Nest intrusions, infanticide, and parental care in the burying beetle, Nicrophorus orbicollis (Coleoptera: Silphidae)

Duration of paternal care in the burying beetle Nicrophorus orbicollis Say is highly variable. Both parents bury and defend mouse-sized vertebrate carcasses as food resources for their offspring, but males abandon their broods several days before females. Nests defended by single female parents were taken over by aggressive conspecifics in live of nine cases, whereas only six of 16 nests defended by both parents were taken over. In the event of a takeover, the intruding beetle replaced the resident beetle of the same sex, destroyed any eggs that were present, and paired with the remaining resident to produce a new clutch. Broods raised by usurpers following takeovers were less successful than broods raised by initial residents on unused carcasses. The majority of takeovers occurred 35 days after carcass burial. The occurrence of nest intrusions by conspecifics did not significantly influence duration of male parental care; when conspecific intruders were excluded from nests males remained with their broods (± S.E.) 11·2 ± 0·8 days ( n = 15), and when intruders were added to nests males remained with their broods 12·2 ± 0·6 days ( n = 8). Conflict for carcasses intensified in response to larger brood mass, but duration of male care was unaffected by brood mass. Overall. brood mass and the presence or absence of intruders explained only 5% of the variance associated with brood abandonment by males.     

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.     

Reproductive biology of the mosquitofish in a permanent natural lagoon in south-west Spain: two tactics for one species

Introduced Gambusia holbrooki in a natural lagoon of southern Spain consisted of two age groups: 1992 cohort, 7-11 months old and 1993 cohort, <4 months old. In the 1992 cohort, females grew even during the gestation period at about 0·30 mm day^-1. In the 1993 cohort, females displayed a high growth rate (0·55 mm day^-1) and reached reproductive size in a few weeks, but stopped growing when they matured. All the 1992 cohort reproduced from mid-May to mid-June, but only 50% of the 1993 cohort reproduced, from mid-August to mid-September. Reproducing females were significantly larger in the 1992 cohort (39·8 mm) than in the 1993 one (34·8 mm). The largest 1992 females cohort had reproduced previously; the 1993 cohort had not. The mean dry weight of intra-ovarian embryos decreased to a minimum immediately before birth. These metabolic costs represented 29·8 and 31·4% of the initial weights of the 1992 and 1993 embryos, respectively. Mean dry weight of full-term embryo was significantly higher in the 1992 cohort (0·80 ± 0·129 mg; 95% CL) than in the 1993 one (0·70 ± 0·086 mg; 95% CL). With more females in 1992, cohort fecundity was considerably higher (number of embryos=7151; 63%) than in the 1993 (4193; 37%) cohort. The population completed two generations each year (spring and summer). The spring stock grew slower than the summer one but continued to grow during the gestation period, reaching larger final lengths, with more synchronous reproduction and clearer evidence of a second reproductive event. Each reproductive stock displayed its own life-history characteristics, with significant differences between mean length of reproducing females, growth rate, mean brood size, offspring size, standard fecundity and minimum length at reproduction.     

Fecundity of the American eel Anguilla rostrata at 45° N in Maine, U.S.A.

The northern portion of the geographic range of the American eel Anguilla rostrata may contribute a great proportion of the reproductive potential to this panmictic species because of apparent increases in average female size and female percentage with latitude. The regressions of fecundity on body length and on body weight of 63 female eels captured at about 45° N latitude on their spawning migration to the sea were log F= 1·2601 + 2·9642 log L and log F= 4·1646+0·9153 log W , where F is fecundity, L is total length (cm), and W is total weight (g). Length and weight each explained about 90% of the variation in fecundity. Estimates of fecundity from counts of aliquots of eggs ranged from 1·84 million to 19·92 million eggs for eels ranging in length from 45 to 113 cm, nearly the range of sizes of migrating females reported in the literature. Fecundities of the American eel were greater than reported in one study at about 37° N and greater than reported for the European eel, A. anguilla , shortfin eel, A. australis , and longfin eel, A. dieffenbachii . If a geographic cline in fecundity does exist in American eels, it is established anew each generation because the species forms a single panmictic population.     

