Natal homing in juvenile loggerhead turtles (Caretta caretta)

Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from ocea...

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Published in:	Molecular ecology Vol. 13; no. 12; pp. 3797 - 3808
Main Authors:	BOWEN, BRIAN W., BASS, ANNA L., CHOW, SHAIO-MEI, BOSTROM, MEREDITH, BJORNDAL, KAREN A., BOLTEN, ALAN B., OKUYAMA, TOSHINORI, BOLKER, BENJAMIN M., EPPERLY, SHERYAN, LACASELLA, ERIN, SHAVER, DONNA, DODD, MARK, HOPKINS- MURPHY, SALLY R., MUSICK, JOHN A., SWINGLE, MARK, RANKIN-BARANSKY, KAREN, TEAS, WENDY, WITZELL, WAYNE N., DUTTON, PETER H.
Format:	Journal Article
Language:	English
Published:	Oxford, UK Blackwell Publishing Ltd 01.12.2004
Subjects:	Analysis of Variance Animal behavior Animal reproduction Animals Aquatic reptiles Atlantic Ocean Bayes Theorem Bayesian Coastal hazards conservation genetics Demography DNA Primers DNA, Mitochondrial - genetics Feeding Behavior - physiology Genetic Variation Habitats Haplotypes - genetics Homing Behavior - physiology Marine marine turtles Mitochondrial DNA mixed stock analysis Nesting North America Population structure Reproduction - physiology Reptiles & amphibians Sequence Analysis, DNA Sexual Behavior, Animal - physiology Turtles Turtles - genetics Turtles - physiology North America Atlantic Ocean
ISSN:	0962-1083, 1365-294X
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Abstract	Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans‐oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences (N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea (N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles (ΦST = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R2 = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats.
AbstractList	Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans-oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences (N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea (N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles (PhiST = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R2 = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats. Juvenile loggerhead turtles ( Caretta caretta ) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans‐oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences ( N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea ( N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles (Φ ST = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R 2 = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats. Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans-oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences (N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea (N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles ( Phi sub(ST) = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R super(2) = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats. Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans-oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences (N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea (N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles (PhiST = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R2 = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats.[PUBLICATION ABSTRACT] Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans‐oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences (N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea (N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles (ΦST = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R2 = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats. Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans-oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences (N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea (N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles (PhiST = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R2 = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats.Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean, whereas larger juvenile turtles occupy shallow (neritic) habitats along the continental coastline of North America. Hence the switch from oceanic to neritic stage can involve a trans-oceanic migration. Several researchers have suggested that at the end of the oceanic phase, juveniles are homing to feeding habitats in the vicinity of their natal rookery. To test the hypothesis of juvenile homing behaviour, we surveyed 10 juvenile feeding zones across the eastern USA with mitochondrial DNA control region sequences (N = 1437) and compared these samples to potential source (nesting) populations in the Atlantic Ocean and Mediterranean Sea (N = 465). The results indicated a shallow, but significant, population structure of neritic juveniles (PhiST = 0.0088, P = 0.016), and haplotype frequency differences were significantly correlated between coastal feeding populations and adjacent nesting populations (Mantel test R2 = 0.52, P = 0.001). Mixed stock analyses (using a Bayesian algorithm) indicated that juveniles occurred at elevated frequency in the vicinity of their natal rookery. Hence, all lines of evidence supported the hypothesis of juvenile homing in loggerhead turtles. While not as precise as the homing of breeding adults, this behaviour nonetheless places juvenile turtles in the vicinity of their natal nesting colonies. Some of the coastal hazards that affect declining nesting populations may also affect the next generation of turtles feeding in nearby habitats.
Author	LACASELLA, ERIN BOSTROM, MEREDITH EPPERLY, SHERYAN BOWEN, BRIAN W. OKUYAMA, TOSHINORI CHOW, SHAIO-MEI WITZELL, WAYNE N. MUSICK, JOHN A. RANKIN-BARANSKY, KAREN TEAS, WENDY BJORNDAL, KAREN A. BASS, ANNA L. SWINGLE, MARK DODD, MARK SHAVER, DONNA BOLKER, BENJAMIN M. HOPKINS- MURPHY, SALLY R. DUTTON, PETER H. BOLTEN, ALAN B.
