Abstract:In social animals, inbreeding depression may manifest by compromising care or resources individuals receive from inbred group members. We studied the effects of worker inbreeding on colony productivity and investment in the ant Formica exsecta. The production of biomass decreased with increasing inbreeding, as did biomass produced per worker. Inbred colonies produced fewer gynes (unmated reproductive females), whereas the numbers of males remained unchanged. As a result, sex ratios showed increased male bias, … Show more
“…Another possibility is that nurse workers can assess the number of queens directly or by colony egg production, and use this as a proxy to adjust sex ratio in polygynous colonies. This is consistent with split-sex ratio theory (Boomsma, 1993), because polygynous colonies will tend to have higher eggproduction and a lower than population-level-average relatedness asymmetry, and also with the idea that specialization in the cheaper sex (males weigh less in F. exsecta; Vitikainen et al, 2011) requires greater initial eggproduction for equal total biomass production. On the other hand, this does not explain the tendency of monogynous/ polyandrous colonies to specialize in male production.…”
Section: Discussionsupporting
confidence: 79%
“…Fletcher and Michener, 1987), but this lack of relationship may be explained by the uniform levels of genetic variation we found among the different colony types. The breeding patterns and the genetic structure of the population, which indicate non-trivial levels of inbreeding Haag-Liautard et al, 2009;Vitikainen et al, 2011), may have contributed to the depauperate chemical profile through genetic purging, a question which will have to be addressed in future studies. We also found that the within-colony CHC variability does not allow accurate assessment of colony kin structure, and that workers do not seem to use any single compound or set of compound as a proxy for sex ratio adjustments.…”
Section: Discussionmentioning
confidence: 98%
“…This is indeed the case in F. exsecta, but many more compounds have been found in F. truncorum (Akino, 2006), which goes against this interpretation. Second, given that inbreeding is rife in the population of F. exsecta studied here Haag-Liautard et al, 2009;Vitikainen et al, 2011), genetic variation for cue diversity may have been purged. We found no significant effects of inbreeding on CHC variability, but the measure we used as a covariate in the analyses does not reflect the absolute level of inbreeding, only the relative level.…”
Section: Discussionmentioning
confidence: 98%
“…The sex of the pupae was determined based on morphology, and the sex ratio was calculated as the proportion of queens of all sexual brood (c.f., Vitikainen et al, 2011).…”
Section: Methodsmentioning
confidence: 95%
“…We included HL in the analysis, given that two earlier studies have indicated a significant effect of inbreeding on sex ratios (Haag-Liautard et al, 2009;Vitikainen et al, 2011). To test the effects of within-colony CHC variability, relatedness, genetic diversity, and inbreeding on colony sex ratio we used a multiple regression with stepwise backward elimination.…”
Split sex ratio theory predicts that when kin structure varies among colonies of social insects, in order to maximize the inclusive fitness, colonies with relatively high sister-sister relatedness should specialize in producing reproductive females, whereas in those with relatively low sister-sister relatedness workers should bias their sex ratio towards males. However, in order to achieve this, workers need to be able to reliably assess the type of colony in which they live. The information on colony kin structure may be encoded in cuticular hydrocarbons (CHCs), assuming that genetic variability translates accurately into chemical variability. However, in genetically heterogeneous colonies, too accurate information may encourage the pursuit of individual interests through nepotistic behavior and reduce colony efficiency or cause social disruption. In this study, we estimated how well variability of CHC recognition cues reflects colony kin structure in the ant Formica exsecta. Our results show that CHC variability does not covary with kin structure or the overall genetic diversity of the colony, and that patrilines and matrilines can have distinct CHC profiles in some but not all colonies. However, within-colony relatedness remains the key determinant of colony sex ratios. Based on our results, CHC variability cannot serve as accurate information on within-colony relatedness, kin structure, or full-sib affiliation, nor do workers seem to use colony CHC variability as a proxy for sex-ratio adjustment. The use of this type of information thus could lead workers to make mistakes, and it remains unclear how colonies of Formica exsecta adjust offspring sex ratio to their optimal value.
