Home About us Contact
|
Home About us Contact | ||
|
|
||
Parental Investment (parental + investment)
Terms modified by Parental Investment Selected AbstractsAdjustment of Parental Investment in the Dung Beetle Onthophagus atripennis (Col., Scarabaeidae)ETHOLOGY, Issue 12 2006Shigeki Kishi If parents can invest resources optimally per offspring, they should adjust the amount of investment in an offspring according to environmental heterogeneity. Many studies have demonstrated changes in egg size or the amount of resource supplied in response to environmental heterogeneity. However, it remains unclear whether parents simply know the resource type a priori or can assess resource quality and adjust the quantity of investment accordingly. We examined the parental capability to adjust the amount of investment per offspring by providing Onthophagus atripennis dung beetle parents with one of three dung types of different quality: monkey dung (high quality), cow dung (low quality), or a mixture of monkey and cow dung (medium quality). The beetle parents cooperatively produce dung brood masses each with one egg under the ground. The size of a brood mass, on which a larva can only feed until adult, represents a large part of the amount of investment. Parents produced a greater number of smaller brood masses given high-quality resource, while they compensated for low quality of the resource by providing a larger amount of the resource, at the cost of offspring number. However, despite this compensation in the amount of food, offspring raised on low-quality food was still smaller than offspring raised on high-quality food. Thus, O. atripennis parents assessed resource quality partly and adjusted the amount of resource provided for their offspring. [source] Incubation Feeding and Nest Attentiveness in a Socially Monogamous Songbird: Role of Feather Colouration, Territory Quality and Ambient EnvironmentETHOLOGY, Issue 7 2010Beata Matysioková Parental investment and environmental conditions determine reproductive success in wild-ranging animals. Parental effort during incubation, and consequently factors driving it, has profound consequences for reproductive success in birds. The female nutrition hypothesis states that high male feeding enables the incubating female to spend more time on eggs, which can lead to higher hatching success. Moreover, both male and female parental investment during incubation might be signalled by plumage colouration. To test these hypotheses, we investigated relationships between male and female incubation behaviour and carotenoid and melanin-based plumage colouration, territory quality and ambient temperature in the Great Tit Parus major. We also studied the effect of female incubation behaviour on hatching success. Intensity of male incubation feeding increased with lower temperatures and was higher in territories with more food supply, but only in poor years with low overall food supply. Female nest attentiveness increased with lower temperatures. Plumage colouration did not predict incubation behaviour of either parent. Thus, incubation behaviour of both parents was related mainly to environmental conditions. Moreover, there was no relationship between male incubation feeding, female nest attentiveness and hatching success. Consequently, our data were not consistent with the female nutrition hypothesis. [source] Parental investment, sexual selection and sex ratiosJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2008HANNA KOKKO Abstract Conventional sex roles imply caring females and competitive males. The evolution of sex role divergence is widely attributed to anisogamy initiating a self-reinforcing process. The initial asymmetry in pre-mating parental investment (eggs vs. sperm) is assumed to promote even greater divergence in post-mating parental investment (parental care). But do we really understand the process? Trivers [Sexual Selection and the Descent of Man 1871,1971 (1972), Aldine Press, Chicago] introduced two arguments with a female and male perspective on whether to care for offspring that try to link pre-mating and post-mating investment. Here we review their merits and subsequent theoretical developments. The first argument is that females are more committed than males to providing care because they stand to lose a greater initial investment. This, however, commits the ,Concorde Fallacy' as optimal decisions should depend on future pay-offs not past costs. Although the argument can be rephrased in terms of residual reproductive value when past investment affects future pay-offs, it remains weak. The factors likely to change future pay-offs seem to work against females providing more care than males. The second argument takes the reasonable premise that anisogamy produces a male-biased operational sex ratio (OSR) leading to males competing for mates. Male care is then predicted to be less likely to evolve as it consumes resources that could otherwise be used to increase competitiveness. However, given each offspring has precisely two genetic parents (the Fisher condition), a biased OSR generates frequency-dependent selection, analogous to Fisherian sex ratio selection, that favours increased parental investment by whichever sex faces more intense competition. Sex role divergence is therefore still an evolutionary conundrum. Here we review some possible solutions. Factors that promote conventional sex roles are sexual selection on males (but non-random variance in male mating success must be high to override the Fisher condition), loss of paternity because of female multiple mating or group spawning and patterns of mortality that generate female-biased adult sex ratios (ASR). We present an integrative model that shows how these factors interact to generate sex roles. We emphasize the need to distinguish between the ASR and the operational sex ratio (OSR). If mortality is higher when caring than competing this diminishes the likelihood of sex role divergence because this strongly limits the mating success of the earlier deserting sex. We illustrate this in a model where a change in relative mortality rates while caring and competing generates a shift from a mammalian type breeding system (female-only care, male-biased OSR and female-biased ASR) to an avian type system (biparental care and a male-biased OSR and ASR). [source] Incubation Feeding and Nest Attentiveness in a Socially Monogamous Songbird: Role of Feather Colouration, Territory Quality and Ambient EnvironmentETHOLOGY, Issue 7 2010Beata Matysioková Parental investment and environmental conditions determine reproductive success in wild-ranging animals. Parental effort during incubation, and consequently factors driving it, has