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Spawning Areas (spawning + area)
Selected AbstractsUse of GIS to predict effects of water level on the spawning area for smelt, Retropinna retropinna, in Lake Taupo, New ZealandFISHERIES MANAGEMENT & ECOLOGY, Issue 4 2002D. K. ROWE A GIS model of the littoral bathymetry and substrate composition of Lake Taupo was created using ArcInfo. Littoral substrates were mapped by aerial photography and confirmed by ground-truthing. Water depths were determined by echosounding linked to a differential GPS. These data were imported into ArcInfo where a 3D GIS model was used to calculate the total area of smelt, Retropinna retropinna Richardson, spawning habitat (i.e. clean sand between depths of 0.5,2.5 m) at each of five lake levels. There was little change in area over the first 50 cm below the natural maximum lake level, but spawning habitat decreased rapidly over the next 1.4 m such that a 30% reduction occurred at the natural minimum level. Anecdotal information on inter-annual variations in lake level and smelt abundance supported the notion that high lake levels in spring result in high recruitment of smelt. The GIS model also predicted effects of lake level change on areas of macrophyte cover and on other littoral substrates, and could be used to assess effects of lake level changes on the habitats of other biota. [source] Growth and movement patterns of early juvenile European anchovy (Engraulis encrasicolus L.) in the Bay of Biscay based on otolith microstructure and chemistryFISHERIES OCEANOGRAPHY, Issue 3 2010NAROA ALDANONDO Abstract Various hypotheses have been put forward to explain the mechanisms in the Bay of Biscay that result in a good recruitment of European anchovy. Anchovy larvae from the spawning area in the Gironde River plume are advected towards off-shelf waters, where juveniles are commonly observed. Otolith microstructural and chemical analysis were combined to assess the importance of this off-shelf transport and to determine the relative contribution of these areas for anchovy survival. Chemical analysis of otoliths showed that anchovy juveniles in the Bay of Biscay can be divided into two groups: a group that drifts towards off-shelf waters early in their life and returns later, and a group that remains in the low salinity waters of the coastal area. The first group presents significantly faster growth rates (0.88 mm day,1) than those remaining in the coastal waters (0.32 mm day,1). This may be due to off-shelf waters being warmer in spring/summer, and to the fact that the lower food concentration is compensated for by higher prey visibility. Furthermore, the group of juveniles that drifted off the spawning area and had faster growth rates represents 99% of the juvenile population. These findings support the hypothesis that anchovy in the Bay of Biscay may use off-shelf waters as a spatio-temporal loophole, suggesting that transport off the shelf may be favourable for recruitment. [source] Ichthyoplankton-based spawning dynamics of blue mackerel (Scomber australasicus) in south-eastern Australia: links to the East Australian CurrentFISHERIES OCEANOGRAPHY, Issue 4 2008FRANCISCO J. NEIRA Abstract We describe findings of three ichthyoplankton surveys undertaken along south-eastern Australia during spring (October 2002, 2003) and winter (July 2004) to examine spawning habitat and dynamics of blue mackerel (Scomber australasicus). Surveys covered ,860 nautical miles between southern Queensland (Qld; 24.6°S) and southern New South Wales (NSW; 41.7°S), and were mainly centred on the outer shelf including the shelf break. Egg identifications were verified applying mtDNA barcoding techniques. Eggs (n = 2971) and larvae (n = 727; 94% preflexion) occurred both in spring and winter, and were confined to 25.0,34.6°S. Greatest abundances (numbers per 10 m2) of eggs (1214,7390) and larvae (437,1172) occurred within 10 nm shoreward from the break in northern NSW. Quotient analyses on egg abundances revealed that spawning is closely linked to a combination of bathymetric and hydrographic factors, with the outer shelf as preferred spawning area, in waters 100,125 m deep with mean temperatures of 19,20°C. Eggs and larvae in spring occurred in waters of the East Australian Current (EAC; 20.6,22.3°C) and mixed (MIX; 18.5,19.8°C) waters, with none occurring further south in the Tasman Sea (TAS; 16.0,17.0°C). Results indicate that at least some of the south-eastern Australian blue mackerel stock spawns during winter-spring between southern Qld and northern NSW, and that no spawning takes place south of 34.6°S due to low temperatures (<17°C). Spawning is linked to the EAC intrusion, which also facilitates the southward transport of eggs and larvae. Since spring peak egg abundances came from where the EAC deflects offshore, eggs and larvae are possibly being advected eastwards along this