陕北淡水涡虫组织形态学初步观察

对陕北常见淡水涡虫的外部形态和石蜡切片进行组织形态学观察,经过绘图、照相、分析、鉴定,结果表明陕北淡水涡虫的常见种主要为日本三角涡虫(Dugesia japonica)。     

Ultrastructural features of oogenesis in some marine neoophoran turbellarians

An ultrastructural study of oogenesis has been undertaken in some marine species of neoophoran turbellarians belonging to the Tricladida, Proseriata, and Prolecithophora. Among marine triclads, Cercyra hastata has oocytes with a remarkable amount of what appears to be autosynthetic proteinaceous yolk, while Procerodes dohrni and P. lobata have alecithal oocytes. Among the Proseriata, several species of the primitive family Monocelididae (subfamily Monocelidinae) have oocytes with a discrete amount of what appears to be autosynthetic yolk, while Parotoplana macrostyla, of the derived family Otoplanidae, has alecithal eggs. Finally preliminary observations on Plagiostomum maculatum (order Prolecithophora) suggest that oocytes have autosynthetic yolk globules.These results support the hypothesis (previously formulated on the basis of similar ultrastructural investigations on freshwater triclads) that the presence of autosynthetic yolk in some neoophoran turbellarians can be interpreted as a primitive character inherited from an ancestor with archoophoran organization. This plesiomorphic character would still be maintained in some species while lost in others following differentiation of vitellaria which are characteristic of the Neoophora.     

Turbellarian assemblages in freshwater lagoons in southern Brazil

Turbellarians, which typically feed on bacteria, algae, rotifers, oligochaetes, dipteran larvae, microcrustaceans, and other organisms, are abundant in diverse types of wetlands. Despite their importance, abundance, and species richness in freshwater environments, turbellarians are seldom considered in studies on biodiversity. We analyzed the structure of turbellarian communities in shore areas of three categories of permanent wetlands classified according to their perimeter as small, intermediate, and large during an annual cycle. In total, 1847 turbellarians were collected representing 42 species and 15 genera, from the orders Catenulida, Macrostomida, Lecithoepitheliata, Rhabdocoela, and Tricladida. Sixteen species were common to the three categories of wetlands, whereas nineteen species were unique to a particular category. Species composition varied among wetlands of different sizes; small, intermediate, and large wetlands had different dominant species. We found seasonal differences in community composition over the year, but no significant differences in mean values of observed species richness among wetlands with different sizes and among seasonal samples. The estimated species richness was, however, higher in the small wetlands, followed by the large and intermediate wetlands. In the summer, abundance was significantly lower in the small water bodies than in the intermediate and large bodies of water. Our results reinforce the need for conservation of wetlands of different sizes.     

Initial morphological diversity as a criterion in deciphering turbellarian phylogeny

The most profound structural variety in morphofunctional systems and morphogenetic mechanisms, i.e. the highest morphological diversity, is observed in those groups where these systems and mechanisms are evolutionarily most primitive. Here, such variety can involve the basic body plan of a given phylum and the types of morphogenesis characteristic of it. This correlation provides a new criterion of evolutionary primitiveness, namely, the criterion of initial morphological diversity.The highest morphological diversity among turbellarian groups is observed in the order Acoela. Acoel turbellarians are archaic in most of their features, apparently being a group near the base of the turbellarian phylogenetic tree. Among other turbellarians there are a few groups that also are archaic in some few features (above all, the Catenulida), although on the whole they are more advanced than the Acoela. The Turbellaria as a whole is notable for its morphological diversity in comparison with other classes of the Scolecida.     

Peptidergic signalization: An immunocytochemical study of FMRF-related peptides in the nervous system of planarians

Free-living freshwater flatworms, planarians, are well known biological object. Due to their unprecedented regenerative ability, planarians attract the particular attention of scientists. From a small body piece planarians can regenerate a whole organism including central nervous system and all organs and tissues. Employment of modern immunocytochemical methods in conjunctions with confocal laser scanning microscopy (CLSM) made it possible to discover a spectrum of neuronal substances in the nervous system of relatively simple animals. In the present study, specific fluorescently labeled antibodies have been used for identification of FMRF-related neuropeptides in the nervous system of three planarian species: Schmidtea mediterranea, Girardia tigrina, and Polycelis tenuis (Platyhelminthes, Turbellaria). The details of the FMRF-like immunostaining have been described and completed. Some previously published data concerning neuronal signalization in turbellarians have been observed.     

