Influence of ambient and thoracic temperatures upon sexual behaviour of the gypsy moth, Lymantria dispar

ABSTRACT. In an ambient temperature ( T _a) range of 18–28°C, thoracic temperatures ( T _th) of individual male Lymantria dispar (L.), caught at flight in the field, ranged from 21 to 36.5°C, with a correlation coefficient of 0.63 between T _th and ambient temperature ( T _a). Ambient temperature (and insolation) altered the insect's body temperature and the probabilities, latencies, and durations of preflight responses to pheromone. In a wind tunnel at 16 and 20°C, quiescent males exposed to pheromone raised their T _th by sustained wing fanning from 17 and 21°C, respectively, to c. 24°C before takeoff. At 24 and 28°C ambient, T _th rose by takeoff to 28 and 31°C, respectively. The latencies of male wing fanning in response to pheromone decreased from 1.44 min at 16°C ambient, to 0.58 min at 20°C, to 0.26 min at 24°C, and to 0.16min at 28°C. The components of behaviour (antennal twitch, body jerk, step and wing tremor) that occurred between quiescence and wing fanning were more frequent at ambients of 16 and 20°C than at 24 and 28°C.     

Thoracic temperature,shivering, and flight in the monarch butterfly,Danaus plexippus (L.)

Summary Monarch butterflies, Danaus plexippus (L.), display a warm-up behavior characterized by wingstrokes of small amplitude. Thoracic temperature during this shivering and during fixed flight was measured by means of a smallbead thermistor inserted into the thorax. At ambient temperatures of 15–16°C, once shivering is initiated the thoracic temperature rises at a maximum rate of 1.3°C/min, and a thoracic temperature 4.0°C greater then ambient is produced (Table 1). Fixed flight at these low ambient temperatures results in a similar rate of increase in thoracic temperature, and a similar temperature excess is produced (Fig. 3). At ambient temperatures between 22 and 35°C the thoracic temperature of an animal starting to fly rises at a faster rate, 3.6°C/min, and reaches a greater excess, 7.9°C (Fig. 4). The wingbeat frequency of animals in fixed flight increases with increasing thoracic temperature (Fig. 2). In the absence of direct solar radiation, shivering typically occurs prior to flight at low ambient temperatures (13–17°C), and the resulting increase in thoracic temperature allows monarch butterflies to fly at these cool temperatures.I thank Miss Janice Ruppert and Mr. C. J. Doughty for their valuable technical assistance. The co-operation of the administrators of New Brighton Beach State Park in permitting me to collect in the park is appreciated. Financial support for this study was provided in part by a faculty research grant from the University of California.     

Thresholds of Response in Nest Thermoregulation by Worker Bumble Bees, Bombus bifarius nearcticus (Hymenoptera: Apidae)

Regulation of nest temperature is important to the fitness of eusocial insect colonies. To maintain appropriate conditions for the developing brood, workers must exhibit thermoregulatory responses to ambient temperature. Because nest-mate workers differ in task performance, thermoregulatory behavior provides an opportunity to test threshold of response models for the regulation of division of labor. We found that worker bumble bees ( Bombus bifarius nearcticus ) responded to changes in ambient temperature by altering their rates of performing two tasks – wing fanning and brood cell incubation. At the colony level, the rate of incubating decreased, and the rate of fanning increased, with increasing temperature. Changes in the number of workers performing these tasks were more important to the colony response than changes in workers' task performance rates. At the individual level, workers' lifetime rates of incubation and fanning were positively correlated, and most individuals did not specialize exclusively on either of these temperature-sensitive tasks. However, workers differed in the maximum temperature at which they incubated and in the minimum temperature at which they fanned. More individuals fanned at high and incubated at low temperatures. Most of the workers that began incubating at higher temperatures continued performing this task at lower temperatures, when additional nest-mates became active. The converse was true for fanning behavior. These data are consistent with a threshold of response model for thermoregulatory behavior of B. bifarius workers.     

