群落结构复杂性的测度方法研究进展

该文对群落结构复杂性的测度方法的研究进展状况进行了综述。根据测度方法建立的方法基础,将现有的方法分成3类:基于多样性的复杂性测度、基于计算复杂性的测度和基于几何学特征的复杂性测度。对每类测度方法进行了介绍,对其优缺点进行了评述。同时提出了未来研究中应给予重视的问题。结果表明,现有群落结构复杂性的测度方法普遍存在区分能力差的问题,对于基于多样性的结构复杂性测度,目前还缺乏确定各测度属性权重的客观方法;现有的一些基于计算复杂性的结构测度与多样性指标关系过于密切,还不完善,同时其生态学的意义还不明确,而另一些计算复杂性指标还缺乏实际检验。今后,如何建立既具有区分力、又与多样性在概念和数值上都有一定区别的群落结构的计算复杂性的测度方法、如何科学合理地确定复杂性测度中的属性权重以及如何建立结构复杂性的测度和功能过程之间的联系等都是需要深入和系统研究的。由于方法的相似性,有关群落结构复杂性的测度方法也可以应用到其它尺度上的结构复杂性的研究中。     

土地生态系统的复杂性研究

运用复杂科学理论,阐述了土地生态系统的复杂性特征,包括多层次性,高维性,子系统关联的复杂性,结构与功能的不确定性,开放性,动态性,自适应性和自组织性等复杂性特征,并进一步探讨了分形,混沌及人工神经网络在土地生态系统复杂性特征研究中的应用。     

佛坪自然保护区植物群落物种多样性和复杂性的海拔格局研究

通过样地调查,利用多样性和复杂性指数分别研究了佛坪国家自然保护区植物群落物种多样性、复杂性沿海拔的变化规律,并对比分析了复杂性与物种多样性之间的关系.结果表明:(1)随着海拔升高,群落结构总复杂性与物种多样性表现出相似的变化规律,均呈现出“低-高-低”的偏正态分布格局,且海拔1 300～1 500 m是植物群落总复杂性和多样性最大区域;植物群落无序结构复杂性与总复杂性沿海拔变化规律相似,而群落有序结构复杂性却没有随海拔升高呈规律性变化.(2)研究区域植物群落物种多样性不仅与海拔变化有关,还与巴山木竹(Bashania fargesii)、秦岭箭竹(Fargesia qinlingensis)分布密度有着密切关系;在2个竹林交汇区域,物种多样性及物种数量都有着明显升高.(3)群落总复杂性、无序结构复杂性分别与多样性各个指数具有极显著的线性关系,物种多样的变化能够完全表达植物群落总复杂性的变化,但植物群落有序结构复杂性与物种多样性之间无显著相关性.因此,物种多样性不能用作植物群落结构复杂性测度方法.     

基于Huffman编码的群落结构复杂性

Anand和Orlóci (1996)提出用Huffman编码的平均码长来衡量群落结构总复杂性,用12阶Rényi熵测度群落无序结构复杂性,用两者之差测度群落有序结构复杂性。这是一种与基于生物多样性的复杂性测度完全不同,至少在思路上不同的结构复杂性测度,但对于这种测度的性质研究还不多。该文模拟建立了具有代表性的各种结构的群落400多万个,计算了这些群落的复杂性测度,对其性质进行了研究。结果表明:1)群落结构总复杂性、无序结构复杂性和有序结构复杂性受群落多样性、变异程度、优势种组成等影响。其中,群落结构总复杂性与Shannon-Wiener指数高度相关(决定系数>0.99),完全可由群落组成的多样性决定。群落无序结构复杂性与群落优势种对数比例或变异系数关系最大,与群落优势种对数比例之间的决定系数>0.99。2)该群落有序结构复杂性可表示为群落生物多样性和优势种对数比例的线性组合。在生态意义上可看作主要由群落中非优势种的组成比例决定,而组成多样性能解释41%~46%的群落有序结构复杂性。3)群落组成物种总数的增加会导致群落复杂性的测度有所增加,但没有像文献(Anand & Orlóci,1996)中描述的那么大,且组成总数对结构复杂性与多样性和优势种的关系等没有影响。     

