Developmental Features of the Primary Phloem in Phaseolus vulgaris L.

Certain developmental features of the primary phloem were examinedin Phaseolus vulgaris L., chiefly by the use of the pulvinusat the base of the petiole. The cells included in the studywere the sieve element, the companion cell, and the tannin cell.In the sieve element, the sieve plate shows the usual sequenceof conversion of plasmodesmatal canals into pores. The endoplasmicreticulum, which appears as flat cisternae associated with ribosomesin younger cells, later becomes in part stacked and in partaligned parallel with the walls as a network. The stacked ERprecedes the anastornosing parietal ER in time of development,but the parietal ER persists longer. Of the two forms of P-proteincharacteristic of a number of Fabaceae, the crystalline bodyappears considerably in advance of the body composed of tubules.Neither form of P-protein disperses completely in the maturecell, although the crystalline protein may spread out into aggregatesof fine fibrils. The companion cells show the typical denseprotoplasts and branched plasrnodesmatal connections with thesieve elements. The vacuome of these cells is dispersed intonumerous small vacuoles, many of which appear to be concernedwith autophagic digestion of protoplasmic material. The tannincells have large vacuoles in which the tannin material is located.The cells form vertical series in which the end walls becomeperforated.     

On the Phloem of Mimosa pudica L.

The phloem of Mimosa pudica L. was examined in view of somereports that the sieve elements in this plant show featuresnot previously described for these cells in Leguminosae. Inthe present study only a usual dicotyledonous type of sieveelement was recognized. The sieve elements pass through stagesof differentiation involving development and dispersal of P-proteinbodies, disintegration of nuclei, and appearance of plastidsstoring a starch staining red with iodine. Callose occurs onthe transverse or moderately oblique sieve plates. The phloemcontains secretory cells. They are wide and long and have transverseor more or less inclined end walls. In younger cells the endwall bears in the centre a conspicuous pit to which the protoplastsof the superimposed cells are firmly attached. In many oldercells the pit region is replaced by a perforation so that thecontents of superimposed cells may be completely merged. Itremains to be determined whether the perforation is presentin an intact plant or results from a rupture during sampling.The secretory cells accumulate material that gives a positivetest for carbohydrates and a negative test for proteins.     

Dilated Endoplasmic Reticulum Cisternae in Differentiating Xylem of Minor Veins of Mimosa pudica L. Leaf

The differentiating tracheary elements in the xylem of minorveins in Mimosa pudica L. contain, as is usual, complete nucleateprotoplasts. Within the latter, dictyosomes with associatedvesicles and endoplasmic reticulum (ER) are prominent components.The ER cisternae show an uncommon feature of developing voluminousdilations accumulating finely fibrous material. Similar dilatedER cisternae occur in parenchyma cells associated with the trachearyelements. Most of the dilated cisternae are elongated, taperingat both ends, and almost circular in transections. They varyin size. The largest measured was 10 µm long and 3 µmwide. In the tracheary elements the cisternae break down asthe protoplast disintegrates. For a time, mature cells containfibrous material, apparently the product of the dilated cisternae,at least in part. In the parenchyma cells the dilated cisternaeare released into the vacuoles after the associated trachearyelements reach maturity. They become structurally modified anddisintegrate. The timing in the appearance and disintegrationof the dilated ER cisternae suggests that these structures havesome function with reference to the differentiation of trachearyelements in the xylem.     

Laticifers in Nelumbo nucifera Gaertn.: Distribution and Structure

The laticifers of Nelumbo nucifera Gaertn. (Nelumbonaceae) occurin vascular bundles and separately from these in the groundparenchyma. In common with laticifers in some other plants,they pass through a stage when they contain numerous small vacuoles,or vesicles, which later merge with the central vacuole. Osmiophilicglobules are formed in the small vacuoles and later releasedinto the central one. Partial disintegration of protoplaststakes place in the central vacuole, apparently by autophagy.The globules are retained. The laticifers are long thin-walledcells. Many show single perforations in the end walls.     

On Vessel Member Differentiation in the Bean (Phaseolus vulgaris L.)

