GRAPTEMYS GIBBONSI (Pascagoula Map Turtle). BASKINGAND PARASITE REMOVAL. The primary physiological roleof basking by turtles is presumed to be for thermoregulation (Boyer1965. Ecology 46:99–118), to increase metabolism and digestionrates (Moll and Legler 1971. Bull. Los Angeles Co. Mus. Nat.Hist. Sci. 11:1–102). However, additional basking hypotheses andsecondary roles of basking have been proposed including to aid invitamin D synthesis (Pritchard and Greenhood 1968. Int. TurtleTortoise Soc. J. 2:20–25, 34) and to rid turtles of ectoparasites(Cagle 1950. Ecol. Monogr. 20:31–54; Neill and Allen 1954. Ecology35:581–584; Vogt 1979. Auk 96:608–609). Here we provideevidence to support the hypothesis that basking aids turtles in parasiteremoval as a secondary role and (to our knowledge) the firstdocumented observation of basking-induced release of a parasitefrom a turtle while basking.On 17 May 2007 (1125 h), WS and DS observed a large femaleGraptemys gibbonsi (>20 cm, ca. 1500 g) emerge on a large logsizedsnag to bask (Leaf River, Forrest Co., Mississippi). The femaleemerged facing the observers and a large leech (Placobdellasp.) was noted on the anterior left pleural scute of the carapace. Atthis time, the leech was in an elongated position. After 10 minutes(1135 h), the leech was observed shortening into a ball-shapedposture; it is presumed that this posture was used by the leech forwater conservation. After 35 minutes of basking (1200 h), the turtlebegan to exhibit ‘gaping’ behavior while basking, evidently reachinga high internal body temperature. Soon after at 1212 h (47minutes after turtle emergence), the leech terminated the ball-shapeand moved slowly toward the left margin of the turtle near thebridge of the shell. At 1214 h (after 49 minutes), the leech removedone end of its body from the margin of the turtle and beganto ‘search’ below toward the log, while the other end was stillattached at the margin of the carapace. The leech attached the freeend of its body to the log and the attached end on the carapacefollowed, thus removing itself from the turtle. At 1215 h (after 50minutes), the leech reentered the water at the edge of the baskinglog.During this time, a G. flavimaculata female was basking on thesame log as the female G. gibbonsi. The surface temperature ofthe G. flavimaculata female was being monitored via a carapacemounted temperature sensitive transmitter (AVM Instruments). Thecarapace temperature of the G. flavimaculata female during thisobservation of the G. gibbonsi female was 40–42°C. Therefore,the carapace temperature of the G. gibbonsi female was probablycomparable to the carapace temperature of the G. flavimaculata,and thus, likely hot enough to induce the leech to voluntarily releaseitself from its host organism. To our knowledge, this is thefirst documented observation of voluntary parasite release duringbasking, and supports the secondary hypothesis of basking as ameans for parasite removal.Submitted by WILL SELMAN, DUSTIN STRONG, andCARL QUALLS, Department of Biological Sciences, Box 5018,University of Southern Mississippi, Hattiesburg, Mississippi39401, USA (e-mail: will.selman@usm.edu).GRAPTEMYS GIBBONSI (Pascagoula Map Turtle). INTER-SPECIFIC COMPETITION FOR BASKING SITES.Graptemys gibbonsi is a highly aquatic freshwater turtle that inhabitsthe Pearl and Pascagoula rivers and tributaries of Mississippiand Louisiana, USA (Ernst et al. 1994. Turtles of the UnitedStates and Canada. Smithsonian Institute Press, Washington, D.C.578 pp.). Very little is known concerning the life history and ecologyof G. gibbonsi, and previous research within the Pearl andPascagoula Rivers has focused predominantly on the two federallythreatened species (G. flavimaculata within the PascagoulaRiver and G. oculifera within the Pearl River) that occur sympatricallywith G. gibbonsi. These observations of G. gibbonsi baskingbehavior were made within the Pascagoula River system.On 14 June 2006 (1200 h), on the Chickasawhay River (GreeneCounty, Mississippi), WS observed a male G. gibbonsi emergefrom the water and position himself above the water’s surface ona low-angled, branch-sized snag. After several minutes, a slightlylarger Apalone sp. approached and climbed onto the submergedportion of the same snag. The Apalone remained partially abovethe surface of the water, but was apparently not in an optimal baskinglocation; it then extended its head forward and proceeded tonudge or bite (unknown due to the observation distance) the posteriorof the male G. gibbonsi. The G. gibbonsi reacted by climbingup the snag. This sequence occurred again until the G. gibbonsimoved far enough up the snag to allow the Apalone to emergefully from the water, presumably achieving a more optimal baskingsite.On 11 April 2007 (1250 h), WS observed a male G. gibbonsi,ca. 9 cm in carapace