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1 January 2013 The Distribution of Larval Fishes of the Charleston Gyre Region off the Southeastern United States in Winter Shaped by Mesoscale, Cyclonic Eddies
J. J. Govoni, J. A. Hare, E. D. Davenport
Author Affiliations +
Abstract

Serial, cyclonic, mesoscale eddies arise just north of the Charleston Bump, a topographical rise on the continental slope and Blake Plateau, and characterize the U.S. outer shelf and upper slope in the region of the Charleston Gyre. This region was transected during the winters of 2000, 2001, and 2002, and hydrographic data and larval fishes were collected. The hydrodynamics of the cyclonic eddies of the Charleston Gyre shape the distribution of larval fishes by mixing larvae from the outer continental shelf and the Gulf Stream and entraining them into the eddy circulation at the peripheral margins, the wrap-around filaments. Over all years and transects (those that intercepted eddies and those that did not), chlorophyll a concentrations, zooplankton displacement volumes, and larval fish concentrations were positively correlated. Chlorophyll a concentrations were highest in filaments that wrapped around eddies, and zooplankton displacement volumes were highest in the continental shelf-Gulf Stream-frontal mix. Overall, the concentration of all larval fishes declined from inshore to offshore with highest concentrations occurring over the outer shelf. Collections produced larvae from 91 fish families representing continental shelf and oceanic species. The larvae of shelf-spawned fishes-Atlantic Menhaden Brevoortia tyrannus, Round Herring Etrumeus teres, Spot Leiostomus xanthurus, and Atlantic Croaker Micropogonias undulatus-were most concentrated over the outer shelf and in the continental shelf-Gulf Stream-frontal mix. The larvae of ocean-spawned fishes-lanternfishes, bristlemouths, and lightfishes-were more evenly dispersed in low concentrations across the outer shelf and upper slope, the highest typically in the Gulf Stream and Sargasso Sea, except for lightfishes that were highest in the continental shelf-Gulf Stream-frontal mix. Detrended correspondence analysis rendered groups of larval fishes that corresponded with a gradient between the continental shelf and Gulf Stream and Sargasso Sea. Eddies propagate northeastward with a residence time on the outer shelf and upper slope of ∼1 month, the same duration as the larval period of most fishes. The pelagic habitat afforded by eddies and fronts of the Charleston Gyre region can be exploited as nursery areas for feeding and growth of larval fishes within the southeastern Atlantic continental shelf ecosystem of the U.S. Eddies, and the nursery habitat they provide, translocate larvae northeastward.

FIGURE 1.

The Charleston Gyre region off the southeastern coast of the United States. Gray-scale gradient represents depth >500 m. Received March 18, 2013; accepted June 21, 2013

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A series of recurrent, cyclonic, mesoscale eddies characterize the Charleston Gyre region off the southeastern coast of the United States, and influences the primary, secondary, and fisheries production of the southeastern Atlantic coastal ecosystem (Govoni and Hare 2001). A bathymetric rise on the continental slope above the Blake Plateau, known as the Charleston Bump (Figure 1), forces an eastward deflection of the Gulf Stream, a major western boundary current (Olson 2001) that borders the southeastern U.S. continental shelf to the east. This deflection, a result of the vertical compression and subsequent expansion of the water column as the Gulf Stream overrides the Charleston Bump, gives repetitive rise to a series of meanders. Meander crests pull Gulf Stream water onto the shelf and into the Gulf Stream Front, and also pull shelf water into the Gulf Stream front. Meanders become unstable and break, spinning off cyclonic eddies. Eddies propagate northeastward and decay or coalesce with the Gulf Stream north of Cape Fear, North Carolina. The residence time of eddies within the region ranges from a week to a month if stranded on the shelf (Pietrafesa et al. 1985; Lee et al. 1991; Blanton et al. 2003). The cyclonic circulation of the eddies upwells nutrient-rich water from deep and off the shelf edge to the euphotic zone, which can result in enhanced primary and secondary production (Verity et al. 1993). These eddies develop most frequently and are more pronounced in winter (Mathews and Pashuk 1984, 1986) when the Gulf Stream is in its strongly deflected mode (Lee et al. 1991).

The survival of fish larvae is the principal determinant of population recruitment and an important contributor to fisheries production (Houde 2008). Most marine fishes are pelagic spawners, while their larvae occupy the upper 200m(Miller and Kendall 2009).While the Charleston Gyre region has the potential to act as spawning and nursery habitat, evidence of the use of the pelagic habitats afforded by cyclonic eddies in this region is limited. Winter is the spawning season for a suite of fishes, many of which are commercially important (Govoni and Hare 2001; Taylor et al. 2009). High concentrations of larval fishes are evident in the Charleston Gyre region (Fahay 1975; Powles and Stender 1976; Yoder 1983), but there is little indication of high concentrations of fish eggs, aside from those reported for Atlantic Menhaden Brevoortia tyrannus (Judy and Lewis 1983). The distribution of larval fishes across the outer shelf and upper slope in association with the passage of the cyclonic eddies is not described, and consequently habitat utilization of these eddies is undetermined.

TABLE 1.

Transects and stations occupied across the outer continental shelf and upper slope in the Charleston Gyre region off the southeastern coast of the United States in the winters of 2000, 2001, and 2002. See Figure 2 for definitions of station abbreviations.

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The objectives of this study were to (1) transect the Charleston Gyre region and intercept eddies that arise there, (2) describe the distribution of chlorophyll a, zooplankton, and larval fishes in and around these eddies, and (3) describe the influence of eddies in shaping the distribution of larval fishes.

