中国科技论文在线. : Q95916 : A : (2001) (Zhao & Adler,1993) (1964,1966)

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2001, Aug. 22 ( 4) : 279 286 CN 53-1040/ Q ISSN 0254-5853 Zoological Research Ξ ( 310036 duweiguo @mail1hz1zj1cn) : ( Eumeces elegans),,,, 50 mm, ; 50 mm,,, 6913 mm,, 614 21783 01554 g : ; ; ; ; : Q95916 : A : 0254-5853 (2001) 04-0279 - 08 (Darwin,1871 ;Shine,1979 ; Greenwood & Wheeler, 1985 ; Parker, 1992 ; Anderson, 1994 ; Bonnet et al1,1998) ( Trivers,1977 ;Powell & Russell,1985 ;Cooper & Vitt, 1989 ;Ji et al1,1997,1998 ;,2000 ;,2000),,, (Anderson &Vitt, 1990 ; Anderson, 1994 ;, 1994 ; Shine, 1994 ; Braga,1996 ; Bonnet et al1, 1998 ;, 2000 ;,2000), : (Brooks,1991) ; (Dunham,1981) ; (Berry & Shine,1980 ;Powell & Russell,1985 ;,2000) ; (Cooper &Vitt,1989), ( Eumeces elegans), ( ) (Zhao & Adler,1993) (1964,1966) 10 (Lue & Chen,1989 ; Kato,1994) (Huang,1996) (Du et al1,2000), 1 111 1998 1999 2000 5,, Met2 tlerb303 ( 01001 g), ( 0101 mm) (snout2vent length,svl) ; (head length,hl) ; (head width,hw) 6913 mm 8 : < 50 mm ; 50 60 mm ; 60 69 mm ; > 6913 mm Ξ : 2000-11 - 17 ; : 2001-03 - 08 : 151 转载

280 22 112 5, (600 mm 300 mm 300 mm), (larvae of Tenebrio molitor) ;, 5 21,,, 2 h, 2 : RCM 1 = / (Shine,1992) ; RCM 2 = / ( + ) (Vitt & Price, 1982 ; Seigel & Fitch,1984) ln (van Damme et al1,1992) 113 1998 5 94, 50 (10 40 ),, 112, 5 25 (12 13 ) 114 Statistica, Kolmogorov2Smirnov F2 max t - (ANCOVA), ANCOVA, = 0105 2 211,, 5, :, 5 212 ( t = 7144, df = 248, P < 010001 ; 1) ( F 3,162 = 1160, P > 0119) ( F 3,162 = 1195, P > 0112) ( F 3,271 = 7123, P < 01001) ( F 3,271 = 13132, P < 010001) ( 1) ANCOVA : < 50 mm ( F 1,42 = 1187, P > 0117) ( F 1,42 = 2107, P > 0115) ; 50 60 mm ( HL, F 1,80 = 16128, P < 01001 ;HW, F 1,80 = 4169, P < 0105) 60 69 mm ( HL, F 1,67 = 50126, P < 010001 ; HW, F 1,67 = 9119, P < 0101) ( F 1,247 = 49123, P < 010001),ANCOVA ANOVA ( HL, F 1,249 = 327123, P < 010001 ;HW, F 1,249 = 323120, P < 010001) ( 1, 1) 213 ( G SVL ) ( : G SVL = - 01079 SVL + 7121, r 2 = 0115, F 1,50 = 8150, P < 0101 ; : G SVL = - 01157 SVL + 11147, r 2 = 0134, F 1,50 = 25116, P < 010001), ( F 1,101 = (juvenile) (adult) 1 Table 1 Body and head sizes of blue2tailed skinks, E1 elega ns (groups) n SVL/ mm HL/ mm HW/ mm (hatchling) 27 2817 013 (2517 3110) 710 011 (615 714) 418 011 (414 512) < 50 ( < 50 female) 26 4512 017 (3816 4919) 912 011 (811 1010) 610 011 (512 619) < 50 ( < 50 male) 19 4519 018 (3819 4918) 914 011 (813 1013) 611 011 (515 618) 50 60 (50-60 female) 40 5517 014 (5014 5914) 1018 011 (919 1118) 711 011 (612 718) 50 60 (50-60 male) 43 5517 015 (5014 5916) 1110 011 (918 1213) 713 011 (614 814) 60 69 (60-69 female) 29 6411 015 (6014 6814) 1212 011 (1112 1312) 812 011 (715 818) 60 69 (60-69 male) 41 6412 015 (6010 6910) 1217 011 (1115 1411) 815 011 (715 918) (female) 75 7618 016 (6913 9319) 1410 011 (1218 1712) 915 011 (813 1114) (male) 176 8313 015 (6914 9819) 1617 011 (1311 2015) 1117 011 (815 1517), (data are expressed as mean SE, and ranges are indicated in parentheses)

