Influence of different rations and water temperatures on the growth rates of shortfinned eels and longfinned eels

Juvenile (12–152 g) shortfinned eels Anguilla australis and longfinned eels A. dieffenbachia caught in New Zealand streams were fed squid mantle Nototodarus spp. 4 days per week in laboratory experiments. A linear multiple regression equation showed the amount of food eaten (0–2·7% w day⁻¹) explained 77·7% of the variation in specific growth rates (–0·60 to +1·07% w day⁻¹) among individual eels, while previous growth rates, water temperature (10·0–20·6°C), and eel weight (12–152 g) explained a further 5·6, 1·4 and 0·8%, respectively. Growth in length ranged from –0·3 to +0·9 mm day⁻¹. Eels which were starved and then given high rations grew substantially faster than expected. Once growth rates were adjusted for differences in ration and other factors, there were no significant differences in growth rates between species or individual fish. Growth of shortfinned eels fed maximum rations of commercial eel food depended on fish size and water temperatures and ceased below 9·0°C. Growth rates in the wild were substantially less than the maximum possible, after seasonal changes in water temperatures were taken into account, indicating that food supplies and not low water temperatures were controlling growth rates in the wild.     

The reproductive tactics of dace in central Siberia: evidence for temperature regulation of the spatio-temporal variability of its life history

Major life history characteristics of dace Leuciscus leuciscus from the R. Yenisei at Mirnoye (66° N, Central Siberia, Russia) were determined in June 1993 and were compared with those available throughout the distribution range of the species. Differences between populations located 25° further south and 8000 km away are smaller than those described for other freshwater fishes, whose distributions fall within that of dace. For all the populations, the growth rates ( K ) are inversely correlated with latitude but these rates for the actual growing season are faster in northern dace. The latitudinal (spatial) variations in the growth rates resemble the temporal variation described for the R. Frome (U.K.). Also, the variations in fecundity between populations are comparable to the temporal variations reported for this British river. Fecundity of the Yenisei dace was correlated with female length [log F=– 3–6284+4–0424 x log L ] but these females spawned lower numbers of eggs than other populations; and the size of their eggs, like those of the Siberian Ust'Ilim dace, did not vary with female length. We hypothesize that a similar spatio-temporal response to low water temperature, coupled with limitations of energy for reproduction, may result in a constant egg size in Siberian dace. The effects of other selective forces cannot, however, be excluded.     

Batch fecundity of Atlantic mackerel, Scomber scombrus L.

The total annual fecundity of mackerel, Scomber scombrus L., during a spawning season is produced by release of discrete batches of eggs. Total fecundity is then the product of the number of batches times the batch fecundity ( F _bw). An extensive trawl survey of the Western mackerel stock in the NE Atlantic was undertaken in the 1989 spawning season. Batch fecundity was estimated for 298 fish by counting hydrated eggs in ovaries just prior to ovulation. F _bw, expressed as eggs g⁻¹ body weight, varied with latitude: south of 51°N, F _bw= 55.49, s.e. = 2.04, n = 227; between 51°N and 55°N, F _bw= 45.72, s.e. = 3.41, n = 52 and north of 55° N, F _bw= 41.33, s.e. = 5.52, n = 19. It is suggested that as spawning fish migrate northwards the batch size decreases with progress of the spawning season.     

Discrepancies between otoliths of larvae and juveniles of the American eel: is something fishy happening at metamorphosis?

The use of otoliths to interpret early life history in fishes depends upon the assumptions that otoliths record past events accurately and consistently and that records of events in otoliths are continuous. Both the number of growth microincrements ( I ), and the radii ( R ,μm) of otoliths of American eel Anguilla rostrata , leptocephali increased linearly and highly significantly with leptocephalus body length ( L , mm), as expected on the above assumptions ( I , =2·29 L , − 5·75 and R , =1·05 L , + 12·02, r ²,=0·938 and 0·931, n , =20). In contrast, the number of increments and the radii of the leptocephalus growth zones of otoliths of glass-phase American eels were not related to body length, and they were lower than predicted by the relationships developed for leptocephali. Thus, otoliths of American eels apparently violate one or both assumptions. Possibly, the margin of the otolith is resorbed during metamorphosis from leptocephalus to glass eel, perhaps as part of calcium metabolism as skeletal elements are being formed.     

