Behaviour is not Reliably Inferred from End-Product Structure in Caddisflies

Many animals engage in elaborate behavioural sequences in order to build structures. The ‘end‐products’ (e.g., nests of birds, cases of caddisflies) of these behaviours have occasionally been used either to infer details of building behaviour or to infer that structures similar in appearance are constructed by similar behavioural sequences. However, behavioural information can be extrapolated from end‐products only if there is congruence between the end‐product structure and the animal's movements. Case building behaviour was studied in caddisflies (Trichoptera) to examine the relationship between end‐products and behaviour. We found examples of taxa that built similar structures using different behavioural patterns, and taxa that built different structures using similar behaviours, regardless of whether these taxa were closely or distantly related. These findings question the reliability of behavioural inferences based solely on details of their associated end‐products and suggest that end‐product structure should be removed from the definition of animal behaviour.     

ADAPTATIONS OF TERRESTRIAL ARTHROPODS TO THE ALPINE ENVIRONMENT

1. The climate changes drastically above the timberline. Diverse adaptations have been evolved by insects and other terrestrial arthropods to survive the alpine environment. The fitness of each species depends on a combination of different factors in accordance with their special habitats. 2. Morphological adaptations such as reduced body-size, are known from a number of alpine insects, increasing their possibility to find sheltered microhabitats. Selection for reduced body size in Andean Phulia spp. butterflies is probably a result of their rigorous environment. Wing atrophy, which is also known in insects from other extreme environments, is widespread in alpine species. In several terrestrial arthropods the absorption of solar radiation is increased by melanism. Increased pubescence, protecting against the loss of heat, is known in alpine butterflies and bumblebees. 3. Several behavioural adaptations are described. Thermoregulatory behaviour is important in many species to raise their body temperatures. Alpine butterflies orient the dark basis of their wings perpendicular to the rays of the sun. Body temperatures of 30 °C may be required for flight. To increase their activities many alpine terrestrial arthropods seek warmer microhabitats in the vegetation and under rocks. The adaptive advantage of nocturnal activity as observed in several species, may be to maintain the water balance or to avoid predation. 4. Tropical alpine terrestrial arthropods are faced with special problems. The large diel temperature fluctuations require cold-hardiness during the night and tolerance to heat during the day. Many species seek sheltered microhabitats under rocks and in vegetation. 5. Due to low precipitation and high evaporation rates many mountain areas are extremely dry. High resistance to desiccation may be very important to alpine species, and in particular to tropical species. Rates of water loss at low relative humidities are comparable to those of desert arthropods. 6. As an adaptation to the cold alpine summers several species of terrestrial arthropods require more than one year to complete their life-cycles. Special to these species is their adaptation to low temperatures in two or more overwintering stages. In spite of their cold surroundings several species have univoltine life cycles, frequently combined with highly specialized adaptations. Increased metabolic rates as a compensation to low temperatures may be widespread in alpine species, but few data are available. 7. Cold tolerance is of particular importance in temperature alpine species. Winter survival in Collembola and Acari depends on supercooling. Great seasonal variations have been observed in a number of species. Freezing tolerance is also known from alpine insects, e.g. in some species of beetles. At high latitudes alpine species must endure periods of up to eight or nine month at low temperatures during hibernation. Anaerobiosis is known from species that are enclosed in ice, with lactate as the main end product of metabolism.     

