Relative pleopod length as an indicator of size at sexual maturity in slipper (Scyllarides squammosus) and spiny Hawaiian (Panulirus marginatus) lobsters

Body size at gonadal maturity is described for females of the slipper lobster (Scyllarides squammosus) (Scyllaridae) and the endemic Hawaiian spiny lobster (Panulirus marginatus) (Palinuridae) based on microscopic examination of histological preparations of ovaries. These data are used to validate several morphological metrics (relative exopodite length, ovigerous condition) of functional sexual maturity. Relative exopodite length (“pleopod length”) produced consistent estimates of size at maturity when evaluated with a newly derived statistical application for estimating size at the morphometric maturation point (MMP) for the population, identified as the midpoint of a sigmoid function spanning the estimated boundaries of overlap between the largest immature and smallest adult animals. Estimates of the MMP were related to matched (same-year) characterizations of sexual maturity based on ovigerous condition — a more conventional measure of functional maturity previously used to characterize maturity for the two lobster species. Both measures of functional maturity were similar for the respective species and were within 5% and 2% of one another for slipper and spiny lobster, respectively. The precision observed for two shipboard collection series of pleopod-length data indicated that the method is reliable and not dependent on specialized expertise. Precision of maturity estimates for S. squammosus with the pleopod-length metric was similar to that for P. marginatus with any of the other measures (including conventional evidence of ovigerous condition) and greatly exceeded the precision of estimates for S. squammosus based on ovigerous condition alone. The two measures of functional maturity averaged within 8% of the estimated size at gonadal maturity for the respective species. Appendage-to-body size proportions, such as the pleopod length metric, hold great promise, particularly for species of slipper lobsters like S. squammosus for which there exist no other reliable conventional morphological measures of sexual maturity. Morphometric proportions also should be included among the factors evaluated when assessing size at sexual maturity in spiny lobster stocks; previously, these proportions have been obtained routinely only for brachyuran crabs within the Crustacea.

Offshore Migratory Corridors and Aerial Photogrammetric Body Length Comparisons of Southbound Gray Whales, Eschrichtius robustus, in the Southern California Bight, 1988–1990

Through most of their annual migration, gray whales, Eschrichtius robustus, remain within 10 km of shore, but in the Southern California Bight many individuals migrate much farther from shore. This paper summarizes aerial survey and photogrammetric efforts to determine body lengths and temporal and spatial distributions of migratory gray whales in the southern portion of the Southern California Bight. Aerial surveys were flown along 13 east–west transects between lat. 32°35′N and 33°30′N during the southbound gray whale migratory seasons of 1988–90 in the Southern California Bight. Photogrammetry was used to obtain body length estimates of animals during some of the surveys. A total of 1,878 whales in 675 groups were sighted along 25,440 km of transect distance flown and 217 body lengths were measured. Using position and heading data, three major migratory pathways or corridors in the southern portion of the bight are defined. Those migrating offshore were split almost evenly between two corridors along the west sides of Santa Catalina and San Clemente Islands. These corridors converge on the mainland coast between San Diego and the United States–Mexico border. No whales larger than 11.5 m were photographed within 30 km of the mainland coast, suggesting that smaller, and presumably younger, whales use the coastal migratory corridor through the California Bight.

Length-weight Relationships of Dolphinfish, Coryphaena hippurus, and Wahoo, Acanthocybium solandri: Seasonal Effects of Spawning and Possible Migration in the Central North Pacific

