Distinct patterns of Arctic cod (<Emphasis Type="Italic">Boreogadus saida</Emphasis>) presence and absence in a shallow high Arctic embayment,revealed across open-water and ice-covered periods through acoustic telemetry

With climate change resulting in unpredictable sea ice conditions between years, it is crucial to gain a more comprehensive understanding of the subsequent effects on Arctic marine ecosystems. Arctic cod (Boreogadus saida) play a key role in the Arctic marine food web, serving as a food source that is estimated to contribute up to 75 % of energy transfer to higher trophic levels. To investigate Arctic cod residency and distribution in Resolute Bay (74°44′N, 095°04′W), 85 individuals from four locations in the bay were captured, measured, weighed, implanted with acoustic tags and subsequently tracked on an acoustic array of 49 receivers. Two main periods of residence in the bay were identified, the first in open water and the second under ice cover, and both concluded with a collective mass departure of fish. A generalised linear mixed model was used to investigate the influence of variables on Arctic cod presence/absence in the bay, indicating that ingress and egress were influenced by environmental changes, particularly those associated with the transition from open-water to the ice-covered period. Timing and distribution, during the study period, appeared to be influenced by a combination of physiological acclimation, and a balance between resource availability and refuge from predators. Receiver site Residence Index (RI) analysis revealed strong site fidelity of fish towards the northern areas of the bay, and this behaviour was consistent between tagging groups and individuals, indicating that the majority of tagged cod were representative of a single school. This study represents the first employment of acoustic telemetry to monitor the movements of individual Arctic cod over 9 months, incorporating both open-water and ice-covered periods.     

Seasonal Distribution of Antlered Sculpin, <Emphasis Type="Italic">Enophrys diceraus</Emphasis> (Cottidae) in Peter the Great Bay,Sea of Japan

The antlered sculpin Enophrys diceraus in Peter the Great Bay is found to inhabit from shallow waters to depths deeper than 600 m. The range of depth where this species occurs is the narrowest, from 12 to 250 m deep, in summer. The greatest depths of inhabitation are characteristic, in all seasons, only of adult fish of this species. In the cold period of the year, the young probably avoid the upper part of the shelf where the temperatures have cooled down to negative numbers. Spawning in the antlered sculpin begins in the second half of November. Females dominate the population of this species inhabiting Peter the Great Bay. Males reach 38 cm long and more; females can be up to 31 cm long. The greatest density of antlered sculpin in the summer period on the preferred substrates is observed in the western part of the bay, primarily on sandy ground.     

应用光合色素研究广西钦州湾丰水期浮游植物群落结构

通过2010年6月现场航次19个站点的调查,应用反相高效液相色谱(RP - HPLC) 并结合二极管阵列检测器分析技术,分析了丰水期广西钦州湾浮游植物光合色素组成,进而由CHEMTAX 软件估算全粒级浮游植物的群落结构。结果表明,钦州湾浮游植物光合色素含量以叶绿素a最高,其次为岩藻黄素;浮游植物的优势类群为硅藻,其次为蓝藻和青绿藻,它们分别平均占据了浮游植物生物量的70.2%、12.6%和9.4%,而其它藻类除了绿藻茅岭江河口占据较高的比例(40.2%)之外在其它站点所占比例很低。钦州湾浮游植物群落结构形成了茅岭江口、内湾、外湾和湾外近海共四种类型,茅岭江口以绿藻为优势类群,内湾以硅藻、蓝藻和青绿藻为主要优势类群,外湾以硅藻为单一优势类群,湾外相对于外湾硅藻比重略为下降。主要光合色素含量及浮游植物类群生物量的分布特征与盐度、营养盐关系密切,浮游植物群落结构的分布变化主要受径流及其输入导致的营养盐变化的影响,而这种影响导致了内湾和外湾之间浮游植物主要类群的生物量多寡及浮游植物群落结构的差异。     

Features of Temporal Differentiation of the Chum Salmon Oncorhynchus ketaof the Anadyr Bay Region at Different Abundance Levels

The temporal heterogeneity of chum salmon stock of the Anadyr Bay region was investigated on the basis of a set of discrete external morphological features and fluctuating asymmetry level of some meristic structures. Differentiation of Anadyr Bay chum salmon during the spawning run was found to be associated with the abundance level of spawning stock in a particular year. Sharply pronounced temporal heterogeneity, based on the investigated characteristics, in the area near the river mouth can be considered as an indicator of the subsequent deficiency of spawners on the spawning grounds of rivers in the Anadyr Bay region.     

