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1.
Males of the seaweed pipefish, Syngnathus schlegeli, take care of their eggs in the brood pouch. These pipefish were periodically collected from the shallow seagrass beds in Otsuchi Bay on the Pacific coast of northern Honshu, Japan, from spring to autumn to investigate the basic reproductive ecology. Appearance of the pipefish in the coastal seagrass beds coincided with the initiation of reproduction. The reproductive season was from May to at least October, with its peak in July. A rearing experiment revealed that the brooding period of the male had a negative correlation with water temperature, and it was estimated to last about 1 month in the bay. Almost all males were brooding during the peak of the reproductive season. Although, the brood pouch of most males was either full or devoid of eggs, 6.2% of the males had a partially filled (20%–90%) brood pouch, and multiple clutches were identified in the brood pouch of some males, indicating that the mating system of the pipefish is polygamous, perhaps polygynous. Sex ratio fluctuated among months, and the overall sex ratio tended to be biased to male. Body size of males with an immature brood pouch had a wide range, from 133 to 215 mm standard length (SL). The smallest brooding male was 134 mm SL. Mean SL of brooding males was significantly larger than that of nonbrooding mature males. The number of males with an immature brood pouch was greater at the beginning than later in the reproductive season. The results seem to collectively indicate that the occurrence of a larger proportion of immature males at the onset of the reproductive season may be ascribed to both new recruitment and larger body size at maturation, resulting from the males trading the reproductive effort to somatic growth, perhaps to increase future reproductive success. Received: April 4, 2000 / Revised: September 21, 2000 / Accepted: January 16, 2001  相似文献   

2.
Notropis longirostris (Hay), the longnose shiner, in Catahoula Creek, Jourdan River drainage, Hancock County, Mississippi, was studied from May 1970 to May 1972. In 1971 reproduction occurred from late March into October, as indicated by gross examination of testes, breeding tubercles and breeding colour in males, and ovarian weights, measurements of ova, and gross examination of ovaries in females. Gross examination of ovaries in 1970 also indicated an extended reproductive season. Generally no significant differences from a 1 : 1 sex ratio or in the size of males and females in collections taken during the reproductive season were indicated. Males and females matured about the same size. Most females were sexually mature when 29–30 mm SL. The smallest female with mature ova was 28 mm; however, the majority of females did not have mature ova until 31–33 mm. The number of mature ova produced prior to spawning ranged from 15 to 129 for females 30.8–44 mm SL. There were significant differences in the number of mature ova with time, two peaks being indicated: the first in late March and April at the beginning of the reproductive period and the second in early July about the middle of the season. This conclusion is also supported by ovarian weight measurements and length frequency histograms. The mean diameters of mature ova ranged from 0.70–1.05 mm, averaging 0.90 mm, and were not significantly correlated with length. Most fish live about 1–1.5 years and do not live through two winters, indicating an annual turnover in the population. Maximum size was about 48 mm SL. Specific characteristics of the life history pattern of N. longirostris are discussed in relation to ecological conditions of the habitat.  相似文献   

3.
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.  相似文献   

4.
We examined the relationships between family (female parentage), body size of females, brood retention time between mating and parturition, female fecundity, and early growth of offspring in the guppy Poecilia reticulata. Mature, virgin females from a single brood were mated with a single male. Results of generalized linear models indicate that the effect of the family on female fecundity and offspring growth was significant, which suggested that these traits are genetically determined to a certain extent. Larger females at the time of mating produced larger broods, although female body size at the time of parturition did not affect brood size, in contrast to the results of some previous studies in guppies. Brood size was negatively associated with the body size of neonates. Results highlighted significant associations between brood retention time and female fecundity as well as offspring growth. In addition, the interaction between the family and brood retention time was significantly associated with female fecundity and offspring growth. Females of some families had longer retention times of larger broods, whereas those of other families had shorter retention times of smaller broods. On the other hand, females with longer brood retention times produced smaller neonates with slower growth. Since the family also affected the brood retention time, selection may work against the duration of brood retention of females via the size, growth and number of offspring, depending on environmental factors such as the intensity of predation or competition in neonates.  相似文献   