Non-lethal effects of predation in birds

Predators can affect individual fitness and population and community processes through lethal effects (direct consumption or ‘density’ effects), where prey is consumed, or through non‐lethal effects (trait‐mediated effects or interactions), where behavioural compensation to predation risk occurs, such as animals avoiding areas of high predation risk. Studies of invertebrates, fish and amphibians have shown that non‐lethal effects may be larger than lethal effects in determining the behaviour, condition, density and distribution of animals over a range of trophic levels. Although non‐lethal effects have been well described in the behavioural ecology of birds (and also mammals) within the context of anti‐predation behaviour, their role relative to lethal effects is probably underestimated. Birds show many behavioural and physiological changes to reduce direct mortality from predation and these are likely to have negative effects on other aspects of their fitness and population dynamics, as well as affecting the ecology of their own prey and their predators. As a consequence, the effects of predation in birds are best measured by trade‐offs between maximizing instantaneous survival in the presence of predators and acquiring or maintaining resources for long‐term survival or reproduction. Because avoiding predation imposes foraging costs, and foraging behaviour is relatively easy to measure in birds, the foraging–predation risk trade‐off is probably an effective framework for understanding the importance of non‐lethal effects, and so the population and community effects of predation risk in birds and other animals. Using a trade‐off approach allows us to predict better how changes in predator density will impact on population and community dynamics, and how animals perceive and respond to predation risk, when non‐lethal effects decouple the relationship between predator density and direct mortality rate. The trade‐off approach also allows us to identify where predation risk is structuring communities because of avoidance of predators, even when this results in no observable direct mortality rate.     

On the evolution of brain size in relation to migratory behaviour in birds

Migratory birds appear to have relatively smaller brain size compared to sedentary species. It has been hypothesized that initial differences in brain size underlying behavioural flexibility drove the evolution of migratory behaviour; birds with relatively large brains evolved sedentary habits and those with relatively small brains evolved migratory behaviour (migratory precursor hypothesis). Alternative hypotheses suggest that changes in brain size might follow different behavioural strategies and that sedentary species might have evolved larger brains because of differences in selection pressures on brain size in migratory and nonmigratory species. Here we present the first evidence arguing against the migratory precursor hypothesis. We compared relative brain volume of three subspecies of the white-crowned sparrow: sedentary Zonotrichia leucophrys nuttalli and migratory Z. l. gambelii and Z. l. oriantha. Within the five subspecies of the white-crowned sparrow, only Z. l. nuttalli is strictly sedentary. The sedentary behaviour of Z. l. nuttalli is probably a derived trait, because Z. l. nuttalli appears to be the most recent subspecies and because all species ancestral to Zonotrichia as well as all older subspecies of Z. leucophrys are migratory. Compared to migratory Z. l. gambelii and Z. l. oriantha, we found that sedentary Z. l. nuttalli had a significantly larger relative brain volume, suggesting that the larger brain of Z. l. nuttalli evolved after a switch to sedentary behaviour. Thus, in this group, brain size does not appear to be a precursor to the evolution of migratory or sedentary behaviour but rather an evolutionary consequence of a change in migratory strategy.     

Egg concealment is an antipredatory strategy in a cavity‐nesting bird

Birds have developed different behavioural strategies to reduce the risk of predation during the breeding period. Bird species that nest in the open often cover their eggs to decrease the risk of predators detecting the clutches. However, in cavity nesters, the potential functions of egg covering have not been explored despite some bird species that nest in cavities also covering their eggs as open nesters do. We analysed whether egg covering is an antipredatory behaviour in the blue tit (Cyanistes caeruleus). We simulated an increase in the perceived risk of predation at experimental nests by adding predator scent inside the nest boxes during the egg‐laying period, whilst adding lemon essence or water to control nest boxes. Birds exposed to predator chemical cues in the nest of experimental pairs more frequently covered their eggs than birds exposed to an odorous control. These results suggest that egg covering may have evolved as an antipredatory behaviour also in cavity nesters to reduce the risk of egg predation and thus increase reproductive success in birds.     

