Size frequency,dispersal distances and variable growth rates of young sharks in a multi-species aggregation

During a mark–recapture survey from November 2014 until April 2017, 333 neonatal and juvenile blacktip reef sharks Carcharhinus melanopterus and 302 neonatal and juvenile sicklefin lemon sharks Negaprion acutidens were tagged and measured at the uninhabited and isolated St. Joseph Atoll (Republic of Seychelles). Both species demonstrated seasonal reproductive synchronicity and relatively large sizes at birth. Despite the extended times at liberty > 2.5 years, the majority of recaptures were found in close proximity to the initial tagging location (< 500 m). Annual growth rates of C. melanopterus (n = 24) and N. acutidens (n = 62) ranged from 6.6 to 31.7 cm year⁻¹ (mean ± SE; 16.2 ± 1.2 cm year⁻¹) and 0.2 to 32.2 cm year⁻¹ (11.8 ± 1 cm year⁻¹), respectively and are to date the most variable ever recorded in wild juvenile sharks. High abundances of both species coupled with long-term and repeated recaptures are indicative of a habitat where juveniles can reside for their first years of life. However, large variability in annual growth rates in both species may suggest high intra and interspecific competition induced by a possibly resource limited, isolated habitat.     

A re-examination of the age and growth of sand tiger sharks, Carcharias taurus, in the western North Atlantic: the importance of ageing protocols and use of multiple back-calculation techniques

Age and growth estimates for sand tiger sharks, Carcharias taurus, in the western North Atlantic were derived from 96 vertebral centra collected from sharks ranging from 94 to 277 cm total length (TL), and compared to previously published age and growth data. The oldest female and male sand tiger sharks aged in this study were 17 and 15 years of age, respectively. von Bertalanffy growth parameters derived from vertebral length-at-age data are L _∞ = 295.8 cm TL, k = 0.11 year⁻¹, and t ₀ = −4.2 years for females, and L _∞ = 249.5 cm TL, k = 0.16 year⁻¹, and t ₀ = −3.4 years for males. Sexual maturity is estimated to be 9–10 years for females and 6–7 years for males. Weight-to-length relationships determined for female and male sand tiger sharks in the western North Atlantic are; W = 1.3 × 10⁻⁴ × L ^2.4 (r ² = 0.84, n = 55) and W = 9.0 × 10⁻⁵ × L ^2.5 (r ² = 0.84, n = 47), respectively, and 7.9 × 10⁻⁵ × L ^2.5 (r ² = 0.84) for the sexes combined. Our results show sand tigers possess a slower rate of growth than previously thought. This information is crucial for accurately assessing this population’s ability to recover, and further justifies the need for this species to be fully protected.     

Three decades of longlining in Bimini,Bahamas, reveals long‐term trends in lemon shark Negaprion brevirostris (Carcharhinidae) catch per unit effort

In Bimini, Bahamas, the consistent employment of longlines, beginning in 1982, provided a rare opportunity to explore population trends for large resident sharks. This study assessed three shallow water longline survey periods at this location; 1982–1989, 1992–2002 and 2003–2014, with the aim of determining trends in annual catch per unit effort (CPUE) for an IUCN listed near‐threatened species, the lemon shark Negaprion brevirostris. A general additive model (GAM) was used to analyse the non‐linear annual CPUE values over the entire 32‐year research period. The GAM displayed high variability of annual CPUE, with a peak value of 0·026 N. brevirostris per hook day (hooks day^?1) in 2000. The temporal pattern of CPUE indicated an abundance trend with a complete cycle, from trough to trough, occurring over a period of approximately 18 years. The 1982–1989 survey period saw the highest proportion of mature individuals (19·8%) and the smallest average pre‐caudal length (L_PC; 124·8 cm). The 1992–2002 survey period had the highest average annual CPUE (0·018 hooks day^?1), while the 2003–2014 research period saw largest average L_PC size (134·8 cm) and the lowest average CPUE values (0·009 hooks day^?1) of the entire research period. The long‐term trend identified in this study provides a baseline for future assessment.     

