中国绿蟹蛛属一新种(蜘蛛目:蟹蛛科)

本文记述采自浙江宁波天童森林公司的蟹蛛科绿蟹蛛属一新种,钳绿蟹蛛Ｏｘｙｔａｔｅ ｆｏｒｃｉｐａｔｕｓ ｓｐ．ｎｏｖ。     

中国绿蟹蛛属一新种记述(蜘蛛目,蟹蛛科)

记述了采自中国湖南省石门县壶瓶山国家自然保护区境内的蟹蛛科Thomisidae绿蟹蛛属Oxytate 1新种:微绿蟹蛛Oxytate minuta sp.nov,新种与冲绳绿蟹蛛Oxytatehoshizuna Ono,1978较为近似,但有以下几点不同:1)身体大小、形状差别较大,本种身体微小2.60,而后者一般在7.00以上,2)本种插入器隆起于生殖球之上,而后者并不如此.模式标本保存在湖南师范大学生命科学学院.文中量度单位为mm.词源:本种以其体型微小而命名.     

尾莫蟹蛛雄蛛的描述（蜘蛛目：蟹蛛科）

对蟹蛛科Ｔｈｏｍｉｓｉｄａｅ的尾莫蟹蛛Ｍｏｎａｅｓｅｓｃａｕｄａｔｕｓ雄蛛作了描述。     

我国2种微蟹蛛记述（蜘蛛目：蟹蛛科）

提出对前报道的蟹蛛科微蟹蛛属２种的修订：西安微蟹蛛ＬｙｓｔｉｅｌｅｓｘｉａｎｅｎｓｉｓＳｏｎｇｅｔＷａｎｇ,１９９１应为小微蟹蛛Ｌｙｓｔｅｌｅｓｍｉｎｉｕｍｕｓ（Ｓｃｈｅｎｋｅｌ１９５３）的异名,唐迎秋等（１９９５）报道的小微蟹蛛雌蛛,改订为１个新种－文微蟹蛛Ｌｙｓｔｅｌｅｓｗｅｎｅｎｓｉｓｓｐ．ｎｏｖ。     

海南3种蟹蛛记述

记述海南尖峰岭3种蟹蛛:海南泥蟹蛛Borboropaclus hainanus Song(雌蛛新发现),大东斜蟹蛛Lox obales dailoensis Ono(中国新纪录)和海南花蟹蛛Xysticus hainanus sp.nov.(新种)。同时对各种的分类地位作简短的讨论。     

中国广西绿蟹蛛属1新种(蜘蛛目:蟹蛛科)

作者在进行中国广西大明山无脊椎动物资源调查研究时,发现了蜘蛛目蟹蛛科绿蟹蛛属1新种,命名为饼绿蟹蛛Oxytate placentiformis sp.nov..所有标本均保存在河北大学生命科学学院.文中测量单位为mm.饼绿蟹蛛,新种Oxytate placentiformis sp.nov.(图1～6)正模♂,广西南宁大明山自然保护区浣纱瀑布,2011-05-23,王英楠采.鉴别特征 在分布于亚洲大陆的本属种类中,本新种与冲绳绿蟹蛛O.hoshizuna Ono,1978,钳绿蟹蛛O.forcipata Zhang&Yin,1998和小头绿蟹蛛O.capitulata Tang&Li,2009外形和触肢器十分相似,但具有以下不同:本种触肢胫节突长,端部弯曲呈"7"字形,而冲绳绿蟹蛛O.hoshizuna的胫节突末端强烈弯曲呈钩状,钳绿蟹蛛O.forcipata胫节突末端呈钳状,小头绿蟹蛛O.capitulata Tang&Li,2009胫节突末端弯曲呈鸟头状.词源学 本新种以雄蛛背甲的形状而拟定.正模 雄蛛体长7.75:头胸部长2.81,宽2.40; 腹部长5.20,宽1.38.背甲黄褐色,中窝纵向线状,颈沟和放射沟不明显; 背甲圆形,头区轻微隆起.8眼2列,背面观两眼列均后凹,后眼列较宽,前侧眼和后侧眼突出; 前中眼直径0.08,前侧眼直径0.10,后中眼直径0.08,后侧眼直径0.10;前中眼距0.13,前中侧眼距0.10,后中眼距0.10,后中侧眼距0.30; 中眼域梯形,前边大于后边(0.30:0.25).螯肢黄褐色,前后齿堤无齿.颚叶黄色,边缘有浓厚的长毛.胸板淡黄色,长大于宽.步足黄褐色,步足测量:Ⅰ 12.40 (3.83+1.38+3.42+2.60+1.17),Ⅱ 12.60 (3.88+1.38+3.57+2.60+1.17),Ⅲ 6.80 (2.09+0.77+1.79+1.33+0.82),Ⅳ7.05 (2.40+0.71+1.79+1.33+0.82); 足式:2143.腹部十分窄长,淡黄色,被有黑色长毛; 腹部背面前端有2对明显的肌痕,腹部后部有横纹,似分节状.触肢胫节腹突拇指状; 外侧突较长,末端骨化程度高,弯曲呈"7"字形状; 生殖球简单,内侧具亚盾板; 插入器刺状,末端较钝.分布:广西.     

