Introduction
Globally, loggerhead marine turtle Caretta caretta populations are declining (Witherington et al., Reference Witherington, Kubilis, Brost and Meylan2009). Within the Western Atlantic five subpopulations have been defined, based on genetic analyses: (1) Northern, (2) Peninsular Florida, (3) Dry Tortugas, (4) Northern Gulf of Mexico, and (5) Greater Caribbean (Shamblin et al., Reference Shamblin, Dodd, Bagley, Ehrhart, Tucker and Johnson2011, 2012). The threatened Dry Tortugas subpopulation is estimated to be the smallest, with 258–496 adult females (Richards et al., Reference Richards, Epperly, Heppell, King, Sasso and Moncada2011). The small population and remoteness of the nesting beaches make Dry Tortugas turtles ideal for studying habitat requirements of nesting loggerhead turtles. To provide adequate protection for marine turtles from in-water threats throughout their nesting phase and inter-nesting period, knowledge of both large- and fine-scale habitat-use patterns is required (Hamann et al., Reference Hamann, Godfrey, Seminoff, Arthur, Barata and Bjorndal2010).
Dry Tortugas National Park encompasses a cluster of islands c. 100 km west of Key West, Florida (Fig. 1), where loggerhead turtles regularly nest on the sandy beaches (Reardon, Reference Reardon2000). Of the seven islands in the Park, the smallest is East Key (c. 400 m long × c. 100 m wide) and the largest is Loggerhead Key (c. 1.5 km long × c. 250 m wide); the majority of turtle-nesting activity occurs on these two islands (Fig. 1). The Park is subdivided into a Natural Cultural Zone, where Park rules apply but where human uses are permitted, and a Research Natural Area, in which most human activities (e.g. anchoring, fishing) are restricted. The Research Natural Area contains an exclusion zone, the Historic Adaptive Use Zone (Fig. 1), within which anchoring and hook-and-line fishing are permitted.
Hart et al. (Reference Hart, Zawada, Fujisaki and Lidz2010) described the first in-water habitat-use patterns for seven Dry Tortugas loggerhead turtles nesting on East Key. They used satellite telemetry to identify core habitat zones, and mapped their benthic composition using the U.S. Geological Survey's Along-Track Reef Imaging System (ATRIS; Zawada et al., Reference Zawada, Thompson and Butcher2008). As Dry Tortugas contains another significant nesting site (Loggerhead Key), an expanded study was warranted to understand fully the behaviours and needs of this subpopulation during critical inter-nesting periods.
Methods
We analysed satellite tracks of an additional 20 loggerhead turtles, of which 10 nested on East and 10 on Loggerhead Key. We tested the hypothesis that loggerhead turtles used in-water habitat in close proximity to nesting beaches, and characterized the core-use benthic habitat selected by turtles. To track turtles we followed the methods described in Hart et al. (Reference Hart, Zawada, Fujisaki and Lidz2010): tagging and sampling were carried out after we intercepted turtles following nesting events or false crawls (Table 1). Satellite positions were determined by Argos, with six location classes of varying accuracies: < 250 m for location class 3; 250–< 500 m for 2; 500–< 1,500 m for 1; and > 1,500 m for 0. For a satellite pass with three or two messages the accuracy was unknown and locations were tagged as location classes A and B, respectively (CLS, 2011, but see also Witt et al., Reference Witt, Åkesson, Broderick, Coyne, Ellick and Formia2010, for on-animal location accuracy estimates). Argos provided Kalman-filtered (Kalman, Reference Kalman1960) data and we manually removed obviously erroneous points (e.g. on land or very distant) and location class Z, as well as points that required straight-line swimming speeds > 5 km per hour, were deeper than 150 m (Hawkes et al., Reference Hawkes, Witt, Broderick, Coker, Coyne and Dodd2011, found that adult female loggerhead turtles in the south-eastern USA did not generally leave the waters of the continental shelf (< 200 