Temporary pools are not `enemy-free'

Temporary pools are traditionally considered as refuges where the conspicuous anostracans are protected from predation. While this is true for the size-selective predation by fish, there is compelling evidence that invertebrate predation is an important biotic stress regulating temporary pool communities. In rock pools in southeastern Botswana, we studied the impact of some suspected invertebrate predators on populations of the freshwater anostracan Branchipodopsis wolfi by means of observations and manipulative experiments. In a survey of 45 pools, the relationship between B. wolfi natural population sizes and the abundance of suspected predators were never negative for turbellarians and mosquito larvae. When dragonfly larvae, notonectids or tadpoles were present, the anostracan populations were generally non-existent or very small. In enclosure experiments with turbellarians, there was a significant effect of predation within one hour of the start; the average daily predation rate was about 1/4 anostracan per turbellarian. Anostracans from a pool with few turbellarians were slightly less vulnerable than those from a turbellarian-rich pool. Furthermore, there was an indication of males being predated on more than females. With dragonfly larvae and notonectids, the predation effect was marked with all six anostracans in an experiment eaten in less than one day by a single predator (predation rate: about one anostracan every 2 h per predator). In a behavioral study, both sexes of B. wolfi avoided swimming above sediment that held more turbellarians than the open patches; there was no evidence for chemical communication with respect to this behavior.     

Freshwater biodiversity in the rivers of the Mediterranean Basin

We review the diversity of freshwater organisms in the Mediterranean Basin (hereafter Med), particularly from streams and rivers. We present available information on the richness, endemicity, and distribution of each freshwater organism group within the Med, and make a comparison with Palearctic diversity. Approximately 35% of known Palearctic freshwater species and more than 6% of the World’s freshwater species are present in the Med. A high degree of endemicity is found in the Med freshwater biota. These data, together with the degree to which many freshwater species are threatened, support the inclusion of the Med among World biodiversity hotspots. Nevertheless, knowledge of Med biodiversity is still incomplete, particularly for some taxa. Regarding to the spatial distribution of species within the Med, the richest area is the North, although patterns differ among groups. A comparison of the ecological and biological traits of endemic and non-endemic species of three riverine groups (Ephemeroptera, Plecoptera, and Trichoptera) revealed that endemic species have several strategies and mechanisms to face typical mediterranean-climate conditions, such as drought, when compared to non-endemic species. We briefly analyse the conservation status of the region’s biodiversity. Finally, we present some future challenges regarding the knowledge and protection of Med freshwater biodiversity.     

On the karyotypes of the Neorhabdocoela species and karyological evolution of Turbellaria

The karyotypes of 10 species belonging to the Neorhabdocoela order (Turbellaria) are described: Proxenetes flabelliger, 2n=6 (Trigonostomidae), Promesostoma rostratum, 2n=12 (Promesostomatidae), Castrada sp., 2n=6, Rhynchomesostoma rostratum, 2n=6, Bothromesostoma esseni, 2n=10, Mesostoma lingua, 2n=8 (Typhloplanidae), Provortex karlingi, 2n=8 (Provorticidae), Halamovortex macropharynx, 2n=16 (Dalyellidae), Macrorhynchus crocea, 2n=16, and Gyratrix hermaphroditus, 2n=4 (Polycystidae). It is proposed that the karyotypes of the ancestral marine neorhabdocoel forms, as well as those of the other groups of turbellarians, must have consisted of 16–20 biarmed chromosomes. The processes of adaptation and speciation in each group seem to be accompanied by a gradual decrease in chromosome number to 2n=8–4, this being due to Robertsonian fusions and translocations. In some freshwater turbellarians the diploid number increased by polyploidisation. The same processes evidently took place in different groups of parasitic worms.     

