Elk survival and mortality causes in the Blue Mountains of Washington

We studied survival of elk (Cervus elaphus) ≥1 yr old and quantified mortality sources in the Blue Mountains of Washington, 2003–2006, following a period of extensive poaching. The population was managed under a spike-only general hunting season, with limited permits for larger males and for females. We radiomarked 190 elk (82 males and 39 females >1 yr old and 65 males 11 months old), most with rumen transmitters and neck radiocollars; 60 elk only received rumen transmitters. We estimated annual survival using known fate models and explored survival differences among sex and age classes and in 2 potentially different vulnerability zones for males. We found little support for differences in survival between younger (2–3-yr old) and older (≥4-yr old) branch-antlered males or zone differences for yearling males. A model with zone differences for branch-antlered males was the second ranked model and accounted for 14% of the available model weight. From the best-supported models, we estimated annual survival for yearling males at 0.41 (95% CI: 0.29–0.53). We estimated pooled adult female survival at 0.80 (95% CI: 0.64–0.93); when an age-class effect was included, point estimates were higher for prime-aged females (2–11 yr: S = 0.81 [0.70–0.88]) than for older females (≥12 yr: S = 0.72 [0.56–0.83]), but confidence intervals broadly overlapped. Only 1 of 7 models with a female age effect on survival was among the competitive models. For branch-antlered males, survival ranged 0.80–0.85, depending on whether zone variation was modeled. We recorded 78 deaths of radiomarked elk. Human-caused deaths (n = 55) predominated among causes and most were of yearling males killed during state-sanctioned hunts (n = 28). Most subadult male deaths were from tribal hunting (n = 5), and most mature males died from natural causes (n = 6) and tribal hunting (n = 5). We detected few illegal kills (n = 4). Our results suggest that increased enforcement effectively reduced poaching, that unreported tribal harvest was not a trivial source of mortality, and that spike-only general seasons were effective in recruiting branch-antlered males. © 2011 The Wildlife Society.     

Age, growth and mortality of red bandfish, Cepola macrophthalma (L.), in the eastern Adriatic Sea (Croatian coast)

Age, growth and mortality were analysed for red bandfish, Cepola macrophthalma, collected in the eastern Adriatic from May 2002 to June 2003. The oldest male was estimated to be age 4, the oldest female age 3. Parameters of the von Bertalanffy growth equation are: L_∞ = 55.0 cm (SE = 0.1), K = 0.445 (SE = 0.074) and t₀ = ?0.1 (SE = 0.001) for males, and L_∞ = 48.9 cm (SE = 0.167), K = 0.395 (SE = 0.062) and t₀ = ?0.009 (SE = 0.02) for females. The overall sex ratio was 1.42 : 1 in favour of males. Total mortality, corresponding to the slope of the descending limb of the catch curve, was Z = 1.20 per year for females and Z = 1.23 per year for males. Exploitation ratios were E = 0.479 for females and E = 0.433 for males.     

Age,growth and mortality of common two‐banded seabream,Diplodus vulgaris (Geoffroy Saint‐Hilaire, 1817), in the eastern Adriatic Sea (Croatian coast)

Age, growth and mortality were analysed for the common two‐banded seabream, Diplodus vulgaris, collected in the eastern Adriatic (Croatian coast) from commercial fishery catches by ‘tramata’ fishing (2005–2006) to obtain growth estimation. The oldest female was estimated to be age 11, the oldest male age 10 years. The von Bertalanffy growth parameters estimated by reading scales were: L_∞ = 48.60 cm (SE = 1.101), K = 0.112 (SE = 0.005) and t₀ = ?2.366 (SE = 0.060) for all specimens; L_∞ = 51.96 cm (SE = 2.153), K = 0.095 (SE = 0.007) and t₀ = ?2.837 (SE = 0.120) for females and L_∞ = 56.25 cm (SE = 2.662), K = 0.084 (SE = 0.067) and t₀ = ?2.920 (SE = 0.117) for males. The overall sex ratio was 1.22 : 1 in favour of males. Total mortality, corresponding to the slope of the descending limb of the catch curve, was Z = 0.81 per year for females and Z = 0.85 per year for males. Exploitation ratios were E = 0.68 for females and E = 0.73 for males.     