METHODS

Study area.—The Charleston Gyre region is dynamic across the outer shelf and upper slope, along the shore and in the vertical dimensions, changing with the formation and northeastward propagation of mesoscale cyclonic eddies. In the absence of eddies, a mix of outer continental shelf and Gulf Stream waters separates water over the continental shelf from the Gulf Stream. During formation of an eddy, the mixture of outer shelf and Gulf Stream water is stretched meridionally and zonally to form wrap-around filaments that appear as a lens of water near the surface and extend to ∼25 m depth. Wrap-around filaments close around an eddy with a core.

With its dynamic character, eddies of the Charleston Gyre region can provide favorable pelagic habitat for larval fishes. Localized frontal convergence in the mixed waters of the outer shelf and the Gulf Stream north of the Charleston Gyre region account for elevated concentrations of larval fishes (Govoni 1993; Govoni and Pietrafesa 1994; Govoni and Spach 1999). Within the eddy core, upwelling from below the Gulf Stream is evident (Bane et al. 2001), and this upwelling stimulates primary and secondary production (Verity et al. 1993). This production can provide food for larval fishes (Govoni et al. 2010).

Data collection and processing.—To determine the influence of cyclonic eddies of the Charleston Gyre region on the distribution of larval fishes, ichthyoplankton collections were taken along transects that nominally began on the outer shelf, extended onto the slope, and continued into the Gulf Stream (and on one transect, in 1 year, into the western edge of the Sargasso Sea). Stations along transectswere occupied in January of 2000, 2001, and 2002; stations were nominally 16.1 km (10 nautical miles) apart along transects (Table 1; Figure 2). Transects extended zonally across the outer shelf and upper slope and meridionally from the Charleston Bump to Cape Fear (Figure 2). Transects were oblique and not perpendicular to the axis of the physical features of the region. Transect and station locations were modified each year to capture eddy formation and propagation. Some transects intercepted formed eddies, some did not, and some intersected eddy formation.

At each station, casts of conductivity, temperature, and depth (CTD) to a maximum depth of 350 m were taken and surface chlorophyll a concentrations were measured. At each station, ichthyoplankton collections were taken with a 60-cm-diameter bongo net fitted with 333-μm-mesh nets fished obliquely from near the bottom on the shelf or from 200 m depth to the surface when they were off the shelf break as described by Powell et al. (2000). Zooplankton displacement volume (including displacement by larval fishes) was measured from ichthyoplankton collections as described by Smith and Richardson (1977). Outer shelf and upper slope sections of temperature were derived from profiles taken from CTD casts.

Larval fishes were sorted from one bongo net and identified to family or order level when specimens could not be referred to family because of their condition. Identification followed that described by Richards (2006); classification, some of which were modified owing to recent systematic revisions, generally followed that of Nelson (1994). The larvae of the herrings (Clupeidae)-Atlantic Menhaden and Round Herring Etrumeus teres-and the drums (Sciaenidae)-Spot Leiostomus xanthurus and Atlantic Croaker Micropogonias undulatus-were identified and selected as indicators of fishes spawned on the shelf. Atlantic Menhaden and Spot larvae are among the most abundant species collected on the shelf in winter south of Cape Hatteras (Checkley et al. 1999; Govoni and Spach 1999; Hare and Govoni 2005). Larvae of the bristlemouths (Gonostomatidae), lightfishes (Phosichthyidae), and lanternfishes (Myctophidae) were selected as indicators of fishes spawned off the shelf in the open ocean. The larvae of these fishes are among the most abundant, open-ocean spawned larvae in the western North Atlantic (Evseenko 1982), as well as in western boundary currents (Sassa et al. 2004).

TABLE 2.

The nominal characteristics of station designations across the outer continental shelf and upper slope in the Charleston Gyre region off the southeastern coast of the United States in the winters of 2000, 2001, and 2002.

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Stations were classified as location-based designations (Table 2) and were not linked to water mass, because water masses are often separated vertically in the region; collections were neither depth nor water-mass discrete. Bongo-net casts obliquely integrated larval fishes within the water column from 200 m to the surface, or from near the bottom to the surface in depths shallower than 200 m. Consequently, larval fishes could be collected vertically from different water masses within retrograde frontal zones or from within eddies of the Charleston Gyre region. Whereas the lack of vertical separation of larval fish collections could result in the combination of larval fishes from different water masses, the spatial scale of stations along transects and location-based station designations ameliorated the effects of the lack of discrete water-mass sampling.

Examination of advanced very high resolution radiometer (AVHRR) images (Figure 2) of sea-surface temperature (SST), temperature (T) and salinity (S) profiles for each station (Figure 3), and sections of T over the outer shelf and upper slope (Figure 4) were used to classify collections along transects. Stations were designated as CS, CS-GS-FM, GS, WAF, EC, and SS (see Table 2 for definitions). Stations WAF and EC were not evident on transects that did not intercept an eddy. Station designations were closely concordant with the surface expression of frontal zones along outer shelf transects north of Cape Fear (Govoni et al. 2010). These location-based designations were consonant with the methods employed for ordination of the larval fish assemblage north of the Charleston Gyre region (Quattrini et al. 2005).

Data analyses.—For analysis, parametric statistics were preferred, but nonparametric methods were used when variances within groups were not homogenous (Zar 1999). Overall concentrations of chlorophyll a, zooplankton displacement volumes, and concentrations of all larval fishes were tested for association with Kendall's correlations. For comparisons, ANOVA was preferred, but Kruskall-Wallis (K-W) nonparametric ANOVA was used when the variances of concentrations were not homogenous (Levene's tests). Multiple comparison tests identified differences among station designations.

Detrended correspondence analysis (DCA) provided ordination (Ter Braak and Prentice 1988; Legendre and Legendre 1998) of station designations and of families and indicator taxa of larval fishes. The DCA minimizes edge effects that can interfere with the interpretation of the ordination by simple correspondence analysis. Concentrations of families and indicator taxa from all station designations were normalized by using percentage composition. Scores from the first and second axes, identified by eigenvalues, were plotted for station designations and concentrations of families and indicator taxa. The proximity families, indicator taxa, and station designation on axis plots indicated the coherence of taxa groups with station designations.

