Reproductive biology of the smooth-hound shark Mustelus mustelus (L.) in the Gulf of Gabès (south-central Mediterranean Sea)

The reproductive biology of the smooth-hound shark Mustelus mustelus was studied in the Gulf of Gabès (southern Tunisia). Females were found to mature between 1075 and 1230 mm total length ( L _T) whereas males matured between 880 and 1120 mm L _T. The L _T at which 50% of the population reached maturity was 971 and 1172 mm for males and females, respectively. Male gonads were symmetrical in terms of mass and both functional, whereas in females only the right ovary was functional. The seasonal changes in the oocytes and testes development, embryo length and the occurrence of near-term and post-partum females showed that this species displayed a clearly defined annual reproductive cycle with parturition occurring during late April and early May, after a gestation period of 10–11 months. Mating took place during May and early June and fertilization occurred from early June to early July. The embryo sex ratio was not significantly different from unity. Litter size varied from four to 18 embryos and was positively correlated with maternal L _T. The young were born with a L _T of 340–420 mm.     

Reproductive biology of the smooth butterfly ray Gymnura micrura

This study provides the first detailed information on the reproductive biology of the smooth butterfly ray Gymnura micrura. A total of 905 individuals were sampled, 377 of which were used for the reproductive study. Juveniles accounted for 75% of the sample, but all life cycle stages were present in the study area. The disc width at which 50% were mature (W(D50) )was estimated at 269 and 405 mm for males and females, respectively. The W(D50V) (based on the onset of vitellogenesis) was estimated at 359 mm. Uterine fecundity (mean ±s.d. = 3·8 ± 1·3; range: 1-6) was positively correlated with female size. A 3564% gain in mean wet mass was observed from egg to full-term embryo in utero. Size at birth ranged from 135 to 175 mm W(D) (19·5 to 55·0 g), with a mean of 165·1 mm W(D) (43·3 g). The embryo sex ratio was not significantly different from 1:1. The ovaries of pregnant females were undergoing vitellogenesis during gestation, with females ready to ovulate soon after parturition. Gymnura micrura may have an asynchronous reproductive cycle, with females reproducing continuously throughout the year.     

Reproductive biology of the lesser guitarfish Zapteryx brevirostris from the south-western Atlantic Ocean

This study provides the first detailed information on the reproductive biology of the lesser guitarfish Zapteryx brevirostris in the south-western Atlantic Ocean between latitudes 34° and 42° S. A total of 320 males (196-647 mm total length, L(T)) and 336 females (200-640 mm L(T)) were analysed. No significant differences were observed in size at 50% maturity between males (499 mm L(T)) and females (506 mm L(T)). Three seasonal patterns were related to the testes mass, the development of spermatocysts and the presence of spermatozoa in genital ducts. Females showed a 3 year reproductive cycle, with 2 years of ovarian maturation and 1 year of gestation, including a mean annual fecundity of one to two embryos. Synchronicity of both ovulating females and males with sperm in genital ducts indicated that ovulation and hence mating occurs during winter. Birth was assumed to occur during winter, but neither ovulation nor mating is simultaneous with this reproductive event. Despite its low economic value, a decline in abundance in the region, together with a low reproductive efficiency, indicates that the Z. brevirostris population should be monitored closely.     

Reproductive biology of the starry smooth-hound shark Mustelus asterias: geographic variation and implications for sustainable exploitation

Examination of the reproductive biology of Mustelus asterias in the north-east Atlantic Ocean highlighted apparent geographical variation in maturity, fecundity and ovarian cycle between Atlantic and Mediterranean populations. The stretch total length (L(ST) ) and age at 50% maturity for Atlantic males and females were estimated at 78 cm L(ST) and 4-5 years and 87 cm L(ST) and 6 years, respectively. Size at maturity of females was considerably smaller than in Mediterranean specimens (96 cm L(ST) ). Ovarian fecundity ranged from eight to 27 oocytes and uterine fecundity from six to 18 embryos. The gestation period was c. 12 months, followed by a resting period of c. 12 months, resulting in a biennial cycle. Females stored sperm in the oviducal gland and, unlike Mediterranean specimens, no uterine compartments were observed in Atlantic specimens. This study reveals the existence of strong, possibly adaptive, divergence in life-history traits in an elasmobranch, whose northern populations may be more susceptible to overexploitation than previously believed.     

