High variability in spawning migration of sea trout,Salmo trutta,in two northern Swedish rivers

Abstract Telemetry was used to examine spawning migration of sea trout, Salmo trutta L. (n = 126), in two rivers in northern Sweden. The spawning areas defined by radio‐tagged fish differed between the river systems. In the River Vindelälven, sea trout spawned in the main stem and 80% of tagged individuals returned to areas where hatchery‐reared juveniles had been previously stocked. In the River Piteälven, 74% of tagged sea trout ascended tributaries for spawning. Tagged fish were categorised into three groups of migratory pattern. cart (classification and regression tree) analysis indicated that distance from tagging location to spawning site (S_dist) explained the migratory patterns. Large S_dist separated fish with stepwise upstream migration from those with up‐ and downstream migrations and one‐directional direct migration. Fish tagged early in the season migrated the longest distance to spawning areas. Stocking locations and sex explained the large search behaviour up‐ and downstream in the rivers. The findings are important for the sustainable management of sea trout in the Gulf of Bothnia.     

Comparative ecologies of domestic and naturalised rainbow trout in northern Lake Huron

Northern Lake Huron (Ontario, Canada) supports the largest concentration of freshwater salmonid cage culture farms in Canada and receives inputs of domestic‐strain rainbow trout (Oncorhynchus mykiss) through escapement. We assessed the potential effects of these domestic fish on the naturalised rainbow trout of this ecosystem by comparing their respective ecologies. Mature adults were sampled from spawning tributaries, primarily in spring, and to a lesser extent in fall. Fish of domestic origin comprised ~80% of rainbow trout sampled from sites near cage culture facilities but <20% of rainbow trout sampled from more distant sites. Domestic adults in spawning condition (gametes free‐flowing) were present in the spawning tributaries in both spring and fall sampling seasons, whereas naturalised fish in spawning condition were only observed in the spring. Domestic adults were younger and smaller (in length), appeared to have shorter lifespan and had a higher male to female ratio compared with their naturalised counterparts. Growth rates (change in length with age) of naturalised and domestic females in the wild were similar, but domestic males grew more slowly than naturalised males. Domestic females also produced smaller eggs than naturalised females. Food web positions (inferred from δ¹³C and δ¹⁵N) of domestic and naturalised fish were very similar but varied more strongly with body size in the former. Domestic‐strain rainbow trout of cage culture origin can survive, grow and attempt to spawn in northern Lake Huron and have the potential to compete for food, mates and spawning habitat with naturalised rainbow trout.     

Water level influences migratory patterns of anadromous brown trout in small streams

Habitats modify the population ecology of species. Here, we show how low water level influences abundance and size of adult anadromous brown trout (Salmo trutta) entering a small, South Norwegian stream for spawning. After smolting, the fish appear chiefly to feed within 10 km of the home stream. In the autumn, South Norwegian streams typically flood because of heavy rainfall, when the anadromous brown trout entered from the sea. Mean annual duration of the upstream migration period was 34 days and ended when the flooding ended and the water temperature dropped to below 4°C. During most of the migration period, on average two trout ascended the river per day. The sexes entered the spawning area concurrently, and the male:female ratio of the anadromous trout was 1.27. No fish entered when the water depth just downstream of the spawning area was below 5 cm, and mean number of fish increased with increasing water depth to ca. 30 cm, but not at higher flows when the ascent gradually decreased. Mean and maximum size of the entering spawners increased with water depth between 5 and 16 cm. Among those that had been to sea, most were recaptured in the home stream, 4% in other streams, but only two of the strays were caught close to spawning time. The present results illustrate that population traits of anadromous brown trout from a small stream differ from those in larger rivers, probably because of selection associated with water flow.     

