Nitrogen and phosphorus content of some temperate and tropical freshwater fishes

The nitrogen and phosphorus content of two temperate fishes, Rutilus rutilus and Perca fluviatilis , and six tropical fishes, Oreochromis niloticus , Cichla monoculus , Serrassalmus rhombeus , Plagioscion squamosissimus , Prochilodus brevis and Hoplias malabaricus , were investigated to test the hypothesis that variation in body P content and N:P ratio is related to body size. Regressions of %P and N:P ratios against fish size (length and mass) confirmed the hypothesis for P. fluviatilis and P. squamosissimus , suggesting that body size is an important factor driving body P content and N:P ratios in some fishes. Moreover, significant increases in %N and N:P ratio with body size was found for H. malabaricus , a common piscivorous fish of the Neotropics. Interspecific variation in %P and N:P ranged two-fold and significant differences ( P < 0·05) were found among the tested species. The mean ± s . d . elemental content across all fishes ( n = 170) was 10·35 ± 1·29% for N and 3·05 ± 0·82% for P, while the N:P ratio was 8·00 ± 2·14. Data on fish body nutrient content and ratio will improve parameterization of bioenergetics and mass balance models and help clarify the role of fishes in nutrient cycles in both temperate and tropical freshwaters.     

Home range size and dispersion in the helmeted guineafowl (Numida meleagris galeata Pallas) of the Waza National Park, Cameroon

Field investigations of the home range size and emigration pattern of wild helmeted guineafowl ( Numida meleagris galeata Pallas) from 1992 to 1995 showed that home range size (±95% confidence limits (CL) ) varied with season from 3·6±1·5 km² for the dry seasons to 3·1±1·5 km² for the rainy seasons. Home range size varied depending on whether it was estimated with data for adult males, adult females or young birds, with a higher home range size for young birds, closely followed by adult males. Group size (±95%CL) varied by month, and was highest between March and April (47·0±8·1 birds/group) and lowest in August 9·0±5·1 birds/group). More young birds (±95%CL) (36·8±19·6%) dispersed than adult males (21·1±1·9%) or adult females (13·5±1·8%). There was a highly significant positive correlation between group size and the number of birds emigrating from the group. There was also a significant negative correlation between the weights of birds at tagging and the percentage that emigrated during the first year of study but not later. This is suggested to be linked to the high number of young birds emigrating, since they weigh relatively less than adults. The lack of correlation between body weight and number of birds emigrating a year or later after birds were tagged was thought to be due to the fact that birds tagged while young attained adult weight within a year.     

Interannual and regional variations in body length, weight and energy content of age-0 Pacific herring from Prince William Sound, Alaska

Age-0 Pacific herring were surveyed in October of 4 years in a large northern Gulf of Alaska estuary, to determine the range of variations in length, weight and whole body energy content (WBEC). These parameters reflect their preparedness for surviving their first winter's fast. During the surveys there were distinct regional and interannual variations in all three parameters for individual groups of herring in Prince William Sound. Likewise, with each collection there was typically a large range of size and WBEC values. The average standard length was (±S.D.) 80±13 mm (range=40–118), the mean whole body wet weight was 5·7±3·0 g (range=0·7–29·2) and the average WBEC of all age-0 herring captured, regardless of year or site (n=1471), was 5·4± 1·0 kJ g⁻¹ wet weight (range=2·4–9·4). The large range of WBEC and size indicates that age-0 herring at different capture sites were not all equally prepared for surviving their first winter.     

Characteristics of egg and larval production in captive bluespotted gobies

Spawning of the Hawaiian coral-reef goby Asterropteryx semipunctata was diurnal, occurring at various times throughout the day. Mean length of eggs deposited in nests was 0·76 mm (range 0·67–0·84); mean egg width was 0·47 mm (range 0·41–0·52). Clutch size varied from 296 to 1552 eggs (mean=886±309), and was independent of standard length, total body weight, and body condition. Mean relative clutch size was 1·59 eggs mg^-1 total body weight (range 0·84–2·43). Clutches hatched 4–5 nights after being deposited in a nest. Mean notochord length of newly-hatched larvae was 1·88 mm (range 1·60–2·04). The minimum period of time that elapsed between egg deposition and subsequent growth of a new batch of oocytes to spawning size was 5–6 days, providing a reasonable estimate of minimum spawning interval. Compared with other gobiids, tropical species tend to have shorter incubation periods, smaller eggs and smaller larvae at hatching.     

