Endokrinologische und genetische Untersuchungen an einer proterandrischen Population des Polychaeten Ophryotrocha labronica

Decerebrate, sexually immature juveniles of Ophryotrocha labronica develop into males and females, although the normal ratio observed in intact worms is not attained. Even without the prostomium, primary males split into secondary females and stable males. Stable males and females do not show any reaction after decerebration as far as sexual differentiation is concerned. The females proliferate new sets of oocytes and the males continue spermatogenesis. In a great number of cases, decerebrate secondary females resume spermatogenesis. Amputation of the prostomium induces the development of the k-jaw. Even in small individuals below the size at which the k-jaw normally appears, the change to the k-jaw is induced. Heterospecific transplantations of prostomia from female O. labronica donors to decerebrate O. puerilis hosts revealed that the prostomia of female O. labronica produce and release a substance which completely compensates the lack of the host's own prostomium. Obviously, this ootropic substance is not necessary in all cases for gaining and/or maintaining female differentiation in O. labronica. Although it is produced both in stable females and secondary females, only a portion of the secondary females requires this substance for female differentiation. It is, therefore, presumed that the strength or stability of female differentiation expresses itself by hormone-dependent or independent oogenesis. In crosses with a gonochoristic population of O. labronica, protandric hermaphroditism is restricted to a few descendants. Crossing experiments within the protandric population of O. labronica seem to indicate a genetic component in the degree of protandry and in sex determination.     

Ist der polychaet Ophryotrocha labronica ein proterandrischer hermaphrodit?

The larvae of an egg-mass of Ophryotrocha labronica differentiate into 60 to 70% males and 15 to 40% females. In the coelom of males, freely floating spermatozoa are visible at a length of 10.5 segments. Oocytes of 5 to 7 m in diameter are released into the coelom of females at 10.7 segments. Males develop the k-jaw (k=complicated) much earlier (at 12.2 segments) than females (at 16.5 segments). As described for O. notoglandulata, O. labronica bears star-shaped glands on the dorsal side of the youngest segments. Males always have more glands (4.4) than females (2.7). These glands and the different appearance of the k-jaw may be considered as sexual characters. At 13.5 segments, 60 to 70% of the males start to proliferate oocytes, thus displaying protandry. The remaining males do not undergo sex reversal and are thus categorised as stable males. The developing oocytes in the so-called secondary females are not shed but ultimately resorbed. Resorption also occurs in isolated females, which display female differentiation from the beginning. The number of glands in secondary females decreases during sex reversal to values as low as those observed in stable females. Rearing experiments revealed the secondary females to be completely infertile. Inhibition of oocyte release in secondary females is permanent, and such release cannot be induced, even by the presence of males. Self-fertilization was not observed.

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Dankenswerterweise unterstützte die DFG die Untersuchung durch eine Reisebeihilfe.     

Bi-directional sex change: testing the growth-rate advantage model

Bi-directional sex change in coral-dwelling fishes (genera Gobiodon and Paragobiodon) has been attributed to a growth-rate advantage for females during the non-breeding season. This model predicts that the smallest individual in a newly formed pair should always be female. To determine if a growth-rate advantage exists for female Gobiodon histrio, I monitored the growth of males and females in natural pairs during the breeding and non-breeding season. I then used a manipulative field experiment to test four predictions of the growth-rate advantage model: (1) the larger individual should change sex to male in new pairs containing two females; (2) the smaller individual should change sex to female in new pairs containing two males; (3) neither individual should change sex in heterosexual pairs where the male is larger than the female; and (4) both individuals should change sex in heterosexual pairs where the female is larger than the male. A growth-rate advantage was detected for female G. histrio during the non-breeding season; however, only the first three of the predicted outcomes were observed in the manipulative experiment. Sex change did not occur in heterosexual pairs where the female was larger than the male. Furthermore, growth did not differ between sex-changed and non-sex-changed fish; therefore, the absence of sex change in these pairs is not due to a growth cost to sex change. I propose that the risk of moving among spatially isolated habitat patches and the low probability of finding a mate have been more important than sex-specific differences in growth rates to the evolution of bi-directional sex change in coral-dwelling gobies.     

