Research was done during 2012 to evaluate the potential exposure of pollinators to neonicotinoid insecticides used as seed treatments on corn, cotton, and soybean. Samples were collected from small plot evaluations of seed treatments and from commercial fields in agricultural production areas in Arkansas, Mississippi, and Tennessee. In total, 560 samples were analyzed for concentrations of clothianidin, imidacloprid, thiamethoxam, and their metabolites. These included pollen from corn and cotton, nectar from cotton, flowers from soybean, honey bees, Apis mellifera L., and pollen carried by foragers returning to hives, preplanting and in-season soil samples, and wild flowers adjacent to recently planted fields. Neonicotinoid insecticides were detected at a level of 1 ng/g or above in 23% of wild flower samples around recently planted fields, with an average detection level of about 10 ng/g. We detected neonicotinoid insecticides in the soil of production fields prior to planting at an average concentration of about 10 ng/g, and over 80% of the samples having some insecticide present. Only 5% of foraging honey bees tested positive for the presence of neonicotinoid insecticides, and there was only one trace detection (< 1 ng/g) in pollen being carried by those bees. Soybean flowers, cotton pollen, and cotton nectar contained little or no neonicotinoids resulting from insecticide seed treatments. Average levels of neonicotinoid insecticides in corn pollen ranged from less than 1 to 6 ng/g. The highest neonicotinoid concentrations were found in soil collected during early flowering from insecticide seed treatment trials. However, these levels were generally not well correlated with neonicotinoid concentrations in flowers, pollen, or nectar. Concentrations in flowering structures were well below defined levels of concern thought to cause acute mortality in honey bees. The potential implications of our findings are discussed.
A monitoring program that used a glass-vial bioassay to detect acephate resistance in populations of the tarnished plant bug, Lygus lineolaris (Palisot de Beauvois) (Heteroptera: Miridae), was carried out with weed-collected populations from 20 sites in the delta of Arkansas, Louisiana, and Mississippi. Additional results from field tests using recommended rates of formulated acephate in cotton showed that plant bug populations with resistance ratio (RR50) values > 3.0 for acephate (from the glass-vial bioassay) would be difficult to control in the field. Over a 4-yr-period from 2001 through 2004, only one population tested with the glass-vial bioassay was found with an RR50 value > 3.0 for acephate, but six populations having RR50 values > 3.0 were found in the delta in 2005. In fall 2005, an additional 10 populations from the hill region (the cotton growing areas outside the delta) were tested and four of these populations had RR50 values > 3.0. The number of populations with RR50 values > 3.0 increased to five of 10 and 18 of 20 in the hills and delta, respectively, in fall 2006. Laboratory tests using resistant populations found that resistance to acephate was not sex-linked and the alleles controlling the resistance were semidominant in nature. Because of the large increase in resistant populations and the nature of the resistance found in this study, along with control problems experienced by growers in 2006, entomologists in the mid-South strongly recommended that alternation of insecticide classes in field treatments for plant bug control be used by growers in 2007. This control strategy probably helped control plant bugs in the hills of MS where plant bug pressure was low in 2007, and only one population was found in the fall with an RR50 value > 3.0. Plant bug pressure was very high in many parts of the delta in 2007, and 15 of the 20 populations tested in the fall had RR50 values > 3.0. In one field test in cotton, a population with multiple resistance was tested and not effectively controlled in treatments using recommended rates of carbamate, organophosphate, and pyrethroid insecticides. Alternation of insecticide classes may not work very well when populations are present that are resistant to three of the four main classes of cotton insecticides. New insecticides in different classes are badly needed for control of tarnished plant bugs in cotton in the mid-South.
