A THREE-DIMENSIONAL RECONSTRUCTION OF THE VASCULAR SYSTEM TO THE LODICULES,ANDROECIUM, AND GYNOECIUM OF A FERTILE FLORET OF PANICUM DICHOTOMIFLORUM (GRAMINEAE)

A three-dimensional reconstruction of a fertile floret stele of Panicum dichotomiflorum approaching anthesis was made by a new technique using superimposition of tracings of 80, 1-μm thick serial sections, cleared tracing film, and mounting adhesive. From a collateral bundle, which also served as the median trace to the fertile lemma, most of the vascular tissue branched adaxially and horizontally to become the sole vascular supply to the two lodicules, three stamens, and pistil. The xylem branched at a low level to form a broad and long vessel plexus. The phloem branched at a higher level to overlay the vessel plexus on the right and left with an arc of horizontal sieve tubes in a phloem plexus. Those sieve tubes and vessels which rose after branching from the horizontal plexi assumed a more vertical course in the floret stele. Traces to the right and left lodicules arose from the lower abaxial portions of the flanks of the floret stele. Vessels ascended vertically from the xylem plexus and passed through the phloem plexi and joined with the sieve tubes there to exit at the same level and become the right and left lodicule traces. The vascular tissues to the three filament traces arose from different higher levels of the stele. The sieve tubes for the median filament trace arose vertically from the abaxial side between but above the lodicule traces. At higher levels the sieve tubes for the lateral filaments rose from the horizontal arcs of the flanks of the stele and departed it tangentially. The vessels destined to the filament traces arose in the center of the floret stele from adaxial portions of the horizontal plexus, ascended between the arcs of phloem, exited the stele simultaneously above the phloem of the traces, and followed the courses of their respective sieve tubes. The adaxially displaced apex of the floret stele then contained the vascular tissue related to the pistil. All the sieve tubes and vessels of the floret stele were embedded in a matrix of intermediary cells. The peripheral intermediary cells associated with the vessel plexus were xylem transfer cells with pronounced wall ingrowths. At higher levels in the floret stele, intermediary cells in scattered locations near sieve tubes or vessels had less conspicuous wall ingrowths. No preferred orientation of transfer cells with any particular trace was noted.     

Ultrastructure of transfer cells in spontaneous nodules of alfalfa (Medicago sativa)

Summary Spontaneous nodules were formed on the primary roots of alfalfa plants in the absence ofRhizobium. Histologically, these white single-to-multilobed structures showed nodule meristems, cortex, endodermis, central zone, and vascular strands. Nodules were devoid of bacteria and infection threads. Instead, the larger cells were completely filled with many starch grains while smaller cells had very few or none. Xylem parenchyma and phloem companion cells exhibited long, filiform and branched wall ingrowths. The characteristic features of both types of transfer cells were polarity of wall ingrowths, high cytoplasmic density, numerous mitochondria, abundant ribosomes, well-developed nucleus and nucleolus, and vesicles originated from rough endoplasmic reticulum. These results were compared with normal nodules induced byRhizobium. Our results suggest that xylem parenchyma and phloem companion transfer cells are active and probably involved in the short distance transport of solutes in and out of spontaneous nodules. Since younger nodules showed short, papillate, and unbranched wall ingrowths, and older tissue showed elongated, filiform and branched wall ingrowths, the development of wall ingrowths seemed to be gradual rather then abrupt. The occurrence of both type-A and -B wall ingrowths suggests that phloem companion transfer cells may be active in loading and unloading of sieve elements. Since there were no symbiotic bacteria and thus no fixed nitrogen, it is tempting to speculate that xylem parenchyma transfer cells may be re-transporting accumulated carbon from starch grains to the rest of the plant body by loading xylem vessels. Fusion of ER-originated vesicles with wall ingrowth membrane indicated the involvement of ER in the membrane formation for elongating wall ingrowths. Since transfer cells were a characteristic feature of both spontaneous andRhizobium-induced nodules, their occurrence and development is controlled by the genetic make-up of alfalfa plant and not by a physiological source or sink emanating from symbiotic bacteria.Abbreviations ATP adenosine triphosphate - ATPase adenosine triphosphatase - EH emergent root hair - EM electron microscope - Nar nodulation in the absence of Rhizobium - RT root tip - RER rough endoplasmic reticulum - YEMG yeast extract mannitol-gluconate     

