青藏高原毛茛科3种特有植物核型和进化研究

对青藏高原高山冰缘地区毛茛科３种特有植物的核型进行了分析。它们的核型公式（Ｋ）、染色体相对长度组成（Ｃ．Ｒ．Ｌ．）和核型不对称系数（Ａｓ．Ｋ％）分别为：青藏金莲花Ｔｒｏｌｉｕｓｐｕｍｉｌｕｓｖａｒ．ｔａｎｇｕｔｉｃｕｓ：Ｋ（２ｎ）＝６ｍ＋８ｓｍ（２ＳＡＴ）＋２ｓｔ,Ｃ．Ｒ．Ｌ．＝４Ｌ＋４Ｍ２＋４Ｍ１＋４Ｓ,Ａｓ．Ｋ％＝６３．５７,核型属２Ｂ型;甘青乌头Ａｃｏｎｉｔｕｍｔａｎｇｕｔｉｃｕｍ为Ｋ（２ｎ）＝６ｍ＋１０ｓｍ,Ｃ．Ｒ．Ｌ．＝４Ｌ＋８Ｍ１＋４Ｓ,Ａｓ．Ｋ％＝６２．５４,２Ｂ型;单花翠雀花Ｄｅｌｐｈｉｎｉｕｍｃａｎｄｅｌａｂｒｕｍｖａｒ．ｍｏｎａｎｔｈｕｍ为Ｋ（２ｎ）＝６ｍ＋８ｓｍ＋２ｓｔ,Ｃ．Ｒ．Ｌ．＝４Ｌ＋４Ｍ２＋４Ｍ１＋６Ｓ,Ａｓ．Ｋ％＝６４．３４,属３Ｂ型。经同相关近缘种核型资料比较,青藏金莲花核型不对称性和进化程度比金莲花Ｔ．ｃｈｉｎｅｎｓｉｓ低;甘青乌头的核型不对称性和进化程度在其近缘类群（乌头组Ｓｅｃｔ．Ａｃｏｎｉｔｕｍ）已报道的种之内最低;单花翠雀花核型不对称性和进化水平比翠雀组（Ｓｅｃｔ．Ｄｅｌｐｈｉｎａｓｔｒｕｍ）已报道的展毛翠雀花Ｄ．ｋａｍａｏｅｎｓｅｖａｒ．ｇｌａｂｒｅｓｃｅｎｓ、     

两种过路黄的核型研究

对国产报春花科（Ｐｒｉｍｕｌａｃｅａｅ）珍珠菜属（Ｌｙｓｉｍａｃｈｉａ）植物过路黄（Ｌ.ｃｈｒｉｓｔｉｎａｅＨａｎｃｅ）和疏节过路黄（Ｌ.ｒｅｍｏｔａＰｅｔｉｔｍ）的核型进行了首次报道。过路黄染色体数目为２ｎ＝２４,核型公式为２ｎ＝２４＝２ｍ＋４ｓｍ＋６ｓｔ＋１２ｔ,核型类型“３Ａ”;疏节过路黄染色体数目为２ｎ＝２２,核型公式为２ｎ＝２２＝４ｍ＋６ｓｍ＋２ｓｔ＋１０ｔ,核型类型“３Ａ”。     

子午岭产4种百合科植物的核型多样性研究

对子午岭产百合科黄精属大苞黄精（Ｐ．ｍｅｇａｐｈｙｌｌｕｍ）、玉竹（Ｐ．ｏｄｏｒａｔｕｍ）,百合属的细叶百合（Ｌ．ｐｕｍｉｌｕｍ）,葱属的糙葶韭（Ａ．ａｎｉｓｏｐｏｄｉｕｍ）４种植物进行了染色体研究。其染色体数目和核型分别为：玉竹２ｎ（２ｘ）＝２０＝１２ｍ（２ＳＡＴ）＋８ｓｍ,核型为２Ｂ型;大苞黄精２ｎ（２ｘ）＝２２＝４ｍ＋１２ｓｍ＋６ｓｔ,核型为３Ｂ型;细叶百合２ｎ（２ｘ）＝２４＝４ｍ＋１０ｓｔ     