岷江干旱河谷植物群落的复杂性

通过对岷江干旱河谷植被及环境因子的系统取样调查,研究了该地区植物群落复杂性及其与环境因子的关系,探讨了群落复杂性与多样性、均匀度、物种丰富度之间的关系.随着海拔的增加,群落总复杂性和结构复杂性均表现为“高-低-高”的变化趋势,表明高海拔和低海拔段有较高的复杂性,中海拔段复杂性较低;位于干旱河谷核心区的样带3、4较北部过渡区样带1、2和南部过渡区样带5、6有着较低的群落总复杂性;不同坡位、坡形及坡向,群落总复杂性和结构复杂性,均表现为上坡位＞下坡位＞中坡位,凹坡＞平破＞凸坡,阴坡＞半阴半阳坡＞阳坡.华帚菊-小黄素馨灌丛的总复杂性最高,西南野丁香灌丛、驼绒藜灌丛的总复杂性最低,橿子栎灌丛和群小花滇紫草灌丛的结构复杂性较高; 群落总复杂性与有机质、全N、土壤含水量、水解N、速效K呈现出显著的二次曲线关系,与全K、全P、速效P、pH值没有明显的相关关系.总复杂性与多样性、均匀度、物种丰富度的关系密切,均呈现显著的线性正相关关系.均匀度和结构复杂性呈现极显著的线性负相关,表明结构复杂性随均匀度的增加而减小.作为群落总复杂性与多样性的区分,结构复杂性对群落内物种数的变化较为敏感,不仅与均匀度有关,还与群落物种数量有关.结构复杂性和多样性作为群落总复杂性的两个组成部分,对总复杂性的影响随着研究区域和群落的不同而不同.     

分区算法复杂性在精神分裂症EEG信号分析中的应用

本文讨论了用Ｋｏｌｍｏｇｏｒｏｖ复杂性和复杂性Ｃ１,Ｃ２来分析精神分裂症脑电时间序列存在的问题,提出了新的分区算法复杂性进行改进,并用临床实验证明,结果使分辨率有了很大的提高。     

系统生物学

分析了生命复杂性问题的产生及其由来,从复杂性问题研究的角度对系统科学与系统生物学的含义及其相互关系进行了深入的讨论。     

生物复杂性研究动态

生物复杂性（biocomplexity或biological complexity）是近年来由Rita Colwell等人积极倡导的一个新的学科领域,旨在更好地了解生命系统及其环境组分间的相互作用以及系统复杂性的动态特征与演化机制,目前,生物复杂性的定义与内涵尚不明确,意见纷呈,而有关研究在美国国家科学基金会（NSF）的支持下已迅速开展起来,并即将成为国际合作研究的热点之一。本文简要介绍了有关生物复杂性的不同观点、生物复杂性与生物多样性研究之间的关系,并以若干生态系统和基因组为例,说明了现阶段生物复杂性研究的主要特点。     

基于土壤食物网的生态系统复杂性-稳定性关系研究进展

复杂性-稳定性关系是生态学核心问题之一。作为模式食物网,土壤食物网在探索生态系统复杂性-稳定性关系中起了极大的作用。总结了以Moore、de Ruiter、Neutel等为代表的理论生态学家以土壤食物网为工具研究生态系统复杂性-稳定性关系的方法、结论及不足之处,并展望了未来的发展方向。Moore、de Ruiter、Neutel等将土壤食物网功能群生物量数据、土壤食物网Lotka-Volterra模型和面向过程模型三者结合起来,描述相互作用强度大小格局、分室、能流组织形式等复杂性特征;将土壤食物网Lotka-Volterra模型与群落矩阵结合起来分析局域稳定性,进而探讨生态系统复杂性-稳定性关系的一般规律。在此基础上,Moore、de Ruiter、Neutel等证明了与随机食物网相比,真实食物网的相互作用强度格局、分室等复杂性特征提高了生态系统稳定性,生产力与稳定性共同决定了食物链的长度,并指出建立在平衡态基础上的静态土壤食物网模型在探索生态系统复杂性-稳定性关系方面具有较大的不足,动态土壤食物网是未来以土壤食物网为工具研究生态系统复杂性-稳定性关系的发展方向。     