ATPase in mature and differentiating phloem and xylem

A cytochemical study using a lead precipitation technique has been made of the distribution of adenosine triphosphatase (ATPase) in mature and differentiating phloem and xylem cells of Nicotiana tabacum and Pisum sativum. The sites of ATPase localization in tobacco phloem were the plasma membrane, endoplasmic reticulum, mitochondria, dictyosomes, plasmodesmata, and the dispersed P proteins of mature sieve elements. In pea phloem sieve elements ATPase was localized in the endoplasmic reticulum, but was not associated with the P proteins or plasma membranes at any stage of their differentiation. In pea transfer cells ATPase activity was associated with the endoplasmic reticulum at all stages of their differentiation and with the plasma membrane of transfer cells that had formed wall ingrowths. In xylem cells of both tobacco and pea the patterns of ATPase activity was similar. At early stages of differentiation ATPase activity was associated with the plasma membrane and the endoplasmic reticulum. At intermediate stages of differentiation ATPase activity continued to be associated with the endoplasmic reticulum, but was no longer associated with the plasma membrane. At later stages of xylem element differentiation ATPase activity was associated with disintegrating organelles and with the hydrolyzing cell walls.     

Structural and ultrastructural characteristics of the vascular apparatus of the sensitive plant (Mimosa pudica L.)

Summary 1. In motor organs ofMimosa pudica xylem contains living fibriform elements limited by a thick lignified highly pitted wall, whereas in other parts of the plant (stem, petiole, rachis), xylem and protoxylem vessels are closely associated with parenchyma cells which possess wall ingrowths. These ingrowths, at the apex of which the plasmalemma and the tonoplast touch, are localized like those of transfer cells of C type described byGunning andPate. Nevertheless, xylem parenchyma cells differ from cells of C type in several characteristics. Moreover, in motor organs, phloem contains cells characterized by wall ingrowths, less abundant on the parts adjacent to the sieve tubes; these cells which are localized near collenchyma cells of primary phloem, look like transfer cells of A type defined byGunning andPate; they are absent from internodes, petioles and rachides. 2. In motor organs, three types of vascular cells (companion cells, living xylem fibriform elements and protoxylem parenchyma cells) are characterized by reduced vacuolar volumes and well developed membrane systems, as compared with homologuous cells belonging to other parts of the plant. 3. A symplastic continuity holds from the middle of motor organs to their cortex: it is provided by the presence, in xylem and phloem respectively, of living fibriform elements and collenchyma cells bearing numerous pit fields containing large numbers of plasmodesmata. Several ultrastructural features suggest that the vascular apparatus ofMimosa pudica would be the site of intensive lateral transfer at different levels, specially in motor organs. Possible functions of certain structures observed are discussed in relation to some hypotheses relative to excitatory conduction pathways.     

Vascular transfer cells in Angiosperm leaves A taxonomic and morphological survey

Summary A study of the fine structure of minor veins of mature leaves of 975 species and 242 families of Angiosperms shows that transfer cells are widespread amongst herbaceous Dicotyledons, are much rarer in woody Dicotyledons, and are virtually absent from the Monocotyledons. The evolutionary significance of the distribution of the cells amongst and within orders, families and minor groupings is discussed.Four types of transfer cell are recognized in minor veins, all possessing irregular ingrowths of wall material protruding into their protoplasts, and all being regarded as modified parenchyma of the minor vein. Two types occur in phloem. One (the A-cell), with ingrowths distributed right round its periphery, is associated specifically with the sieve elements. The other (the B-cell) occurs more generally throughout the phloem and has zones of wall ingrowths oriented towards sieve elements and their associated companion cells or A-cells. Two other types (C- and D-cells) occur in xylem parenchyma and bundle sheath respectively, and have ingrowths only on walls in contact with or in close proximity to vessels or tracheids. Each species has a characteristic combination of types of transfer cell. The variations encountered in the survey are classified. Consistent differences in the frequency and form of ingrowths are to be found between the different types of transfer cell of a single species, and between different species in respect to a particular type of transfer cell.The functional significance of transfer cells in minor veins is discussed in relation to the loading and unloading of the conducting elements and to the retrieval of extra-cytoplasmic solutes from the mesophyll and the transpiration stream.     

