Mackerel icefish size and age differences and long‐term change at South Georgia and Shag Rocks

This study analysed the total length ( L _T)‐frequency distribution of mackerel icefish Champsocephalus gunnari at South Georgia and Shag Rocks from nine bottom trawl surveys at South Georgia and eight at Shag Rocks between 1987 and 2002. The estimated mean L _T of age‐classes 1+, 2+, 3+ and 4+ years during January were, respectively, 14·7, 23·5, 29·8 and 35·1 cm at South Georgia. Age‐classes 1+, 2+ and 3+ years were 18·3, 26·2 and 33·8 cm at Shag Rocks. The derived Bertalanffy growth parameters for South Georgia were: L _∞ = 51·7 cm, k  = 0·27 and t ₀ = −0·26. The mean L _T of each age‐class of C. gunnari at Shag Rocks was significantly larger than at South Georgia, equivalent to c . 5 months growth, although the annual growth in L _T was similar. This is further evidence that C. gunnari hatched earlier at Shag Rocks. At South Georgia, the mean L _T of age‐classes 1+ and 3+ years were correlated, and significantly decreased between 1987 and 2002, and were smaller following warmer summers. This decrease in the size of C. gunnari may be the result of reduced food availability linked to climate warming.     

Age and growth parameters of Siganus sutor in Kenyan marine inshore water, derived from numbers of otolith microbands and fish lengths

Siganus sutor (Valenciennes, 1835) is, together with the Lethrinidae, commercially the most important fish of Kenyan waters. Age and growth parameters of this fish have been estimated for stock assessment purposes, using the von Bertalanffy growth model while taking into account the initial small but finite length of fish, L _o. Microbands on the otoliths were used as a measure of age in days. Data of fish length against numbers of microbands were fitted to the growth formula by a least squares procedure applied to a non-linear fit. This gave an L _∞ of 36.2 cm s.l. and a K of 0.87 on an annual basis. Independently, a curve was fitted by eye to the same data, and values were read off the curve and used in a standard Ford–Walford plot. This gave an L_x of 35 cm and a K of 0.9. The close agreement of the values obtained by the two methods, and of these with values in the literature, demonstrates the value of using microbands for determining growth parameters in a tropical fish.     

Age, growth, mortality and population characteristics of the pearl perch, Glaucosoma buergeri Richardson 1845, from deeper continental shelf waters off the Pilbara coast of north-western Australia

Pearl perch, Glaucosoma buergeri Richardson 1845, from deeper waters (> 100 m depth) on the continental shelf of north-western Australia were aged by examining transverse sections of their sagittal otoliths. Ages were assigned based on counts of alternating opaque and translucent zones (annuli). Otolith length and breadth (width) increased linearly with fish length, whereas otolith weight increased linearly with fish age. The continuous growth of the otoliths provides some evidence that the opaque and translucent zones used to estimate age in this study are formed on a regular basis. Parameters of the length–weight relationship were estimated, along with parameters of the von Bertalanffy growth function. The generalised von Bertalanffy growth function (total length-at-age, both sexes combined) for G. buergeri was L _t=512.7 (1 – e^{–0.139( t  + 0.89)}). There was no significant differential growth between the sexes in observed length-at-age. The oldest individual found was a male G. buergeri estimated to be 26 years of age. The annual instantaneous rate of natural mortality ( M ) was estimated to be 0.14. The slow growth, long life and low natural mortality rate indicate that G. buergeri is vulnerable to overfishing and that harvest strategies for this species should be conservative, given its low production potential.     

Age, growth and cohort composition of 0+ carp in the River Murray, Australia

The age, growth and cohort composition of young-of-the-year (0+) carp, Cyprinus carpio from the River Murray in South Australia were investigated. Daily otolith microincrement formation was validated for the first 5 weeks of life in tetracycline-marked, laboratory-reared fish. Estimation of hatching dates from otolith microincrement counts corroborated the validation method and revealed two major peaks of spawning activity in October and in November. Two main cohorts of carp were distinguished, each consisting of several subcohorts showing variable growth rates. A simple linear regression and a logistic curve best described growth in length and weight, respectively, of wild larvae and juveniles. Two breakpoints, at 16·8 and 26·9 mm L_s , were identified in the length—weight relationship, depending on the procedure followed in fitting a piecewise regression model to the log-transformed variables. The insertion of an additional step of development in the larva period of the early ontogeny of carp is proposed.     

