Environmental Influences on the Abundance and Sexual Composition of White Sharks Carcharodon carcharias in Gansbaai,South Africa

The seasonal occurrence of white sharks visiting Gansbaai, South Africa was investigated from 2007 to 2011 using sightings from white shark cage diving boats. Generalized linear models were used to investigate the number of great white sharks sighted per trip in relation to sex, month, sea surface temperature and Multivariate El Niño/Southern Oscillation (ENSO) Indices (MEI). Water conditions are more variable in summer than winter due to wind-driven cold water upwelling and thermocline displacement, culminating in colder water temperatures, and shark sightings of both sexes were higher during the autumn and winter months (March–August). MEI, an index to quantify the strength of Southern Oscillation, differed in its effect on the recorded numbers of male and female white sharks, with highly significant interannual trends. This data suggests that water temperature and climatic phenomena influence the abundance of white sharks at this coastal site. In this study, more females were seen in Gansbaai overall in warmer water/positive MEI years. Conversely, the opposite trend was observed for males. In cool water years (2010 to 2011) sightings of male sharks were significantly higher than in previous years. The influence of environmental factors on the physiology of sharks in terms of their size and sex is discussed. The findings of this study could contribute to bather safety programmes because the incorporation of environmental parameters into predictive models may help identify times and localities of higher risk to bathers and help mitigate human-white shark interactions.     

Distribution and reproduction of the southern lantern shark from New Zealand

Distribution, population structure and reproduction are described for the southern lantern shark Etmopterus granulosus at the Chatham Rise, New Zealand. Depth of capture for E. granulosus ranged from 744 to 1420 m, with highest catch rates between 800–1200 m. More than twice as many females as males were captured, and the majority of sharks caught were mature, indicating that there may be segregation according to sex and size class. Only 10 of 492 female sharks captured contained ova in uteri, and none contained embryos. The absence of pregnant females suggests that they move to another area or depth prior to pupping. Size of sharks captured ranged from 20·0 to 78·8 cm total length. Females began to mature at 62 cm total length, and males at 52 cm. There was no evidence of a seasonal reproductive cycle. Ovulation appeared to occur when ova reached a diameter of 40–45 mm. The average number of ova in mature females was 12·7. This information is crucial for assessing the impact of fisheries on E. granulosus populations.     

Reproductive biology of the endangered Oxleyan pygmy perch Nannoperca oxleyana Whitley

The reproductive biology of the Oxleyan pygmy perch Nannoperca oxleyana is described from simultaneous studies of wild populations in north-eastern New South Wales and mature fish held in aquaria. In the wild, 50% of males and females matured at total lengths of 24·0–25·9 and 28·0–29·9 mm, respectively. The species displays sexual dichromatism during the spawning season, with males developing more intense red and brown fin and body colouration, and black pelvic fins. Captive male broodfish displayed territoriality during the breeding season, closely guarding sites within artificial, plant-like substrata in which pairs of fish spawned adhesive eggs. Protracted serial spawning of wild and captive fish occurred from September to April and May at mean water temperatures ≥16·6° C and day length ≥10·7 h. Captive broodfish spawned on an average of 57% of days during the 256 day spawning period. Gonado-somatic indices averaged 0·7% for all ripe males and 4·1–4·2% for all ripe females collected. Mean total and batch fecundities of captive females were 1323 eggs per fish and 7·8 eggs per fish per day, respectively, and relative fecundity was 587 eggs g⁻¹ of body mass. Batch fecundity of wild females was estimated at 7·8 eggs per fish. The adaptive significance of this reproductive strategy in a harsh, variable environment is discussed.     

