Growth and crown architecture of two aspen genotypes exposed to interacting ozone and carbon dioxide.

To study the impact of ozone (O3) and O3 plus CO2 on aspen growth, we planted two trembling aspen clones, differing in sensitivity to O3 in the ground in open-top chambers and exposed them to different concentrations of O3 and O3 plus CO, for 98 days. Ozone exposure (58 to 97 microl l(-1)-h. total exposure) decreased growth and modified crown architecture of both aspen clones. Ozone exposure decreased leaf, stem, branch, and root dry weight particularly in the O3 sensitive clone (clone 259). The addition of CO2 (150 microl l(-1) over ambient) to the O3 exposure counteracted the negative impact of O3 only in the O3 tolerant clone (clone 216). Ozone had relatively little effect on allometric ratios such as, shoot/root ratio, leaf weight ratio, or root weight ratio. In both clones, however, O3 decreased the shoot dry weight, shoot length ratio and shoot diameter. This decrease in wood strength caused both current terminals and long shoots to droop and increased the branch angle of termination. These results show that aspen growth is highly sensitive to O3 and that O3 can also significantly affect crown architecture. Aspen plants with drooping terminals and lateral branches would be at a competitive disadvantage in dense stands with limited light.

Haemodynamic changes during laparoscopic anterior fundoplication measured by trans-oesophageal Doppler ultrasound.

We investigated the cardiovascular effects of pneumoperitoneum and steep head-up tilt during laparoscopic fundoplication using an intra-oesophageal Doppler ultrasound probe. Repositioning of the probe proved sufficient to maintain the signal throughout the procedure despite the pneumomediastinum. There was a statistically significant increase in mean arterial blood pressure and a fall in stroke distance but not in systemic vascular resistance. Increasing or decreasing the blood pressure with drugs improved stroke distance. The oesophageal Doppler ultrasound proved a satisfactory method for assessing cardiovascular changes during fundoplication.

Perioperative management of the elderly trauma patient.

This article reviews the physiology and pathology associated with ageing and the impact these may have on the perioperative and anaesthetic care of the elderly trauma patient. The current literature on this subject is summarized and, based on this, recommendations are made for perioperative management.

Anaesthesia for hip fracture: a survey of Scottish practice.

A postal survey of all senior anaesthetists with routine commitment to an acute trauma list in 13 Scottish hospitals was conducted to delineate contemporary anaesthetic practice for hip fracture surgery. Almost equal use of general and regional anaesthesia was reported, however the techniques used for general anaesthesia were different from those described in previous literature in this group. The recently released Scottish Intercollegiate Guidelines Network (SIGN) guidelines for the management of elderly people with fractured hip state that seniority of anaesthetist is important for improved outcome but there is no difference between either general or regional anaesthesia. However these conclusions relate to techniques and drugs which are now rarely used during general anaesthesia for hip fracture surgery. Further work to assess the impact of new techniques and agents on outcome for this group of patients may be required.

Root growth and physiology of potted and field-grown trembling aspen exposed to tropospheric ozone.

We studied root growth and respiration of potted plants and field-grown aspen trees (Populus tremuloides Michx.) exposed to ambient or twice-ambient ozone. Root dry weight of potted plants decreased up to 45% after 12 weeks of ozone treatment, and root system respiration decreased by 27%. The ozone-induced decrease in root system respiration of potted plants was more closely correlated with decreased root dry weight than with specific root respiration, suggesting that aspen root metabolism was less affected by ozone than root growth. We used minirhizotrons to study the appearance and disappearance of roots in the field. Length of live roots of field-grown trees increased rapidly early in the season and peaked by midseason in association with a decrease in root production and an increase in root disappearance. In the twice-ambient ozone treatment, live root lengths were 17% less than those of controls, but the effect was not statistically significant. Seasonal soil CO(2) efflux of field-grown trees decreased significantly in the ozone treatments, but because differences in live root length were not significant and root dry weights were not available, the effect on CO(2) efflux could not be attributed directly to decreased root growth.

Photosynthetic productivity of aspen clones varying in sensitivity to tropospheric ozone.