The costs of keeping cool in a warming world: implications of high temperatures for foraging,thermoregulation and body condition of an arid‐zone bird

Recent mass mortalities of bats, birds and even humans highlight the substantial threats that rising global temperatures pose for endotherms. Although less dramatic, sublethal fitness costs of high temperatures may be considerable and result in changing population demographics. Endothermic animals exposed to high environmental temperatures can adjust their behaviour (e.g. reducing activity) or physiology (e.g. elevating rates of evaporative water loss) to maintain body temperatures within tolerable limits. The fitness consequences of these adjustments, in terms of the ability to balance water and energy budgets and therefore maintain body condition, are poorly known. We investigated the effects of daily maximum temperature on foraging and thermoregulatory behaviour as well as maintenance of body condition in a wild, habituated population of Southern Pied Babblers Turdoides bicolor. These birds inhabit a hot, arid area of southern Africa where they commonly experience environmental temperatures exceeding optimal body temperatures. Repeated measurements of individual behaviour and body mass were taken across days varying in maximum air temperature. Contrary to expectations, foraging effort was unaffected by daily maximum temperature. Foraging efficiency, however, was lower on hotter days and this was reflected in a drop in body mass on hotter days. When maximum air temperatures exceeded 35.5 °C, individuals no longer gained sufficient weight to counter typical overnight weight loss. This reduction in foraging efficiency is likely driven, in part, by a trade‐off with the need to engage in heat‐dissipation behaviours. When we controlled for temperature, individuals that actively dissipated heat while continuing to forage experienced a dramatic decrease in their foraging efficiency. This study demonstrates the value of investigations of temperature‐dependent behaviour in the context of impacts on body condition, and suggests that increasingly high temperatures will have negative implications for the fitness of these arid‐zone birds.     

The Effect of Moonlight on Scopoli's Shearwater Calonectris diomedea Colony Attendance Patterns and Nocturnal Foraging: A Test of the Foraging Efficiency Hypothesis

Moonlight is known to affect the nocturnal behaviour and activity rhythms of many organisms. For instance, predators active at night may take advantage from increased visibility afforded by the moon, while prey might regulate their activity patterns to become less detectable. Many species of pelagic seabirds attend their colony only at night, in complete darkness, avoiding approaching their nest sites under moonlight. This behaviour has been most often interpreted as an antipredator adaptation (‘predation avoidance’ hypothesis). However, it may also reflect a lower foraging efficiency during moonlit nights (‘foraging efficiency’ hypothesis). Indeed, moonlight may reduce prey availability because preferred seabird prey is known to occur at higher depths in moonlit nights. Using high‐accuracy behavioural information from data loggers, we investigated the effect of moonlight on colony attendance and at‐sea nocturnal foraging in breeding Scopoli's shearwaters Calonectris diomedea. We found that birds departing for self‐feeding trips around the full moon performed longer trips than those departing around the new moon. On nights when the moon was present only partly, nest burrow entrances took place largely in the moonless portion of the night. Moreover, contrary to predictions from the ‘foraging efficiency’ hypothesis, nocturnal foraging activity increased according to moonlight intensity, suggesting that birds increased their foraging activity when prey became more detectable. This study strengthens the idea that colony attendance behaviour is strictly controlled by moonlight in shearwaters, which is possibly related to the perception of a predation risk.     

Effects of hunting on the behaviour and spatial distribution of farmland birds: importance of hunting-free refuges in agricultural areas

Hunting is one of the human activities that directly affect wildlife and has received increasing attention given its socioeconomic dimensions. Most studies have been conducted on coastal and wetland areas and showed that hunting activity can greatly affect bird behaviour and distribution. Hunting-free reserves for game species are zones where birds find an area of reduced disturbance. We evaluated the effect of hunting activities on the behaviour and use of hunting-free areas of lapwings Vanellus vanellus , golden plovers Pluvialis apricaria and little bustards Tetrax tetrax in agricultural areas. We compared the habitat use and behaviour of birds on days before, during and after hunting took place. All three studied species showed strong behavioural responses to hunting activities. Hunting activity increased flight probability and time spent vigilant (higher on hunting days than just before and after a hunting day), to the detriment of resting. We also found distributional (use of hunting-free reserve) responses to hunting activities, with hunting-free reserves being used more frequently during hunting days. Thus, reserves can mitigate the disturbance caused by hunting activities, benefiting threatened species in agricultural areas. Increasing the size or number of hunting-free areas might be an important management and conservation tool to reduce the impacts of hunting activities.     

