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A.P. Maloy

Publications and source records attributed to A.P. Maloy.

2 recordsLinked to original sources

Comparison of rainbow smelt age estimates from fin rays and otoliths

Rainbow smelt Osmerus mordax, although nonnative, are an important component of the offshore food web in the Laurentian Great Lakes. In Lake Ontario, we estimate ages of rainbow smelt annually to study population dynamics such as year-class strength and age-specific growth and mortality. Since the early 1980s, we have used pectoral fin rays to estimate rainbow smelt ages, but the sectioning and mounting of fin rays are time and labor intensive. Our objective was to assess the feasibility of using otoliths rather than fin rays to estimate rainbow smelt ages. Three readers interpreted the ages of 172 rainbow smelt (60-198 mm total length) based on thin sections of pectoral fin rays, whole otoliths with no preparation, and whole otoliths that had been cleared for 1 month in a 70:30 ethanol : glycerin solution. Bias was lower and precision was greater for fin rays than for otoliths; these results were consistent for comparisons within readers (first and second readings by one individual; three readers were used) and between readers (one reading for each reader within a pair). Both otolith methods appeared to misclassify age-1 rainbow smelt. Fin ray ages had the highest precision and provided the best approximation of age estimates inferred from the Lake Ontario population's length frequency distribution and from our understanding of this population. ?? American Fisheries Society 2008.

North American Journal of Fisheries Management↗

A PCR-based diagnostic assay for the detection of Roseovarius crassostreae in Crassostrea virginica affected by juvenile oyster disease (JOD)

We have developed a PCR-assay for the diagnosis of juvenile oyster disease (JOD) based on the detection of Roseovarius crassostreae directly from affected oysters. Species-specific primers are used to amplify the 16S-23S rDNA internal transcribed spacer (ITS) of R. crassostreae, and confirmation of product identity is accomplished by restriction enzyme analysis. No false positives were obtained with either closely related bacterial species or from other DNAs present in oyster samples. The assay has the potential to detect as few as 10 cells of R. crassostreae per oyster when samples are taken from the inner valve surfaces of the animal. Inclusion of material from soft body surfaces is not necessary, and may reduce sensitivity approximately 10-fold. In a JOD-affected population, a positive PCR result was obtained from all oysters from which these bacteria were subsequently cultured. The assay also detected the presence of R. crassostreae in 2 oysters from which no R. crassostreae isolates were recovered. No R. crassostreae was detected by either PCR or bacteriology in oysters from a population that was not exhibiting JOD-signs. This assay is expected to advance regional disease management efforts and provide valuable insights into the disease process and epizootiology of JOD. ?? Inter-Research 2005.

Diseases of Aquatic Organisms↗