Herbicides and Plant Physiology. Andrew H. Cobb
Чтение книги онлайн.
Читать онлайн книгу Herbicides and Plant Physiology - Andrew H. Cobb страница 19
Table 1.9 Seed production by a number of common arable weeds and wheat.
Source: Adapted from Radosevich, S.R. and Holt, J.S. (1984) Weed Ecology: Implications for Vegetation Management. New York: Wiley; containing information from Hanf (1983).
Weed | Common name | Seed production per plant |
---|---|---|
Veronica persica | Common field speedwell | 50–100 |
Avena fatua | Wild oat | 100–450 |
Galium aparine | Cleavers | 300–400 |
Senecio vulgaris | Groundsel | 1100–1200 |
Capsella bursa‐pastoris | Shepherd’s purse | 3500–4000 |
Cirsium arvense | Creeping thistle | 4000–5000 |
Taraxacum officinale | Dandelion | 5000 (200 per head) |
Portulaca oleracea | Purslane | 10,000 |
Stellaria media | Chickweed | 15,000 |
Papaver rhoeas | Poppy | 14,000–19,500 |
Tripleurospermum maritimum spp. inodorum | Scentless mayweed | 15,000–19,000 |
Echinochloa crus‐galli | Barnyard grass | 2000–40,000 |
Chamaenerion angustifolium | Rosebay willowherb | 80,000 |
Eleusine indica | Goose grass | 50,000–135,000 |
Digitaria sanguinalis | Large crabgrass | 2000–150,000 |
Chenopodium album | Fat hen | 13,000–500,000 |
Triticum aestivum | Wheat | 90–100 |
Figure 1.2 Some methods of weed seed dispersal with their estimated range in metres.
Source: Liebman, M., Mohler, C.L. and Staver, C.P. (2001) Ecological Management of Agricultural Weeds. Cambridge University Press. Reproduced with permission of Cambridge University Press.
1.5.7 Dormancy and duration of viability
Although the seed production figures of an individual plant are impressive (Table 1.9), the total seed population in a given area is of greater significance. The soil seed reservoir reflects both past and present seed production, in addition to those imported from elsewhere, and is reduced by germination, senescence and the activity of herbivores (Figure 1.3). Estimates of up to 100,000 viable seeds per square metre of arable soil represent a massive competition potential to both existing and succeeding crops, especially since the seed rate for spring barley, for instance, is only approximately 400 m−2! Under long term grassland, weed seed numbers in soil are in the region of 15,000–20,000 m−2, so conversion of arable land to long‐term grassland offers growers a means of reducing soil weed‐seed burden.
The length of time that seeds of individual species of weed remain viable in soil varies considerably. The nature of the research involved in collecting such data means that few comprehensive studies have been carried out, but those that have (see Toole and Brown, 1946, for a 39 year study!) show that although seeds of many species are viable for less than a decade, some species can survive for in excess of 80 years (examples include poppy and fat hen). Evidence from soils collected during archaeological excavations reveals seeds of certain species germinating after burial for 100–600 (and maybe even up to 1700!) years (Ødum, 1965).
Dormancy in weed seeds allows for germination to be delayed until conditions are favourable. This dormancy may be innate and contributes to the periodicity of germination, as illustrated in Figure 1.1. In addition, dormancy may be induced or enforced in non‐dormant seeds if environmental conditions are unfavourable. This ensures that the weed seed germinates when conditions are most conducive to seedling survival.
Figure 1.3 Factors affecting the soil seed population.
Source: Grundy, A.C. and Jones, N.E. (2002) What is the weed seed bank? In: Naylor, R.E.L. (ed.) Weed Management Handbook, 9th edn. Oxford: Blackwell Publishing/BCPC. Reproduced with permission of John Wiley & Sons.
1.5.8 Plasticity of weed growth
The ability of a weed species to make rapid phenotypic adjustment to environmental change (acclimation) may offer a considerable strategic advantage to the weed in an arable context. An example of the consequence of such plasticity is environmental sensing by fat hen (Chenopodium album). This important weed can respond to canopy shade by undergoing rapid stem (internode) elongation, although the plant is invariably shorter if growing in full sun. Similarly,