Ecological Archives E094-237-A2
Hideo Hatase, Kazuyoshi Omuta, Katsumi Tsukamoto. 2013. A mechanism that maintains alternative life histories in a loggerhead sea turtle population. Ecology 94:2583–2594. http://dx.doi.org/10.1890/12-1588.1
Appendix B (Table B1). Life history parameters of adult female loggerhead turtle (Caretta caretta) recruits whose eggs were sampled in 2008 at Yakushima Island, Japan. Data on straight carapace lengths and stable isotope ratios are from Hatase et al. (2010).
Tag number |
Straight carapace length (mm) |
δ13C (‰) |
δ15N (‰) |
Foraging habitat |
Mean clutch size |
Mean emergence success (%) |
61887 |
775 |
-20.02 |
9.24 |
oceanic |
|
|
61884 |
758 |
-20.52 |
9.91 |
oceanic |
118.5 |
57.9 |
61566 |
774 |
-19.38 |
9.92 |
oceanic |
79.0 |
43.0 |
65053 |
748 |
-19.96 |
10.02 |
oceanic |
|
|
61858 |
760 |
-19.69 |
10.10 |
oceanic |
|
|
61281 |
817 |
-20.03 |
10.20 |
oceanic |
116.0 |
69.0 |
61670 |
779 |
-19.73 |
10.21 |
oceanic |
|
|
61916 |
800 |
-19.76 |
10.22 |
oceanic |
|
|
61657 |
739 |
-19.84 |
10.24 |
oceanic |
|
|
61682 |
813 |
-19.46 |
10.37 |
oceanic |
|
|
61690 |
775 |
-19.93 |
10.47 |
oceanic |
89.5 |
76.6 |
61696 |
800 |
-19.71 |
10.51 |
oceanic |
95.0 |
80.0 |
61624 |
839 |
-19.68 |
10.53 |
oceanic |
|
|
61743 |
768 |
-19.47 |
10.56 |
oceanic |
|
|
61717 |
784 |
-19.56 |
10.58 |
oceanic |
|
|
61661 |
812 |
-19.79 |
10.64 |
oceanic |
|
|
61999 |
742 |
-19.12 |
10.65 |
oceanic |
|
|
61600 |
794 |
-19.66 |
10.80 |
oceanic |
|
|
61023 |
812 |
-19.41 |
10.91 |
oceanic |
|
|
61618 |
794 |
-19.26 |
11.15 |
oceanic |
113.0 |
54.9 |
61907 |
747 |
-19.33 |
11.24 |
oceanic |
|
|
61874 |
746 |
-18.80 |
11.62 |
oceanic |
104.0 |
72.1 |
61882 |
764 |
-19.10 |
11.65 |
oceanic |
|
|
61544 |
803 |
-18.55 |
11.70 |
oceanic |
|
|
61932 |
775 |
-18.57 |
11.77 |
oceanic |
|
|
61565 |
872 |
-19.28 |
11.82 |
oceanic |
|
|
61681 |
780 |
-18.60 |
11.90 |
oceanic |
|
|
61485 |
759 |
-17.47 |
12.74 |
neritic |
107.0 |
54.2 |
61260 |
853 |
-17.51 |
13.22 |
neritic |
|
|
61567 |
|
-17.51 |
13.23 |
neritic |
|
|
61540 |
789 |
-18.02 |
13.24 |
neritic |
|
|
61412 |
791 |
-18.46 |
13.32 |
neritic |
|
|
65035 |
770 |
-17.38 |
13.35 |
neritic |
111.0 |
72.1 |
61583 |
902 |
-17.13 |
13.36 |
neritic |
105.0 |
49.5 |
61569 |
799 |
-17.87 |
13.37 |
neritic |
98.0 |
51.0 |
61416 |
|
-17.74 |
13.43 |
neritic |
|
|
61441 |
900 |
-17.61 |
13.43 |
neritic |
|
|
61642 |
795 |
-17.44 |
13.45 |
neritic |
64.0 |
46.9 |
61336 |
925 |
-17.37 |
13.46 |
neritic |
|
|
61341 |
821 |
-17.58 |
13.47 |
neritic |
136.0 |
83.8 |
61439 |
807 |
-17.40 |
13.48 |
neritic |
|
|
61619 |
729 |
-17.68 |
13.56 |
neritic |
|
|
61468 |
|
-17.59 |
13.56 |
neritic |
|
|
61536 |
860 |
-18.03 |
13.56 |
neritic |
|
|
61646 |
840 |
-17.19 |
13.60 |
neritic |
|
|
61400 |
873 |
-17.58 |
13.61 |
neritic |
|
|
61634 |
812 |
-17.38 |
13.67 |
neritic |
84.0 |
82.1 |
61597 |
821 |
-16.92 |
13.68 |
neritic |
