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1.
Tagging of Haliotis iris Martyn at colonies near low water, and subsequent regular observations over 18 months, showed that significant movement tended to occur only in autumn and winter when rough seas disturbed the habitat. These movements may vary from year to year depending on sea conditions. Tn contrast, subtidal colonies dispersed more gradually, seemingly disturbed by the tagging operation and subsequent rehandling. Other colonies which were not tagged remained apparently unchanged for up to 2 years. Individuals in subtidal H. australis Gmelin colonies also did not move to any great extent over this period: this species inhabits narrow crevices and appears to be a much more active animal than H. iris, both in the field and in the laboratory. Drift and attached algae were virtually absent from the crevices inhabited by H. australis and it seems likely that the species must forage to feed. A homing mechanism may be present because many older H. australis are found in deep scars on the rocks or have characteristically worn shell edges fitting the rock of their particular site.

A 24‐hour watch on a tagged, subtidal colony of Haliotis iris at Kaikoura showed that there was very little movement diurnally, and it seems likely that feeding is passive; drift algae are available at most times. No evidence of homing behaviour was detected.  相似文献   

2.
Mean gonad indices of Evechinus chloroticus (Val.) at Kaikoura and Kaiteriteri, South Island, New Zealand, increased during the winter and spring to reach peak values during the summer and then decreased to minimum values in autumn. There was only one major summer peak at Kaikoura, but two at Kaiteriteri. The maximum mean gonad index of Kaiteriteri specimens was little higher than the minimum at Kaikoura. Absolute size of gonads and spawn producton were also lower at Kaiteriteri, perhaps because of less food there.

At both localities gametogenic cycles were correlated with gonad index cycles, progressing from unripe to ripe from late autumn to spring, but Kaikoura urchins held ripe gametes over a longer period than Kaiteriteri urchins. The volume of spawn from females was greater than that from males but males had ripe gametes (and could be artificially induced to spawn) longer. At Kaikoura, some spawning probably occurred throughout summer with a major spawning in late summer or early autumn. Large urchins with small dark gonads were found throughout the year, particularly at Kaiteriteri; these were probably senile individuals.

Although at both localities Evechinus matured at 3–4 years, Kaikoura urchins were larger at maturity.

At Kaiteriteri sex ratios of mature Evechinus did not differ significantly from 1:1, but in some populations at Kaikoura males were significantly more prevalent than females.  相似文献   

3.
The diverse pelagic fish assemblage of sub-tropical southern Queensland includes fishes with predominantly temperate distributions, such as tailor Pomatomus saltatrix, sardine Sardinops sagax, round herring Etrumeus teres, and Australian anchovy Engraulis australis. The peak spawning seasons of P. saltatrix, S. sagax and E. teres occur during late winter and early spring (June–October). Eggs and larvae of these three species are widely distributed in shelf waters and comprise >50% of the ichthyoplankton assemblage during this period. Mean monthly sea surface temperatures (SSTs) during late winter and early spring range from 21 to 23 °C, and are thus similar to those recorded in southern Australia during summer and autumn, which is the spawning season of these three species in those temperate waters. E. australis eggs occur mainly in inshore waters, and comprise >50% of fish eggs collected during summer and autumn when mean monthly SSTs in southern Queensland exceed 27 °C. E. australis also spawns mainly during summer and autumn in temperate Australia. Hence, water temperature may be less important as a determinant of the spawning season of E. australis than it is for the other three species. The suitability of southern Queensland for spawning by predominantly temperate species during late winter and early spring may contribute to the high diversity of the region's pelagic fish assemblage. Adult P. saltatrix, S. sagax and E. teres appear to migrate northwards into southern Queensland during early winter to spawn, and larvae may be transported southwards into temperate waters by the East Australian Current. This dispersal-migration pattern is similar to those observed for several species, including P. saltatrix, in the western boundary current systems off the east coasts of North America and Africa. Hence, pelagic fishes in ecosystems off the east coast of three continents migrate into sub-tropical waters to spawn, and larvae are transported back into temperate nursery areas by the prevailing current.  相似文献   

