Using otolith weight to estimate the age of haddock (Melanogrammus aeglefinus): a tree model application

In this study, we investigated whether otolith weight can be used to estimate fish age with the same level of accuracy as that of the traditional annuli counting technique in a commercially important species such as haddock (Melanogrammus aeglefinus). Results indicate that this method is highly effective for young fish (around 97% correct classification), whereas its powers of prediction decrease with the increasing age of the fish. For older fish, the otolith weight cannot be an accurate estimator of fish age if the weight overlap between the different age classes is too large. Nevertheless, the otolith weight technique is strictly dependent on correct age determination through the counting of annuli of those individuals used in the calibration. Hence, an increase in the accuracy of ageing obviously determines an increase of the power of otolith weight to estimate fish age. Therefore, we suggest that otolith weight could represent a routine technique for determination of the age structure of haddock populations. This technique has the merit to be objective, fast, 100% repeatable and has the same level of accuracy as that of annuli counting.     

Age determination of the Antarctic fishes Champsocephalus gunnari and Notothenia rossii marmorata from South Georgia

Summary Investigations were performed on otoliths from Champsocephalus gunnari and Notothenia rossii marmorata as part of an effort to study the population dynamics of Antarctic fishes. Examination of otoliths by scanning electron microscope (SEM) revealed internal microincrements which were similar to daily increments described for other fish species. No easily identifiable annuli could be discerned and fishes were aged by counting microincrements. Multiple regression analyses relating age to otolith morphometrics and fish size, provided a simpler ageing method. It was determined with these techniques that C. gunnari grew to 50 cm in 15 yrs and N. rossii marmorata grew to 50 cm in 6.5 yrs. The lack of larger-sized individuals for N. rossii marmorata may be indicative of recent overfishing with only the younger age groups remaining. It appears that length-at-age data determined on a yearly basis, could provide valuable scientific and management information for these species.     

软刺裸裂尻鱼的年龄鉴定

检测并比较了软刺裸裂尻鱼（Schizopygopsis malacanthus）鳞片、耳石、脊椎骨和背鳍条的年轮特征。结果表明,这4种材料上均具有年轮特征,以耳石最明显,且易于识别,为最好的年龄鉴定材料;鳞片上的年轮也较明显,但高龄鱼外围的年轮常挤在一起,使鉴定结果偏低;背鳍条上的环纹清晰,但边缘出现轮纹的重叠,影响年龄准确判读;脊椎骨上通常只能观察到比较有限的环纹,不适合用作年龄鉴定。     

Accuracy and repeatability of moose (<Emphasis Type="Italic">Alces alces</Emphasis>) age as estimated from dental cement layers

Optimal research and management of species with age structure often depends on estimates of age-specific population parameters, which in turn depends on reliable methods for age determination. By counting annuli in the cementum of incisor root tips from 51 known-age moose (Alces alces) between 1 and 12 years old, we examined the variation in accuracy and repeatability of age estimates provided by three research technicians with different experiences of aging moose. The most experienced technician estimated the moose age correctly in up to 90% of the cases, while the technician with no prior experience estimated age correctly in up to 73% of the cases. The medium-experienced technician achieved a lower accuracy (up to 53%), indicating that experience alone is not sufficient if the basic training or lack of routine checks against other colleagues or a known-age material are not undertaken. The percentage moose aged within ±1 year from correct age was significantly higher in all technicians (94–98%). After the generally high accuracy, we also found high repeatability (0.980–0.994) within technicians. We conclude that this method of age-determination provides reliable estimates that can be used by management and research to gain information about age-specific patterns in moose populations. However, to obtain estimates of high accuracy the technicians should be well trained, have gained the necessary experience, and most preferably, have access to a sample of teeth from known-age moose.     

Somatic and otolith growth in the oyster toadfish (Opsanus tau L.)

