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In a survey that was conducted during the year 2011, a local strain of Aphid lethal paralysis virus (ALPV) was identified and isolated from a wild population of Aphis nerii aphids living on Nerium oleander plants located in northern Israel. The new strain was tentatively named (ALPV-An). RNA extracted from the viral particles allowed the amplification and determination of the complete genome sequence. The virus genome is comprised of 9835 nucleotides. In a BLAST search analysis, the ALPV-An sequence showed 89 % nucleotide sequence identity with the whole genome of a South African ALPV and 96 and 94 % amino acid sequence identity with the ORF1 and ORF2 of that strain, respectively. In preliminary experiments, spray-applied, purified ALPV virions were highly pathogenic to the green peach aphid Myzus persicae; 95 % mortality was recorded 4 days post-infection. These preliminary results demonstrate the potential of ALPV for use as a biologic agent for some aphid control. Surprisingly, no visible ALPV pathogenic effects, such as morphological changes or paralysis, were observed in the A. nerii aphids infected with ALPV-An. The absence of clear ALPV symptoms in A. nerii led to the formulation of two hypotheses, which were partially examined in this study. The first hypothesis suggest that A. nerii is resistant or tolerant of ALPV, while the second hypothesis propose that ALPV-An may be a mild strain of ALPV. Currently, our results is in favor with the first hypothesis since ALPV-An is cryptic in A. nerii aphids and can be lethal for M. persicae aphids.

The objective of this work was to record the diversity of parasitoid of two aphid species, Brevicoryne brassicae L. and Aphis nerii Boyer de Fonscolombe in a site at Uberlândia, MG, and the relationship between parasitoid size and their mummies size, with reference to the host species. B. brassicae were collected on kale (Brassica oleracea L. var. acephala D.C.) and A nerii on milkweed (Asclepias curassavica L.). Samplings were made monthly from May, 1999 to May, 2000 in two experimental gardens. Morphometric measurements for both aphids and parasitoids were simplified by PCA analysis to achieve a multivariate size index. The parasitic Hymenoptera species associated with A. nerii were also found as parasitoids of B. brassicae, but with distinctive relative frequencies. Diaeretiella rapae (M'Intoch) (93.2%), Aphidius colemani Viereck (4.5%) and Lysiphlebus testaceipes (Cresson) (2.3%) were the parasitoids obtained from B. brassicae. Hyperparasitoids associated with these parasitoids were Alloxysta fuscicornis (Ashmead) (57.8%), Syrphophagus aphidivorus (Mayr) (25.1%) and Pachyneuron sp. (17.1%). The parasitoids found in A. nerii were: L. testaceipes (96.1%), A. colemani (3.9%) and the hyperparasitoids Pachyneuron sp. (85.2%) and S. aphidivorus (14.8%). Parasitoid size was correlated with mummy size for both A. nerii and B. brassicae. S. aphidivorus from A. nerii were significantly larger than those from B. brassicae. However, such differences were not detected for L. testaceipes, A. colemani or for Pachyneuron. Mummies of A. nerii were significantly larger than those of B. brassicae. No sexual dimorphism for size was detected.

Penetration of the stems and leaves ofGomphocarpus physocarpus (E.Mey) by the aphid,Aphis nerii (B. de F.) was studied with light and phase microscopes. Penetration of the epidermis and ground tissues was largely intercellular, that of the phloem tissues partly intercellular and in part intracellular. In the large majority of penetrations the external phloem was bypassed, the stylet tracks terminating in the sieve tubes of the internal phloem. Of 75 pairs of stylet tips encountered in presumably functional sieve tubes 73 were lodged in sieve tubes of the internal phloem. This confirms observations of a preliminary study which indicated thatA. nerii feeds preferentially on sieve tubes of the internal phloem. A satisfactory explanation of this preferential feeding has yet to be provided.