Reproductive biology of Psammobatis extenta

Psammobatis extenta collected from the commercial bottom trawl fishery operating in Puerto Quequén, Argentina, between 2000 and 2001, had a sex ratio of 1:1 (535 specimens). Both the largest male and female measured 313 mm total length ( L _T). The relationship between total body mass and L _T was significantly different between sexes; mature females weighed more than mature males for a given L _T. The size at which 50% of males were sexually mature was 262 mm L _T (83·6% of the maximum size), whereas 50% of females were mature at 249 mm L _T (80·0% of the maximum size). The gonadosomatic index in mature males and females was slightly higher during summer, but did not show significant variation over the sampling period. The hepatosomatic index of males and females was higher during the autumn and winter and followed a distinct seasonal pattern. Evidence suggested a continuous reproductive cycle during the year, with a maximum number of females carrying egg-cases in summer.     

Reproductive parameters of rhinobatid and urolophid batoids taken as by‐catch in the Queensland (Australia) east coast otter‐trawl fishery

Reproductive variables are provided for batoids regularly taken as by‐catch in the east coast otter‐trawl fishery on the inner‐mid continental shelf off the south‐east and central coasts of Queensland, Australia. Total length at maturity (L_T50 and 95% c.i .) for the eastern shovelnose ray Aptychotrema rostrata was 639·5 mm (617·6–663·4 mm) for females and 597·3 mm (551·4–648·6 mm) for males. Litter size (n = 9) ranged from nine to 20 (mean ± s.e. = 15·1 ± 1·2). This species exhibited a positive litter size–maternal size relationship. Disc width at maturity (W_D50 and 95% c.i .) for the common stingaree Trygonoptera testacea was 162·7 mm (155·8–168·5 mm) for females and 145·9 mm (140·2–150·2 mm) for males. Gravid T. testacea (n = 6) each carried a single egg in the one functional (left) uterus. Disc width at maturity (W_D50 and 95% c.i .) for the Kapala stingaree Urolophus kapalensis was 153·7 mm (145·1–160·4 mm) for females and 155·2 mm (149·1–159·1 mm) for males. Gravid U. kapalensis (n = 16) each carried a single egg or embryo in the one functional (left) uterus. A single female yellowback stingaree Urolophus sufflavus carried an embryo in each uterus. A global review of the litter sizes of shovelnose rays (Rhinobatidae) and stingarees (Urolophidae) is provided.     

Reproductive biology of the milk shark Rhizoprionodon acutus and the bigeye houndshark Iago omanensis in the coastal waters of Oman

Female Rhizoprionodon acutus were found to mature between 62 and 74 cm total length ( L _T) whereas males matured between 63 and 71 cm L _T. The L _T at 50% maturity was 64·3 cm for females and 64·7 cm for males. Litter size varied from one to six embryos, and was positively correlated with maternal L _T. Female embryos outnumbered males by a ratio of 2·3:1. The size at birth was c . 37 cm L _T. Full‐term embryos and post‐partum females were observed during all seasons although their occurrence was highest in spring. Spermatozoa were rarely recorded in the oviducal gland, indicating that this species does not store sperm. It was not possible to generate maturity curves for Iago omanensis but it was evident that females matured by the time they reached 35 cm and males were mature by 31 cm L _T. This species displayed a clearly defined reproductive cycle with parturition occurring primarily in spring, after a gestation period of c . 1 year. Maximal embryo size was 19 cm L _T while maximal litter size was 24 embryos. The oviducal gland appeared to act as a seminal receptacle and it appeared that females may utilize these stores by not mating every year.     

