ACT 0274.4 MERFETOLOG |

ISSN 1000-3215 mR TT oF ih ACTA HERPETOLOGICA SINICA

1

1988

FL SC lien) PRES Ss

PR Ne Bh 1988 ”第 1

A.

细胞 研究 .4 C- ee

596000.906606005000005009009000000 900 500000 ond 000000 BSE ODD SoDDDOaSOaIEoO0NC KRK BRR RRR 1 ) 染色 、C- Ag-NORs 研究 pp RE 受精 原核 重建 细胞 研究 :0 24%3£( 10 ) Pee] ee) eel eee ee 2) 000 00000 955.990 ded 96 aNdo 990 cHoboe oo5IDBq396051500 Re = I 18) 广东 ) saaaaoooooeoo

Susana Salas Frazier, John G, Frazier et al( 16 ) Sie GLA. BER) 形态 研究 V. S

形态 比较 研究 ee sdbdodonnor gabndadoce addabechecesen: ( 47 ) 4eHAA FI LA RH—A Sp WS EES BZ AVY BM ve cee cence cece eects cee seeaeeene Eve £2 56 ) Fob LLU BEE AS AR Bee SF BUH WS) SDT iL one eee eee eee ree Bf Hea) 4 K( 60 ) 简报

广西 首次 ( 65 ) 山东 纪录 〈( 66 ) REMI 吸虫 RAE ( 67 ) 温度 决定 爬行 动物 tem (70 )

行动 ”1988 A, 1-4 Acta Herpetologica Sinica

In fy st: 7 i "| :

i 5) ET BE

IV. 4 C-

(图 ) AKA BEE ARK (中 科学 生物 研究 )

材料 方法

1, IR/BTGHE: 1986.4 1987.3, KE AREA MILE. FRR tp AN Te Hh 2760 公里 8

2, Few:

3. SHAS: 1984.10 1986.4

4, PERE. 1985.5 1986.10

标本 采用 骨骼 离心

1985.5 1986.10,

oe

. Individuals and

Table I The summary of materials examined in this study

1983) 蒸汽 固定 ( ,1982) 制备 C- 技术 Sumner (1972) 制备 细胞

结果

1. 染色 :

4 齿 染色 26 (A WI; A- ),13 5 (Nos.1-5)、1 (No.6) 7 染色 tx (Nos,7-13) ,在 No.5 No.6 ,No.6 No.7 存在 比较 界线 No.6

TAR

Numbers of metaphase

Species Sexes Giemsa Stained C-banded

Oreolalax yg 50 20 omeimontis 9 2 30 O. pingii LING 30

Pode 37

haves 105 40 O, popei Ss O, rugosa Se , 10 246 11

rh use 36 3

DnT Pe KE. EPENAA-t

基本 相似

资料 它们 3 染色 排列 2 ,种

SS EB RL IE AR LIN ILI LN TE FE ET IIN TS TOE LIE LE IS I I IN RE IE

差别 查看 2 进行 比较 文中 描述

1987 4 7

Leob, PRE RUEWAB Ah Ae. EAM ANS Ba Be, a RIA Ap On == 97. Gales 9m —_ OO) Ss 7s iw fee ee GLB. Be -K), PH 正常 ree 2 3 Ee, 1B; ENE Tr te py KL), HIRAI eT Sas ae wat fa, (microchromosomes), TE By TA 13 AY TA RR BAS ABS 20 = 261k 相对 差别 APARNA EMH, waa

EY) AS ESE So Tk Hi SE FE: AA EJP Lhak SWB AHS. See ve. oe 3 SOE, TEPPER Se Be, A

Ve *

AN

= br mip

HIRAM SS, 簿 风采 ESL AG BALLET LG A. 2, Cee, 1.B、D PLA)

a a ys ie IX yg Se kA 22 ah C~ a BS = SE

Sie Sh iy Ma sii

SKIL Ree SZ" CRBE, 3% Ab JLT C per tank abe awies :

Re ee ry 2 52 ER NOs) 1-5: Hit @ AE Ke Cn ay iy 55 3 agen Ne 6 32 Bee

ee. cer iad fe Be GF MABE TOR A Rs FER ES LA RESP 7 in Tee |B : MIEN CH Call I. 1); Sesh ve Joule SC a HH

异型 现象 2 Cink 2 238 A, ASS 2/30 Fig. Brwmgen je ee

ay

1, AFA RAR WISER TO Eb KL, AM UNE R SHADERS, AAW 数目 变化 结构 简单, Lay 、s 染色 齿 Ore-

ae ae

olalax rugosa SS 染色体 易于 3 种群 相互 差异 明显 FEMI NO .6 相同 LWA EM Be UGE, (EZ 公历 演化 JL Beas. 标志 共有 特征 8 a HSS 1% HW ASE fel, Pr bic 2 eee, SHWE lS Vibrissaphora GAR oR, as 几乎

唯一 比较 染色 具有 比值 sm 染色 HK. ABS 亲近

=|

ig

清楚 细胞 形态 特征 显示 0

2, 关于 ( “无 antes (Bufonidae), fy e: (Hylidae), @l-(Ranidae), dake (Microhylidae) 7 iW i: (Rhacophoridae) Spray C 资料 AW, FEREWRREMK, MANA PIKE C CC BT Aa (Schmid, 19782, b; 1980), 4) BUS (Pe- lobatidae) C 研究 DRAB HOC DHE, RSMAS Ap, se AI IE LER He BCH {EC ar BEER 显著 ”长 具有 (CC , NO.6 伴随 附近 BC ae 染色 插入 明显 (Megophryinae) Hh B&H) Megophrys nasuta, Pelobates fuscus( WlSchmid ,1980a) FIFC E28 Atympanophrys shapingensis (5 HA, 1987.8) 3 3 4 仍然 揭示 CC 表明 普遍 差别 结构 普遍 认为 进化

ABWMXR, EKHEM, MSAK SI ty BEL, ARATE KM,

Hibs kit C 变化 残迹 (3chmid; 1978a), 数量 估计 它们 少数 染色 Nee ERASERS EKA aE FH 染色 情况 Pyxicephalus ad- spersus (=Rana adspersus) hy ZZ/ZW Ve Be a fkiwit Gtk Kb Schmid, 1980b) 南美 Litoria infrafrenata No.4. K -E(King, 1980) pr DB, BRAM ACh

ro

=.

HSCS LAE Ak MSI, BOIL 22 BAL RIA AER NAT BEEN 根据 King (1980) MUL. 2OARBAREES 进行 调整 fe, CERT H lleca cee hk. canied I, K—-DEM AWA we et PBK L Bt a, BH No.6 形态 ,并 变化 ,但 C 占有 明显 优势 染色 ,虽然 目前 明了 现象 诸如 染色 关系

bable 2 3 The maeiative Lengths and Arm Ratio of f meen best 6 chromosomes of four eol

DO | | O. ined , rf | Rui Uy A iRe Type, | Ro) Rae Gp Type 1 1861.67 13 .2 1.2240.05 om | 38752111 1.29-+0.10 m elu 1292 90st 1,.69+-0.16,,, “ml sm. 139.13 7.5 1.60-+0.13 m ae 3 | 112.53825.4 (ela B 14st | 128.88-56.5 1.9320.27 sm 105.13 5.4 133-0921 sr 113.78-+3.% 1.78-+0.16 sm 5 98.352 2.6 1.5400.14 m | 98.83 6.4 1.80200.17 m, sm I 6 T1TIHL42 a sto. ape | 69.8 214, avi: 2340.11 m T 55.19+3.0 ‘i 45-c0. 20 m AQ, 784 an 1.50260.18 m 8 51.387°2.8 1.6€1-+9:20 m. sm AT. T4-£8.7). -1.802-0.19 sm . 9 29.61 5.0 9 46.0743.1 1.5220.13 m 10 45, 86-b2.6 1 i4oeh TS 41.262°3.7 1.25270.14 m ii Pa ban.) {edplcacOetay sy 10 36.7452.1 | 1.28250-19 m AB, 910°". 48-F4. g aKa Sis oa 83.4°t4.6 2.3820.24 sm 18¢ 4) 1) 36.94 4.0 1. O80. om ia 82.7%: 4.0 1.26200.26 m | QO: ace aa O, rugosa. Roy Ae sro Rn Type 展翅 Rig Type i 158.7210.1 °° 1.47-0.12 | t58.24-410.3 - t.94-b0.18 m 2 132.415¢8,6 £.712-0.19 . > +sm 135.7 2ET.2 1.58 0.25 m, sm i 3 119.67 6.3 工时 0.24 sm 115.39::3.4 1.790.416 sm 4 110.475 .4 1.66+0.19 m. sm 111.08-5.8 1.692-0.13 sm 5 99.21-b4, 0) 1.88-£0.09 m a4. 114, Ay 1.86 0.30 sm ‘I 6 19. esr, 2 1.25-20.15 m 79. +7: 1 1.77+0.22 sm 7 53.0043.1 1.41 0.16 m 53.99-3.2 1.61200.16 m, sm 8 51.49-+3.9 1.42+0.24 .m 51.09-+3.9 1.61-£0.17 m, sm 7 9 47.31+3.4 1.38250.25 m 40 T1251.7 1.00.09) oy aeisis 10 43.39 5.2 3 02 [it ee date Dea 1.24-£0.21 m 11 39.68+3.3 1.311+0.19 m 40.39-42.3 {. SIO 19 a 12, slyly sBlaete-3 <3 1.34-0.28 m 36.42 1.7 1.17 0.16 m seine) 35.62+5.1 1.300. 16 m 33.63 2.6 1.20.18 m aa a

怀疑 染色 染色 质量 增加 转化 例证 染色 C RAHA ARS tia ACH, STA ASABE. SENEHY Cary 反映

HRS: 鉴定 手册 〈1986)

等, 研究 5. 染色 比较 PACT yi 2(1):15-20(1983),

King M, C-Banding Studies on Australian Hylid Frogs, Structure and the Concept of Euchro-

Secondary Constriction

matin Transformation. Chromosoma, 30: 191-217(1980).

Schmid M, Chromosome Banding in Amphibia

J]. Constitutive Heterochromatin and Nucleolus Organizer Regions in Bufo ‘and Hyla. Chromosoma, 66:361-388 (1978 a). Chromosome Banding in Amphibia IV. Differentiation of GC- and AT-Rich Chromosome Regions in Anura, Chromosoma, 77:83-103(1980a) .

Schmid M, Chromosome Banding in Amphibia V. Highly differentiated ZW/ZZ Sex Chromosome and Exceptional Genome Size in Pyxicephalus adspersus, Chromo-

soma, 80:69-96(1980),

CYTOTAXONOMICAL STUDIES ON CHINESE PELOBATIDS IV. THE KARYOTYPES AND C-BANDS OF FOUR SPECIES

IN THE GENUS Oreolalax

Gelategul ») Wu Guanfu Tan Anming Zhao Ermi

(Chengdu Institute of Biology, Academia Sinica)

Abstract

The karyotypes and C-bands of 4 species, Oreolalax omeimontis, O, pingii, O, popei, and O, rugosa are reported for the first time, All these species have the same diploid number, 2n=26, consisting of 5 large (nos, 1-5), 1 medium (no, 6), and 7 small (nos, 7-13) chromosome pairs, There is a secondary constriction at the long arm of chromosome no, 6 in all 4 species, The karyotypic formula of this genus is quite similar to that of Vibrissaphora, C-—banding shows that Oreolalax has less advanced constitutive heterochromatin than other genera in more advanced families of Anura, C-banding techinque reveals heteromorphism in chromatin in the secondary constriction of chromosome no, 6 in O, popei, in which one chro- matin is much larger than the other, suggesting that a euchromatin may have

transformed into a heterochromatin,

ICT ASR ”1988 A, 5-4 Acta Herpetologica Sinica

染色 .C- Ag-NORs

(图 ) WRK BAX (安徽 师范 生物 )

动物 主要 热带 美洲 ERD MAAS, Ep het ite a ap 广 贵州 广 广 西 福建 记载 安徽 生物 ,1978)。 研究 黄山 WY Be ket (Ophisaurus harti Boulenger) fy 3 f& 2A, C- ar AAg-NORs, VIRAXS He 遗传 进化 研究 提供 Fw

材料 方法

Heke eS 2, 2ORA Ree WFR. 1. 染色 制备 ”以 骨髓 细胞 细胞 材料 常规 空气 干燥

1.1 ‘idm: 实验 动物 腹腔 溶液 (5-8 /区 体重 )。5-8 Reais, HO.40K Claim ih bee Be 细胞 20 30 , 然后 离心 (1000 / ), .再 甲醇 (3:1) 固定 固定 15 2 3 1/10Giemsa (0.15M ig 稀释 ,pH6.8) 30-40 be» ART.

1.2 BAR: ERR wy Riga BAAR. 0.250 REA (0.7% NaC lig ye Ac iil) 33 iH (6 2-3

Ra AEM AKEAR DEA. MR BEY 体积 (1000 /分 ) IR. BF 沉淀 进一步 相同

标本 (10x100) 观察 计算 计数 10 细胞 放大 照片 相当 染色 便 相对 计算 染色 染色 百分数 . 确定 Levan et al.(1964) .染色 缩写 符号

行动 命名 Y

染色 ;] 染色 mK Ze phe BK.

2, C-#&e fSumner(1972) i BSG 修改 : 即将 标本 0. 2NHCI 室温 30 蒸馏水 移入 5 Ba (OH),-8H,O 8-10 ,再 60C F2xSSC 温浴 60 5 Giemsa 染色 20

3, Ag-NORs 染色 Be HE ) Howell Black(1980) 进行 ( ,1984)。

1, 染色 染色

ASCRMREBUS HID, FRICBRL. 1987 3 4

Table 1 The chromosomal number of 0 harti baie

Diploid chromosome mm animals obeerved 09K ga ae Mae rf Pan | Ga ay : | a ie i 13 Be ne Sis f uk | 61 | 2 | 2 a | 2 Wi-- Od 5 ee i ee 4 ote 3 | 1h Total | 138 3 3 A Ve 114 Be gb 12.32 | seer) gu07

Se SR WRT A OES

Table 2 The measured data of macrochromosome of Ophisaurus harti Boulenger

Ace, No Relative length Arm ratio Ceniromere ratio Ceniromere position 1 19.73-£0.35 1.62 0.16 38.24 0.20 Vv 2 17.98-F0.26 Hest! Far age) 41.94+0.16 Vv 3 16.63-50.14 1.3940.15 (| 41.860.10 von 4 15.28:40.17 1.72-+0.09 36.710. 11 T 5 12.57 0.08 I 6 10.64 0.21 1.39+0.11 41,820.08 7 1. 16-0. 16 I

染色 测量 结果 1 2。 Whe KE 716-19, 73 5 ,-A4. 染色 (No.1-4,No.6),2 (28) 38, 染色 染色 (No.5 No.7)。 (macrochromosome) 微小 染色 (micro- 染色 差异

chromosome) zeke 染色 : 7 (No.1-7), 微小 染色 : 包括 No.8-19 .

45 10 5 0 CANO MOG Saag Fig 1 The idiogram of macrochromo- Pig 2 The idiogram of C-banding pattern somes of O. harti Boulenger of macrochromosomes of O. harti Boulenger ;

Bese AeA} Hr e738 ay WI BUN HE ee, Oe A 染色 染色 NE. 48(Y oe,

1 ), 染色 表示 10V +41+- 24m 染色 eee tas, RIA

JBAS EAT WER ARE

2. Ae eR BY C- BF a0 AgNORS CaF Ge 结果 表明 结构 染色 染色 染色 Hizs 22 (centromere)C-#, Hm~ Hw No, 2-4 #1 No.6 ane C-i, it

No,1, No 5#1No,7Hig2C-jirs 微小 染色 表现 染色 深浅 程度 差异

c.D 2)。

结果 发现 呈现 清晰 稳定 NORs, 染色 Mie No.8 fiNo.11 染色 (图 T ,sz)。 20 Ag-NORs 7 7 No 11 初步 ) NORs 呈现 染色

PR Ho

1, 染色 结果 SBT By UIE RE pan =38, NF .三 48, (10V 4I 24m) 主要 特点 ; (1) 7 染色 12 微小 染色 (Bimodal Karotypes), fie ke UR 。(2) 报道 数目 22-46, 22 =36, Morescalchi(1976) AW 2n=36 Ei ee 接近 。(3) 动物 存在 复杂 ASAE, IAF 1983), Sei (RHR, 1981) VK King (1977) Bike EBA Ee ii El 15

: soem

染色 8 BL 异型 染色 异型 (XY o/XX), 异型 复合 (XAXBYery AAAXBXB) AME: SAL (ZZ A /ZW) Giemsa 染色 异型 染色 形态 异型

2. 结构 染色 (NORs) 4- 技术 显示 染色 染色 主要 方法 研究 结果 表明 染色 主要 知道

蜡染 特异 侧面 AIA Jel SHE & BX Re B HU. Set ue 28 WN C-aNRIa AR & (Moritz

198423). A Sg (Schmid,1978a; Zuiz3s , 1981) AA, ERPS, BHRLARE

促进 进化 LEE 染色 sy ote ETAWR REA K, AAG

25M ZEAL, . La eMae a wh 2G see He He 68 USHER ARP A ladies: cules 体重 C- 显示 C- Inn hg ese a ie a

HS PS AAT] Bohs Fe 8, 75 EE in ab 2a 22S [a] FB ab Ae ese cst 微小 染色 A & 2B 染色

1981)。 此, - 4fF

, 结构

Ge 68 (AO SE

ean AAJ, Hsu Arsenic eeene 研究 设想 染色 附近 插入

C- 实验 结果 表明 he 贿 显示 C- C- A 染色 相对 稳定

技术 特异 显示 NORs 方法 , Ag-NORs 18s 28SrRNA

7

RANA. ERM, Mee Ag-NORs, 2 。Howell(1977) 染色 体位 代表 IDNA ”schmid(1980) 众多 进行 研究 方法 染色 那些 转录 NORs AgNOs 异地 染色 活性 活性 NORs AgNOs: 因此 Ag-NORs 反映 转录 活性 特点 细胞 重要 指标 比较 研究 ,Ag-NORs rRNA 基因 定位 观察 染色 变异 ?RNA 因数 目的 活性 差异 适当 1-2 棕色 NORs 反映 RAS. |e hee Shinisaurus crocodilurus Ali 研究 。3. 绝色 初步 研究 行动 研究 5(8):59-64(1981) .

