Residence and movement patterns of cownose rays Rhinoptera bonasus within a south-west Florida estuary

Between July 2003 and November 2004, 21 cownose rays Rhinoptera bonasus were tagged and tracked within Pine Island Sound estuary, Florida, using passive acoustic telemetry. Residence time of individuals ranged between 1 and 102 days. No relationship was detected between ray activity and tidal stage or time of day. Minimum convex polygons (MCP) and kernel utilization distributions (KUD) were calculated over several time frames to demonstrate the extent of an animal's home range and core areas of use. Total MCPs ranged between 0·81 and 71·78 km² (mean = 22·01 km²), with daily MCPs as large as 25·8 km². Total 95% KUDs ranged between 0·18 and 62·44 km² (mean = 22·63 km²), while total 50% KUDs were smaller, ranging from 0·09 to 9·68 km² (mean = 3·33 km²). Both MCP and KUD areas exhibited a positive relationship with residence time and R. bonasus size. As mobile, pelagic swimmers capable of traversing large distances, these data show that cownose rays travel extensively throughout this estuary, yet may remain within very small areas for extended periods.     

Distribution and reproduction of the southern lantern shark from New Zealand

Distribution, population structure and reproduction are described for the southern lantern shark Etmopterus granulosus at the Chatham Rise, New Zealand. Depth of capture for E. granulosus ranged from 744 to 1420 m, with highest catch rates between 800–1200 m. More than twice as many females as males were captured, and the majority of sharks caught were mature, indicating that there may be segregation according to sex and size class. Only 10 of 492 female sharks captured contained ova in uteri, and none contained embryos. The absence of pregnant females suggests that they move to another area or depth prior to pupping. Size of sharks captured ranged from 20·0 to 78·8 cm total length. Females began to mature at 62 cm total length, and males at 52 cm. There was no evidence of a seasonal reproductive cycle. Ovulation appeared to occur when ova reached a diameter of 40–45 mm. The average number of ova in mature females was 12·7. This information is crucial for assessing the impact of fisheries on E. granulosus populations.     

Composition, structure and distribution of the ichthyoplankton in a Mediterranean coastal lagoon

The species composition and assemblage structure of the ichthyoplankton from the Mar Menor Lagoon in south‐east Spain are given. The fish larvae were sorted from zooplankton samples collected at 20 stations with a plankton net (50 cm mouth diameter and 500 μm mesh) during 36 surveys between February and December 1997. A total of 39 575 fish larvae representing 14 families, 22 genera and 36 species were identified. Gobiidae was the most dominant family (77·0%) followed by Blenniidae (19·4%) and Atherinidae (1·3%). The most abundant species were Gobius niger and Gobius paganellus , which accounted for 42·7 and 19·3% of the total respectively. These species were followed in order of relative abundance by Pomatoschistus marmoratus (13·9%), Parablennius pilicornis (9·4%), Lipophrys pavo (7·7%), Atherina boyeri (1·3%) and Parablennius tentacularis (1·3%). The high species diversity (2·0–2·8 bits individual⁻¹ for the annual diversity spectra at each sampling station) reflected a diverse assemblage of species. The main commercial species in the lagoon (Sparidae and Mugilidae) were poorly represented among the ichthyoplankton and they probably enter the lagoon on the bottom as recruits. Chlorophyll a concentration in the water column was the main factor explaining the seasonal variation in larval abundance. Spatial distribution of larvae was related to hydrographical circulation patterns in the lagoon and the movement of marine‐spawned larvae through the channels connecting the lagoon with the Mediterranean Sea.     

