Growth of the clupeid fishes, Stolothrissa tanganicae and Limnothrissa miodon, in the Zambian waters of Lake Tanganyika

The age and growth of two endemic Lake Tanganyikan clupeid fishes, Stolothrissa tanganicae and Limnothrissa miodon , were estimated from analysis of otolith microstructure in specimens collected in Zambian waters from October to December 1990. Both species had relatively clear, concentric otolith increments which were believed to represent daily increments based on their similarity to daily increments found in some marine clupeid species. The growth rates estimated from length-at-age data were: for S. tanganicae, L_t = 104·0 (1 – exp (– 0.00512 ( t – 5·8))); for L. miodon, L_t = 155.4 (1 – exp (– 0.00236 ( t +8.1))). In most cases, the growth parameters obtained from otolith analyses generally agreed with those previously estimated from analyses of length-frequency distributions.     

Age at recruitment of Hawaiian freshwater gobies

Synopsis Very little is known about the dynamics of native Hawaiian stream fishes. Five species are restricted, as adults, to freshwater streams and estuaries on the major islands of the Hawaiian archipelago. This paucity of information is partly due to difficulties inherent in determination of age and subsequent determinations of life history characteristics. In the present study, we determined the age of newly recruited Hawaiian gobies,Stenogobius genivittatus andAwaous stamineus using otolith microtechniques. Internal otolith increments were enumerated using scanning electron microscopy (SEM). Increments of newly recruited juveniles were deposited on a daily basis as validated through a marking study. Results showed recruitment at an average age of 135 and 161 days for these two species, respectively, with more rapid growth following recruitment to freshwater. Chemical analyses of otolith carbonate of the Hawaiian gobies by electron microprobe for strontium and calcium concentrations provided valuable insights into a fish's past history. A combination of structural and chemical analyses makes it possible to link growth and recruitment to nutritional and environmental factors. Such information developed as a broad model would be applicable to the management of Hawaiian gobies and would greatly improve the quality of information available for these unique fish populations and other fish populations     

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.     

Dramatic shifts in Hawaiian monk seal distribution predicted from divergent regional trends

Total estimated abundance of Hawaiian monk seals was just 1,161 individuals in 2008 and this number is decreasing. Most monk seals reside in the remote Northwestern Hawaiian Islands (NWHI) where the decline is approximately 4%/yr, whereas relatively fewer seals currently occupy the main Hawaiian Islands (MHI). It is widely accepted that the MHI population is increasing, although there are no formal estimates of total abundance, population growth rate or vital rates. This lack of information has hampered efforts to anticipate future scenarios and plan conservation measures. We present the first estimates of MHI monk seal survival and age‐specific reproductive rates. Using these rates, a conservative estimate of current MHI abundance and a previously published stochastic simulation model, we estimate the MHI population growth rate and projected abundance trend. Analogous estimates for the NWHI are derived from a much richer data set. Estimated survival from weaning to age 1 yr is 77% in the MHI, much higher than recent NWHI estimates ranging from 42% to 57%. Moreover, MHI females begin reproducing at a younger age and attain higher birth rates than observed in the NWHI. The estimated MHI intrinsic rate of population growth is 1.07 compared to a 0.89–0.96 range in the NWHI. Assuming an initial abundance of 152 animals in the MHI, projections indicate that if current demographic trends continue, abundance in the NWHI and MHI will equalize in approximately 15 yr. These results underscore the imperative to mitigate the NWHI decline while devoting conservation efforts to foster population growth in the MHI, where documented threats including fishery interactions, direct killing, and disease could rapidly undo the current fragile positive trend.     

