Effect of Population Density and Female Body Size on Number and Size of Offspring in a Species with Size‐Dependent Contests over Resources

When size‐dependent contests over resources influence reproductive success, the trade‐off between number and size of offspring depends on the frequency of contests. Under these circumstances, clutch size should decrease and offspring size should increase as contests become more frequent. We tested these predictions with the burying beetle Nicrophorus pustulatus through manipulation of rearing densities. Burying beetles reproduce on small vertebrate carcasses, a rare but high quality food source for the larvae. Large beetles are more likely to win contests over carcasses and gain exclusive access to a carcass. The winner of a contest kills eggs and larvae already present on a carcass. As a result of the rarity of carcasses, burying beetles are unlikely to breed more than once. As predicted, brood size of N. pustulatus decreased with increasing rearing density. Despite a negative correlation between brood size and larval mass, larval mass did not increase with increasing rearing density. This may be due to the special biology of N. pustulatus which can use snake eggs for reproduction. Potentially larger supply of resources and generally small population densities of N. pustulatus may weaken selection on body size and thus the correlation between brood size and larval mass. As size‐dependent constraints can limit reproductive phenotypes, we examined whether female size influenced reproductive phenotype. Small females produced larger broods with smaller, but more variable, offspring than large females. Mechanical constraints of egg size seem an unlikely explanation for the differences because burying beetles can compensate for small egg size through parental care. Energetic constraints may impact small females because body mass and brood size of small females decreased with increasing density. Yet, at all density levels small females produced larger, not smaller, broods than large females. The larger and more variable broods of small females seem to be in agreement with a bet‐hedging strategy.     

Nestmate recognition in burying beetles: the "breeder's badge" as a cue used by females to distinguish their mates from male intruders

Burying beetles use small vertebrate carcasses as food for theirlarvae and defend these carcasses against intra- and interspecificcompetitors. Breeding associations on carcasses can consistof single females, heterosexual pairs, or various combinationsof males and females. When a heterosexual pair collaborate ina breeding attempt, they do not typically exhibit aggressivebehavior toward each other, but do attack newly arrived conspecificsthat attempt to usurp the carcass. We investigated the cuesinvolved in discrimination between breeding partners and intrudersby female burying beetles. We found that resident females toleratemales that have cared for a brood, as well as males that havenot cared for a brood but have been on a carcass for a day ortwo. Males that have had no prior contact with a carcass areattacked. Females appear to use a chemical cue, the "breeder'sbadge," an apolar substance on the male's cuticle that can beremoved by washing with pentane. This cue is reliably correlatedwith recent male experience with a carcass that is suitablefor reproduction. The breeder's badge develops as a result ofprolonged contact with such a carcass, and disappears on removalfrom the carcass; its presence does not require contact witha female or with larvae. Female recognition of their male partnersin burying beetles thus does not involve individual recognition,but rather recognition of reproductive condition.     

Calculating males? An empirical and theoretical examination of the duration of paternal care in burying beetles

Summary Male and female burying beetles (Nicrophorus orbicollis) bury and preserve small carcasses which become food for their young. Typically, females remain with the brood until after larval development is complete, but males leave about 3 days after larvae hatch. In the absence of competitors, the effect of male presence throughout larval development is to reduce the size and weight of the brood on small carcasses, but not on larger ones. However, male assistance greatly reduces the probability that a conspecific competitor will usurp the carcass and kill the brood. A dynamic optimization model of the duration of paternal care is developed and the daily probabilities of discovery by conspecific competitors and of finding a new reproductive opportunity are varied. The model predicts that the duration of care should not be very sensitive to either the intensity of competition or the probability of finding another carcass. For a given probability of discovery by an intruder, the probability of finding a new carcass affects the duration of care in a stepwise fashion such that males should either provide no care or remain 10 days on large carcasses and 9 days on small ones (3 days after larvae hatch, in each case). The model also suggests that by providing an average of 9.5 days of care in nature, males act as if there is a negligible chance of having another brood, i.e. they are maximizing their reproductive success with their current brood.     

