Sex and reproduction of the alfonsino Beryx splendens (Pisces, Berycidae) from the Macaronesian archipelagos

This paper provides comparative information on the reproductive biology of the alfonsino, Beryx splendens Lowe, 1834, species with commercial interest in the Azores, Madeira and the Canary Islands. A total of 846 individuals from Azores (14.0–42.0 cm fork length), 621 from Madeira (17.2–50.0 cm fork length) and 643 from the Canaries (18.2–38.9 cm fork length) were used for the study. The alfonsino is gonochoric with no evidence of sexual dimorphism. Females are more abundant than males; this dominance probably reflects certain differences in the spatial distribution and/or the catchability of males and females in the Macaronesian archipelagos. The spawning season was distinct for the three Macaronesian areas, with an observed North–South variation in the reproductive period: September–March in the Azores, March–June in Madeira and July–September in the Canary Islands. The size at sexual maturity estimated for Madeira and the Canary Islands is similar (32 and 30 cm fork length, respectively), while for the Azores it is reached at smaller length (23 cm fork length). The differences observed in the size at sexual maturity can be explained by the different exploitation levels in each archipelago. Life‐history parameters of the alfonsino suggest that this species has a specialistic life‐history strategy and fisheries based on this species are more susceptible to growth overfishing and population depletion.     

Annotated list of demersal fishes occurring at Sedlo Seamount, Azores north-east central Atlantic Ocean

Several fish surveys were carried out in recent years at Sedlo Seamount, Azores, north-eastern central Atlantic Ocean. An objective of the surveys was to determine the species composition of the demersal fish species living in the area. Four types of sampling gears (bottom trawl and three types of longline) were used at Sedlo Seamount resulting in very different species composition by gear and a very complete coverage of the fish fauna of the area. A list of fishes caught with these sampling methods is presented, along with other specific auxiliary information. Altogether 78 species from 43 families were listed for Sedlo Seamount, and as far as is known, 15 species were recorded for the first time for Azorean waters.     

Different growth trends of whitefish (Coregonus lavaretus) forms in the northern Baltic Sea

The sea growth of two whitefish forms, anadromous (Coregonus lavaretus lavaretus) and sea‐spawning (Coregonus lavaretus widegreni), was analysed using samples collected from the commercial sea catch in the Gulf of Bothnia (GoB) in the northern Baltic Sea during 1998–2014. In the GoB area, these two forms are possible to identify because the gill‐raker number and size at maturity vary between forms. The growth rate of the forms is linked to their feeding area. Sea‐spawning whitefish, which has a feeding migration near its home site, was shorter in the northern GoB (66°N–64°N) at the ages of 3–11 than those in the southern GoB (64°N–60°30′N). In the data, most whitefish were caught with gill nets in the GoB. The mesh sizes of gill nets capturing the anadromous form were mostly 35–45 mm, while those capturing the sea‐spawning form were <35 mm in the northern GoB. It is likely that the different growth trends for small and large whitefish were connected with differences in their recruitment for fishing. The length of anadromous females at the age of four sea years increased significantly, but the length of six‐year‐old anadromous female whitefish decreased over the catch years from 1998–2014. In contrast, the length of slow‐growing sea‐spawning whitefish of six years or older increased significantly in relation to the catch year in the gill‐net catch. The increase in the growth of young age groups in both forms was probably associated with the increasing temperature and the low fishing pressure on small fish. The decreasing age at capture for both forms and the depression of the mean size of old anadromous whitefish are signs of high fishing pressure with a high gill‐net effort that selectively removes the largest and oldest individuals of both forms.     

Visual observations of fish at the Whale Ridge (Atlantic Ocean) from the Sever-2 manned underwater vehicle

Research trawling surveys and visual observations aboard manned underwater vehicles carried out at Whale Ridge revealed 116 species of bottom, near-bottom, over-bottom, and over-bottom-pelagic fish of 46 families. The data on the distribution, number, and behavior, along with some data on biology of the mass fish species, are given in the present paper. The following species prevail by number and biomass: splendid alfonsino Beryx splendens; boarfish Pseudopentaceros richardsoni; redbait Emmelichthys nitidus; flintperch Hoplostethus atlanticus; Helicolenus mouchezi; and fish of families Gempylidae, Oreosomatidae, Macrouridae, Moridae, Alepocephalidae, etc. All these species are subject to fisheries but the boarfish and alfonsino are most commercially important.     