The energetic cost of protogynous versus protandrous sex change in the bi-directional sex-changing fish Gobiodon histrio

To investigate the relative cost of protogynous versus protandrous sex change we induced sex change in each direction in Gobiodon histrio (Gobiidae) and then compared growth, body condition and biochemical condition between sex-changed and non-sex-changed fish in treatment and control groups. Sex change in each direction was induced by establishing pairs of adult males and pairs of adult females on isolated coral colonies. Heterosexual pairs were used as controls. For both males and females, growth and body condition did not vary between fish that changed sex and those that did not. The relatively low cost of sex change, compared to the likely costs of searching for a mate of the correct sex, appears to explain the evolution of bi-directional sex change in coral-dwelling gobies. Lipid concentrations in the liver of males and females that changed sex were reduced by similar amounts (34% and 41%, respectively) compared to male and female controls that did not change sex. Therefore, changes in biochemical condition were approximately equal for fish that sex change in each direction and cannot explain the unequal frequency of sex change in each direction in natural populations of G. histrio.     

Breeding Periodicity for Male Sea Turtles,Operational Sex Ratios,and Implications in the Face of Climate Change

Abstract: Species that have temperature‐dependent sex determination (TSD) often produce highly skewed offspring sex ratios contrary to long‐standing theoretical predictions. This ecological enigma has provoked concern that climate change may induce the production of single‐sex generations and hence lead to population extirpation. All species of sea turtles exhibit TSD, many are already endangered, and most already produce sex ratios skewed to the sex produced at warmer temperatures (females). We tracked male loggerhead turtles (Caretta caretta) from Zakynthos, Greece, throughout the entire interval between successive breeding seasons and identified individuals on their breeding grounds, using photoidentification, to determine breeding periodicity and operational sex ratios. Males returned to breed at least twice as frequently as females. We estimated that the hatchling sex ratio of 70:30 female to male for this rookery will translate into an overall operational sex ratio (OSR) (i.e., ratio of total number of males vs females breeding each year) of close to 50:50 female to male. We followed three male turtles for between 10 and 12 months during which time they all traveled back to the breeding grounds. Flipper tagging revealed the proportion of females returning to nest after intervals of 1, 2, 3, and 4 years were 0.21, 0.38, 0.29, and 0.12, respectively (mean interval 2.3 years). A further nine male turtles were tracked for short periods to determine their departure date from the breeding grounds. These departure dates were combined with a photoidentification data set of 165 individuals identified on in‐water transect surveys at the start of the breeding season to develop a statistical model of the population dynamics. This model produced a maximum likelihood estimate that males visit the breeding site 2.6 times more often than females (95%CI 2.1, 3.1), which was consistent with the data from satellite tracking and flipper tagging. Increased frequency of male breeding will help ameliorate female‐biased hatchling sex ratios. Combined with the ability of males to fertilize the eggs of many females and for females to store sperm to fertilize many clutches, our results imply that effects of climate change on the viability of sea turtle populations are likely to be less acute than previously suspected.     

Influence of social factors on sex ratio at birth,maternal investment and young survival in a prosimian primate

