蚂蚁与蚁运植物的互惠共生关系

蚁运植物（myrmecochore)即指种子靠蚂蚁携带散布的植物。在长期的协同进化中,蚂蚁与蚁运植物形成了互惠共生关系。由于蚁运植物种子上附生有蚂蚁喜食的油质体,蚂蚁取食油质体后,将种子丢弃在蚁巢附近,从而使植物得以扩散。蚁运植物广布全世界,但主要分布在澳大利亚和南非。蚂蚁主要搬运草本植物和部分灌木植物的种子。对蚂蚁与蚁运植物互惠共生关系的研究表明：蚂蚁的搬运有利于保护和传播植物种子;蚁巢有利于种子萌发,出苗和建群;蚂蚁的搬运是影响某些温带森林群落结构的重要因素之一;蚂蚁与蚁运植物互惠共生对自然群落的恢复有重要作用。     

红火蚁对蚁运植物种子影响的研究概况

自然界中蚂蚁与蚁运植物的互惠关系是一种普遍的现象。蚁运植物种子的油质体是两者发生联系的纽带,它能为蚂蚁提供营养物质,且蚂蚁在消耗油质体的同时,搬运并散布了种子。红火蚁是近年来在华南地区严重发生的一种入侵性蚂蚁,能在短时间内迅速发展成为优势种,造成入侵地生物多样性降低和生态单一化,是世界范围内最具危险的社会性昆虫之一。由于该入侵蚂蚁极具侵略性、觅食能力强、种群庞大等特点,对蚁运植物具有深远的影响。为了深入、全面地了解红火蚁对蚁运植物种子的影响,本文综述了红火蚁对蚁运植物种子油质体的喜好及搬运行为,以及对蚁运植物种子的直接影响(搬运、取食、划痕或毁坏)及间接影响(排挤本地蚂蚁),最后展望了未来红火蚁对蚁运植物影响的研究方向。     

啮齿类对植物种子的传播作用

种子植物是固着生活的有机体 ,如果能成功地将种子扩散到适宜的生境 ,将会在生存竞争中获得优势。在长期的进化过程中 ,不同的植物依赖不同的媒介传播种子 ,如风传播 ,水传播 ,或自身的力量传播 (重力、弹爆力等 )。在很多情况下也依靠动物完成种子扩散 ,即所谓的动物传播。根据依赖的动物对象不同可以分为蚁传播 ,鸟传播 ,哺乳类传播 ,以及鱼传播 ,爬行类传播等。哺乳类中传播种子的类群主要包括翼手类 ,灵长类和啮齿类。由于能够飞行 ,热带食果实的蝙蝠(属翼手类 )对种子的传播作用最明显 ,研究得也最多 ,源于蝙蝠类的传播特称为ｃｈｉｒ…     

动物对松属植物种子的传播作用研究进展

松属植物约110种,根据种子传播方式可分为风传播松和动物传播松。风传播松占绝大多数,种子多具有适应风力的翅。动物传播松大约23种,都具有大、可食用、无翅或短翅的种子,无法借助风力传播。动物传播松的分布生境多为贫瘠的山地,而且多位于高海拔地区。目前已知9种松树的动物传播种类,其余14种可推测为动物传播。动物传播者包括鸦科鸟类和啮齿类动物,动物将获得的种子分散贮藏,未被重取的种子可能萌发,完成传播。动物传播是定向传播,微生境多适合种子萌发。啮齿类的传播距离可达数10 m,而鸦科鸟类的传播距离可达数公里。动物传播的松树会出现树丛和多树干现象,一般由同一贮点内贮藏的多粒种子萌发造成的。动物贮藏的种子大部分被重取,称传播后取食。一些具有大种子的风传播松在种子落地后,啮齿类和鸟类会再次埋藏而形成二次传播,可看做是一个单独的传播类型,即风-动物传播松。动物传播者与依赖传播松树之间可看作是互利共生关系。     

弓背蚁属蚂蚁初级内共生菌Blochmannia的研究进展

昆虫与其体内细菌的互利共生关系是近十余年来生物学家关注的热点领域,也是研究物种间协同进化的理想模型.Blochmannia是蚁科弓背蚁属Camponotus蚂蚁体内的初级内共生菌,作为最早被描述的动物与细菌之间的共生关系,Blochmannia在帮助宿主蚂蚁合成食物中所缺少的必需营养物质、维持生长发育、繁殖和营养代谢等...     

