Convergence and parallelism among cicadas of Argentina and the southwestern United States (Hemiptera: Cicadoidea)

Cicadas of the genera Derotettix in Argentina and Okanagodes in the south-western United States resemble each other in colour, live on salt-tolerant plants ( Atriplex spp. etc.), nearly match the colour of their respective host plants and produce songs above the range of avian hearing. The Argentine cicadas are smaller, but have nearly identical thermal limits for activity measured by the minimum temperature for flight (20–24 °C) and a body temperature at heat torpor (48–49 °C). The species shift activity from basking sites to shade at temperatures above 37 °C, although O .  gracilis rises to a significantly higher temperature (40.7 °C) than its congener (38.2 °C) or Derotettix (37.2 °C). The thermal tolerances are the highest reported for cicada species. A third group using halophytes in Argentina ( Babras sonorivox ) has similar temperature tolerances and is cryptically coloured. The genera are convergent with respect to morphology, coloration, body size, behaviour, habitat choice and host plant selection. The similarities of thermal tolerances and their influence on behaviour can be viewed as parallelism because the underlying mechanisms are the same in all species studied.  © 2004 The Linnean Society of London, Biological Journal of the Linnean Society , 2004, 83 , 281–288.     

Seed dormancy in Rumex species in response to environmental factors

Abstract. Many Rumex species show similar seed dormancy characteristics but there is more information concerning R. crispus and R. obtusifolius than other species. These species respond positively to red or white light. Far-red light applied for short periods may promote or inhibit germination depending on the timing of the irradiation in relation to temperature change; but long periods of far-red inhibit germination. Seeds may also be stimulated to germinate in the dark by low-temperature stratification at 15°C or less providing the temperature of the seeds is subsequently raised to a minimum of about 15°C. Seeds can, however, germinate at lower temperatures providing they have received other appropriate stimulatory treatment. Seeds also respond to alternating temperatures. In a diurnal cycle the minimum upper temperature required is about 15°C and the maximum lower temperature is about 25°C. The optimum period spent at the upper temperature is about 8 h when it is 15–25°C but the optimum period decreases as the upper temperature is increased above this range so that at 45°C, for example, it is only about 30 min. The period spent at the lower temperature in a diurnal cycle is not critical. Providing these criteria are met, the percentage germination increases with the number and amplitude of the cycles. The warming part of the cycle is necessary for the response but so far there is no convincing evidence that cooling itself is important. Secondary dormancy is induced at constant temperatures at a rate dependent on temperature, but apparently only in the presence of oxygen. This feature affects the optimum timing of a temperature change or exposure to light. Strong positive interactions are shown between stimulatory temperature treatments and white or red light. Unlike many other weed species the seeds respond only slightly to nitrate ions. The implications of these responses are discussed in relation to field behaviour.     

Effect of long-term and rapid cold hardening on the cold torpor temperature of an aphid

Abstract.  The effect of long-term (seasonal) acclimation and rapid cold hardening is investigated on the cold torpor temperature ( CT _min) of adult grain aphids, Sitobion avenae, reared at 20 or 10 °C for more than 6 months before experimentation. Rapid cold hardening is induced by exposing aphids reared at 20 to 0 °C for 3 h and aphids reared at 10 to 0 °C for 30 min (acclimation regimes previously found to induce maximum rapid cold hardening). The effect of cooling aphids from the same rearing regimes from 10 to −10 °C at 1, 0.5 and 0.1 °C min⁻¹ is also investigated. In the 20 °C acclimated population, rapid cold hardening and cooling at 0.1 °C min⁻¹ both produce a significant decrease in CT _min from 1.5 ± 0.3 to –0.9 ± 0.3 and –1.3 ± 0.3 °C, respectively. Rapid cold hardening also results in a significant reduction in CT _min of the population reared at 10 °C from 0.8 ± 0.1 to –0.9 ± 0.2 °C. However, none of the cooling regimes tested reduces the CT _min of the winter-acclimated (10 °C) population. The present study demonstrates that rapid cold-hardening induced during the cooling phase of natural diurnal temperature cycles could lower the movement threshold of S. avenae , allowing insects to move and continue feeding at lower temperatures than would otherwise be possible.     

