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Journal Article↗
Biomedical subjects
J Croxdale
Publications and source records attributed to J Croxdale.
Structure of potato tubers formed during spaceflight.
Potato (Solanum tuberosum L. cv. Norland) explants, consisting of a leaf, axillary bud, and small stem segment, were used as a model system to study the influence of spaceflight on the formation of sessile tubers from axillary buds. The explants were flown on the space shuttle Columbia (STS-73, 20 October to 5 November 1995) in the ASTROCULTURE (TM) flight package, which provided a controlled environment for plant growth. Light and scanning electron microscopy were used to compare the precisely ordered tissues of tubers formed on Earth with those formed during spaceflight. The structure of tubers produced during spaceflight was similar to that of tubers produced in a control experiment. The size and shape of tubers, the geometry of tuber tissues, and the distribution of starch grains and proteinaceous crystals were comparable in tubers formed in both environments. The shape, surface texture, and size range of starch grains from both environments were similar, but a greater percentage of smaller starch grains formed in spaceflight than on Earth. Since explant leaves must be of given developmental age before tubers form, instructions regarding the regular shape and ordered tissue geometry of tubers may have been provided in the presence of gravity. Regardless of when the signalling occurred, gravity was not required to produce a tuber of typical structure.
Culture Techniques↗
Arrest of stomatal initials in Tradescantia is linked to the proximity of neighboring stomata and results in the arrested initials acquiring properties of epidermal cells.
We examined spatial relations of arrested stomatal initials and their differentiated state on leaves of the monocotyledon Tradescantia. The placement and proximity of stomata and arrested stomatal initials to the five nearest stomata were studied to test the hypothesis that if developing stomatal initials occur too close to one another, initials will arrest. The results showed that arrested stomatal initials were not randomly placed, but were closely associated with another stoma, most often in an adjacent cell file. The distance to their nearest stomatal neighbors was less than the equivalent distance between stomata that mature. After stomatal initials form, their position within or across cell files was not adjusted by cell division or expansion. Synergistic effects from several neighboring stomata could not be linked to stomatal arrest; rather, arrest was associated only with the nearest stomatal neighbor. Since the arrest of stomatal initials was distance dependent, a failure intrinsic to the arrested initials is not solely responsible for halting stomatal development. These data show that an inhibitory mechanism adjusts stomatal development to influence the final distribution of Tradescantia stomata. The pigmentation and expansion characteristics of arrested stomatal initials were like those of epidermal cells, indicating that the initials did not remain halted at a specific point in their development. The capacity of arrested initials to differentiate in the epidermal cell pathway indicates that they remain pluripotent after their initial specification and that the opportunity for patterning is long enough to permit their entry into the epidermal cell pathway.
Cell Division↗
Linear aggregations of stomata and epidermal cells in Tradescantia leaves: evidence for their group patterning as a function of the cell cycle.
We tested Charlton's hypothesis (1990) that stomata are present and patterned in linear cell aggregations using the monocot Tradescantia. We examined the following features of the leaf epidermis in support of this theory: linear groups (strings) of stomatal complexes and of epidermal cells were sought in immature and mature regions of entire leaves; the lengths (in cell number) and incidences (numerical occurrence) of both string types were determined; the uniformity and progression of stomatal differentiation within strings were studied; physical characteristics of differentiating strings within cell files were measured. Undifferentiated epidermal cells from the leaf base were stained with DAPI to reveal precursors of stomatal strings immediately proximal to the stomatal initial region. The results indicated that the Tradescantia epidermis in the leaf blade consists of linear groups of stomata and epidermal cells, which did not change in cell number nor incidence during development. The incidence of stomata by length was nonrandom. Although incidence decreased with string length, the decline was not linear nor exponential. Stomatal strings show cell cycle synchrony in DAPI staining of stomatal precursors and synchrony of stomatal differentiation within a string. The irregularity in the length of the stomatal development region, and each differentiation stage in it, by cell file was consistent with the variation in string length and unity in string development. The evidence supports Charlton's hypothesis that cells are patterned based on their position in the cell cycle and that linear groups of stomata reflect cell lineages, which maintain a degree of cell cycle synchrony.
Cell Aggregation↗
NMR detection of a light-induced change in chloroplasts. A new technique to study thylakoid energization in vivo.
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Chloroplasts↗
Stomatal patterning in Tradescantia: an evaluation of the cell lineage theory.
The cell lineage theory, which explains stomatal patterning in monocot leaves as a consequence of orderly divisions, was studied in Tradescantia. Data were collected to test the theory at three levels of organization: the individual stoma; stomata distributed in one dimension, in linear fashion along cell files; and stomata apportioned in two dimensions, across the length and breadth of the leaf. In an attempt to watch the patterning process through regeneration, stomata in all visible stages of development were laser ablated. The results showed that the formation of stomatal initials was highly regular, and measurements of stomatal frequency and spacing showed that pattern was determined near the basal meristem when the stomatal initials arose. Following the origin of initials, the pattern was not readjusted by division of epidermal cells. Stomatal initials were not committed when first present and a small percentage of them arrested. The arrested cells, unlike stomata, were consistently positioned in cell files midway between a developed pair of stomata. At the one-dimensional level of pattern, stomata in longitudinal files were separated by a variable number of epidermal cells and the frequency of these separations was not random. The sequential spacing of stomata also was not random, and stomata separated by single epidermal cells were grouped into more short and long series than expected by chance. The stomatal pattern across the width of the leaf resulted from cell files free of stomata which alternated with cell files containing stomata, but not with a recurring periodicity. Files lacking stomata were found only over longitudinal vascular bundles. Laser ablations of developing stomata did not disrupt the pattern in nearby cells or result in stomatal regeneration. We conclude that the cell lineage theory explains pattern as an individual stomatal initial arises from its immediate precursor and satisfactorily accounts for the minimum spacing of stomata in a cell file, i.e., stoma-epidermal cell-stoma. However, the theory does not explain the collective stomatal pattern along the cell files, at the one-dimensional level of patterning. Nor does the theory account for the for the two-dimensional distribution of stomata in which regions devoid of stomata alternate with regions enriched with stomata, but not in a highly regular nor haphazard manner. We suggest that the grouping of epidermal cells and stomata separated by single epidermal cells in cell files may result from cell lineages at a specific position in the cell cycle as they traverse the zone where stomatal initials form.(ABSTRACT TRUNCATED AT 400 WORDS)
Cell Division↗
Thermal damage to chloroplast envelope membranes.
Nuclear magnetic resonance was used to detect thermal injury to chloroplasts in vivo. A lesion occurs in the chloroplast envelope membrane at temperatures between 53 degrees C and 57 degrees C, depending on species, leaf condition, and heating rate. The injury is associated with a sudden loss of water from the chloroplast.
Journal Article↗
Water is allocated differently to chloroplasts in sun and shade leaves.
Hydrogen-1 nuclear magnetic resonance spectroscopy was used to study water allocation in cell compartments of sun and shade leaves. NMR spectra of Acer platanoides were resolved into two peaks that were assigned to chloroplast and nonchloroplast water. Sun leaves contained 1.7 times more water per unit area of surface than shade leaves, and the water was allocated differently. Chloroplasts in sun leaves contained 17% of the total leaf water versus 47% in shade leaves. Comparing equal leaf surface areas, the chloroplasts in shade leaves contained 60% more water than those in sun leaves.
Journal Article↗