Impact of a long-term mating-disruption management in crops on non-target insects in the surrounding area

Protecting insects in agro-ecosystems may result in substantial benefits assuming that numerous species produce ecological services. The impact of pesticides on non-target insects is a function of the number of treatments, chemical product, amount of active ingredients and the method of application in the fields, together with their persistence in the environment. To reduce the use of these products, several methods of integrated pest management were developed in agriculture. Among them mating-disruption (MD) is widely employed, for example against the codling moth Cydia pomonella L., a key pest in apple orchards. MD should minimize the negative impacts of chemical pest management on non-target insects in the vegetation surrounding the orchards. We investigated this hypothesis in a long-term MD program on insect populations in the edges of managed plots, using five gall-inducing aphid species in 135 Pistacia palaestina trees. The highest aphid species richness was found in trees growing away from orchards followed by trees in orchards close to Kiwi patches which were never sprayed with insecticides. Intermediate aphid species richness was revealed in parcels where MD against codling moth has been carried out during the last 18?years. In these plots, reduced number of chemical treatments was used against secondary pests each year. Trees in orchards with intensive chemical treatment with insecticide had almost no galls. In conclusion, the populations of the five non-target species in the adjacent natural environment did not suffer significantly from the few chemical treatments. The long term MD program of C. pomonella has a minimum disruption on non-target species in the orchards and their immediate surroundings.     

Recommendations on minimum experimental plot size and succession of aphidophaga in West Virginia, USA, apple orchards

Five apple orchards in West Virginia, USA, were managed with five different pest management practices ranging from unsprayed to conventional insecticides. Data were collected on aphid, predaceous insect, and spider abundance every 2 weeks from May to July along one or two randomly selected, 15 consecutive tree transects. A total of 892 individual predaceous insects was observed: 32% wereAphidoletes aphidimyza, 21% wereCoccinella septempunctata and the rest were from 13 other taxa. The most important aphid predator seemed to beC. septempunctata. Of the 32 sample transects with predators, 72 % showed an edge effect in which either the standard error or mean of predator abundance differed from the edge towards the center of the orchard. This edge effect extended a mean of 7 trees (30 m) into the orchard. Only 39% of the 33 transects that had spiders showed an edge effect, extending into the orchard a mean of 8 trees (33 m). However, 75% of the transects with more than one spider per tree had an edge effect of 10 trees (43 m). We recommend a minimum border of seven trees before sampling for aphid predators and 10 trees before sampling for spiders. A recommended experimental plot size, for semi-dwarf, free-standing apple orchards, to eliminate edge effects is 1.25 ha for aphidophaga, 1.5 ha for spiders; a minimum plot size of 0.6 ha for aphidophaga and 0.75 ha for spiders would minimize edge effects.     

Oviposition response of green lacewings (Neuroptera: Chrysopidae) to aphids (Hemiptera: Aphididae) and potential attractants on pecan

Pecan foliage is attacked by three species of aphids [Monellia caryella (Fitch), Melanocallis caryaefoliae (Davis), and Monelliopsis pecanis Bissell], resulting in damage that can reduce tree nut yield. In this study, we assayed the ovipositional response of the green lacewing Chrysoperla rufilabris (Burmeister) to M. caryella and M. caryaefoliae at high and low aphid densities and the development of C. rufilabris larvae when fed solely on each of the three pecan aphid species. During 2004 and 2005, combinations of attractants and food sprays were applied to pecan trees in an orchard to monitor green lacewing ovipositional response. We found that C. rufilabris laid more eggs on seedling trees infested with the M. caryella (at both high and low densities) than on seedlings infested with M. caryaefoliae. Development of C. rufilabris was unaffected by aphid species. At least one attractant/food spray treatment applied to trees in an orchard significantly increased green lacewing oviposition for three of the five treatment dates over both years. These results show that larvae of C. rufilabris will consume all aphid species attacking pecan, even though female ovipositional response can differ for aphid species. It is likely that combinations of attractants and food sprays can be used to enhance green lacewing populations in orchards.     

Temporal and spatial variability of rosy apple aphid Dysaphis plantaginea populations: is there a role of the alternate host plant Plantago major?