Low ambient temperature decreases cadmium accumulation in the liver and kidneys of the bank vole (Clethrionomys glareolus)

The importance of photoperiod and ambient temperature on the accumulation of cadmium in the liver and kidneys of bank voles was determined in the present study. Males and females, aged 1 month, were given 3.0 g Cd ml^–1 drinking water and divided into four groups according to photoperiod (16 h light/8 h dark and 8 h light/16 h dark) and ambient temperature (20 or 5°C); liver and kidneys were removed for cadmium as well as copper, iron and zinc analyses at the end of 6 weeks. Bank voles exposed to 5°C in both photoperiods consumed approximately 30% less water containing cadmium than those kept at 20°C. However, the total accumulation of cadmium in the liver and kidneys of males and females exposed to the low temperatures was 4.3–4.8 and 2.2–3.3 times less than that in animals maintained at room temperature in the long and short photoperiod, respectively. Simultaneously, the low temperature brought about an increase in the copper concentrations in the liver (12–43%) and kidneys (47–78%), giving rise to an inverse correlation between the cadmium accumulation and the tissue copper concentration. In contrast to cadmium and copper, the concentrations of iron and zinc were affected primarily by photoperiod. These findings indicate that ambient temperature is an important determinant of cadmium retention in the bank vole. It appears that low temperature decreases tissue cadmium accumulation not only by reducing cadmium intake but also through changes in copper metabolism.     

Effect of incubation temperature on zearalenone production by strains of Fusarium crookwellense

After 6 weeks incubation on rice 2 strains of Fusarium crookwellense produced more zearalenone (6060–5010 mg/kg dry wt of culture) at ambient temperature (16–29°C) in daylight than at ambient temperature (18–23 °C) in darkness or at controlled temperatures of 11 °C, 20 °C or 25 °C in darkness. Yields at 25 °C were low. Incubation at 11 °C during the second 3 weeks incubation increased yields only when preliminary incubation had been at 25 °C. After 6 weeks incubation at controlled temperatures in darkness, 4 strains produced most zearalenone at 20 °C (2460-21 360 mg/kg), 1 strain at 11 °C (6570 mg/kg). Yields at a temperature oscillating daily from 10–20 °C were less than at 15 °C. One of the 5 strains produced appreciable amounts of a-zearalenol (1645 mg/kg at 20°C) and 2 of nivalenol (340 and 499 mg/kg at 20 °C).     

Thermal physiological ecology of Colias butterflies in flight

Summary As a comparison to the many studies of larger flying insects, we carried out an initial study of heat balance and thermal dependence of flight of a small butterfly (Colias) in a wind tunnel and in the wild.Unlike many larger, or facultatively endothermic insects, Colias do not regulate heat loss by altering hemolymph circulation between thorax and abdomen as a function of body temperature. During flight, thermal excess of the abdomen above ambient temperature is weakly but consistently coupled to that of the thorax. Total heat loss is best expressed as the sum of heat loss from the head and thorex combined plus heat loss from the abdomen because the whole body is not isothermal. Convective cooling is a simple linear function of the square root of air speed from 0.2 to 2.0 m/s in the wind tunnel. Solar heat flux is the main source of heat gain in flight, just as it is the exclusive source for warmup at rest. The balance of heat gain from sunlight versus heat loss from convection and radiation does not appear to change by more than a few percent between the wings-closed basking posture and the variable opening of wings in flight, although several aspects require further study. Heat generation by action of the flight muscles is small (on the order of 100 m W/g tissue) compared to values reported for other strongly flying insects. Colias appears to have only very limited capacity to modulate flight performance. Wing beat frequency varies from 12–19 Hz depending on body mass, air speed, and thoracic temperature. At suboptimal flight temperatures, wing beat frequency increases significantly with thoracic temperature and body mass but is independent of air speed. Within the reported thermal optimum of 35–39°C, wing beat frequency is negatively dependent on air speed at values above 1.5 m/s, but independent of mass and body temperature. Flight preference of butterflies in the wind tunnel is for air speeds of 0.5–1.5 m/s, and no flight occurs at or above 2.5 m/s. Voluntary flight initiation in the wild occurs only at air speeds 1.4 m/s.In the field, Colias fly just above the vegetation at body temperatures of 1–2°C greater than when basking at the top of the vegetation. These measurements are consistent with our findings on low heat gain from muscular activity during flight. Basking temperatures of butterflies sheltered from the wind within the vegetation were 1–2°C greater than flight temperatures at vegetation height.     

