scholarly journals Juvenile hormone affects age polyethism, ovarian status, and cuticular hydrocarbon profile in workers of a Polybia occidentalis wasp

2021 ◽  
Author(s):  
Amanda Prato ◽  
Rafael C. da Silva ◽  
Diego S. Assis ◽  
Sidnei Mateus ◽  
Klaus Hartfelder ◽  
...  
Keyword(s):  
Juvenile Hormone ◽  
Division Of Labor ◽  
Cuticular Hydrocarbon ◽  
Age Polyethism ◽  
Social Hymenoptera ◽  
Polybia Occidentalis ◽  
Ovary Activation ◽  
Social Species ◽  
Ovarian Activation ◽  
Chemical Profiles

Division of labor is one of the most striking features in the evolution of eusociality. Juvenile hormone (JH) mediates reproductive status and aggression among nestmates in primitively eusocial Hymenoptera (species without morphologically distinct castes). In highly social species it has apparently lost its gonadotropic role and primarily regulates the division of labor in the worker caste. Polybia occidentalis, a Neotropical swarm-founding wasp, is an ideal model to understand how JH levels mirror social context and reproductive opportunities because of the absence of a clear morphological caste dimorphism. In this study, we tested the hypothesis that JH influences division of labor, ovary activation and cuticular hydrocarbon profiles of workers. Our observations confirmed that JH analog (methoprene) and precocene affected the cuticular chemical profile associated with the age polyethism. Also, methoprene and precocene-I influenced differently ovarian activation of treated females (individuals treated with methoprene expressed more activated ovaries while precocene treatment did not have significant effect). These results suggest that different hormonal levels induce a differential expression in the cuticular chemical profiles associated with the workers’ age polyethism, which may be essential for keeping the social cohesion among workers throughout their lives in the colony. Furthermore, JH is likely to play a gonadotropic role in P. occidentalis. JH has apparently undergone certain modifications in social Hymenoptera, presenting multifaceted functions in different species.

scholarly journals Chemical Variation among Castes, Female Life Stages and Populations of the Facultative Eusocial Sweat Bee Halictus rubicundus (Hymenoptera: Halictidae)

2021 ◽  
Author(s):  
Iris Steitz ◽  
Robert J Paxton ◽  
Stefan Schulz ◽  
Manfred Ayasse
Keyword(s):  
Chemical Communication ◽  
North American ◽  
Specific Chemical ◽  
Eusocial Insects ◽  
Queen Signal ◽  
Ovarian Activation ◽  
Chemical Profiles ◽  
Reproductive Division Of Labor ◽  
Reproductive Division ◽  
Eusocial Species

AbstractIn eusocial insects, chemical communication is crucial for mediating many aspects of social activities, especially the regulation of reproduction. Though queen signals are known to decrease ovarian activation of workers in highly eusocial species, little is known about their evolution. In contrast, some primitively eusocial species are thought to control worker reproduction through physical aggression by the queen rather than via pheromones, suggesting the evolutionary establishment of chemical signals with more derived sociality. However, studies supporting this hypothesis are largely missing. Socially polymorphic halictid bees, such as Halictus rubicundus, with social and solitary populations in both Europe and North America, offer excellent opportunities to illuminate the evolution of caste-specific signals. Here we compared the chemical profiles of social and solitary populations from both continents and tested whether (i) population or social level affect chemical dissimilarity and whether (ii) caste-specific patterns reflect a conserved queen signal. Our results demonstrate unique odor profiles of European and North American populations, mainly due to different isomers of n-alkenes and macrocyclic lactones; chemical differences may be indicative of phylogeographic drift in odor profiles. We also found common compounds overproduced in queens compared to workers in both populations, indicating a potential conserved queen signal. However, North American populations have a lower caste-specific chemical dissimilarity than European populations which raises the question if both use different mechanisms of regulating reproductive division of labor. Therefore, our study gives new insights into the evolution of eusocial behavior and the role of chemical communication in the inhibition of reproduction.

scholarly journals Distributed nestmate recognition in ants

2015 ◽  
Vol 282 (1806) ◽  
pp. 20142838 ◽  
Author(s):  
Fernando Esponda ◽  
Deborah M. Gordon
Keyword(s):  
Distributed System ◽  
Nestmate Recognition ◽  
Cuticular Hydrocarbon ◽  
Complete Information ◽  
Distributed Model ◽  
Adequate Response ◽  
Chemical Profiles ◽  
The One ◽  
Unique Decision ◽  
Changes Over Time

