Part-Time Mate Guarding Affects Paternity in Male Reed Buntings (Emberiza schoeniclus)

Male mate guarding by close following has been reported in many socially monogamous bird species and is generally believed to function as a paternity guard. Many aspects of the dynamics and effectiveness of this behavior are still however poorly understood. Here, we describe the temporal variation in mate guarding behavior in male reed buntings (Emberiza schoeniclus) with a particular focus on how males allocate their mating effort between mate guarding and extrapair mating in a context of intense sperm competition. In our highly synchronous study population most males have to balance the simultaneous and mutually exclusive demands of mate guarding and seeking extrapair copulations (EPCs). We found that males frequently switched between guarding their mates and performing intrusions to neighboring territories. Both activities seemed to have significant fitness payoffs, as male mate guarding effort had a positive effect on paternity, and a large fraction of extrapair fertilizations occurred during the days when the sire guarded its own female. The reed bunting is thus an example of how discontinuous or part‐time mate guarding can still be effective in securing paternity. Female reed buntings were not particularly active in initiating EPCs as they never were observed performing extraterritorial forays. We argue that the absence of female‐initiated EPCs is a prerequisite for males to trade mate guarding against seeking EPCs. Otherwise, if females circumvent male mate guarding by timing their EPCs to periods of male absence, males should guard their mates almost continuously or rely on alternative paternity guards.     

Age-Related Variation in Mate-Guarding Intensity in the Bluethroat (Luscinia s. svecica)

Female extra‐pair copulations (EPCs) have selected for male paternity guarding strategies in many bird species. In the bluethroat, Luscinia s. svecica, males guard their mates closely during the last 2 d before the start of egg laying, but there is great individual variation in the intensity of mate guarding. Here we show that some of this variation is related to male age. Old males guarded their mates with much lower intensity and sang more than young males, although the latter difference was not statistically significant. Controlling for male age, male and female coloration and size were not significantly related to the intensity of mate guarding. We have previously shown that young and old males had a similar paternity loss in their own broods. On the other hand, old males were far more successful than young males in achieving extra‐pair fertilizations. These patterns suggest that young and old males have different trade‐offs between preventing paternity loss in own nest and gaining paternity in others, because male skills in obtaining EPCs improve with experience and/or because of female preferences for old males as copulation partners. There were no significant relationships between paternity and male mate‐guarding behaviour during the fertile period, indicating that mate guarding is not a very effective paternity‐assurance strategy in the bluethroat.     

Energetic costs of mate guarding behavior in male stream-dwelling isopods

In the stream-dwelling isopod Lirceus fontinalis, males and females engage in a precopulatory mate guarding phase prior to mating. We examined the energetic costs of mate guarding behavior in males by separately assaying glycogen and lipid content at different time increments following mating. We found that males that had recently mated possessed reduced glycogen reserves and that these reserves were fully replenished within 36 h. Conversely, we found that male lipid reserves were unaffected by time since mating. We concluded that precopulatory mate guarding behavior is energetically costly to males and that glycogen is the energy source utilized to pay that cost. We also examined whether food deprivation during the mate guarding phase affected male energy reserves (glycogen) at the end of that phase. We found that males that were held in the laboratory and starved during mate guarding possessed reduced glycogen at the termination of the phase when compared to fed males. This reduced quantity was equivalent to the glycogen reserves of recently mated males collected from the field. We propose that food deprivation during the mate guarding phase explains the reduction in glycogen reserves at the termination of that phase. We discuss these results with reference to patterns of refuge use behavior during the mate guarding phase.     

Size, operational sex ratio, and mate-guarding success of the carrion beetle, Necrophila americana

When male insects guard females until oviposition, the benefitsfrom last-male sperm precedence must outweigh the costs of relinquishingadditional fertilizations. The profitability of guarding isincreased when males guard large, fecund females and when femalesare scarce because fewer fertilizations are sacrificed. However,the male reproductive success is not only determined by theprofitability of guarding but also by his ability to maintainguarding. In this study, we used male carrion beetles (Necrophilaamericana) to examine the effects of sex ratio, male relativesize, and female quality on the ability to guard. First, wepresent a model of mate guarding that explores factors, suchas sperm precedence, sex ratio, male size, and female quality,that influence the profitability of postcopulatory riding. Ourmodel predicts that large N. americana males should preferentiallyguard the largest female only when the sex ratio is male biasedand sperm precedence is above 80%. In contrast, small malesgain little from guarding because they are not likely to maintainit and be the last male to mate. Then, we tested these predictionsby manipulating sex ratio, relative male size, and female quality.All males in equal sex ratio and large males in male-biasedsex ratio guarded females significantly longer than did malesin female-biased sex ratio. In male-biased sex ratio, largemales guarded significantly longer and achieved more takeoversthan small males. Large females were guarded longer. The successof guarding males in this beetle depends on their size relativeto other males and the operational sex ratio.     

Mate Guarding in the Androdioecious Clam Shrimp Eulimnadia texana: Male Assessment of Hermaphrodite Receptivity

Precopulatory mate guarding primarily occurs when males encounter receptive females at a low enough rate that such females become a valuable resource once encountered. Such circumstances are common in aquatic crustaceans wherein females are only receptive for a short period directly after molting. In these species, males commonly mate guard by physically attaching themselves to their prospective mates for hours to days at a time. To be effective in mate guarding, males must be able to assess the time to receptivity in their mates, which is commonly via chemical cues associated with molting. Clam shrimp in the genus Eulimnadia exhibit mate guarding, but with an important variation: these species are mixtures of males and hermaphrodites (androdioecy) rather than males and females. Nonetheless, the mate guarding behaviors of these shrimp are much the same as in other aquatic crustaceans. In this study, three projects were undertaken to determine the ability of Eulimnadia texana males to assess hermaphroditic receptivity. Males were found to be unable to assess receptivity without physically contacting hermaphrodites. However, after physical contact, males spent a significantly greater amount of time guarding receptive relative to non‐receptive hermaphrodites. Additionally, male interest in mate guarding was highest during the period between the dropping of one clutch of eggs and the extrusion of the following clutch. Because this period is also associated with hermaphroditic molting, it is consistent with the notion that males cue into chemicals associated with molting to determine hermaphroditic receptivity. These findings are consistent with previous studies of mating behavior in this species, and we discuss their importance to future tests of optimal mate guarding planned for these shrimp.     

Costs of intersexual conflict in the isopod Idotea baltica

In sexual reproduction one sex can increase its reproductive success at the cost of the other, a situation known as intersexual conflict. In the marine isopod Idotea baltica, males guard females before copulation. The guarding phase is preceded by struggles as females resist males’ attempts to initiate guarding. We determined whether the struggle and/or mate‐guarding result in fitness costs in the form of decreasing fecundity and lower levels of the energy storage compounds, glycogen and lipids. Females that underwent the period of struggles with males had decreased glycogen levels compared with females maintained alone. No such cost was found for males. Females guarded by a male also had smaller eggs than females that were not guarded. Thus the intersexual conflict, imposed by the fitness maximization strategy of the males, gave rise to both a fecundity cost and an energetic cost for females. The fecundity cost confirms the existence of intersexual conflict in I. baltica. This cost is shared by males, suggesting that the intersexual conflict restrains the reproductive output of both sexes.     