RESULTS

Hydrography

Cyclonic eddies were intercepted and traversed in each year with other transects to the south or north of eddies (Table 1). Overall, most collections were taken in the CS-GS-FM (n = 51), followed by the GS (n = 28), WAF (n = 14), CS (n = 7), EC (n = 4), and SS (n = 2).With the exception of CS stations,where the water column was vertically isothermal, the water column was stratified, and the thermocline and halocline occurred at varying depths (Figures 3, 4).

FIGURE 2.

Stations (dots), transects (red numerals), and station designations (black letters) occupied in the Charleston Gyre region off the southeastern United States, superimposed on representative advanced very high resolution images of sea-surface temperatures: (A) 16 January 2000; (B) 10 January 2001; (C) 09 January 2002. CS: continental shelf; CS-GS-FM: continental shelf-Gulf Stream-frontal mix; GS: Gulf Stream; WAF: wrap-around filament; EC: eddy core; SS: Sargasso Sea. Stations occupancy and images are not temporally synoptic; color on images is relative, not absolute, with the temperature scale.

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Chlorophyll a Concentrations, Zooplankton Displacement Volumes, and Larval Fish Correlations

Chlorophyll a concentrations were weakly, but positively, correlated with zooplankton displacement volumes and larval fish concentrations (Table 3). Zooplankton displacement volumes had a stronger, positive correlation with larval fish concentrations than did chlorophyll a concentrations, though zooplankton displacement volume included, volumetrically, larval fishes and therefore was not completely independent of larval fish concentration. Larval fish concentrations had a stronger positive correlation with zooplankton displacement volumes than with chlorophyll a concentration.

FIGURE 3.

Representative temperature (blue) and salinity (red) profiles (downcast and upcast smoothed) for stations designations. See Figure 2 for definitions of station abbreviations.

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Chlorophyll a Concentration, Zooplankton Displacement Volume, and Concentration of Larval Fishes

Over all years and transects (those that intersected the eddies and those that did not), mean chlorophyll a concentrations, zooplankton displacement volumes, and concentrations of all larval fishes differed among years and station designations with no significant interaction between years and station designations (Table 4). Multiple comparison tests indicated significantly higher concentrations of chlorophyll a in WAF than in the GS; concentrations in the CS-GS-FM were significantly higher than in the GS (Figure 5A). Zooplankton displacement volumes were significantly higher in the CS-GS-FM than in the GS (Figure 5B). Concentrations of all larval fishes were significantly higher on the CS than in the GS and EC; concentrations in the CS-GS-FM were significantly higher than in the GS (Figure 5C).

TABLE 3.

Kendall's rank correlations (θ) and test statistics (S) of chlorophyll a concentrations, zooplankton displacement volumes, and concentrations of larval fishes in the winters of 2000, 2001, and 2002 in the Charleston Gyre region off the southeastern coast of the United States (an asterisk [*] denotes significant difference at P < 0.05).

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FIGURE 4.

Representative sections of the outer continental shelf and upper slope of the Charleston Gyre region in 2000: (A) no eddy present; (B) eastward deflection of the Gulf Stream at the Charleston Bump; and (C) eddy present. See Figure 2 for definitions of station abbreviations.

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Taxa of Larval Fishes

Collections produced 91 families of larval fishes representing the larvae of coastal ground, reef, and pelagic fishes and oceanic, meso- and benthopelagic, and benthic fishes (Table 5). Of the indicators of shelf-spawned fishes, Atlantic Menhaden and Round Herring, comprised almost all of the clupeids and were consistently present in high concentrations. Spot and Atlantic Croaker comprised almost all of the sciaenids. Of the indicators of ocean-spawned fishes, most of the bristlemouths were Cyclothone spp., but Diplophos taenia, Bonapartia pedaliota, and Gonostoma spp., were included. Most of the lightfishes were Vinciquerria spp. Lanternfishes included Electrona risso, Gonichthys cocco, Hygophum spp., Myctophum spp., Ceratoscopelus spp., Diaphus spp., and Lepidophanes spp. Lanternfishes and bristlemouths were consistently present.

Overall, concentrations of the indicators of shelf-spawned fishes differed and were highest in the CS or CS-GS-FM (Figure 6), and some significant differences were apparent among station designations (Table 6). Multiple comparison tests indicated that concentrations of Atlantic Menhaden were not significantly different among station designations (Figure 6A). Concentrations of Round Herring larvae were significantly higher in the CS-GS-FM than in the GS and WAF (Figure 6B). Concentrations of Spot larvae were significantly higher in the CS than in CS-GS-FM andWAF (Figure 6C). Concentrations of Atlantic Croaker were not significantly different among station designations. No larvae of shelf-spawned fishes were collected in the SS.

Concentrations of the larvae of ocean-spawned target fishes were low and static across the outer shelf and upper slope (Figure 7), and some significant differences occurred among station designations (Table 6). Concentrations of lanternfishes were significantly higher in the GS than in the CS, CS-GS-FM, andWAF (Figure 7A). Concentrations of lightfishes and bristlemouths did not differ significantly among station designations (Figure 7B, C). No lightfishes were collected in the CS.

