A Survival Estimate of Midwestern Adult Eastern Box Turtles Using Radiotelemetry

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Am. Midl. Nat. 165:143 149 A Survival Estimate of Midwestern Adult Eastern Box Turtles Using Radiotelemetry ANDREA F. CURRYLOW 1 715 West State Street, Department of Forestry and Natural Resources, Purdue University, West Lafayette, Indiana 47907 AND PATRICK A. ZOLLNER, BRIAN J. MACGOWAN AND ROD N. WILLIAMS 195 Marstellar Street, Department of Forestry and Natural Resources, Purdue University, West Lafayette, Indiana 47907 ABSTRACT. Eastern box turtles (Terrapene carolina carolina) are widespread in U.S. eastern deciduous forests, yet many populations are experiencing dramatic declines. Herein, we present an assessment of annual survival for adult eastern box turtles that were radio-tracked over a period of 2 y. Using a known fates Kaplan-Meier estimator, the baseline annual survival for adult eastern box turtles in Indiana s south-central region is 96.2%. Annual survival rates varied slightly between the hibernal period (95.6%) and the active period (96.7%). These initial data provide wildlife managers with a baseline from which a recovery period can be calculated. In areas where road mortality and human interface are high, this should be adjusted to ensure the time for recovery is adequate. Further research is recommended over generations and age-classes to better inform management of this protected species. INTRODUCTION Turtles are among the longest-lived vertebrates studied in nature (Gibbons, 1987). Many species commonly live for more than 30 y and some greater than 100 (Flower, 1937; Gibbons, 1987). Despite the longevity of Testudine species, this taxon is currently experiencing worldwide declines resulting from the food, medicinal and pet trades, disease and habitat alteration (Garber and Burger, 1995; Gibbons et al., 2000; IUCN, 2009). Declines of reproductive adults reduce recovery rates of populations and can preclude recoveries altogether when coupled with certain life-history traits (Heppell, 1998; Dodd et al., 2006). For example, box turtles are known to persist for decades, but have low annual reproduction and juvenile (Shine and Iverson, 1995; Dodd, 2001; Steen et al., 2006), making them especially susceptible to local extirpation if adult decreases. Conservation of the adult age classes in long-lived turtles is critical if populations are to be self-sustaining (Heppell, 1998). Consequently, current and accurate adult annual survival s are needed in order for conservation and management strategies to be implemented (Dodd, 1997; Ricklefs, 1998; Congdon et al., 2001). Eastern box turtles (Terrapene carolina carolina) are geographically widespread throughout eastern North American forests, yet many locations are experiencing precipitous population declines (Stickel, 1978; Williams and Parker, 1987; IDNR, 2007). These declines can be attributed to a variety of age- and sex-related factors such as differential survival rates, growth rates and reproductive contribution (Blair, 1976; Frank and Swingland, 1988; St Clair, 1998; Heppell et al., 2000). Although much box turtle biology has been studied, survival s 1 Corresponding author: e-mail: a.currylow@gmail.com 143

144 THE AMERICAN MIDLAND NATURALIST 165(1) TABLE 1. Studies of Terrapene c. carolina reporting a. Many reported s were informal or did not provide an annual survival rate. MRR 5 Mark-release-recapture Author Allen (1868) Flower (1937) Stickel (1978) Yahner (1974) Williams & Parker (1987) Nazdrowicz (2008) Current Study Location Relocation method Massachusetts Anecdotal reports Various Anecdotal reports Estimator Longevity/ Longevity/ Maryland MRR Longevity/ Tennessee MRR % recovery (informal) Indiana MRR Longevity/ Delaware Radiotelemetry Kaplan-Meier data averaged Indiana Radiotelemetry Kaplan-Meier known-fates staggered entry Survivorship age (years) Ann. surv. Standard error 60+ N/A N/A 20 123 N/A N/A 50 80+ N/A N/A N/A 79.5% 45 50+ N/A N/A N/A 81.3 97.7% N/A 95.4 97.8% 0.023 0.069 0.022 0.044 are dominated by (or longevity) (Allen, 1868; Flower, 1937; Stickel, 1978; Williams and Parker, 1987) as opposed to specific survival rates (annual survival), though some average s for annual survival have been made for this species (Yahner, 1974; Nazdrowicz et al., 2008; Table 1). In the Midwest where population declines are of growing concern, no formal survival analyses have been reported. Moreover, no precise s have been calculated using a known fates model where the same individuals are tracked over time. Known fates models have the advantage over mark-release-recapture (MRR) estimators in that every animal marked is recaptured, dead or alive, thus eliminating assumptions of the hazard function (i.e., the probability of an animal dying during a short interval) and capitalizing on a recapture probability of 1 (White and Garrot, 1990). Using a modified Kaplan-Meier estimator (Kaplan and Meier, 1958) with 2 y of radiotelemetry data, we present an of the adult annual survival rate of eastern box turtles in Indiana. The results of this research will provide a baseline of adult and can serve to compare age class throughout the Midwest. This information can influence management decisions for this legally protected species (Indiana Species of Special Concern) and is important when considering future conservation measures such as reintroduction and head starting (Henry, 2003; IDNR, 2007). METHODS STUDY AREA The study area was located within Morgan, Monroe and Brown counties in south-central Indiana and spans approximately 350 sq km (35,000 ha) in total (Fig. 1). The study area includes sites in Morgan-Monroe State Forest (MMSF) and Yellowwood Sate Forest (YSF).