Summary In order to determine whether social factors influence sex ratio at birth in lesser mouse lemurs, experiments were conducted during 5 successive breeding periods on 51 females. At the beginning of the breeding season, females were either isolated (I) or grouped (G) in heterosexual groups with an increasing number of females (2, 3 or 4). To ensure mating, I females were introduced in a group only during the oestrous period. After mating, both I and G females were isolated during pregnancy and lactation. Reproductive capacities of females in terms of oestrus occurrences (n = 324), impregnations (n–210), pregnancies (n = 136) or abortions (n = 38) or litter sizes (1–3 young) were affected neither by age and parity of females nor by group housing prior to conception. G females produced significantly more sons than daughters (67% males for 189 newborn) while females living alone except during the mating period demonstrated a significant inverse tendency (39.6% males for 96 newborn). Distribution of sexes in litters was statistically different from random and varied according to the shift of sex ratio at birth. In G females, the shift in the sex ratio towards males was consistent across the different groups, independent of the number of females living together, suggesting that the presence of only 1 female is sufficient to induce a bias in the sex ratio. No correlation was found between infant survival at weaning and age, parity or group housing of the mother. The maternal investment allocated to male or female newborn was similar provided the litter contained at least 1 male. In litters without males, growth and survival of female infants were significantly less. These results on sex ratio bias in captive female mouse lemurs agree with directions of bias predicted by the local resource competition model for facultative sex ratio adjustment (Clark 1978). Nevertheless, the pattern observed in mouse lemurs appears to be independent of the nutritional state of the female and of differential maternal investment.     

Bi-directional sex change in a coral-dwelling goby

Bi-directional sex change has recently been reported among obligate coral-dwelling gobies of the genus Gobiodon. However, neither the functional role of this pattern of sex change nor the frequency of sex change in either direction in natural populations is known. We investigated the social structure and pattern of sex change of Gobiodon histrio at Lizard Island on the Great Barrier Reef. The social structure of G. histrio within coral colonies usually consisted of a single juvenile or a heterosexual adult pair. The size of adult social groups was not constrained by coral colony size. In contrast to expectations for pair-forming species, G.␣histrio was primarily a protogynous hermaphrodite. All immature G. histrio were females and sex change from female to male occurred readily when two mature females were placed in a coral colony. In addition, male G. histrio were able to change back to females when two mature males were placed in a coral. Sex change from female to male, however, occurred with over twice the frequency of sex change from male to female. Where two males were placed in a coral colony, heterosexual pairs were most frequently re-established by immigration of females from outside the treatment population. This pattern might be predicted if sex change from male to female is more expensive than sex change from female to male for G. histrio. Where sex change is expensive, movement may be favoured over sex change, particularly where coral densities are high and movement among corals incurs little mortality risk. Received: 10 November 1997 / Accepted after revision: 16 May 1998     

Do sex-changing male snails use mate choice to get a jump on their “size advantage”?

Individuals of species that change sex from male to female may gain a “size advantage” from that sex change; that is, as males become larger, they become female, thus increasing their fecundity with their size. However, males could also gain an early and different reproductive size advantage by choosing large females as mates. While male preference for large females has been observed in many dioecious species, we know little about male size preference in sex-changing species. In choice experiments, we examined whether males of two congeneric species of marine sex-changing snails, Crepidula fornicata and C. convexa, chose large females over small ones as partners. We also used choice tests to see whether males of C. fornicata, a species whose members form long-term, multi-animal stacks, would choose two females in a stack over a single female. Surprisingly, males of neither species showed a preference for large females, in spite of the documented fecundity advantage associated with large female-size. Males of C. fornicata chose slightly, but not significantly, more single females than stacks, suggesting that neither number nor size drives mate choice in these animals. Key factors that may influence this lack of size preference include long association time, the likelihood of sperm competition, and the cost of extended mate search; it may also be that sex-change itself, the very factor that creates female-biased sexual size dimorphism in these species, prevents size preference, as males may gain sufficient reproductive advantage from eventually becoming large females themselves to offset any benefit of choosing large females.     

Population structure and sex-change in the coral-inhabiting snailCoralliophila violacea at Hsiao-Liuchiu,Taiwan

