Effects of body size and timing of reproduction on reproductive success in female natterjack toads (Bufo calamita)

This study estimated variability in components of reproductive success in female natterjack toads ( Bufo calamita , Laurenti, 1768) as a function of their body size and timing of reproduction. Two components of reproductive success were analysed: fecundity and metamorphic success. Fecundity, as a function of body size, tended to increase exponentially. Age had a negligible effect once body size was statistically controlled. Egg size was also related to female body size but showed greater variation. Metamorphic success depended on the timing of reproduction. Later breeders suffered an exponential decline in metamorphic success because females spawned at recently-filled ponds of ephemeral duration. Since female body size decreased as the breeding season progressed, it may be inferred that larger, early-breeding females would have a differential reproductive success. The inverse relationship between the timing of reproduction and body size may be based on the energetic physiology of vitellogenesis, and on the potential trade-offs between the allocation of energy to growth—higher in smaller females—and reproduction.     

SEXUAL SIZE DIMORPHISM AND SELECTION IN THE WILD IN THE WATERSTRIDER AQUARIUS REMIGIS: LIFETIME FECUNDITY SELECTION ON FEMALE TOTAL LENGTH AND ITS COMPONENTS

Darwin's fecundity advantage model is often cited as the cause of female biased size dimorphism, however, the empirical studies of lifetime selection on male and female body size that would be required to demonstrate this are few. As a component of a study relating sexual size dimorphism to lifetime selection in natural populations of the female size-biased waterstrider Aquarius remigis (Hemiptera: Gerridae), we estimated coefficients for daily fecundity selection, longevity selection, and lifetime fecundity selection acting on female body size and components of body size for two consecutive generations. Daily fecundity was estimated using females confined in field enclosures and reproductive survival was estimated by twice-weekly recaptures. We found that daily fecundity selection favored females with longer total length through direct selection acting on abdomen length. Longevity selection favored females with smaller total length. When daily fecundity and reproductive longevity were combined to estimate lifetime fecundity we found significant balancing selection acting on total length in both years. The relationship between daily fecundity and reproductive longevity also reveals a significant cost of reproduction in one of two years. We relate these selection estimates to previous estimates of sexual selection on male body size and consider the relationship between contemporary selection and sexual size dimorphism.     

The interplay between natural and sexual selection in the evolution of sexual size dimorphism in Sceloporus lizards (Squamata: Phrynosomatidae)

Sexual size dimorphism (SSD) evolves because body size is usually related to reproductive success through different pathways in females and males. Female body size is strongly correlated with fecundity, while in males, body size is correlated with mating success. In many lizard species, males are larger than females, whereas in others, females are the larger sex, suggesting that selection on fecundity has been stronger than sexual selection on males. As placental development or egg retention requires more space within the abdominal cavity, it has been suggested that females of viviparous lizards have larger abdomens or body size than their oviparous relatives. Thus, it would be expected that females of viviparous species attain larger sizes than their oviparous relatives, generating more biased patterns of SSD. We test these predictions using lizards of the genus Sceloporus. After controlling for phylogenetic effects, our results confirm a strong relationship between female body size and fecundity, suggesting that selection for higher fecundity has had a main role in the evolution of female body size. However, oviparous and viviparous females exhibit similar sizes and allometric relationships. Even though there is a strong effect of body size on female fecundity, once phylogenetic effects are considered, we find that the slope of male on female body size is significantly larger than one, providing evidence of greater evolutionary divergence of male body size. These results suggest that the relative impact of sexual selection acting on males has been stronger than fecundity selection acting on females within Sceloporus lizards.     

Drought survival and reproduction impose contrasting selection pressures on maximum body size and sexual size dimorphism in a snake, Seminatrix pygaea

The causes and consequences of body size and sexual size dimorphism (SSD) have been central questions in evolutionary ecology. Two, often opposing selective forces are suspected to act on body size in animals: survival selection and reproductive (fecundity and sexual) selection. We have recently identified a system where a small aquatic snake species (Seminatrix pygaea) is capable of surviving severe droughts by aestivating within dried, isolated wetlands. We tested the hypothesis that the lack of aquatic prey during severe droughts would impose significant survivorship pressures on S. pygaea, and that the largest individuals, particularly females, would be most adversely affected by resource limitation. Our findings suggest that both sexes experience selection against large body size during severe drought when prey resources are limited, as nearly all S. pygaea are absent from the largest size classes and maximum body size and SSD are dramatically reduced following drought. Conversely, strong positive correlations between maternal body size and reproductive success in S. pygaea suggest that females experience fecundity selection for large size during non-drought years. Collectively, our study emphasizes the dynamic interplay between selection pressures that act on body size and supports theoretical predictions about the relationship between body size and survivorship in ectotherms under conditions of resource limitation.     