Hydrodynamics and the Distribution of Larval Fishes

The hydrodynamics of the eddies of the Charleston Gyre region shape the outer shelf and upper slope distribution of larval fishes by mixing larval fishes from the CS and the GS into the CS-GS-FM and entraining them into the eddy circulation at the peripheral margins of filaments, the WAF (Figures 2, 4). In eddy formation, the Gulf Stream veers toward the east at the Charleston Bump, the CS-GS-FM and WAF stretches, toward the south, then the east (Figures 2A, 4B), then north as the filament closes (Figure 4C). Larvae, which were in high concentrations on the CS and in CS-GS-FM (Figure 6), were entrained into eddy circulation, the WAF. The overall decrease in concentrations of the larvae of shelf-spawned fishes across eddies and in the WAF and ED (Figure 6), and the more even distribution of the larvae of ocean-spawned fishes (Figure 7), indicated mixing across eddies by the circulation of the eddies and by eddy diffusion.

TABLE 4.

Two-way ANOVA of mean chlorophyll a concentrations, zooplankton displacement volumes, and concentrations of larval fishes among years and station designation in the winters of 2000, 2001, and 2002 in the Charleston Gyre region off the southeastern coast of the United States.

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Ordination of larval Fishes

The assemblage of families and indicator taxa of larval fishes grouped along two axes (Table 7). Overlap in taxa groupings within station designations is indicated by overlapping polygons that encompass station designations (Figure 8). A gradient was evident principally along axis 2. The herrings (Clupeidae) that comprise Atlantic Menhaden and Round Herring, and were the most abundant family, were consistently grouped toward the lower end of axis 2, while the Sciaenidae that comprise Spot and Atlantic Croaker grouped toward the upper end of axis 2 (Figure 8). Spot and Atlantic Croaker typically occupy more inshore habitats, most frequently the station designation CS, whereas Atlantic Menhaden and Round Herring occupy more offshore habitats, the CS-SG-FM. The lanternfishes and bristlemouths grouped toward the far right of axis 1. The CS-GS-FM, EC, and WAF overlap between them and are closer to, or over, the origin, indicating that these stations contained some of the indicator taxa. The EC was more similar to the GS than the CS. Overall, the taxa grouped by the DCA conform with the station classification, which supports the validity of station classification.

DISCUSSION

The action of the eddies of the Charleston Gyre region is to mix larval fishes from the outer continental shelf (CS) and Gulf Stream (GS) into the CS-GS-FM and entrain the CS-GSFM into the water that wraps around the eddy core (WAF). Fronts and eddies of the Charleston Gyre region are areas of elevated abundance of larval fishes. In this region the abundance of larval fishes were greatest on the outer shelf, CS, and CS-GS-FM, and thirdly in the WAF, because the Gulf Stream and continental shelf waters contribute larvae that are concentrated and mixed within this frontal mix. Eddy diffusion (Blanton 1971; Lillibridge et al. 1990; Churchill et al. 1993) affects this mixing, as is evident in frontal zones to the north of the Charleston Gyre region (Govoni 1993; Govoni and Spach 1999).

The dynamics of eddies of the Charleston Gyre region shape the distribution of chlorophyll a, zooplankton, and larval fishes by concentrating these attributes in and about eddies in ways similar to those of other mesoscale cyclonic eddies elsewhere in theworld's oceans. Entrainment of larval fishes and zooplankton into fronts associated with eddies is evident elsewhere, particularly along western boundary currents (Nakata et al. 2000; Everett et al. 2011; Mullaney 2011). In eddies along the western front of the Kuroshio Current extension, Eulerian and Langrangian observations indicated increased chlorophyll a concentrations stimulated by upwelling of nutrients within the eddy core, followed by a decline in chlorophyll a as eddies mature with a concomitant increase in the concentration of copepod nauplii and small copepods (Kimura et al. 1997; Okazaki et al. 2002). Chlorophyll a concentrations, zooplankton abundance, and larval fish concentrations were positively correlated within mesoscale cyclonic eddies of the Loop Current, the progenitor of the Florida Current and the Gulf Stream, in the northern Gulf of Mexico (Biggs and Ressler 2001). Mesoscale eddies formed in the wake of oceanic islands also result in elevated chlorophyll a concentrations (Onitsuka et al. 2009), and positive correlations were evident among chlorophyll a concentrations, zooplankton displacement volumes, and larval fish concentrations. Zooplankton displacement volumes were highest in the eddy core, while concentrations of larval fishes were highest in the periphery of an oceanic, mesoscale, cyclonic eddy formed adjacent to the Hawaiian Islands (Lobel and Robinson 1986). Lagrangian model simulations that conform with empirical observations indicate that invertebrate and vertebrate larvae can aggregate in high-concentration packets randomly distributed along SST fronts associated with filaments that spin off the California Current, an eastern boundary current (Harrison et al. 2013). Lagrangian observations in and about an eddy of the Charleston Gyre region indicated that initially high concentrations of chlorophyll a decreased, while copepod nauplii and small copepodites and some other planktonic invertebrates important in the diets of larval fishes increased as eddies propagated northeastward (Govoni et al. 2010). In the eddies examined, and with the classification of stations used here, chlorophyll a concentrations were highest in theWAF, while zooplankton displacement volumes were highest in the CG-GS-FM; the concentration of all larval fishes was second highest in the CG-GS-FM and third highest in WAF.

FIGURE 5.

Comparison of means grouped by station designation for (A) chlorophyll a concentrations, (B) zooplankton displacement volumes, and (C) larval fish concentrations. See Figure 2 for definitions of station abbreviations. Error bar represents 1 SE of the mean; letters above bar plots indicate the results of multiple comparison tests; the asterisk (*) above the letters “B” or “D” denote significant differences in comparison with the * below the letter “A” or “C” (P < 0.05); the letter “A” above the letter “B” denotes no significant difference.