Genetic differentiation of Pacific cod Gadus macrocephalus in the Sea of Okhotsk and in the Bering Sea

Genetic differentiation of the Pacific cod Gadus macrocephalus was studied. Samples from six regions of the Sea of Okhotsk and the Bering Sea were analyzed with two mtDNA genetic markers-gene of cytochrome 1 and the control region (D-loop). Comparative analysis showed significant genetic differentiation between the two groups of samples. The first group included samples from Tauiskaya Bay and waters of Western Kamchatka. The second group consisted of the samples collected in the waters of the Iturup Island (Sea of Okhotsk), Northern Kurile Islands, Navarin region of the Bering Sea, and Anadyr Bay.     

Comparison of lethal and non-lethal age-based growth estimation methodologies to assess an endemic bay population of Atlantic cod (Gadus morhua)

The Gilbert Bay, Labrador, MPA (Marine Protected Area) was created in 2005 to protect a genomically distinct and locally adapted bay resident population of Atlantic cod (Gadus morhua) from commercial overfishing. Since then research showed that significant numbers of individuals migrate beyond MPA boundaries creating a concern that fishing continues to impact this endemic population. As part of research and MPA monitoring to assess the health of the protected cod population, lethal sampling of Gilbert Bay cod was conducted from 1998 to 2009 to gather length-at-age data from otoliths. Since then only non-lethal sampling methods were used so as to help conserve the protected population. This study was conducted to compare non-lethally (mark-recapture and length-frequency) obtained age and growth data with lethally (otolith-length-at-age) obtained data. The three methods produced similar results for the 1998 to 2009 period, and both of the non-lethal methods considered were consistent over the 20 year study, confirming their preference over lethal methods for this small endemic fish population.     

Mitochondrial DNA sequence variation and genetic stock structure of Atlantic cod (Gadus morhua) from bay and offshore locations on the Newfoundland continental shelf

Bay cod, Atlantic cod (Gadus morhua) that over-winter in the deep-water bays of northeastern Newfoundland, have historically been regarded as distinct in migration and spawning behaviour from offshore (Grand Bank) cod stocks. To investigate their genetic relationships, we determined the DNA sequence of a 307-base-pair portion of the mitochondrial cytochrome b gene for 236 adult cod taken from the waters off northeastern Newfoundland, including fish found over-wintering and spawning in Trinity Bay. Although 17 genotypes were found, a single common genotype occurs at a frequency of greater than 80% in all samples, and no alternative genotype occurs at a frequency of greater than 3%. Genotype proportions did not differ significantly among samples. Measures of genetic subdivision among sampling locations are nil. Cod over-wintering in Trinity Bay are not genetically distinct from offshore cod. In combination with tagging and physiological studies, these data suggest that there is sufficient movement of cod between bay and offshore locations to prevent the development or maintenance of independent inshore stocks. Adult cod that over-winter in Trinity Bay appear to represent an assemblage of temporarily nonmigratory fish that have become physiologically acclimated to cold-water inshore environments. The pattern of genetic variation in northern cod suggests a recent population structure characterized by extensive movement of contemporary individuals superimposed on an older structure characterized by a bottleneck in the population size of cod in the north-western Atlantic.     

