Distribution of leaf assimilates in the stem of Picea abies L.

Summary Autoradiographic and microautoradiographic studies of 2-year-old Picea abies plants show that in summer leaf assimilates from the second-year shoot are translocated basipetally. Leaf assimilates are first transported to the stem via leaf trace phloem, then to the base of the stem in the sieve cells of the latest increment of secondary phloem. On the way down leaf assimilates move radially from sieve cells into cells of the phloem parenchyma, the vascular cambium, the rays, the inner periderm and certain cells of pith and cortex, including the epithelial cells surrounding the resin ducts. Other cells of pith and cortex remain nearly free of label, despite the long translocation time (20 h). With the exception of the vascular cambial cells, the stem cells that gain leaf assimilates by radial distribution coincide with those that contain chlorophyll and starch.     

Ethylene-induced microtubule reorientations: mediation by helical arrays

Pruned source-sink transport systems from predarkened plants of Amaranthus caudatus L. and Gomphrena globosa L. were used to study the localization of ¹⁴C-labeled photosynthate imported into experimentally induced sink leaves by microautoradiography. During a 6-h (Amaranthus) or a 4-h (Gomphrena) transport period, ¹⁴C-assimilates were translocated acropetally from a mature source leaf provided with ¹⁴CO₂, into a younger induced sink leaf (dark/-CO₂). In addition, a young still-expanding source leaf exposed to ¹⁴CO₂ exported ¹⁴C-assimilates basipetally into a mature induced sink leaf (dark/-CO₂). Microautoradiographs showed that imported ¹⁴C-photosynthate was strongly accumulated in the sieve element/companion cell complexes of midveins, secondary veins, and minor veins of both the mature and the expanding sink leaf. Some label was also present in the vascular parenchyma and bundlesheath cells. In petioles, ¹⁴C-label was concentrated in the sieve element/companion cell complexes of all bundles indicating that assimilates were imported and distributed via the phloem. Moreover, a considerable amount of radioactivity unloaded from the sieve element/companion cell complexes of petiolar bundles, was densely located at sites of secondary wall thickenings of differen-tiating metaxylem vessels, and at sites of chloroplasts of the vascular parenchyma and bundle-sheath cells. These observations were more striking in petioles of Gomphrena than Amaranthus.Abbreviation se/cc sieve element/companion cell     

Carbon autonomy of reproductive shoots of Siberian alder (<Emphasis Type="Italic">Alnus hirsuta</Emphasis> var.<Emphasis Type="Italic"> sibirica</Emphasis>)

Carbon autonomy of current-year shoots in flowering, and of current-year shoots plus 1-year-old shoots (1-year-old shoot system) in fruiting of Siberian alder (Alnus hirsuta var. sibirica) was investigated using a stable isotope of carbon, ¹³C. The current-year shoot and 1-year-old shoot systems were fed ¹³CO₂ and the atom% excess of ¹³C in flowers and fruits was determined. The majority of photosynthate allocated to flower buds was originally assimilated in the leaves of the flowering current-year shoots. Of all the current-year shoots on fruiting 1-year-old shoots, only those nearest to the fruits allocated the assimilated photosynthate to fruit maturation. These results indicate that the current-year shoots and 1-year-old shoot systems are carbon-autonomous units for producing flowers and maturing fruits, respectively.     

Structure and development of sieve cells in the secondary phloem of Larix decidua Mill. as related to function

Summary Only one or two layers of sieve cells of the previous year's phloem in lateral branches of Larix decidua persist as fully mature cells. Immature sieve cells or cambial derivatives that have not completed differentiation may also over-winter. Periclinal cell divisions of the vascular cambium were first observed by mid-April. During the short period of greatest cambium activity (mid-April to mid-May), the early phloem is laid down. Late phloem is formed over a much longer period, from mid-May to late September. Microautoradiography revealed that only mature sieve cells of the early phloem are involved in translocation of ¹⁴C assimilates in June. The fine structure of actively translocating sieve cells is described. The impact of structure on long-distance transport of assimilates is discussed.     