Rooted cuttings from three aspen (Populus tremuloides Michx.) clones (216, 271 and 259, classified as high, intermediate and low in O(3) tolerance, respectively) were exposed to either diurnal O(3) profiles simulating those of Michigan's Lower Peninsula (episodic treatments), or diurnal square-wave O(3) treatments in open-top chambers in northern Michigan, USA. Ozone was dispensed in chambers ventilated with charcoal-filtered (CF) air. In addition, seedlings were compared to rooted cuttings in their response to episodic O(3) treatments. Early in the season, O(3) caused decreased photosynthetic rates in mature leaves of all clones, whereas only the photosynthetic rates of recently mature leaves of the O(3)-sensitive Clone 259 decreased in response to O(3) exposure. During midseason, O(3) caused decreased photosynthetic rates of both recently mature and mature leaves of the O(3)-sensitive Clone 259, but it had no effect on the photosynthetic rate of recently mature leaves of the O(3)-tolerant Clone 216. Late in the season, however, photosynthetic rates of both recently mature and mature leaves of Clone 216 were lower than those of the control plants maintained in CF air. Ozone decreased the photosynthetic rate of mature leaves of Clone 271, but it increased or had no effect on the photosynthetic rate of recently mature leaves. Photosynthetic response patterns of seedlings to O(3) treatment were similar to those of the clones, but total magnitude of the response was less, perhaps reflecting the diverse genotypes of the seedling population. Early leaf abscission was observed in all clones exposed to O(3); however, Clones 216 and 259 lost more leaf area than Clone 271. By late August, leaf area in the highest O(3) treatment had decreased relative to the controls by 26, 24 and 9% for Clones 216, 259 and 271, respectively. Ozone decreased whole-tree photosynthesis in all clones, and the decrease was consistently less in Clone 271 (23%) than in Clones 216 (56%) and 259 (56%), and was accompanied by declines in total biomass of 19, 28 and 47%, respectively. The relationship between biomass and whole-tree photosynthesis indicates that the negative impact of O(3) on biomass in the clones was determined largely by lower photosynthetic productivity of the foliage, rather than by potential changes in the carbon relations of other plant organs.

Carbon allocation and partitioning in aspen clones varying in sensitivity to tropospheric ozone.

Clones of aspen (Populus tremuloides Michx.) were identified that differ in biomass production in response to O(3) exposure. (14)Carbon tracer studies were used to determine if the differences in biomass response were linked to shifts in carbon allocation and carbon partitioning patterns. Rooted cuttings from three aspen Clones (216, O(3) tolerant; 271, intermediate; and 259, O(3) sensitive) were exposed to either charcoal-filtered air (CF) or an episodic, two-times-ambient O(3) profile (2x) in open-top chambers. Either recently mature or mature leaves were exposed to a 30-min (14)C pulse and returned to the treatment chambers for a 48-h chase period before harvest. Allocation of (14)C to different plant parts, partitioning of (14)C into various chemical fractions, and the concentration of various chemical fractions in plant tissue were determined. The percent of (14)C retained in recently mature source leaves was not affected by O(3) treatment, but that retained in mature source leaves was greater in O(3)-treated plants than in CF-treated plants. Carbon allocation from source leaves was affected by leaf position, season, clone and O(3) exposure. Recently mature source leaves of CF-treated plants translocated about equal percentages of (14)C acropetally to growing shoots and basipetally to stem and roots early in the season. When shoot growth ceased (August 16), most (14)C from all source leaves was translocated basipetally to stem and roots. At no time did mature source leaves allocate more than 6% of (14)C translocated within the plant to the shoot above. Ozone effects were most apparent late in the season. Ozone decreased the percent (14)C translocated from mature source leaves to roots and increased the percent (14)C translocated to the lower stem. In contrast, allocation from recently mature leaves to roots increased. Partitioning of (14)C among chemical fractions was affected by O(3) more in source leaves than in sink tissue. In source leaves, more (14)C was incorporated into the sugar, organic acid and lipids + pigments fractions, and less (14)C was incorporated into starch and protein fractions in O(3)-treated plants than in CF-treated plants. In addition, there were O(3) treatment interactions between leaf position and clones for (14)C incorporation into different chemical fractions. When photosynthetic data were used to convert percent (14)C transported to the total amount of carbon transported on a mass basis, it was found that carbon transport was controlled more by photosynthesis in the source leaves than proportional changes in allocation to the sinks. Ozone decreased the total amount of carbon translocated to all sink tissue in the O(3)-sensitive Clone 259 because of decreases in photosynthesis in both recently mature and mature source leaves. In contrast, O(3) had no effect on carbon transport from recently mature leaves to lower shoots of either Clone 216 or 271, had no significant effect on transport to roots of Clone 216, and increased transport to roots of Clone 271. The O(3)-induced increase in transport to roots of Clone 271 was the result of a compensatory increase in upper leaf photosynthesis and a relatively greater shift in the percent of carbon allocated to roots. In contrast to those of Clone 271, recently mature leaves of Clone 216 maintained similar photosynthetic rates and allocation patterns in both the CF and O(3) treatments. We conclude that Clone 271 was more tolerant to O(3) exposure than Clone 216 or 259. Tolerance to chronic O(3) exposure was directly related to maintenance of high photosynthetic rates in recently mature leaves and retention of lower leaves.

