The influence of time and temperature on molecular gut content analysis： Adalia bipunctata fed with Rhopalosiphum padi

Gut content analysis is a useful tool when studying arthropod predator-prey interactions. We used polymerase chain reaction （PCR） technique to examine how detection of prey DNA in the gut content of predators was influenced by digestion time and temperature. Such knowledge is critical before applying PCR-based gut content analysis to field collected predators. Larvae of the two-spotted ladybeetle （Adalia bipunctata L.） were fed with the bird cherry-oat aphid （Rhopalosiphum padi L.） at either 21℃ or 14℃. After consuming one aphid, the predators were allowed to digest the prey for a range of time periods up to 24 hours. The influence of temperature on A. bipunctata feeding behavior was also recorded. From the fed larvae, total DNA was extracted and PCR reactions with R. padi specific primers were run. The number ofA. bipunctata that tested positive for R. padi DNA was negatively related to the length of digestion time. Temperature influenced larval feeding behavior but did not have a significant effect on R. padi DNA detection. After pooling the data from both temperature treatments we estimated the time point when R. padi DNA could be amplified from 50% of the fed A. bipunctata by PCR to be 4.87 hours. With such a rapid decrease in prey DNA detection success, positive PCR reactions will most likely be the result of predation events occurring shortly before capture. If a defined digestion temperature range has proven not to influence prey detection, PCR data obtained from predators collected within that particular range can be interpreted in the same way.     

Evaluation of lycosid,micryphantid and linyphiid spiders as predators ofRhopalosiphum padi (Hom.: Aphididae) and their functional response to prey density-laboratory experiments

Laboratory experiments were performed to determine the potential of dominant spider species in winter wheat in Germany,Erigone atra (Blackwall),Lepthyphantes tenuis (Blackwall) andPardosa agrestis (Westring) adults and youngs, in suppressing the population ofRhopalosiphum padi (L.) on wheat plants and their functional response to different aphid densities. The presence of spiders significantly caused between 34 and 58% reduction in aphid population development on wheat plants compared to the aphid population in the absence of spiders. The functional response curves for these spiders as predators ofR. padi seem to descrive a typical type II functional response with the prey consumed increasing to a plateau as aphid densities increased. Prey killed without eating was linear on prey density.     

How glyphosate altered the behaviour of agrobiont spiders (Araneae: Lycosidae) and beetles (Coleoptera: Carabidae)

Cultivation of herbicide-tolerant strain of GM corn involves applications of a non-selective herbicide. Mortality of arthropod natural enemies resulting from the application of herbicides is negligible. But nothing is known how herbicides affect the behaviour of natural enemies and thus alter their pest control efficacy. Aim of the study was to assess the effect of the Roundup residues on the predatory, defensive, locomotory and reproductive behaviour of epigeic spiders and carabid beetles. Specimens of Pardosa agricola (Araneae: Lycosidae) and Poecilus cupreus (Coleoptera: Carabidae) were exposed for 2 h to the fresh and 1-day old residues of Roundup Biaktiv (Monsanto, IPA 480 g/l). Predation rate was similar for all treatments in both spiders and beetles. Spiders did not avoid surface treated with herbicide residues more than the control surface, but beetles slightly avoided surface with fresh residues. The speed of locomotion of spiders was not altered by herbicide residues, but beetles exposed to residues crawled at significantly lower speed than the control group. Herbicide residues did not affect the escape efficacy of spiders from a predator. Residues had no detrimental effect on the courtship, mating frequency and duration in spiders. Roundup Bioaktiv thus appears to be harmless to lycosid spiders and only slightly harmful to carabid beetles. The biological control potential of both predators should not be reduced by the application of Roundup Bioaktiv.     

Improved PCR performance and fidelity of double mutant Neq A523R/N540R DNA polymerase

We previously reported that Neq A523R DNA polymerase is more efficient in PCR than wild-type Neq DNA polymerase, and amplifies products more rapidly. Neq A523R DNA polymerase also amplifies templates more rapidly than Pfu DNA polymerase, but has a lower fidelity than Pfu DNA polymerase. To improve product yield and the fidelity of amplification simultaneously, we constructed and characterized the double mutant Neq A523R/N540R. The yield of PCR products was greater for Neq A523R/N540R DNA polymerase than wild-type and other mutant DNA polymerases, and the Neq double mutant catalyzed amplification of a 12-kb PCR product from a lambda template with an extension time of 3 min. The PCR error rate of Neq A523R/N540R DNA polymerase (6.3 × 10⁻⁵) was roughly similar to that of Pfu DNA polymerase (4.8 × 10⁻⁵), but much lower than those of wild-type Neq DNA polymerase (57.2 × 10⁻⁵), Neq A523R DNA polymerase (13.1 × 10⁻⁵), and Neq N540R DNA polymerase (37.7 × 10⁻⁵). These results indicated that A523R and N540R mutations of Neq DNA polymerase had synergistic effects on its fidelity.     

