Reproductive biology of two co‐occurring mugilids,Liza argentea and Myxus elongatus,in south‐eastern Australia

The reproductive biology of Liza argentea and Myxus elongatus occurring in two estuaries (Lake Macquarie and St Georges Basin) was found to differ. Gonado‐somatic index values and macroscopic staging of gonads identified the peak spawning period of L. argentea occurred between March and November in Lake Macquarie and January and April in St Georges Basin. In contrast, peak spawning of M. elongatus was concentrated between January and March in both estuaries. Spawning of L. argentea probably occurred in the lower reaches of estuaries as well as in nearshore coastal waters, whereas evidence indicated M. elongatus spawned only in ocean waters. The mean fork length at maturity (L_F50) was greater for females than males in both species, and it also occurred at a larger mean L_F in M. elongatus (males = 230 mm and females = 255 mm) than L. argentea (males = 180 mm and females = 207 mm). Estimates of total potential fecundity were also greater for M. elongatus (425 484–1 157 029) compared to L. argentea (159 933–548 954). Both species had determinate fecundity and displayed a group synchronous pattern of oocyte development, with two distinct size classes of oocytes present in mature ovaries. Liza argentea probably release the larger class of oocytes in one spawning event, but this could not be established for M. elongatus.     

Age determination,growth and mortality of Gerres subfasciatus Cuvier, 1830 in southeast Australia

Commercial beach‐seine (30–50 mm cod‐end mesh) catches of Gerres subfasciatus in Lake Macquarie southeast Australia were sampled monthly between December 2000 and April 2002 to investigate species age, growth and mortality characteristics using sectioned sagittal otoliths. Inclusion of fishery‐independent length data of young‐of‐the year collected from littoral seagrass beds with fine meshed beach seines augmented growth analyses. Fifty otoliths each month (total 448 female and 402 male) were examined with sections displaying alternating opaque and translucent zonation. Formation of otolith opaque zones occurred annually between August and December as determined by monthly marginal increment analyses. Spawning occurred between October and February, and a universal birth date of 1 December was assigned that allowed counts of opaque zones to be converted to age estimates in years and months (decimal ages). The von Bertalanffy growth function identified that both genders grew fast for their initial 2 years, but thereafter slowed. Females grew faster, had a greater mean fork length‐at‐age, estimated L_∞ and an observed greater maximum fork length in samples compared to males. Nevertheless, observed longevity was 10⁺ years for both genders. Commercial catches of both genders were dominated by the 2⁺ and 3⁺ year age classes. Catch curve analyses identified the instantaneous rate of total annual mortality to be ~0.8 and an exploitation rate of <0.5 for both genders. The data form a basis for developing assessment and management strategies of G. subfasciatus fisheries.     

Variation in growth,mortality, length and age compositions of harvested populations of the herbivorous fish Girella tricuspidata

Commercial gillnet and beach‐seine catches of Girella tricuspidata from seven estuaries in eastern Australia were examined for differences in fork length (L_F), sex and age composition, and populations were assessed for growth and mortality. Fish 220–350 mm L_F dominated landings across all estuaries sampled, regardless of gear type. Few fish >10 years of age were observed in the catches, with fish aged 3–5 years, and 4–7 years, being most abundant in the catches in the four most northern estuaries and three southern estuaries, respectively. There was considerable variation in the L_F of G. tricuspidata at any given age and the oldest male and female were 21 and 24 years, respectively. There were no consistent differences between sexes or latitudinal regions in the growth and mean L_F at age of fish in each individual age class between 3 and 8 years. Growth of females was greater than males in the northern region, but not elsewhere. Estimates of the instantaneous rate of total mortality (Z) were dependent on estuary and year, ranging from 0·30 to 1·01, whereas the corresponding estimates of fishing mortality (F) ranged from 0·12 to 0·90. Populations of G. tricuspidata appear to have been heavily exploited, primarily relying on young fish recruiting to the fishery. The ecosystem‐wide effects of harvesting this dominant mobile teleost herbivore need to be assessed further.     

