卜氏晶囊轮虫对萼花臂尾轮虫形态及种群生活史对策的短期和长期影响

初步探究了捕食者卜氏晶囊轮虫对其猎物萼花臂尾轮虫形态及种群生活史对策的短期和长期影响。结果表明,在含卜氏晶囊轮虫信号的环境中培养得到的萼花臂尾轮虫所产后代个体较对照组侧棘刺明显增长,体型增大,卵体积增大,净生殖率明显降低。短期接触捕食者信号的萼花臂尾轮虫种群与长期接触捕食者信号的萼花臂尾轮虫种群相比,具有较大的卵体积和较短的侧棘刺,同时具有显著较高的净生殖率。     

萼花臂尾轮虫多态性及形态型转化

在实验室条件下研究了萼花臂尾轮虫3种形态型(双短侧棘刺、单短侧棘刺和无侧棘刺)个体之间的关系。从轮虫的培养水体中随机挑出若干3种形态型雌体的幼轮虫(龄长<24h),分别培养在正常培养液和晶囊轮虫培养液过滤液中。将实验轮虫的后代(F1代)置于200倍显微镜下检查其个体的形态型。实验结果表明,在正常培养液中,每种形态型轮虫个体都可以产生3种形态型的后代。当培养在晶囊轮虫培养液过滤液中时,这3种形态型轮虫的后代都具有2个显著增长的侧棘刺。此外,这3种形态型个体的轮虫能够共存于同一培养环境中,而且每种形态型个体的轮虫都具有3种生殖类型的雌体。由此推测萼花臂尾轮虫是一个由3种基础形态型个体组成的形态型轮虫复合体。     

萼花臂尾轮虫多态性及形态型转化

在实验室条件下研究了萼花臂尾轮虫3种形态型(双短侧棘刺、单短侧棘刺和无侧棘刺)个体之间的关系。从轮虫的培养水体中随机挑出若干3种形态型雌体的幼轮虫(龄长<24 h)，分别培养在正常培养液和晶囊轮虫培养液过滤液中。将实验轮虫的后代(F1代)置于200倍显微镜下检查其个体的形态型。实验结果表明，在正常培养液中，每种形态型轮虫个体都可以产生3种形态型的后代。当培养在晶囊轮虫培养液过滤液中时，这3种形态型轮虫的后代都具有2个显著增长的侧棘刺。此外，这3种形态型个体的轮虫能够共存于同一培养环境中，而且每种形态型个体的轮虫都具有3种生殖类型的雌体。由此推测萼花臂尾轮虫是一个由3种基础形态型个体组成的形态型轮虫复合体。     

盐酸四环素浓度和食物密度对萼花臂尾轮虫生活史特征的综合影响

近年来,抗生素的环境污染问题已引起人们的广泛关注,其在环境中的残留可对水生态系统的结构和功能产生重要影响。迄今,盐酸四环素浓度和食物密度对轮虫生活史特征的影响研究尚未见报道。以萼花臂尾轮虫(Brachionus calyciflorus)为受试动物,研究了在不同斜生栅藻(Scenedesmus obliquus)密度下,不同浓度的盐酸四环素(Tetracycline hydrochloride)对萼花臂尾轮虫生活史特征的影响。结果表明,食物密度和盐酸四环素浓度对轮虫的生命期望、净生殖率、世代时间、内禀增长率、平均寿命和后代混交率,以及食物密度和盐酸四环素浓度间交互作用对除了内禀增长率外的其他5个统计学参数均具有显著影响。在各食物密度下,轮虫的特定年龄繁殖率高峰值随着盐酸四环素浓度的增加呈现先增加后降低的趋势;盐酸四环素对轮虫生长和繁殖参数的影响呈现"低促高抑"的特点。3个食物密度下,高浓度的盐酸四环素显著提高了萼花臂尾轮虫的后代混交率,且在1.0×10~6个/mL藻密度下毒物浓度与轮虫后代混交率间具有显著的剂量-效应关系。食物密度的高低显著影响盐酸四环素对萼花臂尾轮虫的毒性效应。     

