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Anchoa mitchilli and Gobiosoma bosc. Temporal variability in larval abundance and depth distribution. Symbols represent observed values, and lines the fitted relationship based on harmonic regression, including only those predictors that were nominally (p < 0.05) significant. (A) Anchovy larval abundance, for clarity, values for small larvae have been shifted up 1 increment on the y-axis, and values for large larvae have been shifted down 1 increment. (B) Anchovy larvae mean depth, values for small larvae have been shifted up (shallower) 1 increment on the y-axis, and values for large larvae have been shifted down (deeper) 1 increment. (C) Goby larval concentration, values for small larvae have been shifted up 1 increment. (D) Goby larvae mean depth, values for small larvae have been shifted up (shallower) 2 increments on the y-axis. Key applies to all graphs

Anchoa mitchilli and Gobiosoma bosc. Temporal variability in larval abundance and depth distribution. Symbols represent observed values, and lines the fitted relationship based on harmonic regression, including only those predictors that were nominally (p < 0.05) significant. (A) Anchovy larval abundance, for clarity, values for small larvae have been shifted up 1 increment on the y-axis, and values for large larvae have been shifted down 1 increment. (B) Anchovy larvae mean depth, values for small larvae have been shifted up (shallower) 1 increment on the y-axis, and values for large larvae have been shifted down (deeper) 1 increment. (C) Goby larval concentration, values for small larvae have been shifted up 1 increment. (D) Goby larvae mean depth, values for small larvae have been shifted up (shallower) 2 increments on the y-axis. Key applies to all graphs

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Bay anchovy Anchoa mitchilli and naked goby Gobiosoma bosc larvae have been reported to move up-estuary. In the present study, we examined depth preferences and periodic vertical movements that might promote such along-estuary transport in these 2 species. We conducted 2 cruises of 3 d each in the Hudson River estuary, USA. The cruises were 1 wk ap...

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... An effect of season was tested by standardizing date to a mean of 0 and including date and date-squared (date 2 ) as predictors. The effect of moon phase was tested via harmonic regression (Batschelet 1981;Lorda and Saila 1986;Schultz et al. 2003) wherein the 328-h cycle is partitioned into two trigonometric variables that can be used as predictors in linear regression models. Collinearity among the regressors was assessed via correlation tables and eigenanalysis of the design matrix ( Belsley et al. 1980). ...
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We analyzed juvenile anadromous alewife migration at Bride Lake, a coastal lake in Connecticut, during summer 2006 and found that migration on 24-hour and seasonal timescales was influenced by conditions of the environment and characteristics of the individual. To identify environmental cues of juvenile migration, we continuously video recorded fish at the lake outflow and employed information-theoretic model selection to identify the best predictors of daily migration rate. More than 80% of the approximately 320,000 juveniles that migrated from mid-June to mid-August departed in three pulses lasting one or two days. Pulses of migration were associated with precipitation events, transient decreases in water temperature and transient increases in stream discharge. Diel timing of migration shifted over the summer. Early in the season most migration occurred around dawn; late in the season migration occurred at night. To identify individual characteristics associated with migratory behavior, we compared migrating juveniles that we collected as they were exiting Bride Lake to non-migrating juveniles that we collected from the center of the lake. Migrants were a non-random subset of the population; they were on average 1 – 12 mm larger, 2 – 14 d older, had grown more rapidly (11% greater length-at-age), and were in better condition (14% greater mass-at-length) than non-migrant fish. We infer that the amount of accumulated energy has a positive effect on the net benefit of migration at any time in the migratory season.
... It is a predominant member of the estuarine fish assemblage, ranging from tropical and subtropical estuaries in the Gulf of Mexico and the Atlantic coast of the southeastern US (Deegan and Thompson 1985;Castillo-Rivera et al. 1994;Snelson and Johnson 1995;Ayala Perez et al. 1998) to the temperate estuaries of the North Atlantic Bight and southern New England (Dovel 1981;Monteleone 1992;Keller et al. 1999;Dorfman 2000). Early-stage (larvae and juvenile) anchovy are often the most abundant members of the summer ichthyoplankton assemblage (Olney 1983;Setzler-Hamilton 1987;Monteleone 1992;Keller et al. 1999;Schultz et al. 2003). In northern latitudes, anchovy migrate out of estuaries to coastal waters in the autumn, returning in spring as reproduction commences (Dovel 1981;Vouglitois et al. 1987;Schmidt 1992;Wang and Houde 1995). ...
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... Short-term (tidal), seasonal, and longer-term (interannual to decadal) changes in fish distribution and abundance can, at least partially, be ascribed to changes in the salt distribution. Vertical distribution is also affected by salinity preference (e.g., Schultz et al. 2003) and vertical distribution in turn affects predator-prey interactions and alongriver transport, among other processes. ...