House mice bred for many generations in two environments

Wild house mice, Mus musculus L., were trapped, and their descendants reared, in permanently mated pairs, for a number of generations in two laboratory environments, at about 21°C (controls) and -3°C, respectively. All mice had sawdust and cottonwool for bedding; but the nests of those at -3°C were colder than those in the warm, and fluctuated greatly in temperature.
Reproductive performance was inferior in the cold environment: more pairs were barren, and the fecund pairs reared fewer young than the controls. Yet litters at birth were usually larger in the cold, and the young at three weeks were always heavier. Over ten generations nestling mortality declined at -3°C.
From generation 1 on, adult mice at -3°C were heavier than the controls, but there was no corresponding increase in body length. Tails were much shorter relative to body length in the first generations in the cold, but returned to control proportions by generation 10. Most of the structural changes in the cold accord with the "rules" of Bergmann and Allen.
The incidence of abnormal sixth lumbar vertebrae was low in all generations at both temperatures.
After nine generations, some mice were transferred from the cold to the warm environment, and bred for a further three generations. There they outstripped the controls both in reproductive performance and in growth. They also had more fat, and a heavier and longer small intestine; but the heart, stomach and kidneys were lighter than those of the controls. Adrenal weights at 21°C declined over the generations, but those of the mice at -3°C did not.
The secular changes observed, especially those in the cold environment, are attributed principally to differential selection of genotypes, not to inbreeding; but maternal effects may also have been involved.     