Thermoregulation and metabolism in the Cape golden mole (Insectivora: Chrysochloris asiatica)

The Cape golden mole, Chrysochloris asiatica is an insectivore which excavates superficial foraging burrows as it searches for its food. It has a mean (±S.D.) resting metabolic rate (RMR) when newly captured of 1–17±0.17 cm³ O₂g^-1 h^-1 ( n = 14), within the thermoneutral zone (TNZ) of 30–32°C.
The body temperature (Tb) of the mole in the TNZ is low 32.9 ± 0.36 ( n = 14) and remains stable at ambient temperatures (Tas) from 28–32°C. Above 32°C (range 34–37°C), Tb increases albeit slightly to 36 ± 1.75°C ( n = 14). The conductance is high 0.27 ± 006cm³ O₂g^-1 h^-l°C^-1 ( n = 46) at the lower limit of thermoneutrality. The mean RMR at 9°C (the lowest Ta tested) was 4.82±11 cm³ O₂g^-1h^-1, which is 4.1 times that of the RMR in the TNZ.
At an ambient temperature of 9°C, three of the golden moles entered a state of torpor where the RMR was reduced from 5.9±0.56 to 10 1.0 ± 0.69cm³O₂g^-1h^-1.     

Thermoregulation, energy metabolism, and torpor in blossom-bats, Syconycteris australis (Megachiroptera)

Since little information is available on torpor in bats of the suborder Megachiroptera, we investigated whether the small (18 g) blossom-bat Syconycteris australis displays torpor in the laboratory. Bats entered daily torpor when food and water were withheld for one night and the air temperature (T_a) was below about 26°. Torpor began shortly after lights went on in the morning and lasted for a maximum of 12 hours. During torpor at T_a18°, metabolic rates fell to a minimum of about 15% of that in resting individuals at the same T_a, and to about 40% of the basal metabolic rate. The body temperature (T_b) during torpor was metabolically defended at or above about T_b 18°. Individuals that did not enter torpor in the morning reduced their T_b from about 34.5°, observed in resting individuals that had been fed during the previous night, to values between 30.2 and 32.8°, and the resting metabolic rate fell by about 25%. The ability to undergo short periods of torpor may explain why the distribution range of S. australis extends much further south than that of other small Australian megachiropteran bats.     

Respiration and energetics of the bumblebee Bombus terrestris queen

Carbon dioxide production by the Bombus terrestris queen was measured at different temperatures (10–30°C) and during different activities of the bumblebee. During flight the CO₂ production averaged 50 ml g⁻¹ (fresh weight) h⁻¹ and was only slightly affected by temperature. During rest (with a readiness to fly) and incubation the respiration rate clearly increased with decreasing temperature (5–40 and 13–56 ml g⁻¹ h⁻¹, respectively), whilst during torpor it increased with temperature (0.1–1.7 ml g⁻¹ h⁻¹ at temperatures from 10 to 30°C).
The expenditure of energy as calculated from the continuous respiration measurements agreed well with the amount of energy obtained from food (discrepancy 6–19%). The energy budget of an incubating queen was correctly predicted using the measured respiratory functions, prevailing temperatures, and the behaviour of the queen. The number of flower visits needed to fulfil the daily energy requirements of an incubating queen is discussed.     

Biology and life table parameters of the mushroom pest, Pediculaster fletchmanni （Acari： Siteroptidae）, at three constant temperatures

This paper is concerned with the bionomics and demography of Pediculaster fletchmanni Wicht （Acari： Siteroptidae） under controlled conditions （20 ± l, 22 ± 1 and 25 ± 1℃, 70% ± 5% relative humidity and a photoperiod of 16L ： 8D hours）. Glass Petri dishes inoculated with Trichoderma sp. mycelia were used as substrate and food source. The mean developmental time of the egg and the active larva did not differ significantly at the various constant temperatures, but these periods were significantly different for the quiescent larval stage. The preoviposition period ranged from 2.3 to 2.8 days, the ovipositional period increased with temperature increase, and all females died immediately after oviposition. The development of active larvae was the fastest of all life stages. The developmental threshold ranged between 5.25-14.22℃ the highest value being observed for the quiescent larval development. For immature development required 89.29 degree-days. Values of rm （intrinsic rate of increase） were 0.229, 0.398 and 0.386 for 20, 22 and 25℃ respectively. Finite rates of increase （λ） increased along with increasing temperature from 20-25℃ consequently the population doubling time （D） and mean generation time （T） showed significant differences with increasing temperature.     