Evolutionary Modifications of the Spiralian Developmental Program

SYNOPSIS. The Spiralia, an assemblage of phyla united by theirstereotypic pattern of early embryonic cell divisions (spiralcleavage), is an interesting group in which to investigate theevolution of development. This paper examines modificationsof developmental mechanisms within the Spiralia with emphasison the basallybranching forms. Although demonstrating a notabledegree of evolutionary conservation, the equal quartet cleavagepattern, which appears to be the ancestral condition, nonethelessexhibits modifications within the various spiralian groups,such as unequal cleavage, changes in cell size and rate of division,formation of two rather than four quadrants (duet spiral cleavage),and in extreme cases the loss of any trace of the spiral pattern.While the cell lineages of spiralians are remarkably conserved,one can discern evolutionary changes, for example in the cellsthat give rise to mesodenn. Studies of blastomere specificationin many spiralian groups and analyses of axis determinationindicate that embryos with equal versus unequal cleavage typicallyuse different determinative mechanisms to establish cell fatesand the dorsoventral axis. These properties are establishedearly in species exhibiting unequal cleavage. While previousexperiments suggested that equal cleavage was associated withlate specification, there is now evidence of precocious specificationof quadrant fates in some equal-cleaving species, such as thenemerteans and the polyclad turbellarians     

Where Turbellaria? Concerning knowledge and ignorance of marine turbellarian ecology

Present knowledge of marine free-living turbellarians is reviewed in the light of a standard ecological text. Little is known of their ecological adaptations or fitness but they are clearly successful animals. Diversity within communities can be considerable, possibly relating to the small size of individuals and temporal and spatial resource gradients. Little is known about genetic diversity, environmental tolerances and demography. Local distribution patterns are better known but rarely proven with appropriate statistics. New data from work in Northern Ireland on behaviour and habitat choice of Procerodes littoralis and on species richness, population aggregation and microdistribution of meiofaunal turbellarians is presented.Nothing appears known about intra-specific competition but more about inter-specific relationships including responses to biogenic structures. Dietary information is sparse and mostly observational with little known about feeding efficiency. Studies at Sylt have revealed mainly univoltine or polyvoltine annual life cycles partly related to habitat preference and possibly giving some evidence of r and K selection. Factors controlling local abundance are largely uninvestigated and the reasons for the apparent rarity of many species not understood.Lists and counts of turbellarians within particular habitats provide some knowledge of community structure but very few numerical analyses, e.g. of diversity and similarity, exist. Contribution to energy flux and to structuring communities has not been determined in spite of the turbellarians' assumed major role as meiofaunal predators. Nevertheless marine turbellarians appear particularly fitted to studies such as habitat heterogeneity, community stability and biogeography and are surely suitable subjects for field and laboratory experiments. There is no lack of direction for studies to proceed. Impulsion is required.     

淡水鱼类入侵种的分布、入侵途径、机制与后果

生物入侵已经成为全球面临的三大环境问题之一。鱼类入侵现象也随全球经济一体化的进程日益严重。本文综述了全球淡水鱼类入侵的现状和研究进展, 包括鱼类入侵的定义及分布、入侵途径和机制、产生的生态和社会经济影响以及预防措施等。据统计, 目前全球外来鱼类达624种, 该数量超过30年前的两倍。外来鱼类主要通过水产养殖(51%)、观赏渔业(21%)、休闲垂钓(12%)、渔业捕捞运输(7%)等多种途径被引进。入侵鱼类对本地种产生了捕食、种内种间竞争、杂交和疾病传播等负面影响, 破坏本地生态系统, 但是其正面的生态及社会经济影响也不可忽略。近20年来全球鱼类入侵日益受到重视, 相关论文发表数量翻了8倍。值得提出的是, 近10年来全球鱼类入侵风险评价系统的研究显著增加, 一些鱼类入侵模型已应用于五大洲的多个国家。我国淡水外来鱼类共计439种。然而, 我国关于鱼类入侵的研究起步较晚, 发表文献数仅占全球的3.7%, 且主要研究方向仍集中在入侵物种的分布及生物学特性等基础研究上, 缺乏对于鱼类入侵机制及风险评价预测的研究。因此, 我们建议: (1)开展全国范围的本底调查并建立数据库, 实现数据共享, 明确鱼类入侵的历史与分布现状; (2)联合多个政府部门和机构, 对鱼类入侵进行长期观测, 从整个水生生态系统的角度出发, 深入了解其入侵机制及其产生的正面和负面生态和社会经济影响; (3)加强增殖放流的科学研究和管理; (4)构建区域性外来鱼类入侵风险评价系统, 有效预测鱼类入侵活动, 评价入侵种的危害, 并为相关政府部门的决策提供科学依据。     

Global distribution,entry routes,mechanisms and consequences of invasive freshwater fish