Trends in sightings and population structure of white sharks, <Emphasis Type="Italic">Carcharodon carcharias,</Emphasis> at Seal Island,False Bay,South Africa,and the emigration of subadult female sharks approaching maturity

A long-term sightings and photographic identification (photo-ID) database documented the inter-annual and monthly trends in white shark (Carcharodon carcharias) sightings, sex ratios and life-history stages at Seal Island, False Bay, South Africa, over the period 2004–2012. A total of 1105 sightings were recorded during 171 scientific surveys incorporating 577 h of observation (annual mean 64.10 h, range 23.71–178.69 h). The mean annual sighting rate was 1.87 (range 0.90–3.19) sharks per hour and sighting rates declined over the nine-year study period. It is unknown whether the decline resulted from an actual population decline, or was due to changes in shark distribution or environmental conditions, but it highlights the need for ongoing monitoring at this site. The overall sex ratio was 1.0: 1.0: 2.3 for male: female: unsexed sharks, respectively. Of the 1105 sightings, 39% (n = 433) were photo-ID’d, representing 303 individual sharks (112: 111: 80, male: female: unsexed) and 130 resightings. Of the 303 photo-ID’d sharks, 71% were sighted in a single year only, indicative of transient behaviour. Of the 29% of sharks that were resighted in more than one year, 65% were resighted in the following year, indicating site fidelity to Seal Island, whereas 35% skipped one or more years between encounters, indicative of a temporary absence. The majority (60%) of the photo-ID’d sharks were immature, 32% were subadult and only 8% were mature. No young-of-the-year sharks and few adults were recorded, indicating that Seal Island is not an adult aggregation site, nor a pupping or nursery area, but rather is best described as a seasonal feeding ground. Large females were rarely resighted again after they approached length-at-maturity (≥450 cm TL), whereas some adult males were recorded consistently across years. The emigration of subadult female sharks approaching maturity from Seal Island, combined with the small number of mature sharks of both sexes reported from any South African location, indicate that adult aggregation sites, and thus areas of reproductive importance, still remain unknown.     

Age,growth and length–weight relationships of Pinna bicolor Gmelin (Bivalvia: Pinnidae) in the seagrass beds of Sungai Pulai Estuary,Johor, Peninsular Malaysia

Age and growth of Pinna bicolor were examined in the seagrass beds of Merambong shoal (N 1°19′55.62″; E 103°35′57.75″) off the south‐western coast of Johor, Peninsular Malaysia between May 2006 and April 2007. Monthly growth increment data of P. bicolor were analyzed using FiSAT software (FAO‐ICLARM Stock Assessment Tools) to estimate the asymptotic length (L_∞) and growth coefficient (K). Average growth rate of P. bicolor was 1.42 (±0.01) cm per month; the estimated asymptotic length (L_∞) and growth coefficient (K) were 34.66 cm and 0.88 per year, respectively. In their natural habitat, P. bicolor attain shell heights of approximately 17, 25 and 30 cm at the end of their first, second and third years of growth. The length–weight relationship was estimated as Log W = ?5.397 + 3.111Log L, and in exponential form the equation was W = 0.000004L^3.111 (r² = 0.99, P < 0.01). Habitat temperature and salinity ranged between 27.47 and 29.66°C and 28.66–33.00 ppt with a mean of 29.10 (±0.66) m°C and 30.52 (±1.41) ppt, respectively.     