: 染色 初步 研究 NC4T Sh Py FAK2(3) + 27-31(1983)。

研究 .动物 研究 2(3):

2.23-227( 1981), Gorman G C: The

Reptilia, a Cytotaxonomic Interpretations,

chromosomes of the

In “Cytotaxonomy and vertebrate evolu-

tion”, edt. by Chiarelli, A.B. et al., Academic Press, London and New York (1973).

Hsu T C et al.:Distribution of constitutive heterochromatin in mammalian chromo- somes, Chromosoma (Berl.) 34:243-253 (1971).

Howell W M: Visualization of ribosomal Gene activity:silver stained proteins as-

rRNA transcribed from

oocyte chromosomes. Chromosoma §2:261-

267(1977).

King M:The evolution of sex chromosomes

sociated with

in lizards, In: Evolution and Repro- duction, Proc. 4th Int, Conf. on Repro- duction and Evolution, Aust. Acd. Sci, 55-60(1977).

Levan A et al,:Nomenclature for centro- meric position on chromosomes, Hereditas 52: 201-220(1964).

Morescalchi A:Phylogenetic aspects of kar- yological evidence, In “Major Patterns in Evolution” eds. M. K, Hecht et al. Plenum Press New York and London, pp.149-167(1976).

Moritz C:The origin and evolution of par- thenogenesis on Heteronotia binoei, I. Chromosome banding studies, Chromoso- ma $9(2):151-162( 1984).

The evolution of a highly variable sex chromosome in Gehyro purpurascens,

Chromosoma 90(2):111-119(1984).

STUDIES ON THE KARYOTYPE, C-BANDS AND Ag-NORs OF Ophisaurus harti BOULENGER

(Plate 7)

Guo Chaowen

Dong Yongwen

(Department of Biology, Anhui Normal University)

Abstract

The diploid number, 2n, of the glass lizard, Ophisaurus harti Boulenger, is 38,

consisting of 7 pairs of macr- and 12 pairs of microchromosomes,

Among the

macrochromosomes, Nos, 1-4 and 6 are metacentric,and Nos, 5 and 7 acrocentric,

oh S

The karyotype formula may thus be shown as 10V+41+24m, and NEF is 48, No heteromorphic chromosome is observed in the karyotype,

C-bands of various shades are found in all chromosomes, The Ag-NORs observed are located on 2 pairs of microchromosomes, Nos, 8 and 11, Moreover, Ag-NORs association between sister chromatids was observed on 7 chromosomes

of No, 11 during metaphase,

PANO AT BD AR 198846 3A; 10-12 Acta Herpetologica Sinica

CA kk HD

A

《西北 生物 )

关于 受精 原核 重建 〈pronuclear reconstruction) A\|Al Rize > 7B 7b dR TE. Longo PAE RR RUE, AA 80% 受精 同时 认识 重建 形态 变化 eo 详细 报道 进一步 认识 原核 HTK, WA: ala i

EAA Bee a Sh

材料 方法

Be INH PAE A WE Me Bufo raddei Strauch) WAFS. 4AM EER RN BARES. ERMA SHAE RANT, FEzeig 210 FA LR 受精 13 2H, Sy Hie: ASIN. SeHH15, 25, 35, AQ BO. 558 65.75. oe 95. 105° Libay 受精 9-12 受精 BUY Ez (Bataillon) 固定 Ei ApH, ESO. AE, ABA. 绿 染色

[| Pro Pai) 3. dy Zz

fe LRG IR 1 SH Hea Be BE a NTE

0

i. D. SARNIA. Sa 纺锤 皮层 卵黄 颗粒 明显 标记 皮层 直达 上座 原核 显现

受精 15 皮层 周围 许多 色素 颗粒 Kasten, ABR AWK. BAR 20, SRRPER CAH. 2). BER. JREE 细胞 25 形态 消失 自动 色素 颗粒 雄性 原核 活动 色素 AU AGE id. JRA AGE TR

ER iit 结构

原核 染色 表现 形式 清亮

些小 色素 颗粒 (ARI. 3). JERI, SN ab 38 Sik pe SU A, 排出 底层 补体 仿 染色 下,4)。35 原核 开始

文摘 1986 10 召开 yy ee Rite Lins.

* 研究生

1987 3 10

色素 颗粒 卵黄 籽粒。 SDR Hy HEI Re REAR, Rs eA

ener s 红色 ;构成 雄性 Bt eRe

WZ 4M “i

eee Be ee 清晰 ese [il 形成 比较 完整 外周 色素 颗粒 显著 减少 染色 ; 绿 逐渐 形成 周围 卵黄 on Ee eae “图 ,5)。 SIN NESS, EE AI AID pee 45 原核。 雌性 动物 色素 BEEN, AME. HERI RI wi. BALE ADA aaRANAKD CREM). SMR INATER UAB ATI CZ ji >. 6) fis 3 a fecha 进程 oT UT Pe LEE Js 移动 ,内

set oe

5

AUREL E ASG, (Hey eS 638 FERREIRA. 6553, NE

NEARER ERIN, BARE AGE. POAT RMT Ke 755; Fit, BREE BIER, ARETE EE dat Be yma

TAT SN AR) ae o PE RA. PYRE JLEBBRE RM (ERY my. was.

67h, HSS KAH AE IRBERMS

(Aig, 8), 10577 时, 原核 FRE, ANA Re Smee 染色 BREA, DRERM. BAR ENDS 55 Wav 5 DY.

WE Yes FS Es ES f= LH, Hit Te WG Fs J 蛋白 速度

原核 原核 原核 重建 精子 15 进入

BH. (Re SME

> tA PIA GE 1 a Yu Ey Ane 7 Fit METS Fan, BF 0 25

原核 雄性 原核 基本 相同 程度 原核 融合

精子 膨大 Gua yin, a AF Ae EK ek, 重新 酸性 染色 同时

颗粒 减少 参与 重建 进一步 研究

Geman. Bonen eee SRETAR. MERE EERE ZS RNWEEL SMM. £S 35-45 7 Ph, AGEL SIRES, JR 染色 卵黄 颗粒 Kal, Ea SE SSR UL, BERT BURKE.

原核 运动 许多 报道 。60 fe, Longo Anderson 透射 电镜 观察 ia FAA Bite wee; 8046, Harris

SMe ts & A DURE 间接 免疫 荧光 观察 认为 精子 移动

星体 作用 核定 启动 精子 星体 平衡 L. BAVA BERS MTERWE EAI. (ESR S EM 星光 原核 运动 Fis WFP Io

i ee Mer dine (EB RELL WZ eS Bie Sag Nha eA

eC eae oe JHSERERENB. mE. MHRA AZ he fo 2 (he ERT UE IB eT PE Eo

ty

- B

3 OR

q

章鱼 动态 西 )1, (1981). Chen Da-Yuan and F, J, Longo, The Ana-

Record 207:325-334 (1983).

mem-

a5 kbs Wh 1 aS a5 Biz A iE, ORE BS =

tomical

Frank J,

Loago, Derivation of the

Il -

brane comprising the male pronuclear Gerald Schatten, International Review of Cy- envelop in inseminated sea urchin eggs, tology 79:60-156 (1982). Develop. Biol, 49, (2), 347-368 (1976).

A CYTOLOGICAL STUDY ON THE PRONUCLEAR RECONSTRUCTION IN THE FERTILIZED EGG OF Bufo raddei

(Plate J) Wu Yiging Mao Mingting (De pariment of Biology, Northwest Teachers College)

Abstract

At the time of fertilization, the egg of Bufo raddei is in meiotic metaphase 1. and the spindle is located in the cortex, near the centre of the animal pole. The sperm nucleus can be observed at the end of the sperm penetration path marked by pimant granules, 15 minutes after fertilization, the sperm nucleus starts to decondense and migrate towards the centre of the egg, A semitransparent area, which later becomes the site of fusion between the male and female pronuclei, will appear around the male pronucleus during its reconstruction, The female pronu- cleus can readily be found at the end of the female nuclear migration path marked by yolk granules, The female pronucleus reconstructs at a lower speed than does the male pronucleus, During pronuclear reconstruction, both male and female pro-

nuclear proteins turn from acidity to alkalinity,

PRCT yA «1988463; 13-15 Acta Herpetologica Sinica

(徐州 )

目前 世界 报道 6 , Cuora amboinensis(Daudin), Bias aC, flavomar ginata(Gray) , 233) faC, galbinifrons Bourret, BRAS A C. pani Song, =H aC. trifasciata(Bell) FR AC. yunnanensis (Boulenger), 南部 缅甸 印度 西 东南 国产 5 ”。

笔者 1985 10 1986 10

安徽 南陵 3

6 明显 差异 Cuora aurocapitata Luo et Zong, 1-2)

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* 作者 9. B. McDowell(1963) AUX (1986), Cyora flavomarginata(Gray) JF Geoe1yada 〈1987) 认为 se Czwora hainanensis (Li) HS Asc {Cuore galbinifrons Bourret, (HAA 同意 进一步

工作 研究 生物 研究 研究 IVR REBAR, BERS RIE. Fn See PRA. RNIN SRE WA ARERRLBREREWHERBR, HARSAS 帮助 pie, ZEAE, SSRN TAY Aw, 致谢

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参考 XM mM

生物 研究 行动 研究 ,, PET 动物 系统 检索 。9-14(1977)。 3):330

—332(1984), McDowell S B:Partition of the Genus Clem- mys and Related Problems, in The Tax-

onomy of The Aquaitc Testudinidae. 269- 270(1963),

Pope C H: The Reptiles of China. Nat. Hist, Central Asia 10:28-35(1935).

Smith M A: Fauna of British India, Reptiles and Amphibians 1:84-88(1931).

Wermuth H and Mertens R: Schildkroten. Krokodile, Brtickenechsen, 66-72(1961).

A NEW SPECIES OF Cuora—Cuora' aurocapitata Luo Bitao (Xuzhou Thirty-first Middle School, Jiangsu) Zong Yu (Shanghai Museum of Natural History)

Abstract

Cuora aurocapiiaia sp, nov,

Holotype. SMNH 86f[ 012, an adult female,

Paratypes, SMNH 879[910-011, two’male young,

All the type specimens were collected from Nanling County, Anhui by a peasant in October,1985 and 1986 and are preserved, in the Shanghai Museum of Natural History,

Diagnosis, The new species is closely related to C, pani but differs by the possession of,. carapace more convex while flattened at top with a prominent verte- bral keel; nuchal small, bell-shaped; third and fiith vertebrals broader than long, suture between gulars 1,5-2.5 times as long as that between humerals, which, is the shortest; suture between anals the longest; plastron. slightly notched at pos; terior. end; snout \shorter than orbit; head.golden, brownish on the, side, with three black thin streaks, second to fifth vertebrals red-brown; second costal with a spot (red-brown in young and, lighter in adult), plastron yellow, with largely symmetric large, black patches; front lobe with 5 large black patches,

Length of shell 89,3-138,.6mm, breadth 65,7-92,6mm, and. depth 29.2-50,.8mm,

45»

行动 1988463; 16-46

Acta Herpetologica Sinica

SEA TURTLES IN FUJIAN AND GUANGDONG PROVINCES

Susana Salas Frazier John G, Frazier (National Museum of Natural History, Smithsonian Institution, Washington D, C, 20560, USA)

Ding Hanbo (Fujian Teachers University, Fuzhou, PRC)

Huang Zhujian (Institute of Zoology, Academia Sinica, Beijing, PRC)

Zheng Ji (Fujian Teachers University, Fuzhou, PRC)

Lu Ling (Fujian Agricultural College, Fuzhou, PRC)

ABSTRACT

Five species of marine turtles occur in Fujian and in Guangdong Provinces, where a survey of the coast was carried out between June and August 1985, Details of morphometrics, scalation, other body characteristics, and epizoa are given for each species, The major age classes recorded were: Caretta caretta - subadults; Lepi- dochelys olivacea = adults and subadults; Chelonia mydas - adults; Eretmochelys imbricata -subadults; and Deriacea—-adults and subadults, Nesting is reporetd to have once occurred throughout these two provinces, but the only significant nesting known to occur now is by C, mydas, and most of that is in the Xisha Island, with the exception of C, mydas which is fished intensely in the Xisha Islands, incidental capture during offshore fishing operations is the source of nearly all turtles, Most catches are made during the summer and autumn, Beaches, reported to have once

had nesting, are now subjected to so many perturbations that virtually no nesting

This article reports the results of a cooperative project between: Fujian Teachers University, Fuzhou, China; National Program for Advanced Study and Research in China, CSCPRC; and National Academy of Sciences, Washington D. C., USA. Major responsibilities are as follows: Senior sponsorship and obtaining permits (particularly in Fujian—Professor Ding Hanbo; Obtaing permits and logistical planning and support—Zheng Ji; Negotiations and obtaing permits in Guangdong, logistical planning— Huang Zhujian; Translations and Interviews—Lu Ling; Assisting in data gathering, analysis, and writing of preliminary and final reports—Susana Salas Frazier; Data gathering and analysis,

scieatific planning, amd writing of prelimimary and final reports—Joha G, Frazier, 5

* 16

turtle can escape back into the sea, The few inshore marine areas observed suggest that there is little feeding habitat for C, mydas or E. imbricata, It was virtually unanimous among fishermen and other ‘coastal peoples that populations of sea turtles have declined tremendously over the past few decades, and attitudes toward the animals have changed’ from traditional respect and protection to contemporary full-scale exploitation: There is a great need for long-term, detailed studies—even of basi biology; and there is an urgent need for rational conservation and man-. ‘agement of these valuable renewable natural resources and their requisite habitats, The present rate of exploitation on the Xisha Islands will soon result in the whole-

sale destruction of natural resources there, INTRODUCTION

There are some 7 or 8 species of sea turtles (Cheloniidae and Dermochelyidae) living today, and these include some of the largest of ali extant reptiles, as well as some of the most economically valuable of wild animals, Marine turtles represent much appreciated sources of proteins, oils and other products that have been used for nutritional and medicinal purposes for centuries, Some marine turtle products (e, g, tortoise-shell and leather) are much sought after in» industrialized nations and as a result these command high prices and. earn foreign exchange in areas where income is generally low, The effect,on the turtles, is very heavy exploitation, As a tarely broken rule, marine, turtle populations around the, world have been overexploited and their numbers catastrophically reduced-particularly during the last few decades (Frazier 1980; Bjorndal 1982),

In addition, human populations ‘have increased dramatically over the last decades in most cotntries, and.as a result coastal and marine habitats have come under heayy pressure from exploitation of natural. resources and from modification of hab- itats for agricultural and socio-economic development, As a consequence, requisite nesting and feeding habitats for marine turtles in many parts of).the. world have been destroyed or so greatly altered that they do not provide the tequirements of the animals, ;

A further factor which greatly complicates the situation is that all sea turtles have highly ,complicated life cycles, depending on.a variety of habitats from terres- trial :to epipelagic ecosystems, and requiring decades to. reach, maturity, In the course of a normal.life cycle.a single sea turtle, during its;development, may travel over vast areas of ocean, ofice it is mature the turtle may make seasonal migra- tions of thousands of kilometres, across coastal. waters and open ocean, Hence, dur- ing its lifetime, an individual turtle will pass through and live in. many sovereign territories, Despite half a century of detajiled scientific study by, biologists in. dozens

of countries, many basic biological points about sea turtles remain. unknown (Fra-

* Ob ,。

zier, 1984a),

As a consequence, biologists, naturalists and people concerned with the ratio- nal use of natural resources are dedicated to the study of marine turtles. so that mankind can better benefit from a more thorough understanding of the biology and natural history of these intriguing animals and so that we can benefit from rationnal utilisation of these natural resources—in such a way that future generations will be able to enjoy these natural treasures, and not suffer from the greed and misman- agement of former generations, This concern is world-wide, transcending national boundaries,

The goals of the project described herein were to make available basic infor- mation on marine turtles in a poorly studied area; assist in the conception, plan-. ning and guidance of management and conservation programs; and assist in techno-

logy transfer for field, analytical and management procedures,

ITINERARY and METHODS

The survey began on 6 June 1985 in Fujian province, where two weeks were spent, using 8 bases: Shishi, Zhangpu, and Dongshan. During this time 15 coastal sites were visited; 28 interviews were carried out; 6 potential nesting areas were visited; and 13 specimens were examined ¢of which 10 were collected) ,

