Growth of nestling Hamerkops Scopus umbretta in central Mali

Data on growth of nestling Hamerkops Scopus umbretto were analysed with respect to year and season of hatching and to hatch sequence. Quantitative growth characters included weight, culmen, tarsus, tail, third outermost primary quill, standard wing-length and wing span. The growth constant K of weight was 0.179 and time t₁₀-t₉₀ was 21.8 days. Least-squares analyses showed differences in weight gain, culmenlength and tarsus-length related to year and month but not to sequence of hatching. Predictive equations for character against age are provided for all linear measurements. Characters which attained apparent asymptotes before fledging were weight and culmen and tarsus-length whilst other characters varied between 80 and 90% of reported adult size. Qualitative indications of growth discussed are crest development, colouration and the disappearance of the egg-tooth. The rainy and post-rains seasons appear to offer the Hamerkop the best chances of successful breeding and maximum growth rates.     

Growth of nestling Barn Owls Tyto alba in central Mali

Data on growth of 276 young Barn Owls were analysed with respect to the effects of year and month of hatching, hatch order and brood order. Growth characteristics considered were weight; lengths of culmen, tarsus, central tail feathers and quill of third outermost primary; standard wing length; and wing span. For weight the growth constant K was 0151 and time t ₁₀- t ₉₀ was 32-2 days. Least-squares analyses showed that gain in weight and culmen and tarsus length were affected by month of hatching with young hatched in the middle part of the breeding season showing the most rapid growth. Hatch order affected gain in weight. Differences in growth rates of all these characters were not, however, reflected in differences in weight or length at fledging except for the effects of brood on weight with second broods fledging at significantly lighter weights than first ones. Predictive equations for character against age are provided for all linear measurements. All characters examined attained apparent asymptotes before fledging except tail and standard wing length.     

Age and growth of the gulf toadfish Opsanus beta based on otolith increment analysis

In the present study, sagittal otoliths of confirmed male and female specimens of the gulf toadfish Opsanus beta that were collected monthly over the course of a year from Biscayne Bay, Florida, U.S.A. were analysed. The timing and frequency of O. beta spawning seasons are reported by examination of the gonado‐somatic index. The estimated ages of males and females ranged from < 1 year to 6 and 5 years, respectively. Strong sexual dimorphism in growth was apparent with von Bertalanffy parameter estimates for males of L_∞ = 393·8 mm, K = 0·30, t₀ = 0·36 and females of L_∞ = 201·1 mm, K = 0·79, t₀ = 0·47. Comparison with previously published growth trajectories of the more northerly distributed conspecific Opsanus tau showed that O. beta males had a higher growth rate. Female O. beta and O. tau growth trajectories appear similar, with an indication that the former becomes asymptotic at least a year before the latter. Results are discussed in the context of temperature regimes, reproductive energy allocation and waste urea excretion in the two species.     

Nestling growth in the African fish eagle in Uganda

Nestling African fish eagles Haliaeetus vocifer (Daudin, 1858) in Queen Elizabeth National Park (QEP), Uganda, attained and exceeded the adult body weights of their respective sexes by fledging time. The growth curves conformed with the sigmoid form of most animal species. The overall growth rate, K (g/day), was low, averaging 0.077 ± 0.017 g/day and the time t_10–90 required to complete growth from 10 to 90% of the asymptotic weight was c. 42 days. Brood size and hatching order did not significantly influence growth rates but the sex of the young did. The tarsus, femur and humerus reached adult sizes by fledging time but the standard wing did not.     