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BackLink	https://www.ncbi.nlm.nih.gov/pubmed/15548292$$D View this record in MEDLINE/PubMed
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References	Bowen BW, Kamezaki N, Limpus CJ, Hughes GH, Meylan AB, Avise JC (1994) Global phylogeography of the loggerhead turtle (Caretta caretta) as indicated by mitochondrial DNA haplotypes. Evolution, 48, 1820-1828. FitzSimmons NN, Moritz C, Limpus CJ, Pope L, Prince R (1997b) Geographic structure of mitochondrial and nuclear gene polymorphisms in Australian green turtle populations and male-biased gene flow. Genetics, 147, 1843-1854. Limpus CJ, Miller JD, Parmenter CJ, Reimer D, McLachlan N, Webb R (1992) Migration of green (Chelonia mydas) and loggerhead (Caretta caretta) turtles to and from eastern Australian rookeries. Wildlife Research, 19, 347-358. Excoffier L, Slatkin M (1995) Maximum likelihood estimation of molecular haplotype frequencies in a diploid population. Molecular Biology and Evolution, 12, 921-927. Bowen BW, Abreu-Grobois FA, Balazs GH, Kamezaki N, Limpus CJ, Ferl RJ (1995) Trans-Pacific migrations of the loggerhead sea turtle demonstrated with mitochondrial DNA markers. Proceedings of the National Academy of Sciences of the USA, 92, 3731-3734. LaCasella EL, Dutton PH, Epperly SP (2004) Genetic Stock Composition of Loggerheads (Caretta caretta) Encountered in the Northeast Atlantic Distant (NED) Longline Fishery using mtDNA Analysis. NOAA-NMFS-SEFSC Tech Memorandum in press. National Technical Information Service, Springfield, VA. Smouse PE, Long JC, Soka RR (1986) Multiple regression and correlation extensions of the mantel test of matrix correspondence. Systematic Zoology, 35, 627-632. Bass AL, Epperly SP, Braun-McNeill J (2004) Multi-year analysis of stock composition of a loggerhead turtle (Caretta caretta) foraging habitat using maximum likelihood and Bayesian methods. Conservation Genetics, in press. Carr A (1987) New perspectives on the pelagic stage of sea turtle development. Conservation Biology, 1, 103-121. FitzSimmons NN, Limpus CJ, Moritz C (1997a) Philopatry of male marine turtles inferred from mitochondrial DNA markers. Proceedings of the National Academy of Sciences of the USA, 94, 8912-8917. Schneider S, Roessli D, Excoffier L (2000) arlequin , Version 2.0: a Software for Population Genetics Data Analysis. Genetics and Biometry Laboratory. University of Geneva, Geneva Switzerland. Avens L, Braun-McNeill J, Epperly S, Lohmann KJ (2003) Site fidelity and homing behavior in juvenile loggerhead sea turtles (Caretta caretta). Marine Biology, 143, 211-220. Dodd CK Jr (1988) Synopsis of the biological data on the loggerhead sea turtle Caretta caretta (Linnaeus, 1758). United States Fish and Wildlife Service Biology Report, 88, 1-110. Nei M (1987) Molecular Evolutionary Genetics. Columbia University Press, New York. Broderick D, Moritz C, Miller JD, Guinea M, Prince RJ, Limpus CJ (1994) Genetic studies of the hawksbill turtle: evidence for multiple stocks and mixed feeding grounds in Australian waters. Pacific Conservation Biology, 1, 123-131. Rankin-Baransky K, Williams CJ, Bass AL, Bowen BW, Spotila JR (2001) Origin of loggerhead turtle (Caretta caretta) strandings in the northwest Atlantic as determined by mtDNA analysis. Journal of Herpetology, 35, 638-646. Epifanio JM, Smouse PE, Kobak CJ, Brown BL (1995) Mitochondrial DNA divergence among populations of American shad (Alosa sapidissima): how much variation is enough for mixed stock analysis? Canadian Journal of Fisheries and Aquatic Sciences, 52, 1688-1702. Wirgin II, Waldman JR, Maceda L, Stabile J, Vecchio VJ (1997) Mixed stock analysis of Atlantic coast striped bass (Morone saxatilis) using nuclear DNA and mitochondrial DNA markers. Canadian Journal of Fisheries and Aquatic Sciences, 54, 2814-2826. Epperly SP, Braun J, Veishlow A (1995) Sea turtles in North Carolina waters. Conservation Biology, 9, 384-394. Bowen BW (1995) Tracking marine turtles with genetic markers: voyages of the ancient mariners. Bioscience, 45, 528-534. Eckert SA, Martins HR (1989) Transatlantic travel by a juvenile loggerhead turtle. Marine Turtle Newsletter, 45, 15. Norman JA, Moritz C, Limpus CJ (1994) Mitochondrial DNA control region polymorphisms: genetic markers for ecological studies of marine turtles. Molecular Ecology, 3, 363-373. Bjorndal KA, Bolten AB, Martins HR (2000) Somatic growth model of juvenile loggerhead sea turtles Caretta caretta: duration of pelagic stage. Marine Ecology Progress Series, 202, 265-272. Grant WS, Milner GB, Krasnowski P, Utter FM (1980) Use of biochemical genetic variants for identification of sockeye salmon (Oncorhynchus nerka) stocks in Cook Inlet, Alaska. Canadian Journal of Fisheries and Aquatic Sciences, 37, 1236-1247. Laurent L, Casale P, Bradai MN et al. (1998) Molecular resolution of the marine turtle stock composition in fishery bycatch: a case study in the Mediterranean. Molecular Ecology, 7, 1529-1542. Engstrom TN, Meylan PA, Meylan AB (2002) Origin of juvenile loggerhead turtles (Caretta caretta) in a tropical developmental habitat in Caribbean Panama. Animal Conservation, 5, 125-133. Bolker B, Okuyama T, Bjorndal K, Bolten A (2003) Sea turtle stock estimation using genetic markers: accounting for sampling error of rare genotypes. Ecological Applications, 13, 763-775. Resendiz A, Resendiz B, Nichols WJ, Seminoff JA, Kamezaki N (1998) First confirmed East-West trans-Pacific movement of a loggerhead turtle (Caretta caretta), released in Baja California, Mexico. Pacific Science, 52, 151-153. Alfaro-Shigueto J, Dutton PH, Mangel J, Vega D (2004) First confirmed occurrence of loggerhead turtles in Peru. Marine Turtle Newsletter, 103, 7-11. Encalada SE, Bjorndal KA, Bolten AB et al. (1998) Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean regions as inferred from mtDNA control region sequences. Marine Biology, 130, 567-575. Roberts MA, Schwartz TS, Karl SA (2004) Global population structure and male-mediated gene flow in the green sea turtle (Chelonia mydas): analysis of microsatellite loci. Genetics, 166, 1857-1870. Bolten AB, Bjorndal KA, Martins HR et al. (1998) Trans-Atlantic developmental migrations of loggerhead sea turtles demonstrated by mtDNA sequence analyses. Ecological Applications, 8, 1-7. Karl SA, Bowen BW, Avise JC (1992) Global population structure and male-mediated gene flow in the green turtle (Chelonia mydas): RFLP analysis of anonymous nuclear DNA regions. Genetics, 131, 163-173. Mullis KB, Faloona F (1987) Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction. Methods in Enzymology, 155, 335-350. Hatase H, Takai N, Matsuzawa Y et al. (2002b) Size-related differences in feeding habitat use of adult female loggerhead turtles Caretta caretta around Japan determined by stable isotope analyses and satellite telemetry. Marine Ecology Progress Series, 233, 273-281. Tamura K, Nei M (1993) Estimation of the number of substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Molecular Biology and Evolution, 10, 512-526. Casale P, Laurent L, Gerosa G, Argano R (2002) Molecular evidence of male-biased dispersal in loggerhead turtle juveniles. Journal of Experimental Marine Biology and Ecology, 267, 139-145. Okuyama T, Bolker BM (2005) Combining genetic and ecological data