ABNORMAL MIGRATION AND HYBRIDIZATION OF LARUS ARGENTATUS AND L. FUSCUS AFTER INTERSPECIES FOSTERING EXPERIMENTS

Between 1962 and 1966 eggs of Larus argentatus and L. fuscus were interchanged andalmost 900 young were reared by the wrong species. Many of these cross-fostered young were later recovered or retrapped on and away from the colonies.
The British population of argentatus is sedentary and ringed birds are not recovered outside Britain, whereas fuscus normally migrates. Many cross-fostered argentatus migrated to France, Spain and Portugal, areas where fuscus is common, but they did not migrate as far as the control fuscus . It is possible that these cross-fostered argentatus had followed their foster parents when these migrated, but this is unlikely as the cross-fostered fuscus also migrated although their foster parents would have remained in Britain.
Despite wide ecological and behavioural overlaps, interbreeding between L. argentatus and L.fuscus is exceedingly rare. However, as a result of cross-fostering experiments, 31 and 40 mixed pairs were found on Skokholm in 1968 and 1969 respectively. Although some of the birds involved were unringed it is probable that all the adults in mixed pairs had been cross-fostered. Other cross-fostered birds were found mated with their own species and it appears that the sex of the imprinted birds was important. Female gulls will usually only mate with males of their own species, or in the case of the cross-fostered birds, with males of their foster species. Males will mate with either species.
Evidence is given that suggests that the colour of the mantle and wings is important in species recognition at long range, and the colour of eye-ring and join of the mandibles for recognition at short range. The role of voice is uncertain but general behaviour is probably unimportant.     

The adjustment of avian metabolic rates and water fluxes to desert environments

We tested the hypothesis that birds in arid environments, where primary productivity is low and surface water is scarce, have reduced energy expenditure and water loss compared with their mesic counterparts. Using both conventional least squares regression and regression based on phylogenetically independent contrasts, we showed that birds from desert habitats have reduced basal and field metabolic rates compared with species from mesic areas. Previous work showed that desert birds have reduced rates of total evaporative water loss when exposed to moderate environmental temperatures in the laboratory. We tested whether reduced rates of total evaporative water loss translate into low field water fluxes. Conventional ANCOVA indicated that desert birds have reduced water fluxes, but an analysis based on phylogenetically independent contrasts did not support this finding, despite the wide array of taxonomic affiliations of species in the data set. We conclude that the high ambient temperatures, the low primary productivity, and the water scarcity in desert environments have selected for or resulted in reduced rates of energy expenditure and evaporative water loss in birds that live in these climes.     

EXPERIMENTS ON THE LIMITATION OF BIRD NUMBERS BY TERRITORIAL BEHAVIOUR

(1) This paper examines removal and other experimental studies on the role of territorial behaviour in the limitation of bird densities. Experimental design is discussed, as are the types of conclusions that can be drawn. (2) Experiments have been conducted on more than 40 species from a wide range of taxonomic groups. Most provided evidence for density limitation, probably mediated by territorial behaviour, and for the existence of a non-territorial sector able to take territories when territory owners were removed or when additional habitat was made available. Experiments in the breeding season indicated that some surplus birds, although younger on average then territorial birds, were sexually mature and able to breed when given the chance. In some species, replacement birds bred less well than other territorial birds, but in other species no difference was apparent between the two groups. (3) Other experiments indicated that, while density was limited by territorial behaviour in good habitats, this was not the case in poor habitats, and that some individuals would move from poor to good habitat when territory owners were removed from good habitat. (4) In some species, non-territorial birds of breeding age were present in the population despite the existence of vacant territorial sites, while in others replacements were observed on good territories but not on poor ones. The implications were that site quality influenced whether settlement, defence and breeding occurred, and that some individuals had more stringent site requirements than others. In some seabirds' sites in the centre of a colony were more attractive than sites on the edges. (5) Many land-bird species that have been studied show two peaks of territorial activity each year, in autumn and in spring, and a limitation on breeding density can occur at either or both seasons, depending on conditions. (6) The fact that densities of many bird species fluctuate greatly from year to year is not inconsistent with the limitation of density by territorial behaviour. Several mechanisms are apparent through which density might be limited by territorialism at different levels in different years, so that surplus non-territorial birds are present in years of low territorial density, as well as in years of high territorial density. (7) Experiments have shown that density is limited by the presence of territorial birds, in some species at different levels in different areas or years. The next step is to find whether density is regulated by the presence of territorial birds over a period of years in a density-dependent manner. For this, observational data are required to find whether the proportion of birds that is excluded by territorial behaviour each year varies with the total number available for settlement. Such studies can be made only on species in which non-territorial birds can be counted accurately, as well as territorial ones.     