Niche variation and the maintenance of variation in body size in a burying beetle

1. In burying beetles (Nicrophorinae), body size is known to provide both a fecundity advantage (in females) and successful resource defence (in males and females). Despite this, considerable variation in body sizes is observed in natural populations. 2. A possible explanation for the maintenance of this variation, even with intra‐ and inter‐specific resource competition, is that individuals might assort according to body size on different‐sized breeding resources. 3. We tested prediction that ‘bigger is always better’, in the wild and in the laboratory, by experimentally manipulating combinations of available breeding‐resource size (mouse carcasses) and competitor's body size in Nicrophorus vespilloides (Herbst 1783). 4. In the field, large female beetles deserted small carcasses, without breeding, more often than they did larger carcasses, but small females used carcasses indiscriminately with respect to size. In the laboratory, large beetles reared larger broods (with more offspring) on larger carcasses than small beetles, but on small carcasses small beetles had a reproductive advantage over large ones. Offspring size covaried with carcass size independently of parental body size. 5. The present combined results suggest breeding resource value depends on an individual's body size, and variation in body size is environmentally induced: maintained by differences in available carcass sizes. This produces a mechanism by which individual specialisation leads to an increase in niche variation via body size in these beetles.     

Brood discrimination, nest mate discrimination, and determinants of social behavior in facultatively quasisocial beetles (Nicrophorus spp.)

In this study we investigated ecological determinants of socialityin burying beetles (Nicrophorus spp.), potential conflicts ofinterest among reproductive females, and the effects of nestingfailure and costs of fighting on cooperation. Burying beetlesare known to form monogamous pairs when exploiting small vertebratecarcasses. More complex social behavior in this group is poorlyunderstood. We conducted experiments in which one or two females(N. defodiens, N. orbicollis) were provided small or large carcasseson which to breed. On large but not on small carcasses, twofemales often formed cooperative breeding associations (jointlyprepared a carcass and fed young). In N. defodiens, but notN. orbicollis, two females produced a larger brood than singlefemales on large carcasses. In both species, the reproductiveoutput per female was less for two than for one female. Thepresence of a second female did not decrease the preparationtime of a carcass (discovery of resource to egg hatch). Conflictwas evident between females. Trials employing females of similarsize were more likely to result in injury than trials usingfemales of dissimilar size (N. tomentosus, N. defodiens, N.orbicollis). In N. tomentosus, those associations that persistedthe longest resulted in the fewest injuries. After care of youngwas initiated, conflict among familiar nest mates was not observed.There was no evidence that breeding females could discriminatebetween brood; use of a genetic marker (N. orbicollis) demonstratedthat females fed related and unrelated young alike. Femalesof similar size (high potential cost of fighting for the dominantindividual) were not more likely to form cooperative breedingassociations than females of dissimilar size (low cost of fightingfor dominant). Females of a species subject to a high rate ofnest failure (N. defodiens) were more likely to cooperate thanfemales of a species with a low rate of nest failure (N. orbicollis).It is argued that limited reproductive opportunities, difficultyin controlling rivals' access to a large carcass, and the superabundantlarval food supply represented by a large carcass, but not kinselection, have contributed to the evolution of cooperativebehavior in this group. In addition, we hypothesize that beetlesmight initially tolerate consexual rivals on large carcasseswhen there is a high likelihood of nesting failure, therebyavoiding potentially costly conflicts.     