The metabolic and biochemical responses of tropical whitespotted bamboo shark Chiloscyllium plagiosum to alterations in environmental temperature

The capacity of tropical whitespotted bamboo sharks Chiloscyllium plagiosum to metabolically compensate, at both the whole‐animal and biochemical levels, to prolonged exposure to temperatures higher (30° C) and lower (20 and 15° C) than their native temperature (24·5° C) was examined. As expected, whitespotted bamboo shark oxygen consumption increased upon exposure to 30° C and decreased at 20 and 15° C. Initial changes in oxygen consumption were maintained even after months at the experimental temperature, indicating that whitespotted bamboo sharks did not compensate metabolically to the experimental temperatures. Maximal activities and thermal sensitivity of citrate synthase and lactate dehydrogenase from whitespotted bamboo shark white locomotor muscle were similar between control animals maintained at 24·5° C and those maintained at 15° C, indicating that cold‐exposed animals did not compensate at the biochemical level. Similarly, lactate dehydrogenase activity did not change following prolonged exposure to 30° C. White muscle from whitespotted bamboo sharks maintained at 30° C had significantly lower citrate synthase activity than did control animals. This result was surprising given the lack of metabolic compensation at the whole‐animal level. Overall, whole‐animal oxygen consumption measurements supported the hypothesis that animals from thermally stable environments lacked the capacity to metabolically compensate to altered temperatures. Enzymatic results, however, suggested that the metabolic potential of muscle could change following temperature acclimation even in the absence of metabolic compensation at the whole‐animal level.     

Residency,Habitat Use and Sexual Segregation of White Sharks,Carcharodon carcharias in False Bay,South Africa

White sharks (Carcharodon carcharias) are threatened apex predators and identification of their critical habitats and how these are used are essential to ensuring improved local and ultimately global white shark protection. In this study we investigated habitat use by white sharks in False Bay, South Africa, using acoustic telemetry. 56 sharks (39 female, 17 male), ranging in size from 1.7–5 m TL, were tagged with acoustic transmitters and monitored on an array of 30 receivers for 975 days. To investigate the effects of season, sex and size on habitat use we used a generalized linear mixed effects model. Tagged sharks were detected in the Bay in all months and across all years, but their use of the Bay varied significantly with the season and the sex of the shark. In autumn and winter males and females aggregated around the Cape fur seal colony at Seal Island, where they fed predominantly on young of the year seals. In spring and summer there was marked sexual segregation, with females frequenting the Inshore areas and males seldom being detected. The shift from the Island in autumn and winter to the Inshore region in spring and summer by females mirrors the seasonal peak in abundance of juvenile seals and of migratory teleost and elasmobranch species respectively. This study provides the first evidence of sexual segregation at a fine spatial scale and demonstrates that sexual segregation in white sharks is not restricted to adults, but is apparent for juveniles and sub-adults too. Overall, the results confirm False Bay as a critical area for white shark conservation as both sexes, across a range of sizes, frequent the Bay on an annual basis. The finding that female sharks aggregate in the Inshore regions when recreational use peaks highlights the need for ongoing shark-human conflict mitigation strategies.     

Effect of salt concentration and temperature on survival of Legionella pneumophila

The effects of various concentrations of sodium chloride solutions (0·1%–3%) and different temperatures (4, 10, 20, 30 and 37 °C) on survival of Legionella pneumophila were investigated. It was found that at temperatures between 4 °C and 20 °C, Legionella organisms survived in salt solutions up to 3% NaCl. Only the combination of high temperatures, i. e. 30 °C and 37 °C, with NaCl concentrations over 1·5%, reduced cell numbers significantly. It was interesting to note that the addition of small amounts of NaCl (0·1%–0·5%) enhanced survival of Leg. pneumophila , suggesting a protective effect of NaCl. In order to obtain information about conditions encountered in the environment, the survival experiments were repeated in sterile sea water from the Baltic Sea and the North Sea. The marked bacterial die-off, especially at higher temperatures, was not observed in natural sea water. All these results indicate that Leg. pneumophila can survive in the marine environment.     