Seasonal migrations of pacific cod <Emphasis Type="Italic">Gadus macrocephalus</Emphasis> (Gadidae) off the eastern coast of Kamchatka

On the basis of materials of bottom trawl surveys of 1974–1992, data of commercial statistics of 1995–2005, as well as literature sources, on the dynamics of seasonal distributions of cod Gadus macrocephalus and its migrations off eastern Kamchatka are studied. In the southeastern part of the shelf of the peninsula, from Cape Lopatka to Kronotskii Bay inclusively, as compared to its northeastern part, in the cold period of the year, a considerable increase in the density of distribution and the commercial catch of the cod are recorded. In the warm period, the density of its distribution and catch, on the contrary, are higher in the northeastern part of the Kamchatka shelf, in Kamchatka Bay, as well as in the Karaginskaya commercial subzone. This suggests that the cod performs rather extended seasonal migrations during which its considerable part winters and spawns off the southeastern coast of Kamchatka and feeds off the northeastern coast, in Karaginskii and Olyutorskii bays, and, possibly, more to the northeast. At the same time, a noticeable part of cod does not perform extended migrations and throughout the year inhabits eastern Kamchatka bays and adjoining waters. Both types of migratory behavior are characterized by seasonal changes in the habitation depth: in the warm period of the year, cod inhabits comparatively small depths near the coast and, in the cold period, comparatively large depths in the external part of the shelf and the upper section of the continental slope.     

Spatial and temporal variability of juvenile spotted seatrout Cynoscion nebulosus growth in Chesapeake Bay

Juvenile spotted seatrout Cynoscion nebulosus growth in Chesapeake Bay was compared to growth from southerly estuaries to examine the potential for countergradient growth variation, and finer scale growth variation within Chesapeake Bay was investigated further. Because spawning and growing seasons in Chesapeake Bay are much shorter than in southern populations, and the bay population is genetically distinct, it was expected that C. nebulosus in Chesapeake Bay may exhibit faster juvenile growth than their southern counterparts. Within the bay, spatial and temporal growth patterns were examined using a repeated measures linear mixed-effects model on individual retrospective growth histories. Juvenile C. nebulosus were collected from seagrass beds throughout Chesapeake Bay in 1997–1999 and 2002; sagittae were removed for daily growth analysis. The calculated growth rate of 1·44 mm standard length day⁻¹ for Chesapeake Bay fish is two to three times that reported for Florida C. nebulosus . Within the bay from 1997 to 1999 (average rainfall years), growth patterns were similar with the fastest growing fish collected from seagrass beds in the central bay, followed by the eastern shore fish with intermediate growth and western shore fish that exhibited slowest growth. These results were reversed (western shore fish growth > eastern shore > central bay) in 2002 (a drought year) even though temperatures across all years were similar throughout the bay, indicating that growth may be influenced by freshwater inflows.     

Schooling behaviour of arctic cod,Boreogadus saida,in relation to drifting pack ice

Synopsis Concentrations of arctic cod were detected with a hydroacoustic system in Resolute Bay, NWT during 2 weeks in August of 1986. Fish biomass within the bay was about 30 t. The fish were feeding primarily on amphipods, which were abundant. When the daily location of the schools was examined in relation to the extent and position of drifting pack ice, a pattern emerged suggesting that the distribution of the fish was influenced by the amount and location of ice cover. If the bay was relatively ice-free, the density of schooling cod was high and the size of the schools, as 2-dimensional surface area, was generally small. When ice covered the bay, density within the schools was lower and they occupied more area. Arctic cod were most dispersed after the bay had been filled with pack ice for several days. It is postulated that this behaviour is a response to potential predation by seabirds and marine mammals.     