Seasonal variability in growth of larval Japanese anchovy Engraulis japonicus driven by fluctuations in sea temperature in the Kii Channel, Japan

Seasonal variability in the growth of larval Japanese anchovy Engraulis japonicus was examined through otolith microstructure analysis based on the samples collected from the northern side (inner area, IA) and the southern side (outer area, OA) of the Kii Channel from April 2006 to March 2007. Growth trajectories (otolith backcalculated mean standard length of 5 day intervals from 5 days after hatch to 24 days) as well as the most recent 5 day mean growth rate of larvae before capture ( G ₅) differed among months. Growth trajectories showed the same pattern as G ₅. In IA, mean ± s.d. G ₅ ranged from 0·31 ± 0·04 mm day⁻¹ (January) to 0·73 ± 0·06 mm day⁻¹ (October). In OA, mean ± s.d. G ₅ ranged from 0·36 ± 0·05 mm day⁻¹ (January) to 0·79 ± 0·11 mm day⁻¹ (August). G ₅ values declined from November to January and then started to increase. In general, the seasonal patterns of growth were similar between IA and OA, and a clear seasonal pattern in growth was identified. When the relationships among larval growth rate, sea temperature, zooplankton density and larval density were examined, growth rate was positively related with sea temperature in both areas and not related with the other factors. The similar pattern in growth observed between IA and OA was probably due to the low spatial variability in sea temperature compared to its seasonal variability.     

Depth distribution and biological characteristics of the European eel Anguilla anguilla in Lough Ennell, Ireland

Using a longline survey, a total of 196 European eels Anguilla anguilla were collected at different depths in Lough Ennell (maximum depth 30 m), central Ireland. The catch per unit of effort of A. anguilla that were caught from 1 to 25 m depths was lowest at 0·5–5·0 m and greatest at the deepest depth range (22·5–25·0 m). Sub-samples of A. anguilla from depths of <15 m showed little or no difference in size, sex ratio, age, growth rate, condition factor, length–mass relationship, gonado-somatic index, fin index or eye index with fish from depths of >15 m. All fish examined were female yellow-phase A. anguilla that had ages from 7 to 20 years (mean ± s . d . = 10·3 ± 2·9 years), with growth rates from 24·0–60·8 mm year⁻¹ (mean ± s . d . = 40·7 ± 8·5 mm year⁻¹). Variations in the growth rates were greater in the shallow group than that of the deep group. This study suggested that deeper regions are important feeding habitats for A. anguilla and that fish in this lake were growing moderately fast compared to similar habitats and areas in the species' range.     

Effects of different incubation temperatures on the yolk‐feeding stage of Eupallasella percnurus(Pallas)

Embryos and yolk‐feeding larvae of lake minnow Eupallasella percnurus were reared at 13, 16, 19, 22 and 25° C with no access to external food. Time from egg activation to first embryonic movements, hatching, filling of swimbladder and final yolk resorption increased with decreasing temperature. At 13° C, c . 40% of larvae were unable to fill their swimbladder. The predicted lower temperature at which development and growth ceased (biological zero, t ₀) was the same for both processes, c . 7·5–10·5° C. There was no ontogenetic shift in the t ₀ value. Temperature coefficients for development ( Q _10dev.) ranged from 2 to 3 at 19–25° C, but were higher in hatched larvae at lower temperatures. Eggs of E. percnurus had a combination of small size, high hydration and low caloric value of fresh matter. Dry mass of larval tissue on yolk, percentage of dry matter in wet matter, and specific growth rate were maximized at 22 and 25° C. At 19–25° C, energy and matter contained in the initial eggs were converted to body tissue most efficiently. Temperatures from 22 to 25° C are considered optimal for E. percnurus embryos and yolk‐feeding larvae and are recommended for their indoor rearing.     

Thermal tolerance of a northern population of striped bass Morone saxatilis

Thermal tolerance of age 0+ year Shubenacadie River (Nova Scotia, Canada) striped bass Morone saxatilis juveniles (mean ± s . e . fork length, L _F, 19·2 ± 0·2 cm) acclimated in fresh water to six temperatures from 5 to 30° C was measured by both the incipient lethal technique (72 h assay), and the critical thermal method ( C _m). The lower incipient lethal temperature ranged from 2·4 to 11·3° C, and the upper incipient lethal temperature ( I _U) from 24·4 to 33·9° C. The area of thermal tolerance was 618° C². In a separate experiment, the I _U of large age 2+ year fish (34·4 ± 0·5 cm L _F) was 1·2 and 0·6° C lower ( P < 0·01) than smaller age 1+ year fish (21·8 ± 0·5 cm L _F) at acclimation temperatures of 16 and 23° C. Using the C _m, loss of equilibrium occurred at 27·4–37·7° C, loss of righting response at 28·1–38·4° C and onset of spasms at 28·5–38·8° C, depending on acclimation temperature. The linear regression slopes for these three responses were statistically similar (0·41; P > 0·05), but the intercepts differed (25·3, 26·0 and 26·5° C; P < 0·01). The thermal tolerance of this northern population appears to be broader than southern populations.     