5.
瘦尾细额溞是一种出现数量极其稀少的枝角类。关于它的生物学特征尚未见诸文献。本文测量了一次采自云南永胜一池塘的本种300个两性个体的体长和怀卵量,就其幼体与成体的数量、体长与怀卵量、雄性以及性比等问题探讨了种群的生物学状况。 详细观察比较了这个种的重要分类特征——雌体后腹部,并描述了变异范围。对卵鞍和雄体也作了描述。  相似文献   

6.
The reproductive biology of the fanray, Platyrhina sinensis, was examined in Ariake Bay, Japan, from May 2002 until December 2006. Females reached sexual maturity at a larger size than males [total length (TL) at 50% sexual maturity: male, 393 mm; female, 421 mm]. The present data support a distinct annual reproductive cycle for P. sinensis. The gonadosomatic index (GSI) for mature males showed a clear seasonal trend, declining from August to November. Histological observations showed that mature sperm in the testes occurred from August to November when monthly GSI declined. Concomitantly, pre-ovulatory ova were observed in females collected from August to November. These data indicate that mating, ovulation and fertilization occurred from August to November. Near-term embryos, neonates and recent post-partum females also occurred from August to November. Additionally, all post-partum females possessed large pre-ovulatory ova. Parturition occurred from August to November followed immediately by mating, ovulation and fertilization. Mature females become pregnant every year, and the gestation period is almost 1 year. Fertilized uterine eggs without macroscopic embryonic development were present throughout the annual reproductive cycle, indicating that P. sinensis utilizes embryonic diapause as its reproductive strategy. Both reproductive tracts of females were functional, and fecundity ranged from 1 to 12 with a mean of 6.0, increasing with TL.  相似文献   

7.
Female Size Influences Mate Preferences of Male Guppies   总被引:6,自引:1,他引:5  
Guppies (Poecilia reticulata) have a promiscuous mating system in which female choice for brightly coloured males plays an important role. Consequently, much research on guppies has examined how mate choice by females has lead to the evolution of male colour patterns. Much less attention has been devoted to mate choice by males in this species. In this study, we show that male guppies are choosy when selecting a female to associate with, significantly preferring the larger female when presented with two females that differed by ≥2 mm in standard length (SL). The strength of their preference for each female increased with absolute female size. The relative sizes of the females, however, also influenced male mating preferences: males showed stronger preferences for the larger female as the difference in SL between the two females increased. Such a preference for larger females is not unexpected as fecundity generally increases with body size in female fish. Thus, males choosing to mate with the larger female should have higher reproductive success. An apparent, but non‐significant anomaly, whereby males appear to prefer the smaller of the two females when the difference between female SL was <4 mm, deserves further investigation.  相似文献   

8.
We investigated multiple paternity and sperm precedence in the Amarillo fish, Girardinichthys multiradiatus (Goodeidae). We allowed females to mate with two different-sized males consecutively and assessed the paternity of the ensuing broods using allozyme electrophoresis. We presented one-half of the females the larger, and the other half the smaller, male first. Allozyme variation among individuals was low, yielding conservative estimates of multiple paternity. Half the broods were of mixed paternity, but one male always sired more than 70% of the embryos in each brood. The proportion of the brood sired was not related to mating sequence, but when we classified males by relative size, the larger male of each pair usually fathered greater proportions of offspring than the smaller male. This association disappeared when we used the actual size of the males in the analysis. Instead, for any pair of males, the difference in number of offspring sired was correlated to differences in the rate of courtship displays, rather than size differences, suggesting that courtship intensity is a better predictor of paternity than male size. Within a pair, the larger male usually displayed more than the smaller one, but there was no correlation between male size and display rate across all males. Parsimony suggests a correlation between courtship rate and sperm production, but we cannot rule out the possibility that females allocate paternity according to the relative merits of the males.  相似文献   