In the wing dimorphic milkweed-oleander aphid,Aphis nerii, winged aphids begin reproducing about 1.5 days after wingless aphids. The longer maturation period is primarily due to slower development since even adult eclosion by winged aphids takes place after wingless aphids begin reproducing. The delay is not due to a post-eclosion, pre-reproductive flight since, beginning with the fourth instar, larval winged aphids were reared at a density of one per plant and the vast majority were not stimulated to fly under such low-density conditions. Thus, the ability to fly incurs a fitness cost in terms of delayed reproduction, irrespective of whether flight actually occurs. We did not observe a difference between morphs for lifetime fecundity, even though wingless aphids have larger abdomens than winged aphids and for both morphs there is a significant correlation between abdomen width and fecundity. Offspring produced by wingless aphids over the first four days of reproduction are larger than those produced by winged aphids, and the size difference at birth is maintained into adulthood. However, there are no differences in life history traits between these offspring, including maturation period and lifetime fecundity. Thus, reduced body size does not increase the cost of being able to fly, at least under the conditions of these experiments. The cost of being able to fly in this species should favor reduced production of winged individuals in populations that exploit more permanent host plants.

Penetration of the phloem of young and mature leaves ofNerium oleander by stylets of the aphid,Aphis nerii was studied with light, phase and differential interference contrast microscopes. Two of five pairs of stylet tips encountered in young leaves and eleven of sixteen pairs encountered in mature leaves were lodged in sieve tubes of the adaxial phloem. In young leaves, the majority of penetrations originated from the abaxial epidermis; conversely, the majority of penetrations in mature leaves originated from the adaxial epidermis. In all instances, penetration of the epidermis, ground tissue and phloem was largely intercellular.

Populations of the milkweed-oleander aphid,Aphis nerii, were sampled in California, Iowa and Puerto Rico. Among these localities the aphid's host plants differ greatly in permanence. I compared populations for migratory potential, measured as the proportion of winged offspring produced in response to being crowded, and for life history and morphometric traits of the subsequent adult winged aphids. I predicted a negative correlation between degree of host plant permanence and migratory potential. As predicted, aphids from Iowa, where migration on to temporary hosts must occur each year, produce a greater proportion of winged offspring (37.7%) than those from California (25.7%) or Puerto Rico (31.6%) where hosts are more permanent. However, hosts in Puerto Rico appear to be more permanent than those in California, yet the difference between populations for migratory potential was opposite to that predicted. Within California the prediction again held: aphids collected from the most impermanent sites produce the greatest proportion of winged offspring. There were no population differences for any life history or morphometric traits of winged aphids that are important contributors to fitness or migratory ability such as time to reproductive maturity, fecundity or wing length. Nor did any traits covary with migratory potential. Thus, there does not appear to be an association of life history and morphology with migratory potential that could enhance the colonizing ability of migrant aphids. I was unable to detect population differentiation for life history and morphology even though there is ample genetic variation within populations on which selection could act and an absence of constraints arising from genetic correlations that could prevent appropriate evolution of traits within populations. The exploitation of temporary host plants therefore occurs by an increase in the number of colonists produced and not by change in life history or morphology of those colonists.

Penetration of the stems ofAraujia sericofera, Asclepias curassavica, Cynanchum ellipticum andSarcostemma viminale by stylets of the aphidAphis nerii was studied with light and differential interference contrast microscopes. Of a total of 118 stylets and 446 stylet tracks observed in cross-sections of stems of the fourAsclepiadaceae, 97 stylets and 372 stylet tracks terminated within the internal primary phloem. Of the remainder, 15 stylets and 74 tracks terminated within the external primary phloem. 22 stylets and 179 of the stylet tracks penetrated the external phloem on the way to the internal phloem. Of these, only four stylets and 32 of the stylet tracks showed signs of attempted probes of the external phloem. It is suggested thatAphis nerii may obtain not only its essential food requirements but also cardiac glycosides as a basis for chemical aposematism.