Interannual differences in growth and hatch date distributions of age-0 year walleye pollock Theragra chalcogramma (Pallas) sampled from the Shumagin Islands region of the Gulf of Alaska, 1985 – 2001

Daily increments of age-0 year walleye pollock Theragra chalcogramma otoliths from 1985 to 2001 were examined for interannual variability in growth and hatch dates. Fish were collected in summer and autumn surveys near the Shumagin Islands in the western Gulf of Alaska (GOA). Hatch date distributions of these fish were compared with hatch dates of larvae from spawning aggregations located in Shelikof Strait and the Shumagin Islands based on their spawning times. The hatch date distributions of age-0 year fish captured from the Shumagin Islands area were similar to those observed for larvae from the Shelikof Strait spawning group. Age-0 year fish whose hatch dates corresponded to the Shumagin Islands spawning, which occurred earlier in January and February, were not found. Sea surface temperature was associated with variability in hatch date distribution and growth.     

New data on biology of the pearlfish <Emphasis Type="Italic">Maurolicus imperatorius</Emphasis> (Sternopthychidae) from the Emperor Seamount Chain

The pearlfish Maurolicus imperatorius occurs above seamounts of the Emperor Seamount Chain between 30°–40° N and 168°–176° E. It forms dense aggregations at the daytime in the upper mesopelagial above the ground and disperses in the dark period of the day in the surficial layer. Judged by maturation dynamics of gonads, the spawning of this species occurs from January until April with the maximum in March. Catches of this species are characterized by expressed seasonal dynamics of size composition. Juveniles appear in catches in the end of spring-the beginning of summer. The maximum recorded SL is 68 mm. Among large fish, females dominate. The part of females is maximum in winter and minimum in spring. The age of fish with AC 46–63 mm is 265–420 days. The growth rate is abruptly retarded at the fourth month of life when the length 40–45 mm is attained. Life duration of most fish does not exceed 1.5 years, though some specimens may attain the age of two years. It is supposed that the presence of another species—M. japonicus—on the Emperor Seamount Chain may result from passive transfer in the Kuroshio waters.     

Morphology of ovarian changes during the reproductive cycle of the fish, Mystus tengara (Ham.).

A study has been made of the morphological and histological changes of the cat fish (Mystus tengara) ovary during its reproductive cycle in natural and confined waters. This fish is oviparous and breeds once a year during the rainy season (July throught September). Factors responsible for bringing about spawning in fishes are discussed and the onset of spawning in Mystus is attributed to monsoon rains. In the ovarian cycle 7 phases have been recognised, whic are based on the gross morphological changes in the ovary, the percentage and duration of different developmental stages of oocytes, the average diameter and the gonosmatic index. They are: 1) immature virgin (November-February); 2) preparatory virgin (March-April); 3) maturing virgin (April-May); 4) pre-spawning virgin (June); 5) spawning (July-August); 6) depletion (September), and 7) recoupment (October-November). Oocyte growth has been divided into 9 stages. The ova diameter and gonosomatic index are maximum in July and minimum in November and December.     

Reproductive biology and recruitment of the white sea bream in the Azores

The life history of the white sea bream Diplodus sargus in the Azores showed a pattern consistent with digynic hermaphroditism achieving sexual maturity during the second year of life, at 16·7 cm L _T. Spawning occurred from March to June at temperatures between 15 and 17° C and the onset and duration of spawning season in the sea bream appeared to be influenced by sea water temperatures. As latitude decreased, both in the northern and southern hemispheres, the spawning season of D. sargus populations started earlier and extended longer, highlighting the potential importance of temperature to the onset and duration of reproduction in this species. Settlement took place from late May to July, and settlers remained in the nursery area for c . 2·5 months. Emigration from the nursery area to join shoals of juveniles occurred from late July to September.     

Feeding of Fish at the Seamounts of the Whale Ridge (South-Eastern Atlantic Ocean). 2. Splendid alfonsino Beryx splendens (Berycidae)

Journal of Ichthyology - The feeding characteristics of splendid alfonsino Beryx splendens from the seamounts of the Whale Ridge have been studied. A wide range of food organisms in feeding of...     