密度信号对两种臂尾轮虫种群增长的影响

为了更好的了解化学干扰对轮虫种间竞争的影响,分别用萼花臂尾轮虫(Brachionus calyciflorus)和角突臂尾轮虫(Brachionus angularis)研究了同种和异种种群密度信号对种群增长的影响。结果表明,密度信号对轮虫种群增长具有一定的影响。萼花臂尾轮虫的密度信号显著降低了本种和角突臂尾轮虫种群的环境容纳量K并提高了它们的种群增长率r(P0.05),角突臂尾轮虫的密度信号对本种和萼花臂尾轮虫的种群增长都没有显著影响(P0.05)。萼花臂尾轮虫种群增长受同种密度信号抑制十分显著,环境容纳量K降低了50%以上,可能主要受自毒作用的调节,但同种密度信号对高有性生殖的萼花臂尾轮虫种群的混交率影响不明显。角突臂尾轮虫几乎不受自身密度信号的影响。因此,在两种臂尾轮虫的竞争中,由于自身密度信号的抑制作用,萼花臂尾轮虫将更快被角突臂尾轮虫排除。据此可推测密度信号对轮虫的种间竞争具有重要影响。     

五种淡水轮虫种群增长参数的比较研究

在32℃培养条件下,实验研究了5种淡水常见浮游轮虫的种群增长参数。通过编制生命表计算其内禀增长率rm(h-1)、净生殖力(R0)和世代时间T(h)分别为:萼花臂尾轮虫-0.091、14.1和34.1;壶状臂尾轮虫-0.055、6.9和38.4;角突臂尾轮虫-0.035、4.9和50.9;臂尾水轮虫-0.038、4.3和46.1以及裂足臂尾轮虫-0.017、2.1和43.7。其中,萼花臂尾轮虫内禀增长率大,繁殖率高,可作为批量培养的首选种类。       

基于线粒体COⅠ基因序列探讨臂尾轮属的系统发生和几种轮虫的分类地位

通过对萼花臂尾轮虫、角突臂尾轮虫、壶状臂尾轮虫、十指臂尾轮虫、镰形臂尾轮虫、尾突臂尾轮虫和红臂尾轮虫等7种轮虫mtDNA COⅠ序列分析,并以透明囊足轮虫为外群,使用MEGA软件构建臂尾轮属轮虫系统发生树(ME树和NJ树)以探讨臂尾轮属的系统发生和该属中几个种类的分类地位.结果表明本研究所涉及的轮虫mtDNA COⅠ平均序列差异百分比为24%;在两个系统树中,淡水臂尾轮虫和海水臂尾轮虫均独立成枝;用两种方法得到的系统发生树均支持将十指臂尾轮虫作为一个独立的支系分离出来.壶状臂尾轮虫和红臂尾轮虫应属于不同的种;来自芜湖、墨西哥和美国的十指臂尾轮虫以及来自芜湖和澳大利亚的萼花臂尾轮虫应分别互为姐妹种.本研究还首次揭示了角突臂尾轮虫、尾突臂尾轮虫和镰状臂尾轮虫与其它臂尾轮虫间的系统关系.     

基于16S rDNA序列探讨十种臂尾轮虫的系统关系和分类地位

通过对角突臂尾轮虫、尾突臂尾轮虫、裂足臂尾轮虫、剪形臂尾轮虫、方形臂尾轮虫、壶状臂尾轮虫、红臂尾轮虫、镰肜臂尾轮虫、萼花臂尾轮虫和十指臂尾轮虫等十种臂尾轮虫和大肚须足轮虫的线粒体16s rDNA进行扩增和序列测序,结合Genebank 中十指臂尾轮虫的16S rDNA序列,使用MAGE软件构建了NJ(neighbor-joining method)树,使用mrbayes软件构建了贝叶斯树,探讨了十种臂尾轮虫之间的系统关系.结果表明,本研究所涉及的轮虫16S rDNA序列差异百分比均值为14.6%,可作为分子标记应用于轮虫属内种间系统关系研究;系统树均支持将十指臂尾轮虫、裂足臂尾轮虫隶属于臂尾轮属;壶状臂尾轮虫和红臂尾轮虫是两个独立的种.此外,还依据16S rDNA序列变异百分比推测了十种臂尾轮虫的分化时间.     