From 19 June until 2 July and from 19 July until 27 July the survey was based'on the mainland of Guangdong Province, Seven different bases were used; 4 coastal sites were visited; 12 interviews were carried out; one nesting area was visited; and about 16 specimens were examined (of which 3 were collected),

Hainan Island was surveyed between 2 July and 19 July, Four bases were used; 7 coastal sites were visited; 15 interviews were carried out; 6 potential nesting areas were visited; 3 potential feeding habitats were visited; and 102 specimens were examined (of which 10 specimens and additional stomach contents and limb bones were collected) ,

From 9 to 12 August, the survey continued on Pingtan Island, Fujian, where: 6 coastal sites were visited; 4 interviews were carried out; one potential nesting area was visited; and 19 specimens were examined (of which 7 were collected),

During the various stays in Fuzhou 39 specimens were examined, of which 31 were in the Depareneut of Biology, Fujian Teachers University and 8 in the Fujian Provincial Museum,

Identifications of specimens were based on information in Frazier (in press) ; measurements are as described in Frazier (1984b), Abbreviations used in the text are listed in Appendix I, Interviews witlt coastal fishermen and others were con-

ducted using the standard format in Appendix [| (omitted) , “9 18 Ps

RESULTS

The results are treated in 3 parts, Specimens, Habitat Surveys, and Interviews, SPECIMENS

Specimens of 5 species were examined, totaling 189 individuals, Only 4 of these were live, The vast majority of specimens were carapaces (of Chelonia mydas_ espe- cially) that remained after the animal had been killed and consumed, In all but one instance the specimens were easily identified to species; the exception was a small and badly weathered fragment of a carapace (for comments on identification of sea turtles see Frazier, in Press),

Caretta caretta (Linnaeus)—Xi Gui, Loggerhead Turtle,

Specimens examined - A total of 16 specimens (and a fragment of another spec- imen thought to be of this species) were examined, FTU=6; FPM=2, Fujian fish- ermen=5; Hainan fishermen=3,

Distribution-The species was recorded from Hainan Island (19° 40’N) to Pingtan Island (25° 30’N); 819 of the C. caretia were from Fujian and only 19% from Guangdong, Of all the Fujian specimens examined, C, carette comprised 23%; of all the Hainan Island turtle specimens examined, C, caretita comprised only 3%, No C, careita from the Guangdong mainland were seen, Hence, the species is more com- monly captured in the north than in the south (more than half of the specimens of this species came from Pingtan Island alone),

Seasonality - The species is caught through much of the year; records span from March to October, with 3 Hainan specimens in late June/early July and 4 Fujian specimens in October, The few data suggest that in the south the species is caught more commonly in the summer and in the north, more commonly in the autumn, but more data are required to establish seasonal trends,

Morphometrics - Curved carapace length of 16 specimens ranged from 74,5 to 102 .5cm (X +1 St, Dev, =82.0 +6.88cm) (Figure 1), Less than half of the ani- mals were greater than 80cm, so most of the sample were evidently subadults, Curved carapace width varied from 88 to 97% of CCL, averaging 91.4% (42.56%; N=15). Depth of the supracaudal notch varied from 1.0 to 2.8% of the CCL, averaging 1.8% (10.46%; N=15). Head width varied from 19 to 21% of CCL, averaging 19.4% (+0.67%; N=9). Plastron length varied from 69 to 76% of CCL, averaging 72.7% (12.46%; N=9), Length of the postanal scale varied from 2.1 to 7.6% of the PL, averaging 3.9% (+2.06%; N=7).

The sample sizes are too small to make conclusions about sexual differences or ontogenetic variation, although there are indications of allometric decrease in rela- tive, CCW (Figure 2), HW (Figure 3), and PL (Figure.4),

Scalation - Only one of the 15 specimens showed variation in the normal number

e 49

of vertebral scutes; it had 6 instead of the usual 5. Variation in the number of pleural scutes was greater, 12 specimens each had 5 pairs of large scutes; 2 speci- mens each had a greatly reduced Ist right pleural; one specimen had 4 right and 5 left pleurals; and one specimen had 6 right and 5 left pleurals, Hence, 25% of the specimens had abnormal right pleurals; no specimen had abnormal left pleurals, Marginal scutes were relatively variable. 6 specimens each with 11 pairs; dne spec- imen with 10+1 partially divided left and 11 right, 3 specimens each with 12 left and {1 right, specimns each with 12 pairs of marginals, Hence, more than half of the sample’ had non-inodal conditions(viz, other than 11 pairs of marginals), One of the il specimens had a divided cervical scute; in 12 others it was single,

Head scalation also shows considerable variation, The number of postocular scales was most frequently 3 pairs’ (7 of 9 ‘specimens) .Other ‘conditons were, 4 ‘pairs, and’ 2+-1 partially divided left and 4 right, ‘prefrontal scales varied from 4 ‘fo 8 in number, with 5 being most fréquent (4 of 9 cases).

Inframarginal scutes were 3 pairs in the majority of specimens (8 of 9); the exception had 4 pairs, The intergular scute was much reduced in comparison to other species in the Cheloniidae; it was absent in 4 cases and very small (less than 1/4 of a gulat scute) in 4 other cases; The submandibular scales, that gover’ the _-ventral surface of each ramus of the mandible, were always greater than 1 in num-

ber; each side of the jaw had cither two large elliptical scales with a much smaller

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circular scale between them; or 3 large rounded scales of nearly equal size,

Other morphological features, difficult to quantify but characteristic of this species, were present, The notch between the supracaudals was “V”-shaped, A py- geal “knob” was conspicuous at the anterior of the tifth vertebral. scute, |

Epizoa - Filamentous algae were on at least 4 of the 16 carapaces (25%). Bar- nacles were on 50% of the 16 specimens examined,Chelonibia testudinaria on 3, bur- rowing barnacles (Stomatolepas 7?) on 4 (including one male turtle with an extensive infestation that covered about 80% of the carapace), and one animal had Platyle- pas hexasiylos, One carapace had small depressions with what appear to be macro- scopic copepods within, These rates of epizoan occurrence represent minimal values, because these organisms are frequently cleared off of specimens during preparation for museum collections,

Lepidochelys olivacea (Eschscholtz)—Li Gui [ “Beautiful Turtle” 1, Olive Ridley turtle,

Specimens examined - A total of 24 specimens were examined, FTU=5; DSMS= 1; Fujian fishermen=17 (including one carapace said to have been ponent in Zhe- jiang Province); Hainan fishermen=1,

Distribution - The species was recorded from Hainan Island (19° 40’N) to Zhe- jiang Province (about 27°N), Nearly 92% of the Lepidochelys olivacea were from Fujian Province, only one specimen was from Hainan, Guangdong; and one from Zhejiang (captured by Pingtan Island fishermen), Hali of the specimens came from Pingtan Island, north Fujian Province, and of all the Fujian specimens examined,

L. olivacea comprised 31%; of the Hainan Island specimens examined, L. olivacea

- 22+

comprised less than 1%. No turtles of this species were recorded from the mainland of Guangdong Province, Hence, the species is captured more commonly in the north than in the south,

8

NUMBER OF TURTLES

CURVED CARAPACE LENGTH (em)

Seasonality - Specimens were collected between May (1 case) and October (1);

cae

with a preponderance (3) in June, Fishermen reported catches trom February/ March (2) to October (1), with the vast majority (7 of 12) in June and July, The species is evidently captured much more frequently during summer months,

Morphometrics-The 24 specimens measured included adults and subadults, Curved carapace length varied from 43,0 to 70,0cm,averaging 59,3(-+6.70cm;N=23) (Figure 5), Curved carapace width varied from 99 to 108% of the CCl, averaging 102.4% (42.44%; N=20), Head width varied from 18 to 19% of CCL, averaging 18.2% (+0.53%; N=5), Plastron length varied from 70 to 75% of CCL, averag- ing 72,0% (42.16%; N=4). Postanal scale length varied from 2 to 3% of PL, averaging 2.5% (40.51%; N=3). |

The data are insufficient to determine if any sexual differences occur, and they do not indicate any consistent ontogenetic trend, There may be an allometric reduc- tion in relative carapace width (Figure 6), but relative head width (Figure 7) and plastron length (Figure 8) appear to decrease allometrically, More data are needed to determine if these trends are statistically significant,

Scalation-This species shows great variation in carapace scalation, The number

G18 i

of vertebral scutes varied from 5 to 8 in 24 specimens, 5=25%; 5+1 partially di- vided=4%; 6==38%; 7=29%; 8=4%, Variation in pleural scutes was even greater; 63% had symmetric arrangements while 38% had asymmetric arrangements; Of the symmetric arrangements, 6 pairs of pleurals was the most frequent (29% of the to- tal), but there were as few as 5 pairs (8% of the total) and as many as 7 pairs (21% of the total); one animal had 5+1 partially divided on each side, Of the

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asymmetric arrangements, a greater number of left pleurals was more common than a greater number of right pleurals (25% and 13%, respectively). The greatest num- ber of pleurals on any side was 8 and the least, 5,

Data on marginals are available for only 16 specimens, Of these, bi dias had 12 pairs, the remainder had asymmetric arrangements ol 12 on one side and less than 12 on the other, Postocular scales varied from 3 pairs to 4 pairs, asymmetric com- binations of 3 on one side and 4 on the other also occurred, Data from only 5 specimens are available, and there is no mode,

Inframarginals were 4 pairs and the intergular was small (but data on only 2 specimens are available), There was frequently a pygeal swelling (not a knob) at the level of the last vertebral, and the notch between the supracaudals was nor- mally “C”-shaped, A single, exceptionally large elongate scale covers the anterior

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the neurals at the level ot the Ist and 2nd vertebrals,

Other features, common in the East Pacific (Frazier 1984b), were absent, There were never scratches or notches in the anterior “shoulders” of the carapace; nor were there abrasions or gouges on the ventral posterior marginals, These two sorts

of injuries are characteristic of breeding turtles and are evidently made by the male

© 25 ast

during mounting activities, None of the Chinese Lepidochelys olivacea showed a bi- tonal carapace, with the posterior smoother and lighter in colour, This feature is normal in both breeding and nonbreeding populations of the East Pacific,

Epizoa-This species evidently has very low rates of epizoan infestations, at least in China, Only one animal had epizoa, a few small barnacles on the carapace, Chelonia mydas (Linnaeus)—Lu Gui (= “Green Turtle”), Green Turtle,

Specimens examined - A total of 130 specimens were examined, FTU=12; FPM =2: DSMS=1; SCSI=4; ZSU=3,; Fujian fishermen=6; Guangdong nesting beach= about 4; Hainan fishermen=98,

Distribution - The species was recorded from the Xisha Islands (16° N)to Ping: tan Island (25° 30’N). At least 79% of the Chelonia mydas examined were from Hainan-Xisha Islands; only 16% were from Fujian, Of all the Fujian specimens examined, this species comprised 30%; it comprised 95% of the Hainan-Xisha Is- lands specimens, Of all of the sea turtle specimens examined during the present survey, C, mydzs made up 69%, Clearly, this was the most common species, and it is most abundant in the south,

Seasonality - Specimens were collected between April and October, The vast ma- . jority were from June and July, due to the large number of animals examined in early and mid July during the present study in Hainan Island,

Morphometrics - The majority of the 125 animals measured had curved carapace length between 71,5 and 108.0cm; however, turtles as small as 20,0em were mea- sured, There is a conspicuous mode between 90 and 95cm (Figure 9), Curved carapace width is about 90% of CCL, The notch between the supracaudals is nor- mally much less than 1% of the CCL, but in a dozen cases the notch was deep and more than 1% of CCL; never was it more than 2%, Head width varied be- tween 13 and 19% of CCL, averaging 13.8% (+1.36%; N=23), Plastron length varied from 71 to 82% of CCL, averaging 77.9% (+2.23%; N=33). Postanal length varied from 0,0 to 10.5% of PL, averaging 2.5% (+1,.93%; N=23).

Detailed morphometric data will be analised later to test for sexual differences, The data indicate that there are several allometric changes, With increasing CCL, there is a decrease in relative, CCW, HW, and PL (Figures 10-12)

Scalation - Of 123 specimens, 96% had 5 vertebral scutes. Four specimens (3%) had 6 scutes and one (1%) had 7, Pleural scutes were scored for 126 specimens, 95% of which had 4 pairs, Other arrangements were, 5 pairs=i,; 5 left/4 right=1, 6 leit/5 right=1,; 4 left/5 right=3, Marginal scutes were scored for 118 turtles, of which 97% had 11 pairs, Two turtles each had 10+1 partially divided left/11 right, and one had 12 pairs,

Postocular scales were scored for 29 turtles; 76% had 4 pairs, Two had 5 pairs; one had 5 left/4 right, three had 4 left/5 right; one had 2+1 partially di- vided left/3 right, Axillary scales were recorded for 19 specimens, 42% had 3 pairs;

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21% had 4 pairs; 11% had 2 pairs, Four turtles had 4 left/3 right, and one had 4 left/5 right, Inframarginal scales were scored in 32 turtles; 919% had 4 pairs; two turtles had 4 leit/5 right, one turtle had 2+1 partially divided on both sides, In the same 32 turtles the intergular was invariably large. One pair of inguinal scales were present in 22 of 23 turtles, the exception had 2 left/i right,

Coloration - Information on coloration was collected for 103 turtles, Of these, 70% had concentrations of dark pigment in all large carapace scutes; only 7% had no concentrations in the carapace scutes, The occurrence of red-brown “bulls-eyes” within the concentrations was scored for 97 of the turtles, In 35% the bulls-eye was conspictious in all scutes; it was absent from all scutes in 49% of the turtles.

There appears to be a sexually related difference in these color characteristics (see Frazier 1971; 1985a), and detailed data will be analised later. There is a clear ontogenetic sequence of color phases, typical of the species in other areas,

Epizoa - On all the specimens examined, filamentous algae were found on only 9 individuals; green, red and brown forms were evident, Barnacles were recorded on only 21 turtles, at least 4 species were present, Four turtles had heavy infestations of burrowing barnacles in their carapaces,

Eretmochelys imbricata (Linnaeus) —Daimei (frequently, but incorrectly called “Dai- mao”), Hawksbill Turtle,

Specimens examined - A total of 10 specimens were examined, FTU=3,F PM=2 (one live), SCSI=4; ZSU=1,

Distribution The species has been recorded from the Xisha Islands (16° N), to Pingtan Island (25° 30’ N) and Lianjiang (26° 6’ N), on the north side of ‘the Minjiang River, Fujian, About half the specimens of this species were from Xisha Islands and about half from Pingtan and Lianjiang, Eretmochelys imbricata com- prised 7% of all of the Fujian specimens and 4% of all of the Guangdong specimens, The absence of records from southern Fujian and the Guangdong mainland is curi- ous, but at least in part must reflect the lack of collecting effort, '

Seasonality Records (all from northern Fujian) are from: May, July, August and October—summer months with the exception of last named,

Morphometrics - All 10 specimens are well below adult size; the largest was 65 em curved carapace length (Figure 13), Curved carapace width varied from 82 to 91% of CCL, averaging 88.2% (+3,12%; N=i0), Depth of the supracaudal notch varied from 3,6 to 5.8% of the CCL, averaging 4.8% (40.77%; N=10) , Head width varied from 12 to 16% of CCL, averaging 13.7% (11.44%; N=9), las- tron length varied from 68 to 79% of CCL: averaging 71.9% (+4°37%; N=5). Length of postanal scale varied from 1,8 to 4,1% of PL, averaging, 2,62%

(41.03%; N=4) , The data are insufficient to determine if there are sexual differences in mor-

phometric characters, Several allometric changes are apparent; with increasing CCL

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there are relative decreases in CCW and HW and relative increase in PL (Figures 14-16), Statistical verification of these trends must be done when more data are available,

Scalation -Carapace scalation was unvarying in all 10 specimens; each had 5 ver- tebrals, 4 pairs of pleurals and 11 pairs of marginals, Postocular scalation was also unvarying; 3 pairs in 7 of 7 cases, In 6 of 6 cases inframarginals were 4 pairs, Normally the intergular is large and there are 4 prefrontal scales, One animal (JGF 42-87) was unusual in having a very small intergular (less than 25% of a gular) and 7 prefrontal scales,

The position of the most anterior dentate marginal varied from the Ath to the 7th and was inversely related to carapace length, Similarly, the number and strength of dorsal and ventral keels is related to body size; the smaller animals have more prominant keels, This is comparable to the situation in the western Indian Ocean (Frazier 1985),

Epizoa Only one live E, imbricote was examined, and it had two species of balanid barnacle and at least two species of algae, The other museum specimens had evidently been cleaned of epizoa during preparation,

Dermochelys coriacea (Linnaeus)—Leng Pi Gui (“Keeled Turtle”), Leatherback Turtle, :

Specimens examined A total of 9 specimens were examined: FTU=5, FPM 2; ZSU=1; Fujian fishermen=1,

Distribution - Eight of the nine specimens (89%) came from Fujian, between Dong Shan Is, (23°40 N) and Lianjiang (26°6’ N) , The one specimen in Guang- zhou was evidently from Guangdong Province, but it had no specific locality data, Of all the Fujian specimens, Dermochelys coriacea comprises 11%; less than 1% of the Guangdong specimens was D, coriacea, This suggests that the species is caught more commonly in the north, .