profound consequences for reproductive success in birds. The female nutrition hypothesis states that high male feeding enables the incubating female to spend more time on eggs, which can lead to higher hatching success. Moreover, both male and female parental investment during incubation might be signalled by plumage colouration. To test these hypotheses, we investigated relationships between male and female incubation behaviour and carotenoid and melanin-based plumage colouration, territory quality and ambient temperature in the Great Tit Parus major. We also studied the effect of female incubation behaviour on hatching success. Intensity of male incubation feeding increased with lower temperatures and was higher in territories with more food supply, but only in poor years with low overall food supply. Female nest attentiveness increased with lower temperatures. Plumage colouration did not predict incubation behaviour of either parent. Thus, incubation behaviour of both parents was related mainly to environmental conditions. Moreover, there was no relationship between male incubation feeding, female nest attentiveness and hatching success. Consequently, our data were not consistent with the female nutrition hypothesis. [source] Egg Colour Covaries with Female Expression of a Male Ornament in the Spotless Starling (Sturnus unicolor)ETHOLOGY, Issue 10 2007Isabel López-Rull The sexually selected egg colour hypothesis (SSECH) proposes that egg colouration is as a post-mating sexually selected signal of female phenotypic quality, maintained by a higher allocation of paternal care. Similarly, some female traits can reflect genetic quality or condition and males could use this information in mate choice or in modulating parental investment. In our study, we examined the correlation of individual variation in egg colouration with female expression of a male ornament and how male feeding covaried with these two female traits in the spotless starling, in which egg colour varies widely between clutches and where both sexes possess showy throat feathers that are age dependent and that may signal individual quality. According to the SSECH, high-quality females (females with longer throat feathers) are expected to lay more colourful eggs than low-quality females and males should modify their feeding behaviour accordingly. By means of a principal component analysis, we found that most of the variation in egg colouration was due to brightness differences, and in a lower proportion to chromatic variation. Chromatic variation reflected a ultraviolet (UV) vs. greenness trade-off and was positively associated with throat feather length: females with larger throat feathers laid eggs with higher UV and lower green reflectance. However, egg brightness was not related to female feather length, as the SSECH would predict. Male feedings were positively related to female throat feather length and negatively related to chromatic variation, meaning that males contributed more to nests of females with long throat feathers who laid eggs with higher UV and lower green reflectance. In conclusion, our data provide mixed support for the SSECH: although egg chromatic variation was related to female expression of a male ornament and male parental care, we found no evidence that egg brightness was involved in these processes. [source] The Influence of Exogenous Testosterone on the Dynamics of Nestling Provisioning in Dark-Eyed JuncosETHOLOGY, Issue 1 2007Ethan D. Clotfelter In many songbird species, application of exogenous testosterone (T) during the breeding season has the general effects of reducing male parental investment and increasing allocation of time and energy to mating. Most studies record the number of feeding trips made by males as a function of their hormone treatment, but few have investigated the ways in which testosterone affects the dynamics of male and female provisioning behavior or the quantity of food delivered by males. We attempt to fill these gaps in our understanding of testosterone and male parental effort by utilizing data from a long-term study on the behavioral endocrinology of the dark-eyed junco (Junco hyemalis). We found that male and female feeding rates covaried positively, although to different degrees, throughout the nestling period, but that this relationship was degraded in pairs in which males were given T implants. We also found that the coefficients of variation in the duration of intervals between successive feeding trips by males and females were highly positively related in broods of older nestlings. Male hormone treatment, however, had no effect on the coefficients of variation in either male or female feeding intervals. Finally, we examined the quantity of prey delivered by males and found no significant effect of hormone treatment. [source] Nest, but Not Egg, Fidelity in a Territorial SalamanderETHOLOGY, Issue 9 2000Megan G. Peterson Egg recognition and subsequent egg brooding are costly forms of parental investment in many species of vertebrates. Life history factors, such as coloniality or risk of brood parasitism, may constrain egg recognition in vertebrates. Female red-backed salamanders (Plethodon cinereus) from my study site are territorial and do not share nest sites with other females. They are terrestrial and neither they nor their eggs are likely to be displaced by environmental factors such as flooding. I experimentally tested, in the laboratory, the hypothesis that female red-backed salamanders can discriminate between their own eggs and the eggs of unfamiliar females. Each female was allowed to move about a test chamber containing two clutches of eggs, one clutch with which it was found in the forest and one that had been found with a distant female. Most females remained with one clutch of eggs, which they brooded during the entire observation period. However, they did not significantly prefer to brood their own eggs over the eggs of another female. In a corollary field experiment, I tested whether brooding females that were displaced 1 m from their nest sites would return to their territories and commence brooding behaviour within 3 d. All 10 displaced females returned to their own nest within this time period and were found brooding their eggs. Because female red-backed salamanders at my study site do not tend to share nest sites with other females and because their eggs remain in stationary nests, selection may not have favoured egg recognition. However, the results suggest that female salamanders indirectly recognize their own eggs by actively recognizing their territorial nest sites. [source] EVOLUTIONARY PATHWAYS IN SHOREBIRD BREEDING SYSTEMS: SEXUAL CONFLICT, PARENTAL CARE, AND CHICK