MATERNAL PROCESSES IN THE COLD-ADAPTATION OF MICE

• 1 Both laboratory and wild house mice, Mus musculus, given bedding, can breed in captivity in an environment kept at – 3°C. The nest temperature when a young litter is present then fluctuates widely. In a typical laboratory (at 21°C) the temperature of the nest is both higher and more constant.
• 2 The ovaries of pregnant mice breeding at – 3°C have more corpora lute a than controls at 21°C. This is not an index of a higher ovulation rate, but is evidently due to the presence of corpora lutea from a pievious ovulation.
• 3 In the absence of concurrent lactation, weights and numbers of foetuses at the sixteenth day of gestation are little affected by cold; but in both environments foetal weight diminishes with increasing size of litter. This is a systemic effect: foetal weight is hardly if at all influenced by the number of other foetuses in the same uterine horn.
• 4 Cold delays the onset of breeding and lengthens the interval between litters. Mean litter sizes are usually lower than in the warm environment, mainly through absence of large litters.
• 5 The body weights of laboratory mice are usually lower at – 3°C than 21°C at all ages from 3 weeks. This does not, however, apply to strain C57BL, which never stores much fat in adipose tissue. Wild mice bred at – 3°C are heavier than controls at 21°C, possibly because only the heavier individuals survive in early life.
• 6 F ₁ hybrids produced by crossing two inbred strains breed better and more consistently than the parent strains at both temperatures; but the effect of heterozygosis is much greater in the cold environment.
• 7 Food intake changes little during pregnancy, but rises greatly during the first 10 days of lactation at both temperatures.
• 8 At 21°C, body weight, excluding the weight of the litter, increases only slightly during pregnancy; but the weights of the heart and liver are greatly increased. The weight of the stomach also rises; the small intestine lengthens, but becomes lighter. During lactation the liver becomes still heavier, and the small intestine more than restores its loss of weight. The kidneys also become heavier. At – 3°C similar changes occur, but the heart is heavier at all stages of the reproductive cycle than it is at 21°C. The kidneys, too, are consistently heavier in the cold, and so is the small intestine. By contrast, the liver of pregnant or lactating females at – 3°C is no heavier than in the warm environment.
• 9 Pregnancy entails an increase in the absolute amount of nitrogen in the body, in both environments; but females at – 3°C have less nitrogen and collagen than controls. Pregnancy does not alter body fat at either temperature, but lactation is accompanied by some loss. At birth, mice born in the cold environment have more than twice as much body fat as controls.
• 10 When mice are bred for their full reproductive span, the effect of a cold environment depends markedly on genotype. Mice of strain A2G/Tb eventually produce as many young in the cold environment as in the warm, but take longer to do so; C57BL/Tb produce fewer young, Wild mice produce fewer litters at – 3°C, and have a much higher nestling mortality. Most of the mortality is due to loss of whole litters.
• 11 The preceding statements apply to mice of the first two or three generations in a cold environment, There are further effects of breeding for many generations in the cold. Wild mice bred for ten generations lose fewer litters in later than in earlier generations. After ten generations, some wild mice were moved from –3 to 21°C. Their reproductive performance was then much superior to that of controls which had been kept at 21°C throughout. The transferred mice were also quicker than the controls to make a nest of paper.
• 12 Genetically heterogeneous laboratory mice, after twelve generations in the cold, were similarly returned to the warm environment. Their offspring were heavier than controls; but there was no superiority in reproductive performance.
• 13 A2G/Tb mice kept at –3°C, though highly inbred, also improved in reproductive performance over a number of generations: in particular, their infant mortality declined. This was probably not due to a genetical change, but to a cumulative maternal effect.
• 14 Maternal performance was studied by cross-fostering young at birth between these ‘Eskimo’ mice, ‘immigrant’ mice of the first or second generation reared in the cold, and controls at 21°C. There was some evidence of an effect of true parentage, regardless of foster parentage, on body weight: the young of the Eskimo mice tended to be heavier than the others. There was also evidence that this influence persisted into a second generation. Mortality among the fostered young was influenced only by true parentage, not by foster parentage or environmental temperature. Some of the fostered mice were mated. Again, among their young, mortality in the nest was not affected by environmental temperature; but those whose true ancestry was Eskimo displayed a lower mortality than the others.
• 15 If a young mammal is given special treatment (such as exposure outside the nest), the treatment may influence, not only the individual treated, but also the behaviour of the parents; and the altered parental behaviour may in turn affect the development of the young. Enhanced parental attention in the nest has been directly observed after young have been exposed to cold or other treatment. It can probably accelerate maturation, and improve reproductive performance by lowering mortality among the young of the treated mice. Hence the direct effects of treatment in infancy can never be distinguished with certainty from indirect effects through changed parental behaviour, unless the experimental animals are reared artificially.
• 16 A comprehensive theory of ‘stress’, that is, of the response of a species to an environmental change for the worse, requires that attention should be paid to the following: (i) the effects of physiological (ontogenetic) adaptation to one ‘stressor’, such as cold, on response to another, such as infection; (ii) the ways in which conditions of rearing, especially early exposure to mildly adverse conditions such as lower temperature, influence later physiological, reproductive and behaviour al performance; (iii) the relationships of the above with the adaptive changes of pregnancy and lactation.

     

WILD MICE IN THE COLD: SOME FINDINGS ON ADAPTATION

The house mouse, Mus domesticus, can thrive in natural environments much below its optimum temperature. Thermogenesis is then above that at more usual temperatures. In addition, body weight, and the weights of brown adipose tissue and the kidneys, may be higher than usual. In free populations of house mice cold lowers fertility and may prevent breeding. Other possible limiting factors on breeding are food supply, shelter for nesting and social interactions. In captivity, wild-type house mice exposed to severe cold (around 0 degrees C) at first adapt ontogenetically by shivering and reduced activity. But raised thermogenesis is soon achieved without shivering; nest-building improves; and readiness to explore may be enhanced. Endocrine changes probably include, at least initially, a rise in adrenal cortical activity and in catecholamine secretion. Some females become barren, but many remain fertile. The maturity of fertile females is, however, delayed and intervals between births are lengthened; nestling mortality rises. A limiting factor during lactation may be the capacity of the gut. Similar adaptive changes are observed during winter in some species of small mammals that do not hibernate. But neither the house mouse nor other species present a single, universal pattern of cold-adaptation. Wild-type mice bred for about 10 generations in a warm laboratory environment (20-23 degrees C) change little over generations. In cold they become progressively heavier and fatter at all ages; they mature earlier, and nestling mortality declines. The milk of such 'Eskimo' females is more concentrated than that of controls. If 'Eskimo' mice are returned to a warm environment, they are more fertile, and rear heavier young, than controls that remained in the warm. Despite the heavier young, litter size is not reduced: it may be increased, probably as a result of a higher ovulation rate. Parental effects have been analyzed by cross-fostering and hybridizing. Survival, growth and fertility are all favourably influenced by the intra-uterine and nest environments provided by 'Eskimo' females. 'Eskimo' males are also better fathers. Hence after ten generations the phenotype of cold-adapted house mice shows the combined effects of (a) an ontogenetic response to cold, (b) a superior parental environment and (c) a change genotype. The secular changes in the cold that lead to this phenotype give the appearance of evolution in miniature; but it is equally possible that they represent a genetical versatility that allows rapid, reversible shifts in response to environmental demands.(ABSTRACT TRUNCATED AT 400 WORDS)     

