不同栖息地状态下外来种入侵及对本地种生存影响的模拟

外来种入侵引起的生态及经济问题日益严重,人类活动导致大规模栖息地持续变化的背景下,外来种的入侵过程及本地物种多样性的演化更为复杂.在Tilman多物种共存模型基础上,建立了栖息地持续变化条件下的外来种入侵干扰模式,分别模拟了栖息地不变、持续毁坏及持续恢复条件下的外来种入侵及对本地物种多样性的生态影响.模拟结果表明:(1)拓殖率小(入侵性弱)的外来种不能成功定殖,栖息地的持续变化对其没有任何影响.(2)拓殖率增大的外来种入侵过程复杂,栖息地持续毁坏导致其灭绝时间相比于栖息地不变时明显推迟,栖息地持续恢复使其灭绝提前;一定时间内持续增加栖息地可以减小此类外来种入侵危害.(3)拓殖率足够大的外来种能够成功定殖,快速定殖-扩散的入侵过程不会因栖息地毁坏而迅速改变,其响应具有时间滞后性;栖息地持续恢复也有利于其迅速蔓延,占有率呈线性疯狂增长.(4)在具有外来种入侵的本地生态系统中,栖息地持续改变(增加或减少)对本地物种多样性的发展均不利.     

入侵植物喜旱莲子草——生物学、生态学及管理

喜旱莲子草Alternanthera philoxeroides原产于南美洲,属于苋科Amaranthaceae莲子草属Alternanthera。一百多年来,该物种通过压舱水或军马饲料被传播到北美洲、大洋洲、欧洲,以及东南亚和中国等地,成为暖温带-热带湿润气候区淡水生态系统的重要外来入侵种。本文结合对喜旱莲子草在原产地的分布状况的考察、原产地和入侵地喜旱莲子草的比较研究,以及入侵生态学研究的最新成果,对该物种在原产地的地理分布和种内变异、生活史特征、入侵机制和控制策略等方面进行评述,以提高我国科研人员对这一外来入侵种的认识,为科学管理和控制提供依据。     

生物入侵机制研究进展

本文从外来种本身的生物学特性,外来种与新栖息地土著种之间的相互作用,群落生物多样性对入侵种的抵抗能力,新栖息地生态环境变化对入侵种的影响等方面综述了近年来有关生物入侵机制的研究进展,并探讨了研究方法的发展和亟待解决的问题,大量的研究表明生物入侵机制是极为多样的,可能没有一般的,通用的机制,阐明生物入侵的机制,对推动生态学理论的发展和控制有害外来种有重要意义。     

基于栖息地恢复对群落不同种群演化影响的模拟

通过建立基于栖息地恢复的多种群演化动力学模式,模拟了不同群落结构的不同物种种群的演化特点。模拟结果发现了两类灭绝机制,揭示了(1)小规模栖息地的恢复对群落中的弱小物种的影响是非常有限的,不会给弱小物种种群带来灭绝风险。大幅度的栖息地增加几乎使所有的物种种群都在最初数百年中内都有出现一定的增加,特别是竞争能力最强的物种,其幅度的增加最为显著,但次最强的物种种群可能会在千年左右灭绝。群落内幸存的种群将经历3个阶段迅速壮大(增加)阶段震荡阶段稳定阶段;(2)存在着协同现象,栖息地减少所导致种群的协同演化规律与栖息地恢复所导致的种群的演化规律两者之间既有共同点,又有不同点。毁坏是一种破坏,大规模的栖息地的恢复对已适应于破坏后新环境的某些物种也可能是一种威胁,这类似于生态入侵的初始阶段。     

破碎栖息地中物种灭绝机制

栖息地毁坏既会直接降低物种多度,又会间接地降低物种迁移繁殖力,同时还会改变原有的种间平衡.尽管已有研究表明栖息地毁坏是物种灭绝的主要原因之一,但是尚未揭示破碎的栖息地中物种灭绝的驱动机制.通过元胞自动机模拟了物种灭绝对栖息地毁坏空间异质性响应的基础上,进一步研究了栖息地毁坏和种间竞争对物种灭绝的影响.结果发现:强物种的灭绝主要来自栖息地毁坏,而弱物种的灭绝,在随机毁坏下,主要由栖息地毁坏与种间竞争共同决定,而在边缘毁坏下则主要由种间竞争所引起的.栖息地毁坏与种间竞争共同引起的物种灭绝的时间非常短,而栖息地毁坏或种间竞争所引起的物种灭绝时间则较长.     