Otoliths from oyster toadfish were measured and examined for annuli and daily increments. Distinct annual increments made it feasible to determine growth parameters which demonstrated sexual dimorphism in growth. Microincrements, judged to be daily on the basis of two separate criteria, were enumerated and measured to provide verification of annuli. Utilization of multivariate mathematical models relating age to otolith growth and somatic growth simplified age determination. These methods for examining otoliths should be applicable to other fish species and make it possible to link growth and mortality rates to life history and environmental occurrences.     

POPULATION ECOLOGY OF SEALS: RETROSPECTIVE and PROSPECTIVE VIEWS

This review focuses on population ecology, with critical accounts of past work and future possibilities in age determination, body growth and condition, estimating abundances, mortality rates and lifespans, reproduction, comparative life histories, population dynamics, population modelling and seals in ecosystems. We suggest ways to reduce errors in age determination and to improve methods of obtaining and presenting growth data. Generalized von Bertalanffy growth equations are promoted as a basis for analysing species differences and intra-population variation in body lengths. Indices other than blubber thickness may be better for following body condition. Catch-effort and survival-index methods of estimating abundances have limited applicability, total counts are only locally useful, and sample counts may only be accurate for scattered, ice-breeding species. Some new techniques for population indices are promising. Pre-adult mortality remains difficult to assess. Although not always recognized, adult mortality rates do increase with age, as well described by Gompertz functions. Existing estimates of lifespans are unreliable, and a new approach is outlined. There are methodological problems in estimating ages of maturity. Corpora albicantia should not be used for back-extrapolation, and more study is needed of use of teeth annuli as indicators of maturity. Age-specific proportions of females parous based on reproductive tracts may disagree with proportions recruited in breeding groups, suggesting that the former may often be in error. Allometric relationships among body sizes and life-history variables need more reliable data, especially since the residuals of such relationships are of greatest interest. Brain size may be a better scalar. Direct evidence of density dependence in population growth of seals is sparse. Early survival has been more widely shown to be density-dependent, but only among polygynous species where crowding on land may be a byproduct of sexual selection; there is as yet no good evidence of trophic restraints. Evidence of density dependence of ages of maturity is generally unconvincing. Predation, especially by sharks, may be critical in some species. Characteristics of equilibrium populations might profitably be sought in mass remains in middens and historic kill sites. More attention should be paid to the search for density-independent influences. Supposed impacts of fisheries and pollutions are not wholly convincing. Natural epidemics may keep some populations below resource or space saturation, and some high-latitude species may show large year-to-year variations in recruitment and abundances. Evidence for such density-independent effects should be sought in residuals of growth curves and in teeth layers. Although surplus yield and production/biomass models have been tried, realistic pinniped models must be completely age-structured and time-dependent. Simple models have questionably assumed stationarity to derive life-history parameters. The best available estimates of density dependence of such parameters give no resolution when extrapolated toward equilibrium, and only limited efforts have been made to introduce stochasticity. Better data, not improved model structures, are needed for better understanding. Recent work has contradicted the assumed voraciousness of seals, but their system impacts and dependencies are not well understood. Extended Lotka-Volterra equations used to model Antarctic food webs, including seals, are merely heuristic. Fixed seal biomasses enter as top-down, driving functions in a Bering Sea model, which accordingly cannot be used to analyse or manage their populations. Some Soviet models are tantalizing but ill-specified. The introduction of harbor seals in well-chosen lakes might give mote insights into system roles than would more elaborate modelling. We wonder if pinniped ecology is well served by too many enthusiasts operating under too many restraints.     

Patterns of growth and sexual size dimorphism in two species of box turtles with environmental sex determination