Regional variation and the effect of lake: river area on sex distribution of American eels

Silver phase American eels, Anguilla rostrata , were collected while migrating from five rivers in Maine, U.S.A. Sex ratios varied from 49 to 98% male for these rivers and had a range of 46% over a 30 km distance between the mouths of three rivers. The proportion of male eels was inversely related to the amount of lacustrine habitat in the five drainage areas ( r =−0·95, P =0·014). A combination of these sex ratios and published data from two Nova Scotia rivers showed large variation in the proportion of male eels within 1° of latitude. Thus, the hypothesis from the literature that the distribution of the sexes is dependent upon distance of larval transport was not supported. Eels migrating from lacustrine habitats within a river were predominately female, while eels migrating from fluvial habitats were predominately male, regardless of upstream distance. Apparently river habitat influences the distribution of the sexes and may play a role in sex determination.     

亚洲玉米螟体重和体型的地理变异

为探明亚洲玉米螟Ostrinia furnacalis体重和体型地理变异,我们详细比较了来自4个不同地理种群（海南乐东18.8°N, 109.2°E),广西阳朔24.8°N, 110.5°E),江西南昌28.8°N, 115.9°E)和河北廊坊39.5°N, 116.7°E)）亚洲玉米螟的体重、体型大小及其与采集地纬度的关系。结果表明：不同地理种群的亚洲玉米螟卵重随纬度的升高而逐渐增大,符合贝格曼法则(Bergmann’s law), 而雌雄蛹重及成虫体长、后足腿节长和前翅长均随纬度的升高而逐渐减小, 符合反贝格曼法则(Converse Bergmann’s law)。雌虫的前翅显著长于雄虫, 其性体型二型性符合任希法则(Rensch’s rule),即在雌虫体型较大的种群中,雄虫前翅比雌虫前翅增长幅度相对较大。本文结果进一步揭示了即使在同一种类昆虫中,其各个虫态体重和体型的地理变异也可能不同。     

Reproductive biology of Tilapia zillii (Gervais) in Lake Naivasha,Kenya

Synopsis Tilapia zillii breeds all year round in the equatorial Lake Naivasha with slightly high breeding intensity during wet months (March, May and July–August). A sex ratio of 1 : 1.28 was found between males and females. The smallest mature male and female were 9.0 and 11.0 cm respectively. The fecundity ranged from 2990 to 12344 eggs, with a mean of 6606 eggs. Fecundity showed a curvilinear relationship with total length (log F = 1.7034 + 1.6370 log L) and a linear relationship with body weight (F = 2197 + 28.76 W)     

Effects of diet supplementation with carp ovary on gonad differentiation and growth of the European eel

Treating elvers of European eel Anguilla anguilla with mature carp ovary for 3–6 months during early growth induced female differentiation in 51·6–66·7% of treated animals compared with c . 5% in controls. The treatment also induced differentiation of ovaries in eels <13 cm L _T and a higher number of Syrski organs with ambisexual characters, and was most effective when administered at an early growth stage. The results could be attributed to the natural steroid content of the carp ovary. The total weight of treated animals at the end of the farm experiment was 84·7% higher than controls. The specific growth rate for weight was significantly higher in female yellow eels than in males, for both control and treated groups. The enhanced growth was related to induced feminization. A diet supplementation with mature carp ovary could be a good approach to control of sex differentiation and growth in eels.     

Spatial and temporal trends in unexploited yellow eel stocks in two shallow lakes and associated streams

Mean yellow eel density and biomass in two adjacent shallow (mean depth c 1·5 m) lochs varied significantly between years. Temporal patterns of density, biomass and size were similar in both soft and rocky substrata in the lochs, although eels were consistently smaller in the latter habitat. In both substrata, average length and weight showed a non-significant inverse relationship with density, supporting the hypothesis of density-dependent regulation of the yellow eel population. Fyke net catches were size selective, catching no eels <30 cm long, and providing length-frequency information for silver eels. Fyke net catch per unit effort (CPUE) declined consistently each autumn but specific annual trends were different. When eel density increased, fyke net CPUE declined substantially.     