植物种子

种子的主要作用 ,在于保证植物后代的繁衍。依靠种子 ,植物得以到处传播 ;植物大量结子、传宗继代的本领 ,是亿万年自然选择的结果。1　植物种子的传播在夏末秋初时 ,当你走进野草丛生的山野时 ,常会听到“僻拍”、“僻拍”的响声 ,有时甚至会受到突然的袭击。原来这是一些植物的果实已经成熟 ,由于果皮的爆裂 ,产生出一种弹力 ,把种子飞弹出去。以这种方式传播种子的植物有绿豆、大豆和豌豆等。生长在地中海沿岸和非洲北部的有一种叫“喷瓜”的植物 ,它的果实成熟以后 ,只要受外力稍一触动 ,就脱落下来 ,里面的种子随着一股粘液突然地喷射…     

啮齿动物对种子的传播

简要介绍了扩散、传播植物种子的啮齿动物种类、它们传播的植物种子种类,以及啮齿动物对植物种子扩散、传播的主动、被动方式及双方在这一体系中的互惠关系和可能存在的协同进化关系。     

云南无量山黑长臂猿对植物种子的传播作用

2005年9月至2006年4月,对无量山一群黑长臂猿进行观察,研究黑长臂猿在植物种子传播中的作用.观察记录黑长臂猿一天的排便次数并收集粪便.通过直接观察和收集长臂猿粪便确定长臂猿取食的果实种类.以森林中采集的果实种子为对照标本,对粪便中的种子进行鉴定,并记录各种种子的数量,测量其长度、宽度和重量.结果表明观察期间黑长臂猿共取食31种果实,其中有1种在被取食时尚未成熟,另有2种果实的种子在取食后遭到破坏,还有1种植物的种子不能被长臂猿吞食而得不到传播,黑长臂猿可为27种植物传播种子.黑长臂猿个体平均每天排便2次,粪便的平均湿重为22.7 g,每份粪便平均含有1种植物的种子;在不包含小种子(直径<3 mm)的情况下,平均每份粪便中含有12粒种子.总的来说,黑长臂猿是有效的种子传播者.     

南京中山植物园秋冬季鸟类对植物种子的传播作用

1999年10月20日－2000年1月20日,在南京中山植物园内随机收集鸟粪样品160份,共分离出874粒结构完整的种子和果核、3块鞘翅目昆虫残体和1块鸟类羽毛残块。已鉴定出842粒种子和果核,分属于16科20属26种（变种）。在鸟粪样品中出现频率较高的种子依次分别属于冬青（Ilex purpurea)(22.22%)、圆柏（Sabina chinensis)(11.11%)、盐肤木（Rhus chinensis)(10.63%)、朴树（Celtis sinensis)(9．18％）、爬山虎（Parthenocissus tricuspidata)(7.73%)、龙柏（S.chinensis cv.kaizuca)(7.25%)等;种子数量相对较多的植物种类主要有冬青（23．52％）、盐肤木（16．15％）、圆柏（13．54％）、爬山虎（7．96％）、龙柏（7．96％）、小果蔷薇（Rosa cymosa)(5.34%)等。除经鸟粪传播外,鸟类还通过衔取果实以及在吞食果实后将种子呕出的方式传播种子。初步发芽试验表明,鸟粪样品中的爬山虎、盐肤木的种子,以及被鸟呕出的樟树（Cinnamomum camphora)、楝树（Melia azedarach)的种子均可发芽出苗。鸟类传播种子使南京中山植物园内樟树、冬青、海桐（Pittosporum tobira)和红豆杉（Taxus chinensis)等栽培树种成功地侵入到位于植物园北缘的虎山山坡黑松（Pinus thunbergii)、枫香（Liquidambar formosana)群落、以及植物园内山溪边的枫杨（Pterocarya stenoptera)、朴树群落等生境中。鸟类对种子的传播作用扩大了南京中山植物园内那些具有肉质果实、种子具有坚硬种皮或种子包被于坚硬果核中的植物种类的分布范围,促进了它们的自然更新。     

