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Spawning Behaviour (spawning + behaviour)
Selected AbstractsSpawning behaviour, early development and first feeding of the bluestriped angelfish [Chaetodontoplus septentrionalis (Temminck & Schlegel, 1844)] in captivityAQUACULTURE RESEARCH, Issue 9 2010Ming-Yih Leu Abstract Successful natural spawning of Chaetodontoplus septentrionalis in captivity from 19 March to 11 May, 2008 is described for the first time. A single male dominates a harem of two females, spawning with each at dusk, from 10 min before to 20 min after sunset. Each female laid an average 119 × 103 eggs during the spawning period. Fertilized eggs were spherical, buoyant and had a diameter of 0.83 ± 0.02 mm (mean ± SD). Embryonic development lasted 15,18 h at 28.1 °C. Newly hatched larvae were 1.60 ± 0.07 mm in total length (TL) with 27 myomeres. Larvae completed yolk absorption within 3 days post hatching (ph) at 3.01 ± 0.08 mm TL. Ten days ph, the larvae had attained 3.95 ± 0.12 mm TL. Larvae were fed either 100% s-type rotifers (Brachionus rotundiformis), 100% copepods (Microsetella sp.), a combination of the two (50%:50%) or without live feed (starved control) to determine the effect of live feed on the survival rate. The survival was significantly (P<0.001) higher in larvae fed a combination of diet than the others. These results indicate that C. septentrionalis is a potential species for captive breeding programs and the use of a combination of diet (s-type rotifers and copepods) may be a suitable first food for the larvae. [source] Spawning site selection by Eurasian perch (Perca fluviatilis L.) in relation to temperature and wave exposureECOLOGY OF FRESHWATER FISH, Issue 1 2009W. N. Probst Abstract,,, The selection of spawning depth by Eurasian perch Perca fluviatilis was investigated in an experiment using artificial substrata in Lake Constance during the spawning season of 2007. The experiment compared spawning behaviour at substrata between 0.5 and 15 m depth at two sites exposed to different regimes of ship-generated wave action. The total abundance of egg ribbons did not differ significantly between the two sites, but the preferred spawning depth was deeper at the wave exposed site (5 m) compared to the sheltered site (2 m). While water temperatures could not account for the observations, differences in wave exposure may explain the different spawning depth preferences. At both sites, large egg ribbons were generally found in deeper water, and large egg ribbons occurred more frequently at the sheltered site. Because the egg ribbons of perch are likely to have a size-dependent susceptibility to hydrodynamic stress, large females may be expected to select deeper spawning locations where the effects of surface waves are considerably attenuated. [source] Reproduction biology of pikeperch (Sander lucioperca (L.)) , a reviewECOLOGY OF FRESHWATER FISH, Issue 2 2003J. Lappalainen Abstract,,, The present review focuses on the reproduction biology of pikeperch (Sander lucioperca (L.)). Aspects like maturity, fecundity, spawning migrations, spawning habitats, onset of spawning, and development time of eggs were reviewed. The onset of maturity is reached at younger age in southern than northern populations due to higher growth rate in the south. Males mature at smaller size and are on average younger than females. Absolute fecundity is closely related to the length and weight, but no clear relationship could be found between relative fecundity and length. Statistically significant relationships were found between the onset of spawning and latitude, and between the duration of the development time of eggs and stable water temperature. Near the southern limits of distribution, the onset of spawning is in February while near the northern limits it is in June. The interannual variability in fecundity and in the onset of maturity and further the factors affecting them have not been studied much. Furthermore, it is not known whether these variations could affect the population dynamics of pikeperch. Little is also known about the actual spawning behaviour of pikeperch in natural habitats. This is probably due to the typical spawning habitats located at 1,3 m depth in waters with high turbidity and low visibility. Even though the homing behaviour to the same spawning areas is well developed in adults, it is not known whether the adults were actually born in the same area. [source] The influence of environment and spawning distribution on the survival of anchovy (Engraulis encrasicolus) larvae in the Bay of Biscay (NE Atlantic) investigated by biophysical simulationsFISHERIES OCEANOGRAPHY, Issue 6 2007GWENHAEL ALLAIN Abstract A growth and survival model of the early life stages was run along virtual drift trajectories tracked in a hydrodynamic model to simulate the annual recruitment process of anchovy (Engraulis encrasicolus) in the Bay of Biscay (NE Atlantic). These biophysical simulations concerning three different years were analysed in order to investigate the influence of environment and spawning dynamics on the survival of larvae and juveniles. The location of space,time survival windows suggested major environmental