Seasonal changes in the utilization and turnover of assimilation products in 8-year-old Scots pine (Pinus sylvestris L.) trees

Summary The present study aimed at a physiological understanding of the seasonal changes of the carbohydrate patterns and levels in the various tissues of 8-year-old Scots pine (Pinus sylvestris L.) trees growing under ambient climatic conditions in the botanical garden at Bayreuth. The photosynthates of selected twig sections were labelled by ¹⁴CO₂ fixation and after chase periods of 1 h up to 8 months, the distribution of radiocarbon in the whole trees was determined and the labelling of identified carbohydrates was compared with the levels of these compounds in the individual tissues. Bud break and sprouting in spring is exclusively supplied by the recent photosynthates of the previous year's needles. During summer assimilates of the old needles were utilized for secondary growth of the axial system while growth of the recent-year's shoots was supported by their own photosynthesis. In autumn, soluble carbohydrates were produced instead of starch, a major part of which in addition to recent photosynthates was utilized for root growth during the cold season. Another part of the autumnal storage material was incorporated into the cell walls of the latest xylem and phloem elements still in winter. A pronounced starch-oligosaccharide interconversion upon frost hardening, and its reversal in spring as has been described for deciduous trees, could not be observed. This was due to maintenance of photosynthetic capability even in the cold season and the replacement of consumed storage material especially in late winter and early spring by new photosynthates.     

Conductance of needle and twig axis phloem of damaged and intact Norway spruce (Picea abies (L.) Karst.) as investigated by application of14C in situ

Summary Phloem conductance of¹⁴C-labelled assimilates was investigated in natural stands of Norway spruce showing substantial damage from needle yellowing and needle loss disease. Terminal current-year shoots of a branch were allowed to fix¹⁴CO₂ (300–600 ppm in air) and carbon dioxide net uptake was monitored with a gas analyser. The difference between¹⁴C-uptake and the amount of radiocarbon determined in the photosynthesizing needles was interpreted to reflect assimilate export from the needles to the axis of the tree. Compared with an undamaged control tree,¹⁴C-export from the assimilating needles was not impaired in the yellowing tree and only slightly reduced in the tree showing needle loss. Incorporation of¹⁴C into starch increased significantly during autumn particularly in the tree showing needle loss. Import of radiocarbon from the¹⁴C-labelled phloem sap in twig axes and needles older than 1 year was used as a measure of phloem conductivity of older sections of a branch which showed considerable damage. Carbon uptake by these older plant parts was more pronounced than in undamaged twigs. In the case of older needles enhancement of¹⁴C-incorporation suggested an increased sink strength, while the same phenomenon in the twig axes was interpreted as a consequence of partially impaired conductivity of individual sieve elements resulting in an inhomogeneous velocity of phloem transport. The hypothesis is put forward that curtailed viability of the sieve cells is responsible for a delay of transport, which is compensated for by an augmented production of phloem elements from the cambium.     

Control of Adventitious Root Production and Hypocotyl Hypertrophy of Sunflower (Helianthus annuus) in Response to Flooding

Needles of 20-year-old Scots pine trees (Pinus silvestris L.) were permitted to photoassimilate ¹⁴CO₂ for 1 h on different dates during the growing season. The loss of radioactivity from current, 1-year-old, and 2-year-old needles was followed, and the translocation of photoassimilated ¹⁴CO₂ from older needle age-classes to the elongating new needles studied. The effects of good mineral and water supply on translocation were also considered. In the spring, 1-year-old and 2-year-old needles accumulated ¹⁴C. These reserves, together with current photosynthate, were utilized when the trees started growing. The 1-year-old needles exported ¹⁴C to the current needles during the first weeks of elongation of the later, while no such translocation occurred from the 2-year-old needles. Removal of the 1-year-old needles resulted in translocation of assimilates from the 2-year-old needles to the current needles. The general pattern of translocation observed in the control trees was not changed when the trees were fertilized and irrigated. The new needles started to export assimilates in the middle of July when the photosynthetic rate per needle was comparable with that of the older age-classes. This occurred about 4 weeks after positive net photosynthesis was first measured for the current shoot. The current needles of trees with good nutrient and water supply seemed to become self-sufficient in photoassimilates earlier than the current needles of the control trees.     

Biodegradation of Trichloroacetic Acid in Norway Spruce/Soil System

Trichloroacetic acid (TCA) belongs to secondary atmospheric pollutants affecting the forest health. Distribution of [1,2-¹⁴C]TCA-residues and TCA biodegradation were investigated in 4-year-old nursery-grown trees of Norway spruce [Picea abies (L.) Karst.] in the whole plant/soil system. Radioactivity was monitored in needles, wood, roots and soil as well as in the air. During two weeks of exposure TCA was continuously degraded, especially in the soil. Estimates of radioactivity balance showed loss of radioactivity into the atmosphere in the form of ¹⁴CO₂; unincorporated [1,2-¹⁴C]TCA, chloroform, carbon monoxide and methane were not detected at all. TCA degradation to CO₂ was indicated also in the spruce needles. Moreover, it was found that soil litter contained [1,2-¹⁴C]TCA unavailable to microorganisms.     