Cytochemical localization of adenosine triphosphatase in the phloem of Pisum sativum and its relation to the function of transfer cells

The cytochemical localization of ATPase in differentiating and mature phloem cells of Pisum sativum L. has been studied using a lead precipitation technique. Phloem transfer cells at early stages of differentiation exhibit strong enzyme activity in the endoplasmic reticulum (ER) and some reaction product is deposited on the vacuolar and plasma membranes. As the phloem transfer cells mature and develop their characteristic wall structures, strong enzyme activity can be observed in association with the plasma membranes and nuclear envelopes. Mature phloem transfer cells with elaborate cell-wall ingrowths show ATPase activity evenly distributed on plasma-membrane surfaces. Differentiating sieve elements show little or no enzyme activity. When sieve elements are fully mature they have reaction product in the parietal and stacked cisternae of the ER. There is no ATPase activity associated with P-protein at any stage of sieve-element differentiation or with the sieve-element plasma membranes. It is suggested that the intensive ATPase activity on the plasma membranes of the transfer cells is evidence for a transport system involved in the active movement of photosynthetic products through these cells.Key to labeling in the figures ER endoplasmic reticulum - P parenchyma cell - PP P-protein - SE sieve element - SPP sieve-plate pore - TC transfer cell     

A Study of Stelar Ultrastructure in the Heterosporous Water Fern Marsilea quadrifolia L

Sieve tube elements occur in the rhizomes and petioles of Marsileaquadrifolia. These are either thick walled with compound sieveplates in oblique end walls or thin walled with simple sieveplates in transverse end walls. Vessels are restricted to themetaxylem in the roots where the phloem contains sieve cellsonly. The sieve pores are invariably callose lined and as inother pteridophytes, excepting the Lycopsida, refractive spherulesare ubiquitous in the sieve elements of Marsilea. The luminaof the protoxylem tracheary elements in the rhizomes and petiolesare occluded by tyloses but probably remain functional in theroots. Pericycle cells backing on to the root protoxylem armspossess wall ingrowths. Transfer cells are however absent fromthe vascular tissue of the rhizomes and leaves. It is suggestedthat their presence in the root pericycle is related to theretrieval of ions from the xylem sap which may be particularlycritical in water plants. The incidence of transfer cells incryptogams appears to be far more sporadic than in angiosperms.The root endodermis of Marsilea possesses a casparian stripand abundant vacuolar tannin deposits. Plasmalemmasomes arenumerous adjacent to the pericycle transfer cells. vascular ultrastructure, Marsilea quadrifolia L, transfer cells, sieve tube elements, tyloses     

A xylem sap retrieval pathway in rice leaf blades: evidence of a role for endocytosis?