10种鸣禽控制鸣啭神经核团大小与鸣唱复杂性的相关性

为进一步揭示鸣禽鸣唱行为的神经生物学机制 ,本实验先对 8个科 10种鸣禽的鸣唱行为进行了观察和录音 ,并借助声谱软件分析了每种鸣禽的鸣唱复杂性。鸣唱语句复杂性的评价指标包括 :短语总数、每个短语中所含的平均音节数及音节种类数、所有短语的总音节数及音节种类数、最长短语的音节数及音节种类数。然后 ,测定了前脑三个鸣啭学习控制核团和一个与发声无关的视觉参考核团体积 ,分析了鸣唱语句复杂性和这些核团大小间的相关关系。结果表明 :1)HVC和HVC/Rt与 7种鸣唱语句复杂性指标无关 ;RA和RA/Rt与总音节种类数相关 ;AreaX与总音节数及音节种类数相关 ;2 )HVC/RA和HVC/X比值与多个鸣唱语句复杂性指标相关。结果提示 :鸣禽鸣唱复杂性不同特征可能受不同神经控制     

国家大型煤电基地生态环境监测技术体系研究——以内蒙古锡林郭勒盟煤电基地为例

随着我国煤电基地建设进程的不断加快,煤电基地建设与开发活动引起的环境问题也日趋严重。了解生态环境质量现状,评估其对生态系统与人民健康水平的影响,制定合理的保护、治理、恢复策略是煤电基地环境保护工作的重中之重,而生态环境监测是解决上述问题的基础。然而,现有的监测技术体系普遍存在自动化水平较低、成本较高、时空覆盖面较低等问题。鉴于物联网技术在提高信息采集效率和改善信息获取方式方面的作用日益显著,所以将物联网技术应用于煤电基地生态环境监测,从感知层、传输层、支撑层、应用层、用户层的角度明确生态环境监测技术体系,为解决上述问题提供有效途径。     

略论棕榈科与新分出的省藤科的系统分类、演化、区系地理及主要的经济用途

棕榈科原省藤亚科因其子房壁及外果皮被倒生、螺旋状排列的鳞片所覆盖,而区别于其他亚科,因而独立分出成一新科--省藤科。作者讨论了棕榈科的祖先种可能在石炭纪时,自原始裸子植物开以顿目在分化、衍生出苏铁目祖先种的进化干上,于白垩纪时分化出的一个分支。在棕榈科的祖先种出现不久后,在其进化的分支上,于白垩纪后期又分化出一旁支,成为棕榈科的姊妹科--省藤科的祖先种。从两祖先种分别再分化、衍生出现今分布地球上该二科的属与种。两科、尤其前者是被子植物、尤其是单子叶植物中最原始的类群之一。作者还提出棕榈科象牙椰亚科与贝叶棕亚科是该科最原始或较原始的两类群;槟榔亚科和腊材榈亚科是较进化的两类群;而水椰亚科祖先种可能源于象牙椰亚科的祖先种,但又演化为该科最进化与特化的类群。省藤科省藤亚科略比鳞果榈亚科原始。作者讨论了两科为泛热带分布的科,指出两科的"现代分布区"在南北两半球热带地区,少数种还延伸分布到两半球暖亚热带、甚至达中亚热带地区,分布区边缘最北达日本中部、中国长江流域及黄河下游的南部,美国加利佛尼亚州与佛罗里达州和地中海北部;最南达智利中部和新西兰南部;而"现代分布中心"在热带与暖亚热带的亚洲,中、南美洲,大洋洲及非洲的东、南、西部;但分布区的"密集中心"则在热带亚洲、热带中及南美洲、南太平洋群岛及非洲东南部。作者还介绍了近50年我国南方引种驯化成功的两科植物近400种(见^*图谱),其中少数为耐寒的种类,有的种已引种到长江流域或更北的地区。引种的大部分种都有其重要的经济用途,包括:1. 食用,如淀粉和树液可制"西米"或制糖,酿酒、醋或作饮料;果或种子榨油,供食用或工业用;某些种的嫩芽作蔬菜,甚至种子代咖啡饮用;2. 药用,有消炎、止血、活血、驱虫、抗癌等用;3. 建筑、工艺与日用品,包括不少种的树干供建普通房子、桥梁、小船;少数种可提制工业用蜡;许多种的纤维制高级缆绳和编织品;还制工艺品与日用品等;4. 代表热带景观的园林工程、绿化及美化环境的观赏树和人行道树及建造园林景观生态类型的树种等。     