Reproductive biology and implications for management of the painted sweetlips Diagramma pictum in the southern Arabian Gulf

The reproductive biology of the painted sweetlips Diagramma pictum was determined from 487 individuals collected between January and December 2010 in the southern Arabian Gulf. There was no evidence of sex change and the combination of histological results with the sex composition of the size and age structures indicated a gonochoristic sexual pattern. There were peaks in gonado-somatic indices for females in March and October with spawning occurring during two seasons (April to May and November). The mean size and age at sexual maturity (L(m50) and A(m50) ) were 35·7 cm fork length (L(F) ) and 2·9 years for females and 26·7 cm L(F) and 0·5 years for males. The maximum recorded age (11 years) and small mean size and young age at sexual maturity for males may be a direct result of intensive demersal fishing in the southern Arabian Gulf. There was an exponential increase in the cumulative reproductive potential with size and a linear increase with age for both sexes. The mean L(F) (L(c50) ) at which D. pictum became vulnerable to capture was 33·3 cm, which corresponded to only 3 and 7% of the cumulative reproductive potential of males and females, respectively. Size-specific and age-specific reproductive potential indicated that conventional regulations that equate the mean size at first capture to sexual maturation are unsuitable for the management of D. pictum.     

Life-history patterns of the mosquito-fish, Gambusia affinis, in the estuary of the Guadalquivir river of south-west Spain

SUMMARY. 1. The age, growth and reproduction of the small, introduced fish Gambusia affinis (Baird & Girard, 1853) were studied in the estuary of the Guadalquivir river.
2. The life-span was very short, the stock contained only two age groups: with annulus (1+ group; 10–12 months old) and without annulus (0+ group).
3. In both sexes growth restarted in April when the annulus appeared, but whilst 1+ males stopped growth, 1+ females grew steadily to June. Growth of 0+ spawners was only evident in September, the last month of the reproductive period. A differential growth rate between sexes was also evident.
4. 1+ specimens reproduced during May and June and their offspring from July to September. In both age groups somatic condition progressively declined during the spawning period.
5. The loss of condition and the disappearance of 1 + and the larger 04-specimens after reproduction may indicate the cost of a prolonged high level of reproductive effort.
6. The total fecundity (taken as the number of embryos) of 1 + females was represented by the formula: Fec=5.08 T.L. (mm) -170.07 and that of 0+ specimens by: Fec=2.23 T.L. (mm) -42.92. The maximum average monthly fecundity was reached in June when the length of the mother was at its greatest.
7. Length at first maturity was smaller in 0+ group than in the 1 + group; the difference between the two groups was greater in males (≅5 mm, T.L.) than in females (≅3 mm, T.L.). Also the average total length of 14-spawners was greater than 0+ spawners. There were significant differences in the overall sex ratio of 956 males to 2057 females.
8. The differences found in growth and reproduction between the two age groups suggest that life-history tactics may vary not only between different stocks but also within the same stock among its different components.     

Reproductive biology of the crocodile shark Pseudocarcharias kamoharai

From February 2005 to September 2007, a total of 490 crocodile sharks Pseudocarcharias kamoharai, caught as by‐catch in the swordfish and tuna longline fishery that operates in the tropical western Atlantic Ocean, was studied in regard to their reproductive biology. Maximum observed total lengths (L_T) were 1220 and 1090 mm for females and males respectively, with a high proportion of the catch being composed of mature specimens. Sexual maturity was attained at 760–810 mm L_T for males (L_T50 = 800 mm) and 870–980 mm L_T for females (L_T50 = 916 mm). The size at birth was estimated at 415 mm L_T. Temporal variation in gonad morphology and mass suggests that in this region P. kamoharai, an aplacental viviparous species with oophagy, does not show a well‐defined reproductive seasonality, with mating and parturition occurring possibly over an extended period of the year. Mean ±s.d . fecundity was estimated to be 3·9 (± 0·6) pups per reproductive cycle.     