The trout (Salmo trutta) population of the Afon Cwm, a small tributary of the Afon Dyfi, mid-Wales

Data are presented from a 10-year (1984 to 1993) study of a Salmo trutta population in the Afon Cwm, a small tributary of the Afon Dyfi, mid-Wales. The stream is a spawning and nursery area for sea trout. Growth of trout within the stream can be summarized by a von Bertalanffy growth coefficient ( K ) of 0·310, with asymptotic length (1∞) 21·6 cm and with length at age 1 of 7·6 cm. Mean population density in the whole stream varied from year to year between 0·05 and 0·60 0-group trout m⁻² and between 0·05 and 0·70 older trout m⁻². Mean biomass varied, between years, from 0·1 to 3·5 g m⁻² for 0-group and from 1·3 to 10·4g m⁻² for older trout. Loss between 3 and 5 months of age appeared to be proportionate at about 50 to 60% and instantaneous loss rate from 5 to 53 months of age varied from 0·04 to 0·10 month⁻¹ and was positively correlated with cohort number at 3 months of age. Production between 3 and 53 months of age varied between cohorts from 3 to 8 g m ⁻² live weight.     

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.     

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.     

Evaluating the reproductive cost of migration for females in a partially migrating pond-breeding amphibian

Populations of animals with resident and migratory individuals provide an ideal system for addressing questions concerning the evolution of migration. Partially migratory populations may persist because residents and migrants have equal fitness or because migration is based on conditional asymmetries. Studies measuring the costs and benefits of migration provide empirical data to test hypotheses concerning the maintenance of partial migration within a population. In this study, we measured the reproductive differences between resident and migrant females in a pond-breeding amphibian, the red-spotted newt Notophthalmus viridescens . We used large field enclosures to repeatedly sample egg laying over the prolonged breeding season of this species. Resident females did not lay a greater number of eggs or begin laying eggs earlier, despite beginning the breeding season earlier and having a higher mass than migrant newts. The only difference in reproduction we detected was that the eggs of resident females hatched into larger larvae compared with the larvae of migrant females. We discuss this result in the context of other potential trade-offs between residency and migration. This study illustrates the phenology of egg laying of N. viridescens and our results contribute to understanding the population dynamics of partially migratory species.     

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.     

Reproductive biology, length-weight relationship and relative condition of pond raised Tilapia zilli (Gervais)

In 'runted' populations of Tilapia zilli positive correlations were found between maturation stages and the following: gonadosomatic index, gonad weight, fish weight and fish length. The minimum size at maturity was 9·0 cm in males and 11·0 cm in females. The mean fecundity in the 'stunted' females was 2359 eggs and it increased with length ( L ) weight (HO and depth ( D ) of the fish. There was, however, no correlation between fecundity and egg size. The results indicated that growth in this 'stunted' T. zilli population was not isometric. The relative condition factor ( Kn ) which approached one indicates good condition.     

The deposition and mortality of the eggs of the Baltic herring Clupea harengus membras L., on different substrates in the south-west archipelago of Finland

The environmental factors affecting the deposition and mortality of the eggs of the spring-spawning Baltic herring were studied in the inner Archipelago Sea of south-western Finland. On four spawning grounds, 27 study squares (area 1 m²) were surveyed by divers. In each square, one quantitative egg sample was taken and the following data were recorded: depth, temperature, bottom quality of the square and under the eggs, egg substrate, cover (%) of plants and/or the bivalve Mytilus edulis , and the heterogeneity of the environment, expressed as the total number of all bottom materials, plants and Mytilus found in the square.
Eggs were found in the depth zone of 1–4 m. Their density ranged from 6000 to 2·3 millions of eggs per square metre. Egg number had a significant negative correlation with both depth (r=-0·545, P <0·01, d.f. = 25) and temperature of the sea water ( r =-0.479,. P <0·01,d.f. = 25), and a positive correlation with the total cover (%) in the squares ( r = 0·375, P < 0·05, d.f. = 25).
The highest numbers of eggs were found on Cladophora glomerata, which the most preferred spawning substrate of those present. Mortality of the eggs varied according to the substrate. In eggs attached to Cladophora, Potamogeton and Mytilus, the proportion of dead eggs was 0.15·5%; in those attached to red algae it was significantly higher ( Furcellaria , 5·0–63·2%; Phyllophora , 0–95·2%).     