中国瘤蟹蛛属1新纪录种(蜘蛛目:蟹蛛科)

记述我国瘤蟹蛛属1新纪录种,加藤瘤蟹蛛（Phrynarachne katoi Tkiuni,1955)。     

中国蟹蛛科（蜘蛛目）新种记述

记述我国蟹蛛科花蟹蛛属６新种和蟹蛛属２新种,共计８新种,金林花蟹蛛Ｘｙｓｔｉｃｕｓｊｉｎｌｉｎ,玛纳斯花蟹蛛Ｘ．ｍａｎａｓ,林芝花蟹蛛Ｘ．ｎｙｉｎｇｃｈｉｅｎｓｉｓ,拟斑花蟹蛛Ｘ．ｐａｒａｐｕｎｃｔａｔｕｓ,似旋花蟹蛛Ｘ．ｔｏｒｓｉｖｏｉｄｅｓ,吴氏花蟹蛛Ｘ．ｗｕａｅ,广西蟹蛛Ｔｈｏｍｉｓｕｓｇｕａｎｇｘｉｃｕｓ和胡氏蟹蛛Ｔ．ｈｕｉ。     

狼蛛,蟹蛛和跳蛛

狼蛛、蟹蛛和跳蛛分别是蜘蛛目中三个科的蜘蛛的通称。这三类蜘蛛包括了我们日常见到的游猎型蜘蛛的大部分种类,它们在帮助人类消灭害虫中所起作用也较大,所以作为动物学教学中的例子加以介绍。 (一)狼蛛狼蛛在地面或植物上疾驰,凶狠如狼,故名。体长3-25毫米,但多数种类在5-8毫米间。体色多黄褐色,不鲜艳。8眼,排成三列。前列4个小眼,中、后两列各2个眼,较大;后列两眼的间距稍大于中列两眼的间距(图1左)。卵袋扁球形,由两片半圆形丝膜缝合而成。卵袋挂在母蛛腹部后端的纺器上,由母蛛随身携带。幼蛛孵出后不分散,而是爬伏在母蛛腹部     

中国蟹蛛科一新纪录种和一雄性新发现

描述了产于中国广西、云南和福建的2种蟹蛛,锡兰瘤蟹蛛Phrynarachne ceylonica(O.P.-Cambridge,1884)和贵州耙蟹蛛Strigoplus guizhouensis Song et Chai,1990,前1种系中国新纪录,后1种的雄性系首次发现.标本保存在河北大学博物馆.     