山水林田湖草沙一体化保护和修复工程综合成效评估技术框架

我国实施了诸多生态保护修复工程,取得了显著成效。然而,以往工程多以湿地、森林、草原等单一类型的生态系统为保护修复目标,缺乏区域整体性、系统性考虑。2016年以来,我国开始从完整流域的视角出发,系统考虑生态系统完整性、自然地理单元连续性和社会经济可持续性,实施山水林田湖草沙一体化保护和修复工程。该类工程保护修复目标多样、内容庞杂,因而成效评估面临子项目类型多、空间尺度多、目标维度多、项目实施周期短等诸多挑战。就空间尺度而言,评估对象既要涵盖常规评估中相对较大的、确定的空间范围,也要涵盖具有相对类似生态问题或目标的保护修复单元,以及实际采取措施的子项目;就时间尺度而言,既要考虑工程实施结束时的成效,也要考虑实施结束后的成效动态;就评估内容而言,既要关注社会、生态、经济效益,也要考察工程措施与生态效应之间的关系、不同类型子项目的关联性与协同性、工程的整体性与系统性。研究基于上述背景制定了一个新型评估框架,重点强调基于子项目、保护修复单元以及工程范围三个尺度的指标体系,以及生态、社会、经济、管理四个方面的评估内容。新的评估框架将有助于完善山水林田湖草沙一体化保护和修复工程标准体系,为推进国土空...     

黄土高原小叶杨与其他树种枯落叶混合分解对土壤性质的影响

将小叶杨分别与其他11个树种枯落叶粉碎混合后进行室内分解培养,分析不同树种枯落叶混合分解对土壤性质的影响及其相互作用.结果表明:12个树种枯落叶单独混土分解均明显提高了土壤脲酶、脱氢酶、磷酸酶活性和有机质、碱解N含量,但对土壤速效P含量和土壤阳离子交换量(CEC)的影响差异较大,其中柠条和紫穗槐枯落叶改善土壤性质的效果明显.小叶杨分别与油松、侧柏、刺槐、白榆枯落叶混合分解,对土壤微生物数量的影响存在相互促进作用;小叶杨分别与侧柏、柠条枯落叶混合分解对土壤有机质、速效P、速效K含量和CEC的影响存在相互促进作用,但对土壤大部分酶活性的影响却存在相互抑制作用;小叶杨与落叶松枯落叶混合分解对土壤多数酶活性和养分含量的影响存在相互促进作用,而与樟子松枯落叶混合分解时则有抑制作用.总体上,小叶杨分别与白榆、油松、落叶松和刺槐枯落叶混合分解可促进土壤性质的改善,而与侧柏、柠条、樟子松、沙棘和紫穗槐枯落叶混合分解时则相互抑制.     

Relationships Between the Bryoflora of Mt. Wuyi,SE China,and Those of Neighbouring Mountain Regions