Pollen beetles are consumed by ground‐ and foliage‐dwelling spiders in winter oilseed rape

Pollen beetles, Meligethes aeneus (Fabricius) (Coleoptera: Nitidulidae), are major pests in oilseed rape (OSR), Brassica napus L. (Brassicaceae). Among the predator species in the generalist predator complex present in OSR fields, wolf spiders (Araneae: Lycosidae) are found on the ground and cobweb spiders (Araneae: Theridiidae) build webs in the foliage. Here we study the incidence of predation of pollen beetles by these two spider groups using DNA‐based molecular analysis. Wolf spiders of the genus Pardosa and the cobweb spider, Theridion impressum L. Koch, were each collected in three winter OSR fields over a period of about 3 weeks. Pollen beetle densities as well as the occurrence of predators and alternative prey were monitored. In total, 13.8% of the collected Pardosa spp. tested positive for pollen beetle DNA in the PCR analyses, whereas 51.7%T. impressum were positive. The likelihood of detecting pollen beetle DNA in the gut contents of both spider groups was positively related to pollen beetle larval density. The implications of these results for conservation biological control and future studies of food webs in OSR are discussed.     

Predation of Rhopalosiphum padi (Homoptera: Aphididae) by polyphagous predatory arthropods during the aphids' pre-peak period in spring barley

Polyphagous predators (e.g. Araneae, Carabidae and Staphylinidae), collected from spring barley fields during 1981-85, were examined by either gut dissection or a R. padi-specific antiserum in enzyme linked immunosorbent assay (ELISA) in order to detect predation of Rhopalosiphum padi during the aphids' establishment and exponential growth phases. Overall 18% of c. 3000 carabids dissected were shown to feed on R. padi during the aphids' pre-peak period. No overall relationship was found between percentage carabids with R. padi in the diet and peak R. padi densities. Relatively high proportions of Bembidion spp. (particularly B. lampros) and Pterostichus cupreus fed on R. padi during the aphids' establishment phase, and proportions of those predator taxa containing R. padi increased with increasing R. padi densities in both high and low aphid density years. P. melanarius and Harpalus rufipes mainly fed on R. padi during the aphids' exponential growth phase. Overall 11% of c. 1350 predators examined in ELISA gave positive reactions to the R. padi antiserum. Relatively high proportions of linyphiid and lycosid spiders were positive throughout the aphid pre-peak period. Several Acari, Opiliones, Trechus spp. (Carabidae), Philonthus spp. (Staphylinidae), Cantharidae and Chilopoda were positive mainly during the aphids' exponential growth phase. Sample sizes were small, however. Very few of the Bembidion spp. tested in ELISA were positive compared with those examined by gut dissection. The maximum period of R. padi protein (antigen) detection in B. lampros was related to temperature, i.e. 8.5 h at 30°C, 20.5 h at 20°C and 34.5 h at 10°C, respectively. It is suggested that the rate of R. padi protein digestion in B. lampros is faster at higher temperatures than the rate of elimination of prey solids from the guts. Several key predators (in this case B. lampros, P. cupreus and linyphiid spiders) which are abundant in spring cereal fields at a time when R. padi emigrants arrive in the crop and which feed on R. padi during the aphids' establishment phase, are identified. The results are compared with those from similar investigations elsewhere with predators of Sitobion avenae and Metopolophium dirhodum.     

