Duration of Attachment by Mites and Ticks on the Iguanid Lizards Sceloporus graciosus and Uta stansburiana

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Duration of Attachment by Mites and Ticks on the Iguanid Lizards Sceloporus graciosus and Uta stansburiana Authors: Stephen R. Goldberg, and Charles R. Bursey Source: Journal of Wildlife Diseases, 27(4) : 719-722 Published By: Wildlife Disease Association URL: https://doi.org/10.7589/0090-3558-27.4.719 BioOne Complete (complete.bioone.org) is a full-text database of 200 subscribed and open-access titles in the biological, ecological, and environmental sciences published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Complete website, and all posted and associated content indicates your acceptance of BioOne s Terms of Use, available at www.bioone.org/terms-of-use. Usage of BioOne Complete content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research.

Journal of Wildlife Diseases, 27(4), 1991, pp. 719-722 Wildlife Disease Association 1991 Duration of Attachment by Mites and Ticks on the Iguanid Lizards Sceloporus graciosus and Uta stansburiana Stephen R. Goldberg and Charles R. Bursey,2 Department of Biology, Whittier College, Whittier, California 90608, USA; 2 Department of Biology, Pennsylvania State University, Shenango Valley Campus, 147 Shenango Avenue, Sharon, Pennsylvania 16146, USA ABSTRACT: Duration of attachment was determined for the mites Neotrombicula californica and Geckobiella texana and the tick Ixodes pacificus on the iguanid lizards Sceloporus graciosus and Uta stansburiana from southern California. Neotrombicula californica infestations lasted approximately 1 wk. Attachment of Ixodes pacificus larvae and nymphs lasted approximately 8 days on S. graciosus and 16 days on U. stansburiana. Geckobiella texana remained attached to S. graciosus for 5 days and to U. stanshuriana for 28 days. Key words: Ixodes pacificus, Ixodidae, Neotrombicula californica, Trombiculidae, Geckobiella texana, Pterygosomatidae, Ophionyssus natricis, Macronyssidae, Sceloporus graciosus, Uta stansburiana, Iguanidae, infestation, preyalance, attachment. While infestations of mites and ticks on reptiles have long been known (Frank, 1981), the duration of time spent on the host has been little studied. In this note we report the duration of attachment for the chigger Neotrombicula californica (Trombiculidae), the mite Geckobiella texana (Ptenygosomatidae), and the tick Ixodes pacificus (Ixodidae) on the sagebrush lizand (Sceloporus graciosus) and the sideblotched lizard (Uta stansburiana) from southern California. We have previously described the histopathology of lesions produced by these ectoparasites on U. stansburiana (Goldberg and Bursey, 1991). Lizards were collected by hand-held noose in the San Gabriel Mountains (Los Angeles County, California, USA). One hundred Sceloporus graciosus were collected on Windy Gap Trail (elevation 1,889 m; 34#{176}21 N, 117#{176}48 W) in the Crystal Lake area in April and May 1990. Sceloporus graciosus averaged 56.0 mm snout-vent length (SVL), range 32 to 70 mm SVL. One hundred twenty-six Uta stanshuriana were collected at Strawberry Peak (elevation 1,878 m; 34#{176}17 N, 118#{176}07 W) off California Highway 2 in February to May 1990. Uta stansburiana averaged 50.4 mm SVL, range 40 to 59 mm SVL. Representative slides of ticks from U. stansburiana were deposited in the U.S. National Tick Collection (Georgia Southern University, Statesboro, Georgia 30460, USA; Accession numbers 119772 and 119773). Additional specimens were sent to the U.S. National Parasite Collection (Beltsville, Maryland 20705, USA; Accession numbers 80963, 80964, 80965 for G. texana, 0. natricis and N. californica, respectively, from S. graciosus; 81457, 81458, 81459 and 81460 for I. pacificus, N. californica, G. texana and 0. natricis, respectively, from U. stansburiana). On the day of capture, the number, identity and location of mites and ticks were determined with the aid of a dissecting microscope. Lizards were then placed in separate 250 ml glass jars and maintained at 24 C in the laboratory (Department of Biology, Whittier College, Whittier, California 90608, USA) for the duration of the study. Geckobiella texana were counted daily, but the other ectoparasites were counted at 4 day intervals. At capture, 92% (92 of 100) of S. graciosus and 60% (75 of 126) U. stansburiana were infested with N. californica. Monthly sample size, prevalence and intensity of N. californica infestations are presented in Table 1. Uta stanshuriana is active much earlier in the year than S. graciosus. When the two lizard populations were compared on day of capture, there was a significant difference with greater prevalences of N. californica on S. graciosus (x2 = 30.42, 1 df, P < 0.01). 719