Mt. Wuyi, located at 27°37‛-27°54‛ N, 117°27‛-117°51‛ E, is the highest mountain in South-East China. Its main peak, Huanggangshan, is 2158 m above the sea level. In 1955, P. C. Chen organized the first expedition to Mt. Wuyi, and the authors investigated the different ravines and the forests of that area in 1976 and from 1979 to 1984 respectively. Up to now 355 species of the bryophytes have been found in Mt. Wuyi. I. The influence of the factors of geological history on the bryoflora of Mt. Wuyi Fujian Province, belonging to Cathaysian, one of three Chinese ancient lands, was a part of ocean until the end of the lower Tertiary. In the early Devonian, Fujian uplifted above the sea level, but it submerged in the sea later, and then uplifted above the sea level again in the upper Triassic. By the end of the lower Triassic the Himalayan movement influenced the paleogeography of China deeply, and the eastern and central mountains of Fujian uplifted again. In the Tertiary, Fujian was influenced by the hot maritime weather, so the tropical evergreen forests existed in southern Fujian at that time. The conclusion was made by Z. B. Zhao in 1983 after his long period of study on geological history of Fujian Province since the Yanshan movement. According to the morden geographical distribution of Chinese bryophytes, it seems that the above influence might be related to the bryophytes of Mt. Wuyi and also the southern part of Zhejian Province. By the end of the Tertiary the weather became cold in most parts of China. Since then the cold weather and hot weather alternated several times. One kind of the endemic elements of the bryoflora formed in the area from the south-eastern coast of China to the southeastern Xizang (Tibet), including Japan. They are not specialized at the family level or closely related to each other, but they have similar distribution and belong to different families. In the Quaternary, Mt. Wuyi gradually uplifted following the Himalayan movement. As the weather cooled down in the upper part of the mountain, deciduous broad-leaved and needleleaved trees increased there. Meanwhile, temperate genera and species of the bryophytes spread and invaded South China and entered Mr. Wuyi. Rhytidiadelphus and Hvlocomium probably began to grow in Mt. Wuyi at that time, and their distribution is quite different from their primary one. On the other hand, a part of tropical and subtropical bryophytes might enjoy the changed weather and environment in the Quaternary and existed in a few small localities of Mt. Wuyi, and the genera Haplomitrium, Endotrichella and Floribundaria are probably their representatives. From the point of view of geological history we are now living in the interglacial period and the present natural conditions will last continuously, so they will steadily influence the bryoflora of Mt. Wuyi in a long period of time. 2. Essential characteristics of the bryoflora in Mt. Wuyi Due to the geographical position and the other factors of Mt. Wuyi the bryoflora is represented by numerous tropical and subtropical elements (34.1%), but the East-Asiatic endemic ones (79.2%) are characteristic of the bryoflora in Mt. Wuyi (Tab. 1). The tropical and subtropical families of the bryophytes, found south of Changjiang (Yangtzi) River, are Haplomitriaceae (1 genus, 3 species), Porellaceae (2 genera, 8 species), Frullaniaceae (2 genera, 10 species), Lejeun eaceae (21 genera, 35 species), Trachypodaceae (3 genera, 4 species), Meteoriaceae (10 genera, 17 species), Neckeraceae (5 genera, 8 species) and Hookeriaceae (3 genera, 3 species). The above 8 families, including 46 genera and 85 species, represent about 1/4 genera (24.3%) and less than 1/4 species (23.9%) of the bryoflora of Mt. Wuyi. Most species of East-Asiatic elements show very close relationships with Japan, and are widely distributed from the low altitude of Mt. Wuyi to the summit of Mt. Huanggangshan. However, the Holarctic species (26.8%) are also important elements of the bryoflora in Mt. Wuyi, showing its transition nature, although it is located in the subtropics. Moreover, the in fluence of the Himalayas also exists in Mt. Wuyi, and the Himalayan elements cover 14.4% in the bryoflora of Mt. Wuyi. The similarity coefficients between the bryofloras of Central and South America, Africa and Oceania and that of Mt. Wuyi are from 5.0-9.2% respectively. The endemic species are not very many and cosmopolitan species are only 7 there. In 1958, P. C. Chen designated Mt. Wuyi as “the transition region of South and North China rich in East-Asiatic genera and species”. His very important conclusion is essentially in accordance with the fact of the bryoflora on Mt. Wuyi. Recently, some of the new records fur ther show the characteristics of the bryoflora in Wuyi. Two facts are worth being mentioned. One is that East-Asiatic genera are only five in Mt. Wuyi. However, there are 9 East-Asiatic genera in Mt. Huangshan more than in Mt. Wuyi; 4 East-Asiatic genera are recorded in Mt. Shennongjia. The other is that epiphyllous liverworts in Mt. Wuyi, consisting of 7 families, 21 genera and 36 species, are less than on Hainan Island and Xishuangbannan, located in the tro pics in China. 