The frequency and fitness consequences of communal breeding in a natural population of burying beetles: a test of reproductive skew

Abstract.  1. Reproductive cooperation occurs in diverse taxa and a defining characteristic of these social systems is how reproduction is shared. Both male and female burying beetles ( Nicrophorus spp.) facultatively form associations to bury a carcass and rear a single brood, making burying beetles a model system for testing skew theory.
2. In this study, 50% of 40–45 g carcasses and 75% of 55–60 g ones were buried by more than one male and/or female Nicrophorus tomentosus .
3. Females were significantly more likely to cooperate on 55–60 g carcasses than on 40–45 g ones.
4. Analysis of parentage of 13 broods using microsatellite loci as genetic markers showed that maternity analysis of only 2% of the young excluded all females captured leaving the brood chamber after burial. Males previously mated with resident females or displaced by resident males fathered 7% of the young.
5. The male and female remaining the longest were usually the parents of the most offspring, and reproductively dominant individuals also tended to be the largest.
6. Although all but two or three individuals that helped to bury the carcass produced some offspring, reproduction was often not shared equitably. Reproduction of females was significantly skewed on six of nine 40–45 g carcasses but shared fairly equitably on all three 55–60 g ones. Reproduction was skewed among males on 7 of 10 broods.
7. Both males and females relinquished a greater proportion of the brood as the days of assistance from all consexuals increased.     

Burying beetles: intraspecific interactions and reproductive success in the field

Abstract. 1. The discovery and utilization of small carcasses by burying beetles (Silphidae, Nicrophorus ) was studied by placing dead mice at random points on large grids at two Iocations in Michigan, U.S.A.
2. The majority of mice are found within 24 h by more beetles than ultimately will utilize the carcass. If a carcass is likely to be usurped by a larger species of beetle or by a vertebrate, then intraspecific competition may be postponed until the carcass is concealed and buried.
3. Both males and females practice parental care. Maturing broods are tended by no adults, a single female, a single male, or a male—female pair. No differences in brood success were observed among these categories.
4. The female lays a larger clutch than ultimately will survive. Brood size is regulated after the egg stage, such that offspring number varies, but individual offspring size does not.
5. A large amount of unexplained variation exists in brood size, in both the laboratory and the field. This variation is probably caused by the environment, and not the reproductive physiology of the beetles. Competition with microbes is a likely candidate.
6. Differences exist not only between Nicrophorus species, but also between localities for a single species, suggesting adaptation to local environments.     

Maternal nutritional condition and genetic differentiation affect brood size and offspring body size in Nicrophorus

In most animal species, brood size and body size exhibit some variation within and between populations. This is also true for burying beetles (genus Nicrophorus), a group in which the body size of offspring depends critically on the number of offspring competing for food due to the discrete nature of resource used for larval nutrition (vertebrate carcasses). In one species, brood size and body size are correlated with population density, and appear to be phenotypically plastic. We investigated potential proximate causes of between-population variation in brood size and body size in two species, Nicrophorus vespilloides and Nicrophorus defodiens. Our first experiment supported the notion that brood size is phenotypically plastic, because it was affected by environmental variation in adult nutritional condition. We found that the pre-breeding nutritional status of female N. vespilloides affected the number of eggs they laid, the number of surviving larvae in their broods, and the body size of their offspring. We do not know whether this plasticity is adaptive because greater offspring body size confers an advantage in contests over breeding resources, or whether starved females are constrained to produce smaller clutches because they cannot fully compensate for their poor pre-breeding nutritional status by feeding from the carcass. Our second experiment documents that brood size, specifically the infanticidal brood-size adjustment behavior, has undergone genetic differentiation between two populations of N. defodiens. Even under identical breeding conditions with identical numbers of first-instar larvae, females descended from the two populations produced broods of different size with corresponding differences in offspring body size.     