An Introduction to a Special Issue on Large‐Scale Submerged Aquatic Vegetation Restoration Research in the Chesapeake Bay: 2003–2008

The Chesapeake Bay is one of the world's largest estuaries. Dramatic declines in the abundance and distribution of submerged aquatic vegetation (SAV) in the Chesapeake Bay over the last few decades led to a series of management decisions aimed at protecting and restoring SAV populations throughout the bay. In 2003, the Chesapeake Bay Program established a goal of planting 405 ha of SAV by 2008. Realizing that such an ambitious goal would require the development of large‐scale approaches to SAV restoration, a comprehensive research effort was organized, involving federal and state agencies, academia, and the private sector. This effort differs from most other SAV restoration programs due to a strong emphasis on the use of seeds rather than plants as planting stock, a decision based on the relatively low labor requirements of seeding. Much of the research has focused on the development of tools and techniques for using seeds in large‐scale SAV restoration. Since this research initiative began, an average of 13.4 ha/year of SAV has been planted in the Chesapeake Bay, compared to an average rate of 3.6 ha/year during the previous 21 years (1983–2003). The costs of conducting these plantings are on a downward trend as the understanding of the limiting factors increases and as new advances are made in applied research and technology development. Although this effort was focused in the Chesapeake Bay region, the tools and techniques developed as part of this research should be widely applicable to SAV restoration efforts in other areas.     

On the distribution of larvae and localization of spawning stocks of White Sea herring <Emphasis Type="Italic">Clupea pallasii marisalbi</Emphasis>

On the basis of ichthyoplankton surveys made in June 2004–2005 and 2007, June–July 2010, and July 2011 in these bays and beyond them (in open waters of the White Sea Basin and adjacent areas of the Gorlo) larvae of White Sea herring were absent. Principal aggregations of larvae are found in the Kandalaksha Bay in June 2004–2005 and 2007. In the Onega Bay and in the Dvina Bay surveyed in June 2007 abundance of larvae was ratter low and in June–July 2010 and July 2011 in these bays and beyond them (in open waters of the White Sea Basin and adjacent areas of the Gorlo) larvae of White Sea herring were absent. Within the Kandalasksha Bay, from year to year, there were two disconnected aggregations of larvae. The space between them was situated in the open part of the bay along the transect of the Chupa Estuary and the Umba Estuary. One of the aggregations of larvae occupied the tail of the bay, and the second aggregation occupied the ante-mouth and mouth areas of the Chupa Estuary. It is supposed that these aggregations result from spawning of two independent spawning groups of the White Sea herring spawning in isolated regions of the Kandalaksha Bay. Presence of the bulk of larvae of the White Sea herring within the limits of the Kandakaksha Bay and their almost complete absence at the boundary of the bay with the White Sea Basin and at the boundaries between the Onega Bay and the Dvina Bay and the Basin support the hypothesis on the absence of an exchange with larvae between stocks of the White Sea herring spawning in large bays of the White Sea. The larvae are retained within shallow waters of the Kandalaksha Bay by the system of two-layer water circulation in the areas of spawning of herring in bays and gulfs of the estuarine type. Their drift outside of the Onega Bay and the Dvina Bay may be delimited by frontal divides at their boundaries with the Basin.     

Bay-scale population structure in coastal Atlantic cod in Labrador and Newfoundland, Canada

Polymorphisms at five microsatellite DNA loci provide evidence that Atlantic cod Gadus morhua inhabiting Gilbert Bay, Labrador are genetically distinguishable from offshore cod on the north-east Newfoundland shelf and from inshore cod in Trinity Bay, Newfoundland. Antifreeze activity in the blood suggests that Gilbert Bay cod overwinter within the Bay. Gilbert Bay cod are also smaller (weight and length) for their age and consequently less fecund for their age, than cod elsewhere within the northern cod complex. The productivity and recruitment potential of coastal cod off Labrador may thus be much lower than that of offshore northern cod or of inshore cod farther south, implying that a more conservative management strategy may be required for cod from coastal Labrador than traditionally practised for northern cod inhabiting less harsh environments. Relatively high F _ST and R _ST measures of population structure suggest that important barriers to gene flow exist among five components that include two inshore (Gilbert and Trinity Bay) and three offshore cod aggregations on the north-east Newfoundland Shelf and the Grand Bank. D _A and D _SW estimates of genetic distance that involve Gilbert Bay cod are approximately three- and 10–fold larger, respectively, than estimates not involving Gilbert Bay cod. The differences between inshore cod from Gilbert Bay and Trinity Bay raise the possibility that other genetically distinguishable coastal populations may exist, or may have existed prior to the northern cod fishery collapse. Harvesting strategies for northern cod should recognize the existence of genetic diversity between inshore and offshore components as well as among coastal components.     

