. Implanting brains from non-diapausing pupae into diapausing ones had no measurable effect.These results may be explained by postulating that the prothoracic gland is ‘activated’ by exposure to high temperature, but that it reverts to inactivity over a period at 19°C. The ‘active’ gland must then be stimulated by brain hormone for a long period to trigger secretion of its hormone, which results in development. Diapause is thus the result of the failure of the prothoracic gland to secrete.     

Effects of temperature on growth and metabolism in juvenile turbot

The effects of constant temperatures on growth, food efficiency, and physiological status were studied in four different batches of juvenile turbot. The growth responses were studied in three experiments lasting 70–85 days under 8–20° C thermal conditions. There was a positive correlation between growth and temperature from 8 to 17° C and a plateau was observed from 17 to 20° C. In fish fed to satiety, specific growth rate was positively correlated to the food intake, which was double at 20° C, compared with 8° C. Minor changes were observed in food efficiency. Body fat deposition decreased as temperature increased (25% lower at 20° C, compared with 8° C). Apparent food conversion, PER (protein efficiency ratio) and PUC (protein utilization coefficient) ranges were 0.8–0.9, 2.1–2.3 and 33–38% respectively. In 70–300 g fish, routine MO₂ increased (2.5–6.5 μmol O₂ h^?1 g bw^?1) with temperature up to 20° C, while larger turbot (500–600 g) appeared relatively thermo-independent, with a lower oxygen consumption (1.5 ìmol h^?1 g^?1). The average daily total ammonia nitrogen (TAN) and urea-N excretion per fish biomass was positively related to temperature. TAN was 30% lower at 8° C, compared with 20° C. Ingested nitrogen was mainly excreted under the final form of TAN, urea-N representing 26% of the total amount. A post-prandial peak in TAN and a delayed peak in urea-N nitrogen were observed. The hydromineral status [osmolarity, sodium, chloride and potassium blood plasma, gill (Na⁺-K⁺)-ATPase activity] of turbot was not affected by progressive changes in temperature during the acclimation period. Juvenile turbots show remarkable homeostatic capacities and so they have a relatively thermo-independent physiology within the range of temperature studied.     

Effect of temperature and salinity on the oxygen consumption of laboratory produced Penaeus californiensis postlarvae

• 1.1. The oxygen consumption by P. californiensis postlarvae (mean wt = 0.38 g) was determined at five different temperatures and four salinities.
• 2.2. The O₂ in each chamber was recorded at 10 min intervals for 1 hr. The time course of oxygen depletion was independent of O₂ concentration down to 1.6 mg/l.
• 3.3. Oxygen consumption increased with temperature from 0.0045 mg/g/min at 19°C, to 0.0142 mg/g/min at 35°C. The thermal coefficient (Q₁₀) indicated a very high sensitivity of the postlarvae to temperature variations at 19–23°C.
• 4.4. The results show that oxygen consumption significantly depends on temperature (P < 0.001) while salinity has only a marginal effect.

     

Oxygen consumption of engorged nymphs and unfed adults of Hyalomma asiaticum ticks (Acari: Ixodidae) exposed to various photoperiods

The oxygen consumption of engorged nymphs of Hyalomma asiaticum was measured at various intervals after drop-off from mice hosts. Duration of nymphal development to the emergence of adults was 25–32 days at 25°C. The oxygen consumption was high immediately after completing the blood meal (193–248 mm³ g^-1 h^-1 but decreased significantly 18 days later (at 25°C) to 45–65 mm³ g^-1 h^-1. It increased again before ecdysis (81–102 mm³ g^-1 h^-1, and also after ecdysis in freshly moulted adults (177–220 mm³ g^-1 h^-1. The oxygen consumption in 8-month-old adult ticks was very variable ranging from 40–42 to 172 mm³ g^-1 h^-1. Neither engorged nymphs nor unfed adult ticks showed any dependence of their respiratory metabolism on the photoperiodic regimes tested (LD 20:4 and LD 12:12, with or without transfer to an alternative photoperiod after engorgement of nymphs).     