Effect of delayed first feeding on development and feeding ability of Paralabrax maculatofasciatus larvae

The impact of delayed feeding early in development on late feeding ability and development of spotted sand bass Paralabrax maculatofasciatus larvae was examined. Larvae were sampled from hatching until day 19 after delayed feeding for zero (control), 1, 2, or 3 days. Feeding incidence was evaluated as the percentage of larvae with food in the gut and feeding intensity was measured by direct counting of prey after dissection of the gut. Delayed feeding effects due to starvation were observed early in development. By day 5, significant differences ( P  < 0·05) were observed between controls and larvae submitted to degrees of delayed feeding, including total length ( L _T), eye diameter, and the size of the head, liver, gut, muscles and body. Differences were still apparent in L _T, and body, liver and muscle heights at the end of the studied period. Larvae under total starvation did not survive beyond day 5. Initial feeding incidence was 35, 60, 90 and 10% for larvae first fed on day 2, 3, 4 or 5, respectively. Mean ±  s . d . feeding intensity was 3·6 ± 0·8, 2·8 ± 1·3, 5·2 ± 0·3, and 10·2 ± 1·5 rotifers per larva depending on whether larvae were initially fed on day 2, 3, 4 or 5, respectively. The point of no return occurred between 4 and 5 days after hatching.     

Water flux and mass gain during lactation in free-living ringed seal (Phoca hispida) pups

Three ringed seal ( Phoca hispida ) pups were used to calculate water flux and milk intake, based on mass increase and dilution of injected tritiated water. Biological half life of tritium in ringed seal pups was 130 ± 17 h (mean ± S.D.). The plateau level of the isotope indicating equilibrium with the body water was, in all cases (N = 8), reached before the first blood sample was collected after 0·5 h. Daily water flux in the pups was 62·9 ± 21·5 ml kg^-1. Estimated daily milk intake of 1103 ± 388 ml milk resulted in a mass increase of 386 ± 104 g. Neonates had a fat content of 4·75%, and a water content of 70·1% (N = 3). Corresponding figures for a pup close to weaning were 36·5% and 46·3%. Isotope dilution calculations of body water gave an overestimate of 1·6% compared with body water content from desiccation. Ringed seal milk was found to contain 38·1% fat, 9·9% protein, 2·3% lactose and 1% ash.     

The role of the pectoral fins in body trim of sharks

In a large aquarium the leopard shark Triakis semifasciata , sand tiger shark Odontaspis taurus , sandbar shark Carcharhinus plumbeus , and spiny dogfish Squalus acanthias cruised steadily at 0·1-0·7 body lengths s^-1. Relative to the trajectory of the shark, the pectoral fins were maintained at a positive angle of ttack regardless of vertical direction. For level swimming the mean angle of attack for the pectoral fin was 11±1·7, 10·1±1·3°, 9·3±1·3°, and 15·0±0·0 for T. semifasciata , C. plumbeus , O. taurus , and S. acanthias , respectively. The long axis of the body was canted at an angle of attack for T. semifasciata and S. acanthias , but trim was maintained during level swimming for C. plumbeus and O. taurus . Hydrodynamic analysis of the body and fin design of T. semifasciata indicated that the pectoral fins could develop suffcient pitching moment to maintain depth and keep the body in trim. Demonstration of positive angles of attack support the hypothesis that lift is generated in the anterior body to counterbalance the lift produced by the heterocercal tail.     

Morphology and fine structure of the heart of the burbot, a cold stenothermal fish

The ventricle of the burbot Lota lota heart comprised 0·148 ± 0·006% of the body mass which is nearly two-fold heavier than the relative ventricular mass ( M _V) of other similarly sized teleosts. The shape of the ventricle is pyramidal and the wall is exclusively composed of spongious muscle without a distinct compact layer. The atrium forms 0·017 ± 0·002% of the body mass. Length, width, sarcolemmal surface area and volume of enzymatically isolated myocytes from burbot ventricle were 147·2 ± 10·2 μm, 6·3 ± 0·4 μm, 2440·8 · 251·5 μm² and 2356·8 ± 316·6 μm³, respectively. The myofibrils were peripherally located and their volume density was remarkably high: 65 ± 2 and 68 ± 3% in ventricle and atrium, respectively ( P >0·05). Although not particularly conspicuous, some nonjunctional and junctional sarcoplasmic reticulum (SR) was present in both atrial and ventricular myocytes. The SR formed peripheral couplings with the sarcolemma and the junctional clefts were frequently occupied by foot processes. These findings suggest that cold-adaptation is achieved by cardiac enlargement, high volume density of myofibrils and well-developed peripheral couplings in the SR in the heart of stenothermal burbot.     