3. Comparison between the bryoflora of Mt. Wuyi and those of the neighbouring regions As China covers a very large area, bryofloristic elements are quite different in the diffe rent regions. In this section, we are concentrated on making a comparison between the bryof loras of Mt. Wuyi and the regions belonging to the Central China of the bryoflora named by P. C. Chen. Huaping Forest Region, Guangxi Zhuang Autonomous Region in South China, with both latitute and altitude very similar to Mt. Wuyi, is included in this comparison (Fig. 1). According to the rough estimation, the similarity coefficient of moss genera between Mt. Wuyi and Huaping is 56.3%, and those between the mountain and southern Zhejian and Mt. Huangshan, Anhui, are 62.7% and 51.6% respectively, while the similarity coefficient of the genera of the mossfloras between Mt. Shennongjia and Mt. Wuyi is 46.8%. Table 2 shows the statistics of mosses in Mt. Wuyi and the others, but the bryoflora of Huaping needs further study However, it is very interesting to note that Haplomitrium and Pleurozia of liverworts are both found in Mt. Wuyi and Huaping Forest Region, and the similarity coefficient between the mossfloras of Mt. Wuyi and Zhejian Province is also higher than those mentioned above. Tropical and subtropical elements reduce towards the north in China, and temperate ones increase. Huaping is located in the south, and, as expected, some tropical and subtropical genera such as Hookeriopsis and Symphyodon have been found there, but not in Mt. Wuyi; several temperate genera, such as Schwetschkeopsis and Fauriella, have been recorded in Mt. Huangshan, but not in Mt. Wuyi. For some unknown reasons, Octoblepharum and Neckeropsis are only found in southern Zhejiang, but not in Mt. Wuyi. Mt. Shennongjia, with its main peak over 1000 m higher than that of Mt. Wuyi, is located in its northwest, and more than ten temperate genera, such as, Ceratodon, Aulacomnium Myurella, Bryonoguchia and Abietinella have been found there. Generally, Mt. Wuyi belongs to the central subtropical region of China, and East-Asiatic endemic genera are the main elements of its bryoflora, but the bryoflora also consists of tropical and subtropical elements with some temperate ones. 4. East-Asiatic endemic genera in the bryoflora of Mt. Wuyi In the bryoflora of Mt. Wuyi, one of the main elements, East-Asiatic endemic genera, should not be neglected (Tab. 4). East-Asiatic endemic genera in Mt. Wuyi (five) are less than in Mt. Huangshan and Mt. West Tianmu, although the positions of the latter two are very close to Mt. Wuyi. East-Asiatic endemic genera of liverworts are Trichocolea and Macvicaria so far found in Mt. Wuyi, and the mosses are Myuriopsis, Meteoriella, Pseudospiridentopsis (Fig. 1). Myuriopsis is only distributed in Taiwan Province and Mt. Wuyi, and the other four are distributed in Mt. Huangshan or Mt. West Tianmu, and also in Taiwan, besides in Mt. Wuyi. About thirty EastAsiatic endemic genera have so far been known in China, which means that about one sixth of East- Asiatic endemic genera of the bryophytes occur in Mt. Wuyi. We may notice that nine and seven East-Asiatic endemic genera of the bryophytes have been recorded in Mt. Huangshan and Mt. West Tianmu respectively. In Mt. Shennongjia, Central China, there are four East Asiatic endemic genera, but only two have been found in the Huaping Forest Region, South China. In Mt. Dinghua, located south of Mt. Wuyi, on East-Asiatic endemic genus of the bryophytes has so far been found. East-Asiatic endemic genera of the bryophytes are mainly limited to China, Korea and Japan, including the East Himalayas, rarely occur in South Asia, Siberia of the Soviet Union. Therefore, these genera enjoy a warm and moist environment. In Mt. Wuyi, all the East-Asiatic endemic genera are monotypic ones with a disjunct distribution. Now in Taiwan Province five of six recorded East-Asiatic endemic genera are common to Mt. Wuyi. In Japan, about eleven, i.e. one third of, East Asiatic endemic genera so far found are common to China, which shows a long history of the phytogeographical relationships between Japan and China. East Asiatic endemic genera of the bryophytes might therefore exist on islands of Taiwan Province and Japan before they were separated from the mainland of Asia. However the fossil evidence is still lacking in the bryophytes, so we are not able to discuss about the distribution area and the distribution center of the East-Asiatic bryoflora in detail. The above estimation is more or less related to geological history, and we assume that the East-Asiatic endemic genera have existed at least since the end of the Tertiary. Starting from the Quaternary, the climatic change during glacial epoch has been possibly the most important factor affecting the bryoflora in Asia, and the upheaval of the Himalayas has stimulated the diversity and the specialization of the bryophy tes. Considering these factors, East-Asiatic endemic genera might be the “Tertiary fossil plants”. Another problem is difficult to explain, because Mts. Huangshan, West Tianmu and Shen nongjia were once influenced by glaciation directly, although Chinese geologists hold different views. However, no evidence of glaciation has been found in Mt. Wuyi. It is worth to study the close relationships between Mt. Wuyi, Mt. Huangshan and Mt. West Tianmu, where is the distri bution center of the East-Asiatic endemic genera. The above three mountain regions share half of the East-Asiatic endemic genera, and about 32% genera of the others are found in two of them (Fig. 2). Myuriopsis, one of the East Asiatic types, was only recorded in Taiwan Pro vince, Japan and Korea. Neodolichomitra, occuring in Taiwan Province, is endemic to China. More or less the differentiation has taken place in Mt. Huangshan, Mt. West Tianmu and Mt. Wuyi. The number of the East-Asiatic endemic genera is smaller in Mt. Wuyi, so it is possibly located on the border of the distributional center of the East-Asiatic endemic genera. Moreo ver, three of four East-Asiatic endemic genera in Mt. Shennongjia are also found in Mt. Huang shan and Mt. West Tianmu, but the other East-Asiatic genus in Mt. Wuyi is common to the mountain areas in SW China, the Qinglin Range of NW China, and the isolated mountain areas of NE China. Considering all the characteristics of the bryoflora of Mt. Shennongjia, we assume that Mt. Shennongjia may belong to another distribution center, including SW part of Sichuan Province, and the other neighbouring mountains.     

