Search results for "parental investment"

Parental Care and Investment

2017

Parental care is common throughout the animal kingdom, and much variation exists among species in how, and how much, parents care for their offspring. In most species, females care more; in others, males care more and in some, caring is more or less equally shared between the sexes. Several hypotheses have been proposed to explain patterns of parental care within and among species. These hypotheses invoke factors such as the relatedness (parentage certainty) of each parent to the brood; the sex ratio at maturation; the strength of sexual selection faced by each sex and the exact nature of any trade-offs between caring and other activities. Work is still ongoing to develop an overarching hyp…

The evolution of sex roles in mate searching

2016

Searching for mates is a critical stage in the life cycle of most internally, and many externally, fertilizing species. Males usually invest more in this costly activity than females, but the reasons for this are poorly understood. Previous models have shown that female-biased parental investment, including anisogamy, does not by itself select for male-biased mate searching, so it requires additional explanations. Here, we correct and expand upon earlier models, and present two novel hypotheses that might explain the evolution of male-biased mate searching. The "carry-over hypothesis" states that females benefit less from searching if the associated costs affect other stages of the life cyc…

2021

Hosts of brood parasitic cuckoos often employ mobbing attacks to defend their nests and, when mobbing is costly, hosts are predicted to adjust their mobbing to match parasitism risk. While evidence exists for fine-tuned plasticity, it remains unclear why mobbing does not track larger seasonal changes in parasitism risk. Here we test a possible explanation from parental investment theory: parents should defend their current brood more intensively as the opportunity to replace it declines (re-nesting potential), and therefore “counteract” any apparent seasonal decline to match parasitism risk. We take advantage of mobbing experiments conducted at two sites where reed warblers (Acrocephalus sc…

Differential expression and costs between maternally and paternally derived immune priming for offspring in an insect

2011

1. When parasitized, both vertebrates and invertebrates can enhance the immune defence of their offspring, although this transfer of immunity is achieved by different mechanisms. In some insects, immune-challenged males can also initiate trans-generational immune priming (TGIP), but its expressions appear qualitatively different from the one induced by females similarly challenged. 2. The existence of male TGIP challenges the traditional view of the parental investment theory, which predicts that females should invest more into their progeny than males. However, sexual dimorphism in life-history strategies and the potential costs associated with TGIP may nevertheless lead to dissymmetric in…

Male bill colour and age are associated with parental abilities and breeding performance in blackbirds

2005

9 pages; International audience; In monogamous bird species, male parental investment may influence offspring fitness and females may gain advantages through mating with males providing extensive paternal care. However, paternal care is a benefit that can only be assessed indirectly because mate choice precedes paternal activities. Individual quality and age, both signalled by morphological characteristics, may reflect parental abilities. Because they may reflect individual foraging abilities, carotenoid-based colorations have been proposed to honestly signal parental quality. The blackbird (Turdus merula), a socially monogamous species, exhibits biparental care and males show bills that va…

Could male tergal secretions be considered as a nuptial gift in the Madeira cockroach?

2008

International audience; Many male insects provide somatic nuptial gifts that may strongly influence reproductive fitness, ensuring effective copulation or mediating paternal resource benefits in offspring. Although the courtship feeding behaviour on tergal gland secretions has been described in numerous cockroaches, studies on the function of these so-called nuptial gifts are lacking in this group. In this study, we examined, in the Madeira cockroach, Leucophaea maderae, the functional significance of tergal secretions by manipulating their availability on the back of males. We tested whether male tergal secretions function as a form of mating effort, and/or as a form of paternal investment…

Female-female aggression and male polyterritoriality in the pied flycatcher

1994

Assortative mating and female clutch investment in black grouse

1999

Variation in female behaviour has only recently received attention in studies of sexual selection. It has been suggested that females may invest differentially in their offspring in relation to the quality of their mate. This may lead to females that mate with high-quality and/or attractive males laying larger clutches. Females may also differ in their ability to choose between males. For example, females in good physical condition may make better choices. If physical condition and clutch size are positively correlated, this hypothesis could also produce a relationship between male attractiveness and female clutch size. We found, in lekking black grouse, Tetrao tetrix, that females mated to…

Do Pied Flycatcher Females Defend an Extra Nest Hole Against Conspecific Females?

1999

AbstractIn birds, females are often aggressive against conspecific females during the breeding. There are many explanations for this intrasexual aggression by females: e.g., nest site or food resource defence, prevention of intraspecific brood parasitism or infanticide, and monopolization of paternal care. A pair might also benefit by defending an alternative nest site in addition to the current nest site. Here, I study by experimentation whether pied flycatcher (Ficedula hypoleuca) females defend an extra nest box as an alternative nesting site. Further, I examine whether females behave differently when their mate is present vs not present. I measured the reactions by resident females to a…

The evolution of parental care in insects: the roles of ecology, life history and the social environment

2013

Parental care increases the fitness of offspring at a cost to the parents in terms of residual reproductive success. This trade-off may be affected by ecology, life history and the social environment, which raises the question as to how these factors contribute to the evolution of parental care. Here, previous hypotheses concerning the evolution of parental care in insects are summarized and discussed and the underlying empirical evidence is reviewed. Ecological factors such as harsh environments, ephemeral food sources or predation pressure are broadly accepted as evolutionary drivers of parental care. The most consistent evidence supports a role for natural enemies such as predators, micr…