南京中山植物园春夏季节鸟类对植物种子的传播作用

2002年4月至8月,在南京中山植物园内收集了198份鸟粪样品,从中分离、鉴定出9 573粒结构完整的种子及果核,分别隶属于12科15属20种植物,另有1 6粒种子属于1未知种类.单份鸟粪样品中可含有1～4种种子,平均1.5±0.7种;但单份鸟粪样品中种子数量变化很大,约为1～583粒,平均48.4±70.7粒.鸟粪样品中出现频次较高的种类主要有构树(Broussonetia papyrifera)、蛇莓(Duchesnea indica)、桑树 (Morus alba)、山莓(Rubus corchorifolius)、日本珊瑚树(Viburnum awabuki)、蓬FDA1(Rubus hirsutus)和美洲商陆(Phytolacca americana)等7种,并且它们的种子数量也多达9 213粒,占种子总数的96.1%.鸟粪样品中种子出现频次的月份变化也在一定程度上间接地反映出植物果实的成熟期和鸟类对果实的取食频率.白头鹎(Pycn onotus sinensis)、乌鸫(Turdus merula)等鸟类则主要以呕出种子的方式传播桂花(Osmanthus fragrans)、白玉兰(Magnolia denudata)等体积较大的种子.此外,鸟类还以衔取果实的形式传播种子.2000～2002年,已经观察到8种鸟类取食18种植物的肉质果实,其中灰喜鹊(Cyanopica cyana)、乌鸫、白头鹎和山斑鸠(Streptope lia orientalis)等4种留鸟分别取食8～16种植物果实,是春夏季节植物园内取食果实种类数目较多的鸟类,并且也可能是重要的种子传播者.鸟类传播种子已经导致了阔叶十大功劳(Mahonia bealei)、樱桃(Cerasus pseudocerasus)、掌叶复盆子(Rubus chingi i)和桂花等栽培树种逸出植物园,使它们的实生苗及小树成功地侵入到植物园周围的自然生境中,促进了植物园内一些具肉质果实的栽培植物的自然更新.同时,鸟类传播种子也是导致美洲商陆等引种栽培植物逸生为外来杂草并迅速蔓延的重要原因之一.     

Interactions between Fungus-Growing Ants (Attini), Fruits and Seeds in Cerrado Vegetation in Southeast Brazil1

We surveyed the material collected for fungus culturing by attine ants in the cerrado vegetation of southeast Brazil. Six genera of the so-called lower attines (Cyphomyrmex, Mycetarotes, Mycocepurus, Myrmicocrypta, Sericomyrmex and Trachymyrmex) collect a wide variety of plant material as fungal substrate. Plant diaspores of nonmyrmecochorous species comprise a large portion of the items brought to the nest, especially in the rainy season. Removal experiments using fruits of selected plant species revealed that attine ants (including the leaf-cutters Atta and Acromyrmex) not only actively clean the seeds (remove fruit pulp), but also carry them up to 12 m in the cerrado. Germination tests showed that removal of fruit pulp by attine ants increases germination rate in Ocotea pulchella (Lauraceae), Prunus sellowii (Rosaceae), Ouratea spectabilis (Ochnaceae), Rapanea umbellata (Myrsinaceae) and Psychotria stachyoides (Rubiaceae). For P. stachyoides, however, ants had no effect on germination if seeds had already passed the digestive tract of birds. Aril removal by attines also increases germination success of Copaifera langsdorffii (Leguminosae) and Virola sebifera (Myristicaceae) seeds. The results indicate that attine-fruit/seed interactions are particularly conspicuous in the cerrado, suggesting that fungus-growing ants may play a relevant role in fruit/seed biology in this vegetation type. Potential ant-derived benefits to diaspores of nonmyrmecochorous plants in the cerrado would include secondary seed dispersion and/or increased germination success by ant-handled seeds.     