Seasonal migrations of adult and sub‐adult redband trout in a high desert basin of Eastern Oregon,USA

Abstract – Redband trout (Oncorhynchus mykiss gairdneri) migrations were tracked between March 2007 and June 2009 in the Donner und Blitzen River, Oregon, USA, using radio telemetry and PIT tags. We investigated the upstream extent and timing of spawning migrations for two groups of trout, considered the factors that influenced the rate of trout migration and explored the seasonal patterns of redband trout migration related to temperature and flow conditions. We found that trout made long‐distance migrations (up to 91 km) to spawn. Spawning trout from the lower river and middle river migrated to the same reaches, but lower river trout reached spawning habitats later than individuals from the middle river. Migration rate had a positive relationship with fork length and mean river discharge. We also found that redband trout made upstream spring migrations as sub‐adults and as adults. Whereas adult trout migrated to spawn, immature individuals migrated to river segments with more favourable thermal conditions. In both cases, migrations occurred where seasonally appropriate or life‐stage‐specific habitat patches for growth, survival, or reproduction were spatially segregated.     

Reproductive cycle of yellow sea bream <Emphasis Type="Italic">Dentex tumifrons</Emphasis> in Wakasa Bay,the Sea of Japan off central Honshu

ABSTRACT:   To determine the spawning season and reproductive cycle of the yellow sea bream, Dentex tumifrons , in Wakasa Bay, in the Sea of Japan off central Honshu, seasonal change in the gonadosomatic index ( GSI ) was examined and histological observations of both ovaries and testes were conducted. The female GSI gradually increased from May, maintained a high level between August and October and then rapidly decreased. The histological observations of the ovary showed that vitellogenesis began from May and developed until September. Spent fish began to be observed in October and all the fish collected in December were spent. There was only one peak in the seasonal change in GSI of males and females in Wakasa Bay. Thus, yellow sea bream spawn only in autumn in Wakasa Bay. Differences in the reproductive cycle and number of spawning seasons were found between the two different latitudinal areas, Wakasa Bay and the East China Sea (low latitudinal area) where the spawning seasons were spring and autumn. An increase in water temperature is an important factor to initiate gonadal maturation (recrudescence) and is terminated by the short day-length in Wakasa Bay.     

Coastal movement and growth of domesticated rainbow trout (Oncorhynchus mykiss (Walbaum)) in Norway

Between 1979 and 1991, hatchery-reared 1+ and 2+ rainbow trout were released in May and June in the Boknafjord at the mouth of the River Imsa, and from April to June in the Oslofjord, southern Norway. The fish were recaptured in the fjords of release, in rivers emptying there and from rivers and sea further along the Norwegian coast. Of the total recaptures, 35.6% ascended rivers in the year of release. Some fish released at the River Imsa returned to the area of release after spending 1 to 3 years at sea. Among those that were recaptured in rivers, 11.9% were recaptured in other rivers than the Imsa. The growth rate of the fish varied inversely with size at release. The growth rate was higher in the Oslofjord than in the Boknafjord, and in both areas the growth rate decreased with time after release. Rainbow trout that had escaped from local fish farms entered the River Imsa between March and December. Adults ascending in spring remained a shorter time in the river (37 days) than those ascending in autumn (200 days). Fish entering in autumn decreased more in weight during their river stay than those ascending in spring, and females more than males. Spawning took place in April-May. The monthly mean river stay of juvenile entrants ranged from 2 weeks to 6 months. In total, 27.8% of the rainbow trout escaped from fish farms and captured in the Imsa strayed to other rivers for repeat spawning. There is no evidence for continuing survival of escaped Norwegian rainbow trout in the wild.     

Spatial and quantitative patterns of movement in large bull trout (Salvelinus confluentus) from a watershed in north-western British Columbia, Canada, are due to habitat selection and not differences in life history

Abstract –  Movement and habitat use by bull trout ( Salvelinus confluentus ) was examined using radio telemetry in the Morice River watershed, north-western British Columbia, between April 2000 and November 2001. Bull trout principally utilised mainstem habitat. Throughout the watershed, little movement was observed during the winter months. From June to September, movement increased and was correlated with migration into tributaries. We directly observed spawning bull trout only in tributaries of the Morice River and never in the mainstem. Many of the fish ( N  = 48) migrated to the nearest potential spawning sites, but a few fish ( N  = 7) made extensive migrations to other regions of the watershed to spawn. Fish that spawned in both years of the study returned to the same spawning location. Variation in spatial and movement data, therefore, appears to be linked to availability of suitable habitat and not differences in life history that have been observed in large bull trout.     