喜旱莲子草入侵群落土壤对植物生长的影响

分别以受喜旱莲子草(Alternanthera philoxeroides)入侵和未受喜旱莲子草入侵的当地植物群落土壤为生长基质,比较不同基质上入侵植物喜旱莲子草和同属的土著植物莲子草(A.sessilis)的生长指标,探讨喜旱莲子草入侵群落土壤对喜旱莲子草及莲子草生长的影响机制。结果表明,喜旱莲子草入侵群落土壤抑制了莲子草的生长,显著降低了根生物量、茎生物量和总生物;改变了形态特征,显著降低了分枝数量、茎长度、根长、根体积;减少了对根的生物量分配,显著抑制了根质量比与根冠比。喜旱莲子草入侵群落土壤对入侵植物喜旱莲子草的生物量、分枝数量、茎长度、根长、根体积没有显著的抑制作用,而显著增加了其叶片数量和叶质量比。这种效应将有利于喜旱莲子草在入侵地形成单优群落,表明土壤在喜旱莲子草成功入侵中起了重要作用。     

互花米草入侵对鸟类的生态影响

生物入侵威胁本地物种生存,破坏生态系统的结构和功能,是导致全球生物多样性丧失的重要原因之一。外来植物是入侵生物中的重要一类,可以显著改变本地植被群落,并影响其他生物类群。鸟类作为生态系统中的较高营养级,对由入侵植物引起的栖息地变化十分敏感。互花米草自引入中国沿海以来,其分布区域不断扩散,多数研究认为互花米草入侵造成本地生物多样性降低和生态系统退化。系统梳理了互花米草入侵对鸟类栖息地、食物资源、繁殖、群落等方面的生态影响。主要负面影响有:(1)植被群落结构不利于鸟类栖息、筑巢、觅食;(2)鸟类食物资源丰度和多样性下降;(3)本地鸟类种群数量和物种多样性显著下降。在我国东部沿海湿地,互花米草入侵已经显著改变了植被与鸟类分布格局。但随着入侵历史的增长,少数小型雀形目鸟类却可以逐渐适应互花米草生境。互花米草入侵为某些非本地鸟类提供了空白生态位,在一定程度上丰富了本地物种多样性,对互花米草的快速清除反而可能不利于已适应并依赖互花米草生境的鸟类。综上,认为互花米草入侵对鸟类群落甚至整个生态系统的影响可能需要更多研究进行综合评价,应开展长期、大尺度、多因子的监测研究和多物种比较研究,建立生态评价模型并制定科学有效的互花米草管理对策。     

物种多样性对栖息地毁坏时间异质性的响应

栖息地毁坏是物种多样性丧失最重要的因素之一.通过多物种竞争共存的非自治动力模型,利用香农多样性指数,研究并比较了不同结构集合种群群落的物种多样性对不同程度和不同速度的栖息地毁坏时间异质性的响应.结果表明:在栖息地瞬间毁坏下,物种多样性先快速下降,之后得到一定程度的恢复,最终在下降中走向平衡;在栖息地持续完全毁坏下,栖息地毁坏速度对物种多样性随累积栖息地毁坏率变化的影响,只有在最强物种多度 (q)较小时比较明显,而在q较大时较小;对于栖息地持续部分毁坏,栖息地毁坏速度只影响物种多样性振荡的幅度,而不影响其变化的最终结果,并且速度越快,物种多样性振荡幅度越大,越不利于群落的稳定.     