Sexually antagonistic selection on primate size

Abstract Male intrasexual selection in haplorhine primates has previously been shown to increase male size and to a lesser degree also female size. I address the following questions: (1) why does female size increase when the selection is on males, and (2) why does female size not increase to the same extent as that of males. The potential for correlational selection on females through increased resource competition was analysed with independent contrasts analyses. No such effect was found, nor did matched pairs comparisons reveal females to increase in size because of selection to bear larger male offspring. Instead further matched pairs analyses revealed higher female postpartum investment, as indicated by a longer lactation period, in more sexually selected species, also after correcting for body weight. Concerning the second question, independent contrast analyses showed that large size has had negative effects on female reproductive rate across the primate order. Matched‐pairs analyses on haplorhines revealed that females of species in more polygynous clades have lower reproductive rates than females of species in less polygynous clades. This is also true after the effects of body weight are removed. These results, both when correcting for body weight and when not, suggest that sexual selection has shifted female size from one favouring female lifetime fecundity to one favouring male success in competition. This depicts antagonistic selection pressures on female size and a trade‐off for females between the ecologically optimal size of their foremothers and the larger size that made their forefathers successful.     

Quantitative trait locus mapping of fitness-related traits in Drosophila melanogaster

We examined the genetic architecture of four fitness-related traits (reproductive success, ovariole number, body size and early fecundity) in a panel of 98 Oregon-R x 2b3 recombinant inbred lines (RILs). Highly significant genetic variation was observed in this population for female, but not male, reproductive success. The cross-sex genetic correlation for reproductive success was 0.20, which is not significantly different from zero. There was significant genetic variation segregating in this cross for ovariole number, but not for body size or early fecundity. The RILs were genotyped for cytological insertion sites of roo transposable elements, yielding 76 informative markers with an average spacing of 3.2 cM. Quantitative trait loci (QTL) affecting female reproductive success and ovariole number were mapped using a composite interval mapping procedure. QTL for female reproductive success were located at the tip of the X chromosome between markers at cytological locations 1B and 3E; and on the left arm of chromosome 2 in the 30D-38A cytological region. Ovariole number QTL mapped to cytological intervals 62D-69D and 98A-98E, both on the third chromosome. The regions harbouring QTL for female reproductive success and ovariole number were also identified as QTL for longevity in previous studies with these lines.     

Breeding phenology,variation in reproductive effort and offspring size in a tropical population of the woodlouse Porcellionides pruinosus

Summary Most species of woodlice in temperate habitats have discrete breeding seasons. It is hypothesised that breeding synchronises with favourable environmental conditions to maximise offspring growth and survivorship (Willows 1984). We measured the breeding phenology of a species introduced to a tropical environment, primarily to consider the assumption that life histories in the tropics will differ fundamentally from those in temperate habitats. In addition to breeding phenology we considered variation in reproductive effort between individual females and the division of this effort between the size and number of young.A continuous breeding phenology was observed in a synanthropic population of Porcellionides pruinosus within the tropics. Reproductive effort varied between months, showed a weak relationship with female size and was independent of female fecundity. Female sizefecundity relationships varied between samples and when the proportion of reproductive females was high size-fecundity slopes were steeper than at other times. Mean offspring size varied between months and there was a wide range in offspring size within broods. Offspring size was not related to female body mass, reproductive effort or fecundity; consequently brood mass increased linearly with an increase in fecundity. Increased reproductive effort goes into more rather than larger offspring.We propose that the continuous breeding in this population was the result of the constant presence of an environmental cue to reproduction evolved in temperate habitats. Continuous breeding is not necessarily equivocal to high individual reproductive success even though overall population growth may be rapid. However, variation in reproductive effort suggests that individuals respond to current environmental conditions on short time scales.     