Effects of ambient temperature and early open-field response on the behaviour,feed intake and growth of fast- and slow-growing broiler strains

Increased activity improves broiler leg health, but also increases the heat production of the bird. This experiment investigated the effects of early open-field activity and ambient temperature on the growth and feed intake of two strains of broiler chickens. On the basis of the level of activity in an open-field test on day 3 after hatching, fast-growing Ross 208 and slow-growing i657 chickens were allocated on day 13 to one of the 48 groups. Each group included either six active or six passive birds from each strain and the groups were housed in floor-pens littered with wood chips and fitted with two heat lamps. Each group was fed ad libitum and subjected to one of the three temperature treatments: two (HH; 26°C), one (HC; 16°C to 26°C) or no (CC; 16°C) heat lamps turned on. Production and behavioural data were collected every 2 weeks until day 57. For both strains, early open-field activity had no significant effects on their subsequent behaviour or on any of the production parameters measured, and overall, the slow-growing strain was more active than the fast-growing strain. Ambient temperature had significant effects on production measures for i657 broilers, with CC chickens eating and weighing more, and with a less efficient feed conversion than HH chickens, with HC birds intermediate. A similar effect was found for Ross 208 only for feed intake from 27 to 41 days of age. Ross 208 chickens distributed themselves in the pen with a preference for cooler areas in the hottest ambient temperature treatments. In contrast, the behaviour of the slow-growing strain appeared to be relatively unaffected by the ambient temperature. In conclusion, fast-growing broilers use behavioural changes when trying to adapt to warm environments, whereas slow-growing broilers use metabolic changes to adapt to cooler ambient temperatures.     

Leg length and temperature determine the use of unipedal roosting in birds

The function of standing on one leg in birds has long been attributed to reducing heat loss from the unfeathered legs to the external environment. Whilst a handful of single‐species studies correlate the use of the behaviour with ambient temperature, the degree to which it is used across taxa is unknown. Given that leg‐length varies between species, the length of the leg (relative to body size) may mediate the use of this thermoregulatory behaviour, such that birds with longer legs should roost on one leg more than those with relatively shorter legs at any given ambient temperature. We tested this prediction through field observations and comparative analyses of nine shorebird species, with varying tarsi length relative to body size. Six of the nine species examined used unipedal standing more as temperatures decrease, indicating its role as a heat conservation behaviour. We also found that species with relatively longer legs roosted on one leg more frequently across a wide range of temperatures. Species with shorter leg lengths likely rely less on this posture to insulate the relatively smaller surface area of the legs. Our findings showed that the long accepted notion that birds stand on one leg more at colder temperatures holds, and that species with smaller relative leg length were less reliant on this behaviour to minimise heat loss from these bare appendages.     

