J A Harvey’s research while affiliated with Vrije Universiteit Amsterdam and other places

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Publications (41)


Fig. 1. Experimental design. Forty mesocosms of 1 m 3 were created in a raster of 8 by 5 mesocosms with 0.5 m between them. Mesocosms were exposed to three treatments, each with two levels, according to a full factorial design, resulting in a total of 8 unique treatments (n = 5). The two conditioning treatments were plant origin (native or range expanding) and exposure to extreme drought (yes or no), whereas the soil was collected in the Netherlands (local) or from the geographical area where the range expanding plants originated (Hungary). Each mesocosm was dived in four quadrants (a, b, c, d) which all received the same treat. In each quadrant, one plant of each of the 8 species listed in Table 1 was planted.
Plant species pairs, categorized as 'native' or 'range expanding' planted in the mesocosms.
Within-patch and edge microclimates vary over a growing season and are amplified during a heatwave: Consequences for ectothermic insects
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May 2021

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61 Reads

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10 Citations

Journal of Thermal Biology

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K. Li

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J.A. Harvey

Embedded in longer term warming are extreme climatic events such as heatwaves and droughts that are increasing in frequency, duration and intensity. Changes in climate attributes such as temperature are often measured over larger spatial scales, whereas environmental conditions to which many small ectothermic arthropods are exposed are largely determined by small-scale local conditions. Exposed edges of plant patches often exhibit significant short-term (daily) variation to abiotic factors due to wind exposure and sun radiation. By contrast, within plant patches abiotic conditions are generally much more stable and thus less variable. Over an eight-week period in the summer of 2020, including an actual heatwave, we measured small-scale (1 m²) temperature variation in patches of forbs in experimental mesocosms. We found that soil surface temperatures at the edge of the mesocosms were more variable than those within mesocosms. Drought treatment two years earlier, amplified this effect but only at the edges of the mesocosms. Within a plant patch both at the soil surface and within the canopy, the temperature was always lower than the ambient air temperature. The temperature of the soil surface at the edge of a patch may exceed the ambient air temperature when ambient air temperatures rise above 23 °C. This effect progressively increased with ambient temperature. We discuss how microscale-variation in temperature may affect small ectotherms such as insects that have limited ability to thermoregulate, in particular under conditions of extreme heat.

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Habitat complexity reduces parasitoid foraging efficiency, but does not prevent orientation towards learned host plant odours

May 2015

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285 Reads

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44 Citations

Oecologia

It is well known that many parasitic wasps use herbivore-induced plant odours (HIPVs) to locate their inconspicuous host insects, and are often able to distinguish between slight differences in plant odour composition. However, few studies have examined parasitoid foraging behaviour under (semi-)field conditions. In nature, food plants of parasitoid hosts are often embedded in non-host-plant assemblages that confer both structural and chemical complexity. By releasing both naïve and experienced Cotesia glomerata females in outdoor tents, we studied how natural vegetation surrounding Pieris brassicae-infested Sinapis arvensis and Barbarea vulgaris plants influences their foraging efficiency as well as their ability to specifically orient towards the HIPVs of the host plant species on which they previously had a positive oviposition experience. Natural background vegetation reduced the host-encounter rate of naïve C. glomerata females by 47 %. While associative learning of host plant HIPVs 1 day prior to foraging caused a 28 % increase in the overall foraging efficiency of C. glomerata, it did not reduce the negative influence of natural background vegetation. At the same time, however, females foraging in natural vegetation attacked more host patches on host-plant species on which they previously had a positive oviposition experience. We conclude that, even though the presence of natural vegetation reduces the foraging efficiency of C. glomerata, it does not prevent experienced female wasps from specifically orienting towards the host-plant species from which they had learned the HIPVs.


The roles of ecological fitting, phylogeny and physiological equivalence in understanding realized and fundamental host ranges in endoparasitoid wasps

August 2012

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58 Reads

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22 Citations

Journal of Evolutionary Biology

Co-evolutionary theory underpins our understanding of interactions in nature involving plant-herbivore and host-parasite interactions. However, many studies that are published in the empirical literature that have explored life history and development strategies between endoparasitoid wasps and their hosts are based on species that have no evolutionary history with one another. Here, we investigated novel associations involving two closely related solitary endoparasitoids that originate from Europe and North America and several of their natural and factitious hosts from both continents. The natural hosts of both species are also closely related, all being members of the same family. We compared development and survival of both parasitoids on the four host species and predicted that parasitoid performance is better on their own natural hosts. In contrast with this expectation, survival, adult size and development time of both parasitoids were similar on all (with one exception) hosts, irrespective as to their geographic origin. Our results show that phylogenetic affinity among the natural and factitious hosts plays an important role in their nutritional suitability for related parasitoids. Evolved traits in parasitoids, such as immune suppression and development, thus enable them to successfully develop in novel host species with which they have no evolutionary history. Our results show that host suitability for specialized organisms like endoparasitoids is closely linked with phylogenetic history and macro-evolution as well as local adaptation and micro-evolution. We argue that the importance of novel interactions and 'ecological fitting' based on phylogeny is a greatly underappreciated concept in many resource-consumer studies.