DEVELOPMENTEVOLUTION, Issue 10 2005Gavin H. Thomas Abstract Sexual selection, mating opportunities, and parental behavior are interrelated, although the specific nature of these relationships is controversial. Two major hypotheses have been suggested. The parental investment hypothesis states that the relative parental investment of the sexes drives the operation of sexual selection. Thus, the sex that invests less in offspring care competes more intensely and monopolizes access to mates. The sexual conflict hypothesis proposes that sexual selection (the competition among both males and females for mates), mating opportunities, and parental behavior are interrelated and predicts a feedback loop between mating systems and parental care. Here we test both hypotheses using a comprehensive dataset of shorebirds, a maximum-likelihood statistical technique, and a recent supertree of extant shorebirds and allies. Shorebirds are an excellent group for these analyses because they display unique variation in parental care and social mating system. First, we show that chick development constrains the evolution of both parental care and mate competition, because transitions toward more precocial offspring preceded transitions toward reduced parental care and social polygamy. Second, changes in care and mating systems respond to one another, most likely because both influenced and are influenced by mating opportunities. Taken together, our results are more consistent with the sexual conflict hypothesis than the parental investment hypothesis. [source] EVOLUTION OF MOUTHBROODING AND LIFE-HISTORY CORRELATES IN THE FIGHTING FISH GENUS BETTAEVOLUTION, Issue 4 2004Lukas Rüber Abstract The origin of and evolutionary transitions among the extraordinary diverse forms of parental care in teleost fish remain largely unknown. The "safe harbor" hypothesis predicts that the evolution from a "guarding" to a "brooding" form of care in teleost fish is associated with shifts in reproductive and life-history features such as reduced fecundity, and increased egg volume with higher parental investment. Robust phylogenetic hypotheses may help to identify evolutionary changes in key traits associated with differences in the form of parental care. Here, we used reconstruction of ancestral character states to study the evolution of the two forms of parental care, bubble nesting and mouthbrooding in the fighting fish genus Betta. We also applied a comparative analysis using the phylogenetic generalized least-squares method to test the "safe harbor" hypothesis by evaluating differences between the two forms of parental care in standard length, life-history traits, and three habitat variables. Evolutionary hypotheses were derived from the first molecular phylogeny (nuclear and mitochondrial DNA sequence data; 4448 bp) of this speciose group. Ancestral character state reconstructions of the evolution of the form of parental care in the genus Betta, using the methods of unweighted parsimony and maximum likelihood, are uncertain and further indicate a high rate of evolutionary transitions. Applying different weights for the suspected directionality of changes, based on the consistent phenotypic and behavioral differences found between bubble nesters and mouthbrooders, recurrent origin of mouthbrooding in the genus Betta is favored using parsimony. Our comparative analyses further demonstrate that bubble nesters and mouthbrooders do not have a consistent set of life-history correlates. The form of parental care in Betta is correlated only with offspring size, with mouthbrooders having significantly bigger offspring than bubble nesters, but is not correlated with egg volume, clutch size, and broodcare duration, nor with any of the three habitat variables tested. Our results thus challenge the general predictions of the "safe harbor" hypothesis for the evolution of alternative brood care forms in the fighting fish genus Betta. [source] Female zebra finches compromise clutch temperature in energetically demanding incubation conditionsFUNCTIONAL ECOLOGY, Issue 5 2010Andreas Nord Summary 1.,Avian embryos depend on the incubating parent to provide a thermal environment suitable for embryogenesis, but as the maintenance of optimal incubation temperatures is energetically costly, an incubating bird often must trade off embryonic investment against self-maintenance. 2.,We manipulated the energetic cost of incubation in female zebra finches (Taeniopygia guttata Vieillot) by varying ambient temperature and clutch size during nocturnal incubation and recorded the corresponding effects on incubation metabolic rate and clutch temperature. 3.,Females increased their night-time incubation metabolic rate more than twofold when incubating at 10 °C compared to when incubating close to thermoneutrality (28 °C). Furthermore, clutch enlargement caused females to elevate their metabolic rate with 2·8% per additional egg added to the clutch. 4.,However, despite spending more energy, females did not fully cover the increased costs of incubation, because clutch temperature decreased with decreasing ambient temperature and increasing clutch size. 5.,These findings suggest that parental investment in incubation can be energetically constrained and sometimes result in clutch temperatures below the optimal level for embryonic development, at least during nocturnal incubation. [source] Is there a cost of reproduction for Marsh Tits Parus palustris in a primeval forest?IBIS, Issue 1 2006OWSKI TOMASZ We looked for evidence of a cost of reproduction in the Marsh Tit Parus palustris living in the last fragments of primeval temperate forest (Bia,owie,a National Park, eastern Poland). Potential nest-holes were superabundant but the birds had to cope with a diverse set of predators, dangerous both to broods and to parents. Taking advantage of the natural variation in realized reproductive investment that this caused in terms of the loss of nests or mates, we expected to find differences in survival and future fecundity between birds which had lost broods (reduced effort), had reared young (controls) or were either provisioning young single-handed or had laid replacement clutches (increased effort). Despite 13 years of observation, even during seasons with very strenuous conditions, we have failed to demonstrate that the observed range of variation in parental investment caused any demographic cost of reproduction. Incubating females were regularly killed on the nest, which could indicate the existence of a cost operating in the earlier stages of the breeding cycle. Overall, these results suggest that the reproductive rate in Marsh Tits is not controlled proximately by reproductive cost. [source] Selection for birth date in North Sea haddock and its relation to maternal ageJOURNAL OF ANIMAL ECOLOGY, Issue 2 2005PETER J. WRIGHT Summary 1Birth date can be important to lifetime reproductive success. However, selection for birth date has rarely been addressed in fish, despite the opportunity provided by otolith microstructure. 