Variability in growth of longfinned eels among coastal catchments of south‐eastern Australia

Longfinned eels Anguilla reinhardtii were captured by both fishery‐dependent and independent sampling methods from three rivers in New South Wales, south‐eastern Australia. Growth rates were examined in two zones (fresh water and tidal) in the Hacking, Hawkesbury and Clarence Rivers. Mean annual growth increments of sampled longfinned eels ranged from 30 to 60 mm year⁻¹ using age‐length analyses and up to 167 mm year⁻¹ based on tag‐recapture model estimates (GROTAG), with both methods showing high intra‐ and inter‐population variability. Growth was significantly faster in younger (5–15 years) fish than older (>15 years) fish, with females growing an average 10 mm year⁻¹ faster than males of similar age and capture location. Longfinned eels found in tidal areas grew significantly faster than those in non‐tidal freshwater areas as a result of longer growing seasons in the highly productive estuarine habitats. Other possible factors influencing variability in growth rates for this species include habitat preference, density and fishing pressure.     

Long‐term changes in population size and the age structure and sex ratio of waterbuck in a Sudanian savannah of Burkina Faso

The waterbuck (Kobus ellipsiprymnus), though widespread throughout Africa, is suspected to be declining overall. Data on population numbers and structure are lacking for many parts of its range, especially in West Africa, where the subspecies defassa is found. The aim of the present study was to evaluate the abundance, distribution and attributes of waterbuck populations from the Nazinga Forest Reserve, southern Burkina Faso. We investigated waterbuck population trends in the park using transect data collected in 1985–2019. For the more detailed analyses of population structure and distribution of the animals, we used census data gathered during 2019. Most animals were adults (46.6%), and the sex ratio was heavily skewed towards females (5:1). Most animals were concentrated along the larger rivers. There was no influence of poacher activity on waterbuck distribution. In the long term (1985–2019), the population dynamics of waterbuck can be roughly divided into two main periods: a phase of population increase from 1985 to 2005, and one of ongoing population collapse from 2007 to 2019. Although the declining population trend was obvious, coefficients of determination were low indicating that the years explained poorly the number of individuals and the number of sightings obtained. Waterbuck numbers in the Nazinga Forest Reserve are declining, but we found no single reason to explain this trend. It is likely that a combination of factors, including global warming (increased aridity) and illegal activities such as poaching, is responsible. Because there are probably multiple reasons for the observed waterbuck population decline in our study area, we suggest that a multifaceted approach should be adopted in order to enhance the conservation status of the local waterbuck populations.     

The influence of female age and host size on the sex ratio of the parasitoid Opius concolor

The sex ratio of the progeny of single females parasitizing large hosts favoured the females (sex ratio=0.26); but on small hosts favoured the males (0.73). No differences in mortality of the sexes were detected. The sex ratio was independent of female age when large hosts were used. The percentage of males observed in the progeny of the first day of female oviposition was significantly greater than the mean, irrespective of the age at which female oviposition began. When females were exposed to small hosts, a greater percentage of females was observed in the progeny from the last days of oviposition.

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Résumé L'influence de la taille de l'hôteret de l'âge de la femelle sur le taux sexuel de la descendance a été étudiée sur le parasitoïde Opius concolor Szépl.Le taux sexuel de la descendance des femelles isolées est favorable aux femelles (t.s.=0,26) quand elles ont à leur disposition des hôtes de grande taille, tandis qu'avec des hôtes petits le taux sexuel est favorable aux mâles (t.s.=0.73). On n'a pas détecté de mortalité différentielle des sexes.Les pourcentage de mâles obtenu le premier jour de ponte des femelles sur les hôtes de grande taille est significativement différent de la moyenne, indépendamment de l'âge de la femelle à ce moment. Cependant, sur des hôtes petits, bien que restant favorable aux mâles dans l'ensemble, une plus grande proportion de femelles à partir des premiers jours de ponte a pu être observée.