Surveys of the coral-inhabiting snailCoralliophila violacea (Lamarck) (=C. neritoidea Kiener) were made on shallow fringing reefs (<8 m deep) around Hsiao-Liuchiu, Taiwan, between July and October 1990. The snails were aggregated into patches on the surface of massive poritid coral colonies. Coral colonies >40 cm in diameter were more likely to bear patches of snails than smaller colonies, and also to have more snails. The coralliophilids ranged from 5 to 30 mm in aperture length. The sex ratio of the population was biased toward males (539:279), with only a few small individuals of indistinguishable sex. Snails between 6 and 10 mm were all males, while most snails with aperture lengths 20 mm were females. Judging from the distinct size ranges of males and females within patches and from the observed degeneration of the penis, the snails may have changed sex from male to female with increasing size. Sex-change may occur across a wide size range (10 to 20 mm). The correlation of smallest female size and largest male size among patches indicates that snail size at sex-change is peculiar to each individual patch. Those females in patches with a single female (but many males) were significantly smaller than females in multiple-female patches. It is likely that in the absence of females males change sex at a smaller size, whereas in the presence of large females males delay sexchange until they have reached a larger size. The plasticity of size at sex-change may be adaptive and a result of natural selection at the individual level.     

When is a male not a male? Sex recognition and choice in two sex-changing species

For dioecious species, choosing a mate of the same sex can have reproductive costs. For sex-changing animals, however, a lack of sex recognition may not carry a reproductive cost, as pairs that were initially same-sex can become opposite-sex pairs as one partner changes sex. The strength of sex discrimination in sex changers, then, should depend on the duration of mating associations and whether the time of sex change is influenced by social situation (“flexible” sex change). We studied two species of marine snails that change sex from male to female, one with flexible sex change and long-term or permanent mating associations (Crepidula fornicata) and one with short-term pairings and relatively fixed time of sex change (Crepidula convexa), to determine whether either species exhibits sex recognition and whether members of C. convexa show stronger sex discrimination. In laboratory experiments, small males, the choosing animals, were placed with either a male or a female conspecific (no-choice experiments) or given a choice of a male or female (choice experiments). We controlled for shell length in all experiments, as relative size may influence sex change or choice. Males of both species paired more often with females than males, but, as predicted, males of C. convexa showed stronger discrimination: When given a choice, no C. convexa male paired with another male. In contrast, some C. fornicata males always chose other males even when given the choice of a female. These results suggest that sex recognition can be adaptive even for sex changers but demonstrate that the level of sex recognition will depend on other aspects of reproductive behavior.     

Male-male competition selects for delayed sex change in the protandrous shrimp<Emphasis Type="Italic"> Pandalus latirostris</Emphasis>

In most protandrous species, male size advantage is generally regarded as unimportant in determining the timing of protandrous sex change. In pandalid shrimp, the size/age of male sex change often fluctuates among years and populations, but the adaptive significance of late reversing males (LRMs) is not well understood. This study experimentally examined the adaptive significance of LRMs in the protandrous pandalid shrimp Pandalus latirostris Rathbun. Field and laboratory studies were carried out in August–September of 1998–2002 on P. latirostris in Notoro Lagoon, Japan (44°03′N; 144°10′E). Mature females that had molted (i.e. mate receptive) were tethered in the field and their mating behavior with wild males was observed. Copulations occurred with a single male at a time, although other males could sequentially mate with a tethered female. Because tethered females rejected male approaches, males had difficulty transferring their spermatophores. In the laboratory, males copulated with non-tethered, recently molted females for only 15 min after molting. Recently molted females are wary of potential predators, since their soft exoskeleton makes them particularly vulnerable. Fast access by males enhanced fertilization success in this shrimp. The effect of male size on mating success in the laboratory was examined. Both small and large males successfully inseminated females in the absence of competitors. In experiments where large, medium, and small males competed for a female, however, larger males guarded females longer than smaller males, until the female molted and became receptive. Moreover, large males were more successful at copulating once molting occurred. These results imply that male-male competition drives delayed sex change in some situations.     

