WASPnest: A worldwide assessment of social Polistine nesting behavior (original) (raw)

Different axes of environmental variation explain the presence vs. extent of cooperative nest founding associations in Polistes paper wasps

Ecology Letters, 2015

Ecological constraints on independent breeding are recognised as major drivers of cooperative breeding across diverse lineages. How the prevalence and degree of cooperative breeding relates to ecological variation remains unresolved. Using a large data set of cooperative nesting in Polistes wasps we demonstrate that different aspects of cooperative breeding are likely to be driven by different aspects of climate. Whether or not a species forms cooperative groups is associated with greater short-term temperature fluctuations. In contrast, the number of cooperative foundresses increases in more benign environments with warmer, wetter conditions. The same data set reveals that intraspecific responses to climate variation do not mirror genus-wide trends and instead are highly heterogeneous among species. Collectively these data suggest that the ecological drivers that lead to the origin or loss of cooperation are different from those that influence the extent of its expression within populations.

Why Wasp Foundresses Change Nests: Relatedness, Dominance, and Nest Quality

2012

The costs and benefits of different social options are best understood when individuals can be followed as they make different choices, something that can be difficult in social insects. In this detailed study, we follow overwintered females of the social wasp Polistes carolina through different nesting strategies in a stratified habitat where nest site quality varies with proximity to a foraging area, and genetic relatedness among females is known. Females may initiate nests, join nests temporarily or permanently, or abandon nests.

Ecological constraints on independent nesting in facultatively eusocial hover wasps

Proceedings of The Royal Society B: Biological Sciences, 1998

Recent ¢eld experiments suggest that cooperative breeding in vertebrates can be driven by a shortage of breeding territories. We did analogous experiments on facultatively eusocial hover wasps (Stenogastrinae: Liostenogaster £avolineata). We provided nesting opportunities by removing residents from 39 nests within a large aggregation (1995), and by glueing 20 nests obtained from a distant site into a second aggregation (1996). We prevented nest-less £oaters from competing for these opportunities in 1995 but not in 1996. In both years, helpers in unmanipulated groups were given opportunities to nest independently without having to incur nest-building costs and with a reduced wait before potential helpers emerged. Helpers visited the nests we provided, but adopted only a small proportion (5% of 111 vacancies created in 1995). Others were adopted by £oaters, but a signi¢cant proportion of nests were never adopted (9 out of 20 in 1995, 7 out of 20 in 1996). Helpers that visited nests did not originate from particular kinds of social group. Nests containing older broods were more likely to be adopted, and adopting females rarely destroyed older brood. A general feature of social insect, but not vertebrate life histories, namely the long period of o¡spring dependency relative to the short life expectancy of adult carers, may be a key factor constraining independent nesting.

Reproduction in foundress associations of the social wasp, Polistes carolina: conventions, competition, and skew

Behavioral Ecology, 2002

Who reproduces in colonies of social insects is determined by some combination of direct competition and more peaceful convention. We studied these two alternatives in foundresses of the paper wasp, Polistes carolina, by examining two different contexts: what determines who becomes the dominant reproductive and what determines the amount of reproduction obtained by subordinates. The dominant queen on most nests was the foundress to arrive first, rather than the largest foundress, expected to be best at fighting. This suggests that dominance is initially determined by convention, although the persistence of some aggressive conflict throughout the foundress period suggests that this convention is not absolute. Attempts to explain the division of reproduction using several skew theories were generally unsuccessful. Skew was not correlated with relatedness, size differences, colony productivity, and challenges by the subordinate. P. carolina showed high constraints against solitary nesting, with a minority of females attempting to nest alone, and none succeeding. In this situation, most skew theories predict that group stability will be independent of relatedness, yet nearly all collected subordinates were full sisters to the queen. Reproductive partitioning in early P. carolina colonies may have more to do with enhancing worker production than with conflict over direct fitness.