Interaction of genotype and parental environment in the adaptation of wild House mice Mus musculus to cold

Wild House mice, Mus musculus, were bred in two laboratory environments, one warm (controls) and one cold (Eskimo). At the seventh generation, mice of both stocks were cross-fostered at birth in both environments. In the warm environment, differences in both genotype and nest environment influenced growth: (1) Eskimo reared by Eskimo females were the heaviest of the four classes of fostered young; and (2) control foster parentage retarded growth. There was, however, no good evidence of differences in the reproductive performance of the four classes of fostered mice. In the cold environment, the effects of both genetical differences and of fostering were greater. Both the superior growth of Eskimo reared by Eskimo and the retarding effect of control foster parentage were more marked. Moreover, adult males with control foster parents had less fat than had those with Eskimo foster parents. Reproductive performance was also affected: (1) the young of the pairs with Eskimo genotype were heavier than the young of control pairs; (2) the litters of mice with Eskimo foster parents were larger than those of mice with control foster parents, and their young were heavier. Differences among the young of fostered mice represent a grandmother effect. Evidently, selection in a cold environment had led, not only to adaptive genetical changes in the ability to respond directly to cold, but also to changes in parental performance; and the latter enhanced the fitness, in the cold environment, of their offspring and grandoffspring.     

THE DEVELOPMENT AND SURVIVAL OF PODISUS SAGITTUS (HEMIPTERA: PENTATOMIDAE) ON ARTIFICIAL DIETS

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The effects of 4 diets on population parameters of Podisus sagittus (L.), a pentatomid predator of Lepidoptera, were compared. Direct comparisons were made of survival, stadial lengths, generation times and predator weights at 20, 25, and 33°C. Temperature influenced stadial lengths, generation time and survival but not weight. Improved survival compared with controls was recorded for diet I at 20°C and diet I and II at 25°C. On diet III adults were produced only at 33°C, in which survival was similar to that in the controls.     

Actions and interactions of growth hormone and insulin-like growth factor-II: body and organ growth of transgenic mice

To characterize long-term actions and interactions of growth hormone (GH) and insulin-like growth factor-II (IGF-II) on postnatal body and organ growth, hemizygous phosphoenolpyruvate carboxykinase (PEPCK)-human IGF-II transgenic mice were crossed with hemizygous PEPCK-bovine GH transgenic mice. The latter are characterized by two-fold increased serum levels of IGF-I and exhibit markedly increased body, skeletal and organ growth. Four different genetic groups were obtained: mice harbouring the IGF-II transgene (I), the bGH transgene (B), or both transgenes (IB), and non- transgenic controls (C). These groups of mice have previously been studied for circulating IGF-I levels (Wolf et al., 1995a), whereas the present study deals with body and organ growth. Growth curves (week 3 to 12) were estimated by regression with linear and quadratic components of age on body weight and exhibited significantly (p < 0.001) greater linear coefficients in B and IB than in I and C mice. The linear coefficients of male I and C mice were significantly (p < 0.001) greater than those of their female counterparts, whereas this sex-related difference was absent in the bGH transgenic groups. The weights of internal organs as well as the weights of abdominal fat, skin and carcass were recorded from 3.5- to 8- month-old mice. In addition, organ weight-to-body weight-ratios (relative organ weights) were calculated. Except for the weight of abdominal fat, absolute organ weights were as a rule significantly greater in B and IB than in I and C mice. IGF-II overproduction as a tendency increased the weights of kidneys, adrenal glands, pancreas and uterus both in the absence and presence of the bGH transgene. Analysis of relative organ weights demonstrated significant (p < 0.05) effects of elevated IGF- II on the relative growth of kidneys (males and females) and adrenal glands (females), confirming our previous report on organ growth of PEPCK-IGF-II transgenic mice. In females, IGF-II and GH overproduction were additive in stimulating the growth of spleen and uterus, providing evidence for tissue-specific postnatal growth promoting effects by IGF-II in the presence of elevated IGF-I     