Influence of rearing temperature during the larval and nursery periods on growth and sex differentiation in two Mediterranean strains of Dicentrarchus labrax

European sea bass Dicentrarchus labrax of the north‐western (NW) and south‐eastern (SE) Mediterranean Sea strains were exposed to different temperatures (13, 17 or 21° C) during the larval rearing (11–51 days post hatching, dph) or nursery periods (55–95 dph), in order to examine the effects of temperature on sex differentiation and subsequent growth during the first year of life. Higher growth was observed during exposure to higher temperatures, but fish of the NW strain exposed to 13 or 17° C during larval rearing exhibited compensatory growth once exposure to the lower temperatures finished, and as a result their final size at 300 dph was similar or greater to the group exposed to 21° C. Fish exposed to 17° C during the nursery period also had similar size to fish exposed to 21° C after 300 days of rearing, but the fish exposed to 13° C remained significantly smaller (ANOVA, n  = 55–100, P  < 0·05). There were significant differences in the sex ratio among the fish exposed to different temperatures during the two periods of rearing, with high temperature (21° C) resulting in a significantly higher percentage of males in the population, both in the NW (ANOVA, n  = 2, P  < 0·04) and SE populations (ANOVA, n  = 2, P  < 0·01). The masculinization effect of high temperature was significantly stronger during the larval rearing stage, both in the NW (ANOVA, n  = 2, P  < 0·005) and SE populations (ANOVA, n  = 2, P  < 0·01). None of the temperature manipulations could produce 100% females, suggesting that there is a part of the genetic component in sex differentiation which is not labile to environmental influence.     

Influence of pregnancy on the thermal biology of the lizard, Sceloporus jarrovi: why do pregnant females exhibit low body temperatures?

1. Selected body temperatures of female lizards, Sceloporus jarrovi , were measured on a photothermal gradient during late pregnancy and again when postpartum, and pregnant females were subjected to one of three fluctuating temperature regimes that simulated body temperatures of (1) pregnant females, (2) postpartum females or (3) allowed normal thermoregulation.
2. Overall, females selected lower body temperatures when pregnant (mean = 32·0°C) than when postpartum (mean = 33·5°C).
3. Females regulated body temperature more precisely when pregnant than when postpartum as judged by their smaller variances in body temperature throughout the day.
4. When pregnant, females selected a lower mean maximum body temperature (mean: pregnant = 32·8°C; postpartum = 34·5°C) than when postpartum, but selected mean minimum body temperatures did not differ.
5. None of the experimental temperature treatments was detrimental to pregnant females. Female body length increased during pregnancy but the rate of increase did not differ among treatments. Moreover, length-adjusted body mass of postpartum females did not differ among treatments.
6. Pregnant females that experienced postpartum body temperatures produced neonates that were smaller in body mass and length than pregnant females that experienced pregnant body temperatures and females that were allowed to thermoregulate.
7. For neonates resulting from the postpartum body temperature treatment, the disparity in the body length, but not mass, was still observed at 9 days of age, although survival and growth of neonates was high and did not differ among treatments.
8. The results demonstrate that pregnant females could maintain higher postpartum body temperatures without compromising their physical condition, but select relatively low body temperatures, presumably to avoid decrements in offspring fitness.     

Life history of Maurolicus muelleri in fjordic and oceanic environments

Life history parameters are compared for populations of Maurolicus muelleri from Norwegian fjords and the Norwegian Sea in 1995 and 1996. The mortality rate was higher in the oceanic population (2·55 for males, 2·00 for females) than in the fjords (1·15 for males, 0·97 for females). Fish from the Norwegian Sea population occupied a depth with higher light levels, which may have contributed to the higher mortality through increased visibility to predators. Differences in growth, condition and gonad weight indicated different resource levels caused by different population densities. Recruitment was weak in many fjords in 1994, but not in the Norwegian Sea. It is suggested that wind-generated advection may affect recruitment in fjords on the western coast of Norway.     