Biochemical composition of loblolly pine reflects pollutant exposure.

Under experimental conditions, the growth of loblolly pine (Pinus taeda L.) is often responsive to ozone at near-ambient concentrations. However, little is known of the biochemical changes associated with this or other pollutants. Loblolly pine seedlings in open-top chambers were exposed to combinations of ozone (sub-ambient, ambient, or twice-ambient), acidic precipitation (pH 3.8 or pH 5.2) and soil magnesium (0.15 or 0.32 microg g(-1) exchangeable Mg) for three growing seasons. The effects of these treatments were greater in foliage than in stems or roots. The largest treatment effect was a 50% decrease in the starch concentration of current-year foliage from the twice-ambient ozone treatment compared with current-year foliage from the sub-ambient ozone treatment. Responses to ozone were consistent with the hypothesis that ozone-induced growth reductions are associated with depletion of carbohydrate reserves resulting from injury compensation and repair processes or reduced carbon fixation or both. Addition of acidic precipitation, and to a small extent Mg, decreased sugar concentrations of tissues; however, this effect appeared to be mediated by nutrient addition rather than by acidity per se. Given the role of carbohydrates in plant resistance to environmental stress, the sensitivity of carbohydrates to experimental treatments demonstrates the potential for indirect effects of ozone, acidic precipitation, and soil properties on stress resistance. Noncarbohydrate constituents were largely unresponsive to the experimental treatments. These findings imply that tissue carbohydrate analysis may be useful for assessing the impacts of pollutants in forest ecosystems.

ECOPHYS: An ecophysiological growth process model for juvenile poplar.

The ECOPHYS model is an ecophysiological growth process model of juvenile poplar clones growing under near optimal conditions. The theoretical basis for the ECOPHYS model is that (1) individual leaves drive and control growth; (2) the microenvironment at the leaf exerts primary control of photosynthetic rates; (3) leaf orientation is a major determinant of that microenvironment, (4) photosynthates produced by leaves are allocated among meristematic and respiratory sinks: and (5) the plant's genome and microenvironment regulate photosynthate allocation. The major driving variables are solar radiation, temperature, and clonal morphological and physiological factors. The user can interact or override any or all of the input variables to examine the effects of such changes on photosynthetic production and growth. Verification and sensitivity analyses of ECOPHYS are presented and discussed. The use of ECOPHYS as a research tool is illustrated with several examples. Model potential and limitations are discussed.

Regulation of human breast cancer by secreted growth factors.

Laboratory evidence is presented that estrogens are able to induce the production of numerous growth factors which can act in an autocrine or paracrine fashion in estrogen dependent breast cancer. Estrogen independent tumors can produce these same growth factors constitutively and so escape the need for estrogen stimulation. Growth inhibitory factors such as TGF-beta can also be controlled by estrogens and antiestrogens. It is unclear at present, however, how much of the cytostatic effect of antiestrogens in vivo is explained by the production of growth inhibitors. The overall control of breast cancer growth is mediated by the combined effects of these growth stimulatory and inhibitory factors in both breast stroma and epithelium. Interruption of the action of growth factors and the use of growth inhibitors may provide opportunities for new approaches to the treatment of breast cancer.

Diurnal changes in leaf chemical constituents and (14)C partitioning in cottonwood.