Sperm Quantity Explains Age-Related Variation in Fertilization Success in the Hide Beetle

Age-related variation in sperm quality and quantity may have a dramatic impact on female fecundity and fertilization success. Despite this, the relationships between these parameters are rarely investigated. Moreover, studies exploring age-related variation in male mating success generally fail to consider the entire lifespan of an individual male; instead they restrict analyses to a small number of defined age classes. As a consequence they are unable to assess the impact of early and late life history components on male reproductive success. In this study, we explore these questions using the hide beetle, Dermestes maculatus , a model species for investigating age-related male mating success. We first employed a longitudinal design to explore whether patterns of sperm transfer and subsequent reproductive success varied over the reproductive lives of a cohort of males. Secondly, we investigated age-related variation in sperm viability, a surrogate measure of sperm quality. Finally, we combined these data and assessed whether the observed patterns of sperm transfer were correlated with fertilization success. We found that the quantity of sperm varied with male age: the amount of sperm transferred to a female increased with male age until 9 wk and then started to decline. Similarly, female fecundity and fertilization success were related to male age: females mating with males when they were relatively young (1 wk) or relatively old (13 wk) suffered reductions in fecundity and fertilization. Our data suggest that fertilization success is driven at least in part by the quantity of sperm transferred during mating.     

Body size and fecundity in the waterstrider Aquarius remigis: a test of Darwin's fecundity advantage hypothesis

The general female bias in body size of animals is usually attributed to fecundity selection. While many studies have demonstrated a positive relationship between body size and fecundity, the most common interpretation of fecundity selection is that larger females have larger abdomens and can hold more eggs, yet the relationship between abdomen size and fecundity has rarely been examined. For the waterstrider, Aquarius remigis, we find a significant relationship between body size and fecundity and demonstrate that the target of fecundity selection is abdomen size. Thus, larger females have higher fecundities because they have larger abdomens and not because of their total size per se. The rate at which fecundity increases with increasing abdomen size exceeds that which would be expected due to a simple volume constraint and suggests that other factors, such as increased ability to obtain resources, may contribute to the increase in fecundity with body size. Selection intensities estimated from our data indicate that fecundity selection could be a significant selective force on both total and abdomen lengths. Previous studies have found that abdomen size increased faster than body size and thus, larger females had relatively larger abdomens. The relationship of abdomen length and thorax length in A. remigis is hypoallometric and indicates that larger females have relatively smaller abdomens. We hypothesize that this may reflect conservation of abdomen size in females developing under poor conditions. Finally, while egg size is not directly related to body size, we find a trade-off between egg size and number when female abdomen length is held constant, suggesting that selection on egg size may influence abdomen length only indirectly through its effects on fecundity.     

No evidence for costs of being large in females of Orgyia spp. (Lepidoptera, Lymantriidae): larger is always better

Strong correlation between female body size and potential fecundity is often observed in insects. Directional selection favouring increased body sizes is thus predicted in the absence of opposing selection pressure. The evolutionary forces capable of counterbalancing such a 'fecundity advantage' are poorly documented. This study focuses on revealing the costs of large body size in the wingless females of Orgyia antiqua and O. leucostigma, two related species of lymantriid moths. Extreme behavioural simplicity of these animals allows systematic assessment of various fitness components in conditions that are close to natural. A linear relationship between pupal weight and potential fecundity was observed. This association was found to be independent of particular rearing conditions. There was no evidence that the relationship between fecundity and body mass becomes asymptotic when body sizes increases. No component of fitness showed a negative phenotypic correlation with body size; some displayed a weakly positive one. In particular, pupal mortality, adult longevity, mating and oviposition success, as well as egg hatching rate and egg size, were established as independent of body size in a series of field and laboratory experiments. There was a very high overall efficiency of converting resources accumulated during the larval stage to egg masses. With no costs of large adult size, selective forces balancing the fecundity advantage should operate in the course of immature development. The strong dependence of realized fecundity on body size is considered characteristic of the capital breeding strategy.     