4.
The New Zealand abalone fishery produces about 1200 t annually, mostly from southern New Zealand. The fishery, based on Haliotis iris, is managed over broad management areas within which fishing intensity is spatially dispersed. The size composition of the commercial catch depends on location within a management area but is similar for divers fishing individual populations of H. iris and reflects the size composition of natural populations. For most populations, length‐frequency distributions of abalone were normally distributed: the mean shell length of H. iris was found to vary within populations over small spatial scales (100s m). The relative abundance of juvenile H. iris was low in relation to adults suggesting, at least for exposed populations, that rates of recruitment to populations of H. iris may be low. The relative abundance and mean shell length of juveniles and adults of H. australis was much less than that of H. iris. The scarcity of H. australis and the lack of separate catch quotas for the two species are factors which explain the low to zero catch of H. australis. The spatial variation in the size composition of H. iris suggests that management would be more appropriate over spatial scales which reflect local populations rather than the large spatial areas which are used to manage the New Zealand abalone fishery.  相似文献   

5.
Growth rates of three species of abalone in New Zealand were estimated by fitting data to the von Bertalanffy growth equation. Length‐frequency analysis and tagging were used for Haliotis iris Martyn, and shell growth‐checks were used for H. australis Gmelin and H. virginea Gmelin. The relative growth coefficient (K) and the asymptotic length (L8) were found to be 0.3104 and 146.2 mm respectively for H. iris, 0.3205 and 86.75 mm for H. australis, 0.4460 and 61.5 mm, and 0.3231 and 64.4 mm for H. virginea from two separate localities. An absolute growth curve could be calculated only for Haliotis iris.  相似文献   

6.
Abstract

In September 1986, dense concentrations of freshly spawned hoki (Macruronus novaezelandiae) eggs were located in eastern Cook Strait. A follow‐up exploratory trawl survey of Cook Strait and the east coast of the South Island, in August and September 1987, located concentrations of spawning hoki in canyon features in Cook Strait, off the Kaikoura coast, and off Banks Peninsula. The largest concentration, 14 km long, 4 km wide, and up to 150 m thick occurred in Cook Strait Canyon, with catch rates of hoki up to 48 t h?1. Gonad conditions of male and female hoki showed they were actively spawning. Catch rates in Cook Strait Canyon were comparable to the main fishery on the west coast of the South Island but were much lower off Kaikoura and Banks Peninsula. Hoki associated with spawning concentrations were not feeding. Bycatch species were mostly ling (Genypterus blacodes) and spiny dogfish (Squalus acanthias), and both were preying on hoki. Spiny dogfish were also feeding on spawned fish eggs. The possible stock structure of hoki is discussed.  相似文献   

7.
Mustelus lenticulatus is a non‐placental ovoviviparous shark with a gestation period of about 11 months. Young are born at a total length of 30–32 cm from September to December. Copulation, and ovulation of a further set of eggs, rapidly follows parturition. Fecundity increases with the length of the female; the most eggs found in one female was 24; the mean for all females was 10.73.

Males mature at about 85 cm total length and females at 95 cm at Kaikoura. Nelson males probably mature at a smaller size than do Kaikoura males. Nelson females mature at about 85 cm. Maximum observed lengths were 137 cm for females and 115 cm for males.  相似文献   

8.
Twelve Galaxias postvectis (shortjaw kokopu) and four G. fasciatus (banded kokopu) spawning sites were found on the margins of the Katikara Stream, Taranaki, New Zealand. This is the first time G. postvectis spawning sites have been documented. G. fasciatus spawning sites discovered in this study confirm previous observations elsewhere in New Zealand. These spawning sites were all found out of water, variable distances from the base flow water level amongst stony substrate, vegetation, and debris. Most G. fasciatus appeared to lay their eggs, and subsequently hatch, c. 3 weeks earlier than G. postvectis, which spawned from 9 to 17 May 2001. G. brevipinnis (koaro) larvae were also identified drifting downstream in late May and mid June 2001. Deposition of eggs and subsequent hatching were found to be associated with elevated flows.  相似文献   

9.
Larvae of Boccardia knoxi (Rainer) were reared in the laboratory after dissection from brood capsules extracted from the outer shell and perio‐stracum of Cookia sulcata and Haliotis iris collected from Tasman Bay, New Zealand. All the eggs within each brood capsule developed into embryos. The dissected larvae had provisional setae and fed on phytoplankton. Larval development is described through to metamorphosis.  相似文献   