720 JOURNAL OF WILDLIFE DISEASES, VOL. 27, NO. 4, OCTOBER 1991 TABLE 1. Prevalence and intensity (range) of Neotrombicula callfornica on Sceloporus graclosus and Uta stansburiana. Month Prevalence Intensity Prevalence Intensity February - - 100% (4/4) 41 (30-74) March - - 62% (21/34) 7 (1-34) April 95%(37/39) 40(10-93) 58%(39/67) 8(1-46) May 90%(55/61) 20(1-66) 52%(11/21) 14(1-72) Infestations in both species lasted approximately 1 wk (Table 2). By day 8 the mean number of chiggers remaining was 1.5 on S. graciosus and 0.9 on U. stansburiana. Chiggers were found most often on the upper and lower eyelids, around the tympanic membrane and in the gular region. Fifteen percent (15 of 100) of S. graciosus and 29% (37 of 126) of U. stansburiana were infested with I. pacificus at capture. Prevalence and intensity of I. pacificus are presented in Table 3. Both larvae and nymphs were present; no adults were found. Adult I. pacificus are typically found on mammals (Furman and Loomis, 1984). There was a significant difference in prevalence of I. pacificus when the two lizard populations were compared on day of capture with greaten numbers on U. stansburiana (x2 = 6.49, 1 df, P < 0.05). By day 12 the mean number of ticks remaining was 0.5 on S. graciosus and 1.0 on U. stansburiana (Table 4). Ticks nemained longer on U. stansburiana (ap- TABLE 2. Mean number and prevalence of Neotrombicula californica on 92 captive Sceloporus graciosus and on 75 captive Uta stansburiana at four day intervals. Day Number of Number of lizard Preva- lizard Preva- lence lence Mean (Range) % Mean (Range) % 0 30.5 (1-93) 100 8.4 (1-72) 100 4 20.9 (0-90) 90 4.7 (0-36) 77 8 1.5 (0-14) 61 0.9 (0-7) 34 12 0.4 (0-3) 18 <0.1 (0-1) 2 proximately 16 days) than S. graciosus (approximately 8 days). Ticks were most commonly attached to the gular regions or the outer edge of the tympanic membranes. Eight percent (8 of 100) of S. graciosus were infested with Ophionyssus natricis; none were found on U. stansburiana. These mites are highly mobile and wander freely over the body. We were unable to estimate the length of time they remained on their hosts. One Geckobiella texana was found on S. graciosus; it remained attached for 5 days. Twelve G. texana were found on nine U. stansburiana: the mean attachment time was 28.3 days. Melvin et a!. (1943) reported that Trombicula aifreddugesi remained attached for an average of 30 days and a maximum of 65 days on horned lizards (Phrynosoma sp.). Jones (1950) reported that Trombicula autumnalis fed on its bird and mamma! hosts for 3 to 5 days. Frank (1981) reported larval trombiculids fed on reptiles for 2 to 10 days. Loomis and Stephens (1973) suggested that Neotrombicula harperi remained on its lizard hosts for as long as three months. Because we were only able to measure attachment time from the day of capture, we consider our data to represent a minimum attachment time. Neotrombicula californica remained attached for approximately the same length of time on both S. graciosus and U. stansburiana. We have previously reported maximum numbers of N. californica at the beginning of the spring activity period (Goldberg and Bursey, 1991) which suggests to us that