Age-based life history of humpback red snapper,Lutjanus gibbus,in New Caledonia

This paper examines the life history of humpback red snapper Lutjanus gibbus, an important fishery species for coastal communities across the Indo-Pacific, in southern New Caledonia, where the species is lightly exploited. A total of 243 L. gibbus were sampled between January 2013 and December 2016 from occasional harvests of commercial fishers. Examination of sectioned otoliths revealed that opaque increment formation occurred annually between November and March, coinciding with the species' spawning season. Estimates of maximum age were similar between sexes, with observed ages of 38 and 36 years for females and males, respectively, extending the reported longevity of this species by at least 11 years. Growth differed significantly between sexes, with males reaching greater length at age and greater asymptotic length than females (38.88 v. 31.46 cm fork length (L_F). Total mortality for all samples was estimated as 0.13 and was slightly higher for males (0.16) than females (0.11). Estimates of natural and fishing mortality were low and slightly higher for males than females. Male L. gibbus were found to mature at slightly greater lengths and younger ages than females, with the length and age at which 50% of individuals attained maturity estimated to be 25.8 cm L_F and 3.9 years of age for females and 26.8 cm L_F and 3.4 years of age for males. The results provide key baseline information from which to assess the effect of fishing on the species for populations in New Caledonia and adjacent locations and, when viewed with those of other studies, highlight the importance of understanding spatial patterns in demography of harvested fish species across gradients of exploitation and environmental influences.     

Population biology and assessment of the white-spotted spinefoot, Siganus canaliculatus (Park, 1797), in the southern Arabian Gulf

The age, growth, mortality, reproduction and resource status of Siganus canaliculatus in the southern Arabian Gulf were investigated using a combination of size frequency, biological and size‐at‐age data. Defined structural increments consisting of alternating translucent and opaque bands in transverse sections of sagittal otoliths were validated as annuli. The maximum absolute age estimate was 7.8 years. Parameter values of the von Bertalanffy growth function fit to size‐at‐age data (males and females combined) were: k = 1.0, L_∞ = 24.8 cm (L_F), t_o = −0.1 years. Fish in spawning condition were only observed between April and July although patterns in gonadosomatic indices suggested a second but less well defined spawning event in November. The mean sizes and ages at first sexual maturity were 21.5 cm L_F (1.9 years) for males and 25.7 cm L_F (2.1 years) for females. Fish were fully recruited to the fishery at a size (L₁₀₀ = 19.7 cm L_F) that was smaller than the sizes at which sexual maturity was attained. The annual instantaneous rate of fishing mortality (F = 0.85 year⁻¹) (0.26–1.44 year⁻¹ 95% CI) was considerably greater than the target (F_opt = 0.33 year⁻¹) and limit (F_limit = 0.44 year⁻¹) biological reference points, indicating that the stock is overexploited.     

Age‐based demographic and reproductive assessment of orangespine Naso lituratus and bluespine Naso unicornis unicornfishes

Bluespine unicornfish Naso unicornis and orangespine unicornfish Naso lituratus were sampled in Pohnpei and Guam, Micronesia, over 13 months to identify reproductive and age‐based demographic features necessary for informed management. Age and reproductive information were derived from analysis of sagittal otoliths and gonads. Both species had moderate life spans [maximum ages of 23 (N. unicornis) and 14 years (N. lituratus)] compared with published estimates of conspecifics from other locations (>30 years) and of other Naso species. Length at maturation for N. unicornis was similar between Pohnpei and Guam while females consistently matured at a larger size [c. 30 cm fork length (L_F)] than males (c. 27 cm L_F). This sex‐specific pattern was reversed in N. lituratus for which estimates of maturation length (females: 15 cm L_F; males: 18 cm L_F) were only obtained from Guam. Developmental patterns in female gonads of both species suggested that initiation of maturation occurs very early. Growth patterns of N. lituratus displayed rapid asymptotic growth compared with N. unicornis and other congeners as well as slight sex‐specific patterns of length‐at‐age. Results highlight the considerable spatial variation that may occur in the population biology of these species across various scales. Additionally, proper management remains complicated without improved knowledge of fishery trends and reproductive behaviour in unicornfishes, species that are prime fishery targets in Micronesia and elsewhere.     

