Biomedical subjects

C P Andersen

Publications and source records attributed to C P Andersen.

9 recordsLinked to original sources

PubMed2001

Seasonal changes in above- and belowground carbohydrate concentrations of ponderosa pine along a pollution gradient.

Seasonal patterns of carbohydrate concentration in coarse and fine roots, stem or bole, and foliage of ponderosa pine (Pinus ponderosa Laws) were described across five tree-age classes from seedlings to mature trees at an atmospherically clean site. Relative to all other tree-age classes, seedlings exhibited greater tissue carbohydrate concentration in stems and foliage, and greater shifts in the time at which maximum and minimum carbohydrate concentration occurred. To determine the effect of environmental stressors on tissue carbohydrate concentration, two tree-age classes (40-year-old and mature) were compared at three sites along a well-established, long-term O3 and N deposition gradient in the San Bernardino Mountains, California. Maximum carbohydrate concentration of 1-year-old needles declined with increasing pollution exposure in both tree-age classes. Maximum fine root monosaccharide concentration was depressed for both 40-year-old and mature trees at the most polluted site. Maximum coarse and fine root starch concentrations were significantly depressed at the most polluted site in mature trees. Maximum bole carbohydrate concentration of 40-year-old trees was greater for the two most polluted sites relative to the cleanest site: the bole appeared to be a storage organ at sites where high O3 and high N deposition decreased root biomass.

Air Pollution↗

PubMed2001

Blue wild-rye grass competition increases the effect of ozone on ponderosa pine seedlings.

Individual ponderosa pine (Pinus ponderosa Dougl. ex Laws.) seedlings were grown in mesocosms with three densities of blue wild-rye grass (Elymus glaucus Buckl.) (equivalent to 0, 32 or 88 plants m-2) to determine if the presence of a natural competitor alters the response of ponderosa pine seedlings to ozone. After 3 years of ozone exposure, grass presence reduced total ponderosa pine dry mass by nearly 50%, whereas ozone alone had no significant effect on ponderosa pine growth. The combination of ozone and grass further reduced needle, stem and branch dry mass significantly below that induced by grass competition alone. Root:shoot ratios increased in response to the combined grass and ozone treatments. Grass competition significantly reduced soluble sugar concentrations in all ponderosa pine tissue components examined. Starch concentrations were highly variable but did not differ significantly between treatments. Ozone significantly reduced soluble sugar concentrations in fine roots and stems. In the absence of grass, ozone-treated seedlings tended to have higher tissue N concentrations than controls. In the presence of grass, ozone-treated seedlings had lower N concentrations than controls, resulting in a significant interaction between these two stresses in 1- and 2-year-old needles. Needle C:N ratios decreased in response to grass competition, as a result of increased N concentration and no change in C concentration. The opposite response was observed in ozone-treated seedlings as a result of decreased N concentrations, indicating that ozone-treated seedlings were unable to take up or retain as much nitrogen when grown in the presence of grass. We conclude that ponderosa pine seedlings are more susceptible to ozone when grown in competition with blue wild-rye grass.

California↗

PubMed2000

The effect of ozone on below-ground carbon allocation in wheat.

Short-term (14)CO(2) pulse and chase experiments were conducted in order to investigate the effect of ozone on below-ground carbon allocation in spring wheat seedlings (Triticum aestivum L. 'ANZA'). Wheat seedlings were grown in a sand-hydroponic system and exposed to either high ozone (38-40 ppm-h) or low ozone (23-31 ppm-h) for 21 days in a series of replicated experiments. Following the ozone exposures, the plants were pulsed with (14)CO(2) and allocation of (14)C-labeled photosynthate was measured in the plant and growth media. Soluble root exudates were measured, without disturbing the plant roots, 24 h after the (14)CO(2) pulse. Shoot biomass was reduced by 17% for the high ozone and 9% for the low ozone exposures, relative to control treatments. Root biomass was reduced by 9% for the high ozone exposures, but was not significantly different than the controls for the low ozone. The amount of (14)C activity in the shoot and root tissue 24 h after the (14)CO(2) pulse, normalized to tissue weight, total (14)CO(2) uptake, or the total (14)C retention in each plant, was not affected by either high or low ozone exposures. The amount of (14)C activity measured in the growth media solution surrounding the roots increased 9% for the high ozone exposures, and after normalizing to root size or root (14)C activity, the growth media solution (14)C activity increased 29 and 40%, respectively. Total respiration of (14)CO(2) from the ozone-treated plants decreased, but the decrease was not statistically significant. Our results suggest that soluble root exudation of (14)C activity to the surrounding rhizosphere increases in response to ozone. Increased root exudation to the rhizosphere in response to ozone is contrary to reports of decreased carbon allocation below ground and suggests that rhizosphere microbial activity may be initially stimulated by plant exposure to ozone.