SHORT COMMUNICATIONS 721 TABLE 3. Prevalence and intensity (range) of Ixodes pacificus on Sceloporus graciosus and Uta stansburiana. Sceloporus graciosus Uta stanshuriana Month Prevalence Intensity Prevalence Intensity February - - 0% (0/4) - March - - 21% (7/34) 2 (1-5) April 21%(8/39) 4(1-8) 43%(29/67) 2(1-5) May 11% (7/61) 2 (1-5) 5% (1/21) 1 lizards acquire their infestations during the winter inactivity period. The greater preyalences and mean intensities of N. calif ornica on S. graciosus as compared to U. stansburiana may be related to the longer period of inactivity of S. graciosus. A portion of the U. stansburiana population is active during February and March (Goldberg and Bunsey, 1991). In contrast, S. graciosus in the San Gabriel Mountains enters hibernation in early October and remains inactive until March (Goldberg, 1975). Thus, chiggers have a longer time to infest inactive S. graciosus. We found significantly more male lizands were infested with I. pacificus than female lizards; 10 of 15 infested S. graciosus and 32 of 41 infested U. stansburiana were males (x2 = 14.6, 3 df, P < 0.01). We attribute these differences to increased movement by males during the spring breeding season. A male moving frequent- TABLE 4. Mean number and prevalence of Ixodes pacificus (larvae and nymphs) on 15 captive Sceloporus graciosus and on 37 captive Uta stansburiana at four day intervals. Number of Number of lizard Prevalence lizard Prevalence Day Mean (Range) % Mean (Range) (%) 0 2.7 (1-7) 100 2.0 (1-6) 100 4 2.2 (0-7) 87 1.7 (0-5) 93 8 0.7 (0-4) 40 1.5 (0-5) 78 12 0.5 (0-3) 33 1.0 (0-4) 61 16 <0.1 (0-1) 6 0.7 (0-4) 51 20 - - - 0.1 (0-i) 17 24 - - - 0.7 (0-1) 7 ly through his territory has a greater chance of acquiring ticks than does a more sedentany female. It is not clear why ticks should remain attached longer to U. stanshuriana. A similar pattern was seen for G. texana which also remained longer on U. stansburiana. We assume the answen to this may lie in host physiology. Wright et a!. (1988) reported decreased engorgement times in mice with repeated exposure to the chigger Eutrombicula cinnabaris. Uta stansburiana has a life expectancy of 1.1 to 1.4 yr (Tinkle, 1967) while S. graciosus has a life span of approximately three years (Tinkle, 1973) and is thus a potential host for a much longer period of time. Whether a similar phenomenon exists in lizards has to our knowledge, not been examined. Our finding of 29% prevalence for U. stansburiana infested with I. pacificus in this study versus a 16% prevalence in 1989 (Goldberg and Bursey, 1991) for lizards of the same population during the same season one year later suggests there may be considerable annual variation in tick preyalence for a given population. These diffenences may reflect yearly variations in precipitation and/on temperature. It has been shown that tick life histories are intimately associated with climatic cycles (Auffenberg and Auffenberg, 1990) and lack of precipitation has been correlated with a decrease in chiggers (Loomis and Stephens, 1973). We thank M. L. Goff, University of Hawaii, Manoa for identification of ectopanasites and 0. Rivas for assistance in the field.

722 JOURNAL OF WILDLIFE DISEASES, VOL. 27, NO. 4, OCTOBER 1991 LITERATURE CITED AUFFENBERG W., AND T. AUFFENBERG. 1990. The reptile tick Aponomma gervalsi (Acarina: Ixodidae) as a parasite of monitor lizards in Pakistan and India. Bulletin of the Florida Museum of Natural History, Biological Sciences 35: 1-34. FRANK, W. 1981. Ectoparasites. In Diseases of the Reptilia, Vol. 1, J. E. Cooper and 0. F. Jackson (eds.). Academic Press, London, England, pp. 359-383. FURMAN, D. P., AND E. C. LooMis. 1984. The ticks of California (Acari: Ixodida). Bulletin of the California Insect Survey, Vol. 25. University of California Press, Berkeley, California, 239 pp. GOLDBERG, S. R. 1975. Reproduction in the sagebrush lizard, Sceloporus graciosus. American Midland Naturalist 93: 177-187., AND C. R. BURSEY. 1991. Integumental lesions caused by ectoparasites in a wild population of the side-blotched lizard, Uta stansburiana (Iguanidae). Journal of Wildlife Diseases 27: 68-73. JONES, B. M. 1950. The penetration of the host tissue by the harvest mite, Trombicula autumnalis Shaw. Parasitology 40: 247-260. LooMIs, R. B., AND R. C. STEPHENS. 1973. The chiggers (Acarina, Trombiculidae) parasitizing the side-blotched lizard (Uta stansburlana) and other lizards in Joshua Tree National Monument, California. Bulletin of the Southern California Academy of Sciences 72: 78-89. MELVIN, R., C. L. SMITH, AND 0. H. GRAHAM. 1943. Some observations on chiggers. Journal of Economic Entomology 36: 940. TINKLE, D. W. 1967. The life and demography of the side-blotched lizard, Uta stansburlana. Miscellaneous Publications No. 132, Museum of Zoology, University of Michigan, Ann Arbor, Michigan, 182 pp.. 1973. A population analysis of the sagebrush lizard, Sceloporus graclosus in southern Utah. Copeia 1973: 284-296. WRIGHT, S. M., S. K. WIKEL, AND W. J. WRENN. 1988. Host immune responsiveness to the chigger, Eutrombicula cinnabaris. Annals of Tropical Medicine and Parasitology 82: 283-293. Received for publication 11 January 1991.