Seasonality - Four specimens were collected in May call in 1984), two in July and one each in August and October, The species appears to be caught more com- monly during summer and autumn,

Morphometrics - The 7 specimens with measurements include adults and sub- adults, Curved carapace length (taken along the medial keel) varied from 115.5 to 152.5 cm, averaging 131,8 (112.62%) (Figure 17), Curved carapace width varied from 66 to 75% of CCL, averaging 70.4% (+3.30%: N=7), Head width varied from 14 to 16% of CCL, averaging 14.6 (40.57; N=7).,

The largest and smallest animals were both males, and there are insufficient data to determine what sexual differences exist, There are clear cases for allome- tric changes; both relative carapace width and relative head width decrease with increasing CCL (Figures 18 and 19),

Osteoderms-—In at least 3 of the Fujian specimens large osteoderms were con-

32

spicuous in the anterior of the paramedial keels of the plastron, Small osteoderms in these keels were as far anterior as the level of the axillae,

Epizoa None of the museum specimens examined had any evidence of epizoa,

HABITAT SURVEYS

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A total. of 14 beaches were visited: 7 in Fujian, one on the Guangdong main- land, and 6 on Hainan Island, Three potential feeding habitats were visited—all on Hainan, Although beach visits were brief—usually only half an hour in duration— an attempt was made to assess the status of strand vegetation and the potential value of each beach as a sea turtle nesting habitat,

Fujian beaches

Pingtan— A long sandy beach stretches from Dafa west to Da’ao, on the north east of Pingtan, It was reputed to have once had nesting, some 30 years ago (al- though it seems that only one nest was ever seen), The intertidal area ends abruptly at vertical cliffs of soil and sand. These cliffs have been, and are, undergoing ac- tive erosion, The beach provides poor, if any, nesting habitat, Its badly degraded status appears to be a result of extensive and prolonged sand mining, The Dafu-—

Da’ao beach is today unimportant as a sea turtle nesting area,

e 33 e

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Zhangpu - Five beaches in this county were reported to have had turtles nest-

ing; two were visited, Liaozhua beach is on the east, or ocean, side of Liu’ao

peninsula; Kishan and Liaozui are evidently alternate names for the same beach, It has a wide terrestrial area: a lower terrace without vegetation, and an upper vegetated terrace with half a dozen typical strand species, Some 25 to 35 m irom the high water mark (HWM) is a dense plantation of Casuarina, evidently planted about the year 1980, Although there is a small human settlement at its north end, the beach provides good to excellent nesting habitat, If, however, the Casuarina are planted farther seaward, the nesting habitat will be destroyed,

At the south eastern end of Gulei peninsula, near Xia’an village, is Houjiang beach, Here there are low dunes inland of a wide intertidal zone, Half a dozen typical strand species grow on the dunes, helping to stabilize them, Thirty metres inland of the beach is a plantation of Casuarina, Settlements are both west and north of the beach, but there is good nesting habitat, Like the previous beach, there was no evidence of nesting,

Dongshan-Six beaches were reported to have had nesting on this island, four were visited, In the north east, Nanmen and Yulan, two contiguious beaches here considered as one, are near to the township, Nanmen actually forms the seaward limit of much of the town; breakwaters and other constructions line the beach, At its. south end, free from human habitations, the intertidal zone ends abruptly at actively eroding cliffs of sand and soil, Extensive and prolonged sand mining has evidently been done on this beach, and whatever value it once may have had as a nesting habitat has long since been destroyed, Yulan, which extends to the south, has a few dwellings, Sand. is being mined in the north, creating vast depressions and beginning an irreversible erosional process, Other activities

Fae

‘on the beach include rope making, and the omnipresent Casuarina plantation lines the beach, At the southern end the beach is relatively undisturbed, and a vegetated beach platform provides good nesting habitat, However, the base of the littoral zone has numerous large rocks, obstructing the approach to this part of the beach, All things considered, there seems to be little significant nesting habi- tat left here, There was no sign of nesting,

“Luoshanxu beach, near Huidong village in the east centre of Dong shan, was “reported to have had turtles nesting on it as recent as 1981 or 1982, A narrow platform, vegetated with half a dozen typical strand species, is all that is left of the original coastal habitat, for Casuarina has been planted along the beach and cultivation taken to the edge of the Casuarina, A vestigeal hedge of Pandanus indi- cates that this beach once had an “oceanic” type strandline vegetation, and that the nesting habitat was once good or excellent. The high beach habitat that re- mains provides fair nesting habitat, |

~Guizitou beach is at the southern end of the island, immediately west of Ao- jiao villace. Turtles are said to have nested about 1980. An undulating beach plat- form has an open Casuarina plantation within 10 to 15 m of the HWM, Little re- mains of the strand vegetation, and there is considerable pedestrian traffic on and along the beach. Although there is fair nesting habitat, there is little chance that a nesting turtle would be able to escape from the beach before being detected and killed, a

Houjiang beach is in the extreme south, just east of Gonggian village, Here also it was said that turtles had nested since 1980. The south end of the beach is next to the village and is actively used for fish drying, There is little (if any) natural strand vegetation left. The north end is more isolated, but Casuarina have been planted to within 20 m of the HWM, A few strand species occur, and there is a strip with good nesting habitat, As before, no signs of nesting were evident. Guangdong mainland beaches |

Huidong This county was first visited in the midst of a typhoon on 24 June, and then again a month later with normal weather. Haigui Bay, with a sandy beach less than 2 km long, is on the east side of a stubby peninsula about 100 km north east of Hong Kong, A dune ridge about 10 m high runs the length of most of the beach; it is covered by an intact Pandanus hedge, As many as 3 fter- races occur between the HWM and dune base, the two seaward platforms are with- out vegetation and together as much as 50 m wide in the north of the beach, The inland, vegetated terrace (ideal for nesting) is about 10 m wide in the north and nearly 30 'm wide in thé south, There are ‘about a dozen species of conspicuous strand plants.

In 1984 this area was declared a sea turtle conservation area, and at the major

points of entry to the beach large signs proclaim that it is a protected area. A

s $5 e

temporary shelter at the center of the dune ridge houses 1 to 4 beach wardens that patrol the beach and record nesting events by turtles, Before its declaration as a. reserve, this beach was subject to human predation, and the skeletal remains of half a dozen C, mydas are scattered about, On 26 July there were i7 recent nest- ing pits, at least 13 of which appeared to contain eggs, these spoors were consis- tent with those of C, mydas, Considering the nesting cycles normally exhibited by this species, there had probably been no more than 6 individual turtles nesting on this beach before 25 July, We were told that general reports about the conservation area and the turtles were top security aud secret and could not be shown to us; however, Mr, Zheng and Mr, Huang were given access to the relevant reports and they were allowed to extract from them, : Hainan beaches

Qionghai - This county is known for its turtles, but the majority of the animals we saw were imported from the Xisha Islands, indicating that the local breeding population has been decimated, Seven beaches were reputed to have had nesting, and 5 of these were visited, Fentoulin is north of Taimen village, A vast expanse of sand stretches both northeast and south as far as the eye can see, The off- shore bay has a shallow sandy bottom that extends out for about 1 km; it serves as an anchorage for fishing vessels and provides protected waters for dozens. of dip net fishing stands. At the south end of the beach an erosional cliff as much as 1 m high has encroached into a small coconut plantation; sand mining has evident- ly been carried out here, A dense forest of Casuarina has been planted along nearly all of the beach to within a few metres of the beach crest, Seaward of the Casuarina is a zone about 3 to 5 m wide with a low colonizing vegetation consistiog of about half a dozen typical strand species, This narrow vegetated zone provides good nest- ing habitat, but the amount of human activity in the offshore and onshore areas greatly decreases the chances of any turtles nesting here, there were no signs of nesting ,

Xilu beach is on the south side of Taimen village; the sand beach here extends as far as the eye can see, both to north and south, Dense plantations of , coconut and Casuarina are within 25 m of the HWM, The vegetated beach platformiis domi- nated by spiny grass, Near to the beach are human habitations and considerable pedestrian traffic, There is a vast emergent tide flat at the base of the beach, and this extends about 100 m seaward; this flat is a major impediment to turtles that attempt to ascend the beach, nest and return safely to the sea. The nesting habitat available is fair to poor, and there was no sign of nesting,

Sutan beach is between Taimen and Bo’ao on a stretch of coast that is an uninterrupted sand beach, Rising from the beach crest about 1 to 2 m is a. zone about 3 m wide vegetated with typical strand species, At the landward edge a ter-

race rises and extends inland for at least 10 m; at its seaward edge is. an intact

+ 36

hedge of Pandanus that runs for a total distance of several km, The narrow zone between beach crest and terrace provides good nesting habitat, Although it was stated that as recently as 1983 turtles had nested here, there was no evidence of nesting, There is a well established Casaurina plantation inland of the Pandanus hedge, but otherwise little human traffic or disturbance, The Sutan beach was one of the two places seen during the entire survey that has a significant remanent of natural coastal vegetation along the beach.

Beimen beach is just north of Bo’ao port, seaward of the village, Not only is it close to a center of human activities, but it is the site of a mechanized mining operation that digs up and washes sand for rare metals, The mouth of the Wan- quan River is a few hundred metres south, and this river has evidently been depos- iting large amounts of sand along the coast here, for there are open rolling dunes on the high beach platform that is nearly 100 m wide and sparsely covered by low colonizing species typical of the strand, Apparently a turtle nested here in 1980, but at present there is poor nesting habitat available—notably because of the mining operation, It is not known if the mining activities will proceed northward along the beach of Sutan; if they do, they will destroy the remanent of beach vegeta- tion that is there,

Donghai (formerly Nangang) beach is south of Bo’ao port; it once again is part of a vast uninterrupted stretch of sandy beach. A wide, gently undulating open dune, some 300 m from beach crest to Casuarina plantation, has sparse cover of typical strand species and dune colonizers, The seaward edge of the vegetation is dominated by a spiny grass, There is some pedestrian traffic on and near the beach, but there is a large area of good nesting habitat, It was claimed that as late as 1984 turtles had nested here (and been caught and slaughtered), However, no Sign of nesting was seen,

Sanya- There are reported to be at least 4 places with turtles nesting; two are on Xidao Island, It was only possible to visit Haiguishi on the south east of the island, This was the shortest beach visited during the entire survey, about 200 m long, An emergent fringing reef lies about 40 m offshore, The littoral and su- pralittoral beach are littered with wave worn coral rubble, which is being extracted from the north end of the beach, A zone, some 5 m wide that runs about 10 to 15 m from the HWM, has cover provided by nearly a dozen plant species, typical of the strand. The colonizing vegetation is in succession to shrubs and woody forms, whick dominate the beach immediately inland of the strand zone, Pandavus, and aa Asclepiadaceae (Pleurosteima 7) dominate the woody hedge, An Opuntia, evi- dently naturalized on the island, is also conspicuous in the hedge, and it is colo- nizing the zone of strand vegetation, A few old nest pits, the size of Chelonia mydas pits, were in the centre of the beach, and we were told that at least one turtle

had nested in 1985, This beach was named “Sea Turtle. Market” because of the

ey ek

large number of turtles that nested here; it now appears that the market has been abandoned. Hainan marine habitats _

Qionghai-Only one marine pasture was seen during the survey, that which grows immediately to the south of a sea wall that extends out from Taimen inlet, To landward is a wide emergent tide flat covered with Halodule sp, On a _ sub- strate of coarse sand, coral rubble and silt, a mixed species pasture extends from afew msouth to the sea wall southward for at least 300 m, At low tide it is cov- ered by about 50 cm of water, Clumps of Enhalius acaroides are in slightly deeper water that forms small channels,or depressions, The flat shallower area has Thalas- sia hemprichii, Cymodocee sp,, Halophila sp., Halodule spp, and Syriogodium isoeti- folium, The last named forms nearly species pure swards some 50. m from the sea wall, and on 14 July 1985 there. were numerous flowers, In many, tropical | seas, pastures of this type provide feeding habitat for Chelonia mydas,, There were few algae in evidence, The rubble covered depressions had few angiosperms but 3 brown algae were evident, including Padina sp,,and Sargasum sp,

Sanya - South of Sanya city a peninsula extends toward the southwest, A bay on the east side has a “C”-shaped beach that extends for several km; at its south- west end is a fringe reef about 300 m long, Surge channels perforate the platform at the north end, The south end has an emergent reef platform, The platform is widest (nearly 150 m) in the centre, and narrowest (about.15 m).at the north and south ends, At the outer edge of the platform there is an abrupt drop off to 3 to 6 m deep, Scattered to seaward of the edge are numerous granite boulders, The most active scleractinian coral growth is on these boulders and on the edge of the platform; the most conspicuous species belong to the groups: Acropora spp., Pocitl- lopore spp,, meandrines and faviids. Porites spp, were not conspicuous, At the south end of the reef platform Alcynarian type soft corals are conspicuous and in localized places these seem to be dominating the hard corals, Few thalloid algae were evi- dent; there was moderate diversity of coral reef fishes, There was a great abundance of crinoids, and the textural diversity of this reef was good, In conclusion, there was fair feeding habitat and good sheltering habitat for Hreimochelys imbricata, It is not known to what level of exploitation this reef is subjected; there was evidence of unnatural breakage to some of the branching hard corals, and fishermen and fish- ing boats were seen here in ones and twos,

On the west side of the same peninsula, facing Sanya harbour, is a protected bay with long gentle “C”-shaped beach, A vast submergent reef flat extends out 300 to 500 m. from the shore, lt is covered with coral rubble, sand and silt, there is very little live coral, Shrimp burrows with symbiotic gobies are common, At the edge of the reef flat is a slope from about 1 m of water at mid tide to several metres

below the surface, Shoreward of the slope are a few live hard corals, but the ma-

es 38 *

jority of these are broken, solitary, unsupported branches (e.g. Acropora sp.) that

appear to have been washed in from actively growing colonies elsewhere, Slabs and | blocks of dead coral are also common near the slope, Large solitary corals (e.g, Fungia sp.) are common on the reef flat, but they, like the branching coral pieces and coral blocks, have evidently been washed in from elsewere, At the slope there are growing colonies of table forms of Acropora, but there is only about 25% cover by live corals, There are very few algae on either the reef flat or the slope, and there are very few live mollusks evident, In conclusion, this reef appears to have been very heavily mined for coral and shells, there has evidently been repeated breakage and removal of live coral, It is a habitat poor in species diversity, poor in textural diversity and with very little value. as feeding or sheltering habitat for marine turtles, Tourists frequent this bay, for it is next to the grounds of a large hotel, .

It must be noted that in and around Sanya large amounts of hard coral are sold as souvenirs; these are eagerly purchased by visitors from the Chinese mainland and from overseas. There is no apparent control on, or concern for, the amount of coral destroyed and sold, This is symptomatic of large scale destruction of the near shore marine environment,

INTERVIEWS

There is no substitute for direct examination and investigation of specimens and habitats, However, untrained people during their lives accumulate a wealth of knowledge, and although this is often subjective, mixed with superstitions, and not organized scientifically, the information provides unique and valuable opportu- nities to make inferences about situations outside the scope of an individual scien- tist’s personal experiences, In the case of sea turtles, the experiences of professional fishermen and people who live along the sea coast provide valuable sources of in- formation, After several days trying different methods at questioning fishermen, we made up a standarized interview form, this was translated into Chinese and dupli- cated (see Appendix If) (omitted),

Language is a tremendous barrier in China - not only to those who speak no Chinese but also to natives, The diversity of dialects and pronunciations, in a lan- guage that depends on subtle differences in tones, makes it difficult —if not impo- ssible—for neighbors to communicate efficiently with each other, When one is trying to extract precise, objective information from people not trained in the sci- entific method, this further complicates an already difficult situation, It was, thus, not uncommon to have 10-minute discussions to get a two word answer to a specific question, Because each question was asked three times (English - Mandarin - local dialect, and back by the reverse route), the chances of misunderstandings and erroneous, or misinterpreted end products were very great, Nonetheless, a major

effort was put into interviewing coastal people and fishermen in an effort to learn:

«? 96P..°

species occurrene, seasonality and abundance; status, past and present, rates of ex- ploitation, past and present; reproductive sites and seasons, and economic value, A total of 59 interviews were conducted, some under makeshift conditions on a beach, but most around a table, In Fujian 32 interviews were recorded, 12 on the Guang- dong mainland, and 15 on Hainan Island, The number of common names used for sea turtles in just Fujian and Guangdong provinces is at least 75; of these, 25 can be assigned with certainty to a certain species of sea turtle, The remaining 50 names are used for several species and/or, have imprecise definitions so that. they are of limited use, |

The names that can be individual species are those that refer to the distinctive Dermochelys coriccea and the economically important Eretmochelys imbricata, Some 13 names apply to the former and 10 to the latter, Six names were related to a large-headed turtle, probably Caretta caretta,

There were reports of nesting from Pingtan Island to Hainan Island, but the only place where there was any evidence for recent nesting (and this was very little), and the only place where the species nesting could be identified, was in. Huidong, Guangdong province,

With but 1 or 2 exceptions (and these exceptions are of questionable reliability) . it was unanimously stated that sea turtles had become much less abundant \over the last few decades, It was usual to hear that once sea turtles had been revered, ven- erated or respected in some way, and that they were released when accidentally caught, However, in recent years most turtles that are caught are killed, Given that a single turtle may sell for the equivalent of a month’s wages, this is not hard to understand, It is also relevant that in recent years new markets have appeared in China; nowadays all parts of the turtle can be sold for a handsome profit, whereas formerly certain parts like the shell and bones were useless and thrown away, (It seems that in the last few years the shells of turtles have been bought to make wine)

Direct exploitation on sea turtles in China is of 3 kinds: capturing animals intentionally at sea with trammel nets, harpoons, and other means; capturing ani- mals specifically on nesting beaches; and capturing animals accidently, or incidental to other fishing activities, in fishing nets, trawls or with other fishing gear not designed to catch turtles, This last phenomenon occurs throughout coastal Fujian and Guangdong, ,ia varying degrees depending on place, season, gear and other variables, At any one place the incidental capture may seem insignificant, but the annual catch of sea turtles in Fujian and Guangdong may approach 1000, Although the absolute number of nesting animals caught on the mainland is surely very small, the percent of nesting animals that are caught must be very high; nesting females were said to be caught in Fujian and Hainan, and formerly they were captured in

Huidong before the creation of a conservation area, The only places today where

.。 40°

sea turtles are purposefully caught at sea are Hainan and Xisha Islands. It is likely that nesting turtles are caught in large numbers in Xisha, The majority of sea turtle specimens that were seen during the present survey were Chelonia mydas in Wenchang and Qionghai Counties, Hainan Island; the vast majority of these were said to have come from the Xisha Islands, Given the enormous amounts of coral, giant clams (Tridacna sp.), sea snails (Strombus sp. etc.) that are also mined from the Xisha: Islands, it is clear that there is rampant, unchecked exploitation of potentially renewable natural resources in the Xisha Islands.