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.     

Assessing patterns of hybridization between North Atlantic eels using diagnostic single-nucleotide polymorphisms

The two North Atlantic eel species, the European eel (Anguilla anguilla) and the American eel (Anguilla rostrata), spawn in partial sympatry in the Sargasso Sea, providing ample opportunity to interbreed. In this study, we used a RAD (Restriction site Associated DNA) sequencing approach to identify species-specific diagnostic single-nucleotide polymorphisms (SNPs) and design a low-density array that combined with screening of a diagnostic mitochondrial DNA marker. Eels from Iceland (N=159) and from the neighboring Faroe Islands (N=29) were genotyped, along with 94 larvae (49 European and 45 American eel) collected in the Sargasso Sea. Our SNP survey showed that the majority of Icelandic eels are pure European eels but there is also an important contribution of individuals of admixed ancestry (10.7%). Although most of the hybrids were identified as F1 hybrids from European eel female × American eel male crosses, backcrosses were also detected, including a first-generation backcross (F1 hybrid × pure European eel) and three individuals identified as second-generation backcrosses originating from American eel × F1 hybrid backcrosses interbreeding with pure European eels. In comparison, no hybrids were observed in the Faroe Islands, the closest bodies of land to Iceland. It is possible that hybrids show an intermediate migratory behaviour between the two parental species that ultimately brings hybrid larvae to the shores of Iceland, situated roughly halfway between the Sargasso Sea and Europe. Only two hybrids were observed among Sargasso Sea larvae, both backcrosses, but no F1 hybrids, that points to temporal variation in the occurrence of hybridization.     

Evolution of freshwater eels of the genus Anguilla: a probable scenario

We present a molecular phylogeny of freshwater eels from three oceans and give hypotheses to address major questions about the evolution and geographic distribution of this group. A phylogenetic tree obtained from mitochondrial cytochrome b sequences of eight species of Anguilla suggests that the African species A. mossambica and Australian species A. australis form a clade together with the two Atlantic species, the European eel, A. anguilla, and American eel, A. rostrata , whereas A. marmorata in the Indo-Pacific Ocean, A. reinhardti in northeastern Australia and the Japanese eel, A. japonica, in the northwestern Pacific are placed in another. Most speciation among the lineages is proposed to have occurred during the Eocene to Oligocene (45–30 million years ago, Ma). However, the two Atlantic species are estimated to have separated much later, approximately 10 Ma. The following evolutionary scenario for the dispersal and speciation of these species of anguillid eels is proposed based on general global paleogeography and paleo-circulation. Ancestral eels evolved during the Eocene or earlier, in the western Pacific Ocean near present-day Indonesia. A group derived from this ancestor dispersed westward, by transport of larvae in the global circum-equatorial current through the northern edge of the Tethys Sea. This group split into the ancestor of the European and American eels, which entered the Atlantic Ocean, and a second group, which dispersed southward and split into the east African species and Australian species.     

The length weight relationship, age, growth and reproduction of the roach Rutilus rutilus (L.) in Lake Volvi

The length-weight relationship of a sample of 233 roach ( Rutilus rutilus ) can be described by the following equations: y =0·0356 x ^3·405 and y =0·0215 ×^3·606 for males and females respectively. In both equations y equals the body weight in grams and × is the standard length in centimetres. The average condition factor K was 2·01 with a range of 1·71 to 2·26. The roach's span of life was 13 years for both sexes. The growth increment is greater during the first year of life (about 56 mm), decreasing to approximately 17 mm at the end of the sixth year of life and then becoming constant at about 12 mm per year. Roach become sexually mature at age 1 + for males and one year later for females. The mean absolute fecundity was 9294 eggs; with a range from 920 to 32 810. The growth of the gonads is related to the age of the fish. Spawning occurs during the first half of April, at a mean water temperature of 10° C.     