三种毛茛的核型研究

对３种（含１变种）毛莨属植物进行了核型研究,其染色体数目及核型资料为首次报道。三叶毛莨（ＲａｎｕｎｃｕｌｕｓｊａｐｏｎｉｃｕｓＴｈｕｎｂ．ｖａｒ．ｔｅｒｎａｔｉｆｏｌｉｕｓＬ．Ｌｉａｏ．）有两种核型。即基本型２ｎ＝２ｘ＝１４＝６ｍ＋４ｓｍ＋４ｓｔ（２ＳＡＴ）和杂合型２ｎ＝２ｘ＝１４＝６ｍ＋４ｓｍ＋４ｓｔ（１ＳＡＴ）,前者核型的特征是其随体较大,而后者核型变异发生在第２对和第３对同源染色体异形上,并     

湖南6种毛莨科植物的核型研究

本文对产于湖南的６种毛莨科植物的染色体进行了研究。裂叶星果草［Ａｓｔｅｒｏｐｙｒｕｍｃａｖａｌｅｒｉｅｉ（Ｌｅｖｌ．ｅｔＶａｎｔ）Ｄｒｕｍｍ．ｅｔＨｕｔｃｈ．）的染色体属于Ｒ型,核型公式为２ｎ＝１６＝１２ｍ＋２ｓｍ＋２ｔ,核型类型属于ＺＢ;打破碗花花（ＡｎｅｍｏｎｅｈｕｐｅｈｎｓｉｓＬｅｍ．）的核型公式为２ｎ＝１６＝１０ｍ＋４ｓｔ＋２ｔ（２ｓａｔ）,核型类型属于２Ａ;粗齿铁线莲［Ｃｌｅｍａｔｉｓａｐｉｉｆｏｌｉａｖａｒ．ａｒｇｅｎｔｉｌｕｃｉｄａ（Ｌｅｖｌ．ｅｔＶａｎｔ）Ｗ．Ｔ．Ｗａｎｇ］的核型公式为２ｎ＝１６＝１０ｍ＋２ｓｔ＋４ｔ（２ｓａｔ）或２ｎ＝１６＝１０ｍ＋２ｓｔ＋４ｔ（４ｓａｔ）随体染色体数目在居群之间有变化,核型类型属于２Ａ;扬子铁线莲［Ｃｌｅｍａｔｉｓｇａｎｉｐｉｎｉａｎａ（Ｌｅｖｌ．ｅｔＶａｎｔ）Ｔａｍｕｒａ］的核型公式为２ｎ＝１６＝１０ｍ＋２ｓｔ＋４ｔ（４ｓａｔ）,核型类型属于２Ｂ;毛莨（ＲａｎｕｎｃｕｌｕｓｃａｎｔｏｎｉｅｎｓｉｓＤＣ．）的核型公式为２ｎ＝１６＝６ｍ＋４ｓｔ＋６ｓｔ（２ｓａｔ）,核型类型属于３Ａ;毛莨（ＲａｎｕｎｃｕｌｕｓｊａｐｏｎｉｃｕｓＴｈｕｎｂ．）的核型公式为２ｎ＝?     

安徽黄精属的细胞分类学研究

本文首次报道黄精属ＰｏｌｙｇｏｎａｔｕｍＭｉｌｌ我国三种特有植物的染色体数目和核型,结果如下：安徽黄精Ｐ．ａｎｈｕｉｅｎｓｅ发现两个细胞型：（１）２ｎ＝２４＝４ｍ＋６ｓｍ＋１４ｓｔ;（２）２ｎ＝２０＝４ｍ十６ｓｍ＋１０ｓｔ;　　黄精Ｐ．ｌａｎｇｙａｅｎｓｙ２ｎ＝１８＝６ｍ＋８ｓｍ＋４ｔ;距药黄精Ｐ．ｆｒａｎｃｈｅｔｉｉ有三个细胞型：（１）２ｎ＝２２＝８ｍ＋８ｓｍ（２ｓｃ）＋６ｓｔ;（２）２ｎ＝２０＝２ｍ＋１４ｓｍ＋４ｓｔ;（３）２ｎ＝１８＝４ｍ＋８ｓｍ＋４ｓｔ＋２Ｔ,全部属３Ｂ核型。黄精属植物安徽共有１０种,本文对９种黄精的染色体数目、核型进行了比较研究,发现它们可划分成三个类群,与中国植物志（第十五卷）的形态分类基本相符。     

