Biological structures and bottom type influence habitat choices made by Alaska flatfishes

Habitats of flatfishes are ordinarily characterized on the basis of depth, sediment type, and temperature. However, features of the benthic environment such as structures created by sessile organisms and different bedforms may also influence habitat suitability. In this investigation, we tested the hypothesis that habitat choices made by juveniles of two economically important flatfishes, Pacific halibut (Hippoglossus stenolepis Schmidt) and northern rock sole (Lepidopsetta polyxystra Orr and Matarese), are influenced by structures on the sea floor. In the laboratory, age-0 individuals of both species demonstrated high positive selectivity for habitats with structure (natural sponges, bryozoan mimics, bivalve shells, and sand waves) over smooth sand substratum. The degree of choice was influenced significantly by density of structures, particularly sponges. Small halibut (48-77 and 90-144 mm) were more selective than larger juveniles (270-337 mm), and in sponge habitat juvenile halibut were more selective than comparably sized rock sole. Preference for habitat with structure increased significantly with increasing light level, suggesting that choices were made partially on the basis of visual cues or as related to perceived threat. However, the preference for structured habitat was maintained in darkness. Beam trawl collections made in a flatfish nursery ground near Kodiak, Alaska, revealed that the abundances of age-0 Pacific halibut and rock sole were closely correlated with amounts of shell and echinoderm bycatch in the tows, corroborating the laboratory observations of affinity for habitat structure. Strong preferences for structured habitat in young halibut and rock sole indicate the importance of benthic structures that are frequently removed by fishing gear.     

Sediment preferences and size-specific distribution of young-of-the-year Pacific halibut in an Alaska nursery

A combination of laboratory experiments and field surveys was used to test the hypotheses that responses to sediments change with fish size and that sediment grain-size is the predominant environmental factor affecting small-scale distribution in young-of-the-year (yoy) Pacific halibut Hippoglossus stenolepis . Laboratory tests showed that the smallest fish (31–40 mm L _T) chose fine sediments (muddy and fine sands), fish 51–70 mm had high selectivity (primarily medium sand), and the largest fish (80–150 mm) were not selective although they avoided the largest grain-sizes (pebbles and granules). Sediment preferences were correlated with size-dependent burial capabilities. Beam trawl collections were made over a 6 year period in Kachemak Bay, Alaska, to examine the distribution of yoy Pacific halibut (14–120 mm L _T) using small size classes (e.g. 10 mm intervals). Canonical correlation analysis showed that the per cent of sand in the sediment was a highly significant variable for all but one size and date combination. Catch per unit of effort (CPUE) for newly settled fish (<30 mm L _T) was highest on very fine sand, fish 41–80 mm were most abundant on fine sand, and the largest yoy fish (81–120 mm) were abundant over a range of sediments from fine sand to mud. Except for the smallest fish, Pacific halibut in the field were associated with sediments somewhat finer than predicted from the laboratory experiments; however, virtually all were captured where they could bury easily. The ability of flatfish to bury and shelter in sediment is related to fish size; consequently, habitat associations shift rapidly during the first year of life. Habitat models for yoy flatfishes should consider size-dependent shifts in capabilities and preferences.     

Risk sensitivity in three juvenile (Age-0) flatfish species: Does estuarine dependence promote risk-prone behavior?

Pleuronectid flatfish are generally thought to use stereotypical anti-predator behavior to reduce encounters with potential predators, including burial, maintaining a low profile on the bottom, cryptic coloration, and reduced activity. However, a series of laboratory experiments demonstrate significantly different predation rates on juvenile (Age-0) English sole (Parophrys vetulus), northern rock sole (Lepidopsetta polyxystra), and Pacific halibut (Hippoglossus stenolepis) by Age-2 Pacific halibut predators, suggesting differing anti-predator strategies and/or capabilities among species. In this study, behavioral attributes that control how conspicuous juvenile flatfish are to their predators, such as burial, body posture, and activity levels, were examined both in the presence and absence of perceived predation risk. English sole exhibited risk-prone behavior; they tended to bury less, exhibit an arched body posture (with head elevated off the bottom), and were more active in both the absence and presence of predators when compared to the other two species. Conversely, rock sole exhibited risk-averse behavior, being buried, inactive, with a flat body posture regardless of predation risk. Halibut demonstrated risk-sensitive behavior; behaving like English sole in the absence of predation risk, and shifted to behavior similar to that of rock sole in the face of predation risk. As an estuarine dependent species, English sole recruit to an environment that tends to be highly turbid reducing encounters with predators. As a result English sole, may have “relaxed” anti-predator behaviors in comparison to northern rock sole and Pacific halibut which recruit to less turbid coastal nurseries.     