Growth, reproduction and recruitment patterns of the wide-eyed flounder, Bothus podas Delaroche (Pisces: Bothidae), from the Azores

The wide-eyed flounder, Bothus podas, occurs in many East Atlantic sub-tropical and temperate inshore areas and is the dominant flatfish in shallow-water areas around the Azores. The aim of this study was to examine the growth, reproductive biology and recruitment patterns of the wide-eyed flounder in the Azores. Adult fish samples were obtained by spear fishing and SCUBA hand netting at Faial Island. Juveniles were obtained from a complementary monthly beach-seining programme undertaken at Porto Pim Bay, Faial. Sex and development stage were determined by macroscopic examination of gonads, whereas age estimates were obtained by counting the number of opaque bands in the otoliths. In the Azores, B. podas reaches 6 years old, which is more than reported for the central Mediterranean, the only other population of this species that has been studied. The studied population has a sex ratio biased to males, which contrasts to a previous observational study, which noted a female-biased sex ratio. Spawning time, as determined from the gonadosomatic ratio and the macroscopic examination of gonads, was between July and September. This time period agrees with behavioural observations in the same area. Sexual maturity was estimated at a total length (TL₅₀) of 14.1 cm and at an age (A₅₀) of 1.7 years. Small juveniles occur on sandy inshore nursery areas for most of the year, but mainly between July and August each year. The presence of small fish throughout most of the year could suggest a protracted settlement period or slow growth on occasions on the shallow-water nursery grounds.     

Age validation and growth of Micropogonias furnieri (Pisces – Sciaenidae) in a temporally open coastal lagoon (South‐western Atlantic – Rocha – Uruguay) based on otolith analysis

In this work 228 individuals of the whitemouth croaker Micropogonias furnieri collected in the Rocha coastal lagoon (Uruguay) from October 1997 to September 1998 were analysed. The species formed annuli in the otolith (sagitta) associated with the opaque zone (narrow opaque annulus), mainly in early winter when water temperature decreased, and reached the lowest values in July–August. The period of greatest growth occurred from December to June, partially overlapping with the spawning period (December–March) and in coincidence with the increase in marginal increment. Growth parameters determined for all individuals were K = 0.19, L _∞ = 30.2 and t₀ = ?2.12. Annual growth increments showed that individuals grew rapidly and attained over 50% of their maximum observed size in the second year of life. In the third year, individuals attained sizes of first maturity at 11–12 cm less than estimates for the Río de la Plata spawning area and coastal areas of Brazil. The increment in length‐at‐age in the Rocha coastal lagoon was smaller than in individuals inhabiting the continental shelf (up to 50 m depth).     

Ichthyoplankton of the Azores seamounts

Species composition and quantitative distribution of ichthyoplankton in the region of the oceanic seamounts of the Azores complex from 2000 to 2004 are considered. The spawning biomass of the main fishery item of this region—Atlantic jack Trachurus picturatus—is calculated. The ichthyoplankton of the Azores seamounts in the period under consideration included eggs and larvae of 60 fish species from 26 families. In the summer, 20 species of eggs and larvae from 11 families and, in winter, 57 species from 24 families were recorded. Larval Myctophidae and Gonastomatidae have the most mass in the plankton in both seasons. The eggs and larvae of commercial fish species (T. picturatus and Pacific mackerel Scomber japonicus) were recorded mainly in the cold period. The species and quantitative composition of ichthyoplankton of the South Azores seamounts is far more numerous than in the North Azores seamounts. The region of the seamounts of the South Azores complex, judging from the estimation of biomass of commercial fish with different methods, can be regarded as a reserve for the fishery of Russian vessels in the central eastern Atlantic.     

