Selectivity Parameters and Size at First Maturity in Deep-Water Shrimps, Aristaeomorpha foliacea (Risso, 1827) and Aristeus antennatus (Risso, 1816), from the North-Western Ionian Sea (Mediterranean Sea)

Selectivity experiments were carried out during trawling targeting deep-water shrimps Aristaeomorpha foliacea (Risso, 1827) and Aristeus antennatus (Risso, 1816) (Crustacea, Decapoda, Aristeidae) in the North-Western Ionian Sea (Eastern-Central Mediterranean). Different criteria were employed to analyse maturity; however, the proportion at 50% of retained, mated and mature specimens was always used to indicate the size, expressed as Carapace Length (CL, mm), at first capture (CL_c), mating (CL_sp) and at first maturity (CL_m), respectively. In order to estimate the size at 50% maturity (CL_m) for females of both species, three criteria were adopted. In particular, CL_m was computed for the mature females not considering the presence of spermatophores, for the mature females with spermatophores and for the mature females intersected by the decreasing proportion with size of females without spermatophores. Three diamond stretched mesh codends of 40, 50 and 60 mm were tested using a cover of 20 mm. The 40-mm stretched mesh size (European Union legal size in the Mediterranean) was not selective for the sampled population of each species. The size at first capture (CL_c), calculated in both species for the two sexes combined, increased significantly with mesh size. Even for the mesh size of 60 mm, the size at first capture was still smaller than the sizes at 50% maturity, whatever the criterion adopted. Since the differences between the size at first maturity and the sizes at first capture are greater in A. foliacea than A. antennatus, the former species appears in this respect to be more vulnerable to trawling than the latter.     

Size composition, growth and sexual maturity of Callinectes latimanus (Rath.) in two Ghanaian lagoons

Blue crabs Callinectes latimanus (Rath.) trapped from two lagoons were sexed, measured and weighed. The eggs of the mature females were counted to determine fecundity, and the spermatophores of the males were counted to determine the size of sexual maturity. Sizes at maturity of both male and female crabs were determined. The methods employed and the results are discussed.     

Relative Growth and Sexual Maturity of the Hermit Crab Paguristes erythrops (Anomura, Diogenidae) from South Atlantic

Some morphometric relationships were studied in the hermit crab Paguristes erythrops to describe its relative growth and the size at which sexual maturity is reached, as well as the shell influence on this process. Individuals were collected monthly from January to December/1999, by SCUBA diving and 12 different characters were measured on males and females. Sexual size dimorphism was observed in length and width of left cheliped. Size at sexual maturity was estimated between 2.8 and 3.5 mm shield length based on the left cheliped relations of the males and on the endopod and exopod of the second pleopod of the females. Differences in the allometry of individuals occupying different shell species were observed. The present work demonstrated the importance of characterizing the type of growth of some parts (pleopods) not yet used in other studies on relative growth of hermit crabs that may correspond to indicators of the size at sexual maturity.     

First evidences of sexual selection by mate choice in marine zooplankton

Sexual selection is potentially important in marine zooplankton, presumably the most abundant metazoans on earth, but it has never been documented. We examine the conditions for sexual selection through mate choice and describe mating preferences in relation to size in a marine zooplankter, the pelagic copepod Acartia tonsa. Males produce spermatophores at a rate (~1 day⁻¹) much lower than known female encounter rates for most of the year and the decision to mate a particular female thus implies lost future opportunities. Female egg production increases with female size, and males mating larger females therefore sire more offspring per mating event. Similarly, females encounter males more frequently than they need to mate. Large males produce larger spermatophores than small males and the offspring production of female increases with the size of the spermatophore she receives. Additionally, large spermatophores allow females to fertilize eggs for a longer period. Thus, mating with large males reduces the female’s need for frequent matings and she may sire sons that produce more offspring because size is heritable in copepods. Finally, we show that both males and females mate preferentially with large partners. This is the first demonstration of sexual selection by mate choice in a planktonic organism.     