青海南部七种翠雀属植物的核型

报道了采自青海南部７ 种翠雀属（ Ｄｅｌｐｈｉｎｉｕｍ Ｌ．） 植物的染色体数目和核型。大通翠雀花Ｄ．ｐｙｌｚｏｗｉｉ 的核型公式为２ｎ＝ １６ ＝ ２ｍ ＋ ４ｓｍ ＋ １０ｓｔ; 毛翠雀花Ｄ． ｔｒｉｃｈｏｐｈｏｒｕｍ 的核型公式为２ｎ＝ １６ ＝ ２ｍ ＋ ４ｓｍ ＋ １０ｓｔ; 蓝白翠雀花Ｄ．ａｌｂｏｃｏｅｒｕｌｕｍ 的核型公式为２ｎ ＝ １６ ＝ ２ｍ ＋ ４ｓｍ（２ＳＡＴ） ＋ １０ｓｔ; 囊谦翠雀花Ｄ． ｎａｎｇｃｈｉｅｎｅｎｓｅ 的核型公式为２ｎ ＝ １６ ＝ ２ｍ ＋ ６ｓｍ ＋ ８ｓｔ; 唐古拉翠雀花 Ｄ．ｔａｎｇｋｕｌａｅｎｓｅ 的核型公式为２ｎ ＝ １６ ＝ ２ｍ （２ＳＡＴ） ＋ ６ｓｍ ＋ ８ｓｔ; 单花翠雀花 Ｄ．ｃａｎｄｅｌａｂｒｕｍ ｖａｒ． ｍｏｎａｎｔｈｕｍ 的核型公式为２ｎ ＝ １６ ＝ ２ｍ ＋ ６ｓｍ ＋ ８ｓｔ; 展毛翠雀花Ｄ． ｋａｍａｏｅｎｓｅｖａｒ． ｇｌａｂｒｅｓｃｅｎｓ 的核型公式为２ｎ ＝ １６ ＝ ２ｍ ＋ ６ｓｍ ＋ ８ｓｔ; 前５ 种植物的染色体数目与核型为首次报道。     

浙江鸭跖草属植物的核型研究

本文报道了浙江二种鸭跖草属植物──饭包草ＣｏｍｍｅｌｉｎａｂｅｎｇａｌｅｎｓｉｓＬ．和鸭跖草ＣｏｍｍｅｌｉｎａｃｏｍｍｕｎｉｓＬ．的染色体数目与核型：ＣｏｍｍｅｌｉｎａｂｅｎｇａｌｅｎｓｉｓＬ．核型为Ｋ（２ｎ）＝２２＝１８ｍ＋４ｓｍＣｏｍｍｅｌｉｎａｃｏｍｍｕｎｉｓＬ．核型为Ｋ（２ｎ）＝２２＝４Ｍ＋１２ｍ＋４ｓｍ＋２ｓｔ     

吉林省产5种百合的核型研究

报道了吉林省产５种百合科植物的染色体数目和核型：①毛百合Ｌｉｌｉｕｍ ｄａｕｒｉｃｕｍ Ｋｅｒ．－Ｇｅｗ１．２ｎ＝２４＝２ｍ（２ＳＡＴ）＋２ｓｍ（２ＳＡＴ）＋８ｓｔ（２ＳＡＴ）＋１２ｔ（２ＳＡＴ）;②有斑百合Ｌ．ｃｏｎｃｏｌｏｒ Ｓａｌｉｓｂ．ｖａｒ．ｂｕｓｃｈｉａｎｕｍ（Ｌｏｄｄ．）Ｂａｋｅｒ ２ｎ＝２４＝２ｍ（２ＳＡＴ）＋４ｓｍ（４ＳＡＴ）＋６ｓｔ（２ＳＡＴ）＋１２ｔ;③兰州百合Ｌ．ｄａｖｉｄ     