An adaptive explanation for environmental sex determination is that it promotes sexual size dimorphism when larger size benefits one sex more than the other. That is, if growth rates are determined by environment during development, then it is beneficial to match developmental environment to the sex that benefits more from larger size. However, larger size may also be a consequence of larger size at hatching or growing for a longer time, i.e., delayed age at first reproduction. Therefore, the adaptive significance of sexual size dimorphism and environmental sex determination can only be interpreted within the context of both growth and maturation. In addition, in those animals that continue to grow after maturation, sexual size dimorphism at age of first reproduction could differ from sexual size dimorphism at later ages as growth competes for energy with reproduction and maintenance. I compared growth using annuli on carapace scales in two species of box turtles (Terrapene carolina and T. ornata) that have similar patterns of environmental sex determination but, reportedly, have different patterns of sexual size dimorphism. In the populations I studied, sexual size dimorphism was in the same direction in both species; adult females were, on average, larger than adult males. This was due in part to males maturing earlier and therefore at smaller sizes than females. In spite of similar patterns of environmental sex determination, patterns of growth differed between the species. In T. carolina, males grew faster than females as juveniles but females had the larger asymptotic size. In T. ornata, males and females grew at similar rates and had similar asymptotic sizes. Sexual size dimorphism was greatest at maturation because, although males matured younger and smaller, they grew more as adults. There was, therefore, no consistent pattern of faster growth for females that may be ascribed to developmental temperature. Received: 20 March 1996 / Accepted: 10 March 1998     

太湖似刺鳊(鱼句)年龄和生长的研究

本文较为详细地研究了太湖似刺鳊(鱼句)(Paracanthobrama guichenoti Bleeker)的年龄和生长,并对种的繁殖保护措施作了探讨。共积累756尾标本的生物学资料。     

Comparison of ageing methods and growth rates for largemouth bass,Micropterus salmoides Lacépède,from northern latitudes

Synopsis Ages determined by counts of apparent annuli on scales, sagittae, vertebrae, pectoral fin ray and dorsal fin spine cross sections of largemouth bass from northern populations, which are older and slower growing fish than in the southern parts of its native range, were compared to establish the accuracy of each method. Linear regression techniques indicated strong agreement (r> 0.9) among ages assigned from the examination of scales, sagittae, and vertebrae. The pattern of growth zones on pectoral fin ray and dorsal fm spine cross sections proved too variable for accurate age determination. Limited data suggest that ages greater than 7+ assigned from scales were more likely to underestimate true ages than the other body parts used, although none of these methods gave satisfactory results. Examination of scales from recovered tagged fish, and the similarity between back-calculated lengths of fish through age 7+ to annulus I and observed lengths of juvenile largemouth bass near the end of their first growing season, support the validity of ages determined from scales. Despite a very limited amount of habitat suitable for largemouth bass and severe climatic conditions, growth of this species in Tadenac Lake was similar to growth in other waters north of the Great Lakes. Differences in physical characteristics among these waters does not appear to influence growth rates of largemouth bass, but probably affects production and biomass.     

青海湖裸鲤不同年龄鉴定材料的年轮特征

通过各种年龄鉴定材料比较研究了青海湖裸鲤的年轮特征。微耳石和星耳石可用于鉴定年龄,而矢耳石易碎,不适合鉴定年龄。4种年龄鉴定材料对青海湖裸鲤年龄的判别能力为:背鳍条>微耳石>臀鳞>脊椎骨。对8龄以下个体,用背鳍条磨片鉴定年龄效果较佳;对8龄以上个体,臀鳞、背鳍条磨片和脊椎骨上的年轮计数明显低于微耳石磨片,微耳石磨片是高龄青海湖裸鲤较为可靠的年龄鉴定材料。       

Life-history strategies of Acrossocheilus fasciatus (Barbinae, Cyprinidae) in the Huishui Stream of the Qingyi watershed, China

Life-history traits of Acrossocheilus fasciatus were examined using 384 specimens collected monthly during May 2009 and April 2010 in the Huishui Stream of the Qingyi watershed, China. Using scales for age determination, female and male fish comprised five and four age groups, respectively. The monthly changes in marginal increment ratio suggested that annuli on scales were formed during March through May. Total lengths back-calculated significantly increased with age for both sexes and varied significantly between the two sexes at each age. The fact that females had larger body size and grew faster than males indicated the sexual size dimorphism for this species. Both sexes got their 50% maturity at age 3, when females and males were 105.3 and 112.1?mm total length, respectively. Based on the monthly changes in the gonado-somatic index and egg-development process, fish spawned from April through August. Absolute fecundity ranged from 295 to 3,573 eggs per fish and increased significantly with age. But relative fecundity, ranging from 11.77 to 69.96?eggs/g, was not significantly different among age groups. Compared with the life-history traits of an upstream population in the Puxi Stream (a headwater stream within this study watershed), the downstream population of A. fasciatus in the Huishui Stream (a 4th-order stream) exhibits larger body size, faster somatic growth, later sexual maturity, and lower reproductive investment. These variations in life-history strategies between the two populations could perhaps be explained by the spatial heterogeneity in habitat environment along the upstream–downstream gradient in this watershed.     