Adaptive coloration, behavior and predation vulnerability in three juvenile north Pacific flatfishes

Adaptive color change in flatfish has long been of interest to scientists, yet rarely studied from an ecological perspective. Because color change can take a day or so in some species, movement between sediments with differing color or texture may render fish more conspicuous to predators. We conducted laboratory experiments to test the following hypotheses related to adaptive color change in flatfish: 1) fish which do not cryptically match sediment will be more vulnerable to predation, 2) fish will reduce activity and bury to minimize conspicuousness when on a sediment they mismatch, and 3) fish will choose a sediment they match when given a choice. Experiments were conducted using three co-occurring north Pacific juvenile flatfishes: English sole Parophrys vetulus, northern rock sole Lepidopsetta polyxystra and Pacific halibut Hippoglossus stenolepis. As per expectations, juvenile flatfish were more vulnerable to visual predators when they mismatched sediment. Mismatched fish tended to behave differently than fish which matched the sediment. Rather than burying and becoming inactive, they became more active and less likely to bury, perhaps contributing to their predation vulnerability. This increased activity may have represented search for better matching sediment, a stress response, or conspicuousness-related density dependent behavior. Fish which had acclimated to light colored sediment preferred light over dark sediment in choice trials. In contrast, fish acclimated to dark sediment demonstrated no preference. These experiments demonstrate that adaptive coloration is an integral part of the flatfish detection minimization strategy and that movement between habitats can increase risk of predation.     

Biological features of common fish species in Olyutorsky-Navarin region and the adjacent areas of the Bering Sea: 3. Righteye flounders (Pleuronectidae)

Biological features of the seven abundant commercial species—the Pacific halibut Hippoglossus stenolepis, the Greenland halibut Reinhardtius hippoglossoides, the Alaska plaice Pleuronectes quadrituberculatus, the northern rock sole Lepidopsetta polyxystra, the yellowfin sole Limanda aspera, the flathead sole Hippoglossoides elassodon, and the Bering flounder H. robustus (Pleuronectidae)—have been studied for a 20-year period (1995?2015). These species are present in the northwestern Bering Sea in the summer–autumn season; they form the gatherings in Olyutorsky-Navarin region. The size-weight spectra of the fish caught by different fishing gear has been analyzed, the peculiarities of the linear growth and the weight gain, as well as the spawning period and scale and the spawning conditions, have been described. The largest halibut specimens have been registered in the bottom setlines and gill nets, while flounders were in snurrevad catches; the smallest specimens have been observed in trawl catches. The abundant year-class in most of the studied species is seen well on the long-term plots of the fish size spectra and is tracked by the decrease of their biological parameters. The species that demand vast growing grounds (Pacific halibut, Alaska plaice, northern rock sole, and yellowfin sole) are characterized by a smaller average body size of the fish sampled in the coastal waters due to the prevalence of the young specimens in this area.     

Behavioral responses to food odor in juvenile marine fish: Acuity varies with species and fish length

This study tested the hypothesis that acuity of behavioral responses to food odor in three commercially important species of marine fish would increase as juvenile length increased. Swimming activity among two size groups of fish was measured in the presence of a series of squid extract dilutions. Increased swimming activity in juvenile Pacific halibut Hippoglossus stenolepis Schmidt, walleye pollock Theragra chalcogramma Pallas, and sablefish Anoplopoma fimbria Pallas was stimulated above threshold concentrations of squid extract, expressed as dilution from full strength. Maximum chemosensory acuity was observed in smaller (8-14 cm total length, TL) Pacific halibut and walleye pollock, while larger sablefish (15-23 cm TL) continued to develop acuity. Response thresholds were highest (10^− 3 dilution) in Pacific halibut, at intermediate levels (10^− 4-10^− 6 dilution) in walleye pollock and smaller sablefish and reached the lowest levels (10^− 13 dilution) in larger sablefish. The widely held view that dissolved free amino acids (DFAA) are the primary chemosensory stimulants for fish food searching may not be valid for sablefish, as they detected squid extract at dilutions containing DFAA that appeared to be far below ambient sea water DFAA concentrations.     