10.
Seasonal dynamics and feeding of scyphomedusae, Aurelia aurita, were investigated monthly from 1999 to 2002 in relation to environmental conditions in Tapong Bay, a eutrophic tropical lagoon in southwestern Taiwan. Medusae appeared throughout the year but exhibited seasonal dynamics that were correlated with hydrographic features in the bay. Most ephyrae of A. aurita occurred mainly in the lower flushed and eutrophic inner bay, and during the cold, dry season between November and February. They grew to young medusae with a maximum abundance in spring (March–May), but their numbers abruptly decreased during the warm and rainy summer season in June–September. The remaining medusae then grew rapidly to a maximal size of 29 cm. Mature females spawned in the following autumn when precipitation decreased but zooplankton food was still abundant. These mature individuals decreased in size after spawning and in winter. Gut content analysis revealed that A. aurita fed mainly on copepods and copepod nauplii and less on bivalve larvae and fish eggs. Prey selectivity indices indicated that larger medusae selected positively for copepods while small size medusae preferred copepod nauplii. The overall feeding effect of A. aurita on the standing stock of zooplankton was significant (27%) in the bay. Our results suggest that tidal flow and dense oyster culture pens were the two most important factors influencing the spatial distribution pattern of A. aurita in the bay, while precipitation affected the population abundance seasonally; decreasing water temperature coincided with the mass release of ephyra in late autumn and winter.  相似文献   

11.
Discovery that the subarctic Pacific copepods previously grouped as Neocalanus plumchrus belong to two species required reanalysis of the life histories of both. After correction of the abundance estimates for N. plumchrus s.str., our concept of its life history remains much as previously described, because it makes up about 90% of the summed populations. Fifth copepodites of the new species, Neocalanus flemingeri, descend from the surface layer in late May to early June and mature immediately. Males are only present for about two months, and females carrying spermatophores are found during that period. Throughout the summer and autumn the entire population is constituted of females with small, dormant ovaries. This appears to be a diapause phase. Ovarian development begins in November, and spawning occurs at the end of January. Copepodite stages develop in surface layers from February through May.  相似文献   

12.
Life histories for the dominant, larger copepods of the subartic Pacific have been constructed by sampling from weatherships patrolling Ocean Station P (50°N, 145°W) during 1980 and 1981. Neocalanus plumchrus reproduced at depths below 250 m from July through February. Copepodite stages were present in surface layers from October through August with a large peak in numbers and biomass in spring. Fifth copepodites prepared for diapuse in 38 days during spring and descended to depths below 250 m. They commenced immediately to mature, and the females reproduced without renewed feeding. This schedule contrasts with that of the population in the Strait of Georgia, which remains in diapause from July to January and matures exclusively in January and February. There appears to be a difference between the coastal and oceanic habitats in preparing the diapausing individuals for maturation.Maturation of the diapausing stock of N. plumchrus maintained constant adult populations, averaging 714 males m?2 from June through October and 1,434 females m?2 from August through January. This constancy, together with the exponential pattern of decline in the diapause stock from September through February, suggests that density of adults may regulate maturation of fifth copepodites. Offspring of individuals delaying maturation and, thus, reproduction would benefit from the resulting moderation of intraspecific competition, probably that among copepodites.Reproduction of Neocalanus cristatus also occurred below 250 m, and, while spawning was continuous through the year, there was a substantial peak in November. That resulted in a peak of abundance for early copepodite stages in mid-winter, and a peak for the fifth copepodite stage in June. Stocking of the population of fifth copepodites in diapause below 250 m occurred from July through October. Some fifth copepodites were present in surface layers through the entire summer, and some younger copepodites persisted through the summer in progressively declining abundance just below the mixed layer. In autumn 1980 resurgence of early copepodite populations was rapid, occurring during the course of a prolonged October storm. The storm may have improved the habitat either by cooling the mixed layer or by resupplying nutrients to the euphotic zone.Eucalanus bungii reproduced in the mixed layer in early May and in early July. The first event was a spawning by females that had previously spawned in 1979 and then had returned to diapause. The second, heavier spawning (more females, more eggs per female) was by newly matured females from stocks that had overwintered as fifth copepodites. Nauplii peaked sharply in abundance on 19 July, one week after the peak in spawning. First and second copepodites peaked on 1 August, and all had advanced to the third copepodite stage by September. The diapause stock was established by September, principally between 250 and 500 m, and consisted of copepodite stages from third to sixth. Duration of the E. bungii life cycle appears to be typically two years. New nauplii develop as far as the third or fourth copepodite stage during their first summer, then enter diapause. The second summer they advance to the fifth copepodite stage and reenter diapause. Fifth copepodites mature in their third summer at two years of age. The males remain at depth and mate without subsequent feeding. Females migrate at night to the mixed layer where spawning occurs. About 20% of females that had already spawned in 1980 reentered diapause. They would reproduce again in their fourth summer at three years of age. All aspects of the life cycle suggest low mortality rates for copepodite stages, particularly at depth in the habitat occupied during diapuse. There can be no premium on rapid reproduction for E. bungii in the subartic Pacific, and there must even be benefit from spreading reproduction between years. This iteroparity may amount to a “bet-hedging” tactic, the young from a given mother having more than one chance to find sustaining conditions. It also produces gene flow between the year classes of the biennial life cycle.  相似文献   