SEASONAL VARIATION IN THE ONSET OF EGG LAYING IN A PRIMITIVELY EUSOCIAL WASP: IMPLICATIONS FOR THE EVOLUTION OF SOCIALITY

Entomon, 1991

When freshly eclosed females of the primitively eusocial wasp, Ropalidia marginata are isolated into individual cages, only about half of tliem build nests and lay eggs and those that do so take a long and variable amount of thne (Mean ± S D = 66 ± 37 days) before they lay their first egg. Part of the reason for this delay is because, when kept in isolation, no wasp begins to lay eggs during a period of approximately 82 days from mid-October to early January. Wasps maintained at a constant temperature of 26±1°C however initiate egg laying throughout the year, suggesting that the low temperatures during mid-October to early January may be at least one factor that makes this period unfavourable for wasps maintained at room temperature. Egg laying continues more or less normally throughout October-January however, in all natural and laboratory colonies studied. Natural colonies of R. marginata are initiated throughout the year and often by groups of females. Huddling together is a striking feature of the wasps especially on cold mornings. We therefore suggest that the isolated animals in our experiment are unable to lay eggs during the coldest part of the year because of their inability to huddle together, share metabolic heat and perform "co-operative thermoregulation". Such "co-operative thermoregulation" may thus be another factor that facilitates the evolution of sociality.

Colony life history and demography of a swarm-founding social wasp

Behavioral Ecology and Sociobiology, 1997

Colonies of social insects are sometimes viewed as superorganisms. The birth, reproduction, and death of colonies can be studied with demographic measures analogous to those normally applied to individuals, but two additional questions arise. First, how do adaptive colony demographies arise from individual behaviors? Second, since these superorganisms are made up of genetically distinct individuals, do conflicts within the colony sometimes modify and upset optima for colonies? The interplay between individual and superindividual or colony interests appears to be particularly complex in neotropical, swarm-founding, epiponine wasps such as Parachartergus colobopterus. In a long-term study of this species, we censused 286 nests to study colony-level reproduction and survivorship and evaluated individual-level factors by assessing genetic relatedness and queen production. Colony survivorship followed a negative exponential curve very closely, indicating type II survivorship. This pattern is defined by constant mortality across ages and is more characteristic of birds and other vertebrates than of insects. Individual colonies are long-lived, lasting an average of 347 days, with a maximum of over 4.5 years. The low and constant levels of colony mortality arise in part from colony initiation by swarming, nesting on protected substrates, and an unusual expandable nest structure. The ability to requeen rapidly was also important; relatedness data suggest that colonies requeen on average once every 9–12 months. We studied whether colony optima with respect to the timing of reproduction could be upset by individual worker interests. In this species, colonies are normally polygynous but new queens are produced only after a colony reaches the monogynous state, a result which is in accord with the genetic interests of workers. Therefore colony worker interests might drive colonies to reproduce whenever queen number happens to cycled down to one rather than at the season that is otherwise optimal. However, we found reproduction to be heavily concentrated in the rainy season. The number of new colonies peaked in this season as did the percentages of males and queens. Relatedness among workers reached a seasonal low of 0.21–0.27, reflecting the higher numbers of laying queens. This seasonality was achieved in part by a modest degree of synchrony in the queen reduction cycle. Worker relatedness reached peaks of around 0.4 in the dry season, reflecting a decrease to a harmonic mean queen number of about 2.5. Thus, a significant number of colonies must be approaching monogyny entering the rainy season. Coupled with polygynous colonies rearing only males (split sex ratios), this makes it possible for a colony cycle driven by selfish worker interests to be consistent with concentrating colony reproduction during a favorable season.

The habitat saturation hypothesis and sociality in an allodapine bee: cooperative nesting is not "making the best of a bad situation

