Melissa B. Riley

Mycotoxins in Root Extracts of American and Asian Ginseng Bind Estrogen Receptors α and β

The estrogenic activity of ginseng has been the subject of conflicting reports. Cell proliferation, induction of estrogen-responsive genes, and isolated cases of adverse reactions such as postmenopausal vaginal bleeding and gynecomastia have been reported after ginseng treatment. Other studies report antiproliferative effects with no induction of estrogen-responsive genes. We developed estrogen receptor (ER) α and ERβ competitive binding assays using recombinant receptors and [3H]-17β-estradiol to detect phytoestrogens in extracts of Asian ginseng root (Panax ginseng C. A. Meyer) and American ginseng root (Panax quinquefolius L.). Root extracts contained substances that bound both receptor isoforms. These substances had a two to three times greater affinity for ERβ. Significantly higher binding was found in methanol extracts than in hot water extracts. Subsequent analysis of the extracts revealed significant ER binding attributable to zearalenone, the estrogenic mycotoxin produced by several Fusarium species. The ER showed no binding affinity for Rb1 and Rg1, the major ginsenosides found in P. quinquefolius and P. ginseng, respectively. Thus, ginseng extraction methods, plant species tested, and mycotoxin contaminants may help to explain the disparate literature reports. The prevalence and health significance of fungal contamination in herbal products used for medicinal purposes should be further investigated.

Use of Wild Radish (Raphanus raphanistrum) and Rye Cover Crops for Weed Suppression in Sweet Corn

Abstract Field experiments were conducted near Blackville, SC, and Tifton, GA, in 2004 and 2005, to evaluate the effect of wild radish and rye cover crops on weed control and sweet corn yield when used in conjunction with lower-than-recommended herbicide rates. Cover crop treatments included wild radish, rye, and no cover crop, alone and in conjunction with half and full rates of atrazine (0.84 and 1.68 kg ai ha−1) plus S-metolachlor (0.44 and 0.87 kg ai ha−1) applied before sweet corn emergence. Florida pusley, large crabgrass, spreading dayflower, ivyleaf morningglory, and wild radish infested the test sites. Wild radish and rye cover crops without herbicides reduced total weed density by 35 and 50%, respectively, at 4 wk after planting (WAP). Wild radish in conjunction with the full rate of atrazine plus S-metolachlor controlled Florida pusley, large crabgrass, and ivyleaf morningglory better than rye or no cover crop treated with a full herbicide rate in 2004 at Blackville. In 2005, at Blackville, weed control in sweet corn following wild radish cover crop plots alone was not different from that following rye. Wild radish or rye in conjunction with a half or full rate of atrazine and S-metolachlor controlled > 95% Florida pusley, wild radish, and large crabgrass in sweet corn at Tifton during both years. Ten glucosinolates, potential allelopathic compounds, were identified in wild radish, including glucoiberin, progoitrin, glucoraphanin, glucoraphenin, glucosinalbin, gluconapin, glucotropaeolin, glucoerucin, glucobrassicin, and gluconasturtin. Sweet corn yields at Blackville and Tifton following wild radish or rye cover crops were similar between the half and full rates of atrazine plus S-metolachlor. Sweet corn in wild radish or rye cover crop plots without herbicides produced less-marketable ears than herbicide-treated plots, indicating that a combination of cover crops and herbicides are required to optimize yields and to obtain desirable weed control. Nomenclature: Atrazine; S-metolachlor; Florida pusley, Richardia scabra L. RCHSC; ivyleaf morningglory, Ipomoea hederacea Jacq. IPOHE; large crabgrass, Digitaria sanguinalis (L.) Scop. DIGSA; spreading dayflower, Commelina diffusa Burm. f. COMDI; wild radish Raphanus raphanistrum L. RAPRA; rye, Secale cereale L. ‘Wrenz’; sweet corn, Zea mays L. ‘Silver Queen’, ‘Summer Sweet’, ‘Prime Plus’.

Influence of Glyphosate Timing and Row Width on Palmer Amaranth (Amaranthus palmeri) and Pusley (Richardia spp.) Demographics in Glyphosate-Resistant Soybean

