Seasonal occurrence of sea lice Lepeophtheirus salmonis on sea trout in two north Norwegian fjords

Seasonal occurrence of the parasitic copepod Lepeophtheirus salmonis (sea lice) was studied from March to December 2001 in two large north Norwegian sill fjords without fish farming activity, the Ranafjord and the Balsfjord. Anadromous brown trout Salmo trutta (sea trout) in both fjords had a low infestation rate during all sampling periods, but followed a seasonal pattern. During early and late winter (November to December and March to April) and spring (May to June), the prevalence varied from 0 to 25% and the abundance was <0·5 sea lice. Adults dominated (92%) during this period, particularly gravid females. In both fjords, the highest prevalence was during September (80–81%, all stages represented). In Ranafjord, the abundance and mean intensity during this month was 6·8 and 8·6 sea lice, respectively, while in Balsfjord it was 3·6 and 4·5 sea lice, respectively. Fish were captured at temperatures down to 1° C and at full strength sea water which is supposed to cause osmoregulatory problems for the fish. This observation has implications for the understanding of high‐latitude sea trout behaviour and can also make the fish more vulnerable to heavy sea lice infestation during this period. It is suggested that winter running sea trout help to maintain a self replicating local population of sea lice within such fjord systems where other possible hosts ( e.g . farmed Atlantic salmon Salmo salar ) are not present during a whole year cycle.     

Life history characteristics of brown trout in lakes at different stages of acidification

In 66 Norwegian lakes with allopatric populations of brown trout Salmo trutta that ranged from highly acidified to non-acid (pH 4·7–6·6) there was a significant inverse correlation between mean age and relative abundance (CPUE). As mean annual survival rates were not significantly related to CPUE, this population response may indicate that recruitment was lower in low-density lakes. Age-specific masses were significantly higher in populations that had declined in abundance than in unaffected populations. Mean body mass at sexual maturity in both males and females was inversely correlated with CPUE. Between populations, high age at maturity was associated with high survival rates in both sexes. Age at maturity correlated positively with specific growth rate between the ages of 1 and 2 years in females only.     

The morphometric variation of Actinomma boreale (Radiolaria) in Atlantic boreal waters

A morphometric study on the polycystine radiolarian species Actinomma boreale (Cleve) from ten trigger weight core-tops from the Norwegian-Iceland Seas, three piston cores taken offshore western Norway and three surface sediment samples from Lygrepollen, Sogndalsfjord and Høyangsfjord (western Norwegian fjords) shows a variation in morphology that groups A. boreale into three distinct clusters, interpreted to be related to different oceanographic settings. The largest specimens of A. boreale are found in the western Norwegian fjords, the smallest in the Iceland Sea, giving an apparent positive correlation with temperature.Down core studies in piston cores from the Norwegian Sea demonstrate a considerable size variation of the cortical shell of A. boreale. In the eastern Norwegian Sea, the climatically cold Younger Dryas had a population of A. boreale that was characterized by large cortical shells, while the climatically warm Holocene population was dominated by small sized cortical shells, showing a negative correlation with temperature. We suggest that the large sized conical shell population of A. boreale in the Younger Dryas is not reflecting precisely the sea-surface water temperature. Another factor must play the dominant role here, probably nutrients.     

Egg cannibalism in Barents Sea capelin in relation to a narrow spawning distribution

The spawning distribution of Barents Sea capelin Mallotus villosus off northern Norway in 2002 was restricted to a narrow area at the easternmost spawning grounds. There was an increase in abundance and a marked shift in aggregation area from east towards west during 11 March to 4 April, as the capelin went from prespawning through spawning to spent stages. The capelin stomachs were either empty or contained capelin eggs, often mixed with sand. Both the occurrence of cannibals and stomach fullness increased with stage of maturity, being highest in spent fish, and higher in males than in females. No differences were found between cannibals and non-cannibals of the same sex when adjusted for total length ( L _T), age, L _T at age and condition factor. At similar stomach fullness, the females had consumed more eggs than the males. This was attributed to a higher proportion of empty and broken eggs and less sand in females compared to males. In the full stomachs, the mean consumption in females and males was 623 and 334 eggs, respectively, whereas the respective maximum egg consumption was 871 and 683 eggs. The minimum estimates (given no digestion) of mean ± 95% CL egg consumption in spent females and males were 75·4 ± 6·9 and 58·4 ± 12·0 eggs, respectively, implying a minimum mortality of 1–2% of the total egg production caused by cannibalism.     