The angle of attack of the body of common bream while swimming at different speeds in a flume tank

The body attack angle of common bream Abramis brama varied with swimming speed and was best described by θ = −3·32 (±0·24) − 9·23 (±0·54)e^{− u} ( r ² = 0·56, P  < 0·0001; ±1 s . e . given in parentheses), where θ is the body attack angle and u is swimming speed. The hypothesis that neutrally buoyant fishes may swim with body attack angles deviating increasingly from 0° as the swimming speed decreases is supported.     

三线闭壳龟繁殖生态的研究

在暨南大学爬行动物养殖场对三线闭壳龟的繁殖生态进行了研究。结果显示:三线闭壳龟每年产卵1次,每次产卵平均3.6枚。受精卵长径为48.00±2.63mm,短径为26.42±1.66mm,卵重为23.89±3.34g。未受精卵长径为44.35±4.36mm,短径为25.39±2.71mm,卵重为20.39±4.96g。卵的受精率为50.9%,孵化率为83.3%,孵化期平均88d,估计积温为59.581℃·h。稚龟的背甲长为44.83±2.41mm,背甲宽为36.90±1.86mm,体重为15.85±2.07g。     

Escape manoeuvres of schooling Clupea harengus

The escape behaviour of schooling herring startled by an artificial sound stimulus was observed by means of high speed video filming. Response latencies showed two distinct peaks, at 30 ms and c . 100 ms. Escape responses belonging to the two latency groups showed different turning rates during the first stage of the response, and showed different escape trajectories. We suggest that long latency escapes may be responses to startled neighbours or simply weak responses to the sound stimulus. In addition, the different contraction rates during the C-bend formation seen in the two latency groups may imply differences in the neuronal commands. The escape responses of herring were directed away from the stimulus more often than towards it (88% of the total). These away responses were more common in long latency responses, suggesting that the latter enable herring to be more accurate in discerning the direction of the threat. Startled fish contracting their body towards the stimulus (performing a towards response) appear to correct their escape course, since their escape trajectory distribution is non-uniformty distributed around 360° and directed away from the stimulus. We hypothesize that when herring are schooling, the ability of each fish to correct its trajectory following turns towards the stimulus is enhanced.     

KINETICS OF GROWTH OF HAEMOPOIETIC COLONY CELLS IN AGAR

Cell kinetic parameters of mouse granulocytic and mononuclear cells growing in colonies in agar cultures have been measured. Analysis of flash and continuous labelling studies with ³H-thymidine together with determinations of colony size, growth fraction and mitotic indices, gave the following values for the phases of the cell cycle: G₁= 6·3 1·6 hr, S = 5·8 ± 1·4 hr, G₂= 1·7 ± 0·1 hr and M = 0·7 ± 0·1 hr (42 ± 8 min). No difference in the cell cycle parameters of granulocytic and mononuclear cells were found in this study.
Colonies of different size from cultures of the same age group had similar labelling indices, indicating that the size of a colony is not a function of the rate of proliferation of cells in the colony. Rather, variation in colony size is probably representative of an initial delay in the onset of colony development.     

Autotriploid tench Tinca tinca (L.) larvae obtained by fertilization of eggs previously subjected to postovulatory ageing in vitro and in vivo

Eggs of diploid tench Tinca tinca were half-stripped out and stored for 0 (control batch), 1, 3 and 5 h at mean ± s . d . 17·0 ± 0·4 and 21·9 ± 0·5° C or for 0, 1, 2, 3, 4 and 5 h at 24·0 ± 0·0° C in vitro prior to fertilization. The eggs remaining in vivo in the fish kept at 17·0 ± 0·4 and 21·9 ± 0·5° C were collected and fertilized in the same time intervals. Fertilization rate and larval yield mostly decreased after 3–5 h storage of eggs both in vitro and in vivo and only the diploid larvae were found in all control batches. Triploid larval yields increased to a maximum 5·26% after 5 h in vitro storage at 24·0° C and 1·07 and 1·60% after 3 h in vitro storage at 21·9 and 17·0° C, respectively. Triploid larval yield during in vivo storage at 21·9° C reached a maximum 0·91% after 5 h. As the spontaneous autotriploid larvae arose solely from fertilized eggs previously subjected to postovulatory egg ageing by means of prolongated storage, the autotriploidy was probably caused by failure of extrusion of the second polar body.     