4 : 281 < 50 ( < 50 female), < 50 ( < 50male), 50 60 (50260 female), 50 60 (50260 male), 60 69 (60269 female), 60 69 (60269 mate), (adult female), g (adult male) 1 Fig11 Relationships of head length and width to snout2vent length in E1elgans = 0124, P > 016), ( F 1,47 = 8110, P < 0101) ( G HL ) ( : G HL = - 01015 SVL + 1117, r 2 = 0122, F 1,50 = 12159, P < 01001 ; : G HL = - 01017 SVL + 1149, r 2 = 0118, F 1,50 = 10187, P < 0101) ( F 1,50 = 4106, P < 0105) ( 2) 3 25,,, 214, 6913 mm,, 6 2 7 12 2 ( r 2 = 0137, F 1,37 = 21161, P < 010001) ( r 2 = 0135, F 1,10 = 5134, P < 0105) ( r 2 = 0146, F 1,10 = 8151, P < 0105) ( 4), ( r = 0126, t = 0180, df = 10, P = 0144) 2 Table 2 Snout2vent length and reproductive characteristics of female E1 elega ns ( n) (mean SE) (range) / mm (snout2vent length) 39 7717 017 6913 9319 / g (post2oviposition body mass) 12 819 015 613 1210 / (clutch size) 39 614 014 210 1110 / g (egg mass) 12 0155 0103 0142 0171 / mm (egg length) 12 1412 013 1310 1519 / mm (egg width) 12 814 011 717 913 / g (clutch mass) 12 2178 0138 0185 4162 (relative clutch mass) RCM 1 12 01314 01046 01088 01619 RCM 2 12 01229 01026 01081 01382 3 Huang (1996), : ; ;,,

282 22 2 Fig12 Growth rates of snout2vent length and head length in E1 elegans 3 Fig13 Growth of body size and mass and head size in juvenile E1elegans ( 2) Vitt, 1989), (Cooper &,

4 : 283 4 Fig14 Relationships of clutch size, egg mass and clutch mass to snout2vent length of female E1elegans ;, ( Huang, 1996),,, 3 : ; ; ( Powell & Russell, 1985) 1, ( Eumeces chinensis) (, 2000) 2, ( Sphenomorphus indicus ) ( Takydromus septentrionalis) 2 (, 2000) 3 (Ji et al1, 1998 ;, 2000),, (, 2000),,, (, 2000) (Ji et al1, 1998 ;, 2000) (Carothers,1984 ;Powell & Russell,1985 ;Vitt & Coop2 er, 1985, 1986 ; Anderson & Vitt, 1990 ;, 1994 ; Braga,1996 ;Ji et al1,1998 ; 2000 ;,2000 ;,2000 ;Braga &Ji, 2000),, 50 mm,,, : [ = ( 2817 013) mm, n = 27 ] 50 mm, [ = (2718 011) mm, n = 257 ] 40 mm (,2000) ; [ = (2918 011) mm, n = 437] 70 mm ; [ = (2414 011) mm, n = 532 ] ( Podarcis muralis) [ = (2515 011) mm, n = 60 ] (,2000 ; Braga &Ji,2000),, ( 1,2),