Weight-on-length (W-L) relationships for 2,482 dolphinfish, Coryphaena hippurus, and 1,161 wahoo, Acanthocybium solandri, were examined. Data on fork length, whole (round) weight, and sex were collected for dolphinfish at the Honolulu fish auction from March 1988 through November 1989. Unsexed weight and length data for wahoo were collected at the auction from July 1988 through November 1989. We also used sex specific weight and length data of 171 wahoo collected during 1977–1985 research cruises for analysis. Coefficients of W-L regressions were significantly different between the sexes for dolphinfish. Coefficients did not significantly differ between the sexes for wahoo based on research cruise data. In a general linear model evaluating month as a categorical factor, month was significant for female dolphinfish, male dolphinfish, and wahoo with sexes pooled. W-L and length-on-weight (L-W) relationships were fitted by nonlinear regression for all dolphinfish, female dolphinfish, male dolphinfish, and all wahoo sexes pooled. W-L relationships for monthly samples of female dolphinfish, male dolphinfish, and all wahoo with sexes pooled were also fitted by nonlinear regression. Predicted mean weight at length for wahoo was highest at the beginning of the spawning season in June and lowest after the spawning season in September. Maximum and minimum predicted mean weight at length for both sexes of dolphinfish did not correspond with the peak spawning period (March–May). Plausible migration models in conjunction with reproductive behavior were examined to explain the variability in monthly predicted mean weight at length for dolphinfish.

Comparison of Standard Length, Fork Length, and Total Length for Measuring West Coast Marine Fishes

Measurements of adult marine fishes on the U.S. west coast are usually made using one of three methods: standard length, fork length, or total length. Each method has advantages and disadvantages. In this paper we attempt to determine whether one method is faster and/or more reliable than the other methods. We found that all three methods were comparable. There was no appreciable difference in the time it took to measure fish using the different methods. Fork length had the most reproducible results; however, it had the highest level of bias between researchers. We therefore suggest that selection of measurement type be based on what other researchers have used for the species under study. The best improvement in measurement reliability probably occurs by adequate training of personnel and not type of measurement used.

Efeito do reforço estrutural em cimentos de ionômero de vidro com fibras de vidro em restaurações classe II de molares decíduos: estudo in vitro

Os objetivos deste estudo foram medir o efeito do reforço estrutural com a adição de fibras de vidro, na resistência ao teste de tração diametral e no selamento marginal de restaurações classe II com cimento de ionômero de vidro em molares decíduos. Fibras de vidro foram incorporadas ao pó do cimento de ionômero de vidro (CIV) na concentração de 40%. As fibras usadas foram do tipo E com comprimentos que variavam de 50m a 210m. A propriedade mecânica foi verificada através do teste de tração diametral, após 15 minutos, 24 horas e 15 dias de estocagem em água. Corpos de prova foram preparados com as dimensões de 4x8 mm para cada intervalo de tempo de acordo com as normas do fabricante e padrões internacionais. Para o teste de microinfiltração foram usados segundos molares decíduos hígidos, onde foram preparadas cavidades classe II padronizadas em dois grupos: a) controle com CIV Ketac Molar Easymix (3M/ESPE); e b) teste Ketac Molar Easymix (3M/ESPE); reforçado com fibras. Estes dentes foram restaurados e deixados em água por 24h e, a seguir, imersos em solução de nitrato de prata a 50% pelo mesmo período. Para que houvesse a precipitação de sais de prata os dentes foram colocados em solução reveladora de radiografias por 15 minutos. Para analisar a microinfiltração os espécimes foram seccionados na direção mesio-distal obtendo duas amostras de observação para cada cavidade restaurada. Os resultados do teste mecânico foram analisados através dos testes de variância ANOVA e de múltiplas variáveis de Tukey. Os resultados da microinfiltração foram analisados através do teste de MANN-WHITNEY. Com a metodologia empregada foi possível concluir que houve aumento dos valores de tração diametral no CIV com a adição de fibras de vidro. Para os intervalos de 24 horas e 15 dias, o CIV reforçado com fibras apresentou valores de tração diametral superiores àqueles do CIV não reforçado, havendo diferença significativa estatística (p<0,05) para os intervalos testados. No teste de microinfiltração os grupos mostraram valores semelhantes de infiltração marginal. A adição das fibras de vidro tipo E aumentou a resistência à tração diametral do CIV testado em relação ao grupo controle e as fibras de vidro não alteraram a adesão do cimento reforçado.

