Difficulties associated with modeling growth in the Atlantic angel shark (Squatina dumeril)

Several methods were used in an attempt to develop an age and growth model for the Atlantic angel shark (Squatina dumeril). Band counts from vertebral sections, which were fit to the traditional von Bertalanffy growth equation, the Gompertz growth equation, and the two-parameter von Bertalanffy growth equation, did not produce realistic parameter estimates. Additionally, a length-based Bayesian model was applied to fishery-independent length–frequency data, and a full Bayesian model was fitted to length-at-age data to estimate parameters for von Bertalanffy growth equation. Both the length-based and full Bayesian models failed to converge; the length–frequency data showed high bimodality unrelated to season, year, or other factors, and band counts were not predictable by length. Vertebral band counts were not valid for ageing Atlantic angel sharks, and length-based methods, which require normally distributed length–frequencies, were not appropriate for this data set. This study represents the first attempt at modeling age and growth for this species and provides research guidelines for future research initiatives.     

Growth of juvenile chub mackerel Scomber japonicus in the western North Pacific Ocean: with application and validation of otolith daily increment formation

The growth of juvenile chub mackerel Scomber japonicus collected in the western North Pacific Ocean in 2007 and 2009 was examined based on the evidence of otolith daily increment formation in captive specimens. There was a significant difference in the relationship between known age and number of increments in the frontal and sagittal planes. Repeated markings on the otolith using Alizarin complexone and the coefficient of variation in number of increments suggest that the increments in the frontal plane of the otolith are more suitable for age estimation than those in the long and short axes of the sagittal plane. The increments in the frontal plane formed daily, and the first ring was usually deposited 3 days after hatch. Age of wild juveniles ranged from 24 to 211 days after hatch based on the frontal plane method. The estimated hatching periods of specimens ranged from February to June, but the April-hatched specimens were collected throughout the sampling periods of 2007 and 2009. The Gompertz growth model showed a difference in growth pattern in specimens between 2007 and 2009. The juveniles in 2009 appeared to grow more quickly than those in 2007 until summer, but thereafter the 2009 specimens seemed to grow more slowly.     

Geographic influences on and the accuracy and precision of age estimates for the red bass, Lutjanus bohar (Forsskal 1775): A large tropical reef fish

The red bass is a large tropical reef fish (Lutjanidae, tropical snappers) that is harvested to varying extents throughout a widespread Indo-Pacific distribution. The aims of this study were to investigate the accuracy and precision of age estimates from transverse sections of sagittal otoliths and to assess effects on these of the geographic area of collection and otolith preparation method. Two independent validation studies suggested an approximately annual formation of annuli in otoliths, predominantly for otoliths with 4–10 annuli but also for one otolith with 29 annuli. Otolith sections produced exceptionally high annulus counts: up to 56 annuli for samples from the Great Barrier Reef (GBR), Australia; and up to 55 annuli from the Seychelles, indicating a high longevity for this species. The precision of otolith readings from the GBR (index of average percent error, IAPE = 3.21 ± 0.26 S.E.) was within commonly accepted bounds for age estimation (IAPE up to 5%) but precision of readings from the Seychelles was significantly lower (IAPE = 9.18 ± 0.47 S.E.) and outside of this “acceptable” range. Age-based biological parameters for red bass from the Seychelles should thus be applied with greater caution than those for red bass from the GBR. If basic demographic properties are assumed relatively constant across the wide geographic range sampled, however, results from the GBR could be used as more reliable preliminary data for precautionary management strategies in the Seychelles and elsewhere.     

Using otolith weight–age relationships to predict age based metrics of coral reef fish populations across different temporal scales