Age determination and growth of the pollan, Coregonus autumnalis pollan Thompson, of Lough Neagh, Northern Ireland

Scales from Lough Neagh pollan display a large number of checks, making age determination difficult. Sclerite counts showed that an annual check is formed on scales in May and a second accessory check in most young fish in October. The method of ageing from scales was supported by inspection of length-frequency plots and by following the growth of pollan in their first 2 years of life. The body-scale relationship was curvilinear. Back-calculation showed that pollan of both sexes attain a fork length of 29 cm in 5 years (1 ∞=28.9 cm; k = 0.65; l ₀= -0.06 year). There is no evidence that annual growth rates have changed since 1965. Possible environmental causes of scale check formation are discussed.     

Distribution, growth, diet and foraging behaviour of the yellow-fin notothen Patagonotothen guntheri (Norman) on the Shag Rocks shelf (Southern Ocean)

The distribution, total length ( L _T) frequency and diet of Patagonotothen guntheri are described from 14 bottom trawl surveys conducted on the Shag Rocks and South Georgia shelves in the austral summers from 1986 to 2006. Patagonotothen guntheri (80–265 mm L _T) were caught on the Shag Rocks shelf from depths of 111 to 470 m, but no specimens were caught on the South Georgia shelf. Multiple cohorts were present during each survey and L _T-frequency analysis of these cohorts suggests that growth was slow (von Bertalanffy K = 0·133). Evidence from stomach contents and acoustic data (2005 and 2006) showed that P. guntheri is primarily a pelagic feeder, migrating from the sea floor towards the surface to feed during daylight. The diet of smaller fish (<140 mm) was dominated by copepods, predominantly Rhincalanus gigas , whilst larger fish principally consumed the pelagic hyperiid amphipod, Themisto gaudichaudii and Antarctic krill Euphausia superba . Some larger fish also took benthic prey.     

Observations on the age, growth, reproduction and food of the pike Esox lucius (L.) in two rivers in southern England

Opercular bones of 261 pike from the River Stour and 117 from the River Frome were used for age and back-calculated growth determinations. The annuli were laid down during late April and early May and most growth occurred between May and September. Pike growth in the two rivers was comparable with the fastest growth in other waters, though Frome pike grew slightly faster than Stour pike. Spawning occurred from the end of March into May. Elaboration of the ovaries commenced in September and was virtually completed by February, whereas the testes reached their maximum weight in October and maintained it until spawning. Immature pike had an annual cycle of condition reaching a maximum in May and a minimum during the winter. The gonad cycle affected the condition of mature females which had their minimum condition in mid-summer. The fecundity of Stour pike is expressed by the formula: log₁₀ egg number =3.56 log₁₀ fish length (mm) – 5.40. Approximately 75% of all Stour pike were sexually mature by age II and these fish were, on average, larger than immature pike of the same age. The most numerous items in the diet of pike were small cyprinids, 30–80 mm fork length, although pike over 700 mm long ate larger fish. Few salmonids appeared in the diet of either Frome or Stour pike. The percentage of empty stomachs was highest in Stour samples taken during the summer, shorter digestion times and longer feeding periods in this period are suggested as reasons for the apparent anomaly.     

Population ecology of pike-cichlid, Crenicichla lepidota, in two streams of the Brazilian Pampa subject to a severe drought

Scales were valid for age determination of pike-cichlid Crenicichla lepidota Heckel in two Brazilian streams, since, for every age-class, annual rings (annuli) were formed once a year, in August. Back-calculated Jengths-for-age coincided with those obtained by inspecting the monthly length-frequency distributions. Only 11 reproductive females were captured (length range 9.6–16 cm, age 1+ and 2 + ) and their fecundity ( F ) increased with fish length ( L ) according to: F= 2.4027 L^2.3631. Average annual density and biomass in four localities of Zanga do Campus were 2194, 1676, 1824 and 1071 individuals ha⁻¹ and 17.2, 12.1, 13.8 and 18.7 kg ha⁻¹and about 1000 individuals ha⁻¹ and 8.5 kg ha⁻¹ in three combined sites of Zanga do Barbará. The annual production ranged between 18.5 and 32.7 kg ha⁻¹ a ⁻¹ in the first stream and 8.7 kg ha ⁻¹a ⁻¹ in the other. Feeding tactics differed between streams and age-classes (0+ v . 1+/2+). In winter, the 0+ age-class in Zanga do Campus fed mainly upon Ephemeroptera (Baetidae) but in other months also fed on zooplankton. In winter, these age-classes in Zanga do Barbara preyed upon benthic species but the contribution of different taxa varied between months. In January, these fish preyed exclusively upon Chydoridae and fish. The effects of a severe drought (November-February) upon these parameters are discussed.     