9.
1. Fecundity of a Dikerogammarus villosus population at Spitz was studied in the Austrian Danube during the 3‐year period 2002–2004. Ovigerous females were absent in October and November, and extremely scarce in December when the reproductive season started again slowly. From January to September pre‐copulatory pairs and egg‐carrying females were present. The reproductive cycle lasted for 9–10 months. 2. Various pigmentation phenotypes of D. villosus have been described in the literature. However, no significant differences were found between the reproductive variables studied here and several colour morphs. Mating was size‐assortative; mean body length of males was about 1.3 times greater than that of their potential mates, and the wet weight was approximately twice as heavy. 3. The relationship between the number of embryos per clutch and the wet weight of females was described by a 3‐parameter power equation. The population mean was 43 eggs with a range of five to 194 eggs. Eighty‐two specimens from 1359 D. villosus females had more than 100 eggs: the smallest of these females was 12 mm long (30 mg) wet weight, and the largest, which was 18 mm long (91 mg), had 194 eggs in embryonic development stage 4. 4. Numbers of embryos in developmental stages 2 (early egg stage) and 7 (newly hatched neonates) differed significantly with body wet weight of ovigerous females (P < 0.05). For an average female in the range 10–12 mm (20–30 mg) the number of juveniles in the brood pouch was 74% of the number of stage 2 eggs. This value can be interpreted as the survival rate of eggs. 5. The overall mean egg volume (EV, ±95% CL) of stage 2 eggs of D. villosus was 0.05 ± 0.001 mm3, and EV increased significantly at each stage of development. At stage 6, egg volume had increased by a factor of 2.6, and averaged 0.13 ± 0.001 mm3. In comparison, G. fossarum and G. roeseli had significantly larger eggs in all developmental stages. 6. Mean egg size of D. villosus (0.063 mm3) was maximal in January. For D. villosus (and G. roeseli) the minimum mean egg size occurred in September. In contrast to G. fossarum and G. roeseli, a second peak in egg size was not observed for D. villosus, and egg size fell more or less successively from January to September. 7. A simple index of fecundity was calculated from the number of stage 2 eggs divided by the female's wet weight. The highest values were observed in April and May, when females from the overwintering generation grew to their maximum body size. Thus the release of a large number of neonates corresponds with the availability of plentiful food and rising water temperatures for juvenile growth in the spring. The lowest value occurred in December. In June the small females of a summer generation appeared, with a naturally low fecundity. 8. The relationship between brood development time and water temperature was studied in the laboratory at a series of constant temperatures. At 16 °C, mean brood development time was 14 days for D. villosus, compared with about 3 weeks for the indigenous species. At 10 °C, mean brood development time was 24 days in D. villosus, compared with 40 days in G. fossarum and 44 days in G. roeseli. At 4 °C it was 1.8 and 3.5 times longer in G. fossarum and G. roeseli. 9. The number of offspring produced by a single clutch from a large female D. villosus is considerably higher than the total numbers produced by the indigenous freshwater gammarids, such as G. fossarum, G. roeseli and G. pulex, during their life‐spans of 1.5–2 years in seven to nine successive broods. Only one or two large ovigerous D. villosus would probably be enough to start a new population. A potentially high reproductive capacity, comparatively small eggs, optimal timing to release the maximum number of neonates per female in April/May, and a long reproductive cycle, together with rapid development of eggs, rapid growth to sexual maturation, short life span, tolerance to a wide range of environmental conditions, and exceptional predatory capabilities, all give the invasive Ponto‐Caspian gammarid an opportunity to become globally distributed in freshwater ecosystems of the temperate climate zone.  相似文献   

10.
Sexual dimorphism and the female reproductive cycle were studied in a population of the viviparous lizard Trachylepis vittata at 2000 m a.s.l. on Mount Sannine, Lebanon. Females have larger body sizes than males and males have relatively larger heads than females. Females reach maturity at 56 mm snout-vent length. They spend at least six months in hibernation, from October to March. Adult females emerge from hibernation in April. Fertilization occurs mid-May and gestation lasts for 8-10 weeks. All females collected on the same date had embryos at the same embryonic developmental stage. Females produced 1-4 embryos. There is a significant positive relationship between female body size and number of embryos. Parturition lasts for two weeks and new-borns achieve adult size within about ten months.  相似文献   

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