2This study examined the relationship between maternal age, spawning time and early survivorship in the North Sea haddock stock. Temporal changes in egg production were compared with the birth date distribution of progeny surviving to the demersal phase in 1994, 1996 and 1999, when the age structure of the spawning stock differed. 3Estimates of intra-annual variation in stock egg production indicated that first-time spawning 2-year-olds began spawning much later than older age-classes. 4The form and magnitude of selection on birth date varied between years, indicating that the production of multiple batches of eggs over an extended period has some adaptive significance to progeny survival. 5Survivorship was consistently poor from the late spawning period when age 2 females contributed most to stock egg production. This persistent selection against late hatched offspring could reflect either low parental investment, as age 2 females produce smaller eggs, or the short length of the growing season prior to settlement. 6Variability in birth date selection, particularly with respect to first vs. subsequent years of spawning, implies a strong selection pressure for a long reproductive lifespan. As such, reproductive potential in this and other exploited fish species with a similar reproductive trait may have been affected adversely by the general decline in repeat spawning females in recent years. [source] Manipulation of offspring number and size: benefits of large body size at birth depend upon the rearing environmentJOURNAL OF ANIMAL ECOLOGY, Issue 2 2003Tuula A. Oksanen Summary 1Allocation of reproductive effort between the number and size of offspring determines the immediate rearing environment for the growing young. As the number of offspring increases, the amount of parental investment per individual offspring decreases, and the quality of the rearing environment is expected to decrease. This may result in a lower quality of offspring reared in such conditions. 2We studied the effects of the rearing environment on the quality of juvenile bank voles, Clethrionomys glareolus, with different initial body sizes at birth in a 2 × 2 factorial experiment. The rearing environment was manipulated by enlarging both the litter size by two extra pups, and mean offspring body size at birth by replacing the original litter with heavier pups from smaller litters. Offspring quality was estimated from body size measurements, parasitic infection with Eimeria spp. and the level of immune response to a novel antigen. 3The analyses revealed that large body size at birth was an advantage in ,normal' rearing environments, but a disadvantage in poor ones. The initially normal sized offspring grown in enlarged litters had a relatively good capacity for growth and high immune function confirming that a poor rearing environment alone does not reduce their quality. 4Our findings that the benefits of large body size depend on the rearing environment suggest that offspring body size is adjusted in relation to litter size, and thus the evolution of these two traits is combined. [source] A fixed energetic ceiling to parental effort in the great tit?JOURNAL OF ANIMAL ECOLOGY, Issue 2 2000J. M. Tinbergen Summary 1.,To elucidate the links between avian brood size, parental effort and parental investment, we measured daily energy expenditure (DEEfem), condition (residuals of mass on tarsus) and feeding rate in female great tits Parus major L. rearing broods in which the number of young was either reduced, unmanipulated or enlarged. 2.,Female condition was negatively correlated with manipulation when measured at the nestling age of 8 days (measured during the day), which suggests a shift in allocation from self-feeding to chick-feeding. However, there was no detectable manipulation effect on condition measured at the nestling age of 12 days (measured during the night). Either female condition was only affected by manipulation in the early nestling phase or the females adjusted their diurnal mass trajectory in response to brood size manipulation. More detailed data are required to verify this point. There were no indications of a fitness cost associated with the condition during the day, but condition at night was positively related to winter survival. Since manipulation only affected condition during the day, there was no link between manipulation and winter survival. 3.,The duration of the working day was not affected by manipulation and female feeding rate tended to flatten off with manipulated brood size. Similarly, brood reduction resulted in a lower DEEfem, whilst brood enlargement had no effect. This suggests that females worked at an energetic ceiling when rearing an unmanipulated brood. However, the level of this ,ceiling' in DEEfem was not fixed: it differed between years. This leads us to conclude that the observed ceiling was imposed by extrinsic factors (e.g. available foraging time) and not by an intrinsic factor such as maximum energy assimilation rate. We hypothesize that time limitation was the cause for the observed ceiling in energy expenditure and that the annual variation in the level of this ceiling was due to annual variation in ambient temperature. 4.,A cost of reproduction was previously demonstrated in this population: brood enlargement caused a reduction in the incidence of second clutches. However, since DEEfem did not differ between control and enlarged broods, we judge it unlikely that daily energy expenditure is a general predictor for parental investment. [source] Sex-dependent response of primary moult to simulated time constraints in the rock sparrow Petronia petroniaJOURNAL OF AVIAN BIOLOGY, Issue 3 2010Lorenzo Serra There is growing evidence that moult speed affects plumage quality. In many bird species, males and females differ in terms of breeding effort, survival expectation and the relationship between fitness and plumage quality. Consequently, differences in moult strategies between the sexes can be expected. The aim of this study was to assess whether, under simulated time constraints and with no parental investment in the previous breeding season, males and females differed in: a) timing and duration of primary moult, b) growth rates of individual primary feathers, and c) number of concurrently growing feathers. We investigated the effect of time constraints generated by a treatment consisting of two