Fish community responses to ecosystem stressors in coastal estuarine wetlands: a functional basis for wetlands management and restoration

Functional responses of estuarine fish species to environmental perturbations such as wetland impoundment, changes in water quality, and sediment accretion are investigated. The study focuses on the feeding, growth and habitat use by California killifish (Fundulus parvipinnis), topsmelt (Antherinops affinis), and juvenile California halibut (Paralichthys californicus) in impacted coastal wetlands to provide an ecological basis for guidance on the management and restoration of these ecosystems. The ecology of California killifish, Fundulus parvipinnis, is closely tied with the marsh surface, which they access at high tide to feed and grow. Field estimates of food consumption show that killifish can increase their food intake by two-fold to five-fold by adding marsh surface foods to their diet. Bioenergetics modeling predicts that killifish can grow over an order of magnitude faster if they add intertidal marsh surfaces to their subtidal feeding areas. Tidal inlet closures and increased marsh surface elevations due to sediment accretion can restrict killifish access to the marsh surface, affecting its growth and fitness. An open tidal inlet and tidal creek networks that allow killifish to access the marsh at high tide must be incorporated into the restoration design. Topsmelt and California halibut are also adversely affected by tidal inlet closures. Food consumption rates of topsmelt are 50% lower when the tidal inlet is closed, compared to when the estuary is tidally-flushed. Tidal inlet closures inadvertently induce variations in water temperature and salinity and negatively affect growth of juvenile California halibut. Tidal creek networks which consist of channels and creeks of various orders are also important to halibut. Large halibut (>200 mm TL) inhabit deeper, high order channels for thermal refuge, while small halibut (<120 mm TL) are abundant in lower order channels where they can feed on small-sized prey which are typically less abundant in high order channels. Maintaining an open tidal inlet, implementing sediment management programs and designing coastal wetlands with tidal creek networks adjacent to intertidal salt marsh habitat (for fish access) are key elements that need to be considered during the planning and implementation of coastal wetland restoration projects.     

Temperature and state‐dependence of feeding and gastric evacuation in juvenile Pacific halibut

Relationships between nutritional state, behavioural response to prey and gastric evacuation rates were examined in juvenile Pacific halibut Hippoglossus stenolepis feeding on squid. Pacific halibut reared at 2, 6 and 10° C were fasted for 1 or 7 days to generate variation in energetic state. The 7 day fast resulted in measurable declines in condition indices at 10 and 6° C but not at 2° C. At 10° C, all Pacific halibut consumed the first meal offered, but fish previously fasted for 7 days took significantly longer to locate and consume the meal than fish fasted for only 1 day. At 2° C, Pacific halibut fasted for 7 days did not generally consume the first meal offered, but resumed feeding 2·1 days sooner, on average, than fish fasted for only 1 day. The gastric evacuation rate of the squid meal was best described by a power model with near‐exponential curvature ( a  = 1·011). The evacuation rate was strongly temperature‐dependent ( Q ₁₀ = 3·65) but displayed the same degree of variability at each temperature. The evacuation rate in Pacific halibut was not affected by feeding history, body size or energetic state. Furthermore, individual variation in gastric evacuation rate was not correlated with feeding responsiveness at any temperature. These results indicate a general plasticity in the behavioural but not physiological aspects of energy acquisition.     

Effect of rearing temperature on sex ratio in juvenile Atlantic halibut, Hippoglossus hippoglossus

Several flatfish species exhibit temperature-dependent sex determination. This research investigated the effects of rearing temperature on sex ratio in Atlantic halibut, Hippoglossus hippoglossus, a species in which females grow larger and faster than males under culture conditions. Previous research has shown that ovarian differentiation occurs in Atlantic halibut in the size interval of 38–50 mm, and precedes the differentiation of testes. In the current study, triplicate groups of juvenile Atlantic halibut were reared at each of three temperatures (7, 12 and 15°C) from an initial mean size of 21 mm to a final mean size of 80 mm (total length). The sex of each fish was then determined by macroscopic and histological examination of the gonads. Sex ratios were not significantly different from 1:1 in any group, suggesting that sex in this species is not influenced by temperature.     