Respiration,energy balance and development during growth and starvation of Carcinus maenas L. larvae (Decapoda:Portunidae)

In all larval stages of Carcinus maenas L. oxygen consumption was measured at three temperatures (12,18,25 °C). Values increased during development and were in the range of 0.037 ± 0.01 (zoea-1, 12°C, $\text{x}\text{?}\text{± 95\% CL}$) to 0.734 ± 0.047 μl O₂ · h^?1 · ind^?1 (megalopa, 25 °C). Growing larvae showed temperature dependent trends in weight specific respiration rates (referred to dry wt; DW), with values between ≈2.4 and 9.4 μl O₂· h^?1·mg DW^?1. Increase in oxygen consumption of megalops did not differ much at temperatures between 18 and 25 °C. This points to an exceptional physiological position of this stage. Fed zoea-1 of C. maenas (18 °C) revealed growth rates in terms of 40% DW, 20% carbon (C), 30% nitrogen (N) and 65% hydrogen (H). At the same time larvae gained individual energy by 13% (J · ind^?1), while weight specific energy dropped by ≈ 19% (J · mg DW^?1) during the first day and remained constant until the moult. Starved zoea-1 of C. maenas (18 ° C) gained ≈ 20 % in DW through the first day, probably caused by inorganic salts which enter the organism after the moult of the prezoea. DW dropped to ≈ 25 % of initial value, when starvation continued. Single components decreased by ≈50% (C), 54% (N), 57% (J · ind^?1). Weight specific energy (J · mg DW^?1) decreased by 40% during the first 4 days of starvation, remaining constant thereafter. Individual respiration rate (R) dropped by 61 %, weight specific respiration rate (QO₂) by 55 %. Individual energy loss in starved zoea-1 was 0.077 J over a period of 11 days. In this period ≈ 9.3 μl O₂·ind^?1 were consumed. Thus effective oxygen capacity was lower than in growing larvae. It dropped to 5.3 J·mlO₂^?1 after 4 days and remained constant if starvation continued, i.e. 65 % of possible energy loss occurred during the first 4 days. Decrease in requirement for oxygen and its effective capacity were both recognized as independent components of survival during starvation. Partitioning of energy through individual larval development of C. maenas was investigated for all five larval stages. The cumulative budget could be calculated: consumption (C) = 28.23 J, growth (G) = 0.92 J, exoskeleton (Ex) = 0.20 J, metabolism (M) = 5.30 J, egestion and excretion (E) = 21.82 J. Mean gross and net growth efficiency were, K₁ = 3.3% and K₂ = 14.8%, respectively.     

The effect of temperature on feeding,growth, and metabolism during the last larval stadium of the female house cricket, Acheta domesticus

Eighth instar female house crickets at 35°C developed faster, gained slightly more wet weight, and consumed less food, water, and oxygen than at 25°C. The duration of the 8th stadium at 25°C was 13 days (undisturbed), but was 14 days when disturbed by daily weighing. The duration of the 8th stadium at 30°C was 8 days and at 35°C was 6 days. During the first half of the 8th stadium at 25, 30, and 35°C, there was a high rate of food and water consumption resulting in statistically equal maximum dry weight achievement (124 mg). Respiratory quotients greater than one during this time indicated the conversion of ingested carbohydrate to fat. During the latter half of the 8th stadium, food and water consumption declined and the crickets lost weight. The period of weight loss was proportionally much longer at 25°C than at 30 or 35°C. Respiratory quotients lower than 1.0 during the latter half of the 8th stadium at 30 and 35°C indicated the metabolism of stored lipids. The respiratory quotient at 25°C never fell below 1.0, possibly because some food remained in the gut. The absorption efficiency was not influenced by temperature (25–35°C). Though the caloric content of the faeces was lower at 25°C than at 30 or 35°C, which correlated to the much longer time for food passage at 25°C than at 35°C, the difference in total calories egested was insufficient to alter the absorption efficiency. A longer period of reduced feeding and greater dry weight loss during the latter half of the 8th stadium at 25°C resulted in a lower metabolic efficiency at 25°C than at 30 or 35°C. Eighth instar crickets in response to a step-function transfer from 30°C–25 or 35°C showed an immediate (<1 hr) and complete metabolic adjustment which was not affected by the temperature history during the 7th stadium. House crickets did not exhibit temperature acclimation in the range 20–40°C, the metabolic rate being determined by ambient temperature. The Q₁₀ for oxygen consumption in the range 20–40°C was about 2.     