decreasing photoperiods (slow changing photoperiod, SCP=2,min,day,1 and fast changing photoperiod, FCP=8,min,day,1) on the primary post-nuptial moult of captive rock sparrows Petronia petronia. Females started to moult on average 14 and 15,days later than males in both experimental groups. Primary moult duration was 10 (FCP) and 24 (SCP) days longer in males than in females, and, within sex, 34 (females) and 48 (males) days longer in SCP birds than in FCP ones. Females renewed a larger number of primaries simultaneously (5.7% in FCP and 12.8% in SCP) and had a higher total daily feather mass grown (9.9% in FCP and 22.4% in SCP), even though daily growth rates of individual primaries did not differ between sexes. As a result, males and females completed their primary moult at the same time within treatment. The observed differences in timing, duration and energy allocation for primary moult between the sexes probably have a genetic basis, as birds did not engage in reproduction during the preceding breeding season. [source] Why is violent crime so common in the Americas?AGGRESSIVE BEHAVIOR, Issue 5 2006Nigel BarberArticle first published online: 11 JUL 200 Abstract Violent crimes, including murders, rapes, and assaults are substantially higher in the Americas than other regions of the world. This study investigated the role of single parenthood ratios in accounting for this regional variation in violent crime of 39 countries using INTERPOL data. It pitted the prediction of parental investment (calling for a delayed relationship between single parenthood and crime) against a mating aggression hypothesis that predicted a contemporaneous effect. Regression analyses found that current single parenthood ratios were strongly and consistently predictive of violent crimes whereas single parenthood ratios 18 years earlier were not and this conclusion remained following controls for income inequality and the population sex ratio. The results indicate that the regional difference in violent crime is best explained in terms of mating competition rather than reduced parental investment. Aggr. Behav. 32:1,9, 2006. © 2006 Wiley-Liss, Inc. [source] Are parental care trade-offs in shorebirds driven by parental investment or sexual selection?JOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2009V. A. OLSON Abstract Sexual selection, mating systems and parental behaviour are closely linked, although the exact nature of their relationship is controversial. The parental investment hypothesis (PIH) states that parental care disparity drives sexual selection intensity, because the sex providing less care competes for the sex that provides more. In contrast, the sexual selection hypothesis (SSH) asserts that more intense sexual selection on males leads to reduced male parental investment. We tested these hypotheses using directional phylogenetic comparative methods in shorebirds, which have an unusually diverse array of breeding systems. Changes in parental care and sexual selection intensity were tightly correlated, and we carried out three sets of analyses focusing on changes in male behaviour, female behaviour and in either sex. The results from the analyses were consistent with both PIH and SSH, although the patterns in male transition were sensitive to model values. We propose two explanations for these results. First, phylogenetic transitions may be idiosyncratic so that they depend on the ecological circumstances of individual species. Second, transitions in social traits, such as breeding systems, may be rapid and take place in ecological time, so directional phylogenetic methods that work through longer time scales may not infer accurately the timing and direction of all changes. [source] Parental investment, sexual selection and sex ratiosJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 4 2008HANNA KOKKO Abstract Conventional sex roles imply caring females and competitive males. The evolution of sex role divergence is widely attributed to anisogamy initiating a self-reinforcing process. The initial asymmetry in pre-mating parental investment (eggs vs. sperm) is assumed to promote even greater divergence in post-mating parental investment (parental care). But do we really understand the process? Trivers [Sexual Selection and the Descent of Man 1871,1971 (1972), Aldine Press, Chicago] introduced two arguments with a female and male perspective on whether to care for offspring that try to link pre-mating and post-mating investment. Here we review their merits and subsequent theoretical developments. The first argument is that females are more committed than males to providing care because they stand to lose a greater initial investment. This, however, commits the ,Concorde Fallacy' as optimal decisions should depend on future pay-offs not past costs. Although the argument can be rephrased in terms of residual reproductive value when past investment affects future pay-offs, it remains weak. The factors likely to change future pay-offs seem to work against females providing more care than males. The second argument takes the reasonable premise that anisogamy produces a male-biased operational sex ratio (OSR) leading to males competing for mates. Male care is then predicted to be less likely to evolve as it consumes resources that could otherwise be used to increase competitiveness. However, given each offspring has precisely two genetic parents (the Fisher condition), a biased OSR generates frequency-dependent selection, analogous to Fisherian sex ratio selection, that favours increased parental investment by whichever sex faces more intense competition. Sex role divergence is therefore still an evolutionary conundrum. Here we review some possible solutions. Factors that promote conventional sex roles are sexual selection on males (but non-random variance in male mating success must be high to override the Fisher condition), loss of paternity because of female multiple mating or group spawning and patterns of mortality that generate female-biased adult sex ratios (ASR). We present an integrative model that shows how these factors interact to generate sex roles. We emphasize the need to distinguish between the ASR and the operational sex ratio (OSR). If mortality is higher when caring than competing this diminishes the likelihood of sex role divergence because this strongly limits the mating success of the earlier deserting sex. We illustrate this in a model where a change in relative mortality rates while caring and competing generates a shift from a mammalian type breeding system (female-only care, male-biased OSR and female-biased ASR) to an avian type system (biparental care and a male-biased OSR and ASR). [source] The influence