Mated pairs of owl monkeys (Aotus nancymaae) exhibit sex differences in response to unfamiliar male and female conspecifics

In socially monogamous species, mate‐guarding could be a reproductive strategy that benefits both males and females, especially when males contribute to parental care. By actively guarding mates, males may reduce their chances of being cuckolded, whereas females that mate‐guard may reduce the likelihood that their mates will desert them or acquire additional mates, and hence limit or reduce paternal care of offspring. Owl monkeys (Aotus spp.) are socially monogamous with biparental care of young and, hence, potential beneficiaries of mate‐guarding. We presented mated pairs of captive owl monkeys (A. nancymaae) with unfamiliar male and female conspecifics, to determine if either member of the pair exhibits intraspecific aggression toward an intruder or stays close to its mate, behaviors indicative of mate‐guarding. Male mates were more responsible for the maintenance of close proximity between mates than females. Male mates also exhibited elevated levels of behavior that signify arousal when presented with a male conspecific. These responses by mated male owl monkeys are consistent with patterns that may help prevent cuckoldry. Am. J. Primatol. 72:942–950, 2010. © 2010 Wiley‐Liss, Inc.     

Factors influencing mate guarding and territory defence in the stitchbird (hihi)

Socially monogamous male birds are predicted to maximise their reproductive success by pursuing extra-pair copulations (EPCs) while engaging in anti-cuckoldry behaviour such as mate guarding. In the stitchbird, Notiomystis cincta, high levels of forced EPCs and a high proportion of nestlings resulting from extra- pair fertilisations lead to the prediction that males of this species should exhibit intense paternity guarding behaviours. While studying an isolated stitchbird population on Tiritiri Matangi Island New Zealand (3636'S, 17453'E), I collected daily behavioural data throughout the breeding season from 15 males in 2000/01 and 27 males in 2001/02. In this study, male stitchbirds demonstrated clear paternity guarding by exhibiting: (1) an increased likelihood of being close to their mate during her fertile period, (2) an increased initiation of mate contact during her fertile period, (3) switching from site-specific territorial defence during the pre-fertile period to defending an area centring on the their female partners location during her fertile period, and (4) an increased following of the female to communal feeding sites outside the territory during her fertile period. For polygynous males, mate guarding and territorial defence were conditional on which of their females was fertile. Additional evidence supporting the hypothesis that mate guarding in this species is a form of paternity assurance, rather than protection from harassment, is that males protected their partner from harassment by other stitchbird males but did not intervene when females were harassed by male bellbirds, Anthornis melanura. While mate-guarding intensity in many species is conditional on the stage of female fertility, male stitchbirds also modified their behaviour depending on the location of the female and the rate of intrusions by extra-pair males. Resident males adopted a best-of-a-bad-job tactic when they were unable to locate their female by defending an area around her last known location. Furthermore, when the rate of intrusions by extra-pair males increased they traded-off the area they could defend within their territory against their ability to guard the female. Territory takeovers were uncommon, but when they did occur older males displaced younger males and healthy birds displaced sick ones. Contrary to the prevailing view that mate guarding is a male response to female infidelity, male stitchbirds appear to use mate guarding primarily to prevent paternity losses from forced EPCs. Future assessments of mate guarding function should consider the possibility that mate guarding involves a combination of conflict and co-operation between the sexes.     

Effects of density experience on mate guarding behavior by adult male Kanzawa spider mites

In the Kanzawa spider mite, Tetranychus kanzawai (Acari: Tetranychidae), adult males guard pre-reproductive quiescent females. I experimentally examined the effects of density experience during development and/or after adult emergence on precopulatory mate guarding behavior by T. kanzawai males. Mate guarding behavior was modified by density experience after adult emergence. When males had previously experienced high density after adult emergence (n = 71), 73.2% of them engaged in precopulatory mate guarding. In contrast, when males had previously experienced low density after adult emergence (n = 82), 61.0% of them did not guard females. Mate guarding with physical contact occurred more frequently when males had previously experienced a high density of potential rivals than when they had not, but the difference in behavior between the two groups of males was marginally not significant. Nevertheless, these results suggest overall that T. kanzawai males change mate guarding behavior in response to previously experienced density.     