Reproductive investment in the Silurus meridionalis

A comparison of pre- and postspawning Silurus meridionalis showed that 20·7% of body stored energy was utilized during spawning for a standard male (74·5 cm) and 23·8% for a standard female (85·3 cm). About one-third of the loss of the stored energy was released as eggs by females, and almost all of the energy loss for males and about two-thirds for females were expended in metabolism. Stored lipid as fuel for metabolism supplied 90·0% of energy in males and 95·2% in females, and protein supplied the rest of the energy. Models for predicting energy in released gametes ( G _g), deposited in the body as somatic growth ( G _s), utilized in spawning activity ( S _a), expended in maintenance ( M , including metabolism, faeces and excretion), and food energy ( C ) were developed, and annual energy budgets were compiled. The balanced budget for a male aged 4 was: 100 C =0·06 G _g+11·17 S _a+19·5 G _s+69·2 M , and for a female aged 5: 100 C =5·48 G _g+8·51 S _a+15·8 G _s+70·2 M .     

Mass transfer efficiency between harp seal (Phoca groenlandica) mothers and their pups during lactation

We investigated the efficiency of mass transfer in lactating harp seals through serial measurements on individual mother-pup pairs during the whelping seasons of 1988 and 1989. We also compared the influence of longitudinal versus cross-sectional sampling on estimates of the efficiency of mass transfer. Among longitudinally sampled pairs, pups grew at an average rate of 2·3 ± 0·5 (mean ± S.D.) kg/d (N = 20). The concomitant mass loss by females averaged 3·1 ± 0·8 kg/d (N = 19). The mean efficiency of mass transfer was 77·0 ± 13·6% (N= 19 pairs).
Estimates of pup growth and female mass loss from regressions of cross-sectional data were 2·0 kg/d and 3·1 kg/d, respectively. These values produce an estimate of 65% for the efficiency of mass transfer.
Consistent with the high efficiency of mass transfer, harp seal females contribute less of their total body mass to nursing ( c. 28%) than most other phocids examined. The resulting energy savings may be important for females of an ice-breeding species, which migrate a long distance shortly after weaning their pups     

Reproductive strategy of a primitive temperate notothenioid Eleginops maclovinus

The reproductive biology of Eleginops maclovinus was examined in the Falkland Islands between October 2000 and December 2002. Males predominated at total lengths ( L _T) of 10 to 52 cm and females at >53 cm L _T. Length frequency analysis showed a bimodal distribution with females representing the larger mode for every month during the study period. Gonad histology revealed that 19% of the histological samples studied were considered to be those from hermaphrodites: morphologically as male gonads but containing protoplasmic oocytes. It was therefore concluded that E. maclovinus is a protandrous hermaphrodite. The size of first (male) maturation of E. maclovinus was 30·73 cm L _T. Males and females matured from August onwards and spawning occurred between September and December at depths of >40 m. Eleginops maclovinus has the smallest eggs and highest fecundity among the notothenioids. The highest potential fecundity was attained at maturity stage III with c . 48 million eggs. Because of further oocyte resorption, this value gradually decreased until the final fecundity ranged from 1·1 to 7·3 million eggs. Oocyte length frequencies in ovaries suggested that E. maclovinus was a batch spawner. Hydrated oocytes were found to contain a large perivitelline space indicating that the egg had a pelagic development.     

Infection of sardine eggs by the protistan endoparasite Ichthyodinium chabelardi off Portugal

In 1997 and 1999 around 30% of the stations off Portugal sampled for sardine eggs Sardina pilchardus included eggs infected with Ichthyodinium chabelardi. A randomization test on the mean nearest neighbour distances of parasitized stations did not reveal evidence of significant spatial clustering. The mean prevalence of infection was c. 0·05 for both years, but the probability of parasite detection increased considerably with egg age. Eggs in their first day of development (before the embryo is formed) were not parasitized; most parasitized eggs were in the cohorts close to hatching. Although the reasons for age-dependent detection are unknown, if all parasitized eggs of the cohort ready to hatch were to die, infection by Ichthyodinium chabelardi would lead to mortality rates similar to those reported for the average daily mortality of sardine eggs and early larvae.     

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.     