Behavioural thermoregulation by subyearling fall (autumn) Chinook salmon Oncorhynchus tshawytscha in a reservoir

This study investigated behavioural thermoregulation by subyearling fall (autumn) Chinook salmon Oncorhynchus tshawytscha in a reservoir on the Snake River, Washington, U.S.A. During the summer, temperatures in the reservoir varied from 23° C on the surface to 11° C at 14 m depth. Subyearlings implanted with temperature-sensing radio transmitters were released at the surface at temperatures >20° C during three blocks of time in summer 2004. Vertical profiles were taken to measure temperature and depth use as the fish moved downstream over an average of 5·6–7·2 h and 6·0–13·8 km. The majority of the subyearlings maintained average body temperatures that differed from average vertical profile temperatures during most of the time they were tracked. The mean proportion of the time subyearlings tracked within the 16–20° C temperature range was larger than the proportion of time this range was available, which confirmed temperature selection opposed to random use. The subyearlings selected a depth and temperature combination that allowed them to increase their exposure to temperatures of 16–20° C when temperatures <16 and >20° C were available at lower and higher positions in the water column. A portion of the subyearlings that selected a temperature c. 17·0° C during the day, moved into warmer water at night coincident with an increase in downstream movement rate. Though subyearlings used temperatures outside of the 16–20° C range part of the time, behavioural thermoregulation probably reduced the effects of intermittent exposure to suboptimal temperatures. By doing so, it might enhance growth opportunity and life-history diversity in the population of subyearlings studied.     

Male signalling and lek attractiveness in the Mediterranean fruit fly

I tested the null hypothesis that females of the Mediterranean fruit fly, Ceratitis capitata, were equally likely to visit leks composed of males with high versus low mating success. In laboratory trials, the observed distribution of matings among males differed significantly from that expected by chance, owing primarily to the higher than expected numbers of individuals with low (mated 0-1 days over 6 consecutive observation days) or high (mated 4 or more days) mating scores. I termed these two groups as 'low' and 'high' maters, respectively. In the field, greater numbers of female sightings were made at artificial leks of high maters than low maters. This result apparently reflected a greater calling propensity among high maters. Slopes of female sightings versus calling level did not differ significantly between leks of low and high maters, suggesting that the observed relationship between calling activity and female sightings was independent of male mating status. Following the same protocol, I conducted a second experiment to examine whether males used the signals of conspecific males to locate lek sites and, if so, whether signal attractiveness varied with male mating ability. Attraction of males to calling conspecifics was far weaker than that observed for females, and over five different trials a total of only seven male sightings were made at any of the established leks. Copyright 2000 The Association for the Study of Animal Behaviour.     

Phenotypic sex differentiation of blue tilapia under constant and fluctuating thermal regimes and its adaptive and evolutionary implications

Oreochromis aureus exposed during the first 28 days of exogenous feeding to constant 35° C, or fluctuating temperatures (day at 35° C, night at 27° C, and vice versa) showed significantly ( P <0·05) faster growth, least size heterogeneity and better survival rates than siblings under constant 27° C. Constant high temperatures had a strong masculinizing effect (M: F sex ratios of 7·33–19·00: 1·00 v . 0·75–0·82: 1·00 in controls reared at 27° C). Fluctuating temperatures had less masculinizing potential but still produced sex ratios significantly skewed to the detriment of females (M: F sex ratios of 2·33–11·50: 1·00). This suggests that ambient temperature may have represented a sufficient environmental pressure for the selection of thermolabile sex-determinism in this species, and presumably in other Oreochromis spp. The evolutionary advantage of thermosensitivity in Oreochromis spp. is discussed, considering a framework where individual advantages oppose, to some degree, to the population or species interest.     