Analysis of digestion of rice planthopper by Pardosa pseudoannulata based on CO-I gene

In order to systematically study the predatory behavior and digestion regularity of spiders, real-time fluorescence quantification PCR technique was used to detect the number of CO-I genes in Pardosa pseudoannulata after it preyed on rice planthoppers in different temperatures within different periods. At 28 °C, 0, 1, 2, 4, 8, 16, and 24 h after P. pseudoannulata preyed on rich planthopper, DNA was extracted from cephalothorax and abdomen of P. pseudoannulata. Routine PCR and real-time fluorescence PCR techniques were employed for CO-I gene amplification. The results show that: The prey liquid was temporarily stored in the sucking stomach of the spider head within 2 h after prey, and gradually transferred to the midgut of the abdomen with the prolongation of time. After 4 h, CO-I gene residues of rice planthopper in the cephalothorax gradually decreased. The CO-I gene of rice planthopper was basically transferred to the abdomen after 16 h. During 0–1 h, food contained in abdominal midgut and other digestive organs was very small, CO-I gene detection was not obvious. Over time, food entered into the midgut from the sucking stomach for digestion. During 2–4 h, CO-I gene amount increased, at 2–4 h, detected CO-I gene residue reached the peak; but rapidly declined after 8, 16, and 24 h, even it is still detectable. The results at different temperatures reveal that: As the temperature increased from 26 °C to 32 °C, CO-I gene residues of rich planthopper in cephalothorax and abdomen of P. pseudoannulata gradually decreased, which indicated that the digestion rate increased with the increase of temperature with some range. However, when the temperature continued to increase to 34 °C, the digestion rate decreased.     

Seasonal,spatial and diel partitioning of Acyrthosiphon pisum (Hemiptera: Aphididae) predators and predation in alfalfa fields

Predators are important natural enemies, often responsible for preventing pest population outbreaks of in many crops. Complementarity in resource use involves spatial or temporal segregation of predators, which can result in better biological control when several species of natural enemies share a prey. In this study, we investigated the seasonal, spatial and diel segregation of Acyrthosiphon pisum predators and its predation in alfalfa fields, by setting out cards with sentinel aphids, and making observations every 3 h for a 24 h period. A temporal and spatial segregation of predators was observed. Coccinellids were the most abundant predators, representing 51% of the total observations, followed by syrphid larvae. Coccinellids were also responsible for high levels of predation throughout the year, although the species responsible varied from spring to summer and autumn. On the other hand, syrphids were only found in spring and summer, while spiders only in autumn. Predator species also differed on their preferred sites for predation, with Heteropterans and syrphids found on the foliage, the spider Neomaso articeps only on the ground, and coccinellid and Anyphaenidae species on both sites. The two main predator groups also showed distinct diel patterns, with coccinellids observed only during day and syrphids only during night. This predatory activity corresponded with aphid predation, observing more predation in spring, on the foliage and during the day time. The proportion of predators observed preying on cards in the different seasons did not corresponded tightly with their field abundance, particularly in the case of coccinellids, which maintained high levels of predation in spite of great variations in its field abundance. Our results support the hypothesis of a spatio-temporal segregation of the predators associated with A. pisum in alfalfa, which might be beneficial for the outcome of biological control of this pest.     

Comparison of the RE and B1 gene for detection of Toxoplasma gondii infection in children with cancer

Early, accurate and effective diagnosis of toxoplasmosis can make an important contribution to the prevention and control of disease, especially in people who are at risk. In this study, two commonly used genomic repeats of Toxoplasma gondii, RE (GenBank accession number AF146527) and B1, were compared to each other in nested-PCR assay. Five hundred and thirty-five blood samples from children with leukemia were tested for the presence of T. gondii antibodies using enzyme immunoassays. One hundred and ten DNA samples of these patients (50 IgM +, IgG +, 10 IgM −, IgG +, and 50 IgM −, IgG −) were analyzed by nested-PCR. The specificity of two nested PCR assays was determined using the DNA samples of other parasites and human chromosomal DNA. As a result, 82% (41/50) and 68% (34/50) of the IgM +, IgG + samples were positive on duplicate RE and B1-nested PCR analyses, respectively. None of the 10 IgM −, IgG + seropositive samples was detected positive after testing RE and B1-nested PCR assays in duplicate. One (2%) of the 50 seronegative samples was positive by duplicate RE-nested PCR but none of them were positive by duplicate B1-nested PCR. The detection limit of the RE-nested PCR assay was 640 fg of T. gondii DNA whereas this rate for B1-nested PCR was 5.12 pg of the DNA template. No cross-reactivity with the DNA of other parasites and human chromosomal DNA was found. The results indicate that an RE-based nested PCR assay is more sensitive than B1 genomic target, of those tested, for detection of T. gondii. It is noteworthy that in comparison with B1-nested PCR, RE-nested PCR could detect the T. gondii DNA in seronegative samples too.     

