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Tree Roots (tree + root)

Distribution by Scientific Domains

Life Sciences	66%

Selected Abstracts

Modelling Tree Roots in Mixed Forest Stands by Inhomogeneous Marked Gibbs Point Processes

BIOMETRICAL JOURNAL, Issue 3 2009
Stefanie Eckel
Abstract The aim of the paper is to apply point processes to root data modelling. We propose a new approach to parametric inference when the data are inhomogeneous replicated marked point patterns. We generalize Geyer's saturation point process to a model, which combines inhomogeneity, marks and interaction between the marked points. Furthermore, the inhomogeneity influences the definition of the neighbourhood of points. Using the maximum pseudolikelihood method, this model is then fitted to root data from mixed stands of Norway spruce (Picea abies (L.) Karst.) and European beech (Fagus sylvatica L.) to quantify the degree of root aggregation in such mixed stands. According to the analysis there is no evidence that the two root systems are not independent. [source]

Tree root and soil heterotrophic respiration as revealed by girdling of boreal Scots pine forest: extending observations beyond the first year

PLANT CELL & ENVIRONMENT, Issue 8 2003
BHUPINDERPAL-SINGH
ABSTRACT Limitations in available techniques to separate autotrophic (root) and soil heterotrophic respiration have hampered the understanding of forest C cycling. The former is here defined as respiration by roots, their associated mycorrhizal fungi and other micro-organisms in the rhizosphere directly dependent on labile C compounds leaked from roots. In order to separate the autotrophic and heterotrophic components of soil respiration, all Scots pine trees in 900 m2 plots were girdled to instantaneously terminate the supply of current photosynthates from the tree canopy to roots. Högberg et al. (Nature 411, 789,792, 2001) reported that autotrophic activity contributed up to 56% of total soil respiration during the first summer of this experiment. They also found that mobilization of stored starch (and likely also sugars) in roots after girdling caused an increased apparent heterotrophic respiration on girdled plots. Herein a transient increase in the ,13C of soil CO2 efflux after girdling, thought to be due to decomposition of 13C-enriched ectomycorrhizal mycelium and root starch and sugar reserves, is reported. In the second year after girdling, when starch reserves of girdled tree roots were exhausted, calculated root respiration increased up to 65% of total soil CO2 efflux. It is suggested that this estimate of its contribution to soil respiration is more precise than the previous based on one year of observation. Heterotrophic respiration declined in response to a 20-day-long 6 °C decline in soil temperature during the second summer, whereas root respiration did not decline. This did not support the idea that root respiration should be more sensitive to variations in soil temperature. It is suggested that above-ground photosynthetic activity and allocation patterns of recent photosynthates to roots should be considered in models of responses of forest C balances to global climate change. [source]

Below-ground competition between trees and grasses may overwhelm the facilitative effects of hydraulic lift

ECOLOGY LETTERS, Issue 8 2004
F. Ludwig
Abstract Under large East African Acacia trees, which were known to show hydraulic lift, we experimentally tested whether tree roots facilitate grass production or compete with grasses for below-ground resources. Prevention of tree,grass interactions through root trenching led to increased soil water content indicating that trees took up more water from the topsoil than they exuded via hydraulic lift. Biomass was higher in trenched plots compared to controls probably because of reduced competition for water. Stable isotope analyses of plant and source water showed that grasses which competed with trees used a greater proportion of deep water compared with grasses in trenched plots. Grasses therefore used hydraulically lifted water provided by trees, or took up deep soil water directly by growing deeper roots when competition with trees occurred. We conclude that any facilitative effect of hydraulic lift for neighbouring species may easily be overwhelmed by water competition in (semi-) arid regions. [source]

Seasonal variation in habitat use by salmon, Salmo salar, trout, Salmo trutta and grayling, Thymallus thymallus, in a chalk stream

FISHERIES MANAGEMENT & ECOLOGY, Issue 4 2006
W. D. RILEY
Abstract, A portable multi-point decoder system deployed in a tributary of the River Itchen, a southern English chalk stream, recorded the habitats used by PIT-tagged juvenile salmon, Salmo salar L., trout, Salmo trutta L. and grayling, Thymallus thymallus L., with a high degree of spatial and temporal resolution. The fishes' use of habitat was monitored at 350 locations throughout the stream during September/October 2001 (feeding period) and January/February 2002 (over-wintering period). Salmon parr tended to occupy water 25,55 cm deep with a velocity between 0.4 and 1.0 m s,1. During both autumn and winter, first year salmon (0+ group) were associated with gravel substrate during the daytime and aquatic weed at night. In autumn, 1+ salmon were strongly associated with hard mud substrates during the day and with marginal tree roots at night. In winter, they were located on gravel substrate by day and gravel and mud at night. Trout were associated with a greater range of habitats than salmon, generally occupying deeper and faster water with increasing age. During the autumn, 0+ trout were located along shallow (5,10 cm) and slow (,0.1,0.4 m s,1) margins of the stream, amongst tree roots by day and on silty substrates at night. During winter the 0+ trout occupied silty substrates at all times. As age increased, trout increasingly used coarse substrates; hard mud, gravel and chalk, and weed at night. All age groups of grayling (0+, 1+ and 2+) tended to occupy hard gravel substrate at all times and used deeper and faster water with increasing age. The 1+ and 2+ groups were generally found in water 40,70 cm deep with a velocity between 0.3 and 0.5 ms,1, whilst the 0+ groups showed a preference for shallower water with reduced velocity at night, particularly in the winter. There were greater differences in the habitats used between species and age groups than between the autumn and winter periods, and the distribution of fish was more strongly influenced by substrate type than water depth or velocity. The results are discussed in relation to the habitat requirements of mixed salmonid populations and habitat management. [source]

