Recovery of terrestrial plants in vegetative vigor and seedling emergence tests from exposure to atrazine.

Ten species of terrestrial plants, including 6 dicotyledonous and 4 monocotyledonous species, were exposed to a direct overspray of atrazine according to US Environmental Protection Agency seedling emergence and vegetative vigor study guidelines and subsequently evaluated for potential recovery. For each species, no-observed-effect rate (NOER), 10% effect rate, 25% effect rate, and 50% effect rate values were calculated (where possible) for a variety of guideline-required endpoints (but focusing on growth rate) for both the standard experimental phase and a recovery phase; and the rates subsequently were compared. For the seedling emergence study, the standard experimental (designated test 1) and recovery (designated test 2) phases encompassed days 0 to 14 and days 14 to 28, respectively. Similarly, for the vegetative vigor study, test 1 and test 2 encompassed days 0 to 21 and days 21 to 42, respectively. Plants were exposed to atrazine at nominal application rates ranging from 1.1 g active ingredient (a.i.)/ha (0.0010 lb a.i./A) to 28,000 g a.i./ha (25 lb a.i./A), depending on the species; the 28,000 g a.i./ha rate is greater than 12 times the maximum application rate of 2250 g a.i./ha (2 lb a.i./A) registered on corn. For seedling emergence, only 2 of 10 species tested, cabbage and tomato, provided clear rate responses in the initial 14 d of exposure (test 1). Based on a comparison of x% effect rate (ERx) and NOER values for growth rates of shoot length and shoot dry weight for days 0 to 14 relative to days 14 to 28, recovery was apparent for cabbage shoot length growth rate and tomato shoot length and shoot dry weight growth rates. Test application rates selected for the remaining 8 species showed either a weak response that did not allow a clear assessment of recovery or no response at all. For the vegetative vigor study, 9 of the 10 species tested provided clear rate responses in test 1 (days 0-21); corn did not demonstrate any herbicidal response up to the highest rate tested, 28,000 g a.i./ha. Based on comparison of day 0 to 21 (test 1) relative to day 21 to 42 (test 2) ERx and NOER values for shoot length, average growth rates indicated that 8 of 9 species clearly demonstrated an increase in 2 or more metrics (cabbage did not demonstrate a response based on shoot length). Clear recovery was also indicated by an increase in ERx and/or NOER values from test 1 to test 2 for shoot dry weight average growth rates for 7 of the 9 species (corn did not show a response, and oat and soybean showed variable responses). Thus, in most species, where initial herbicidal effects were observed, the effects are largely ameliorated over time.

Influence of light intensity on the toxicity of atrazine to the submerged freshwater aquatic macrophyte Elodea canadensis.

Light intensity can have a profound influence on the degree of phytotoxicity experienced by plants exposed to photosystem II (PSII) inhibiting herbicides. This relationship was evaluated in the submerged aquatic macrophyte Elodea canadensis exposed to three different concentrations of atrazine (510, 1000 and 2000 µg a.i./L) plus an untreated control at three different light intensities (0, 500 and 6000 lx) under static-renewal conditions for 14 days. Under 500 lx light intensity, control plants demonstrated a rapid increase in shoot length but minimal increase in dry shoot weight, suggesting limited photosynthesis. Based on shoot-length and biomass, growth was not affected by any atrazine exposure relative to controls under dark conditions (0 lx). Under low-light conditions at 500 lx, exposures to 510, 1000 and 2000 µg a.i./L atrazine significantly decreased net shoot lengths by 34%, 38% and 35%, respectively, relative to corresponding (500 lx) controls. However, atrazine exposure under this light condition did not significantly decrease biomass (dry shoot weight). Compared to 6000 lx, only approximately 8% of photosynthetically active radiation (PAR) was measured under 500 lx intensity, indicating that minimal PAR was available for photosynthesis. Under optimal light conditions (6000 lx), net shoot lengths significantly decreased in the treated atrazine groups by 48%, 51% and 68%, and net dry shoot weights (biomass) were significantly decreased by 79%, 81% and 91%, respectively, relative to corresponding (6000 lx) controls. These data show that under low light conditions, atrazine-induced effects on dry shoot weight (biomass) are dependent on available PAR and active photosynthesis.

ICON rice seed treatment toxicity to crayfish (Procambarus clarkii) in experimental rice paddies.

Outdoor pools (2.3 x 2.3 m) were used to simulate typical rice agricultural practices in Louisiana, USA, to evaluate the toxicity of ICON (active ingredient [a.i.] fipronil) and its degradates to crayfish (Procambarus clarkii). Six paddies were planted with seed treated with ICON 6.2 FS at an exaggerated application rate of 0.05 kg a.i./ha (recommended rate, 0.042 kg a.i./ha), simulating three rice-planting scenarios. Two reference paddies were planted with untreated seed. Crayfish were exposed to tail water within 24 to 48 h after seeding, simulating standard Louisiana agricultural and water management practices. At 50 d after planting, a separate group of crayfish was caged in situ for 14 d to evaluate toxicity. An additional 50 crayfish were added to two paddies approximately 100 d after rice planting and held for 29 weeks to evaluate bioaccumulation. Residues of fipronil and its degradates in water and soil were similar to residue concentrations measured from rice fields in Louisiana. Tail water from the treated paddies was not toxic to crayfish. The fipronil 96-h median lethal concentration (LC50) for adult crayfish was 180 microg/L, which would provide at least a sixfold safety factor between the maximum fipronil concentration in tail water and the crayfish LC50. In situ exposures of crayfish also were not toxic. Concentrations of fipronil and its degradates after 29 weeks of exposure were less than 5 microg/kg in crayfish tail muscle tissue. These results demonstrate that label instructions adequately protect crayfish in a rice-crayfish cropping scenario when ICON is applied at maximum application rates as a seed treatment.

Identification of chromosomal translocations in leukemias by hybridization with oligonucleotide microarrays.

BACKGROUND AND OBJECTIVES: Identification of chromosomal rearrangements is important for a precise risk-stratified diagnosis of hematologic malignancies. As the number of known translocations, specific for different types of leukemia increases, it takes ever more time and increasing amounts of patient's material to screen a single patient with individual polymerase chain reactions (PCR). The aim of this study was to develop a new approach combining specificity with high-throughput sufficient for rapid screening of clinical samples for the presence of numerous translocations. DESIGN AND METHODS: We designed an oligonucleotide microarray and used hybridization with microarrays in combination with multiplex reverse transcription-polymerase chain reaction (RT-PCR) assay for accurate and rapid identification of some major leukemias. The following translocations were used as prototypic: t(9;22) p210 and p190, t(4;11), t(12;21), and t(15;17). This approach was tested on five different cell cultures carrying translocations and on 22 clinical samples from leukemic patients. RESULTS: Distinctive hybridization signals were obtained for all types of chimeric transcripts from cell lines with translocations. Both the type of translocation and the splice variant were determined. The data demonstrated high specificity and reproducibility of the method. Analysis of the 22 clinical samples using the microarray-based approach showed complete agreement with standard PCR analysis. INTERPRETATION AND CONCLUSIONS: Our data suggest that oligonucleotide microarrays can be used as an efficient, alternative approach to the traditional post-PCR Southern blot analysis. The oligonucleotide microarray approach appears suitable for clinical screening of major risk-stratifying translocations in patients with leukemia.