Effects of the timing of initial feeding on growth and survival of spotted mandarin fish Siniperca scherzeri larvae

The effects of delayed first feeding on growth and survival of spotted mandarin fish Siniperca scherzeri larvae were examined under controlled conditions. Morphometric characters [yolk‐sac volume, oil globule volume, head depth (H_D), body depth (B_D), eye diameter (E_D), musculature height (M_H), mouth diameter (M_D) and total length (L_T)], body mass (M), specific growth rate (S_GR) and survival were evaluated under different first‐feeding time (2, 3, 4 and 5 days after hatching). Larvae began to feed exogenously at 2 days after hatching (DAH) and the point of no return (P_NR) occurred between 5 and 6 DAH at 23° C, range ±1·0° C. The yolk volume of larvae first‐fed at 2 days had a significant difference compared with that of larvae first‐fed at 3, 4 and 5 days on 3 and 4 DAH. The larvae first‐fed at 2 days achieved comparatively better growth performance than that of 3, 4 and 5 days. On 5 DAH, all morphometric characters had significant differences between 2 and 5 days and 2 and 4 days initial feeding, respectively. Total mortality was recorded on 9 DAH for the larvae first‐fed at 5 days. On 12 DAH, significant differences were observed between 2 and 4 days and 3 and 4 days initial feeding for all morphometric characters. From 16 DAH to the end of experiment, all growth variables of the larvae first‐fed at 2 days were significantly higher than those in other treatments. The S_GR (2–9 DAH) first‐fed at 2 and 3 days were significantly higher than 4 and 5 day treatments, and the S_GR (9–16 DAH) first‐fed at 2 days was significantly higher than 3 and 4 day treatments. There was no significant difference, however, of S_GR (16–28 DAH) among treatments. Survival rate was significantly higher at 2 days initial feeding (27·42%) when compared with 3 (15·96%) and 4 days (7·92%) initial feeding at the end of experiment. The present study suggests that the first feeding of S. scherzeri larvae should be initiated at 2 days after hatching for achieving good growth and survival.     

Factors affecting estimates of size at age and growth in grey triggerfish Balistes capriscus from the northern Gulf of Mexico

Growth zones in dorsal spines of grey triggerfish Balistes capriscus from the northern Gulf of Mexico were utilized to estimate growth and examine factors that may affect estimates of size at age. Age was estimated from dorsal‐spine sections of 4687 individuals sampled from U.S. waters during 2003–2013, including both fishery‐independent (n = 1312) and fishery‐dependent (n = 3375) samples. Ninety‐six per cent (n = 4498) of these sections were deemed suitable for ageing; average per cent error between two independent readers was 10·8%. Fork length (L_F) ranged from 65 to 697 mm and age estimates from 0 to 14 years. Both sex and sample source (fishery‐independent v. recreational) significantly affected estimated size at age for 2–6 year‐old fish. Data were pooled between sources to fit sex‐specific von Bertalanffy growth functions. Results for the female model were L_∞ = 387 mm L_F, k = 0·52 year^?1 and t₀ = 0·01 year, while for males L_∞ = 405 mm L_F, k = 0·55 year^?1 and t₀ = 0·02 year. These results were significantly different between sexes and indicate clear sexual dimorphism. Thus, growth should be modelled separately by sex when examining population parameters or conducting stock assessment modelling. The positive bias in estimates of size at age computed for recreational v. fishery‐independent samples also has clear implications for stock assessment as growth functions computed with fishery‐dependent samples would tend to overestimate stock productivity.     

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

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

Morphological and morphometric aspects of early life stages of piabanha Brycon gouldingi (Characidae)

Adult specimens of piabanha Brycon gouldingi were collected from Rio das Mortes (Mato Grosso, Brazil), adapted to captivity and induced to spawn at Buriti Fisheries (Nova Mutum, MT, Brazil). The early developmental stages of B. gouldingi were then characterized. Samples were collected at pre‐determined times from oocyte extrusion to total yolk absorption. Oocyte diameter, total larval length (L_T) and yolk‐sac volume were measured. The mean ± s.d . duration of embryo developmental of B. gouldingi was 13·90 ± 0·06 h at 26·40 ± 1·13° C. The mean ± s.d . oocyte diameter was 1·13 ± 0·06 mm with 54% of oocytes ranging from 1·11 to 1·20 mm. Seven stages characterized the early developmental phase of this species: zygote, cleavage, morula, blastula, gastrula, histogenesis–organogenesis and hatching, with unique features related to each stage. At hatching, the larvae measured 3·40 ± 0·07 mm, presented an elongated shape with yolk‐sac volume of 0·46 ± 0·08 µl, non‐pigmented eyes and exhibited swimming ability. When the yolk was completely absorbed at 55 h post‐hatch, mean ± larval L_T was 6·68 ± 0·65 mm, the eyes were highly pigmented and the teeth were visible. These are the first reported findings on the initial developmental stages of B. gouldingi and could be used to improve captive breeding management and conservation practices.     