Movements by adult cutthroat trout in a lotic system: implications for watershed-scale management

Abstract  Movements by adult cutthroat trout, Oncorhynchus clarkii (Richardson), were assessed from autumn to summer in the Salt River watershed, Wyoming-Idaho, USA by radio telemetry. Adult cutthroat trout were captured during September and October 2005 in the main stem of the Salt River, surgically implanted with radio transmitters, and tracked through to August 2006. Adult cutthroat trout were relatively sedentary and resided primarily in pools from October to March, but their movement rates increased during April. Higher movement rates were observed among tagged fish during May and early June. Among 43 fish residing in the Salt River during April 2006, 44% remained in the river, 37% moved into mountain tributaries and 19% moved into spring streams during the spawning season. Fish did not use segments of mountain tributaries or the upstream Salt River where fish passage was blocked by anthropogenic barriers or the channel was dewatered during summer. Almost all the fish that moved into spring streams used spring streams where pools and gravel–cobble riffles had been constructed by landowners. The results suggest that adult Snake River cutthroat move widely during May and early June to use spawning habitat in mountain tributaries and improved spring streams. Maintaining the ability of adult fish to move into mountain streams with spawning habitat, preserving spawning habitat in accessible mountain tributaries and removing barriers to upstream movements, and re-establishing summer stream flows in mountain tributaries affected by dams appear to be habitat management alternatives to preserve the Snake River cutthroat trout fishery in the Salt River.     

Effect of habitat fragmentation on spawning migration of brown trout (Salmo trutta L.)

Abstract –  Human-induced habitat alteration is one of the main causes of the decline of freshwater fish populations. The watershed of the River Bidasoa (Spain) is an example of heavily fragmented habitat. The local brown trout ( Salmo trutta L.) population is disturbed, with evidence of poor recruitment as well as low adult densities in the main stem. Forty male and female adult migratory trout were tagged with external or internal radio transmitters and released. Fixed stations with data loggers and mobile antennae were used with daily surveys to track fish movements during the migration and spawning period (3 months). Migration distances did not exceed 10 km, and half of the fish never entered a tributary in the study area. Fragmentation because of weirs on the main stem apparently prevented fish from reaching their spawning destination. Fish that entered the tributaries were first confronted with an accessibility problem because of low discharge. However, each fish chose one tributary, without making attempts to run up in other tributaries. Once in the tributary, fish were restrained in their upstream movements by dams. The study area appeared to be isolated from the vast upper part of the watershed. Within the study area, upper parts of tributaries also seemed strongly disconnected from the main stem. This study illustrates the negative impact of river fragmentation on S. trutta migration pattern. Population sustainability can be directly affected through the low availability of spawning grounds for migratory fish. Long-term effects of fragmentation may cause reproductive isolation within watersheds, which in the case of trout also means isolated phenotypic population units.     

Relationships between water temperatures and upstream migration, cold water refuge use, and spawning of adult bull trout from the Lostine River, Oregon, USA