Figure 2 Conceptual diagram showing the potential effects of invasive plants on a four-trophic-level interaction involving plants, herbivores, a parasitoid, and hyperparasitoid. (A) A native plant species grows in patches where it is dominant. A specialist herbivore (in this case a moth) oviposits on the plant which, through feeding damage from the caterpillar, releases volatiles (blue plumes) that attracts one of its specialist natural enemies, a primary endoparastioid. In turn, plant-related cues attract a primary hyperparasitoid of the primary endoparasitoid. (B) A larger unrelated invasive plant species fragments patches in which the native plant grows. The plant provides structural and perhaps chemical barriers, such as repellents (red plumes) that interfere with the foraging behavior of the moth, its primary parasitoid and hyperparasitoid. (C) The invasive plant species is a close relative of the native plant species, and invades the same patches where the native plant normally occurs. The invasive plant produces volatiles that are attractive to the herbivore and its parasitoid, but the plant tissues are toxic to both of them and the plant thus represents a potential evolutionary 'trap' for these consumers. Another generalist herbivore readily feeds on both plants, increasing the level of volatiles emitted that are attractive to the herbivore and its parasitoid. This may increase the detection or 'associational susceptibility' of the invasive plant to the specialist herbivore and its parasitoid. Ultimately, the effects of structural and chemical impediments imposed by invasive plants on native insects will critically depend on how different species and trophic levels respond to them.
Figure 3 Flow diagram showing various scenarios describing the potential effects of plant volatiles on arthropod communities based on the diversity of the native (N) plant communities where the invasive (I) plant is introduced. Attractive volatiles emitted by the invaded plant community may lead to a plant shift by local fauna if the invasive plant is suitable or to an evolutionary trap if the invasive plant is not suitable. Alternatively, if invasive plant volatiles trigger a repellent response on local arthropods, the patch will hold few or no plant enemies, and the invasive plant may find a time window that enables it to spread and eventually become dominant, supporting the Enemy Release Hypothesis.
Chemical and structural effects of invasive plants on herbivore-parasitoid/predator interactions in native communities

January 2012

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901 Reads

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50 Citations

The introduction and/or spread of exotic organisms into new habitats is considered a major threat to biodiversity. Invasive plants have been shown to negatively affect native communities, competing with and excluding other plants and disrupting a wide range of trophic interactions associated with them. In spite of this, thus far, few studies have explicitly studied the mechanisms underlying the displacement and potential local extinction of native herbivores and their natural enemies up to the third trophic level and even higher. Here, we formulate hypotheses on how structural and chemical characteristics of invasive plants may affect the plant-finding abilities of herbivores and the host- or prey-finding behavior of predators and parasitoids. The sudden incursion of an invasive plant into a native plant community may fragment native habitats and thus create structural barriers that impede dispersal and plant-finding ability for herbivores and prey- or host-finding ability for predators and parasitoids. At the same time, invasive plants may produce odors that are attractive to native insects and thus interfere with interactions on native plants. If invasive plants are both attractive and toxic to native insects, they may constitute ‘traps’ that are possibly beneficial against insect pests in agro-ecosystems, but have conservation implications for native herbivores and their natural enemies. However, we also suggest that some herbivores, and by association their parasitoids, may benefit from the establishment and spread of exotic plants because they increase the amount of available resources for them to exploit.