小檗科鬼臼亚科植物的核型研究

本文首次报道了中华山荷叶与川八角莲的核型,分别为Ｋ（２ｎ）＝１２＝８ｍ（４ＳＡＴ）＋２ｓｔ＋２ｔ及Ｋ（２ｎ）＝１２＝４ｍ（２ＳＡＴ）十４ｓｍ＋２ｓｔ（２ＳＡＴ）＋２ｔ,核型类型均为ＺＡ型。本文报道的桃儿七及八角莲的核型与前人的结果有一定差异,前者为：Ｋ（２ｎ）＝１２＝６ｍ（４ＳＡＴ）＋２ｓｍ＋２ｓｔ＋２ｔ,２Ｂ型,后者为Ｋ（２ｎ）＝１２＝８ｍ（２ＳＡＴ）＋２ｓｔ（２ＳＡＴ）＋２ｔ,为２Ａ型。本文分析了小檗科鬼臼亚科４个属共７种植物的核型,结果是该类植物的核型极为相似,染色体数目均为２ｎ＝１２,由８条ｍ或ｓｍ,２条ｓｔ以及２条ｔ染色体组成。核型的相似性反映了这类植物的亲缘关系,这４个属的植物是一个自然类群。但随着系统发育,核型的不对称性有所增加,其中以山荷叶属最为对称,八角莲属居中,桃儿七属与足叶草属最不对称。笔者认为,核型上的高度相似是该类植物在系统发育上不发达,属内种类稀少,通常为寡种属或单种属的重要原因。     

The Discovery of Diploid Lycoris radiata (L′Her.) Herb. from Anhui

Lycoris radiata (L′Her. ) Herb. containing wild and cultural types, is distributed in China and Japan. The karyotype variation in three populations of the species from Anhui is studied in this paper. (1) Wuhu wild population has a karyotype 2n=21+1B= 1m+12st +8t+1B. The chromosomes range in length from 7.50 to 14.10 µm with the ratio of the longest to the shortest 1.88. The karyotype belongs to Stebbins’(1971) 3A. (2) Huangshan wild population has two cytotypes: 2n=22 and 2n=22+1B. Type Ⅰ: The karyotype formula is 2n=22=12st+10t. The chromosomes range in length from 6.85 to 9.95 µm. with the ratio of the longest to the shortest 1.45. The karyotype belongs to 4A. Type Ⅱ: The karyotype formula is 2n=22+1B=6st+14t+2T+1B (plate 1: 7,8). The chromosomes range in length from 6.50 to 11.02 µm. with the ratio of the longest to the shortest 1.70. The karyotype belongs to 4A. (3) Wuhu cultural type has a karyotype 2n=33=30st +3t. The chromosomes range in length from 7.10 to 9.35 µm with the ratio of the longest to the shortest 1.32. The karyotype belongs to 4A. This result agrees well with the previous reports. The diploid types of Lycoris radiata (L´Her.) Herb. are found in Anhui for the firsttime.     

The discovery of triploid Lycoris sprengeri Comes ex Baker from Anhui,China

Lycoris sprengeri Comes ex Baker is endemic to China. Reported in the present paper are the chromosomes number and karyotypes for two wild populations of the species from Anhui. ( 1 )Caishi population has a karyotype 2n=33=9st+21t+3T. The length of chromosomes ranges from 5.58～9.15μm. The karyotype belongs to Stebbin’s (1971) “4A”. (2)Longyashan populations have two karyotypes. The karyotype formula of the type I is 2n=22=8st+14t, with chromosomes ranging from 6.88～9.15μm. The karyotype belongs to “4A”. The karyotype formula of the type Ⅱ is 2n＝22＝1m+1sm+14st+6t, with chromosomes ranging from 7.20～15.80μm. The karyotype belongs to “3B”. The triploid type of L. sprengeri was discovered in Anhui for the first time. The karyotype 2n=22 =1m+1sm+14st+6t in diploid type of this species is here reported for the first time.The Robertsonian change plays a key role in karyotype evolution of Lycoris.     

二倍体石蒜在安徽发现

本文以根尖细胞为材料,观察了石蒜Lycoris radiata(L′Her．)Herb．三个不同居群植物的染色体数目和核型,发现石蒜为一复合体,包括两种不同类型：(1)三倍体类型,主要包括一群以鳞茎无性繁殖的园艺栽培植株,其染色体数目和核型为2n＝33=33t(st),属“4A”核型,且极其稳定。(2)二倍体类型,主要包括一群野生植株,变异较大,我们发现有下列几种情况：一是芜湖产石蒜(L．radiata)的野生材料,其染色体数目和核型为2n=21+1B=1m+12st+8t+1B,属“3A”核型,在石蒜种内迄今未见有类似报道;另一是黄山产野生材料,观察到两个细胞型,绝大多数细胞为2n=22＝12st+1Ot,极个别细胞出现2n＝22+1B=6st+14t+2T+1B的情况,均属“4A”核型。芜湖和黄山野生材料的染色体数目和核型均为首次报道。石蒜(L．radiata)的二倍体类群也是首次在安徽发现。     

