具有阶段结构和Leslie-Gower HollingⅡ功能性反应的脉冲食饵-捕食系统(英文)

我们考虑了一个具有阶段结构和Leslie-Gower HollingⅡ功能性反应的时滞脉冲食饵-捕食系统.运用脉冲微分方程的比较定理和小扰动的方法,我们得到了保证系统食饵灭绝周期解的全局渐近稳定性和系统永久持续生存的条件.     

具Holling第Ⅱ类功能性反应的捕食者--食饵系统的定性分析

考虑捕食者无密度制约,食饵具有非线性密度制约的第二类Holling功能性反应捕食者－食饵系统。对该系统给出了完整的定性分析,证明了该系统至多有一个极限环,存在极限环的充要条件是平衡点不稳定。     

捕食系统时空动态对非对称的Allee效应的响应

虽然具有Allee效应的捕食系统动态已得到了广泛的研究,但很少有研究关注同一系统中不同种群受Allee效应影响情况.本文将考虑捕食、食饵种群分别受.Allee效应的影响,利用常微分方程与元胞自动机建立空间隐含(非空间)与显含的捕食模型,并讨论了Allee效应对捕食、食饵种群相互作用的非对称影响.空间隐含模型的模拟结果显示,捕食系统的稳定性与哪一个种群受Allee效应影响有关.当食饵种群受到中等强度Allee效应影响时,系统从稳定变为振荡状态.然而,捕食种群受Allee效应影响可使系统振动减弱并迅速达到稳定.空间显含模型的模拟结果表明,在概率转化模式下Allee效应可促使空间异质化,而捕食种群受Allee效应影响时空间异质化比食饵种群受影响时更强.此外,考虑统计随机性后发现两种群分别受Allee效应影响时种群呈现出两种分布模式:聚集型和界限型.特别当食饵受Allee效应,加之空间结构及统计随机性的作用,捕食系统出现一种矛盾的现象.     

具有Holling Ⅳ类功能反应的三维顺环捕食者-食饵模型

考虑具有Holling Ⅳ类功能反应三维顺环捕食者一食饵系统,利用常微分方程比较定理及Liapunov函数方法,得到了该系统持久性的充分条件,并且对于周期系统在一定条件下。系统存在唯一一个全局渐进稳定的周期正解,最后讨论了概周期解现象,得出了概周期正解的唯一存在性和全局渐进稳定性的充分条件。     

带有食饵保护的Gause型扩散捕食系统的稳定性分析

考虑了具有扩散项和食饵保护的Gause型捕食系统.该模型带有齐次Neumann边界条件.讨论了系统的全局吸引性以及系统非负常数平衡态的局部稳定性和全局稳定性.其条件依赖于食饵保护参数,表明了食饵保护对系统动力学行为的影响.     

一类具非单调泛函响应的状态-依赖型时滞捕食者-食饵系统的周期性

考虑一类具非单调泛函响应的状态-依赖型时滞捕食者-食饵系统,利用重合度和延拓定理,得到了一系列易检验的类方程至少存在一个严格正周期解的充分条件．     

具性别偏食的二种群捕食者-食饵系统模型

本文根据生态学实验现象研究了一类二种群捕食者－食饵系统,其中捕食者对食饵有性别偏食情形。建立了相应的数学模型,并对该模型的有关性状进行了分析。     

一类具有非单调增长率和功能反应的捕食者-食饵系统的定性分析

考虑一类食饵密度具有非单调增长率,捕食者具有功能性反应的捕食者一食饵系统。得到系统在第一象限内正平衡点的区域稳定的条件和极限环存在唯一的条件,完整地讨论了系统(1)的拓扑结构。     

具有捕食正效应的捕食-食饵系统

在经典的捕食食饵系统中考虑到由于捕食效应对食饵种群带来的正向调节作用后,提出了具有捕食正效应的捕食-食饵系统.通过对模型的动力学行为的分析,从理论上说明了正向调节作用对系统的影响,并就第一象限内平衡点存在时的相图解释了捕食正效应的作用.结果表明:(1)捕食系统中适当的正向调节作用会增加系统的稳定性;(2)当捕食正效应达到一定的程度后系统拥有一个不稳定的极限环;(3)当捕食正效应过大时会使系统的稳定性发生变化,使捕食者种群与食饵种群同时趋向无穷,出现了调节放纵现象.这些结果在保护生物学中具有重要的意义.     