Size Matters: Individual Variation in Ectotherm Growth and Asymptotic Size

Body size, and, by extension, growth has impacts on physiology, survival, attainment of sexual maturity, fecundity, generation time, and population dynamics, especially in ectotherm animals that often exhibit extensive growth following attainment of sexual maturity. Frequently, growth is analyzed at the population level, providing useful population mean growth parameters but ignoring individual variation that is also of ecological and evolutionary significance. Our long-term study of Lake Erie Watersnakes, Nerodia sipedon insularum, provides data sufficient for a detailed analysis of population and individual growth. We describe population mean growth separately for males and females based on size of known age individuals (847 captures of 769 males, 748 captures of 684 females) and annual growth increments of individuals of unknown age (1,152 males, 730 females). We characterize individual variation in asymptotic size based on repeated measurements of 69 males and 71 females that were each captured in five to nine different years. The most striking result of our analyses is that asymptotic size varies dramatically among individuals, ranging from 631–820 mm snout-vent length in males and from 835–1125 mm in females. Because female fecundity increases with increasing body size, we explore the impact of individual variation in asymptotic size on lifetime reproductive success using a range of realistic estimates of annual survival. When all females commence reproduction at the same age, lifetime reproductive success is greatest for females with greater asymptotic size regardless of annual survival. But when reproduction is delayed in females with greater asymptotic size, lifetime reproductive success is greatest for females with lower asymptotic size when annual survival is low. Possible causes of individual variation in asymptotic size, including individual- and cohort-specific variation in size at birth and early growth, warrant further investigation.     

Relatedness,body size and paternity in the alpine newt,Triturus alpestris

Sexual selection has traditionally been investigated assuming that male quality is as skewed as patterns of male reproductive success can sometimes be. Recently, female choice has been investigated under the model of genetic compatibility, which assumes that each individual female has her own 'best' mate and there is no overall optimal choice for all females. We investigated female mate choice in the newt species Triturus alpestris, a member of a genus where female choice has been investigated only within the context of the optimal male (female choice for condition-dependent traits). We provided females with two males that differed in one condition-dependent trait (body size) and overall genetic composition. Both male body size and female body size did not influence paternity, but the degree of genetic relatedness between females and potential mates did. Two components of fitness (fecundity and hatching success) did not differ between singly and multiply sired clutches, indicating that females do not employ polyandry as a means of increasing offspring fitness through genetic bet-hedging. Instead, we hypothesize that females may mate initially for fertility assurance, but prefer less-related males as the most genetically compatible mates.     

Monogenean body size,but not reproduction,increases with infracommunity density

Body size reveals a plethora of life-history, ecological, and evolutionary information about a species. It plays a critical role in success or failure during competitive, reproductive, or predator–prey interactions. Typically, there is a negative relationship between body size and population density in natural populations and communities. I analysed this relationship within and among multiple populations of two prominent monogenean parasites (>90% prevalence) on Lepomis macrochirus in three lakes in New Jersey (USA), using multiple regression models. To elucidate the causes and benefits of this relationship, I also measured host body condition via a regression index, and reproductive output of the parasite community by measuring parasite eggs shed from the host. The relationship between body size and density of infrapopulations (parasites of a single species on a single host) was positive, and the strength of this relationship for both species depended on which lake they occupied, indicating the potential for Allee effects. This relationship persists at the infracommunity level, where there was a similar positive relationship between a community weighted mean body size and density. However, this relationship did not result in greater reproductive success as measured by infracommunity egg production per individual per 24 h or egg size. The cause of this relationship also remains elusive; it was not explained by host condition or age. The results suggest that there is either no reproductive advantage to this increase in body size or the advantage conferred was not related to these measured fitness components. These findings indicate that researchers should be cautious using body size as a proxy for fitness or reproduction, while also raising further questions about the nature of the relationship between parasites on a host and that between those parasites and the host.     

Fecundity Selection and the Evolution of Reproductive Output and Sex-Specific Body Size in the <Emphasis Type="Italic">Liolaemus</Emphasis> Lizard Adaptive Radiation

Fecundity is a primary component of fitness. Theory predicts that the evolution of fecundity through increased brood size results from fecundity selection favouring larger female size to accommodate more offspring and to store more energy. This is expected to generate asymmetric selection on body size between the sexes, ultimately driving evolution of female-biased sexual size dimorphism. Additionally, it has been predicted that the intensity of fecundity selection increases when the opportunities for reproduction are reduced by the limiting thermal effects of increasing latitude-elevation (i.e. decreasing environmental temperatures) on the length of the reproductive season. This later factor would be particularly strong among ectotherms, where reproduction is heavily temperature-dependent. However, this integrative perspective on reproductive evolution by fecundity selection has rarely been investigated. Here, we employ a comparative approach to investigate these predictions in Liolaemus, a prominent lizard radiation. As expected, Liolaemus reproductive output (i.e. offspring number per reproductive episode) increases predictably with increasing female size. However, contrary to predictions, we found that increased fecundity does not translate into female-biased SSD, and that combined latitude-elevation does not impose a detectable effect on fecundity. Finally, our allometric analyses reveal that SSD scales with body size, which supports the occurrence of Rensch’s rule in these lizards. We discuss the evolutionary implications of our results, and the assumptions of the investigated hypotheses.     