deflection front. This proposition is discussed based on recent data on blue mackerel larvae found apparently entrained along the Tasman Front. [source] Fluctuations in European eel (Anguilla anguilla) recruitment resulting from environmental changes in the Sargasso SeaFISHERIES OCEANOGRAPHY, Issue 1 2008SYLVAIN BONHOMMEAU Abstract European eel decline is now widely observed and involves a large number of factors such as overfishing, pollution, habitat loss, dam construction, river obstruction, parasitism and environmental changes. In the present study, we analyzed the influence of environmental conditions in the Sargasso Sea and Atlantic ocean circulation on European glass eel recruitment success. Over a recent 11-yr period, we showed a strong positive correlation between an original index of glass eel recruitment and primary production (PP) in eel spawning area. Moreover, PP was negatively correlated with temperature in the Sargasso Sea. Therefore, we used sea temperature as an inverse proxy of marine production. A close negative relationship has been found over the last four decades between long-term fluctuations in recruitment and in sea temperature. These findings were reinforced by the detection of a regime shift in sea temperature that preceded the start of the decline in glass eel recruitment in the early 1980s. By contrast, variations in integrative indices measuring ocean circulation, i.e. latitude and strength of the Gulf Stream, did not seem to explain variations in glass eel recruitment. Our results support the hypothesis of a strong bottom-up control of leptocephali survival and growth by PP in the Sargasso Sea on short and long time scales. We argue that sea warming in the eel spawning area since the early 1980s has modified marine production and eventually affected the survival rate of European eels at early life stages. [source] Advection of anchovy (Engraulis encrasicolus) larvae along the Catalan continental slope (NW Mediterranean)FISHERIES OCEANOGRAPHY, Issue 2 2007A. SABATÉS Abstract The Gulf of Lions is one of the main anchovy (Engraulis encrasicolus) spawning areas in the NW Mediterranean. During the spring, low-salinity surface water from the outflow of the Rhône is advected by the shelf-slope current along the continental slope off the Catalan coast. In June 2000, a Lagrangian experiment tracking these low-salinity surface waters was conducted to assess the importance of this transport mechanism for anchovy larvae and to determine the suitability of the tracked surface waters for survival of anchovy larvae. The experiment consisted of sampling the tracked water parcel for 10 days with three drifters launched at the core of the shelf-slope current where low-salinity surface waters were detected. The survey was completed by sampling the surrounding waters. Anchovy larvae from the spawning area in the Gulf of Lions were advected towards the south in the low-salinity waters. The size increase of anchovy larvae throughout the Lagrangian tracking closely followed the general growth rate calculated by otolith analysis (0.65 mm day,1). However, advection by the current was not the only mechanism of anchovy larval transport. A series of anticyclonic eddies, originated in the Gulf of Lions and advected southwards, seemed to play a complementary role in the transport of larvae from the spawning ground towards the nursery areas. These eddies not only contributed to larval transport but also prevented their dispersion. These transport and aggregation mechanisms may be important for anchovy populations along the Catalan coast and require further study. [source] Modelling the effect of buoyancy on the transport of anchovy (Engraulis capensis) eggs from spawning to nursery grounds in the southern Benguela: an IBM approachFISHERIES OCEANOGRAPHY, Issue 3 2003C. Parada Abstract An individual-based model (IBM) was used to investigate the effects of physical and biological variables on the transport via a jet current of anchovy (Engraulis capensis) eggs from spawning to the nursery grounds in the southern Benguela ecosystem. As transport of eggs and early larvae is considered to be one of the major factors impacting on anchovy recruitment success, this approach may be useful to understand further the recruitment variability in this economically and ecologically important species. By coupling the IBM to a 3D hydrodynamic model of the region called Plume, and by varying parameters such as the spatial and temporal location of spawning, particle buoyancy, and the depth range over which particles were released, we could assess the influences of these parameters on transport success. A sensitivity analysis using a General Linear Model identified the primary determinants of transport success in the various experimental simulations, and model outputs were examined and compared with patterns observed in field studies. Model outputs