Figure 1: The composition of nematode communities underneath individual plants is influenced by the identity of the plant species and by the plant community in which the species was embedded. For eight different plant species a consistent pattern emerges: The similarity (Bray-Curtis) between two nematode communities is highest when two plant individuals of the same species and growing in the same plant community are compared, and lowest when two plants belonging to two different plant species and growing in two different plant communities are compared. Means are shown with standard errors for plant individuals of grass species (G) Festuca rubra, Holcus lanatus, and Anthoxanthum odoratum (Anthox.); forb species (F) Leucanthemum vulgare (Leucanth.), Plantago lanceolata, and Tanacetum vulgare; and legume species (L) Vicia cracca and Lotus corniculatus.
Figure 2: Plant species identity (L. corniculatus or P. lanceolata) and surrounding plant community (originally sown with 15, 4, or 0 species) influence the composition of soil communities underneath individual plants. Results are from multivariate analyses of the composition of different taxonomic groups of soil organisms, phospholipids (PLFA), and microbial functioning (Biolog), and on the food web structure (the composition of the carbon biomasses of all feeding groups within the food web as depicted in ); AMF stands for arbuscular mycorrhizal fungi. The amount of variation within the 58 food webs that is explained by host plant identity (df = 1) and plant community identity (sowing treatment, df = 2) is shown. The number following each bar shows the number of identified categories (e.g., species or genus) included in the analysis. Asterisks indicate significance of the effect based on permutation tests. * P < 0.05; ** P < 0.01; *** P < 0.001.
Figure 4: Schematic representation of the soil food web. Soil organisms were grouped into feeding groups, and the biomass of each group was calculated (g carbon per g soil). Boxes represent feeding groups, and their surface areas represent feeding group biomass, based on the average of all food webs. Biomass of roots and soil organic matter are not scaled to their actual amounts, but the ratio is shown. Arrows indicate feeding relations with the arrow head pointing toward the consumer. AMF stands for arbuscular mycorrhizal fungi.
Divergent composition but similar function of soil food webs of individual plants: Plant species and community effects

October 2010

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469 Reads

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175 Citations

Soils are extremely rich in biodiversity, and soil organisms play pivotal roles in supporting terrestrial life, but the role that individual plants and plant communities play in influencing the diversity and functioning of soil food webs remains highly debated. Plants, as primary producers and providers of resources to the soil food web, are of vital importance for the composition, structure, and functioning of soil communities. However, whether natural soil food webs that are completely open to immigration and emigration differ underneath individual plants remains unknown. In a biodiversity restoration experiment we first compared the soil nematode communities of 228 individual plants belonging to eight herbaceous species. We included grass, leguminous, and non-leguminous species. Each individual plant grew intermingled with other species, but all plant species had a different nematode community. Moreover, nematode communities were more similar when plant individuals were growing in the same as compared to different plant communities, and these effects were most apparent for the groups of bacterivorous, carnivorous, and omnivorous nematodes. Subsequently, we analyzed the composition, structure, and functioning of the complete soil food webs of 58 individual plants, belonging to two of the plant species, Lotus corniculatus (Fabaceae) and Plantago lanceolata (Plantaginaceae). We isolated and identified more than 150 taxa/groups of soil organisms. The soil community composition and structure of the entire food webs were influenced both by the species identity of the plant individual and the surrounding plant community. Unexpectedly, plant identity had the strongest effects on decomposing soil organisms, widely believed to be generalist feeders. In contrast, quantitative food web modeling showed that the composition of the plant community influenced nitrogen mineralization under individual plants, but that plant species identity did not affect nitrogen or carbon mineralization or food web stability. Hence, the composition and structure of entire soil food webs vary at the scale of individual plants and are strongly influenced by the species identity of the plant. However, the ecosystem functions these food webs provide are determined by the identity of the entire plant community.


Climate range-expanding plant species experience lower herbivore loads, but higher predator pressure

August 2009

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11 Reads

Ecosystems worldwide are increasingly being invaded by plants from exotic origins. It has been stressed that these invaders perform better than similar native species in the invaded communities. Although some plant invasions have taken place for more than a century, the mechanisms explaining the success of these invaders are not well understood yet. The release from aboveground natural enemies has been widely stressed as one of the most important factors accounting for the ability of invaders to become successful. Novel biotic interactions, if favorable, enable many invasive plants to become dominant in their new community, thereby displacing native species. Currently, the consequences of climate warming are being noticed in range shifts of plants and animals to higher elevations and latitudes. Although biotic interactions strongly affect responses to warming, they are generally not included in climate studies. Also, top-down effects mediated by natural enemies in the third trophic level have not yet been taken into account in these studies. Hence, when plants spread faster than their natural enemies or than the enemies of their enemies, multi-trophic interactions can become, at least temporarily, disrupted. These changes in relations may create invasion opportunities for species within geographical regions. In order to test whether release from enemies may be applicable to the natural situation of range-expanding plants we studied the arthropod community on 2 range-expanding plant species (exotic to the Netherlands) and their native congeners. All species co-occur in riverine habitat and insects were sampled in 3 different populations in 3 consecutive periods in the growing season (early, mid and late summer). Insects were classified to different herbivorous guilds providing insight on the specificity of enemy release. Furthermore, we discriminated between phytophagous and carnivorous insects to determine the control potential of the third trophic level. As expected, we found higher aggregate loads of herbivorous insects on both range-expanding plants than on the native species. Depending on the species pair, either the chewing and sap-sucking insects or the galling insects showed the strongest differences, which in some cases depended on the temporal context. Surprisingly, we found higher predator pressure for the range-expanding plants, indicating an additional advantage over their native congeners. These results suggest that climate range-expanding plants are, at least partially, released from natural enemies, and that they experienced indirect positive feedback from carnivorous arthropods in the third trophic level