Size at the onset of sexual maturity in the anomuran crab, Aegla uruguayana (Aeglidae)

The size at maturity was studied in the crab Aegla uruguayana from the Areco River (31°14′ S, 59°28′ W), Argentina. Size at sexual maturity was determined according to three criteria: morphometric (change in the relative growth of reproductive characters), histological (first maturation of gonads) and functional (capability to mate and carry eggs). Regarding females, morphometric maturity occurred at a carapace length (CL) of 11.50 mm, considering abdomen width as a reproductive character. Gonad maturity of females could be observed at a minimum size ranging from 15 to 17 mm CL. The smallest ovigerous female observed in the field was 15.60 mm CL, although a relevant population incidence of ovigerous females (86.6%) has just been observed at values higher than 17 mm CL. As for males, the relative growth of the left chela length changed at a value of 15.40 mm CL, while morphological changes in sexual tube occurred between CL of 14 and 16 mm. Testicular maturation occurred at a CL ranging from 17 to 19 mm. The smallest size of males having spermatozoids in their vasa deferentia was 18.70 mm CL. The results obtained indicated that, in both sexes, functional maturity occurred after morphometric maturity and at a size similar to that of gonad maturity. Comparing sexes, females acquired sexual maturity (morphometric, gonad and functional maturity) at sizes statistically smaller than those of males.     

Effects of Ocean Acidification on Juvenile Red King Crab (Paralithodes camtschaticus) and Tanner Crab (Chionoecetes bairdi) Growth,Condition, Calcification,and Survival

Ocean acidification, a decrease in the pH in marine waters associated with rising atmospheric CO₂ levels, is a serious threat to marine ecosystems. In this paper, we determine the effects of long-term exposure to near-future levels of ocean acidification on the growth, condition, calcification, and survival of juvenile red king crabs, Paralithodes camtschaticus, and Tanner crabs, Chionoecetes bairdi. Juveniles were reared in individual containers for nearly 200 days in flowing control (pH 8.0), pH 7.8, and pH 7.5 seawater at ambient temperatures (range 4.4–11.9 °C). In both species, survival decreased with pH, with 100% mortality of red king crabs occurring after 95 days in pH 7.5 water. Though the morphology of neither species was affected by acidification, both species grew slower in acidified water. At the end of the experiment, calcium concentration was measured in each crab and the dry mass and condition index of each crab were determined. Ocean acidification did not affect the calcium content of red king crab but did decrease the condition index, while it had the opposite effect on Tanner crabs, decreasing calcium content but leaving the condition index unchanged. This suggests that red king crab may be able to maintain calcification rates, but at a high energetic cost. The decrease in survival and growth of each species is likely to have a serious negative effect on their populations in the absence of evolutionary adaptation or acclimatization over the coming decades.     

Sexual size dimorphism, growth and maturity of the Japanese fluvial sculpin,Cottus pollux (large egg type), in the Inabe River, Mie prefecture, central Japan

The population structure of the Japanese fluvial sculpin,Cottus pollux (large egg type), in the upper reaches of the Inabe River, Mie Prefecture, central Japan, was investigated by a mark-and-recapture method from July 1989 to January 1991. Breeding of the species occurred from mid February to early May, peaking from mid February to late March. The mean size of mature males observed in March 1990 was significantly larger than that of females, showing apparent sexual size dimorphism. Data analysis of the growth of 1658 marked individuals revealed that the species matured at 2 years of age in both sexes. Whereas 1 year old males reached ca. 50–70 mm SL, females were less than 50 mm SL at the same age, size dimorphism already being apparent. Immature males exhibited higher growth rates than females during their first and second years, some of the former outstripping mature males of the preceding year class in total length. After attaining sexual maturity, both males and females grew mainly from July to December, with no significant differences in mean growth rate between them. Sexual size dimorphism of the species seems to be attributable to different growth rates between the sexes during their immature stage.     