川金丝猴肠,肝,胰的观察

对川金丝猴（Rhinioithecusrozxellane的肠、肝、胰作了观察。小肠全长284．0-296．0cm,其中十二指肠9．0－12．0cm,呈V形,余为空回肠。大肠长约120．0－130．0cm;无阑尾;升结肠短,仅7．0－8．0cm,横结肠19．0－20．0cm,降结肠及乙状结肠达80．0－90．0cm。肝分背、腹侧二部,腹侧部又分作上、下二部。胆总管开日于十二指肠上部。胰呈T形,胰头为十二指肠降、升部围绕,胰管由胰头发出,开口于十二指肠升部。对个体间的差别、盲结肠发达程度的相关因素、肝叶愈合与进化的关系作了讨论。     

菱臼齿兽((犭亚)目、哺乳纲)耳区的骨骼结构

本文详细描述了菱臼齿兽耳区各个部分的基本结构;并指出了耳区结构与某些啮齿类的相似性,以及中耳鼓泡组成成份与戈壁(犭亚)兽(Anagale gobiensis)的区别。     

An Ultrastructural Study on the Development of Egg- apparatus in Rice Embryo Sac

The development of the egg-apparatus (consisted of an egg cell and two synergids) of rice ( Oryza sativa L. ) was studied at the uhrastructural level. The walls of the egg cell and synergids, immediately after their formation, possessed numerous plasmodesmata. Plasmodesmata were also present on walls between the egg cell and synergids. During the enlargement phase of the egg cell and synergids, the walls at the tip region began to loosen and vesiculate. By the time the embryo sac became mature, the part of the wall of the egg cell and synergids, facing the chalaza, disappeared. Consequently, the tip regions of the egg cell and synergids were only protected by a plasma membrane. When the embryo sac reached full maturity, the upper and middle region of the wall of the synergids broke up into pieces. At that time one synergid began to degenerate. Plasmodesmata persisted at the hook region of the wall of both the egg cell and synergids. Most plastids in the egg cell contained starch grains that persisted throughout the period of the embryo sac development. Starch grains in the plastids of the synergids appeared only before the time when the two polar-nuclei moved into the region above the egg-apparatus. They then disappeared and did not appear again until the embryo sac had reached full maturity. The size and location of the vacuoles in the egg cell were different from those in the synergids. The time of formation was also different. Vacuoles in the egg cell formed late in comparison with the synergids. Vacuoles in the chalazal region of the egg cell (especially at the early stage of the embryo sac development) were much larger than those in the micropylar region. Vacuoles in the synergids tended to concentrate mainly in the chalazal region. There was a peak period of lipid formation in the two synergids. The peak appeared when the embryo sac neared maturity. At the early stage of development, the nuclei of the synergids were elliptical in shape and were situated at the central region near the micropyle. The shape of the nuclei at the late stage of development became less regular and tended to move more towards the micropylar region. Changes in the uhrastructure of the egg cell and synergids of rice appeared to be closely related to the metabolic processes controlling the embryo sac formation and development.     

Circular-dichroic properties and secondary structure of Pseudomonas aeruginosa soluble cytochrome c oxidase.

The c.d. spectra of Pseudomonas aeruginosa cytochrome c oxidase in the oxidized state and the reduced state are reported in the visible- and u.v. absorption regions. In the visible region the comparison between the spectra of reduced cytochrome c oxidase and ferrocytochrome c-551 allows the identification of the c.d. bands mainly due to the d1 haem chromophore in cytochrome c oxidase. In the near-u.v. region the assignment of some of the observed peaks to the haem groups and to the aromatic amino acid residues is proposed. A careful analysis of the data in the far-u.v. region leads to the determination of the relative amounts of alpha-helix and beta-sheet in the enzyme, giving for the first time a picture of its secondary structure. A significant difference in this respect between the reduced and the oxidized species is observed and discussed in the light of similar conclusions reported by other workers.     