The daily onset of flight in the crepuscular dung beetle Onitis alexis

The role of light intensity and temperature in determining the onset of flight in the crepuscular dung beetle Onitis alexis Klug (Coleoptera: Scarabaeidae) was examined. Flight under natural light was highly synchronized, with two-thirds of the beetles that flew flying over a period of 10–12 min. In six flights on different days, the mean time of onset varied by up to 13 min, but mean onset occurred at fixed light intensity. Absolute light intensity therefore appears to be a vital cue in determining flight onset. Mean onset remained at this intensity when dusk was advanced artificially by up to about 8 min. However, when dusk was brought further forward, mean flight occurred at lower intensities and onset of flight took place over a longer period. This is interpreted as an overlapping of the period of light intensities suitable for flight with the circadian rhythm that brings the beetles to the surface. No beetles flew when kept under constant bright light or in the dark during the dusk period. Under conditions of constant dusk, the beetles appeared uncoordinated and, although the median time of onset of flight was only 3 min later than in the control flight, onset of flight was spread out over a much longer period. At soil temperatures of 20–22 °C, over 90% of the beetles flew. This percentage decreased with decreasing temperature, and less than 10% flew at temperatures of 16–17 °C.

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L'incitation quotidienne au vol chez e bousier crépusculaire Onitis alexis Klug (Col. Scarabaeidae)

Résumé L'examen a porté sur le rôle de l'intensité lumineuse et de la température sur l'incitation au vol chez Onitis alexis. Le vol en lumière naturelle est fortement synchronisé, avec les deux tiers des adultes qui s'envolent en 10–12 min. Sur six vols pour différents jours, le moment moyen d'envol variait de 13 min, mais l'envol moyen avait lieu à une intensité lumineuse déterminée. La valeur absolue de l'intensité lumineuse paraît ainsi un signal crucial dans la détermination et l'incitation au vol. Le moment d'envol se maintient à cette intensité quand le crépuscule est artificiellement avancé jusqu'à 8 min environ. Cependant, quand le crépuscule est rendu encore plus précoce, l'envol moyen se produit à des intensités plus basses et est étalé. Ceci peut être interprété comme un chevauchement de la période des intensités lumineuses favorables à l'envol avec le rythme circadien qui conduit les bousiers à la surface. Aucun adulte ne vole quand il y a maintien de lumière constante ou d'obscurité à l'heure du crépuscule. En présence de crépuscule constant, les réponses sont hétérogènes, et, bien que le moment médian d'envol ne soit retardé que de 3 min, par rapport aux témoins, l'incitation à l'envol est étalée sur une période plus longue. Avec des températures au sol de 20–22 °C, plus de 90% des adultes s'envolent. Le pourcentage diminue avec la température, et moins de 10% s'envolent à 16–17 °C.

     

Thermoregulation in four species of tropical solitary bees: the roles of size,sex and altitude