Certain ultrastructural features of vessel member differentiationwere examined in the primary xylem of petiole of bean (Phaseolusvulgaris L.). The cells used had helical secondary wall thickeningsand simple perforation plates. The primary cell wall increasesin thickness before the helices of secondary wall develop. Ina common wall between two vessel members of different ages,theprimary thickening occurs first in the older cell so thatfor a time the middle lamella is located closer to the youngercell rather than medianly. Apparently the helix is depositedafter the primary wall of a given cell reaches maximum thickness.The perforation of the end wall is preceded by primary thickeningof the part of the wall that is later removed. The marginalregion remains relatively thin and becomes covered with a rimof secondary wall. Vesicles with fibrous content appear nearthe surface within the end wall shortly before the perforationoccurs. A highly vacuolated protoplast with a much enlargednucleus and numerous organdIes is present during cell wall differentiation.After that process is completed, the protoplast disintegratesand the primary wall bearing the helix is hydrolysed where itis exposed to the cell lumen and, under certain conditions,also under the secondary wall.     

Floral biology of 'Bulida' apricot trees subjected to postharvest drought stress

Drip irrigated ‘Búlida’ apricot trees (Prunus armeniaca L., on Real Fino apricot rootstock) were submitted to drought stress by withholding irrigation for two different postharvest periods for two consecutive years. The first treatment (T–1) started immediately after harvest, and lasted 11/2 months, while the second treatment (T–2) started when the first treatment finished and lasted 2 months. These stress treatments were compared with a control treatment (T–0), which was irrigated throughout the year so that it received an amount of water equivalent to 100% of the crop evapotranspiration (ETc) demand. Flowers from the three treatments showed similar quality (fresh weight, petal surface area and pistil length) and frequent macrostyle (stigma located above the anthers). A lower percentage of pollen germination was observed in grains from the following year's bloom in plants from the T–1 treatment. The T–1 drought stress also induced a significant decrease in fruit yield, due to an increase in fruitlet drop, which led to significantly lower fruit set. The T–2 treatment did not affect these processes and was not critical as regards apricot yield. The fruits harvested met the required standards of quality in all treatments.     

Changes in the Nucleus and the Endoplasmic Reticulum during Differentiation of a Sieve Element in Mimosa pudica L.

The differentiating sieve element in stem and leaf phloem ofMimosa pudica L. was examined with the electron microscope.The nucleus of a sieve element at first resembles that of acompanion cell, except that its nucleolus is smaller. The firstindication of approaching disintegration is a change in theappearance of the nuclear envelope. With the fixatives used,its profile becomes wider and clearer, giving the impressionof having been dilated. Subsequently, the nuclear contents disintegrateand the envelope breaks apart. No nuclear remnants are discerniblein mature sieve elements. The endoplasmic reticulum (ER) ofyoung sieve elements consists of cisternae-bearing ribosomes.At the beginning of nuclear disintegration ER cisternae becomestacked, with electron-dense material accumulating between thecisternae. The stacking assumes various forms. Some of the stackedER is independent of cell organelles and occurs next to theplasmalemma along the cell wall. Part of the ER becomes stackedagainst the plastids or the nucleus. There is also unstackedER which forms an anastomosing system along the plasmalemma.All of the modified ER bears no ribosomes. The anastomosingER appears to persist longer than the stacked ER.     

Ultrastructure of Secretory Cells in the Phloem of Mimosa pudicaL.

The secretory cells arc a prominent component of the phloemtissue of Mimosa pudica L. They form longitudinal files in whichthe common end walls of the cells are perforated. The originof the perforations in relation to protoplast differentiationwas the objectof the study. As the cells emerge from the meristematicstate, portions of cytoplasm including some organelles aretransferredinto the central vacuole and are apparently lysed. This phenomenonis accompanied by an accumulation of flocculent material, possiblythe secretory product referred to in the literature as a carbohydrate.The tonoplast ceases to be definable so that the flocculentmaterialand degraded and non-degraded protoplast componentsare intermingled inthe cell lumen. The perforation of the endwall OCCUR while the tonoplast is still intact. Theplasmalemmasof the contiguous cells withdraw from the part of the wall undergoingdegradation. The space becomes filled with fibrous debris ofthe apparently lysed wall. The degraded wallpart becomes brokenpossibly by a unidirectional pressure flow in the cells, forthe remnants of the wall are pushed into one of the two superimposedcells. At this presumably mature stage, the cells contain someintactprotoplast components among which ribosomes are especially conspicuous.