Demographic parameters and status assessments of Lutjanus ehrenbergii,Lethrinus lentjan,Plectorhinchus sordidus and Rhabdosargus sarba in the southern Arabian Gulf

Demographic parameters and status assessments for L. ehrenbergii, L. lentjan, P. sordidus and R. sarba in the southern Arabian Gulf were established using a combination of size frequency, biological and size‐at‐age data. Defined structural increments consisting of alternating translucent and opaque bands in transverse sections of sagittal otoliths were validated as annuli. The maximum age estimates ranged from 5 years for R. sarba to 14 years for P. sordidus. Growth trajectories were significantly different between sexes for L. ehrenbergii and L. lentjan with females achieving a larger asymptotic size than males. Estimates of fishing mortality rates were less than the target (F_SB40) and limit (F_SB30) biological reference points for L. ehrenbergii, L. lentjan and P. sordidus indicating that these species were exploited within sustainable limits. Conversely, R. sarba was found to be heavily overexploited and recruitment overfishing may have occurred as the fishing mortality rate was considerably greater than the limit reference point and the relative spawner biomass per recruit was 6.4% of the theoretical unexploited level. Due to restrictions in the available data set, the presented results require confirmation from specific studies on natural mortalities and from growth estimates based on more extended size spectra, avoiding any size selective sampling method.     

Comparative biology of tropical Lethrinus species (Lethrinidae): challenges for multi‐species management

Life‐history characteristics of six tropical Lethrinus species sampled from the Great Barrier Reef World Heritage Area were compared. Two species groups were identified based on fork length (L_F): large species with maximum L_F > 640 mm (longface emperor Lethrinus olivaceus, yellowlip emperor Lethrinus xanthochilus and spangled emperor Lethrinus nebulosus) and small species with maximum L_F < 480 mm (Pacific yellowtail emperor Lethrinus atkinsoni, pink ear emperor Lethrinus lentjan and ornate emperor Lethrinus ornatus). Lifespan was not correlated with L_F. Early growth for all species was rapid and similar during the first few years of life, but coefficients of the von Bertalanffy growth function varied considerably among species. Growth also differed between sexes for L. atkinsoni. Reproductive characteristics varied among species, with peak periods of spawning occurring in November to December for L. atkinsoni, July to August for L. nebulous, September to October for L. olivaceus and a protracted season for L. lentjan, although fewer samples were available for the last two species. Sex‐specific L_F and age distributions and gonad histology of L. lentjan were suggestive of a functional protogynous reproductive pattern, as observed in other lethrinids. Gonad histology indicated non‐functional protogynous hermaphroditism for L. atkinsoni and L. nebulosus. The diversity of life histories among these closely related species emphasizes the difficulty in devising single management strategies appropriate for multi‐species fisheries and illustrates the importance of understanding species‐specific life histories to infer responses to exploitation.     

Age,growth and mortality of scaldfish (Arnoglossus laterna Walbaum, 1792) from the Adriatic Sea

The population dynamics parameters of scaldfish, Arnoglossus laterna, from the Adriatic Sea were studied. Specimens ranging from 4.5 to 17.1 cm in total length were collected from commercial bottom‐trawl catches (2000–2006). Spawning from April through the end of August with a peak in May, A. laterna is one of the non‐target species usually present in mixed bottom trawl catches. The overall male to female ratio was 1.00 : 0.61. The oldest individual was 6 years of age. Length–weight relationships showed positive allometric growth (b = 3.36 for males and b = 3.39 for females). Parameters of the von Bertalanffy growth equation were: L_∞ = 17.3 cm; K = 0.258 per year; t₀ = ?1.0026 year; R² = 0.925. The relatively low value of total mortality (Z = 0.90) and relatively high value of constant rate of natural mortality (M = 0.64) was estimated. Presumed calculated fishing mortality (F = 0.26) and the consequently estimated exploitation ratio (E = 0.29) indicated no danger of an over‐exploitation of this species in the study area at the current level of fishing pressure. The low T max and correspondingly high M suggest that this small benthic predator plays an important role in the Adriatic ecosystem as a prey species for large benthic predators. However, the estimates include uncertainties and require further confirmation, especially with regard to natural mortality.     