Morpho- und Thermogenese nestjunger Blaukehlkolibris (Lampornis clemenciae)

Zusammenfassung Mit einer konstanten Wachstumsrate K von 0,444 und 0,481 wachsen Blaukehlkolibris (Lampornis clemenciae; Körpermasse 7,5 g) ähnlich schnell wie andere Vogelarten der gemäßigten Zone (K = 0,384–0,680). Der t_10–90-Wert der beiden untersuchtenLampornis-Nestlinge beträgt 9,1 bzw. 9,9 Tage. Die Körpertemperatur kann am 10. Tag reguliert werden. Am Ende der Nestlingszeit erreicht die Schnabellänge der Jungvögel 90 % der eines Adultvogels. Die Morphogenese entspricht den Beobachtungen beim kleineren ZimtkolibriSelasphorus rufus.

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Morpho- and thermogenesis in nestling Blue-throated Hummingbirds (Lampornis clemenciae)

Summary The study was conducted at the Southwestern Research Station of the American Museum of Natural History (N. Y.) in June/July 1981. Cumulative growth, thermogenesis, monitored in one chick only, morphogenetic characters and behavioral patterns in 2 nestlings were constantly recorded from hatching to fledging. The growth rate K and the inverse growth rate t_10–90 (s. Fig.) are presented for both nestlings. Until the 9th day both nest-mates accumulated 67 % and 86 % respectively of their maximum weight (asymptote). The data suggest, as already observed inSelasphorus rufus, another temperate trochilid, that growth rates extend those of tropical species, e.g.Amazilia sp. (seeRicklefs 1976). However, further data are needed to confirm this geographical trend for hummingbirds.Thermogenetical homeostasis was observed in one chick at an age of 10 days. Simultaneously, the shafts of primaries appeared in both chicks after 7 days, the eyes opened at the 9th day, primaries are completely open at the 13th day. Wing exercises were observed at the 20th day, and both nestlings fledged at an age of 25 days. The bill length by then is 90 % of an adult bird.

     

Life‐history traits of the long‐nosed skate Dipturus oxyrinchus

This work investigates life‐history traits of the long‐nosed skate Dipturus oxyrinchus, which is a common by‐catch in Sardinian waters. The reproductive variables were analysed from 979 specimens sampled during scientific and commercial hauls. Females (10·4–117·5 cm total length, L_T) attained larger sizes than males (14·5–99·5 cm L_T). To evaluate age and growth, a sub‐sample of 130 individuals (76 females and 54 males) were used. The age was estimated by annuli counts of sectioned vertebral centra. Four models were used for the length‐at‐age data: the von Bertalanffy, the exponential, the Gompertz and the logistic functions. According to the Akaike's information criterion, the Gompertz model seemed to provide the best fitting curve (L_∞ mean ± s.e. : 127·55 ± 4·90 cm, k: 0·14 ± 0·09, IP: 3·97 ± 0·90 years). The oldest female and male were aged 17 (115·5 cm L_T) and 15 years (96·0 cm L_T), respectively. Lengths at maturity were 103·5 cm for females and 91·0 cm for males, corresponding to 90% of the maximum observed length in both sexes. The monthly distribution of maturity stages highlighted an extended reproductive cycle, with spawning females and active males being present almost throughout the year, as confirmed by the gonado‐somatic index. Ovarian fecundity reached a maximum of 26 yolked follicles with a mean ± s.e. size of 19·7 ± 6·5 mm.     

MORPHOMETRICS AND SEXING OF THE AFRICAN BLACK OYSTERCATCHER

Summary

Hockey, P. A. R. 1981. Morphometries and sexing of the African Black Oystercatcher. Ostrich 52: 244–247.