Age estimation, growth, maturity and distribution of the roundnose grenadier from the Rockall trough

This paper summarizes the history of commercial exploitation of roundnose grenadier Coryphaenoides rupestris in the North Atlantic. Length frequencies of C. rupestris in 1993, from 400 to 1200 m on the slopes of the Rockall trough indicate a reduction since the 1970s in the modal length of fish found at 700–1000 m. Ages ranged from 2 to 50 years for males and 2 to 60 years for females, with most between 10–38 years. Females attained a greater asymptotic pre-anus length ( L _∞=19.5 cm) than males ( L _∞=15.5 cm) and had a greater weight for a given age (male W _∞=761g, female W _∞=1132g). This species may have a protracted spawning period. Using pre-anus lengths, 50% of male fish were mature at 10 cm (ages 8–10) while 50% of female fish were mature at 12 cm (ages 9–11). At the greatest depths sampled the length frequency of fish was bimodal with a hiatus between 9 and 11 cm (ages 8–12). Highest catch rates occurred on the Donegal slope in September at a depth of 800–1000 m.     

Growth, diet and metabolism of common wolf–fish in the North Sea, a fast–growing population

The von Bertalanffy growth parameters for common wolf–fish Anarhichas lupus in the North Sea were: male: L ∞=111·2 cm, t ₀=–0·43 and K =0·12; and female: L ∞=115·1 cm, t ₀=–0·39 and K =0·11, making this the fastest growing stock reported. Resting metabolic rates (RMR±S.E.) and maximum metabolic rates (MMR±S.E.) for six adult common wolf–fish (mean weight, 1·39 kg) at 5° C were 12·18±1·6 mg O₂ kg^–1 h^–1 and 70·65±7·63 mg O₂ kg^–1 h^–1 respectively, and at 10° C were 25·43±1·31 mg O₂ kg^–1 h^–1 and 113·84±16·26 mg O₂ kg^–1 h^–1. Absolute metabolic scope was 53% greater at 10° C than at 5° C. The diet was dominated by Decapoda (39% overall by relative occurrence), Bivalvia (20%) and Gastropoda (12%). Sea urchins, typically of low energy value, occupied only 7% of the diet. The fast growth probably resulted from summer temperatures approximating to the optimum for food processing and growth, but may have been influenced by diet, and reduced competition following high fishing intensity.     

Lifetime consequences of variable 0 year group length in riverine populations of chub Leuciscus cephalus (L.)

The fork length ( L _F) of individual chub Leuciscus cephalus in English riverine populations at the end of their first growth season varied considerably, ranging from <25 to >70 mm. This had a significant influence on the subsequent growth of individuals over their lifetime. Chub of small L _F at age 1 year generally produced smaller annual growth increments throughout life than those of longer L _F at age 1 year, although they had the potential to attain greater ultimate L _F. This variability in L _F at age 1 year resulted, at least in part, from multiple spawning events over a protracted period, that caused variation in the growing seasons for 0 year group chub of the same year class. Since the adult population contained individuals that only attained L _F of <25 mm at the end of their first growing season, it is possible that L _F at age 1 year may not be such a major precursor to strong chub recruitment as previously thought.     

Biometrics of Sardinella longiceps Val. in relation to upwelling in the Gulf of Aden

Growth, size composition, condition factor and gonad index of the oil sardine, Sardinella longiceps Val., oscillated over an annual cycle in relation to upwelling. Growth in length was modelled using the formula of Pauly & Gaschütz (1979): where L _t= length cm at age t years, L_∞= 23.8cm, K=0.97, t_o=0.70, C=1.08 and t_s=−0.08. The relationship of growth rate, spawning, and condition factor, to upwelling and plankton blooms is discussed.     