     

Movements of Macquaria ambigua, in the Murray River, south‐eastern Australia

A 2 year (2000–2001) radio‐tagging study was undertaken to investigate the movements of 51 golden perch Macquaria ambigua in the Murray River at Nyah in north‐western Victoria, Australia. During the winter of both years, golden perch did not undertake movements >5 km and displayed strong home range fidelity. In the first year of the study there was an increase in the distance of golden perch movement during late spring which coincided with increasing water temperature and river discharge. Nineteen golden perch were tracked during this period, of which 10 travelled downstream between 11 and 290 km. Seven of these fish moved to an area below the junction of the Murray and Wakool Rivers. Five golden perch travelled upstream between 13 and 35 km, four of which travelled to an area around the junction of the Murray River and Speewa Creek. The remaining four golden perch undertook localized movements of <5 km. Many of the long distance movements undertaken in spring 2000 were rapid and 53% of these golden perch returned to within 3 km of their release locations, indicating homing behaviour. Given that the rapid movements of golden perch in spring coincided with the known spawning season of this species, these long distance movements may be associated with reproductive strategy.     

Home range size and distribution in a wild population of Cape pangolins, Manis temminckii, in north‐west Zimbabwe

The aim of this study was to estimate the size of the home range used by individual Cape pangolins ( Manis temminckii ). The study was conducted in 1991–95 at Sengwa Wildlife Research Institute, Gokwe, Zimbabwe. Radio‐telemetry was used to repeatedly locate study pangolins. Home range area was estimated from the location of the burrows used by each pangolin. It was established that pangolins must be tracked for 85+ days to generate a reliable estimate of home range. The size of home ranges, determined from 1141 tracking days of data for 10 pangolins (3·0–15·8 kg body mass) that were each tracked for at least 85 days, was from 0·17 to 11·07 km². Larger (older) pangolins used more burrows and had larger home ranges than smaller (younger) pangolins. The data indicate that large adult males had larger home ranges than large adult females. Within each sex, the home ranges were adjacent to each other with only slight overlap at the boundaries. There was clear overlap of home ranges between males and females.     

Age, growth, and sexual maturity of the yellownose skate Dipturus chilensis in the south‐eastern Pacific

The age and growth parameters of Dipturus chilensis were estimated by counting growth rings from thin sections of vertebral centra from 400 fish (246 females and 154 males), ranging from 23 to 124 cm total length (L_T), and backcalculating fish lengths at previous ages. Marginal increment analysis lent support to the hypothesis of annual deposition of band‐pairs, which formed during the winter months. The oldest female D. chilensis aged in this study was 21 years and 117 cm L_T, whereas the oldest male was 18 years and 93 cm L_T. A 4·7% index of average per cent error (I_APE) suggested that this is a precise method for calculating the age of D. chilensis. Observed L_T were lower than backcalculated L_T, which implies the influence of Lee's phenomenon. The von Bertalanffy growth equations, based on mean length‐at‐age data, were estimated as L_t = 128·3 (1 ? e^{?0·112 (t + 0·514)}) for females and L_t = 107·8 (1 ? e^{?0·134 (t + 0·862)}) for males where t is age (years). Growth was significantly different between sexes: females reached a larger adult size. Ages and lengths at 50% maturity were estimated at 14 years of age and 106 cm L_T for females and 11 years of age and 86 cm L_T for males. At c. 14 years, there was a decline in growth rates in females. The factor most likely responsible for this was sexual maturity, which caused a discontinuity in growth of female fish. These results show that this species is slow‐growing, long‐lived, relatively large and of delayed maturity, characteristics that make it vulnerable to exploitation.     

Proximate causes of sexual size dimorphism in Colorado pikeminnow, a long‐lived cyprinid