Muscle fine structure reflects ecotype in two nototheniids

The fine structure of swimming (pectoral) and myotomal (axial) skeletal muscle and myocardium of two species of Antarctic nototheniid fishes were studied by electron microscopy, comparing the cryopelagic Pagothenia borchgrevinki and the benthic Trematomus bernacchii . Mean fibre size varied by a factor of four among muscles within each species and may have reflected the locomotory power available, being larger in pectoral oxidative (red) and axial glycolytic (white) muscle of P. borchgrevinki . Both species use labriform locomotion, and the more active P. borchgrevinki had a greater capillary supply, expressed as a capillary to fibre ratio, than T. bernacchii to both red (3·48 ± 0·36 v . 1·63 ± 0·14, mean ±  s . e .; P  < 0·01) and white (2·70 ± 0·20 v . 1·53 ± 0·18, mean ±  s . e .; P  < 0·01) regions of the pectoral musculature. The greater aerobic scope of P. borchgrevinki was strikingly demonstrated in the higher mitochondrial content of all skeletal muscle types sampled, and the ventricular myocardium (0·269 ± 0·011 v . 0·255 ± 0·012 mean ±  s . e .; P  < 0·05). Minor differences were found in other elements of fibre composition, with the exception of a five‐fold greater lipid content in pectoral red fibres of P. borchgrevinki (0·074 ± 0·014 mean ±  s . e .) v . T. bernacchii (0·010 ± 0·003; P  < 0·05). Differences in muscle fine structure among species clearly reflected differences in their ecotype.     

Morphometry of some structural parameters affecting oxgyen diffusion in body trunk red muscle at different sizes of a tilapia, Oreochromis niloticus

Morphometric measurements were carried out on some of the structural parameters affecting oxygen diffusing capacity in red muscle of 15 specimens of O. niloticus body weight (b.w.) 0.65–812.3 g. Total capillary length and surface area and total morphometric oxygen diffusing capacity in body trunk red muscle had average values of 4792·7 (± 1740.7 s.e.) m, 415·4 (± 157·3 s.e.) cm² and 0·0213 (± 0·0075 s.e.) ml⁻¹ min⁻¹ cm⁻² mmHg respectively. When expressed as functions of b.w. these parameters had scaling values of 1·02, 1·07 and 0·993 respectively. These figures show a slight increase or almost no change in these structural parameters (which affect diffusion of oxygen to mitochondria in red muscle) per unit weight of fish. This should be important as the role of sustained swimming (by red muscle) becomes more important in larger tilapia. Oxygen diffusion distances were short [3·11 (±0·16 s.e.) μm] which facilitates diffusion of oxygen to mitochondria. The scaling value for oxygen diffusion distances of 0·067 (with respect to body weight) shows a slight increase in this parameter with development. This value is significantly different from zero.     

Poikilothermic traits and thermoregulation in the Afrotropical social subterranean Mashona mole-rat (Cryptomys hottentotus darlingi) (Rodentia: Bathyergidae)

When acclaimated for two months at 26 C the social Mashona mole-rat Cryptomys hottentotus darlingi (±S.D.) resting metabolic rate (RMR) of 0·98±0.·14cm²O₂g _-1 h_-1 ( n =21), within a thermal neutral zone (TNZ) of 28 31·5 C ambient temperature (Ta). The body temperature (Tb) of the mole-rat is very low. 33·3±0·5 C, and remained stable between 25 31·5 C ( n =28). Above 33 C. Tb increased to a mean of 34·±0· C (n=28) (Ta range 33 39 C). Below Ta 25 C. Tb showed strong poikilothermic tendencies, with Tb dropping to a mean of 26·8±1·16 C. whereas above Ta25 C. Tb varied in a typically endothermic pattern. The conductance is high 0·19±0·03 cm² O_2g¹ C ¹ (n=28) at the lower limit of thermoneutrality. The mean RMR at 18 C (the lowest Ta tested) was 2·63 ± 0·55 cm³ O₂g ¹ h ¹ (n=7) which is 2·6 times that of the resting metabolic rate in the TNZ.     