Body temperatures during free flight in the field, warm-up rates during pre-flight warm-up, and temperatures during tethered flight are measured for four tropical solitary bee species at three sites of differing altitude in Papua New Guinea. All four species are capable of endothermic preflight warm-up; three species give slopes of thoracic temperature on ambient temperature of significantly less than 1, indicating regulation of thoracic temperature. In the kleptoparasitic Coelioxys spp. (Megachilidae) and Thyreus quadrimaculatus (Anthophoridae), warm-up rates and thoracic temperatures in flight are low by comparison with the two provisioning species Creightonella frontalis (Megachilidae) and Amegilla sapiens (Anthophoridae). In both C. frontalis and A. sapiens thoracic temperatures correlate positively and significantly with both ambient temperature and body mass. In A. sapiens, body mass increases with altitude; this can be interpreted as a response to lower ambient temperatures at higher altitude, an example of Bergmann's rule. In both A. sapiens and C. frontalis populations at higher altitude have higher thoracic temperatures independent of differences of body mass, suggestive of additional morphological or physiological adaptation to lower ambient temperatures. In A. sapiens there is no qualitative difference in body temperatures between males and females after controlling for body mass, while male C. frontalis have significantly lower thoracic temperatures than females of the species. This difference between A. sapiens and C. frontalis is discussed with reference to variation in mating systems found in the Apoidea.Abbreviations C.R.I. Christensen Research Institute - P.N.G. Papua New Guinea - SFT stable flight temperature - T _a ambient air temperature - T _ab abdominal temperature - T _dif the temperature difference between thorax and abdomen - T _ex thoracic temperature excess - VFT voluntary flight temperature     

Homeothermy in adult salmon sharks, <Emphasis Type="Italic">Lamna ditropis</Emphasis>

Salmon sharks, Lamna ditropis, belong to a small group of sharks that possess vascular counter-current heat exchangers (retia mirabilia) allowing retention of metabolically generated heat, resulting in elevated body temperatures. The capacity of free-swimming lamnid sharks to regulate rates of heat gain and loss has not been demonstrated. Using acoustic telemetry, we recorded swimming depth and stomach temperature from four free-swimming salmon sharks in Prince William Sound, Alaska. Temperature data were obtained over time periods ranging from 3.8 to 20.7 h. Temperature profiles of the water column were obtained concurrently for use as estimates of ambient temperature. Mean stomach temperature among four individuals tracked ranged from 25.0 to 25.7°C. These sharks defended specific elevated temperatures regardless of changes in ambient temperature, which ranged from about 5–16°C. The maximum observed elevation of stomach temperature over ambient was 21.2°C. Because stomach temperatures were so strictly maintained relative to changes in ambient temperature, a thermal rate coefficient, k, (°C min^–1 °C thermal gradient^–1) for cooling of 0.053 min^–1 was obtained via a `control' experiment with a dead salmon shark. We show that free-swimming adult salmon sharks maintain a specific stomach temperature independent of changes in ambient temperature through a combination of physical and physiological means, and essentially function as homeotherms. This unique ability is probably the underlying factor in the evolutionary niche expansion of salmon sharks into boreal waters and in their ability to actively pursue and capture highly active prey such as salmon.     

Movement of plum curculio adults toward host trees and traps: flight versus walking

Adult plum curculios, Conotrachelus nenuphar (Herbst), were dislodged from branches of apple trees by tapping on 14 days between blossom petal fall and 3 weeks thereafter. They fell onto a small square of framed white cloth that was quickly but carefully moved to a position beneath or adjacent to the canopy of another apple tree.There, adults were observed for 50-min periods from 0800–1950 h for propensity to fly from or walk off the cloth or move to hide beneath foliage on the cloth. At each position, the mean time from observation initiation until flight, walking off or hiding did not differ significantly among these behaviors (averaging 21–30 min), but significantly more flew (31–40%) than crawled off (16–19%) or hid (18–20%). Substantial walking off but no flights occurred at air temperatures below 20 °C, whereas at temperatures of 20 °C or greater, propensity for flight was usually significantly greater than that for walking off.Flights were predominantly toward the tree canopy or inter-tree space, with only a small proportion (17% or less) toward the tree trunk or (in a parallel study) toward an unbaited black pyramid trap (mimicking a tree trunk). Walking was overwhelmingly toward the tree trunk or a black pyramid trap adjacent to the trunk. Our observations lead us to conclude that unbaited black pyramid traps next to trunks of host trees (the most attractive position) can be effective at air temperatures below 20 °C by attracting plum curculio adults that would have entered host trees by walking toward and up tree trunks.Such traps appear to be less effective at 20 °C or greater because under such conditions, adults tend to enter host trees by flight into the canopy.     