Conclusive evidence for panmixia in the American eel

Eels are unique species in the biological world. The two North Atlantic eel species, the American eel (Anguilla rostrata) and the European eel (A. anguilla), occupy a broad range of habitats from the Caribbean to Greenland in the western Atlantic and from Morocco to Iceland in the eastern Atlantic, respectively. North Atlantic eels have a catadromous life cycle, spawning only in the Sargasso Sea and spending the majority of their lives in continental (fresh, brackish and coastal) waters. Despite such a wide distribution range, North Atlantic eels have been regarded as a textbook example of panmictic species. In contrast with the large amount of population genetic studies testing the panmixia hypothesis in the European eel, a relatively modest effort has been given to study the population structure of the American eel. In this issue of Molecular Ecology, Côté et al. ( 2013 ) present the most comprehensive American eel data set to date, which includes samples of different life stages obtained throughout all its distribution range in North America. Results show a total lack of genetic differentiation among samples and provide decisive evidence for panmixia in the American eel.     

The influence of growth rate on the size of migrating female eels in Lake Ellesmere, New Zealand

Lake Ellesmere, a large coastal lake in the South Island of New Zealand, supports an important commercial eel fishery, based mainly on migrating (silver) male Anguilla australis . Lengths of silver female eels from samples collected in 1942, 1974–1982 and 1998–1999 showed an initial decline between 1942 and 1974 but an increase from 1979 onwards. Back-calculated growth rates of 50 female silver eels caught in 1998 showed that most (90%) exhibited a period of accelerated linear growth commencing at lengths between 380 and 660 mm (mean 598 mm); this accelerated growth coincided with a change in diet to piscivory. The onset of maturity was more closely associated with length than age, condition, or growth rate. The increase in average length of female silver eels of 250 mm over the past 20 years is consistent with the hypothesis that female eels adopt a size-maximizing growth strategy to ensure maximum fecundity; this is the first time this hypothesis has been demonstrated from temporal changes within a single population.     

Some morphometric and biochemical features of ready-to-migrate silver and pre-migratory yellow stages of the shortfin eel of south-eastern Australian waters

The mean total length ( L _T), mass and age of ready to migrate female silver shortfin eels Anguilla australis from the Hopkins River estuary and the mouth of the Merri River in south-eastern Australia, were 83·2 ± 1·2 cm, 1051 ± 51 g, and 17·2 ± 1·79 years, respectively. The eye index ( I _E) of the silver shortfin eels was < 5·2 (mean 7·64 ± 0·29) and differed significantly from that of the yellow shortfin eels collected from two other sites. The I _E increased with L _T (mm) and was related by log I _E= 2·656 log L _T6·925. The per cent moisture, protein and ash content of the liver of silver shortfin eels was significantly lower than in yellow shortfin eels, but lipid content was significantly higher in the former (35·5 ± 2·0%). The mean mass μg mg lipid ⁻) of saturates (230·4 ± 2·6 v . 181·7 ±2·6), monoenes (367·4 ± 6·3 v . 290·8 ± 8·9) and PUFA (177·3 ± 5·3 v . 159·7 ± 4·6) in muscle was significantly higher, and the great majority of individual fatty acids was found also in higher quantities in silver shortfin eels. In the liver, the PUFA found in the highest quantity was 22:6n-3, except in shortfin eels from Hopkins River estuary, and the amount of 18:2n-6 in the liver of silver shortfin eels was significantly higher than that in yellow shortfin eels but the reverse was true of 20:4n-6. In both muscle and liver tissues the saturate 16:0 and the monoene 18:ln-9 collectively accounted for >50% of all the fatty acids in the lipid.     