Growth-band counts from elephantfish Callorhinchus milii fin spines do not correspond with independently estimated ages

Fin spines from elephantfish Callorhinchus milii were sectioned and viewed with transmitted white light under a compound microscope. The sections displayed growth bands but their interpretation and significance were unclear. Three different methods were used for counting growth bands. The results were compared with reference growth curves based on length-at-age estimates for six juvenile year classes derived from length-frequency distributions, and tagging data that showed longevity is at least 20 years. None of the three ageing methods showed good correspondence with the reference curves and all methods departed markedly from the reference curves at ages above 2 years old. Therefore, growth bands present in C. milii spines are not useful for ageing, at least with the three methods tested here. Spine bands may not represent age marks, but instead may be layers of material deposited irregularly to strengthen the spine.     

Demographic patterns in the peacock grouper (Cephalopholis argus), an introduced Hawaiian reef fish

This study took advantage of a unique opportunity to collect large sample sizes of a coral reef fish species across a range of physical and biological features of the Hawaiian Archipelago to investigate variability in the demography of an invasive predatory coral reef fish, Cephalopholis argus (Family: Epinephelidae). Age-based demographic analyses were conducted at 10 locations in the main Hawaiian Islands and estimates of weight-at-length, size-at-age, and longevity were compared among locations. Each metric differed among locations, although patterns were not consistent across metrics. Length-weight relationships for C. argus differed among locations and individuals weighed less at a given length at Hilo, the southernmost location studied. Longevity differed among and within islands and was greater at locations on Maui and Hawaii compared to the more northern locations on Oahu and Kauai. Within-island growth patterns differed at Kauai, Oahu, and Hawaii. This work provides a case study of fundamental life history information from distant and/or spatially limited locations that are critical for developing robust fishery models. The differences observed both among and within islands indicate that variability may be driven by cross-scale mechanisms that need to be considered in fisheries stock assessments and ecosystem-based management.     

Age estimation and validation for South Pacific albacore Thunnus alalunga

Validated estimates of age are presented for albacore Thunnus alalunga, sampled from a large part of the south‐western Pacific Ocean, based on counts of annual opaque growth zones from transverse sections of otoliths. Counts of daily increments were used to estimate the location of the first opaque growth zone, which was completed before the first assumed birthday. The periodicity of opaque zones was estimated by marginal increment analysis and an oxytetracycline mark–recapture experiment. Both validation methods indicated that opaque zones formed over the austral summer and were completed by autumn to winter (April to August). The direct comparison of age estimates obtained from otoliths and dorsal‐fin spines of the same fish indicated bias, which was assumed to be due to poor increment clarity and resorption of early growth zones in spines, resulting in imprecise age estimates. As such, age estimates from otoliths are considered to be more accurate than those from spines for T. alalunga. This is consistent with results for a growing number of tropical and temperate tuna Thunnini species. It is recommend that validated counts of annual growth zones from sectioned otoliths is used as the preferred method for estimating age‐based parameters for assessment and management advice for these important stocks.     

Otolith shape analysis and daily increment validation during ontogeny of larval and juvenile European chub Squalius cephalus

This assesses features of otoliths from laboratory-reared embryos, larvae and juvenile European chub Squalius cephalus from hatching to 180 days post-hatching (dph). We observed the development of the three pairs of otoliths (lapilli, sagittae and asterisci) and more precisely shape changes, as well as timing and deposition rate of increments of the lapilli. The lapilli and the sagittae were present at hatching, whereas the asterisci formed between 20 and 30 dph. The lapillus and sagitta shapes were round until 20 dph. From 60 dph the anterior and the posterior rostra of the sagittae were well developed, but very thin, making this otolith too fragile to manipulate for further studies of shape and validation of otolith increment deposition rate. The lapilli provided reliable age estimates for free embryos, larvae and juveniles up to 120 dph. However, caution should be taken when ageing fish older than 150 dph as an underestimation was noticeable. The regression of the number of otolith increments on age showed a slope and an intercept not significantly different from 1 and 0, respectively, which indicated that otolith growth increments were deposited on a daily basis, with the first microincrement occurring at hatching. Increment counts were consistent between three interpreters, indicating a consistent and reliable age estimate. This study validates that the otolith increment deposition rate can be used to assess hatching dates and daily growth of wild S. cephalus under 150 dph and in environments similar to the conditions used in this study.     