Biological invasion is now considered one of the three major environmental issues worldwide. Freshwater fish invasion becomes more serious with globalization of the world economy. We reviewed the current status of global freshwater fish invasions and discussed the definitions, distributions, introduction pathways, mechanisms, ecological and economic impacts, and risk assessments of freshwater fish invasions. Non-native fish are mainly introduced through food aquaculture (51%), as ornamental fish (21%), or for sport fishing (12%) and fisheries (7%). The number of introduced fish has reached 624 species, doubled the number found thirty years ago. Successful invasions may bring many negative ecological consequences, such as predation, hybridization, structure and function alteration of local freshwater ecosystems, as well as diseases transmission. However, it also brings positive biological and economic values. The number of fish invasion studies has increased eight times over the last 20 years, with studies mainly focusing on biology and the biological impact of invasive fish species. Risk assessments of freshwater fish invasions were studied over the last 10 years, and fish invasiveness screening models have been applied in countries of five continents. The number of non-native freshwater fish in China totaled 439. However, research papers on freshwater fish invasions in China was only 3.7% of the global total, and these researches were mainly on the distribution and biology of invasive fish species, and very few studies included risk assessments. Therefore, we suggest investigating the history, distribution, and mechanisms of invasive species at the national level, evaluating both the positive and negative effects of freshwater fish invasions, and also reinforcing studies of risk assessments in China.     

Nahrungsbeziehungen der Turbellarien in Küstensalzwiesen

Turbellarians represent one of the most characteristic and often also most numerous elements of the salt-marsh biocoenosis. The analysis of their food relations promised, therefore, insights into the food web in salt marshes. Two questions are of particular importance: (1) Is autochthonous or allochthonous food more important? (2) Are there noticeable relations to the aerial phase of the biotope? Gut-content surveys, feeding-experiments and information from literature indicate, that the main food of salt-marsh turbellarians consists of oligochetes, nematodes and diatoms. There exist certain relations between the taxonomic categories of turbellarians and their food sources, and, furthermore, between the type of pharynx and the kind of food. Oligochetes are 4 and nematodes up to 14 times more abundant than turbellarians. Nematodes are also likely to be the most important food competitors for turbellarians. Enemies of salt-marsh turbellarians are the polychaeteNereis diversicolor and sporozoan parasites. The main food of salt-marsh turbellarians consists of organisms existing in sufficient numbers in the biotope; a dependency on allochthonous food is therefore unlikely. Allochthonous food (e. g. copepods from adjacent mud flats) may, however, at times enlarge the food resources available. Little evidence for the use of air-living organisms as food, and no evidence for air-living enemies, was found. The aquatic food chain in salt marshes ends at the level of flatworm-eating polychaetes or, where these are absent, already at that of the turbellarians themselves. Although the biomass (standing crop) of primary producers reaches its maximum in the most protected part of the beach (salt marshes), maximum population density of turbellarians is found in parts of maximum exposure. This fact is considered to be due to the great amount of allochthonous food available at the upper edge of the surf zone.     

An assessment of animal species diversity in continental waters

There is a need for monitoring the status and trends of freshwater biodiversity in order to quantify the impacts of human actions on freshwater systems and to improve freshwater biodiversity conservation. Current projects carrying assessment of freshwater biodiversity focus mainly on leading-better-known groups such as fish, or identify keystone species and/or endemic freshwater systems for conservation purposes. Our purpose is to complete these existing projects by providing quantitative estimates of species number for all freshwater groups on each continent and/or major eco-regions. This article present the results of the first implementation phase carried out from September 2002 to June 2003 and which addressed only freshwater animal species. The project consisted of: (1) compiling existing data from literature, web sites and museum collections; (2) contacting scientific experts of each group to provide a ‘to the best of their knowledge, estimates of species numbers. In this study, we consider as true freshwater species, those that complete part or all of their life cycle in freshwater, and water-dependant species those that need freshwater for food or that permanently use freshwater habitats. The current order of magnitude for known freshwater animal species world wide is 100 000, of which half are insects. Among other groups, there are some 20 000 vertebrate species; 10 000 crustacean species and 5000 mollusc species that are either true freshwater or water-dependant species. The study highlighted gaps in the basic knowledge of species richness at continental and global scales: (1) Some groups such as Protozoa, nematodes or annelids have been less studied and data on their diversity and distribution is scarce. Because current richness estimates for these groups are greatly biased by knowledge availability, we can expect that real species numbers might be much higher. (2) Continents are not equal in the face of scientific studies: South America and Asia are especially lacking global estimates of species richness for many groups, even for some usually well-known ones such as molluscs or insects. The second phase of the project will address freshwater plants and algae. The present status should be considered as a first sketch of the global picture of freshwater biodiversity. We hope that this project will initiate interactive exchange of data to complete and update this first assessment.     