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The high taxa richness of larval fishes registered in collections from the Charleston Gyre region with 91 families was higher than in cross-shelf collections that penetrated the Gulf Stream to the north and to the south off the southeastern United States. Year-round between Cape Canaveral, Florida, and Cape Fear, Fahay (1975) recognized 51 families and Powles and Stender (1976) recognized 48. North of the Charleston Gyre region, Powell and Robbins (1994), Powell et al. (2000), and Quattrini et al. (2005) recognized 85 families from April through December, and Govoni and Spach (1999) recognized 75 families in the coalesced outer shelf and Gulf Stream fronts in similar areas in winter. Marancik et al. (2005) recognized 34 families along a cross-shelf transect south of the Charleston Gyre region, from near shore to the Gulf Stream in spring and winter. To the south, over the Florida Keys and proximal Gulf Stream, Limouzy-Paris et al. (1994) recognized 91 families in May and June, and Sponaugle et al. (2005) recognized 66 families yearround. Farther south in the Florida Straits and along transects across the Florida current (the progenitor of the Gulf Steam), Richards et al. (1993) recognized 52 families. While advances in larval fish taxonomy and changes in systematic classification through time influence the number of families recognized, mixing of Gulf Stream water and shelf water in the outer shelf front can explain much of the high taxa richness of larval fishes in the Charleston Gyre region.

The distribution of taxa and of taxa groups within eddies and associated fronts of the Charleston Gyre region indicates mixing of shelf and oceanic water. This observation is consonant with observations in and about anticyclonic, mesoscale eddies in the Gulf of Alaska, wherein ordination of taxa of larval fishes resulted in grouping by location inside and outside of eddies and associated frontal zones (Atwood et al. 2010). Elsewhere, Lobel and Robinson (1988) found the larvae of pelagic and mesopelagic fishes and coastal and shore fishes in an eddy off the Hawaiian Islands, and Sabatés and Olivar (1996) found the larvae of coastal and mesopelagic fishes displaced by the position of the shelf-slope front in the Mediterranean Sea. The dynamics that drive elevated concentrations of larval fishes are evident also in the Mediterranean Sea (Sabatés 1990; Sabatés and Masó 1990; Sabatés and Olivar 1996; Olivar et al. 2010), eddies along the margins of western boundary currents (Okazaki et al. 2002; Sponaugle et al. 2005), and eddies juxtaposed to deepwater currents (Brandt 1983; Lobel and Robinson 1986, 1988; Smith et al. 1999).

TABLE 5.

Abundance of the families of larval fishes collected in the Charleston Gyre region off the southeastern United States in the winters of 2000, 2001, and 2002.

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continued

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FIGURE 6.

Comparison of means grouped by station designation for indicator taxa of the larvae of shelf-spawned fishes in the Charleston Gyre region off the southeastern coast of the United States. See Figure 2 for definitions of station abbreviations. Error bar represents 1 SE of the mean: letters above bar plots indicate the results of multiple comparison tests; the asterisk (*) above the letter “B” denotes significant differences in comparison with the * below letter “A” (P < 0.05); the letter “A” above the letter “B” denotes no significant difference.

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Upwelling and eddy diffusion within eddies and fronts of western boundary currents (Olson 2001) can provide enhanced primary and secondary productivity, as well as favorable habitat for feeding and consequent growth of larval fishes (Bakun 2006; Richardson et al. 2009). For larval fishes, enhanced feeding could shorten larval duration, lower cumulative mortality, and increase population recruitment (Houde 2008). The enhanced trophic environments in and about the mesoscale cyclonic eddies of the Charleston Gyre region as they propagate northeastward (Govoni et al. 2010) indicate the potential importance of these pelagic habitats to the growth, survival, and subsequent population recruitment of larval fishes (Munk et al. 2003; Godø et al. 2012). The residence time on the outer shelf and upper slope is ∼1 month, the same duration as the larval period of most fishes. These eddies also translocate larvae to the east and north.

TABLE 6.

Results of one-way ANOVAs of the mean concentrations of the larvae of indicator taxa among station designations and Kruskal-Wallis tests of the ranks of the median concentrations among station designations.

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TABLE 7.

Detrended correspondence analysis (DCA) (axes and eigenvalues) of families of larval fishes collected in the Charleston Gyre region off the southeastern United States in the winters of 2000, 2001, and 2002.

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FIGURE 7.

Comparison ofmeans grouped by station designation for indicator taxa of the larvae of ocean-spawned fishes in the Charleston Gyre region off the southeastern coast of the United States. See Figure 2 for definitions of station abbreviations. Error bar represents 1 SE of the mean: letters above bar plots indicate the results of multiple comparison tests; the asterisk (*) above letter “B” denotes significant differences in comparison with the * below the letter “A” (P < 0.05); the letter “A” above the letter “B” denotes no significant difference.

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FIGURE 8.

Detrended correspondence analysis (axes and eigenvalues) of families of larval fishes collected in the Charleston Gyre region off the southeastern United States in the winters of 2000, 2001, and 2002. Polygons encompass groupings and symbols denote groupings of station designations; see Figure 2 for definitions of station abbreviations.

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ACKNOWLEDGMENTS

We thank M. L. Burton, M. D. Greene, D. E. Hoss, L. R. Settle, H. J. Walsh, and all of the NOAA Beaufort Laboratory for their recurrent participation and assistance on cruises. P. A. Tester provided chlorophyll a analysis. Larval fishes were sorted and identified to family by M. Konieczna and H. Skolska of the Sea Fisheries Institute, Plankton Sorting and Identification Center, Szczecin and Gadynia, Poland. G. Bath-Martin and D. S. Vaughan reviewed drafts of themanuscript and provided helpful comments. The U.S. Government has the right to retain a nonexclusive, royalty-free license in and to any copyright covering this paper.

REFERENCES

1.

E. Atwood , J. T. Duffy-Anderson , J. K. Horne , and C. Ladd . 2010. Influence of mesoscale eddies on ichthyoplankton assemblages in the Gulf of Alaska. Fisheries Oceanography 19:493–507. Google Scholar

2.

