-Japalura brevipes is an oviparous lizard native to high elevations of Taiwan, Republic of China. A total of 105 lizards (72 males; 33 females) were collected from March, 1992 to September, 1993. Males exhibited testicular recrudescence in spring; maximum spermiogenesis occurred in March-April. Testis somatic indices declined to a minimum in June and July. Fat body somatic indices were smallest in spring. Females lay eggs in late spring and summer. The average clutch size is 5.4. There was no correlation between maternal SVL and clutch size. Female fat body somatic indices declined to a minimum during March and July. Rainfall and temperature are considered the most important environmental factors that regulate J. brevipes reproductive cycles. Data on reproductive cycles, coupled with life history information, help us understand the evolution of lizard life history strategies (Tinkle et al., 1970; Vitt, 1981). Until 1960, research on the 1Present Address: Department of Zoology, National Museum of Natural Science, 1, Kuan Chien RD., Taichung, Taiwan, ROC. ctive cycles, coupled with life atio , help us understand the evoi life history strategies (Tinkle et ; i , 81). ntil 1960, research on the ess: epart ent of Zo logy, Nar productive biology of lizards was conducted almost entirely in north temperate regions (Clerke and Alford, 1993). Recently, there have b en extensive studies of tropical and Australian lizards (James and Shine, 1985; Joss and Minard, 1985; James, 1991; James et al., 1992; Clerke and Alford, 1993); however, investigations of the reproductive biology of lizards from subtropical regions remain scarce (Lin and Cheng, 1986). 22 This content downloaded from 207.46.13.25 on Mon, 12 Sep 2016 04:32:57 UTC All use subject to http://about.jstor.org/terms REPRODUCTIVE CYCLE IN LIZARD The genus Japalura is widespread in southeast Asia, north Borneo, Taiwan, and Ryukyu island (Lin and Cheng, 1990). Reproductive cycles of two species of this genus are known (Japalura swinhonis mitsukurii, Lin and Cheng, 1986; male J. swinhonis formosensis, Cheng and Lin, 1977). The purpose of this study is to provide information on the reproductive cycle of Japalura brevipes in relation to environmental factors that may influence it. MATERIALS AND METHODS The study site was located at Chunyang, Nantou County, about 90 km east of Taichung in central Taiwan (23? 30' N, 121? 08' E; ca. 1100 m above sea level). The site consists of 43 ha of man-made reforestation. The major plant species are the Gymnosperms Pinus taiwanensis, Cryptomeria japonica, and Cunninghamia lanceolata, the Dicotyledons Rhus semialata, Aralia taiwaniana, Rhododendron lasiostylum, Cinnamomum camphora, and Machilus zuihoensis. The average annual rainfall for Chunyang is about 2500 mm, most of which falls from February to September. The maximum air temperature in summer (June-August) ranges from 24 to 26?C, with minimum temperatures ranging from 14?-18?C during winter (November to January). Lizards were caught by noosing at monthly intervals between January 1992 and September 1993. The stage of maturity of males was judged by the appearance of the testes and epididymides which have free sperm in tubules, and were small and without convolutions in immature specimens. Females were considered immature if they had only small follicles in the ovary (diameter 3 mm. The estimation of clutch size was based on the number of vitellogenic follicles and/or oviductal eggs. The presence of vitellogenic follicles and oviductal eggs in the same female was considered evidence of the production of at least two clutches. The male reproductive state was estimated according to the GSI (Gonad-Somatic-Index) and spermatogenetic activity. The right testis from each male was fixed in Bouin's solution, embedded in paraffin, sectioned at 6 um, and stained with hematoxylin and eosin. Spermatogenetic activity was qualitatively assessed according to the classification system of Licht (1967). The stages are: (1) seminiferous tubules involuted with spermatogonia only; (2) primary spermatocytes appearing; (3) secondary spermatocytes and early spermatids abundant; (4) transforming spermatids with few spermatozoa; (5) spermatids and spermatozoa abundant; (6) spermatozoa abundant, (maximal level of spermiogenesis); and (7) spermatozoa abundant, (spermatids and spermatocytes greatly reduced). The presence of spermatozoa in the epididymis was noted. The relationship between clutch size and female body size was examined using a Pearson's correlation analysis. Monthly changes in fat body, liver, and testis mass were assessed using analysis of covariance (ANCOVA) with snout vent length (SVL) as the covariate.
Read full abstract