高维“食饵—捕食者”模型周期解的存在性

一、引言文献对“Ⅱ类功能反应模型”进行了详细、完整的分析,给出了存在周期解的充分条件.但是在自然界中,就某一生态环境而言,往往同时存在上千种,甚至上万种“食饵-捕食者”系统,在食饵和捕食者之间都存在竞争关系.考虑到这些因素,本文将考虑更一般的高维“食饵-捕食者”模型.     

Concentration of 17 trace elements in serum and whole blood of plains viscachas (Lagostomus maximus) by ICP-MS, their reference ranges, and their relation to cataract

The reference ranges of the trace elements Al, As, Be, B, Cd, Co, Cu, Fe, Mn, Mo, Ni, Pb, Li, Rb, Se, Sr, and Zn were determined by inductively coupled plasma-mass spectrometry (ICP-MS) in sera of a group of free-ranging plains viscachas of the pampa grasslands of Argentina. The values were compared with those of a small group of captive plains viscachas of the Zurich Zoo with diabetes and bilateral cataracts. In addition, a method for digestion of whole-blood samples is described for the trace element determination. Significant differences in the concentration of trace elements in the two groups of animals are discussed. No correlation was found between the levels of selenium and of other trace elements compared to the formation of cataracts.     

Molecular phylogeny of the gobioid fishes (Teleostei: Perciformes: Gobioidei)

The phylogeny of groups within Gobioidei is examined with molecular sequence data. Gobioidei is a speciose, morphologically diverse group of teleost fishes, most of which are small, benthic, and marine. Efforts to hypothesize relationships among the gobioid groups have been hampered by the prevalence of reductive evolution among goby species; such reduction can make identification of informative morphological characters particularly difficult. Gobies have been variously grouped into two to nine families, several with included subfamilies, but most existing taxonomies are not phylogenetic and few cladistic hypotheses of relationships among goby groups have been advanced. In this study, representatives of eight of the nine gobioid familes (Eleotridae, Odontobutidae, Xenisthmidae, Gobiidae, Kraemeriidae, Schindleriidae, Microdesmidae, and Ptereleotridae), selected to sample broadly from the range of goby diversity, were examined. Complete sequence from the mitochondrial ND1, ND2, and COI genes (3573 bp) was used in a cladistic parsimony analysis to hypothesize relationships among the gobioid groups. A single most parsimonious topology was obtained, with decay indices indicating strong support for most nodes. Major phylogenetic conclusions include that Xenisthmidae is part of Eleotridae, and Eleotridae is paraphyletic with respect to a clade composed of Gobiidae, Microdesmidae, Ptereleotridae, Kraemeriidae, and Schindleriidae. Within this five-family clade, two clades are recovered. One includes Gobionellinae, which is paraphyletic with respect to Kraemeriidae, Sicydiinae, Oxudercinae, and Amblyopinae. The other contains Gobiinae, also paraphyletic, and including Microdesmidae, Ptereleotridae, and Schindleriidae. Previous morphological evidence for goby groupings is discussed; the phylogenetic hypothesis indicates that the morphological reduction observed in many goby species has been derived several times independently.     