135.0 |
70.4 |
61551 |
849 |
-17.44 |
13.68 |
neritic |
164.0 |
37.2 |
61548 |
815 |
-17.51 |
13.71 |
neritic |
92.0 |
72.8 |
61935 |
817 |
-17.11 |
13.73 |
neritic |
|
|
61332 |
884 |
-17.45 |
13.80 |
neritic |
|
|
61557 |
883 |
-17.45 |
13.83 |
neritic |
|
|
65130 |
803 |
-17.06 |
13.87 |
neritic |
|
|
61611 |
853 |
-16.85 |
13.89 |
neritic |
91.0 |
86.8 |
61543 |
801 |
-17.48 |
13.89 |
neritic |
85.5 |
70.5 |
61685 |
844 |
-17.42 |
13.90 |
neritic |
117.0 |
71.8 |
61327 |
902 |
-17.30 |
13.90 |
neritic |
118.8 |
54.1 |
61714 |
836 |
-17.36 |
13.94 |
neritic |
|
|
61591 |
851 |
-17.58 |
13.96 |
neritic |
|
|
61604 |
802 |
-17.67 |
13.97 |
neritic |
|
|
61442 |
845 |
-17.19 |
13.97 |
neritic |
|
|
61554 |
878 |
-17.54 |
13.97 |
neritic |
131.0 |
77.1 |
61721 |
789 |
-17.05 |
13.99 |
neritic |
100.0 |
70.0 |
61589 |
|
-17.09 |
14.06 |
neritic |
|
|
61507 |
865 |
-17.59 |
14.06 |
neritic |
71.0 |
56.3 |
61299 |
838 |
-17.32 |
14.08 |
neritic |
|
|
61492 |
862 |
-17.00 |
14.08 |
neritic |
108.0 |
81.5 |
61471 |
857 |
-17.23 |
14.09 |
neritic |
|
|
61547 |
846 |
-16.75 |
14.09 |
neritic |
|
|
61713 |
|
-17.29 |
14.11 |
neritic |
138.0 |
60.1 |
61805 |
757 |
-17.17 |
14.12 |
neritic |
|
|
61495 |
902 |
-17.13 |
14.13 |
neritic |
113.0 |
85.8 |
61464 |
768 |
-17.10 |
14.16 |
neritic |
91.0 |
82.4 |
61418 |
865 |
-16.93 |
14.17 |
neritic |
|
|
61461 |
843 |
-16.86 |
14.19 |
neritic |
|
|
61330 |
813 |
-17.52 |
14.21 |
neritic |
123.0 |
85.4 |
61659 |
848 |
-16.76 |
14.23 |
neritic |
|
|
61620 |
828 |
-16.99 |
14.30 |
neritic |
|
|
61702 |
829 |
-16.96 |
14.32 |
neritic |
103.0 |
69.9 |
61715 |
|
-16.94 |
14.33 |
neritic |
|
|
61704 |
826 |
-17.28 |
14.38 |
neritic |
|
|
61709 |
856 |
-17.06 |
14.40 |
neritic |
|
|
61605 |
807 |
-16.39 |
14.47 |
neritic |
109.5 |
50.7 |
61556 |
825 |
-16.84 |
14.48 |
neritic |
|
|
61665 |
865 |
-16.77 |
14.48 |
neritic |
|
|
61497 |
840 |
-16.76 |
14.60 |
neritic |
97.0 |
60.8 |
61718 |
811 |
-16.68 |
14.61 |
neritic |
|
|
61650 |
873 |
-17.48 |
14.67 |
neritic |
116.0 |
57.4 |
61574 |
|
-16.83 |
14.70 |
neritic |
103.0 |
23.3 |
61363 |
865 |
-16.59 |
14.71 |
neritic |
90.0 |
26.7 |
61241 |
875 |
-16.36 |
14.80 |
neritic |
|
|
61214 |
843 |
-16.22 |
14.91 |
neritic |
119.0 |
63.9 |
61570 |
879 |
-15.66 |
15.21 |
neritic |
|
|
61683 |
871 |
-15.54 |
15.23 |
neritic |
117.0 |
30.7 |
61512 |
874 |
-16.51 |
15.32 |
neritic |
141.0 |
73.0 |
61542 |
881 |
-16.01 |
15.33 |
neritic |
129.0 |
51.9 |
61283 |
895 |
-15.95 |
15.46 |
neritic |
|
|
61406 |
903 |
-16.50 |
15.50 |
neritic |
|
|
61259 |
|
-16.40 |
15.55 |
neritic |
|
|
61613 |
815 |
-16.12 |
15.80 |
neritic |
|
|
61478 |
870 |
-16.39 |
18.09 |
neritic |
|
|
Literature cited
Hatase, H., K. Omuta, and K. Tsukamoto. 2010. Oceanic residents, neritic migrants: a possible mechanism underlying foraging dichotomy in adult female loggerhead turtles (Caretta caretta). Marine Biology 157:1337–1342.