Age and growth of the round stingray Urobatis halleri at Seal Beach, California

The age and growth of the round stingray Urobatis halleri was determined using vertebral sections from animals collected at Seal Beach, California from 2002 to 2005. Annual periodicity was validated from U. halleri injected with oxytetracycline and maintained in captivity over a 2 year period ( n = 7). The coefficients estimated by the von Bertalanffy growth model were the disc width asymptote ( W _D∞) (286 mm for males and 224 mm for females) and K (0·09 year⁻¹ for males and 0·15 year⁻¹ for females). The age structure of the population consisted of mostly older, mature males and females. Age at maturity was estimated at 3·80 years for females and 3·75 years for males, and the maximum assessed age was 14 years old. Males were more numerous than females throughout the year; however, from May to September, females outnumbered males. The U. halleri age and growth coefficients were comparable to other species in the family Urolophidae. Based on the seasonality and age structure of this population, Seal Beach offers warm-water refuge for U. halleri of reproductive maturity, and the U. halleri at Seal Beach may garner some behavioural thermoregulation benefit.     

The reproductive biology of the crystal goby with a comparison to that of the transparent goby

A histological analysis of the gonad of the pelagic crystal goby Crystallogobius linearis , from the coastal central area of the Adriatic Sea, showed it to be a truly semelparous species; after the first spawning the mature gonads of both males and females appeared to have lost the capability for further spawning. Mature females had very low fecundity (200–700 mature oocytes) and small egg size (0·2–0·55 mm) similarly to other progenetic species. This reproductive strategy is compared with that of Aphia minuta , and a possible cause for the post-reproductive mortality of the two gobies is suggested and discussed.     

Sexual and geographical variation in life history parameters of the shorthorn sculpin

A total of 293 shorthorn sculpins Myoxocephalus scorpius from Tromsø, northern Norway, were sampled between November 1998 and April 1999 to determine sex, total length, age, growth, maturity and mortality. Females grew to larger sizes ( L _∞=26·9 v. 18·5 cm), matured later (2 v. 1 year of age) at larger size (maturation length=16 v. 14 cm L _T), and had lower instantaneous mortality rates (0·93 v. 1·20 year⁻¹) than males. The life history parameters of shorthorn sculpins in northern Norway were more similar to the parameters of short-lived central European populations than to the parameters of the long-lived population of Newfoundland. This study confirms that northern Norwegian shorthorn sculpins exhibit sexual dimorphism as in other shorthorn sculpin populations. The relationships between growth pattern, age at maturity and mortality rates observed in the Tromsø population and in other shorthorn sculpin populations, correspond well with the predictions from a published life history model.     

Plasma non-esterified fatty acid profiles in wild Atlantic salmon during their freshwater migration and spawning

Total plasma non-esterified fatty acid (NEFA) levels increased significantly in adult Atlantic salmon during the first months of their upstream migration and spawning in the Exploits River, Newfoundland, Canada. The highest levels occurred in May and were 5467±270·43 nmol ml⁻¹ for females and 4617±334·70 nmol ml⁻¹ for males. Significantly higher levels were maintained by females compared with males for most of the upstream migration. Between August and October, total plasma NEFA levels declined by 61% in females but only 23% in males. The decline in plasma monounsaturated and polyunsaturated fatty acid levels accounted for 74% of the loss of NEFAs in females. Specific plasma NEFAs such as 16: 0 (palmitic), 16: 1 (palmitoleic), 18: 1n9 (oleic) and 20: 5n3 (eicosapentaenoic acid) differed significantly between males and females during migration and spawning. The mean gonadosomatic index ( I _G) values of females in May and just prior to spawning were 0·37±0·01 and 10·25±0·32, respectively. The rapid decline in the plasma NEFA content of females coincided with the largest increase in their I _G (1·85±0·02–10·25±0·32). Corresponding I _G values for males were 0·34±0·01 in May and 3·33±0·78 prior to spawning. Plasma NEFA levels of spent salmon did not differ between sexes and were significantly lower than those of salmon preparing to spawn.     

