Effect of Phosphorus Nutrition on the Cellular Distribution of Acid Phosphatase in the Leaves of Lycopersicon esculentum L.

A histochemical study using light microscopy has been made ofthe distribution of acid phosphatase (EC 3.1.3.2 [EC] ) activity intransverse sections of fully expanded leaves of Lycopersiconesculentum grown in phosphate-deficient or sufficient media.Leaf tissues were prepared by two methods and were embeddedin paraffin wax. The location of acid phosphatase activity inleaf sections was determined by trapping orthophosphate releasedfrom p-nitrophenyl phosphate with lead acetate and subsequentlyconverting the lead phosphate to optically dense lead sulphide.In leaf sections from control tissue lead sulphide depositswere larpely confined to the spongy mesophyll cells. Whereasthe staining of the palisade cells was limited and of a granularnature, the staining of the spongy mesophyll cells was heavierand coincident with the outline of the individual cells. Moreover,the minor veins were more heavily stained than the surroundingmesophyll cells. Sections of phosphorus-deficient tissues wereheavily stained in both the palisade and spongy mesophyll layersand heavy deposits of lead sulphide were present in the regionsof the minor veins. It is suggested that the enhanced acid phosphataseactivity of the mesophyll cells in fully expanded leaves couldbe involved in the remobilization of phosphate within phosphorus-deficientplants, or be part of a phosphate transporting system, concentratingthe intracellular phosphate from the limiting supply in thesolution bathing the mesophyll cells. Lycopersicon esculentum L., tomato, acid phosphatase, phosphorus nutrition     

Anatomical considerations related to photosynthesis in cotton (Gossypium hirsutum L.) leaves, bracts, and the capsule wall

Light and electron microscopy was used to relate histologicaland ultrastructural differences of cotton (Gossypium hirsutumL.) leaves, bracts, and capsule walls to their different photosyntheticactivities. Light microscopy revealed that the leaf thicknesswas approximately 152µm, had a well-defined internal organizationwith elongated palisade mesophyll cells and loosely packed spongymesophyll cells. In contrast, the bract was thinner (111 µm),lacked a defined palisade layer, and was largely composed ofinternal air spaces. The capsule wall was very thick (1013µm)and composed of numerous tightly packed, paren-chymatous corticalcells with little or no intercellular air space. Chloroplastswith well-defined granal stacks and extensive stroma lamellaewere observed in each of these three tissues, however, theirdensity was always greater in the palisade cells of the leafcompared to spongy mesophyll cells of the bract and the parenchymatouscells of the capsule wall. The low rates of photosynthesis inthe bracts and the capsule wall were associated with the internalorganization of these tissues. Key words: Cotton, photosynthesis, anatomy, cuticle, tissues     

Anthocyanin Influence on Water Proton NMR Relaxation Times and Water Contents in Leaves of Evergreen Woody Plants During the Winter

An investigation was made to determine the effect of anthocyaninin red-colored evergreen leaves during the mid-winter on waterproton NMR relaxation times (T₁). Water contents, anthocyanincontentsand histologic localization of red-coloration in mesophyllswere determined by using both red-colored and green leaves fromthe same branches of Rhododendron, Viburnum and Mahonia, respectively.Although the decrease of water contents in the red-colored leavesin Mahonia was insignificant, decreases in the former two specieswere clearly observable. T₁ differences between red-coloredand green leaves for the three species were insignificant. Increasesof anthocyanin contents and histologic localization of red colorationin mesophylls for the red-colored leaves were more pronouncedin Rhododendron and Viburnum than in Mahonia. These observationssuggest that the pronounced increases of histologic localizationof red-colored mesophyll cells and anthocyanin contents in red-coloredleaves for the former two species contribute to maintenanceof T₁ relaxation times in spite of the marked decrease of watercontents in leaves. It is assumed that the increase of localizationareas of red-colored parenchymatous cells in mesophylls is moreeffective than the total contents of anthocyanins in leavestowards the maintenance of the T₁ level in red-colored leaves,and this appears to be dependent on the vacuolar compartmentationof anthocyanin in mesophyll cells. (Received August 3, 1991; Accepted December 12, 1991)     

Chloroplast fine structure in the japonica-2 maize mutant exposed to continuous illumination. 1. The green tissues.

Exposure to continuous illumination causes the appearance of numerous plastoglobuli in the stroma of both the mesophyll and bundle sheath chloroplasts of the green tissues of the leaves of the japonica-2 mutant of maize. In the pale green tissues the thylakoids have markedly swollen membranes. Another feature of the plastids exposed to continuous illumination is the heavy accumulation of starch. The japonica-2 chloroplasts show a different sensitivity to light, the chloroplasts of the pale green tissues being affected more markedly than the ones of the dark green tissues, and the bundle sheath chloroplasts more than those of the mesophyll. The effects of continuous illumination may be interpreted as an acceleration of chloroplast ontogenesis.     