Plasticity in juvenile hormone in male burying beetles during breeding: physiological consequences of the loss of a mate

Burying beetles, Nicrophorus orbicollis, have facultative biparental care. They bury and prepare small vertebrate carcasses that provide food for their young. Here we establish the juvenile hormone (JH) profiles of paired females, paired males and single males and investigate some of the environmental and social factors that may affect these profiles. Before larvae hatch JH profiles of paired males and females were similar. However, after larvae hatch and during brood care, JH titers of females were very high and those of single males were significantly higher than those of paired males. We tested the hypothesis that higher JH was a response to the need for increased parental care by manipulating brood size. Although JH titers of single males caring for small versus large broods were not significantly different, when comparing JH titers and larval growth (a measure of parental effort), a significant positive correlation emerged. In contrast, we found that food quality had no effect on JH levels suggesting that increased feeding by males and females after carcass discovery cannot explain the elevation of JH. The regulation of JH in male burying beetles appears thus to be dependent on the presence of a mate and on critical stimuli from young.     

Harsh nutritional environment has positive and negative consequences for family living in a burying beetle

Harsh environmental conditions in form of low food availability for both offspring and parents alike can affect breeding behavior and success. There has been evidence that food scarce environments can induce competition between family members, and this might be intensified when parents are caring as a pair and not alone. On the other hand, it is possible that a harsh, food-poor environment could also promote cooperative behaviors within a family, leading, for example, to a higher breeding success of pairs than of single parents. We studied the influence of a harsh nutritional environment on the fitness outcome of family living in the burying beetle Nicrophorus vespilloides. These beetles use vertebrate carcasses for reproduction. We manipulated food availability on two levels: before and during breeding. We then compared the effect of these manipulations in broods with either single females or biparentally breeding males and females. We show that pairs of beetles that experienced a food-poor environment before breeding consumed a higher quantity of the carcass than well-fed pairs or single females. Nevertheless, they were more successful in raising a brood with higher larval survival compared to pairs that did not experience a food shortage before breeding. We also show that food availability during breeding and social condition had independent effects on the mass of the broods raised, with lighter broods in biparental families than in uniparental ones and on smaller carcasses. Our study thus indicates that a harsh nutritional environment can increase both cooperative as well as competitive interactions between family members. Moreover, our results suggest that it can either hamper or drive the formation of a family because parents choose to restrain reproductive investment in a current brood or are encouraged to breed in a food-poor environment, depending on former experiences and their own nutritional status.     

Delayed benefits of paternal care in the burying beetle Nicrophorus vespilloides

Burying beetles, Nicrophorus spp., inter the carcasses of small vertebrates as a food source for their offspring. Females can bury a carcass and rear a brood on it alone, but are frequently assisted by a male whose presence reduces the risk of the carcass being taken over by other beetles. However, the male often stays for longer than the carcass is vulnerable to take-over, and he cares for the brood without conferring any further benefits on it. In a laboratory experiment using N. vespilloides, we found that, in the absence of competitors, male assistance conferred no advantages on the brood for which he was caring, but significantly increased the subsequent reproductive success of his mate, in terms of the mass and rate of development of a second brood, reared alone. We suggest that this is due to a reduced parental effort of assisted females, who spent less time feeding offspring and more time resting than unassisted females whilst rearing their first broods. In the field, a female is unlikely to pair with the same male for consecutive broods, so we discuss the possible benefits a male may accrue from increasing his mate's reproductive success. We also discuss the relevance of these results to our understanding of the evolution of biparental care in birds. Copyright 2000 The Association for the Study of Animal Behaviour.     

Carcass maintenance and biparental brood care in burying beetles: are males redundant?

1. Burying beetles inter small vertebrate carcasses that ultimately serve as a food source for their developing young. The male remains with the female on the carcass after the brood has been produced, purportedly to aid in the feeding and protection of larvae. However, numerous laboratory experiments have failed to demonstrate a beneficial effect of the male on the growth and survival of offspring.
2. A potential difficulty with laboratory studies is that beetles are typically held under relatively benign conditions, protected from the biotic and environmental challenges that they normally encounter. In nature, males may enhance offspring survival by aiding the female in ridding the carcass of mould, and by helping to preserve the carcass through the secretion of antibiotic substances in the beetles' saliva. To examine more rigorously the potential benefits of male parental care, an experiment was conducted under field conditions in which the reproductive output of male–female pairs was compared to that of single females.
3. Beetles were induced to bury carcasses in soil inside rigid plastic tubes that had been inserted into the ground. The experiment was a paired design involving pairs of sisters reproducing in adjacent tubes; one sister reproduced alone, whereas the other reproduced with the assistance of a male. Soil cores were recovered about 1 month later, and examined for viable pupae.
4. There was no significant difference in the number of offspring produced by single females and those reproducing with the assistance of the male, nor was there any significant difference in total brood mass. These results suggest that any benefits of extended male residency on the carcass do not stem from male participation in carcass maintenance or provisioning young.     