Abstract The influence of soybean row width and glyphosate application timing was determined on survival, biomass, and seed production of cohorts from a mixed population of Palmer amaranth and pusley species (Florida and Brazil pusley) along with soybean seed yield. The first Palmer amaranth and pusley cohort comprised plants that emerged from soybean planting through the V3 (3 wk after soybean emergence [WAE]) soybean stage (cohort 1). The second cohort comprised plants that emerged between the V3 to V6 (5 WAE) soybean stages (cohort 2), and the third cohort emerged after the V6 through the R2 soybean stage (cohort 3). Glyphosate at 840 g ae ha−1 was applied at V3; V6; V3 and V6; and V3, V6, and R2 in rows either 19 or 97 cm wide. A nontreated control was included for comparison in each row width. Sequential glyphosate applications at V3 and V6 or at V3, V6, and R2 soybean stages resulted in 1 to 3% survival of cohort 1 compared with 23 to 28% survival after a single glyphosate application. Vegetative biomass production by cohort 1 accounted for 71% of the total pusley biomass produced in the nontreated plots. Cohort 1, 2, and 3 contributed 68, 31, and 1%, respectively, of the total 37,900 seeds m−2 produced by pusley plants in nontreated plots. Delaying a glyphosate application to the V6 stage resulted in higher biomass and more than twice the seed produced from cohort 1 when compared with cohort 2. Glyphosate applied at V3 and V6 stages prevented pusley seed production from cohort 1, and an additional glyphosate application at the R2 stage prevented seed production from cohorts 2 and 3. No Palmer amaranth emergence occurred after the V6 soybean stage in either row width. A single glyphosate application at the V3 or V6 stage eliminated cohort 1 of Palmer amaranth in narrow rows. Palmer amaranth plants from cohort 1 in wide rows that survived the V3 glyphosate application produced 3.3 g m−2 biomass and 600 seeds m−2. Averaged over years and row widths, soybean yields after sequential glyphosate applications were 2,490 to 2,640 kg ha−1 compared with 1,850 to 2,020 kg ha−1 after a single glyphosate application at the V3 or V6 stage. This research confirms that sequential glyphosate applications are superior to a single application for minimizing pusley and Palmer amaranth survival, biomass, and seed production along with an improvement in soybean yields.

Acclimation of Palmer Amaranth (Amaranthus palmeri) to Shading

Abstract Experiments were conducted to investigate the acclimation of Palmer amaranth to shading. Plants were grown in the field beneath black shade cloths providing 47 and 87% shade and in full sunlight (no shading). All photosynthetic measurements were taken 4 wk after initiating the shade treatments. Photosynthetic rates of Palmer amaranth grown under 47% shade increased with increasing photosynthetic active radiation (PAR) similar to 0% shade-grown plants. Light-saturated photosynthetic rates were predicted beyond the highest measured PAR of 1,200 µmol m−2 s−1 for plants grown under 0 and 47% shade. Plants acclimated to increased shading by decreasing light-saturated photosynthetic rates from 60.5 µmol m−2 s−1 under full sun conditions to 26.4 µmol m−2 s−1 under 87% shade. Plants grown under 87% shade lowered their light compensation point. Rate of increase in plant height was similar among shade treatments. Plants responded to increased shading by a 13 to 44% reduction in leaf appearance rate (leaf number growing degree days [GDD]−1) and a 22 to 63% reduction in main-stem branch appearance rate (main-stem branch number GDD−1) compared with full sunlight. Palmer amaranth specific leaf area increased from 68 to 97 cm2 g−1 as shading increased to 87%. Plants acclimated to 47% shade by increasing total leaf chlorophyll from 22.8 µg cm−2 in full sunlight to 31.7 µg cm−2 when shaded; however, the increase was not significant at 87% shading. Thus, it is concluded that Palmer amaranth shows photosynthetic and morphological acclimation to 87% or less shading. Nomenclature: Palmer amaranth, Amaranthus palmeri S. Wats. AMAPA.

Annual Changes in Temperature and Light Requirements for Germination of Palmer Amaranth (Amaranthus palmeri) Seeds Retrieved from Soil

Abstract Experiments were conducted on Palmer amaranth seeds collected in 2004 and 2006 from a natural population near Pendleton, SC, to determine the temperature and light requirements for germination of seeds retrieved from soil surface or from 10-cm depth in the field. A cyclic change in seed germination of Palmer amaranth in response to temperature and light occurred during a 12-mo after-ripening period. Freshly matured seeds collected in November required mean temperatures ≥ 25 C, and natural or red (R) light for increased germination. Following after-ripening in winter, seeds experienced a reduction in dormancy and germinated higher at 25 to 35 C mean compared with 10 to 15 C mean. With after-ripening for an additional 3 mo in May, seeds experienced a broadening of thermal range (10 to 40 C mean), and germination in natural light or R light was more than twice the germination in the absence of light. Fluctuating temperatures (7.5 C amplitude) improved germination over constant temperatures, except in summer and fall (9 and 12 mo after seed maturation). Exposure of seeds to high temperatures during summer caused secondary dormancy induction. Averaged over thermal amplitudes, seeds retrieved in fall required mean temperatures > 25 C for increased germination. Burial in spring for 3 to 6 mo induced seed dormancy, and the relative germination in fall (12 mo after seed maturation) was at least 50% higher for seeds retrieved from soil surface compared to seeds exhumed from 10-cm soil depth. Seeds retrieved in late summer and fall required natural light or R light for promoting germination, whereas far-red (FR) light or darkness inhibited germination. Furthermore, the effect of R and FR light was reversible, indicating a partially phytochrome-mediated germination response of Palmer amaranth seeds following 9 to 12 mo of after-ripening in the field. Nomenclature: Palmer amaranth, Amaranthus palmeri S. Wats. AMAPA.

Glucosinolate profile variation of growth stages of wild radish (Raphanus raphanistrum).