United in adversity: Aridity and cold influence aggregation behaviour in a social lizard,Egernia stokesii

Sociality has evolved independently many times in a diverse array of animal taxa. While sociality in some invertebrates, birds and mammals is relatively well understood, complex social behaviour in Squamate reptiles is a comparatively recent discovery. The extent to which social behaviour is phylogenetically constrained, or free to respond to environmental conditions is a key question in understanding sociality. We sampled 74 aggregations involving 137 individuals of a social lizard (Egernia stokesii) from 13 sites across a 96 250 km² area showing a wide range of environmental conditions. Over all locations, 70% of the lizards were found in aggregations, supporting the previous suggestion that aggregation in this species is phylogenetically constrained. However, the size of aggregations was negatively related to spatial variation in aridity and daily variation in maximum temperature, suggesting that social behaviour also varied in response to harsh environmental conditions. Lizards aggregated more in arid areas and on cold days. Our results show that it is overly simplistic to regard social behaviour in E. stokesii as either phylogenetically constrained or environmentally determined. A more nuanced appreciation of the extent to which social behaviour is free to vary in response to environmental conditions improves our understanding of social behaviour in Squamate reptiles.     

Urbanization and its effects on personality traits: a result of microevolution or phenotypic plasticity?

Human‐altered environmental conditions affect many species at the global scale. An extreme form of anthropogenic alteration is the existence and rapid increase of urban areas. A key question, then, is how species cope with urbanization. It has been suggested that rural and urban conspecifics show differences in behaviour and personality. However, (i) a generalization of this phenomenon has never been made; and (ii) it is still unclear whether differences in personality traits between rural and urban conspecifics are the result of phenotypic plasticity or of intrinsic differences. In a literature review, we show that behavioural differences between rural and urban conspecifics are common and taxonomically widespread among animals, suggesting a significant ecological impact of urbanization on animal behaviour. In order to gain insight into the mechanisms leading to behavioural differences in urban individuals, we hand‐raised and kept European blackbirds (Turdus merula) from a rural and a nearby urban area under common‐garden conditions. Using these birds, we investigated individual variation in two behavioural responses to the presence of novel objects: approach to an object in a familiar area (here defined as neophilia), and avoidance of an object in a familiar foraging context (defined as neophobia). Neophilic and neophobic behaviours were mildly correlated and repeatable even across a time period of one year, indicating stable individual behavioural strategies. Blackbirds from the urban population were more neophobic and seasonally less neophilic than blackbirds from the nearby rural area. These intrinsic differences in personality traits are likely the result of microevolutionary changes, although we cannot fully exclude early developmental influences.     

Weighing the cost: the impact of serial heatwaves on body mass in a small Australian passerine

Rising temperatures pose a grave risk to arid zone birds because they are already living close to their physiological limits and must balance water conservation against the need for evaporative cooling. We assess how extreme temperatures affect a wild population of small passerines by monitoring daily mass change in individual jacky winters Microeca fascinans (a small Australasian robin) across a series of severe heatwaves that afflicted southern Australia in the summer of 2018–2019. Daily maximum temperature and duration of heat exposure were negatively related to the birds’ ability to maintain body mass. At maximum temperatures ≥ 42°C, birds lost 2.0% of their body mass daily and at ≥ 45°C, 2.6%. Apparent mortality increased almost three‐fold, and all breeding birds abandoned their nests. Nevertheless, net daily mass loss was less than might be expected from laboratory‐based findings, presumably because wild jacky winters undertook behavioural thermoregulation. The birds also regained some mass between heatwave events and suffered no long‐term reduction in body condition.     

Maternal care and subsocial behaviour in spiders

While most spiders are solitary and opportunistically cannibalistic, a variety of social organisations has evolved in a minority of spider species. One form of social organisation is subsociality, in which siblings remain together with their parent for some period of time but disperse prior to independent reproduction. We review the literature on subsocial and maternal behaviour in spiders to highlight areas in which subsocial spiders have informed our understanding of social evolution and to identify promising areas of future research. We show that subsocial behaviour has evolved independently at least 18 times in spiders, across a wide phylogenetic distribution. Subsocial behaviour is diverse in terms of the form of care provided by the mother, the duration of care and sibling association, the degree of interaction and cooperation among siblings, and the use of vibratory and chemical communication. Subsocial spiders are useful model organisms to study various topics in ecology, such as kin recognition and the evolution of cheating and its impact on societies. Further, why social behaviour evolved in some lineages and not others is currently a topic of debate in behavioural ecology, and we argue that spiders offer an opportunity to untangle the ecological causes of parental care, which forms the basis of many other animal societies.     