Interspecific Interactions Among Larval Trematode Parasites of Freshwater and Marine Snails

Freshwater and marine snails serve as intermediate hosts fornumerous species of larval trematodes. Any particular populationof snails may be infected by several species. It is commonlyobserved that mixed species infections are less frequent thanexpected by change in collections of host snails from naturalpopulations. While several mechanisms might generate such negativeassociations, laboratory studies of freshwater snail-trematodeassociations have demonstrated the presence of strong antagonisticinteractions between intramolluscan larval stages (rediae andsporocysts) of species that infect the same host individual.Both predatory and non-predatory antagonism has been observed,the former taking the form of predation by large, dominant redialforms on the sporocysts and rediae of subordinate species. Theseinteractions are largely hierarchical, although in some systemspriority effects have been observed, and in one case a sporocystspecies replaced a redial species by strong non-predatory antagonism.Several instances of positive association between larval trematodespecies have also been observed. In such cases, interferencewith host defense mechanisms by the first parasite appears toenhance superinfection by the second. My own study of the larvaltrematode guild that infects the salt marsh snail, Cerithideacalifornica, has revealed patterns of association and interactionthat are very similar to those demonstrated by laboratory studiesof freshwater systems. Ultimately, the frequency of interactionsamong larval trematodes depends on the availability, relativeto the numbers of susceptible snails, of infective eggs andmiracidial larvae transmitted from definitive hosts.     

Recent trends in Lake Ladoga ice cover

This contribution reviews diversity of turbellarian species by biogeographical regions, with comments on species biology. The review draws on the database available at http://www.devbio.umesci.maine.edu/styler/turbellaria. Comparisons between regions suggest that species richness may be at least one order of magnitude higher than the currently reported number of species. In the context of the recent reconstructions of phylogeny of Platyhelminthes based on molecular data, the paper allows inferences as to the history of colonization of freshwaters by turbellarians. Specifically, four, or perhaps six, major invasions of freshwater habitats may have occurred in the Pangean period, each of which gave rise to a monophyletic freshwater taxon. In addition, several occasional invasions by representatives of marine taxa must have taken place.     

Responses of freshwater ecosystems to global change: research progress and outlook

全球变化已经通过提高水温、改变降水格局和水流状况、促进物种入侵、增加极端事件, 对不同的淡水生态系统造成严重的威胁。该文将全球变化背景下淡水生态学的主要研究内容归纳为: (1)全球变化各要素对个体、种群、群落及至生态系统水平的影响; (2)全球变化过程中生态系统生物地球化学循环的改变; (3)淡水生态系统对全球变化的适应对策。最近10-15年淡水生态系统与全球变化研究快速发展, 取得的重要突破有: (1)阐明淡水生态系统结构与功能对全球气候变化尤其是水温升高的响应过程与机制; (2)揭示淡水生态系统(湿地、湖泊、河流等)是全球碳循环的重要组成部分, 在全球变化因素的影响下呈现有机碳埋藏减少和矿化速率提高。今后的研究中, 需要进一步加强对淡水生态系统全要素的系统观测与整合; 开展以“河流”为介质耦合多系统的碳输运和转化过程研究; 强化基础理论研究揭示淡水生态系统对全球变化的适应机制。     

On some commensal Turbellaria of the Canadian East Coast

The brachyurans Chionoecetes opilio and Hyas araneus collected from the east coast of Canada harbour two species of commensal turbellarians. Ectocotyla hirudo (Levinsen) and E. multitesticulata Fleming & Burt are found on the gills and branchial chambers of male and female crabs. The molluscs Crassostrea virginica and Mytilus edulis collected from several locations where they are cultured along the Northumberland strait carry two commensal eulecithophoran turbellarians, both on the gills, viz., Urasloma cyprinae (Graff) and Paravortex gemellipara (Linton), the latter being a new host record. Aspects of the biology and life-history of these turbellarians are discussed, especially in relationship to the biology of their hosts.Abbreviations in the figures A Atrium - An Antrum - C Capsule - CO Common Oviduct - E Embryo - Ep Egg-laying pore - GP Genital Pore - I Intestine - O Ovary - Od Oviduct - Og Ora-genital Pore - Ph Pharynx - Sp Sperm - SV Seminal Vesicle - T Testes - Va Vagina - Y Yolk     