Howell PJ, Dunham JB, Sankovich PM. Relationships between water temperatures and upstream migration, cold water refuge use, and spawning of adult bull trout from the Lostine River, Oregon, USA.
Ecology of Freshwater Fish 2010: 19: 96–106. This article is a US Government work and is in the public domain in the USA Abstract – Understanding thermal habitat use by migratory fish has been limited by difficulties in matching fish locations with water temperatures. To describe spatial and temporal patterns of thermal habitat use by migratory adult bull trout, Salvelinus confluentus, that spawn in the Lostine River, Oregon, we employed a combination of archival temperature tags, radio tags, and thermographs. We also compared temperatures of the tagged fish to ambient water temperatures to determine if the fish were using thermal refuges. The timing and temperatures at which fish moved upstream from overwintering areas to spawning locations varied considerably among individuals. The annual maximum 7‐day average daily maximum (7DADM) temperatures of tagged fish were 16–18 °C and potentially as high as 21 °C. Maximum 7DADM ambient water temperatures within the range of tagged fish during summer were 18–25 °C. However, there was no evidence of the tagged fish using localized cold water refuges. Tagged fish appeared to spawn at 7DADM temperatures of 7–14 °C. Maximum 7DADM temperatures of tagged fish and ambient temperatures at the onset of the spawning period in late August were 11–18 °C. Water temperatures in most of the upper Lostine River used for spawning and rearing appear to be largely natural since there has been little development, whereas downstream reaches used by migratory bull trout are heavily diverted for irrigation. Although the population effects of these temperatures are unknown, summer temperatures and the higher temperatures observed for spawning fish appear to be at or above the upper range of suitability reported for the species.     

Drift diving: A quick and accurate method for assessment of anadromous salmonid spawning populations

The accuracy of drift diving surveys of Atlantic salmon, Salmo salar L. and sea trout, Salmo trutta L., was evaluated by comparing the abundance and size distribution with catches in a fish trap over 6 years in the River Etneelva, western Norway. The population count from drift diving accounted for on average 96.3% of the salmon in the trap after accounting for the catches during fishing. Size structure registered during drift diving corresponded with trap catches of salmon, but the number of small salmon (<3 kg) appeared to be somewhat underestimated, while large salmon (>7 kg) were overestimated in drift diving. For sea trout, the match between drift diving counts and trap registrations was poorer (average 76.3%), but may have been affected by the surveys being performed too late with regards to sea trout spawning time. The study illustrates the utility of drift counting for estimating the entire population of anadromous salmonids in a river.     

Linking habitat characteristics with juvenile density to quantify Salmo salar and Salmo trutta smolt production in the river Sävarån,Sweden

Abstract Habitat mapping along 85 km of river was related to juvenile (15 years of electric fishing) and smolt (3 years of screw‐trapping) abundance data to estimate salmon, Salmo salar L., and sea trout, Salmo trutta L., smolt production in the River Sävarån, northern Sweden. Spawning site selection by radio‐tagged salmon (n = 12) and sea trout (n = 4) was also assessed. Fifty‐one hectares of potential spawning and nursery habitat was found in the main stem river, representing 25% of the total river area. These areas were estimated to yield 1300–7580 salmon and 630–3540 sea trout smolts based on juvenile densities, equating with 3 years of screw‐trap data (2990–5080 salmon and 680–2520 trout smolts, respectively). A hypothetical maximum production of about 19 900 salmon smolts was predicted for the river at a density of 40, 0+ salmon 100 m^?2. Tracking adults during the spawning period identified optimal and potential reproductive areas.     

The effect of short-term starvation on ovarian development and egg viability in rainbow trout (Salmo gairdneri)

Adult female rainbow trout (Salmo gairdneri) were fed a commercial trout production diet until approximately 40 days prior to spawning at which time the fish were divided in two groups. One group continued to be fed while the other group was starved until spawning. Egg size, egg number, ovary weight, and egg proximate composition were examined periodically starting 5 months before spawning. Muscle tissues of the fish were sampled at spawning to measure somatic depletion of proximate consituents in the two groups. Egg hatchability was determined by incubating test lots from each spawning female. No significant differences (P > 0.05) were found in egg hatchability between the fed and starved groups. Changes in proximate composition were observed in the eggs during the months prior to spawning, but no differences were detected between the eggs of the starved and the fed groups. Short-term starvation did not significantly alter the proximate composition of muscle tissue of the spawned female trout.     

The commercial exploitation of sea trout, Salmo trutta L.