Differences in Fecal Androgen Patterns of Breeding and Nonbreeding Kori Bustards (Ardeotis kori)

To better understand breeding conditions to promote reproduction in captive kori bustards, fundamental endocrine studies measuring fecal androgen metabolites in male and female kori bustards were conducted. Feces collected weekly from males and females were analyzed for testosterone using enzyme‐linked immunoassay. Results from adult males (n = 5), adult females (n = 10), immature males (n = 10), and immature females (n = 10) revealed seasonally elevated testosterone concentrations in fertile, but not nonfertile adult males and females (P > 0.05). Adult females that were not maintained in a breeding group, or that did not produce eggs, did not demonstrate increases in testosterone compared to egg laying counterparts. In males, but not females, seasonal testosterone increases were accompanied by weight gain. Peaks in male fecal androgen metabolites ranged from 10‐ to 22‐fold higher than nonbreeding season (181.5 ± 19.1 vs. 17.0 ± 0.94 ng/g; P < 0.05). Mean breeding season values for adult males were 83.6 ± 6.1 ng/g vs. nonbreeding season values of 12.3 ± 0.73 ng/g (P < 0.05). In females, average breeding season testosterone concentrations were approximately 4‐fold higher than nonbreeding season (55.9 ± 6.0 vs. 14.5 ± 1.8 ng/g), with peaks 10‐ to 30‐fold higher. Results show that noninvasive fecal androgen metabolite analysis can provide a means of predicting fertility potential of male and female kori bustards and might be utilized to assess effects of modifying captive environments to promote reproduction in this species. Zoo Biol. 32:54‐62, 2013. © 2012 Wiley Periodicals, Inc.     

Teeth emergence in wild olive baboons in Kenya and formulation of a dental schedule for aging wild baboon populations

Teeth emergence schedules are presented from analysis of 95 wild olive baboons Papio anubis (age range 2–120 months) and compared to recently published results for wild and captive yellow baboons (P. cynocephalus; Phillips-Conroy and Jolly: American Journal of Primatology 15:17–29, 1988). Age at emergence of M1 (20.5 months males, 19.5 months females), I1 (32.5 and 33.5 months) and I2 (40.0 and 39 months) of olive baboons was earlier than in the wild yellow baboons and similar to captive yellow baboons. However, the later emerging teeth were delayed considerably relative to the captive animals and were similar in age of emergence to those of wild yellow baboons. Considerable variation in age of emergence occurred in the later emerging teeth especially among males. Regression analysis of dental scores with age demonstrated differences between olive baboons and captive yellow baboons but not between olive baboons and wild yellow baboons. Combined data on dental scores for wild yellow, olive, and hamadryas baboons provide schedules of AGE (months) = {SCORE – 11.79} ÷ 0.4405 and AGE (months) = {SCORE – 11.24} ÷ 0.4797 for males and females, respectively, which may be used for aging wild baboons. Full permanent dentition in wild baboons is predicted to occur over 1 year later than in captive animals.     

Reproductive Parameters of Female<Emphasis Type="Italic">Pan paniscus</Emphasis> and <Emphasis Type="Italic">P. troglodytes</Emphasis>: Quality versus Quantity

We investigated intra- and interspecific differences in life history and reproductive parameters in bonobos (Pan paniscus) and chimpanzees (Pan troglodytes). We compare the parameters of wild and captive females in order to shed light on the influence of habitat or specific differences or both on reproduction. We present new and additional information on reproductive parameters from captive bonobos and chimpanzees. Captive chimpanzees birth more live offspring and have a shorter interbirth interval, but experience higher infant mortality than captive bonobos. Although captive bonobo females tend to start reproduction at a younger age than chimpanzees, this is effectively only so for wild-born females of both species. Ultimately both species reach the same rate of production of offspring surviving to 5 yr. These results contrast with data from the wild. Wild bonobos tend to have higher reproductive success, a higher fertility rate and a shorter interbirth interval than wild chimpanzees. Reproduction is similar for wild and captive bonobos, which suggests that they are producing at their maximum under both conditions. Overall captive chimpanzees perform better than their wild conspecifics, probably because of lower feeding competition. Infant survival is the only specific difference not affected by captivity. Bonobo infants survive better, which suggests that chimpanzee infants are more at risk. We argue that the interspecific variation in reproductive parameters in captivity is related to the different influence of captivity on reproduction and different pressures of external sources of infant and juvenile mortality.     