Ichthyoplankton of Rockall-Hutton seamounts

Species composition and quantitative distribution of ichthyoplankton in areas of the Rockall-Hutton seamounts are considered in a comparative aspect, and the spawning biomass of the blue whiting Micromesistius poutassou, the main commercial item of this region, is calculated. Maximal catches of eggs and larvae were recorded in spring 2006 and minimal catches were recorded in spring 2003. The highest number of species was recorded in March–April 2006 and the lowest number was recorded in March–April 2003. In the seasons under consideration, M. poutassou had the most mass of the commercial fish in the plankton; haddock Melanogrammus aeglefinus and gurnard Eutrigla gurnardus were less numerous. Of the noncommercial species, the larvae of myctophids (fam. Myctophidae) and of other mesopelagic fish occurred more frequently in the ichthyoplankton. The species and quantitative composition of ichthyoplankton was considerably more numerous at the Rockall Seamount than at the Hutton Seamount, which is explained by specific oceanographic features of the region and the more southern location of this seamount. According to the data of the ichthyoplanktonic method, the spawning biomass of M. poutassou exhibited a tendency for an increase in the period of 2002 to 2006.     

Thermal heterogeneity,migration, and consequences for spawning potential of female bull trout in a river–reservoir system

The likelihood that fish will initiate spawning, spawn successfully, or skip spawning in a given year is conditioned in part on availability of energy reserves. We evaluated the consequences of spatial heterogeneity in thermal conditions on the energy accumulation and spawning potential of migratory bull trout (Salvelinus confluentus) in a regulated river–reservoir system. Based on existing data, we identified a portfolio of thermal exposures and migratory patterns and then estimated their influence on energy reserves of female bull trout with a bioenergetics model. Spawning by females was assumed to be possible if postspawning energy reserves equaled or exceeded 4 kJ/g. Given this assumption, results suggested up to 70% of the simulated fish could spawn each year. Fish that moved seasonally between a cold river segment and a warmer reservoir downstream had a greater growth rate and higher propensity to spawn in a given year (range: 40%–70%) compared with fish that resided solely in the cold river segment (25%–40%). On average, fish that spawned lost 30% of their energy content relative to their prespawn energy. In contrast, fish that skipped spawning accumulated, on average, 16% energy gains that could be used toward future gamete production. Skipped spawning occurred when water temperatures were relatively low or high, and if upstream migration occurred relatively late (mid‐July or later) or early (early‐May or earlier). Overall, our modeling effort suggests the configuration of thermal exposures, and the ability of bull trout to exploit this spatially and temporally variable thermal conditions can strongly influence energy reserves and likelihood of successful spawning.     

Contemporary ocean warming and freshwater conditions are related to later sea age at maturity in Atlantic salmon spawning in Norwegian rivers

Atlantic salmon populations are reported to be declining throughout its range, raising major management concerns. Variation in adult fish abundance may be due to variation in survival, growth, and timing of life history decisions. Given the complex life history, utilizing highly divergent habitats, the reasons for declines may be multiple and difficult to disentangle. Using recreational angling data of two sea age groups, one‐sea‐winter (1SW) and two‐sea‐winter (2SW) fish originated from the same smolt year class, we show that sea age at maturity of the returns has increased in 59 Norwegian rivers over the cohorts 1991–2005. By means of linear mixed‐effects models we found that the proportion of 1SW fish spawning in Norway has decreased concomitant with the increasing sea surface temperature experienced by the fish in autumn during their first year at sea. Furthermore, the decrease in the proportion of 1SW fish was influenced by freshwater conditions as measured by water discharge during summer months 1 year ahead of seaward migration. These results suggest that part of the variability in age at maturity can be explained by the large‐scale changes occurring in the north‐eastern Atlantic pelagic food web affecting postsmolt growth, and by differences in river conditions influencing presmolt growth rate and later upstream migration.     

Life history of the silverside Atherinomorus lacunosus (Atherinidae) in New Caledonia

The abundance, the seasonal variation and the life history of the silverside, Atherinomorus lacunosus , are studied from fish caught in the lagoons around New Caledonia. About 270 nights of fishing were carried out between 1980 and 1983. The silverside is present in most of the fishing hauls but seldom in large quantities. Fish reproduce from September to December at 1 year of age. At this time their size is about 10 cm. Mortality is high and a few individuals can survive a second year and reach 13 cm. Results from other studies indicate that in a less seasonally contrasted environment than the lagoons of New Caledonia, A. lacunosus has several spawning periods during the year. This species is thus able to adjust its phenology to the environmental conditions.     