The structure and transport properties of pit membranes at the interface between the metaxylem and xylem parenchyma cells and the possible role of these pit membranes in solute transfer to the phloem were investigated. Electron microscopy revealed a fibrillar, almost tubular matrix within the pit membrane structure between the xylem vessels and xylem parenchyma of leaf blade bundles in rice (Oryza sativa). These pits are involved primarily with regulating water flux to the surrounding xylem parenchyma cells. Vascular parenchyma cells contain large mitochondrial populations, numerous dictyosomes, endomembrane complexes, and vesicles in close proximity to the pit membrane. Taken collectively, this suggests that endocytosis may occur at this interface. A weak solution of 5,6-carboxyfluorescein diacetate (5,6-CFDA) was applied to cut ends of leaves and, after a minimum of 30 min, the distribution of the fluorescent cleavage product, 5,6-carboxyfluorescein (5,6-CF), was observed using confocal microscopy. Cleavage of 5,6-CFDA occurred within the xylem parenchyma cells, and the non-polar 5,6-CF was then symplasmically transported to other parenchyma elements and ultimately, via numerous pore plasmodesmata, to adjacent thick-walled sieve tubes. Application of Lucifer Yellow, and, separately, Texas Red-labelled dextran (10 kDa) to the transpiration stream, confirmed that these membrane-impermeant probes could only have been offloaded from the xylem via the xylem vessel-xylem parenchyma pit membranes, suggesting endocytotic transmembrane transfer of these membrane-impermeant fluorophores. Accumulation within the thick-walled sieve tubes, but not in thin-walled sieve tubes, confirms the presence of a symplasmic phloem loading pathway, via pore plasmodesmata between xylem parenchyma and thick-walled sieve tubes, but not thin-walled sieve tubes.     

Function of transfer cells in the nodal regions of stems,particularly in relation to the nutrition of young seedlings

Summary The distribution and time course of development of transfer cells in the hypocotyl region of lettuce (Lactuca sativa L.) and groundsel (Senecio vulgaris L.) are examined by light microscopy of serial sections through a sequence of ages of hypocotyls. Investments of xylem transfer cells occur in departing traces to the cotyledons and, later, in the traces to foliage leaves; phloem transfer cells are widely distributed but particularly prominent in those bands of protophloem in the plumule vasculature which lie alongside xylem of the cotyledonary traces. Both classes of transfer cell are well endowed with wall ingrowths before differentiation of xylem and perforation of stomata occurs in the plumule. Autoradiographic evidence is obtained of a transport pathway from cotyledonary trace xylem elements to xylem transfer cell to plumule, and analyses of xylem sap collected from above or below the zones of transfer cells in the hypocotyl show that certain materials can be removed from the xylem sap by transfer cells as it moves towards the cotyledons. From these findings it is concluded that the seedling transfer cells play an important role in nutrition of the young plumule, particularly before the latter has become adequately connected with the vascular systems of cotyledons and root.Experiments on the experimental modification of transfer cell development in the hypocotyl suggest that both photosynthetic fixation of carbon dioxide and a transpirational loss of water by a cotyledon must take place before the presumptive xylem transfer cells in its traces can develop normal sets of wall ingrowths.Discussion is extended to the general role of transfer cells in the nodal regions of stems. Possible functions envisaged are, the general nutrition of young tissues of the apical region, the abstraction of assimilates for local storage, the transfer of assimilates to axillary buds released from apical dominance, and the interchange of assimilates between adjacent vascular traces running through the node.     

Multinucleate transfer cells induced in coleus roots by the root-knot nematode,Meloidogyne arenaria

Summary The occurrence and position of wall protuberances in giant cells induced in coleus roots by the root-knot nematodeMeloidogyne arenaria is described, and the structure and function of giant cells is compared with that of syncytia induced by cyst-nematodes.Extensive protuberance development occurs on walls of giant cells adjacent to xylem vessels. Protuberances are less well developed next to sieve elements, and almost absent next to parenchyma cells. On walls between giant cells they occur on both sides or only one side. The formation of protuberances indicates that giant cells are multinucleate transfer cells. The position of protuberances marks the wall area where solutes enter the cell. Solutes are obtained from xylem and phloem elements, and the position of protuberances at the junction between giant cells and vascular elements indicates an extensive flow of solutes along cell walls. The observations support the hypothesis that wall protuberances form as a result of selective solute flow across the plasmalemma.No cell wall dissolution was observed, although wall gaps may occur between giant cells as a result of breakage during rapid cell expansion.     