长江干流圆筒吻鮈的年龄与生长

根据 5 5 1尾标本研究了生活在长江干流中圆筒吻的年龄与生长 ,并提出了资源合理利用建议。圆筒吻的鳞片可作为年龄鉴定的依据 ,年轮形成期主要在 2～ 5月。圆筒吻的体长与鳞长呈直线关系 ,与体重呈幂指数关系 ,生长适合VonBertalanffy生长方程。在 1～ 2龄生长最快 ,为保护圆筒吻资源 ,应限捕体长 2 0 0mm以下的个体     

长江干流圆筒吻(鱼句)的年龄与生长

根据551尾标本研究了生活在长江干流中圆筒吻(鱼句)的年龄与生长,并提出了资源合理利用建议.圆筒吻(鱼句)的鳞片可作为年龄鉴定的依据,年轮形成期主要在2～5月.圆筒吻(鱼句)的体长与鳞长呈直线关系,与体重呈幂指数关系,生长适合Von Bertalanffy生长方程.在1～2龄生长最快,为保护圆筒吻(鱼句)资源,应限捕体长200 mm以下的个体.     

珍稀濒危植物长蕊木兰种群的年龄结构与空间分布

珍稀濒危植物长蕊木兰为国家Ⅰ级保护植物。然而,由于受研究尺度和分析方法的限制,对其种群生态特征等方面仍不清楚。以云南高黎贡山原生的中山湿性常绿阔叶林4 hm2样地调查数据为基础,应用Ripley的L函数分析了长蕊木兰种群的年龄结构与空间分布格局。研究发现:(1)长蕊木兰种群的年龄结构为反"J"型,属稳定型种群。(2)长蕊木兰种群个体的空间分布格局与空间尺度关系密切,空间尺度小于75 m时为聚集分布,大于75 m时为随机分布。生境异质性在长蕊木兰种群空间分布格局的形成中可能发挥了重要的作用。(3)不同发育阶段个体的空间分布格局存在明显的差异,中树和小树阶段的分布格局在中、小尺度上呈聚集分布,在较大尺度上呈随机分布;大树阶段在整个空间尺度上均呈现随机分布。(4)长蕊木兰不同发育阶段的空间关联性主要表现为中、小尺度上的负相关,在较大尺度上则趋向于无关联。     

Age determination and body growth of the Common duiker Sylvicapra grimmia(Mammalia)

Age determination in the Common duiker Sylvicapra grimmia was investigated by analysis of tooth eruption and replacement sequence, incremental lines of tooth cementum and tooth wear in a unique collection of 48 known-age skulls, and also by analysis by post-natal body growth in known-age duiker. In both the mandible and maxilla, permanent molariform teeth were fully erupted and in wear by 26 months of age. There was little variation in the age of eruption and replacement of all molariform teeth, making this a particularly useful feature of the duiker for age determination purposes. In contrast, the variability in eruption of the incisiforms, coupled with the difficulty in distinguishing deciduous incisiforms from the permanent counterparts, placed an unexpected limitation on the use of these teeth. Although the apparent linear relationship between tooth attrition and age has potential for further investigation as an age determination technique, the cementum annuli were not correlated with chronological age. Theoretical Von Bertalanffy equations were used to analyse body growth with age. It was concluded that because the asymptote of growth was reached at such an early age, and because there is so much individual variation in growth, body growth, including horn growth, is of very limited value for age determination. Female duiker were significantly larger than males.     