Age and length composition of Columbia Basin chinook, sockeye, and coho salmon at Bonneville Dam in 2001

In 2001, representative samples of adult Columbia Basin chinook (Oncorhynchus tshawytscha), sockeye (O. nerka), and coho salmon (O. kisutch) populations at Bonneville Dam were collected. Fish were trapped, anesthetized, sampled for scales and biological data, revived, and then released adult migrating salmonids. Scales were examined to estimate age composition; the results contributed to an ongoing database for age class structure of Columbia Basin salmon populations. Based on scale analysis of chinook salmon, four-year-old fish (from brood year [BY] 1997) comprised 88% of the spring chinook, 67% of the summer chinook, and 42% of the Bright fall chinook salmon population. Five-year-old fish (BY 1996) comprised 9% of the spring chinook, 14% of the summer chinook, and 9% of the fall chinook salmon population. The sockeye salmon population at Bonneville was predominantly four-year-old fish (81%), with 18% returning as five-year-olds in 2001. The coho salmon population was 96% three-year-old fish (Age 1.1). Length analysis of the 2001 returns indicated that chinook salmon with a stream-type life history are larger (mean length) than the chinook salmon with an ocean-type life history. Trends in mean length over the sampling period for returning 2001 chinook salmon were analyzed. Chinook salmon of age classes 0.2 and 1.3 show a significant increase in mean length over time. Age classes 0.1, 0.3, 0.4, 1.1, 1.2, and 1.4 show no significant change over time. A year class regression over the past 12 years of data was used to predict spring, summer, and Bright fall chinook salmon population sizes for 2002. Based on three-year-old returns, the relationship predicts four-year-old returns of 132,600 (± 46,300, 90% predictive interval [PI]) spring chinook and 44,200 (± 11,700, 90% PI) summer chinook salmon for the 2002 runs. Based on four-year-old returns, the relationship predicts five-year-old returns of 87,800 (± 54,500, 90% PI) spring, 33,500 (± 11,500, 90% PI) summer, and 77,100 (± 25,800, 90% PI) Bright fall chinook salmon for the 2002 runs. The 2002 run size predictions should be used with caution; some of these predictions are well beyond the range of previously observed data.

Age and length composition of Columbia Basin chinook, sockeye, and coho salmon at Bonneville Dam in 2000

In 2000, representative samples of adult Columbia Basin chinook (Oncorhynchus tshawytscha), sockeye (O. nerka), and coho salmon (O. kisutch), populations were collected at Bonneville Dam. Fish were trapped, anesthetized, sampled for scales and biological data, allowed to revive, and then released. Scales were examined to estimate age composition and the results contribute to an ongoing database for age class structure of Columbia Basin salmon populations. Based on scale analysis, four-year-old fish (from brood year (BY) 1996) were estimated to comprise 83% of the spring chinook, 31% of the summer chinook, and 32% of the upriver bright fall chinook salmon population. Five-year-old fish (BY 1995) were estimated to comprise 2% of the spring chinook, 26% of the summer chinook, and 40% of the fall chinook salmon population. Three-year-old fish (BY 1997) were estimated to comprise 14% of the spring chinook, 42% of the summer chinook, and 17% of the fall chinook salmon population. Two-year-olds accounted for approximately 11% of the fall chinook population. The sockeye salmon population sampled at Bonneville was predominantly four-year-old fish (95%), and the coho salmon population was 99.9% three-year-old fish (Age 1.1). Length analysis of the 2000 returns indicated that chinook salmon with a stream-type life history are larger (mean length) than the chinook salmon with an ocean-type life history. Trends in mean length over the sampling period were also analysis for returning 2000 chinook salmon. Fish of age classes 0.2, 1.1, 1.2, and 1.3 have a significant increase in mean length over time. Age classes 0.3 and 0.4 have no significant change over time and age 0.1 chinook salmon had a significant decrease in mean length over time. A year class regression over the past 11 years of data was used to predict spring and summer chinook salmon population sizes for 2001. Based on three-year-old returns, the relationship predicts four-year-old returns of 325,000 (± 111,600, 90% Predictive Interval [PI]) spring chinook and 27,800 (± 29,750, 90% PI) summer chinook salmon. Based on four-year-old returns, the relationship predicts five-year-old returns of 54,300 (± 40,600, 90% PI) spring chinook and 11,000 (± 3,250, 90% PI) summer chinook salmon. The 2001 run size predictions used in this report should be used with caution, these predictions are well beyond the range of previously observed data.