109 African Black Oystercatchers Haematopus moquini were caught, measured and sexed by cloacal examination during the 1979/1980 breeding season. Six standard taxonomic variables were measured. Females were larger than males in all dimensions considered. The most dimorphic characters were mass and exposed culmen length. The data were subjected to stepwise discriminant analysis and a linear function was derived which allowed birds of unknown sex to be sexed. The function is D = ?0,391x₁ ?0,016 x₂ +0,218 x₃ +0,714 x₄ +15,946 where x₁ = exposed culmen length (mm), x₂ = body mass (g), x₃ = length of tarsometatarsus (mm) and x₄ = culmen depth at the gonys. Values of D from the above equation less than zero indicate a female while those greater than zero indicate a male. The greater the divergence of D from zero, the higher the probability of correctly sexing an unknown individual: once D> ± 1,2, p>0,99.     

Sap flow in Scots pines growing under conditions of year-round carbon dioxide enrichment and temperature elevation

Starting in rrrr, individual trees of Scots pine (Pinus sylvestris L.) aged 30 years were grown in closed-top chambers and exposed to normal ambient conditions (CON), elevated CO₂ (Elev. C), elevated temperature (Elev. T) and a combination of elevated CO₂ and temperature (Elev. C + T). Using the constant-power heat balance method, sap flow was monitored simultaneously in a total of 16 trees, four for each treatment, over a 32 d period (after the completion of needle expansion and branch elongation in 1997). An overall variation in diurnal sap flow totals (F_t) was evident during the period of measurement (days 167–198, 1997) regardless of the treatments, with a range from 0·15 to 2·82 kg tree^–1 d^–1. Elev. C reduced F_t by 4·1–13·7% compared with CON on most days (P varies from 0·042 to 0·108), but slightly increased it on some days (P≥ 0·131), depending on the weather conditions. Although the decrease in F_t caused by Elev. C was statistically significant on only a few days (P≤ 0·042), the cumulative F_t for the 32 d decreased by 14·4% (P = 0·047), indicating that Elev. C may have an important influence on seasonal water use of the Scots pine. Analysis of the diurnal courses of sap flow combined with corresponding weather factors indicated that the CO₂-induced decrease in F_t could be largely attributed to an increase in stomatal sensitivity to vapour pressure deficit (VPD), whereas the CO₂-induced increase in F_t related to an increase in stomatal sensitivity to low light levels. Elev. T increased F_t by 11·2–35·6% throughout the measuring period and the cumulative F_t for the 32 d by 32·5% (P = 0·019), which could be largely attributed to the temperature-induced increase in current-year needle area and decrease in stomatal sensitivity to high levels of VPD. There were no significant interactive effects of CO₂ and temperature on sap flow, so that Elev. C + T had approximately the same F_t as Elev. T and similar diurnal patterns of sap flow, suggesting that the temperature factor played a dominant role in the case of Elev. C + T.     

Temperature and prey quality effects on growth of juvenile walleye pollock Theragra chalcogramma (Pallas): a spatially explicit bioenergetics approach

A bioenergetics model for juvenile age‐0 year walleye pollock Theragra chalcogramma was applied to a spatially distinct grid of samples in the western Gulf of Alaska to investigate the influence of temperature and prey quality on size‐specific growth. Daily growth estimates for 50, 70 and 90 mm standard length (L_S) walleye pollock during September 2000 were generated using the bioenergetics model with a fixed ration size. Similarities in independent estimates of prey consumption generated from the bioenergetics model and a gastric evacuation model corroborated the performance of the bioenergetics model, concordance correlation (r_c) = 0·945, lower 95% CL (transformed) (L₁) = 0·834, upper 95% CL (transformed) (L₂) = 0·982, P < 0·001. A mean squared error analysis (M_SE) was also used to partition the sources of error between both model estimates of consumption into a mean component (M_C), slope component (S_C), and random component (R_C). Differences between estimates of daily consumption were largely due to differences in the means of estimates (M_C= 0·45) and random sources (R_C= 0·49) of error, and not differences in slopes (S_C= 0·06). Similarly, daily growth estimates of 0·031–0·167 g day^?1 generated from the bioenergetics model was within the range of growth estimates of 0·026–0·190 g day^?1 obtained from otolith analysis of juvenile walleye pollock. Temperature and prey quality alone accounted for 66% of the observed variation between bioenergetics and otolith growth estimates across all sizes of juvenile walleye pollock. These results suggest that the bioenergetics model for juvenile walleye pollock is a useful tool for evaluating the influence of spatially variable habitat conditions on the growth potential of juvenile walleye pollock.     