Stomatal Responses and the Senescence of Leaves

Guard cell responses were examined in green and senescing leavesof Victa faba using detached epidermal strips to eliminate influencesfrom the mesophyll. Stomatal opening was greater in epidermalstrips from mature leaves than from senescing leaves althoughthe latter still retained the ability to respond to CO₂ andto kinetin. It was concluded that the decline in stomatal activityduring senescence is an independent but parallel process tochanges occurring in the mesophyll. Vicia faba, leaf senescence, stomata, kinetin     

Digitoxin Biosynthesis in Isolated Mesophyll Cells and Cultured Cells of Digitalis

In the laminae of Digitalis, most of the digitoxin present isfound in the mesophyll. A new method for determining the amountof digitoxin biosynthesis using a digitoxin antibody was devisedto estimate this activity in isolated mesophyll cells and culturedcells. Isolated mesophyll cells showed significant activity,which suggests that the site of biosynthesis and the accumulationof cardenolides in a lamina of Digitalis is mainly in the mesophyllcells. Of five liquid cultures of D. purpurea; green shoot-formingcultures, white shoot-forming cultures, root-forming cultures,undifferentiated green cells and undifferentiated white cells,the green shoot-forming cultures had the highest activity. Thewhite shoot-forming cultures had about one-third the activityof the green shoot-forming cultures, and the other three cultureshad very low activity. No stimulatory effect of light was foundduring the 48-h incubation. (Received January 19, 1984; Accepted June 8, 1984)     

The Structure of the Mesophyll of Flag Leaves in Three Triticum Species

Flag leaves of Triticum urartu, T. monococcum and T. aestivumcv. Professeur Marchal were examined by light and electron microscopyand by separating cells to determine whether differences inleaf anatomy could be related to known differences in theirlight-saturated rates of photosynthesis. Mesophyll cells fromthe three species were lobed and orientated with their longaxis parallel to the veins. The longest, most-lobed cells flankedthe sclerenchyma associated with the veins. Mean cell dimensionswere greatest in Professeur Marchal, but there was no significantdifference in the ratio of the mesophyll cell surface area tocell volume amongst the three species. Flag leaves of T. urartushowed the highest rates of photosynthesis and were also thethickest, with closely-spaced veins from which many of the mesophyllcells radiated. These flag leaves also had significantly more(21.9 per cent) air-filled space, and the highest ratio (15.2)of mesophyll cell surface exposed to this air-filled space perunit leaf area. Ways in which these anatomical characteristicsmay contribute to the higher rate of photosynthesis are discussed. Triticum urartu, Triticum monococcum, Triticum aestivum, flag leaves, morphology, mesophyll     

Free Sugars and Organic Acids in the Leaves of Various Plant Species and their Compartmentation Between the Tissues4

The distribution of free sugars and organic acids between theepidermis and mesophyll of Tulipa gesneriana L., Vicia fabaL., and Commelina communis L. leaves was studied using mainlygas-liquid chromatography. Fructose, glucose, sucrose, and myo-inositol were found in theepidermis and mesophyll of all three species. In T. geenerianaleaf tissues arabinose (trace levels), stachyose, tuliposidesA and B (mainly in the mesophyll), and xylose (trace levelsalso in V. faba tissues) were also detected. The acids were more difficult to detect and identify, beingat considerably lower concentrations than the sugars in bothtissues. Fumaric, citric, malic, ascorbic (trace levels), andan unidentified acid were common to the epidermis and mesophyllof all three species. Of special interest was the detectionof large amounts of glyceric acid in the epidermis and mesophyllof V. faba; this acid was not detected in the tissues from theother species. Fumaric acid was also very abundant in the epidermisof V.faba. A special study was made of the compartmentation of acids andsugars between the epidermis and mesophyll of T. geenerianaleaves after light and dark treatments. No changes in free acidor sugar levels were detected in the epidermis or mesophyllafter these treatments. Except for suceinic acid (P < 0·05),there were no statistically significant differences in acidlevels between the epidermis and mesophyll but for most of thesugars (myo-inositol, arabinose, and xylose being exceptions)differences were highly significant (P < 0·001), highestlevels occurring in the mesophyll. The differences in sugarlevels and the similarity in acid levels between epidermis andmesophyll of tulip leaves were considered to be essentiallydue to the different CO₂ fixing mechanisms and capacities ofthe two tissues. The energy source for the essentially non-greenepidermal tissue was discussed.     