2011 CURRYLOW ET AL.: EASTERN BOX TURTLE SURVIVAL ESTIMATE 145 FIG. 1. Local and regional map of the study area in Indiana, USA. Turtles were radio-tracked in forested habitats of south-central Indiana in Morgan, Monroe and Brown counties (within the approximated dotted rectangle in the center of the local map) MMSF was established in 1929, comprising nearly 10,000 ha and YSF was created in 1940, comprising nearly 9500 ha. This area was chosen because it was suspected to have a stable population of box turtles based on the relative contiguity of the forest habitat (Fig. 1). The location is characterized by hills and ravines of hardwood, deciduous forests with scattered harvest areas managed for multiple purposes, including research. Dominant canopy species include Quercus spp., Carya spp., Fagus grandifolia, Acer saccharum, A. rubrum, Nyssa sylvatica and Liriodendron tulipifera. Herbaceous understory consists of Smilax spp., Parthenocissus quinquefolia, Carex spp., Viola spp. and Desmodium nudiflorum. DATA COLLECTION Meandering transect, visual encounter surveys were used to find adult turtles between May 2007 and Jul. 2009. Surveys were conducted during the active period of box turtles (daylight hours of Apr. through Oct.) and captured adults were subsequently radio-tagged and tracked. Holohil RI-2B Transmitters (14.5 g each) were epoxied to the carapace of the turtles. Transmitters did not exceed 5% of the animal s total body weight.

146 THE AMERICAN MIDLAND NATURALIST 165(1) Radio-tagged box turtles were monitored from May 2007 to Nov. 2009. Tracking consisted of using a homing technique (White and Garrot, 1990) with portable receivers (Advanced Telemetry Systems, Isanti, MN, USA) to approach and visually locate each turtle. All tracking dates and locations were recorded. Turtles were continually added to the study following a staggered entry design. During the 2007 season, 23 turtles were located and incorporated into the study and by the end of the 2009 season, 45 turtles had been incorporated. All animals were tracked two to three times per week from approximately May to Oct. each year. SURVIVAL ESTIMATE We calculated survival of adult box turtles (Nov. 2007 to Nov. 2009) using a modified Kaplan-Meier estimator. Assumptions of survival over specified time intervals and constant survival rates among individuals and are often unrealistic. To account for this, we used the modifications of the Kaplan-Meier procedure outlined by Pollock et al. (1989a) that allows for staggered entry and right-censoring. Modeling for staggered entry enables us to continually add individuals, increasing our number tracked and thus, our precision (while decreasing standard error). The d survival function (Ŝ) for a given time (t) used in StagEnt program (Pollock et al., 1989a) is calculated as follows: ^S t ~P 1{d j rj where j rjvt: Active season and hibernal season s were calculated separately using the radiotelemetric data across two consecutive years. Active season s were grouped by total number of turtles alive (number at risk; r) at the end of each tracking week (sample period; j). The hibernal period data were taken singly, as the animals were not disturbed during this period and any deaths could not be confirmed until the following spring, resulting in sample periods of approximately 6 mo. All censored [deaths or losses (d) and removals] individuals were recorded as censored for the sample period that they were discovered dead, missing or removed from the study. RESULTS Over the 2 y period of the study, 48 eastern box turtles were located and subsequently monitored. Approximately 36 locations were collected for each turtle in the 2008 active period and approximately 70 locations per turtle in 2009. Seven turtles were censored over the course of the study (Table 2). Of the three deaths, one was attributed to a known predation attempt, one to severe emaciation, and one to apparent overexposure to freezing temperatures. The average annual survival was 96.3% with a standard error of 0.04 and a 95% confidence interval of 0.89 1.03. Survival s varied little over each of the 6 mo intervals. The average survival rate during the hibernal period is 95.7% (SE 5 0.04) whereas that of the active period is 97.0% (SE 5 0.03; Table 2). If all s are combined, the 2 y survival for adult eastern box turtles in Indiana was 86.4% (SE 5 0.05). Due to the small number of total deaths, no individual s were made for sexes or for causes of deaths. DISCUSSION Previous studies that include a survival for eastern box turtles often lack formal computation due to recapture methods (Table 1). Until recently, s were made using long-term MRR where individuals cannot be followed over time. Without following animals to ensure their recapture (and thus, their survival), the resulting s are less reliable. It is time-prohibitive to use MRR and exhaustively sample in order to avoid