A study of some autoecological parameters of southern barbel (Barbus meridionalis R.) in the Rentina stream, Greece

In our effort to give some information which investigates autecological parameters for southern barbel, a study of age, growth and reproduction for this species was carried out in the Rentina stream, northeastern Greece. The length-weight relationship can be described by the equations W = 0.008 L^3.159 and W = 0.0583 L^2.428 for females and males, respectively (W = body weight in g, L = fork length in cm). The most rapid growth in length occured during the first year of life (7.3 cm) after which growth decreased and remained constant at approximately 3.4 cm per year. The average density and biomass were 0.25 fish. m^-2 and 9.35 g. m^-2, respectively. The southern barbel becomes sexualy mature at the second year of life for both sexes. The mean absolute fecundity was 9119 ± 322 eggs with mean diameter 1.2 ± 0.2 mm. Spawning of this species, in the study area, occurs in June at mean temperature 19°C.     

Body composition and energy allocation in life-history stages of brown trout

Energy contents of immature parr and smolts, and mature resident and anadromous brown trout Salmo trutta sampled from a small stream in southern Norway were estimated from lipid, protein and carbohydrate concentrations. In immatures the lipid concentrations were highest in parr in the autumn. Mean lipid concentrations increased significantly with age in parr sampled in autumn (1·3% in age 0+ to 3·4% in age 3+), whereas they did not in smolts. The lipid concentrations of parr in spring were not significantly different from those of similarly aged smolts. By contrast, the relative water content (%) decreased with age in parr in the autumn and increased with age in smolts, mean values being slightly higher in smolts (78%) than in parr (77%). Protein and carbohydrate concentrations did not vary with age in the immature fish, mean protein concentrations being 18·0, 17·5 and 16·8% in parr in the autumn and spring, and in smolts, respectively. In residents, the concentrations of lipids were lower and of water higher, in age group 1 than in older fish, whereas there was no significant variation with age amongst anadromous trout. The energy concentration of 2+ smolts (349 kJ 100 g^-1) was similar to that of 0+ parr in the autumn. Mean somatic energy density in autumn was 1·1 times higher in freshwater residents than in parr at age 1+ (407 and 387 kJ 100 g^-1) and marginally different at age 2+ (462 and 426 kJ 100 g^-1, respectively). The energy contents per unit mass of residents were 1·3–1·6 times that of similar aged smolts. Mean somatic energy density of anadromous trout (504 kJ 100 g^-1) was higher than that of residents (455 kJ 100 g^-1). Somatic energy, lipid and protein concentrations were correlated highly with water contents of all life stages, age and sex groups.     

Reproduction of the blue-spotted maskray Neotrygon kuhlii (Myliobatoidei: Dasyatidae) in south-east Queensland, Australia

This study examined the reproduction and population structure of the blue-spotted maskray Neotrygon kuhlii within Moreton Bay, a subtropical embayment in south-east Queensland, Australia. Mean sizes at maturity were 314 mm disc width ( W _D) in females ( n = 140, 115–465 mm W _D) and 294 mm W _D in males ( n = 123, 129–381 mm W _D). Female N. kuhlii had a synchronous annual reproductive cycle, with one litter of one to three pups (mean ± s.d . 1·67 ± 0·71) produced per year. Mating behaviours were observed in October and November, and ovulation occurred early in the Austral summer, overlapping with the start of embryonic development. Gestation took c. 4 months with parturition occurring in late February and March. Size at birth was 115–170 mm W _D. The population showed a significant female bias, particularly in larger size classes. Tagging studies produced a total recapture rate of 16·1% and indicated that N. kuhlii were site resident for up to 1081 days.     

Differences in susceptibility to sea lice infection between a sea run and a freshwater resident population of brown trout

Two experimental groups comprising mixed Norwegian sea run and freshwater resident brown trout Salmo trutta were infected with sea lice Lepeophtheirus salmonis in replicate tanks. Comparison of mean abundance and louse development between the sea run and resident groups revealed highly significant differences in lice abundance. The resident trout had an average abundance ± of 6·3±0·37 and 6·6±0·43 lice whilst the sea trout had an average abundance of 3·5 ±0·25 and 3·3 ±0·28 lice 29 days post infection at 9° C. No differences in development of lice, of either sex, were detected between the groups. As host groups were naive to sea lice at the start of the experiment, this suggests that there was a significant difference in susceptibility to sea lice infection between them, which may be genetically determined.