Oxygen consumption and haemocyanin function in the freshwater snail Marisa cornuarietis (L.)

• 1.1. The MO₂ for branchial respiration in adult snails increased from 0.24 mmol/l/O₂ kg/hr at 18°C to 0.83 mmol/l/O₂ kg/hr at 40°C. Q₁₀ values were 2.75 between 35 and 40°C and 1.8 between 18 and 30°C.
• 2.2. The haemocyanin (31.9 ± 5.8 mg/ml) has a high oxygen affinity (6.28 ± 0.8 at 25°C) with a reversed Bohr effect measured between a pH of 6.80 and 7.95 with gelchromatographed haemolymph, and measured between a pH of 7.34 and 8.10 for native haemolymph.
• 3.3. Growth rate is optimal between 27 and 30°C whilst at 24°C stunted growth was found.
• 4.4. At 25°C the same MO₂ values were found for aerial and aquatic respiration.

     

The dependence of oxygen consumption of the common whelk (Buccinum undatum) on hypoxia,salinity and air exposure

• 1.1. Oxygen consumption of low salinity (20‰) acclimated whelks decreases markedly upon acute exposure to hypoxia (P_WO₂ = 35 Torr), but almost regenerates its original level within 48 hr exposure to the hypoxic condition.
• 2.2. This ability to regain the original level of oxygen consumption is not seen in high salinity (35‰) acclimated whelks.
• 3.3. Oxygen consumption in air at 10°C is more than twice the rate shown by low salinity acclimated whelks in normoxic water (P_WO₂ = 150 Torr).
• 4.4. Q₁₀ for oxygen consumption in air is about 1.0 in the temperature range 10–20°C.

     

Effect of low temperature on emergence, fecundity, longevity and host-feeding by Trichogramma brassicae

The occurrence of sub-optimal temperatures during development of immature parasitoids can have important consequences on adult fitness. We investigated the impact of different regimes of low temperature on emergence, differential mortality, longevity and fecundity in Trichogramma brassicae Bezdenko (Hymenoptera: Trichogrammatidae). The host-feeding behaviour of adult females was also measured as an indicator of energy reserve at emergence. Acclimation of 30 days at 10 °C or 24 days at 13 °C allowed T. brassicae immatures to develop with a lower mortality than those exposed directly at 5 °C. Longevity and fecundity of females decreased at a lower rate with acclimation at 10 °C suggesting that acclimation at 13 °C may have depleted the energy reserves of individuals more than acclimation at 10 °C. Short photoperiod exposure during the maternal generation had no effect on progeny’s fitness. We found no difference among the treatments in females’ host-feeding behaviours, in differential mortality at emergence, in female’s mobility and in F1 sex ratio.     

Susceptibility of the cigarette beetle Lasioderma serricorne (Coleoptera: Anobiidae) to hypoxia