Territorial and non-territorial spawning behaviour in the bream

The spawning behaviour of bream Abramis brama was studied in 1993, in a harbour on the River Meuse, Belgium. Fish spawned from 22 to 27 April and from 11 to 14 May, when the water temperature rose to 14.5) C. The reproductive behaviour of the bream was studied within a 15 m long part of the harbour using a video camera. Territorial males with tubercles (33–43 cm total length; >5 years old) defended bank areas of diameter 80–150 cm which included spawning substratum, i.e. roots of alder and willow trees and aquatic plants. Water depth ranged from 25 to 50 cm. Non-territorial males without tubercles (24–33 cm; 3–4 years old), remained 2–4 m away from the bank. Aggressive behaviour between males was frequent and, occasionally, males with tubercles were unable to defend a territory. Mature females (25–43 cm; >3 years old), coming from the deeper water of the surrounding area, were followed by non-territorial males before spawning in territories near the bank.     

The relationship between mosaic muscle fibres and size in rainbow trout (Salmo gairdneri)

The dynamics of increase of the mosaic muscle in hatchery reared rainbow trout (2·3 to 61·3 cm fork length) are investigated. In trout <5 cm, all fibres are <40 μm in diameter; from 5 to 20 cm the diameter mode remains in the 0–39·9 μm class and there is some extension in range of diameter, thereby suggesting that mosaic muscle increase up to 20 cm is mainly by recruitment of new (small) fibres. When trout exceed 20 cm, mode of fibre diameter shifts to the 40–79·9 um class and fibres of larger diameter (> 100 μrn) appear but the subsequent overall fibre diameter frequency distribution changes little until 50 cm. Increase in muscle during the phase 20–50 cm seems partly attributable to increase in fibre diameter, but remains largely the result of recruitment of small fibres, although the mechanism of the latter process appears less clear than in fish of <20 cm. The recruitment of new fibres stops at 55 cm and further increase in mosaic muscle evidently depends upon the ability of existing fibres to increase in diameter. Possible means by which increasing muscle fibre diameter may limit the ultimate size which trout may achieve are discussed. A phenomenon of apparent reduction in fibre diameter in winter among fish 20–39·9 cm long is noted and its significance is considered.     

THE PROLIFERATION OF LYMPHOID CELLS IN GUINEA-PIG BONE MARROW

A double isotope DNA labelling method has been used to determine the duration of DNA synthesis (S) in bone marrow lymphoid cells classified by their nuclear diameters in smears. Incorporation of ³H-thymidine was confined almost entirely to marrow lymphoid cells of 8·0-15·0 μm nuclear diameter (large lymphoid cells). After exposure to ³H-thymidine in vivo and ¹⁴C-thymidine 40-104 min later in vitro , the proportion of cells labelled with ³H alone to those labelled with ¹⁴C(±³H) in radioautographic smears, plotted against time indicated the efflux from S per hour. Collectively, 28·3 ± 1·1% of all large lymphoid cells were in S and the efflux from S was 15·1% per hour. With decreasing cell size (nuclear diameter) the efflux fell progressively from 28·3% per hour (11·0 μm) to 9·2% per hour (8·0-8·9 μm) and the proportion of cells in S declined from 54·9 ± 2·3% to 14·8 ± 1·6%. Influx into S, measured in vitro by reversing the sequence of isotopes, closely resembled the corresponding efflux values in vivo relative to cell size. Most DNA synthesizing marrow large lymphoid cells belonged to a subgroup with deeply basophilic cytoplasm. The results demonstrate that basophilic large lymphoid cells in the marrow are actively proliferating and have a mean S phase duration of 6·6 hr. The largest marrow lymphoid cells (11·0 μm) proliferate most rapidly (S phase, 3·5 hr; maximum cell cycle time, 6·4 hr) while S duration is prolonged progressively to 10·9 hr for the smaller cells (8·0-8·9 μm).     