to estimate sea turtle origins. Ecological Applications, in press. Epperly SP, Braun J, Chester AJ et al. (1996) Beach strandings as an indicator of at-sea mortality of sea turtles. Bulletin of Marine Science, 59, 289-297. Bowen BW, Avise JC, Richardson JI, Meylan AB, Margaritoulis D, Hopkins-Murphy SR (1993) Population structure of loggerhead turtles (Caretta caretta) in the northwestern Atlantic Ocean and Mediterranean Sea. Conservation Biology, 7, 834-844. Nichols WJ, Resendiz A, Seminoff JA, Resendiz B (2000) TransPacific migration of a loggerhead turtle monitored by satellite telemetry. Bulletin Marine Science, 67, 937-947. Pella J, Masuda M (2001) Bayesian methods for analysis of stock mixtures from genetic characters. Fishery Bulletin, 99, 151-167. Witzell WN (2002) Immature Atlantic loggerhead turtles (Caretta caretta): suggested changes to the life history model. Herpetological Review, 33, 266-269. Witzell WN, Bass AL, Bresette MJ, Singewald DA, Gorham JC (2002) Origin of immature loggerhead turtles (Caretta caretta) from Hutchinson island, Florida: evidence from mtDNA markers. Fishery Bulletin, 100, 624-631. Hatase H, Kinoshita M, Bando T et al. (2002a) Population structure of loggerhead turtles, Caretta caretta, nesting in Japan: bottlenecks on the Pacific population. Marine Biology, 141, 299-305. Allard MW, Miyamoto MM, Bjorndal KA, Bolten AB, Bowen BW (1994) Support for natal homing in green turtles from mitochondrial DNA sequences. Copeia, 1994, 34-41. Bjorndal KA, Bolten AB, Dellinger T, Delgado C, Martins HR (2003) Compensatory growth in oceanic loggerhead sea turtles: response to a stochastic environment. Ecology, 84, 1237-1249. Owens DW, Ruiz GW (1980) New methods of obtaining blood and cerebrospinal fluid from marine turtles. Herpetologica, 36, 17-20. Seutin G, White BN, Boag PT (1991) Preservation of avian blood and tissue samples for DNA analysis. Canadian Journal of Zoology, 69, 82-90. 1993; 7 1987; 1 2004; 166 1989; 45 1986; 35 2003; 13 1992; 19 2003a 1980; 37 1980; 36 2003b; 2 1987; 155 2001 2000; 202 2000 1997; 54 2002; 267 2002b; 233 2002; 100 1987 1994; 1994 1988; 88 1997a; 94 2001; 99 1998; 52 2002a; 141 2003; 84 1995; 52 1995; 9 1995; 92 2004; 103 2000; 67 2002; 5 1995; 12 2002; 33 1996 2005 2004 1994; 48 1993 2003 1992 1996; 59 1997b; 147 1998; 130 1999 1991; 69 1992; 131 1995; 45 1993; 10 1994; 1 1998; 7 1994; 3 2001; 35 2003; 143 1998; 8 Resendiz A (e_1_2_6_55_1) 1998; 52 e_1_2_6_32_1 Karl SA (e_1_2_6_40_1) 1992; 131 Bolten AB (e_1_2_6_10_1) 2003 e_1_2_6_19_1 e_1_2_6_36_1 e_1_2_6_59_1 FitzSimmons NN (e_1_2_6_31_1) 1997; 94 e_1_2_6_11_1 e_1_2_6_34_1 e_1_2_6_17_1 e_1_2_6_15_1 e_1_2_6_43_1 e_1_2_6_60_1 Schneider S (e_1_2_6_57_1) 2000 FitzSimmons NN (e_1_2_6_30_1) 1996 Epperly SP (e_1_2_6_28_1) 1996; 59 e_1_2_6_5_1 e_1_2_6_7_1 Bolten AB (e_1_2_6_9_1) 2003 e_1_2_6_24_1 e_1_2_6_3_1 Van Dyke JM (e_1_2_6_62_1) 1993 Hopkins‐Murphy SR (e_1_2_6_38_1) 2003 e_1_2_6_45_1 e_1_2_6_26_1 e_1_2_6_52_1 Margaritoulis D (e_1_2_6_44_1) 2003 e_1_2_6_54_1 Pella J (e_1_2_6_53_1) 2001; 99 Alfaro‐Shigueto J (e_1_2_6_2_1) 2004; 103 e_1_2_6_50_1 Owens DW (e_1_2_6_51_1) 1980; 36 LaCasella EL (e_1_2_6_41_1) 2004 Eckert SA (e_1_2_6_22_1) 1989; 45 Ehrhart LM (e_1_2_6_23_1) 2003 Dutton PH (e_1_2_6_21_1) 1996 Bowen BW (e_1_2_6_13_1) 2003 Hykle DJ (e_1_2_6_39_1) 1992 Dodd CK (e_1_2_6_20_1) 1988; 88 Witzell WN (e_1_2_6_64_1) 2002; 33 e_1_2_6_14_1 e_1_2_6_35_1 Hillis DM (e_1_2_6_37_1) 1996 e_1_2_6_12_1 e_1_2_6_18_1 FitzSimmons NN (e_1_2_6_33_1) 1999 e_1_2_6_56_1 e_1_2_6_16_1 e_1_2_6_63_1 e_1_2_6_42_1 e_1_2_6_61_1 Schroeder BA (e_1_2_6_58_1) 2003 Nichols WJ (e_1_2_6_47_1) 2000; 67 e_1_2_6_8_1 Norrgard JW (e_1_2_6_49_1) 1996 e_1_2_6_4_1 e_1_2_6_6_1 e_1_2_6_25_1 e_1_2_6_48_1 Witzell WN (e_1_2_6_65_1) 2002; 100 Excoffier L (e_1_2_6_29_1) 1995; 12 e_1_2_6_27_1 e_1_2_6_46_1