Environment, competition and reproductive performance of female monkeys

In most wild and captive monkey groups, some females are clearly dominant over others. Dominant animals have priority of access to resources, and well fed animals generally outreproduce poorly fed ones. So why is it that only in some social groups are dominant female monkeys more fecund than subordinate ones? The distribution of food influences the intensity of competition between group members, and it appears that dominants do better only when interference competition is intense. In addition, dominance influences reproductive performance via reproductive parameters other than simple fecundity. Analysis of the different components of reproductive success, and of the environmental conditions under which dominants outreproduce subordinates, should help our understanding of the biological processes by which differential reproductive performance arises.     

The Costs of Confronting Infanticidal Intruders in a Burying Beetle

Infanticide by unrelated adults is a complex behavior in burying beetles (Nicrophorus spp.) serving multiple functions (resource competition, access to mates, cannibalism). The costs of confronting an infanticidal intruder are likely to vary with context. To assess these costs for a single female parent (Nicrophorus pustulatus), we systematically manipulated the sex of a conspecific intruder and the timing of the intrusion. Male intruders were a greater takeover threat than female intruders, and infanticidal takeovers were more common earlier in the breeding cycle. Even though a male intruder posed a greater threat to the brood, a female intruder was a greater threat to the reproductive success of the resident female. Female intruders that took over a carcass excluded the resident female from the resource. When a male intruder took over a carcass, the resident female was able to recover much of her loss by producing a replacement brood. Even when females successfully defended their broods, they suffered decreased reproductive output relative to control females that never had to confront an intruder (expt 1), but the mechanisms underlying this cost were unclear. To test the hypothesis that defeated female intruders attempt to parasitize late‐stage broods, female intruders whose eggs could be identified by a fat‐soluble dye were introduced to resident females caring for larvae (expt 2). Fifteen of 20 intruders oviposited eggs and the number of eggs were related to intrusion pressure. Because resident females rarely produced eggs while caring for larvae, it is uncertain whether the behavior of the defeated female should be characterized as brood parasitism, a failed takeover attempt, or an attempt to use the remains of the depleted resource. This study provides the most complete picture of the changing costs of confronting an infanticidal threat throughout the vulnerable period of offspring development.     

Host shift by the burying beetle, Nicrophorus pustulatus, a parasitoid of snake eggs

Recent work [Ecoscience (2000) vol. 7, 395-397] suggests that the burying beetle Nicrophorus pustulatus may have undergone a remarkable host shift, exploiting snake eggs rather than carrion as resources for breeding. We conducted behavioural and physiological experiments to examine the hypothesis of a host shift and to formulate hypotheses on its origin. Two congeners of N. pustulatus, Nicrophorus orbicollis and Nicrophorus defodiens did not respond to snake eggs with typical breeding behaviour. When N. pustulatus male-female pairs (n = 14) were presented with clutches of snake eggs, the number of offspring but not the mean size of offspring varied with snake egg mass, indicating effective regulation of brood size. When breeding on turtle eggs, N. pustulatus had a more variable response than when exploiting snake eggs, suggesting that turtle eggs are not a primary resource for breeding. Nicrophorus pustulatus presented with both snake eggs and a mouse carcass combined and exploited the two resources within the same nest (10 of 12 trials). Mouse carcasses and snake eggs were treated differently. Carcasses were moved, buried and stripped of hair in a manner characteristic of burying beetles, whereas snake eggs were not moved or buried. Females that discovered a mouse carcass also had a significantly greater juvenile hormone increase than did females discovering snake eggs. Some responses to the two resources, however, were similar. Female N. pustulatus oviposited rapidly in response to either a mouse carcass or snake eggs, and males elevated sex pheromone emission in response to either resource. The efficient use of snake eggs, the ability to regulate brood size and the different responses to snake eggs and carrion suggest that N. pustulatus is well adapted to exploiting snake eggs for breeding. The use of snake eggs by N. pustulatus has potential implications for conservation of oviparous reptiles.     