Stable-isotope analysis reveals sources of organic matter and ontogenic feeding shifts of a mangrove-dependent predator species,New Granada sea catfish,Ariopsis canteri

To gain a better understanding on the trophic ecology of New Granada sea catfish, Ariopsis canteri, and their linkage to mangroves, nitrogen and stable carbon isotopes (δ¹⁵N and δ¹³C), as well as Bayesian mixing models, were used to explore trophic dynamics and potential ontogenic feeding shifts across different size classes: class I (8–20 cm), class II (21–32 cm) and class III (>32 cm). The study area was the estuary of the Atrato River Delta, where information about fish ecology is scarce. The δ¹³C of size class I was lower (mean ± s.d . = −24.96 ± 0.69‰) than that of size classes II (−22.20 ± 0.90‰) and III (−22.00 ± 1.96‰). The δ¹⁵N of size class I was lower (mean ± s.d . = 8.50 ± 0.67‰) than that of size classes II (9.77 ± 0.60‰) and III (10.00 ± 0.66‰). Body size was positively and significantly correlated to δ¹⁵N and δ¹³C. Individuals with L_T > 32 cm presented the highest estimated trophic position (3.8). Five-source mixing models indicated that for class I, the mean estimated contribution of macroalgae was the highest (6%–57% c.i. ), and for classes II and III, the mean estimated contribution of macrophytes was the highest (3%–53% c.i. and 4%–53% c.i. , respectively). Ontogenetic feeding shifts of A. canteri were confirmed evidencing decreasing intraspecific competition between small and large individuals. Results suggest that mangroves are a nursery and feeding ground habitat for this species and that mangroves support A. canteri mainly due to the substrate/habitat that supports sources in the food webs. These results can be used in ecosystem-based fishery management focused on the protection of extensive mangrove areas in the southern Caribbean Sea.     

Age and growth of the sandbar shark, Carcharhinus plumbeus, in Hawaiian waters through vertebral analysis

Age and growth estimates were determined for the sandbar shark, Carcharhinus plumbeus, from Oahu, Hawaii in the central Pacific Ocean. Age estimates were obtained through vertebral centra analysis of 187 sharks. We verified our age estimates through marginal increment analysis of centra and oxytetracycline marking methods of at liberty sandbar sharks. Sizes of sampled sharks ranged from 46 to 147 cm pre-caudal length. Four growth models were fitted to length-at-age data; two forms of the von Bertalanffy growth model, the Gompertz growth model, and a logistic growth model. Males and females exhibited statistically significant differences in growth, indicating that females grow slower and attain larger sizes than males. Growth parameter estimates revealed slower growth rates than previously estimated (based on captive specimens) for Hawaiian sandbar sharks. The von Bertalanffy growth model using empirical length-at-birth provided the best biological and statistical fit to the data. This model gave parameter estimates of L _∞ = 138.5 cm PCL and k = 0.12 year⁻¹ for males and L _∞ = 152.8 cm PCL, k = 0.10 year⁻¹ for females. Male and female sandbar sharks mature at approximately 8 and 10 years of age, respectively.     

Unique osmoregulatory morphology in primitive sharks: an intermediate state between holocephalan and derived shark secretory morphology

Discovery of an unusual rectal gland in the Atlantic sixgill shark Hexanchus vitulus led us to examine the rectal glands of 31 species of sharks to study diversity in rectal-gland morphology. Twenty-four of 31 species of sharks had digitiform glands (mean width–length ratio ± SD = 0.17 ± 0.04) previously assumed to be characteristic of all elasmobranchs regardless of habitat depth or phylogenetic age. Rectal glands from the family Somniosidae were kidney bean-shaped (mean width: length ± SD = 0.46 ± 0.05); whereas those from families Echinorhinidae and Hexanchidae were lobulate (mean width: length ± SD = 0.55 ± 0.06). Rectal gland width: length were different among species with digitiform morphology and lobulate morphology (ANOVA; R² = 0.9; df = 15, 386; 401, F = 219.24; P < 0.001). Histological and morphological characteristics of the digitiform morphology from deep-sea sharks were similar to those from shallow-water sharks. Histology of lobulate rectal glands from hexanchids were characterised by tubule bundles separated by smooth muscle around a central lumen. Additionally, we examined plasma chemistry of four species of sharks with digitiform rectal glands and two species with lobulate rectal-gland morphology to see if there were differences between morphologies. Plasma chemistry analysis showed that urea and trimethylamine N-oxide (TMAO) followed the piezolyte hypothesis, with TMAO being highest and urea being lowest in deep-sea sharks. Among electrolytes, Na⁺ was highest in species with lobulate rectal glands. Hexanchids and echinorhinids both have lobulate rectal glands similar to those of holocephalans, despite the more than 400 million years separating these two groups. The morphological similarities between the lobulate rectal-gland anatomy of primitive sharks and the secretory morphology of holocephalans may represent an intermediate state between Holocephali and derived shark species.     