Pediatric stress: hormonal mediators and human development

Stress activates the central and peripheral components of the stress system, i.e., the hypothalamic-pituitary-adrenal (HPA) axis and the arousal/sympathetic system. The principal effectors of the stress system are corticotropin-releasing hormone (CRH), arginine vasopressin, the proopiomelanocortin-derived peptides alpha-melanocyte-stimulating hormone and beta-endorphin, the glucocorticoids, and the catecholamines norepinephrine and epinephrine. Appropriate responsiveness of the stress system to stressors is a crucial prerequisite for a sense of well-being, adequate performance of tasks and positive social interactions. By contrast, inappropriate responsiveness of the stress system may impair growth and development, and may account for a number of endocrine, metabolic, autoimmune and psychiatric disorders. The development and severity of these conditions primarily depend on the genetic vulnerability of the individual, the exposure to adverse environmental factors and the timing of the stressful event(s), given that prenatal life, infancy, childhood and adolescence are critical periods characterized by increased vulnerability to stressors. The developing brain undergoes rapid growth and is characterized by high turnover of neuronal connections during the prenatal and early postnatal life. These processes and, hence, brain plasticity, slow down during childhood and puberty, and plateau in young adulthood. Hormonal actions in early life, and to a much lesser extent later, can be organizational, i.e., can have effects that last for long periods of time, often for the entire life of the individual. Hormones of the stress system and sex steroids have such effects, which influence the behavior and certain physiologic functions of individuals for life. Exposure of the developing brain to severe and/or prolonged stress may result in hyperactivity/hyperreactivity of the stress system, with resultant amygdala hyperfunction (fear reaction), decreased activity of the hippocampus (defective glucocorticoid-negative feedback, cognition), and the mesocorticolimbic dopaminergic system (dysthymia, novelty-seeking, addictive behaviors), hyperactivation of the HPA axis (hypercortisolism), suppression of reproductive, growth, thyroid and immune functions, and changes in pain perception. These changes may be accompanied by abnormal childhood, adolescent and adult behaviors, including excessive fear ('inhibited child syndrome') and addictive behaviors, dysthymia and/or depression, and gradual development of components of the metabolic syndrome X, including visceral obesity and essential hypertension. Prenatal stress exerted during the period of sexual differentiation may be accompanied by impairment of this process with behavioral and/or somatic sequelae. The vulnerability of individuals to develop varying degrees and/or components of the above life-long syndrome is defined by as yet unidentified genetic factors, which account for up to 60% of the variance. CRH has marked kindling and glucocorticoids have strong consolidating properties, hence both of these hormones are crucial in development and can alone produce the above syndrome. CRH and glucocorticoids may act in synergy, as in acoustic startle, while glucocorticoids may suppress or stimulate CRH, as in the hypothalamus and amygdala, respectively. A CRH type 1 receptor antagonist, antalarmin, inhibits both the development and expression of conditioned fear in rats, and has anxiolytic properties in monkeys. Profound stressors, such as those from sexual abuse, may elicit the syndrome in older children, adolescents and adults. Most frequently, chronic dysthymia and/or depression may develop in association with gastrointestinal complaints and/or the premenstrual tension syndrome. A lesser proportion of individuals may develop the classic posttraumatic stress disorder, which is characterized by hypocortisolism and intrusive and avoidance symptoms; in younger individuals it may present as dissociative personality disorder.     