compared well with observed patterns of vertical and horizontal egg distribution. Particle buoyancy and area of particle release were the major single determinants of transport success, with an egg density of 1.025 g cm,3 maximizing average particle transport success and the western Agulhas Bank being the most successful spawning area. This IBM may be useful as a generic prototype for other upwelling ecosystems. [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] Ovary development in Greenland halibut Reinhardtius hippoglossoides in west Greenland watersJOURNAL OF FISH BIOLOGY, Issue 5 2005C. S. Simonsen Maturity in adult female Greenland halibut Reinhardtius hippoglossoides was studied in three areas in west Greenland waters: the inshore area in Disko Bay and two offshore areas, Baffin Bay and Davis Strait. The aim was to monitor maturity changes in the inshore fjords of Disko Bay over an extended period from winter to autumn and compare these findings with specimens from Baffin Bay and the presumed spawning area in Davis Strait. A significant difference in maturity level was observed in and between the three areas. In Disko Bay maturity indices increased significantly in August and September both with respect to the gonado-somatic index (IG) and the size in the leading oocyte cohort. In the period February to May no significant changes were observed. Mature ovaries were only observed among fish >80 cm total length and only among a fraction of these large fish. Offshore areas of Baffin Bay, even though poorly sampled, showed similar signs in the maturity indices as in Disko Bay. Relative to Disko Bay and Baffin Bay, female fish in Davis Strait had more progressed maturity indices. Furthermore, almost all fish in Davis Strait showed signs of progressed maturity contrary to Disko and Baffin Bay. A large proportion of the Greenland halibut in Disko and Baffin Bay apparently did not begin the maturation cycle until very late in their life history or were repeat spawners with a multi-year maturation cycle. These observations could thus support the hypothesis that Greenland halibut have a prolonged adolescent phase. Atresia was highest in the early phases of maturation in Greenland halibut but relatively high levels of atresia were also observed in fish in more advanced maturity phase. The first was ascribed to fecundity regulation while the latter could be linked to the fish's fitness condition but it was not possible to show this with the available condition index. [source] Reproductive migration of brown trout in a small Norwegian river studied by telemetryJOURNAL OF FISH BIOLOGY, Issue 1 2004A. Rustadbakken The movement of 34 large (39,73 cm standard length) brown trout Salmo trutta was monitored using radio telemetry for up to 74 days in Brumunda, a small Norwegian river (mean annual discharge 3·3 m3 s,1) flowing into the large Lake Mjøsa. The maximum range of movement in the river was 20 km. No clear relationships existed between individual movement and water discharge, temperature and barometric pressure. Brown trout migrated at all levels of water discharge. At low discharge (<2 m3 s,1) movements were nocturnal. A weir 5·3 km from the outlet restricted ascending brown trout at low (c. 6° C), but not at high (c. 8° C) water temperatures. Spawning occurred in September to October and tagged individuals spent 2,51 days at the spawning sites. Mean migration speed from tagging to when the fish reached the spawning area, and from when they left the spawning areas and reached the lake was 1·0 and 2·3 km day,1, respectively. All tagged brown trout that survived spawning returned to the lake after spawning. [source] Reproduction of Micropogonias funieri in a shallow temperate coastal lagoon in the southern AtlanticJOURNAL OF FISH BIOLOGY, Issue 2002D. Vizziano The white croaker Micropogonias furnieri, in the coastal Rocha Lagoon, spawned during 5 months, in late spring and summer. It was eurythermic (gonad growth at 12·5 to 25·5° C, spawning at 20 to 27° C) and mesoxic (living at 5·2 to 9·1 mg l -1). The spawning occurred in brackish (8,18 salinity), basic (c. 8 pH) and oxygenated (c. 8·0 mg l -1) waters. The temperature appeared to be an important environmental factor affecting the timing of reproduction. The size at first maturity (19,20 cm) was 11,12 cm lower than the reported for the Río de la Plata spawning area (Uruguay). Juveniles were observed throughout most of the year suggesting that the lagoon is also a nursery area. In Brazil, M. furnieri spawns in marine areas while in Uruguay it spawns in estuaries. This is the first time that a coastal lagoon of the subtropical and temperate western coast of the South Atlantic Ocean has been shown to be a spawning area of a marine species. [source] Salinity tolerance in young Allis shad larvae (Alosa alosa L.)ECOLOGY OF FRESHWATER FISH, Issue 1 2008A. Bardonnet Abstract,,, Estuarine migration