Microautoradiographic studies of phloem loading and transport in the leaf of Zea mays L.

Microautoradiographs showed that [¹⁴C]sucrose taken up in the xylem of small and intermediate (longitudinal) vascular bundles of Zea mays leaf strips was quickly accumulated by vascular parenchyma cells abutting the vessels. The first sieve tubes to exhibit ¹⁴C-labeling during the [¹⁴C]sucrose experiments were thick-walled sieve tubes contiguous to the more heavily labeled vascular parenchyma cells. (These two cell types typically have numerous plasmodesmatal connections.) With increasing [¹⁴C]sucrose feeding periods, greater proportions of thick- and thin-walled sieve tubes became labeled, but few of the labeled thin-walled sieve tubes were associated with labeled companion cells. (Only the thin-walled sieve tubes are associated with companion cells.) When portions of leaf strips were exposed to ¹⁴CO₂ for 5 min, the vascular parenchyma cells-regardless of their location in relation to the vessels or sieve tubes-were the most consistently labeled cells of small and intermediate bundles, and label (¹⁴C-photosynthate) appeared in a greater proportion of thin-walled sieve tubes than thick-walled sieve tubes. After a 5-min chase with ¹²CO₂, the thin-walled sieve tubes were more heavily labeled than any other cell type of the leaf. After a 10-min chase with ¹²CO₂, the thin-walled sieve tubes were even more heavily labeled. The companion cells generally were less heavily labeled than their associated thin-walled sieve tubes. Although all of the thick-walled sieve tubes were labeled in portions of leaf strips fed ¹⁴CO₂ for 5 min and given a 10-min ¹²CO₂ chase, only five of 72 vascular bundles below the ¹⁴CO₂-exposed portions contained labeled thick-walled sieve tubes. Moreover, the few labeled thick-walledsieve tubes of the transport region always abutted ¹⁴C-labeled vascular parenchyma cells. The results of this study indicate that (1) the vascular parenchyma cells are able to retrieve at least sucrose from the vessels and transfer it to the thick-walled sieve tubes, (2) the thick-walled sieve tubes are not involved in long-distance transport, and (3) the thin-walled sieve tubes are capable themselves of accumulating sucrose and photosynthates from the apoplast, without the companion cells serving as intermediary cells.     

Involvement of Exported Photosynthetic Products in the CO2Exchange of the Skeletal Shoots of Pine

CO₂exchange in the leafy and skeletal parts of attached shoots of Pinus sylvestrisL. was measured with an infrared gas-analyzer in an open differential system during daylight hours. The ¹⁴CO₂assimilation rates in the leafy parts of shoots and ¹⁴CO₂evolution from current photosynthetic products in the lower skeletal part of shoots were measured in afternoons. Chlorophyll content was measured in the needles of the same shoot. The carbon of exported assimilates contributed only about 4% to CO₂exchange in the heterotrophic tree tissues. Only this component of CO₂evolution from the surface of the skeletal part of the tree was related to the losses of the net primary photosynthetic production (NPP) in the aboveground part of the pine stand during the current growth period.     

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 ¹⁴C-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 ¹⁴CO₂, label was exported through specific bundles in the petiole associated with that vein. When the whole lamina of a mature source leaf was fed ¹⁴CO₂, 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.Abbreviations C central leaf trace - L left leaf trace - LPI leaf plastochron index - R right leaf trace     

Apoplastic Transport of 14C-Photosynthates Measured under Drought and Nitrogen Supply

Using water infiltration of the plant and individual shoots with the subsequent intercellular liquid extraction by the pressure chamber, dynamics of the movement ¹⁴C-photosynthates from cell to apoplast, and ¹⁴C distribution among photosynthetic products in mesophyll cells and apoplast were studied. The relative quantity of ¹⁴C-photosynthetes in leaf apoplast depended on growing conditions; drought increased, and nitrate supply decreased it. When the middle leaves absorbed ¹⁴CO₂, photosynthates moving down in stem phloem appeared in intercellular space, where they were transported up by transpiration stream. ¹⁴C-photosynthates entering to the apex and young leaves were utilized a accumulated, and photosynthates transported to the mature leaves were reloaded into the phloem and reexported. Thus, photosynthates circulated through the plant and were redistributed to the plant organs according to their transpiration. In leaf apoplast photosynthetic sucrose was partly hydrolyzed to glucose and fructose. This increased under high nitrogen supply. The result indicate that apoplast sucrose hydrolysis is the basic cause of the reduction of photosynthate flux from leaves when the nitrate concentration in soil increases.     