The susceptibility of the cigarette beetle Lasioderma serricorne (F.) to hypoxia was examined at three different oxygen concentrations (0.5?C0.8, 1.0?C1.3, and 2.0?C2.3?%) and four different temperature/humidity (RH) conditions: 30?°C/75?% RH, 25?°C/75?% RH, 20?°C/43?% RH, and 15?°C/43?% RH. The influence of humidity on mortality was also examined at three humidity levels (21, 43, and 75?% RH) at 1.0?C1.3?% oxygen (O₂) and 25?°C. Our results revealed that adult beetles were the most tolerant at 2.0?C2.3?% O₂ and that the larvae were the most tolerant at O₂ levels <1.0?C1.3?%. Mortality increased with increasing temperatures and decreasing O₂ concentrations. At 30?°C, 75?% RH, and 0.5?C0.8?% O₂, the 99?% lethality (LT₉₉) of larvae was 6.9?days; however, it increased to 20?days when the temperature was decreased to 25?°C or when O₂ levels were increased to 1.0?C1.3?%. Humidity also influenced mortality of both larval and adult beetles. LT₉₉ values for larvae at 25?°C and 1.0?C1.3?% O₂ were 24.0, 44.6, and 50.2?days at 21, 43, and 75?% RH, respectively. Results of this study indicate that a controlled atmosphere (CA) with reduced oxygen levels (<0.5?C0.8?% O₂) represents an effective measure for disinfesting stored tobacco as an alternative to conventional phosphine fumigation at temperatures >30?°C.     

Adult diapause ofCybocephalus nigriceps nigriceps [Col.: Cybocephalidae]

During autumn and winter (October–February)Cybocephalus nigriceps nigriceps (J. Sahlberg) adults undergo a facultative diapause. The diapausing adults agregate in hiding places, development of the ovaries is arrested, and prey consumption is lowered. Diapause can be prevented by exposure to a long-day photoperiod (16 hr light) at high temperatures (29° and 32°C). Diapause is induced mainly by short-day conditions, but the termination of diapause is affected by both photoperiod (long-day conditions) and temperature (29°, 32° and 34°C). In mature females, diapause induction causes ovarian degeneration. The induction or inhibition of adult diapause is affected by photoperiods occurring during larval development as well as during adult life.     

Effect of photoperiod and temperature on diapause in a Florida strain of the tropical warehouse moth Ephestia cautella

A photoperiodically-controlled diapause of the long-day, short-day type was identified in a brown-winged, yellow-eyed strain of Ephestia cautella (Walker). The proportion of larvae diapausing in very long photoperiods was less than in short photoperiods. The mean critical photoperiod, here defined as that photoperiod giving half the maximum percentage of insects that diapause in response to photoperiod at a given temperature, was between 12 and 13 hr for the long-day reaction at both 20 and 25°C. The principal sensitive phase occurred near the time of the last larval moult. The mean duration of diapause was 2–3 months at 20°C and slightly longer at 25°C. The optimum temperature for diapause development was near 15°C, all larvae pupating within 24 days after a 45-day exposure at this temperature. Diapause could be terminated whenever larvae diapausing at 20°C were exposed to as few as five long (15 hr) photoperiods at 25°C. Long photoperiods at 20°C, or short photoperiods (9 hr) at 25°C were less effective in terminating diapause.     

Reproduction,survival, and life table parameters of the predatory mite <Emphasis Type="Italic">Cheyletus malaccensis</Emphasis> (Acari: Cheyletidae) at various constant temperatures

Reproduction, survival, and life table parameters of the predatory mite Cheyletus malaccensis Oudemans were evaluated at six constant temperatures: 17.5, 20, 25, 30, 32.5 and 35°C, feeding on Tyrophagus putrescentiae (Schrank). Preoviposition period of fertilized and virgin females varied with temperature from ca. 9 days at 17.5°C to ca. 1.5 day at 32.5°C and then increased to ca. 3 days at 35°C. Virgin female oviposition period was significantly shorter than for fertilized females at the temperatures examined with the exception of 17.5°C. The mean total number of eggs per fertilized (169.7 ± 6.6) and virgin female (60.7 ± 4.3) was highest at the temperature of 30°C. The data indicated a significant positive and nearly doubling effect of fertilization on female fecundity at the temperatures examined with the exception of 17.5°C. Age-specific fecundity was described by a temperature dependent model from which the maximum daily fecundity rate was estimated for fertilized and virgin females at 10.3 (at 30°C) and 6.8 (at 32.5°C) eggs/female, respectively. Virgin female longevity was significantly shorter than for fertilized females at 20, 30 and 32.5°C, and decreased from ca. 57 days at 17.5°C to ca. 17 days at 35°C. The Weibull function that was used to describe the age specific survival of fertilized and virgin females produced excellent fits to the survival data. Estimates of intrinsic rate of increase, net reproductive rate, mean generation time, doubling time and finite rate of increase, were obtained. The r_m value increased with temperature from 0.03 (day⁻¹) at 17.5°C to 0.21 (day⁻¹) at 32.5°C, after which it decreased to 0.15 (day⁻¹) at 35°C. These data indicate that C. malaccensis can reproduce at temperatures between 17.5 and 35°C and can be used for biological control of astigmatid mites within the temperature range where the pest occurs.     