Plants use volatile organic compounds (VOCs) to cue natural enemies to their herbivore prey on plants. Simultaneously, herbivores utilize volatile cues to identify appropriate hosts. Despite extensive efforts to understand sources of variation in plant communication by VOCs, we lack an understanding of how ubiquitous belowground mutualists, such as arbuscular mycorrhizal fungi (AMF), influence plant VOC emissions. In a full factorial experiment, we subjected plants of two milkweed (Asclepias) species under three levels of AMF availability to damage by aphids (Aphis nerii). We then measured plant headspace volatiles and chemical defenses (cardenolides) and compared these to VOCs emitted and cardenolides produced by plants without herbivores. We found that AMF have plant species-specific effects on constitutive and aphid-induced VOC emissions. High AMF availability increased emissions of total VOCs, two green leaf volatiles (3-hexenyl acetate and hexyl acetate), and methyl salicylate in A. curassavica, but did not affect emissions in A. incarnata. In contrast, aphids consistently increased emissions of 6-methyl-5-hepten-2-one and benzeneacetaldehyde in both species, independent of AMF availability. Both high AMF availability and aphids alone suppressed emissions of individual terpenes. However, aphid damage on plants under high AMF availability increased, or did not affect, emissions of those terpenes. Lastly, aphid feeding suppressed cardenolide concentrations only in A. curassavica, and AMF did not affect cardenolides in either plant species. Our findings suggest that by altering milkweed VOC profiles, AMF may affect both herbivore performance and natural enemy attraction.

The aim of this work was to examine, both in the field and in the laboratory, ecological aspects of selected plant–aphid–parasitoid interactions to evaluate their potential for the open rearing of the parasitoid Lysiphlebus testaceipes (Cresson) (Hymenoptera: Aphidiinae) for the control of Aphis craccivora (Koch) (Hemiptera: Aphididae) in alfalfa agroecosystems. To this end quantitative samplings of parasitoids and aphids were made fortnightly in three alfalfa crop fields and their spontaneously vegetated edges, in Rafaela (Santa Fe, Argentina), during three years (2009–2011). Three sink webs based on L.testaceipes, on a per-year basis, were constructed to assess the strength of the interactions established by aphids and parasitoids, the host ranges of alternative aphid species, and the tendencies in parasitoid host use across years. In the laboratory, emergence rates, parasitism rates, larval and pupal development times, and adult lifespan of L. testaceipes were analyzed by means of choice tests, including the alternative and the target aphid species in the assays. About 84 % of adults of L. testaceipes obtained in the samples came from Aphis nerii (Boyer de Fonscolombe), an innocuous aphid species only associated with plants of the genus Araujia Brotero (Apocynaceae). Based on our results, the system proposed has many features that support its feasibility to be used as an open rearing system of L. testaceipes: unrisky alternative aphid, easy reproduction of the banker plant and similar suitability of innocuous and pest aphid species for the parasitoid to oviposit and complete their development without noticeably preference for specific hosts. Fil: Zumoffen, Leticia. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Santa Fe. Estación Experimental Agropecuaria Rafaela; Argentina Fil: Tavella, Julia Rita. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina Fil: Signorini, Marcelo. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Santa Fe. Estación Experimental Agropecuaria Rafaela; Argentina Fil: Salvo, Silvia Adriana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina

Trophic cascades occur when predators benefit plants by consuming herbivores, but the overall strength of a trophic cascade depends upon the way species interactions propagate through a system. For example, plant resistance to, or tolerance of, herbivores reduces the potential magnitude of a trophic cascade. At the same time, plants can also affect predator foraging or consumption in ways that either increase or decrease the strength of trophic cascades. In this study, we investigated the effects of plant variation on cascade strength by manipulating predator access to aphid populations on two species of milkweed: the slower-growing, putatively more-defended Asclepias syriaca and the faster-growing, putatively less-defended Asclepias incarnata. Predatory insects increased plant growth and survival for both species, but the strength of these trophic cascades was greater on A. incarnata, which supported more aphid growth early in the season than did A. syriaca. More predators were observed per aphid on A. incarnata, and cage treatments generated significant patterns consistent with predator aggregation on A. incarnata, but not A. syriaca. Although predators strongly affected aphids, this effect did not differ consistently between milkweed species. Plant tolerance to herbivory may therefore be the primary driver of the difference in trophic cascade strength observed. Importantly, we observed that the timing of predator exclusion affected plant growth and survival differently, indicating that measures of “cascade strength” may change with phenology and plant physiological responses. Together, our results suggest a mechanism by which differences in resource allocation patterns could explain differences in growth, phenology, and cascade strength between species.