• 1 The rosy apple aphid Dysaphis plantaginea (Passerini) (Homoptera: Aphididae) is a pest of economic importance to the apple industry worldwide, particularly in organic apple orchards where no acceptable controls are available. In the Similkameen Valley of British Columbia, Canada, the rosy apple aphid population size varies widely between orchards and between years. To explain this variation, potential environmental correlates of aphid density were evaluated. The architecture of the alternate host was also evaluated for its effect on rosy apple aphid summer survival and reproduction.
• 2 The percentage of trees infested by rosy apple aphids among orchards was in the range 8–94% for trees having at least one cluster with more than ten aphids in 2007 and in the range 0–39% in 2008.
• 3 A general linear model correlating aphid densities to the environmental variables of abundance of the alternate host (plantain Plantago spp.), foliar nitrogen, tree age and planting density, and reduced by stepwise regression, indicated that foliar nitrogen and tree age explained 33% of the variation. Abundance of the summer, alternate food plant, plantain, was not related to later aphid densities on apple trees.
• 4 Plantain architecture, however, influenced aphid numbers and 25‐fold more aphids were found on low‐lying plantain leaves than on more upright leaves. Experimental manipulation of leaf angle and leaf size showed that significantly more aphids occurred on low angle, large leaves. Finally, mowing that encouraged low lying plants prior to spring aphid migration was associated with a four‐fold greater number of both winged and wingless aphids on the plantain.

     

Effect of trap color and orientation on the capture of Aphelinus mali (Hymenoptera: Aphelinidae), a parasitoid of woolly apple aphid (Hemiptera: Aphididae)

The factors affecting trap capture of adult Aphelinus mali (Haldeman) (Hymenoptera: Aphelinidae) were studied in 2010-2011 in eastern Washington apple (Malus spp.) orchards infested with its host woolly apple aphid, Eriosoma lanigerum (Hausmann) (Hemiptera: Aphididae). The initial study of white sticky cards indicated that traps stapled to the trunk in a vertical orientation had the highest capture. A factorial experiment of three colors (clear, white, and yellow) by three orientations (trunk, scaffold, and hanging) indicated that yellow traps and traps on trunks caught higher numbers ofA. mali. For this reason, the recommended trap for this natural enemy is a yellow trap stapled to the trunk. Having a readily available and effective sampling method for this species may be helpful in implementing biological control programs and assessing the impact of different spray regimes.     

Use of arthropods for the evaluation of the olive-orchard management regimes

Abstract 1 The presence and abundance of arthropods were compared in three olive orchards under organic, integrated and conventional management regimes. In each olive orchard, trees were sampled in the canopy by beating branches and soil arthropods by placing pitfall traps. Contrary to expectations, the highest abundance of arthropods occurred in the integrated management orchard. The most abundant groups were Formicidae and the species Euphyllura olivinae (Homoptera: Psyllidae). 2 Canopies and the soil under the tree canopy (interior soil) were selected as the most informative sites for sampling. The months with the strongest differences were May, June and July, especially June. In the canopy, Araneae, Coleoptera, Diptera, Heteroptera, Hymenoptera, Homoptera, Lepidoptera, Neuroptera and Thysanoptera were the most abundant, and showed significant differences in abundance among orchards with different management regimes. Moreover, in the canopies, Coleoptera and Lepidoptera showed a seasonal pattern of abundance and consistent significant differences between the organic orchard vs. the integrated and conventional ones in both years of study. In the soil, 12 orders showed significant differences in abundance among management regimes at some point of the sampling season. 3 In a search for biological indicators that could help to distinguish between management regimes, a discriminant analysis applied to the data indicated that only the samples from the canopy were classified according to their management regime in a consistent way over time. The groups selected by the analysis to establish differences among management regimes were Coleoptera, Diptera, Heteroptera, Lepidoptera and Thysanoptera. The analysis applied to compare organic vs. non‐organic olive orchards, again identified Coleoptera and Lepidoptera as suitable groups. The results suggest that these two orders are potential bioindicators to distinguish, in a simple way, organic olive orchards from non‐organic ones.     