We assess the use of otolith weight to predict population age structure of an important harvested coral reef fish at different temporal scales up to 4 years, and explore the implications of age prediction for estimates of key fishery parameters. Fish age and otolith weight relationships were estimated for common coral trout, Plectropomus leopardus (Serranidae: Epinephelinae), at 24 coral reefs located in four different regions spanning 7° of latitude along the Great Barrier Reef of Australia from 1995 to 1999. We explored the robustness of predictions of population age structures from otolith weights where age structure in 1 year was derived from otolith weights using the age–otolith weight relationships derived in another year up to 4 years earlier. The accuracy of predictions of age structure varied depending upon the temporal scale over which the prediction was made. Predictive accuracy was highest for predictions in the same year as the age–otolith weight relationship was derived and worst at the longest scale, when predictions spanned 4 years. Predictions of age based on the age–otolith weight relationships generally overestimated the minimum age of a population and underestimated the maximum age. Mean predicted age was generally within ±1% difference of the mean observed age while mean predicted length at modal age (growth index) was largely within ±5% difference of mean observed length at modal age. Predicted age structures gave less accurate estimates of total mortality rate than those estimated from directly determined age structures. Fish age–otolith weight relationships generally predicted modal age within ±1 year at all temporal scales. These results have significance for making rapid, initial estimates of key parameters for long-term monitoring of tropical reef fish stocks, especially in circumstances where available resources are insufficient for a comprehensive program of direct age estimation.     

Seasonal changes in otolith and somatic growth in age-0 Pacific saury <Emphasis Type="Italic">Cololabis saira</Emphasis>

We evaluated the seasonal changes in otolith and somatic growth of age-0 Pacific saury Cololabis saira in 223 fish collected between June and November 2002. We calculated the age in days of each individual by measuring otolith growth increments under a scanning electron microscope. The age was correlated with body length and otolith radius. We also observed seasonal changes in the rate of increase in body length and otolith radius and in the pattern of otolith growth. Until August, both body length and otolith radius increased with age. Thereafter, the otolith radius continued to increase, whereas the rate of somatic growth decreased. As a result, the ratio of otolith radius to body length increased. After August, the percentage of otoliths with unreadable increments on their edge increased due to the formation of hyaline zones. Otoliths grew both radially and in thickness until July, but gradually stopped growing in thickness after August. Beginning in October, more than 80% of otoliths only grew radially. After August, the otolith not only continued growing but the morphological growth pattern also changed.     

Population structure of bigeye tuna (Thunnus obesus) in the Indian Ocean inferred from mitochondrial DNA

Population structure of bigeye tuna (Thunnus obesus) in the Indian Ocean, Western Pacific Ocean and Eastern Atlantic Ocean were investigated using mitochondrial (mt) DNA sequence data. A total of 380 specimens were sampled from four regions in the Indian Ocean (Cocos Islands, Southeastern Indian Ocean, Southwestern Indian Ocean and Seychelles), and one region each from the Atlantic (Guinea) and the Western Pacific Oceans, respectively. The reconstructed neighbor-joining phylogeny based on the first hypervariable region (HVR-1) of the mitochondrial control region sequence data showed that haplotypes from the Indian and the Western Pacific Oceans could be grouped into two clades (Clades I and III), whereas in the Atlantic Ocean, two divergent clades (Clades I and II) coexisted. A single stock of bigeye tuna in the Indian Ocean was supported by hierarchical AMOVA tests and pairwise Φ_ST analyses. Clade I was the dominant population in the Indian and the Western Pacific Oceans which consisted of more than 96% of the specimens and Clade II was a specific group exclusively restricted to the Atlantic Ocean which made up 77% of its specimens. A new minor Clade, Clade III was discovered in the Indian and the Western Pacific Ocean. Overall, these analyses indicated that bigeye tuna of the Indian Ocean constituted a single panmictic population.     

Validation of daily increment formation in otoliths of immature and adult Japanese anchovy <Emphasis Type="Italic">Engraulis japonicus</Emphasis>

In order to validate daily increment formation in otoliths of immature and adult Japanese anchovy Engraulis japonicus, three rearing experiments using chemical marking of otoliths were conducted on adult anchovy in summer 2004 and immature anchovy in summer 2005 and in winter 2006. In the two experiments conducted in summer, the number of otolith microincrements between alizarin complexone (ALC) marks showed that microincrements were formed daily. In the summer 2005 experiment, immature anchovy under conditions of reduced daily food rations also showed daily microincrement formation. Average increment width was 0.9 μm in adults and 1.8–3.1 μm in immature anchovy. In contrast, no clear increments were observed between ALC marks on the otoliths from the experiment in winter 2006, and scanning electron microscope (SEM) observations failed to confirm clear increment formation. We consider that low water temperatures (<13–14°C) restricted otolith growth and lowered the contrast between the discontinuous and the incremental zones of the otolith increments. For age estimation of Japanese anchovy, clear increments wider than about 1 μm in the otolith can be regarded as daily increments. However, daily age estimation of immature and adult anchovy that experience low water temperatures in winter may be difficult due to the obscurity of the increments.     