Abnormally High Nourishment During Sensitive Periods Results in Body Weight Changes Across Generations

Objective : This study asked whether a brief period of over-nutrition during a developmentally sensitive time could impact the individual's adult weight and that of succeeding generations. Research Methods and Procedures : Female rat pups (F₁ generation) were randomly assigned to 1 of 3 groups: (1) a control group that was naturally reared by mothers; (2) another control group implanted with chronic gastric fistulas on postnatal day 4 and fed enough formula to match the growth of the mother-reared group; and (3) an experimental group gastrostomized and infused from day 8 through day 16 with a greater quantity of food than gastrostomy-reared controls (OF). On postnatal day 16, both gastrostomy-reared groups were returned to normal litters. Adult F₁ females from overfed and mother-reared groups were bred with normal males to yield an F₂ generation. F₂ adult females were bred to normal males to produce an F₃ generation. Results : When adult, the F₁ experimental group was heavier than control groups. F₂ adults from OF mothers were smaller than those from the control group. F₃ animals from OF grandmothers were heavier at weaning than F3 descendants from mother-reared animals. Discussion : Excess nourishment during a developmentally sensitive period changed the metabolic phenotype of one generation so dramatically that the gestational development and subsequent phenotype of two succeeding generations were also changed. The experiment models fetal effects of gestational diabetes in humans and may help to elucidate how, independent of genetic anomalies, secular changes can be detected across generations.     

Fast life in cold water: Diamesa incallida (Chironomidae)

Development times of Diamesa incallida and its numbers of generations per vear were studied using in situ reanngs in conjunction with continuous collection of egg masses from the field The evidence suggested that the crenophilous D incallida laid eggs throughout the year and produced eight to ten generations per year, depending on water temperature (76°C to 80°C) This is the first proof for a muitivoltine Diamesinae as well as for continuous egg laying behaviour by a non–troprcal chironomid The comparatively large mature larvae (96 mm, 710 μ.g a f d weight) and the numerous generations per year indicate that D incallida is a highly productive component of crenal communities The importance of rearing chironomids over a sufficient number of generations is emphasized as a basis for the reliable interpretation of field data     

Cloning and expression of swine myostatin gene and its application in animal immunization trial

An important performance trait target in swine breeding is the percentage of the lean meat within the total consumable pork. China has numerous indige-nous swine breeds, but the percentage of the lean meat percentage is generally low. Thus, increasing the per-centage of the lean meat would improve the pork qual-ity, which would have great importance in the devel-opment of our livestock industry as well as the opti-mization of the consumers’ dietary. Throughout the years researchers have been …     

Baseline and stress-induced plasma corticosterone concentrations of mice selectively bred for high voluntary wheel running

