A simple age verification method is presented for centrum edge analysis (CEA) of elasmobranch species. In this method, a binomial model is linked with a von Mises distribution for circular data, taking the characteristics of the CEA data into account. The periodicity of growth band pairs is categorized as no cycle, an annual cycle, or a biannual cycle. Three models are then constructed according to different periodicities. We use the Akaike information criterion (AIC) to determine which model is the best. The models were applied to the shortfin mako shark ( Isurus oxyrinchus ) data collected in the North Pacific to identify the best periodicity model. The AIC best-fitting model was one involving an annual cycle. The general performance of the method was evaluated using simulated data of various sample sizes, formation times, and durations of growth band pairs. The simulation trials showed that the performance of the method was satisfactory with moderate sample sizes. This method should improve the accuracy of age determination and could be applied to all species that have periodic growth band pairs.

We determined the age and growth rates of male and female shortfin makos, (Isurus oxyrinchus), from the western and central North Pacific Ocean. Growth band pairs were counted on half-cut vertebral centra using a shadowing method. In this method, we focused on the ridges on the surface of the centra, consisting of a convex and concave structure. After comparing four enhancing methods, we decided on the use of shadowing method for aging. Vertebrae from 128 males and 147 females were examined. The centrum edge analysis suggested annual band pair formation. Von Bertalanffy growth curves were fitted separately to the length-at-age data for males and females with birth length fixed. Until approximately 7 years of age, both sexes showed similar growth rates; thereafter, males showed a significantly slower growth rate compared to females. It was suggested males and females mature at approximately 6 years and 16 years, respectively. These life-history characteristics suggest relatively low productivity for this species, which agrees with reports on populations in other geographic regions.

Shortfin mako, Isurus oxyrinchus, is a highly migratory shark with a worldwide distribution. Despite recent global concern and intensive ecological studies on this species, little is known about its reproduction, owing to a paucity of information on mature females. We investigated the size-at-maturity and reproductive traits of shortfin mako in the western and central North Pacific. Males attain maturity at a much smaller size (156 cm) than females (256 cm). The positive relationship between maternal size and litter size indicates that fecundity increases as the female grows. The seasonal trends in the gonadosomatic index of mature individuals and the presence of females in early pregnancy confirmed that mating occurs from spring to summer. From monthly changes in embryonic body lengths, averaged per litter, and the seasonal occurrence of neonates, we infer that parturition occurs from winter to spring and the gestation period is 9–13 months. There was a negative correlation between embryonic developmental stages and environmental temperature for females in various stages of pregnancy. The productivity of this species may be higher than previously thought, considering the estimated gestation period and size-related fecundity.

This paper proposes a new and flexible statistical method for marginal increment analysis that directly accounts for periodicity in circular data using a circular-linear regression model with random effects. The method is applied to vertebral marginal increment data for Alaska skate Bathyraja parmifera. The best fit model selected using the AIC indicates that growth bands are formed annually. Simulation, where the underlying characteristics of the data are known, shows that the method performs satisfactorily when uncertainty is not extremely high.

We evaluated the behavior of skipjack (Katsuwonus pelamis), yellowfin (Thunnus albacares) and bigeye tuna (T. obesus) associated with drifting fish aggregating devices (FADs) in the equatorial central Pacific Ocean. A total of 30 skipjack [34.5–65.0 cm in fork length (FL)], 43 yellowfin (31.6–93.5 cm FL) and 32 bigeye tuna (33.5–85.5 cm FL) were tagged with coded transmitters and released near two drifting FADs. At one of the two FADs, we successfully monitored the behavior of all three species simultaneously. Several individuals remained around the same FAD for 10 or more days. Occasional excursions from the FAD were observed for all three species, some of which occurred concurrently for multiple individuals. The detection rate was higher during the daytime than the nighttime for all the species, and the detection rate for bigeye tuna was higher than for yellowfin or skipjack tuna. The swimming depth was deeper during the daytime than nighttime for all species. The fish usually remained shallower than 100 m, but occasionally dived to around 150 m or deeper, most often for bigeye and yellowfin tuna during the daytime. The swimming depth for skipjack tuna was shallower than that for bigeye and yellowfin tuna, although the difference was not large, and is probably not sufficient to allow the selective harvest of skipjack and yellowfin tuna by the purse seine fishery. From the detection rate of the signals, bigeye tuna is considered to be more vulnerable to the FAD sets than yellowfin and skipjack tuna.

This article documents the addition of 139 microsatellite marker loci and 90 pairs of singlenucleotide polymorphism sequencing primers to the Molecular Ecology Resources Database. Loci were developed for the following species: Aglaoctenus lagotis, Costus pulverulentus, Costus scaber, Culex pipiens, Dascyllus marginatus, Lupinus nanus Benth, Phloeomyzus passerini, Podarcis muralis, Rhododendron rubropilosum Hayata var. taiwanalpinum and Zoarces viviparus. These loci were cross-tested on the following species: Culex quinquefasciatus, Rhododendron pseudochrysanthum Hay. ssp. morii (Hay.) Yamazaki and R. pseudochrysanthum Hayata. This article also documents the addition of 48 sequencing primer pairs and 90 allele-specific primers for Engraulis encrasicolus. et al.

The reproductive biology of the blue shark (Prionace glauca) in the western North Pacific Ocean was investigated to contribute to future stock assessments because of limitations of recent studies and the lack of information about the reproductive cycle. Reproductive data were obtained from 490 males (precaudal length (PCL), 33.4–252.0cm) and 432 females (PCL, 33.4–243.3cm). Size at 50% maturity was estimated to be 160.9cm for males and 156.6cm PCL for females. Litter size varied from 15 to 112 (mean 35.5) and was positively correlated with maternal PCL. Parturition, ovulation and mating occurred sequentially from spring to summer. The gestation period was estimated to be 11 months. The ovarian follicles of pregnant females developed synchronously throughout the gestation period along with embryonic growth, indicating that females reproduce annually. Our results showed that the productivity of North Pacific blue sharks is higher than previously thought, based on larger fecundity and a shorter reproductive cycle. These new findings will improve future stock assessments and provide management advice.

Longline surveys have been conducted in the Northwest Pacific Ocean from 2000 to 2014 using chartered commercial longline vessels. Each year, two cruises were conducted offshore of northeastern Japan from mid‐April to mid‐June. For each longline set during the surveys, onboard scientists collected detailed biological information about the species caught, such as the size and sex, and recorded the catch numbers for all species. Blue shark (Prionace glauca) and shortfin mako (Isurus oxyrinchus) have eurythermal distributions, but the application of a generalized additive model (GAM) showed that the sea surface temperatures (SSTs) at catch sites positive for shortfin mako were warmer than those for blue shark. On the basis of the GAM, the probabilities of occurrence of both sharks differed by size category: small sharks had a narrower SST range than that of large sharks. Most catches of both sharks were juveniles, and the nominal catch rate of blue shark was more than 10 times that of shortfin mako. The standardized catch per unit effort (CPUE) for both species was calculated using a generalized linear model (GLM) with negative binomial errors, or a delta‐lognormal GLM. The standardized CPUE for blue shark in the second quarter of the year peaked in the mid‐2000s and then decreased, but it has been increasing since 2012. The CPUE for shortfin mako in the second quarter generally increased, with fluctuations.