Summary 1.A high dose ⁄ refuge strategy has been adopted in the USA to manage the risk of Bacillus thuringiensis (Bt) resistance in target pests such as the cotton bollworm (CBW), Helicoverpa zea (Boddie) in transgenic Bt cotton Gossypium hirsutum L. Structured refuges, consisting of non-Bt cotton, have been a mandated part of this strategy to produce non-selected insects that are temporally and spatially synchronous with insects from the Bt crop, diluting Bt resistance alleles through mating. However, the bollworm is highly polyphagous and exploits a large number of crop and weedy hosts concurrently with Bt cotton. 2. A study was carried out in five major US cotton-producing states during 2002 and 2003 using the ratios of 13 C to 12 C in bollworm moths to estimate the proportions of the population originating from C 3 or C 4 plants. A separate study measured gossypol residues in moths from four states in 2005 and 2006, enabling the identification of moths whose natal hosts were cotton rather than other C 3 hosts. 3. C 4 hosts served as the principal source of bollworm moths from mid-to-late June to early September, depending on the state. Beginning in late August ⁄ early September and lasting 1-4 weeks, the majority of moths exhibited isotopic compositions characteristic of C 3 hosts. During this period, however, the minimum percentage of moths that developed as larvae on C 4 hosts was typically >25%. By mid-September and through October and November, the majority of the bollworm population exhibited C 4 isotopic compositions. 4. Between late June and early August, cotton-derived bollworm moths (moths with gossypol residues) comprised <1% of moths in all states, and remained below this level throughout the season in North Carolina. In other states, cotton-derived moths increased between early August and early September to peak at an average of 19AE1% of all moths. 5. Synthesis and applications. Data on 13 C ⁄ 12 C ratios and gossypol residues in CBW moths were used to assess the importance of structured non-Bt cotton refuges for the management of Bt resistance risk in H. zea. Weekly estimates of bollworm breeding on cotton, C 3 plants other than cotton and C 4 plants showed that, throughout the season, the majority of bollworm moths caught in pheromone traps adjacent to cotton fields did not develop as larvae on cotton. This result implies that management practices in cotton such as the use of structured cotton refuges will play a relatively minor role -particularly compared with maize Zea mays L. -in managing potential resistance to Bt cotton in populations of the CBW in the US Cotton Belt.
Downed (i.e., fallen, dead) wood was sampled in 1-, 15-, 50-, and 100-year-old managed stands, an uneven-aged, managed stand, and an uncut stand of northern hardwoods in New Hampshire. Mass of downed wood ranged from a mean of 32 t/ha in the 15- and 50-year-old stands to 86 t/ha in the recently cut stand. Mean estimates varied significantly among stands, although most of the variation was due to the large amount of downed wood in the recently cut stand. The range of downed-stem diameters was greatest in the 100-year-old and uncut stands. Large (>38 cm) logs were notably absent from the uneven-aged, managed stand, indicating that selective cutting utilizes mature stems efficiently. Comparison of our data with other estimates shows that the amount of downed wood in northern hardwood stands declines to about 20 t/ha within 20–30 years after logging. Quantities remain relatively stable for up to an additional 30 years and then begin to increase. They stabilize at 35–40 t/ha after approximately 100 years. Large-diameter logs become an increasingly important component of downed wood as stands mature beyond 50 years of age. Rapid decomposition of even the largest logs precludes continued accumulation of downed wood in uncut, old-growth stands. The data suggest that less downed wood and fewer large-diameter logs are likely to accumulate under short-rotation (<50 years) harvest, whole-tree harvests, and selection cuts than under long rotations or in uncut forests.