The hypothalamic-pituitary-adrenal (HPA) axis is important in regulating energy metabolism and in mediating responses to stressors, including increasing energy availability during physical exercise. In addition, glucocorticoids act directly on the central nervous system and influence behavior, including locomotor activity. To explore potential changes in the HPA axis as animals evolve higher voluntary activity levels, we characterized plasma corticosterone (CORT) concentrations and adrenal mass in four replicate lines of house mice that had been selectively bred for high voluntary wheel running (HR lines) for 34 generations and in four nonselected control (C) lines. We determined CORT concentrations under baseline conditions and immediately after exposure to a novel stressor (40 min of physical restraint) in mice that were housed without access to wheels. Resting daytime CORT concentrations were approximately twice as high in HR as in C mice for both sexes. Physical restraint increased CORT to similar concentrations in HR and C mice; consequently, the proportional response to restraint was smaller in HR than in C animals. Adrenal mass did not significantly differ between HR and C mice. Females had significantly higher baseline and postrestraint CORT concentrations and significantly larger adrenal glands than males in both HR and C lines. Replicate lines showed significant variation in body mass, length, baseline CORT concentrations, and postrestraint CORT concentrations in one or both sexes. Among lines, both body mass and length were significantly negatively correlated with baseline CORT concentrations, suggesting that CORT suppresses growth. Our results suggest that selection for increased locomotor activity has caused correlated changes in the HPA axis, resulting in higher baseline CORT concentrations and, possibly, reduced stress responsiveness and a lower growth rate.     

Adaptation to sub- and supraoptimal temperatures of inbred maize lines differing in origin with regard to seedling development and photosynthetic traits

Six inbred lines of maize ( Zea mays L.) from cool temperate regions (C) and from warm regions (W) were grown at 14, 22, 30 and 38°C up to the same physiological age, the full expansion of the third leaf. Generally, plants developed smaller shoot dry weights and leaf areas at extreme temperatures. The shoot:root ratio was lowest at 22°C and highest at 30°C. Most lines had a minimum for specific leaf dry weight at 30°C, but W lines had a second lower minimum at 14°C. Phosphofructokinase activity scarcely reacted to temperature between 22° and 38°C; at 14°C one C line and all W lines had rather low activities. Generally, the chlorophyll content increased steeply from 14 to 22°C and decreased somewhat from 30 to 38°C. In C lines the carotenoid level decreased from 14 to 38°C. No uniform temperature response was found for PEP carboxylase activity, but the highest activity was mostly attained at 38°C. RuBP carboxylase activity increased considerably from 14 to 22°C and remained comparatively constant at higher temperatures. The highest activity of NADP malate dehydrogenase was found at 22°C, with a decrease up to 38°C and with second lowest values at 14°C. C lines possessed larger leaf areas, shoot dry weights and higher shoot:root ratios than W lines at 14 and 22°C, and higher specific leaf dry weights over the whole temperature range. The genotypic pattern of shoot dry weight at 14°C corresponded reasonably well with that of phosphofructokinase activity. A better adaptation of C lines to suboptimal temperatures was mostly clearly indicated for photosynthetic traits which have a well proven relationship with the chloroplast membranes: chlorophyll, carotenoids and RuBP carboxylase. The least distinct effects of origin were observed at 38°C; a tendency prevailed for a better performance of C lines with regard to phosphofructokinase, carotenoids, RuBP carboxylase and NADP malate dehydrogenase.     

Biochemical and metabolic effects of a six-month exposure of small animals to a helium-oxygen atmosphere

Rats and mice were exposed for periods of up to six months and two successive generations of mice were raised in a ground-level chamber system filled with 80% helium –20% oxygen, at 24°C. A duplicate chamber for controls contained a comparable nitrogen-oxygen mixture, and in both the other environmental parameters were well-controlled and nearly identical. Animals adapted to helium showed no greater increase in oxygen consumption (P>0.05) when placed in helium-oxygen than did those raised in air. Growth rates were identical, but the helium mice consumed more food and water.Selected biochemical analyses were made on the parent and two successive generations of mice. These included blood indices; electrophoretically separated tissue protein patterns from liver, skeletal muscle, and cardiac muscle; quantitative determinations of LDH, MDH, and G6PDH from the same tissues; serum insulin; and semi-quantitative histochemical estimates of liver glycogen. No cases of statistically significant difference or consistent trends were seen between the experimental environmental groups. Additional analyses of liver nucleotides and redox-coenzymes also failed to show a significant difference.The relative weights of liver, heart, kidney, and diaphragm (wet and dry) were the same in both groups. Histopathological examination of kidney and adrenal tissue produced unremarkable findings and none that were attributable to the nature of the gaseous environment.It must be concluded that prolonged exposure to helium-oxygen, relative to air, does not produce detectable changes in several key subcellular factors which might be altered by serious metabolic disturbances, and therefore the helium exposure is well tolerated.Prepared under Contract No. NAS 2-3900 for Union Carbide Corporation, Linde Division Research Laboratory, Tonawanda, N.Y. for Ames Research Center.     

