SUMMARYBracken {Pteridium aquilinum (L.) Kuhn) and heather {Calluna vulgaris (L.) Hull) are important upland species which often grow in close proximity in the UK. The effects of factorial treatments of elevated atmospheric COj (539/
Mass loss, together with nitrogen and carbon loss, from above‐ground material and roots of Festuca vivipara were followed for 13 months in a high Arctic polar semi‐desert and a low Arctic tree‐line dwarf shrub heath. Festuca vivipara for the study was obtained from plants cultivated at two different CO2 concentrations (350 and 500 μL L–1) in controlled environment chambers in the UK. Each of the four resource types (shoots or roots from plants grown in elevated or ambient CO2 concentrations) was subsequently placed in an experiment simulating aspects of environmental change in each Arctic ecosystem. Air, litter and soil temperatures were increased using open‐topped polythene tents at both sites, and a 58% increase in summer precipitation was simulated at the high Arctic site. Mass loss was greatest at the low Arctic site, and from the shoot material, rather than the roots. Shoots grown under an elevated CO2 concentration decomposed more slowly at the high Arctic site, and more quickly at the low Arctic one, than shoots grown at ambient CO2. After 13 months, greater amounts of C and N remained in above‐ground litter from plants grown under elevated, rather than ambient, CO2 at the polar semi‐desert site, although lower amounts of C remained in elevated CO2 litter at the low Arctic ecosystem. In the high Arctic, roots grown in the 500 μL L–1 CO2 concentration decomposed significantly more slowly than below‐ground material derived from the ambient CO2 chambers. Elevated CO2 concentrations significantly increased the inital C:N ratio, % soluble carbohydrates and α‐cellulose content, and significantly decreased the inital N content, of the above‐ground material compared to that derived from the ambient treatment. Initially, the C:N ratio and percentage N were similar in both sets of roots derived from the two different CO2 treatments, but soluble carbohydrate and α‐cellulose concentrations were higher, and percentage lignin lower, in the elevated CO2 treatments.The tent treatments significantly retarded shoot decomposition in both ecosystems, probably because of lower litter bag moisture contents, although the additional precipitation treatment had no effect on mass loss from the above‐ground material. The results suggest that neither additional summer precipitation (up to 58%), nor soil temperature increase of 1 °C, which may occur by the end of the next century as an effect of a predicted 4 °C rise in air temperature, had an appreciable effect on root decomposition in the short term in a high Arctic soil. However, at the low Arctic site, greater root decomposition, and a lower pool of root N remaining, were observed where soil temperature was increased by 2 °C in response to a 4 °C rise in air temperature. These results suggest that decomposition below‐ground in this ecosystem would increase as an effect of predicted climate change. These data also show that there is a difference in the initial results of decomposition processes between the two Arctic ecosystems in response to simulated environmental change.
Domestication and subsequent genetic enhancement in lentil (Lens culinaris Medik.) have involved changes in plant structure and DM distribution. These changes were examined using a “genetic gradient” comprising three representatives each of Lens orientalis (Boiss.) progenitors, landraces, pre‐1980 cultivars, and modern germplasm. All 12 genotypes were sown at Pullman, WA, in 1996 and 1997, and at Reading, UK, in 1997. The biomass (all genotypes) and N concentration (four genotypes) of above‐ground tissues were measured at 50% flowering (leaf and stem) and at reproductive maturity (leaf, stem, pod wall and seed). The progenitors produced meager biomass (averaging 0.72 Mg ha−1) and poor HI (0.19), and consequently small seed yields (0.11 Mg ha−1). Productive landraces had substantially higher biomass (3.52 Mg ha−1), improved HI (0.34), and larger seed yields (1.13 Mg ha−1). Biomass and seed yield were increased further by the selection of cultivars (5.11 and 1.32 Mg ha−1, respectively). The development of modern germplasm by hybridization further increased seed yields (1.95 Mg ha−1). Consistent seed yield improvements have not been associated with consistent increases in HI. Instead a strong, positive correlation between seed yield and biomass has persisted. NHI increased more rapidly than HI and is unlikely to increase further in the future. Future seed yield improvement will therefore depend on increased N accumulation. Reliance on N2 fixation must be supported by increased photosynthetic capacity and therefore by vegetative biomass. An advantageous correlation between seed yield and residue production seems likely to persist as crop improvement continues.
Summary The encroachment of bracken (Pteridium aquilinum (L.) Kuhn) into areas previously dominated by heather represents a threat to the ecology, agricultural economy and landscape value of many UK upland areas, including the moorland of the North York Moors National Park. The morphology of bracken, within a mature stand and at several bracken‐heather interfaces, has been studied at a number of sites within the National Park. Differences have been found in the frond growth of bracken in a mature stand, at stationary stand margins, and at advancing stand margins where bracken is encroaching into heather. Frequency of fronds present on bracken rhizome growing at a stationary stand margin close to the interface with heather (1–2 m behind the boundary) are approximately the same as those found within a mature stand. At advancing margins (again 1–2 m behind the boundary), maximum frond densities were often found to exceed those present in either a mature stand or at a stationary margin. Frond numbers decline rapidly at the stand margins as distance from the stand increases. This is especially true where the front is stationary and bracken is not encroaching into heather at a significant rate. Maximum frond heights in a mature stand consistently exceed those at stand margins (even 1–2 m into the stand) and are greater at stationary margins than at advancing margins. Outlying fronds at the edges of bracken stands are generally present in greater numbers, and further into the area dominated by heather, where the margin is advancing. Heights of outlying fronds fall as distance from the bracken stand increases, as does stipe length. Fronds at the edges of bracken stands emerge each spring before those further into the stand and are therefore particularly vulnerable to frost damage. Outlying fronds are not, however, the first to emerge. Early emerging fronds reach their maximum height and eventually become senescent before later emerging fronds. Whilst most fronds emerge before the end of June a few fronds continue to emerge throughout the summer. Frond densities close to the edges of bracken stands (1–2 m into the stand) are comparable to those in a mature stand. At advancing stand margins frond densities generally exceed those in a mature stand, suggesting that a large number of potential entry points for foliage‐applied herbicides are available for bracken control at the stand margins. The ratio of potential uptake points to biomass of rhizome is also greatest at the edges of the stand, and the canopy 1–2 m into the stand is usually almost completely closed. It is possible therefore, the efficacy of herbicides could be improved by the use of small scale applications, using tractors or hand‐held sprayers, close to the margins of bracken stands.
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