A. Bakun 2006. Fronts and eddies as key structures in the habitat of marine fish larvae: opportunity, adaptive response, and competitive advantage. Scientia Marina 70(Supplement 2):105–122. Google Scholar

3.

J. M. Bane Jr. , L. P. Atkinson , and D. A. Brooks . 2001. Gulf Stream physical oceanography at the Charleston Bump: deflection, bimodality, meanders, and upwelling. Pages 25–36 in G. R. Sedberry , editor. Island in the stream: oceanography and fisheries of the Charleston Bump . American Fisheries Society, Symposium 25, Bethesda, Maryland. Google Scholar

4.

D. C. Biggs , and P. H. Ressler . 2001. Distribution and abundance of phytoplankton, zooplankton, ichthyoplankton, and micronekton in the deepwater Gulf of Mexico. Gulf of Mexico Science 19:7–29. Google Scholar

5.

B. O. Blanton , A. Aretxabaleta , F. E. Werner , and H. E. Seim . 2003. Monthly climatology of the continental shelf waters of the South Atlantic Bight. Journal of Geophysical Research: Oceans 108:3264. DOI:  10.1029/2002JC001609Google Scholar

6.

J. Blanton 1971. Exchange of Gulf Stream water with North Carolina shelf water in Onslow Bay during stratified conditions. Deep-Sea Research, Part A18:167–178. Google Scholar

7.

S. B. Brandt 1983. Temporal and spatial patterns of lanternfish (family Myctophidae) communities associated with a warm-core eddy. Marine Biology 74:231–244. Google Scholar

8.

D. M. Checkley Jr. , P. B. Ortner , F. E.Werner , L. R. Settle , and S. R. Cummings . 1999. Spawning habitat of the Atlantic Menhaden in Onslow Bay, North Carolina. Fisheries Oceanography 8(Supplement 2):22–36. Google Scholar

9.

J. H. Churchill , E. R. Levine , D. N. Connors , and P. C. Cornillon . 1993. Mixing of shelf, slope and Gulf Stream water over the continental slope of theMiddle Atlantic Bight. Deep-Sea Research, Part I 40:1063–1085. Google Scholar

10.

J. D. Everett , M. E. Baird , and I. M. Suthers . 2011. Three-dimensional structure of a swarm of the salp Thalia democratica within a cold-core eddy off southeast Australia. Journal of Geophysical Research: Oceans 116:C12046. DOI:  10.1029/2011JC007310Google Scholar

11.

S. A. Evseenko 1982. Ichthyoplankton of slope and Gulf Stream waters off Nova Scotia in late autumn 1974. Journal of Northwest Atlantic Fishery Science 3:127–139. Google Scholar

12.

M. P. Fahay 1975. An annotated list of larval and juvenile fishes captured with surface-towed meter net in the South Atlantic Bight during four RV dolphin cruises between May 1967 and February 1968. NOAA (National Oceanic and Atmospheric Administration) Technical Report NMFS (NationalMarine Fisheries Service) SSRF-685. Google Scholar

13.

O. R. Godø , A. Samuelsen , G. J. Macaulay , R. Patel , S. S. Hjøllo , J. Horne , S. Kaartvedt , and J. A. Johannessen . 2012. Mesoscale eddies are oases for higher trophic marine life. PLoS (Public Library of Science) ONE [online serial] 7(1):e30161. DOI:  10.1371/journal.pone.0030161Google Scholar

14.

J. J. Govoni 1993. Flux of larval fishes across frontal boundaries: examples from the Mississippi River plume front and the western Gulf Stream front in winter. Bulletin of Marine Science 53:538–566. Google Scholar

15.

J. J. Govoni , and J. A. Hare . 2001. The Charleston Gyre as a spawning and larval nursery habitat for fishes. Pages 123–136 in G. R. Sedberry , editor. Island in the stream: oceanography and fisheries of the Charleston Bump. American Fisheries Society, Symposium 25, Bethesda, Maryland. Google Scholar

16.

J. J. Govoni , J. A. Hare , E. D. Davenport , M. H. Chen , and K. E. Marancik . 2010. Mesoscale, cyclonic eddies as larval fish habitat along the southeast United States shelf: a Lagrangian description of the zooplankton community. ICES Journal of Marine Science 67:403–411. Google Scholar

17.

J. J. Govoni , and L. J. Pietrafesa . 1994. Eulerian views of layered water currents, vertical distribution of some larval fishes, and inferred advective transport over the continental shelf off North Carolina, USA, in winter. Fisheries Oceanography 3:120–132. Google Scholar

18.

J. J. Govoni , and H. L. Spach . 1999. Exchange and flux of larval fishes across the western Gulf Stream front south of Cape Hatteras, USA, in winter. Fisheries Oceanography 8(Supplement 2):77–92. Google Scholar

19.

J. A. Hare , and J. J. Govoni . 2005. Comparison of average larval fish vertical distributions among species exhibiting different transport pathways on the southeast United States continental shelf. U.S. National Marine Fisheries Service Fishery Bulletin 103:728–736. Google Scholar

20.

C. S. Harrison , D. A. Siegel , and S. Mitarai . 2013. Filamentation and eddy-eddy interactions in marine larval accumulation and transport. Marine Ecology Progress Series 472:27–44. Google Scholar

21.

G. L. Hitchcock , T. Rossby , J. L. Lillibridge , E. J. Lessard , E. R. Levine , D. N. Connors , K. Y. Børsheim , and M. Mork . 1994. Signatures of stirring and mixing near the Gulf Stream front. Journal of Marine Research 52:797–836. Google Scholar

22.

E. D. Houde 2008. Emerging from Hjort's shadow. Journal of Northwest Atlantic Fishery Science 41:53–70. Google Scholar

23.