A new technique to gather 3‐D spatial information using a single camera

A new technique using a single camera and shadows to determine 3‐D spatial positions of fishes in the laboratory is described. The apparatus consisted of a large aquarium (2·0 × 1·5 × 0·4 m), a wide‐angle camera mounted above and two light sources to cast shadows to either side of the fish. Using image analysis and vector mathematics, aquarium objects were plotted within 1·5 cm of their actual location along the x ‐, y ‐ and z ‐axis. The technique was also successful in quantifying changes in 3‐D spatial pattern of juvenile fish, Atlantic cod Gadus morhua (7·4–8·6 cm standard length, L _S) and cohabitant piscivorous shorthorned sculpin Myoxocephalus scorpinus (12·0–25·8 cm L _S), at these same viewing fields. The new technique should have a wide application, largely because it is potentially less expensive, laborious and invasive than alternative methods for determining 3‐D positions of fishes.     

Some aspects of the biology of a cyprinid, Aspius vorax Heckel

Scales were used for the determination of age with back-calculation of length. The oldest fish was VII + years old. Back-calculation did not exhibit Lee's phenomenon. The most rapid growth occurred in summer at water temperatures over 25°C. The growth in weight was c . 331 g year^-1 after IV vears of life. Growth was well described by von Bertalanffy equation : l_l - 91·0 [ l= ^{0·122(l0·25)}] The length-weight relationship followed the cube law (b = 3·0601) K_n ranged from 0·74 to 1·18 with a mean value of 1·0. Spawning occurred in January, fecundity was 74 509 with a mean of 1157 eggs -¹ body weight. Mean diameter of eggs was 1071 (pm). A developed ovary had ova of two sizes, immature oocytes and mature ova. The fish is a carnivorous feeder.     

Effects of hanging ice dams on winter movements and swimming activity of fish

Formation of a hanging dam, a large, thick sub-surface accumulation of frazil ice that blocked river flow, altered physical environmental conditions dramatically and common carp Cyprinus carpio , and brown trout Salmo trutta , evacuated the pool in which the dam developed. A mean of 80·1% of the pool volume was filled with frazil ice. Mean and bottom water velocities in the pool increased from 6 to 27 cm s⁻¹ and from 4 to 21 cm s⁻¹, respectively, when the hanging dam formed, and water depth decreased from a mean of 2·25 to 0·45 m. Activity levels of fish leaving the pool varied. Two carp had higher swimming activities when in the over wintering pool, compared to the period when they were out of it, and a third showed opposite results.     

Hydroacoustic measurement of swimming speed of North Sea saithe in the field

Saithe Pollachius virens , tracked diurnally with a split-beam echosounder, showed no relationship between size and swimming speed. The average and the median swimming speeds were 1·05 m s⁻¹(±0·09 m s⁻¹) and 0·93 m s⁻¹, respectively. However, ping-to-ping speeds up to 3·34 m s⁻¹ were measured for 25–29 cm fish, whose swimming speeds were significantly higher at night (1·08 m s⁻¹) than during the day (0·72 m s⁻¹). The high average swimming speed could be related to the foraging or streaming part of the population and not to potential weakness of the methodology. However, the uncertainty of target location increased with depth and resulted in calculated average swimming speeds of 0·15 m s⁻¹ even for a stationary target. With increasing swimming speed the average error decreased to 0 m s⁻¹ for speeds >0·34 m s⁻¹. Species identity was verified by trawling in a pelagic layer and on the bottom.     