Differences in size and growth rates of male and female migrating Japanese eels in Pearl River, China

The Sr/Ca ratios in otoliths of silver Japanese eels Anguilla japonica , in Pearl River, China, indicated that both sexes did not stay in brackish water and grew in fresh water from the glass eel stage until spawning migration. This did not support the hypothesis that females tended to distribute upstream and males might be restricted to estuaries. The back-calculated total length of males at glass eel stage was not significantly different from that of females, indicating that the hypothesis that small glass eels became males and larger ones became females may not be true. The mean (±S.D.) age and total length of males at migration were 6·4±1·6 years and 48·3±4·5 cm, which were significantly smaller than for females, 8·3±1·6 years and 61·4±4·1 cm. The age of migration was related inversely to growth rate for both sexes. Growth parameters of the von Bertalanffy growth equation were K =0·21 cm year°1, L _∞=55·7 cm and t _o=-0·55 year for males and K =0·14 cm year⁻¹, L _∞=77·5 cm and t _o=-0·60 year for females. The difference in asymptotic length ( L _∞) between males and females may be because females postpone migration to achieve larger size for maximizing reproductive success.     

Genetic response to human‐induced habitat changes in the marine environment: A century of evolution of European sprat in Landvikvannet,Norway

Habitat changes represent one of the five most pervasive threats to biodiversity. However, anthropogenic activities also have the capacity to create novel niche spaces to which species respond differently. In 1880, one such habitat alterations occurred in Landvikvannet, a freshwater lake on the Norwegian coast of Skagerrak, which became brackish after being artificially connected to the sea. This lake is now home to the European sprat, a pelagic marine fish that managed to develop a self‐recruiting population in barely few decades. Landvikvannet sprat proved to be genetically isolated from the three main populations described for this species; that is, Norwegian fjords, Baltic Sea, and the combination of North Sea, Kattegat, and Skagerrak. This distinctness was depicted by an accuracy self‐assignment of 89% and a highly significant F _ST between the lake sprat and each of the remaining samples (average of ≈0.105). The correlation between genetic and environmental variation indicated that salinity could be an important environmental driver of selection (3.3% of the 91 SNPs showed strong associations). Likewise, Isolation by Environment was detected for salinity, although not for temperature, in samples not adhering to an Isolation by Distance pattern. Neighbor‐joining tree analysis suggested that the source of the lake sprat is in the Norwegian fjords, rather than in the Baltic Sea despite a similar salinity profile. Strongly drifted allele frequencies and lower genetic diversity in Landvikvannet compared with the Norwegian fjords concur with a founder effect potentially associated with local adaptation to low salinity. Genetic differentiation (F _ST) between marine and brackish sprat is larger in the comparison Norway‐Landvikvannet than in Norway‐Baltic, which suggests that the observed divergence was achieved in Landvikvannet in some 65 generations, that is, 132 years, rather than gradually over thousands of years (the age of the Baltic Sea), thus highlighting the pace at which human‐driven evolution can happen.     