Development of guidelines for assessing obesity in captive chimpanzees (Pan troglodytes)

Many captive chimpanzees (Pan troglodytes) are subjectively considered to be overweight or obese. However, discussions of obesity in chimpanzees are rare in the literature, despite the acknowledged problem. No study to date has systematically examined obesity in captive chimpanzees. This project develops guidelines for defining obesity in captive chimpanzees through the examination of morphometric and physiologic characteristics in 37 adult female and 22 adult male chimpanzees. During each animal's biannual physical exam, morphometric data was collected including seven skinfolds (mm), body mass index (BMI), waist‐to‐hip ratio (WHR), and total body weight (kg). The morphometric characteristics were correlated with triglycerides and serum glucose concentration, to test the utility of morphometrics in predicting relative obesity in captive chimpanzees. Abdominal skinfold (triglyceride: F=3.83, P=0.05; glucose: F=3.83, P=0.05) and BMI (triglyceride: F=10.42, p=0.003; glucose: F=6.20, P=0.02) were predictive of increased triglycerides and serum glucose in females; however no morphometric characteristics were predictive of relative obesity in males. Results suggest that no males in this population are overweight or obese. For females, there were additional significant differences in morphometric (skinfolds, BMI, WHR, total body weight) and physiologic measurements (systolic and diastolic blood pressure, red blood cells) between individuals classified overweight and those classified non‐overweight. Skinfold measurements, particularly abdominal, seem to be an accurate measure of obesity and thus potential cardiovascular risk in female chimpanzees, but not males. By establishing a baseline for estimated body fat composition in female captive chimpanzees, institutions can track individuals empirically determined to be obese, as well as obesity‐related health problems. Zoo Biol 0:1–12, 2007. © 2007 Wiley‐Liss, Inc.     

The locus Om,responsible for the DDK syndrome,maps close to Sigje on mouse Chromosome 11

The DDK inbred strain of mouse has a striking particularity: when DDK females are crossed to males of other strains they exhibit a reduced fertility, whereas the reciprocal crosses (non-DDK females x DDK males) are fertile (Wakasugi et al. 1967; Wakasugi 1973). The low fertility results from an early embryonic lethality, the F₁ embryos dying near the late morula-early blastocyst stage. Genetic analyses (Wakasugi 1974) and nuclear and cytoplasmic transfers (Renard and Babinet 1986; Babinet et al. 1990; Mann 1986), have shown that the failure of the embryos to develop is due to an incompatibility between a DDK maternally encoded cytoplasmic product and the non-DDK paternal genome. In order to elucidate the genetic determinism of this embryonic lethality, we have analyzed the fertility of male progeny from a backcross BALB/c females x (BALB/c x DDK)F₁ males and that of males from a set of recombinant inbred (RI) strains, established from DDK and BALB/c progenitors, when mated with DDK females. Our results indicate that a single locus, Om, is responsible for the DDK syndrome and is located on Chromosome (Chr) 11, very close to the Sigje locus.     

Comparison of techniques for sex determination of American martens

Accurate determination of sex in harvested species is critical for understanding demography and developing population models for management. We used genetic-based sex identification to assess accuracy of external carcass and pelt examination at registration and maximum canine root area (MRA) to determine sex of American martens (Martes americana) trapped in the Upper Peninsula of Michigan, 2000–2004. Overall percent similarity between MRA and genetic-based sex determination was 98.4% (n = 188). In contrast, only 84.6% (n = 421) of martens were similarly classified using external examination. For external examination, percent similarity to genetic-based sex determination for juveniles (<1-yr old) and adults (≥1-yr old; Wald χ²₁ = 2.168, P = 0.141), as well as for males and females (Wald χ²₁ = 0.005, P = 0.946), was similar. We recommend MRA as a suitable technique for sex determination of martens; thus, marten sex and age (using cementum annuli counts) can be obtained from one lower canine tooth. We do not recommend use of external examination at registration to identify sex of martens without implementing additional quality assurance measures. © 2010 The Wildlife Society.     