Interspecific competition and torpor in golden spiny mice: two sides of the energy-acquisition coin

We studied the occurrence of torpor in golden spiny mice in a hot rocky desert near the Dead Sea. In this rodent assemblage, a congener, the nocturnal common spiny mouse, competitively excluded the golden spiny mouse from the nocturnal part of the diel cycle and forced it into diurnal activity; this temporal partitioning allows the two species to partition their prey populations, particularly in summer when the diet of the two species is comprised mainly of arthropods, and largely overlap. We studied the effect of the presence of the common spiny mice at two resource levels (natural food availability and food added ad libitum) on populations of golden spiny mice in four large outdoor enclosures: two with common spiny mice removed and two enclosures with populations of both species. We hypothesized that with interspecific competition and/or reduced resources, golden spiny mice will increase their use of torpor. As we expected, supplemented food reduced the total time spent torpid. In summer, when the different activity periods of the two species results in prey species partitioning, removal of the congener did not affect torpor in the golden spiny mouse. However, in winter, when insect populations are low and the two species of mice overlap in a largely vegetarian diet, removal of the common spiny mouse reduced torpor in golden spiny mice, whether food was supplemented or not. This result suggests that torpor, a mechanism that allows small mammals to sustain periods of low availability of resources or high energetic requirements, may also help them to tolerate periods of enhanced interspecific competition. This may be a significant short-term mechanism that reduces competition and hence increases fitness, in particular of individuals of the subordinate species whose accessibility to resources may be limited.     

The roles of temperature and diapause in the life history of a temperate-zone dragonfly: Argia vivida (Odonata: Coenagrionidae)

Abstract. 1. The life cycle of Argia vivida Hagen generally took longer to complete in the field than was predicted on the basis of the thermal sum accumulated in laboratory rearing.
2. The prediction of a bivoltine life-cycle from geothermal sites with either a constant annual temperature of 26°C or thermal range of 11–31°C was not borne out because the intervention of short-day induced developmental delays in later larval instars extended the life cycle to 1 year.
3. This diapause, which synchronizes adult emergence with favourable summer temperatures, was also present in larvae from sites with annual temperature ranges of 0–33°C and 5–20°C.
4. At these colder sites completion of the life cycle takes 2 and 3 years respectively and dragonflies must be in cold-resistant stages during the winter. A long-day diapause, principally affecting late-instar larvae below a certain size during the summer, achieves this.
5. Large diurnal temperature fluctuations at the 0–33°C site markedly increase the useful thermal energy available to larvae for growth over that predicted by the thermal sum equation.
6. The interaction between the effects of temperatures favourable for growth and day-length-governed diapause, synchronize the emergence of the low-temperature sensitive adult stage of this tropical dragonfly with northern-latitude summers at a variety of habitats.     

Plant mitochondria electron partitioning is independent of short-term temperature changes

We tested the hypotheses that relative activity of the less efficient alternative oxidase (AOX) path changes with diurnal temperature changes, and thus changes carbon use efficiency with temperature. The activities of the alternative and cytochrome oxidase (COX) paths in plant tissues of three species were determined by measuring ¹⁸O/¹⁶O discrimination and total respiration from 17 to 36 °C. A new, more accurate method for calculating oxygen uptake rate from the mass spectrometry data was developed. Total carbon use efficiency was calculated from the ratio of respiratory heat and CO₂ rates measured from 10 to 35 °C. Oxygen isotope discrimination (22.9 ± 0.4‰) and AOX participation were invariant with temperature in leaf tissue of Cucurbita pepo , Nicotiana sativa and Vicia faba , thus falsifying the first part of the hypothesis. Stress responses of respiration at the temperature extremes limited the range for which carbon use efficiency could be accurately measured to 15–30 °C in N. sativa , to 10–25 °C in C. pepo and to 20–30 °C in V. faba . Carbon-use efficiency was invariant at these temperatures in these species, demonstrating that changes in other pathways that would vary carbon-use efficiency were also invariant with temperature.     