Demography of the vegetable ivory palm Phytelephas seemannii in Colombia, and the impact of seed harvesting

1. The demography of the vegetable ivory palm Phytelephas seemannii was studied on the Pacific coast of Colombia and a female-based matrix model was used to determine the proportion of seed that can be sustainably harvested from the population.
2. The density of the palm stands ranged from 240 to 420 adult palms ha⁻¹. The sex ratio was 1:1 and palms of both sexes produced leaves at the same rate. Seedlings produced 1·2 leaves per year on average, juveniles 1·8, and adults 6·1–7·4.
3. Adult females had fewer leaves than males (18·5 vs. 21·3 on average). Leaves of females lasted about 2·7 years in the crown, those of males about 3·2 years.
4. Stems creep on the ground, growing at the apex and often dying behind, the extant portion not always reflecting the palm's total age. The longest stem of a female palm in the study plots was 2·5 m, corresponding to an 'extant' age of 85 years; the longest stem recorded was that of a male (outside the plots) 10·5 m long, corresponding to an 'extant' age of 184 years. These figures reflect differences in growth habit, not in longevity.
5. Reproduction began at about 24 years, when the palm still lacked an above-ground stem.
6. The population growth rate λ was 1·059, and was most sensitive to changes in survival of juveniles and adults, and relatively insensitive to changes in fecundity and growth.
7. River channel migration is the most important cause of adult mortality. Phytelephas seemannii is apparently an efficient colonizer of the understorey in the late phases of riverine forest succession.
8. The population can tolerate a harvest intensity of 86% of all seeds before λ decreases to the equilibrium level of 1·00. Monitoring of the populations under intensive harvesting is required.     

Environmental variables affecting the sexual segregation of great white sharks Carcharodon carcharias at the Neptune Islands South Australia

The seasonal temporal sexual segregation of white sharks Carcharodon carcharias , at the Neptune Islands, South Australia, is described in relation to environmental variables. A significant sexual segregation was found at this site with sex ratios strongly favouring males overall. Males were more prevalent than females in all months in a 3 year sampling period, aside from April and May. There was a significant difference between the sexes in terms of mean daily numbers over the months of the study. It was also observed that sexual segregation fluctuated for unknown reasons on a temporal scale. Predictive models for estimating male and female numbers based on a series of abiotic factors were generated. Sea surface temperature, tidal height, tidal range, moon phase, cloud cover, underwater visibility and swell height were related to daily sightings of male and female white sharks to determine the influence of these variables on sexual segregation. Visibility and sea surface temperature affected male numbers, however, visibility did not affect sexual segregation. Tidal height was significantly different between males and females. Sea surface temperature also appeared to be related to sexual segregation in this species. Females were present when temperatures ranged from 15·7 to 18·1° C whereas males were observed at temperatures ranging from 14·3 to 17·8° C, with a peak in sightings in September, when sea surface temperatures were at their lowest. Since parturition is thought to occur in spring or summer, it is suggested that females are absent at this time and only return during prime feeding periods or times at which temperatures are elevated in order to increase developmental growth rates of their young. The significantly lower temperatures in 2003 may explain the absence of females in this year. Hypotheses related to temperature regulation in this species are put forward to explain the sexual segregation observed.     

Bird predation as a sex- and size-selective agent of the arboreal spider Pityohyphantes phrygianus

1. The solitary sheetweb spider Pityohyphantes phrygianus (Araneae: Linyphiidae) lives in canopies of coniferous trees. Earlier studies in Scandinavia have shown that bird predation affects the spider abundance negatively.
2. In a large-scale, 2-year field experiment, passerine birds were excluded from foraging on spruce branches. The experimental branches were net-enclosed, which prevented bird predation but left spiders free to leave and enter. Samples were taken in the autumn and spring for 2 years.
3. Removal of bird predation increased the mean number of subadult P. phrygianus per branch between 2·1 and 10·6 times the control number for each sex. Bird predation had approximately similar effects on the sexes, except in the second experimental spring when males were affected twice as much as females, and there was a significantly lower proportion of males on control branches exposed to bird predation than on net-enclosed branches.
4. The mean size of females was larger on net-enclosed branches than on controls in both spring samples. In males, this was the case in the first spring sample only.
5. This study shows that there are also mortality costs for both sexes associated with large size in the non-mating season. In certain winters, however, there is an additional mortality risk to males, presumably caused by a higher activity level than in females.     