Diurnal changes in concentrations of leaf chemical fractions and partitioning of photosynthetically fixed (14)C within the plant and among chemical fractions were studied in rapidly growing cottonwood (Populus deltoides Bartr. ex Marsh.) seedlings. During the light period, leaf weight (mg cm(-2)) increased by about 25% primarily as a result of the accumulation of starch and sucrose, and to a lesser extent because of an increase in the content of amino acids and the chloroform fraction (pigments plus lipids). In contrast, reducing sugars and organic acids decreased in concentration. The partitioning of (14)C within the plant also changed during the light period. Acropetal transport to developing leaves and stem decreased from 81 to 55% of the total (14)C translocated from a source leaf in 4 hours, whereas basipetal transport to stem and roots increased from 13 to 37%. Although assimilation rate ((14)C fixed in 0.5 h) remained constant during the light period, the percentage of fixed (14)C translocated out of the source leaf in 4 h decreased from 27 to 9%. This change in transport rate of recently fixed (14)C was caused by a shift in (14)C partitioning from transport sucrose to storage starch. During the light period, the incorporation ratio ((14)C-sugar/(14)C-starch) decreased from 40 at 0700 h to 2 at 1900 h. The partitioning of carbon to different chemical fractions within the source leaf and the interactions or feedback between different sinks and the source leaf have a major influence on plant growth and development. Control of this carbon partitioning is located in both source and sink leaves.

A morphological index of Quercus seedling ontogeny for use in studies of physiology and growth.

Attempts to relate plant metabolic activity with developmental stage are often hindered by lack of an appropriate developmental index. Existing indices of morphological development are unsuitable for use with plants having a semideterminate, recurrently flushing pattern of growth as displayed by Quercus seedlings. We propose the following morphological index (QMI) to define the stages of Quercus seedling ontogeny: (1) radicle emergence; (2) epicotyl emergence from the soil; and (for each flush) (3) termination of elongation of the second internode, which corresponds with the period of most rapid stem elongation; (4) completion of elongation by all internodes, which corresponds with the period of most rapid leaf elongation; and (5) completion of elongation of the last leaf but one, which usually precedes closely the pause between one growth flush and another. The relationship between QMI and net photosynthesis by individual leaves of Quercus rubra L. seedlings was determined. Net photosynthesis increased with QMI during a flush, but at a particular QMI stage, generally decreased from one flush to the next.

Glutamine Transfer from Xylem to Phloem and Translocation to Developing Leaves of Populus deltoides.

The distribution of (14)C from xylem-borne [(14)C]glutamine, the major nitrogen compound moving in xylem sap of cottonwood (Populus deltoides Bartr. ex Marsh), was followed in rapidly growing shoots with a combination of autoradiographic, microautoradiographic, and radioassay techniques. Autoradiography and (14)C analyses of tissues showed that xylem-borne glutamine did not move with the transpiration stream into mature leaves. Instead, most of it was transferred from xylem to phloem in the upper stem and then translocated to young developing tissues. Microautoradiography showed that metaxylem parenchyma, secondary xylem parenchyma, and rays were the major areas of uptake from xylem vessels in the stem. Accumulation in phloem (high (14)C concentrations in sieve tubes) took place in internodes subtending recently mature leaves. Little (14)C from xylem-borne glutamine was found in phloem of mature leaves, which indicates restricted retransport of glutamine that did enter the leaf. In the primary tissues of the upper stem, most (14)C was found in the phloem. Cottonwood stems have an efficient uptake and transfer system that enhances glutamine movement to developing tissues of the upper stem.

Comparative Distribution and Metabolism of Xylem-Borne Amino Compounds and Sucrose in Shoots of Populus deltoides.

The transport and metabolism of xylem-borne amino compounds and sucrose were investigated in rapidly growing shoots of cottonwood (Populus deltoides Bartr. ex Marsh.). (14)C-labeled glutamine, threonine, alanine, glutamic acid, aspartic acid, and sucrose were applied to the base of severed stems for transport in xylem. Distribution and metabolism of the compounds were followed with autoradiography, microautoradiography, and radioassay. Three utilization patterns were observed: (a) little alanine and sucrose was transported to the laminae of either mature leaves or developing leaves. These compounds were taken up from xylem free-space and utilized in adjacent tissue; (b) threonine also did not move into mature leaves but was translocated to developing leaves or utilized in the stem; (c) glutamic acid and aspartic acid were transported directly into the laminae of mature leaves via the xylem. Relatively less (14)C was retained in stems compared to the other compounds.Metabolism of the test compounds also differed considerably. (14)C from amino acids moved primarily into organic acids and protein. The (14)C from sucrose was widely distributed among the chemical fractions, with a high percentage found in structural carbohydrates. Clearly, cottonwood stems contain efficient uptake and transfer systems that differentiate among various compounds moving from root to shoot in xylem.