Abstract. The net and coble catch of sea trout in the River North Esk was sampled between 1977 and 1979. A comparison of the length frequency distribution of these samples with those of sea trout taken in a trap which was assumed to be unselective revealed that the net and coble fishery was very selective. Only isolated fish below 35·0 cm were encountered in the commercial catch samples, yet between 25% and 41% of the upstream migratory sea trout taken in the trap during the netting season were below this length. The sea trout in the commercial catch samples were predominantly maiden, one-sea-winter fish. The dominant age class each year was the 2·1 + group, 3·1 + fish comprising the other major age class. The freshwater age of the maiden sea trout sampled declined as the season progressed. The proportion of previously spawned fish in the samples ranged between years from 12% to 15%. The mean length and mean weight of sea trout sampled from each year's catch showed little variation, ranging from 42·9 cm to 43·3 cm and 971 g to 972 g, respectively. The ratio of males to females in the 1979 sample was 1·00:2·18. The use of morphometric characteristics, including head length, pectoral fin length and adipose fin length was investigated with the aim of distinguishing the sex of fish taken early in the season from external features alone. Although in each month the mean head length as a percentage of fork length of males was greater than that of females, this difference was not sufficient to enable the rapid determination of sex during commercial catch sampling routines. The exploitation rate of sea trout reaching the most upstream major fishing station, Morphie Dyke, was estimated from the recapture of upstream adult sea trout removed from a trap and released in the main river 2 km downstream of Morphie Dyke. The percentage exploitation rate at this fishing station was found to range between 6·4% and 12·2%, and the percentage exploitation rate for the entire net and coble fishery was at a level of approximately 30% during the period of the study. The sea trout statistics of the North Esk net and coble fishery for the period 1925–1979 were examined, and the effect of a change in fishing effort on these figures is described. Recent catch figures, although below those reported during the mid-1960s, are above the level of catches reported prior to 1952.     

Induction of Spawning in the Sea Cucumber Holothuria scabra (Echinodermata: Holothuroidea)

With the advent of sea cucumber aquaculture in the South Pacific region, a reliable method is needed to induce large numbers of animals to spawn in captivity. Broodstock of the sea cucumber Holothuria scabra , collected from Stradbroke Island, Moreton Bay (27°90'N, 153°24'E) Australia, during the reproductive season from October to January, were used in spawning trials. During the 1997–1998 summer between one to five weeks of captivity, 100% of animals were induced to spawn in four trials at dusk on or close to a new or full moon, using nine males and nine females contained in a Reln tank and 30 cm of filtered sea water, using a 3–5 C temperature shock. H. scabra was induced to spawn in small numbers during the 1996–1997 summer despite a marked degree of weight loss, and all animals spawned during 1997–1998 with minimal loss of weight. The difference in the number of spawned eggs between animals of similar size and mean numbers of spawned eggs in consecutive trials decreased the longer animals were held in captivity before spawning. The hatch rate of eggs was reduced significantly for broodstock held for more than one month. Hatch rate and numbers of spawned eggs are important indicators of egg viability of broodstock maintained in captivity for an extended period.     

Observations on the Contribution of Planted Brown Trout (Salmo trutta L.) to Spawning Stocks in Four Irish Lakes

The relative proportions of mature wild and stocked brown trout in four Irish lakes were compared with their subsequent occurrence in spawning runs. Data indicate that stocked trout, of two strains, did not run the streams to spawn in significant numbers. Considerable stocks of introduced fish, which had shed their milt or eggs, were present in these lakes in springtime. The failure of brown trout stocked in lakes to run spawning streams subsequently has not been recorded previously.     