Changes in the body composition of mice selected for high and low eight week weight

Summary Body composition was studied in three lines of mice, one selected for high (H) and one for low (L) 8 week weight, and one maintained as an unselected control (C). After 25 generations 8 week weights were 41.2g, 30.6 g and 20.5g for the H, C and L lines. Mice were sampled from the lines and analysed for fat, protein, ash and water at generations 14 and 25. Apart from fat in the H line, there was little alteration due to selection in the relationships between individual body components and total body weight. In the H line, the contribution of fat to body weight gain was considerably increased. Although leaner than the C and L mice at low body weights, H line mice rapidly became fatter with increasing body weight. Selection appeared to reduce the body weight at which fat was deposited at its maximum rate in the H line. The H and C lines were equally fat at body weights of 29.0 g and 21.6 g at generations 14 and 25 respectively. Body weights at points of inflection of the growth curves of the H, C and L lines at generation 25 were 18.3 g, 14.3 g and 12.8 g. The implications of these findings for meat species slaughtered at set weights are discussed.     

Intergenerational acclimation in aphid overwintering

Abstract.  1. When first instar nymphs and adults of the grain aphid Sitobion avenae (Fabricius) (Hemiptera: Aphidiae) were maintained in long-term cultures (>6 months) at 20 °C and 10 °C, the LT₅₀ decreased from −8 and −8.8 °C to −16.0 and −13.5 °C, respectively.
2. When aphids from the 20 °C culture were transferred to 10 °C, there was a progressive increase in cold tolerance through three successive generations. Transfer of newly moulted pre-reproductive adults reared at 10 °C for three generations back to 20 °C resulted in a rapid loss of cold hardiness in their nymphal offspring.
3. In all generations reared at 10 °C, first born nymphs were more cold hardy than those born later in the birth sequence. The LT₅₀ of nymphs produced on the first day of reproduction in the first, second and third generations maintained at 10 °C were −14.8, −17.0 and −16.6 °C, respectively. Thereafter, nymphal cold hardiness decreased over the subsequent 14 days of reproduction in each generation at 10 °C with mean LT₅₀ values of −10.3, −12.6 and −14.8 °C, respectively. By contrast, the cold tolerance of first born nymphs of aphids reared continuously at 20 °C did not differ in comparison with later born siblings. The LT₅₀ of adult aphids was also unaffected by ageing.
4. The ecological relevance of these findings is discussed in relation to the overwintering survival of aphids such as S. avenae .     

Genetic-statistical analysis of growth in selected and unselected mouse lines

The growth of males sampled from two mouse lines long-term selected for over 86 generations on body weight (DU6) or on protein amount (DU6P) was analysed from birth till 120 days of age and compared to the growth of an unselected control line (DUKs). Animals from the selected lines are already approximately 40 to 50% heavier at birth than the controls. This divergence increases to about 210 to 240% at the 120 day of age. With birth weights of 2.2 and 2.4 g and weights of 78 and 89 g at the 120 day these selection lines are the heaviest known mouse lines.

The fit of three modified non-linear growth functions (Gompertz function, Logistic function, Richards function) was compared and the effect of three different data inputs elucidated. The modification was undertaken to use parameters having a direct biological meaning, for example: A: theoretical final body weight, B: maximum weight gain, C: age at maximum weight gain, D (only Richards function): determines the position of the inflection point in relation to the final weight. All three models fit the observed data very well (r² = 0.949–0.998), with a slight advantage for the Richards function. There were no substantial effects of the data input (averages, single values, fitting a curve for every animal with subsequent averaging the parameters).