The effects of low summer flow on wild salmon (Salmo salar), trout (Salmo trutta) and grayling (Thymallus thymallus) in a small stream

FRESHWATER BIOLOGY, Issue 12 2009
W. D. RILEY
Summary 1.,The effects of an experimentally imposed low summer flow on habitat use, displacement and survival of wild populations of juvenile salmon (Salmo salar), trout (Salmo trutta) and grayling (Thymallus thymallus) were investigated in a chalk stream. The habitat use and mobility of the fish in response to reduced flow was determined using passive integrated transponder-tag detector systems. 2.,Habitat use was compared to that available under different flow regimes. These consisted of an initial control phase of normal summer flow, an abrupt step change to 21 days of low flow, followed by a second control phase when normal summer flow was reinstated. First year (0+) salmon showed little change in their preferred substratum during low flow, whilst 1+ salmon increased their use of gravel and reduced that of mud during the day. Both 0+ and 1+ salmon were found in relatively deep water by day under low flow, whilst 1+ salmon preferred relatively shallow water at night. First year trout increased their use of gravel and reduced their use of mud and submerged tree roots under low flow, using relatively deep and fast flowing water by day. Older trout increased their use of gravel and occupied relatively deep, slow flowing water by day and relatively fast and shallow water at night. Grayling showed little change in their preferred substratum, but occupied relatively shallow water following the introduction of low flow. 3.,The range of movement of juvenile salmon increased at night under low flow, and was greater by day under normal flow. There was also an initial increase in the range of movement of 0+ trout following the introduction of low flow. Older trout initially moved less under low flow. With reduced flow, the range of movement by grayling increased significantly during the day. 4.,There was no net downstream displacement of any species with reduced flow, but the mortality rate in 0+ salmon, trout and grayling increased. This may be related to their small size and increased vulnerability to predation under low flow, and due to the reduction in depth and loss of the stream margins that are normally the preferred habitat of 0+ trout and grayling. 5.,The findings of this field study have implications for the management of braided, and highly regulated, chalk stream systems. In particular, they underline the importance of the stream margins as juvenile salmonid habitat, and suggest that a flow management strategy is required to mitigate for drought conditions. Such a strategy might include pre-emptive controls on abstraction and the maintenance of river flow via a prioritised route, predetermined using fish or habitat surveys, to minimise the effects of drought conditions on the more vulnerable or valued fish groups. [source]

Quantifying root lateral distribution and turnover using pine trees with a distinct stable carbon isotope signature

FUNCTIONAL ECOLOGY, Issue 1 2005
K. JOHNSEN
Summary 1In order to help assess spatial competition for below-ground resources, we quantified the effects of fertilization on root biomass quantity and lateral root distribution of mid-rotation Pinus taeda trees. Open-top chambers exposed trees to ambient or ambient plus 200 µmol mol,1 atmospheric CO2 for 31 months. 2Tank CO2 was depleted in atmospheric 13C; foliage of elevated CO2 trees had ,13C of ,42·9, compared with ,29·1 for ambient CO2 trees. 3Roots 1 m from the base of elevated CO2 -grown trees had more negative ,13C relative to control trees, and this difference was detected, on average, up to 5·8, 3·7 and 3·7 m away from the trees for 0,2, 2,5 and >5 mm root-size classes, respectively. Non-fertilized tree roots extended as far as fertilized trees despite the fact that their above-ground biomass was less than half that of fertilized trees. 4These results are informative with respect to root sampling intensity and protocol, and the distances required between experimental manipulations to evaluate below-ground processes of independent treatments. 5Fine-root turnover has usually been estimated to range from weeks to 3 years, representing a major avenue of carbon flux. Using a mixing model we calculated that 0,2 mm roots had a mean residence time of 4·5 years indicating relatively slow fine-root turnover, a result that has major implications in modelling C cycling. [source]

Fungal specificity bottlenecks during orchid germination and development

MOLECULAR ECOLOGY, Issue 16 2008
MARTIN I. BIDARTONDO
Abstract Fungus-subsidized growth through the seedling stage is the most critical feature of the life history for the thousands of mycorrhizal plant species that propagate by means of ,dust seeds.' We investigated the extent of specificity towards fungi shown by orchids in the genera Cephalanthera and Epipactis at three stages of their life cycle: (i) initiation of germination, (ii) during seedling development, and (iii) in the mature photosynthetic plant. It is known that in the mature phase, plants of these genera can be mycorrhizal with a number of fungi that are simultaneously ectomycorrhizal with the roots of neighbouring forest trees. The extent to which earlier developmental stages use the same or a distinctive suite of fungi was unclear. To address this question, a total of 1500 packets containing orchid seeds were buried for up to 3 years in diverse European forest sites which either supported or lacked populations of helleborine orchids. After harvest, the fungi associated with the three developmental stages, and with tree roots, were identified via cultivation-independent molecular methods. While our results show that most fungal symbionts are ectomycorrhizal, differences were observed between orchids in the representation of fungi at the three life stages. In Cephalanthera damasonium and C. longifolia, the fungi detected in seedlings were only a subset of the wider range seen in germinating seeds and mature plants. In Epipactis atrorubens, the fungi detected were similar at all three life stages, but different fungal lineages produced a difference in seedling germination performance. Our results demonstrate that there can be a narrow checkpoint for mycorrhizal range during seedling growth relative to the more promiscuous germination and mature stages of these plants' life cycle. [source]