COMPARISON OF SWEEP-NET AND STEM-COUNT TECHNIQUES FOR SAMPLING PEA APHIDS IN ALFALFA

1989 ◽  
Vol 24 (3) ◽  
pp. 344-347
Author(s):  
G. David Buntin ◽  
David J. Isenhour

The accuracy, precision and efficiency of stem-count and sweep-net techniques were compared for sampling the pea aphid, Acyrthosiphon pisum (Harris), in alfalfa. Density estimates by both techniques were highly correlated (r = 0.87). Both techniques were similar in sample precision and efficiency, but stem counts provided more accurate density estimates than the sweep net technique. The stem count technique is an accurate and efficient alternative to the sweep net for sampling pea aphids in alfalfa.

1986 ◽  
Vol 118 (6) ◽  
pp. 601-607 ◽  
Author(s):  
G.A. Maiteki ◽  
R.J. Lamb ◽  
S.T. Ali-Khan

AbstractPea aphids, Acyrthosiphon pisum (Harris), were sampled from 1980 to 1983 in field peas, Pisum sativum (L.), in Manitoba. Sweep and foliage samples were taken in commercial fields and plots. Aphids were found in late May or early June soon after the crop emerged, but populations were low throughout June. Populations increased in July, when the crop was flowering and producing pods, and peaked in the latter half of July or early August in 3 of the 4 years, when pods were maturing. Populations decreased rapidly after the peak, as the plants senesced. In 1980, a drought year, aphid densities were low and the populations peaked in the middle of August. From 1981 to 1983, densities exceeded the economic threshold in all commercial fields and all but one of the plots that were sampled.


1992 ◽  
Vol 124 (1) ◽  
pp. 87-95 ◽  
Author(s):  
K.L. Kouamé ◽  
M. Mackauer

AbstractThe influence of nutrient stress on growth, development, and reproduction in apterous virginoparae of the pea aphid, Acyrthosiphon pisum (Harris), was investigated in the laboratory. We tested the hypothesis that species with a high reproductive investment have low resistance to starvation. Aphids in two groups were starved daily from birth for 4 h and 6 h, respectively, and compared with feeding counterparts reared on leaves of broad beans, Vicia faba L. Aphid wet weight increased as an exponential function of age in all groups. Starved aphids had lower adult weight and required longer from birth to parturition than feeding aphids. These effects increased with the length of daily starvation. The number of offspring produced was correlated with adult dry weight. Aphids were unable to compensate, or to compensate completely, for water and nutrient loss resulting from starvation. It is suggested that pea aphids allocate resources first to maintenance and then to reproduction when deprived of food.


1982 ◽  
Vol 60 (10) ◽  
pp. 2245-2252 ◽  
Author(s):  
J. M. Clegg ◽  
C. A. Barlow

Pea aphids respond most effectively to the threat of a predator by walking away or dropping from their host plant. Simulating threat by using vibration and alarm pheromone, both separately and together, we found no evidence that escape responses are heritable, nor that individual aphids have characteristic escape behaviours. On the contrary, the amount of alarm pheromone influenced responses: the more pheromone, the more likely an immediate and effective escape. Vibration preceding alarm pheromone greatly increased responsiveness to pheromone, and aphids were more responsive to pheromone after vibration when feeding on stems than when feeding on the undersides of leaves.


2002 ◽  
Vol 80 (12) ◽  
pp. 2131-2136 ◽  
Author(s):  
Edward B Mondor ◽  
Bernard D Roitberg

Aphids possess unique anatomical structures called cornicles through which a defensive secretion containing alarm pheromone is often emitted when a predator attacks an aphid. The levels of alarm pheromone in cornicle droplets from the pea aphid, Acyrthosiphon pisum (Harris), vary considerably during development; however, it is not clear how the length of the cornicle changes during ontogeny. The length of the cornicle relative to the lengths of other body structures may have profound effects on aphid defense and alarm signal diffusion. Using previously published morphological measurements of pea aphids and observing interactions between pea aphids and multicolored Asian ladybird beetles, Harmonia axyridis Pallas, it was observed that pea aphid cornicles elongate proportionally more than other body parts during the first four instars, when alarm-pheromone levels have peaked, than during the fifth (adult) instar, when pheromone levels decline. Pea aphids also are more likely to emit cornicle droplets and daub them onto a predator when the cornicles are undergoing such rapid growth. We suggest that because of a high risk of predation, rapid cornicle growth in juveniles has evolved both for individual defense and for the inclusive fitness benefits of alarm signaling.