基于28S rDNA基因序列研究十种臂尾轮虫的系统关系和分类地位

通过对角突臂尾轮虫、尾突臂尾轮虫、裂足臂尾轮虫、剪形臂尾轮虫、方形臂尾轮虫、壶状臂尾轮虫、红臂尾轮虫、镰形臂尾轮虫、萼花臂尾轮虫和十指臂尾轮虫等10种臂尾轮虫以及透明囊足轮虫、大肚须足轮虫和晶囊轮虫等其他3种轮虫的28S rDNA序列分析,使用MAGE软件构建这13种轮虫系统发生树(NJ树、ME树、UPGMA树和MP树),探讨了臂尾轮属、须足轮属、晶囊轮属和囊足轮属之间以及10种臂尾轮虫之间的系统关系.结果表明,本研究所涉及的轮虫28S rDNA序列差异百分比均值为30.15%,可作为分子标记应用于轮虫属间和属内种间系统关系研究;系统树均支持将十指臂尾轮虫作为一个独立的支系从臂尾轮属中分离出来;裂足臂尾轮虫应隶属臂尾轮属;壶状臂尾轮虫和红臂尾轮虫是两个独立的种;透明囊足轮虫与臂尾轮属亲缘关系较近.     

基于 rDNA ITS 1序列探讨臂尾轮属轮虫的系统发生关系

本文通过对剪形臂尾轮虫、矩形臂尾轮虫、十指臂尾轮虫、红臂尾轮虫、角突臂尾轮虫、双棘臂尾轮虫、裂足臂尾轮虫和萼花臂尾轮虫等八种臂尾轮虫rDNAITS 1序列分析,并以西氏晶囊轮虫为外群,使用PAUP和贝叶斯软件分别构建臂尾轮属轮虫系统发生树( MP树、NJ树、ML树和贝叶斯树) ,以探讨臂尾轮属的系统发生关系,并解决其中的一些分类问题。结果表明:本研究所涉及的轮虫rDNAITS 1平均序列差异百分比较高,为29 %;海水和淡水臂尾轮虫被明显分为不同的进化枝;除双棘臂尾轮虫外,在淡水臂尾轮虫中具有三对前棘刺且营附着生活的种类与前棘刺少于三对且营浮游生活的种类聚在不同支系中,这与以形态特征为主所进行的系统发生研究结果基本一致;所有的系统树均支持将十指臂尾轮虫作为一个独立的支系分离出来,裂足臂尾轮虫应归入臂尾轮属。     

Chimpanzee and felid diet composition is influenced by prey brain size

Prey use a wide variety of anti-predator defence strategies, including morphological and chemical defences as well as behavioural traits (risk-modulated habitat use, changes in activity patterns, foraging decisions and group living). The critical test of how effective anti-predator strategies are is to relate them to relative indices of mortality across predators. Here, we compare biases in predator diet composition with prey characteristics and show that chimpanzee (Pan troglodytes) and felid show the strongest and the most consistent predator bias towards small-brained prey. We propose that large-brained prey are likely to be more effective at evading predators because they can effectively alter their behavioural responses to specific predator encounters. Thus, we provide evidence for the hypothesis that brain size evolution is potentially driven by selection for more sophisticated and behaviourally flexible anti-predator strategies.     

Multiple predator defence strategies in Daphnia pulex and their relation to native habitat

Daphnia may respond with an array of anti-predator defences(behavioural, morphological and life history) to a chemicalcue (kairomone) exuded by its predators: fish and Chaoborus.Given the wide array of potential responses, it is an interestingquestion whether anti-predator defences are coupled or independentof each other. Since anti-predator responses are costly andeven possessing the genetic information to respond to a certainpredator might involve a cost, clones may only react to predatorsthey co-occur with in nature. In this study, we provide evidencefor an uncoupling of responses by Daphnia pulex in several anti-predatordefences against Chaoborus. We were unable to detect a correlationbetween behavioural (migration), morphological (neck-spine induction)and life history [growth rate, neonate size and size at firstreproduction (SFR)] responses. Furthermore, anti-predator responsesdid not always comply with what is commonly believed. We foundthat Daphnia clones can migrate up or down when exposed to fishor Chaoborus kairomone and that population growth rate, neonatesize and SFR can increase or decrease in response to Chaoboruskairomone. We also show patterns in anti-predator defences thatseem to relate to the habitat from which clones were derived.Daphnia clones that were collected in habitats with Chaoborusas the dominant predator tended to react strongly to Chaoboruskairomone by migrating upward and producing neck-spines. Themigration behaviour against fish kairomone in these clones wasoften an unexpected upward migration. The Daphnia clone thatco-existed with fish predators showed a downward migration inthe presence of fish as well as Chaoborus kairomone. Clonesthat had occurred with either both or no predators had mixedresponses. We sometimes found an upward migration in combinationwith smaller body size as a response to Chaoborus kairomone.This may be interpreted as a behavioural defence against Chaoborusand a life-history defence against fish. Daphnia seem not toexhibit defence behaviour against predators they do not co-occurwith. It might be costly for Daphnia to maintain genetic informationto respond to these predators and protect that information fromgenetic drift.     