Infection of the gonads of Glaucosoma hebvaicum by the nematode Philometva lateolabracis: occurrence and host response

The prevalence of infection of the West Australian dhufish Glaucosoma hebraicum off the lower west coast of Australia by Philometra lateolabracis was greater among females than males, which contrasts with the situation with Pagrus auratus in waters off New Zealand. Live P. lateolabracis were represented solely by females and were found only in the gonads of fish of mature size ( L ₅₀ at first maturity = c . 300 mm) caught between December and April and thus during the spawning period of dhufish. Since the gonads were largest during that period, they, and particularly ovaries, would provide an abundant food source in the form of blood. The prevalence of the parasite (live + dead individuals) increased with host body size to reach a maximum of c . 80% in the 700–799 mm length class of females and c . 50% in the largest length class of males. During the spawning period of G hebraicum, P. lateolabracis developed from small, non-gravid females to large gravid females, representing an increase in mass of more than 200 times. The maximum length of P. lateolabracis (470 mm) in G hebraicum is the greatest yet recorded for this species. Gonadosomatic indices provided no evidence that infection by P. lateolabracis leads to a conspicuous atrophy of the ovaries, which contrasts with the situation with the gonads of some of the teleosts infected by Philometra species, and presumably reflects, in part, the small volume of the ovary occupied by P. lateolabracis (c . 3%) and the low intensity of infection (mean = 2.0, maximum = 7). Although the presence of live P. lateolabracis did not stimulate an obvious tissue response by the ovaries during the spawning period of G. hebraicum , both the dead and any live parasites that remain after spawning become encapsulated in fibrous tissue.     

Reproductive biology of Carcharhinus acronotus in the coastal waters of South Carolina

The reproductive biology of blacknose sharks Carcharhinus acronotus in the western North Atlantic Ocean was studied by examining specimens collected in the coastal waters of South Carolina. Males begin the maturation process between 875 and 910 mm fork length ( L _F), as indicated by the presence of functional claspers and siphon sacs. The presence of vitellogenic oocytes and developing oviducal glands and uteri indicated that females begin to mature at c . 870 mm L _F. Length at which 50% of the population reached maturity was 896 and 964 mm L _F, equivalent to 4·3 and 4·5 years, for males and females, respectively. Gonado‐somatic indices suggested that spermatogenesis and vitellogenesis began after December. Mating took place during the end of May and the beginning of June. Fertilization occurred during late June and early July, suggesting that female blacknose sharks were capable of sperm storage. Based on the timing of fertilization and occurrence of females carrying near‐term pups in late May and early June, the gestation period for blacknose sharks was c . 11 months. Female blacknose sharks reproduced biennially based on the absence of vitellogenic oocytes in near‐term females and there being no indication of vitellogenesis in postpartum females. Male blacknose sharks were capable of reproducing annually as indicated by turgid genital ducts, which were observed in all mature males collected during late May and early June.     

Reproductive biology of the freshwater goby Knipowitschia croatica Mrakovčić, Kerovec,Mišetić & Schneider 1996 (Actinopterygii,Gobiidae)

The reproductive biology and gonadogenesis cycle of the Vrgorac goby, Knipowitschia croatica is described [Conservation of Endangered Freshwater Fish in Europe, Birkhauser Verlag, Basel]. The species displays sexual dimorphism during the spawning period. Sexual maturity is achieved at an early age, with 50% of males and females sexually mature at total lengths of 40–45 mm. Fecundity of gravid females ranged from 188 to 593 eggs, with an egg diameter of 0.22–1.11 mm. Though the extended spawning period lasts from March to November, the highest intensity is observed from April to September. A comparison is made of the reproductive biology of this species with other sand goby species of the genera Knipowitschia and Pomatoschistus.     