Energy and ration requirements of juvenile Pacific halibut (Hippoglossus stenolepis) based on energy consumption and growth rates

Growth of captive juvenile Pacific halibut was linearly related to energy consumption (J g⁻¹ day⁻¹) at 4°C by the following equation: growth (% body weight (b.w.) day⁻¹)=0–007 (consumption J g⁻¹ day⁻¹)– 0.192; r² =0.81. Weight gain was independent of size for fish between 9 and 7000 g when growth was expressed as a function of consumption in J g⁻¹ day⁻¹. Maintenance ration determined in feeding–growth experiments averaged 27.4 J g⁻¹ day⁻¹ at 4–0°C. Small halibut ate significantly more food than large fish. Single meals following 2 day fasts averaged 4.1% b.w. for halibut under 100 g, 1.72% b.w. for 1.2 kg fish and 1.1% B.W. for 6.8 kg fish. Both large and small size categories of halibut tended to evacuate their meal in about 3 days even though small fish ate relatively larger meals. Minimum estimates for daily ration to achieve growth rates observed in the Gulf of Alaska were approximately 0.5 to 2.4% b.w. day⁻¹ depending on fish size and whether northern shrimp or yellowfin sole were their prey.     

Scale formation in selected fundulid and cyprinodontid fishes

Patterns of scale formation (onset, points of origin, completion, and spatial pattern) were examined for six species of killifishes in two families (Cyprinodontidae: Cyprinodon variegatus, and Fundulidae: Fundulus confluentus, F. heteroclitus, F. luciae, F. majalis, and Lucania parva) to determine if the patterns are another useful indicator for the transition from the larval to juvenile periods. In some species, the patterns were very similar, with scale formation originating on/near the caudal peduncle, then the dorsal surface of the head (in fundulids only), and later on the lateral surfaces of the head, and on the ventral surface of the trunk at the level of the pectoral fin. The timing of scale formation, relative to fish size, was later than or overlapped with other morphological characters (e.g., fin ray formation, juvenile/adult body shape) often used to mark the larval/juvenile transition. The onset of scale formation, across all species, occurred between 8 and 13 mm TL. Completion of scale formation occurred between 18 and 23 mm TL. At completion, scales covered 86–99% of the trunk and head. Completion of scale formation in these fishes is one of the last external morphological changes to occur during the larval to juvenile transition. For these species, and other flatfishes we have examined in detail, it appears that scale formation may be useful in helping to define the end of the larval period and the beginning of the juvenile period. Further studies, of divergent groups of teleosts, are necessary to determine if this length-based approach has broad validity.     

August diet of age-0 Pacific halibut in nearshore waters of Kodiak Island,Alaska

Synopsis The objective of this study was to describe the diet of age-0 Pacific halibut,Hippoglossus stenolepis, for the inshore waters of Kodiak Island, Alaska during August 1991. Stomach contents were identified from 170 age-0 halibut captured inshore of the eastern and southern coasts of Kodiak Island, and were analyzed in relation to halibut size, location, depth and substrate of capture. One hundred sixty-eight of 170 fish had eaten crustaceans, of which the predominant prey taxa were Mysidacea (34.3%), Cumacea (33.1%), Gammaridea (26.6%) and Caridea (3.9%). In five of six capture locations, mysids and amphipods were predominant prey. In the remaining area, Sitkinak Strait, cumaceans were the primary food source. At depths less than 10 m, mysids were the predominant prey taxa. Gammarid amphipods were of primary importance at depths of 10–30 m. Halibut captured from 30–70 m fed mainly on cumaceans. Cumaceans and gammarid amphipods were consumed by halibut caught on gravel substrate. Fish caught on substrates of sand and mud fed mainly on mysids and amphipods. Cumaceans were also consumed on sandy substrates. Fish 45 mm fed on cumaceans. An ontogenetically related shift in diet occurred at 46–55 mm TL, at which size the halibut's primary prey began to shift from cumaceans to mysids. Fish of 46–75 mm consumed increasingly greater proportions of mysids, amphipods and shrimps. The diet of age-0 Pacific halibut along the Kodiak coast during August was related to predator size, and location, depth, and substrate type of capture.     