Journal Article↗

PubMed1999

Understanding plant-soil relationships using controlled environment facilities.

Although soil is a component of terrestrial ecosystems, it is comprised of a complex web of interacting organisms, and therefore can be considered itself as an ecosystem. Soil microflora and fauna derive energy from plants and plant residues and serve important functions in maintaining soil physical and chemical properties, thereby affecting net primary productivity (NPP), and in the case of contained environments, the quality of the life support system. We have been using 3 controlled-environment facilities (CEF's) that incorporate different levels of soil biological complexity and environmental control, and differ in their resemblance to natural ecosystems, to study relationships among plant physiology, soil ecology, fluxes of minerals and nutrients, and overall ecosystem function. The simplest system utilizes growth chambers and specialized root chambers with organic-less media to study the physiology of plant-mycorrhizal associations. A second system incorporates natural soil in open-top chambers to study soil bacterial and fungal population response to stress. The most complex CEF incorporates reconstructed soil profiles in a "constructed" ecosystem, enabling close examination of the soil foodweb. Our results show that closed ecosystem research is important for understanding mechanisms of response to ecosystem stresses. In addition, responses observed at one level of biological complexity may not allow prediction of response at a different level of biological complexity. In closed life support systems, incorporating soil foodwebs will require less artificial manipulation to maintain system stability and sustainability.

Biological Transport↗

PubMed1997

Carry-over effects of ozone on root growth and carbohydrate concentrations of ponderosa pine seedlings.

Ozone exposure decreases belowground carbon allocation and root growth of plants; however, the extent to which these effects persist and the cumulative impact of ozone stress on plant growth are poorly understood. To evaluate the potential for plant compensation, we followed the progression of ozone effects, with particular emphasis on the development of new roots. Ponderosa pine (Pinus ponderosa Dougl. ex Laws.) seedlings were exposed to ozone for 2 years. Following removal of the seedlings from ozone, root growth was assessed to characterize the carry-over effects on new root production, and carbohydrate concentrations were measured to determine if allocation strategies differed among ozone treatments. Four months after removal from ozone, dormant seedlings had significantly lower starch concentrations in stems, coarse roots and fine roots than control seedlings. Following root flushing, starch concentrations in all seedlings decreased, with ozone-treated seedlings containing significantly less starch, sucrose, fructose, glucose and total monosaccharides than control seedlings. There was some evidence that stem starch was mobilized to compensate partially for the lower concentrations of root starch in ozone-treated seedlings; however, there was significantly less new root production in seedlings previously exposed to ozone for 2 years than in control seedlings. Early senescence of older needle age classes, perhaps resulting in inadequate available photosynthate, may be responsible for the reduction in new root production during the year following exposure to ozone. Stored carbohydrate reserves, which were depleted in seedlings previously exposed to ozone, were insufficient to compensate for the ozone-induced reduction in canopy photosynthate. We conclude that there are carry-over effects of ozone exposure on ponderosa pine seedlings, including an enhanced potential for seedling susceptibility to other stresses even in respite years when ozone concentrations are low.

Journal Article↗

PubMed1997

Nutrient availability alters belowground respiration of ozone-exposed ponderosa pine.

Exposure to ozone (O(3)) and changes in soil fertility influence both the metabolism of plant roots and their interaction with rhizosphere organisms. Because one indication of altered root metabolism is a change in belowground respiratory activity, we used specially designed measurement chambers to assess the effects of O(3) and nutrient availability on belowground respiratory activity of potted three-year-old ponderosa pine (Pinus ponderosa Dougl. ex Laws.). Seedlings were exposed to a factorial combination of three O(3) treatments and three fertilization treatments in open-top O(3) exposure chambers. Ozone exposure decreased and high nutrient supply increased total plant dry weight, but root/shoot ratios were not affected. In general, exposure to O(3) increased rates of belowground O(2) uptake and CO(2) release and the respiratory quotient (RQ, CO(2)/O(2)), although seasonal differences were detected. In October, following the second season of O(3) exposure, rates of belowground O(2) uptake and CO(2) release and RQ were increased in trees in the high-O(3) exposure treatment by 22, 73 and 32%, respectively, over values in control trees in charcoal-filtered air. Increasing nutrient supply resulted in decreasing rates of belowground O(2) uptake and CO(2) release but it had little effect on RQ. In the high-nutrient supply treatment, rates of belowground O(2) uptake and CO(2) release were decreased by 38 and 39%, respectively, compared with rates in the low-nutrient supply treatment. At the end of the second growing season, the high-nutrient supply treatment had decreased lateral root total nonstructural carbohydrates by 22% compared with the low-nutrient supply treatment. Nutrient availability altered the belowground respiratory response to O(3), such that the response to O(3) was greatest in the low-nutrient supply treatment. Significant O(3) effects on belowground respiratory activity were apparent before any reduction in total plant growth was found, suggesting that roots and rhizosphere organisms may be early indicators of physiological dysfunction in stressed seedlings.