Role of light and jasmonic acid signaling in regulating foliar phloem cell wall ingrowth development

Phloem cells adjacent to sieve elements can possess wall invaginations. The role of light and jasmonic acid signaling in wall ingrowth development was examined in pea companion cells (CCs), Arabidopsis thaliana phloem parenchyma cells (PCs), and in Senecio vulgaris (with ingrowths in both cell types). Features characterized included wall ingrowths (from electron microscopic images), foliar vein density and photosynthetic capacity. In Arabidopsis, wall ingrowths were bulky compared with finger-like invaginations in pea and S. vulgaris. Relative to low light (LL), wall invagination in both CCs and PCs was greater in high light (HL). Treatment with methyl jasmonate in LL had no effect on CCs, but increased PC wall ingrowths. LL-to-HL transfer resulted in significantly less wall ingrowth in the fad7-1 fad8-1 (jasmonate-deficient) Arabidopsis mutant relative to the wild type. These results suggest that chloroplast oxidative status, via chloroplast-derived jasmonates, may modulate phloem structure and function. While CC wall ingrowths facilitate phloem loading by expanding the membrane area available for active uptake, one can speculate that phloem PC ingrowths may have two potential roles: to increase the efflux of sugars and/or protons into the apoplast to augment phloem loading; and/or to protect the phloem against pathogens and/or insects.     

Transfer cells and nematode induced giant cells inHelianthemum

Summary The morphology of wall ingrowths in xylem and phloem transfer cells inHelianthemum is different. It is possible to use nematode infection to induce the formation of giant cells which abut both xylem and phloem elements to test whether ingrowth morphology is controlled by the solutes presumed to be transported across the plasmalemma of the cells. This experiment has been done and it is found that although wall ingrowths develop against both xylem and phloem, the giant cells exhibit only the ingrowth structure characteristic of xylem transfer cells.     

THE TIME COURSE OF SIEVE TUBE AND VESSEL REGENERATION AND THEIR RELATION TO PHLOEM ANASTOMOSES IN MATURE INTERNODES OF COLEUS

Quantitative counts of regenerative sieve tubes and vessels were made in a large number of samples of mature internode #5 of C. blumei, with concomitant study of the fine details of vascular regeneration and the occurrence of the normally developing phloem anastomoses. Such anastomoses were found in many of the plants, but their average number in the small regenerating area was low (viz., 0.9 ± 0.2). With the phloem anastomoses excluded from the counts, the time course of regeneration was clear cut—no strands completed their regeneration around the wound until three days after wounding. More regenerative sieve tubes completed their differentiation under all conditions than did regenerative vessels. The number of sieve tubes and vessels regenerated by four days was closely related to the number of preexisting bundles of that type of vascular cell that had been severed by the transverse wound. The ratio of bundles severed by the wound in the phloem to those in the xylem was 2.14, and the ratio of the regenerative sieve tubes to the regenerative vessels was 2.24. For both tracheary and sieve tube cells the initial regeneration was strongly polar (mostly above the wound), as expected from earlier IAA transport data. The path of tracheary regeneration was obviously related to that of the sieve tubes on the other side of the cambium.     

Immunogold localization of callose and other cell wall components in pea nodule transfer cells

Summary Transfer cells are located adjacent to xylem and phloem elements in pea nodule vascular tissues. The composition of the labyrinthine wall intrusions was investigated by immunogold labeling using specific antibody probes. Callose antigen was found at the base of newly formed cell wall intrusions and also in adjacent plasmodesmata. Sections through developed labyrinthine intrusions revealed that wall ingrowths had an internal structure with small domains of callose suggesting the presence of channels or vents. Xyloglucan and pectin antigens were uniformly distributed within the wall, but the distribution of extensin antigens was variable, with different antigens being detected in different regions of the wall ingrowth. A lectinlike glycoprotein, PsNLEC-1, was localized in intercellular spaces associated with nodule transfer cells. Previously, expression of this component was observed in other types of cells showing complex involution of the plasma membrane, namely root cortical cells harboring arbuscular mycorrhizae and nodule cells harboring nitrogen-fixing rhizobia.     