Mate Guarding in Male Dall's Porpoises (Phocoenoides dalli)

Mate guarding, whereby a male closely attends and defends a fertile female from extra‐pair matings, is one mating tactic males of many species use to protect their paternity. Although female defense occurs in many species of terrestrial mammal, comparable examples among cetaceans are largely absent, potentially as a result of the wide dispersion and mobility of females and their prey. Here, we investigate whether the close association of individual male Dall's porpoises with individual females during the breeding season is consistent with mate guarding. As mate guarding is predicted to be costly, and in other taxa is often associated with a reduction in foraging efficiency, we also examine whether males trade‐off this activity with time at depth. Males maintained longer associations and closer distances with female partners than with male ones. They also surfaced in greater synchrony with, and more often approached, their female partners than male ones. In contrast to males with male partners, males paired with females engaged in agonistic interactions with other adult males, and infrequently affiliated with extra‐pair individuals. These data suggest males are actively attempting to maintain their associations with females, while also acting to reduce female extra‐pair copulations and increase their own paternity. Guarding males also undertook shorter dives than non‐guarding males, suggesting that they trade‐off time at depth with guarding. Such a trade‐off is likely to involve a reduction in foraging opportunities, due to a decrease in time spent at foraging depth. Mate guarding in this species may be facilitated by the relatively smaller size and decreased mobility of newly calved, estrous females, particularly if females also benefit from guarding.     

Energetically costly precopulatory mate guarding in the amphipod Gammarus pulex: causes and consequences

Precopulatory mate guarding (PCMG) is thought to have evolved as a male mating strategy in species in which female receptivity is limited to a short time. It is common among crustaceans, and energetic costs associated with PCMG are thought to promote size-assortative pairing in such species, although direct evidence is lacking. Using both field surveys and laboratory experiments, we assessed the energetic costs of PCMG in Gammarus pulex and investigated their possible causes. Energetic costs were measured as differences in lipid and glycogen reserves. In field-collected samples, size-corrected lipid and glycogen reserves of paired males were both significantly higher than those of unpaired ones. In the laboratory, the energetic cost of PCMG was unrelated to its duration, but was strongly positively correlated with female size (relative to the size of the male). In addition, the increased energetic cost of guarding a larger female was independent of an induced starvation cost. Our results show for the first time an energetic cost of PCMG in male G. pulex, and indicate that such a cost is more likely to result from pair formation than from the cost of carrying the female, as has previously been assumed. We discuss our results in relation to sexual conflict over PCMG duration and the ability of males to overcome female resistance. Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour      

Increased predation risk while mate guarding as a cost of reproduction for male broad-headed skinks (Eumeces laticeps)

We investigated antipredatory costs associated with mate guarding as potential costs of reproduction for male broad-headed skinks. Mate guarding by male lizards may increase fitness by preventing loss of fertilizations of the guarded female's eggs to other males, but it may have several costs. In addition to lost opportunities to search for additional females, risk of injury while fighting other males, and energetic expenditures while following females and fighting, guarding males might suffer increased risk of predation and reduction of opportunities to forage. We studied potential antipredatory costs of mate guarding by simulating predators searching for and approaching pairs of lizards in the field. Among pairs of lizards in close proximity to each other, males were detected before females 10 times more frequently than females were detected before males, and females fled before males much more frequently than males fled before females when pairs were approached, leaving the males exposed to the predator. After one or both lizards fled, males frequently followed females by scanning visually and scent trailing, exposing themselves to the predator while the female hid. Females never followed males. The implications of these findings for antipredatory costs of mate guarding are discussed. Electronic Publication     