Biomimetic nanosystems and novel composite nanobiomaterials

Biophysicochemical approaches to the solution of nanotechnology problems associated with the design of functional biomimetic nanosystems, hybrid and composite nanobiomaterials and study of their structure-function relationships. The results of studies concerned with physicochemical mechanisms of the formation of organized biomimetic nanostructures and bioinorganic nanomaterials in systems involving a bulky liquid phase and the interface (gas-liquid, solid-liquid, liquid-liquid)during the synthesis and structure formation with the participation of the components of colloid systems, inorganic nanoparticles of various composition and clusters of metals, surfactants, polyelectrolytes and their complexes are discussed. In the development of the methods for the formation of composite bioinorganic nanosystems containing inorganic nanocomponents, two major approaches were used: adsorption and incorporation into the biomolecular matrix or colloid system of presynthesized inorganic nanoparticles, as well as the synthesis of the inorganic nanophase immediately in the biomolecular system. The methods of obtaining biomaterials and nanosystems are based on the principles of biomimetics, biomineralization, self-assembly and self-organization, combination and integration of a number of synthetic and physicochemical methods (physical and chemical adsorption, Langmuir technique, the formation of polycomplexes, chemical linking, competitive interactions, and substitution of ligands in supramolecular and coordination complexes) and nanocomponents of different nature. In particular, a novel approach to the preparation of highly organized nanofilm materials was developed, which is based on the effect of self-assembly and self-organization of colloid nanoparticles during the formation of their complexes with polyfunctional biogenic ligands in the volume of the liquid phase in the absence of any surfaces and interfaces. The physical and chemical factors responsible for the formation of structurally ordered biomolecular and composite nanosystems including nano-sized components of different nature and the possibilities to control the composition, structure, and properties of resulting nanomaterials and nanosystems are discussed. The experimental methods and approaches developed may be useful in studies of structure-property relationships and basic mechanisms of structural organization and transformation at the nanoscales level in biological, artificial, and hybrid nanosystems. The problems of practical application of the synthetic methods and the corresponding nanomaterials are discussed.     

不同生态地理区域杉木人工林土壤微生物及生化活性的研究

 本文研究了广西龙胜县里骆林区、宜山县庆远林区、岑溪县七坪林区和田林县老山林区四种不同生态地理区域杉木人工林土壤微生物及其生化活性。研究结果表明：1．土壤微生物的总数及各类群数量均以龙胜县里骆林区和田林县老山林区杉木人工林土壤最高,岑溪县七坪林区次之,宜山县庆远林区最低。2．土壤生化活性包括土壤氮的转化强度,土壤碳的氧化代谢能力和土壤酶活性,也均以龙胜县里骆林区和田林县老山林区杉木人工林土壤最强,岑溪县七坪林区次之,宜山县庆远林区最弱。3．四种不同生态地理区域杉木人工林生长状况与土壤微生物的数量分布和生化活性表现相似规律,龙胜县里骆林区和田林县老山林区杉木人工林林木生长最好,岑溪县七坪林区次之,宜山县庆远林区最差。     

Phylogenetic analysis of Adephaga (Coleoptera) based on characters of the larval head

Abstract. Characters of the head of adephagan larvae were examined and analysed phylogenetically. A labrum which is completely fused to the clypeofrons and the presence of a closed prepharyngeal tube are autapomorphies of Adephaga. Partial reduction of the fossa maxillaris, cardo and stipes forming a functional unit, the immobilization of the lacinia, attachment of M. craniolacinialis to the lateral stipital wall, and loss of one stipitopalpal muscle, are considered autapomorphies of Adephaga excluding Gyrinidae. Complete reduction of the fossa maxillaris and the presence of M. craniostipitalis medialis are possible autapomorphies of Adephaga excluding Gyrinidae and Haliplidae. The presence of caudal tentorial arms, insertion of the galea on the mesal side of palpomere I, and absence of the lacinia are considered synapomorphies of Trachypachidae and Dytiscoidea (Noteridae, Amphizoidae, Hygrobiidae, Dytiscidae). The presence of a slender, elongated process of the head capsule, which articulates with a corresponding socket of the cardo, is a possible autapomorphy of Dytiscoidea. The sinuate frontal sutures, distinctly protruding prementum, shortened M. craniostipitalis medialis, and absence of M. submentopraementalis are considered autapomorphies of Geadephaga excluding Trachypachidae. The presence of a regular row of hairs along the anterior hypopharyngeal margin is a possible autapomorphy of Geadephaga excluding Trachypachidae and Rhysodidae. Improvement of the hypopharyngeal filter apparatus suggests the monophyly of Anisochaeta. Presence of a penicillum and partial reduction of the lacinia are possible autapomorphies of Anisochaeta excluding Omophronini. Larvae of Cychrini, Carabini, Nebriini and Notiophilini are characterized by a strongly developed, cone-shaped hypodon. Postocular and cervical ridges, crosswise arrangement of antennal muscles, and a completely flattened hypopharynx are considered autapomorphies of Caraboidea Limbata.