Dark respiration of the stipe of Ecklonia cava (Laminariales, Phaeophyta) in relation to temperature

Sporophytes of Ecklonia cava Kjellman (Laminariales, Phaeophyta) with a stipe length of 22–102 cm were collected at 6–9 m depth in Nabeta Bay, Shimoda, central Japan by scuba diving in February (winter) and in August (summer) 1998. Dark respiration of the intact stipe of E. cava was measured at various water temperatures ranging from 15 to 27.5°C in winter and 15–30°C in summer in a closed system by using a dissolved oxygen meter. The stipe respiration was compared on whole stipe, length, surface area, volume, wet weight and dry weight bases. On each basis, the stipe respiration always increased with a rise in water temperature within the temperature range investigated. The stipes showed similar respiration rates on each basis of length, surface area, volume, wet weight and dry weight at each temperature, irrespective of the stipe length. The mean respiration rates in winter (at 15–27.5°C) were: length, 16.7–32.5 μL O₂ cm^?1 h^?1; surface area, 3.2–6.2 μL O₂ cm^?2 h^?1; volume, 7.6–15.0 μL O₂ cm^?3 h^?1; wet weight, 6.2–12.2 μL O₂ g (wet weight)^?1 h^?1; and dry weight, 43.8–88.0 μL O₂ g (dry weight)^?1 h^?1. Those for summer (at 15–30°C) were: length, 17.1–32.0 μL O₂ cm^?1 h^?1; surface area, 3.6–6.8 μL O₂ cm^?2 h^?1; volume, 9.7–18.7 μL O₂ cm^?3 h^?1; wet weight, 7.6–14.6 μL O₂ g (wet weight)^?1 h^?1; and dry weight, 49.4–95.8 μL O₂ g (dry weight)^?1 h^?1. This is the first report of the intact stipe respiration of E. cava at various temperatures.     

Diapause in the mite Metaseiulus occidentalis: Stages sensitive to photoperiodic induction

Stages of Metaseiulus occidentalis sensitive to photoperiod induction of diapause were determined by transferring various stadia into diapause-inducing conditions, and rearing them until adult females could be scored for reproductive condition. When eggs were transferred to 10 hr light at 19°C from 24 hr light at 25°C and the mites reared to adults, 92 per cent entered diapause. When larvae and all subsequent stages were kept under the inductive conditions, 62 per cent of adult females diapaused. Mites transferred as protonymphs into inductive conditions yielded only 10 per cent in diapause, and mites transferred as deutonymphs or newly emerged females did not enter diapause.However, adult females reared from eggs at 19°C under 12 hr light (which is near the critical photophase of 11·2 hr at 19°C) showed an unexpected sensitivity to photoperiod. Some newly emerged females oviposited upon transfer to an 8 hr photophase at 19°C. Some then stopped ovipositing and apparently entered diapause; these females resumed ovipositing after intervals ranging from 34 to 100 days. This was termed ‘switching’ into diapause. Some females reared under a 16 hr photophase at 19°C ‘switched’ also upon transfer as adults to shorter photophases—either 8 or 12 hr at 19°C. Thus, ‘switching’ may be due to transfer to shorter photophases. Promptness of mating vs delayed mating allowed ‘switching’ to be more easily detected.     