Effect of production system and pruning on Aphis sambuci dynamics over time and on elderberry yield

In a 2‐year study, elder aphid (Aphis sambuci) dynamics over time and berry yield were evaluated in two production systems (integrated and organic) and in two winter pruning treatments (trees pruned to four and eight scaffolds) in two black elderberry orchards in Hungary. In the organic production system, the first aphid colony was observed 1–2 weeks earlier (late‐March) in both years and locations compared to the integrated programme. The number of aphid colonies then increased until mid‐May in both years, reaching a maximum number of aphid colonies of 11.2 on 100 scaffolds in the integrated production system and of 38.9 in the organic programme. Then, the number of colonies decreased and reached a zero value at mid‐June in the integrated production system and 2 weeks later (early July) in the organic one in both years and locations. First autumn aphid colonies were observed in early September in the integrated production system but 2 weeks earlier (late August) in the organic one in both years and locations. The number of aphid colonies between mid‐April and mid‐June indicated a larger increase on trees pruned to eight scaffolds compared to trees pruned to four scaffolds. Both the total number of aphid colonies and the area under the aphid colony curves (AUACC) were significantly lower (P < 0.001) in the integrated treatments compared with organic ones. Across all treatments, both measures were significantly lower (P < 0.05) on trees pruned to four scaffolds compared with trees pruned to eight scaffolds. However, when the effect of pruning on the number of aphid colonies was analysed separately for integrated and organic plots, pruning caused significant differences in aphid colony numbers and AUACC in the organic plots. Berry yield was significantly higher (P < 0.05) in the integrated treatments compared with the organic ones, but pruning showed no significant effect on yield. Overall, pruning to four scaffolds resulted in a lower aphid colony number in the organic production system compared to the integrated one. Thus, winter pruning may be useful as an aphid control strategy in organic elderberry orchards.     

Aphid (Hemiptera: Aphididae) species composition and potential aphid vectors of plum pox virus in Pennsylvania peach orchards

Plum pox, an invasive disease recently identified in Pennsylvania stone fruit orchards, is caused by the aphid-transmitted Plum pox virus (genus Potyvirus, family Potyviridae, PPV). To identify potential vectors, we described the aphid species communities and the seasonal dynamics of the dominant aphid species within Pennsylvania peach orchards. Aphids were trapped weekly in 2002 and 2003 from mid-April through mid-November within two central Pennsylvania orchards by using yellow and green water pan traps. In total, 42 aphid species were identified from both orchards over 2 yr. Within orchards, actual species richness ranged from 24 to 30 species. The Abundance Based Coverage Estimator predicted species richness to range from 30 to 36 species, indicating that trap catches were identifying most aphid species expected to occur in the orchard. Three species, Rhopalosiphum maidis (Fitch), Aphis spiraecola Patch, and Myzus persicae (Sulzer), were consistently dominant across locations and years. Orchard-trapped populations of these three species peaked in a similar chronological sequence each year. As expected, trap color influenced the total number and distribution of the predominate species collected. However, the same dominant species occurred in both yellow and green traps. Based on the seasonal population dynamics reported here and on published vector efficacy studies, the most probable significant PPV vector was identified as A. spiraecola. If the PPV pathogen escapes current quarantine or if subsequent reintroductions of PPV occur, these data will be useful for developing plum pox management strategies.     

Baseline susceptibilities to imidacloprid for green apple aphid and spirea aphid (Homoptera: Aphididae) collected from apple in the Pacific northwest

Susceptibilities to the neonicotinyl insecticide imidacloprid were determined for clones of apple aphid, Aphis pomi De Geer, and spirea aphid, Aphis spiraecola Patch, collected from conventional and organic apple orchards and from crab apple and wild apple in Washington state and British Columbia over a period of 6 yr. For aphids collected during 1996--1998, adults were dipped in test solutions by using the Food and Agriculture Organization protocol, and third instars and adults were reared on treated apple leaf disks. During the final 3 yr of study, bioassays involved only third instars on treated leaf material. Tests showed that A. spiraecola was significantly more tolerant to imidacloprid compared with A. pomi. Depending on the bioassay method and aphid developmental stage, average LC50 values for A. spiraecola were 4.4 -5.7 times higher than those for A. pomi established under the same test conditions. Clones of both species from Washington were marginally more tolerant to imidacloprid than clones from British Columbia, but the differences were generally not significant. Average measures of susceptibility for clones from organic orchards or unsprayed trees also did not differ from those for clones from conventional orchards, and there was no evidence for increasing LC50 values over the 6 yr of study. Differences in susceptibility to insecticides between these two anatomically similar species should be considered during the testing of new products for use on apple.     