A simple regression model to assess environmental effects on fish growth

Multiple regression was used to assess relationships between annular growth and environmental variables. This approach (1) tests for the significance of environmental changes on fish growth and (2) can be successfully used to predict fish growth using different environmental conditions. Age usually explains a large proportion of the variation in growth increments measured in length, and these two variables are inversely related. Since length increments decline as age increases, environmental impacts on growth will be reduced as fish grow older. To account for within-age growth variation and incorporate this age-dependent factor, the inverse of age (1/age in years) is multiplied by the value of an environmental variable (ENV) that may be related to growth. This interaction term and age are regressed against mean annular growth increments in length (TLINC; l _{t +1}— l ₁):
TLINC = b₀—b₁AGE±b₂(1/AGE)*ENV
where b₀, b₁, and b₂ are the regression coefficients for intercept and slope, respectively. Additional variables that measure environmental factors can be added to the model. Environmental effects associated with growth rates of black crappie, Pomoxis nigromaculatus (LeSueur), are presented as an example.     

Growth rates of Lutjanidae (snappers) in tropical Australian waters

Growth rates of three commercial species of Lutjanidae were estimated from sections of vertebrae cross-checked with scales. The von Bertalanffy growth constants for Lutjanus malabaricus were K =0.168, L_∞ =70.7 cm standard length (S.L.). For Pristipomoides multidens these were K = 0.219, L _∞= 59.1cm, and for Pristipomoides typus K =0.254, L _∞= 51.5 cm. Length/weight was analysed in the form W= aL^b where W was fresh weight (g) and L = S.L. (cm). The constants were: L. malabaricus, a = 0.041, b = 2.842; P. multidens, a =0.032, b = 2.897; P. typus, a = 0.038, b = 2.822. The growth rates were considered low in comparison with demersal fish counterparts from temperate seas.     

Compensatory growth of juvenile brown flounder Paralichthys olivaceus (Temminck & Schlegel) following thermal manipulation

The compensatory growth of juvenile brown flounder Paralichthys olivaceus (body mass c. 12 g) following different thermal exposure was investigated. Fish were exposed to one of the five temperatures: 8·5 ( T _8·5), 13·0 ( T _13·0), 17·5 ( T _17·5), 22·0 ( T _22·0) and 26·5° C ( T _26·5) for 10 days and fish grew best at 22·0° C. Then the water temperature in all treatments was equably adjusted to 22·0° C over 3 days. At the end of the following 30 days after temperature adjustment, there were no significant differences between body masses of fish in the different treatments (wet body mass at the end of the experiment ranged from 22·13 to 24·56 g). Results indicated that the juvenile P. olivaceus achieved complete compensatory growth. Analysis of the dynamics of the feeding rates and feed conversion efficiencies indicated that compensatory growth of the fish experienced low temperature ( T _8·5, T _13·5 and T _17·5) or high temperature ( T _26·5) exposure was mainly dependent on increasing feed intake (hyperphagia) and possibly by improvement in feed conversion efficiency. The moisture content was not affected by different temperature exposure significantly. The lipid and energy content of juvenile P. olivaceus in T _8·5, however, were significantly lower than other treatment. Results of the current study indicate that a short period of low or high temperature exposure may not affect annual growth, but may affect lipid and energy deposition.     

Regional, interannual and size-related variation of age 0 year walleye pollock whole body energy content around the Pribilof Islands, Bering Sea

Mean whole energy content ( E _wb) of age 0 year walleye pollock Theragra chalcogramma was 19.928 KJ g⁻¹ dry mass in 3943 fish collected from different habitats around the Pribilof Islands frontal structure, south-east Bering Sea, during September 1994–1996 and 1999. It varied, however, with habitat type. Fish residing offshore had higher E _wb than fish residing inshore of the frontal regions. Age 0 year walleye Pollock E _wb changed in a non-linear fashion with fish size, with larger juveniles typically having higher E _wb. Size thresholds were identified at which the relationship between age 0 year walleye pollock E _wb and L _S changed. One such threshold was found at 46 mm where E _wb reached a local minimum. Another threshold was found at 80 mm beyond which E _wb tended to remain constant with size. Overall mass-length and E _wb-length residuals were highly correlated with each other ( r =0.73, P ≪0.0001). The slope of the regression, however, was higher for smaller fish. Possible mechanisms are proposed to explain the observed ontogenetic variation in nutritional status and the role of age 0 year walleye pollock late summer E _wb on survival over their first critical winter of life.     