Successful mass production of biocontrol agents is a prerequisite to their effective use in the field. Thus in the present study the suitability of ten aphid species of a ladybird beetle Anegleis cardoni (Weise) in terms of growth, development, survival and mortality life table attributes was assessed for the purpose of mass production. The study revealed that the developmental duration of the immature stages of A. cardoni was shortest when fed on Uroleucon compositae (Theobald), Rhopalosiphum maidis (Fitch), Hyadaphis coriandri (Das) and Myzus persicae (Sulzer) in comparison with other aphid species. Immature survival, development rate, adult weight and growth index were also highest when A. cardoni larvae were fed on these aphids, while lowest when fed on Hysteroneura setariae (Thomas) and Ceratovacuna silvestri (Takahashi). Any larva of A. cardoni did not reach adult stage when fed on Aphis nerii Boyer de Fonscolombe; therefore it may be considered as a toxic prey. Life table data revealed that the overall mortality prior to adult stage was lowest in U. compositae and highest in C. silvestri. The first instars suffered the highest mortality in comparison with other instars on all the aphid species tested. However, the life expectancy for each aphid species as prey revealed a continuous decline with the advancement of age. Thus among all the ten aphid species tested, U. compositae, R. maidis, H. coriandri and M. persicae were found equally suitable for mass production of A. cardoni.

The pea aphid U-type symbiont (PAUS) was investigated to characterize its microbiological properties. Fluorescence in situ hybridization (FISH) and electron microscopy revealed that PAUS was a rod-shaped bacterium found in three different locations in the body of the pea aphid Acyrthosiphon pisum: sheath cells, secondary mycetocytes, and hemolymph. Artificial transfer experiments revealed that PAUS could establish stable infection and vertical transmission when introduced into uninfected pea aphids. When 28 aphid species collected in Japan were subjected to a diagnostic PCR assay, four species of the subfamily Aphidinae (Aphis citricola, Aphis nerii, Macrosiphum avenae, and Uroleucon giganteus) and a species of the subfamily Pemphiginae (Colopha kansugei) were identified to be PAUS-positive. The sporadic incidences of PAUS infection without reflecting the aphid phylogeny can be best explained by occasional horizontal transfers of the symbiont across aphid lineages.

Pre-imaginal development, immaturesurvival, and reproduction of a ladybird, Coccinella septempunctata Linnaeus, werestudied in response to six aphid species, Aphiscraccivora Koch, Aphis gossypii Glover,Aphis nerii Boyer de Fonscolombe,Lipaphis erysimi (Kaltenbach), Myzuspersicae (Sulzer) and Uroleuconcompositae (Theobald) to quantify theirrelative suitability as prey. Pre-adultdevelopment was shortest (13.93 ± 0.12 days)when fed on L. erysimi and longest(22.85 ± 0.10 days) on A. nerii. Immaturesurvival, adult emergence, growth index,relative growth rate, development rate, maleand female longevity, oviposition period,fecundity and hatching percent were maximal, i.e. 73.47 ± 0.89%, 90.07 ± 1.43%,8.62 ± 0.23, 1.52 ± 0.02, 0.07,81.10 ± 1.26 days, 85.70 ± 1.45 days,69.80 ± 1.32 days, 1764.10 ± 8.46,and 87.88 ± 1.05, respectively when C.septempunctata were fed on L. erysimi.The same parameters were minimal, i.e.43.86 ± 1.33%, 71.65 ± 2.75%,2.02 ± 0.08, 0.49 ± 0.02, 0.04,44.40 ± 1.39 days, 53.50 ± 1.00 days,16.40 ± 0.60 days, 203.20 ± 11.83, and48.68 ± 2.06, respectively on A. nerii. Theweights of different ladybird life stages weremaximal after feeding on L. erysimi and minimalon A. nerii. Regression analyses of thedata revealed linear relationships betweendevelopment rate and weight of adult; dailyprey consumption and relative growth rate; logweight of adult male and female; and longevityand fecundity of female. On the basis of thesefindings, the order of suitability of aphidspecies for C. septempunctata is L. erysimi >M. persicae > A. craccivora > A. gossypii >U. compositae > A. nerii. Thus, the presentinformation can be utilized for the massrearing of C. septempunctata by supplyingthe best food and can also help in theprediction of the relative abundance of theladybird on different aphid infestations in thefields.