The Effect of Rearing Temperature on Flight Initiation of Trichogramma sibericum Sorkina at Ambient Temperatures

Trichogramma sibericum Sorkina was reared in the laboratory at three temperatures: 16, 21, and 26°C. Individuals from each of these treatments were then tested for propensity to initiate flight at one of four ambient temperatures: 16, 19, 21, or 26°C. Both rearing and ambient temperatures had significant effects on flight initiation. Insects reared at 16°C had the highest mean proportion of flyers; insects reared at 26°C had the lowest. The proportion of insects initiating flight increased with increasing ambient temperature. Also, the interaction of these two temperature experiences was significant. Insects reared at 16°C were more likely to initiate flight at 16°C than insects reared at 21 or 26°C. These results indicate that performance (as assessed by flight initiation) at ambient temperature is dependent on the temperature previously experienced during rearing.     

Responses and song pattern copying of Omega-type I-neurons in the cricket,Gryllus bimaculatus,at different prothoracic temperatures

Summary Omega-type I-neurons (ON/1) (Fig. 1A) were recorded intracellularly with the prothoracic ganglion kept at temperatures of either 8–9°, or 20–22° or 30–33 °C and the forelegs with the tympanal organs kept at ambient temperature (20–22 °C). The neurons were stimulated with synthetic calling songs (5 kHz carrier frequency) with syllable periods (SP in ms) varying between 20 and 100, presented at sound intensities between 40 and 80 dB SPL. The amplitude and duration of spikes as well as response latency decreased at higher temperatures (Figs. 1 B, 2, 6). At lower prothoracic temperatures (8–9 °C) the neuron's responses to songs with short SP (20 ms) failed to copy single syllables, or with moderate SP (40 ms) copied the syllable with low signal to noise ratio (Fig. 3). The auditory threshold of the ON/1 type neuron, when tested with the song model, was temperature-dependent. At 9° and 20 °C it was between 40 and 50 dB SPL and at 33 °C it was less than 40 dB SPL (Fig. 4). For each SP, the slope of the intensity-response function was positively correlated with temperature, however, at low prothoracic temperatures the slope was lower for songs with shorter SPs (Fig. 5). The poor copying of the syllabic structure of the songs with short SPs at low prothoracic temperatures finds a behavioral correlate because females when tested for phonotaxis on a walking compensator responded best to songs with longer SPs at a similar temperature.Abbreviations epsps excitatory postsynaptic potentials - ON/1 omega-type I-neuron - SP syllable period - SPL sound pressure level     

The energetics of the common mole rat Cryptomyś, a subterranean eusocial rodent from Zambia