References_xml	– reference: Hatase H, Kinoshita M, Bando T et al. (2002a) Population structure of loggerhead turtles, Caretta caretta, nesting in Japan: bottlenecks on the Pacific population. Marine Biology, 141, 299-305. – reference: Pella J, Masuda M (2001) Bayesian methods for analysis of stock mixtures from genetic characters. Fishery Bulletin, 99, 151-167. – reference: Encalada SE, Bjorndal KA, Bolten AB et al. (1998) Population structure of loggerhead turtle (Caretta caretta) nesting colonies in the Atlantic and Mediterranean regions as inferred from mtDNA control region sequences. Marine Biology, 130, 567-575. – reference: Dodd CK Jr (1988) Synopsis of the biological data on the loggerhead sea turtle Caretta caretta (Linnaeus, 1758). United States Fish and Wildlife Service Biology Report, 88, 1-110. – reference: Witzell WN, Bass AL, Bresette MJ, Singewald DA, Gorham JC (2002) Origin of immature loggerhead turtles (Caretta caretta) from Hutchinson island, Florida: evidence from mtDNA markers. Fishery Bulletin, 100, 624-631. – reference: Engstrom TN, Meylan PA, Meylan AB (2002) Origin of juvenile loggerhead turtles (Caretta caretta) in a tropical developmental habitat in Caribbean Panama. Animal Conservation, 5, 125-133. – reference: Epperly SP, Braun J, Chester AJ et al. (1996) Beach strandings as an indicator of at-sea mortality of sea turtles. Bulletin of Marine Science, 59, 289-297. – reference: Witzell WN (2002) Immature Atlantic loggerhead turtles (Caretta caretta): suggested changes to the life history model. Herpetological Review, 33, 266-269. – reference: Bowen BW, Kamezaki N, Limpus CJ, Hughes GH, Meylan AB, Avise JC (1994) Global phylogeography of the loggerhead turtle (Caretta caretta) as indicated by mitochondrial DNA haplotypes. Evolution, 48, 1820-1828. – reference: Rankin-Baransky K, Williams CJ, Bass AL, Bowen BW, Spotila JR (2001) Origin of loggerhead turtle (Caretta caretta) strandings in the northwest Atlantic as determined by mtDNA analysis. Journal of Herpetology, 35, 638-646. – reference: Bjorndal KA, Bolten AB, Dellinger T, Delgado C, Martins HR (2003) Compensatory growth in oceanic loggerhead sea turtles: response to a stochastic environment. Ecology, 84, 1237-1249. – reference: Carr A (1987) New perspectives on the pelagic stage of sea turtle development. Conservation Biology, 1, 103-121. – reference: Mullis KB, Faloona F (1987) Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction. Methods in Enzymology, 155, 335-350. – reference: Wirgin II, Waldman JR, Maceda L, Stabile J, Vecchio VJ (1997) Mixed stock analysis of Atlantic coast striped bass (Morone saxatilis) using nuclear DNA and mitochondrial DNA markers. Canadian Journal of Fisheries and Aquatic Sciences, 54, 2814-2826. – reference: Epperly SP, Braun J, Veishlow A (1995) Sea turtles in North Carolina waters. Conservation Biology, 9, 384-394. – reference: FitzSimmons NN, Limpus CJ, Moritz C (1997a) Philopatry of male marine turtles inferred from mitochondrial DNA markers. Proceedings of the National Academy of Sciences of the USA, 94, 8912-8917. – reference: Schneider S, Roessli D, Excoffier L (2000) arlequin , Version 2.0: a Software for Population Genetics Data Analysis. Genetics and Biometry Laboratory. University of Geneva, Geneva Switzerland. – reference: Alfaro-Shigueto J, Dutton PH, Mangel J, Vega D (2004) First confirmed occurrence of loggerhead turtles in Peru. Marine Turtle Newsletter, 103, 7-11. – reference: Bowen BW, Avise