Hormone Induced Spawning of Summer Flounder Paralichthys dentatus

During their first year in captivity, summer flounder Paralicthys denratus were induced to spawn with gonadotropin releasing hormone analogue (GnRHa) implants, injected carp pituitary extract (CPE) or human chorionic gonadotropin (hCG) injections. The percentage of fertile eggs was greatest (69%) in CPE-treated females. CPE, but not GnRHa or hCG, was capable of stimulating oocyte growth (increased follicle diameter during vitellogenesis) followed by ovulation. Fish with maximum ovarian follicle diameters between 180 and 435 μm at the initiation of CPE injections produced the greatest percentage of fertile eggs. For most females, fertilization rate was greatest for the first batch of eggs ovulated. The mean fertilization rate for the first spawn of CPE-treated fish was 42% compared with 14% for the second spawn from the same fish. Fish with maximum initial follicle diameters of 585 40 μm that were implanted with GnRHa ovulated the greatest number of eggs, but fertility was low and variable. Approximately 35% of females injected with hCG ovulated a limited number of eggs, but only one hCG-treated female produced fertile eggs. Only a limited number of spermiating males were available for spawning trials. Hormone treatments used on females were ineffective for inducing or maintaining spermiation in male summer flounder.     

Variation in growth rate,liver weight and body composition at first sexual maturity in rainbow trout

Rainbow trout around 743 g were fed four different diets over an 8-month period. Maturing males grew faster in the period before spawning (Sept.–Dec.) than maturing females, and significantly faster than immature fish. Mature fish stagnated in growth while the immature fish surpassed the growth of mature fish during the spawning season. The condition factor was moderately influenced by the maturation process. In the period before spawning (Sept.–Jan.) maturing females had a significantly higher hepatosomatic index than males and immature fish. An increase in dry matter and fat and a decrease of protein were observed in the muscle of maturing males and immature fish towards the spawning season, while maturing females had a slight fall in dry matter and fat and a small increase in protein in the same period. Dry matter and fat in muscle of rainbow trout were positively correlated.     

Temporal segregation in spawning between native Yellowstone cutthroat trout and introduced rainbow trout

Hybridisation with introduced taxa poses a threat to native fish populations. Mechanisms of reproductive isolation can limit or prevent hybridisation between closely related species. Understanding how these mechanisms interact between the same species across geographically distinct occurrences of secondary contact, and how regional factors influence them, can inform our understanding of hybridisation as a threat and management actions to mitigate this threat. We used data collected on adult fish migration timing and approximate emergence timing of subsequent juvenile fish paired with genomic data to assess whether temporal isolation in the timing of spawning exists between Yellowstone cutthroat trout, rainbow trout and hybrids in the North Fork Shoshone River drainage in northwest Wyoming. We found evidence that Yellowstone cutthroat trout spawn, on average, two to four weeks later than rainbow trout and hybrids and two environmental covariates related to water temperature and discharge were associated with differences in spawning migration timing. Despite statistical support for Yellowstone cutthroat trout spawning later, disproportionately high numbers of rainbow trout and hybrids, paired with extended spawning seasons, lead to substantial overlap between all genotypes. Our results provide further evidence of temporal segregation in the timing of spawning as a mechanism of reproductive isolation between closely related species, but substantial spawning overlap suggests temporal segregation alone will not be enough to curtail hybridisation in conservation populations.     

Conservation of spawning time between years in lumpfish Cyclopterus lumpus and potential impacts from the temporal distribution of fishing effort

Lumpfish, Cyclopterus lumpus L., has an extended ovary development period and a relatively long spawning season. It therefore seems unlikely that individuals spawning later in the season would be able to recover from spawning and develop their gonads in time to spawn during the early part of the season the following year. The hypothesis that individuals spawning early or late in a spawning season would spawn early or late the following year was tested using fish tagged in Iceland between 2008 and 2017. The tagging date and recapture date the following year were positively correlated with an average of 356 days at large (DAL). Fish sampled from the fishery indicate that tagging/recapture date gives an indication of spawning time. From this, it was concluded that spawning time in the current year can be used to predict spawning time the following year. As fishing effort was greatest at the end of April/beginning of May, it seems likely that fish that come to spawn at this time will be subject to a higher fishing mortality. Therefore, they will be less likely to spawn successfully than fish spawning earlier or later in the year. If spawning time is under genetic control, then this could have consequences for the spawning phenology of lumpfish.