2011 CURRYLOW ET AL.: EASTERN BOX TURTLE SURVIVAL ESTIMATE 147 TABLE 2. Number of adult eastern box turtles (Terrapene carolina carolina) monitored between 2007 and 2009 in south-central Indiana, USA. Standard error 5 SE and confidence interval 5 CI Time period Total tracked # Censored Survival SE 95% CI Hibernal 2007 23 1 (R lost) 0.954 0.044 0.87 1.04 Active 2008 26 1 (R died) 0.963 0.036 0.89 1.03 Hibernal 2008 26 1 (R died) 0.960 0.039 0.88 1.04 Active 2009 42 1 (R died), 0.978 0.022 0.93 1.02 3(= removed) Annual Average 0.964 0.035 0.89 1.03 2-year Total 0.864 0.048 0.77 0.96 recapture bias. Radiotelemetry methods and known-fates models have eliminated this problem. By following the same individuals over time to ensure recapture, we are able to calculate more realistic and accurate s of annual survival rates. In addition, the estimator (Pollock et al., 1989a) allows for the staggered entry of individuals into the study, increasing precision and reducing standard error (Pollock et al., 1989b). Individual s for sex could not be constructed due to the high of the study animals. Considering this, longer-term monitoring should be conducted to better assess adult eastern box turtle over generations. It has been suggested that box turtle populations with d adult annual survival rates as high 81.3% may not be viable (Nazdrowicz et al., 2008) due to skewed sex ratios and low juvenile abundance, aspects of the population dynamics that were not studied here. In eastern box turtles, hatchlings rarely survive to adulthood and decades are necessary to replace adults in a population (Congdon et al., 1994; Belzer, 2002). Even with an apparently high annual survival such as 90%, only one in a population of 100 turtles would be expected to survive after 44 y (Wilbur and Morin, 1988). Moreover, previous studies suggest that there is no guarantee that recovery can be achieved even with population protection or husbandry (Stickel, 1978; Belzer, 2008). In addition, it should be noted that our annual survival was made from data collected on a relatively undisturbed population. Therefore, the presented here is relatively conservative and could be dramatically reduced in areas of increased wildlife-human interface (Budischak et al., 2006) or during widespread stochastic events such as flooding or disease. This study has shown that relatively undisturbed populations of eastern box turtles in the Midwest have high adult, a life history trait important for a species with low annual reproductive rates. However, this species continues to decline throughout Indiana (IDNR, 2007). Road mortality, habitat destruction and collection for pets are the purported leading causes (IDNR, 2007; Iglay et al., 2007). Declines of this species within Indiana suggest that further research is necessary at development edges and where the human interface with box turtle habitat is greatest. Information presented herein can aid in management decisions for this protected species and is essential when considering future conservation measures. Acknowledgments. This paper is a contribution of the Hardwood Ecosystem Experiment, a partnership of the Indiana Department of Natural Resources (IDNR), Purdue University, Ball State University, Indiana State University, Drake University and the Nature Conservancy. Funding for the