Age, growth, maturity, mortality, and yield-per-recruit for annular sea bream (Diplodus annularis L.) from the eastern middle Adriatic Sea

The population dynamics parameters of Diplodus annularis from the eastern middle Adriatic Sea were studied. Total lengths of 1704 specimens ranging from 3.3 to 23.0 cm were obtained from commercial and fishery‐independent catches (2000–2002). The species spawns from April through the end of August, with a peak in May. Overall male to female ratio was 1.00 : 1.05. The species is a rudimentary hermaphrodite in the Adriatic Sea. Total lengths (TL) at 50% maturity were 9.0 cm for males and 10.0 cm for females. These estimated sizes were smaller than the minimum legal landing size (MLS = 15 cm) and greater than the actual minimum landing size (L_c = 7.1 cm) for the bottom trawl net. All specimens sampled were fully mature above 13 cm TL. The oldest individual was 13 years old. Length–weight relationship showed close to isometric growth (b = 3.073). Parameters of the von Bertalanffy growth equation were: L_∞ = 23.95 cm; K = 0.126 per year; t₀ = −1.664 year; r² = 0.896. The low value of total mortality (Z = 0.72) was a consequence of the relatively low rate of natural mortality (M = 0.39) and fishing mortality (F = 0.33). The exploitation ratio was E = 0.46. Estimated parameters and the relative yield‐per‐recruit analysis did not indicate any overexploitation of the species in the study area. However, the estimates include uncertainties and require further confirmation, especially of the natural mortality.     

Ontogenetic shifts in morphology and resource use of cisco Coregonus artedi

Two previously described lacustrine cisco Coregonus spp. morphs [i.e. a small (<300 mm fork length, L_F), low‐gillraker (≤44) morph and a large (≥300 mm L_F), high‐gillraker (≥45) morph] from Great Slave Lake, NT, Canada, were found to be synonymous with cisco Coregonus artedi. Geometric body shape did not differ between the two size classes nor could they be differentiated by 24 size‐corrected linear measurements, indicating that the two groups had similar phenotypes. Strong, positive correlations between all linear characters and geometric centroid size (a composite variable of fish body length, mass and age) suggested that body morphology changed with age as fish grew. Total gillraker number (N_GR) increased with L_F according to: N_GR = 36·3 + 0·034L_F. Differences in gillraker number and phenotype with age and size were explained by shifts in habitat and trophic resource use. Relative abundance within 0–30, 30–60, 60–90 and >90 m depth strata differed between size classes suggesting that morphology changed when fish shifted their habitat as they grew older. Large C. artedi had lower δ¹³C and slightly higher δ¹⁵N, indicating greater reliance on pelagic prey resources (i.e. more or larger zooplankton, such as Mysis spp.), compared to small C. artedi, which relied slightly more on benthic prey. Gillraker shape and number have always been used as key diagnostic characters in coregonine taxonomy; based on the findings presented here, ontogenetic shifts should be accounted for in resulting classifications.     

Growth patterns and age validation from otolith ring deposition in New Zealand longfin eels Anguilla dieffenbachii recaptured after 10 years at large