A new method to study the functional response of Scymnus syriacus (Coleoptera: Coccinellidae) to different densities of Aphis gossypii

Functional response is basic to any investigation of predator–prey relationships. In this study, the functional response of female Scymnus syriacus Marseul (Col.: Coccinellidae) to different densities (10, 20, 40, 60, 80, 100) of third instar nymphs of Aphis gossypii Glover as prey was studied in an open patch experiment in a growth chamber (25 °C, 65 ± 5% RH and a photoperiod of 16L:8D h ). Using logistic regression, a type II functional response for female Scymnus syriacus was determined. The searching efficiency (a') and handling time (T_h) of the female predator using non linear least-square regression were estimated as 0.0769 ± 0.0136 h^? 1 and 0.3103 ± 0.0438 h., respectively. Mean times required for the female predator to settle in a patch were 10.20 ± 4.28, 6.58 ± 2.58, 12.58 ± 4.50, 4.53 ± 1.48, 5.14 ± 2.59, 3.87 ± 3.52 min at different prey densities, respectively. Maximum theoretical predation rate (T/T_h) estimated by Rogers' model for the female predator was 77.34. The proportion of female predators remaining in open patches at the end of the experiment was dependent on prey density (R² = 0.876). The type of functional response obtained here agrees with studies on this predator in closed patches.     

Consumption of aphids by spiders and the effect of additional prey: evidence from microcosm experiments

Spiders are common generalist predators in agroecosystems and have been suggested to lower herbivore abundance in crops. It is not clear, however, if spiders can effectively suppress pest populations, and if so, by what mechanisms. In a microcosm experiment, we examined the consumption of the bird cherry-oat aphid, Rhopalosiphum padi L. (Homoptera: Aphididae), a pest species in wheat fields, by three spider species that differ in their hunting methods. We then tested the effect of additional prey type on the ability of erigonid spiders to reduce aphids. In a 48-h experiment Mermessus denticulatus (Banks) (Araneae: Linyphiidae; Erigoninae) consumed more aphids than did Enoplognatha gemina Bosmans and Van Keer (Araneae: Theridiidae) and Bathyphantes cf. extricatus (O·P.-Cambridge) (Araneae: Linyphiidae; Linyphiinae). This difference may be due to the ability of erigonids to forage actively on the vegetation in addition to using their webs to catch prey. In a 7-week experiment, we provided springtails (Collembola) in high and low densities as additional prey to mated erigonids, prior to aphid introduction. Spiders in the low-density springtail treatment built more webs on the vegetation, and caused a 50% reduction in aphid populations. There were significantly fewer aphids in the low-density springtail treatment, but not in the high-density treatment, in comparison to the control (high-density springtails without spiders). The results suggest that additional prey density affects predatory interactions between M. denticulatus and R. padi and that erigonids, which occur in high densities in wheat fields in the Negev desert, may be involved in aphid suppression in these agroecosystems.

Detection of secondary predation by PCR analyses of the gut contents of invertebrate generalist predators

Predation by generalist predators is difficult to study in the field because of the complex effects of positive and negative interactions within and between predator species and guilds. Predation can be monitored by molecular means, through identification of prey DNA within predators. However, polymerase chain reaction (PCR) amplification of prey DNA from predators cannot discriminate between primary and secondary predation (hyperpredation), in which one predator feeds on another that has recently eaten the target prey. Here we quantify, for the first time, the potential error caused by detection of prey DNA following secondary predation, using an aphid-spider-carabid model. First, the aphid Sitobion avenae was fed to the spider Tenuiphantes tenuis and the carabid Pterostichus melanarius, and the postconsumption detection periods, for prey DNA within predators, were calculated. Aphids were then fed to spiders and the spiders to carabids. Aphid DNA was detected in the predators using primers that amplified 245- and 110-bp fragments of the mitochondrial cytochrome oxidase I gene. Fragment size and predator sex had no significant effect on detection periods. Secondary predation could be detected for up to 8 h, when carabids fed on spiders immediately after the latter had consumed aphids. Beetles tested positive up to 4 h after eating spiders that had digested their aphid prey for 4 h. Clearly, the extreme sensitivity of PCR makes detection of secondary predation more likely, and the only reliable answer in future may be to use PCR to identify, in parallel, instances of intraguild predation.     