云冷杉天然次生林死木分布格局及空间关联性

为揭示天然次生林群落演替规律,以吉林省汪清林业局金沟岭林场的云冷杉天然次生林为对象,采用相邻网格法调查样地(100 m×100 m)内每株林木(DBH≥1 cm)的基本特征及坐标位置,研究死木的分布格局及空间关联性。结果表明: 死木的径级分布呈左偏单峰山状分布,其中枯倒木呈多峰山状分布;各树种的死木株数与该树种的总株数没有必然联系;树种死木株数与树种混交度之间存在显著负指数关系;死木主要在0～8 m尺度上呈聚集分布,随着尺度的增大,逐渐转变为随机分布或均匀分布,以随机分布为主;中(10 cm≤DBH＜20 cm)、小径级(1 cm≤DBH＜10 cm)死木在8 m以下的小尺度上的聚集分布是造成死木总体在小尺度上呈聚集分布的主要原因。不同径级死木与不同径级活立木的空间关联性差异较大,死木与幼树(1 cm≤DBH＜5 cm)的关系较为明显,尤其是大径级死木与幼树在2～25 m尺度上呈显著正关联性;死木与小树(5 cm≤DBH＜15 cm)没有明显的关联性;中、小径级死木与中树(15 cm≤DBH＜25 cm)在0～3 m尺度上呈正关联性,与大树(DBH≥25 cm)分别在9、11～14 m以及15、42～45 m尺度上呈负关联性。树种在生物学特性、径级分布和空间布局上的差异影响着死木的株数和径级分布;混交程度低的树种可能出现较多的死木;死木空间分布格局随林木径级和研究尺度的大小产生变化;死木与活立木的空间关联性在不同径级和不同尺度上呈现出明显差异。     

The use of pulse‐echo acoustic microscopy to non‐invasively determine the sex of living larval sea lampreys

A rapid, accurate and non‐invasive method to determine the sex of larval sea lampreys Petromyzon marinus , using wide‐field pulse‐scanning acoustic microscopy, is described. Cross‐sectional pulse‐echo scans were made with a high‐resolution acoustic microscope in 48 larvae (110–130 mm total length, L _T), and the acoustic images generated showed such internal body structures as the gonad, intestine, kidneys, cardinal veins, notochord and musculature. Females were identified by the presence of a relatively large (1–1·5 mm diameter) ovary, which was considerably less reflective to the 15 to 25 MHz acoustic signals than the surrounding kidney tissue. Males were recognized by the lack of the large non‐reflective ovary and, in some cases, the appearance of a small (0·2–0·3 mm) testis with slightly stronger reflective properties than the kidney. Identification of sex was confirmed by optical microscopy following dissection, and in a blind test on an additional 10 specimens (121–168 mm L _T), the acoustic method reliably identified sex in 100% of the larvae. These results indicate that acoustic microscopy can determine the sex of live sea lamprey larvae in c . 30 s per animal, a process which until now required dissection or invasive surgery.     

Reproductive biology of the threatened golden galaxias Galaxias auratus Johnston and the influence of lake hydrology

Golden galaxias Galaxias auratus (31–235 mm fork length, L _F) were collected monthly from littoral habitats in Lakes Crescent and Sorell, Tasmania, Australia, between July 2000 and December 2002. Spawning habitats were identified and monitored in both lakes, and surveyed in Lake Crescent. Trends in gonado-somatic indices and reproductive stages of development indicated that gonad development in both sexes begins in midsummer and peaks in late autumn to early winter. Males mature at smaller sizes (50% at 52 mm L _F) than females (50% at 76 mm L _F), larger individuals are predominately females (95% of fish ≥138 mm L _F), and overall male to female ratios are female biased ( c . 1:2). Spawning occurs late autumn to early spring (water temperatures = 1·4–9·7° C) with peaks in spawning activity in winter (mean water temperatures <5° C). Demersal adhesive eggs ( c. 1·5 mm diameter) were found on cobble substrata ( c. 20–250 mm diameter) in littoral areas ( c. 0·2–0·6 m deep) and fecundity of fish 71–181 mm L _F ranged from 619 to 14 478 eggs. The rate of change in water level over the 20 days prior to monthly sampling was important in explaining the occurrence of spent fish and this accounted for temporal differences in spawning between the populations. Lake hydrology influences the reproductive cycle of G. auratus by possibly providing a stimulus for spawning and it controls the availability of spawning habitat in Lake Crescent. Seasonal hydrological cycles ( i.e. rises during late autumn to winter) and a minimum water level of 802·20 m Australian Height Datum in Lake Crescent during autumn (above which littoral areas of cobble substratum are inundated) are critical to G. auratus populations.     