Life‐history characteristics of the large Amazonian migratory catfish Brachyplatystoma rousseauxii in the Iquitos region,Peru

The main life‐history traits of the dorado Brachyplatystoma rousseauxii, a large Amazonian catfish undertaking the largest migration known for a freshwater fish species (from the nursery area in the estuary of the Amazon to the breeding zones in the head waters of the western Amazon basin close to the Andes), were determined from a 5 year sampling of >15 000 specimens in the Peruvian Amazon. The breeding season occurred during the falling and low‐water periods, which is hypothesized to be an adaptation to maximize the chances of young stages to reach the estuary. The size at first sexual maturity was slightly larger for females than males, c. 91 and 83 cm standard length (L_S), respectively. Both males and females reproduce for the first time at >3 years old. The fecundity per spawning event ranged from 481 734 to 1 045 284 oocytes for females weighing 25 and 34 kg, respectively. Seasonal variations of body condition were similar among sexes, but differed between immature specimens that had a higher condition during the low‐water period and lower condition during rising waters, and mature individuals that showed the opposite pattern. The growth characteristics were estimated by L_S frequency analysis. For females, the best fitting models gave a mean birth date in August, during the height of the breeding cycle, with the following von Bertalanffy growth function parameters: L_S∞ = 153·3, K = 0·29 and t₀ =– 0·37 years. For males, the best fitting model gave a mean birth date in July, also during the height of the breeding period, with L_S∞ = 142, K = 0·30 and t₀ =– 0·36 years. At a given age, females were systematically larger than males and the size difference increased with age. The largest females sampled (148 cm L_S) was 11 years old and the largest male (134 cm L_S) was 9 years old. The mortality estimates were higher for males total (Z) = 1·34, natural (M) = 0·52 and fishing (F) = 0·82 than for females (Z = 0·98, M = 0·50, F = 0·48). The life‐history patterns of B. rousseauxii are discussed in light of the available knowledge about this species and the understanding of its complex life cycle.     

Age and growth of Carcharhinus leucas in the northern Gulf of Mexico: incorporating variability in size at birth

Age and growth rates of bull shark Carcharhinus leucas[n = 255; 555–2230 mm fork length (L_F)] from the northern Gulf of Mexico were estimated from ring counts on vertebral sections collected from fishery‐dependent and ‐independent surveys. Two growth models were fitted to observed data: the von Bertalanffy growth model (VBGM) with t₀ as the third parameter and a modified version of the VBGM using a fixed size‐at‐birth intercept as the third parameter. To address the variability in size‐at‐birth, a Monte Carlo simulation was incorporated into the size‐at‐birth intercept. The sex‐specific growth models were not significantly different, allowing a sexes combined model to be generated. The traditional VBGM predicted a theoretical maximum size (L_∞) of 3007·1 mm L_F, a growth coefficient (K) of 0·042 year^?1 and a theoretical age at zero length (t₀) of –6·844 years. The modified VBGM with a fixed size‐at‐birth intercept of 565 mm L_F predicted an L_∞ of 2289·2 mm L_F and a K value of 0·089 year^?1. When comparing model estimates to previously published information, the traditional VBGM predicted a significantly lower theoretical maximum size and a higher growth coefficient than those produced using data collected during the 1980s. Overall, results obtained using the VBGM with a fixed size‐at‐birth produced more biologically realistic parameters than that of the VBGM with t₀. The Monte‐Carlo simulation incorporating variability in size‐at‐birth produced similar results to the VBGM using a fixed size‐at‐birth. This study provides the first attempt to incorporate variability at size‐at‐birth and provide measurements of variability around the individual parameter estimates for an elasmobranch.     