Habitat-based submersible assessment of macro-invertebrate and groundfish assemblages at Heceta Bank, Oregon, from 1988 to 1990

Exploitation of groundfish off the U.S. Pacific coast reached maximum levels during the 1990s, resulting in severe declines in at least nine species of groundfish. From 1988 to 1990, we used the 2-man submersible Delta to make 42 dives and run replicate visual belt transects at six stations ranging from 67-360 m in depth at Heceta Bank on the outer continental shelf of Oregon. We identified four major habitats and associated benthic macroinvertebrate and groundfish assemblages: (1) shallow rock ridges and large boulders (< 100 m deep) dominated by basket stars, juvenile rockfishes, yelloweye rockfish, and lingcod; (2) mid-depth small boulder-cobbles (100-150 m) dominated by crinoids, brittle stars, rosethorn, pygmy/Puget sound, and canary rockfishes; (3) deep cobble (150-200 m) dominated by crinoids, brittle stars and various small rockfish species, and (4) deep mud slope (> 200 m) dominated by fragile urchins, sea cucumbers, shortspine thornyhead, and flatfishes. Although substantial interannual variation in groundfish abundance among seafloor types was evident in the 12 most abundant and/or commercially important fish taxa sampled, high variance resulted in statistically significant differences among years only in juvenile rockfishes. These data provide a baseline for future comparisons exploring long-term change this continental-shelf ecosystem.     

School Formation and Concurrent Developmental Changes in Carangid Fish with Reference to Dietary Conditions

The ontogeny of schooling behaviour was studied in comparison to the development of sensory and swimming organs and taxis in carangid fish. Striped jack, Pseudocaranx dentex, larvae showed strong phototaxis at 3 days after hatching (3.5 mm in TL) when they developed pigmentation in the retina. Rheotaxis and optokinetic responses were apparent at 4.0-6.0 mm TL as larvae completed development of the basic structure of their eyes. A major inflection of allometric growth occurred at 9 mm, and fin ray formation was completed at these stages. Schooling behaviour, represented by one TL of inter-individual distance and parallel orientation, only appeared at 16 mm TL, and just prior to this behaviour, fish showed mutual attraction through vision at 12 mm TL. Canalization of buccal lateral lines was complete at 18 mm TL, whereas that of trunk lateral lines started at 23 mm TL and was complete at 30 mm TL. With these results, we assumed that critical factors of the ontogeny of schooling behaviour in carangid fish include not only the development of sensory or swimming organs, but also other factors such as development of the central nervous system. To show this, we reared another carangid species, the yellowtail Seriola quinqueradiata, with dietary depletion of DHA (docosahexaenoic acid), which is indispensable for the development of the central nervous system. Although DHA-free fish showed optokinetic response, they did not show schooling behaviour when they attained their schooling size. Tracer experiments using radioisotope labelled DHA showed that DHA is incorporated into the brain, spinal cord, and retina of juvenile fish. Under natural conditions, carangid fish larvae should intake enough DHA through diet to develop schooling behaviour, the fluctuation of dietary quality in zooplankton might therefore influence the development of indispensable antipredatory behaviour. Morphological changes of striped jack occurred in two steps; first at 9-12 mm (fin formation and inflection of allometric growth) and then second at 20-30 mm (scale and lateral line formation), and these changes corresponded with the development of schooling and recruitment to coastal waters, respectively. Since the onset of schooling is the first step of active antipredatory behaviour, we considered that 12 mm TL is the size at which they attain the juvenile period.     