length, climb vertically 19.5 cm to get to adesired basking location on a low-angled snag (Leaf River, ForrestCounty, Mississippi). No other turtles occupied the log at this time.This chosen basking location was 1.5–1.8 m from the lowest angleat the air/water interface where most turtles would emerge ontothe snag. It could have chosen this “easier” location to emerge andonly climb a 10–15° angle rather than the chosen vertical climb. Itis unclear why the G. gibbonsi male chose this more difficult routeto get to a desired basking location. However, it is possible that hetook this route to avoid larger turtles that may emerge to baskfrom the lower angle at the air/water interface.Submitted by WILL SELMAN and CARL QUALLS, Departmentof Biological Sciences, Box 5018, University of SouthernMississippi, Hattiesburg, Mississippi 39401, USA (e-mail:will.selman@usm.edu).GRAPTEMYS GIBBONSI (Pascagoula Map Turtle). INTERAC-TIONS WITH DUCKS. Graptemys gibbonsi is an aquatic turtlethat inhabits the Pearl and Pascagoula rivers and tributaries ofMississippi and Louisiana, USA (Ernst et al. 1994. Turtles of theUnited States and Canada. Smithsonian Institute Press, Washington,D.C. 578 pp.). Very little is known about the life history of G.gibbonsi following its description as a species in 1992 (Lovichand McCoy 1992. Ann. Carnegie Mus. 61:293–315). Observationswere made on two occasions of interactions between adult femaleG. gibbonsi and Wood Ducks (Aix sponsa).On 11 May 2006 (1500 h), on Oakohay Creek (CovingtonCounty, Mississippi), WS observed a basking adult female G.gibbonsi on a horizontal log-sized snag, along with a pair of WoodDucks. The two Wood Ducks were startled by the approachingboat, but the female G. gibbonsi was not startled off the log whenthey flew away. However, the turtle vacated the log ca. 30 seconds216 <strong>Herpetological</strong> <strong>Review</strong> 39(2), 2008
after the ducks flew away, apparently in response to the boat’sapproach. On 16 April 2007 (1450 h), on the Leaf River (ForrestCounty, Mississippi) WS observed from shore via spotting scopea female G. gibbonsi basking on a large log-sized snag with threePseudemys concinna. A female Wood Duck was also perched abovethe four turtles on the same log. Upon noticing their observer, thefemale Wood Duck, and a male Wood Duck (that was previouslyunnoticed nearby on the water), flew away but none of the turtleswere startled by this event. The turtles remained on the log andwere only startled once they were approached by boat ca. 5 minuteslater. From these observations, it appears that Wood Ducksare not viewed as a potential predator by these turtles and further,do not serve in any ‘sentinel’ capacity to alert turtles of dangerwhile these turtle species are basking.Submitted by WILL SELMAN and CARL QUALLS, Departmentof Biological Sciences, Box 5018, University of SouthernMississippi, Hattiesburg, Mississippi 39401, USA (e-mail:will.selman@usm.edu).KINOSTERNON SCORPIOIDES ABAXILLARE (CentralChiapas Mud Turtle). SIZE, GROWTH, AND REPRODUC-TION. Since its description (Baur, in Stejneger 1925. J. WashingtonAcad. Sci. 15[20]:462–463) the only published growth or reproductivedata for Kinosternon scorpioides abaxillare were thoseof Alvarez del Toro (1983. Los Reptiles de Chiapas. TerceraEdición, Corregida, y Aumentada. Instituto Historia Natural, LosTuxtlas, Chiapas. 248 pp.), who reported that 6–12 eggs are laidin March or April, and they hatch after three months. The presentreport is based on 23 specimens trapped between 1700 h 30 Apriland 0800 h 1 May 1981 (15 in the first two hours) near the RioCintalapa bridge on Hwy 190 in Chiapas, Mexico, as well as 52examined museum specimens of this subspecies (see acknowledgments).Males did not differ significantly from females in carapace length(CL: males, 122.4 ± 15.7 mm, 88–149, N = 21 versus females,118.6 ± 14.6 mm, 84–153, N = 36; t = 0.93, P = 0.35) or plastronlength (PL: males, 116.1 ± 15.6 mm, 83–143, N = 20 versus females,115.8± 14.8 mm, 81–149, N = 36; t = 0.8, P = 0.94), butdiffered significantly for the ratio PL/CL (males, 0.95 ± 0.02, 0.91–0.99, versus females, 0.98 ± 0.02, 0.93–1.01; t = 3.6, P = 0.0007).Females outnumbered males in the field collection (12:7) and themuseum collections (24:14). Body mass (in grams) for the fieldcollectedanimals was related to CL (in mm) by the equation BM= 0.000506CL 2.727 (r = 0.994; P < 0.0001; N = 23), and the equationsfor males and females were nearly identical. A single neonate(CU 48847) was available, collected 25 June 1971, and measured29.6 mm CL and 24.1 mm PL.Although K. s. abaxillare was originally diagnosed as lackingan axillary scute, of 66 specimens examined for the trait, 8 hadpartial medial axillary seams, and 6 had complete axillary seams.In addition, I have observed the absence of axillary scutes in