JC, Richardson JI, Meylan AB, Margaritoulis D, Hopkins-Murphy SR (1993) Population structure of loggerhead turtles (Caretta caretta) in the northwestern Atlantic Ocean and Mediterranean Sea. Conservation Biology, 7, 834-844. – reference: Broderick D, Moritz C, Miller JD, Guinea M, Prince RJ, Limpus CJ (1994) Genetic studies of the hawksbill turtle: evidence for multiple stocks and mixed feeding grounds in Australian waters. Pacific Conservation Biology, 1, 123-131. – reference: Smouse PE, Long JC, Soka RR (1986) Multiple regression and correlation extensions of the mantel test of matrix correspondence. Systematic Zoology, 35, 627-632. – reference: Eckert SA, Martins HR (1989) Transatlantic travel by a juvenile loggerhead turtle. Marine Turtle Newsletter, 45, 15. – reference: LaCasella EL, Dutton PH, Epperly SP (2004) Genetic Stock Composition of Loggerheads (Caretta caretta) Encountered in the Northeast Atlantic Distant (NED) Longline Fishery using mtDNA Analysis. NOAA-NMFS-SEFSC Tech Memorandum in press. National Technical Information Service, Springfield, VA. – reference: Bass AL, Epperly SP, Braun-McNeill J (2004) Multi-year analysis of stock composition of a loggerhead turtle (Caretta caretta) foraging habitat using maximum likelihood and Bayesian methods. Conservation Genetics, in press. – reference: Bowen BW, Abreu-Grobois FA, Balazs GH, Kamezaki N, Limpus CJ, Ferl RJ (1995) Trans-Pacific migrations of the loggerhead sea turtle demonstrated with mitochondrial DNA markers. Proceedings of the National Academy of Sciences of the USA, 92, 3731-3734. – reference: Nei M (1987) Molecular Evolutionary Genetics. Columbia University Press, New York. – reference: Bjorndal KA, Bolten AB, Martins HR (2000) Somatic growth model of juvenile loggerhead sea turtles Caretta caretta: duration of pelagic stage. Marine Ecology Progress Series, 202, 265-272. – reference: Karl SA, Bowen BW, Avise JC (1992) Global population structure and male-mediated gene flow in the green turtle (Chelonia mydas): RFLP analysis of anonymous nuclear DNA regions. Genetics, 131, 163-173. – reference: Nichols WJ, Resendiz A, Seminoff JA, Resendiz B (2000) TransPacific migration of a loggerhead turtle monitored by satellite telemetry. Bulletin Marine Science, 67, 937-947. – reference: Limpus CJ, Miller JD, Parmenter CJ, Reimer D, McLachlan N, Webb R (1992) Migration of green (Chelonia mydas) and loggerhead (Caretta caretta) turtles to and from eastern Australian rookeries. Wildlife Research, 19, 347-358. – reference: Epifanio JM, Smouse PE, Kobak CJ, Brown BL (1995) Mitochondrial DNA divergence among populations of American shad (Alosa sapidissima): how much variation is enough for mixed stock analysis? Canadian Journal of Fisheries and Aquatic Sciences, 52, 1688-1702. – reference: Norman JA, Moritz C, Limpus CJ (1994) Mitochondrial DNA control region polymorphisms: genetic markers for ecological studies of marine turtles. Molecular Ecology, 3, 363-373. – reference: Grant WS, Milner GB, Krasnowski P, Utter FM (1980) Use of biochemical genetic variants for identification of sockeye salmon (Oncorhynchus nerka) stocks in Cook Inlet, Alaska. Canadian Journal of Fisheries and Aquatic Sciences, 37, 1236-1247. – reference: FitzSimmons NN, Moritz C, Limpus CJ, Pope L, Prince R (1997b) Geographic structure of mitochondrial and nuclear gene polymorphisms in Australian green turtle populations and male-biased gene flow. Genetics, 147, 1843-1854. – reference: Casale P, Laurent L, Gerosa G, Argano R (2002) Molecular evidence of male-biased dispersal in loggerhead turtle juveniles. Journal of Experimental Marine Biology and Ecology, 267, 139-145. – reference: Excoffier L, Slatkin M (1995) Maximum likelihood estimation of molecular haplotype frequencies in a diploid population. Molecular Biology and Evolution, 12, 921-927. – reference: Bowen BW (1995) Tracking marine turtles with genetic markers: voyages of the ancient mariners. Bioscience, 45, 528-534. – reference: Roberts MA, Schwartz TS, Karl SA (2004) Global population structure and male-mediated gene flow in the green sea turtle (Chelonia mydas): analysis of microsatellite loci. Genetics, 166, 1857-1870. – reference: Laurent L, Casale P, Bradai MN et al. (1998) Molecular resolution of the marine turtle stock composition in fishery bycatch: a case study in the Mediterranean. Molecular Ecology, 7, 1529-1542. – reference: Bolker B, Okuyama T, Bjorndal K, Bolten A (2003) Sea turtle stock estimation using genetic markers: accounting for sampling error of rare genotypes. Ecological Applications, 13, 763-775. – reference: Tamura K, Nei M (1993) Estimation of the number of substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Molecular Biology and Evolution, 10, 512-526. – reference: Allard MW, Miyamoto MM, Bjorndal KA, Bolten AB, Bowen BW (1994) Support for natal homing in green turtles from mitochondrial DNA sequences. Copeia, 1994, 34-41. – reference: Seutin G, White BN, Boag PT (1991) Preservation of avian blood and tissue samples for DNA analysis. Canadian Journal of Zoology, 69, 82-90. – reference: Owens DW, Ruiz GW (1980) New methods of obtaining blood and cerebrospinal fluid from marine turtles. Herpetologica, 36, 17-20. – reference: Okuyama T, Bolker BM (2005) Combining genetic and ecological data to estimate sea turtle origins. Ecological Applications, in press. – reference: Resendiz A, Resendiz B, Nichols WJ, Seminoff JA, Kamezaki N (1998) First confirmed East-West trans-Pacific movement of a loggerhead turtle (Caretta caretta), released in Baja California, Mexico. Pacific Science, 52, 151-153. – reference: Avens L, Braun-McNeill J, Epperly S, Lohmann KJ (2003) Site fidelity and homing behavior in juvenile loggerhead sea turtles (Caretta caretta). Marine Biology, 143, 211-220. – reference: Bolten AB, Bjorndal KA, Martins HR et al. (1998) Trans-Atlantic developmental migrations of loggerhead sea turtles demonstrated by mtDNA sequence analyses. Ecological Applications, 8, 1-7. – reference: Hatase H, Takai N, Matsuzawa Y et al. (2002b) Size-related differences in feeding habitat use of adult female loggerhead turtles Caretta caretta around Japan determined by stable isotope analyses and satellite telemetry. 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Snippet	Juvenile loggerhead turtles (Caretta caretta) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean,... Juvenile loggerhead turtles ( Caretta caretta ) from West Atlantic nesting beaches occupy oceanic (pelagic) habitats in the eastern Atlantic and Mediterranean,...
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SubjectTerms	Analysis of Variance Animal behavior Animal reproduction Animals Aquatic reptiles Atlantic Ocean Bayes Theorem Bayesian Coastal hazards conservation genetics Demography DNA Primers DNA, Mitochondrial - genetics Feeding Behavior - physiology Genetic Variation Habitats Haplotypes - genetics Homing Behavior - physiology Marine marine turtles Mitochondrial DNA mixed stock analysis Nesting North America Population structure Reproduction - physiology Reptiles & amphibians Sequence Analysis, DNA Sexual Behavior, Animal - physiology Turtles Turtles - genetics Turtles - physiology
Title	Natal homing in juvenile loggerhead turtles (Caretta caretta)
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