2019 ◽  
Author(s):  
Brian D. Heinold ◽  
Dan A. Kowalski ◽  
R. Barry Nehring

AbstractTraditional methods of collecting and sorting benthic macroinvertebrate samples are useful for stream biomonitoring and ecological studies; however, these methods are time consuming, expensive, and require taxonomic expertise. Estimating larval densities through collection of post-emergent exuvia can be a practical and time efficient alternative. We evaluated the use of multiple pass depletion techniques of the post-emergent exuvia of Pteronarcys californica to estimate larval densities at ten sites in three Colorado rivers. Exuvia density was highly correlated with both final-instar larval density (R2 = 0.90) and total larval density (R2 = 0.88) and the multiple pass removal technique performed well. Exuvia surveys found P. californica at three low density sites where benthic sampling failed to detect it. At moderate and high density sites the exuvia surveys always produced lower density estimates than benthic surveys. Multiple pass depletion estimates of exuvia proved to be an accurate and efficient technique at estimating larval densities and provided an effective alternative for traditional benthic sampling when objectives are monitoring P. californica and detecting populations, especially at low density sites.


1999 ◽  
Vol 202 (19) ◽  
pp. 2639-2652 ◽  
Author(s):  
G. Febvay ◽  
Y. Rahbe ◽  
M. Rynkiewicz ◽  
J. Guillaud ◽  
G. Bonnot

The fate of sucrose, the major nutrient of an aphid's natural food, was explored by radiolabeling in the pea aphid Acyrthosiphon pisum. To investigate the influence of nitrogen quality of food on amino acid neosynthesis, pea aphids were reared on two artificial diets differing in their amino acid composition. The first (diet A) had an equilibrated amino acid balance, similar to that derived from analysis of aphid carcass, and the other (diet B) had an unbalanced amino acid composition similar to that of legume phloem sap. Aphids grown on either diet expired the same quantity of sucrose carbon as CO(2), amounting to 25–30 % of the ingested sucrose catabolized in oxidation pathways. On diet A, the aphids excreted through honeydew about twice as much sucrose carbon as on diet B (amounting to 12.6 % of the ingested sucrose for diet A and 8.4 % for diet B), while amounts of sucrose carbons incorporated into exuviae were almost identical (1.9 % of the ingested sucrose on diet A and 2.7 % on diet B). There was also no difference in the amounts of sucrose carbon incorporated into the aphid tissues, which represented close to 50 % of the ingested sucrose. Sucrose carbons in the aphid tissues were mainly incorporated into lipids and the quantities involved were the same in aphids reared on either diet. On diet B, we observed neosynthesis of all protein amino acids from sucrose carbons and, for the first time in an aphid, we directly demonstrated the synthesis of the essential amino acids leucine, valine and phenylalanine. Amino acid neosynthesis from sucrose was significantly higher on diet B (11.5 % of ingested sucrose carbons) than on diet A (5.4 %). On diet A, neosynthesis of most of the amino acids was significantly diminished, and synthesis of two of them (histidine and arginine) was completely suppressed. The origin of amino acids egested through honeydew was determined from the specific activity of the free amino acid pool in the aphid. Aphids are able to adjust to variation in dietary amino acids by independent egestion of each amino acid. While more than 80 % of excreted nitrogen was from food amino acids, different amino acids were excreted in honeydew of aphids reared on the two diets. The conversion yields of dietary sucrose into aphid amino acids determined in this study were combined with those obtained previously by studying the fate of amino acids in pea aphids reared on diet A. The origin of all the amino acid carbons in aphid tissues was thus computed, and the metabolic abilities of aphid are discussed from an adaptive point of view, with respect to their symbiotic status.