Body temperature, oxygen consumption, respiratory and cardiac activity and body mass loss were measured in six females and four males of the subterranean Zambian mole rat Cryptomys sp. (karyotype 2 n=68), at ambient temperatures between 10 and 35°C. Mean body temperature ranged between 36.1 and 33.2°C at ambient temperatures of 32.5–10°C and was lower in females (32.7°C) than in males (33.9°C) at ambient temperatures of 10°C but dit not differ at thermoneutrality (32.5°C). Except for body temperature, mean values of all other parameters were lowest at thermoneutrality. Mean basal oxygen consumption of 0.76 ml O₂·g^-1· h^-1 was significantly lower than expected according to allometric equations and was different in the two sexes (females: 0.82 ml O₂·g^-1·h^-1, males: 0.68 ml O₂·g¹·h^-1) but was not correlated with body mass within the sexes. Basal respiratory rate of 74·min^-1 (females: 66·min¹, males: 87·min^-1) and basal heart rate of 200·min^-1 (females: 190·min^-1, males: 216·min^-1) were almost 30% lower than predicted, and the calculated thermal conductance of 0.144 ml O₂·g^-1·h¹·°C^-1 (females; 0.153 ml O₂·g^-1·h^-1·°C^-1, males: 0.131 ml O₂·g^-1·h^-1·°C^-1) was significantly higher than expected. The body mass loss in resting mole rats of 8.6–14.1%·day^-1 was high and in percentages higher in females than in males. Oxygen consumption and body mass loss as well as respiratory and cardiac activity increased at higher and lower than thermoneutral temperatures. The regulatory increase in O₂ demand below thermoneutrality was mainly saturated by increasing tidal volume but at ambient temperatures <15°C, the additional oxygen consumption was regulated by increasing frequency with slightly decreasing tidal volume. Likewise, the additional blood transport capacity was mainly effected by an increasing stroke volume while there was only a slight increase of heart frequency. In an additional field study, temperatures and humidity in different burrow systems have been determined and compared to environmental conditions above ground. Constant temperatures in the nest area 70 cm below ground between 26 and 28°C facilitate low resting metabolic rates, and high relative humidity minimizes evaporative water loss but both cause thermoregulatory problems such as overheating while digging. In 13–16 cm deep foraging tunnels, temperature fluctuations were higher following the above ground fluctuations with a time lag. Dominant breeding females had remarkably low body temperatures of 31.5–32.3°C at ambient temperatures of 20°C and appeared to be torpid. This reversible hypothermy and particular social structure involving division of labour are discussed as a strategy reducing energy expenditure in these eusocial subterranean animals with high foraging costs.Abbreviations BMR basal metabolic rate - br breath - C thermal conductance - HR neart rate - LD light/dark - M _b body mass - MR metabolic rate - OP oxygen pulse - PCO₂ partial pressure of carbon dioxide - PO₂ partial pressure of oxygen - RMR resting metabolic rate - RR respiratory rate - T _a ambient temperature - T _b body temperature - TNZ thermal neural zone - O₂ oxygen consumption     

Phenotypic plasticity across 50 MY of evolution: Drosophila wing size and temperature

We studied the response in wing size to rearing at different temperatures of nine strains of Drosophila representing six species. The species varied in their natural habitats from tropical to temperate and one cosmopolitan. The evolutionary divergence of the species spans 50 million years. While some quantitative differences were found, all species responded to temperature very similarly: females increased an average of ∼11% and males ∼14% when reared at 19 °C compared to 25 °C. The phenotypic plasticity in wing size in response to temperature appears to be a fixed trait in Drosophila across long evolutionary time and diverse ecological settings. This likely reflects the close relationship between wing area (and thus wing loading) and insect body mass that is a crucial factor for flight regardless of ecology and is, thus, maintained across long evolutionary time.     

Body surface temperatures of jerboas (Allactaga) in uniform thermal environments

Summary Body surface temperatures of threeAllactaga elater and oneA. hotsoni were measured by infrared radiography at ambient temperatures of 1° to 42°C. In each test the radiant temperature of environmental surfaces was the same as air temperature.At ambient temperatures of 40–42°C, the temperature of the entire body surface was close to ambient temperature. As ambient temperature was lowered toward 1°C, forehead and back temperatures became increasingly greater than ambient temperature (Fig. 3), indicating an increasing thermal flux across these parts of the body. Forehead and back temperatures were linear functions of ambient temperature below thermoneutrality and behaved as expected according to a model of thermal exchange developed here. The surface temperature of the extraordinarily large pinnae remained close to ambient temperature down to 10°C (Fig. 3), indicating that deep pinna temperature likely falls with decreasing ambient temperature and that the pinnae, despite their size, are not major sites of heat loss at low ambient temperatures.     

Response characteristics of cold cell on the antenna ofLocusta migratoria L.