Neural function in an alpine grylloblattid: a comparison with the house cricket, Acheta domesticus

ABSTRACT. The effect of temperature on evoked activity in giant interneurons was compared in Grylloblatta sp. (an alpine insect with a temperature preference close to 0°C) and Acheta domesticus. The response to sound and air-puff stimulation of the abdominal cerci was monitored with extracellular electrodes placed under the ventral nerve cord. Responses to air puffs were elicited in Grylloblatta while the animal was supercooled to -6°C. The supercooling point was reached and freezing occurred in the range -5.5 to 8.5°C. The upper extinction temperature could not be determined due to massive spontaneous giant fibre activity in the 12–15°C range masking responses to air puffs. Lethal heat coma occurred at 15–20°C, although most animals did not recover from the spontaneous CNS activity which preceded it. The extinction ranges for Acheta giant neurons were 3.5-4.0°C and 42–44°C. Spike number peaked at 33–36 C and amplitude levels diminished as heat or cold coma was approached; -7.5 C was the mean supercooling point. Both species recovered from cold coma if supercooling was avoided; in Acheta , heat coma was also reversible. Giant fibre latencies in Acheta displayed a Q₁₀ of 1.2 above 11–14°C, below which a break occurred in the curve and delays increased sharply. Latencies for the grylloblattid exhibited a Q₁₀ of 2 but no break in the curve was observed until 0° C was approached. Spike number and amplitude increased with temperature until spontaneous CNS activity obliterated responses to air puffs. The potential role of unsaturated fatty acids in low temperature adaptation in Grylloblatta is discussed.     

Effects of temperature on the growth and survival of the European eel, Anguilla anguilla L.

Experiments to determine the growth rate of eels ( Anguilla anguilla L.) at different temperatures are described and show the optimum temperature for growth to be 22–23° C. The ultimate upper lethal temperature was found to be 38° C and the critical thermal maximum varied from 33 to 39° C for fish acclimated at 14 to 29° C. An attempt was also made to determine lower lethal temperatures. Eels enter a state of torpor at temperatures varying from 3° C for fish acclimated at 29° C to less than 1° C for fish acclimated at 23° C or below. The results have been used to estimate the growth rates expected from eels cultured in power station cooling water using different types of temperature control.     

Confirmation of pleisiomorphic daily torpor in mammals: the round-eared elephant shrew Macroscelides proboscideus (Macroscelidea)

The characteristics of daily torpor were measured in the round-eared elephant shrew Macroscelides proboscideus (Macroscelidea) in response to ambient temperature and food deprivation. Elephant shrews are an ancient mammal order within a superordinal African clade including hyraxes, elephants, dugongs and the aardvark. M. proboscideus only employed torpor when deprived of food; torpor did not occur under an ad libitum diet at ambient temperatures of 10, 15 and 25?°C. Torpor bout duration ranged from <1?h to ca. 18?h. The times of entry into torpor were restricted to the scotophase, despite normothermic body temperature patterns indicating a rest phase coincident with the photophase. Full arousal was always achieved within the first 3?h of the photophase. When food deprived, the onset of the rest phase, and hence torpor, advanced with respect to the experimental photoperiod. The lowest torpor body temperature measured was 9.41?°C. Daily torpor in M. proboscideus confirms a pleisiomorphic origin of daily heterothermy. Torpor facilitates risk-averse foraging behaviour in these small omnivores by overcoming long-term energy shortfalls generated by the inherent variability of food availability in their semi-arid, El Niño-afflicted habitats.     

Evaporative water loss in two sympatric species of vespertilionid bat, Plecotus auritus and Myotis daubentoni: relation to foraging mode and implications for roost site selection