Evidence for sexual size dimorphism (SSD) and its possible causes were examined in the endangered Colorado pikeminnow Ptychocheilus lucius, a large, piscivorous, cyprinid endemic to the Colorado River system of North America. Individuals representing 18–24% of the upper Colorado River population were captured, measured, sexed and released in 1999 and 2000. Differing male and female total length‐(L_T) frequency distributions revealed SSD with females having greater mean and maximum sizes than males. Although both sexes exhibit indeterminate post‐maturity growth, growth trajectories differed. The point of trajectory divergence was not established, but slowed male growth might coincide with the onset of maturation. Differing growth rate was the dominant proximate cause of SSD, accounting for an estimated 61% of the observed difference in mean adult L_T. The degree of SSD in adults, however, was also related to two other factors. Evidence suggests males become sexually active at a smaller size and earlier age than females; a 2 year difference, suggested here, accounted for an estimated 12% of the between‐sex difference in mean adult L_T. Temporal shifts in gender‐specific survival accounted for an additional 27% of the observed between‐sex difference in mean adult L_T. Estimated age distributions indicated a higher number of older females than older males and more younger males than younger females in the population during the period of sampling. Dissimilarity of age distributions was an unexpected result because the male : female population sex ratio was 1 : 1 and estimates of long‐term annual survival for adult males and females were equal (88%). Future assessments of SSD in this population are apt to vary depending on the prior history of short‐term gender‐specific survival. Without recognizing SSD, non‐gender‐specific growth curves overestimate mean age of adult females and underestimate mean age of adult males of given L_T. Assuming age 8 years for first reproduction in males and age 10 years for females, the adult male : female ratio was estimated as 1·1 : 1 and mean adult age, or generation time, was estimated as 16·4 years for males and 18·4 years for females.     

Sex ratio, sex-specific chick mortality and sexual size dimorphism in birds

It has been suggested that sexual size dimorphism (SSD) may influence sex ratios at different life stages. Higher energy requirements during growth associated with larger body size could lead to a greater mortality of the larger sex and ultimately to an overproduction of the smaller sex. To explore the associations between SSD and hatching and fledging sex ratio we performed a species-level analysis and a phylogenetically controlled analysis, based on 83 bird species. Overall, there was a significant inverse relationship between the degree of SSD and the proportion of males at hatching and fledging. Sex-specific mortality related to SSD showed a weak but persistent negative tendency, suggesting a mortality bias towards the larger sex. These results suggest that changes in relation to SSD may take place mainly at the conception stage, but could be adjusted during growth. However, conclusions should be treated cautiously as these relationships weaken when additional variables are considered.     

Relative abundance, sex ratio and population structure of the Japanese eel Anguilla japonica in the Tanshui River system of northern Taiwan

From the Gong-Shy-Tyan (GST) Stream and the Tanshui River, Taiwan, eels ranged from 5.53 cm t.l . (elvers) to 72.5 cm t.l . Anguilla japonica accounted for 93-99%, A. marmorata 1-7% and A. bicolor pacifica less than 1% of all eels caught. Mean eel lengths increased from 10 cm t.l . at the downstream sites to 50 cm t.l . at the upstream sites. Females made up 92.8% of the sex-determined eels. Population density, averaged approximately 0.14 eel m⁻² (2.42 g m⁻²) and 0.25 eel m⁻² (0.92 g m⁻²) in downstream sites of the GST and Tanshui River, respectively, and decreased substantially with upstream distance. Eels were rarely found in the heavily polluted and dam constructed areas in the midstream site of the Tanshui River.     

Hatching order and sex ratio in Southern Grey Shrike Lanius meridionalis in relation to clutch size

Despite major advances in sex ratio theory, how offspring sex should vary with hatching order remains unclear. We examine nestling sex ratio in the Southern Grey Shrike Lanius meridionalis according to hatching order and clutch size. Southern Grey Shrike nestlings present a different sex ratio with body‐mass rank order depending on clutch size. When the clutch size was five eggs (with a very low risk of brood reduction; 13%) the less costly sex (male) was found at the end of the body mass hierarchy. However, when clutch size was six eggs (with a high risk of brood reduction; 42%) the larger sex (female) was found at intermediate positions in the hatching order, possibly to decrease competitive asymmetries.     