Summary The dendritic outer segment of the cell which is most likely the cold unit in the poreless coeloconic sensilla onLocusta migratoria antennae, has finger-like projections up to 1.5 m long and 0.13 m thick (Fig. 1). This unit responds to constant temperature, to slowly changing temperature and to step changes. Under stationary conditions impulse frequency attained 35 imp/s. Between 14 °C and 41 °C the higher frequencies were associated with the higher temperatures (Fig. 5). In this range the differential sensitivity is positive but not large: + 0.8 (imp/s)/°C. Its resolving power for steady temperature is 4.7 °C.Downward step changes produced by shifting between airstreams at different temperatures yield far higher frequencies (Figs. 2, 3). Step amplitudes were between –0.1 °C and –12 °C; the conditioning temperature from which the steps were initiated, was between 16 °C and 33 °C. Frequency peaked during the first 50 ms after stimulus onset (Fig. 2) and reached its highest values (310–340 imp/s) at initial temperatures above 30 °C and steps larger than –10 °C (Fig. 4). The mean differential sensitivity from 23 curves was –19 (imp/s)/°C and the resolving power 0.6 °C.During slowly changing temperature the impulse frequency was governed by two parameters simultaneously: ambient temperature and its rate of change. Rates were between 0.001 °C/s or less, and 0.03 °C/s in either direction. Frequency was higher during slow cooling at a given temperature than during slow warming (Fig. 6). The average differential sensitivity to the rate of change was –210 (imp/s)/(°C/s). Further, the larger responses to cooling developed at lower ambient temperatures (differential sensitivity: –1.0 (imp/s)/°C). It is to be noted that this sign is negative, in contrast to the sign for differential sensitivity to constant temperature and also for the influence of initial temperature on the response to downward step changes.Abbreviations b Slope of characteristic curve, differential sensitivity - F impulse frequency in imp/s - imp/s impulses/s - P _w partial pressure of water vapor in torr - r correlation coefficient - T temperature in °C - T T-step - x resolving power in °C     

Partial arousals from hibernation in hedgehogs in outdoor hibernacula

Summary Thermal properties of hibernacula and sequences of arousals have been studied in four adult hedgehogs for seven months starting in October. Departures and entries to the nesting chamber were continuously monitored together with ambient temperature and the temperature in the hibernacula.During the two first months of the experimental period nest departures were intermittently recorded, predominantly in the two females which also occasionally foraged. The longest periods spent continuously in the hibernaculum ranged from 129 to 178 days. The natural hibernation season for Danish hedgehogs was found to comprise the six months from October onwards when there is little shelter where hedgehogs normally roam.Ambient temperatures recorded were —11 to +13° C being subzero for half the total time measured. The nest temperatures generally were higher, and above 0° C during 78–99% of total time, most commonly ranging from 0° to 4° C and thus reflecting deep hibernation.Between December and May spontaneous increases in nest temperatures amounting to 7–26° C (average 18° C) and bringing these temperatures to 10–29.5° C were recorded in 58 cases. Fiftyfour arousals did not involve departure from the hibernaculum (partial arousals). In the remaining cases (full arousals) the preceding rewarming lasted 4 1/2–6 1/2 h and nest departures amounted to 10,2 and 5 min in one female hedgehog and 90 min in another.The hedgehogs showed 12–18 arousals, the mean duration of which was 34–44 h. The high energy expenditure associated with arousals however, was found to last on average 21 h during each arousal. It is hypothesized that the body temperature during arousals chiefly was below 35–37° C.The time between arousals was 3–15 days. Periods in hibernation averaged 7–8 days in the females and 9–10 days in the heavier males, being generally longest in January-February. Neither arousals nor re-entries into deep hibernation occurred at any particular time of the day. It is suggested that for undisturbed hedgehogs arousals are induced and controlled by endogenous factors. In conclusion it is stressed that future studies on hibernation should recognize the importance of individual variability in the response pattern and focus interest on the endogenous factors which govern this important process.     