Minor vein structure and sugar transport in Arabidopsis thaliana

Leaf and minor vein structure were studied in Arabidopsis thaliana (L.) Heynh. to gain insight into the mechanism(s) of phloem loading. Vein density (length of veins per unit leaf area) is extremely low. Almost all veins are intimately associated with the mesophyll and are probably involved in loading. In transverse sections of veins there are, on average, two companion cells for each sieve element. Phloem parenchyma cells appear to be specialized for delivery of photoassimilate from the bundle sheath to sieve element-companion cell complexes: they make numerous contacts with the bundle sheath and with companion cells and they have transfer cell wall ingrowths where they are in contact with sieve elements. Plasmodesmatal frequencies are high at interfaces involving phloem parenchyma cells. The plasmodesmata between phloem parenchyma cells and companion cells are structurally distinct in that there are several branches on the phloem parenchyma cell side of the wall and only one branch on the companion cell side. Most of the translocated sugar in A. thaliana is sucrose, but raffinose is also transported. Based on structural evidence, the most likely route of sucrose transport is from bundle sheath to phloem parenchyma cells through plasmodesmata, followed by efflux into the apoplasm across wall ingrowths and carrier-mediated uptake into the sieve element-companion cell complex. Received: 5 October 1999 / Accepted: 20 November 1999     

HISTOLOGICAL STUDIES ON THE COLEOPTILE. I. TISSUE AND CELL TYPES IN THE COLEOPTILE TIP

The uppermost 1-4 mm of 25-mm coleoptiles of oats and wheat have been studied at the optical microscope level, using newer histological methods and sections 1-4 μ thick. The outer epidermal wall, which shows very fine wrinkling, is continuous with the thinner wall of the inner epidermis through the pore. The cells of both epidermal layers have acidophilic cytoplasm with long transvacuolar strands. Both inner and outer epidermis have stomata, those of the outer epidermis having kidney-shaped guard cells like those of dicotyledons. The guard-cell walls are lignified in their inner layers only and are thinly cuticularized. In the vascular bundles the sieve tubes terminate apically about 250 μ below the end of the xylem; the xylem in turn terminates about 400 μ below the extreme apex. A number of clearly undifferentiated cells, with highly basophilic cytoplasm and many mitochondria, separate the xylem elements from the inner epidermis. Towards the outer epidermis there are a few sieve elements, each of which is associated with a special cell having an elongated nucleus supported on fine cytoplasmic strands. The parenchyma of both the tip and the shaft of the coleoptile are generally interpenetrated by air-spaces, but where they are adjacent to the inner epidermis there is heavy interposition of readily stained intercellular material, especially in Triticum. Plastids are widely distributed throughout the tissue, but their greening in light takes place preferentially towards the phloem side of the vascular bundles. The observations are discussed in reference to earlier literature and with regard to the function of the coleoptile as a protecting and guiding organ for the shoot system of the seedling.     

CO2浓度加倍对辽东栎维管组织结构的影响

 以辽东栎(Quercus liaotungensis)的13年生幼树为材料,分别培养在大气CO2浓度加倍(700μl·L-1)与对照(350μl·L-1)的开顶式熏气室中,研究CO2浓度升高对其茎次生木质部和次生韧皮部结构的影响。结果表明：经CO2浓度加倍处理的两个生长季内,辽东栎的年轮宽度明显增加,为对照的300％～370％,其中晚材宽度的增加更为显著,为对照的750％～830％。另外,晚材中导管的密度和径向直径分别比对照增加50％和20％;木纤维细胞的比例约为对照的170％。但早材的导管分子和木纤维细胞与对照相比均无显著变化。在CO2浓度加倍条件下,辽东栎的次生韧皮部中含晶韧皮薄壁细胞的数目,每条韧皮纤维切向带中韧皮纤维细胞的数目,以及韧皮纤维长度均有显著增加(p≤0.05)。相反地,韧皮纤维细胞的直径和筛管分子长度却无明显变化。值得提出的是,在CO2浓度加倍的条件下,次生韧皮部的宽度、筛管分子的直径、以及每年形成的韧皮部细胞总数分别为对照的82％、87％和80％。综上所述,大气CO2浓度加倍对辽东栎次生木质部的生长发育具明显的正效应,而对次生韧皮部的细胞总数与筛管分子的影响则呈负效应。     

