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Live Seed (live + seed)
Selected AbstractsImpact of seeding rate on annual ryegrass performanceGRASS & FORAGE SCIENCE, Issue 1 2004B. C. Venuto Abstract Annual ryegrass (Lolium multiflorum Lam.) is a primary forage resource for livestock producers throughout the south-eastern USA during the winter-growing season. It is important for livestock producers to begin grazing annual ryegrass as early as possible and any management practices maximizing early season production could be beneficial. To assess the impact of seeding rate on subsequent yield, yield distribution, quality, seedling density, and end-of-season plant and tiller density, a 2-year study was initiated at four locations in Louisiana. Three annual ryegrass cultivars, varying in seed size, were established at four seeding rates based on pure live seed (PLS) rates of 400, 800, 1200 and 1600 PLS m,2. There was no advantage in total yield from increasing seeding rates beyond 800 PLS m,2. However, first-harvest yields increased from 360 to 930 kg dry matter (DM) ha,1 as seeding rate increased from 400 to 1600 PLS m,2. Crude protein and neutral-detergent fibre concentrations, and in vitro DM digestibility, were not affected by seeding rate. Seedling density and end-of-season plant numbers increased as seeding rate increased. However, stems per plant decreased as seeding rate increased, indicating compensatory tillering for the reduced plant numbers observed at the lower seeding rates. These results indicate first-harvest yield can be increased by planting at higher seeding rates but total yields are not increased. [source] Seed variation among annual ryegrass cultivars in south-eastern USA and the relationship with seedling vigour and forage productionGRASS & FORAGE SCIENCE, Issue 4 2002B. C. Venuto Abstract Annual ryegrass (Lolium multiflorum Lam.) is grown on more than one million ha in the south-eastern USA each year. Recommended and actual seeding rates vary substantially within the region. The objective of this study was to evaluate variation in seed weight, germination, seedling vigour and seasonal yield performance among annual ryegrass cultivars. During 1997, 1998 and 1999, seed from fourteen commercial cultivars was weighed and germinated to determine numbers of pure live seed (PLS) m,2 before yield evaluation at four locations. Seed from ten cultivars was planted at 0·7 and 2·0 cm depth in a greenhouse study to evaluate relative seedling vigour. Cultivar mean single-seed weight ranged from 2·4 to 4·8 mg in 1997, 1·8 to 4·5 mg in 1998, and 2·6 to 4·6 mg in 1999. Seed germination ranged from 78·8% to 98·0% in 1997, 82·3 to 98·3% in 1998 and 77·8 to 98·3% in 1999. Seed number, PLS m,2, ranged from 675 to 1289 in 1997, 710 to 1550 in 1998, and 717 to 1179 in 1999. Among the ten cultivars evaluated for seedling vigour, seedling weight differed between planting depths and a significant cultivar by year interaction was observed. Seedling weight was highly correlated with seed weight at each seeding depth. The effect of increasing number of PLS m,2 on subsequent yield performance, although small, was consistently negative. These results indicate that target plant populations may be obtained more economically by adjusting seeding rates for seed size differences among cultivars and seed lots of annual ryegrass. [source] Wyoming Big Sagebrush Density: Effects of Seeding Rates and Grass CompetitionRESTORATION ECOLOGY, Issue 2 2002Mary I. Williams Abstract The mining industry commonly seeds shrubs and grasses concurrently on coal-mined lands of northeastern Wyoming, but ecological interactions between seeded shrubs and grasses are not well documented. Artemisia tridentata Nutt. ssp. wyomingensis (Beetle and Young) (Wyoming big sagebrush) is the dominant pre-mining shrub on many Wyoming mine sites. Despite past failures to establish Wyoming big sagebrush, the Wyoming Department of Environmental Quality, Land Quality Division's rules and regulations require establishment of 1 shrub per m2 on 20% of post-mined land in Wyoming. A study was established at the Belle Ayr Coal Mine south of Gillette, Wyoming to evaluate the effects of sagebrush seeding rates and grass competition on Wyoming big sagebrush seedling density. Three sagebrush seeding rates (1, 2, and 4 kg pure live seed [pls]/ha; 350, 700, and 1,400 pls/m2, respectively) and seven cool-season perennial grass mixture seeding rates (0, 2, 4, 6, 8, 10, and 14 kg pls/ha; 0, 187, 374, 561, 750, 935, and 1,309 pls/m2, respectively) were applied during winter 1998,1999. Pascopyrum smithii (Rydb.) A. Love (western wheatgrass), Elymus lanceolatus (Scribner & J.G. Smith) Gould (thickspike wheatgrass), and Elymus trachycaulus (Link) Gould ex Shinners (slender wheatgrass) comprised the grass seed mix (equal seed numbers of each species). Sagebrush seedling density differed among sagebrush seeding rates but not among grass seeding rates. On all sampling dates in 1999 and 2000, sagebrush seedling density differed among sagebrush rates and was greatest at the 4 kg pls/ha sagebrush seeding rate. All sagebrush seeding rates provided densities of at least 1 shrub per m2 after two growing seasons. Grass density and production in 2000 suggest that adequate grass production (75 g/m2) was achieved by seeding at 6 to 8 kg pls/ha. Within these grass seeding rates, four or more sagebrush seedlings per m2 were attained when sagebrush was seeded at 2 to 4 kg pls/ha. Use of these seeding rate combinations in mine reclamation can achieve Wyoming big sagebrush standards and reduce reseeding costs. [source] Dynamics of Neotyphodium endophyte infection in ageing seed pools: incidence of differential viability loss of endophyte, infected seed and non-infected seedANNALS OF APPLIED BIOLOGY, Issue 2 2010P.E. Gundel Symbiotic associations between grasses and vertically transmitted endophytic fungi are widespread in nature. Within grass populations, changes in the frequency of infected plants are driven by influence of the endophyte on the fitness of their hosts and by the efficiency of endophyte transmission from parent plants to their offspring. During the seed stage, the endophyte might influence the fitness of its host by affecting the rate of seed viability loss, whereas the efficiency of endophyte transmission is affected by losses of viability of the fungus within viable seeds. We assessed the viability losses of Lolium multiflorum seeds with high and low level of infection of the endophyte Neotyphodium occultans, as well as the loss of viability of the fungus itself, under accelerated seed ageing and under field conditions. Starting with high endophyte-infected accessions of L. multiflorum, we produced their low endophyte-infected counterparts by treating seeds with a fungicide, and subsequently multiplying seeds in adjacent plots allowing pollen exchange. In our accelerated ageing experiments, which included three accessions, high endophyte-infected seeds lost viability significantly faster than their low endophyte-infected counterpart, for only one accession. High endophyte-infected seeds of this particular accession absorbed more water than low endophyte-infected seeds. In contrast, the endophyte lost viability within live seeds of all three accessions, as the proportions of viable seeds producing infected seedlings decreased over time. In our field experiment, which included only one accession, high endophyte-infected seed lost viability significantly but only slightly faster than low endophyte-infected seed. In contrast, the loss of viability of the endophyte was substantial as the proportions of viable seeds producing infected seedlings decreased greatly over time. Moving the seeds from the air to the soil surface (simulating seed dispersion off the spikes) decreased substantially the rate of seed viability loss, but increased the rate of endophyte viability loss. Our experiments suggest that, in ageing seed pools, endophyte viability loss and differential seed mortality determine decreases in the proportions of endophyte-infected seeds in L. multiflorum. Endophyte viability loss within live seeds contributes substantially more to infection frequency changes than differential viability losses of infected and non-infected seeds. [source] | ||||||||||