Only 3 people had any knowledge of tags on sea turtles, but it was impossible to decipher which species of turtle had been tagged or what the tags had inscribed on them, Several people had knowledge of turtles bearing chinese words engraved

on their shells,

CONCLUSIONS

Five species of sea turtles frequent the South and East China Seas; 3 of these have been recorded in scientific writings since the early part of the present century: Chelonia, mydas, Eretmochelys imbricata, and Dermochelys coriacea, The 2 members of the subfamily Carettinae (Caretta coretic and Lepidochelys olivacea), as in other parts of the world have been confused and often misidentified as a single species (“Caretta olivaces”), combining the characteristics of the two (see Zhou 1983, Fra- zier 1985b), It is now clear that both Caretie caretta and Lepidochelys olivacee are relatively common, at least in the East China Sea, Dermochelys coriacea is also a regular visitor to the East China Sea, although captured less often, Chelonia mydas is common in the South China Sea, where Er etmochelys imoricata is also found most often, Vet, all 5 species occur from Hainan Island to the north of Fujian,

Captures of all 5 species appear to be most common during summer months, C, careita are evidently caught mostly during summer in the south but mostly during the autumn in the north. However, the records are not standardized and are likely to be effected by biases in both fishing and collecting efforts,

The size classes that are caught most often, for all species except Eretmochelys imbricata, are subadults and adults, Immatures of C, mydas and E., imbricata are caught with notable frequency,

There are indications of ontogenetic variation in several body proportions, be- cause of allomeiric growth, and this point needs to be investigated in more detail, Although there are some sexually related differences in several morphometric varia- bles and proportions, the data are too few to describe the differences statistically, The meristics of Chinese sea turtles are consistent with those of other populations for the respective species,

Although there may be some small regional differences, on the whole other

° Al

external characterisitcs, e.g., scalation and coloration, are also comparable to those of other populations of the respective species, Even epizoa and rates of colo- neeaitd conform to the general situation—except, however, the occurrence of heavy infestations of Stomatolepas sp,, and resultant disease—like conditions,

One of the most important biological questions to be answered is “From whence come the Chinese sea turtles Chelonia reproduces in China, but there is no verified record of reproduction by other species, Nesting by Dermochelys is most unlikely, It is possible that the remaining species nest in China, but most unlikely that there are large Chinese breeding populations still to be discovered,

There is potentially good nesting habitat on isolated beaches from southern Fujian to Hainan Island, Although turtles are said to have once nested from Ping- tan to Hainan, the number of animals now nesting annually on this coast of nearly 4000 km in length, is very few (possibly a dozen or two), and mainly (if not entirely) Chelonic, The annual number of Chelonia nesting in the Xisha ‘Islands is evidently large, but no detailed studies have been done,

Except for Cheloniz, which evidently breeds in fair numbers on the oceanic Xisha Islands, any reproduction which occurs in China is unlikely to produce a significant part of the populations found in Chinese waters, This was probably not true before the impact of Man was as great as it is now, and nesting by other che- loniid turtles may have once been widespread, |

Despite a lack of quantified information, there can be little doubt that the populations of (Chinese séa turtles have undergone major declines; this is the opinion of virtually every fisherman and fisheries official interviewed, and this is, sadly enough, consistent with the general pattern around the world,

Several factors are likely to be related to (if not the main cause of) the decrease of Chinese sea turtles, The exponential increase in human populations and their technology is at the base of the problem, Direct exploitation of sea turtles has in- creased from several factors, greater numbers of people fishing, motorized vessels and gear that enables fishermen to travel farther and faster; modern net fibers (nylon and monofilament) that have greater catch efficiencies than natural fibers, modern techniques such as trawling and purse seining that effectively entrap organisms in: vast volumes of water, capturing many non-target species; and also contemporary attitudes that now generally accept complete utilization of sea turtles in a profit- based economy (rather than the old traditional custom of respecting the live turtles and releasing them for religious reasons),

Coupled with this is massive habitat degradation, Many beaches, as well as coastal areas, have been destroyed by uncontrolled sand mining and resultant erosion, After-the-fact checks, to control this erosion (viz sea walls) are rare, but these constructions completely destroy the high littoral and supralittotal beach

habitat, as well as the dynamic nature of sand movement, Vegetation modification

e 42 e

by cutting natural strand plants as well as by developing plantations of Casuarina and coconut down to the strand line greatly reduce the area and quality of nesting habitats, Human habitation on, or near to, beaches, and the resulting activities and disturbance are likely to drive away breeding turtles (if they are not first caught and killed), Of the entire coast of Fujian and Guangdong, which totals nearly 4000km, there are only a few km of coast that are reserved and protected; less than 2km in Huidong county and probably less than 2km in Sanya county, Virtu- ally the entire coast has beea modified in some form or another,

The situation in the Xisha Islands is alarming to say, the very least, It appears that there is not only no control of exploitation of marine resources, but intense exploitation of resources which are potentially’ renewable, These natural resources

will soon be squandered if the overexploitation continues,

RECOMMENDATIONS

There is an urgent need to gather basic information in a quantitative and standardized way, Particularly valuable will be fisheries statistics, e,g,, dates, local- ities, conditions of environment, capture techniques, species, weight, length and sex, Information on tagged turtles is desperately needed, data as above in addition to tag type, number and address, !

Every effort should be made to reduce the incidental capture of sea. turtles— particularly in breeding areas, Trawl efficiency devices (= TED = turtle ex- cluder device) should be tested by Chinese fishermen, modified if necessary, and in- stalled on all trawls, Fishing near breeding areas should be prohibited during the breeding seasons,

Detailed, non intrusive, studies on nesting beaches should be initiated on a long term basis with trained personnel, incorporating postgraduate students that can make a long term commitment for research purposes, The design of these studies should be developed on the basis of progress made in programs in other regions that have been going on for 30 years; there is no reason to repeat. the mistakes made many years ago, These studies should include nest habitat ecology, repro- ductive ecology, and intense tagging, |

In Xisha Islands all of the above approaches are needed, It is ironic that Xisha Islands seems to be the most important area in China for marine turtles, yet it is the area that has been least studied and is subjected to the highest level of exploi- tation,

The agencies best situated for this work, and the agencies with responsibility to manage and protect the sea turtle resources, are the Aquatic Products Bureaux, lt is of the greatest importance that personnel in the Aquatic Products Bureaux be

informed about the sea turtle situation and how best to solve the conservation pro-

we

blem, Cooperation and communication between counties and provinces is also of the highest priority, Full cooperation and collaboration with academic and research professionals is just as important; inthis way the greatest benefits will be derived from different professionals with different specialities,

The present survey, as those that have gone before it, represents a small. but significant beginning, A great deal of basie information still needs to be docu- mented and recorded quantitatively; basic conservation problems need to be solved with some urgency; critical habitats must be given the fullest protection—ideally as reserves; fundamental descriptions of the status of the populations and their habitats need to be distributed and explained to policy makers; nationally important laws made by the central government need te be enforced in the various counties where they are now being ignored,

Yet, the results of this survey show that China has a great diversity of turtle species, some of which occur in considerable abundance, There is a great eagerness for different agencies to collaborate, including management, academic and research organizations; this cooperation has also transcended geographic boundaries between 17 counties, 2 provinces and 2 nations, All the signs are that successful programmes are being developed by counties, provinces and the central government, With the present rate of advance the future for sea turtle conservation and research in China 8

bodes well,

ACKNOWLEDGEMENTS

The survey would not have been possible without the generous assistance of a great many people and organisations, Political and academic leaders in the Fujian Province Government, Fujian Teachers University, and Department of Biology gave generous support, Local political officials and other authorities, notably leaders and staff of the Aquatic Products Bureaux, provided valuable pesiskanes in, Pingtan, Shishi, Zhangzhou, Zhangpu, Dongsha, (Fujian); Shantou, Haifeng, Huidong, Guangzhou, Yangjiang, Zhanjiang, Haikang, Xuwen, Haikou, Wenchang, Qionghai, and Sanya (Guangdong), ‘Various museums assisted with specimens, Fujian Teachers University (Mr, Zheng Ji), Fujian Provincial Museum (Mr, Lee Shuging), Dong- shan 2nd Middle School (Mr, Au Yingmon), South China Sea Institute of Oceano- logy (Dr, Chen Zhenran), and Zhong Shan University (Dr, Lin Haoren), Count- less fishermen in coastal Fujian and Guangdong gave generously of their time and knowledge, Invaluable assistance with translations was given by Fan Yen, Liw Zhendeng, Zhao Jianzhong, Chen Huanan, Zheng Zhiping, Chen Guoming, Wen Jianghua, Zhu -Zhiwen, Yin Dahu, Wang Mu, Xiu Xiu, Yang Qinlan, Xu Xiu, Lin Qiuping, Lin Xinyun, and many others, Generous support was also provided by

Mr, John Lundin, USIS, Guangdong, Funding for the study was provided by the

A4 +

Fujian Provincial Government, Fujian Bureau of Higher Education, Fujian Tea- chers University-Department of Biology, and the National Program for Advanced Study and Research in China, CSCPRC, National Academy of Sciences (Washing- ton. D. Ci USA) :

To these many people and organizations we are deeply grateful, LITERATURE CITED

BIORNDAL, K, (Ced,) 1982. Biology and Conservation of Sea Turtles, Smithsonian Institation Press, Washington, D, C,

FRAZIER, J, 1971, Observations on sea turtles on Aldabra Atoll, Philisophical Transactions of the Royal Society (B) 260, 373-410.

FRAZIER, J, 1980, Exploitation of marine turtles in the Indian Ocean, Human Ecology. 8(4); 329-370.

FRAZIER, J. 1984a, Contemporary problems in sea turtle biology and conservation, Madras 27-29 February 1984, Sulletin of the Central marine Fisheries Research Institute, Special Publication, Cochin 18, 77-91,

FRAZIER, J, 1984b, Analisis estadistico de la tortuga golfina Lepidochelys olivacea (Eschscholtz) de Oaxaca, Mexico, Ciencia Pesquera 4(1983); 49-75,

FRAZIER, J, 1985a, Marine turtles in the Comoro Archipelago, Koninklijke Nederlandse Akedemie van Wetenschappen 84, 177 pp, 18 pls,

FRAZIER, J, 1985b, Misidentification of marine turtles, Coreita caretta and Lepi- dochelys olivacea in the East Pacific, J, of Herpetology 19(1); 1-11,

FRAZIER, J, in press, A key to sea turtle identification in the field,

ZHOU K, 1983, Caretta, Lepidochelys and Dermochelys from coastal waters of Jiangsu Province, Acia Herpetologica Sinica 2(3), 57-62, pls 7 & 8.

APPENDIX 1, ABBREVIATIONS

Measurements, Curved carapace length =GCl, Curved carapace width baie hp =CCW Head. width : =HW Plastron length yee al

Museums,

Dongshan 2nd Middle School = DSMS Fujian Provincial Museum =FPM Fujian. Teachers. University =FTU South China Sea Insitute of Oceanology =SCSI Zhongshan University =Z5U

a Ad 2

CAPTIONS TO FIGURES

Figure 1, Size frequency histogram for curved carapace length in Caretta caretta, Figure 2, Relationship between log curved carapace width and log curved carapace length in Coretta ccretic,

Figure 3, Relationship between log head width and log curved carapace length in Caretta caretia. :

Figure 4, Relationship between log plastron length and log curved carapace length in Caretta caretta,

Figure 5, Size frequency histogram for curved carapace length in Lepidochelys oli- vacea,

Figure 6, Relationship between log curved carapace width and log curved carapace length in Lepidochelys olivacea,

Figure 7, Relationship between log head width and log curved carapace length in Lepidochelys olivacea, . )

Figure 8, Relationship between log plastron length and log curved carapace length in Lepidochelys olivecec, :

Figure 9, Size frequency histogram for curved carapace length in Chelonia mydas,

Figure 10, Relationship between log curved carapace width and log curved cara- pace length in Chelonia mydas,

Figure 11, Relationship between log head width and log curved carapace length in Chelonia mydas, | .

Figure 12, Relationship between log plastron length and log curved carapace length in Chelonia mydas., 3

Figure 13, Size frequency histogram for curved carapace length in FEretmochelys imbricata,

Figure 14, Relationship between log curved carapace width and log curved cara- pace length in Eretmochelys imbricata,

Figure 15, Relationship between log head width and log curved carapace length in Eretmochelys imbricata, '

Figure 16, Relationship between log plastron length and log curved carapace l2ngth in Eretmochelys imbricata,

Figure i7, Size frequency histogram for curved carapace length in Dermochelys coriacea.,

Figure 18, Relationship between log curved carapace width and jog curved carapace length in Dermochelys coriaceca,

Pigure 19, Relationship between log head width and log curved carapace length in

Dermochelys coriacea,

- ae

PURIET Wik 198842 34, 47-55

Atoa Herpetologica Sinica

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Fig, 1 The shapes of ridges and the bilateral transverse processes in the parietal bone

Zaocys dhumnades

Ptyas mucosus

Elaphe taeniura

E, radiata

E, p. porphyracea

FE, mandarina

E, rufodorsata

Entechinus major

the ridge of the parietal 2. the transverse process of the parietal 3, the ridge of the supraoccipital

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Fig. 2 The lateral process in the prefrontal bone A-H as same as Fig,1

OA

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pig of Fig. 3 The nasal bone and the ascending process of the premaxillae A-H as same as Fig. 1 the dorsal view of the nasal the anterior view of the premaxilla

1.2 便 2)

差异 主要 突起。 CEB WARE, MOMS AI. 存在 状态 :; ALICE RD, IIR ARIE HR ASE MIE. SBIR KAILERRIE.

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Fig. 4 The palato-maxillary component A-H the same as Fig, 1 i. the palatine 2. the pterygoid 3, the maxilla 4, the ectopterygoid 5, the medial process §, the maxillary process 7, the palatine process 8, the ectopterygoid process 9, the medial process of the ectopterygoid 10, the lateral process of the ectopterygoid 11. the ectopterygoid process extending posteriorly and the elongate lateral process of the ectopterygoid in E, major

a PARTE SB ALAA RR, RULER IN RAS TPE 突起 2. 鼻腔 (iasal component)

差异 主要 鼻骨

2.1 Beh2e 3)

鼻骨 背面 形状 程度 差异 鼻骨 NCS. SRR Sae er. 27

. 鼻骨 角形

角形

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249" «

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1, (adductores' mandibulae)

包括 3 、I 。2 1 RC HL. 差异 走向 方式 比较 清楚 ( 6)

后方

Fig. 8 The cephalic glands of Z. dhumnades

premaxillary gland nasal gland supralabial gland infralabial gland Harderian gland Duvernoy's gland anterior temporal gland se

a1 Ol eo he Sale ae = eee HO

Fig. 6 The adductores mandibulae

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aAv>

+50.

D, Entechinus major 1-2 m, adductor mandibulae, Pars anterior

Fig. 7 The intermandibular muscles

A-D the same as in Fig. 6

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结构 初步

任何 变异 适应 联系 形态 特点 显然 特殊 方式 关系 复杂 主要 扩张 独立 交错 运动 上颌 配合 运动 左右 扩张

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:

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整个 作用 方向 头骨 联结 形式 使 垂直 扩张

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较为 退化 缘故 解剖

骨骼 皮肤 鼻骨 鼻骨 联系 联系 松弛 鼻骨 退 彼此 皮肤 推测 具有 相对 左右 活动 余地 补充 直面 活动 。, 扩张

亲缘 关系 形态 结构 食性 生活 JA eR. EME, ENA AAAI BAR, ae LP Al 垂直 扩张 KEP RAE RABY KA. ATER HERA TERA ER AMR SU BY Ze 结构 差异

参考 M Mm

BAR AE HUES Ra: BUF IL A Colubrinae (HEA, Colubridac) 形态 比较 研究 演化 关系 探讨 行动 3(3):

Or

23-44,

: Sees GLB. wee) 形态 研究 [ . 骨骼 肌肉 研究 行动 6(3):52-62( 1987),

, SE COLE. eee) 形态 HAN. 形态 初步 研究 PAI To wk 6(4):1-11(1987)。

Albright RG and EM Nelson: Cranial Ki- netics of the generalized colubrid snake Elaphe obsoleta quadrivitiata, Journal of Morphology 195(2):241-291(1959).