Age and growth of Saurenchelys (Nettastomatidae) and Dysomma (Synaphobranchidae) leptocephali in the East China Sea

The otolith microstructures of the leptocephali of Saurenchelys stylura and Dysomma sp., collected in November and December 2000 in the East China Sea, were examined to determine their larval ages and growth rates, and the spawning times of these two species of outer shelf and slope marine eels. Leptocephali ranging in size from 8 to 48 mm total length were examined, and the nettastomatid, S. stylura , and the synaphobranchid, Dysomma sp., had estimated ages that ranged from 16 to 75 days and 17 to 66 days, respectively. The overall growth rate of S. stylura was 0·68 mm day⁻¹( n  = 21), and of Dysomma sp. was 0·44 mm day⁻¹( n  = 22). These growth rates were similar or slightly faster than those observed for anguillid leptocephali in offshore areas of the western Pacific. The backcalculated hatching dates for these two species were from September to November. The otolith increment widths of S. stylura showed an increase before 20 to 30 days that were similar to those in anguillid species, but in Dysomma sp. there were no remarkable increases.     

Winter behaviour of juvenile Atlantic salmon Salmo salar L. in experimental stream channels: effect of substratum size and full ice cover on spatial distribution and activity pattern

Activity and choice of areas offering different cover (substratum or surface ice) for juvenile Atlantic salmon Salmo salar were studied in experimental stream channels during winter. Channels were completely ice covered between December and March. During this period, the ice thickness increased from 50 to 300 mm after which 50% of the ice was experimentally removed and followed by c. 2·5-fold increase in discharge to simulate the effects of spring flood. Large substrata provided preferred habitats but areas with small substratum sizes were also used when full surface ice provided above-stream cover and the stream discharge was relatively low. The fish remained nocturnal throughout the study but the level of day activity significantly increased as the surface ice became thicker. Maximum movement distance during a 24 h period and homing-at-dawn behaviour remained at a constant level throughout the main winter, but significantly changed during the simulated spring flood (mean ± s . e . maximum extent of movements within 24 h increased from 1·1 ± 0·1 to 3·0 ± 0·5 m; homing behaviour decreased from the highest level of 89·3 to 34·6% during spring flood). Overwinter survival was high (92·9%). Relative mass increase during the study ranged from –8·3 to 28·5%, and 84% of the juvenile Atlantic salmon gained mass. The highest rates of mass increase were associated with frequent movements between areas of different substratum size. The results indicate that during winter: (1) Atlantic salmon parr preferred large substratum cover compared with surface ice cover at the fish densities studied here, (2) juvenile Atlantic salmon were predominantly nocturnal but diurnal activity increased as surface ice became thicker and (3) increase in water discharge during spring altered the behaviour of juvenile Atlantic salmon and may have caused additional habitat shifts.     

Early development and growth of the laboratory reared north-east Atlantic mackerel Scomber scombrus L.

The early development, growth and morphological changes of mackerel Scomber scombrus were investigated at different incubation temperatures (8, 10, 13, 15 and 18° C). Details on the early life history are illustrated with special reference to morphological transformations. Culture techniques to rear larval mackerel stages are described using laboratory cultured foods. Artificially fertilized eggs were hatched after 80·6 h at 18·4° C and 256·8 h at 8·7° C. The standard length ( L _S) of the individuals at first feeding was 4·71 ± 0·18 mm. Four mortality critical periods and cannibalistic behaviour were identified. A maximum average larval size of 37·5 ± 4·41 mm L _S was attained 30 days post-hatch (dph) at 18·4° C. Development and growth were affected significantly by temperature during both endogenous and exogenous feeding periods. Larvae grew more rapidly at high, than at low temperatures. Daily specific growth rate (in mass) ranged from 2·4% at 10·6° C to 16·9% at 18·4° C. Likewise, average growth rate (in length) ranged from 0·05 mm day⁻¹ at 8·4° C to 0·37 mm day⁻¹ at 18·4° C. The allometric relationship of L _S, with several body measurements was not affected by temperature. Comparison with larvae collected in the Bay of Biscay did not show any significant difference in the dry mass and L _S relationship; conversely, the growth rate in length differed significantly between both laboratory and field conditions. The trends observed in the laboratory are described in relation to some aspects of the year-class strength regulation.