Floral elaiophore structure in four representatives of the Ornithocephalus clade (Orchidaceae: Oncidiinae)

Background and Aims A significant number of species assigned to the Neotropical orchid sub-tribe Oncidiinae reward insect pollinators with oil produced in floral glands termed elaiophores. The latter may be glabrous (epithelial elaiophores) or hirsute (trichomal elaiophores). Although the detailed anatomy and ultrastructure of epithelial elaiophores have been studied for a number of genera, such as Oncidium Sw., Gomesa R. Br. and Trichocentrum Poepp. & Endl., hitherto, trichomal elaiophores have been investigated only for a single species of Oncidiinae, Ornithocephalus ciliatus Lindl. Furthermore, this is the only representative of the Ornithocephalus clade to be investigated to date. Here, an examination is made of the elaiophore anatomy and ultrastructure of a further four species currently assigned to this clade (Ornithocephalus gladiatus Hook., Phymatidium falcifolium Lindl., Zygostates grandiflora (Lindl.) Mansf. and Zygostates lunata Lindl.) and the results compared with those obtained for other Oncidiinae. Methods Elaiophore structure was examined for all species at three stages of flower development: closed bud, first day of anthesis and final stage of anthesis, using light microscopy, fluorescence microscopy, scanning electron microscopy, transmission electron microscopy and histochemistry. Key Results Elaiophores of O. gladiatus occur upon the lateral lobes of the labellum and display characters intermediate between those of typical epithelial and trichomal elaiophores, in that they are largely glabrous, consisting mainly of cuboidal epidermal cells, but bear short, unicellular hairs proximally. By contrast, the elaiophores of all the other species investigated occur on the callus and are of the trichomal type. In P. falcifolium, these unicellular hairs are capitate. In all species, oil secretion commenced at the closed floral bud stage. Ultrastructurally, the mainly trichomal elaiophores of the four representatives of the Ornithocephalus clade closely resembled the epithelial elaiophores of other Oncidiinae, in that their cells displayed an organelle complement typical of lipid-secreting cells. However, in some taxa, a number of noteworthy characters were present. For example, the elaiophore cuticle of O. gladiatus and P. falcifolium was bi-layered, the outer layer being lamellate, the inner reticulate. The cuticle of Z. grandiflora and Z. lunata was also lamellate, but here, a reticulate layer was absent. Accumulation of secreted oil resulted in the localized distension of the cuticle. Cuticular cracks and pores, however, were absent from all species. The walls of the secretory cells of Z. grandiflora were also atypical in that they had short protuberances or ingrowths, and contained cavities which are thought to be involved in the secretory process. Conclusions Of the species investigated, most displayed similar anatomical organization, their trichomal elaiophores occurring on the labellar callus. They, thus, differ from many other members of the Oncidiinae, where epithelial elaiophores are found either on the callus, or on the lateral lobes of the labellum. However, ultrastructurally, all elaiophores, whether those of representatives of the Ornithocephalus clade, or those of other oil-secreting Oncidiinae, possessed a similar complement of organelles, regardless of whether the elaiophores were trichomal or epithelial. In view of the latter, and the similar chemical composition of oils derived from all Oncidiinae investigated to date, it is probable that position and type of elaiophore, and possibly the structure of the overlying cuticle, play an important role in pollinator selection in these oil-secreting orchids.     

Comparative morphology and evolutionary pathways of the mouthparts in spore-feeding Staphylinoidea (Coleoptera)