Behavioural and life history effects of predator diet cues during ontogeny in damselfly larvae

A central issue in predator–prey interactions is how predator associated chemical cues affect the behaviour and life history of prey. In this study, we investigated how growth and behaviour during ontogeny of a damselfly larva (Coenagrion hastulatum) in high and low food environments was affected by the diet of a predator (Aeshna juncea). We reared larvae in three different predator treatments; no predator, predator feeding on conspecifics and predator feeding on heterospecifics. We found that, independent of food availability, larvae displayed the strongest anti-predator behaviours where predators consumed prey conspecifics. Interestingly, the effect of predator diet on prey activity was only present early in ontogeny, whereas late in ontogeny no difference in prey activity between treatments could be found. In contrast, the significant effect of predator diet on prey spatial distribution was unaffected by time. Larval size was affected by both food availability and predator diet. Larvae reared in the high food treatment grew larger than larvae in the low food treatment. Mean larval size was smallest in the treatment where predators consumed prey conspecifics, intermediate where predators consumed heterospecifics and largest in the treatment without predators. The difference in mean larval size between treatments is probably an effect of reduced larval feeding, due to behavioural responses to chemical cues associated with predator diet. Our study suggests that anti-predator responses can be specific for certain stages in ontogeny. This finding shows the importance of considering where in its ontogeny a study organism is before results are interpreted and generalisations are made. Furthermore, this finding accentuates the importance of long-term studies and may have implications for how results generated by short-term studies can be used.     

Predator recognition and defence strategies in crucian carp, Carassius carassius

Crucian carp from populations that lack piscivores are extremely vulnerable to predation. However, in the presence of piscivores these fish develop an inducible morphological defence, a deep body. This switch from a vulnerable, shallow-bodied morph to a morphologically defended morph makes this species very suitable for investigations of anti-predator strategies, and trade-offs between morphological and behavioural defences. To address these questions, we performed eight different experiments. We found that crucian carp exhibited fright responses to chemical cues from unfamiliar predators (northern pike, perch) when these were fed prey that contained alarm substance (for northern pike: crucian carp, roach; for perch: crucian carp). Cues from small pike that were fed prey that lacked alarm substance (swordtails) caused no significant fright response whereas cues from larger pike with the same diet did. Perch on a chironomid diet elicited weaker but significant fright responses. Starved predators caused as strong fright reactions as recently fed ones did, whereas no response was exhibited towards nonpredatory fish (roach, crucian carp). Crucian carp were able to detect the presence of pike after cues had been diluted to an equivalent of 21 000 l, and larger predators elicited stronger fright responses. Prior experience of predators decreased fright responses. In particular, individuals from populations that coexisted with northern pike responded less to chemical cues from northern pike than individuals without prior experience did. Thus, crucian carp may use both alarm-substance related and predator-related cues to identify predators. Further, they were able to discriminate between large and small predators. Finally, individuals from populations that coexist with predators exhibit less pronounced fright responses. These fish have an induced morphological defence, a deep body, which most likely decreases the need for strong antipredator behaviour.     