of mating system on the intensity of parent,offspring conflict in primatesJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 3 2005T. A. F. LONG Abstract An evolutionary conflict of interest exists between parents and their offspring over the partitioning of parental investment (PI) among siblings. When the direct fitness benefits to offspring of increased PI, outweigh the inclusive fitness costs from lost future sibling fitness, selection should favour the evolution of offspring selfishness over altruism. In theory, this conflict is heightened when females are not strictly monogamous, as current offspring should be less altruistic towards future half-siblings than they would be towards full-siblings. Using data collected on foetal growth rate (representing prenatal PI) in primates, I test the prediction from theory that the resolution of the parent-offspring conflict will be closer to the offspring's evolutionary optima in polyandrous species than in more monandrous species. Using phylogenetic comparative analysis, and controlling for allometry, I show that offspring are able to obtain more PI when the probability of future full-siblings decreases, and that this is most pronounced in taxa where there is the opportunity for direct foetal access to the maternal bloodstream. These results support the hypothesis that the resolution of prenatal PI conflict is influenced by both a species' mating system and by its placental structure. [source] Genetic monogamy despite social promiscuity in the pot-bellied seahorse (Hippocampus abdominalis)MOLECULAR ECOLOGY, Issue 11 2007A. B. WILSON Abstract Sexual selection theory predicts a positive correlation between relative parental investment and mate choice. In syngnathid fishes (seahorses and pipefish), males brood offspring in specialized brooding structures. While female-female mating competition has been demonstrated in some pipefishes, all seahorses (genus Hippocampus) studied to date have been found to have conventional sex roles with greater male,male competition for access to mates despite possessing the most complex brood structures in the family. Although multiple mating is common in pipefish, seahorses are again exceptional, exhibiting strict genetic monogamy. Both demographic and behavioural explanations have been offered to explain the lack of multiple mating in seahorse species, but these hypotheses have not yet been explicitly addressed. We investigated mating systems and brood parentage of the pot-bellied seahorse, Hippocampus abdominalis, a temperate-water species that is socially promiscuous with conventional sex roles in laboratory populations. We observed promiscuous courtship behaviour and sex-role reversal in high density, female-biased field populations of H. abdominalis. We hypothesize that sex roles are plastic in H. abdominalis, depending on local population density and sex ratio. Despite promiscuous courtship behaviour, all assayed male seahorses were genetically monogamous in both laboratory and wild populations. Physiological limitations associated with embryo incubation may explain the absence of multiple mating in seahorses and may have played an important role in the development of the unique reproductive behaviour typical in these species. [source] A model of triploid endosperm evolution driven by parent-offspring conflictOIKOS, Issue 3 2001Roger Härdling The parental investment in angiosperms comprises the endosperm, a nutrient reserve that is used during seed development. The endosperm contains genes from both parents. The most common endosperm form is the 3n Polygonum -type with more maternal genetic influence than paternal, i.e. with two maternal nuclei and one paternal nucleus. The evolutionary original state is thought to be a diploid endosperm with equal influence of the parents. We focus on the evolution of the triploid endosperm and show that a gene for triploid endosperm would have an initial advantage in a population of diploid endosperm type plants, and increase to fixation. We assume that endosperm amount is controlled by endosperm genes. Then a gene causing triploid endosperm will increase the influence of the mother plant on parental investment. The production of endosperm with two copies of the maternal genes will modify the inheritance of endosperm amount and cause an increased production of seeds. [source] Intraclutch egg-size variation in acanthosomatid bugs: adaptive allocation of maternal investment?OIKOS, Issue 2 2001Shin-ichi Kudo If there are differences in predation risk among the offspring within a clutch, parents may allocate less resources to the offspring facing higher risk. I examined parental investment in terms of egg size within clutches in five species of stink bugs (Heteroptera, Acanthosomatidae). In subsocial Elasmucha and Sastragala species, the female guards her eggs and first-instar nymphs against invertebrate predators by covering her clutch with her body. Large differences in survival from predation between offspring at the centre and offspring at the periphery of the clutch have been reported in such subsocial insects. I found that Elasmucha and Sastragala females laid significantly smaller eggs in the peripheral (and thus more vulnerable) part of the clutch. Phenotypic trade-offs between egg size and clutch size were detected in these subsocial species. Egg size was positively correlated with hatched first-instar nymph size: smaller nymphs hatched from smaller peripheral eggs. In asocial Elasmostethus humeralis, however, no significant difference in size was detected between the eggs at the centre of and those at the periphery of the clutch. Thus, in subsocial acanthosomatid bugs, females seem to allocate their resources according to the different predation risks faced by the offspring within the clutch. [source] Sex differences in child nutritional and immunological status 5,9 years post contact in fringe highland Papua New GuineaAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 5 2010Jason A. Decaro Objectives: This study examines sex differences in vulnerability among children experiencing rapid culture change that may reflect distinct microecologies driven by differential parental investment and/or sex-specific life history strategies. Apparent female growth canalization may be a life history strategy favoring growth over maintenance but also may reflect sex-differentiated selection for resilience based on unequal treatment during early life. Methods: Stature, weight, and serum measures of C-reactive protein (CRP, an inflammation marker) and Epstein-Barr Virus antibodies (EBV, a humoral immune response marker) were collected longitudinally among children/adolescents ages 5,20 years (N = 65), 5,9 