The effects of osmotic experiments and prolactin on the mucous cells in the skin and the ionocytes in the gills of the teleost Cichlasoma biocellatum

Summary Adult Cichlasoma biocellatum were kept in deionized water, 25% sea-water and tap-water. The mucous cells in the epithelium of the gills and the buccal floor were not affected by the osmotic experiments. In animals kept in deionized water the mucous cells in the skin remained unaffected, but the ionocytes (chloride cells) in the gills were strongly stimulated. Keeping the animals in salt water led to a strong regression of the epidermis including the mucous cells, and of the ionocytes. The regression could be counteracted by prolactin injections. The changes in the skin and the ionocytes could be correlated with the activity of the prolactin producing cells in the adenohypophysis. It is suggested that the epidermis and its mucous cells as well as the ionocytes are under prolactin control.The authors gratefully acknowledge the interest and helpful suggestions of Prof. Dr. P. G. W. J. van Oordt. Thanks are also due to Mr. H. van Kooten for making the photographs, to Dr. L. Boomgaart for correcting the english, and to the N. I. H., Bethesda, Maryland (U.S.A.) for presenting the ovine prolactin.     

高寒草甸退化对鹅绒委陵菜克隆生长特征的影响

为了揭示高寒草甸典型匍匐茎克隆植物对不同生境的生态适应对策,验证生境适应假说,并为高寒草地的退化演替机理研究提供依据,以调查统计和比较样地法研究了江河源区高寒草甸退化对鹅绒委陵菜克隆生长特征的影响。研究表明,重度退化草甸的植物群落结构、功能以及土壤特征发生了明显的变化,继而对鹅绒委陵菜无性系的克隆生长行为和形态特性产生了影响。高寒草甸退化后鹅绒委陵菜的匍匐茎增多,分支强度加大。退化草甸内鹅绒委陵菜的基株高度小于未退化草甸,根长大于未退化草甸,基株的叶片数目问没有明显差别。退化草甸的分株高度显著小于未退化草甸,而分株叶数大于未退化草甸,根长小于未退化革甸且差异不显著。未退化草甸内鹅绒委陵菜无性系的问隔子长度、粗度和匍匐茎长度大于退化草甸,间隔子平均数目少于退化草甸,差异都不显著。随着鹅绒委陵菜无性系匍匐茎数目的增加,不论重度退化草甸与未退化草甸,用于鹅绒委陵菜克隆繁殖的能量投资也逐渐增加。鹅绒委陵菜在未退化草甸用于克隆繁殖的能量投资比例高于退化草甸,其中未退化草甸内鹅绒委陵菜基株的干重占无性系总生物量的比例略低于退化草甸,分株和匍匐茎的干重占无性系总生物量的比例高于退化草甸。高寒草甸退化对鹅绒委陵菜克隆生长特征的这些影响,与植物群落结构和功能的变化导致生境变异密切相关,是其对高寒草甸退化导致的资源和生境差异的反应,也是对资源利用达到的最合理状态,是一种选择适应的结果,有利于克隆繁殖潜力的发挥。同时为生境适应假说提供了又一例证。     

以礼草属的地理分布

根据植物类群的地理分布与系统发育相统一的原理,本文讨论了以礼草属的分布中心、起源地、 起源时间和现代分布格局的形成。以礼草属全世界约26种、6变种,隶属于3个组,主要分布于中国,哈萨克斯坦、吉尔吉斯斯坦、塔吉克斯坦、阿富汗和伊朗也有分布。其中,中国的青藏高原汇聚了该属的大多数种类,且不同等级和演化水平的类群均集居于此,使其成为该属的现代分布中心;而该属的原始类群、以及与原始类群很近缘的鹅观草属却分布在这一中心之外的天山地区,加之天山地区自新生代的晚第三纪再次抬升以来,具备了以礼草属发生和繁衍的自然条件,因而天山地区很可能就是该属的起源地,起源时间也可能在晚第三纪或第四纪初。以礼草属自天山起源后,扩散的途径大概有3条,其中西南向途径和东南向途径从东、西两侧侵入青藏高原,在青藏高原得到极度发展,并随着高原的继续隆起,进一步衍生出最高级的类群短穗组,从而形成了以礼草属现今的分布格局。     

Influence of light and darkness on the hypothalamo-hypophysial system of Rana temporaria L.