mechanisms involved in simulated recruitment variability at the different scales , retention of larvae and juveniles in favourable habitats over the shelf margins and turbulence effects. These small-scale and meso-scale mechanisms were related to the variations in wind direction and intensity during spring and summer. Survival was also variable according to the origin of the drift trajectories, that is spawning distribution in space and time. The observed spawning distribution (according to field surveys) was compared with the spawning distribution that would maximize survival (according to the biophysical model) on a seasonal scale, which revealed factors not considered in the biophysical model (e.g. spawning behaviour of the different age classes). The variation of simulated survival according to spawning distribution was examined on a multi-annual scale and showed a coherent pattern with past and present stock structures. The interaction processes between the population (influence on spawning) and its environment (influence on survival) and its implications on recruitment and stock dynamics are discussed. [source] A link between sound producing musculature and mating success in Atlantic codJOURNAL OF FISH BIOLOGY, Issue 3 2008S. Rowe Individual variability in the mating success of male Atlantic cod Gadus morhua was quantified within an aggregation (n= 59) breeding undisturbed in a large (684 m3) mesocosm tank. Observational and morphometric data were examined to assess the degree to which this mating variation could be explained by aspects of morphology, condition and spawning behaviour. The number of ventral mounts initiated (i.e. mating success) was highly variable; most mounts were initiated by a very small percentage of available males. The significant correlate of male mating success was mass of the sound producing musculature, i.e. drumming muscles. Neither body size, condition, pelvic and median fin morphology nor aggression influenced the number of ventral mounts initiated by a male. The present study suggests a possible link between sound production and mating success in Atlantic cod. [source] Reproductive behaviour of a temperate serranid fish, Paralabrax clathratus(Girard), from Santa Catalina Island, California, U.S.A.JOURNAL OF FISH BIOLOGY, Issue 1 2006B. E. Erisman The reproductive behaviour of the kelp bass Paralabrax clathratus was studied on Santa Catalina Island, California, U.S.A. from April 2000 to September 2002. Adults formed aggregations of three to > 200 individuals, and spawning occurred within subgroups of three to 23 individuals that contained a single female. The gonado-somatic index (IG) of collected ripe males (mean = 5·8%, range = 0·5,13·1%) indicated a large investment in sperm production that is common in group-spawning fishes characterized by intense sperm competition. Spawning occurred 32 min before sunset to 120 min after sunset, and both males and females were capable of spawning multiple times during a single evening. Behavioural observations of adults and estimates of spawning periodicity from the collection of females with hydrated oocytes suggested that spawning occurred continuously throughout the summer months and showed no significant relationship with the lunar cycle. In general, the spawning behaviour of kelp bass was similar to other functionally gonochoric, group-spawning serranids. The dynamics of P. clathratus spawning aggregations, however, were inconsistent with that of tropical reef fish spawning aggregations, including the transient spawning aggregations of some tropical serranids. Aggregation spawning appeared to be an important component of the annual reproduction of this species. [source] Variation of reproductive behaviour and success of males adopting different tactics in Atlantic salmonJOURNAL OF FISH BIOLOGY, Issue 2003B. De Gaudemar Six males and five females anadromous Atlantic salmon were released in two sections of the Lapitxuri experimental stream (Southwest France), where they could reproduce naturally. Females had all the same size and age, contrary to males. We focussed our attention on the variation with time of spawning tactics and success of males. Two factors affected male spawning behaviour in the short term. An increase of the OSR increased the level of male competition around redds which resulted in a larger number of males adopting sneaking rather than fighting tactics. Changes in female activities also seemed to be detected by males, since male aggressiveness increased when females were close to oviposition. But whatever their activities, males preferentially courted the earlier spawning female when two females were active at the same time. Fighting in males was confirmed to be the most successful tactic at a given time. However, males adopting sneaking tactic at the beginning of the spawning season could dramatically increase their reproductive success in the long-term. Fighting males invested much more energy in contests than secondary males, which may constitute a handicap in terms of longevity. They could quickly lose their status or strength with time which, although placed in a situation of high OSR, resulted in greater numbers of previously low-ranking