Behavioural and physiological adaptations to a burrowing lifestyle in the snake blenny, Lumpenus lampretaeformis, and the red band-fish, Cepola rubescens

Observations have been made on the mode of burrow construction in the snake blenny, Lumpenus lampretaeformis , under laboratory conditions. It appears that head probing and lateral oscillations of the body are principally responsible for the excavation of the burrow which is completed within 24 h. The burrow structure has been analysed in detail, showing a mean depth of 7.2 cm with a maximum observed length of 73 cm, with most systems between 20 and 35 cm in length. Initially linear burrows with two openings are usually provided with a small side tunnel, giving the system a characteristic Y-shape.
Burrow irrigation was investigated for the first time in L. lampretaeformis. The mean duration of burrow irrigation, by flexions of the tail of the fish, was 21 s with over 13 min h⁻¹ spent in irrigating the burrow. The mean water displacement per irrigation period was 3.1 ml. The PO ₂ and PCO ₂ were measured in both surface water and within the burrow system of L. lampretaeformis. Surface water values for PO ₂ were high (> 150 Torr) and PCO ₂ low (<0.4 Torr). Hypoxic and hypercapnic conditions were measured in the burrow system itself, with PO ₂ values ranging between 57 and 129 Torr and PCO ₂ rising to > 1.3 Torr in some burrows.
A comparative study of Cepola rubescens burrows indicated similar surface water PO ₂ and PCO ₂ values as in L. lampretaeformis. Burrow water PO ₂ values ranged between 60 and 94 Torr, with PCO ₂ values as high as 1.5 Torr being recorded. These results are discussed in relation to the adaptation of both species to a burrowing lifestyle.     

Validation of the periodicity of increment formation in the otoliths of a cichlid fish from Lake Tanganyika, East Africa

Tetracycline was used as a chemical tag in a mark‐recapture study to examine the pattern of increment formation in the otoliths of Tropheus moorii , a rock‐dwelling cichlid from Lake Tanganyika. A total of 256 fish were captured by divers and injected with tetracycline. Of these, nine were recaptured after either 1 or 2 years at liberty and eight retained tags within their otoliths. Comparison of the number of growth increments formed after the tag and the time at liberty demonstrated that increments were deposited on an annual basis in the otoliths of this species. Furthermore, there was a strong relationship between otolith mass and age suggesting that otoliths grew at a predictable rate throughout the life of the fish. Validation of an annual pattern of increment deposition allowed age and growth information to be derived from otoliths. This showed that T. moorii grew rapidly to attain adult size by 3 years of age. Males grew faster than females and also attained a larger size than females (8·74 v . 7·91 cm L _S respectively). The longevity of some of these small freshwater fish was surprising; the oldest individual had an age of 10 years, while the average age of adults was 4 years.     

Taxonomy of the deep-sea eel genus, Histiobranchus (Synaphobranchidae, Anguilliformes), with notes on the ecology of H. bathybius in the eastern North Atlantic

The eel genus Histiobranchus Gill occurs benthopelagically over the continental rise and abyss of the World Ocean, primarily beneath temperate and subpolar surface waters. Its generic status within the subfamily Synaphobranchinae is confirmed by comparison of the structure and topography of its cephalic sensory system and skeletal features with Synaphobranchus. At least three species of Histiobranchus are recognized: H. bathybius (panoceanic), H. bruuni (Tasman Sea and waters south-east of New Zealand) and H. australis (two geographical forms; South Atlantic and south-western Indian Ocean, and South Indo-West Pacific Oceans). Collections totalling 319 specimens of H. bathybius from the eastern North Atlantic (1790–5440 m depth) yielded a size range of 99–1370 mm total length ( L _T), with no apparent sexual dimorphism. Length–frequency distributions indicate a mode of juvenile fish at around 100–200 mm L _T and a further two around 600–700 and 1300–1400 mm L _T among adults. Generally smaller fish occur in shallower regions, although the size range is broad over the whole depth range. No apparent trend occurs in the size distribution with latitude over the range 17–54) N. Females outnumber males (1 male : 1·7 females) and both sexes are largely distinguishable from 300 mm L _T. Ripening eggs occur in females from both adult length modes, with running ripe and spent females of very different size indicating iteroparity.