Validated age,growth and maturity of the bonnethead Sphyrna tiburo in the western North Atlantic Ocean

The age, growth and maturity of bonnetheads Sphyrna tiburo inhabiting the estuarine and coastal waters of the western North Atlantic Ocean (WNA) from Onslow Bay, North Carolina, south to West Palm Beach, Florida, were examined. Vertebrae were collected and aged from 329 females and 217 males ranging in size from 262 to 1043 mm and 245 to 825 mm fork length, L_F, respectively. Sex‐specific von Bertalanffy growth curves were fitted to length‐at‐age data. Female von Bertalanffy parameters were L_∞ = 1036 mm L_F, k = 0·18, t₀ = ?1·64 and L₀ = 272 mm L_F. Males reached a smaller theoretical asymptotic length and had a higher growth coefficient (L_∞ = 782 mm L_F, k = 0·29, t₀ = ?1·43 and L₀ = 266 mm L_F). Maximum observed age was 17·9 years for females and 16·0 years for males. Annual deposition of growth increments was verified by marginal increment analysis and validated for age classes 2·5+ to 10·5+ years through recapture of 13 oxytetracycline‐injected specimens at liberty in the wild for 1–4 years. Length (L_F50) and age (A₅₀) at 50% maturity were 819 mm and 6·7 years for females, and 618 mm and 3·9 years for males. Both female and male S. tiburo in the WNA had a significantly higher maximum observed age, L_F50, A₅₀ and L_∞, and a significantly lower k and estimated L₀ than evident in the Gulf of Mexico (GOM). These significant differences in life‐history parameters, as well as evidence from tagging and genetic studies, suggest that S. tiburo in the WNA and GOM should be considered separate stocks.     

Critical swimming speeds of wild‐caught sand‐smelt Atherina presbyter larvae

Swimming abilities of wild‐caught sand‐smelt Atherina presbyter larvae were assessed as critical swimming speed (U_crit) throughout ontogeny. The mean U_crit increased with size, ranging from 3·6 to 18·7 cm s^?1, over the size range of 6·6–21·0 mm L_T. This indicates that at hatching A. presbyter larvae, far from being passive floaters, are already capable of active behaviours, which may influence their dispersal patterns.     

Life history of an unusual marine fish: survival, growth and movement patterns of Hippocampus guttulatus Cuvier 1829

The life history of the long‐snouted seahorse Hippocampus guttulatus was characterized using mark‐recapture data collected within a focal study site and catch data from 53 additional sites in the Ria Formosa coastal lagoon, southern Portugal. Population structure in benthic habitats was characterized by high local densities (0·3–1·5 m^?2), equal sex ratios and few juveniles <70 mm. Adult H. guttulatus maintained small (19·9 ± 12·4 m²), strongly overlapping home ranges during multiple reproductive seasons. Recruited (benthic) juveniles exhibited significantly lower site fidelity than adults. A Ford‐Walford plot of standard length (L_S) at time t against L_S measured during the previous year from tagged juveniles and adults led to estimates of the von Bertalanffy parameters K = 0·571 and L_∞ = 197·6 mm. The growth rate of planktonic juveniles (inferred from previous studies), was greater than predicted by the von Bertalanffy model, providing evidence of an ontogenetic shift in growth trajectory. The instantaneous rate of natural mortality, M, ranged from 1·13 to 1·22 year^?1(annual survival rate = 29·4–32·2%). Sexes did not differ in movement, growth or survival patterns. On average, H. guttulatus measured 12·2 ± 0·8 mm at birth. Planktonic juveniles recruited to vegetated habitat at 96·0 ± 8·0 mm (0·25 years), had mature brood pouches (males only) at 109·4 mm (0·49 years), began maintaining home ranges and reproducing at 125–129 mm (0·85–0·94 years), and lived for 4·3–5·5 years. Early age at maturity, rapid growth rates, and short generation times suggested that H. guttulatus may recover rapidly when direct (e.g. exploitation) and indirect (e.g. by‐catch and habitat damage) effects of disturbance cease, but may be vulnerable to extended periods of poor recruitment.     