Wild radish (Raphanus raphanistrum L.) produces glucosinolates (GSL), which are important for its use as a biofumigation or allelopathic plant for weed management. Total GSL concentrations and individual GSLs were quantified in different plant parts at different developmental stages. Eight GSLs were found in various plant tissues but glucoerucin, glucoraphenin, and glucotropaeolin comprised >90% of the total GSLs. All three are degraded to isothiocyanates, which are associated with weed suppression. Maximum GSL concentration (1942.2 micromol/plant) occurred at 50% flowering stage prior to the time of maximum biomass production, when GSL concentration was 1246.65 mumol/plant. Roots contributed <15% of the total GSL. The highest concentration of GSLs was in flowers at flowering stage, but due to the low biomass they contributed only 11.83% to the total GSL. On the basis of these results, wild radish should be incorporated into soil at 50% flowering to provide the most GSLs for weed suppression.

Variation of glucosinolates in wild radish (Raphanus raphanistrum) accessions.

Glucosinolate composition was determined in wild radish accessions from eight states in the northeastern and southern United States to determine the variability of production among accessions. Glucosinolates were evaluated from roots, leaves, flowers, primary, and secondary branches. Seventeen glucosinolates were identified, with glucoerucin, glucoraphenin, glucobrassicin, and gluconasturtiin contributing 90% to 100% of the total glucosinolates. Flowers contained the highest glucosinolate concentrations, 12.07 to 55.36 μmol/g, but flowers contributed only 5.3 to 21.3% to the total glucosinolates. Of the eight accessions, the Mississippi accession produced significantly higher levels of total glucosinolates and glucosinolates which can be degraded to isothiocyanates per plant, totals of 618.97 and 563.53 μmol/plant, respectively. Total plant biomass did not differ between accessions indicating a difference in the ability of the Mississippi accession to produce glucosinolates. Further studies are needed to determine if this accession would consistently produce higher glucosinolate levels under different environmental conditions.

Microbial degradation of mefenoxam in rhizosphere of Zinnia angustifolia.

The fate of the fungicide mefenoxam was studied in a containerized rhizosphere system. The rhizosphere system used Zinnia angustifolia (Tropic Snow) in a bark/sand potting mix and was compared to bulk potting mix (no plants). Rhizosphere microbial populations were allowed to establish for 3 weeks prior to fungicide addition (20 microg per g mix). Mefenoxam and degradation product concentrations were determined by High HPLC or capillary electrophoresis after extraction. Seventy eight percent of the fungicide originally applied to the rhizosphere was degraded after 21 days compared to 44% in bulk system (no plant). The primary degradation product was the free acid N-(2,6-dimethylphenyl)-N-(methoxyacetyl)-DL-alanine, which accounted for 71% of the applied parent chemical after 30 days. N-(2,6-dimethylphenyl)-acetamide was also detected, but in lesser amounts. Bacterial populations in the rhizosphere increased during the 30-day period, which correlated with an increase in degradation of the parent compound. Pure cultures of Pseudomonas fluorescens and Chrysobacterium indologenes isolated from the rhizosphere system could degrade the applied fungicide (10 microg/ml) almost completely to the free acid within 54 h.

Temperature and Light Requirements for Wild Radish (Raphanus raphanistrum) Germination over a 12-Month Period following Maturation

Abstract Knowledge of the germination requirements of wild radish will help in determining the favorable conditions for germination and emergence and allow better management of this weed. Experiments were conducted during 2005 to 2006 and 2006 to 2007 to evaluate wild radish temperature and light requirements over a 12-mo period beginning in July on seeds placed on the soil surface and at a 10-cm depth. Germination response was influenced by temperature, light, duration of burial, and burial depth. Freshly harvested seeds (July) had no more than 18% germination whereas seeds allowed to after-ripen in the field for 3 to 6 mo (October to January) had up to 40% germination. The germination of wild radish retrieved from the soil surface was 1.2 to 1.5 times greater at alternating temperatures (2.5/17.5, 7.5/22.5, and 12.5/27.5 C) than at constant temperatures (10, 15, and 20 C) at 0, 3, and 6 mo after maturation. The light requirement for germination varied by time of year with no differences in germination between light and dark conditions for freshly harvested seeds. Far-red light inhibited germination of wild radish, indicating that wild radish may become sensitive to light following an after-ripening period. Nomenclature: Wild radish, Raphanus raphanistrum L. RAPRA

Post-production stability of parthenolide in feverfew (Tanacetum parthenium)

ABSTRACT The influence of pH, temperature and light on parthenolide (PRT) content of feverfew was investigated. Feverfew powder and PRT standards mixed in citrate buffers at selected pH (2.4-7.2) were stored for four months. PRT declined in all treatments with greatest loss in solutions with pH below 5, and highest stability in solutions with pH 7.2. PRT in dry samples declined 30 percent after 320 days of storage. Degradation of PRT in feverfew solutions exposed to 40, 60, and 80°C for 24 h increased with increasing temperature. Dry samples exposed to various temperatures revealed stability of PRT at temperatures up to 130°C for short time periods.