M. H. Judy , and R. M. Lewis . 1983. Distribution of eggs and larvae of Atlantic Menhaden, Brevoortia tyrannus, along the Atlantic coast of the United States. NOAA (National Oceanic and Atmospheric Administration) Technical Report NMFS (National Marine Fisheries Service) SSRF-774. Google Scholar

24.

S. Kimura , A. Kasai , H. Nakata , T. Sugimoto , J. H. Simpson , and J. V. S. Cheok . 1997. Biological productivity of meso-scale eddies caused by frontal disturbances in the Kuroshio. ICES Journal of Marine Science 54:179–192. Google Scholar

25.

T. N. Lee , J. A. Yoder , and L. P. Atkinson . 1991. Gulf Stream frontal eddy influence on productivity of the southeast U.S. continental shelf. Journal of Geophysical Research: Oceans 96:22191–22205. Google Scholar

26.

P. Legendre , and L. Legendre . 1998. Numerical ecology. Elsevier, Amsterdam. Google Scholar

27.

J. L. Lillibridge III, G. Hitchcock , T. Rossby , E. Lessard , M. Mork , and L. Golmen . 1990. Entrainment and mixing of shelf/slope waters in the nearsurface Gulf Stream. Journal of Geophysical Research: Oceans 95:13065–13087. Google Scholar

28.

C. Limouzy-Paris , M. F. McGowan , W. J. Richards , J. P. Umaran , and S. S. Cha . 1994. Diversity of fish larvae in the Florida Keys: results from SEFCAR. Bulletin of Marine Science 54:857–870. Google Scholar

29.

P. S. Lobel , and A. R. Robinson . 1986. Transport and entrapment of fish larvae by ocean mesoscale eddies and currents in Hawaiian waters. Deep-Sea Research, Part A33:483–500. Google Scholar

30.

P. S. Lobel , and A. R. Robinson . 1988. Larval fishes and zooplankton in a cyclonic eddy in Hawaiian waters. Journal of Plankton Research 10:1209–1223. Google Scholar

31.

K. E. Marancik , L. M. Clough , and J. A. Hare . 2005. Cross-shelf and seasonal variation in larval fish assemblages on the southeast United States continental shelf off the coast of Georgia. U.S. NationalMarine Fisheries Service Fishery Bulletin 103:108–129. Google Scholar

32.

T. D. Mathews , and O. Pashuk . 1984. Shelfwater response to the cold winters of 1977 and 1978 in the South Atlantic Bight (SAB). Litoralia 1:41–58. Google Scholar

33.

T. D. Mathews , and O. Pashuk . 1986. Summer and winter hydrography of the U.S. South Atlantic Bight (1973–1979). Journal of Coastal Research 2:311–336. Google Scholar

34.

D. J. McGillicuddy Jr. , R. Johnson , D. A. Siegel , A. F. Michaels , N. R. Bates , and A. H. Knap . 1999. Mesoscale variations of biogeochemical properties in the Sargasso Sea. Journal of Geophysical Research: Oceans 104:13381–13394. Google Scholar

35.

B. S. Miller , and A. W. KendallJr. 2009. Early life history of marine fishes. University of California Press, Berkeley. Google Scholar

36.

T. J. Mullaney , A. G. Miskiewicz , M. E. Baird , P. T. P. Burns , and I. M. Suthers . 2011. Entrainment of larval fish assemblages from the inner shelf into the East Australian Current and into the western Tasman Front. Fisheries Oceanography 20:434–447. Google Scholar

37.

P. Munk , B. W. Hansen , T. G. Nielsen , and H. A. Thomsen . 2003. Changes in plankton and fish larvae communities across hydrographic fronts off west Greenland. Journal of Plankton Research 25:815–830. Google Scholar

38.

H. Nakata , S. Kimura , Y. Okazaki , and A. Kasai . 2000. Implications of mesoscale eddies caused by frontal disturbances of the Kuroshio Current for anchovy recruitment. ICES Journal of Marine Science 57:143–152. Google Scholar

39.

J. S. Nelson 1994. Fishes of the world, 3rd edition. Wiley, New York. Google Scholar

40.

Y. Okazaki , H. Nakata , and S. Kimura . 2002. Effects of frontal eddies on the distribution and food availability of anchovy larvae in theKuroshio Extension. Marine and Freshwater Research 53:403–410. Google Scholar

41.

M. P. Olivar, M. Emelianov , F. Villate , I. Uriarte , F. Maynou , I. Aívarez , and E. Morote . 2010. The role of oceanographic conditions and plankton availability in larval fish assemblages off the Catalan coast (NWMediterranean). Fisheries Oceanography 19:209–229. Google Scholar

42.

D. B. Olson 2001. Biophysical dynamics of western transition zones: a preliminary synthesis. Fisheries Oceanography 10:133–150. Google Scholar

43.

G. Onitsuka , A. Morimoto , T. Takikawa , A. Watanabe , M. Moku , Y. Yoshikawa , and T. Yanagi . 2009. Enhanced chlorophyll associated with island-induced cyclonic eddies in the eastern channel of the Tsushima Straits. Estuarine, Coastal and Shelf Science 81:401–408. Google Scholar

44.

L. J. Pietrafesa , G. S. Janowitz , and P. A. Wittman . 1985. Physical oceanographic processes in the Carolina capes. Pages 23–32 in L. P. Atkinson , D.W. Menzel , and K. A. Bush , editors. Oceanography of the southeastern U. S. Continental Shelf, volume 2. American Geophysical Union, Washington, D.C. Google Scholar

45.

A. B. Powell , D. G. Lindquist , and J. A. Hare . 2000. Larval and pelagic juvenile fishes collected with three types of gear in Gulf Stream and shelf waters in Onslow Bay, North Carolina, and comments on ichthyoplankton distribution and hydrography. U.S. National Marine Fisheries Service Fishery Bulletin 98:427–438. Google Scholar

46.