Differences in size and growth rates of male and female migrating Japanese eels in Pearl River, China

The Sr/Ca ratios in otoliths of silver Japanese eels Anguilla japonica , in Pearl River, China, indicated that both sexes did not stay in brackish water and grew in fresh water from the glass eel stage until spawning migration. This did not support the hypothesis that females tended to distribute upstream and males might be restricted to estuaries. The back-calculated total length of males at glass eel stage was not significantly different from that of females, indicating that the hypothesis that small glass eels became males and larger ones became females may not be true. The mean (±S.D.) age and total length of males at migration were 6·4±1·6 years and 48·3±4·5 cm, which were significantly smaller than for females, 8·3±1·6 years and 61·4±4·1 cm. The age of migration was related inversely to growth rate for both sexes. Growth parameters of the von Bertalanffy growth equation were K =0·21 cm year°1, L _∞=55·7 cm and t _o=-0·55 year for males and K =0·14 cm year⁻¹, L _∞=77·5 cm and t _o=-0·60 year for females. The difference in asymptotic length ( L _∞) between males and females may be because females postpone migration to achieve larger size for maximizing reproductive success.     

Age and growth of Anguilla anguilla in the Camargue lagoons

Age and total length ( L _T) data from a 11 year monitoring of the Anguilla anguilla eel population of the Camargue lagoons (Rhône delta, southern France) were collected for glass, yellow and silver eels. Three distinct models were calibrated to describe the growth process of undifferentiated eels, females and males, respectively. Uncertainty of parameter estimates was evaluated by bootstrapping. Females were characterized by larger asymptotic body size ( L _T) than males (580 ± 50 v . 388 ± 13 mm) and faster growth, whilst the Brody growth coefficient was larger for males than for females (means ±  s . d . 3·00 10⁻³ ± 1·68 10⁻³ v . 1·73 10⁻³ ± 0·50 10⁻³). Sexual differentiation was estimated to begin at 204 ± 38 mm mean ±  s . d ., i.e . at the end of the second year in the lagoons, well before the L _T at which macroscopic differentiation became possible ( c . 300 mm). Males probably leave the lagoon or die (due to either natural or fishing mortality) within the first 3 years, whilst females can remain up to 5 years. Sexual differentiation and maturation have a major role in shaping the L _T structure of the population. The L _T and mass ( M ) data were fitted by allometric curves     . The calibration of distinct curves for data from different years indicated that the allometric coefficient a was subject to wider interannual fluctuations than the allometric exponent b . A negative correlation linked the average L _T and the allometric exponent ( r  = −0·58, P  < 0·01).     

Short‐term freshwater exposure benefits sea lice‐infected Atlantic salmon

Atlantic salmon Salmo salar were infected with sea lice Lepeophtheirus salmonis (0·08 ± 0·007 sea lice g⁻¹) over a period of 4 h. Both infected and non‐infected fish were swim tested in sea water (SW) and fresh water (FW). The ventral aorta of each fish was fitted with a Doppler cuff in order to measure cardiac output, stroke volume and heart rate during swim testing. Blood samples were taken at rest and after exercise. Critical swimming speed of infected fish in SW (2·14 ± 0·08 body lengths, bl s⁻¹) was significantly lower ( P  < 0·05) than infected fish switched to FW (2·81 ± 0·08 bl s⁻¹) and non‐infected fish in SW (2·42 ± 0·04 bl s⁻¹) and FW (2·61 ± 0·08 bl s⁻¹). Cardiac and blood results indicated infected fish exposed to FW did experience stress, but relief from osmotic and ionic distress probably reduces energy expenditure, allowing the increase in performance. As the performance of sea lice‐infected fish improved upon transfer to FW, it is likely that heavily infected salmonids do return to FW to restore compromised osmotic and ionic balance, and remove sea lice in the process.     

Latitudinal variability in lunar spawning rhythms: absence of a lunar pattern in the northern mummichog Fundulus heteroclitus macrolepidotus

In this study, the natural spawning season of the northern mummichog Fundulus heteroclitus macrolepidotus was examined from May to July in the lower St John River, New Brunswick, Canada (45° N), through measurements of gonado-somatic index ( I _G), liver-somatic index ( I _L) and condition factor ( K ). I _G increased during the prespawning phase (mean ± s.e. 5·49 ± 0·20%), peaked during the spawning phase (14·68 ± 0·51%) and dropped during the regression phase (3·23 ± 0·29%). A single peak of spawning was observed in F. h. macrolepidotus , contrasting with multiple peaks observed in studies south of 41° N in North America. Within the prespawning phase, there were significant differences between sampling dates in female body mass, gonad mass, liver mass and K . On the basis of results from this study, water temperature is believed to be the predominant factor controlling initiation of spawning in F. h. macrolepidotus .