Life history parameters for Nesidiocoris tenuis (Reuter) (Het., Miridae) under different temperature regimes

The development time for eggs and nymphs and female fertility were determined for Nesidiocoris tenuis Reuter (Het., Miridae: Dicyphini) at 15, 20, 25, 30, 35 and 40 ± 1°C, using tomato, Solanum esculentum (Miller), as substrate and eggs of Ephestia kuehniella Zeller as substitute prey. At 40°C, N. tenuis was unable to develop and barely reproduced. Egg development ranged from 30.8 days at 15°C to 6.3 days at 35°C. The cumulative thermal requirements for the eggs were 148.6 degree days (°d) and the lower thermal threshold, 10.3°C. The duration of the nymphal instar decreased from 55.9 days at 15°C to 8.6 days at 35°C. The thermal constant for the nymphs was 182.3 °d and the lower thermal threshold 11.7°C. No nymphs survived at 40°C, and the highest mortalities were at extreme temperatures (15 and 35°C). Female and male weights were influenced significantly by temperature. The fertility of N. tenuis females was reduced greatly at 15 and 40°C. The highest fertility during an observation period of 18 days following female emergence (79.5–60.0 nymphs per female) was within the temperature range of 20 to 35°C. Fertility was related directly to female weight and temperature (r² = 0.932). Based on development, reproduction data and thermal requirements, the optimum temperature range for N. tenuis was established as being between 20 and 30°C. Overall, N. tenuis is the most thermophilous of all dicyphines from vegetable crops in the Mediterranean area studied so far.     

Changes in the oxygen consumption of cysts of Globodera rostochiensis associated with the hatching of juveniles

The oxygen consumption of single cysts (90–110 /tg dry wt) was measured with an oxygen electrode microrespirometer. The mean oxygen consumption of nine cysts after 7 days in tap-water, was 0–48 + 0–05 mm³ 0₂ mg dry wt^-1 h^-1. After transfer to potato root diffusate for 1 day the mean oxygen consumption of the same cysts showed a significant increase to 159±7% of the rate recorded before they were removed from water. After 3 and 7 days in diffusate the corresponding means were 131±9% and 127±12% respectively. Cysts that remained in water throughout the experiments did not show any significant change in their oxygen consumption from the rate recorded after 7 days. The initial increase in oxygen uptake after the addition of diffusate was shown not to be due to the presence of microorganisms. Comparison of hatching data with the changes in oxygen consumption of similar cysts after 24 h in diffusate suggests that the increased oxygen uptake cannot be attributed solely to locomotor activity of the juveniles during the hatching process. The increased rate of respiration may precede other known changes that follow after the juveniles within a cyst are stimulated to hatch.     

Thermal tolerance and standard metabolic rate of juvenile gilthead seabream (Sparus aurata) acclimated to four temperatures

Temperature variation affects the growth, maturation and distribution of fish species due to increasing constraints on physiological functions therefore, the aim of the present study is to evaluate effect of temperature on thermal tolerance and standard metabolic rate (SMR) of gilthead seabream (Sparus aurata). For this purpose, tolerable temperature ranges of juvenile gilthead seabream acclimated at 15, 20, 25, and 30 °C for 30 days were estimated using dynamic and static thermal methodologies. The SMRs of the fish were also determined based on oxygen consumption rate (OCR). The dynamic and static thermal tolerance zones of gilthead seabream were calculated as 737 °C² and 500 °C², respectively, with a resistance zone area of 155.5 °C². The SMR of the fish at the above acclimation temperatures (AT) was determined as 138, 257, 510, and 797 mg O₂ h⁻¹ kg⁻¹, respectively and were significantly different (P < 0.01, n = 10). The temperature quotient (Q₁₀) in relation to the SMR of the fish was calculated as 3.45, 3.91, and 2.44 for acclimation temperature ranges of 15–20, 20–25, and 25–30 °C, respectively. The fact that the SMR increased with rising temperatures and then decreased gradually after 25 °C indicates that the temperature preference of juvenile gilthead seabream lies between 25 and 30 °C. This study shows that gilthead seabream tolerates a relatively narrow temperature range, and consequently, a low capacity for acclimatisation to survive in aquatic systems characterised by temperature variations.