Microautoradiography of water-soluble compounds in plant tissue after freeze-drying and pressure infiltration with epoxy resin.

It is difficult to retain and localize radioactive, water-soluble compounds within plant cells. Existing techniques retain water-soluble compounds with varying rates of efficiency and are limited to processing only a few samples at one time. We developed a modified pressure infiltration technique for the preparation of microautoradiographs of (14)C-labeled, water-soluble compounds in plant tissue. Samples from cottonwood (Populus deltoides Bartr. ex Marsh.) labeled with (14)C were excised, quick frozen in liquid N(2), freeze-dried at -50 degrees C, and pressure-infiltrated with epoxy resin without intermediate solvents or prolonged incubation times. The technique facilitates the mass processing of samples for microautoradiography, gives good cellular retention of labeled water-soluble compounds, and is highly reproducible.

Translocation pathways in the petioles and stem between source and sink leaves of Populus deltoides Bartr. ex Marsh.

Microautoradiography was used to follow the translocation pathways of (14)C-labeled photosynthate from mature source leaves, through the stem, to immature sink leaves three nodes above. Translocation occurred in specific bundles of the midveins and petioles of both the source and sink leaves and in the interjacent internodes. When each of six major veins in the lamina of an exporting leaf was independently spot-fed (14)CO2, label was exported through specific bundles in the petiole associated with that vein. When the whole lamina of a mature source leaf was fed (14)CO2, export occurred through all bundles of the lamina, but acropetal export in the stem was confined to bundles serving certain immature sink leaves. Cross-transfer occurred within the stem via phloem bridges. Leaves approaching maturity translocated photosynthate bidirectionally in adjacent subsidiary bundles of the petiole. That is, petiolar bundles serving the lamina apex were exporting unlabeled photosynthate while those serving the lamina base were simultaneously importing labeled photosynthate. The petioles and midveins of maturing leaves were strong sinks for photosynthate, which was diverted from the export front to differentiating structural tissues. The data support the idea of bidirectional transport in adjacent bundles of the petiole and possibly in adjacent sieve tubes within an individual bundle.

(14)C fixation, metabolic labeling patterns, and translocation profiles during leaf development in Populus deltoides.

The incorporation of photosynthetically fixed (14)CO2 and the distribution of (14)C among the main chemical constituents of laminae and petioles were examined in cottonwood (Populus deltoides Bartr. ex Marsh.) leaves ranging in age from Leaf Plastochron Index (LPI) 3 (about one-quarter to one-third expanded) to LPI 30 (beginning of senescence). In addition, carbon flow among chemical fractions and translocation from leaves of LPI 7 and 14 were examined periodically up to 24 h after labeling. Specific activity of (14)C (on dry-weight basis) increased in developing laminae to full leaf expansion, decreased in the mature leaves to LPI 16, then remained constant to LPI 30. In developing leaves (LPI 3-5), after 2 h, most of the (14)C was found in protein, pigments, lipids, and other structural and metabolic components necessary for cell development; only 28% was in the sugar fraction of the lamina. In fully expanded leaves (LPI 6-8), after 2 h, the sugar fraction contained 50-60% and about 90% of fixed (14)C in the lamina and the petiole, respectively. In a pulsechase "kinetic series" with recently mature leaves, 60% of the (14)C was found in the sugar fraction after 15 min of (14)CO2 fixation. Over the 24-h translocation period, (14)C decreased in sugars to 23% and increased in the combined residue fraction (protein, starch, and structural carbohydrates) to about 60% of the total activity left in the lamina. Within 24 h after labeling, the turnover of (14)C-organic acids,-sugar, and-amino acids (either metabolzed or translocated from the leaf) was 30, 70 and 80%, respectively, of that initially incorporated into these fractions by a leaf at LPI 7 (turnover was 55% of (14)C-organic acids, 80% of (14)C-sugar, and 95% of (14)C-amino acids at LPI 14). Anatomical maturity in cottonwood leaves is closely correlated with physiological maturity and with production of translocatable sugar.