Ontogenic changes in tolerance to hypoxia and energy metabolism of larval and juvenile Japanese flounder Paralichthys olivaceus

Changes in tolerances to hypoxia and sodium azide, an indicator of cellular respiration, and activities of various energy metabolism-related chemical components were studied in Japanese flounder Paralichthys olivaceus during its early life stages from 3.5 to 20.5 mm in total length (TL). They showed flexion stage around 10.4 mm TL. Lethal levels of hypoxia increased with growth from 3.5 to 8 mm total TL, and the levels remained high in larvae, until 10.4 mm TL, decreased significantly thereafter. The 50% lethal concentration of sodium azide temporarily increased at 4.5 mm TL, diminished drastically between 4.5 and 10.4 mm TL, and then increased again in post-flexion larvae. Cytochrome c oxidase activity was highest in larvae around flexion, at 10.4 mm TL, and subsequently decreased. In post-flexion larvae at 13.0 mm TL, lactate dehydrogenase (LDH) and creatine kinase activities increased; LDH activity decreased at the juvenile stage. The adenosine triphosphate content and energy charge in fish were consistently higher in the larval stage than in the juvenile stage. These results indicated that, from just before flexion to the post-flexion stage, the energy metabolism of larvae is higher due to activated aerobic and subsequent anaerobic metabolism for metamorphosis; as a consequence, hypoxia tolerance in fish is the lowest during the increase of aerobic metabolism just before and around flexion.     

Juvenile Greenland sharks <Emphasis Type="Italic">Somniosus microcephalus</Emphasis> (Bloch &amp; Schneider, 1801) in the Canadian Arctic

Life-stage-based management of marine fishes requires information on juvenile habitat preferences to ensure sustainable population demographics. This is especially important in the Arctic region given very little is known about the life histories of many native species, yet exploitation by developing commercial and artisanal fisheries is increasing as the ice extent decreases. Through scientific surveys and bycatch data from gillnet fisheries, we document captures of rarely reported juvenile Greenland sharks (Somniosus microcephalus; ≤200 cm total length [TL]) during the ice-free period in the Canadian Arctic. A total of 22 juvenile animals (42 % of total catch; n = 54), including the smallest reliably measured individual of 117 cm TL, were caught on scientific longlines and bottom trawls in Scott Inlet and Sam Ford Trough over three consecutive years. Molecular genetic nuclear markers confirmed species identity for 44 of these sharks sampled; however, two sharks including a juvenile of 150 cm TL were identified as carrying a Pacific sleeper shark (Somniosus pacificus) mitochondrial cytochrome b (cyt b) haplotype. This represents the first record of a Pacific sleeper shark genetic signature in Greenland sharks in Eastern Arctic waters. Juvenile sharks caught as bycatch in gillnet fisheries were only observed offshore in Baffin Bay surrounding a fishery closure area, while larger subadult and mature Greenland sharks (>200 cm TL) were caught in all fishing locations, including areas where juveniles were observed. The repeatable occurrence of juvenile Greenland sharks in a fjord and their presence at two offshore sites indicates that these smaller animals either reside in nurseries or have defined home ranges in both coastal and offshore regions or undertake large-scale inshore–offshore movements.     

Parasitology of the English Sole, Parophrys vetulus Girard in Oregon, U.S.A.

A total of 877 juvenile English sole ( Parophrys vetulus Girard) from the Yaquina Bay estuary and742 juvenileandadultsole from the Pacific Ocean off Oregon were examined forparasites. Fifteen species of parasites were found in juvenile English sole on the estuarine nursery ground. Differences in the prevalence and intensity of parasite infection between size classes of juvenile sole and between sole occupying the upper and lower estuary were determined. An additional 14 parasite species were found in offshore English sole, bringing the total observed in all fish to 29 species. Parasites acquired only in the estuary included the microsporidan Glugea stephani , the acanthocephalan Echinorhynchus lageniformis , and the nematode Philometra americana . Those acquired only in offshore areas included the trematodes Otodistomum veliporum and Zoogonus dextrocirrus , the leech Oceanobdella sp. and three species of copepods. An attempt to use parasite data to indicate the presence of distinct English sole stocks along the Oregon coast was inconclusive.     