Relationships between otolith microstructure, otolith growth, somatic growth and ontogenetic transitions in two cohorts of windowpane

Otolith increments in larval and juvenile windowpane Scophthalmus aquosus can provide an estimate of daily age for spring-spawned individuals held under summer conditions. Otolith increments for spring- and autumn-spawned individuals occurred at intervals >1 day under winter conditions. A significant decrease in the slope of the linear relationship between otolith size and somatic size at 40 mm L_S coincided with significant habitat, morphological and behavioural transitions. In smaller, field-captured windowpane belonging to spring- and autumn-spawned cohorts, the formation of accessory growth centres coincided with a transitional settlement period and the completion of eye migration (c. 8–20 mm L_S). Back-calculated growth rate estimates for spring-spawned windowpane were significantly faster than those for autumn-spawned windowpane and these differences could produce differential rates of survival for the two cohorts during the first year of life.     

耳石在鱼类年龄与生长研究中的应用

有关鱼类耳石的研究已有100多年的历史,目前已形成一个相对独立的研究领域,在多个研究层面上深入开展,但年龄与生长至今仍然是鱼类耳石研究的主要方面。本文分别从耳石的年轮、日轮和重量方面,介绍了当前耳石在鱼类年龄与生长研究中的应用与发展。我们认为,对耳石日轮的研究仍将会是耳石研究的重要方向;相关研究将会逐渐由个体尺度向种群尺度发展,并可为渔业资源的可持续利用提供科学依据。     

Growth estimates from otolith increment widths of juvenile chinook salmon (Oncorhynchus tshawytscha) reared in changing environments

For otolith increments to provide useful estimates of fish growth, otolith growth must covary closely with somatic growth. We reared groups of juvenile chinook salmon ( Oncorhynchus tshawytscha Walbaum) for 70 days, changing ration or temperature during a 20-day treatment period. Restricted rations halted somatic growth, however increment widths decreased gradually; somatic growth was overestimated from increment width. Otolith growth followed changes in water temperature more closely than changes in ration, supporting a hypothesized effect of metabolic rate on otolith growth. Increment growth was only loosely coupled to fish growth rate, and may also be affected by past growth histories. For juvenile fish, increment widths may not be sensitive indicators of short-term changes in growing conditions.     

Hawaiian biogeography and the islands' freshwater fish fauna

Aim This paper describes known patterns in the distributions and relationships of Hawaiian freshwater fishes, and compares these patterns with those exhibited by Hawaii's terrestrial biota. Location The study is based in Hawaii, and seeks patterns across the tropical and subtropical Indo‐west Pacific. Methods The study is based primarily on literature analysis. Results The Hawaiian freshwater fish fauna comprises five species of goby in five different genera (Gobiidae). Four species are Hawaiian endemics, the fifth shared with islands in the western tropical Pacific Ocean. All genera are represented widely across the Indo‐west Pacific. All five species are present on all of the major Hawaiian islands. All five species are amphidromous – their larval and early juvenile life being spent in the sea. Although there has been some local phyletic evolution to produce Hawaiian endemics, there has been no local radiation to produce single‐island endemics across the archipelago. Nor is there evidence for genetic structuring among populations in the various islands. Main conclusions In this regard, the freshwater fish fauna of Hawaii differs from the well‐known patterns of local evolution and radiation in Hawaiian Island terrestrial taxa. Amphidromy probably explains the biogeographical idiosyncrasies of the fish fauna – dispersal through the sea initially brought the fish species to Hawaii, and gene flow among populations, across the archipelago, has hitherto inhibited the evolution of local island endemics, apparently even retarding genetic structuring on individual islands.     

Validation of daily increment deposition and early development in the otoliths of Sarotherodon melanotheron

A one-to-one relationship was found between days of rearing and counted daily increments in the otoliths of Sarotherodon melanotheron verifying daily increment deposition. A marked hatch check was found in all otoliths from both the reared fish and the wild specimens. Five to 10 faint prolarval increments were visible but the rate of their formation was not investigated. The rate of increment deposition of S. melanotheron is apparently independent of somatic growth and increments found in the otoliths of this species can therefore be used for ageing.     