A. B. Powell , and R. E. Robbins . 1994. Abundance and distribution of icthyoplankton along an inshore-offshore transect in Onslow Bay, North Carolina. NOAA (National Oceanic and Atmospheric Administration) Technical Report NMFS (National Marine Fisheries Service) 120. Google Scholar

47.

H. Powles , and B. W. Stender . 1976. Observations on composition, seasonality and distribution of icthyoplankton from MARMAP cruises in the South Atlantic Bight in 1973. South Carolina Wildlife and Marine Resources Department, Technical Report 11, Charleston. Google Scholar

48.

A. M. Quattrini , D. G. Lindquist , F. M. Bingham , T. E. Lankford , and J. J. Govoni . 2005. Distribution of larval fishes among water masses in Onslow Bay, North Carolina: implications for cross-shelf exchange. Fisheries Oceanography 14:413–431. Google Scholar

49.

W. J. Richards , editor. 2006. Early stages of Atlantic fishes: an identification guide for the western central North Atlantic, volume 2. CRC Press, Boca Raton, Florida. Google Scholar

50.

W. J. Richards, M. F. McGowan , T. Leming , J. T. Lamkin , and S. Kelley . 1993. Larval fish assemblages at the Loop Current boundary in the Gulf ofMexico. Bulletin of Marine Science 53:475–537. Google Scholar

51.

D. E. Richardson , J. K. Llopiz , K. D. Leaman , P. S. Vertes , F. E. Muller-Karger , and R.K. Cowen . 2009. Sailfish (Istiophorus platypterus) spawning and larval environment in a Florida Current frontal eddy. Progress in Oceanography 82:252–264. Google Scholar

52.

A. Sabatés 1990. Changes in the heterogeneity of mesoscale distribution patterns of larval fish associated with a shallow coastal haline front. Estuarine, Coastal and Shelf Science 30:131–140. Google Scholar

53.

A. Sabatés , and M. Masó . 1990. Effect of a shelf-slope front on the spatial distribution of mesopelagic fish larvae in the western Mediterranean. Deep- Sea Research, Part A37:1085–1098. Google Scholar

54.

A. Sabatés , and M. P. Olivar . 1996. Variation of larval fish distributions associated with variability in the location of a shelf-slope front. Marine Ecology Progress Series 135:11–20. Google Scholar

55.

C. Sassa , K. Kawaguchi , Y. Oozeki , H. Kubota , and H. Sugisaki . 2004. Distribution patterns of larval myctophid fishes in the transition region of the western North Pacific. Marine Biology 144:417–428. Google Scholar

56.

W. J. Schmitz Jr. , J. R. Luyten , and R.W. Schmitt . 1993. On the Florida Current T/S envelope. Bulletin of Marine Science 53:1048–1065. Google Scholar

57.

K. A. Smith , M. T. Gibbs , J. H. Middleton , and I. M. Suthers . 1999. Short term variability in larval fish assemblages of the Sydney shelf: tracers of hydrographic variability. Marine Ecology Progress Series 178:1–15. Google Scholar

58.

P. E. Smith , and S. L. Richardson . 1977. Standard techniques for pelagic fish egg and larva surveys. FAO Fisheries Technical Paper 175. Google Scholar

59.

S. Sponaugle , T. Lee , V. Kourafalou , and D. Pinkard . 2005. Florida Current frontal eddies and the settlement of coral reef fishes. Limnology andOceanography 50:1033–1048. Google Scholar

60.

J. C. Taylor , W. A. Mitchell , J. A. Buckel , H. J. Walsh , K. W. Shertzer , G. B. Martin , and J. A. Hare . 2009. Relationships between larval and juvenile abundance of winter-spawned fishes in North Carolina, USA. Marine and Coastal Fisheries: Dynamics,Management, and Ecosystem Science 1:11–20. Google Scholar

61.

C. J. F. Ter Braak , and I. C. Prentice . 1988 A theory of gradient analysis. Advances in Ecological Research 34:235–282. Google Scholar

62.

P. G. Verity , T. N. Lee , J. A. Yoder , G. A. Paffenhöfer , J. O. Blanton , and C. R. Alexander . 1993. Outer shelf processes. Pages 45–74 in D.W. Menzel , editor. Ocean processes: U.S. southeast Continental Shelf: a summary of research conducted in the South Atlantic Bight under the auspices of the U.S. Department of Energy from 1977 to 1991. U.S. Department of Energy, Office of Scientific and Technical Information, Oak Ridge, Tennessee. Google Scholar

63.

L. Xie , and L. J. Pietrafesa . 1995. Shoreward intrusion of upper-layer warm water by prescribed shelf-break temperature perturbation and surface wind stress. Geophysical Research Letters 22:2585–2588. Google Scholar

64.

J. A. Yoder 1983. Statistical analysis of the distribution of fish eggs and larvae on the southeastern U.S. Continental Shelf with comments on oceanographic processes thatmay affect larval survival. Estuarine, Coastal and Shelf Science 17:637–650. Google Scholar

65.

J. H. Zar 1999. Biostatistical analysis, 4th edition. Prentice-Hall, Upper Saddle River, New Jersey.  Google Scholar
© American Fisheries Society 2013
J. J. Govoni, J. A. Hare, and E. D. Davenport "The Distribution of Larval Fishes of the Charleston Gyre Region off the Southeastern United States in Winter Shaped by Mesoscale, Cyclonic Eddies," Marine and Coastal Fisheries: Dynamics, Management, and Ecosystem Science 5(5), 246-259, (1 January 2013). https://doi.org/10.1080/19425120.2013.820245
Published: 1 January 2013
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