Simultaneous measures of oxygen consumption and evaporative water loss (EWL) were made in two species of temperate-zone vespertilionid bat ( Plecotus auritus and Myotis daubentoni ; mean body mass 9.12 and 10.12g, respectively) at ambient temperatures (T_a) of 5, 15 and 25°C and variable vapour pressure deficit. EWL was directly dependent on vapour pressure deficit and oxygen consumption and inversely dependent on T_a. EWL was significantly greater in P. auritus than in M. daubentoni. A model for EWL in P. auritus under a variety of environmental conditions (5–25°C and 20–80% relative humidity) suggested that EWL from bats in shallow summer torpor will be lowest at low T_a, and that, except at low (> 50%) relative humidity, EWL from euthermic bats will be lowest at high T_a. At low relative humidity (< 20%), resting bats could lose over 30% of body mass per day (24 h) through evaporation. At high T_a (> 25°C), EWL from euthermic bats could be over 65% lower at high (> 80%) compared to low (< 20%) relative humidity. In bats in shallow summer torpor at low (5°C) T_a the equivalent saving was > 96%. At low relative humidity predicted EWL from bats in shallow summer torpor was 34 to 81% of that from euthermic bats, and at low T_a and high relative humidity was only 2%. In the wild, M. daubentoni has freer access to drinking water than does P. auritus and yet EWL at rest was higher in the latter species. We suggest that post-prandial dumping of urinary water by M. daubentoni leads to a limit in the amount of body water available to this species to cover evaporative losses once within the day roost, which in turn has led to an adaptation of physiology towards the minimization of EWL when at rest.     

Germination Responses of Taraxacum platycarpum Seeds to Temperature

Abstract Germination responses of Taraxacum platycarpum seeds to temperature were examined under laboratory conditions to investigate the emergence-season choice mechanism of the seeds. Almost all the newly collected seeds were non-dormant. Under constant temperature conditions, maximum percentage germination (approximately 90%) was attained at temperatures 6–16°C, where simple linear relationships were observed between the temperature and the rates of germination, i.e. the reciprocals of the time taken to germinate by seed subpopulations with 10–80% germination. Thermal time required for germination of the subpopulations ranged from 600 Kh (degree Kelvin × hours) to 1500 Kh with a relatively constant base temperature of about 2.5°C. Lower limit temperature for germination was slightly below 6°C. Higher limit temperature for germination has the normal distribution with the mean ±SD of 19±2.5°C. Pre-exposure of imbibed seeds to temperatures higher than the higher limit temperature for germination, 25 and 30°C, had no effect on the germinability and the rate of germination at a circa-optimum temperature. Moist chilling treatment at 4°C caused an increase in the variation of germination rate within the seed population, but no evidence for dormancy-inducing or breaking effects was obtained.     

THE EFFECT OF TEMPERATURE ON EGGS AND IMMATURE STAGES OF CULEX ANNULIROSTRIS SKUSE (DIPTERA: CULICIDAE)

Abstract
No immature stages of Culex annulirostris were found during field sampling in 1979–1980 when the average water temperature was < 17 °C; they reappeared when the average water temperature was 19 °C and reached the peak density (mean 107 immatures/cylinder) at 26.5 °C.
The effect of 6 temperatures (15–40°C) on egg hatching, development and survival of the immature stages of Cx annulirostris in the laboratory showed that at 15 and 40°C, eggs failed to hatch and larvae died in the first instars. The optimum temperatures for egg hatching and the survival of immature stages were 25 and 30°C. At these temperatures, 85 and 82% respectively of egg rafts hatched, the mean number of larvae per raft was 258 ± 9.8 and 260 ± 11.4 with immature survival of 83.5 and 79.0% respectively. Mean time to hatch at 20–35°C ranged from 1.2 d (35°C) to 2.9 d (20 °C). Developmental times from first instar to adult ranged from 7.1 d (35 °C) to 25.2 d (20 °C). The threshold for development of the immatures was 15.6 ± 2.5°C and the thermal constant was 142.9 ± 26.5 day—degrees (incubation temperatures 20–35°C). At less suitable temperatures of 20 and 35 °C, hatching (57.5 and 45%), number larvae per raft (mean 139.8 ± 9.8 and 102.6 ± 14.2) and survival were low.     

Working for food shifts nocturnal mouse activity into the day

Nocturnal rodents show diurnal food anticipatory activity when food access is restricted to a few hours in daytime. Timed food access also results in reduced food intake, but the role of food intake in circadian organization per se has not been described. By simulating natural food shortage in mice that work for food we show that reduced food intake alone shifts the activity phase from the night into the day and eventually causes nocturnal torpor (natural hypothermia). Release into continuous darkness with ad libitum food, elicits immediate reversal of activity to the previous nocturnal phase, indicating that the classical circadian pacemaker maintained its phase to the light-dark cycle. This flexibility in behavioral timing would allow mice to exploit the diurnal temporal niche while minimizing energy expenditure under poor feeding conditions in nature. This study reveals an intimate link between metabolism and mammalian circadian organization.     