Early growth and development of reciprocal hybrids of the starry flounder Platichthys stellatus and stone flounder Kareius bicoloratus

Larval growth and development of hybrid flounder were observed and compared with those of their parent species. The reciprocal hybrids of female starry flounder Platichthys stellatus and male stone flounder Kareius bicoloratus (hybrid Sb) and of female K. bicoloratus and male P. stellatus (hybrid Bs) both survived and grew to juveniles. Development was divided into nine stages (A–I). Many of the hybrids' traits were identical and intermediate to those of their parents. The position of the eye, however, was primarily sinistral in both hybrids (80% in Sb and 76% in Bs), a trait possessed by P. stellatus (80%) in the western Pacific Ocean. The daily growth rates of the larvae were similar. In the parent species, development was more rapid in P. stellatus than in K. bicoloratus whereas rate of development was intermediate in both Sb and Bs hybrids. The size at settlement [standard length (L_S) at stage H (mean ± s.d. )] was 9·82 ± 1·47 mm for the hybrid Sb and 9·99 ± 0·90 mm for the hybrid Bs, while the minimum age at metamorphosis (initial age at stage H) was 29 days after hatching (DAH) in both hybrids. In comparison, L_S at settlement in parent species was 6·43 ± 0·25 mm for P. stellatus and 12·87 ± 1·29 mm for K. bicoloratus. Minimum age at metamorphosis for the parents was 23 DAH at stage G in P. stellatus and 34 DAH at stage H in K. bicoloratus. Thus, the timing of settlement of hybrids was different from that of their parent species. These traits may occur with high frequency in a natural habitat.     

Scaling relationships for woody tissue respiration in two tropical rain forests

The relationship between gross primary productivity (GPP) and net primary productivity (NPP) is not fully understood. One of the uncertainties relevant to this issue is the magnitude of woody tissue respiration. Although some data exist for temperate and boreal zones, measurements of woody tissue respiration in tropical forests are sparse. We made in situ chamber measurements of woody tissue respiration in two tropical rain forests, one in the Brazilian Amazon (Reserva Jarú) and one in Central Cameroon (Mbalmayo Reserve). We made measurements on a wide range of species at each site and over a range of stem diameters from 0·02 to 1·4 m. The rate of efflux of carbon dioxide (CO₂) from bark at 25 °C, R_t, varied from 0·1 to 5·2 µmol m^?2 s^?1 across the two sites, and the efflux was related to both volume and surface area components of the measured stem sections. The temperature response in R_t was slightly higher at Jarú than at Mbalmayo, with Q₁₀ values of 1·8 (± 0·1 SE) and 1·6 (± 0·1 SE), respectively. A log–log regression showed that R_t was significantly related to stem diameter, D (P < 0·001; r² = 0·58–0·62) and was significantly higher at Mbalmayo than at Jarú (P < 0·001), but that the rate of increase in R_t with stem diameter, D, was similar between sites. At the Mbalmayo site, tree growth measurements made over a 4 month period were used to make two estimates of the maintenance (R_m) and construction (R_c) components of respiration embedded in R_t. The two methods agreed closely, suggesting that R_m was approximately 80% of R_c at this site. R_m could be strongly related to D using a sigmoidal relationship that described both surface area and volume components as sources of respiratory CO₂ (r² = 0·71). This functional model was combined with inventory, growth and climate data for the Mbalmayo site to make a first estimate of annual above‐ground woody tissue respiration, R_A, which was 257 (± 18 SE) g C m^?2 year^?1. This value corresponds to approximately 10% of GPP, slightly lower than that found for another tropical rain forest, but higher than for temperate forests. When combined with data from six other sites in tropical, temperate and boreal settings, a very strong relationship was found between R_A and leaf area index (LAI), and between R_A/GPP and LAI (P < 0·001, r² = 0·98). This indicates that R_A exerts an appreciable constraint on NPP and that this constraint varies closely with LAI across widely differing types of woody vegetation.