Generalization of predator recognition: Velvet geckos display anti-predator behaviours in response to chemicals from non-dangerous elapid snakes

Many prey species detect chemical cues from predators and modify their behaviours in ways that reduce their risk of predation. Theory predicts that prey should modify their anti-predator responses according to the degree of threat posed by the predator. That is, prey should show the strongest responses to chemicals of highly dangerous prey, but should ignore or respond weakly to chemicals from non-dangerous predators. However, if anti-predator behaviours are not costly, and predators are rarely encountered, prey may exhibit generalised antipredator behaviours to dangerous and non-dangerous predators. In Australia, most elapid snakes eat lizards, and are therefore potentially dangerous to lizard prey. Recently, we found that the nocturnal velvet gecko Oedura lesueurii responds to chemicals from dangerous and non-dangerous elapid snakes, suggesting that it displays gen-eralised anti-predator behaviours to chemicals from elapid snakes. To explore the generality of this result, we videotaped the be-haviour of velvet geckos in the presence of chemical cues from two small elapid snakes that rarely consume geckos: the nocturnal golden-crowned snake Cacophis squamulosus and the diurnal marsh snake Hemiaspis signata. We also videotaped geckos in tri-als involving unsceted cards (controls) and cologne-scented cards (pungency controls). In trials involving Cacophis and Hemi-aspis chemicals, 50% and 63% of geckos spent long time periods (> 3 min) freezing whilst pressed flat against the substrate, re-spectively. Over half the geckos tested exhibited anti-predator behaviours (tail waving, tail vibration, running) in response to Ca-cophis (67%) or Hemiaspis (63%) chemicals. These behaviours were not observed in control or pungency control trials. Our re-sults support the idea that the velvet gecko displays generalised anti-predator responses to chemical cues from elapid snakes. Generalised responses to predator chemicals may be common in prey species that co-occur with multiple, ecologically similar, dangerous predators.     

Interspecific infanticide deters predators

It is well known that young, small predator stages are vulnerable to predation by conspecifics, intra-guild competitors or hyperpredators. It is less known that prey can also kill vulnerable predator stages that present no danger to the prey. Since adult predators are expected to avoid places where their offspring would run a high predation risk, this opens the way for potential prey to deter dangerous predator stages by killing vulnerable predator stages. We present an example of such a complex predator–prey interaction. We show that (1) the vulnerable stage of an omnivorous arthropod prey discriminates between eggs of a harmless predator species and eggs of a dangerous species, killing more eggs of the latter; (2) prey suffer a minor predation risk from newly hatched predators; (3) adult predators avoid ovipositing near killed predator eggs, and (4) vulnerable prey near killed predator eggs experience an almost fourfold reduction of predation. Hence, by attacking the vulnerable stage of their predator, prey deter adult predators and thus reduce their own predation risk. This provides a novel explanation for the killing of vulnerable stages of predators by prey and adds a new dimension to anti-predator behaviour.     

Winter Stephanodiscus bloom development in the Nakdong River regulated by an estuary dam and tributaries

Planktonic organisms exhibit diverse morphological, behavioural and life-history responses to the chemical presence of potential predators. Prey organisms have been found to sense such predators via predator-derived kairomones. The induced reactions are assumed to reduce predation risk and thus to be adaptive. Numerous studies have investigated various aspects of inducible defences in different crustaceans, in rotifers, planktonic ciliates and algae. As a first step, we summarise recent work on chemically induced anti-predator defences in morphology, life history and behaviour. Morphological defences have been found in a wide range of different plankton organisms and recent studies on predator-induced morphologies mainly addressed the question of costs for these changes. Life-history responses were mainly studied in cladocerans and several studies have recently addressed some novel topics, such as diapause induction and the influence of predator kairomones on hatching of resting stages. Behavioural anti-predator defences also have been found for several plankton species and are characterised by relatively fast induction times. We further identified four research directions in which substantial progress has been made recently: (I) The effects of simultaneous exposure to infochemicals from different predators and the consequences of a complex chemical environment. Some environmental contaminants, such as synthetic chemicals or heavy metals, have been found to potentially disturb natural chemical communication in aquatic predator-prey systems. (II) The influence of genetic variation on the reaction to infochemicals and its implications. Clonal differences have not only been found for the presence or absence of a certain trait but also with respect to the type of response. (III) The degree to which different types of responses to a specific kairomone are coupled. Recent studies underline the uncoupling of different anti-predator responses of which some have been considered to be coupled. (IV) Studies on the chemical properties and on the metabolic origin of predator kairomones. Substantial progress has been made recently, especially with respect to the identification of predator kairomones that are important for planktonic ciliates. The identification and isolation of kairomones are an important step towards studies addressing the consequences of predator-induced defences on the level of populations, communities and ecosystems. So far most studies have considered effects and consequences on the level of individual prey organisms and studies taking the consequences at higher ecological levels into account are rare.     