Effects of the concurrent exclusion of ants and earwigs on aphid abundance in an organic citrus grove

Based on the well-known mutualism between ants (Hymenoptera: Formicidae) and aphids (Homoptera: Aphididae), we conducted a five-year experiment of ant-exclusion from the canopies of citrus trees as a possible method of biological control of aphids. However, our results showed that the exclusion of ants from the canopies increased, instead of reducing, aphid abundance. To explain this unexpected result, we reasoned that the exclusion of ants from the canopies might also have excluded crawling insects that prey on aphids, such as the European earwig (Forficula auricularia L., Dermaptera: Forficulidae). Such a possibility is supported by the negative relationship between aphid density and the abundance of earwigs, consistent with a top-down control of aphids by earwigs. In contrast, the abundance of other aphid predators (Coleoptera: Coccinellidae, and Heteroptera) had no such negative effect on aphid density but a positive one, suggesting a bottom-up control, and showed no differences between control and ant-excluded trees. Thus, the most likely explanation for the increase in aphid abundance in the ant-excluded trees is the absence of earwigs from the canopies of the experimental trees, providing further evidence of the major role that earwigs play as control agents of aphids in cultivated trees.     

Influence of the margin vegetation on the conservation of aphid biological control in apple orchards

The influence of three margin strip treatments (wildflower strips, grass strips and spontaneous vegetation) adjacent to apple orchards on the biological control of Dysaphis plantaginea Passerini (Hemiptera: Aphididae) was compared during two consecutive years. The wildflower strips provided the highest amount of floral resources. Within the margin strips, hoverflies responded positively to higher resource provisioning whereas ladybird abundance did not differ between strip treatments. Within the orchards, the presence of parasitoids, hoverflies, and ladybirds in aphid colonies and the predation of sentinel aphids were not significantly affected by the adjacent strip treatments. The number of natural enemies observed in aphid colonies was mainly driven by aphid number. Aphid numbers were higher close to the margin strips suggesting that aphid colonization from orchard edges may counteract the positive effect of wildflower strips on natural enemy abundance and on a reduction of aphid infestation. The results confirm the positive influence of floral resource provisioning by wildflower strips on the conservation of aphid natural enemies, but also suggest that effects of wildflower strips on aphid regulation inside orchards are not very strong compared with spontaneous vegetation naturally occurring in the margins.     

Dispersion patterns and sampling plans for Diaphorina citri (Hemiptera: Psyllidae) in citrus

The abundance and spatial dispersion of Diaphorina citri Kuwayama (Hemiptera: Psyllidae) were studied in 34 grapefruit (Citrus paradisi Macfad.) and six sweet orange [Citrus sinensis (L.) Osbeck] orchards from March to August 2006 when the pest is more abundant in southern Texas. Although flush shoot infestation levels did not vary with host plant species, densities of D. citri eggs, nymphs, and adults were significantly higher on sweet orange than on grapefruit. D. citri immatures also were found in significantly higher numbers in the southeastern quadrant of trees than other parts of the canopy. The spatial distribution of D. citri nymphs and adults was analyzed using Iowa's patchiness regression and Taylor's power law. Taylor's power law fitted the data better than Iowa's model. Based on both regression models, the field dispersion patterns of D. citri nymphs and adults were aggregated among flush shoots in individual trees as indicated by the regression slopes that were significantly >1. For the average density of each life stage obtained during our surveys, the minimum number of flush shoots per tree needed to estimate D. citri densities varied from eight for eggs to four flush shoots for adults. Projections indicated that a sampling plan consisting of 10 trees and eight flush shoots per tree would provide density estimates of the three developmental stages of D. citri acceptable enough for population studies and management decisions. A presence-absence sampling plan with a fixed precision level was developed and can be used to provide a quick estimation of D. citri populations in citrus orchards.     