A macroecological perspective of diversity patterns in the freshwater realm

1. The aim of this paper is to review literature on species diversity patterns of freshwater organisms and underlying mechanisms at large spatial scales. 2. Some freshwater taxa (e.g. dragonflies, fish and frogs) follow the classical latitudinal decline in regional species richness (RSR), supporting the patterns found for major terrestrial and marine organism groups. However, the mechanisms causing this cline in most freshwater taxa are inadequately understood, although research on fish suggests that energy and history are major factors underlying the patterns in total species and endemic species richness. Recent research also suggests that not all freshwater taxa comply with the decline of species richness with latitude (e.g. stoneflies, caddisflies and salamanders), but many taxa show more complex geographical patterns in across‐regions analyses. These complexities are even more profound when studies of global, continental and regional extents are compared. For example, clear latitudinal gradients may be present in regional studies but absent in global studies (e.g. macrophytes). 3. Latitudinal gradients are often especially weak in the across‐ecosystems analyses, which may be attributed to local factors overriding the effects of large‐scale factors on local communities. Nevertheless, local species richness (LSR) is typically linearly related to RSR (suggesting regional effects on local diversity), although saturating relationships have also been found in some occasions (suggesting strong local effects on diversity). Nestedness has often been found to be significant in freshwater studies, yet this pattern is highly variable and generally weak, suggesting also a strong beta diversity component in freshwater systems. 4. Both geographical location and local environmental factors contribute to variation in alpha diversity, nestedness and beta diversity in the freshwater realm, although the relative importance of these two groups of explanatory variables may be contingent on the spatial extent of the study. The mechanisms associated with spatial and environmental control of community structure have also been inferred in a number of studies, and most support has been found for species sorting (possibly because many freshwater studies have species sorting as their starting point), although also dispersal limitation and mass effects may be contributing to the patterns found. 5. The lack of latitudinal gradients in some freshwater taxa begs for further explanations. Such explanations may not be gained for most freshwater taxa in the near future, however, because we lack species‐level information, floristic and faunistic knowledge, and standardised surveys along extensive latitudinal gradients. A challenge for macroecology is thus to use the best possible species‐level information on well‐understood groups (e.g. fish) or use surrogates for species‐level patterns (e.g. families) and then develop hypotheses for further testing in the freshwater realm. An additional research challenge concerns understanding patterns and mechanisms associated with the relationships between alpha, beta and gamma components of species diversity. 6. Understanding the mechanistic basis of species diversity patterns should preferably be based on a combination of large‐scale macroecological and landscape‐scale metacommunity research. Such a research approach will help in elucidating patterns of species diversity across regional and local scales in the freshwater realm.     

Induced defences in marine and freshwater phytoplankton: a review

Many organisms have developed defences to avoid predation by species at higher trophic levels. The capability of primary producers to defend themselves against herbivores affects their own survival, can modulate the strength of trophic cascades and changes rates of competitive exclusion in aquatic communities. Algal species are highly flexible in their morphology, growth form, biochemical composition and production of toxic and deterrent compounds. Several of these variable traits in phytoplankton have been interpreted as defence mechanisms against grazing. Zooplankton feed with differing success on various phytoplankton species, depending primarily on size, shape, cell wall structure and the production of toxins and deterrents. Chemical cues associated with (i) mechanical damage, (ii) herbivore presence and (iii) grazing are the main factors triggering induced defences in both marine and freshwater phytoplankton, but most studies have failed to disentangle the exact mechanism(s) governing defence induction in any particular species. Induced defences in phytoplankton include changes in morphology (e.g. the formation of spines, colonies and thicker cell walls), biochemistry (such as production of toxins, repellents) and in life history characteristics (formation of cysts, reduced recruitment rate). Our categorization of inducible defences in terms of the responsible induction mechanism provides guidance for future work, as hardly any of the available studies on marine or freshwater plankton have performed all the treatments that are required to pinpoint the actual cue(s) for induction. We discuss the ecology of inducible defences in marine and freshwater phytoplankton with a special focus on the mechanisms of induction, the types of defences, their costs and benefits, and their consequences at the community level.