This study surveys the external morphology of the mouthparts in the guild of spore‐feeders among the coleopterous superfamily Staphylinoidea, evaluating the influence of different phylogenetic and ecological starting points on the formation of their mouthparts. Our emphasis is on a scanning electron microscope analysis (SEM) of the involved trophic structures in spore‐feeding larvae and adults of the Ptiliidae, Leiodidae and Staphylinidae, describing the fine structure of their main functional elements. Functionally, mouthpart structures resemble brushes, brooms, combs, rakes, rasps, excavators, knives, thorns, cram‐brushes, bristle troughs, blocks and differently structured grinding surfaces. Their different involvement in the various aspects of the feeding process (i.e. food gathering, transporting, channelling and grinding) is deduced from our SEM analyses plus direct video observations. We infer five different patterns of food transport and processing, discriminating adults of ptiliids, leiodids plus staphylinids (excluding some aleocharines), several aleocharine staphylinids, and the larvae of leiodids and staphylinids. The structural diversity of the mouthparts increases in the order from (1) Ptiliidae, (2) Leiodidae towards (3) Staphylinidae, reflecting the increasing systematic and ecological diversity of these groups. Comparisons with non‐spore‐feeders show that among major lineages of staphylinoids, shifts from general microphagy to sporophagy are not necessarily constrained by, nor strongly reflected in, mouthpart morphology. Nevertheless, in several of these lineages the organs of food intake and grinding have experienced particular fine‐structural modifications, which have undergone convergent evolution, probably in response to specialized mycophagy such as spore‐feeding. These modifications involve advanced galeal rakes, galeal or lacinial ‘spore brushes’ with arrays of stout bristles, reinforced obliquely ventrad orientated prosthecal lobes and the differentiations of the molar grinding surfaces into stout teeth or tubercles. In addition, several staphylinids of the tachyporine and oxyteline groups with reduced mandibular molae have evolved secondary trituration surfaces, which in some aleocharines are paralleled by considerable re‐constructions of the labium–hypopharynx.     

Phylogenetic relationships and character evolution in New Zealand and selected Australian Gnaphalieae (Compositae) inferred from morphological and anatomical data

Most of the estimated 70–80 species of New Zealand Gnaphalieae are endemic. Those of Anaphalioides , Ewartia , Helichrysum , Leucogenes , Rachelia and Raoulia belong to a putatively monophyletic group which is supported by analysis of nuclear ITS DNA sequences and is virtually confined to New Zealand. All species of Craspedia , Euchiton , Ozothamnus and Pseudognaphalium are excluded from this group. A phylogenetic analysis of 42 species of Gnaphalieae, using 57 morphological, anatomical and palynological characters, was conducted to test the monophyly of this group and to seek evidence of generic relationships. The analysis does not resolve basal relationships among the Gnaphalieae studied here. The putative monophyletic New Zealand group is not retrieved. Monophyly is supported for each of Euchiton , Leucogenes , the whipcord species of Helichrysum , the pulvinate species of Raoulia , and Raoulia subg. Raoulia (excluding the aberrant R. cinerea ), but not for Anaphalioides or Raoulia s.l. There are these two distinct groups in Raoulia s.l. but also a substantial number of isolated species. The sole New Zealand species of Ewartia is not a sister species to Australian Ewartia . The Australian species Ewartia planchonii is the sister species to Euchiton rather than to the other Australian species of Ewartia .  © 2003 The Linnean Society of London, Botanical Journal of the Linnean Society , 2003, 141 , 183–203.     

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。     

利用培养特征和生理特性鉴别担子菌菌种的研究

担子菌菌种多是菌丝型的培养物,在长期保藏中如发生错误也较难辨别。本文报道了以培养特征和生理特性作为保藏的担子菌菌种的特征集要,并根据集要制定出鉴别他们的检索表。通过对48属、71种、142株菌种的实验结果,利用培养特征和生理特性鉴别保藏的担子菌菌种是可行的。     

The effect of aging on the mineral status of female mice

To clarify the effect of aging on the mineral status of female mice, mineral concentrations in their tissues were determined. Five 2-mo-old, five 6-mo-old, and five 10-mo-old female B10BR mice were fed a commercial diet. Iron, zinc, copper, calcium, magnesium, sodium, and potassium concentrations in the blood, liver, kidney, heart, brain, lung, and spleen of the mice were determined using a flame atomic absorption spectrophotometer. Iron concentrations in the liver, kidney, heart, brain, and spleen increased with age. Significant differences were detected between mice 2 and 6 mo of age and between mice 2 and 10 mo of age. Zinc concentrations in the heart and lung decreased significantly with age. Zinc concentrations in the heart and lung of 10-mo-old mice were significantly lower than those of 2-mo-old mice. It is noteworthy that the copper concentration in the brain of 10-mo-old mice was markedly higher compared with that of younger mice. Calcium accumulation was apparent in the kidney of mice at 10 mo.