m), and the depths throughout Dry Tortugas are ≤ 100 m), occurred on the capture date, and were considered to be outside the inter-nesting time period (i.e. after obvious migration away from the study site, such as the last point within 25 km of Dry Tortugas or after 31 August, the end of the breeding period for Dry Tortugas loggerhead turtles). For filtered locations with at least 20 days of data we generated the mean number of daily locations, to minimize autocorrelation, and used them in the kernel density estimation, a non-parametric method for identifying one or more core areas within a home-range boundary (White & Garrott, Reference White and Garrott1990), with appropriate weighting of outlying observations. We used ArcGIS v. 9.3 (ESRI, Redlands, USA) to calculate the in-water area within 50% kernel density estimates to represent the core area of activity during inter-nesting (Hooge et al., Reference Hooge, Eichenlaub and Hooge2001; Supplementary Material 1), and overlaid each turtle's core area to determine an overlap area where turtles co-occurred. Turtle site-fidelity to inter-nesting areas was determined with Monte Carlo Random Walk simulations (100 replicates), using the Animal Movement Analysis extension for ArcView v. 3.2 (Supplementary Material 2). We also calculated the number of days within each grid cell (0.5 × 0.5 km) for individual turtles (Fig. 2), using only filtered locations with location classes 3, 2 and 1, as these accuracy estimates matched the spatial scale of the selected grid.
* Site-fidelity tests were run to determine if movements within inter-nesting areas were random. Passed indicates rejection of the null hypothesis that the movements were random. The proportion of the random movement paths with higher mean square distance values than the observed path was > 0.99 for all turtles except turtle G, which had a proportion > 0.88.
To assess habitat diversity around Loggerhead Key we conducted benthic surveys in July 2011 using ATRIS, which simultaneously acquired geo-referenced, colour digital images and measurements of water depth (Fig. 3a). We assigned ATRIS images to one of five categories based on the predominant substrate type: rubble, sand, seagrass, senile coral reef, or unclassifiable. We grouped categorized images into a 0.5 × 0.5 km grid (Fig. 3a) and computed the inverse of Simpson's index, a measure of habitat diversity (Fig. 3b; see equation in Hart et al., Reference Hart, Zawada, Fujisaki and Lidz2010). Cells containing < 50 images were excluded from analyses. To investigate turtle–habitat associations we calculated the total number of turtle tracking days per cell (high-quality locations only), and overlaid this on the habitat-index plot (Fig. 3b).
Results
Our turtle-tracking data revealed that 17 of 18 turtles (94%) showed site-fidelity to core inter-nesting habitats (50% kernel density estimates; Table 1). Distance to the nearest land from the centroids of these 50% kernel density estimates was 0.5–10.5 km (Supplementary Material 1), which supports previous findings (Miller, Reference Miller, Lutz and Musick1997; Schroeder et al., Reference Schroeder, Foley, Bagley, Bolten and Witherington2003; Hart et al., Reference Hart, Zawada, Fujisaki and Lidz2010). The 10 East Key loggerhead turtles used an area almost identical to that reported in Hart et al. (2010; Fig. 2), demonstrating consistency of inter-nesting habitat-use across years and turtles.
The ATRIS surveys (Fig. 3a) yielded 264,100 permanently archived colour digital images; every fifth image (47,312 images) was used for analysis because of extensive overlap. Carbonate sand was the dominant cover type (32.3%) and seagrass was the least represented (3.6%). Senile coral reef was present throughout the surveyed area but was most prevalent and dominant in the western half (Fig. 3a, rows A–E, columns 1–9). Patches of rubble were found all around Loggerhead Key and represented the predominant cover type on the shoals west and south of the island (Fig. 3a, blue area).