Sexuality, sex change and maturation patterns in the yellowfin seabream, Acanthopagrus latus (Teleostei: Sparidae) (Houttuyn, 1782)

Macroscopic and histological studies were carried out to describe the reproductive styles and sex reversal and to follow gonadal changes in captive yellowfin seabream during the second year of life. Four reproductive styles are found in Acanthopagrus latus (Houttuyn, 1782): (i) males and females (gonochorism), (ii) functional males, (iii) transitionals and (iv) functional females. The species is a protandric hermaphrodite and begins life as a functional male with testicular zone undergoing active spermatogenesis, while the ovarian zone is arrested at the primary growth (perinucleolar) phase. Males and females were encountered in virtually all size‐classes. Functional males outnumbered the functional females in all size‐classes in which they were encountered. Sex reversal begins in the transitionals from July to August, after spawning in the functional males, at 14.9–20.2 cm standard length (SL) and, by November, maturation of the ovarian tissue begins. A. latus in cages in Kuwait waters spawns from January to April with a peak in February for males, and a peak in March for females and transitionals. Spawning begins in the 18.3–20.2 cm size‐range fish, peaking in the 20.3–22.2 cm size‐range in both males and females and also in the transitionals, although a few of the latter spawn from 14.9 cm SL. In relation to age, spawning begins at 20 months in males and peaks at 21 months. Females begin to spawn at 21 months with a peak at 22 months, while transitionals generally begin to spawn at 20 months, although a few 14–15‐month‐old sex‐changing individuals were encountered. Temperature, either alone or in combination with other unknown factors, triggers spawning in A. latus.     

Divergence in juvenile growth and life history in two recently colonized and partially isolated chinook salmon populations

In 47 families of New Zealand chinook salmon, Oncorhynchus tshawytscha derived from two populations, differing in mean spawning date by 11–17 days and in juvenile life history, neither mean ovum weight nor mean time to hatch differed between the two populations, but substantial differences in mean family weight were apparent from 6 months after fertilization. Differences in growth rates from 12 to 24 months were relatively small, suggesting that most of the divergence in size and growth occurred during the first 6 months of life. There were differences in mean weight for families spawned 11–17 days apart, the approximate interval by which peak spawning date differs between the two populations, but these did not persist beyond 7 months. Differences between the two populations are consistent with their natural life history. The slower growing population experiences cooler temperatures during stream residence and is dominated by fish which spend a year in fresh water before seaward migration, whereas the faster growing population normally experiences warmer temperatures and migrates to sea in the first year of life. These results provide further evidence of life history evolution in partially isolated chinook salmon populations within 90 years ( c. 30 generations) of becoming established.     

Mitochondrial DNA structure and colony expansion dynamics of New Zealand fur seals (Arctocephalus forsteri) around Banks Peninsula

New Zealand fur seals are one of many pinniped species that survived the commercial sealing of the eighteenth and nineteenth centuries in dangerously low numbers. After the enforcement of a series of protection measures in the early twentieth century, New Zealand fur seals began to recover from the brink of extinction. We examined the New Zealand fur seal populations of Banks Peninsula, South Island, New Zealand using the mitochondrial DNA control region. We identified a panmictic population structure around Banks Peninsula. The most abundant haplotype in the area showed a slight significant aggregated structure. The Horseshoe Bay colony showed the least number of shared haplotypes with other colonies, suggesting a different origin of re-colonisation of this specific colony. The effective population size of the New Zealand fur seal population at Banks Peninsula was estimated at approximately 2500 individuals. The exponential population growth rate parameter for the area was 35, which corresponds to an expanding population. In general, samples from adjacent colonies shared 4.4 haplotypes while samples collected from colonies separated by between five and eight bays shared 1.9 haplotypes. The genetic data support the spill-over dynamics of colony expansion already suggested for this species. Approximate Bayesian computations analysis suggests re-colonisation of the area from two main clades identified across New Zealand with a most likely admixture coefficient of 0.41 to form the Banks Peninsula population. Approximate Bayesian computations analysis estimated a founder population size of approximately 372 breeding individuals for the area, which then rapidly increased in size with successive waves of external recruitment. The population of fur seals in the area is probably in the late phase of maturity in the colony expansion dynamic.