A Study on Karyotypes of the Genus Lycoris

The genus Lycoris (Amaryllidaceae) consists of about 20 species, all of which are confined to temperate China, Japan and Korea. Cytological investigations, including a reexamination of the karyotypes of 14 taxa, measurements of relative nuclear DNA content, and meiotic configuration observations on some specific forms and interspecific hybrids, have been carried out by the present authors in order to re-evaluate the mode of karyotype evolution and the role of hybridization in the speciation of Lycoris. These have resulted in a new theory for explaining the karyotype evolution in the genus, which will be considered elsewhere. The present paper deals with observations on karyotypes of 11 species, 1 variety and 2 artificial hybrids. Results obtained through karyotype analysis, as shown by the data in Table 1, Plates I-VI and Figs. 1-2, reveal that: (1) the karyotypes of Lycoris rosea, L. radiata var. pumila, L. sprengeri, L. haywardii, L. caldwellii, L. squamigera and L. radiata are, on the whole, consistent with those reported by the previous authors^{[1,2,3,4,5,8,10,12]};(2) the I (rodshaped) chromosomes of L. chinensis and L. longituba are all T’s (telocentric) instead of t’s (acrocentric) or t(Sat)’s; (3) the three materials of L. aurea of different sources have shown a karyotypic differentiation: one with 2n=14=8m+6T, and the others with 2n=16=6m+10T: (4) both of the karyotypes of L. straminea and L. albiflora are 2n=19=3V+6I, inconsistent with 2n=16=6V+10I for the former and with 2n=17=5V+12I for the latter as reported by Inariyama (1953), Bose and Flory (1963) and Kurita (1987). The following aspects are worthwhile discussing: 1. The types of chromosomes. Karyotype analyses reveal the existence of three major chromosome types in Lycoris: (1) m (metacentric) chromosomes: (2) t (acrocentric) chromosomes, with short arms, (3) T (telocentric) chromosomes, sometimes with dot-like terminal centromeres. To distinghish t’s from T’s is of paramount importance for solving the problem of karyotype evolution in Lycoris. Bose (1963) pointed out that in the species with 2n=22, all I chromosomes were t’s, while in species with 2n=12-16, all I chromosomes were T’s. Our results of chromosome observations are consistent with Bose’s remarks. Some authorst^[3,6] have probably mistaken the dot-like terminal centromeres of T’s of L. longituba and L. chinensis as the short arms of t’s. 2. The significance of Robertsonian change in karyotype evolution. Although chromosome numbers and karyotypes are very variable in Lycoris, as shown in Table 1, the total number of arms of a chromosome complement of any species is always multiples of 11. Hence, it seems likely that Robertsonian changes have taken part in karyotype alteration, The genus has a series of basic chromosome numbers: 6, 7, 8 and 11. But which is the most primitive one? It is uncertain whether a successive decrease in chromosome numbers as a result of Robertsonian fusion or a gradual increase in chromosome numbers brought about by fission (fragmentation) has been the essential mechanism for karyotype evolution and speciation in Lycoris. These problems are of crucial importance and will be discussed in our subsequent papers. 3. The origin of polyploids. As evident from Table 1, there are two levels of ploidy differentiation in Lycoris: (1) di ploids with 2n=22 or the equivalent of 22, (2) triploids with 2n=33 or the equivalent of 33. The most common way of origination of triploids in plants is the hybridization of diploids with Tetraploids. But tetraploids have never been found in Lycoris. Thus, it is suggested that the triploids have originated from the combination of an unreduced gamete of a diploid with a normal gamete of another diploid. 4. The role of hybridization in speciation. Results of karyotype analyses show that hybridization has taken an important part in the speciation of Lycoris. Two types of hybrids have been found: (1) 2n=19= 3V+ 16I, L. straminea, L. albiflora and the two artificial hybrids L. sprengeri×L. chinensis and L. haywardii× L. chinensis all possess this karyotype. It could be seen from the above chromosome number and karyotype that this sort of karyotype is exactly half of the total sum of 2n=22I and 2n=16= 6V+10I. It is, therefore, quite evident that taxa possessing this karyotype are all diploid hybrids of 2n=22 and 2n=16, (2) 2n=27=6V+21I, L. caldwellii and L. squamigera possess this karyotype. It is reasonable to assume, too, that they are segmental allotriploids and have arisen from the combination of an unreduced diploid gamete of 2n=16 and a normal haploid gamete of 2n=22. The origin of the hybrid karyotype 2n=17=5V+12I reported by Inari- yama (1953) is similar to that of 2n=19, except that one of the parents possesses 2n=12= 10V+2I instead of 2n=16=6V+10I. The origin of the other hybrid karyotype 2n=30=3V+ 27I reported by Bose (1963) is similar to that of 2n=27, but the diploid gamete comes from taxa possessing 2n=22 instead of 2n=16.     