Some biological parameters of the Mediterranean sand smelt Atherina (Atherina) hepsetus, Linnaeus, 1758 (Pisces: Atherinidae) from the middle eastern Adriatic (Croatian coast)

Data on the length–weight relationship, age, growth, sex ratio and mortality were analysed for the Mediterranean sand smelt, Atherina (Atherina) hepsetus L. (total = 2805; males = 1258; females = 1547) collected in the eastern middle Adriatic island area during the reproductive period (February to April) in 2002. The total length of sampled specimens ranged from 3.8 to 14.5 cm and the weight from 0.28 to 22.39 g. The overall sex ratio was 1.23 : 1 in favour of females, significantly different from the expected 1 : 1 ratio (χ² = 29.76; P < 0.05). All individuals >13.4 cm were females. The oldest collected male and female specimens were 5 years old. The von Bertalanffy growth formula was estimated for females (L_∞ = 15.79 (1−e^{−0.43(t+0.049)}) and males (L_∞ = 15.25 (1−e^{−0.43(t+0.018)}). The power values (b) of the length–weight relationship were very similar for both sexes (b = 3.14) and indicated a slightly allometric growth. The instantaneous rates of mortality for all collected fish were Z = 1.44 year⁻¹; M = 0.94 year⁻¹ and F = 0.50 year⁻¹. The exploitation ratio was E = F/Z = 0.35. The value for M is highly uncertain, however, as well as those values for F and E.     

Basic characteristics of the population dynamic and state of exploitation of Moroccan white seabream Diplodus sargus cadenati (Sparidae) in the Canarian archipelago

Moroccan white seabream Diplodus sargus cadenati (n = 603) were caught off the Canary Islands from April 2000 to March 2001. Total length ranged from 46 to 404 mm. The subspecies was characterized as being dygynous with partial protandry. Overall ratio of males to females was 1 : 2.9. The reproductive season extended from December to May, with a peak in spawning activity in January–February. Fifty per cent maturity was reached at 201 mm total length in males and 216 mm in females. The length–weight relationship for all individuals was described by the following parameters: a = 0.000023, and b = 2.96, when length is given in millimeters and weight in grams. Fish of 0–12 years in age were found. The von Bertalanffy growth parameters for the entire population were: L_∞ = 467 mm, k = 0.143 year^?1 and t₀ = ?2.14 year. Growth parameters differed between males and females. For all fish, instantaneous rates of mortality were Z = 0.68 year^?1, M = 0.31 ± 0.6 year^?1 and F = 0.37 ± 0.6 year^?1; the exploitation ratio was E = 0.54 ± 0.9. Length at first capture for all individuals was 173 mm. The stock exploited above is an assumed optimum.     

Male-biased sex ratios,female promiscuity,and copulatory mate guarding in an aggregating tropical bug,Dysdercus bimaculatus

The ecological and social bases of the mating system of the seed-feeding bug, Dysdercus bimaculatus(Hemiptera: Pyrrhocoridae), were studied in the lab and in aggregations at the host tree, Sterculia apetala(Malvales: Malvaceae), in Panama. On theoretical grounds, two factors are predicted to be of importance in determining the evolution of male mating tactics in Ms species: the operational sex ratio and the probability that undefended females will mate with other males, subjecting the gametes of deserters to sperm competition. Results of a study of a related species suggested that sperm displacement is probably substantial. Adult sex ratios at numerous sites were significantly male biased, and females whose mates were removed remated before oviposition (i. e., sperm utilization). These results predict that a mate defense tactic is likely to be superior to a nondefense tactic. The biological significance of the parameters is supported by observations that captive pairs often remained in copulafor several days, until just before oviposition. However, substantial variation in copulation duration was also observed, and possible causes of this variation are considered. Causes of male biased adult sex ratios were investigated by monitoring demographic changes within a single aggregation over 2 months. Both female juvenile and adult mortality rates were greater than male. In addition, dissections of reproductive adults showed that the flight muscles of females, but not males, had histolyzed, so that female reproduction is physiologically limited to a single site. Greater rates of immigration among both mature and young males suggests that an excess of males may also be found in the populations of bugs that subsequently colonize other host plants, so that female scarcity is typical of aggregations in all stages of development. The evolution of sex-limtied flight muscle histolysis may be explained by greater patchiness of females than males as mating resources, plus a lower energetic benefit/cost ratio of histolysis for males.     

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.     