Heterogeneous communities with lognormal species abundance distribution: Species-area curves and sustainability

Heterogeneous species abundance models are models in which the dynamics differ between species, described by variation among parameters defining the dynamics. Using a dynamic and heterogeneous species abundance model generating the lognormal species abundance distribution it is first shown that different degrees of heterogeneity may result in equivalent species abundance distributions. An alternative to Preston's canonical lognormal model is defined by assuming that reduction in resources, for example reduction in available area, increases the density regulation of each species. This leads to species-individual curves and species-area curves that are approximately linear in a double logarithmic plot. Preston's canonical parameter gamma varies little along these curves and takes values in the neighborhood of one. Quite remarkably, the curves, which define the sensitivity of the community to area reductions, are independent of the heterogeneity among species for this model. As a consequence, the curves can be estimated from a single sample from the community using the Poisson lognormal distribution. It is shown how to perform sensitivity analysis with respect to over-dispersion in sampling relative to the Poisson distribution as well as sampling intensity, that is, the fraction of the community sampled. The method is exemplified by analyzing three simulated data sets.     

Pest management systems affect composition but not abundance of phytoseiid mites (Acari: Phytoseiidae) in apple orchards

We examined the faunal composition and abundance of phytoseiid mites (Acari: Phytoseiidae) in apple orchards under different pest management systems in Hungary. A total of 30 apple orchards were surveyed, including abandoned and organic orchards and orchards where integrated pest management (IPM) or broad spectrum insecticides (conventional pest management) were applied. A total of 18 phytoseiid species were found in the canopy of apple trees. Species richness was greatest in the organic orchards (mean: 3.3 species/400 leaves) and the least in the conventional orchards (1.4), with IPM (2.1) and abandoned (2.7) orchards showing intermediate values. The phytoseiid community’s Rényi diversity displayed a similar pattern. However, the total phytoseiid abundance in the orchards with different pest management systems did not differ, with abundance varying between 1.8 and 2.6 phytoseiids/10 leaves. Amblyseius andersoni, Euseius finlandicus, and Typhlodromus pyri were the three most common species. The relative abundance of A. andersoni increased with the pesticide load of the orchards whereas the relative abundance of E. finlandicus decreased. The abundance of T. pyri did not change in the apple orchards under different pest management strategies; regardless of the type of applied treatment, they only displayed greater abundance in five of the orchards. The remaining 15 phytoseiid species only occurred in small numbers, mostly from the abandoned and organic orchards. We identified a negative correlation between the abundance of T. pyri and the other phytoseiids in the abandoned and organic orchards. However, we did not find any similar link between the abundance of A. andersoni and E. finlandicus.     

Abundance and spatial distribution of aphids and scales select for different life histories in their ladybird beetle predators

Abstract:  Life history parameters tend to differ between aphidophagous and coccidophagous ladybird beetles. It seems that the nature of prey, in particular the abundance, number and size of the colonies and their spatial distribution, may have been selected for the evolution of the life histories in these two groups of coccinellids, leading the aphidophagous ladybird beetles to develop at a fast pace and the coccidophagous beetles at a slower pace. To study the abundance, number and size of the colonies and the spatial distribution of aphid and coccid species, 100 sampling plots regularly spaced along four parallel transects were surveyed in the summer of 2004. At each sampling plot, species abundance, and the number and size of colonies of aphid and coccid species were recorded. Iwao's patchiness regression was used to assess the spatial distribution of aphids and coccids. From this study, it was found that coccids are much rarer than aphids but formed more colonies. Whereas aphids display a stonger tendency to crowding, aphid colonies are randomly distributed in space while coccid groups are aggregated. So, it seems that the abundance and spatial distribution of prey distribution may be factors selecting for the evolution of different life histories among aphidophagous and coccidophagous ladybird beetles.     

A population dynamics perspective on effect of irrigation regimes and plant densities on greenbug abundance in grain sorghum using regression

• 1 A dataset generated from previous experiments on greenbug Schizaphis graminum (Rondani) (Hemiptera: Aphididae) response to irrigation and plant density in grain sorghum was reanalyzed using a recently‐developed mechanistic ecological model for describing aphid population density curves. The model was used to estimate seven response variables: observed peak aphid abundance, predicted peak aphid abundance, time of peak abundance, per capita birthrate, death rate coefficient, final cumulative density and duration of substantial aphid infestation across three irrigation regimes and five plant densities.
• 2 Using regression, the observed peak aphid abundance, predicted peak aphid abundance, per capita birthrate and final cumulative abundance were shown to decrease significantly, whereas the death rate coefficient and duration of the infestation were shown to increase significantly for each 100 000 plant/ha increase.
• 3 Although significant results were found for a number of variables generated from the specific data set used in the analyses, of perhaps greater importance is the potential use of these equations in future predictions of aphid population dynamics. An example of projecting population curves based on estimated peak and cumulative counts and an example of projecting population curves based on estimated birth and death rate coefficients are provided.