Population genetic substructure in blue whiting based on allozyme data

The genetic population structure of the pelagic gadoid blue whiting Micromesistius poutassou throughout its east Atlantic distribution range was explored using polymorphisms at the tissue enzyme loci IDHP-2 * and PGM-1 *. The study included 5025 individuals from 65 locations in the east Atlantic and the Mediterranean. Significant geographic heterogeneity in allele frequencies was demonstrated at both loci ( IDHP-2 *: P=0·030, PGM-1 *: P=0·005). The degree of genetic differentiation ( F _ST= 1·1%) in blue whiting appears to be at the same level as for the demersal gadoids cod and haddock. Several separate reproductive units were indicated at the fringes of the distribution range, i.e. in the Barents Sea, and in one Norwegian fjord (Romsdalsfjord).     

A demographic comparison of two Nordic populations of Greylag Geese Anser anser

Greylag Geese Anser anser have been neck-banded on an annual basis in Scania, southern Sweden since 1984 and in Norway since 1986 as part of a Nordic Greylag project. This has yielded a large database of resightings, which we used here to estimate and compare survival rates between the two populations by means of mark–recapture models. Estimated adult survival was sex-dependent in the Scanian population, probably a result of differential neck band retention rates in this population. Mean juvenile survival was about 12% higher in the Scanian population (0.603 vs. 0.485). Adult survival in the Norwegian population was 0.728 (males 0.733; females 0.725), and in males and females from the Scanian population was 0.711 (0.752 after accounting for higher neck band loss in males) and 0.771, respectively. Over the course of the study, juvenile survival in the Scanian population increased substantially, and adult survival was constant, whereas both these parameters declined in the Norwegian population. This study demonstrates that the two Nordic populations are demographically distinct and gives further support to the notion that they should be treated as separate management units. The decline of 10% in adult survival in the Norwegian population, the cause of which still remains uncertain, is likely to have had a major impact on the growth of this population.     

Influence of sex, body size, and reproduction on overwinter lipid depletion in brook trout

Expressed as percentages of total fresh body weight, lipids of brook trout Salvelinus fontinalis declined between October and April: reproductive males from 2·89 to 1·22%, reproductive females from 3·19 to 1·84%, and non-reproductive males and females from 2·75 to 2·08%. The absolute and proportional overwinter reduction in lipids among reproductive trout was more than twice that of non-reproductive trout, with reproductive males losing significantly more lipids than reproductive females. Larger reproductive individuals lost more lipids during winter, relative to body size, than smaller individuals, although such an effect was not evident among non-reproductive trout. The average overwinter reduction in lipids for reproductive males (58%), females (42%), and non-reproductive trout (24%) was negatively associated with mark-recapture estimates of overwinter survival probabilities of 0·27, 0·36, and 0·58, respectively, providing support for the hypothesis that energy is allocated to reproduction to the detriment of post-reproductive survival. Our emergent hypothesis that reproductive costs differ between sexes, and the life history consequences thereof, merit further study.     

Sexual differences in reproductive phenology and their consequences for the demography of Baccharis dracunculifolia (Asteraceae), a dioecious tropical shrub

Patterns of phenological variation and reproductive investment were studied in the dioecious shrub Baccharis dracunculifolia DC (Asteraceae), and possible consequences on survivorship were evaluated. The sex ratio was determined in a natural field population (n = 921) of B. dracunculifolia in Belo Horizonte, Brazil. Fifty-two males and 56 females were sampled at random from this population. During the reproductive season of 1999, inflorescence production, shoot growth and mortality, and xylem water potential were recorded for each individual. The population sex ratio was male-biased (1.27 : 1, P < 0.05), and was associated with a higher mortality of female shoots (38.4 vs. 23.1 %, P < 0.05), and individuals (17.8 vs. 11.5 %, P < 0.1), despite lower water stress in female plants. Flowering phenology also differed between the sexes, with males producing more inflorescences, and earlier, than females. Owing to fruit maturation, the number of inflorescences supported by females was higher than that supported by males later in the reproductive season. This occurred during the dry season, and drought stress may have been responsible for the greater female mortality. Thus, the male-biased sex ratio in this population of B. dracunculifolia is probably due to different reproductive functions of males and females. Intersexual differences in reproductive phenology had consequences for plant demography.     