Dominance and reproductive success in primates

Theoretical models of the relationship between competition and differential reproduction in primates share the premise that agonistic dominance hierarchies determine differential access to those limited resources which are essential to reproduction. In particular, the priority-of-access-to-estrous-female model is based on the postulate that high rank in males enhances reproductive success. Tests for a correlation between rank and reproductive success in males have produced mixed results. Problems in measuring male reproductive success and in conceptualizing dominance systems are implicated in the diversity of conclusions reached. Other attributes which affect reproductive success have been proposed, and alternative models of mating systems, based on the concepts of reproductive strategies, social skills, and life histories have also been developed. Studies of differential reproduction in female primates are fewer, but have the advantage over male studies of directly measuring infant production and offspring survival. Research on the relationship between rank and reproductive success in females has shown that under conditions of low resource availability, subordinate females sometimes suffer reduced fecundity and infant survival as a result of restricted access to food and water. Under conditions of social stress, low-ranking females may suffer from disruption of their reproductive cycles, resulting in lowered fecundity. Dominant females may also incur reproductive costs as well as benefits for their social position. Better insights into the relationship between dominance and reproduction are potentially offered by improved genetic paternity measures, new models of social and demographic processes, and the recent availability of life history data from field studies.     

Female-biased sexual size dimorphism in the yellow-pine chipmunk (Tamias amoenus): sex-specific patterns of annual reproductive success and survival

Sexual size dimorphism is ultimately the result of independent, sex-specific selection on body size. In mammals, male-biased sexual size dimorphism is the predominant pattern, and it is usually attributed to the polygynous mating system prevalent in most mammals. This sole explanation is unsatisfying because selection acts on both sexes simultaneously, therefore any explanation of sexual size dimorphism should explain why one sex is relatively large and the other is small. Using mark-recapture techniques and DNA microsatellite loci to assign parentage, we examined sex-specific patterns of annual reproductive success and survival in the yellow-pine chipmunk (Tamias amoenus), a small mammal with female-biased sexual size dimorphism, to test the hypothesis that the dimorphism was related to sex differences in the relationship between body size and fitness. Chipmunks were monitored and body size components measured over three years in the Kananaskis Valley, Alberta, Canada. Male reproductive success was independent of body size perhaps due to trade-offs in body size associated with behavioral components of male mating success: dominance and running speed. Male survival was consistent with stabilizing selection for overall body size and body size components. The relationship between reproductive success and female body size fluctuated. In two of three years the relationship was positive, whereas in one year the relationship was negative. This may have been the result of differences in environmental conditions among years. Large females require more energy to maintain their soma than small females and may be unable to maintain lactation in the face of challenging environmental conditions. Female survival was positively related to body size, with little evidence for stabilizing selection. Sex differences in the relationship between body size and fitness (reproductive success and survival) were the result of different processes, but were ultimately consistent with female-biased sexual size dimorphism evident in this species.     

Mate choice, egg cannibalism and reproductive success in the river bullhead, Cottus gobio L.

The seasonal pattern and individual variation in reproductive success was studied in a population of the river bullhead, Cottus gobio L. Female fecundity and male reproductive success were correlated with body size. Large males were found to breed early in the season when most of the large females spawned. The diameter of eggs found in male nests indicates that females tend to mate with males larger than themselves. The analysis of stomach contents suggests that guarding males cannibalize some of their own eggs. During parental care, the rate of filial cannibalism increases as guarding male body condition deteriorates.     