MOBILIZATION BY PINUS RESINOSA CONES AND SHOOTS OF C14-PHOTOSYNTHATE FROM NEEDLES OF DIFFERENT AGES

Current-year, 1-year-old, 2-year-old, and 3-year-old needles of 25- to 30-year-old Pinus resinosa trees were separately exposed to C¹⁴O₂ at various times during the growing season. Currently produced C¹⁴-photosynthate was preferentially mobilized in the following order: second-year cones > current needles > current internodes > first-year conelets. A changing seasonal pattern was shown in sources of current photosynthate for growth of cones and shoots. One-year-old needles were the major source of current photosynthate for growth of both cones and shoot internodes. During June the 2- and 3-year-old needles contributed appreciable amounts of current photosynthate to both cones and developing shoots, but after late June their contribution was slight. The supply of carbohydrates to all tissues, except 2nd-year cones, from the three age classes of old needles declined late in the season as tissues mobilized increasingly more carbohydrates from current-year needles. Nevertheless, the bulk of the C¹⁴-photosynthate produced by current-year needles was retained by them. The preferential mobilization of carbohydrates by reproductive tissues over vegetative tissues is emphasized as is the importance of both reserve and currently produced carbohydrate for growth of various tissues.     

Das Phloem der Haustorien vonCuscuta

Summary Haustoria ofCuscuta odorata R. & P. andC. grandiflora H.B.K. show continuous traces of sieve elements, connecting the phloem of the host with that of theCuscuta shoot. The continuity of this haustorial phloem is discernible by callose fluorescence after staining with aniline blue. The fine structural criteria for sieve tubes are analyzed electronmicroscopically, with special respect to sieve pores, P-protein, and a distinct wall-standing smooth surfaced ER. Within the central part of the haustorium sieve tubes are elongated, while the elements abutting the phloem of theCuscuta shoot are nearly isodiametric in shape. Both elements are associated with rather large companion cells, derived from an unequal division.

     

宁夏枸杞果实韧皮部及其周围细胞超微结构研究

应用透射电镜技术研究了宁夏枸杞果实韧皮部细胞的超微结构变化。结果表明:(1)随着枸杞果实的发育成熟,果实维管组织中的韧皮部筛分子筛域逐渐变宽,筛孔大而多,通过筛孔的物质运输十分活跃;筛分子和伴胞间有胞间连丝联系,伴胞属传递细胞类型,与其相邻韧皮薄壁细胞和果肉薄壁细胞连接处的细胞界面发生质膜内突,整个筛分子/伴胞复合体与韧皮薄壁细胞之间形成共质体隔离,韧皮部糖分的卸载方式主要以质外体途径进行。(2)韧皮薄壁细胞间的胞间连丝较多,而韧皮薄壁细胞与果肉薄壁细胞的胞间连丝相对较少,但果肉薄壁细胞间几乎无胞间连丝;果肉薄壁细胞之间胞间隙较大,细胞壁和质膜内突间形成较大的质外体空间,为质外体的糖分运输创造了条件。(3)筛管、伴胞、韧皮薄壁细胞和果肉薄壁细胞中丰富的囊泡以及活跃的囊泡运输现象,暗示囊泡也参与了果实糖分的运输过程。研究推测,枸杞果实韧皮部同化物的卸载方式以及卸载后的同化物运输主要以质外体途径为主。     

Simultaneous inhibition of translocation of photosynthate and of the floral stimulus by localized low-temperature treatment in the short-day plant Pharbitis nil

There is considerable evidence to indicate that the floral stimulus moves along with photosynthate in the phloem. In the present study the effect of cooling a localized region of the stem of the short-day plant Pharbitis nil Chois. on translocation was investigated. This low-temperature treatment simultaneously inhibited translocation of photosynthate and of the floral stimulus, thus further supporting the idea that the floral stimulus is transported concurrently with assimilates in the phloem.     