in Allis shad (Alosa alosa) usually does not take place before mid-summer, but exposure to salinity in brackish water may occur earlier as many spawning areas are of necessity located in upper estuarine zones due to the placement of dams. Therefore, Allis shad conservation programmes need to consider the risk of mortality due to the ability of young Allis shad to tolerate salinity. To evaluate larval mortality due to the inability of larvae to withstand salinity during early ontogeny, we exposed larvae of different ages (from few days old to 27 days old) to salinities ranging from 0 to 30 g·l,1. Results indicate that direct seawater exposure induces high mortality in young larvae whatever the ontogenetic stage. However, young larvae can easily deal with upper estuary salinity conditions. [source] Migration of landlocked brown trout in two Scandinavian streams as revealed from trap dataECOLOGY OF FRESHWATER FISH, Issue 3 2004J. Carlsson Abstract,,, Anthropogenic barriers that may interfere or prevent fish migration are commonly found in streams throughout the distribution of salmonids. Construction of fish passages in streams is a common solution to this problem. However, the goal with fish passages is often, at least in Scandinavia, to allow Atlantic salmon (Salmo salar L.) and migratory brown trout (S. trutta L.) to get access to spawning areas above these barriers. Hence, the fish passages may often only be open during the spawning migration of salmonids (late summer to autumn). We present data, on wild brown trout migration, from two trapping systems in two Scandinavian streams showing that intra- and interstream migrations are common throughout the summer and autumn. Moreover, differences in size were found between trap-caught trout and electrofished trout where trapped trout were generally larger than electrofished trout. We suggest that the current regime with fish passages only open parts of the year can have negative effects on populations by depriving trout from the possibility to perform migrations throughout the year. Resumen 1. Barreras de origin antrópico que pueden interferer o prevenir las migraciones de los peces son frecuentes a lo largo de las áreas de distribución de los salmónidos. Una solución común a este problema es la construcción de pasos. Si embargo, el fin general de estos pasos es, por lo menos en Escandinavia, permitir el acceso a las áreas de reproducción por encima de las barreras tanto a salmones (Salmo salar L.) como a truchas migratorias (S. trutta L.). Frecuentemente, estos pasos están solamente abiertos durante el período de migración reproductiva (final del verano y otoño) porque se piensa que este régimen no tiene consecuencias negativas ya que estas especies muestran movimientos muy limitados en otros periodos del año. 2. Presentamos datos sobre migraciones de truchas colectados en dos sistemas de trampas de dos ríos escandinavos. Un río localizado por encima de una catarata inaccesible. El segundo, con una población migratoria de truchas. Los datos indicaron claramente migraciones intensivas a lo largo de todo el período en el que las trampas estuvieron operativas. Ambos ríos mostraron un pico de migración aguas arriba a mediados de Julio. Migraciones aguas abajo fueron raramente observadas en la población por encima de la catarata aunque migraciones aguas abajo en la población del río fueron intensivas al final del otoño. 3. Sugerimos que el régimen actual de pasos de peces que abren solamente partes del año puede tener efectos negativos sobre las poblaciones, al privar a las truchas de la posibilidad de migrar a lo largo del año. Esto puede extenderse a otros sistemas con barreras ya que observamos también migraciones intensivas en la población localizada por encima de la catarata. [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] Visualisation of standardized life-history patternsFISH AND FISHERIES, Issue 4 2001Dirk Zeller Abstract The life-history patterns of fish and invertebrate species are complex. But much of this complexity can be captured in simple diagrams of coastal transects, where juveniles usually occur in larger numbers in shallow waters, while adults generally inhabit deeper, offshore waters. Iconographic representations of generalized life-history patterns and depth profiles, with specific key life-history parameters can capture much of these standardized patterns, including spawning areas, nursery/juvenile distributions, adult distributions and spawning migrations. Several examples presented here from a wide range of habitats and ecosystems (temperate and tropical waters, demersal, deep water, pelagic and coral reefs), including an example of different stocks of the same species, illustrate some general patterns with regard to water depth and distance from shore. The present approach should be viewed as a first step towards obtaining standardized patterns about key