The spatial distribution of the inverse of Simpson's index revealed that regions of highest habitat diversity (≥ 2.4) were situated in close proximity to the beach (Fig. 3b, rows A–C, columns 7–13) and to its south-west (rows C–F, columns 4–8). Turtle observations per cell (20 of 37, 54%) showed turtles that nested on Loggerhead Key were most often located within areas of high habitat-diversity. All cells with turtle counts represented various combinations of our tagged turtles, with the exception of the two cells with five counts (Fig. 3, rows B–C, column 9), where turtle I was detected twice in each cell, and the one cell with four counts (Fig. 3, row B, column 11), where turtle J was detected four times. For the duration of the study three turtles (D, E and G) only registered sufficiently high-quality location data within the grid boundary west of Loggerhead Key.
Discussion
As in the previous study of loggerhead turtles around East Key (Hart et al., Reference Hart, Zawada, Fujisaki and Lidz2010) the highest-quality turtle-location data occurred within areas of highest habitat-diversity (Fig. 3b). The kernel density estimates exhibit a similar orientation to the south of Loggerhead Key, suggesting these tagged turtles are primarily accessing the nesting beaches from the south and leaving them along similar paths. Previously we observed a westward bias among the core-areas of East Key nesters (Hart et al., Reference Hart, Zawada, Fujisaki and Lidz2010); these areas were adjacent to a deep-water channel, with low habitat diversity and dominated by sand and rubble, but they were interspersed between regions of high diversity. At Loggerhead Key the east side offers the most direct access to deep water but is essentially devoid of suitable structure for hiding or resting. Loggerhead Key's west side offers more diverse habitat, including a medium-profile patch reef (Little Africa; Fig. 3a, row A, column 10) and numerous shallow ledges oriented parallel to the island and extending south (row B, columns 8–9 to row E, columns 5–6). Isolated clusters of living coral heads occur on top of and to the west of the ledges. For our tagged turtles nesting on Loggerhead Key, greater habitat diversity and a more topographically complex benthos seem to be more important than proximity to deep water.
Our group of 27 loggerhead turtles (20 in this study, seven in Hart et al., Reference Hart, Zawada, Fujisaki and Lidz2010) represents c. 10% of the estimated nesting population in Dry Tortugas, a genetically distinct subpopulation. Tracking data revealed high site-fidelity to the chosen nesting beach and nearby waters during inter-nesting, and preferred corridors between them. Benthic mapping (here and in Hart et al., Reference Hart, Zawada, Fujisaki and Lidz2010) showed both nesting beaches are adjacent to diverse habitat, which may contribute to the turtles remaining within c. 10 km of their nesting beach during breeding periods. This behaviour has implications for evaluating current protected-area boundaries as well as regulating human activities in areas near loggerhead turtle nesting beaches at Dry Tortugas. Protecting diverse benthic areas that are located adjacent to loggerhead turtle nesting beaches here and elsewhere could provide benefits for overall biodiversity conservation.
Acknowledgements
We thank National Park Service (NPS) staff at Dry Tortugas National Park, and U.S. Geological Survey (USGS) staff, for field and laboratory assistance. The USGS Coastal and Marine Geology, Priority Ecosystem Studies, and Ecosystems Programs provided funding. We acknowledge the use of STAT at www.seaturtle.org. All research on loggerhead turtles was conducted according to institutional and animal-care protocols (USGS/SESC 2011-05), NPS permits DRTO-2008-SCI-0008, DRTO-2009-SCI-0005, DRTO-2011-SCI-0012, DRTO-2012-SCI-0008, and Florida Marine Turtle Permit 176. Any use of trade, product or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
Biographical sketches
Kristen Hart's research focuses on the population biology of rare and threatened reptiles, including several species of marine turtles, to promote their conservation. David Zawada's research interests include underwater imaging systems, image-processing algorithms, and the optical properties of marine organisms, especially corals. Autumn Sartain has been involved in various research concerning wildlife ecology and conservation, with a particular focus on animal movement patterns. Ikuko Fujisaki's research interests include population ecology, spatial ecology and quantitative ecology, focusing on marine and wetland species.