Sex ratio varies with egg investment in the red-necked phalarope (Phalaropus lobatus)

Fisher’s sex ratio theory predicts that on average parents should allocate resources equally to the production of males and females. However, when the cost/benefit ratio for producing males versus females differs, the theory predicts that parents may bias production, typically through underproduction of the sex with greater variation in fitness. We tested theoretical predictions in the red-necked phalarope, a polyandrous shorebird with sex-role reversal. Since females are larger and therefore potentially more expensive to produce and may have greater variation in reproductive success, we predicted from Fisher’s hypothesis a male bias in population embryonic sex ratio, and from sex allocation theory, female biases in the clutches of females allocating more resources to reproduction. We measured eggs and chicks and sexed 535 offspring from 163 clutches laid over 6 years at two sites in Alaska. The embryonic sex ratio of 51.1 M:48.9 F did not vary from parity. Clutch sex ratio (% male) was positively correlated with clutch mean egg size, opposite to our prediction. Within clutches, however, egg size did not differ by sex. Male phalarope fitness may be more variable than previously thought, and/or differential investment in eggs may affect the within-sex fitness of males more than females. Eggs producing males were less dense than those producing females, possibly indicating they contained more yolk relative to albumen. Albumen contributes to chick structural size, while yolk supports survivorship after hatch. Sex-specific chick growth strategies may affect egg size and allocation patterns by female phalaropes and other birds.     

Gonad morphology, sexual development, and colony composition in the obligate coral-dwelling damselfish Dascyllus aruanus

Gonad morphology and colony composition support the existing supposition that the obligate coral-dwelling damselfish Dascyllus aruanus has a protogynous hermaphroditic sexual pattern. Adults had either an active ovary containing vitellogenic oocytes, an ovotestis, or a spermiated testis and were classified as adult female, hermaphrodite, or adult male, respectively. Among individuals having male function, the testis (or testis portion of the ovotestis) takes the form of an unrestricted spermatogonial lobular testis. Among hermaphrodites having an ovotestis, a small proportion of individuals had a gonad in which both the ovarian and testicular portions were inactive (inactive hermaphrodites), whereas the majority had a predominantly testicular ovotestis that contained spermatozoa (male-active hermaphrodites). The size range of individuals within gonadal classes indicates that all D. aruanus first develop an ovariform gonad. Some individuals then undergo ovarian maturation to become adult females while others develop testicular tissue to form an ovotestis and become male-active hermaphrodites. Subsequently, progressive loss of ovarian tissue results in the development of a secondary testis from an ovotestis with the retention of a residual, afunctional lumen among adult males. The wide size range of individuals having an ovotestis suggests that some hermaphrodites function as adult females before developing testicular tissue while other individuals do not pass through an adult female stage. If this is the case, D. aruanus exhibits a diandric protogynous hermaphroditic sexual pattern. The apparent prolonged retention of an ovotestis with both healthy oocytes and an ovarian-type lumen in a spermiated ovotestis, as well as a functional sex ratio of 1:1 for adult females:adult males plus male-active hermaphrodites also raises the possibility that D. aruanus may be capable of bidirectional sex change during the hermaphroditic stage. Such a capability would be highly adaptive for a species having limited mobility and unpredictable recruitment of new colony members resulting in unpredictable mating opportunities.     

Sex ratio response to conspecifics in a parasitoid wasp: test of a prediction of local mate competition theory and alternative hypotheses

Maternal manipulation of offspring sex ratio in response to conspecifics is considered in relation to sex ratio theory using the parasitoid wasp Spalangia endius. Females produced a greater proportion of sons in response to mated but not virgin females. This is the first demonstration of a differential sex ratio response to virgin versus mated females and provides support for local mate competition theory. More recent sex ratio models that predict sex ratio responses to conspecifics, specifically constrained, perturbation, and crowding models, were not supported. An increased proportion of sons in response to another mated female occurred on the second day of oviposition but not on the first, and the day effect resulted from experience not age. When females oviposited alone after 2 days' exposure to another female, they still produced a greater proportion of sons than if they had always been alone, but only if the other female was mated, not if she was virgin. Females do not seem to assess the presence of virgin versus mated females indirectly by using a low density of males or a long latency to mate as an indicator for virgin females: neither affected offspring sex ratio. That mated females adjusted their sex ratios in response to other mated females, but not virgin females or males, may be due proximally to mated females not often encountering the latter. Virgin females and males are not located as deep in the oviposition substrate as mated females.     