Litter size and fetal sex ratio adjustment in a highly polytocous species: the wild boar

For species in which reproductive success is more variable inone sex than the other, the Trivers and Willard model (TWM)predicts that females are able to adjust their offspring sexratio. High-quality mothers should provide greater investmentto one sex than the other. Previous tests of the TWM have beeninconsistent, and whether the TWM applies to species with severaloffspring per litter is unclear due to possible trade-offs betweensize, number, and sex of the offspring. Williams' model (WM)accounts for confounding effects of these trade-offs on sexratio variation. Lastly, the "extrinsic modification hypothesis"predicts changes in offspring sex ratio in relation to climaticconditions and population density. Using wild boar as a model,we tested 1) whether the WM fitted observed sex ratio variationand 2) whether sex ratio variations were related to maternalattributes (test of the TWM) and/or to resource availability(test of the extrinsic modification hypothesis). Females adjustedtheir litter size rather than their litter composition, so thatthe WM was not supported. Likewise, changes in resource availabilitydid not influence the fetal sex ratio, so that the extrinsicmodification hypothesis was not supported. The fetal sex ratiowas negatively related to increasing litter size, providingsome support for the TWM. Sex ratio was male biased for littersizes up to 6 and then became female biased in larger litters.Our results provide the first case study showing marked changesin sex ratio in relation to litter size in a large mammal.     

Effects of oestradiol—enriched diet and of feeding with porcine testicular tissue on macroscopic gonadal sex in European eels

Oestradiol–enriched food (25 mg kg^-1 oestradiol) fed for 91 days to small eels (2 or 7 g) with undifferentiated gonads (UD) significantly favoured development of gonads with the macroscopic appearance of ovaries (♀-gonads) during the next 8 months. Fifty-four and 51% of control eels and 75 and 78% ofoestradiol-treated eels developed ♀-gonads. Minced porcine testicular tissue fed to 2-g eels for up to 371 days had effects similar to oestradiol-enriched food (68% with ♀-gonads), whereas feeding for only 91 days had no effect during the next 8 months. Oestradiol-enriched food was also fed to larger eels with already macroscopically differentiated gonads (30–70 g; 95% with ♀-gonads, 5% with ♀-gonads). After 27 days significantly more eels with a ♀-gonad or with a mixture of ovary-like and testis-like regions in the gonads (♂+♀-gonads) were found. After 96 days there were 44% with ♀-gonads, 40% with ♂+♀-gonads and 16% with ♀-gonads. Oestradiol thus had a feminizing effect, not only on morphologically undifferentiated gonads but also on morphologically differentiated ♀-gonads. The presence of sex steroid hormones or their precursors in porcine testicular tissue may also exert a feminizing influence. In all experiments the hormone-fed groups showed a tendency (not significant) towards increased growth rate. In small eels early rapid growth and differentiation of ♀-gonads were clearly correlated, both in hormone treated and in control eels. Otherwise no correlation was found between growth rate and gonadal sex.     

Covariation of sexual size dimorphism and adult sex ratio in parasitic nematodes

Females are larger than males in most invertebrate taxa, a phenomenon believed to result from the pressures exerted on female body size by size-dependent fecundity. Male-male competition, which can act on male body size, is not thought to play as important a role in the evolution of sexual size dimorphism in invertebrates as it apparently does in some vertebrate groups. Here, using a comparative approach, the relationship between sexual size dimorphism and adult sex ratio is examined across 46 natural populations (41 species) and 30 experimental populations (21 species) of parasitic nematodes. If male-male competition via physical contests is important, relative male size should increase as the sex ratio becomes less female-biased. This is exactly what was found in the analyses, where residuals of male size regressed on female size were used as measures of sexual size dimorphism. This result was independent of any phylogenetic influences, and was obtained for both natural and experimental nematode populations. In addition, there was no evidence of any Allometric relationship between male and female body size. The average ratio of male size to female size was roughly constant across all species and independent of body size. The results are consistent with a role for male-male competition in explaining specific deviations from the average ratio of male to female body size, suggesting a significant role for sexual selection in the evolution of nematode body sizes.     