The high growth of the selected mice is connected with very substantial changes in the final weight and in the maximum weight gain, whereas the changes of the age at the point of inflection were, although partially significant, relatively small and dependent on the model used.     

Effect of a 12 HZ and of a 460 HZ pulsed magnetic field on the weight of AKR mice

AKR mice were exposed to a 6 mT, 12 Hz or 460 Hz pulsed magnetic field (PMF) 30 minutes twice a week. The exposure took placein utero and/or during the life span for four consecutive generations. The adult mice exposed to the 460 Hz PMF only after the birth time were lighter than the controls; for the two frequencies the decrease in weight with the ageing was less pronounced than in the controls. When the exposure took placein utero the exposed new-born mice were heavier than the controls. The difference in weight progressively disappeared when the mice were exposed to the 12 Hz PMF, persisted when the mice were exposed to the 460 Hz PMF.     

Morphology, growth and reproduction in the Australian house mouse: differential effects of moderate temperatures

The house mouse ( Mus musculus domesticus ) was introduced into Australia two centuries ago and is now succeeding in a wide range of habitats and climatic regions. To explore how mice exploit such extreme environments, we compared growth rate, morphology and reproductive success of animals reared under differing thermal regimes (13 °C 'cool', 22 °C 'moderate' and 30 °C 'warm') in laboratory mice derived from wild stock. 'Warm' group young were smaller and grew more slowly than those from other groups. At 6 weeks of age, body mass was less in 'warm' than in 'cool' treatment individuals; and liver mass/body mass also was less in 'warm' than in 'cool' treatment individuals. Paired kidney mass/body mass and paired adrenal mass/body mass were less in 'warm' than in 'cool' and 'moderate' treatment mice. Low heritability values indicate that these effects were from the temperature treatments rather than genetic influences. Irrespective of temperature treatment, females were more likely to produce a litter from post-partum matings if they were experienced, rather than young or reproductively naïve, and also bore more young from post-partum matings. These observations contribute to understanding of the sudden plague activities of mice in some parts of Australia and also their sparse distribution in the interior of the continent.  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 21–30.     

Does maternal condition or predation risk influence small mammal population dynamics?

There is strong debate over whether the intrinsic traits of individuals or the extrinsic environment exert the greater influence on small mammal population dynamics. We test the roles of maternal effects (an intrinsic factor) and predation risk (an extrinsic factor) in the population dynamics of wild strain house mice using a 2-factor enclosure experiment. Pre-release supplemental feeding with a high-fat diet created female treatment founders that were 6–10% heavier than controls, a condition that we predicted would be passed on as a maternal effect. Predation risk was enhanced using regular application of predator (red fox Vulpes vulpes ) scats. Founder populations of six females and six males released into eight, 15×15 m enclosures showed near exponential population growth over 17 weeks (maximum 3 generations). But there were no responses to either treatment in terms of survival, inherited body weights, fecundity or population size. We suggest that elevated maternal condition may have only minor and transient intergenerational effects with little long-term consequence. We also suggest that the general significance of predator scats as a cue to predation risk to alter prey behaviour may have been overestimated. Hence our results question the role of either factor in causing long-term responses that influence condition to affect population processes.     

Progeny of male rats treated with methadone: physiological and behavioural effects

Male rats were injected with methadone HCl (METH) at 5 mg/kg s.c. for 4 days prior to mating with drug-free females. Offspring resulting from these matings were compared with offspring of drug-free males. The progeny of METH-treated males gained less weight after weaning and had lighter thymuses as adults (but not in infancy). Gonadal weights did not differ in infancy or adulthood, and adrenal weights were heavier in female offspring in adulthood. In adulthood METH offspring were significantly different from controls on all behavioural tests used (open field activity, activity cage activity, passive avoidance latencies, shuttle box avoidances, and rotarod latencies), with the differences frequently affected by test order, days of testing, or sex of offspring. The effects in progeny of METH-treated males in the absence of differences in litter size or neonatal mortality indicate that paternal drug ingestion prior to mating can produce physiological and behavioural changes in progeny that are not dependent on detectable effects on early viability or growth.