Gonadal development in the coral reef damselfish<Emphasis Type="Italic"> Dascyllus flavicaudus</Emphasis> from Moorea,French Polynesia

The present study investigated the sexual pattern of the yellow-tailed dascyllus, Dascyllus flavicaudus (Randall and Allen), through histological examination of the process of gonadal differentiation and maturation and through male-removal experiments in the laboratory. The study was conducted in Moorea, French Polynesia (17°32S; 149°50W), from 31 December 1994 to 11 March 1995. For gonadal histology, two populations were sampled, one consisting of large aggregations (n=54) and the other consisting of small- to medium-sized groups around isolated corals (n=55). An additional small sample (n=21) was also collected from a population that consisted of small groups around isolated corals. After an initially undifferentiated state, gonads of D. flavicaudus developed an ovarian lumen, followed by oocytes in the primary growth stage. From this ovarian state or from more developed ovaries with cortical-alveolus stage oocytes, some gonads developed into testes through degeneration of oocytes and development of spermatogenic tissue. In all three populations, spermatogenic tissue developed only in gonads that contained pre-vitellogenic oocytes (termed as mixed stage 1–2 gonads). The two main populations did not differ in their expression of sex change despite differences in their social organization. In both populations, size of individuals with mixed stage 1–2 gonads overlapped mainly with the size range of immature females, which suggests that functional female-to-male sex change was rare. The hypothesis that D. flavicaudus is primarily gonochoristic is further supported by removal experiments in laboratory groups, in which removal of a dominant male(s) failed to induce sex change in any of the high-ranking females. Yet, in all three field populations, some fish with mixed stage 1–2 gonads were found within the size ranges of mature females, which indicates possible occurrences of functional sex change. These conflicting results indicate that it may be premature to draw any definitive conclusions about the sexual pattern of D. flavicaudus.Communicated by T. Ikeda, Hakodate     

Gametogenesis in Harmothoe imbricata (Polychaeta: Polynoidae)

The processes of gametogenesis in Harmothoe imbricata are described and illustrated. For most of their development the gametes are attached to the walls of segmental blood vessels. In males, only meiosis and sperm differentiation occur while the cells are free in the coelom. In females, oocytes are only released into the coelom briefly, after vitellogenesis has been completed. H. imbricata thus differs from most polychaete species so far described — where in males the spermatogonia divide mitotically to form rosettes after they have been released into the coelom, and in females the whole of vitellogenesis occurs after release of oocytes into the coelom. The oocytes of H. imbricata enter the first metaphase of meiosis before they are shed at spawning. The elongated head of the sperm in H. imbricata is atypical of polychaetes in general.     

Male influence on sex allocation in the parasitoid wasp Nasonia vitripennis

Sex allocation is an important reproductive decision for parents. However, it is often assumed that females have substantial control over sex allocation decisions, and this is particularly true in haplodiploid insects, in which females apparently determine sex by deciding whether to fertilise an egg (and produce a diploid daughter) or not (and produce a haploid son). Mechanisms by which males may influence sex allocation are not so straightforward, and their potential influence on sex ratios has been somewhat neglected. Here, we test whether males influence offspring sex ratios in the parasitoid wasp Nasonia vitripennis. We show that some of the variation in observed sex ratios can be attributed to males when comparing the affect of male strain on sex ratio. We did not find among-male variation in sex ratio with a less powerful experiment using males from only one strain or an effect of male mating environment. Our data suggest that males can influence female sex ratios and contribute to the variation around the sex ratios optimal for females. However, the influence is not large, suggesting that females have more influence on sex allocation than do males. We conclude by considering whether male influences on sex ratio represent differences in male reproductive competence or deliberate attempts by males to increase their fitness by influencing daughter production.     

Tests of the mate-guarding hypothesis for social monogamy: does population density, sex ratio, or female synchrony affect behavior of male snapping shrimp (Alpheus angulatus)?