国产毛茛属三种植物的核型研究

对国产三种毛茛属 (Ranunclus)植物进行了核型研究 ,其中昆明毛茛 (RanunculuskunmingensisW .T .Wang)染色体数目 2n=1 4及核型 2n =1 4 =6m +4sm +4st为首次报道 ;匍枝毛茛 (R .repenceL .)核型公式为 2n =4x =3 2 =8m +1 2sm +1 0st+2t,它是由两个不同的染色体组组成 ;刺果毛茛 (R .muricatusL .)核型公式为 2n=8x=64=1 0m +2 2sm +2 8st+4t,它也是由两个不同的染色体组组成     

石蒜新核型及染色体数目在安徽的发现

对安徽省马鞍山的石蒜居群进行了核型分析 ,发现了石蒜的一种新的染色体数目及核型。按Levan等 (1 964)标准 ,核型公式为 2n =2 4=6m +8sm +6st+4t,为 3A核型 (Stebbin,1 971 )。与目前国内外学者的观察结果差异很大。马鞍山居群的新染色体数目及核型均为首次报道。     

珍珠菜属三种植物的核型研究

对国产三种珍珠菜属 (Lysimachia)植物进行了核型研究 ,其中点腺过路黄 (LysimachiahemsleyanaMaxim .)染色体核型 2n =2 2 =2m +4sm +8st+8t,聚花过路黄 (L .congestifloraHesmsl.)核型 2n =2 4=2m +2sm +1 0st+1 0t及山萝过路黄 (L .melampyroidesR .Knuth)染色体数目 2n =2 2 ,核型 2n =2 2 =4m +6sm +4st+8t,为首次报道。本文还分析了黄连花亚属 (subgen.Lysimachia) 2组 8种植物的核型 ,结果表明黄连花组(sect.Lysimachia)核型类型 1A ,过路黄组 (sect.Nummularia)核型类型 3A或 3B。     

五种苏铁属植物的核形态

报道了苏铁属（Cycas L.)5种植物的染色体数目和核型,除多歧苏铁外,其他种均为首次报道。5个种的体细胞中期染色体核型公式分别为：滇南苏铁C.diannanensis K(2n)=2x=22=2m 4sm 4st 12T;潭清苏铁C.tanqingii K(2n)=2x=22=2m 8sm 2st 10T;多歧苏的Cmultipinnata K(2n)=2x=22=4m 8st 2st 8T;巴兰萨苏铁C.balansae K(2n)=2x=xx=2m 4sm 6st 10T。石山苏铁C.miquelii K(2n)=22=2m 6sm(1SAT) 4st 10T;核型均属于3B型。本研究结果支持苏铁属植物的核型从不对称进化的观点;同时,支持将巴兰萨苏铁和石山苏铁归入攀枝花苏铁组的台湾苏铁亚组的观点。     

安徽产石蒜两个居群的核型研究

观察了石蒜(Lycoris radinta)两个不同居群植物的染色体数目和核型,发现野生石蒜在一个植株的不同根尖细胞里,存在两种倍性的细胞,如生于宣城敬亭山的居群既有正常三倍体：2n=33=18st 15T,属于“4A”核型;还有异常二倍体：2n=20 1B=2st 18T 1B,属于“4B”核型;生于芜湖的居群核型为：2n=20 1B=lm 9T 4t 6st 1B和2n=20 1B=1M 9T 10st 1B,属于“3B”和“3C”核型。