life-history parameters, and will hopefully lead to incorporation into management of life-history interconnectivity between different fishery sectors or gears. This may contribute to sustainable, ecosystem-based approaches to management by informing policy options when faced with decisions to rationalize overcapitalized fisheries. [source] Introducing size limits as a management tool for the recreational line fishery of silver kob, Argyrosomus inodorus (Griffiths and Heemstra), in Namibian watersFISHERIES MANAGEMENT & ECOLOGY, Issue 3 2001C. H. Kirchner Individual silver kob Argyrosomus inodorus (Griffiths and Heemstra) first mature at just over 1 yr of age and the median age at maturity is approximately 1.5 yr. Spawning of silver kob was observed in the southern and central region of the stock's range, but little spawning activity was found in silver kob sampled from the northern region. The spawning period is protracted over 6 months (October,March), which coincides with warmer water temperatures (>15 °C) and the occurrence of large-sized spawning silver kob in the southern and central part of Namibia. Implementing a minimum size limit for the silver kob fishery is not recommended as it will have serious economic implications for the coastal communities. The protection of the spawning areas, Meob Bay and Sandwich, should be continued and a strict bag limit on large-sized silver kob is recommended for the Namibian silver kob recreational fishery. [source] Advection of anchovy (Engraulis encrasicolus) larvae along the Catalan continental slope (NW Mediterranean)FISHERIES OCEANOGRAPHY, Issue 2 2007A. SABATÉS Abstract The Gulf of Lions is one of the main anchovy (Engraulis encrasicolus) spawning areas in the NW Mediterranean. During the spring, low-salinity surface water from the outflow of the Rhône is advected by the shelf-slope current along the continental slope off the Catalan coast. In June 2000, a Lagrangian experiment tracking these low-salinity surface waters was conducted to assess the importance of this transport mechanism for anchovy larvae and to determine the suitability of the tracked surface waters for survival of anchovy larvae. The experiment consisted of sampling the tracked water parcel for 10 days with three drifters launched at the core of the shelf-slope current where low-salinity surface waters were detected. The survey was completed by sampling the surrounding waters. Anchovy larvae from the spawning area in the Gulf of Lions were advected towards the south in the low-salinity waters. The size increase of anchovy larvae throughout the Lagrangian tracking closely followed the general growth rate calculated by otolith analysis (0.65 mm day,1). However, advection by the current was not the only mechanism of anchovy larval transport. A series of anticyclonic eddies, originated in the Gulf of Lions and advected southwards, seemed to play a complementary role in the transport of larvae from the spawning ground towards the nursery areas. These eddies not only contributed to larval transport but also prevented their dispersion. These transport and aggregation mechanisms may be important for anchovy populations along the Catalan coast and require further study. [source] Seasonal maturity development of Baltic cod in different spawning areas: importance of the Arkona Sea for the summer spawning stockJOURNAL OF APPLIED ICHTHYOLOGY, Issue 1 2009M. Bleil Summary We investigated the seasonal maturity development of cod in four areas of the Baltic Sea. Two different spawning peaks were identified and found to be consistent over the period 1992,2005. In the Kiel Bight and Mecklenburg Bight (ICES SD 22) a spawning peak was observed from March to April (spring spawning). In the areas of the Arkona Sea (ICES SD 24) and Bornholm Sea (ICES SD 25) the spawning peak occurred during summer. In the Bornholm Sea, the main spawning activities began in June and ended in September, with a spawning peak in June,August (summer spawning). In the Arkona Sea, which is a transition area between the Mecklenburg Bight and the central Baltic Sea, spawning began in March and lasted until July, with a spawning peak in June,July (summer spawning). Seasonal maturity development and proportions of spawning cod in June in the Arkona Sea were similar to that of the Bornholm Sea. In addition, the proportion of spawning cod in the Arkona Sea was positively correlated with the size of the spawning stock in the Bornholm Sea. Our results provide evidence of a spatial expansion of spawning activities of the summer spawning stock from the eastern Baltic Sea into the Arkona Sea. Therefore, the Arkona Sea should be considered as one of the spawning habitats of the summer spawning stock of Baltic cod. [source] Spatial distribution of spawning sites of pikeperch [Sander lucioperca (L.)] in a highly eutrophic clay-turbid lake , implications for managementJOURNAL OF