Bogert CM: The status of the genus Lepto- drymus Amaral, with commeats on mod- ifications of colubrid premaxillae, Amer-

ican Museum Noviiaies 1352:1-14(1947).

Campbell JA and LS Ford: Phylogenetic

relationships of the colubrid snakes of the genus Adelphicos in the highlands of middle America, Occasional Papers (100): 1-22(1982).

Cundall D: Cranial osteology of the colu- brid snake genus Opheodrys. Copeia (2): 353-371(1981).

Dowling HG: Classification of pentes: A critical review. Copeia (1):

38-52( 1959).

the ser-

Johnson RG: The origin and evolution of the

venomous snakes, Evolution 19: 56-$5 (1956),

Kardong KV: Kinesis of the jaw apparatus during the strike in the cottonmouth snake, Agkistrodon piscivorus, Forma et functio 7:327-354(1974) .

————, Kinesis of the jaw apparatus dut-

in the

Agkistrodon

(2):338-348 (1977).

Maglio VJ: West Indian xenodontine colubrid

ing swallowing cottonmouth

snake, biscivorus,

Copeia

snake: Their probable origin, phylogeny, and zoogeogtaphy, Bull, Mus, Comp. Zool. 141(1):1-54(1970),.

Marx H and GB Rabb: Phyletic analysis of fifty characters of advanced snakes. Fieldiana Zoology 63:1-320(1972).

Rossman DA and WG Eberle: Partition of the genus Natrix, with preliminary ob- servations on evolutionary trends in natricine snakes, 34-43(1977).

Voris HK: A phylogeny of the sea snakes (Hydrophiidae), Fieldiana Zoology 70 (4): 79-169(1977). |

Herpetological 33 :

STUDIES ON THE CRANIAL MORPHOLOGY OF Zaocys (SERPENTES: COLUBRIDAE) V. A COMPARATIVE STUDY ON THE CRANIAL MORPHOLOGY OF CHINESE | Zaocys, Piyas, Elaphe AND E'ntechinus, WITH PRELIMINARY DISCUSSIONS ON THE FUNCTION AND PHYLOGENY -

Zhang Fuji

(Chengdu Institute of Biology, Academia Sinica)

Abstract

The cranial structures of 10 species of Chinese snakes, Zaocys dhumnades, Z.

nigromar ginatus, Piyas mucosus, P, korros, Elaphe taeniura, 已, porphyracea por phyra-

cea, E, mandarina, E’, rufodosaia, E, radiaia, and Euiechinus doriae, in 4 genera

(Colubrinae) are morphologically compared through anatomy,

The characters of their skulls, head muscles, and cepualic glands are discussed,

The skulls of all 10 species examined display a generalized colubrid pattern and

are essentially similar, though some intergeneric and even interspecific differences

e 5A

may be observed (Figs, 1-5), These species are different in the shapes of the pari- etal ridge, the lateral process of the prefrontal, the nasal, the ascending process of the premaxillae, the quadrate, and the articular processes of the palato-maxillary arch, the size of orbit, the pattern of squamo-quadrate articulation, and the length of the hyoid apparatus, The main differences in muscles consist in the adductors mandibulae and the intermandibular muscles (Figs, 6-7), The direction of muscle fibers and the pattern of function of the adductors mandibulae are different, For example, when the mouths of Zaocys and a few other snakes are closed, the angle between the mandible and the pars anterior of m, adductor mandibulae externus is larger than that in E, taeniura, FE, radiata, and E, p, porphyracea, and the line of action is almost vertical to the mandible, In Zaocys and a few other snakes, the m, intermandibularis anterior is comparatively thick and consists of 3 bunches, while in Elaphe this muscle is narrow, The pars posterior of the m, intermandibularis posterior of Elaphe is so degenerate that it cannot be determined, Although constrictor colli is generally present in most snakes, it is absent is some Elaphe snakes, e, ¢. taeniura, radiata, and EF, p, porphyracea, Besides, the size of m, hyoglossus is also different among these snakes, Among the cephalic glands, Duvernoy’s gland pre- sents the most remarkable difference, There is no such gland in EF, taeniura, E, p, por phyracec, and Entechinus major, and the size of it is different from species to species in the other snakes observed, It is discovered that the degree of development of this gland is correlated to the degree of development of the posterior maxillary teeth, There are at least 4 types of head structures based on comparison: 1. Zaocys and Ptyas type; 2, Eniechinus type; 3, E, taeniura, E, radiata and FE, p, por phyra- cea type; and 4. EF mandarina and E, rufodorsata, The relationship of the two snakes of type 4 deserves further study, as considerable differences can be distin- guished between them, especially between FE, rufodorsata and other species of the same genus, It is regarded that among these related species, type 3, which is rep- resented by F, taeniurc, is a primitive group, whereas the genus of Zaocys, to which Ptyas is closely related, is a derived group, Entechinus is probably an off- shoot derived from a common ancestor at a primitive stage long ago,

The relationship between the structure and function is preliminarily studied, using Zaocys and FE’, taeniura as research objects, These animals are all terrestrial and feed mainly on mice, birds, lizards, frogs, and fish, However, various species of Zaocys inhabit waterside and favour frogs and fish, while E, taeniura lives around human houses and consumes mice as staple food, It is presumed that the volume of the mouth cavity of snakes, when swallowing, depends mainly on their ability to move the maxilla and mandible vertically and horizontally, as well as to move the cervix horizontally, The ability of E, taeniura to move its maxilla and mandi- ble vertically is preater than that of Zaocys, while Zaocys is more capable of

moving them horizontally,

PINGICT Mw 1998473, 56-59 Acta Herpetdogica Sinica

+LHRH-Axtees

RAE is Be he 89 Fe

CK Piya He ( )

释放 A (Luteinizing hor- mone releasing hormone, LHRH)

FERIA RAD WTB. TEIE

生理 状态 作用 垂体 细胞 使

A easy LH, FSH, Smee MEE ARAQIE BPLBE.

哺乳 动物 剂量 LHR 活性 (LHRS-A), 雄性 动物 ATE MASE: FUGUE A EI We (CorbinS:, 1975; Beattie2¢, 1977; xi ,1979, mE ,1978、 1985), 使 雄性 动物 精子 生成 障碍 ( ,1986;

Yves ,1985)、 激素 降低

(Sandow, 1983; 77H iF =e. 1986) ARSE, LHRH LHRH-A 作用 尚未 见报 {11 ZED tg 2S HAE es as (Bufo gar garizans) 指标 细胞 观察 剂量 LHRH-A 作用 探讨 作用 制作 初步

材料 方法

He WR ES 50-70 Fe HU HE PEWS 34 A, aD 室温 进行 实验

AA. hokey, SRSA, MA

Ye FES PR EEE L00pg_LH REA (上 生产 )。 ® DO

B ,6 注射 HCG501.U..

C44. 6 注射 (0.25ml) 生理 盐水 Ate

EHS 2) ANDRA. UW

反应

A 持续 注射 反应 动物 进行 : 1, 6 注射

(SER EAD, WATCH RRM.

2, 6 ,每 注射 CG50Iu, 反应

3. 4 , SAMAK, LHRH-A 100kg, 反应

4. A C 动物 6 ,3 垂体 Zenker ike, Oh oe, 垂体 Slidder 染色 Masson -〈 ,1982) 观察 ,3 垂体 2.5 2 Ea

ne

1, 剂量 LHRH-A BSH Rw

A 动物 开始 注射 LHRH-A 5 活动 精子 现在 尿 精子 14 动物

* 现在 ,山东 医学 科学 基础 1987 3 30

15 6 AAW ERR BADR, PAN NRX Sa 精子

Ea HCG i 6 RRR BHI 精子

注射 LHRH- A, 注射 ,4 3 反应

2, HCG 反应

B 注射 SG 动物 精子 , :之 逐渐 减少 直到 少量 活动 精子 排出 动物 注射 生理 盐水 精子

3, 观察

3.1 《4 ) ap i B. 管内 精子 EE Sertoli (图 WV ,1).

3.2 LHRH-ASa mii: Hae 管内 精子 基本 Sertoli 游离 细胞 WV, 2).

3.3 HHCSG 动物 : 管内 精子 作用 活路 Bis (ARV. 3).

4. ERA SE ie

细胞 细胞 ) 紫红 酸性 细胞 剂量 注射 -A 动物 细胞 颗粒 减少 细胞 Dy ate AH LARA; HCG 动物 细胞 情况 相似

5. 垂体 电镜 观察

正常 动物 垂体 细胞 密度 颗粒

《图 ,4), 物质 ;内 线

LHRH-A 动物 细胞 含有 BRC, RHA MMA, Aafia 残留 形态 规则 物质 肉质 基体 线粒体

Bis: Hee

剂量 LHRH LHRH-A 哺乳 动物 作用 方面 生育 作用 主要 解释 : 认为 垂体 细胞 完整 动物 (Sandow,1983)、 Fel iit (i) By (Belchetz, 1978), WHR 动物 (Koiter 3, 1981; Schuiling 1984) Bt ER OPS FE BES i (Mark, 1981; Mcintosh , 1985) 实验 ;, 认为 垂体 释放 (Labrie, 1978; Hsueh 1976; ,1984)。 认为 LHRH LHRH-A 性腺 具有 垂体 制作 (Hsueh ,1983, Clayton 1980,Rosario ,1984)。 #J 91, LHRH LHRH-A ILE RA, LHRAAKRS AE ENE AL ve VERA SSL 2) Yy tH 1. fe We Be 0. Sug LHRH-A BUay (28 100% BY HE te. Im LHRH-A 3x hi SSR AR ENDL Gl 通过 垂体 释放 作用 ,1983)。 实验 结果 BH. KS 剂量 LHRH-A 脊椎 动物 具有 作用 生育 作用 环节 垂体 LHRH-A FHSS RMS. 12 RHCG RA S| HH ML, 表明 KRG LHRH-A 2 SRLS AE Se WHEE , ARE LER EAR RRS. TEBE A Pew IERA RET

as (are

EK PERR SS ER Kile LHRH_-A 作用 释放 减少 原因 垂体 电镜 观察 垂体 细胞 合成 速率 释放 速率 细胞 线粒体

. 实验 结果 指出 ee SVE RAY, 7 felS AK OS

动物 恢复 LHRHAA Yves 《1985) 实验 结果 动物 反应 恢复 垂体 形态 同时 变化 进一步 研究

S$ 4 xX

EX, DAB: GAARA RBORE A Uy (LRE- A) S| USHERS VLEET. WRK ik (〈 ) 1:109 (1983),

EME. SURES: 病理 手册 468 。468(1982)。

MILI. SRR: LARA LARS aT BBN: | WEEK MNSe. sys fz 25(3): 201(1979),

8 BRA. MISH. sha, MR. RBA VES EDA KF Se ALI ZS 2 2 2a SA EME, AE SHEAR, 6(1)+53( 1986),

Peet Ol: 功能 激素 调节 男性 生育 iT Za WAS. AWS SRS 4(2): 60(1984),

黄体 释放 激素 BUFO EGE DRE, AE BAe He 30(2) 99 19ve ee

RE, See. Ke, Sa. 黄体 生成 生育 作用 生殖 避孕 5(3):41(1985)。

Beattie CW, A Corbin, G Cole, S Corry, RC

K Kock, and J Tracy: Mechanism

Jones, of the post-coital contraceptive effect of LHR Ain the cats) levels during chronic LHRH administra- Reprod, 16:322 (1977), Belchetz PE, TM Plant, Y Nakai, EJ Keogh, and E Knobil: Hypophyseal responses to

setum hormone

tion, Biol,

continuous and intermitent delivery of

° 58s

Labrie F,

hypothalamic gonadotropin releasing hor- mone, Science, 202:630 (1978),

Clayton RW, M Katikineni, V Chan, ML Pufau and KJ Catt: Direct inhibition of testicular function by gonadotropin-

releasing hormone: Mediation of testicular

function by specific gonadotropin-releasing hormone receptors in interstitial cells, Proc, Natl, Sci, USA, 17:4459 (1980),

Corbin A and CW Beattie: Post-coital contra- ceptive and uterotrophic effects of lu- teinizing hormone releasing hormone, Endocri, Res, Commun, 2:445 (1975).

Hsueh AJW, ML Dufau \ and. KJ < Catt: Regulation of LH receptors’ in testicular interstitial cells by gonadotropin, Bio- chem, Biophysi, Res, Commun, 72:1145 (1976).

Hsueh AJW, C Wang and GF Erickson: Direct inhibitory effects of gonadotropin releasing hormone upon follicle-stimula- tion hormone induction of luteinizing

hormone recepters and aromatase activity

in rat granulosa cells, Endocri, 106:1679 (1980), Hsuek AJW, TH Bamibion, L-Z Zhuang,

JR Welsh end NC Ling: Mechanism of the direct action of gonadotropin-releasing hormone and its antigonist on androgen biosynthesis by cultured rat testicular cells, Endocrinology 112:1653 (1983). TR, N Pols-Valkhof, . and CA Schuiling: Recovery of the pituitary gland from LHRH-induced LHRH in the ovariectomized rat, Acta, Endocrinologica, 96:315 (1981). C Auclair, L Cusan, RA G Pelletier, and F Ferland: Inhibitory effects of LHRH and

gonadotropin

Koiter

refracteriness to

Kelly

its agonists on testicular . receptors and spermatogenesis in the rat, Int, J, Andor- logy. (suppl 2)303 (1978), | Mark AS and WV Wylie: Desensitization ‘to gonadotropin

releasing hormone ob-

served in superfused pituitary cells on Cy- its analogue, Clini, Endocri, 182571

todex beads, Endocrinology 108:752(1981), (1983),

Mcintosh RP and JEA: Mcintosh: Dynamic Schuiling G A, N Pols-Valkhof, GC J Van- characteristics of luteinizing hormone der Schaaf-Verdonk, and TR: Koiter release from perifused sheep anterior cells Blockade of LH and FSH secretion by

stimulated by combined pulsatile and LH-releasing hormone, by the LH-rele-

continuous gonadotropin-releasing hor-

asing hormone analogue, buserelin, and mone, Endocrinology 117:169 (1985).

by combined treatment with LH-releasing

Rosario D, T Cassorla, AK Munabi, V hormone and oestradiol benzoate, J, Mericq, MC, Gekato, BD Albertson, Endocri, 103:303 (1984), | and L Lorianx : Direct effect of the Yves T, and A Belanger: Reversible inhibi- LHRH analog: 6-D-tryptophan-10-proline tion of gonadal functions by a potent

-LHRH-N-ethylamide on rat testicular gonadotropin-releasing hormone agonist in

steroidogenesis, Steroid 43(2):201 (1984), adult dog, Contraception 30(5):483 (1985), Sandow J: Clinical application of LHRH and .

EFFECTS OF CHRONIC LARGE DOSES OF AN LHRH ANALOGUE ON THE SPERMIATION RESPONSE IN THE TOADS (Plate IV)

Wang Shili Wang Long (Department of Biology, Snangdong University, Jinan)

Abstract

An analogue of luteinizing hormone releasing hormone (LHRH), D-Ala®-des- Gly"-LHRH-ethylamide, was administered subcutaneously 100ug twice per day in each of 22 toads for a period of 14 consecutive days, The spermiation of the toads was initially accelerated, and then inhibited during the course of treatment, These animals resumed spermiation after an injection of either normal toad pituitary homogenate or human chorionic gonadotropin (HCG) (501U), A lot of sperms were observed to remain in the seminiferous tubules in the testis slice under microscope, Gonadotropic cells contained large numbers of endoplasmic reticula, mitochondria, and Golgi bodies, as revealed by observation of pituitary gland under electron microscope, while the secretory granules could hardly be observed, The results reveal that after repeated large doses of LHRH analogue the inhibition of sper- miation occurs, This may results from the exhaustion of gonadotropin stored in the

pituitary gonadotropic cells after the administrations,

* 309 «.