Effect of Chronic Caloric Restriction on the Circadian Regulation of Physiological and Behavioral Variables in Old Male B6C3F1 Mice

The circadian rhythms of food and water consumption, the number of feeding and drinking episodes, oxygen consumption, carbon dioxide production, respiratory quotient, gross motor activity, and body temperature were measured in male B6C3F, mice that were fed ad libitum (AL) or fed a caloric-restricted diet (CR). The CR regimen (60% of the normal AL consumption) was fed to mice during the daytime (5 hr after lights on). CR animals exhibited fewer feeding episodes but consumed more food per feeding bout and spent more total time feeding than AL mice. It appears that CR caused mice to change from their normal “nibbling behavior” to meal feeding. Compared to AL animals, the mean body temperature was reduced in CR animals, while the amplitude of the body temperature rhythm was increased. Spans of reduced activity, metabolism, and body temperature (torpor) occurred in CR mice for several hours immediately before feeding, during times of high fatty acid metabolism (low RQ). The acute availability of exogenous substrates (energy supplies) seemed to modulate metabolism shifting metabolic pathways to promote energy efficiency. CR was also associated with lower DNA damage, higher DNA repair, and decreased proto-oncogene expression. Most of the circadian rhythms studied seemed to be synchronized primarily to the feeding rather than the photoperiod cycle. Night-time CR feeding was found to be better than daytime feeding because the circadian rhythms for AL and CR animals were highly synchronized when this regimen was used.     

Gastric emptying in Limanda limanda (L.) and the return of appetite

Limanda limanda (35–225 g) fed during daytime when trained to use demand feeders under natural photoperiods. Under continuous illumination different feeding rhythms developed which were detected by periodogram analysis. Interfeeding periods (P hours) varied with body weight (W grams) and temperature (T° C) over the range 6.5–15° C as: In P=4.4 – 0.167 (In W) – 0.05 T. Daily food intake (D grams increased with both temperature and size (In D = 0.099 T + 0.579 In W – 3.49). Relative daily intake (R as % body weight, b.w) increased with temperature but decreased with size (In R = 0.099T–0.41 In W + 1.05). These changes in daily intake are primarily caused by changes in feeding frequency; the amount eaten at a meal is relatively constant save at low temperatures (6.5° C) when appetite is suppressed. Dilution of the food with kaolin (from 4.8 to 2.2 kcal/g) did not cause a compensatory increase in meal size or frequency. Gastric emptying time (GET hours) measured by X-radiography changed with body weight, temperature and relative meal size (M % b.w.) as In GET = 0.68 In M + 0.39 In W – 0.035T + 1.46. With the exception of the lowest temperature (6.5° C) interfeeding periods closely followed GET (P = 1.09 GET – 2.6) supporting the proposal that stomach fullness is a major factor controlling appetite in the dab.     

Interactive effects of diet and thermal regime on growth of the midge Pseudochironomus richardsoni Malloch

1. Larvae of Pseudochironomus richardsoni were reared to pupation in individual enclosures, in one of three thermal habitats in a northern California stream. The average temperature range in cold seeps was 15–21 °C, while the main channel ranged from 20 to 27 °C, and side pools ranged from 18 to 33 °C. Diet consisted of either diatoms or algal detritus.
2. Specific growth rate ranged from 0.057 to 0.267 day^–1. Specific growth and developmental rates were highest on a diatom diet, and increased with temperature. Regressions of growth rate on mean microsite temperature were also significantly altered by diet. Differences in specific growth rate due to diet are magnified at higher temperatures.
3. Pupae reared on diatoms were larger than those reared on detritus. The mass of pupae reared on detritus decreased with increasing temperature. However, there was no significant relationship between pupal mass and temperature for larvae reared on diatoms.
4. The combined effects of food quality and thermal environment on growth of the midge P. richardsoni are significantly different from the independent effects of diet and temperature. Interactive effects of food quality and temperature may influence the contribution of certain aquatic habitats (algal mats) to invertebrate secondary production.