The authors acknowledge financial support from the California Table Grape Commission, the California Competitive Grants Program for Research in Viticulture and Enology, and from Valent BioSciences. Ms. Celia M. Cant´ın was supported by a FPU fellowship from Spanish MEC (Ministerio de Educación y Ciencia). We also acknowledge the assistance of M.
Experiments were conducted in 2006 to 2008 to study growth, phenology, and competitive ability of glyphosate-resistant (GR) and -susceptible (GS) biotypes of horseweeds from San Joaquin Valley (SJV), CA. When grown alone, in pots, the GR horseweeds consistently developed more rapidly than the GS weeds, as evidenced by their earlier bolting, flowering, and seed set; the GR horseweeds set seeds nearly 25 d (approximately 190 fewer growing degree days) sooner than the GS horseweed. At seed set, the relatively slow-developing GS horseweeds had amassed 40% more shoot dry matter than the GR weeds at the same phenological stage, but neither biotype was consistently more fecund than the other. Although the GR biotype had lower shoot dry mass than the GS biotype when grown alone, in mixed populations under increasing levels of competition (in a replacement series design) and limited resources (mainly moisture), the GR weeds were not only taller, but also accumulated more dry matter than the GS weeds. Thus, the GR biotype was more competitive than the GS biotype, particularly when grown at high densities and under moisture-deficit stress. Therefore, under California conditions there is no apparent fitness penalty for this particular GR horseweed biotype, and it is likely to persist in the environment and outcompete the GS biotypes regardless of further glyphosate selection pressure. If so, this biotype of GR horseweed is likely to become increasingly common in the SJV until effective management strategies are developed and adopted.
Hybrid (Vitis vinifera ×Vitis labrusca) table grape cultivars grown in the subtropics often fail to accumulate sufficient anthocyanins to achieve good uniform berry color. Growers of V. vinifera table grapes in temperate regions generally use ethephon and, more recently, (S)-cis-abscisic acid (S-ABA) to overcome this problem. The objective of this study was to determine if S-ABA applications at different timings and concentrations have an effect on anthocyanin regulatory and biosynthetic genes, pigment accumulation, and berry color of the Selection 21 cultivar, a new V. vinifera ×V. labrusca hybrid seedless grape that presents lack of red color when grown in subtropical areas. Applications of S-ABA 400 mg/L resulted in a higher accumulation of total anthocyanins and of the individual anthocyaninsanthocyanins: delphinidin-3-glucoside, cyanidin-3-glucoside, peonidin-3-glucoside, and malvidin-3-glucoside in the berry skin and improved the color attributes of the berries. Treatment with two applications at 7 days after véraison (DAV) and 21 DAV of S-ABA 400 mg/L resulted in a higher accumulation of total anthocyanins in the skin of berries and increased the gene expression of CHI, F3H, DFR, and UFGT and of the VvMYBA1 and VvMYBA2 transcription factors in the seedless grape cultivar.
The foundation of a successful revegetation or restoration program is quality native seed. This requires careful collection, processing, and storage. Mature seed should be collected from healthy, local stands with a sufficiently broad genetic base. Careful identification of the site characteristics and seed‐lot tracking are essential. Yearly variation in seed production and seed quality can be very high, and an early determination of seed quality can prevent expensive failures. Nondestructive evaluation using X‐rays is effective and economical, but techniques such as staining, inspection, and germination tests can also be helpful. Cleaning, dewinging, and upgrading seed before storage can (1) reduce weight and bulk, (2) improve storage life, (3) increase germination, and (4) make greenhouse production and field planting easier and more economical. The seeds of many native plants can lose their viability quickly if they are not stored under controlled conditions. Seeds in storage must also be protected from rodents, pests, and disease. Dormancy is common in the seeds of many native species, and experimentation is often necessary to determine the best way to break seed dormancy. This can be complicated by year‐to‐year and plant‐to‐plant variation.
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