In laboratory bioassays, whole-body homogenates and fresh cornicle wax of Rhopalosiphum padi(L.) (the bird-cherry oat aphid) elicited antennal examination and attack behavior in naive females of the polyphagous aphidiid parasitoid, Lysiphlebus testaceipes (Cresson). No such response was elicited by either homogenates or cornicle wax of Aphis nerii(Boyer de Fonscolombe) (another known host of the parasitoid) or by preparations of the aphid alarm pheromone, (E)-β-farnesene. The response to R. padiproducts was independent of rearing host and appears to be innate. Application of R. padicornicle wax to the dorsum of a nonhost aphid [Acythosiphum pisum(Harris)] increased the frequency with which this species was attacked by L. testaceipes.There was a tendency for the kairomonal activity of the cornicle secretion to decline as the wax dried, although parasitoid attack behavior was still elicited by wax which had been allowed to dry for up to 30 min before testing.

Oleander aphids, (Aphis nerii), which are sporadically tended by ants, were used as a moded system to examine whether host plant factors associated with feeding site influenced the formation of ant-aphid associations. Seasonal patterns of host plant utilization and association with attendant ants were examined through bi-weekly censuses of the aphid population feeding on thirty ornamental oleander plands (Nerium oleander) in northern California in 1985 and 1986. Colonies occurred on both developing and senescing plant terminals, including leaf tips, floral structures, and pods. Aphids preferentially colonized leaf terminals early in the season, but showed no preference for feeding site during later periods. Argentine ants (Iridomyrmex humilis) occasionally tended aphid colonies. Colonies on floral tips were three to four times more likely to attract ants than colonies on leaf tips, even though the latter frequently contained more aphids. Ants showed a positive recruitment response to colonies on floral tips, with a significant correlation between colony size and number of ants. There was no recruitment response to colonies on leaf tips. These patterns were reproducible over two years despite large fluctuations in both aphid population density and ant activity. In a laboratory bioassay of aphid palatability, the generalist predator,Hippodamia convergens, took significantly more aphids reared on floral tips compared to those reared on leaf tips. The patterns reported here support the hypothesis that tritrophic factors may be important in modifying higher level arthropod mutualisms.

Cardenolide sequestration by a hemimetabolous aphid and a holometabolous butterfly from the neotropical milkweed,Asclepias curassavica L., is compared. The oleander aphid,Aphis nerii B. de F., sequestered a similarly narrow range of cardenolide concentrations to the monarch butterfly,Danaus plexippus (L.), from the wide range of concentrations available in leaves of A.curassavica. However, A.nerii sequestered significantly less cardenolide (269 µg/0.1 g) thanD. plexippus (528 µg/0.1 g). The honeydew excreted by A.nerii was comprised of 46% cardenolide. The complete polarity range of 25 cardenolides detected by thin layer chromatography in A.curassavica was represented in the 17 whole aphid cardenolides and the 20 aphid honeydew cardenolides detected. D.plexippus sequestered a narrower polarity range of 11 cardenolides, having eliminated low polarity cardenolide genins and glycosides. It is suggested that these chemical differences may be related to interactions among the broad feeding tactics of sucking or chewing milkweed leaves, life history constraints of holometabolyversus hemimetaboly, the distribution of milkweed food resources in space and time, and the dynamics of natural enemies.