Delaying insect access alters community composition on small carrion: a quantitative approach

We present a study of interactions in the highly competitive insect communities inhabiting the carrion of small mammals. Via manipulation in a fully quantitative design, we delayed community development by excluding insect colonization in mouse and rat carcasses for 3 days, to study the role of early competitively dominant colonizers [burying beetles (Nicrophorus spp.; Coleoptera: Silphidae) and blowfly larvae (Diptera: Calliphoridae)] in the course of heterotrophic succession on small cadavers. Earlier studies demonstrated that in the case of large mammalian carrion, exclusion of insects’ access to the carcass in the early stages of decomposition altered the successional trajectory and species assemblages. However, the effect of such manipulation in easy monopolizable small vertebrate carrion remained unknown. Our results demonstrate that delaying insect access to carrion significantly lowered blowfly larvae abundances, while it simultaneously had no effect on colonization and carrion burial by burying beetles. Higher abundances of blowfly larvae seem to deter necrophagous beetles, whereas they are not harmful to the larvae of flesh flies, at least in larger rat carcasses. Predatory beetle species preferred the lower abundances of blowfly larvae, presumably due to better accessibility of their prey. Our results therefore suggest that in the course of the entire season, larvae of blowflies are the dominant competitors in small carcasses, and significantly affect the assembly of other insect groups, whereas burying beetles may exhibit a more temporal pattern of dominance.     

Residency Time as an Indicator of Reproductive Restraint in Male Burying Beetles

The cost of reproduction theory posits that there are trade-offs between current and future reproduction because resources that are allocated to current offspring cannot be used for future reproductive opportunities. Two adaptive reproductive strategies have been hypothesized to offset the costs of reproduction and maximize lifetime fitness. The terminal investment hypothesis predicts that as individuals age they will allocate more resources to current reproduction as a response to decreasing residual reproductive value. The reproductive restraint hypotheses predicts that as individuals age they will allocate fewer resources to current reproduction to increase the chance of surviving for an additional reproductive opportunity. In this study, we test for adaptive responses to advancing age in male burying beetles, Nicrophorus orbicollis. Burying beetles use facultative biparental care, but the male typically abandons the brood before the female. Previous work in male burying beetles has suggested several factors to explain variation in male residency time, but no study has observed male behavior throughout their entire reproductive lifetimes to determine whether males change residency time in an adaptive way with age. We compared residency time of males that reproduced biparentally, uniparentally, and on different-sized carcasses to determine if they used an adaptive reproductive strategy. Males did not increase residency time as they aged when reproducing biparentally, but decreased residency time with age when reproducing uniparentally. A decrease in parental care with age is consistent with a reproductive restraint strategy. When female age increased over time, males did not increase their residency time to compensate for deteriorating female condition. To our knowledge, this is the first test of adaptive reproductive allocation strategies in male burying beetles.     