Offspring allocation in externally ovipositing fig wasps with varying clutch size and sex ratio

The simultaneous optimization of clutch size and sex ratio isa tricky problem. Unless parameters such as host size or fecundityexist to pin down the optimal clutch size, this problem remainselusive to analytical analysis. This is because the fitnesslandscape with respect to clutch size and sex ratio does nothave one single evolutionarily stable peak toward which thepopulation can evolve. To solve this problem, I used a computeremulation to optimize both clutch size and sex ratio using externallyovipositing fig wasps as a model taxon. The simulation approachallows the use of integer numbers of eggs rather than assumingthat females can produce any sex ratio between 0 and 1. Whenfemales have no information about the patches on which theyoviposit, they produce either large clutches with a strong femalebias or clutches of a single male egg. When females have completeknowledge of their oviposition site, a set of conditional substrategiesis evolutionarily stable. Again, these substrategies are eitherlarge clutches with a female bias or dutches consisting of asingle male egg. This dichotomous oviposition pattern resultsin unrelated males sharing a fig, a condition conducive to theevolution of fatal fighting. Selection on female ovipositionstrategies may therefore be an important driving force behindhigh levels of fighting observed between male fig wasps.     

The effect of size and sex ratio experiences on reproductive competition in Nicrophorus vespilloides burying beetles in the wild

Male parents face a choice: should they invest more in caring for offspring or in attempting to mate with other females? The most profitable course depends on the intensity of competition for mates, which is likely to vary with the population sex ratio. However, the balance of pay‐offs may vary among individual males depending on their competitive prowess or attractiveness. We tested the prediction that sex ratio and size of the resource holding male provide cues regarding the level of mating competition prior to breeding and therefore influence the duration of a male's biparental caring in association with a female. Male burying beetles, Nicrophorus vespilloides were reared, post‐eclosion, in groups that differed in sex ratio. Experimental males were subsequently translocated to the wild, provided with a breeding resource (carcass) and filmed. We found no evidence that sex ratio cues prior to breeding affected future parental care behaviour but males that experienced male‐biased sex ratios took longer to attract wild mating partners. Smaller males attracted a higher proportion of females than did larger males, securing significantly more monogamous breeding associations as a result. Smaller males thus avoided competitive male–male encounters more often than larger males. This has potential benefits for their female partners who avoid both intrasexual competition and direct costs of higher mating frequency associated with competing males.     

基于粪便DNA的马鹿种群数量和性比

为分析黑龙江省完达山林区马鹿种群生存状态,制定科学有效地保护措施,从分子水平研究了种群数量和性比。2006、2007两年冬季跟踪马鹿足迹链,于五泡林场共搜集210份粪便,以成功提取DNA的167份作为分析样本。通过多态性较高的7个微卫星位点进行了基因分型分析,显示167份粪便DNA分属66只个体。基于非损伤性标志重捕法,统计出林场内马鹿数量2a平均47(39—60)只,密度0.302(0.251—0.386)只/km2,与2002年大样方法调查结果相比有减无增。SRY基因性别鉴定显示,种群雌雄性比1.00∶2.00(22♀,44♂),存在较多雄性个体,分析认为偷猎是导致性比失衡的最主要原因。数量的持续下降和性比失衡提示完达山林区马鹿种群数量的恢复需要更好地保护工作。     

Age, sex ratio and timing of the catch of kelts and ascending Atlantic salmon in the subarctic River Teno

By 15 June, 82% of the catch of Atlantic salmon Salmo salar kelts had been taken from the middle part of River Teno, northern Scandinavia. The median date of capture was 4 June for males and 8 June for females. Salmon of 1–4 sea–winters (SW) of both sexes survived spawning to return to sea as kelts. Among males, 1 SW kelts were caught earliest in the spring and 3 SW latest, but among females 4 SW were earliest, then 3 SW and finally 1 and 2 SW. There were 17 river and sea–age combinations among the kelts compared with 23 among the ascending salmon. The smolt age distribution and the mean smolt age differed significantly only between female 2 SW ascending salmon (3·97 years) and kelts (4·14 years). The proportion of 1 SW females was higher and that of 3 SW males lower among kelts than among ascending salmon. The proportion of males among 1 SW ascending salmon was 80% but among kelts only 57%. Similarly, the proportion of males among 3 SW fish was 21% for ascending salmon but only 7% for kelts. Hence overwinter mortality was higher among males. Male and female kelts of 1 and female kelts of 2 SWhad a greater mean length than ascending salmon in corresponding groups indicating a better survival of larger fish within an age group. Grilse ascend rivers after most kelts have left, but the main catch of ascending 2–3 SW salmon takes place concurrently with kelts leaving the river, inadvertently targeting kelts in the fishery.