Age, sex ratio and timing of the catch of kelts and ascending Atlantic salmon in the subarctic River Teno

By 15 June, 82% of the catch of Atlantic salmon Salmo salar kelts had been taken from the middle part of River Teno, northern Scandinavia. The median date of capture was 4 June for males and 8 June for females. Salmon of 1–4 sea–winters (SW) of both sexes survived spawning to return to sea as kelts. Among males, 1 SW kelts were caught earliest in the spring and 3 SW latest, but among females 4 SW were earliest, then 3 SW and finally 1 and 2 SW. There were 17 river and sea–age combinations among the kelts compared with 23 among the ascending salmon. The smolt age distribution and the mean smolt age differed significantly only between female 2 SW ascending salmon (3·97 years) and kelts (4·14 years). The proportion of 1 SW females was higher and that of 3 SW males lower among kelts than among ascending salmon. The proportion of males among 1 SW ascending salmon was 80% but among kelts only 57%. Similarly, the proportion of males among 3 SW fish was 21% for ascending salmon but only 7% for kelts. Hence overwinter mortality was higher among males. Male and female kelts of 1 and female kelts of 2 SWhad a greater mean length than ascending salmon in corresponding groups indicating a better survival of larger fish within an age group. Grilse ascend rivers after most kelts have left, but the main catch of ascending 2–3 SW salmon takes place concurrently with kelts leaving the river, inadvertently targeting kelts in the fishery.     

Factors affecting early mortality in the South American fur seal (Arctocephalus australis) in Peru: density-related effects and predation

Early mortality in the South American fur seal ( Arctocephatus australis ) in Peru is considerably higher than that seen in any other population of fur seal; 31–49% in the first month as opposed to a maximum of 20% in other populations. In 1987 and 1988, pup mortality was found to be enhanced by density-related effects and predation on pups by the southern sea-lion ( Olaria byronia ). At a high density beach, where 60% of the fur seals bred, mortality correlated with the number of females ashore as did aggression. Female aggression was driven to high levels by a combination of high density and movement within the colony to thermoregulate. However, even at a low density, beach mortality remained high due to a high level of predation by male southern sea-lions (low density beach 5·0–8·3% of all pups; high density beach 0·2%). Predation rates were lower at the high density beach because male fur seals expelled most attacking sea-lions during the breeding season (low density beach 10·0% of attacking sea-lions expelled; high density beach 58·8%).     

Age and growth of Anguilla anguilla in the Camargue lagoons

Age and total length ( L _T) data from a 11 year monitoring of the Anguilla anguilla eel population of the Camargue lagoons (Rhône delta, southern France) were collected for glass, yellow and silver eels. Three distinct models were calibrated to describe the growth process of undifferentiated eels, females and males, respectively. Uncertainty of parameter estimates was evaluated by bootstrapping. Females were characterized by larger asymptotic body size ( L _T) than males (580 ± 50 v . 388 ± 13 mm) and faster growth, whilst the Brody growth coefficient was larger for males than for females (means ±  s . d . 3·00 10⁻³ ± 1·68 10⁻³ v . 1·73 10⁻³ ± 0·50 10⁻³). Sexual differentiation was estimated to begin at 204 ± 38 mm mean ±  s . d ., i.e . at the end of the second year in the lagoons, well before the L _T at which macroscopic differentiation became possible ( c . 300 mm). Males probably leave the lagoon or die (due to either natural or fishing mortality) within the first 3 years, whilst females can remain up to 5 years. Sexual differentiation and maturation have a major role in shaping the L _T structure of the population. The L _T and mass ( M ) data were fitted by allometric curves     . The calibration of distinct curves for data from different years indicated that the allometric coefficient a was subject to wider interannual fluctuations than the allometric exponent b . A negative correlation linked the average L _T and the allometric exponent ( r  = −0·58, P  < 0·01).