A study of some autoecological parameters of southern barbel (Barbus meridionalis R.) in the Rentina stream, Greece

In our effort to give some information which investigates autecological parameters for southern barbel, a study of age, growth and reproduction for this species was carried out in the Rentina stream, northeastern Greece. The length-weight relationship can be described by the equations W = 0.008 L^3.159 and W = 0.0583 L^2.428 for females and males, respectively (W = body weight in g, L = fork length in cm). The most rapid growth in length occured during the first year of life (7.3 cm) after which growth decreased and remained constant at approximately 3.4 cm per year. The average density and biomass were 0.25 fish. m^-2 and 9.35 g. m^-2, respectively. The southern barbel becomes sexualy mature at the second year of life for both sexes. The mean absolute fecundity was 9119 ± 322 eggs with mean diameter 1.2 ± 0.2 mm. Spawning of this species, in the study area, occurs in June at mean temperature 19°C.     

Landings of whale sharks Rhincodon typus Smith, 1828 in Indian waters since protection in 2001 through the Indian Wildlife (Protection) Act, 1972

Since 28^th May 2001, Whale shark Rhincodon typus Smith, 1828 have received the highest protected status for an animal in India through the Indian Wildlife (Protection) Act, 1972 Schedule-1. However, landings have still been recorded off the Indian coast since 2001, mostly as incidental bycatch in commercial fishing operations, and other sightings have also been reported. In the 1990’s, a targeted whale shark fishery existed off the Gujarat coast following increased demand for the flesh in some other Asian countries. Since the ban, landings of whale sharks have decreased substantially with only 79 recorded between 2001 and 2011. Landings were recorded in each year and in each month of the year with the highest landings in January and February. Between 2001 and 2011, the smallest specimen reported from Indian waters was a 94 cm TL individual and the largest was a 13.7 m TL individual, with most individuals recorded in the 4–6 m TL size class. Small juveniles of less than 3 m TL are rarely recorded in the literature and appear to be rarely observed globally. Between 2006 and 2011, seven juveniles of less than 3 m TL were recorded from two landing sites. Despite the continued landing of whale sharks along the Indian coasts since 2001, the protection of this species appears to have substantially reduced the catches with only incidental landings and strandings now evident. The protection status of whale sharks in India is generally well understood by fishers, but still there is need for further education regarding the current national legislation and vulnerability of the species.     

Population ecology of rhesus monkeys (Macaca mulatta) at Nanwan Nature Reserve,Hainan, China

Rhesus monkeys (Macaca mulatta) at the Nanwan peninsula of Hainan Island, China, have been observed in the field for 25 years, and have been studied intensively for eight years, beginning in 1981. There were about 115 monkeys in 5 natural groups when the Nanwan Reserve was founded in 1965. From 1965 to 1984, the number of groups increased from 5 to 19, and the total population increased from 115 to 930 individuals, an annual population increase of 12.7%. From 1984 to 1987, the population continued a slower rate of increase (8.9%) to approximately 1200 monkeys in 20 groups. The home ranges of each monkey group at Nanwan varied from 0.16 to 0.72 km², with a mean and standard deviation of 0.37 ± 0.18. The size of the home range of the rhesus was affected by the quality of vegetation and rhesus population density. The average birth rate per year was 77.8 ± 13.9%, varying from 53.8% to 100% since 1978. From 1978, the birth rates of two food provisioned groups were higher in alternate years (x? = 91.7%) and lower in intervening years (x? = 68.8%; P = <0.01). A minority (26.5%) of females have given birth at 4 years of age, most at 5 years. The sex ratio of newborns in any one year varied from 0.3 to 3.5 males to females, with a mean and standard error of 1.09 ± 0.37 males to females.     