FAIA «1988423, 60-64

Acta Herpetologica Sinica

ocd | | as ie y a ii ae

眼镜

He TOR at 3)

《华东 师范 生物 )

ILA Wee te ab, EA 19 AEE WERE IS HH, DBR he By ke Caja naja) Rieke Pe we (Piyes mucosus) i) Be at Be .我 1984 4 .5 7 1985 7 9 繁殖 情况 进行 研究

材料 方法

材料 浙江 收购 背山 邻近 岛屿 ,先后 327 ( 119, 208) 205 4 (2100, 105). ill 解剖 38 条, 119 ; 7h BN 18 100

阶段 根据 同时 MA), MAKE ORK. ADRA

—B, APR RER RAN) FAN CONTE ) (简称 外) ANALY EH BE Baer 1, HERE TERR HEE TR BNE ERE A HE RS

EER WH

FN F7I90, 3+ 14, 4(75-130) em#ti82, 4+ 19.8 (144-225)cm, PRAPIE NS GS te ap BA 43.7+10,6(26-63) mm 71,3 + 14.1 (45- 95)mm, SKE BAZ4. 748. 4(20-55) mmFi60,0+10,8(42-73)mm, Fe 2K

THE a BAL. 72,783 BRS wk

HAR Ry Al Ar = 0/792 Fr =0,585, FASS AR ESE OLR EAR 14.4% , 7G Se sinh ye ela a Zs (6-15)em, $2

较为 一致 ,平均 7.7 1.6

4 5 初出 5 .下 繁殖 阶段 ,它们 A 相对 体积 Tie iE, BAL RE SARE R440 3.9% ; BRD AASB E20. 8% F110, 7% -

2. MESE TROD Ta oe

2.1 . HRs Pi HE HR) PRU 4 DG UN Lay 1984 425 A16-28 5 Wea OLAS EAR ee, Eh (EEK 68, 81AIS4emy 3 AON, HK 4 474-91icemsy 23 Za Re CAD 55 K93cm KSHEMETA, (22 KAKIN, 440%, INR

-分别 20 23 ,2 95cm

怀 ,95czm 怀

Tabs i Fes number of Meds 28, May 1984) Total No. of (No. Sot baakal Sidel of Taree Ay. No, | Av, Ne, Av; No, length samples conceiving eggs of large of small of total (em), large eggs (mm) eggs eses(6mm) eggs | 68- 80 19 0 | re 12. T2242 1242 81-99 Tah ee oe 9 pitien | 13.58.42) 18.548.4 91-160 15 | 1¢6(87.9%) 8.3-+9.9"4.62:0.7 Qbear 5.2 Onder 23.728.5 101-110 27 25(92.6%) Saale ee ac0 51 21.4¢5.5 13.625. 2 33.1+8.6 111-120 20 |, 19(95.0%) | 16.5 2.8 “5.4 0.9 22.2 4 | 16.028.9 38.02:7.2 121-128. 4 14}, 14G00.07%) 10.2:11.9%5.350.5 | 23.048.8 | 16.646.2 | 37.2+8.0 101 | 68(67, 3%) 9.7°5.3 21 ots. 8 14162 28.1 141.9

FR EN I EE LT 一人

i987 8 21

are See RE PE IS ST

2.2 JERUEN ARR RA 1984 明显 4 28 解剖 25 怀 …( 4)。

72cm,

Tab.4 state of Eaves mucosus, 28 Apa 1984

rere ON TT SETI IT rrzuramrnrr eS eet Se SOS Se eee cone eS

Total length No. of ‘Size of large No, Pag Size of small | “Total No, (cm) large eggs eggs(mm) small eggs | eggs (mim) | of eggs 72 = = 49 | <4%3 40 144 7 x, 51 | <5*3 | 51 153 = = 15 | <6*5 | 15 167 17 8x6.5 | 28 | <5x3 | 45 167 | 34 <6%5 34 168 = 34 <6*4 | 34 168 34 <<6x4 | 34 169 19 8x6 22 | <4%3 | At 171 = 53 <6%5 | 53 1T1 11 8x5 | 14 | <3%2 | 25 180 12 9x5 42 | <5#4 | 54 182 28 | <5x4 | 28 183 22 8*5 12 <Ax3 | 34 184 37 <5*3 37 189 15 <6*5 15 193 21 8*5. 55 <4%3 16 193 16 9x5 11 <3%2 21 193 49 <5x4 49 194 17 8x6 . 35 <Ax3 52 195 18 9x6 10 <4%4 28 201 = = 31 <6%4 31 204 34 <5x3 34 205, 25 | Be5 19 <4%3 44 205 8 8x5 20 <4*3 28 207 49 -<<584 49

178.8227.2 | 16.9:5.0 8.2*5.2 30.9 14.1 4.8#*3.6 38 .2 12.9

Te 52.9 ,170cama 当年

1984 5 24-29 解剖 61 怀 5

180cm 怀 比例 超过 93

Tab. 5 Pregnant state of Ptyas mucosus during 24-29, May

ar TES A EB NE BI SER IF IE EEE

EAE LE TE cron zs a

een

* 62 «

Total body No, of | No, of snake Size of Av. No. of | “Av. No, of | | Av, No, conccving small eggs | of total length (cm) samp, large cggs large eges(mm) large eggs (<6mm) | eggs 164-170 10 (40%) 10.8+1.3*5.5+0.5 22.8 3.3 25.5 11.5 34.6+13.8 171-180 17 9(52.9%) | 10.4+1.5*6.0-+0.7 19.7+3.2 36.619.0 | 47.0+13.4 181-190 16 15(9¢.7%) 11.1+1.5*6.1+0.6 | 23.944.3 27. TE11.5 48.0+9.3 191-200 12 12(100%) 11.4+3.0*5.9-0.5 28.9+4.5 31.611.6 60.3212.7 201-215 6 6(100%) 13.1 3.4x6.9 1.0 | 25.5 4 8 22.8+9.7 44,8-12.0 61 . 46(75.4%) 11.3*6.0 23.6 4.0 30.4+13.4 | 49.9+10.3

9 0% (#1). AAAS KK 95cm

同时 1 可见 怀 显著 ,7r 0.7200 0 |

1984427 7A, HRA 11 Awe ( 2)。 归纳 DA. RASA, ATARI, RAB 4ommeG, Ky NSAI BIS HBEE; (2) Fc OPH BZD 5 21.9 5.8 9.0 2.2 ) 增加

营养 营养 情况 《〈 进食 ) 继续 RA, A 停止 推测

. 食物

范围 饥饿 9 (4-12 BOs (3) 103-110cam 8 ,No-。 1. 4. 5. BEAR, RASH 62.5 1, 范围 怀 92.6 7 Ea i

Tab. 2 Pregnant state of Naja naja, 7 July 1984

Total length

| Size of

| No, of | No, of | Size of small | No, of (cm) _ large eggs _ large eggs(mm) small eggs | eggs (mm) total eggs 103 = = 22 | 12*5 22 107 40 47*19 45 - 85 | ”2950 108 9 47*23 35 6*4 44 108 = 36 9*5 | 36 110 = <q 31 8*5 | 31 110 9 39*22 29 10*4 38 110 9 aT 2a Ad | T*5 50 110 10 40*17 34 : 10*6 - Ad 115 12 35*18: 30- 11*4 ; 42 118 8 46*20 36 | 9*5 | 4A 122 11 40*22 25 | 10*5 ly BUBB ia

111.0 5.7 | 9,012.2 | 42.6*20.3 SR 1 8.8*4.6 Ta 1256

1985 7 23 解剖 3 9 19-25 解剖 4 ( 3) RE

现象 1985 7 22 10 量度 51.0 3.2x24.1 0.7 。Moriguchi 〈1982) 记录 台湾 5 肉眼 产儿 情况 台湾 3 5 10 ,5 20 6 15 2 眼镜 &% 10 气候

Tab. 3 Pregnant state of Naja naja, in uly and REDE. , 1985

Date Total Size” se! No. al Uae: No.of

(cm) | eggs | eggs | eggs

eB SOM27 <tem | 27

eV moses <10cm | 34

te23 145 <9cm 21 | 23.8+9.1 S19 | 4. wat \<5em “| 29 |

9.19 145 <Tem 23

9,25 129 <6cm 32

9.25 155 |<ioem | 21

« 6L -

TH PRE OOD SIR BIE 范围 191-200cm

0281,

SRRAT HR, r= RNB RB RK #250 200cm 反而

198442 7A 7A, MHZ 151cm iy ° ae ADF I He

1160em 170czma

ZU ME , ETB 2%, RRK

A PE Mp 24 aE sere eae ae Tab.6 Prengant state of Ptyas mucosus, 7 July 1984 aS OUR ERS CTI STN RE RIT RTI A NOR NT NNT NR SR ore oe CUE A ELSES = SENATE PRA AS ORCA BIEN US SPT EO NTI TE Total No. of Jarge Size of large No, of Size of small Total No , length (cm) eggs eggs (mm) small eggs eges(mm) of eggs 151 ae Tr 27 <4x3 27 160 rap : PRG 4} <12*7 Ai 167 12 36#20 17 <8¥4 29 168 8 46x20 22 | <beg 30 180 9 39x22 29 | <i0%4 39 182 6 58*18 17 | <9H5. 23 194 1 44%18 34 | <10*5 Al im. Ha: 5 ha shes o poe ey 6 28. 148, on &.3%4.4 323 Tae ton 浙江 医科 生物 教研 1975 ,, 现象 必须 引起 重视

江南 8 1 15 45-50X25- 30mm, FORMER, SURE IE, (Etre 7 AR

1985 9 17- ghee 押解 ue. AON RES eB 5e GRD. 6 NS 26,74 8.8 #7 Hy 27.6 16.75%) Bee (AMI A) BN--, AAI BE WIR KEE

近年 造成 使 严重

Tab. 7 Pregnant state of Piyas mucosus

during 17-21 Sept. i985

(a ETE NS EPI i IRIN EA ROT LE = a PT

Bay 7

CT

Date of Total | Maximum | Total Nol | | dissection | length i(em) (she of cggs | of ges DAG diy 156 a lee aTae Gul 42 9.18 159 | 885 bas | if 9.20 162 5x3 (Peceet 9.24 167 i 8#6 Ly 26 OTe Lbs 95#5 2T 9:20", a acenan T#A 21 9.29 183 10*5 | 21 1612 Samael Ganee Gr: | 27.6007

2 TRS MASAI LES REE ERA OSE ES IT AST CET SII ETD

FGI MOB

ne et iy SS PME, FAR SS 5 AEA PVA RE AAA, ON BE as BE BY BB inkl. AAR SM mba. HEAR eas

破坏 资源 ee ee 提供 利用 限制 措施 眼镜 收购 110cm 收购 190c 放宽

a 4 3 ik

WILESAMED SAHA: —PIIA ET NR TSG. HEAT FEB} (3) + 32(1976),

Moriguchi H, M, Toeoriba H, Miyata A Sakai and H Sugano, Notes on reproductions of captive snakes observed in the Japan snake institute during the years 1980-1981. The Snake vol, 14. 57-60, 1982,

- * 63°

THE REPRODUCTIONS OF Naja naja AND Piyas mucosus ON ZHOUSHAN AND NEARBY ISLANDS Sheng Helin Xie Shengxun Feng Ruiben (Department of Biology, East China Normal University) Abstract

During April and May 1984 and July and September 1985, 327 Naja naja (119 females and 208 males) and 205 Ptyas mucosus (100 females and 105 males) were captured from the, main island) of. Zhoushan and.its nearby islands, Zhejiang pro- vince, and were analized through observation and dissection,

The results show that the right testes in the males of both species were long- er than the left ones and the difference is significant (P<0,01), The average leng- ths of the right and left testes in Naja naja are 43,7 and 34,7mm,_ respectively (t=10.7); and data for the other species are 71,3 and 60,0mm (t=2,78),

As for the females of Naja naja, those which were as long as or shorter than 91cm could not lay eggs in that year; 50% of those that reached a length of 93-95cm could lay eggs; and 90% of those that measured over 95cm could lay eggs, The average number of eggs in the body, which had a linear correlation with the body length (r=0,.720, P<0,01), was 28,1+11,9; whereas the average clutch number was 9, Egg-laying occured in early and mid July,

Half of the female Ptyas mucosus with a length of 171-180cm had an ability of laying eggs; and 90% of those longer than 180cm could lay eggs, The average number of eggs found in the body, not correlated with the body length, was 47,9 +10,3 (r=0,281, P>0,05), Clutch number was 8.3, however, Egg-laying occured

in mid and late July,

PUHIeTT ay Aik 1988463; (1):65 Acta Herpetologica- Sinica

AAA AAT AN AAS Aun

y ital Fh)

Dae ew ve ew

ENE TES PE Se BL

Rana cancrivora Gravenhorst Discovered in Guangxi

Ygic:R ana cancrivora Gravenhorst 主要 东南 报道 BS, 笔者 1987 7 2 7 AIR A) Babys 盐田 采集 15 海星 标本 ,, 存放 北海

生活 背面 浅黄 绿色 部、 AMA

规则 斑纹 绿色

雄性 ;

栖息 水浴 , 隐蔽 海滩 活动 海星 容易 :

广西 A, eS ”了 人防 营盘 海边 :

th (广西 北海 ) Sun Jianyun

(Beihai Museum of Aquatic Products, Guanxi)

1987 8

“e 65 “。

PUBIC ship ik 1988463 A; Acta Herpetologica Sinica

(3):66

1 纪录

Elaphe davidi A Record New to Shandong

行动 系统 检索 >》(〈1977) ee

11 1963 6 济南 进行 动物 调查 整理 标本 mh, 鉴定 He Elaphe davidi (Sau- vage), 山东 纪录

标本 1o,? 平均 298.0 66.3mm, +7, BALA. RSS, kB MASA /448 47; SAR2, TAKER: HAR 2, HA SRR KTH, RA LE 8, 3-2-3 5h; IGE, IEZEG, AME; BRR (BK2); HEBISe1-2; HESEIERS, Ae S38, Hi4ree ,25-23-19 174-180, 64 Whee, BLE 神色 褐色 BARA, AG 70 规则 交界 ALE E, ECR IRS Bi) BER.

EVA Ki OL ee 茂盛 丰富 645059 6372 645071 泗水 RA, RoE

» 66 »

活泼 ,行动 迅速 夏季 1963 7 8 6372 SAS A hy, AA 东北 河北 山西 AR 首次 纪录

Al 76 op Be

SSRIS RE RE STS RE ES ED

编号 ”性别 ek se ns ee

6372 ATF 301.0 65.0 25-23-19 183 64 645059 oo 295.0 72.0 25-23-19 169 64 Beane AE 298. 0 62.0 25-23-19 183 64

MY a RYN EE ES TERE IM SE TOM co

(单位 : min)

R RK (而 德州 农学 BSE) ~ Jia Zhenxu (Dezhou Specialized Class of Agriculture, Shandong University of Agriculture)

A THERRURAKSEDAR Ral 教授 指导 提供 资料 致谢 1987 4 21

PUI a= 1988423 A; (1)26%

Acta Herpetologica Sinica

)

VERE He 5 HE We HE

Digenetic Trematodes from Common Snakes of Tianjin

1986 5 解剖 12 BEBE MISA AA, AR 找到 吸虫 9 41 个, 鉴定 认为 重合 th die, EH WW Diplodiscidae Skrjabin, 1949 AEB Schizamphistomum 1912 寄生 动物 目前 1

Looss,

”是 FEischthal et Kuntz 1975427 GIS Kye ta lon

EIN, ZEZAGEAA Ke Schizamphistomum taiwanensis, 7¢)T j= Amuroiroema Achmerov, 1959 1 1959 找到 黑龙 4oruro- trema dombrovskajae; ##; Diplodiscus Die- sing, 1836292:-F PUNE, ILE ATE 10th (#1). RPKECKALAGAER, eR K 记录 测量 毫米 单位 保存 南开 生物

1 Diplodiscus amphichrus Tu- 1935 (1),

= Achmerov

bangui,

Al 吸虫 Diplodiscus amphichrus Tubangui

宿主 “虎斑 Natrix tigrina lateralis 寄生

“1986 5

感染 解剖 12 1 9

记载 宿 AW, HE

BEE, RSS HEME, Se MA, Zee 首次 报道 3.04- 3.76, 标本 1.131-1.658, DO, RUA 1:2.5, ORHRK, SHS RA #2, Weh, HORE. Be 相对 相符 原因 体内 抑制 MM BAA, (Ase, 1973466 山东 烟台 ENDER MASEA RAIN 标本 1.951=-2.968, 东方 Jw 找到 标本 0.916-1.198。 鉴定 标本 DEH, =A Ree 接近 紧密 明显 相关 因素 变化 准确 鉴定

3.5mm

A2 .日 吸虫

Diplodiscus japonicus Yamaguti 20 ABA Diplodiscus japonicus Yama- guti, 1936 (图 2)。 = EBT Natrix tigrina lateralis SEM ”1986 5

科学 科学 基金 资助 课题 1987 6 24

67

1 宿

be Zo 1a ES “fe | RRR. FEE | 福建、 山东 | Rr = Ja = D, amphichrus Tubangui, 1933 ARATE pS HOR Fey BE 缅甸 RSE EERIE | 斯里兰卡 Tf 印度 Rana cyano phlyctis D, amphichrus magnus Srivastava, Rana tigrine 1934 Hylarana Kassina | Dicer Be Be | Eh tae kia by aap ie bufonis VEE 1977 | RM Dek | BAR KAE, Pelee, pk | RE, BAK D. japonicus (Yamayuti, 1936) | FADE, DESH, 7H Scie Pee | | RBEREE GE BHIER) HA PABA Dh | Hyla aurea ”澳大利亚 15M LEGER GTS Helnas nas (1912 ae | Pie aes | rE KURA, BBE | 福建 D. mehrai Pande, 1937 Bufo bufo viridis | 印度 Rana cyanop DES | Asses a ewingii j | 澳大利亚 D, microchrus OI 1912 te Se ee tasmaniensis | Mek 微小 Rae 北京 D, minutus Li et Gu, 1978 | EYE HE LW oh HEME Le RS D, melanosticti Yamaguti et | BEG 1943, | BBE A Uhh, a: gis | ae D, DOOR Wang, 1977 | ine Sar Ba Refer | 非洲 D, pallascatus Manter et Peitchard, | 1964 | DSi e amas | Rana erythraea D, sacculosus Yuen, 1962 | aE, |. MRO D, sinicus Li, 1937 | OL, Tee le ae SRS. Nye 德国 SAWS. EB FE pe e eee ee: D, subclavatus (Goeze, 1782) | Bombinator igneus Bufo regularis

e 68 e

FOS ATT RT TE LS EN TN

= 4

B, vulgaris

bie, Sa

Dendrodryas sp, 德国 Diplocotyle mutabile |

{ies BM D, subclavatus (Goeze, 1782)