The role of fecundity and reproductive effort in defining life‐history strategies of North American freshwater mussels

Selection is expected to optimize reproductive investment resulting in characteristic trade‐offs among traits such as brood size, offspring size, somatic maintenance, and lifespan; relative patterns of energy allocation to these functions are important in defining life‐history strategies. Freshwater mussels are a diverse and imperiled component of aquatic ecosystems, but little is known about their life‐history strategies, particularly patterns of fecundity and reproductive effort. Because mussels have an unusual life cycle in which larvae (glochidia) are obligate parasites on fishes, differences in host relationships are expected to influence patterns of reproductive output among species. I investigated fecundity and reproductive effort (RE) and their relationships to other life‐history traits for a taxonomically broad cross section of North American mussel diversity. Annual fecundity of North American mussel species spans nearly four orders of magnitude, ranging from < 2000 to 10 million, but most species have considerably lower fecundity than previous generalizations, which portrayed the group as having uniformly high fecundity (e.g. > 200000). Estimates of RE also were highly variable, ranging among species from 0.06 to 25.4%. Median fecundity and RE differed among phylogenetic groups, but patterns for these two traits differed in several ways. For example, the tribe Anodontini had relatively low median fecundity but had the highest RE of any group. Within and among species, body size was a strong predictor of fecundity and explained a high percentage of variation in fecundity among species. Fecundity showed little relationship to other life‐history traits including glochidial size, lifespan, brooding strategies, or host strategies. The only apparent trade‐off evident among these traits was the extraordinarily high fecundity of Leptodea, Margaritifera, and Truncilla, which may come at a cost of greatly reduced glochidial size; there was no relationship between fecundity and glochidial size for the remaining 61 species in the dataset. In contrast to fecundity, RE showed evidence of a strong trade‐off with lifespan, which was negatively related to RE. The raw number of glochidia produced may be determined primarily by physical and energetic constraints rather than selection for optimal output based on differences in host strategies or other traits. By integrating traits such as body size, glochidial size, and fecundity, RE appears more useful in defining mussel life‐history strategies. Combined with trade‐offs between other traits such as growth, lifespan, and age at maturity, differences in RE among species depict a broad continuum of divergent strategies ranging from strongly r‐selected species (e.g. tribe Anodontini and some Lampsilini) to K‐selected species (e.g. tribes Pleurobemini and Quadrulini; family Margaritiferidae). Future studies of reproductive effort in an environmental and life‐history context will be useful for understanding the explosive radiation of this group of animals in North America and will aid in the development of effective conservation strategies.     

Group Structure,Nest Size and Reproductive Success in the Cooperatively Breeding Cichlid Julidochromis ornatus: A Correlation Study

The effect of group size on reproductive success has long been studied in cooperatively breeding species, as it might provide an adaptive explanation for group‐living in social species. Numerous studies have shown positive effects of subordinates on reproductive success (‘helper effect’), but these studies have also revealed the importance of controlling statistically, or experimentally, for the effect of other factors that might affect reproductive success. Here, we first examine the relationships between group size, body size of group members and nest size in the cooperatively breeding cichlid Julidochromis ornatus, in which unrelated helpers frequently participate in reproduction and their breeding nests inside rock crevices may be crucial for reproduction and survival of all group members. Then, we subsequently investigate the relationship between group size and reproductive success, while controlling for these factors. The results showed that group size was significantly related to body size of group members rather than nest size; and larger breeders had larger helpers. It was found that group size significantly increased group reproductive output. More importantly, reproductive success of male breeders did not depend on the presence of mature helpers, whereas female reproductive success increased when two males assisted her and tended to decrease when two females bred cooperatively. We conclude that breeding groups of J. ornatus have size hierarchical societies that relate to group size, and group composition of genetically unrelated and co‐breeding members affects their reproductive success.     

Reproduction in the North Atlantic oceanic ichthyofauna and the relationship between fecundity and species' sizes

Synopsis The pelagic (589 spp.) and demersal (505 spp.) oceanic ichthyofaunas of the North Atlantic Basin have very different compositions at ordinal and family level. Yet the pattern of relationships between species' maximum size and maximum fecundity from data available (10% of the pelagic, 19% of the demersal species) was similar. A positive relationship between fecundity and weight was confirmed among most teleosts, but was not followed by the elasmobranchs represented. Species' reproductive styles are reviewed in ordinal groupings within a framework of the overall body size/fecundity distribution. Species size (maximum weight) spectra were synthesized for both pelagic and demersal assemblages to assess the allocation of potential reproductive effort throughout the North Atlantic oceanic ichthyofauna. The only available examples of species size spectra and biomass spectra from the pelagic and demersal ichthyofauna in this ocean basin imply geographic and bathymetric variation in overall reproductive effort among fishes whose fecundity is size dependent. Further implications concerning reproductive effort are discussed in the light of food availability.