Reproductive biology and population dynamics of the shortfin mako, Isurus oxyrinchus Rafinesque, 1810, off the southwest Portuguese coast, eastern North Atlantic

A total of 262 shortfin mako sharks, Isurus oxyrinchus, was sampled from the swordfish longliners operating in the eastern North Atlantic. Most were juveniles, with only 3.4% mature. Based on cohort analysis, average growth was determined as 61.1 cm year⁻¹ for the first year and 40.6 cm year⁻¹ for the second year. There was a marked seasonality in growth, with average monthly rates of 5.0 cm month⁻¹ in summer and 2.1 cm month⁻¹ in winter. Cohort analysis also indicated summer as the probable parturition season, with sharks close to birth size caught in May 2003 and July 2004. Length at maturity for males was estimated at 180‐cm fork length using the Schnute model. No females between 210 and 290‐cm fork length were caught, although this appears to be the interval where maturation occurs. Gear selectivity was considered as the probable cause for the low number of mature females sampled.     

Tidal Influence on Spatial Dynamics of Leopard Sharks, Triakis semifasciata, in Tomales Bay, California

We used ultrasonic telemetry to determine the movement directions and movement rates of leopard sharks, Triakis semifasciata, in Tomales Bay, California. To analyze tide and time of day effects, we surgically implanted transmitters in the peritoneal cavities of one male and five female leopard sharks, which we located during summer for three to five sampling sessions lasting 12 to 24h each. All leopard sharks showed strong movement direction patterns with tide. During incoming tides, sharks moved significantly (p<0.0001) towards the inner bay, apparently to exploit the extensive inner bay muddy littoral zones' food resources. On outgoing tides, sharks showed significant (p<0.0001) movements towards the outer bay. During high tide, there was no discernible pattern to their movements (p=0.092). Shark movement rates were significantly (p<0.0001) greater during dark periods (mean±SE: 10.5±1.0m min^–1), compared with fully lighted ones (6.7±0.5m min^–1). Movement rates of longer sharks tended to be greater than those of shorter ones (range means±SE: 5.8±0.6m min^–1 for the 91cm shark, to 12.8±1.6m min^–1 for the 119cm shark), but the leopard sharks' overall mean movement rate (8.1±0.5m min^–1) was slower than other (more pelagic) sharks.     

Waist Circumference,BMI, and Visceral Adipose Tissue in White Women and Women of African Descent

Although waist circumference (WC) is a marker of visceral adipose tissue (VAT), WC cut‐points are based on BMI category. We compared WC‐BMI and WC‐VAT relationships in blacks and whites. Combining data from five studies, BMI and WC were measured in 1,409 premenopausal women (148 white South Africans, 607 African‐Americans, 186 black South Africans, 445 West Africans, 23 black Africans living in United States). In three of five studies, participants had VAT measured by computerized tomography (n = 456). Compared to whites, blacks had higher BMI (29.6 ± 7.6 (mean ± s.d.) vs. 27.6 ± 6.6 kg/m², P = 0.001), similar WC (92 ± 16 vs. 90 ± 15 cm, P = 0.27) and lower VAT (64 ± 42 vs. 101 ± 59 cm², P < 0.001). The WC‐BMI relationship did not differ by race (blacks: β (s.e.) WC = 0.42 (.01), whites: β (s.e.) WC = 0.40 (0.01), P = 0.73). The WC‐VAT relationship was different in blacks and whites (blacks: β (s.e.) WC = 1.38 (0.11), whites: β (s.e.) WC = 3.18 (0.21), P < 0.001). Whites had a greater increase in VAT per unit increase in WC. WC‐BMI and WC‐VAT relationships did not differ among black populations. As WC‐BMI relationship did not differ by race, the same BMI‐based WC guidelines may be appropriate for black and white women. However, if WC is defined by VAT, race‐specific WC thresholds are required.     