Lissotriton

Emys orbicularis

Molge al pestris

M , vulgaris

Natrix natrix Pelophylax, Phyrne, friturus

Pot te

Redia gracilis

pee

D, tigrinus Wang, 1977 ANBAR Triton palusttis 西

D., unguiculaius (Rud, ,1819)

= er TCR EE I EN ETT TE ES ETT -

感染 解剖 12 1 1

宿 EAA AK HL RO tee, ADEE, FESCEA RE, FEE

标本 0.245, AK BAERS, WRS252ZAA—E IER, Nie

LF MRAM MRR AMREN, BAAR is. WE Ae Baez oh he WR Gyraulus prashadi, HABARENDE BEER AMS 12 Planorbis compressus Ff ka #2 Se gmentina

SE I TN EBL IE I EL ITE ae

mica, Feke TE TKTKIY ES AT ASB te 直接 宿 宿主 问题 进一步 研究 FRE KBE We 《南开 生物 ) Kit KR 《天津 博物 ) Li Qingkui Zhang Runsheng Qiu Zhaozhi (Depariment of Biology, Nankai University)

Chen Xiqin Liang Zhong (Tianjin Museum of Natural History)

2 Oo «

MTS lessees A; 70-74 Acta Herpetologica Sinica

Po Ge # 简报 Weleacbindeis

温度 决定

爬行 动物

Temperature-Dependent Sex Determination in Reptiles

决定 ? 理论 认为 : F 染色 表现 独立 相关 问题 : 遗传 决定 ; 胚胎 ; 生态

Big, KSA MME (S/S4+Q)H1/2,

存在 遗传 决定 密切 关系 BE, RAD Moles, ARENA WEES. 近年 认识 ee ee 因素 (如 温度 ) HBR. B96 LK 广泛 细胞 遗传 研究 室内 试验 野外 观察 FT; 生变 行动 遗传 决定 (Temperature-dependent Sex determination, 简称 TSD)。 客观 现象 许多 关注 国内 ADWARE NTE.

行动 决定 方式

目前 行动 物性 方式 :一 异型 染色 ; 温度 决定

1, 染色 决定 NTA, TER 比较 复杂 生殖 6 :8 22 动物 生殖 动物 复杂 AZZ-2W 异型 程度 染色 X-XY 22-2W X-XY 决定

九州 理学 参考 资料 “特此 致谢 1986 1 27

« 70 «

1 Ritalin eis (根据 Bull, 1980 补充 )

eer SES SURE TRAE

BA iceman PIC CIEM Senate

2Z-ZW 2 we XX-XY FS 壁虎 2/54 ZZ-ZW 2 Sa aT EY 5/6 DP. 0, ey. CD. Gian = eRe Ve 45/145° XiXiX,X,-KiX.Y Ris BE} 1/46 RK-KV a 4/33 ZZ-ZW 2. 2 KE 3/25 X:X:X,X,-KiX,Y ss" : 4/18 ZZ-ZW 2

Sa aS en a ee ne

2 Teale a IS Aah BEA AES RES

sy # TSD 研究 He RE BR} 2 Bull (1978) fee (1986) HRB BL 2 Rayaatud (1972) Bale tet (1982) = 1 Osgood(1980) aS 1 Muth (1981) Lor | i ‘pipes se ie ~ Bo tot ae oe rf y ok | See eee ee a) 5 SE ee 20 22 24 26. 28), 30 32, 34 36° 88

ett (°C)

1 SeiRe Sete

PEAS RES Mea, MebeA1/2 Behe Muth#iBull(1981) @ ke - AEB ull (1980)

”中华 ( ) fe BE(1986)

RS EY Sa ER ENE Bl 4 MEF BN Hy ALE Bull 4h Fe)

SST SR NL NY 1A SNA RE TENE NE TE TL TRE RN TI IN BST OKIE 2

fF |

Bll (1979,1981),Pieau(1971 1978,1982) 1985):

Yetema 〈1979) ,Morreale (1982)

Wanger (1980) fate (1885)

TSD 研究 ee ec) T | i Pieau (1971.1975) se 8 + 2 Yetema (1976,1979) ue fy 3 + 2 Bull (1980) BY TS F753} = 1 Pieau (1982) Be WK a Oe + fi Charnier (1966) + 2 - =| ie RY 1 bs Ferguson (1982)

A iid 8

Ae i

=. 0-5 oa ay 8 | (HEEL) EN / F

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B, 4322:

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eee cece!

2 Sars mera | a=

C ese ()

if ] (3 of --?

i A poe renee soci neramenp ace iors cemrcracnncrtnrs cmon irae adlencearcaecl

36 0g 2 2A re 26 Tf 2B) BOI 32 ht Bt

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O Ate (8%)

@ ike (Hee) Mrosovsky (1980) A St Ga) fz Be (1985 )

12 e798 Sieg

O vent Vogt 2 (1982) @ Fe HM) Yetema(1978)

71

AT ITS UTE

染色 较为 复杂 ( 12。 BARMERA, Enews SR ima, SUR Se iE a all MRA Fa eA Ee I, 2. 温度 决定 (TSD) AMERTRARHR AUER, TESA, RABI, BM Fy WP AI FS Le fa, PTA Me ae Wins. Charnier(i9)SKRMNT mew DOERR EZ. thie tht (Agama agame)

BY SP THE 26-27 0 HEL FANOT. 8% HEE, FE29T

100 雄性 28-430 YOR, FH 50 许多 生物 兴趣 决定 爬行 动物 进行 研究 ( 3 )。

3 相当 _ 行动

定性 温度 关系 怎样? 2 | 温度 动物

影响 完全 相同 .

BRA, SZAAHE MAREE, SHAS MM 21—3 CLEC). FEB 温度 反应 Ge ei F (30-350) AOA ME GEE RE IE Mim F(20-27C) RABE GEE RE ime (2, C), sss ywAM SER, & im THEE, (im 7 HEHE C2, A, B). mss meBAy Wyte, (Chelydra serpeniina) BH RR, 24306 M20CH, FRA AMEE, TOZE 20-30 Zia 代为 雄性 (图 ?2,D )。

环境 影响

1. 温度 ”温度 决定 主要 胚胎 作用 决定 作用 便 温度 敏感 进度 作用 .REergtsoa Joameak19352) 西西 (Alligator mississippiensis) 温度 敏感 2-3 Bull fa Vogt(igsi) (Chrysemys picta) 温度 敏感 Se LM. Gaara Bee Ce 4).

DMB ihin F (250) 产生 雄性 ,高远 (30.5 PPM. 16 低温 改变 im, FT PERT E, MMM SHEE. ia 19

oa TBs

py) Bed RIE A Ae CB 改变 温度 方式 ( 2 调配 16 O/1T 25 ->320.5T 19 18/16 LO | 3/9 30.50 >25T 21 5/27 23 f/18 改变 温度 :

2. 野外 决定 ”野外 实验 密切 关系 野外 Al, 温度 变化 。Eergusona Joanea 《1982) 野外 试验 西西 完全 温度 决定 30 347 雄性 S2CRHLN, AREA, (HME EES. te 沼泽 阴凉 30 ) 代为 阳光 充足 CF ty im BE7E34T ) 99 雄性 IB Ear NIG APA, WEE 31234% ) ALE NE CGEM, HET Sn cy az DLS Oe Oe Le BSE 平均 6 Sth RARE. ABER RESP DL, MERE, BUA A ASIMEMAHSTAEN SERA, DEAT AQIS BY iia SE SG ES Ac A ee 72 ell, PR BE HE (1983) AMF SSH Sl 6 Ree RA BES. PRES BERN AEB 数目 雄性 4 乌龟 增多 动物 繁殖 雄性 交配 繁衍 温度 决定

SNF RES EN URE EB RT SES, 结果 取决 环境 温度 选择 决定 胚胎 控制 相互 作用 公园 北方 南方 情况 怎样 ?根据 温度 关系 相同 北方 南方 产生 雌性 Vogt (1982) 现在 Se. 北方 比例 反而 什么 方法 平衡 ? A, HT UPR: C1 IR imEe CEES /2A mM BE) :发 生变 ABA ; C2 ) BB, Jb BGR: C3 )

北方 ,在 阳光 充足 .Bull (19827 进行 研究 美国 PAW KS (Chrysemys picta) & (Grapte- mys pseudogeogra phicajitty J AACA 3 ).

10r Q tre. | gig 4 FP, \ i ay \ e | \ \ x i" | \ : ie ce 1 \ 0-5 / Ny Pia gahiun a+ ¢ | \ \ Sa | \ eon \ \ NA | RN { \ Dees « \ oY tN 0 b jer Cen Ses DS | EE a hg Ee Us ae eS Ra UO) 25 28 29 30

温度 ( °C) AS RAW SIAR O-—O 2 CHAE APE) @-----@ Ke (北方 威斯康星 ) A---A 西 ) A A Alfa Cha RRB) -

3 ; COSTE, dba heat HERMES, NR Bea SIAN A WARES Sala: 因此 平衡 41 2), 根据 场所 选择 控制 通过 选择 差异 温度 控制 存在 差异

温度 决定 原因

Swe Re EAS, Rabe BBA 染色 它们 环境

温度 影响 变化 染色 决定 原始 动物 同体 进化 异体 染色 进化 动物 环境 影响 方向 进化 温度 决定 定性 进化 解释

1. Charnov Bu 理论 “Charmaov Btll(1977) 受精 环境 决定 受精 受精 遗传 决定 环境 , 环境 问题 环境 变化 天, 因此 环境 形成 适合 《fitnaess) 环境 雄性 适合 ”外 育成 雄性 ;友之 性。 认为 适合 形成 ME, Ferguson Joanen( 1982 Ky es HT ER AS. Haff Es aS Leal BS ULES C FN34°C FH #4REmin PRB REE, HRT RB “:. REAANBE ES, AEZHABESH SA, (AA ANS SSK, MAAS, BEE ‘ADR 5). ARTDDAAR RA Eta 营养 生长

推论 雌性 生长 繁殖

自身 环境 适合 Charaov Bull 理论 解释 体内 减少 雄性 理论 目前 解释 何在 低温 雄性 ? 难道 fei PPE? 什么 TSD ? 温度 雌性 雄性 适合 ? 差异 怎样 影响

#€ 5 FL RAF Stl, ABMAADRENAA Fergtson ,1982 )

《1 ) 室内 :

aip 38 FES ERAS 体内 卵黄

Retake Bg =| (#) te Fill (g) (gz) (g) (z) 30T ST 2. 65.1-5.7 47.6-3.1 37.8+3.9 8.12.2 34 94 J 65.2-+6.1 43.7+4.0 38.2+4.6 5.3 1.9 32 es 2 65 8 6.8 46-2b4.5 36.8 4.2 T.7H2.5

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A Re a te eR EL A NY RIS EE ST NE TREE ECE ST A RNS IE PTE

BY HE RBA? )

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温度 决定 染色 定性 温度

决定 动物 共存 凡是

染色 影响 ”凡是 温度 定性 动物 异型 染色 | 课题 怎样 控制 〈1984) 设想 爬行 动物 Re : RCT PEE AON SERIE GL-YHuROeE) |

y

| 环境 (RR. EES) AREA | RNY | 生活 环境 温度 适应 |

m PURE, RPE | (SHAE, 4825, SBI, Kay mRHRZE) 模型 理解 温度 定性 别提

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Th

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7 2 ANVIL RANE (根据 ,1984 )

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SS SN DS ET RE IS EE

SaRH-YiiR i. erry SONS FE BCRLEMARE, 0CRLEMAMR, £ 5-290 PEAS UL HERE, SBS PERE 广 -Y ,个 细胞 H2Y 关系 细胞 H-Y 再- 抗原 存在 胚胎 育成 ;胚胎 存在 - 抗原 事实 便 没有 异型 染色 具有 哺乳 同样 遗传 决定 背景 温度 影响 考虑 ”可 温度 决定 因素 作用 胚胎

”性 因素 孵化 温度 影响 H-Y

活动 ) ,从 进一步 影响 表现

温度 决定 性别 揭示 极其 深奥 决定 因素 ;尽管 目前 HY 抗原 ) 激素 作用 基因 温度 决定 作用 ,水 潜在 温度 决定 (ASAD GREER ER ERA SES #, LESMEREMSR SATEEN.

a) a (湖南 师范 生物 ) Hou Ling (Department of Biology,

Hunan Normal University)

~

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O

O. jorge Wi:

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is rugosa,

t

O

The number variation of the chromosomes of O, rugosa,

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Showing C-bands heteromorphism,

7mon

G. lal

The Karyotypes and C-bands of four Oreolalax spec

O ome

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ie

Fig,

9. I-K: 2n

I

Fig.

29.

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染色 、C- Ag-NORSs

(A,B)、,C= (C,D) Ag=NORS (E) The karyotype (A, B), C-banding pattern (C, D) and Ag-NORs (E) of Ophisaurus harti Boulenger

BE: FEY SR SC Ten ER EY LR

The unfertilized ezg is in meiotic meitapase |. X1329

Fifteen minutes after fertilization, the sperm has penetrated into the cortex of the egg, X729

Twenty-five minutes after fertilization, the sperm head

starts to decondense, X1320

Twenty-five minutes after fertilization, the egg is in the end

of meiotic metaphase I. X720

The male pronucleus, fifty-five minutes after fertilization, X720 The female pronucleus, fifty-five minutes after fertilization, X720 Two pronuclei in the clear area, seventy-five minutes

after fertilization, X720

Two pronuclei conjugate, ninety-five minutes after

fertilization, X720

ERT, KA AELURE-AHERAE

Flg 4,

Fig 5.

The spermary histology of the normal toads, (X490) Observation on the spermary of the toads administered

twice daily with large doses of LHRH analogue for 14d. (X496). A lot of sperms remained in the seminiferous tubules can be seen when thier spermiation was inhibited, Observation on the spermary of the contrast toads injected twice daily with 501U HCG for 15d. (X490). Spermiogenesis is active (——) , and spermatic cell is proliferative,

Portion of gonadotropic cell of the normal toads. (X28000). GTH: gonadotropin; Nu: nucleus,

Gonadotropic cell of the toads administered twice daily with large doses of LHRL analogue for 14d. (X11600). Nu: nucleus; G: Golgi body; RE: rough endoplasmic reticulum; V: vesicle; Mt: mitochondria,

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ACTA HERPETOLOGICA SINICA 1988 NO,1 CONTENTS

Cytotaxonomical studies on Chinese pelobatids WV, The karyotypes and C-bands

of four species in the genus CO ooopa6600800 0 Guanfu, Tan Anming & Zhao Erm 人)

Studies on the karyotype,C=bands and Ag=-NORS of Ophisaurus hartis Bou- Guo Chaowen & Dong Yongwen( 5 ) A cytological study on the pronuclear reconstruction in the fertilized egg of

Bufo “Gyolel ilocos 040000.000.000000000000000 000000000000 000000000000 Wu Viging & Mao Mingting( 10)

A new species of Cuora—Cuora aurocapitata odp 000000000000 006600 D00 GOD 000000 000000000000000

Sea turtles in Fujian and Guangdong proVimceSs cee eee cer ceeceenee Steet teen eee ete eens een eteeteecesese ess Susan Salas Frazier, John G, Frazier et al,( 16 ) Studies on the cranial morphology of Zaocys (Serpentes, Colubridae) V . A comparative study on the cranial morphology of Chinese Zaocys, Ptyas, Elaphe and Entechinus, with preliminary discussions on the function and phylogeny-:. + Zhang Fuji( 47 ) Effects of chronic is a doses of an LHRH analogue on the spermiation response in the toadS Wang Shili & Wang Long( 56 ) The reproductions of Naja naja and Ptyas mucosus on Zhoushan and nearby islands pp Sheng Helin, Xie Shengxun & Feng Ruiben( 60

~—S

Herpetological Notes

Rana cancrivora Gravenhorst discovered in Guangxi—Sun Jianyun( 65 ). Elaphe davidi—a record new to Shandong—Jia Zhenxu( 66 ). Digenetic trematodes from common snakes

of Tianjin—Li Qingkui et al .( ). Temperature-Dependent sex determination in rep-

tiles—Hou Ling( 70 ).

行动 (= TD) | 19884 3 1

行动 ca ras ae Oc) 2 (北京 朝阳 137 ) zetT HO A ml 3 邮电

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报刊 临时 登记 1065

ACTA HERPETOLOGICA SINICA

(Quaterly) 1988 March, Number 1

Edited by: Chinese Society of Herpetologists by Science Press (137 Chaoyangmen Nei St,, Beijing, PRC) ee: |

KE, 62-60 Sk ee