Sublethal effects of spirodiclofen on life history and life-table parameters of two-spotted spider mite (<Emphasis Type="Italic">Tetranychus urticae</Emphasis>)

Laboratory bioassays were conducted to evaluate the effects of spirodiclofen on life history and life-table parameters of two-spotted spider mite (Tetranychus urticae Koch) females treated at pre-ovipositional period with a series of acaricide concentrations starting with the concentration discriminative for eggs and immatures i.e. the lowest concentration that causes 100% mortality of those stages. After a 24 h exposure, the proportion of females that survived treatments was 0.71 (6 mg/l), 0.51 (12 mg/l), 0.41 (24 mg/l), 0.30 (48 mg/l) and 0.25 (96 mg/l). At the end of the trial, the survival rate of females treated with the lowest concentration was significantly lower than the survival rate of untreated females but it remained above that of females treated with higher concentrations. Total fecundity/fertility significantly decreased as concentrations of spirodiclofen increased. Viable eggs were laid by females treated with 6, 12 and 24 mg/l, and total fertility was reduced by 42, 84 and 97%, respectively. Compared with control, the gross fecundity/fertility of the treated females was significantly reduced throughout the trial, except in females treated with 6 mg/l. All concentrations caused a significant reduction in the net fecundity/fertility throughout the trial. The females treated with 12 mg/l had significantly reduced net reproductive rate (R ₀ = 6.45), compared to females treated with 6 mg/l (R ₀ = 23.35) and to untreated females (R ₀ = 28.92); there was no significant difference between the last two treatments. The intrinsic rate of increase (r _m ) and finite rate of increase (λ) were significantly reduced in treated females (r _m = 0.141, λ = 1.156 and r _m = 0.214, λ = 1.232; 12 and 6 mg/l, respectively), compared to control (r _m = 0.251, λ = 1.276). The reduction was significantly greater in females treated with the highest concentration. As a result of the lowered r _m , the doubling time in treated females was significantly extended. Sublethal effects of spirodiclofen and its impact on T. urticae management are discussed.     

Aging and Loss of Fertility in Male and Female Brachionus plicatilis (Rotifera)

Summary

The decline with age of mictic female susceptibility to fertilization and male capacity for fertilization is characterized for the rotifer Brachionus plicatilis. All mictic females were susceptible to fertilization until age 4 hr. Susceptibility then declined non-linearly according to the quadratic equation Y = 140.6—14.3X + 0.36X ². By age 24 hr, sexual females no longer could be fertilized. Only 83% of newborn males were capable of fertilization. This level of fertility held until age 8 hr, then declined linearly. The age when 50% of individuals were no longer fertile was termed the length of fertilizability ₅₀(LF₅₀) and is 7.9 hr (16.7% of lifespan) and 18.8 hr (26.1% of lifespan) for females and males, respectively. Newborn males had an average of 30.1 ± 1.40 motile sperm. Males transferred a mean of 2.3 motile sperm into the pseudocoelom of females on each insemination. Sperm inseminated per copulation closely corresponds to the mean number of resting cysts produced by fertilized females. It is not likely that resting cyst production is limited by sperm availability.     

Artificial insemination of captive European brown hares (Lepus europaeus PALLAS, 1778) with fresh and cryopreserved semen derived from free-ranging males

This study aimed to establish artificial insemination (AI) protocols to predictably initiate pregnancy during the breeding season in the European brown hare (EBH) (Lepus europaeus PALLAS, 1778). Semen was collected from seven captive and eight free-ranging males by means of electroejaculation. Semen from the free-ranging males was cryopreserved using directional freezing. Total motility/integrity of fresh and frozen-thawed semen was 91.6%/87.7% and 46.9%/53.8%, respectively. Ovulation was induced in ultrasonographically preselected females using a gonadotropin-releasing hormone analogue. Each female was inseminated with 1 mL fresh (Group A, n = 16) or frozen-thawed semen (Group B, n = 9) at a concentration of 100 × 10⁶ spermatozoa/mL. The use of ultrasonography (10 to 22 MHz) confirmed the intracervical semen deposit, the success of artificial ovulation induction (formation of postovulatory corpus luteum), and permitted the monitoring of individual pregnancies. Although sperm motility/integrity was significantly different between groups, no significant difference was detected in conception rates (A, 87.50%; B, 77.78%). Because of embryonic resorption, there was a slight difference in fertility rate between groups (A, 62.5%; B, 77.78%). Overall, AI in captive EBH using fresh and frozen-thawed semen achieved successful fertility rates. Long-term cryopreserved semen was used to bring new genetic material from the wild into a genetically limited captive population without extensive animal transport. Therefore, AI has the potential to enhance breeding programs for EBH especially when cryopreserved semen from wild donors is used.     