13.
Spawning grounds and spawning times of the sand flounder, Rhombosolea plebeia (Richardson), and the yellow‐belly flounder, Rhombosolea leporina Gunther, in the Hauraki Gulf are described. The occurrence of female fish at different stages of ovarian development at different stations during the year, the distribution of eggs in the plankton, and changes in ovary weight during the year were used as indicators of spawning grounds and spawning times.

The sand flounder was found to spawn in the waters to the east of Waiheke and Ponui Islands, at the northern end of the Firth of Thames, from June to November.

Yellow‐belly flounders spawned during September, October, and November, slightly to the south of the sand flounder spawning grounds in a belt extending from Tapu, on the eastern side of the Firth of Thames, north‐westwards towards Ponui Island.

Fecundity of both species was approximately proportional to the weight of the fish, or to the length cubed, and less than proportional to the ovary weight. The mean fecundity of sand flounders in the Hauraki Gulf varied from approximately 100,000 eggs in a fish of 18 cm to 500,000 in a 30 cm fish. That of yellow‐belly flounders varied from approximately 250,000 eggs in a fish of 30 cm to 1.25 million in a 45 cm fish.  相似文献   

14.
Two experiments were performed to assess the effect of photoperiod and temperature on spawning of Panulirus ornatus. In experiment 1, sexually mature lobsters taken from the wild during summer were held at one of two photoperiods, winter (13 Light: 11 Dark) and summer (14.5 Light:9.5 Dark). Additionally, lobsters were also exposed to either summer (29°C) or winter (24°C) average water temperatures. Spawning was significantly greater when animals were exposed to summer photoperiod than to winter photoperiod, irrespective of temperature. Although a higher percentage of lobsters spawned when placed under a higher temperature, this trend was not statistically significant. In experiment 2, sexually mature lobsters were taken from the wild during winter and exposed to the same two photoperiods as in experiment 1, at a summer equivalent temperature of 29°C. Breeding started earlier and was more successful at the summer photoperiod. Time to first breeding was 17 weeks after exposure to summer photoperiod, compared with less than 1 week in experiment 1, and did not occur until individuals had moulted. Moulting occurred in 81% of lobsters, primarily after an increase in temperature to 29°C. The time between moulting and mating was varied and there was no significant difference in moult frequency between the two experimental photoperiods. After the lobsters had moulted, breeding success was reached earlier if photoperiod was lengthened. Results suggest photoperiod is the primary cue for the onset of gonad maturity and mating activity, with temperature playing a less important role. Physiological rest and possibly a moult may be required between breeding seasons before spawning can occur. Furthermore, temperature may be an important cue for pre‐reproduction moulting.  相似文献   

15.
A spawning site of Galaxias brevipinnis Giinther was located in a New Zealand stream for the first time. It was at the edge of a riffle and only partially submerged. The habitat used for spawning matched that described for G. brevipinnis in Australia. Spawning was estimated to have occurred between late April and early May and the eggs hatched in late May. The species of fish spawning was identified by rearing the eggs through to identifiable juveniles and by DNA sequencing of one individual.  相似文献   