Opisthorchis viverrini and Haplorchis taichui: Development of a multiplex PCR assay for their detection and differentiation using specific primers derived from HAT-RAPD

Specific primers for the detection of Opisthorchis viverrini and Haplorchis taichui were investigated by using the HAT-RAPD PCR method. Fourteen arbitrary primers (Operon Technologies) were performed for the generation of polymorphic DNA profiles. The results showed that a 319 bp fragment generated from the OPA-04 primer was expected to be O. viverrini-specific while a 256 bp fragment generated from the OPP-11 primer was considered to be H. taichui-specific. Based on each sequence data, two pairs of specific primers were designed and sequences of each primer were as follows; H. taichui; Hapt_F5′-GGCCAACGCAATCGTCATCC-3′and Hapt_R1 5′-CTCTCGACCTCCTCTAGAAT-3′ which yielded a 170 bp PCR product. For O. viverrini, OpV-1F: 5′-AATCGGGCTGCATATTGACCGAT-3′ and OpV-1R: 5′-CGGTGTTGCTTATTTTGCAGACAA-3′ which generated a 319 bp PCR product. These specific primers were tested for efficacy and specific detection for all parasites DNA samples. The results showed that 170 and 319 bp specific PCR products were generated as equivalent to positive result in H. taichui and O. viverrini, respectively by having no cross-reaction with any parasites tested. PCR conditions are recommended at 68 °C annealing temperature and with 0.5 mM magnesium chloride (Mg Cl₂). Additionally, specific primers developed in this study were effective to determine the presence of both parasites in fish and snail intermediate hosts, which the DNA of O. viverrini was artificially spiked since it is rarely found in northern Thailand.The H. taichui and O. viverrini-specific primers successfully developed in this study can be use for epidemiological monitoring, preventing management and control programs.     

Food quality of Ephestia eggs,the aphid Rhopalosiphum padi and mixed diet for Orius majusculus

We studied the food quality of the aphid Rhopalosiphum padi to the pirate bug Orius majusculus using Ephestia eggs as high-quality comparison prey. Several performance parameters were tested on individuals that had been reared and maintained on each of the two single-prey diets or on a mixed diet. All fitness parameters were lower in individuals fed aphids only, indicating poor food quality of this prey. Compared with the pure Ephestia egg diet, the mixed diet enhanced teneral mass, while adult survival and female starvation tolerance were negatively affected and all other traits were unaffected. Body protein proportions were constant across diets, whereas lipid proportion was low in the aphid treatment. Preference for aphids was lower following a monotypic aphid diet than when reared on Ephestia eggs or a mixed diet. The results confirm that R. padi is low-quality food for O. majusculus as it is for other generalist predators, even though O. majusculus may contribute significantly to population suppression of the aphid.     

Characterization and PCR application of a new high-fidelity DNA polymerase from Thermococcus waiotapuensis

The family B DNA polymerase gene from the euryarchaeon Thermococcus waiotapuensis (Twa) contains an open reading frame of 4404 bases that encodes 1467 amino acid residues. The gene is split by two intein-coding sequences that forms a continuous open reading frame with the three polymerase exteins. Twa DNA polymerase genes with (whole gene) and without (genetically intein-spliced) inteins were expressed in Escherichia coli Rosetta(DE3)pLysS. The inteins of the expressed whole gene were easily spliced during purification. The molecular mass of the purified Twa DNA polymerase was about 90 kDa, as estimated by SDS-PAGE. The optimal pH for Twa DNA polymerase activity was 6.0 and the optimal temperature was 75 °C. The enzyme was activated by magnesium ions. The half-life of the enzyme at 99 °C was about 4 h. The optimal buffer for PCR with Twa DNA polymerase was 50 mM Tris–HCl (pH 8.2), 2.0 mM MgCl₂, 30 mM KCl, 2.0 mM (NH₄)₂SO₄, 0.01% Triton X-100, and 0.005% BSA. The PCR fidelity of Twa DNA polymerase was higher than Pfu, KOD and Vent DNA polymerases. A ratio of 15:1 Taq:Twa DNA polymerase efficiently facilitated long-range PCR.     