Importance of multiple mating to female reproductive output in Diaphorina citri

Abstract The importance of multiple mating to female reproductive output in Diaphorina citri Kuwayama (Hemiptera: Psyllidae) is evaluated by grouping individual females with one or three males for 24 h (short duration) or 2 weeks (long duration) and examining oviposition over 18–19 days. For the short‐duration treatments, females lay more eggs per day when grouped with multiple males, whereas females in the long‐duration treatments lay more eggs when paired with one male. When held for 24 h with one or three males, females show a decline in fecundity beginning 10 and 15 days after mating, respectively. Total fecundity is relatively high for females paired with one male for 2 weeks, but fecundity is low and mortality high when females are held with three males for 2 weeks. In treatments in which females are held with males for 2 weeks, oviposition increases dramatically in the days after removal of males. For females paired with a male for 24 h and re‐paired for 24 h, 9 days later, fecundity remains high throughout the 18–19‐day observation period. Egg fertility does not differ among treatments, but varies over time in a manner that is similar among treatments. The present study demonstrates that, in D. citri, females require multiple matings over time to achieve high reproductive output, but oviposition is constrained by the presence of males.     

Generalized stable population theory

In generalizing stable population theory we give sufficient, then necessary conditions under which a population subject to time dependent vital rates reaches an asymptotic stable exponential equilibrium (as if mortality and fertility were constant). If x ₀(t) is the positive solution of the characteristic equation associated with the linear birth process at time t, then rapid convergence of x ₀(t) to x ₀ and convergence of mortality rates produce a stable exponential equilibrium with asymptotic growth rate x ₀–1. Convergence of x ₀(t) to x ₀ and convergence of mortality rates are necessary. Therefore the two sets of conditions are very close. Various implications of these results are discussed and a conjecture is made in the continuous case.     

Growth and derived life-history characteristics of the Brazilian electric ray Narcine brasiliensis

The majority of batoids are listed as Threatened (20.4%) or Data Deficient (41%) by the IUCN Red List. A key challenge to assessing Data-Deficient species is obtaining estimates of key life-history characteristics. Here, a Bayesian approach was used to estimate derived life-history characteristics from a growth model applied to the Data-Deficient Brazilian electric ray Narcine brasiliensis. The age of 170 specimens (107 females, 63 males) was estimated from vertebral centra, and total length, disc width, total weight and birth size were used in a joint estimation of sex-specific length-weight models and two-dimensional von Bertalanffy growth models. Estimates of age at length zero, age at maturity, longevity and mortality at age were derived simultaneously. The Bayesian joint modelling approach was robust to small sample sizes by adding a likelihood to constrain L₀ and sharing parameters, such as Brody growth coefficient between length measurements. The median growth parameter estimates were a shared L₀ = 38.8 mm, female L_∞ = 515 mm, 𝑘 = 0.125 and male L_∞ = 387 mm, 𝑘 = 0.194. Age at maturity was estimated to be 7.40–7.49 years for females and 4.45–4.47 years for males, whereas longevity was 22.5–22.6 years for females and 14.2 years for males depending on length measurement. Age-1 natural mortality was estimated to be 0.199–0.207 for females and 0.211–0.213 for males. The derived life-history characteristics indicate N. brasiliensis is earlier maturing, but slower growing relative to other Torpediniformes. These characteristics along with the species’ endemism to southern Brazil and high by-catch rates indicate that one of the IUCN Red List threatened categories may be more appropriate for the currently Data-Deficient status. The Bayesian approach used for N. brasiliensis can prove useful for utilizing limited age-growth data in other Data-Deficient batoid species to inform necessary life characteristics for conservation and management.     

Life history of the red-banded seabream Pagrus auriga (Sparidae) from the coasts of the Canarian archipelago

Red‐banded seabream Pagrus auriga (N = 615) were caught off the Canary Islands from January 2003 to December 2004. Total length ranged from 120 to 780 mm. The species was characterized by protogynous hermaphroditism. The male :female ratio was in favour of females (1 : 8.2). The reproductive season extended from September to February, with a peak in spawning activity in October–November. Fifty percentage maturity was reached at 387 mm total length by females and 533 mm by males. The length–weight relationship for all individuals was described by the parameters: a = 0.0086 and b = 3.014, when length is given in mm and weight in grams. Otolith age readings indicated that the population consists of 19 age groups, including a very high proportion of individuals between 0 and 7 years old. Growth analysis reveals that the species is slow‐growing and relatively long lived (18 years). The von Bertalanffy growth parameters for the entire population were: L_∞ = 803 mm, k = 0.081 year⁻¹ and t₀ = −2.17 year. Growth differed between males and females. The instantaneous rate of natural mortality for all fish was: M = 0.164 year⁻¹.