Size distribution,length–weight relationship and size at the onset of sexual maturity of the orange mud crab,Scylla olivacea,in Malaysian waters

The size distribution, length–weight relationship and size at the onset of sexual maturity of the orange mud crab (Scylla olivacea) from four geographically distinct locations (Taiping, Setiu, Kota Marudu and Lundu) representing Malaysian waters were analysed and estimated. Scylla olivacea was found in the size range of 47–134?mm carapace width. Males were significantly smaller in size but heavier than females. Geographical variation in carapace width and body weight were significant, but no interaction was found between sexes and locations. As shown by the length–weight relationships of S. olivacea, the males exhibited positive growth allometry whereas the females exhibited negative growth allometry. Males mature physiologically prior to attaining morphometric sexual maturity. Females, however, achieve physiological and morphometric sexual maturity in synchrony. No significant variation was found in the estimates of size at the onset of sexual maturity of males and females among different locations. We recommend the use of the third right walking leg merus length and carapace width to estimate the size at the onset of sexual maturity (morphometric maturity) for S. olivacea. Data obtained in this study serve as important baseline data for future mud crab resource management in Malaysia and were used to recommend minimum landing sizes for S. olivacea in each respective location based on the largest size at the onset of sexual maturity estimates were suggested.     

Pairing and insemination patterns in a giant weta (Deinacrida rugosa: Orthoptera; Anostostomatidae)

Positive size assortative mating can arise if either one or both sexes prefer bigger mates or if the success of larger males in contests for larger females leaves smaller males to mate with smaller females. Moreover, body size could not only influence pairing patterns before copulation but also the covariance between female size and size of ejaculate (number of spermatophores) transferred to a mate. In this field study, we examine the pre-copulatory mate choice, as well as insemination, patterns in the Cook Strait giant weta (Deinacrida rugosa). D. rugosa is a large orthopteran insect that exhibits strong female-biased sexual dimorphism, with females being nearly twice as heavy as males. Contrary to the general expectation of male preference for large females in insects with female-biased size dimorphism, we found only weak support for positive size assortative mating based on size (tibia length). Interestingly, although there was no correlation between male body size and the number of spermatophores transferred, we did find that males pass more spermatophores to lighter females. This pattern of sperm transfer does not appear to be a consequence of those males that mate heavier females being sperm depleted. Instead, males may provide lighter females with more spermatophores perhaps because these females pose less of a sperm competition risk to mates.     

Nuptial gifts and sexual selection in photinus fireflies

The phenomenon of nuptial gift transfer during mating occursacross a remarkably wide range of taxa, and such male donationsare likely to influence both pre-copulatory and post-copulatorysexual selection. This paper reviews what is known about nuptialgifts in Photinus fireflies (Coleoptera: Lampyridae), and discussesthe adaptive significance of spermatophores in firefly matingsystems. During copulation Photinus males transfer a spiral,gelatinous spermatophore to the female: sperm are released intothe female's spermatheca for storage, while the remainder ofthe spermatophore disintegrates within a specialized gland.Radiolabelling studies indicate that male-derived protein isused to help provision the female's developing oocytes, andmultiply-mated females show increased fecundity. As most Photinusadults do not feed, these studies suggest that females shouldcontinue to forage for matings to supplement their diminishinglarval reserves, even after they have gained sufficient spermto fertilize their eggs. Male spermatophore mass declines acrosssequential matings, and smaller spermatophores are associatedwith lower paternity success in situations where males competefor fertilizations. Declining spermatophore size across sequentialmatings may thus lead to diminishing reproductive returns forfirefly males. Taken together, these results suggest that seasonalchanges in nuptial gift availability may contribute to reversalsof traditional courtship roles, with male choice and female-femalecompetition occurring as spermatophore availability declines.     

Growth and maturity of the spider crab Halicarcinus planatus (Brachyura: Hymenosomatidae) females in the southwestern Atlantic Ocean. Can these parameters be influenced by the population sex ratio?