males adopting satellite and fighting tactics during the period preceding oviposition. Age more than size affected male status and reproductive success. Females seemed to select their mate directly in relation to their physiological condition, since they only attacked dull coloured males showing obvious wound marks. They also could indirectly choose their mate by repeatedly leaving the redd during the period preceding oviposition in a situation of high OSR. This behaviour might incite male competition and also promoted, by incessant attempts of secondary males to rob the more successful status of primary males, their chance to spawn with fitter males. These results emphasized the importance of environment, physiological condition and energy expenditure in allocation tactics and variations in salmon reproductive success throughout the spawning season. This led us to hypothesize that the choice of sneaking through conditional strategies might provide greater average fitness in salmon alternative life histories. [source] Spatial partitioning and asymmetric hybridization among sympatric coastal steelhead trout (Oncorhynchus mykiss irideus), coastal cutthroat trout (O. clarki clarki) and interspecific hybridsMOLECULAR ECOLOGY, Issue 9 2004CARL O. OSTBERG Abstract Hybridization between sympatric species provides unique opportunities to examine the contrast between mechanisms that promote hybridization and maintain species integrity. We surveyed hybridization between sympatric coastal steelhead (Oncorhynchus mykiss irideus) and coastal cutthroat trout (O. clarki clarki) from two streams in Washington State, Olsen Creek (256 individuals sampled) and Jansen Creek (431 individuals sampled), over a 3-year period. We applied 11 O. mykiss -specific nuclear markers, 11 O. c. clarki -specific nuclear markers and a mitochondrial DNA marker to assess spatial partitioning among species and hybrids and determine the directionality of hybridization. F1 and post-F1 hybrids, respectively, composed an average of 1.2% and 33.6% of the population sampled in Jansen Creek, and 5.9% and 30.4% of the population sampled in Olsen Creek. A modest level of habitat partitioning among species and hybrids was detected. Mitochondrial DNA analysis indicated that all F1 hybrids (15 from Olsen Creek and five from Jansen Creek) arose from matings between steelhead females and cutthroat males implicating a sneak spawning behaviour by cutthroat males. First-generation cutthroat backcrosses contained O. c. clarki mtDNA more often than expected suggesting natural selection against F1 hybrids. More hybrids were backcrossed toward cutthroat than steelhead and our results indicate recurrent hybridization within these creeks. Age analysis demonstrated that hybrids were between 1 and 4 years old. These results suggest that within sympatric salmonid hybrid zones, exogenous processes (environmentally dependent factors) help to maintain the distinction between parental types through reduced fitness of hybrids within parental environments while divergent natural selection promotes parental types through distinct adaptive advantages of parental phenotypes. [source] Oceanic migration and spawning of anguillid eelsJOURNAL OF FISH BIOLOGY, Issue 9 2009K. Tsukamoto Many aspects of the life histories of anguillid eels have been revealed in recent decades, but the spawning migrations of their silver eels in the open ocean still remains poorly understood. This paper overviews what is known about the migration and spawning of anguillid species in the ocean. The factors that determine exactly when anguillid eels will begin their migrations are not known, although environmental influences such as lunar cycle, rainfall and river discharge seem to affect their patterns of movement as they migrate towards the ocean. Once in the ocean on their way to the spawning area, silver eels probably migrate in the upper few hundred metres, while reproductive maturation continues. Although involvement of a magnetic sense or olfactory cues seems probable, how they navigate or what routes they take are still a matter of speculation. There are few landmarks in the open ocean to define their spawning areas, other than oceanographic or geological features such as oceanic fronts or seamounts in some cases. Spawning of silver eels in the ocean has never been observed, but artificially matured eels of several species have exhibited similar spawning behaviours in the laboratory. Recent collections of mature adults and newly spawned preleptocephali in the spawning area of the Japanese eel Anguilla japonica have shown that spawning occurs during new moon periods in the North Equatorial Current region near the West Mariana Ridge. These data, however, show that the latitude of the spawning events can change among months and years depending on oceanographic conditions. Changes in spawning location of this and other anguillid species may affect their larval transport and survival, and appear to have the potential to influence recruitment success. A greater understanding of the spawning migration and the choice of spawning locations by silver eels is needed to help conserve declining anguillid species. [source] | |||||||||||||