Fig. 1 a Average leaf concentration of aucubin (percent of dry weight) and b average number of leaves on Plantago lanceolata plants with (black bars) and without (hatched bars) oviposition by Melitaea cinxia in experiments 1 and 2. Note that experiment 1 represents a 1- day dual-choice test, whereas experiment 2 represents a multiplechoice test of longer duration. See text for a detailed description of the experiments. *P<0.05  
Table 1 Characteristics of ten Plantago lanceolata genotypes selected for low (L1-L5) or high (H1-H5) leaf IG in the Tvärminne field site and occurrence of Melitaea cinxia on them (exp. 3)
Oviposition Cues for a Specialist Butterfly–Plant Chemistry and Size

August 2008

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206 Reads

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76 Citations

Journal of Chemical Ecology

The oviposition choice of an insect herbivore is based on a complex set of stimuli and responses. In this study, we examined the effect of plant secondary chemistry (the iridoid glycosides aucubin and catalpol) and aspects of size of the plant Plantago lanceolata, on the oviposition behavior of the specialist butterfly Melitaea cinxia. Iridoid glycosides are known to deter feeding or decrease the growth rate of generalist insect herbivores, but can act as oviposition cues and feeding stimulants for specialized herbivores. In a previous observational study of M. cinxia in the field, oviposition was associated with high levels of aucubin. However, this association could have been the cause (butterfly choice) or consequence (plant induction) of oviposition. We conducted a set of dual- and multiple-choice experiments in cages and in the field. In the cages, we found a positive association between the pre-oviposition level of aucubin and the number of ovipositions. The association reflects the butterfly oviposition selection rather than plant induction that follows oviposition. Our results also suggest a threshold concentration below which females do not distinguish between levels of iridoid glycosides. In the field, the size of the plant appeared to be a more important stimulus than iridoid glycoside content, with bigger plants receiving more oviposition than smaller plants, regardless of their secondary chemistry. Our results illustrate that the rank of a cue used for oviposition may be dependent on environmental context.


Citations (25)


... However, it is a perfect multidisciplinary field for the species-specific analysis of climate-species interactions and the dynamics of species distribution (Pincebourde and Woods 2020). As the exposure of insects to environmental conditions is determined by small-scale local conditions that can have an impact on the biology and ecology of species, the collection of climate data at finer scales is important (Gols et al. 2021). ...

Reference:

Can Monitoring Data of Forensically Important Blow Flies Be Transferred Between Cities?
Within-patch and edge microclimates vary over a growing season and are amplified during a heatwave: Consequences for ectothermic insects

Journal of Thermal Biology

... Plants also show both interand intraspecific variation in volatile composition, which affects the apparency of cues from individual host-infested plants through herbivore-induced plant volatiles (Bukovinszky et al., 2005;Degen et al., 2012;Kuramitsu et al., 2019;Lamy et al., 2018;Li et al., 2018;Mody et al., 2017;Ode & Crompton, 2013). Also, plumes of plant volatiles from neighbouring plants might mix to create new odour blends, further affecting parasitoid host location efficiency (Bukovinszky et al., 2007;Kostenko et al., 2015;Kruidhof et al., 2015). Apparency of profitable patches for parasitoids is thus determined by how well plant volatile cues stand out in the context of other cues derived from the plant community and is determined by plant genotypic variation in volatile emission as well as its relative difference from volatile emissions by neighbouring plants. ...

Habitat complexity reduces parasitoid foraging efficiency, but does not prevent orientation towards learned host plant odours

Oecologia

... At that time, caterpillars parasitized by C. glomerata were in the early fifth instar stage, while cater pillars par asitized b y C. rubecula w ere in the late thir d instar stage. Cotesia rubecula is known to arrest host development at the third instar stage (Harvey et al. 1999 ), while C. glomerata allows its host to r eac h the final instar sta ge (Harv ey et al. 2012 ). Nonparasitized P. brassicae and P. rapae cater pillars wer e in the early fifth instar sta ge. ...