Fine-scale population genetic structure in Alaskan Pacific halibut (<Emphasis Type="Italic">Hippoglossus stenolepis</Emphasis>)

Pacific halibut collected in the Aleutian Islands, Bering Sea and Gulf of Alaska were used to test the hypothesis of genetic panmixia for this species in Alaskan marine waters. Nine microsatellite loci and sequence data from the mitochondrial (mtDNA) control region were analyzed. Eighteen unique mtDNA haplotypes were found with no evidence of geographic population structure. Using nine microsatellite loci, significant heterogeneity was detected between Aleutian Island Pacific halibut and fish from the other two regions (F _ST range = 0.007–0.008). Significant F _ST values represent the first genetic evidence of divergent groups of halibut in the central and western Aleutian Archipelago. No significant genetic differences were found between Pacific halibut in the Gulf of Alaska and the Bering Sea leading to questions about factors contributing to separation of Aleutian halibut. Previous studies have reported Aleutian oceanographic conditions at deep inter-island passes leading to ecological discontinuity and unique community structure east and west of Aleutian passes. Aleutian Pacific halibut genetic structure may result from oceanographic transport mechanisms acting as partial barriers to gene flow with fish from other Alaskan waters.     

Relationship between body size and habitat complexity preference in age-0 and -1 year winter flounder Pseudopleuronectes americanus

The interaction between body size, habitat complexity and interstice width on habitat preference of age-0 and -1 year Pseudopleuronectes americanus was examined using continuous remote video observation. The habitat choices of juvenile P. americanus were recorded over a 6 h period in tanks with four treatments: bare sand, sand with low complexity cobble, sand with intermediate complexity cobble and sand with high complexity cobble. Both age-0 and -1 year fish preferred cobble to bare sand. Within cobble treatments, age-0 year fish preferred intermediate complexity cobble, with a 1.59 ratio of interstitial space to body width. The largest age-1 year fish (123-130 mm standard length, L(S) ) preferred low complexity cobble. While a significant preference was not detected, medium age-1 year fish (83-88 mm L(S) ) tended to select low complexity cobble, whereas small age-1 year fish (73-82 mm L(S) ) tended to select low and intermediate cobble, with an interstitial space to body width ratio of 1.05. For medium and large age-1 year fish, there was an increased selection of low complexity cobble, corresponding to larger interstitial space to body size ratios. This study indicates that juvenile P. americanus prefer complex habitat to unstructured habitat and that this preference is mediated by a relationship between fish body size and the size of structure interstices. These results contribute to the growing body of knowledge of complex habitat selection and drivers of habitat choice in flatfishes.     

Morphogenesis in hatchery-reared larvae of the black rockfish,Sebastes schlegeli,and its relationship to the development of swimming and feeding functions

The developmental sequence of morphological characteristics related to swimming and feeding functions was investigated in hatchery-reared larvae and juveniles ofSebastes schlegeli, a viviparous scorpaenid. The fish were extruded at an early larval stage, when the mean body size was 6.23 mm TL. Fin-ray rudiments became visible at 9.0 mm TL in the dorsal and anal fins, at 8.0 mm TL in the pectoral and pelvic fins and 6.0 mm TL (size at extrusion) in the caudal fin. Completion of segmentation of soft rays in the dorsal and anal fins was attained by 14 mm TL and in all fins by 17 mm TL. Branching of soft rays in the respective fins started and was completed considerably later than the completion of segmentation, as well as ossification of the fin-supports. Morphological transformation from larva to juvenile was apparently completed by about 17 mm TL. Although the completion of basic juvenile structures was attained by transformation at that body size, succeeding morphological changes occurred between 17 mm and 32 mm TL. Newly-extruded larvae possessed one or two teeth on the lower pharyngeal and pharyngobranchials 3 and 4, but lacked premaxillary, dentary, palatine and prevomer teeth. The fish attained full development of gill rakers and gill teeth by 15 mm TL, the upper and lower pharyngeal teeth subsequently developing into a toothplate. Development of the premaxillary, dentary and palatine teeth was completed at about 30 mm TL, by which time loop formation of the digestive canal and the number of pyloric caeca had attained the adult condition. The developmental sequence of swimming and feeding functions during larval and early juvenile periods appeared to proceed from primitive functions to advanced or complex ones, from the ability to produce propulsive force to that of swimming with high maneuverability and from development of the irreducible minimum function of passing food into the stomach to the ability to actively capture prey via passive food acquisition with the gill rakers and gill teeth. The relationship of morphological development to the behavior and feeding activity of artificially-produced hatchlings is also discussed.