To combat an increasing abundance of sucking insect pests, >40 pesticides are currently recommended and frequently used as foliar sprays on row crops, especially cotton. Foraging honey bees may be killed when they are directly exposed to foliar sprays, or they may take contaminated pollen back to hives that maybe toxic to other adult bees and larvae. To assess acute toxicity against the honey bee, we used a modified spray tower to simulate field spray conditions to include direct whole-body exposure, inhalation, and continuing tarsal contact and oral licking after a field spray. A total of 42 formulated pesticides, including one herbicide and one fungicide, were assayed for acute spray toxicity to 4-6-d-old workers. Results showed significantly variable toxicities among pesticides, with LC50s ranging from 25 to thousands of mg/liter. Further risk assessment using the field application concentration to LC1 or LC99 ratios revealed the risk potential of the 42 pesticides. Three pesticides killed less than 1% of the worker bees, including the herbicide, a miticide, and a neonicotinoid. Twenty-six insecticides killed more than 99% of the bees, including commonly used organophosphates and neonicotinoids. The remainder of the 13 chemicals killed from 1-99% of the bees at field application rates. This study reveals a realistic acute toxicity of 42 commonly used foliar pesticides. The information is valuable for guiding insecticide selection to minimize direct killing of foraging honey bees, while maintaining effective control of field crop pests.
Selection pressure on bollworm, Helicoverpa zea (Boddie) (Lepidoptera: Noctuidae), by cotton, Gossypium hirsutum (L.) (Malvaceae), that produces one or more Bacillus thuringiensis Berliner (Bt) proteins is reduced by plantings of non‐Bt refuge cotton that produce non‐selected individuals. However, the contributions of non‐Bt, non‐cotton crop hosts to the overall effective refuge for H. zea on Bt cotton have not been estimated. A 2‐year, season‐long study was conducted in five US cotton‐producing states to assess the spatial and temporal population dynamics and host use of H. zea. Helicoverpa zea larval estimates in commercial crop fields demonstrated that non‐cotton crop hosts, such as maize, Zea mays L. (Poaceae), grain sorghum, Sorghum bicolor (L.) Moench (Poaceae), peanut, Arachis hypogaea L. (Fabaceae), and soybean, Glycine max (L.) Merrill (Fabaceae), collectively support much larger larval populations than cotton throughout the season. Larval populations were almost entirely restricted to maize in the middle part of the season (June and portions of July), and were observed in non‐cotton crop hosts more frequently and typically in larger numbers than in cotton during the period when production would be expected in cotton (July and August). Numbers of H. zea larvae produced in replicated strip trials containing various crop hosts paralleled production estimates from commercial fields. In contrast, the number of H. zea adults captured in pheromone traps at interfaces of fields of Bt cotton and various crop hosts rarely varied among interfaces, except in instances where maize was highly attractive. With the exception of this early season influence of maize, moth numbers were not related to local larval production. These data demonstrate that H. zea adults move extensively from their natal host origins. Therefore, non‐cotton crop hosts, and even relatively distant hosts, contribute significantly to effective refuge for H. zea on Bt cotton. The results presented here demonstrate that substantial natural refuge is present for Bt‐resistance management of H. zea throughout the mid‐South and Southeast portions of the US cotton belt.
A major goal in evolutionary biology is to understand how and why populations differentiate, both genetically and phenotypically, as they invade a novel habitat. A classical example of adaptation is the pale colour of beach mice, relative to their dark mainland ancestors, which colonized the isolated sandy dunes and barrier islands on Florida's Gulf Coast. However, much less is known about differentiation among the Gulf Coast beach mice, which comprise five subspecies linearly arrayed on Florida's shoreline. Here, we test the role of selection in maintaining variation among these beach mouse subspecies at multiple levels-phenotype, genotype and the environments they inhabit. While all beach subspecies have light pelage, they differ significantly in colour pattern. These subspecies are also genetically distinct: pair-wise F ST -values range from 0.23 to 0.63 and levels of gene flow are low. However, we did not find a correlation between phenotypic and genetic distance. Instead, we find a significant association between the average 'lightness' of each subspecies and the brightness of the substrate it inhabits: the two most genetically divergent subspecies occupy the most similar habitats and have converged on phenotype, whereas the most genetically similar subspecies occupy the most different environments and have divergent phenotypes. Moreover, allelic variation at the pigmentation gene, Mc1r, is statistically correlated with these colour differences but not with variation at other genetic loci. Together, these results suggest that natural selection for camouflage-via changes in Mc1r allele frequency-contributes to pigment differentiation among beach mouse subspecies.
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