APPLIED ICHTHYOLOGY, Issue 6 2006H. Lehtonen Summary The spawning sites of pikeperch were mapped using artificial spawning nests in the clay-turbid Lake Tuusulanjärvi in southern Finland to protect the most important spawning areas. Altogether 272 artificial spawning nests were set before actual spawning on potential spawning grounds. The first observations of eggs were made on 26 May at a surface water temperature of 12°C. No new eggs were found after 10 June at water temperature of 16°C. The nests were removed on 18 June when the larvae had already hatched. The study demonstrated that artificial spawning nests could be used to evaluate both duration and spatial dimensions of spawning of pikeperch. [source] Spawning dynamics and biomass estimates of an anchovy Engraulis australis population in contrasting gulf and shelf environmentsJOURNAL OF FISH BIOLOGY, Issue 7 2009W. F. Dimmlich The spawning biomass of Australian anchovy Engraulis australis in gulf and shelf waters of South Australia was compared using the daily egg production method (DEPM). The total survey area was 128 700 km2 with recorded spawning areas in gulf and shelf waters of 4898 and 44 618 km2, respectively. High egg densities in the warm, shallow gulf waters were produced by small, young (<1 year old) E. australis that spawned relatively small batches of eggs (c. 855) approximately every 3 days. In cooler, deeper shelf waters, where larger, older E. australis are found, lower egg densities occurred despite individuals producing much larger batches of eggs (c. 15 572) approximately every 7 days. In shelf waters, the highest densities were recorded at inshore sampling stations. Spawning appeared to peak between 0000 and 0100 hours. Females were more abundant than males in samples from both gulf and shelf waters with sex ratios of 0·61 and 0·56, respectively. The spawning biomass of E. australis in shelf waters was 101 522 t, whereas the estimate for gulf waters was 25 374 t. Due to the differences in mean size of the spawning females, however, c. 6 × 109E. australis were present in each region. The results support the hypothesis that variability in habitat conditions may directly influence E. australis reproduction. A large reserve of young fish in the relatively stable gulf environment may increase the resilience of the E. australis population in South Australia to unfavourable interannual changes in offshore environmental conditions. [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] Sympatric spawning of Anguilla marmorata and Anguilla japonica in the western North Pacific OceanJOURNAL OF FISH BIOLOGY, Issue 9 2009M. Kuroki Extensive collections were made of the larvae of the temperate Japanese eel Anguilla japonica and the tropical giant mottled eel Anguilla marmorata in an overlapping area of the North Equatorial Current region of the western North Pacific Ocean. Collections of 189 A. marmorata and > 2500 A. japonica larvae during nine surveys from 1991 to 2007 showed that these two anguillid eels have similar spawning areas just west of the southern West Mariana Ridge. In July to August 2006 and August 2007, morphologically and genetically identified A. marmorata preleptocephali were mainly collected between 14·5,15° N and 142,142·5° E, where A. japonica preleptocephali were also caught in some of the same net tows. Fewer A. marmorata preleptocephali, however, were collected (n = 31) compared to those of A. japonica (n = c. 165), and fewer small larvae of A. marmorata were collected per tow than A. japonica (n = 1,10 and 1,294, respectively), suggesting relatively smaller spawning aggregations of A. marmorata. The distribution of preleptocephali and small larvae was wider in longitude in A. marmorata (131, 143° E) than in A. japonica (137,143° E), while the latitudinal range was almost the same (12,17° N). Although spawning by these two species overlaps both spatially and temporally, the tropical eels of the North Pacific population of A. marmorata probably have a much longer spawning season with fewer spawners, at least in summer, and recruit to a much wider latitudinal range of growth habitats. [source] Energetics and morphology of sockeye salmon: effects of upriver migratory distance and elevationJOURNAL OF FISH BIOLOGY, Issue 3 2004G. T. Crossin Depending on population, wild Fraser River sockeye salmon Oncorhynchus nerka travel distances of <100 km to >1100 km and ascend elevations ranging from near sea-level to 1200 m to reach spawning areas. Populations embarking on distant, high elevation migrations (i.e. Early Stuart, Chilko and Horsefly populations) began their upriver spawning migrations with higher densities of somatic energy (c. 9·2 to 9·8 MJ kg,1) and fewer eggs (c. 3200 to 3800) than populations making shorter, low elevation migrations (i.e. Weaver and Adams; c. 7·1 to 8·3 MJ kg,1 gross somatic energy and c. 4300 to 4700 eggs). Populations