Development of the parasitoid, Cotesia rubecula (Hymenoptera: Braconidae) in Pieris rapae and Pieris brassicae (Lepidoptera: Pieridae): evidence for host regulation
  • Citing Article
  • January 1999

Journal of Insect Physiology

... Among the aboveground plant structures are stems, branches, leaves, shoots, flowers, and seeds, whereas belowground plant parts are represented by roots and tubers. These distinct plant structures enable indirect interactions between organisms that rarely interact directly with one another (Soler et al., 2008). In both the belowground and aboveground environments, various organisms are associated with the plants, including vertebrates, arthropods, and microorganisms, which exert beneficial, neutral, or negative effects on plants. ...

Plants as green phones: Novel insights into plant-mediated communication between below- and aboveground insects

Plant Signaling & Behavior

... Combining analyses of seedling distribution relationships to conspecific adult plants with analyses of soil community feedbacks, enables examination of the role of soil biota in the conspecific distanceand density-dependent plant recruitment (Bever et al., 2010;Mangan et al. 2010). Negative plant-soil feedback effects are often associated with changes in the density or composition of soil organisms, and in particular with changes in microbial communities which occur more rapidly than changes in plant communities (Bezemer et al., 2006(Bezemer et al., , 2018Ke et al., 2015). Besides conditioning soil communities in pots, host-specific soil communities can also be obtained by sampling in proximity to adult plants (e.g. ...

Interplay between population dynamics of Senecio jacobaea and plant, soil and aboveground insect herbivore community composition
  • Citing Article
  • January 2006

Ecology

... Plants grown in amended soil had an increased plant width, greater maximum leaf length both with and without herbivores, but only increased height in the absence of herbivores (Fig. 1). Herbivory by P. brassicae early in B. nigra's development has been shown to reduce the height of this species (Blatt et al., 2008), even when other growth variables showed compensation. These results indicate a positive effect of the soil amendment on B. nigra's ability to tolerate herbivory, perhaps due to compensation for lost biomass (Blatt et al., 2008). ...

Tolerance of Brassica nigra to Pieris brassicae herbivory

... Tricondyla tiger beetle species in studied habitats in Lanao sel Sur Province, Mindanao, Philippines as for now there is a lack of such data for Philippine arboreal tiger beetles, similar results are obtained in case of epigeic species studied in this country (Jaskuła et al., in prep.). Moreover, there are numerous published examples of negative impact of alien/invasive plant species on animal/insect diversity in areas where they were introduced (e.g., Dostál et al., 2013;Harvey & Fortuna, 2012), even if gradually some of insect species start to use alien plants as food or habitat (e.g., Brändle et al., 2008;Karolewski et al., 2014;Meijer et al., 2012;Novotny et al., 2003). Taking all these facts into consideration, one can note that high abundance of endemic predatory tiger beetles (Cabras et al., 2016) occurring not only on native but also on invasive/alien tree species in Lanao del Sur is unusual and surprising, until we will pay attention on biology and ecology of both arboreal Cicindelidae and tree species on which these beetles were recorded in current study. ...

Chemical and structural effects of invasive plants on herbivore-parasitoid/predator interactions in native communities

... The pheromone of N. sertifer has been identified as (2S, 3S, 7S)-3,7-dimethyl-2-pentadecanol esterified with acetic acid (Jewett et al. 1976;Wassgren et al. 1992), thus differing from the D. pini pheromone by its stereochemistry and the chain length of the alcohol component of the ester. Especially in parthenogenetically reproducing parasitoids, local adaptation to the environment may facilitate maintenance of within-species genetic variance and support successful development in host species of different quality (Godfray 1994;Harvey et al. 2012;Hopper et al. 2019;Harrison et al., 2022). In our previous studies, which showed attraction of C. ruforum to D. pini sex pheromones (Hilker et al. 2000) and to pine odor induced by D. pini eggs (Hilker et al. 2002;Schröder et al. 2008), we also used individuals collected from N. sertifer eggs at the same locations in Finland as the parasitoids used in our current study. ...

The roles of ecological fitting, phylogeny and physiological equivalence in understanding realized and fundamental host ranges in endoparasitoid wasps
  • Citing Article
  • August 2012

Journal of Evolutionary Biology

... Subterranean organisms such as nematodes, arbuscular mycorrhizal fungi (AMF), and decomposers also affect the degree of parasitism of foliar herbivory (13,(25)(26)(27)(28). Root herbivore-induced systemic changes in above-ground defense levels affected herbivores and their natural enemies (13). ...

Soil community composition drives aboveground plant-herbivore-parasitoid interations
  • Citing Article
  • April 2005

Ecology Letters