16.
Seasonal changes in ovarian activity were investigated in New Zealand turbot Colistium nudipinnis (Waite 1910) and brill Colistium guntheri (Hutton 1873), collected by commercial trawlers along the west coast of the South Island of New Zealand. Both species demonstrated group synchronous oocyte development, with a capacity for multiple ovulations within a reproductive season. During a 17‐h trawl survey, ovulated turbot were caught between 1500 and 2030 h, indicating a daily spawning rhythm. The turbot and brill spawning seasons were prolonged (late autumn to mid summer). A protracted spawning season confers some advantages in aquaculture.  相似文献   

17.
A population model is developed and used in conjunction with the results of a study of an unexploited population of paua (Haliotis iris Martyn) to examine the historical pattern of recruitment and yield per recruit. As H. iris cannot yet be aged, the population model uses size rather than age classes, but is structurally similar to the Leslie matrix model. Simulations suggest that the observed population size structure resulted from a short (about 5 year) period of high recruitment, preceded and followed by longer periods of low recruitment. Yield per recruit analysis shows that the present minimum legal size for the fishery (127 mm) provides close to the maximum yield per recruit for most stocks, although yield per recruit could be increased in some areas by a reduction in minimum legal size.  相似文献   

18.
The reproductive biology of a shelf morid, red cod (Salilota australis) was investigated in the Falkland Islands, in order to expand our knowledge of the reproductive strategy of this relatively unstudied family of fishes. Red cod spawn to the south and south-west of West Falkland between August and October. Length frequency and sex ratio data suggest that females arrive at the spawning grounds first. The greatest spawning activity occurred in early evening and this timing may be an adaptation to reduce predation on eggs. Ripe egg size varied from 0.95 to 1.26 mm and was not dependant on female size. There was no regulative atresia during maturation and the formation of fecundity and fecundity increased with increasing fish total length (LT) from 300,000 (42-45 cm LT) to 4.5-9.0 million eggs (75-83 cm LT). The fecundity of most of the population was between 2 and 5 million eggs. Red cod releases small batches of eggs over the spawning period. Batch size ranged from 30,000-90,000 (39-42 cm LT) in smaller animals to 400,000-800,000 (>75 cm LT) in larger animals and the batch size of first spawners was significantly higher than for advanced spawners. The study allows us to discuss the evolutionary relationships between the Gadiformes.  相似文献   

19.
Spawning, phases of embryonic development, intracapsular feeding mechanism and development mode of banded murex Hexaplex trunculus (Linnaeus, 1758) were examined using specimens from the Aegean Sea. In addition, the numbers and characteristics of non‐viable nurse eggs during different phases were examined in relation to the development phases of viable embryos. Females spawned between 59 and 162 egg capsules containing 306.76 ± 50.74 eggs. Trochophore larvae first appeared on the 15th day after spawning. Nurse egg consumption began on the 17th day after spawning when the embryos reached the early veliger stage. In the beginning, veligers consumed the nurse eggs by mechanically disintegrating them with velar cilia movement. From the 18th day after spawning, embryos began to consume whole nurse eggs, although mechanical disintegration continued until hatching. Viable embryos consumed the most developed nurse eggs first. The average number of nurse eggs consumed per embryo was 24.67 by the end of the intracapsular period. The average number of hatchlings was 11.95 ± 3.81 per capsule with 1321.48 ± 133.1 μm shell length. According to our observations H. trunculus shows dispersal polymorphism, with most of the hatchlings completing metamorphosis after a short planktonic non‐feeding period (up to 2 days), while others metamorphose prior to hatching. Planktonic hatchlings had both foot and well developed four‐lobed velum and minimum 1 3/4 whorls. Both hatchling types could be seen in the capsule mass from the same female.  相似文献   

20.
Seasonal trends in spawning, derived from ovary-weight data of four length classes of pilchard Sardinops ocellatus, are compared. Ovary-weight data were obtained from some 9 000 females collected between June 1973 and September 1974. The number of ovaries beyond the commencement of hydration was used to estimate the incidence of advanced ovaries. There were peaks in the incidence of advanced ovaries during both spring and summer for all four length classes, and the lowest incidence was during late autumn and early winter. Spawning incidence was high over a longer period during summer 1973/74 than during spring 1973. The reproductive potential for the entire spawning season (the total number of spawnings) of the larger length classes was considerably more than that of the smaller ones, the increase in the number of spawnings being about 50–70 per cent for each 1-cm increase in length.  相似文献   

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