Reproductive biology,multiple paternity and polyandry of the bull shark Carcharhinus leucas

To improve understanding of bull shark Carcharhinus leucas reproductive biology, we analysed reproductive traits from 118 bull sharks caught along Reunion Island coasts (Western Indian Ocean), including 16 gravid females. Specific microsatellite loci were used to investigate the frequency of multiple paternity. Males and females reached maturity at c. 234 cm and 257 cm total length (L_T), respectively, and litter sizes ranged from 5 to 14 embryos. Analysis of the 16 litters collected in various months of the year indicated that parturition occurs between October and December, with a size at birth c. 60–80 cm L_T and that the gestation period is probably c. 12 months. Assuming a 1 year resting period and a period of sperm storage (4–5 months) between mating (in June–September) and fertilisation, the reproductive cycle of bull sharks at Reunion Island would be biennial. At least 56.25% of the litters investigated were polyandrous, sired by 2–5 males. Several males that each sired several litters conceived during the same or distinct mating seasons were detected, suggesting both a seasonal aggregation of sharks to mate and some male fidelity to mating site. Altogether, these findings provide valuable information for both shark risk management and conservation of the species in the Western Indian Ocean.     

Size composition and reproductive cycle of Pseudupeneus grandisquamis (Pisces: Mullidae) in the Central Mexican Pacific

Size composition and reproductive cycle of Pseudupeneus grandisquamis (Pisces: Mullidae) in the Central Mexican Pacific. From June 1995 to December 1998 we used shrimp trawl nets to capture 492 Pseudupeneus grandisquamis in soft-bottom grounds off the central Mexican Pacific (Jalisco and Colima). The ength-weight ratio indicates allometric growth (p = 0.0035L(3.46) y r2 = 0.97). The total sex ratio was 1:1.15 (females: males). Mean total length was 153.8 mm (range 77-236 mm). A progression in length was found: the highest means were observed at the end of 1996 and during 1997. The mean length of females (162 mm) was longer than in males (150 mm). Four gonadic maturity stages were observed in both sexes; in females the most frequently stage was stage IV (mature gonads, 48.6%), while in males it was stage III (gonads in maturation, 45.0%). Seven microscopic oocyte development stages were identified. Oocyte development seems to be asynchronous. The mature testicle showed sperm inside the lobular lumen and in the duct. The highest values of the gonadosomatic index, as well as the largest percentages of individuals with mature gonads (at macroscopic and microscopic levels), were observed during winter and summer, suggesting that this species has two reproduction peaks by year. The length at which 50% of the individuals show gonads in maturation (L50) was 183 mm for the females and 181 mm for the males.     

Population structure and sexual maturity of Aegla castro (Decapoda,Anomura), an endemic freshwater crab from Brazil

Specimens of Aegla castro Schmitt, 1942 were monthly sampled from June 2012 to May 2013 from Couro stream (23°57′15″S 51°06′00″W), located in the Upper Paraná river region, southern Brazil. Population structure, morphometric and functional maturity were analyzed. Allometric growth analysis on chela dimension versus carapace length (CL) was employed to recognize juveniles and adult individuals. Two sequential groups of adult males (morphotypes I and II) were recognized according to the state of development of the pair of claws. The CL where 50% of the population of individuals are adults (CL₅₀) was used to estimate the size at the onset of morphometric maturity. Males attain morphometric maturity at same size class of females (8.0–9.0 mm CL). Males and females are heterochelous and they often show the left chela more developed. The reproductive period was extended from June to September 2012 and April to May 2013 (six months) with record of 22 ovigerous females. The recruitment occurred in the months following the reproductive period, with higher records in October and December 2012. All the information gathered here should be useful to better understand the biology of the species studied.     

Reproductive biology of the spotback skate Atlantoraja castelnaui in the south-west Atlantic Ocean

This study provides information on the reproduction of spotback skate Atlantoraja castelnaui. A total of 232 individuals (119 females and 113 males) were obtained from surveys carried out between 2003 and 2006, from the south-west Atlantic Ocean, between 34 and 42° S and <50 m deep; another 514 specimens (241 females and 273 males) were obtained between 2005 and 2007 from commercial fishery operations carried out in the same area and landings in the port of Mar del Plata, Argentina. Males ranged from 185 to 1250 mm total length (L(T) ) and females from 243 to 1368 mm L(T) . Length at maturity was estimated to be 980 mm for males and 1089 mm L(T) for females. Lack of variation of testis mass together with the continuous production of mature spermatocyst and spermatozoa in deferent ducts suggested that males can reproduce throughout the year. Females reproduced year-round with peaks of reproductive activity an integral part of a continuous cycle. This conclusion is corroborated by the seasonal variation of ovaries, oviducal gland and the occurrence of females with eggs in the uterus throughout the year. Results from this study indicate that A. castelnaui is very susceptible to fishery pressure.     