Transfer cells and flange cells in sinkers of the mistletoePhoradendron macrophyllum (Viscaceae), and their novel combination

Summary The unusual thick-walled cells in contact with host and parasite vessels, first noted by Calvin 1967 in sinkers (structures composed of tracheary elements and parenchyma that originate from parasite bark strands that grow centripetally to the host vascular cambium and become embedded by successive development of xylem) of the mistletoePhoradendron macrophyllum (Englem.) Cockerell, have been investigated by modern methods of microscopy. The wall is thickest in cells abutting large-diameter host vessels, less so against smaller host vessels and those abutting sinker vessels. Transmission electron microscopy reveals the wall to be complex, consisting of a basement primary wall, upon which two developments of secondary-wall material occur. These are represented by lignified thickenings, in the form of flanges, and a labyrinth of wall ingrowths characteristic of a transfer cell. The wall ingrowths occur mostly in the primary-wall regions between the flanges, but when in contact with a large host vessel the ingrowths also differentiate on top of the flanges. Cells with such a transfer cell labyrinth have not been previously reported in the endophytic system of a mistletoe. The cells are confined to the xylary portion of the primary haustorium and sinkers. InP. macrophyllum, however, the cells differ from ordinary transfer cells in that they have differentiated as part of a flange parenchyma cell. This arrangement represents a novel anatomical situation. The name flange-walled transfer cell is used for these cells. The xylem of primary haustorium and sinkers also contain numerous ordinary flange cells. In both flange-walled transfer cells and ordinary flange cells the flanges are lignified and form a reticulate pattern of thickenings, separated by rounded areas of primary pit fields. The extent of development of the flange wall can vary in different parts of a sinker. At the host interface, the existence of a flange-walled transfer cell in direct contact with a vessel reflects a site associated with high loading into the parasite. Similarly, a labyrinth against a sinker vessel indicates a site of unloading from surrounding sinker tissue into the vessel for subsequent longdistance transport within the parasite.Dedicated to the memory of Dr. Katherine Esau (1898–1997)     

Relationship between development of endosperm transfer cells and grain mass in maize

The most basal endosperm cells of maize (Zea mays L.) began differentiating into transfer cells in 10 days after pollination (DAP). The thickening and ingrowths forming in the transfer cell wall were slow during 10 and 15 DAP. There were many vesicles, silky and string ball objects in cytoplasm, and the number of mitochondria and rough endoplasm reticulum increased. After 15 DAP, the wall thickening and ingrowths forming in the transfer cells sped up. By 20 DAP, the transfer cell zone had developed, there appeared 65 - 70 rows of cells in width and 3 - 4 layers of cell in depth, the obvious cell wall ingrowths presented strong positive reaction with periodic acid Schiff's reagent. After 20 DAP, no significant change appeared in the shape and structure of the transfer cells, and the transfer cells entered function stage. In the mature kernels (53 DAP), the most basal transfer cells were filled with ingrowths, however, dense cytoplasm was also found in these cells. The nuclei had quite irregular shapes in these cells. Some transfer cells contained black grains and crystals. A black layer formed in the pericarp tissue adjacent to the transfer cell zone. Full development of endosperm transfer cells was important for reduction of kernel abortion and increase of kernel mass. This revised version was published online in July 2006 with corrections to the Cover Date.     

嫁接早期IAA在西葫芦／南瓜嫁接面处薄壁细胞和维管分子中的免疫 …

Immuno-gold localization of IAA in cells of the graft union in the explant internode graft of Cucurbita pepo/Cucurbita moschata were investigated with electron microscopy. In parenchyma cells near the graft union, the gold particles were mainly accumulated in nucleus, plastid and endoplasmic reticulum, while no gold particles was detected in Golgi body, mitochondrion, cell wall and vacuoles. In the differentiating xylem element, the gold particles were labeled in secondary wall and cytoplasm. In the sieve element gold particles were found in the sieve plate, sieve pore and cytoplasm. There was a dense label of the gold particles in the companion cell. The role of IAA in the differentiation of the vascular elements was discussed.