In 1998, 9500 juvenile New Zealand longfin eels Anguilla dieffenbachii (mean total length, L_T, 42 cm) captured from the lower Clutha River were transferred upstream to Lake Hawea, a high‐country oligotrophic lake in the same catchment where recruitment of juvenile eels has been prevented by hydroelectric dams since 1958. A total of 2010 of the transferred A. dieffenbachii were tagged with coded wire tags. Ten years later in 2008, the A. dieffenbachii population in Lake Hawea was sampled resulting in 399 recaptures (distinguishable by the presence of tags and by L_T from the remnant resident population of large old A. dieffenbachii) of the 1998 transfers; 79 (19·2%) of the recaptured fish had tags compared with 21·3% at release, indicating good tag retention and low mortality due to tagging. All recaptured tagged A. dieffenbachii were female. Mean annual growth over the 10 years since release was 3·80 cm year^?1 for all recaptures and 3·65 cm year^?1 for tag recaptures, and both were significantly greater than the estimate of 2·38 cm year^?1 at release. After release, mean condition (K) increased significantly (P < 0·001) for all recaptures and tag recaptures. Annual length growth increment was linear. Tag recaptures showed significant increases in somatic growth rate post‐transfer, and otoliths from the 2008 recaptured A. dieffenbachii were examined to see whether any similar enhanced growth after transfer was incorporated into the otolith structure that would serve as a date stamp. Measurement of otolith ring radii indicated that an increase in the radius occurred on most otoliths corresponding to the year after transfer. Because there was 9 years of completed growth following the observed growth inflection on the otoliths, this was strong evidence that opaque rings were formed annually.     

Little evidence for morphological change in a resilient endemic species following the introduction of a novel predator

Human activities, such as species introductions, are dramatically and rapidly altering natural ecological processes and often result in novel selection regimes. To date, we still have a limited understanding of the extent to which such anthropogenic selection may be driving contemporary phenotypic change in natural populations. Here, we test whether the introduction of the piscivorous Nile perch, Lates niloticus, into East Africa's Lake Victoria and nearby lakes coincided with morphological change in one resilient native prey species, the cyprinid fish Rastrineobola argentea. Drawing on prior ecomorphological research, we predicted that this novel predator would select for increased allocation to the caudal region in R. argentea to enhance burst‐swimming performance and hence escape ability. To test this prediction, we compared body morphology of R. argentea across space (nine Ugandan lakes differing in Nile perch invasion history) and through time (before and after establishment of Nile perch in Lake Victoria). Spatial comparisons of contemporary populations only partially supported our predictions, with R. argentea from some invaded lakes having larger caudal regions and smaller heads compared to R. argentea from uninvaded lakes. There was no clear evidence of predator‐associated change in body shape over time in Lake Victoria. We conclude that R. argentea have not responded to the presence of Nile perch with consistent morphological changes and that other factors are driving observed patterns of body shape variation in R. argentea.     

Growth and mortality of larval Myctophum affine (Myctophidae,Teleostei)

The growth and mortality rates of Myctophum affine larvae were analysed based on samples collected during the austral summer and winter of 2002 from south‐eastern Brazilian waters. The larvae ranged in size from 2·75 to 14·00 mm standard length (L_S). Daily increment counts from 82 sagittal otoliths showed that the age of M. affine ranged from 2 to 28 days. Three models were applied to estimate the growth rate: linear regression, exponential model and Laird–Gompertz model. The exponential model best fitted the data, and L₀ values from exponential and Laird–Gompertz models were close to the smallest larva reported in the literature (c. 2·5 mm L_S). The average growth rate (0·33 mm day^?1) was intermediate among lanternfishes. The mortality rate (12%) during the larval period was below average compared with other marine fish species but similar to some epipelagic fishes that occur in the area.     

Intra‐population trends in the maturation and reproduction of a temperate marine herbivore Girella elevata across latitudinal clines

Latitudinal variation in the reproductive characteristics of a temperate marine herbivore, rock blackfish Girella elevata, was examined from three regions of the south‐eastern Australian coast. Biological sampling covered 780 km of coastline, including the majority of the species distribution. The sampling range incorporated three distinct oceanographic regions of the East Australian Current, a poleward‐flowing western boundary current of the Southern Pacific Gyre and climate‐change hotspot. Girella elevata are a highly fecund, group synchronous (multiple batch)‐spawner. Mean fork length (L_F) and age at maturity were greater for females than males within all regions, with both male and female G. elevata of the southern region maturing at a greater size and age than those from the central region. Estimates of batch fecundity (F_B) were greatest in the northern and southern regions, relative to the central region where growth rates were greatest. Significant positive relationships were observed between F_B and L_F, and F_B and total fish mass. Gonado‐somatic indices indicated latitudinal synchrony in spawning seasonality between G. elevata at higher latitudes, spawning in the late austral spring and summer. A late or prolonged spawning period is evident for G. elevata from the northern region. Juvenile recruitment to intertidal rock pools within the central and southern regions was synchronous with the spawning season, however, no juveniles were found within the northern region. The implications of latitudinal variation in reproductive characteristics are discussed in the context of climate and oceanographic conditions of south‐east Australia.     