Effects of constant and fluctuating temperatures on life span of Aedes taeniorhynchus adults

Male and virgin female Aedes taeniorhynchus were maintained on a sugar solution at constant temperatures, at split-temperatures, and at alternating temperatures from immediately after emergence until death in order to study the effect of temperatures on their longevity. Life spans were found to be temperature dependent at constant temperatures of 22, 27, and 32°C, but they were divided into ‘ageing’ and ‘dying’ phases at split-temperatures. The rate of ageing, which was independent of temperatures, was the same in males whether they were transferred from low to high or high to low temperatures. The rate of ageing was the same in females transferred from 22°C or 27 to 32°C, but much longer than expected when transferred from 22 to 27°C. Also, the rate of ageing was the same for females transferred from 32°C to either 22 or 27°C and from 27 to 22°C. The rate of dying was essentially temperature dependent in both males and females with slight temperature compensation occurring in some cases. Life spans were the same in males when alternated between 22?27°C, 27?32°C, and 22?32°C. In females they were same at 27?32°C and 22?32°C, but were much longer than expected at 22?27°C. It is concluded that the threshold theory is confirmed when mosquitoes are maintained at split-temperatures and at alternating temperatures in their optimum range of temperatures.     

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.     

Photoperiod and temperature effects on gametogenesis in winter flounder Pseudopleuronectes americanus

The winter flounder is an in‐shore flatfish living in shallow waters on the east coast of North America from Labrador to Georgia. In the St Lawrence estuary, the reproductive season is May and June. Our objective was to test the effects of winter‐spring photoperiod and temperature conditions on the timing of sexual maturation in both males and females. Groups (16 animals each) of winter flounder breeders were maintained from mid‐January to mid‐May under five different experimental conditions: (1) natural photoperiod and temperature conditions; (2) natural photoperiod, 6° C; (3) 15L : 9D, natural temperature conditions; (4) 15L : 9D, 6° C; (5) accelerated photoperiod increase from winter to spring conditions, 6° C. Natural photoperiod and temperature conditions correspond to a gradual increase in light period from 8L : 16D (January) to 15L : 9D (May) and in temperature from −1° C (January to April) to 6° C (May). GSI and condition factor did not differ among the treatments ( P  > 0·05). In males, milt production occurred simultaneously in the different treatments and histological examination did not indicate any significant effect of either photoperiod or temperature on testes development. In females, seven stages of oocyte development were observed. Both the number of oocytes at the cortical alveoli stage and number of atretic oocytes increased at 6° C (warm temperature conditions). Overall, neither photoperiod nor temperature modified the reproductive period. Warm winter‐spring temperature conditions, however, may decrease egg numbers and egg quality.     

Ontogenetic variations of thermal optimum for growth, and its implication on thermolabile sex determination in blue tilapia

Knowledge of how the optimum temperature for growth ( T °_opt) varies during ontogeny, and how close it is to the temperatures that induce phenotypic masculinization is fundamental to the understanding of the evolution of thermolabile sex determinism (TSD) in fishes. In blue tilapia Oreochromis aureus , T °_opt is 32·6° C at the start of exogenous feeding (10mg fish) and it decreases by c . 1° C each time that the fish body mass increases by an order of magnitude. Temperatures <35° C are not sufficient to induce complete phenotypic masculinization. Based on a multiple-regression model ( r ²=0·938) plotting growth against body mass and water temperature, genotypically female tilapia living at high temperatures during the thermosensitive period (21–28 days) and being reversed into phenotypic males would incur an initial growth disadvantage over fish living at T °_opt, but not over those living at slightly colder temperatures (27–29° C). This initial disadvantage would be later compensated for by faster growth because of between-sex growth dimorphism to the detriment of phenotypic females. These arguments suggest that there is no definite pressure against the selection of TSD in blue tilapia and probably other Oreochromis spp.     