Mate guarding, male attractiveness, and paternity under social monogamy

Socially monogamous species vary widely in the frequency ofextrapair offspring, but this is usually discussed assumingthat females are free to express mate choice. Using game-theorymodeling, we investigate the evolution of male mate guarding,and the relationship between paternity and mate-guarding intensity.We show that the relationship between evolutionarily stablemate-guarding behavior and the risk of cuckoldry can be complicatedand nonlinear. Because male fitness accumulates both throughpaternity at his own nest and through his paternity elsewhere,males evolve to guard little either if females are very faithfulor if they are very unfaithful. Attractive males are usuallyexpected to guard less than unattractive males, but within-pairpaternity may correlate either positively or negatively withthe number of extrapair offspring fertilized by a male. Negativecorrelations, whereby attractive males are cuckolded more, becomemore likely if the reason behind female extrapair behavior appliesto most females (e.g., fertility insurance) rather than thesubset mated to unattractive males (e.g., when females seek"good genes") and if mate guarding is efficient in controllingfemale behavior. We discuss the current state of empirical knowledgewith respect to these findings.     

Mate Choice in Male Mandrills (Mandrillus sphinx)

Male primates that attempt to monopolize access to receptive females by mate‐guarding expend time and energy and risk injury, making reproduction costly. Males should therefore show mate choice and preferentially allocate mating effort to females that are likely to be fertile and those that will produce high‐quality offspring. Specifically, males should preferentially mate‐guard high‐ranking females rather than low‐ranking females, as such females are more likely to be fertile and are able to invest more in offspring. Males should also prefer parous females to nullipares, for similar reasons. Finally, males should avoid mating with close relatives, to avoid the deleterious effects of inbreeding. We investigated 13 group‐years of mate‐guarding observations for two semi‐free‐ranging groups of mandrills to examine the influence of these factors on male investment in mate‐guarding. We found that males mate‐guarded higher‐ranking females more than lower‐ranking females, and parous females more than nullipares. Female age, true relatedness and maternal kinship did not influence male mate‐guarding. Our results suggest that male mandrills do exercise mate choice for higher‐quality females, in the form of higher‐ranking and parous females. As alpha males are responsible for the great majority of mate‐guarding, this can lead to assortative mating, where high‐ranking males reproduce with high‐ranking females, and has important implications for social relationships and kin selection.     

The relationship between mating system and penis morphology in ischnuran damselflies (Odonata: Goenagrionidae)

Zygopterans belonging to the genus Ischnura are unusual amongst damselflies because of the variety of mate guarding techniques employed by males of different species. The lack of post-copulatory guarding combined with lengthy copulations in one group of ischnuran species suggest that these males guard females in copula. An examination of the accessory penes of species in this group indicates that all but one species have considerable microspination on the distal end (the flagella) of their penes that can function in sperm displacement. The flagella of these species are long and thin compared to those of other ischnurans. This is likely an adaptation to gain access to the spermatheca of the female. Two species tandem guard their mates during ovipositing. These species are the only ischnurans missing a stout pair of basal spines on the penultimate segments of their penes. They have considerable microspination over much of their penes but their flagella are of only moderate length and stout. Ischnurans that do not mate guard have short, stout flagella and most species examined from this group (5 of 7) have litde microspination on their flagella tips. It is proposed that females of these species mate only once and therefore their males do not displace sperm.     

Flexible Mate Guarding Tactics in the Dragonfly Sympelrum Internum (Odonata: Libellulidae)

Mate guarding–a behaviour prevalent in odonates–is a post copulatory association during which males prevent females from re-mating. Some species use two forms of guarding: contact mate guarding, which is energetically costly but highly effective and non-contact mate guarding, which is less costly but less effective. This study aimed to determine if male Sympetrum internum (Odonata:Libellulidae) adjust the duration of contact mate guarding according to environmental, temporal and physiological factors. There was a significant interaction between male density and season on duration of contact mate guarding. Early in the season males increased the duration of contact guarding as the density of rivals increased. Later in the season males guarded mates longer irrespective of male density. Wind and temperature did not detectabiy alter the duration of contact mate guarding, suggesting that the trade-off between current and future reproductive success was more important than were physiological costs.     