Age,growth and maturity of the pelagic thresher Alopias pelagicus and the scalloped hammerhead Sphyrna lewini

Indonesia has the greatest reported chondrichthyan catches worldwide, with c.110,000 t caught annually. The pelagic thresher (Alopias pelagicus) and scalloped hammerhead (Sphryna lewini) together comprise about 25% of the total catches of sharks landed in Indonesia. Age and growth parameters were estimated for A. pelagicus and S. lewini from growth‐band counts of thin‐cut vertebral sections. Alopias pelagicus (n = 158) and S. lewini (n = 157) vertebrae were collected from three Indonesian fish markets over a 5 year period. A multi‐model analysis was used to estimate growth parameters for both species. The models of best fit for males and females for A. pelagicus was the three‐parameter logistic (L_∞ = 3169 mm L_T, k = 0·2) and the two‐parameter von Bertalanffy models (L_∞ = 3281 mm L_T, k = 0·12). Age at maturity was calculated to be 10·4 and 13·2 years for males and females, respectively, and these are the oldest estimated for this species. The samples of S. lewini were heavily biased towards females, and the model of best fit for males and females was the three‐parameter Gompertz (L_∞ = 2598 mm L_T, k = 0·15) and the two‐parameter Gompertz (L_∞ = 2896 mm L_T, k= 0·16). Age at maturity was calculated to be 8·9 and 13·2 years for males and females, respectively. Although numerous age and growth studies have previously been undertaken on S. lewini, few studies have been able to obtain adequate samples from all components of the population because adult females, adult males and juveniles often reside in different areas. For the first time, sex bias in this study was towards sexually mature females, which are commonly lacking in previous biological studies on S. lewini. Additionally, some of the oldest aged specimens and highest age at maturity for both species were observed in this study. Both species exhibit slow rates of growth and late age at maturity, highlighting the need for a re‐assessment of the relative resilience of these two globally threatened sharks at current high levels of fishing mortality throughout the eastern Indian Ocean.     

Population biology and vulnerability to fishing of deep‐water Eteline snappers

Deep‐water fish in the tropical and sub‐tropical Pacific Ocean have supported important fisheries for many generations. Observations of localised depletions in some fisheries have raised concerns about the sustainability of current fishing rates. However, quantitative assessments of deep‐water stocks in the Pacific region have been limited by the lack of adequate biological and fisheries data. Estimates are provided of age‐based demographic parameters for two important deep‐water snapper species in the Pacific, Etelis carbunculus and E. coruscans. A spawner biomass‐per‐recruit (SPR) model was applied to determine fishing mortality rates for each species that would achieve specified biological targets (40% unexploited levels, SPR₄₀) and limit (30% unexploited levels, SPR₃₀) reference points, and examine the sensitivity of the model to variation in natural mortality and age at first capture. The maximum observed age, based on increment counts from sectioned otoliths, was 21 years for E. carbunculus and 18 years for E. coruscans. Total mortality (Z), estimated from the Hoenig regression, was 0.21 year^?1 for E. carbunculus and 0.25 year^?1 for E. coruscans. The best approximating growth models were the von Bertalanffy model (L_∞ = 896 mm fork length, k = 0.28, t₀ = 0.51) for E. carbunculus and the logistic model (L_∞ = 879 mm fork length, k = 0.32 year^?1, t₀ = 3.42) for E. coruscans. The spawner biomass‐per‐recruit analysis demonstrated that lower rates of fishing mortality were required for E. coruscans than for E. carbunculus to maintain spawning biomass above estimated biological reference points. Estimates of spawner biomass‐per‐recruit were more sensitive to variation in natural mortality than in the age at first capture, suggesting that regulating fishing mortality rather than gear selectivity would be a more effective management measure for both species. Maintaining fishing mortality <0.1 for both species is recommended as a cautious approach to management, given the uncertainty in estimates of natural mortality and mixed fishery considerations.     