Distribution of Japanese temperate bass, <Emphasis Type="Italic">Lateolabrax japonicus</Emphasis>, eggs and pelagic larvae in Ariake Bay

We collected eggs and larvae of the Japanese temperate bass, Lateolabrax japonicus, and present horizontal and temporal changes of distribution relative to development and growth during the species pelagic life history in Ariake Bay. Sampling was conducted from the inner to central region (11 sampling stations) of Ariake Bay using a plankton net (80 cm diameter, 0.5-mm mesh) from November 2000 to February 2001. Both eggs and larvae were collected most abundantly in mid-December. The CPUE of eggs in the surface layer was higher than the middle layer, which is in contrast to that at the larval stage. Most eggs were collected around the central and western regions of the bay. The distribution of eggs shifted vertically to the middle layer with development. Yolk-sac larvae were collected in the central region of the bay, and preflexion and flexion larvae were more abundantly collected in the inner region of the bay. The body length of larvae around the inner bay was larger than in the central region. The pelagic life history can be summarized as follows: eggs are distributed around the central region of the bay and eggs and larvae expand their distribution to the inner and shallower waters with growth. We conclude that the shift of vertical distribution in pelagic stages and the hydrographic features of the middle layer form one of the mechanisms enabling the inshore migration of L. japonicus.     

Satellite telemetry reveals population specific winter ranges of beluga whales in the Bering Sea

At least five populations (stocks) of beluga whales (Delphinapterus leucas) are thought to winter in the Being Sea, including the Bristol Bay, Eastern Bering Sea (Norton Sound), Anadyr, Eastern Chukchi Sea, and Eastern Beaufort Sea (Mackenzie) populations. Belugas from each population have been tagged with satellite‐linked transmitters, allowing us to describe their winter (January–March) distribution. The objectives of this paper were to determine: (1) If each population winters in the Bering Sea, and if so, where? (2) Do populations return to the same area each year (i.e., are wintering areas traditional)? (3) To what extent do the winter ranges of different populations overlap? Tagged belugas from all five populations either remained in, or moved into, the Bering Sea and spent the winter there. Each population wintered in a different part of the Bering Sea and populations with multiple years of data (four of five) returned to the same regions in multiple years. When data were available from two populations that overlapped in the same year, they did not occupy the shared area at the same time. Although our sample sizes were small, the evidence suggests belugas from different populations have traditional winter ranges that are mostly exclusive to each population.     

Spatiotemporal occurrence and feeding habits of tonguefish,Cynoglossus lighti Norman, 1925, larvae in Ariake Bay,Japan

Spatiotemporal occurrence and feeding habits of tonguefish (Cynoglossus lighti Norman, 1925) larvae were investigated in an offshore area (>5 m in depth) of the inner part of Ariake Bay, Japan. All specimens were symmetric, free‐swimming larvae. Although their seasonal abundance and distribution in the study site varied from year to year, spawning started in June and the larval abundance was high in August and September with a wide distribution in the inner part of the bay. Both present and previous study results strongly suggest that larvae may settle primarily in the estuary and near‐shore areas of Ariake Bay after their wide distribution in the offshore area of the bay during the free‐swimming stage. Larvae showed a clear feeding rhythm in which they fed on prey mainly during the daytime. Larvae fed exclusively on copepods, and identified prey were mostly Paracalanidae (mainly Parvocalanus crassirostris), Microsetella norvegica, and Oithona davisae. Pre‐metamorphosis larvae fed primarily on Paracalanidae and O. davisae, whereas O. davisae formed a smaller proportion of the early‐metamorphosis diet. In early metamorphoses, larvae fed preferentially on Paracalanidae and M. norvegica.     