Common milkweed (Asclepias syriaca) has been identified as a potential whole-plant source of poly phenol, oil, and polymeric hydrocarbon. Based on in situ sampling, a range of 4.7-14.4% (dry weight) polyphenol + oil (variation significant at 1% level) and 0.2-1.2% polymeric hydrocarbon (variation significant at 5% level) were found among 48 Maryland and northern Virginia populations. In a 2-yr replicated evaluation of progenies from 41 populations, significant differences (5% level) in vigor,Aphis nerii feeding preference, numbers of plants surviving the seeding year, and numbers of tillers produced the second year were observed. Genetic variation for agronomic traits was generally small, but appeared sufficient to justify a breeding program. Excluding aphid feeding-preference, all agronomic variables were positively correlated with each other (significant at 1% level); aphid feeding-preference was weakly, negatively correlated with the remaining agronomic variables (significant at 1% level). Chemical and agronomic data were not significantly correlated. Factor analysis indicated that plants which performed well early in their life cycle would be expected to perform well on a long term basis. Based on cluster analysis, the environment in which some populations developed may have affected in situ production of poly phenols + oil and polymeric hydrocarbon as well as the subsequent agronomic performance of their progenies.

This paper describes the influence on predator behaviour, and the survival of an aposematic aphid, Aphis nerii, in comparison with a palatable, cryptic aphid, Acyrthosiphon pisum, when offered to two predators with different foraging tactics. The experiments were designed to test Fisher's (1930) suggestion that aposematism could evolve by kin selection, since aposematic animals often occur in aggregations of relatives. Initially, spiders (Zygiella x-notata) and birds (Parus major) killed high proportions of distasteful A. nerii (60% and 54% respectively). With experience, the predators killed and ate fewer A. nerii. The decreasing mortality of A. nerii after initial encounters with predators, coupled with its apparently obligate parthenogenesis, indicate that the evolution of aposematism in this soft-bodied insect is consistent with kin selection.

Investigations carried out on the relationship of Bittergourd Mosaic virus and its vectors indicated that the pre-acquisition fasting threshold, acquisition threshold and inoculation feeding threshold were 15 minutes, 5 seconds and 60 seconds respectively forMyzus persicae; 15 minutes, 20 seconds and 5 minutes respectively for Aphis gossypii; 30 minutes 30 seconds and 5 minutes respectively for Aphis nerii and Brevicoryne brassicae; 30 minutes, 20 seconds and 5 minutes respectively for A. malvae. The optimum number of viruliferous aphids per plant for transmission was 15 for all the five aphid vectors; increasing the number of aphids above the optimum decreased the percentage of transmission. Persistence of the virus during fasting was 4 hours, 90, 60, 45 and 30 minutes respectively for M. persicae, A. gossypii, A. malvae, B. brassicae and A. nerii while persistence during feeding was 40, 30, 20, 15 and 10 minutes respectively for the same aphid vectors. Though both alate and apterous forms of the vectors transmitted the virus, the apterous forms were more efficient than the alate ones.

La valeur alimentaire pour la Coccinelle aphidiphage,Adonia 11-notata des œufs deAnagasta kuehniella a ete comparee a celle d'une nourriture tres favorable (Aphis fabae) et d'une alimentation peu satisfaisante (Aphis nerii). Les criteres retenus pour cette comparaison ont ete la duree de developpement larvaire, la taille et le poids des larves, le taux de mortalite pendant la vie larvaire ainsi que la fecondite des adultes. D'apres ces criteres les œufs d'A. kuehniella constituent une mediocre alimentation pourA. 11-notata et ne permettent pas de faciliter l'elevage de masse de ce predateur.