Population density, body size, and phenotypic plasticity of brood size in a burying beetle

Theory predicts that organisms living in heterogeneous environmentswill exhibit phenotypic plasticity. One trait that may be particularlyimportant in this context is the clutch or brood size becauseit is simultaneously a maternal and offspring characteristic.In this paper, I test the hypothesis that the burying beetle,Nicrophorus orbicollis, adjusts brood size, in part, in anticipationof the reproductive environment of its adult offspring. N. orbicollisuse a small vertebrate carcass as a food resource for theiryoung. Both parents provide parental care and actively regulatebrood size through filial cannibalism. The result is a positivecorrelation between brood size and carcass size. Adult bodysize is an important determinant of reproductive success forboth sexes, but only at higher population densities. I testthree predictions generated by the hypothesis that beetles adjustbrood size in response to population density. First, averageadult body size should vary positively with population density.Second, brood size on a given-sized carcass should be larger(producing more but smaller young) in low-density populationsthan in high-density populations. Third, females should respondadaptively to changes in local population density by producinglarger broods when population density is low and small broodswhen population density is high. All three predictions weresupported using a combination of field and laboratory experiments.These results (1) show that brood size is a phenotypically plastictrait and (2) support the idea that brood size decisions arean intergenerational phenomenon that varies with the anticipatedcompetitive environment of the offspring.     

Adaptive consequences and heritable basis of asynchronous hatching in Nicrophorus vespilloides

Asynchronous hatching is an important component of animal reproductive strategies, yet it has been studied almost exclusively in altricial birds. In this study, we provide evidence on the adaptive consequences and the heritable basis of asynchronous hatching in an insect, the burying beetle Nicrophorus vespilloides . Parents of this species breed on carcasses of small vertebrates and provide food in the form of predigested carrion for their offspring. We found that the size of the carcass used for breeding had a significant effect on hatching skew towards the earlier part of the hatching period, suggesting that female parents adjust hatching skew facultatively to the amount of resources available for breeding. Using a full sibling breeding design, we also found that parent family had a significant effect on both hatching skew and hatching spread, suggesting that there is a heritable basis to asynchronous hatching. Finally, we found that hatching spread affected offspring survivorship, providing evidence that asynchronous hatching patterns have adaptive consequences in N. vespilloides . Our study provides valuable new insights into the evolution and ecological significance of asynchronous hatching by providing evidence on the adaptive consequences and the heritable basis of asynchronous hatching in a non-avian species.     

Group composition affects male reproductive partitioning in a cooperatively breeding cichlid

Individuals within groups of cooperatively breeding species may partition reproduction, with the dominant pair often taking the largest share. The dominant's ability to reproductively control subordinates may depend on differences in competitive ability, due to, e.g. body size differences, but may also depend on the number of same‐sex competitors inside the group. We tested experimentally whether subordinates reproduce more when these subordinates are large or when a second subordinate of the same sex need to be controlled by the dominants, using the cooperatively breeding cichlid Neolamprologus pulcher. Dominant pairs were assisted by a large and a small unrelated subordinate; sexes of these fish were varied in a full‐factorial design (giving four treatments). Dominant males lost significantly more parentage to the large subordinate male when a small subordinate male was also present, compared to when a small subordinate female was present. However, subordinate paternity was generally low and did not significantly curb total dominant male reproductive output, which was more affected by the sizes and numbers of reproductive females present inside his group. Dominant female maternity, clutch sizes and total output did not depend on the treatments. Subordinate–subordinate reproduction was virtually absent (one out of 874 offspring). Female subordinates were more likely to provide care for their own broods. In contrast, male subordinates did not adjust their level of care to their parentage. Variability in female subordinate alloparental brood care was particularly high, with females showing more care than males in general. We also detected effects of growth rate and food ration on parentage independent of the treatments, most notably: (i) a trade‐off between dominant male growth rate and paternity; (ii) a decrease in dominant male paternity with increasing food ration; (iii) a positive effect of growth rate on paternity in small males. We conclude that dominant males should be sensitive to the number and sizes of subordinate males present in their group, particularly when these subordinates are not helpful or grow fast, and food is plentiful. Dominant females should be less sensitive, because female subordinates do not appear to impose reproductive costs and can be helpful through alloparental brood care.