A simple regression model to assess environmental effects on fish growth

Multiple regression was used to assess relationships between annular growth and environmental variables. This approach (1) tests for the significance of environmental changes on fish growth and (2) can be successfully used to predict fish growth using different environmental conditions. Age usually explains a large proportion of the variation in growth increments measured in length, and these two variables are inversely related. Since length increments decline as age increases, environmental impacts on growth will be reduced as fish grow older. To account for within-age growth variation and incorporate this age-dependent factor, the inverse of age (1/age in years) is multiplied by the value of an environmental variable (ENV) that may be related to growth. This interaction term and age are regressed against mean annular growth increments in length (TLINC; l _{t +1}— l ₁):
TLINC = b₀—b₁AGE±b₂(1/AGE)*ENV
where b₀, b₁, and b₂ are the regression coefficients for intercept and slope, respectively. Additional variables that measure environmental factors can be added to the model. Environmental effects associated with growth rates of black crappie, Pomoxis nigromaculatus (LeSueur), are presented as an example.     

Comparison of growth rate and formation of otolith increments in age-0 red snapper

For wild red snapper Lutjanus campechanus , mean otolith increment deposition rate after marking with oxytetracycline dihydrate (OTC) was daily (0.97 increments day⁻¹) when growth rates were fast (0.63 mm fork length, L _F day⁻¹), but were not daily (0.82 increments day⁻¹) when somatic growth was slow (0.2 mm L _F day⁻¹). For reared larvae ( n =8), increment deposition rates were daily (0.99–1.03 increments day⁻¹), and growth rates ranged from 0.6 to 0.9 mm L _F day⁻¹. Growth rate affected increment deposition rate as a threshold function, i.e. when growth rate was <0.3 mm L _F day⁻¹, deposition was less than daily, but above this level increment deposition did not exceed a daily rate. As growth rates increased increment widths increased. Examination of a sub-sample ( n =8) of the otoliths from the slowest growing wild fish by scanning electron microscopy did not increase increment counts. Because L. campechanus are late spring-early summer spawners, young fish can expect maximum growth due to warm summer temperatures. Thus, daily ageing methods should be well suited to this species.     

The Morphology and Periodic Structures of the Otolith of the Chinook Salmon (Oncorhynchus tshawytscha), and Temperature-dependent Variation in Otolith Microscopic Growth Increment Width

The otolith (sagitta) of the chinook salmon (Oncorhynchus tshawytscha) has a variable external crystalline morphology which is related to differences in the growth rate of crystals in different parts of the otolith. The internal crystal structure of the otolith is complex with different mineral phases in different growth fields of the otolith and a well-defined series of microscopic growth increments in both the dorsal and the ventral parts (orientation in situ) of the otolith. The period of the microscopic growth increments was shown, by both a rearing experiment and interpolation from fish of known age, to be daily. By rearing sibling chinook salmon at different temperatures (while still maintaining them on the same diet) it was shown that the width of the daily growth increment varies with temperature, but neither multi- nor sub-daily increments appear in the area of regular, daily growth incrementation. Inclusions of the vaterite morph of calcium carbonate crystallizing in the botryoidal habit occur in the otherwise aragonitic otolith. Regularly spaced check rings in the sulcul part of the otolith are homologous with those occurring in the dorsal and ventral growth axis and are. on average, separated by about 28 microincrements.     