入侵种喜旱莲子草——主要天敌昆虫

喜旱莲子草是一种水陆两栖的重要入侵杂草,中国首批16种重要入侵物种之一.本文介绍了生物防治喜旱莲子草的天敌昆虫莲草直胸跳甲Agasicles hygophila、Vogtia malli、Amynothrips andersoni、阿根廷跳甲Disonycha argentinensis、Systena nitentula和虾钳菜披龟甲Cassida piperata等天敌的分类地位、形态特征、生物学、生态学特性以及国内外寄主专一性研究、释放效果与评价.     

植物群落的生物多样性及其可入侵性关系的实验研究

 生物入侵已经成为一个普遍性的环境问题,并为许多学者所关注。尽管一些理论研究和观察表明生物多样性丰富的群落不容易受到外来种的入侵,但后来有些实验研究并没能证实两者的负相关性,多样性 可入侵性假说仍然是入侵生态学领域争论比较多的一个焦点。人为构建不同物种多样性和物种功能群多样性（C3 禾本科植物、C4植物、非禾本科草本植物和豆科植物）梯度的小尺度群落,把其它影响可入侵性的外在因子和多样性效应隔离开来,研究入侵种喜旱莲子草(Alternanthera philoxeroides)在不同群落里的入侵过程来验证多样性 可入侵性及其相关假说。研究结果显示,物种功能群丰富的群落可入侵程度较低,功能群数目相同而物种多样性不同的群落可入侵性没有显著性差异,功能群特征不同的群落也表现出可入侵性的差异,生活史周期短的单一物种群落和有着生物固氮功能的豆科植物群落可入侵程度较高,与喜旱莲子草属于同一功能群且有着相似生态位的土著种莲子草(A. sessilis)对入侵的抵抗力最强。实验结果表明,物种多样性和群落可入侵性并没有很显著的负相关,而是与物种特性基础上的物种功能群多样性呈负相关,群落中留给入侵种生态位的机会很可能是决定群落可入侵性的一个关键因子。     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

A Unique Protease Cleavage Site Predicted in the Spike Protein of the Novel Pneumonia Coronavirus (2019-nCoV) Potentially Related to Viral Transmissibility

正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases     

Curcuminoids as inhibitors of thioredoxin reductase: A receptor based pharmacophore study with distance mapping of the active site

Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.     

Comparative morphology of the carpel in the Liliaceae: Hewardieae, Petrosavieae, and Tricyrteae

The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.     

Synthesis and antimicrobial studies of hydrazone derivatives of 4-[3-(2,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid and 4-[3-(3,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid

Microbial resistance to antibiotics is an unresolved global concern, which needs urgent and coordinated action. One of the guidelines of the Centers for Disease Control and Preventions (CDC) to combat antibiotic resistance is the development of new antibiotics to treat drug-resistant bacteria. In our effort to find new antibiotics, we report the synthesis and antimicrobial studies of 30 new pyrazole derivatives. These novel molecules have been synthesized by using readily available starting materials and benign reaction conditions. Some of these molecules have shown activity with MIC values as low as 0.78?µg/mL against four bacterial strains; Staphylococcus aureus, methicillin-resistant S. aureus, Bacillus subtilis, and Acinetobacter baumannii. Furthermore, active molecules are non-toxic to mammalian cell line.

     

Novel compounds with potent CDK9 inhibitory activity for the treatment of myeloma

Cyclin-dependent kinases (CDKs) and Polo-like kinases (PLKs) play key role in the regulation of the cell cycle. The aim of our study was originally the further development of our recently discovered polo-like kinase 1 (PLK1) inhibitors. A series of new 2,4-disubstituted pyrimidine derivatives were synthesized around the original hit, but their PLK1 inhibitory activity was very poor. However the novel compounds showed nanomolar CDK9 inhibitory activity and very good antiproliferative effect on multiple myeloma cell lines (RPMI-8226).