Effect of temperature on the ovipositional biology and egg viability of the cattle tickBoophilus annulatus (Acari: Ixodidae)

The effect of temperature on the ovipositional biology ofBoophilus annulatus (Say) was determined under laboratory conditions. Engorged females subjected to constant temperatures of 12 and 45°C died without ovipositing, while females held at 15 and 40°C laid eggs which did not hatch. The preoviposition period at 25–40°C was 2–3 days; however, significant increases occurred at 20°C (5.2 days) and at 15°C (16.3 days). The number of eggs laid per female was ca. 2700 at temperatures of 25–35°C, but decreased significantly at 20°C (ca. 2300 eggs/female), 15°C (ca. 1800 eggs/female), and at 40°C (ca. 300 eggs/female). No differences were observed in the Conversion Efficiency Index (CEI) values at temperatures of 20–30°C (ca. 50%), while temperatures of 15 and 40°C produced the lowest CEI values at 35.6 and 4.9%, respectively. Hatch-ability of eggs was ca. 80% at temperatures of 20–35°C. Incubation period of eggs ranged from 52.2 days at 20°C to 16.2 days at 35°C. The thermal threshold for egg development determined by linear regression was 12.9°C. Females subjected to four fluctuating temperature regimes produced no differences in number of eggs/female (ca. 2400), CEI (ca. 50%), or hatchability of eggs (ca. 75%). Preoviposition period and incubation were significantly affected by a change in the thermoperiod, becoming longer in duration as the temperatures were decreased. From studying females exposed for various intervals from 0 to 105 days at 12°C, indications were that the longer the exposure period the more adverse the effects were on oviposition and egg-hatch. Correspondingly, exposure of eggs to a temperature of 15°C for up to 105 days gave indications that the longer the eggs remained at 15°C, the lower the hatch would be after transfer back to a temperature of 25°C.     

Effects of ambient Lake Mohave temperatures on development,oxygen consumption,and hatching success of the razorback sucker

Synopsis Spawning of razorback suckers,Xyrauchen texanus, in Lake Mohave occurred from 10–22°C and larvae were collected at water temperatures from 10–15°C in 1982 and 1983. In the laboratory, hatching success was similar from 12–20°C, but reduced hatching success was found at 10°C while none hatched a 8°C. Development rate and oxygen consumption were positively related to incubation temperature. Direct effects of ambient Lake Mohave water temperatures on hatching success of razorback sucker embryos are considered minimal. Historical spawning temperatures for the species are hypothesized based upon successful incubation temperatures and comparison to the white sucker,Catostomus commersoni.     

Thermal investigations of a honey bee colony: thermoregulation of the hive during summer and winter and heat production of members of different bee castes

Summary The temperature at the centre, the periphery and the entrance of a honey bee colony (Apis mellifera carnica) was continuously determined during the summer season and the broodless time in winter. During the summer season the temperature in the brood nest averages 35.5°C with brief excursions up to 37.0°C and down to 33.8°C. Increasing environmental temperatures resulted in linear increases in the temperature of the hive entrance, its periphery and its centre. The temperature in the centre of an overwintering cluster is maintained at an average value of 21.3°C (min 12.0°C, max 33.5°C). With rising ambient temperatures the central temperature of a winter cluster drops whereas the peripheral temperature increases slightly. With decreasing external temperatures the peripheral temperature is lowered by a small amount while the cluster's centre temperature is raised. Linear relationships are observed between the central and the ambient temperature and between the central temperature and the temperature difference of the peripheral and the ambient temperatures. The slopes point to two minimum threshold values for the central (15°C) and the peripheral temperature (5°C) which should not be transgressed in an overwintering cluster. Microcalorimetric determinations of the heat production were performed on the three castes of the honey bee: workers, drones and queens of different ages. Among these groups single adult workers showed the highest heat production rates (209 mW·g^–1) with only neglectible fluctuations in the heat production rate. Juvenile workers exhibited a mean heat production rate of 142 mW·g^–1. The rate of heat production of adult workers is strongly dependent upon the number of bees together in a group. With more than 10 individuals weight-specific heat dissipation remains constant with increasing group sizes at a level approximately 1/17 that of an isolated bee. Differences are seen between the rates of virgin (117 mW·g^–1) and laying (102 mW·g^–1) queens. Laying queens showed less thermal fluctuations than virgin queens. High fluctuations in heat production rates are observed for drones. In both groups (fertile, juvenile) phases of high and extremely low activity succeed one another. The heat production of juvenile drones was 68 mW·g^–1, that of fertile drones 184 mW·g^–1 due to stronger locomotory activities.