There are at least two mechanisms by which social monogamy in the absence of biparental care may evolve: as a form of territorial cooperation, in which one or both sexes benefits by sharing a territory with a partner, and as a form of extended mate guarding, in which males guard females through entire, and perhaps multiple, reproductive cycles. I examined the effects of population variables (density, sex ratio, female synchrony) on male pairing behavior in the snapping shrimp, Alpheus angulatus, to test the hypothesis that social monogamy in this genus has evolved as a result of selection on males for long-term mate guarding of females. There was no evidence that pairing behavior changes with differences in population density; in a natural population, there was a 1:1 relationship between the number in pairs and local population density. In a laboratory experiment, males altered their pairing behavior in response to manipulated differences in sex ratio. Males in female-biased sex ratios were significantly more likely to abandon recently mated females than males in equivalent sex ratios, though there was no significant difference in the duration of pairing or the number of times males switched females. Observations of shrimp maintained for an extended period in the laboratory revealed no evidence that females molt and become sexually receptive synchronously, which would reduce the likelihood that a searching male would encounter additional receptive females. These data suggest that sex ratio may have contributed to the evolution of social monogamy in snapping shrimp, but provide no evidence that population density or female synchronous receptivity have contributed to the evolution of social monogamy.     

Host choice and offspring sex allocation in a solitary parasitic wasp

Summary Females of the parasitic wasp Antrocephalus pandens can detect differences in the quality of their hosts (pupae of Corcyra cephalonica, a stored-product moth) and allocate offspring of either sex accordingly. Larger and younger hosts are accepted more often in both dead and live hosts; more female offspring emerge from the perceived better hosts, while more males emerge from the smaller, older ones. These patterns are consistent with a sex allocation strategy by the mother, since females from a given size host tend to be larger than males and larger females produce more eggs. However, when wasps lay their eggs in groups of hosts of different size and age rather than encountering them one at a time, no difference in number or sex ratio of offspring is detected between groups. This result and evidence from the change in offspring sex ratio with female age and with numbers of females foraging on a group of hosts are interpreted and discussed in the context of sex allocation (Charnov 1979) and local mate competition (LMC, Hamilton 1967) theories.     

Sex ratio manipulation and decreased growth of male offspring of undernourished golden hamsters (Mesocricetus auratus)

Summary The theory that female mammals in poor condition may increase individual fitness by skewing the sex ratio of their offspring toward daughters and by investing more resources in daughters than in sons was tested in hamsters. Newly mated experimental females were food-restricted during pregnancy and lactation (RR) or during lactation only (AR). Controls received food ad libitum. Maternal body weights were assessed daily from mating to 25 days postpartum. Litter survival (% litters with at least one pup surviving on any day), litter size, offspring sex ratios (=% males), and pup weights were monitored daily from birth (Day 1) to Day 25. All control and AR dams gave birth 16 days after mating. Gestation was extended by 1–3 days for 35.4% of RR dams. RR dams weighed significantly less at parturition than controls and AR females. During lactation, AR females showed the greatest weight loss and control females the least. AR weight loss exceeded that of RR females, possibly because the former maintained larger litters. Survival was highest for controls, intermediate for AR, and lowest for RR litters. Mean sex ratio at birth was significantly less for RR (40.7%) than for control (49.6%) and AR (48.8%) litters. RR sex ratio did not change significantly postnatally. Sex ratios of control and AR litters never differed statistically from 50%. Control male pups were significantly heavier than their sisters throughout the experiment. No significant gender differences were observed for AR pup weights after Day 2 postpartum. RR female offspring weighed more than their brothers throughout the experiment, and this difference was statistically significant immediately prior to the time that pups began to feed independently (Days 14–17). RR female pup weights were similar to, and sometimes significantly greater than, weights of control daughters during the period of postnatal maternal investment. Control males were always heavier than males from the other treatments. Patterns of weight gain by AR and RR males varied with age. We conclude that underfed female hamsters are able to adjust the sex ratio of offspring prenatally and parental investment postnatally to favor daughters.