2005 ◽  
Vol 95 (2) ◽  
pp. 125-131 ◽  
Author(s):  
G. Kunert ◽  
W.W. Weisser

AbstractThe pea aphidAcyrthosiphon pisumHarris has been shown to produce an increasing proportion of winged morphs among its offspring when exposed to natural enemies, in particular hoverfly larvae, lacewing larvae, adult and larval ladybirds and aphidiid parasitoids. While these results suggest that wing induction in the presence of predators and parasitoids is a general response of the pea aphid, the cues and mechanisms underlying this response are still unclear. Tactile stimuli and the perception of chemical signals as well as visual signals are candidates for suitable cues in the presence of natural enemies. In this paper the hypothesis that the aphids' antennae are crucial for the wing induction in the presence of natural enemies is tested. Antennae of pea aphids were ablated and morph production was scored when aphids were reared either in the presence or the absence of predatory lacewing larvae over a six-day period. Ablation of antennae resulted in a drastic drop in the proportion of winged morphs among the offspring, both in the presence and the absence of a predator whereas predator presence increased wing induction in aphids with intact antennae, as reported in previous experiments. The results show that antennae are necessary for wing induction in the presence of natural enemies. Critical re-examination of early work on the importance of aphid antennae and tactile stimuli for wing induction suggests that a combination of tactile and chemical cues is likely to be involved not only in predator-induced wing formation but also for wing induction in response to factors such as crowding in the aphid colony.


1984 ◽  
Vol 116 (7) ◽  
pp. 923-932 ◽  
Author(s):  
A. P. Gutierrez ◽  
J. U. Baumgaertner ◽  
C. G. Summers

AbstractA simple age-specific energetics (calories or biomass) model for the growth and development, reproduction, respiration, ageing, and intrinsic survivorship as a function of temperature and per capita energy availability for pea aphid (Acyrthosiphon pisum (Harris)) is reported. The ratio of energy supply–demand is used to scale all of the rates in the model. The maximum demand for energy based upon current state values is used to drive the Frazer–Gilbert functional response model (i.e. food acquisition), which is a component of the metabolic pool model used to assimilate energy to growth, reproduction, respiration, and egestion. The extensive data sets on pea aphid energetics published by Randolph et al. (1975) were used to develop the model. As the model estimates reproduction (Mx) and survivorship (Lx) values, extensive published age-specific life-data sets on pea aphids are used to test it. The results suggest:(1) the lower thermal threshold for development is raised and the upper threshold is lowered as food resources are decreased(2) the temperature-dependent rate of development is slowed with decreasing energy resources(3) the size of individuals and reproduction become smaller as temperature approaches the upper and lower thermal thresholds.A simple model for multitrophic level interactions incorporating the acquisition and assimilation functions is presented.


2019 ◽  
Vol 151 (3) ◽  
pp. 365-377 ◽  
Author(s):  
Bradley S. Stokes ◽  
Edward J. Bechinski ◽  
Sanford D. Eigenbrode

AbstractEmpirically-based economic injury levels are lacking for pea aphid, Acyrthosiphon pisum Harris (Hemiptera: Aphididae), as a direct pest of dry peas, Pisum sativum Linnaeus (Fabaceae). To address this need, the relationship between pea aphid density and yield of dry pea (cultivar Aragorn) were quantified by encaging pea aphids at varying densities for 17-day infestation periods during 2009 and 2010 in Moscow, Idaho, United States of America. Pea aphid density after infestation at the early reproductive stage of the crop (x) significantly reduced dry pea seed yield (relative weight of US #1 dry peas, y): y = 0.7733 − 0.00998x + 0.000037x2. Economic injury levels were computed based on this relationship and incorporating the cost of control, crop market value, insecticide efficacy, and crop yield potential. The resulting economic injury levels ranged from five to 19 pea aphids per plant at the start of early reproductive growth stages of dry peas. For usability these were converted to sweep net sample size equivalents of 86–307 pea aphids per twenty-five 180-degree sweeps with a standard sweep net. These economic injury levels are applicable in the inland Pacific Northwest, United States of America, where they were developed and likely in other regions with similar climatic and agronomic conditions.


1965 ◽  
Vol 45 (6) ◽  
pp. 571-577 ◽  
Author(s):  
H. B. Specht ◽  
D. Chisholm

Furrow applications of Di-syston (O,O-diethyl S-2- (ethylthio)ethyl phosphorodithioate) for control of pea aphids, Acyrthosiphon pisum (Harris), on peas under greenhouse conditions showed that the Di-syston content of the plants reflected the application rates; absorption of Di-syston by the plants was greater on sandy loam than on clay loam; concentrations of Di-syston tended to be highest in the basal third of the pea vines and progressively lower in the middle and top thirds of the plants; slight phytotoxicity occurred on the lower leaves at 4 and 32 lb per acre (4.48 and 35.87 kg/ha) of toxicant but yields were not affected; soil moisture did not affect the uptake of Di-syston in the plant. Differences in uptake may be attributed to differences in the base exchange capacity of the soils.


Sign in / Sign up

Export Citation Format

Share Document