Age,growth and mortality of Lutjanus alexandrei in estuarine and coastal waters of the tropical south‐western Atlantic

Otolith‐based methods were used to determine life history traits of the endemic Brazilian snapper (Lutjanus alexandrei) in estuarine and coastal environments in the south‐western Atlantic. Fishes were caught as juveniles inside mangrove‐bordered estuaries by traditional corral fisheries whereas adults were captured at sea using motorboats with trap and gill nets. Fish were sampled during landings and 331 otolith pairs were extracted from L. alexandrei. Inshore mangroves comprised individuals of 0–4 years (mean: 2 years), while individuals in deeper reef environments were older (range: 3–22; mean: 8 years), indicating an ontogenetic shift at approximately age 3 or 4. Edge analysis was used to validate the annual deposition in the otoliths, suggesting that opaque growth rings were formed between April and September. Age‐at‐length data were used to predict L. alexandrei growth rates using the von Bertalanffy growth model from where the parameters were calculated: L_∞ = 31 cm, k = 0.24, t₀ = ?1.26, r² = 0.97. Mortality rates were estimated for coastal habitats, with Z = 0.22 and S = 0.78 year^?1, based on ages 7–17. Additionally, evidence of ontogenetic migration is provided by age and size structure.     

The growth ofOreochromis andersonii (Pisces: Cichlidae) from the Okavango Delta,Botswana, and a comparison of the scale and otolith methods of ageing

Synopsis Otoliths and scales were used for age and growth determination ofOreochromis andersonii from the Okavango Delta, Botswana. Marginal increment analysis showed that an annulus was formed in both the scales and otoliths during the dry summer period. Using scales, the growth ofO. andersonii was described by L_t = 285.27(1-e^{-0.26(t+2.02)}) mm SL and using otoliths by the equation L_t = 267.48(1-e^{-0.25(t+2.18)}) mm SL. Maximum age estimates of 10 years using scales and 13 years using otoliths were obtained and the growth curves were significantly different (p < 0.01). Age estimation using scales tended to over-emphasise growth inO. andersonii resulting in larger predicted lengths-at-age. For this reason, otoliths are considered to be more reliable and suitable than scales in determining the age and growth of this species.     

Latitudinal and altitudinal growth patterns of brown trout Salmo trutta at different spatial scales

Spatial variation in growth of stream‐dwelling brown trout Salmo trutta was explored in 13 populations using a long‐term study (1993–2004) in the Bay of Biscay drainage, northern Spain. The high variability in fork length (L_F) of S. trutta in the study area was similar to the body‐size range found in the entire European distribution of the species. Mean L_F at age varied: 0+ years, 57·4–100·7 mm; 1+ years, 111·6–176·0 mm; 2+ years, 155·6–248·4 mm and 3+ years, 194·3–290·9 mm. Average L_F at age was higher in main courses and lower reaches compared with small tributaries and upper reaches. Annual specific growth rates (G_L) were: 0+ to 1+ years, 0·634–0·825 mm mm⁻¹ year⁻¹; 1+ to 2+ years, 0·243–0·342 mm mm⁻¹ year⁻¹; 2+ to 3+ years, 0·166–0·222 mm mm⁻¹ year⁻¹, showing a great homogeneity. Regression models showed that water temperature and altitude were the major determinants of L_F at age variability within the study area. A broader spatial analysis using available data from stream‐dwelling S. trutta populations throughout Europe indicated a negative relationship between latitude and L_F of individuals and a negative interaction between latitude and altitude. These findings support previous evidence of the pervasive role of water temperature on the L_F of this species. Altitude appeared as the overall factor that includes the local variation of other variables, such as water temperature or food availability. At a larger scale, latitude was the factor that encompassed these environmental gradients and explained the differences in L_F of S. trutta. In summary, L_F at age in stream‐dwelling S. trutta decreases with latitude in Europe, the converse of Bergmann's rule.