The effect of temperature, pH and medium in a surface adhesion immunofluorescent technique for detection of Listeria monocytogenes

A rapid surface adhesion-based immunofluorescence technique was used to detect Listeria monocytogenes from inoculated culture systems. The effect of culture type (pure, mixed and meat), pH (7·00, 6·40, 4·76 and 3·13), acids (citric and HCl) and temperature (25°, 30° and 37°C) on the adhesion of Listeria to the polycarbonate membrane used in this technique was determined. It was found that pH had a significant effect ( P < 0·05) with higher numbers of Listeria adhering at low pH values (4·76). Culture type was also important with significantly higher numbers of Listeria ( P < 0·05) adhering to membranes immersed in meat cultures than in pure or mixed cultures. This effect was seen at 30°C but not at 25° or 37°C. The total viable count (TVC) on the membrane was unaffected by pH but temperature had an influence with optimum adhesion occurring at 25°C. The reasons for observed differences and their implications for the surface adhesion immunofluorescent rapid method are discussed.     

Observations on mass atresia and skipped spawning in northern Atlantic cod, from Smith Sound, Newfoundland

Atlantic cod Gadus morhua were collected from Smith Sound, Newfoundland in January 1999. Visual examination of females (n=150) and males (n=126) revealed that some large fish (42–79 cm) had underdeveloped gonads. Histological examination of underdeveloped ovaries indicated that the majority of these females were undergoing mass resorption of oocytes and would not have spawned in 1999. Fish in this condition included females that were aborting their first attempt at maturation and females that had spawned the previous year but were failing to re-ripen. Somatic and liver condition were significantly lower (P<0·05) for fish undergoing mass oocyte resorption than ripening females, suggesting that the interruption in the maturation cycle may have been related to insufficient nutrient storage. In males, testes of some adult fish were considered to be non-reproductive as they showed no signs of ripening and probably would not have spawned in 1999. Liver condition was significantly higher (P<0·05) for non-reproductive males than those that were ripening. Disruptions in male and female reproductive cycles may also have been related to water temperatures that were too cold (0–0·5° C) for successful gamete development. Immature gametes (perinucleolar oocytes in females; spermatogonia in males) showed no signs of breakdown in non-reproductive individuals, suggesting that they retained the potential to develop and spawn gametes in 2000.     

Reproductive biology of Carcharhinus acronotus in the coastal waters of South Carolina

The reproductive biology of blacknose sharks Carcharhinus acronotus in the western North Atlantic Ocean was studied by examining specimens collected in the coastal waters of South Carolina. Males begin the maturation process between 875 and 910 mm fork length ( L _F), as indicated by the presence of functional claspers and siphon sacs. The presence of vitellogenic oocytes and developing oviducal glands and uteri indicated that females begin to mature at c . 870 mm L _F. Length at which 50% of the population reached maturity was 896 and 964 mm L _F, equivalent to 4·3 and 4·5 years, for males and females, respectively. Gonado‐somatic indices suggested that spermatogenesis and vitellogenesis began after December. Mating took place during the end of May and the beginning of June. Fertilization occurred during late June and early July, suggesting that female blacknose sharks were capable of sperm storage. Based on the timing of fertilization and occurrence of females carrying near‐term pups in late May and early June, the gestation period for blacknose sharks was c . 11 months. Female blacknose sharks reproduced biennially based on the absence of vitellogenic oocytes in near‐term females and there being no indication of vitellogenesis in postpartum females. Male blacknose sharks were capable of reproducing annually as indicated by turgid genital ducts, which were observed in all mature males collected during late May and early June.     

Reproductive cycles and spawning periods of two Lessepsian siganid fishes on the Lebanese coast

A total of 1048 specimens of Siganus rivulatus and Siganus luridus were collected from the Batrun area of the Mediterranean Sea from January 1999 to August 2000. The sex-ratio in both species did not differ significantly from 1 : 1 between size classes or months. For S. rivulatus , the estimated mean length at first maturity ( L _T50) was 132·5 mm for males and 136·5 mm for females, and 139·0 and 142·0 mm, respectively, for male and female S. luridus . Spawning occurred in June in S. rivulatus and from May to July in S. luridus . High temperature in summer appeared to be a limiting factor in the gonadal development of both siganid species, which have reduced their breeding seasons on the Lebanese coast compared to their native Red Sea.