Vulnerability to longline fisheries of three hammerhead shark Sphyrna species in the south‐western and equatorial Atlantic Ocean

Catch and effort data from 29 418 longline sets from Brazilian tuna longline vessels operating in the south‐western and equatorial Atlantic Ocean between 2004 and 2011 were analysed to investigate the distribution, catch rate and size of three species of hammerhead sharks (Sphyrna lewini, Sphyrna mokarran and Sphyrna zygaena). During that period, 6172 hammerhead sharks were caught. Among the elasmobranchs, the highest percentage of hammerhead sharks were caught in 2007, when they accounted for 3·90% of the group, while the lowest value of 0·40% was recorded in 2010. In general, the spatial distribution of the mean catch per unit effort (CPUE) by years and quarters showed a trend of higher catches near the equatorial region and in southern Brazil. The nominal mean CPUE was 0·12 Sphyrna spp. 1000⁻¹ hooks, with the highest value being recorded in 2007 (0·30 Sphyrna spp. 1000⁻¹ hooks). The standardized yearly CPUE estimated by a generalized linear model assuming a zero inflated negative binomial (ZINB) distribution were not much different from nominal values. Of the 205 sexed specimens, 117 were females and 88 were males, resulting in a sex ratio with a predominance of females (1·30:1·00), although not statistically significant. The total length of females ranged from 1200 to 2800 mm and of males from 1100 to 3100 mm. Juvenile hammerhead sharks represented 82 and 54% of the sexed female and male specimens, respectively.     

Haemodynamics using transthoracic echocardiography in healthy pregnant and non-pregnant baboons (Papio hamadryas)

Background To determine systolic and diastolic function using transthoracic echocardiography in the baboon (Papio hamadryas). Methods Transthoracic echocardiography was performed in eight non‐pregnant female and six pregnant baboons according to American Society of Echocardiography recommendations. Results Haemodynamic measurements were obtained from fourteen baboons. Compared to non‐pregnant baboons, pregnant baboons demonstrated: (mean ± SD, pregnant vs. healthy) increased cardiac output (1615 ± 121 ml/minutes vs. 1317 ± 134 ml/minutes P = 0.001) due to an increased heart rate [120 ± 11 beats per minute (BPM) vs. 105 ± 6 BPM P = 0.018]. The inter‐observer and intra‐observer variability (mean difference ± SD) for the left ventricular outflow tract diameter was 0.05 ± 0.07 cm and 0.01 ± 0.03 cm respectively. There was minimal impact to the animal’s daily activities. Conclusions Transthoracic echocardiography was applicable and reproducible for the assessment of haemodynamics in baboons thus enabling translation of animal results to human studies.     

Trophic ecology of juvenile bull sharks (Carcharhinus leucas) in the Coyote estuary,Costa Rica

Bull shark (Carcharhinus leucas) is a near-threatened elasmobranch species capable of moving between the fresh and salty waters of tropical and subtropical coastal areas, for which we still lack important ecological information. During their first years of life, bull sharks use estuarine systems as nursery areas, making them highly susceptible to environmental and anthropogenic pressures. We studied the trophic ecology of juveniles found in the Coyote estuary, a potential nursery area in Costa Rica, to understand the potential impact of further bull shark declines and gain knowledge that could aid in their conservation. We analysed the trophic ecology of juvenile bull sharks [81–103 cm total length (TL)] in the Coyote estuary, Costa Rica, using stable isotopes of δ¹⁵N and δ¹³C. Since one problem using this technique in juveniles is the confounding effect of the maternal signature, we sampled different tissues (muscle and plasma), verified the status of the shark's umbilical scar and identified the size at which the isotope signature is a result of the animal's current diet. The isotopic values of the muscle tissue reflected the maternal isotopic signature. In contrast, plasma values reflected the diet of juvenile bull sharks >95 cm TL and with a closed umbilical scar. Juvenile bull sharks fed primarily on teleost fishes of the order Anguilliformes and Siluriformes, and have a high trophic position (≥4.0) in the Coyote estuary. Our findings suggest that this estuary is an important feeding site for juvenile bull sharks of the Pacific of Costa Rica. Thus, the protection of essential habitats such as the Coyote estuary will benefit not only bull shark conservation, but also the conservation of an array of fish species that also use this habitat as a rookery, many of which are of commercial interest.     