Uncertainty in determination of sex from harvested bobcats

Considerable uncertainty often exists in estimates of demographic parameters based on data collected from harvested furbearer species. We used molecular genetic techniques to estimate rates of error in 2 methods of sex determination of harvested bobcats (Lynx rufus): manual examination of the carcass (field sex) and laboratory-based maximum canine root area (MRA sex). Error rates were high for both sexing techniques, and were associated with age and an age–sex interaction for the field and MRA sexing methods, respectively. These findings do not support the use of the field methods for identifying sex of harvested bobcats. The MRA method may be effective for determining sex of older bobcats but is limited by considerable overlap between sexes in juveniles and yearlings. If critical demographic parameters are estimated from harvest data, efforts should be made to identify and reduce rates of error before data are used to assess population status. © 2011 The Wildlife Society.     

The effects of marking and capture on recapture frequencies of butterflies

Summary As a preliminary to a population study using markrelease-recapture techniques, specimens of the Satyrid buttfly Melanargia galathea (L.) were subjected to a number of marking and capture techniques. Although the adults are thought to display both aposematic and cryptic coloration, the use of marks of different sizes and colours had no significant effect on recapture frequencies. However, repeated disturbance due to capture was found to significantly reduce recapture frequency. The influence of the different techniques on recapture frequencies could not be detected reliably by excessively low recapture rates, or by comparisons to Poisson distributions. It is suggested that these comparisons are of limited value as measures of the suitability of a marking or handling scheme. Subsequent work showed that capture affected recapture rates of several other species. Moreover, these effects could not be readily predicted from knowledge of the biology of these species. The implications of these findings are discussed.     

Use of the frontal bone in age determination of Labeo horie (Pisces,Cyprinidae) in Jebel Aulia Reservoir,Sudan

In spite of the exuberance of recent approaches to age determination of fish, many ecologists are convinced that the most valid method is age reading from permanent marks or growth rings laid on skeletal parts. Of the known structures used, only the vertebrae are suitable and readable for a large variety of species and sizes. Examination of different skeletal structures of Labeo horie, a Cyprinid collected from Jebel Aulia reservoir, revealed that the frontal bone carried well-defined growth rings. The validity of these rings was checked against other direct and indirect methods of age determination. Results proved to be statistically valid, and the frontal bone offers an additional device of age determination of L. horie.     

Review of the Methods Frequently Used to Estimate the Abundance of Orthoptera in Grassland Ecosystems

Ecologists have quantified Orthoptera (grasshoppers and crickets) density in a wide variety of conservation studies. Objective determination of Orthoptera population size is possible using mark-release recapture techniques but these are time-consuming and of little use for all but the smallest scale studies. Therefore, a wide range of sampling techniques have been devised to quantify population density and the most commonly used methods include sweep netting and quadrat counts. It is the aim of this paper to critically review studies that have used these techniques and to provide useful suggestions for non-specialists on which method may be most applicable to their study site. This paper reviews a selection of the extensive literature reporting studies estimating the abundance of grasshoppers (Acrididae) in a wide range of grassland ecosystems. Where possible, studies on bush-crickets (Tettigoniidae) and crickets (Gryllidae) are included reflecting their overall contribution to assemblage diversity in grassland ecosystems and to highlight the need for further investigations of sampling efficiency on these two under-researched families.The most rapid and inexpensive sampling methods, such as quadrat and transect counts, involve ‘flushing’ grasshoppers from the sward. These techniques are fairly accurate in short, open swards (<50 cm sward height) where grasshopper densities are low (<2 adults per m²). At higher population densities (>2 adults per m²), methods which require the capture of grasshoppers such as box quadrats and sweep netting may be more appropriate. Sampling grasshopper populations in taller vegetation (>50 cm sward height) is more problematic as the efficiency of many techniques may be reduced by vegetation structure. Methods such as timed counts can be used at low densities (<2 adults per m²) and night trapping might be most applicable where high numbers of grasshoppers are present (>2 adults per m²).There is an urgent need for development of a standardised sampling technique that can produce comparable data from studies with a wide variety of observers in grasslands with differing vegetation structures and grasshopper densities.