years after sustained contact in a fringe highland hunter-horticulturalist group from the Schrader Range in Papua New Guinea exhibiting male preference and sex-biased survival. It was hypothesized that girls would exhibit canalization, with better nutritional status than boys; lower maintenance investment would yield lower female immune activation; and because of differential survivorship, females would appear increasingly canalized as early conditions for girls worsened relative to boys. Results: Girls had greater arm circumference z -scores than boys, less frequent stunting, and lower CRP despite high pathogen load. Average nutritional status for girls improved over time as the sex ratio became increasingly male biased and the condition of female infants reportedly worsened. Conclusions: Both canalization and survivorship effects were found. Although a life history perspective on female canalization can help explain developmental outcomes in populations undergoing rapid culture change amid adversity, possible sex differences in the strength of survivorship effects that select for resiliency should not be ignored. Am. J. Hum. Biol. 22:657,666, 2010. © 2010 Wiley-Liss, Inc. [source] Reproductive development and parental investment during pregnancy: Moderating influence of mother's early environmentAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 2 2010David A. Coall The association between a woman's age at menarche and the birth weight of her children is highly variable across human populations. Life history theory proposes that a woman's early environment may moderate this association and thus account for some of the variation between populations. According to one life history theory model, for individuals who develop in a childhood environment of high local mortality rates (experienced subjectively as psychosocial stress), it can be adaptive to mature earlier, have more offspring during their reproductive lifetime, and reduce investment in each offspring. In an environment of low psychosocial stress, however, it may be adaptive to mature later, have fewer offspring, and invest more in each. In this study, birth weight and proportionate birth weight (neonate's birth weight as a percentage of its mother's prepregnancy weight) were used as measures of parental investment during pregnancy. In a sample of 580 first-time mothers, we tested the hypothesis that the psychosocial stress experienced as a child would moderate the association between age at menarche and investment during pregnancy. We found that earlier menarche in those women who experienced stressful life events before 15 years of age was associated with a lower birth weight and proportionate birth weight. Conversely, in those who reported no childhood stressors, earlier menarche was associated with increased birth weight and proportionate birth weight. Our data suggest that the moderating influence of the childhood psychosocial environment on the association between age at menarche and parental investment throughout gestation operates in a dose-dependent manner. Am. J. Hum. Biol., 2010. © 2009 Wiley-Liss, Inc. [source] Breastfeeding structure as a test of parental investment theory in Papua New Guinea,AMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 5 2009David P. Tracer Evolutionary parental investment theory predicts that parents invest preferentially in offspring best able to translate investments into fitness payoffs. It has also been proposed that where the reproductive prospects of offspring are directly correlated with parental investment and variance in fertility is higher for males than females, parents in better condition should bias investment toward males while those in poorer condition should bias investment toward females. Lactation is arguably among the costliest forms of investment expended by mothers and is thus expected to be allocated in ways consistent with fitness payoffs. Quantitative data collected among 110 Papua New Guinean mother-infant pairs during 470 h of focal follows on nursing frequency and duration and responses to infant demands by maternal and offspring characteristics are presented to provide empirically-based descriptions of infant care and tests of evolutionary parental investment theory. Results indicate that mothers show very high levels of investment in offspring. However, although breastfeeding in developing countries is often characterized as on-demand, fussing and crying by infants were only attended to with breastfeeding about 30% of the time. Contrary to expectations of parental investment theory that parents should invest less in poorer quality offspring, mothers increased investment in offspring in poorer condition. The expectation that mothers in better condition would bias investment toward male offspring was also not supported; better nourished mothers biased investment toward female offspring. This study illustrates how infant feeding data may be used for testing larger evolutionary questions such as those derived from parental investment theory. Am. J. Hum. Biol. 2009. © 2009 Wiley-Liss, Inc. [source] Short- and long-term consequences of early parental loss in the historical population of the Krummhörn (18th and 19th century)AMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 4 2009Kai P. Willführ The impact of the early loss of one's father or one's mother on the survival and age at death of children was investigated on the basis of a historical reconstitution of families from the Krummhörn (East Frisia/Ostfriesland; Germany) with the aid of Kaplan-Meier plots and the Cox regression. In our analyses, we took into account the changed situation of the family after the death of a parent by incorporating the surviving spouse's remarriage or relationships with stepparents. We find that the impact on survival of the children was sex-specific and also depended on whether and at what point in time during childhood their father or mother had died. As expected, children's immediate survival was strongly affected by maternal loss. A few results can be construed as survival diminishing long-term consequences of the early loss of a parent. Daughters who lost their fathers before their first birthday proved to have increased mortality over a longer period of their youth. The age at death of daughters was also lowered if they had to live with a step-mother during early childhood. To interpret these results, three hypotheses, including an (intrinsic) trade-off, compensation and a selection scenario, were tested. Other approaches, which are based, for example, on the extrinsic trade-off between mating effort and parental investment of the surviving parent, also appear to be suitable as an explanation for the