The Halicarcinus planatus populations of the southwestern Atlantic Ocean show a highly variable sex ratio and a large size overlapping between females in the last immature instar (ADO) and mature (MAT) females. We hypothesized that these facts are related and that female impregnation has a central role in this relation. Non-impregnated ADO females delay maturity and would continue to grow, leading to size overlapping. This scenario is most probable in populations with a scarcity of males and could affect the growth, maturity and population structure. The sex ratio and female size distribution of several populations of the southwestern Atlantic Ocean were analysed. Growth and maturity were studied in two populations with different sex ratios (Camarones, a population with males, and Rada Tilly, a population where no males were found). Size overlapping was not related to the population sex ratio. Size overlapping was due to a variable moult increment and, to a lesser extent, to delayed maturity. Females mated before terminal moult in both populations. However, in Camarones, physiological maturity was not related to impregnation, while in Rada Tilly, vitellogenic oocytes were observed only in impregnated females. Also, differences in the number of spermatophores in female spermathecae were related to the sex ratio. Our results showed that the morphological maturity pattern of females was not influenced by the population sex ratio. However, physiological maturity was related to female impregnation and sex ratio. Also, the variation in the number of spermatophores suggests differences in the mating system related to the sex ratio.     

Female‐biased dimorphism in size and age at maturity is reduced at higher latitudes in lake whitefish Coregonus clupeaformis

Female‐biased sexual dimorphism in size at maturity is a common pattern observed in freshwater fishes with indeterminate growth, yet can vary in magnitude among populations for reasons that are not well understood. According to sex‐specific optimization models, female‐biased sexual size dimorphism can evolve due to sexual selection favouring earlier maturation by males, even when sexes are otherwise similar in their growth and mortality regimes. The magnitude of sexual size dimorphism is expected to depend on mortality rate. When mortality rates are low, both males and females are expected to mature at older ages and larger sizes, with size determined by the von Bertalanffy growth equation. The difference between size at maturity in males and females becomes reduced when maturing at older ages, closer to asymptotic size. This phenomenon is called von Bertalanffy buffering. The predicted relationship between the magnitude of female‐biased sexual dimorphism in age and size at maturity and mortality rate was tested in a comparative analysis of lake whitefish Coregonus clupeaformis from 26 populations across a broad latitudinal range in North America. Most C. clupeaformis populations displayed female‐biased sexual dimorphism in size and age at 50% maturity. As predicted, female‐biased sexual size dimorphism was less extreme among lower mortality, high‐latitude populations.     

Daily cycle and body characteristics of mating Litopenaeus vannamei shrimps (Decapoda: Penaeidae) in the wild off southern Sinaloa, Mexico

Mating behavior has been described for very few species of penaeoid shrimps. We describe some of the environmental conditions under which mating of Litopenaeus vannamei took place in the ocean, as inferred by the presence of attached spermatophores on the thelycum of females, combined with the presence of mature males with empty ampulla terminalis, both evidence of recent copulation. Out of a total of twelve 24 hr samplings on board the research vessel B/O "EL PUMA", one was selected to examine mating. There were four periods of observation. The highest frequency of females with attached spermatophores were found during the daytime whilst the lowest was registered during the night. Females with attached spermatophore were mostly at stages IV and V of ovarian maturity and fell within the 30-50 mm of C.L. range. Copulating male size ranged between 30 and 40 mm of C.L. and there was a close relation between the percentage of mating females and males. Male to female ratio varied throughout the sampling period but it was never 1:1. The female mean size was, in all cases, bigger than the male mean size. Among the environmental factors, salinity and oxygen varied very slightly throughout the sampling period; temperature variation was more pronounced and those changes were attributed to the tidal oscillation.     