A community-level evaluation of the impact of prey behavioural and ecological characteristics on predator diet composition

Although predation avoidance is the most commonly invoked explanation for vertebrate social evolution, there is little evidence that individuals in larger groups experience lower predation rates than those in small groups. We compare the morphological and behavioural traits of mammal prey species in the Taï forest, Ivory Coast, with the diet preferences of three of their non-human predators: leopards, chimpanzees and African crowned eagles. Individual predators show marked differences in their predation rates on prey species of different body sizes, but clear patterns with prey behaviour were apparent only when differences in prey habitat use were incorporated into the analyses. Leopard predation rates are highest for terrestrial species living in smaller groups, whereas eagle predation rates are negatively correlated with group size only among arboreal prey. When prey predation rates are summed over all three predators, terrestrial species incur higher predation rates than arboreal species and, within both categories, predation rates decline with increasing prey group size and decreasing density of groups in the habitat. These results reveal that it is necessary to consider anti-predator strategies in the context of a dynamic behavioural interaction between predators and prey.     

Responses of tadpoles to hybrid predator odours: strong maternal signatures and the potential risk/response mismatch

Previous studies have established that when a prey animal knows the identity of a particular predator, it can use this knowledge to make an ‘educated guess'' about similar novel predators. Such generalization of predator recognition may be particularly beneficial when prey are exposed to introduced and invasive species of predators or hybrids. Here, we examined generalization of predator recognition for woodfrog tadpoles exposed to novel trout predators. Tadpoles conditioned to recognize tiger trout, a hybrid derived from brown trout and brook trout, showed generalization of recognition of several unknown trout odours. Interestingly, the tadpoles showed stronger responses to odours of brown trout than brook trout. In a second experiment, we found that tadpoles trained to recognize brown trout showed stronger responses to tiger trout than those tadpoles trained to recognize brook trout. Given that tiger trout always have a brown trout mother and a brook trout father, these results suggest a strong maternal signature in trout odours. Tadpoles that were trained to recognize both brown trout and brook trout showed stronger response to novel tiger trout than those trained to recognize only brown trout or only brook trout. This is consistent with a peak shift in recognition, whereby cues that are intermediate between two known cues evoke stronger responses than either known cue. Given that our woodfrog tadpoles have no evolutionary or individual experience with trout, they have no way of knowing whether or not brook trout, brown trout or tiger trout are more dangerous. The differential intensity of responses that we observed to hybrid trout cues and each of the parental species indicates that there is a likely mismatch between risk and anti-predator response intensity. Future work needs to address the critical role of prey naivety on responses to invasive and introduced hybrid predators.     

Costs and benefits of defences induced by predators differing in dangerousness

While theoretical studies predict that inducible defences should be fine-tuned according to the qualities of the predator, very few studies have investigated how dangerousness of predators, i.e. the rate at which predators kill prey individuals, affects the strength of phenotypic responses and resulting benefits and costs of induced defences. We performed a comprehensive study on fitness consequences of predator-induced responses by involving four predators (leech, water scorpion, dragonfly larva and newt), evaluating costs and benefits of responses, testing differences in dangerousness between predators and measuring responses in several life history traits of prey. We raised Rana dalmatina tadpoles in the presence of free-ranging predators, in the presence of caged predators, and exposed naive and experienced tadpoles to free-ranging predators. Tadpoles adjusted the intensities of their behavioural and morphological defences to predator dangerousness. Survival was lower in the nonlethal presence of the most dangerous predator, while we could not detect costs of induced defences at or after metamorphosis. When exposed to free-ranging predators, small, but not large, tadpoles benefited from exhibiting an induced phenotype in terms of elevated survival when compared to naive tadpoles, but we did not observe higher survival either in tadpoles exhibiting more extreme phenotypes or in tadpoles exposed to the type of predator they were raised with. These results indicate that while predator-induced defences can mirror dangerousness of predators, costs and benefits do not necessarily scale to the magnitude of plastic responses.