Ants,Stem Borers,and Pubescence in Endospermum in Papua New Guinea1

The stems of the ant-plant, Endospermum labios Schodde, serve as colonization sites for the ant, Camponotus quadriceps F. Smith. They are also subject to damage by insect borers. We sampled young E. labios trees in distutbed forest to compare evidence of stem boring insect and stem miner damage in plants with and without colonies of C. quadriceps. Dissections of a subsample of plants showed that dipteran stem borers and stem miner damage were significantly more common in plants lacking C, quadriceps colonies than in plants with established colonies. Evidence from these dissections and from field counts of meristem damage caused by emerging borers suggested that coleopteran stem borers were also more abundant when ants were not present. In addition to the incidence of stem boring insects and ant colonies, we examined relative levels of leaf pubescence by measuring trichome density and leaf size for E. labios trees. We found that trichome density was significantly greater in trees with evidence of prior shoot damage (presumably from stem borer emergence at the meristem) but was not significantly related to the presence or absence of an ant colony. This prompted us to compare trichome density on leaves of nearby small trees and of different branches of the same tree, pairing a stem/branch that appeared damaged with one that appeared healthy. Trichome densities on leaves from damaged stems and branches were significantly greater than were trichome densities on healthy branches and stems. Based on these empirical data, we present several possible explanations for the patterns of association between ants, stem borers, and pubescence. Although feeding preference tests with a common folivore showed no effect of trichome densities on leaves, we suggest further study on how trichomes may affect ovipositing stem borers.     

Variations in abiotic defense within myrmecophytic and non-myrmecophytic species of Macaranga in a Bornean dipterocarp forest

We examined the interspecific variations in intensity of total abiotic (chemical and physical) defenses in five sympatric Macaranga (Euphorbiaceae) species, including three myrmecophytic species. The intensity of the total abiotic defense for each Macaranga species was estimated by measuring inhibiting effects on the growth performance of the common cutworm, Spodoptera litura (Fabricius) (Lepidoptera: Noctuidae) when the cutworm larvae were fed fresh leaves of each Macaranga species. Indices of the growth performance, number of dead larvae, pupal weight and length of larval period were obtained. We found that the intensities of total abiotic defense of the two non-myrmecophytic species were significantly stronger than those of the three myrmecophytic species, and that there was a significant difference in intensity even within the three myrmecophytic species. The former result supports the hypothesis that, unlike non-myrmecophytic species, myrmecophytic species cannot invest so many metabolic resources in abiotic defense, because they have to allocate nutrients to biotic defense (toward biotic defense agents). Moreover, the latter result suggests the possibility that the three sympatric myrmecophytes have different defense strategies, with a trade-off between abiotic and biotic defense, and/or with a trade-off between defense and other life-history traits such as growth and reproduction. Abiotic defense can be roughly separated into physical and chemical mechanisms. To assess the intensity of the physical defense of Macaranga leaves, we measured the leaf toughness of each species. In addition, to assess the intensity of the plants general chemical defense, cutworm larvae were reared on an artificial diet containing dry leaf powder of each Macaranga species, and their growth performances were compared. The estimated orders of intensity of both leaf toughness and general chemical defense coincided with that of the total abiotic factors measured by the growth performance of cutworm on fresh leaves. This suggests the presence of both physical defenses, represented by leaf toughness, and a general chemical defense affecting the intensity of the total abiotic defense in similar ways.