148 THE AMERICAN MIDLAND NATURALIST 165(1) project was provided by the Indiana Department of Forestry Grant #E-9-6-A558 and IDNR Division of Fish and Wildlife, Wildlife Diversity Section, State Wildlife Improvement Grant #E2-08-WDS15. The authors thank J. MacNeil, S. Kimble, H. Powell, N. Burgmeier, S. Johnson, K. Lilly, M. Cross, K. Norris, K. Powers, L. Woody, Z. Walker, A. Hoffman, A. Krainyk, B. Tomson, M. Turnquist, G. Stephens, N. Engbrecht, J. Faller, A. Garcia and B. Geboy for assisting in field data collection. We also thank members of the Williams lab for providing helpful comments on previous versions of this manuscript. Research activities associated with this project fall under the Purdue Animal Care and Use Protocols and amendments, PACUC 07-037 and IDNR Scientific Purposes License 10-0083. LITERATURE CITED ALLEN, J. A. 1868. Catalogue of the reptiles and batrachians found in the vicinity of Springfield, Massachusetts, with notices of all other species known to inhabit the state. Boston Soc. Nat. Hist. Conf. Proc., 12:1 38. BELZER, B. 2002. A nine year study of eastern box turtle courtship with implications for reproductive success and conservation in a translocated population. Turtle Tortoise Newsl., 6:17 26.. 2008. Field observations of North America s eastern box turtle (Terrapene carolina carolina). Cheloniens, 12:12 25. BLAIR, F. W. 1976. Some aspects of the biology of the ornate box turtle, Terrapene ornata. Southwest. Nat., 21:89 103. BUDISCHAK, S. A., J. M. HESTER, S. J. PRICE AND M. E. DORCAS. 2006. Natural history of Terrapene carolina (box turtles)in an urbanized landscape. Southeast. Nat., 5:191 204. CONGDON, J. D., A. E. DUNHAM AND R. C. V. SELS. 1994. Demographics of common snapping turtles (Chelydra serpentina): Implications for conservation and management of long-lived organisms. Am. Zool., 34:397 408., R. D. NAGLE, O.M.KINNEY AND R. C. V. SELS. 2001. Hypotheses of aging in a long-lived vertebrate, Blanding s turtle (Emydoidea blandingii). Exp. Gerontol., 36:813 827. DODD, C. K., JR. 1997. Population structure and the evolution of sexual size dimorphism and sex ratios in an insular population of Florida box turtles (Terrapene carolina bauri). Can. J. Zool./Rev. Can. Zool., 75:1495 1507.. 2001. North American box turtles: A natural history. University of Oklahoma Press, Norman. 231 p., A. OZGUL AND M. K. OLI. 2006. The influence of disturbance events on survival and dispersal rates of Florida box turtles. Ecol. Appl., 16:1936 1944. FLOWER, S. S. 1937. Further notes on the duration of life in animals. III. Reptiles. Proc. Zool. Soc. London, 1:1 39. FRANK, S.AND I. SWINGLAND. 1988. Sex ratio under conditional sex expression. J. Theor. Biol., 135:415 418. GARBER, S. D. AND J. BURGER. 1995. A 20-yr study documenting the relationship between turtle decline and human recreation. Ecol. Appl., 5:1151 1162. GIBBONS, J. W. 1987. Why do turtles live so long? Bioscience, 37:262 269., D. E. SCOTT, T. J. RYAN, K. A. BUHLMANN, T. D. TUBERVILLE, B. S. METTS, J. L. GREENE, T. MILLS, Y. LEIDEN, S. POPPY AND C. T. WINNE. 2000. The global decline of reptiles, deja vu amphibians. Bioscience, 50:653 666. HENRY, P. F. P. 2003. The eastern box turtle at the Patuxent Wildlife Research Center 1940s to the present: Another view. Exp. Gerontol., 38:773 776. HEPPELL, S. S. 1998. Application of life-history theory and population model analysis to turtle conservation. Copeia, 1998:367 375., H. CASWELL AND L. B. CROWDER. 2000. Life histories and elasticity patterns: Perturbation analysis for species with minimal demographic data. Ecology, 81:654 665. IDNR. 2007. Reptiles of Indiana, http://www.ai.org/dnr/fishwild/3307.htm. Indiana Department of Natural Resources, Wildlife Diversity Section. IGLAY, R. B., J. L. BOWMAN AND N. H. NAZDROWICZ. 2007. Eastern Box Turtle (Terrapene carolina carolina) movements in a fragmented landscape. J. Herpetol., 41:102 106.

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