Journal Article↗

PubMed1991

Stress interactions and mycorrhizal plant response: understanding carbon allocation priorities.

In this paper, a framework is presented for studying responses of mycorrhiza to external stresses, including possible feedback effects which are likely to occur. The authors review recent literature linking carbon allocation and host/fungal response under natural and anthropogenic stress, and present a conceptual model to discuss how carbon may be involved in singular and multiple stress interactions of mycorrhizal seedlings. Due to an integral integral role in metabollic processes, characterizing carbon allocation in controlled laboratory environments could be useful for understanding host/fungal responses to a variety of natural and anthropogenic stresses. Carbon allocation at the whole-plant level reflects an integrated response which links photosynthesis to growth and maintenance processes. A root-mycocosm system is described which permits spatial separation of a portion of extramatrical hyphae growing in association with seedling roots. Using this system, it is shown that root/hyphal respiratory release of pulse-labeled 14C follows a sigmoidal pattern, with typical lag, exponential and saturation phases. Total respiratory release of 14C per mg root and the fraction respired of total 14C allocated to the root is greater in ponderosa pine inoculated with Hebeloma crustuliniforme than in noninoculated controls. Results illustrate the nature of information than can be obtained using this system. Current projects using the mycocosms include characterizing the dynamics of carbon allocation under ozone stress, and following the fate of organic pollutants. The authors believe that the system could be used to differentiate fungal- and host-mediated responses to a large number of other stresses and to study a variety of physiological processes in mycorrhizal plants.

Journal Article↗

PubMed1991

Seasonal changes in shoot water relations of Picea rubens at two high elevation sites in the Smoky Mountains.

Seasonal changes in water relations of current-year shoots of red spruce (Picea rubens Sarg.) were examined in relation to climatic conditions in trees growing at elevations of 1720 and 1935 m on Clingman's Dome, Tennessee, USA, where increment core data have shown that red spruce decline increases with elevation. Relative height growth of trees at 1720 m was 68% greater than in trees at 1935 m. Following two weeks in July with only traces of precipitation, trees at both sites showed decreased saturated osmotic potentials. The magnitude of the reduction was greater in trees at the high elevation site than in trees at the low elevation site. However, during August and September, shoot water relations of trees at both sites were similar. Precipitation patterns and water relations measurements suggested that, at both sites, trees experienced water stress only briefly during the growing season and to a degree that could not account for the lower growth rates of trees at the high elevation site. During the period of cold hardening in October and November, trees at the low elevation site exhibited saturated osmotic potentials that were lower by 0.2 MPa and solute accumulation (osmol kg(dw) (-1)) that was 48% greater than in trees at the high elevation site.

Journal Article↗

PubMed1979

[Dictyocaulus viviparus in Denmark. A survey of 15 years' diagnostic examination of faeces samples (author's transl)].

On the basis of routine diagnostic examinations of 12424 bovine faeces samples for larvae of Dictyocaulus viviparus, performed during the period 1963 through 1977, some calculations and reflections have been made on the incidence and epidemiology of lungworm infection in cattle in Denmark. It seems justified to conclude that dictyocaulosis is an important disease in heifers and cows as well as in calves. A distinct seasonal variation in the incidence of lungworm infection is apparent, in that more than 85% of the faeces samples were submitted within the period July through October. Lungworm larvae could be demonstrated in faeces samples from cattle during the winter and spring- This is considered to be of great importance with a view to re-establishment of the infection in the following grazing season. Overwintering of larvae on pastures seems possible. too, since patent infections among calves were demonstrated already in May and June. A comparison of meteorological data with totals of samples submitted and with relative numbers of positive samples seems to confirm, that both the level and the spread of lungworm infections are influenced by the amount of rainfall during the period June through August.

Animals↗