Forensic biological pursuits of exotic fish origins: piranha in Hawaii

Synopsis The otoliths of an adult red-bellied piranha, Pygocentrus nattereri, captured from a reservoir in Hawaii were scrutinized to determine the fish's origin and growth history. Sagittal otoliths of the piranha, P. nattereri, contained internal microincrements visible by Scanning Electron Microscopy. The medial cross sectional plane of the sagitta was resolved to provide counts for the most visible micro-increments. An opportune spawning of confiscated adults provided samples for verification of daily increment formation. Daily formation of microincrements was verified from hatched individuals, and confirmed the suitability of otoliths for revealing daily patterns in the age and growth of piranhas. The central area of the sagitta was diffuse in regards to otolith microstructure and indicated the fish was held in an unchanging environment (aquarium). Therefore, otoliths provide important life history or forensic information incorporated within their structural components. The visualization of daily microincrements in the otolith of a juvenile allowed the determination of age at and since release. Fish grew rapidly after being released into the wild. From otolith increments the date of release for an individual fish can be calculated with acceptable accuracy. As presented, otolith structural information can provide age and growth data which are essential to the management of introduced species.     

Enhancing the contrast and visibility of daily growth increments in fish otoliths etched by proteinase K buffer

The otoliths of the amphidromous gobies Stiphodon elegans and Sicyopterus japonicus , a marine eel Strophidon sathete and a freshwater fish Varicorhinus barbatulus were digested by proteinase K buffer (PKb), which removed the proteins and retained the major calcified structure to reveal conspicuous daily increments. Compared with etching by ethylenediaminetetraacetate (EDTA), etching with PKb revealed more visible daily increments and enhanced the contrast. Moreover, by using PKb, both the daily increments and annuli could be observed simultaneously. The better performance of PKb as an etching agent can be attributed to digesting of predominantly only the organic matrix and leaving the calcified structure almost intact. PKb provides another effective means to reveal otolith microstructure so as to examine and count daily growth increments.     

Growth and production of the dominant pelagic fish, Acanthobrama terraesanctae, in subtropical Lake Kinneret, Israel

Acanthobrama terraesanctae (local name lavnun), an endemic planktivorous cyprinid, dominates total fish numbers (>80%) in Lake Kinneret, and may have a significant top-down impact on the lake ecosystem. The length of young-of-the-year fish calculated from the von Bertalanffy equation agreed with field observations of juvenile growth. An unusual bi-modal length-frequency distribution observed in May 1993 provided additional help in age identification. Males grew more slowly than females and reached a lower maximum length. Total mortality coefficients (exponents) of males and females >12 cm (minimal legal size of fish in the catch) were similar ( c. 1·52). An average cohort reaches maximum biomass during its second year. Maximum production is created at the end of the second year. The production: biomass ratio of the population was 1·16, and 36% of total lavnun standing stock was taken by fishing. From the late 1980s to early 1990s, when standing stock and population structure were stable, the average harvest of 1000 t was consistent with a total lavnun biomass of 2800 t, which constitutes 50–70% of the total fish stock measured acoustically in the lake. Such a biomass could be sustained by the known production of zooplankton. Absence of verified growth data for lavnun contributed to the collapse of the fishery in 1993, because it hampered timely revision of fishery policy in response to the drastic changes in the lavnun stock in 1992.     

Studies on the age and growth of the bata,Labeo bata (Ham.) (Cyprinidae,Teleostei) from the river Kali,India

Age and growth of Labeo bata (Ham.) was studied by the analysis of annuli found on the scale and by length-frequency distribution. The fish attained lengths of 131, 194, 236, 277, 314, 341 and 364 mm at the end of the 1st, 2nd, 3rd, 4th, 5th, 6th and 7th years of life respectively. The increase in length of scale bears a constant relationship with the increase in length of fish, and regression analysis yielded a straight line between scale and body length. Calculated values could be expressed as: Y = –2.534 + 0.064 XThe growth rate of the fish was found high during the 1st and 2nd years and decreased gradually afterwards till the 7th year. Both sexes showed more a or less similar growth rate and attained a similar longevity. Growth trend of the fish confirmed the von Bertalanffy growth equation: Lt = 450(l–e^{–0.2165(t+0.5963))} The seasonal growth curve was chiefly influenced by feeding intensity in fishes of 1st year class while in adults it was affected by feeding intensity as well as by maturation of the gonads.