long-term consequences, which eventually draws the conclusion that the compensation scenario is the most likely explanation for the consequences of early parental loss. Am. J. Hum. Biol., 2009. © 2009 Wiley-Liss, Inc. [source] Women's autonomy and its relationship to children's nutrition among the Rendille of northern KenyaAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 1 2009Emily K. Brunson This study explores the effect of women's autonomy on children's health. Research was conducted among the Rendille, a traditionally nomadic pastoralist population living in northern Kenya. Using data collected from 435 women and 934 of their children, we tested the hypothesis that women with higher levels of autonomy would have children with better nutrition. Results of our study indicated that while women's autonomy had no effect on younger,ages 0,35 months,children's nutrition as measured by WHZ scores, greater levels of women's autonomy were significantly associated with improved nutrition among older,ages 3,10 years,children. These results suggest that women's autonomy is an important factor in relation to children's health in some circumstances. In addition to exploring the applied aspects of our findings, we also suggest how considering the concept of women's autonomy may add to the existing literature on parental investment. Am. J. Hum. Biol., 2009. © 2008 Wiley-Liss, Inc. [source] Fetal programming: Adaptive life-history tactics or making the best of a bad start?AMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 1 2005James Holland Jones Fetal programming is an ontogenetic phenomenon of increasing interest to human biologists. Because the downstream consequences of fetal programming have clear impacts on specific life-history traits (e.g., age at first reproduction and the general age-pattern of reproductive investments), a number of authors have raised the question of the adaptive significance of fetal programming. In this paper, I review in some detail several classical models in life-history theory and discuss their relative merits and weaknesses for human biology. I suggest that an adequate model of human life-history evolution must account for the highly structured nature of the human life cycle, with its late age at first reproduction, large degree of iteroparity, highly overlapping generations, and extensive, post-weaning parental investment. I further suggest that an understanding of stochastic demography is essential for answering the question of the adaptive significance of fetal programming, and specifically the finding of low birth weight on smaller adult body size and earlier age at first reproduction. Using a stage-structured stochastic population model, I show that the downstream consequences of early deprivation may be "making the best of a bad start" rather than an adaptation per se. When a high-investment strategy entails survival costs, the alternate strategy of early reproduction with relatively low investment may have higher fitness than trying to play the high-investment strategy and failing. Am. J. Hum. Biol. 17:22,33, 2005. © 2004 Wiley-Liss, Inc. [source] Fallback foods, eclectic omnivores, and the packaging problemAMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 4 2009Stuart A. Altmann Abstract For omnivorous primates, as for other selective omnivores, the array of potential foods in their home ranges present a twofold problem: not all nutrients are present in any food in the requisite amounts or proportions and not all toxins and other costs are absent. Costs and benefits are inextricably linked. This so-called packaging problem is particularly acute during periods, often seasonal, when the benefit-to-cost ratios of available foods are especially low and animals must subsist on fallback foods. Thus, fallback foods represent the packaging problem in extreme form. The use of fallback foods by omnivorous primates is part of a suite of interconnected adaptations to the packaging problem, the commingling of costs and benefits in accessing food and other vital resources. These adaptations occur at every level of biological organization. This article surveys 16 types of potential adaptations of omnivorous primates to fallback foods and the packaging problem. Behavioral adaptations, in addition to finding and feeding on fallback foods, include minimizing costs and requirements, exploiting food outbreaks, living in social groups and learning from others, and shifting the home range. Adaptive anatomical and physiological traits include unspecialized guts and dentition, binocular color vision, agile bodies and limbs, Meissner's corpuscles in finger tips, enlargement of the neocortex, internal storage of foods and nutrients, and ability internally to synthesize compounds not readily available in the habitat. Finally, during periods requiring prolonged use of fallback foods, life history components may undergo changes, including reduction of parental investment, extended interbirth intervals, seasonal breeding or, in the extreme, aborted fetuses. Am J Phys Anthropol 140:615,629, 2009. © 2009 Wiley-Liss, Inc. [source] Social bonds in birds are associated with brain size and contingent on the correlated evolution of life-history and increased parental investmentBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2010SUSANNE SHULTZ In birds, large brains are associated with a series of population-level phenomena, including invasion success, species richness, and resilience to population decline. Thus, they appear to open up adaptive opportunities through flexibility in foraging and anti-predator behaviour. The evolutionary pathway leading to large brain size has received less attention than behavioural and ecological correlates. Using a comparative approach, we show that, independent of previously recognized associations with developmental constraints, relative brain size in birds is strongly related to biparental care, pair-bonding, and stable social relationships. We also demonstrate correlated evolution between large relative brain size and altricial development, and that the evolution of both traits is contingent on biparental care. Thus, biparental care facilitates altricial development, which permits the evolution of large relative brain size. Finally, we show that large relative brain size is associated with pair-bond strength, itself a likely consequence of cooperation and negotiation between partners under high levels of parental investment. These analyses provide an evolutionary model for the evolution of and prevalence of biparental care, altricial development, and pair-bonding in birds. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 111,123. [source] | |||||||||||||||||||||||||