Investment in Mate Guarding May Compensate for Constraints on Ejaculate Production in the Cricket Gryllodes sigillatus

Although there is a corpus of evidence that females of many taxa are choosy about males, there is less information on how males may react to females of different 'quality' (i.e. potential fecundity). The cricket Gryllodes sigillatus shows distinct mate guarding behaviour. We examined how long males mate guard females of different sizes (reflecting egg load and potential fecundity). We also examined the sperm number in ampullae donated to females of different sizes to see if males make a concomitant difference in investment in ejaculate. We also examined mate-guarding behaviour and ejaculate size of males mated to virgin and nonvirgin females of the same size to see if males equate size with increased age and increased likelihood of mating (increased sperm competition). The results showed that males mate guard larger females for longer but make no difference in ejaculate investment between sizes of female. Males make no significant difference in mate guarding investment or ejaculate investment between virgins and nonvirgins of the same size. There is evidence that other species of crickets do alter their ejaculate depending on the female size and mating history, but have less distinct guarding behaviour. We suggest that mate-guarding investment in G. sigillatus may serve a similar function to that of ejaculate investment in other crickets.     

The effectiveness of mate guarding by male black-throated blue warblers

In many socially monogamous birds, males maintain close proximityto their mates during the fertile period. This is often consideredan effort on the male's part to prevent other males from copulatingwith his mate, but other functions have been suggested andthe effectiveness of males in preventing extrapair fertilizationshas come into question. Moreover, it is unclear whether mateguarding conflicts with other male activities, particularlythe pursuit of extrapair fertilizations. We examined mate guardingby male black-throated blue warblers (Dendroica caerulescens).Behavioral observations showed that males that guarded theirmates more closely were less likely to have extrapair youngin their nests. Moreover, the experimental detention of a malefor 1 h during the fertility risk period increased the probabilitythat a brood would contain extrapair young. Thus, male mate guarding was effective in reducing the risk of extrapair fertilization.Males with many opportunities for extrapair copulations appearedto guard their mates less and consequently had more extrapairyoung in their broods than males with few such opportunities.This suggests that mate guarding may conflict with the pursuitof extrapair fertilizations.     

Do male paternity guards ensure female fidelity in a duetting fairy-wren?

Most socially monogamous bird species engage in extra-pair mating,and consequently males may adopt various behavioral strategiesto guard paternity. However, the relationship between mate guardingand extra-pair paternity is unclear: low levels of extra-pairpaternity can be associated either with no mate guarding orwith intense mate guarding. We investigate paternity guardsin the purple-crowned fairy-wren (Malurus coronatus), a duettingspecies where extra-pair paternity is rare. This species isunusual in a genus known for extremely high levels of extra-pairmating. We examine the behavioral interactions between the sexesunderlying these low rates of extra-pair paternity and showthat male purple-crowned fairy-wrens do not use frequent copulationor courtship feeding to assure paternity or guard females acousticallyby duetting. Males maintain close proximity to females bothwhen they are fertile and when they are not breeding and donot invest in courtship displays to extra-pair females. Consistentwith predictions of theoretical models, low extra-pair paternityin this species may be related to female fidelity rather thanmale paternity assurance strategies, but short-term removalof males would be necessary to test this experimentally.     

Absence of Mate Guarding in the Yellowhammer (Emberiza citrinella)?

The mate guarding behaviour of male yellowhammer (Emberiza citrinella) was studied with special reference to the effects of age, body size (tarsus length) and coloration of males. Measurements of intra-pair distance do at the most provide evidence for relatively lax mate guarding. On the other hand, patterns of male song activity and inter-male aggression were more in agreement with the predictions of the mate guarding hypothesis. The reasons for the comparatively low mate guarding intensity in the yellowhammer may be that males do not need to guard their mates intensely. Age differences were found in song and aggressive activity, older males singing and fighting the most. Size had no effect on guarding behaviour. Coloration was correlated with inter-male aggressiveness and conflict initiation propensity. Less colourful males fought the most in the pre-fertile period of their mates, whereas colourful and old males fought the most during the fertile period. This suggests that coloration may be an indicator of individual fighting and guarding ability.