Population densities,group size and biomass of ungulates in a lowland tropical rainforest forest of the eastern Himalayas

Large ungulate population monitoring is a crucial wildlife management tool as ungulates help in structuring and maintaining the large carnivore populations. Reliable data on population status of major ungulate prey species are still non-existent for most of the protected areas in the Indian part of the eastern Himalayan biodiversity hotspot. Twenty transects were monitored over a period of three years (2009–2011) totaling 600 km with an average length of 2 km. The estimated mean density of ungulates was 17.5 km⁻² with overall density of 48.7 km⁻². The wild pig Sus scrofa had the highest density (6.7 ± 1.2 km⁻²) among all the prey species followed by barking deer Muntiacus muntjak (3.9 ± 0.6 km⁻²), sambar Rusa unicolor (3.8 ± 0.5) and gaur Bos gaurus (3.5 ± 0.9 km⁻²). The estimated total ungulate biomass density was 2182.56 kg km⁻². This prey biomass can support up to 7.2 tigers per 100 km⁻². However, with two other sympatric carnivores sharing the same resources, the actual tiger numbers that can be supported will be lower. The estimated minor prey species was 31 km⁻² significantly 30.6% crop damages were reported by wild pig (p = 0.01) and 35.4% was elephant (p = 0.004). This data on ungulate densities and biomass will be crucial for carnivore conservation in this understudied globally significant biodiversity hotspot.     

Association between hypermethylation of DNA repetitive elements in white blood cell DNA and pancreatic cancer

Pancreatic cancer is a leading cause of cancer-related deaths worldwide. Methylation of DNA may influence risk or be a marker of early disease. The aim of this study was to measure the association between methylation of three DNA repetitive elements in white blood cell (WBC) DNA and pancreatic cancer.DNA from WBCs of pancreatic cancer cases (n = 559) and healthy unrelated controls (n = 603) were tested for methylation of the LINE-1, Alu and Sat2 DNA repetitive elements using MethyLight quantitative PCR assays. Odds ratios (ORs) and 95% confidence intervals (95%CI) between both continuous measures of percent of methylated sample compared to a reference (PMR) or quintiles of PMR and pancreatic cancer, adjusted for age, sex, smoking, BMI, alcohol and higher education, were estimated.The PMR for each of the three markers was higher in cases than in controls, although only LINE-1 was significantly associated with pancreatic cancer (OR per log unit = 1.37, 95%CI = 1.16–1.63). The marker methylation score for all three markers combined was significantly associated with pancreatic cancer (p-trend = 0.0006). There were no associations between measures of PMR and either presence of metastases, or timing of blood collection in relation to diagnosis, surgery, chemotherapy or death (all p > 0.1).We observed an association between methylation of LINE-1 in WBC DNA and risk of pancreatic cancer. Further studies are needed to confirm this association.     

Enhancing biological control by an omnivorous lacewing: Floral resources reduce aphid numbers at low aphid densities

The availability of plant resources to omnivorous arthropod predators may have a positive, negative or negligible effect on their population densities and predation rates, depending on the availability of prey. At high prey densities, flowering buckwheat has been shown to negatively impact populations of the brown lacewing, an omnivorous predator, due to the probable increase in parasitism rate of lacewing larvae by their primary parasitoid, Anacharis zealandica. However, little is known about the effect of buckwheat flowers on this insect community at low prey densities. We used field cages to assess the effects of nectar provision by flowering buckwheat on the population dynamics of the pea aphid, the brown lacewing and its parasitoid A. zealandica in an alfalfa field, under low aphid densities in the New Zealand summer. The insects were sampled every 2 weeks with a suction device, then counted and released on each sampling date from 15 January to 15 March 2007. Buckwheat significantly increased lacewing populations and significantly decreased aphid numbers by 70% and 39%, respectively. The buckwheat had its greatest effect at the end of summer (February/March) for both these species. It had no effect on A. zealandica abundance.     

Attraction of the predator,Harmonia axyridis (Coleoptera: Coccinellidae), to its prey,Myzus persicae (Hemiptera: Aphididae), feeding on Chinese cabbage

The predatory multicolored Asian lady beetle, Harmonia axyridis, was attracted to volatiles released from Chinese cabbage infested by the green peach aphid, Myzus persicae, in T-tube olfactometer choice tests. However, lady beetle adults and larvae did not respond to clean air, Chinese cabbage alone or green peach aphid alone. Of different prey densities, H. axyridis adults were most attracted to Chinese cabbage infested by 60 M. persicae adults after 24 h. However, H. axyridis larvae were not attracted to Chinese cabbage infested by M. persicae. Mechanically damaged Chinese cabbage attracted neither lady beetle adults nor larvae. Predatory adults were attracted to 60 M. persicae adults after 24 and 48 h, and to 90 M. persicae adults after 12 h, suggesting that the predatory response depends on the prey density. Lady adult beetles did not prefer the volatiles induced by Diamondback moth, Plutella xylostella, indicating that specific host insect specificity attracts respective natural enemies. It can be explained that the volatile compounds emitted from the host plant as a result of herbivore attack preferred by the specific insect species.