Behavioral Ecology and Sociobiology, 1996

The habitat saturation hypothesis and sociality in an allodapine bee: cooperative nesting is not "making the best of a bad situation" Abstract Several factors thought to be important for the evolution of cooperative breeding in vertebrates have received little attention in facultatively social insects. One of these, the "habitat saturation hypothesis" of Selander (1964), predicts that colony sizes will be greater in breeding units where dispersal opportunities are limited, suggesting that group living is a secondary option to independent reproduction. The Australian allodapine bee Exoneura bicolor exhibits a number of traits that occur in cooperatively breeding bird species, including long life-span, repeated opportunities for reproduction, and vulnerability to brood predation and parasitism. We experimentally examined the effect of a potentially limiting environmental factor, nesting substrate availability, as an agent influencing sociality in E. bicolor. We manipulated nesting substrate availability in two separate locations during a time when foundress dispersal is common. No significant difference was found between colony sizes in cases where dispersal options were abundant and cases where dispersal options were limited. An increase in opportunities for dispersal did not lead to higher rates of independent nesting, suggesting that cooperative nesting is a preferred strategy regardless of distance-related costs of dispersal. Reproductivity per female and brood survival were examined as factors selecting for group living. Low survival of brood in single-female nests has the potential to select for cooperative nesting in this bee.

Neighbourhood Society: Nesting Dynamics, Usurpations and Social Behaviour in Solitary Bees

PLoS ONE, 2013

Intraspecific cleptoparasitism represents a facultative strategy advantageous for reducing time and energy costs. However, only a few studies about nesting dynamics have described intraspecific cleptoparasitic behaviour in obligate solitary bees. We focused on nesting dynamics with the characterisation of nest owner replacements and frequency of true usurpation in four aggregating species belonging to different phylogenetic lineages -Andrena vaga (Andrenidae), Anthophora plumipes (Apidae), Colletes cunicularius (Colletidae), and Osmia rufa (Megachilidae). Our study, based on the regular observation of individually marked females, shows that nest owner replacement affects 10-45% of nests across all of the studied species and years. However, 39-90% of these nests had been abandoned before owner change and thus true nest usurpations represent only a part of observed nest replacement cases. Females tend to abandon their nests regularly and found new ones when they live long enough, which is in accordance with risk-spreading strategy. We suggest that the original facultative strategy of observed solitary bees during nest founding is not cleptoparasitism per se but rather reuse of any pre-existing nest (similar to ''entering'' strategy in apoid wasps). This is supported by gradual increase of nests founded by ''entering'' during the season with an increase in the number of available nests. Although the frequent reuse of conspecific nests results in frequent contact between solitary females, and rarely, in the short-term coexistence of two females in one nest, we detected unexpectedly low level of conflict in these neighbourhood societies. We suggest that nesting dynamics with regular nest switching and reusing reduces long-term and costly intraspecific aggression, a key factor for the origin and evolution of sociality.

Causes and Consequences of Reproductive Conflicts in Wasp Societies

2020

Wasps are a true model in studies on the origin and evolution of cooperative behavior and the mechanisms that help to stabilize sociality and resolve internal conflicts. Indeed, the wide variety of social organizations found in the group-ranging from solitary to highly social-provides unique opportunities to test how cooperation evolved and how conflicts are suppressed in societies with different degrees of social complexity. As the individuals in wasp colonies are not genetic clones of each other, inclusive fitness theory predicts that there should often be significant scope for conflicts between the queen and worker castes arising from specific genetic relatedness asymmetries within the colony. In many species, for example, the workers retain the ability to develop their ovaries and lay unfertilized male-destined eggs, thereby allowing them to challenge the reproductive monopoly of the queen. The amount of worker reproduction that is tolerated within the colony is a function of the genetic relatedness patterns within the colony and the costs and benefits of cheating, which under some circumstances can drive social enforcement mechanisms, whereby eggs laid by workers are selectively cannibalized or "policed" by the queen herself or by other workers. In some wasp species, such policing is so effective that workers are better off not trying to reproduce in the first place because nearly all the workers' eggs would be policed anyway. The fact that policing can align the evolutionary interests of the queens and workers in turn has selected for queen signaling systems, i.e. queen pheromones that act as honest signals for the presence of a healthy and fertile queen, which in many species cause the workers to refrain from reproducing in her presence. In many other species though, queen-worker conflict can be severe, with workers sometimes even engaging in matricide-killing their own mother queen to be able to reproduce without interference. This chapter provides an overview of both current and past research on reproductive conflicts within the Vespidae wasps and how their study has been instrumental in testing some key predictions of inclusive fitness theory.