Summary The influence of a long daily photoperiod and continuous darkness was studied on the hypothalamo-hypophysial system of Rana temporaria. After six weeks of treatment (December-January 1968/1969) the secretory activity of the hypothalamo-hypophysial system of the light-treated animals was enhanced.The amount of aldehyde-fuchsin positive material in the preoptic nucleus increased as a result of the light treatment, and decreased in the median eminence, whereas in the posterior lobe no difference could be observed between the light- and dark-treated animals.The karyometric results showed an increase of the nuclear volume of the cells of the preoptic nucleus after light treatment; small differences were noticed between distinct areas of the preoptic nucleus.Autoradiographic data especially showed that light influenced the hypothalamo-hypophysial system to a high degree. Half an hour after the injection of ³⁵S-cysteine, the incorporation of the isotope in the preoptic nucleus of the light-treated animals was five times as much as in the dark-treated animals. In the median eminence and in the posterior lobe, the autoradiographic results confirmed the results found with regard to the amount of aldehyde-fuchsin positive material. Labelled material is released only from the median eminence and not from the posterior lobe.The author is indebted to Prof. Dr. J. C. van de Kamer and Dr. F. C. G. van de Veerdonk for their interest and helpful encouragement. Thanks are also due to Ir. J. J. Bezem for his assistance in solving the statistical problems and to Mr. H. van Kooten and his staff for making the illustrations. The co-operation of the student Mr. E. Schenk is gratefully acknowledged. Dr. L. Boomgaart was so kind to check and amend the English writing.     

Sublingual structures in primates. Part 1: Prosimiae, Platyrrhini and Cercopithecinae

1. The sublingual structures of primates have been studied light-microscopically. There are 3 different sublingual structures in the species studied. The plica sublingualis occurs in all primates. The sublingual organ is a topographically modified plica sublingualis which occurs exclusively in Callicebus. A sublingua is present only in the prosimians. 2. The plica sublingualis contains the excretory ducts of the submandibular and sublingual salivary glands. The sublingua is ventrally adherent to the body of the tongue and is, with a few exceptions in Tupaia, characterized by a skeleton of cartilage tissue. A sublingua never exhibits excretory ducts or salivary glands. 3. In some Platyrrhini (Ateles, Aotus, Lagothrix, Alouatta, Callicebus), there are taste buds in the epithelium of the plica sublingualis. They are especially concentrated near the orifices of the salivary glands. 4. The fresh saliva of the submandibular and sublingual gland can be tested by the taste buds on the plica sublingualis, because there is a topographical coincidence. 5. There is a complete absence of taste buds at the plica sublingualis of the prosimians and the Cercopithecinae. 6. There are no taste buds in the epithelium of the sublingua. In the Lorisiformes and in the Lemuriformes the sublingua is a cleaning device of the anterior dentition, most probably in connection with a tactile sensibility. In the Tupaiformes and in the Tarsiiformes the sublingua is less developed. 7. There is no anatomical connection between the skeleton of cartilage tissue in the sublingua and the lytta, or the skeleton of the hyoideum. 8. In some Cercopithecinae (Macaca, Papio) a glandula apicis linguae is present.     

扬子鳄皮肤腺结构与发育的初步观察

扬子鳄有三种皮肤腺:背腺、泄殖腔麝腺和下颌腺。背腺位于背中线左右两侧第二行鳞片下方,其确切位置个体间差异很大,如表1。幼鳄背腺形态多种多样,但显示出是一种退化器官,未观察到腺开口,也未观察到半成鳄和成鳄的背腺,因此扬子鳄背腺可能不具功能。泄殖腔麝腺位于泄殖腔腹唇内,梨形,腺管开口于泄殖腔腹壁,成体腺腔很大,腺的底部壁较厚,腺细胞明显地分成若干小叶,其它部位壁较薄,小叶不明显,属全泌腺,分泌油脂物,繁殖期特别发达,但性未成熟个体亦具功能,是一种信息素下颌腺位于下颌后方两侧皮肤内,圆柱状,脉管开口于下颌腹侧皮肤表面,成体腺腔不规则,腺壁厚,从包囊到腺腔,腺细胞可明显地分成三个区,属全泌腺,分泌油脂物,在繁殖期特别发达,此腺到性成熟才具功能。