We propose a distributed model of nestmate recognition, analogous to the one used by the vertebrate immune system, in which colony response results from the diverse reactions of many ants. The model describes how individual behaviour produces colony response to non-nestmates. No single ant knows the odour identity of the colony. Instead, colony identity is defined collectively by all the ants in the colony. Each ant responds to the odour of other ants by reference to its own unique decision boundary, which is a result of its experience of encounters with other ants. Each ant thus recognizes a particular set of chemical profiles as being those of non-nestmates. This model predicts, as experimental results have shown, that the outcome of behavioural assays is likely to be variable, that it depends on the number of ants tested, that response to non-nestmates changes over time and that it changes in response to the experience of individual ants. A distributed system allows a colony to identify non-nestmates without requiring that all individuals have the same complete information and helps to facilitate the tracking of changes in cuticular hydrocarbon profiles, because only a subset of ants must respond to provide an adequate response.

scholarly journals Hormone-mediated dispersal and sexual maturation in males of the social paper wasp Polistes lanio

2020 ◽  
Vol 223 (23) ◽  
pp. jeb226472
Author(s):  
Robin J. Southon ◽  
Andrew N. Radford ◽  
Seirian Sumner
Keyword(s):  
Sexual Maturation ◽  
Paper Wasp ◽  
Social Hymenoptera ◽  
Natal Nest ◽  
Male Dispersal ◽  
Accessory Glands ◽  
Social Species ◽  
The Social ◽  
Males And Females

ABSTRACTSex-biased dispersal is common in social species, but the dispersing sex may delay emigration if associated benefits are not immediately attainable. In the social Hymenoptera (ants, some bees and wasps), newly emerged males typically disperse from the natal nest whilst most females remain as philopatric helpers. However, little information exists on the mechanisms regulating male dispersal. Furthermore, the conservation of such mechanisms across the Hymenoptera and any role of sexual maturation are also relatively unknown. Through field observations and mark–recapture, we observed that males of the social paper wasp Polistes lanio emerge from pupation sexually immature, and delay dispersal from their natal nest for up to 7 days whilst undergoing sexual maturation. Delayed dispersal may benefit males by allowing them to mature in the safety of the nest and thus be more competitive in mating. We also demonstrate that both male dispersal and maturation are associated with juvenile hormone (JH), a key regulator of insect reproductive physiology and behaviour, which also has derived functions regulating social organisation in female Hymenoptera. Males treated with methoprene (a JH analogue) dispersed earlier and possessed significantly larger accessory glands than their age-matched controls. These results highlight the wide role of JH in social hymenopteran behaviour, with parallel ancestral functions in males and females, and raise new questions on the nature of selection for sex-biased dispersal.

scholarly journals Speed and accuracy in nest-mate recognition: a hover wasp prioritizes face recognition over colony odour cues to minimize intrusion by outsiders

2015 ◽  
Vol 282 (1802) ◽  
pp. 20142750 ◽  
Author(s):  
D. Baracchi ◽  
I. Petrocelli ◽  
L. Chittka ◽  
G. Ricciardi ◽  
S. Turillazzi
Keyword(s):  
Visual Cues ◽  
Cuticular Hydrocarbon ◽  
Mate Recognition ◽  
Social Wasp ◽  
False Alarms ◽  
Nest Mate ◽  
Colony Odour ◽  
Sensory Modalities ◽  
Chemical Profiles ◽  
Serious Injury

Social insects have evolved sophisticated recognition systems enabling them to accept nest-mates but reject alien conspecifics. In the social wasp, Liostenogaster flavolineata (Stenogastrinae), individuals differ in their cuticular hydrocarbon profiles according to colony membership; each female also possesses a unique (visual) facial pattern. This species represents a unique model to understand how vision and olfaction are integrated and the extent to which wasps prioritize one channel over the other to discriminate aliens and nest-mates. Liostenogaster flavolineata females are able to discriminate between alien and nest-mate females using facial patterns or chemical cues in isolation. However, the two sensory modalities are not equally efficient in the discrimination of ‘friend’ from ‘foe’. Visual cues induce an increased number of erroneous attacks on nest-mates (false alarms), but such attacks are quickly aborted and never result in serious injury. Odour cues, presented in isolation, result in an increased number of misses: erroneous acceptances of outsiders. Interestingly, wasps take the relative efficiencies of the two sensory modalities into account when making rapid decisions about colony membership of an individual: chemical profiles are entirely ignored when the visual and chemical stimuli are presented together. Thus, wasps adopt a strategy to ‘err on the safe side’ by memorizing individual faces to recognize colony members, and disregarding odour cues to minimize the risk of intrusion from colony outsiders.