“…Another possibility is that nurse workers can assess the number of queens directly or by colony egg production, and use this as a proxy to adjust sex ratio in polygynous colonies. This is consistent with split-sex ratio theory (Boomsma, 1993), because polygynous colonies will tend to have higher eggproduction and a lower than population-level-average relatedness asymmetry, and also with the idea that specialization in the cheaper sex (males weigh less in F. exsecta; Vitikainen et al, 2011) requires greater initial eggproduction for equal total biomass production. On the other hand, this does not explain the tendency of monogynous/ polyandrous colonies to specialize in male production.…”
Section: Discussionsupporting
confidence: 79%
“…Fletcher and Michener, 1987), but this lack of relationship may be explained by the uniform levels of genetic variation we found among the different colony types. The breeding patterns and the genetic structure of the population, which indicate non-trivial levels of inbreeding Haag-Liautard et al, 2009;Vitikainen et al, 2011), may have contributed to the depauperate chemical profile through genetic purging, a question which will have to be addressed in future studies. We also found that the within-colony CHC variability does not allow accurate assessment of colony kin structure, and that workers do not seem to use any single compound or set of compound as a proxy for sex ratio adjustments.…”
Section: Discussionmentioning
confidence: 98%
“…This is indeed the case in F. exsecta, but many more compounds have been found in F. truncorum (Akino, 2006), which goes against this interpretation. Second, given that inbreeding is rife in the population of F. exsecta studied here Haag-Liautard et al, 2009;Vitikainen et al, 2011), genetic variation for cue diversity may have been purged. We found no significant effects of inbreeding on CHC variability, but the measure we used as a covariate in the analyses does not reflect the absolute level of inbreeding, only the relative level.…”
Section: Discussionmentioning
confidence: 98%
“…The sex of the pupae was determined based on morphology, and the sex ratio was calculated as the proportion of queens of all sexual brood (c.f., Vitikainen et al, 2011).…”
Section: Methodsmentioning
confidence: 95%
“…We included HL in the analysis, given that two earlier studies have indicated a significant effect of inbreeding on sex ratios (Haag-Liautard et al, 2009;Vitikainen et al, 2011). To test the effects of within-colony CHC variability, relatedness, genetic diversity, and inbreeding on colony sex ratio we used a multiple regression with stepwise backward elimination.…”
Split sex ratio theory predicts that when kin structure varies among colonies of social insects, in order to maximize the inclusive fitness, colonies with relatively high sister-sister relatedness should specialize in producing reproductive females, whereas in those with relatively low sister-sister relatedness workers should bias their sex ratio towards males. However, in order to achieve this, workers need to be able to reliably assess the type of colony in which they live. The information on colony kin structure may be encoded in cuticular hydrocarbons (CHCs), assuming that genetic variability translates accurately into chemical variability. However, in genetically heterogeneous colonies, too accurate information may encourage the pursuit of individual interests through nepotistic behavior and reduce colony efficiency or cause social disruption. In this study, we estimated how well variability of CHC recognition cues reflects colony kin structure in the ant Formica exsecta. Our results show that CHC variability does not covary with kin structure or the overall genetic diversity of the colony, and that patrilines and matrilines can have distinct CHC profiles in some but not all colonies. However, within-colony relatedness remains the key determinant of colony sex ratios. Based on our results, CHC variability cannot serve as accurate information on within-colony relatedness, kin structure, or full-sib affiliation, nor do workers seem to use colony CHC variability as a proxy for sex-ratio adjustment. The use of this type of information thus could lead workers to make mistakes, and it remains unclear how colonies of Formica exsecta adjust offspring sex ratio to their optimal value.
Chemical recognition cues are used to discriminate among species, con-specifics, and potentially between patrilines in social insect colonies. There is an ongoing debate about the possible persistence of patriline cues despite evidence for the mixing of colony odors via a “gestalt” mechanism in social insects, because patriline recognition could lead to nepotism. We analyzed the variation in recognition cues (cuticular hydrocarbons) with different mating frequencies or queen numbers in 688 Formica exsecta ants from 76 colonies. We found no increase in the profile variance as genetic diversity increased, indicating that patriline effects were absent or possibly obscured by a gestalt mechanism. We then demonstrated that an isolated individual's profile changed considerably relative to their colony profile, before stabilizing after 5 days. We used these isolated individuals to eliminate the masking effects of the gestalt mechanism, and we detected a weak but statistically significant patriline effect in isolated adult workers and also in newly emerged callow workers. Thus, our evidence suggests that genetic variation in the cuticular hydrocarbon profile of F. exsecta ants (n-alkanes and alkenes) resulted in differences among patrilines, but they were obscured in the colony environment, thereby avoiding costly nepotistic behaviors.
In a subarctic climate, the seasonal shifts in temperature, precipitation, and plant cover drive the temporal changes in the microbial communities in the topsoil, forcing soil microbes to adapt or decline. Many organisms, such as mound‐building ants, survive the cold winter owing to the favorable microclimate in their nest mounds. We have previously shown that the microbial communities in the nest of the ant
Formica
exsecta
are significantly different from those in the surrounding bulk soil. In the current study, we identified taxa, which were consistently present in the nests over a study period of three years. Some taxa were also significantly enriched in the nest samples compared with spatially corresponding reference soils. We show that the bacterial communities in ant nests are temporally stable across years, whereas the fungal communities show greater variation. It seems that the activities of the ants contribute to unique biochemical processes in the secluded nest environment, and create opportunities for symbiotic interactions between the ants and the microbes. Over time, the microbial communities may come to diverge, due to drift and selection, especially given the long lifespan (up to 30 years) of the ant colonies.
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