making difficult upriver migrations also had morphologies that were smaller and more fusiform than populations making less difficult migrations, traits that may facilitate somatic energy conservation by reducing transport costs. Indeed, fish travelling long distances expended less somatic energy per unit of migratory difficulty than those travelling shorter distances (2·8 to 3·8 kJ v. 10,1400 kJ). Consistent with evolutionary theory, difficult migrations appear to select for energy efficiency but ultimately fish making more difficult migrations produce fewer eggs, even when differences in body length have been accounted for. Despite large among-population differences in somatic energy at the start of upriver migration, all populations completed migration and spawning, and subsequently died, with c. 4 MJ kg,1 of energy remaining, a level which may reflect a threshold to sustain life. [source] Reproductive migration of brown trout in a small Norwegian river studied by telemetryJOURNAL OF FISH BIOLOGY, Issue 1 2004A. Rustadbakken The movement of 34 large (39,73 cm standard length) brown trout Salmo trutta was monitored using radio telemetry for up to 74 days in Brumunda, a small Norwegian river (mean annual discharge 3·3 m3 s,1) flowing into the large Lake Mjøsa. The maximum range of movement in the river was 20 km. No clear relationships existed between individual movement and water discharge, temperature and barometric pressure. Brown trout migrated at all levels of water discharge. At low discharge (<2 m3 s,1) movements were nocturnal. A weir 5·3 km from the outlet restricted ascending brown trout at low (c. 6° C), but not at high (c. 8° C) water temperatures. Spawning occurred in September to October and tagged individuals spent 2,51 days at the spawning sites. Mean migration speed from tagging to when the fish reached the spawning area, and from when they left the spawning areas and reached the lake was 1·0 and 2·3 km day,1, respectively. All tagged brown trout that survived spawning returned to the lake after spawning. [source] Specific gravity and vertical distribution of sprat eggs in the Baltic SeaJOURNAL OF FISH BIOLOGY, Issue 2 2003A. Nissling During peak spawning of sprat Sprattus sprattus in the Baltic Sea in May,June egg specific gravity averaged ±s.d. 1·00858 ± 0·00116 g cm,3 but was significantly higher in the beginning and significantly lower towards the end of the spawning season. A close relationship was found between egg diameter and egg specific gravity (r2 = 0·71). This relationship, however, changed during the spawning season indicating that some other factor was involved causing the decrease in specific gravity during the spawning period. The vertical egg distribution changed during the spawning season: eggs were distributed mainly in the deep layers early in the season, occurred in and above the permanent halocline during peak spawning, and above the halocline towards the end of the spawning season. Consequently, poor oxygen conditions in the deep layers and low temperatures in layers between the halocline and the developing thermocline may affect egg development. Thus, opportunities for egg development vary over the spawning season and among spawning areas, and depending on frequency of saline water inflows into the Baltic Sea and severity of winters, between years. [source] Effects of temperature on disease progression and swimming stamina in Ichthyophonus -infected rainbow trout, Oncorhynchus mykiss (Walbaum)JOURNAL OF FISH DISEASES, Issue 10 2009R Kocan Abstract Rainbow trout, Oncorhynchus mykiss, were infected with Ichthyophonus sp. and held at 10 °C, 15 °C and 20 °C for 28 days to monitor mortality and disease progression. Infected fish demonstrated more rapid onset of disease, higher parasite load, more severe host tissue reaction and reduced mean-day-to-death at higher temperature. In a second experiment, Ichthyophonus -infected fish were reared at 15 °C for 16 weeks then subjected to forced swimming at 10 °C, 15 °C and 20 °C. Stamina improved significantly with increased temperature in uninfected fish; however, this was not observed for infected fish. The difference in performance between infected and uninfected fish became significant at 15 °C (P = 0.02) and highly significant at 20 °C (P = 0.005). These results have implications for changes in the ecology of fish diseases in the face of global warming and demonstrate the effects of higher temperature on the progression and severity of ichthyophoniasis as well as on swimming stamina, a critical fitness trait of salmonids. This study helps explain field observations showing the recent emergence of clinical ichthyophoniasis in Yukon River Chinook salmon later in their spawning migration when water temperatures were high, as well as the apparent failure of a substantial percentage of infected fish to successfully reach their natal spawning areas. [source] |