Distribution,Abundance and population structure of the Antarctic krill (Euphausia superba Dana) in the Prydz Bay region,Antarctica

Summary This paper presents results of net sampling carried out on four marine science cruises, between 1981 and 1985, in the Prydz Bay region of Antarctica by the Australian Antarctic Division. Krill exhibited a patchy distribution and overall low abundance. The majority of sampling sites in January 1985 returned no post-larval krill or densities of <1 individual 1000 m^-3. The estimated mean abundance of E. superba in January 1985 was 6 individuals or 2 g (wet wt.) 1000 m^-3 integrated for the upper 200 m of the water column which represented 3.4% of the total zooplankton biomass. No more than five years-groups, including the larvae, were observed in Prydz Bay, with mean lengths of groups 1+, 2+, 3+ and 4+ being 24, 38, 46 and 53 mm (standard 1), respectively in the middle of January. A high proportion of naupliar stages observed in January 1985 indicated that spawning in Prydz Bay begins in January and examination of adult maturation showed that the spawning continues at least to March.     

Mitochondrial DNA Variation in Northwestern Bering Sea Walleye Pollock, Theragra chalcogramma (Pallas)

Genetic variability of the highly valuable gadid species, walleye pollock, Theragra chalcogramma (Pallas 1811), from five spatially separated northwestern Bering Sea areas (Ozernoi Bay, Olutorskyi Bay, Koryak shelf, Navarin region, and Anadyr Gulf) was investigated. Haplotype diversity within the samples ranged from 0.8788±0.0393 to 0.9436±0.0162. Nucleotide diversity within the samples ranged from 0.0108 to 0.0127. Nucleotide diversity among the regional collections ranged from 0% to 0.18%. Walleye pollock from the Anadyr Gulf appeared genetically separate from the other four samples in a clustering of genetic distances. Total heterogeneity among all five samples was significant, while there was no heterogeneity among the four samples excluding that from the Anadyr Gulf. Pair-wise comparisons using tests for heterogeneity and F_st supported the dendrogram of genetic distances in that only the collection from the Anadyr Gulf was significantly different from the others. The observed pattern of genetic differentiation among walleye pollock from the northwestern Bering Sea presumably emerged as a result of a population of the species subdividing in the northernmost part of its geographic range, though further analysis is needed to verify this supposition.     

Captures of Pacific halibut <Emphasis Type="Italic">Hippoglossus stenolepis</Emphasis> (Pleuronectidae) in Anadyr estuary of the Bering Sea

Pacific halibut Hippoglossus stenolepis is registered in the Anadyr estuary (Bering Sea basin) for the first time: 20 specimens, 18.5–160.5 cm in length, were caught by trawl and longline within the sea portion of the Anadyr River estuary in August 2010 and September 2015 in highly desalted (23.5‰ on average) and heated (6.5°С) water at a depth of 14–30 meters. Halibut is suggested to form feeding groups within the Anadyr Estuary. An opportunity for organized fishing in this region is discussed.     

Ovarian morphology of the Japanese eel in Mikawa Bay

Annual changes in gonadal maturation of female Japanese eel Anguilla japonica in sea water were investigated histologically over 5 years in the Mikawa Bay, Japan, where they occurred throughout the year except in March. Almost all immature Japanese eels (yellow eels) occurred mainly from April to September, and they were rare after November. In contrast, maturing Japanese eels (silver eels) occurred from October to February. The gonado‐somatic index ( I _G) and oocyte diameters of yellow eels were <1·0 and 150 μm, respectively, and oocytes were at the peri‐nucleolus or the oil droplet stages. The I _G and oocyte diameters of silver eels were greater than those of yellow eels and most oocytes developed to the primary yolk globule stage. The numbers of silver eels lacking oocytes at the primary yolk globule stage increased after January in Mikawa Bay, although I _G and oocyte diameters remained unchanged. In contrast, silver eels caught at the mouth of the bay in January possessed oocytes that had advanced to the secondary yolk globule stage. These observations indicate that oocyte development changes seasonally, especially after winter in Mikawa Bay.