     

Epiphytic lichen is associated with species richness of gall-inducing aphids but not with niche differentiation among them

The presence of epiphytic foliose lichen amplifies the heterogeneity of habitat by creating shelters for insects living on tree bark. It thus should enhance species number and spatial niche segregation among these canopy insects. We studied this hypothesis in a field experiment using four aphid species that induce galls on Pistacia atlantica trees covered with Xanthoria parietina lichen. In autumn 2008, 3 months after aphid fundatrices were oviposited, we marked six branches on each of 29 trees. Two served as a control, whereas the other four were isolated with insect glue; two of them were scraped with sandpaper to remove epiphytic foliose lichens. We therefore obtained three treatments comprising control branches, isolated branches with lichen, and isolated branches without lichen. In summer 2009, we counted all the galls developing on five new annual shoots on each of 174 branches. We observed more cecidogenic aphid species on all the branches with lichens than without, but each species at different proportions. The different frequencies of utilization of the lichen did not lead to habitat partitioning between species. In conclusion, although habitat heterogeneity itself was associated with species richness and population abundance, it did not induce spatial niche segregation. Considering that many economically important insect species, pests and natural enemies, oviposit or spend some portion of their lives in bark cracks, it is possible that some can use lichens too for protection or/and oviposition sites. As a consequence, lichens may affect management of agrosystems and their impacts should be investigated more deeply in such contexts.     

Flower strips increase the control of rosy apple aphids after parasitoid releases in an apple orchard

Mass releases of two parasitoid species, Aphidius matricariae and Ephedrus cerasicola, may provide an alternative measure to pesticides to control the rosy apple aphid Dysaphis plantaginea in organic apple orchards. As an exploratory study, we tested if the presence of flower strips between apple tree rows could improve the action of three early parasitoid releases––and of other naturally present aphid enemies––on the control of aphid colonies and the number of aphids per tree. Apple trees located at various distances from parasitoid release points were monitored in plots with and without flower strips in an organic apple orchard over two years, along the season of aphid infestation (March to July). Our case study demonstrated that the presence of flowering plant mixes in the alleyways of the apple orchard reduced the presence of D. plantaginea by 33.4%, compared to plots without flower strips, at the infestation peak date. We also showed a negative effect of increasing the distance to parasitoid release points on aphid control. However, our results at the infestation peak date suggest that the presence of flower strips could marginally compensate for the detrimental effect of increasing distance to the release point, probably by improving the persistence and dispersal capacities of natural enemies. Despite high variations in aphid population dynamics between years, we conclude that combining flower strips with early parasitoid releases in apple orchards is promising for biological control of the rosy apple aphid, although the method merits to be further refined.     

Conservation biological control of rosy apple aphid, Dysaphis plantaginea (Passerini), in eastern North America

Because of the potentially serious damage rosy apple aphid, Dysaphis plantaginea (Passerini) (Homoptera: Aphididae), can cause to apple fruit and branch development, prophylactic insecticides are often used for control. If biological control could be relied on, the amount of pesticide applied in orchards could be reduced. This study examined biological control of rosy apple aphid in eastern West Virginia and the potential for enhancement through conservation biological control, in particular, the effect of interplanting extrafloral nectar-bearing peach trees. By 20 d after first bloom, only 2% of fundatrices initially present survived to form colonies based on regression of data from 687 colonies. Exclusion studies showed that many of the early colonies were probably destroyed by predation; the major predator responsible seemed to be adult Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae). Mortality before apple bloom was most important in controlling rosy apple aphid population growth but by itself is not sufficiently reliable to prevent economic injury. Interplanting of extrafloral nectar-bearing trees did not increase biological control, and interplanting with 50% trees with extrafloral nectar glands reduced biological control. The number of leaf curl colonies in the 50% interplanted orchards was lower than in monoculture orchards, suggesting a preference of alate oviparae for more diverse habitats, supporting the resource concentration hypothesis but not at a level sufficient to prevent injury. Predation and parasitism after the formation of leaf curl colonies was not adequate to control rosy apple aphid populations.