Translocation and incorporation of (14)C into the petiole from different regions within developing cottonwood leaves.

The ability of a developing cottonwood (Populus deltoides Bartr.) leaf to export (14)C-labeled assimilates begins at the lamina tip and progresses basipetally with increasing LPI. This progression indicates that portions of leaves function quasi-independently in their ability to export (14)C-photosynthate. Although most of the exported radioactivity was recovered in the petiole as water-80% alcohol-soluble compounds, there was also substantial incorporation into the chloroform and insoluble fractions. This observation indicates that assimilates translocated from the lamina are used in structural development of the petiole. Freeze substitution and epoxy embedding were used to prepare microautoradiographs for localization of water-soluble compounds. Radioactivity was found in all cell types within specific subsidiary bundles of the petiole. However, radioactive assimilates appeared to move from the translocation pathway in the phloem toward active sinks in the walls of the expanding metaxylem cells. Translocation in the mature xylem vessels was not observed.

Incorporation of C-photosynthate into major chemical fractions of source and sink leaves of cottonwood.

The incorporation and distribution of photosynthetically fixed (14)CO(2) was followed for 48 hours in a recently matured source leaf (LPI 7) and in young expanding source and sink leaves (LPI 4) of cottonwood (Populus deltoides Bartr.). The major chemical constituents of leaf laminae and petioles were separated by sequential solvent extractions and enzyme hydrolyses. Two hours after labeling, about 80% of the (14)C was found in water-alcohol-soluble constituents in the mature source lamina as compared to about 45% in those of the young expanding leaf. In both mature and expanding source leaves the water-alcohol-soluble constituents decreased while the CHCl(3)-soluble and -insoluble compounds increased with time. After 48 hours, 7 and 37% of the total (14)C was recovered from structural carbohydrates and from protein + CHCl(3)-soluble fractions, respectively, in the mature source leaf; and 4 and 65%, respectively, in the young source leaf. When the distribution of (14)C among major chemical fractions was calculated on per cent dpm/mg basis, the data showed that a young sink leaf incorporated over twice as much (14)C into structural carbohydrates as a young source leaf (11% versus 4%). However, when calculated on an absolute dpm/mg basis, activity in this fraction of the young source leaf exceeded that in the sink leaf by a ratio of about 11:1 (9528 versus 845 dpm/mg). Thus, most of the material for synthesis of structural carbohydrates was derived from in situ photosynthate.The distribution of (14)C in chemical fractions recovered from petioles was similar to that recovered from their respective laminae, except that petioles incorporated greater amounts (up to 24% of total (14)C) into structural carbohydrates. In contrast to lamina tissue, most of the photosynthate for synthesis of structural carbohydrates in the petioles of young developing leaves was imported from mature leaves farther down the stem.

Distribution of imported (14)C in developing leaves of eastern cottonwood according to phyllotaxy.

Individual leaves of eastern cottonwood (Populus deltoides Bartr.), representing an ontogenetic series from leaf plastochron index (LPI) 3.0 to 8.0, were fed (14)CO2 and harvested after 2-24 h. Importing leaves from LPI-1.0 through 8.0 on each plant were sectioned into 9 parts, and each part was quantitatively assayed for (14)C activity. The highest level of (14)C import was by leaves from LPI 1.0 to 3.0, irrespective of source-leaf age. (14)C was translocated preferentially to either the right or left lamina-half depending on the position of the importing leaf in the phyllotactic sequence and its stage of development. For example, import was high when the importing leaf and the source leaf had two vascular bundles in common, moderately high with one bundle in common, and low with no bundles in common. The distribution of (14)C within young importing leaves was highest in the lamina tip and decreased toward the base. With increasing leaf age, incorporation declined in the lamina tip and increased in the base.It may be concluded that each cottonwood leaf progresses through a continuum of importing and exporting stages as its lamina expands. The photosynthate imported by a given leaf is compartmentalized, with different exporting leaves supplying photosynthate to rather restricted regions of the lamina. Such localization within the importing leaf depends on its vascular connections with each of the exporting leaves, and these are predictable from a knowledge of the phyllotaxy.