THE EVOLUTION OF FEMALE-BIASED SEXUAL SIZE DIMORPHISM: A POPULATION-LEVEL COMPARATIVE STUDY IN HORNED LIZARDS (PHRYNOSOMA)

Female-biased sexual size dimorphism is uncommon among vertebrates and traditionally has been attributed to asymmetric selective pressures favoring large fecund females (the fecundity-advantage hypothesis) and/or small mobile males (the small-male advantage hypothesis). I use a phylogenetically based comparative method to address these hypotheses for the evolution and maintenance of sexual size dimorphism among populations of three closely related lizard species (Phrynosoma douglasi, P. ditmarsi, and P. hernandezi). With independent contrasts I estimate evolutionary correlations among female body size, male body size, and sexual size dimorphism (SSD) to determine whether males have become small, females have become large, or both sexes have diverged concurrently in body size during the evolutionary Xhistory of this group. Population differences in degree of SSD are inversely correlated with average male body size, but are not correlated with average female body size. Thus, variation in SSD among populations has occurred predominantly through changes in male size, suggesting that selective pressures on small males may affect degree of SSD in this group. I explore three possible evolutionary mechanisms by which the mean male body size in a population could evolve: changes in size at maturity, changes in the variance of male body sizes, and changes in skewness of male body size distributions. Comparative analyses indicate that population differentiation in male body size is achieved by changes in male size at maturity, without changes in the variance or skewness of male and female size distributions. This study demonstrates the potential of comparative methods at lower taxonomic levels (among populations and closely related species) for studying microevolutionary processes that underlie population differentiation.     

Sexual cannibalism, competition, and size dimorphism in the orb-weaving spider Nephila plumipes Latreille (Araneae: Araneoidea)

The degree and direction of sexual dimorphism varies widely,but in several taxa of orb-weaving spiders, including Nephila,males may be less than one-tenth the size of females. This differenceis commonly attributed to selection through precopulation sexualcannibalism: females may either fail to detect very small males,or ignore them as potential prey items. However, there is oftenthe potential for male-male competition in these species becauseseveral males can be found on the web of a single female. Weinvestigated experimentally the effects of sexual cannibalismand male-male competition on male body size and hence sexualdimorphism in the Australian golden orb-weaver (Nephila plumipes).Small males were less likely to be detected and cannibalizedthan larger males. However, larger males excluded small malesfrom the central hub of the web, where mating takes place. Theconflicting effects of sexual cannibalism and male-male competitionmay be responsible for the relatively large variation in malebody size in this species.     

Reaction norms of size and age at maturity of Pomacea canaliculata (Gastropoda: Ampullariidae) under a gradient of food deprivation

Pomacea canaliculata, an apple snail native to South America,has become a serious pest of aquatic crops and a promoter ofecosystem changes in natural wetlands worldwide. Its successas an invader has been attributed to its great phenotypic plasticityin life-history traits. Our aims were to determine the reactionnorms of size and age at maturity under a gradient of food deprivation.Full sibling experimental snails were reared in isolation fromhatching and maintained until maturity under seven differentlevels of relative food deprivation based on size-specific ingestionrates. To detect the onset of sexual activity of experimentalsnails, fully mature virgin snails reared in the laboratorywere used as consorts. The reaction norms for age and size atmaturity of P. canaliculata showed marked sexual dimorphism.Shell length was the main component of variation in the malereaction norms for both copulation and egg-laying by femaleconsorts, whereas age was the main component of variation forfemales. Irrespective of the intensity of food deprivation,males mature at the same age at the expense of size, since sizeis apparently irrelevant in the access to females and male fitnesscan be maximized through fast maturation. In contrast, a minimumsize is required for females to reach maturity, perhaps as aresult of their higher reproductive costs. The highly dimorphicreaction norms lead to an increasing lag between male and femalematurity as deprivation increases; in temperate regions, malesborn early in the reproductive season would mature in the sameseason irrespective of food availability, while most femaleswould have to overwinter before attaining sexual maturity inunproductive habitats or those dominated by unpalatable macrophytes.The great life-history plasticity reported in invaded areascould be a heritage from populations in the native range. (Received 10 August 2007; accepted 30 July 2008)     

Effects of gamma radiation on spermatophore production and reception and subsequent fecundity and egg viability inAcarus siro L. (Acari: Acaridae)