occasionalspecimens of K. s. cruentatum from Veracruz (BCB-SM7852) and Cozumel (UF 24135, 24138).The largest immature (no eggs, corpora lutea, or ovarian follicles> 3 mm), field-collected females were 99, 102, 110, 110,121, and 126 mm CL. The smallest mature females were 124 mmCL (two 9 mm follicles), and 130 mm (one 8 mm follicle). Othermature females were 130 mm CL (follicles, 15, 15, 10, 10 mm),130 mm CL (9, 9, 8, 8, 8, 8, 8 mm), 131 mm CL (9, 9, 8, 8 mm),and 133 mm CL (8, 8, 8, 7). These data suggest sexual maturity at120–130 mm CL. Another 132 mm CL female (UIMNH 39373;27 December 1955) bore 5 partially shelled oviducal eggs (3crushed, the others 32.3 × 16.5 mm, and 28.75 × 17.5 mm), andfollicles of 14, 13, 13, 9, and 8 mm, but counts of corpora luteawere not possible because of preservative effects. These preliminarydissection data suggest that clutch sizes might range fromone to five eggs, and that the clutch sizes reported by Alvarez delToro (op. cit.) may be exaggerated. The presence of preovulatoryand enlarged follicles in females at the beginning of May suggestthat the production of clutches might be possible in May and June,in addition to March and April as suggested by Alvarez del Toro(op. cit.). Furthermore, the ovaries of the UIMNH female suggestthat eggs could also be laid in January. Whether K. s. abaxillareexhibits as long a reproductive season as captive K. scorpioidesfrom Honduras (Goode 1994. In Murphy and Adler [eds.], CaptiveManagement and Conservation of Amphibians and Reptiles,pp. 275–295. Soc. Study Amphib. Rept., Lawrence, Kansas) or K.s. cruentatum on the Yucatan Peninsula (Iverson, unpubl.) remainsto be determined. In addition, whether K. s. abaxillare also exhibitsdelayed embryonic development, with hatching synchronizedto the onset of the summer rainy season, like other populations ofMexican and Central American K. scorpioides (Ewert 1991. InDeeming and Ferguson [eds.], Egg Incubation: Its Effect on EmbryonicDevelopment in Birds and Reptiles, pp. 173–191. CambridgeUniv. Press, Cambridge, UK), also deserves attention.Measurements of right abdominal scute annuli were used to estimateprevious plastral lengths following the method of Ernst etal. (1973. Herpetologica 29:247–250). Three estimates of PL forage one year were 34.2, 40.9, and 39.3 mm; four estimates for twoyears were 45.2, 52.1, 62.0, and 66.4 mm; one for three years was64.2 mm; and one for four years was 70.7 mm. A crude extrapolationof those data suggests that 8–10 years would be required toapproach maturity at 120 mm PL (ca. 122 mm CL).I thank T. Leithauser, R. Magill, P. A. Meylan, P. Moler, and C.R. Smith for field assistance, and the American Museum of NaturalHistory (AMNH; D. Frost, C. W. Myers, R. G. Zweifel), theUniversity of Colorado Museum (CU; T. P. Maslin, H. M. Smith),the University of Kansas Museum of Natural History (KU; J. T.Collins, W. E. Duellman), the Museum of Comparative Zoologyat Harvard University (MCZ; J. Rosado, the late E. E. Williams),the Strecker Museum (BCB-SM; B. Brown), the Texas CooperativeWildlife Collection (TCWC; J. R. Dixon), the University ofArizona collection (UAZ; the late C. W. Lowe), the University ofFlorida-Florida State Museum (UF; the late W. Auffenberg, P. A.Meylan), the University of Illinois Museum of Natural History(UIMNH; D. Hoffmeister, D. Smith), the University of MichiganMuseum of Zoology (UMMZ; A. G. Kluge, R. Nussbaum, thelate D. W. Tinkle), the United States Natural History Museum(USNM; R. Crombie, R. W. McDiarmid, R. Reynolds, G. R. Zug),and the University of Utah (UU; J. F. Berry, J. M. Legler) for theloan of specimens. La Dirección General de la Fauna Silvestre deMéxico provided permits for the field work. Treatment of all animalswas in accordance with the ethical principles outlined in theSSAR Guidelines for Use of Live Amphibians and Reptiles inField Research. Support for the project was provided by Earlham<strong>Herpetological</strong> <strong>Review</strong> 39(2), 2008 217
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About Our Cover: Zonosaurus maramai
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Prey-specific Predatory Behavior in
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acid water treatment than in the co
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TABLE 1. Time-line history of croco
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we call it, is in flux.Forty years
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poles (Pond 1 > 10,000, Pond 2 4,87
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FIG. 2. Responses of adult Regal Ho
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PIANKA, E. R., AND W. S. PARKER. 19
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BUSTAMANTE, M. R. 2005. La cecilia
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