Seasonal dynamics in population characteristics of European bitterling Rhodeus amarus in a small lowland river

The seasonal dynamics of biological traits in a population of European bitterling Rhodeus amarus from a small river in central Europe (River Kyjovka, Czech Republic) were investigated from April 2007 to March 2008. The reproductive season lasted from early April to mid-June, with a peak in late April when > 50% of females possessed ripe eggs in their ovaries. The sex ratio was female-biased, with a higher bias following the peak in reproduction, suggesting higher mortality of males than females over the reproductive period. The population was effectively annual, with a major decrease in adult fish abundance at the end of the reproductive period. Highest relative lipid content and condition factor were observed in February, both decreasing with an increase in investment into gonads. Seasonal dynamics in somatic condition, relative lipid content and gonad mass, and their comparison with other R. amarus populations, suggest that the study population allocated a disproportionally high level of resources to reproduction.     

三峡水库秀丽白虾生长与繁殖生物学特征研究

2012 年11 月至2013 年10 月逐月对三峡水库木洞江段秀丽白虾的生长和繁殖生物学特征进行了研究。结果显示秀丽白虾是一年生的虾类, 寿命为1214 个月。雌性个体的平均体长(37.727.92) mm 显著大于雄性(37.086.59) mm, 具有明显的雌雄异形现象。秀丽白虾的渐近体长(L)为59.33 mm, 生长系数(K)是1.6/年, 生长方程为:Lt=59.33-e-1.6(t+0.081)。雌虾繁殖季节从4 月上旬持续至9 月下旬, 繁殖高峰期为4 月中旬至6 月中旬, 由越冬虾和当年虾两个世代的繁殖群体组成。抱卵雌虾的体长为27.0753.71 mm, 平均体长(L50)为37.06 mm。雌雄性比月变化为1.112.36, 平均为1.46, 群体中雌性个体数量显著多于雄性(P 0.001)。绝对繁殖力(FA)为31294 粒, 相对繁殖力(FR)为(11522)粒/g。绝对繁殖力与体长呈幂函数关系(FA=0.0031L2.8632, r=0.72, n=106), 而与体重呈直线关系(FA=104.63W+9.9534, r=0.79, n=106)。卵径(D)平均值为(1215102) m。为合理保护和利用三峡水库秀丽白虾种群资源, 建议加强虾类捕捞管理, 繁殖期间(49 月)禁止捕捞虾类或限制捕捞强度。       

Reproductive biology and population variables of the Brazilian sharpnose shark Rhizoprionodon lalandii (Müller & Henle, 1839) captured in coastal waters of south-eastern Brazil

Throughout 1 year, from October 2003 to September 2004, 88 visits to the landing site of a small urban fishery (APREBAN) in Rio de Janeiro city were conducted and 816 specimens of Rhizoprionodon lalandii were analysed. The sample, mostly females, was composed of two cohorts: young-of-the-year were abundant in spring and summer and adults predominated in autumn and winter. Gravid females were most abundant from April to June, whereas post-partum females composed most of the catch in August to September. Adult males were present all year although were more abundant between February and July. No neonates were captured during the study and most embryos collected measured slightly below the reported total length ( L _T) at time of birth ( L ₀) for the species, suggesting that parturition may occur slightly outside the main fishing grounds or that neonates were not captured in commercial gillnets set at this time of the year. The mean L _T at maturity ( L _T50) for males was 578 mm and females matured between 620 and 660 mm, although a precise estimate of L _T50 for females could not be determined. The total length ( L _T) and total mass ( M _T) relationship     was calculated for both sexes and showed no significant differences. The mean condition factor increased steadily from February to July followed by a steep decrease in values relative to females in August and September, suggesting a pupping season. The present study area can be classified as a coastal juvenile habitat and a probable mating ground for R. lalandii .