Gamma radiation at doses higher than 10 krad significantly lowered the fecundity of the grain mite,Acarus siro. The fecundity of irradiated females was inversely correlated with dose, both when control or irradiated males were used in the pairing.Irradiation with ionizing radiation affected sexual activity of males. At doses above 10 krad the number of formed or observed spermatophores was lowered significantly.Sexual attractiveness of irradiated and control females to irradiated males was similar. However, non-irradiated males were observed mating more often with non-irradiated than with irradiated females.No correlation was found between the numbers of spermatophores present in the spermathecae of the female and the fecundity of the female. Irradiation had a greater effect on fecundity of the female than on sexual activity of the male; it did not affect the shape or behavior of spermatophores in the spermathecae of the female.Viability of eggs laid by females decreased by at least 50% when females or males were irradiated with doses above 20 krad. Irradiation also affected the survival of adults, but females were more sensitive than males. Net sterility index indicates that doses higher than 20 krad induce more than 90% sterility.     

Sexual Dimorphism and Facial Growth Beyond Dental Maturity in Great Apes and Gibbons

The great apes and gibbons are characterized by extensive variation in degree of body size and cranial dimorphism, but although some studies have investigated how sexual dimorphism in body mass is attained in these species, for the majority of taxa concerned, no corresponding work has explored the full extent of how sexual dimorphism is attained in the facial skeleton. In addition, most studies of sexual dimorphism combine dentally mature individuals into a single “adult” category, thereby assuming that no substantial changes in size or dimorphism take place after dental maturity. We investigated degree and pattern of male and female facial growth in Pan troglodytes troglodytes, Pan paniscus, Gorilla gorilla gorilla, Pongo pygmaeus, and Hylobates lar after dental maturity through cross-sectional analyses of linear measurements and geometric mean values of the facial skeleton and age-ranking of individuals based on molar occlusal wear. Results show that overall facial size continues to increase after dental maturity is reached in males and females of Gorilla gorilla gorilla and Pongo pygmaeus, as well as in the females of Hylobates lar. In male Pongo pygmaeus, adult growth patterns imply the presence of a secondary growth spurt in craniofacial dimensions. There is suggestive evidence of growth beyond dental maturity in the females of Pan troglodytes troglodytes and Pan paniscus, but not in the males of those species. The results show the presence of statistically significant facial size dimorphism in young adults of Pan paniscus and Hylobates lar, and of near statistical significance in Pan troglodytes troglodytes, but not in older adults of those species; adults of Gorilla gorilla gorilla and Pongo pygmaeus are sexually dimorphic at all ages after dental maturity. The presence of sex-specific growth patterns in these hominoid taxa indicates a complex relationship between socioecological selective pressures and growth of the facial skeleton.     

COMPARISONS OF LIFE-HISTORY TRAITS AND SEXUAL DIMORPHISM BETWEEN ASSIMINEA JAPONICA AND ANGUSTASSIMINEA CASTANEA (GASTROPODA: ASSIMINEIDAE)

Life histories of two sympatric assimineid gastropods, Assimineajaponica and Angustassiminea castanea, were investigated ata reed marsh in northern Japan. Size frequency distributionsrevealed that growth curves of females and males differed inboth species resulting in sexual dimorphisms in shell size.In A. japonica, the shell height of females was larger thanthat of males, whereas in A. castanea males attained a biggershell than females. Mating behaviour of A. japonica was observedmainly from February to June, while that of A. castanea wasobserved from May to August. The diameter of deposited eggsof A. japonica was 200 to 250 mm, whereas that of A. castaneawas 125 to 150 mm. The length of the veliger larva of A. japonicaat hatching was approximately 200 mm, whereas that of A. castaneawas approximately 125 mm. Longevity, age at sexual maturityand opportunities for reproduction during life time were estimatedin the field. For A. japonica, sexual maturity was establishedby the age of 17 months and longevity was about three years.Opportunities for reproduction of A. japonica occurred twiceduring a lifetime. For A. castanea, sexual maturity was establishedby the age of 10 months and longevity was almost five years.Opportunities for reproduction of A. castanea occurred fivetimes during a lifetime. The differences of life-history traitsand sexual dimorphism between species and possible explanationsof evolutionary factors are discussed. To whom correspondence should be addressed. (Received 21 January 1999; accepted 8 September 1999)