Chemical profiles, division of labor and social status in Pachycondyla queens (Hymenoptera: Formicidae)

2001 ◽  
Vol 88 (4) ◽  
pp. 175-178 ◽  
Author(s):  
Tentschert J. ◽  
Kolmer K. ◽  
Hölldobler B. ◽  
Bestmann H.-J. ◽  
Delabie J. ◽  
...  
Keyword(s):  
Social Status ◽  
Division Of Labor ◽  
Chemical Profiles

scholarly journals Recombination mapping of the Brazilian stingless bee Frieseomelitta varia confirms high recombination rates in social hymenoptera

BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Prashant Waiker ◽  
Fabiano Carlos Pinto de Abreu ◽  
Danielle Luna-Lucena ◽  
Flávia Cristina Paula Freitas ◽  
Zilá Luz Paulino Simões ◽  
...  
Keyword(s):  
Linkage Map ◽  
Social Evolution ◽  
Stingless Bee ◽  
Recombination Rates ◽  
Social Hymenoptera ◽  
Social Species ◽  
A Genome ◽  
Study Results ◽  
Worker Caste ◽  
Genomic Recombination

Abstract Background Meiotic recombination is a fundamental genetic process that shuffles allele combinations and promotes accurate segregation of chromosomes. Analyses of the ubiquitous variation of recombination rates within and across species suggest that recombination is evolving adaptively. All studied insects with advanced eusociality have shown exceptionally high recombination rates, which may represent a prominent case of adaptive evolution of recombination. However, our understanding of the relationship between social evolution and recombination rates is incomplete, partly due to lacking empirical data. Here, we present a linkage map of the monandrous, advanced eusocial Brazilian stingless bee, Frieseomelitta varia, providing the first recombination analysis in the diverse Meliponini (Hymenoptera, Apidae). Results Our linkage map includes 1417 markers in 19 linkage groups. This map spans approximately 2580 centimorgans, and comparisons to the physical genome assembly indicate that it covers more than 75 % of the 275 Megabasepairs (Mbp) F. varia genome. Thus, our study results in a genome-wide recombination rate estimate of 9.3–12.5 centimorgan per Mbp. This value is higher than estimates from nonsocial insects and comparable to other highly social species, although it does not support our prediction that monandry and strong queen-worker caste divergence of F. varia lead to even higher recombination rates than other advanced eusocial species. Conclusions Our study expands the association between elevated recombination and sociality in the order Hymenoptera and strengthens the support for the hypothesis that advanced social evolution in hymenopteran insects invariably selects for high genomic recombination rates.

scholarly journals The cuticular hydrocarbon profiles of honey bee workers develop via a socially-modulated innate process

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Cassondra L Vernier ◽  
Joshua J Krupp ◽  
Katelyn Marcus ◽  
Abraham Hefetz ◽  
Joel D Levine ◽  
...  
Keyword(s):  
Honey Bee ◽  
Social Insect ◽  
Cuticular Hydrocarbon ◽  
Specific Chemical ◽  
Behavioral Interactions ◽  
Age Dependent ◽  
Chemical Profiles ◽  
Group Members ◽  
Environmentally Sensitive ◽  
Honey Bee Workers

Large social insect colonies exhibit a remarkable ability for recognizing group members via colony-specific cuticular pheromonal signatures. Previous work suggested that in some ant species, colony-specific pheromonal profiles are generated through a mechanism involving the transfer and homogenization of cuticular hydrocarbons (CHCs) across members of the colony. However, how colony-specific chemical profiles are generated in other social insect clades remains mostly unknown. Here we show that in the honey bee (Apis mellifera), the colony-specific CHC profile completes its maturation in foragers via a sequence of stereotypic age-dependent quantitative and qualitative chemical transitions, which are driven by environmentally-sensitive intrinsic biosynthetic pathways. Therefore, the CHC profiles of individual honey bees are not likely produced through homogenization and transfer mechanisms, but instead mature in association with age-dependent division of labor. Furthermore, non-nestmate rejection behaviors seem to be contextually restricted to behavioral interactions between entering foragers and guards at the hive entrance.

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