Age and growth of the spotted goatfish, Pseudupeneus maculatus (Bloch, 1793) in Brazil, validated through marginal increment and oxytetracycline dyes in the sagittae

A sample composed of 4973 specimens of the spotted goatfish, Pseudupeneus maculatus (4.5–29.2 cm fork length) was collected off northeastern Brazil from 1999 to 2002. Sagittae (398) were analyzed for age and growth estimation using both annuli and microincrements. For the first approach, the mean monthly marginal increment ratio analysis suggested that one band is formed annually from May to June. With the microincrements analysis, 15 specimens were reared (3–71 days) for validation of periodicity using oxytetracycline. Fluorescent dyes were observed in 10 specimens (7.5–16.9 cm). After testing, one microincrement was found to form daily. Otolith sections were polished and analyzed using a light microscope (100–1200× magnifications). Individuals larger than 22.6 cm (4 years) showed heavily overlaid increments on the otolith edge, which hampered the counts. There was agreement on the size from counts on an annual and daily basis. The von Bertalanffy function provided the following parameters: L_∞ = 33.23 cm; K = 0.265; t₀ = 0.0883 year. The sample was composed of 0⁺ to >5‐year‐old specimens. Age at first maturity was 3.6 years (20 cm), whereas the recruitment age for fisheries was 3.9 years. Juveniles represented about half of the catch (48.7%), which may have implications for population equilibrium.     

Bioenergetics of juvenile whitespotted bamboo shark Chiloscyllium plagiosum [Anonymous (Bennett)]

This study establishes the bioenergetics budget of juvenile whitespotted bamboo shark Chiloscyllium plagiosum by estimating the standard metabolic rate (R_S), measuring the effect of body size and temperature on the R_S, and identifying the specific dynamic action (R_SDA) magnitude and duration of that action in juvenile whitespotted bamboo sharks. The mean ±s .d . (R_S) of six fish (500–620 g) measured in a circular closed respirometry system was 30·21 ± 5·68 mg O₂ kg^?1 h^?1 at 18° C and 70·38 ± 14·81 mg O₂ kg^?1 h^?1 at 28° C, respectively. There were no significant differences in R_S between day and night at either 18 or 28° C (t‐test, P > 0·05). The mean ±s .d . Q₁₀ for 18–28° C was 2·32 ± 0·06 (n = 6). The amount of oxygen consumed per hour changed predictably with body mass (M; 295–750 g) following the relationship: (n = 40, r²= 0·92, P < 0·05). The mean magnitude of R_SDA was 95·28 ± 17·55 mg O₂ kg^?1 h^?1. The amount of gross ingested energy (E_I) expended as R_SDA ranged from 6·32 to 12·78% with a mean ±s .d . of 8·01 ± 0·03%. The duration of the R_SDA effect was 122 h. The energy content of juvenile whitespotted bamboo shark, squid and faeces determined by bomb calorimeter were 19·51, 20·3 and 18·62 kJ g dry mass^?1. A mean bioenergetic budget for juvenile whitespotted bamboo sharks fed with squid at 18° C was 100C = 29·5G + 31·9R_S+ 28·2R_SDA+ 6·7F + 2·1E + 1·6U, where C = consumption, G = growth, F = egestion, E = excretion and U = unaccounted energy.