284 22 ( 1), :, (Castilla et al1,1991 ; P rez2mellado et al1,1991 ;Webb & Shine,1994) ;, (Vial & Stewart,1989), (,2000) ( Ptyas korros) (,2000), ( Dinodon rufozona2 tum) ( Elaphe taeniura), (,2000 ;,2000),, (Avery et al1, 1982 ; Garland et al1,1990 ; Sinervo,1990 ;Braga & Ji,2000),, ( Ferguson & Fox, 1984 ; Sinervo et al1, 1992),,,,,,, (,2000 ;,2000) Anderson M,1994. Sexual Selection[M]. New Jersey :Princeton Universi2 ty Press. Anderson R A,Vitt L J,1990. Sexual selection versus alternative causes of sexual dimorphism in teiid lizards[j ]. Oecologia,84 :145-157. Avery R A,Bedford J D,Newcombe C P,1982. The role of thermoregula2 tion in lizard biology :predatory efficiency in a temperature diurnal basker[j ]. Behav. Ecol. Sociobiol.,11 :261-267. Berry J F,Shine R,1980. Sexual size dimorphism and sexual selection in turtle (order Chelonia) [J ]. Oecologia,44 :185-191. Bonnet X, Shine R, Naulleau G et al, 1998. Sexual dimorphism in snakes :different reproductive roles favour different body plans [J ]. Proc. R. Soc. Lond. B.,265 :179-183. Braga F,1996. Sexual dimorphism in lacertid lizards :male head increase vs female abdomen increase[j ]. Oikos,75 :511-523. Braga F,Ji X,2000. Influence of incubation temperature on morphology, locomotor performance, and early growth of hatchling wall lizards ( Podarcis muralis) [J ]. J. Exp. Zool.,286 :422-433. Brooks M J,1991. The ontogeny of sexual dimorphism :quantitative models and a case study in Labrisomid blennies (Teleostei :Paraclinus) [J ]. Syst. Zool.,40 :237-255. Carothers J H,1984. Sexual selection and sexual dimorphism in some her2 bivorous lizards[j ]. Amer. Nat.,124 :244-254. Castilla A M,Bauwens D,Llorente G A,1991. Diet composition of the lizard Lacerta lepida in central Spain[J ]. J. Herpetol.,25 :30-36. Cooper W E,Vitt L J,1989. Sexual dimorphism of head and body size in an iguanid lizard :paradoxical results [J ]. Amer. Nat.,133 : 729-735. Darwin C,1871. The Descent of Man and Selection in Relation to Sex [M].London :John Murray. Dunham A E,1981. Populations in a fluctuating environment :the compar2 ative population ecology of the iguanid lizards Sceloporus merriami and Urosaurus ornatus [J ]. Misc. Publ. Univ. Mich. Mus. Zo2 ol.,158 :1-62. Du W G, Yan S J,Ji X,2000. Selected body temperature,thermal toler2 ance and thermal dependence of food assimilation and locomotor performance in adult blue2tailed skinks, Eumeces elegans [J ]. J. Therm. Biol.,25 :197-202. Ferguson G W,Fox,S F,1984. Annual variation and survival advantage of large juvenile sideblotched lizards, Uta stansburiana :its causes and evolutionary significance[j ]. Evolution,38 :342-349. Garland T Jr,Hankins E,Huey R B,1990.Locomotor capacity and domi2 nance in adult male lizards[j ]. Func. Ecol.,4 :243-250. Greenwood P J,Wheeler P,1985. The evolution of sexual size dimorphism in bird and mammals :a hot blooded hypothesis[a ]. In : Greenwood P J, Harvey P H, Slatkin M. Evolution : Essays in Honour of John Maynard Smith[M]. Cambridge :Cambridge Univ. Press. 287-299. Huang W S,1996. Sexual size dimorphism in the five2striped blue2tailed skink, Eumeces elegans,with notes on its life history in Taiwan [J ]. Zool. Stud.,35 :188-194. Ji X,1994. Sexual dimorphism in body and head size in the skink Eume2 ces chinensis [J ]. J. Hangzhou Normal Coll. Natural Sciences, 94 (6) :80-85. [,1994.. ( ),94 (6) :79 84. ] Ji X,Du W G,2000. Sexual dimorphism in body size and head size and female reproduction in a viviparous skink, Sphenomorphus indicus [J ]. Zool. Res.,21 (5) :349-354. [,,2000.., 21 (5) :349 354. ]

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286 22 emerged young did not show sex difference in SVL, and male and female juveniles ( SVL < 6913 mm) ex2 hibit isometric growth pattern of SVL. Male and female adults (SVL > 6913 mm) showed allometric growth pat2 tern of SVL, as male adults grew faster than female adults. Therefore, It was concluded that sexual dimor2 phism in body size of E1 elegans occured only in adults. Our data revealed that male and female juve2 niles larger than 50 mm SVL began to diverge in head size, with males having larger heads than female s. This sexual dimorphism resulted from the greater head growth rate relative to SVL in males when their SVLs were larger than 50 mm SVL, and became increasingly pronounced in adults. The sexual dimorphism in body and head size suggested that the strategy of energy par2 tition of adult males and females was different. Adult males partition relatively more energy into body and head growth so as to improve the reproductive fitness, in contrast, adult females partition relatively more en2 ergy into reproductive investment other than body growth. Morever, adult females partition relatively less energy into head growth but more into carcass growth, thereby leaving a larger space for containing more eggs. The smallest reproductive female in our sample is 6913 mm SVL, and all females larger than this size lay a single clutch of eggs per breeding season. Clutch size, clutch mass and clutch mean egg mass were all positive2 ly correlated with maternal SVL, with average 614 eggs, 21783 g and 01554 g, respectively. Females of E1 elegans increase reproductive output mainly through increasing clutch size ( egg number ) and egg size as well. Key words : Eumeces elegans ; Growth ; Sexual dimorphism ; Female reproduction 2002 1980 ;, ; ; ; 1996, 2000,, 3 ; ( CSCI ) 1999 300, 181, 012024 2000, 01311 BA ( ) ZR ( ) CA ( ) AE ( ) P ( ) ( ) 30, 11, 23 75, 22 16, 80 10100, 60100 : 64-20, ( ), : 32 : 650223 : (0871) 5199026 E2mail : zoores @mail1kiz1ac1cn