CO2 fixation in stem slices of Picea abies (L.) Karst: microautoradiographic studies

Summary Microautoradiography was used to show that chlorophyllous cells of young Picea abies stem slices are able to fix ¹⁴CO₂, in the dark as well as in the light. The amount of ¹⁴CO₂ fixed in the dark is much lower than that in the light. In the dark the concentration of radioactive label is equally high in all chlorophyllous cells of the stem. In the light, however, a gradient of radioactive assimilates extends from the stem surface to its centre, with the highest concentration being located in the phelloderm and the outer one-third of the cortex. This is in spite of even illumination and CO₂ supply across the whole stem slice. In the dark, stem slices with and without bark show the same amount of radioactive label in the chlorophyllous cells of xylem, perimedullary region and pith. In the light, however, the concentration of radioactive assimilates in these cells is much higher in stem slices with bark than in stem slices without bark. It is assumed therefore that light fixation products of phelloderm and cortex are transported radially into the tissue inside the cambium.     

Photosynthesis and distribution of photosynthates in apple shoots treated by pinching and bark ringing

Individual leaves on apple shoots treated by pinching and/or ringing were supplied with¹⁴CC₂ and the rate of photosynthesis and the pattern of photosynthate distribution was studied. The ringing of the shoots as well as the ringing and pinching done together reduces the rate of photosynthesis almost by half. Pinching itself had no effect on the rate of photosynthesis. Removing the main sink — the growing shoot apex — by pinching leads to the accumulation of photosynthates in the shoot, mainly in the first internode below the pinching point. Accumulated assimilates were soon used up by the axillary meristems which were stimulated to grow by pinching. Very small amounts of assimilates (about 1 %) were translocated to adjacent shoots which were supplied by their own leaves. When adjacent shoots were defoliated, more assimilates were translocated there (nearly 8%), however, a strong tendency to accumulate the assimilates in the internode below the pinching point was observed. Assimilates are not located in matured leaves. The presence of an active sink located near the donor stimulates the mobilization of assimilates present in the donor leaf.     

Carbon allocation in shoots of alpine treeline conifers in a CO<Subscript>2</Subscript> enriched environment

With a new approach we assessed the relative contribution of stored and current carbon compounds to new shoot growth in alpine treeline conifers. Within a free air CO₂ enrichment experiment at the alpine treeline in Switzerland, ¹³C-depleted fossil CO₂ was used to trace new carbon in the two tree species Larix decidua L. and Pinus uncinata Ramond over two subsequent years. The deciduous L. decidua was found to supply new shoot growth (structural woody part) by 46% from storage. Surprisingly, the evergreen P. uncinata, assumed to use current-year photosynthates, also utilized a considerable fraction of storage (42%) for new wood growth. In contrast, the needles of P. uncinata were built up almost completely from current-year photosynthates. The isotopic composition of different wood carbon fractions revealed a similar relative allocation of current and stored assimilates to various carbon fractions. Elevated CO₂ influenced the composition of woody tissue in a species-specific way, e.g. the water soluble fraction decreased in pine in 2001 but increased in larch in 2002 compared to ambient CO₂. Heavy defoliation applied as an additional treatment factor in the second year of the experiment decreased the lipophilic fraction in current-year wood in both species compared to undefoliated trees. We conclude that storage may play an important role for new shoot growth in these treeline conifers and that altered carbon availability (elevated CO₂, defoliation) results in significant changes in the relative amount of mobile carbon fractions in woody tissue. In particular, stored carbon seems to be of greater importance in the evergreen P. uncinata than has been previously thought.     

Seasonal Changes in the Distribution of Photo-assimilated C in Young Pine Plants

Pinus strobus L. plants in their third year of growth were permitted to photoassimilate ¹⁴CO₂ for about 1 hour at monthly intervals between April and October, and the subsequent distribution of ¹⁴C in these plants was determined 8 hours, 1 month, 2 months or 4 months after photo-assimilation. In this way, the fate of ¹⁴CO₂ photo-assimilated during different months of the growing season was observed.

In the spring, old needles played a significant role in photo-assimilating ¹⁴CO₂ and exporting current photosynthate to the developing new shoots and roots. By July, the new shoot had replaced the old shoot both as the primary photo-assimilating part of the plant and as an exporter, particularly to the root.

The root received current photosynthate from the shoot throughout the entire growing season, although plant analysis only 8 hours after photo-assimilation did not always reveal this. Translocation of recent photosynthate from shoot to root was particularly high in August, September, and October.

The amounts of photo-assimilated ¹⁴C lost from the plants over a 4 month interval, principally through respiration and photorespiration, were about one-half of that absorbed during photo-assimilation, with the greatest loss occurring within the first month.