近海张网对黄鲫和小黄鱼的年龄选择性研究

渔具对捕捞对象的年龄选择性对于渔业资源评估等工作是至关重要的,但相关研究较少。使用套网法对网囊网目尺寸分别为35 mm和45 mm的近海张网对黄鲫(Setipinna taty)和小黄鱼(Larimichthys polyactis)的年龄选择性进行分析。数据分析采用2种年龄选择性曲线模型:即估算网囊对个体体长选择性后根据个体生长方程换算和直接使用Logistic曲线代表年龄选择性曲线;通过对渔获体长分布和年龄分布数据的拟合,结果显示,2种年龄选择性曲线均能较好地拟合数据,网囊对黄鲫和小黄鱼的50%选择年龄t50和年龄选择范围SRt均随着网目尺寸的增加而增加,35 mm和45 mm网目尺寸的网囊对黄鲫的t50分别约为4月龄和8月龄,对小黄鱼的t50分别约为0.6龄和1.5龄,明显小于黄鲫和小黄鱼的推荐开捕年龄,反映出目前近海张网渔具网目过小,可能会对幼鱼资源产生不利的影响。     

Age and growth of sea perch (Helicolenus percoides) from two adjacent areas off the east coast of South Island,New Zealand

A validated ageing methodology using otolith thin sections is presented for sea perch (Helicolenus percoides) in two adjacent areas off the east coast of South Island, New Zealand. Oxytetracycline marking of two adult fish held in captivity for 1 year suggested that a single dark growth increment formed during winter, commencing May or June. The annual formation of growth increments was confirmed by the observed progression of year classes in comparable samples from three different years, and the progression of length modes in several consecutive years that matched the estimated growth curves. Otolith interpretation was difficult because of a central dense region and the presence of many fine bands within each growth increment, but the latter could be counted, and it is considered that a validated ageing procedure is presented. Von Bertalanffy growth parameters were calculated for east coast South Island (ECSI) and Chatham Rise males and females. In both areas the growth rate of males is slightly but significantly faster than for females. Growth is relatively slow throughout life. From the maximum observed ages for ECSI and Chatham Rise fish of 35 and 59 years, the respective natural mortality rates are estimated to be 0.12 and 0.07 year^?1, but the most plausible value for the species is likely to be at the lower end of this range. Some stock differentiation between the two areas is indicated, based primarily on differences in length-frequency distributions implying different patterns of year class strengths, but also on apparent differences in growth rates between areas. This supports the present management regime of separate commercial catch quotas.     

Interannual variability in hatching period and early growth of juvenile walleye pollock, Theragra chalcogramma, in the Pacific coastal area of Hokkaido

Juvenile walleye pollock of the Japanese Pacific population were collected from the Funka Bay [spawning ground; 16–64 mm fork length (FL)] in spring and the Doto area (nursery ground; 70–146 mm FL) in summer. Hatch dates were estimated by subtracting the number of otolith daily increments from sampling dates, and their early growth was back‐calculated using otolith radius–somatic length relationships. Interannual change of the hatching period was observed during 2000–02, and the peaks ranged from mid‐February in 2000 to early‐April in 2002. In 2000, when a strong year class occurred, early life history of the surviving juveniles could be characterized by early hatching and slower growth in the larval stage (<22 mm length). Higher growth rate in 2001 and 2002 did not always lead to good survival and recruitment success. Even though their growth was slow in 2000, the larvae hatched early in the season had larger body size on a given date than faster‐growing larvae hatched in later season in 2001 and 2002. Bigger individuals at a certain moment may have advantage for survival. The delay of hatching period may result in higher size‐selective mortality, and as a necessary consequence, back‐calculated growth in 2001 and 2002 could shift towards higher growth rate, although abundance of such a year class would be at the lower level. Variability in spawning period, early growth and their interaction might have a strong relation to larval survival through cumulative predation pressure or ontogenetic changes in food availability.