Metabolic response to changes in temperature in northern wheatears from an arctic and a temperate populations

Until recently it had been widely accepted that birds are energetically adapted to the latitude they inhabit, having an increased basal metabolic rate (BMR) at higher latitudes. Latterly, this general view has been questioned and the influence of phenotypic flexibility, due to factors such as habitat, life‐history or acclimatization has received increased attention. In particular, focus has been directed towards comparing species from arid and mesic habitats, but less attention has been given to species which breed in cold climates. We chose to study northern wheatears Oenanthe oenanthe from two populations at different latitudes (southern Norway, Iceland), but with similar life‐histories and habitat requirements throughout the year, in a common‐garden experiment. In order to assess true latitudinal trends in metabolic rate, we estimated the nocturnal resting metabolic rate (RMR) of northern wheatears from southern Norway and Iceland at different temperatures from 0° to 30°C. We found that Norwegian birds had overall lower metabolic rates than Icelandic birds, which were also slightly larger. This difference was not observed at 0°C, which might indicate that Icelandic birds might rely on better feather insulation reducing metabolic costs at very low temperatures. At temperatures above 10°C birds of both populations had constant metabolic values, indicating that their thermoneutral range almost completely covered the temperatures experienced during the breeding period. This study shows that the northern wheatear, which is one of only a few insectivorous long‐distance migratory songbirds occurring at such high latitudes, has evolved metabolic adaptations to life at cold temperatures which are endogenously determined.     

Megapodes: Recent ideas on origins, adaptations and reproduction

Some birds don't incubate their eggs using the warmth of their bodies. The megapodes have evolved a markedly different method of incubation. By making use of environmental heat, adult megapodes are emancipated from most of the usual constraints to reproductive success associated with parental care. Consequences of this unique incubation method are evident in all aspects of megapode development and behaviour. Recently, renewed interest in these birds from a number of disciplines has led to significant advances, especially in aspects associated with reproduction. Both eggs and embryos exhibit remarkable adaptations to the physiologically stressful incubation environment. The use of various types of incubation heat may also shape the mating systems of the species involved.     

Age affects the expression of maternal care and subsequent behavioural development of offspring in a precocial bird

Variations of breeding success with age have been studied largely in iteroparous species and particularly in birds: survival of offspring increases with parental age until senescence. Nevertheless, these results are from observations of free-living individuals and therefore, it remains impossible to determine whether these variations result from parental investment or efficiency or both, and whether these variations occur during the prenatal or the postnatal stage or during both. Our study aimed first, to determine whether age had an impact on the expression of maternal breeding care by comparing inexperienced female birds of two different ages, and second, to define how these potential differences impact chicks' growth and behavioural development. We made 22 2-month-old and 22 8-month-old female Japanese quail foster 1-day-old chicks. We observed their maternal behaviour until the chicks were 11 days old and then tested these chicks after separation from their mothers. Several behavioural tests estimated their fearfulness and their sociality. We observed first that a longer induction was required for young females to express maternal behaviour. Subsequently as many young females as elder females expressed maternal behaviour, but young females warmed chicks less, expressed less covering postures and rejected their chicks more. Chicks brooded by elder females presented higher growth rates and more fearfulness and sociality. Our results reveal that maternal investment increased with age independently of maternal experience, suggesting modification of hormone levels implied in maternal behaviour. Isolated effects of maternal experience should now be assessed in females of the same age. In addition, our results show, for first time in birds, that variations in maternal care directly induce important differences in the behavioural development of chicks. Finally, our results confirm that Japanese quail remains a great laboratory model of avian maternal behaviour and that the way we sample maternal behaviour is highly productive.