Migratory patterns and contribution of stocking to the population of European eel in Lithuanian waters as indicated by otolith Sr:Ca ratios

Otolith Sr:Ca ratios were examined to evaluate the contribution of the stocked eel Anguilla anguilla elvers, which have been stocked in Lithuanian waters and mixed with naturally recruited eels for several decades, to the native eel population. Stocked eels were identified by the freshwater signature (Sr:Ca ratios <2·24 × 10⁻³) on the otolith after the glass eel stage. Naturally recruited eels, that had migrated through the North and Baltic Seas, were characterized by an extended seawater and brackish-water signature (Sr:Ca ratios >3·23 × 10⁻³) after the glass eel stage. Of 108 eels analysed, 21 eels had otolith Sr:Ca ratio profiles consistent with stocking while 87 showed patterns of natural recruitment. The ages of naturally recruited eels arriving in Lithuanian fresh waters varied from 1 to 10 years, with a mean ±  s.d . age of 5·2 ± 2·1 years. Eels from the inland Lake Baluošai were all freshwater residents of stocked origin. Stocked eels, however, accounted for only 20% of the eels from the Curonian Lagoon and 2% of eels sampled in Baltic coastal waters. This finding does not support the hypothesis that the eel fishery in the Curonian Lagoon depends mostly on stocking.     

Reproductive biology of the endangered Oxleyan pygmy perch Nannoperca oxleyana Whitley

The reproductive biology of the Oxleyan pygmy perch Nannoperca oxleyana is described from simultaneous studies of wild populations in north-eastern New South Wales and mature fish held in aquaria. In the wild, 50% of males and females matured at total lengths of 24·0–25·9 and 28·0–29·9 mm, respectively. The species displays sexual dichromatism during the spawning season, with males developing more intense red and brown fin and body colouration, and black pelvic fins. Captive male broodfish displayed territoriality during the breeding season, closely guarding sites within artificial, plant-like substrata in which pairs of fish spawned adhesive eggs. Protracted serial spawning of wild and captive fish occurred from September to April and May at mean water temperatures ≥16·6° C and day length ≥10·7 h. Captive broodfish spawned on an average of 57% of days during the 256 day spawning period. Gonado-somatic indices averaged 0·7% for all ripe males and 4·1–4·2% for all ripe females collected. Mean total and batch fecundities of captive females were 1323 eggs per fish and 7·8 eggs per fish per day, respectively, and relative fecundity was 587 eggs g⁻¹ of body mass. Batch fecundity of wild females was estimated at 7·8 eggs per fish. The adaptive significance of this reproductive strategy in a harsh, variable environment is discussed.     

Lunar spawning in Siganus canaliculatus

A major spawning of the seagrass rabbitfish Siganus canaliculatus occurred 4 days after the new moon in both May and June 1993, and 7 days after the new moon in 1994. The gonadosomatic index ( I _G) and serum vitellogenin (VTG) levels fluctuated according to the lunar cycle; IG and VTG levels showed peaks at around the new moon and the waning moon, respectively, suggesting that spawning of this species is synchronized with the lunar cycle. Vitellogenic oocytes appeared on day 2 after the first spawning and were fully mature on day 30. When a greater percentage of the most advanced oocytes attained the tertiary yolk stage, they formed a batch and separated from the adjacent group of smaller pre-vitellogenic oocytes, indicating that S. canaliculatus is a multiple spawner with an ovary belonging to the group-synchronous type of oocyte development. Batch fecundity, assessed using batches of oocytes at and after the tertiary yolk stage, ranged from c. 0·52 to 2·56 million eggs. The relationship between batch fecundity (F) and fork length (1) can be represented as F=0·0536854L^5·07292.     

Maturation patterns in female European eel: age and size at the silver eel stage

The maturation pattern in the female European eel Anguilla anguilla was studied by investigating age and size patterns of silver eels in different aquatic environments in Sweden, covering limnic, brackish and marine waters. The results neither supported the hypothesis that there is a critical size or age when eels enter the silvery stage, nor that size and age at maturity are positively related. Age at maturity, however, was observed to be negatively related to growth rate in all localities, i.e. the female reproductive tactic apparently is to become sexually mature at the earliest possible opportunity. Furthermore, it was recognized that a significant amount of variation was due to habitat differences, since the female eel maturation pattern deviated systematically between sampling sites, as it did also when the effect of growth rate was eliminated. Thus, the ability of the female eel to adjust maturation to an optimal size and age can be questioned, because the panmictic nature of the eel means local adaptations are unlikely Growth rate dependent differences suggest that variations in maturation patterns between eel environments are linked more to the opportunity for nutrient accumulation than to other aspects of growth.