Light Environment within a Leaf I. Optical Properties of Paradermal Sections of Camellia Leaves with Special Reference to Differences in the Optical Properties of Palisade and Spongy Tissues

The attenuance (apparent absorbance), angular distribution oftransmitted light (scattering) and reflectance of paradermalsections of Camellia leaves were measured spectrophotometricallyand the data for the palisade and spongy tissues were compared. Attenuance in tissues could be expressed by Beer's law onlyfor wavelengths of strong absorption. At 680 nm, the apparentextinction coefficient of chlorophyll (e) for the spongy tissuewas about 1.4 times that for the palisade tissue. The largere for the spongy tissue is attributable mostly to the more effectiveincrease in the pathlength of light due to scattering at theinterfaces between the air space and cells because the differencebetween e for the two tissues was minimized by infiltrationof the air space in the tissues with a medium whose refractiveindex was similar to the index of the leaf cells. Scatteringwas larger for wavelengths of weak absorption, and the relativeincrease in attenuance caused by elongating the optical pathlengthwas even more prominent. Based on these data, we report an ecophysiological discussionof the internal light environment of a leaf and the meaningof the differentiation of mesophyll into the palisade and spongytissues. (Received May 18, 1983; Accepted September 21, 1983)     

Ultrastructural aspects of leaves inFestuca ovina andPoa sphondylodes (C-3 Poaceae)

Structural aspects of the leaves of two common festucoids,Festuca ovina andPoa sphondylodes, have been examined employing the electron microscopy. The nature of vascular bundles and of sheaths that surround vascular tissues was discussed in the study. The festucoids exhibited a non-Kranz C-3 anatomy with more than four mesophyll cells separating the bundle sheaths of a leaf blade. Vascular tissues in theseFestuca andPoa leaves were surrounded by a double sheath: an inner distinct mestome sheath (MST) and an outer indistinctive layer of parenchymatous bundle sheath (PBS) cells. The PBS cells were much larger than the MST and had thin walls. The MST cells were relatively small and rectangular inP. sphondylodes and more or less hexangular in transverse sections ofF. ovina. InP. sphondylodes, MST had conspicuously thickened inner tangential walls with asymmetrically uninterrupted suberized lamellae in radial and tangential walls. In most differentiated MST cells, all walls were highly suberized. During suberin deposition, MST cells were quite vacuolated and most of the cytoplasm was present as a thin peripheral layer. However, MST walls inF. ovina revealed very thin suberized lamellae with translucent striations. No chloroplasts were detected inP. sphondylodes, whereas the MST inF. ovina contained small chloroplasts. Plasmodesmata were well developed in the primary pit fields of walls between MST and vascular cells, and between adjacent MST cells. Plasmodesmata were less frequent in the walls between the inner and outer sheath cells. Suberized lamellae were totally absent from the PBS cell walls in all veins. External to the PBS, the mesophyll comprised thin walled cells with abundant intercellular spaces. Peripherally arranged chloroplasts in the mesophyll were numerous and often larger than those of PBS and MST cells. Characteristics associated with C-3 and other ultrastructural features were also discussed in the study.     

Promotion of flowering and morphological alterations in Atropa belladonna transformed with a CaMV 35S-rolC chimeric gene of the Ri plasmid

Summary Kanamycin-resistant plants of belladonna (Atropa belladonna) were obtained after Agrobacterium mediated transformation. When a rolC gene, which is one of the loci located on Ri plasmid of Agrobacterium rhizogenes, was co-introduced with a kanamycin resistant (NPT II) gene under control of a cauliflower mosaic virus 35S promoter, the rolC gene was expressed strongly in leaves, flowers, stems and roots. The transformed plants exhibited dramatic promotion of flowering, reduced apical dominance, pale and lanceolated leaves and smaller flowers. On the other hand, when native rolC gene was co-introduced with NPT II, the transgenic plants obtained did not exhibit the altered phenotypes observed in 35S-rolC transformants, and the expression level of the rolC gene was much lower than in 35S-rolC transformants. These results suggest that the morphological changes in transgenic Atropa belladonna were related to the degree of expression of the rolC gene.Abbreviations native rolC rolC gene under control of its own promoter - 35S-rolC rolC gene under control of a cauliflower mosaic viras 35S promoter     

Major Element Composition of Epidermal and Mesophyll Tissues2Commelina Communis L. and Vicia Faba L.: Some Further Considerations of the Role of Ions in Stomatal Functioning

Epidermal and mesophyll tissues of Commelina communis L. andVicia faba L. were analysed by atomic absorption spectrometryfor the major plant inorganic cations and anions (K, Na, Ca,Mg, P, NO₃-N, Cl) when stomata of the leaf were open and closed.Water-soluble and residual levels of the elements were estimatedand a charge balance of the soluble fraction made. The major portion of K, Na, Cl, and P was extracted in the water-solublefraction of the epidermal and mesophyll tissues of both species.In both species the bulk of Ca remained in the insoluble residueof the epidermis whereas in mesophyll tissue it was equallydistributed be-between the two fractions in C. communis butmainly in the insoluble residue in V. faba. Magnesium was predominantlyfound in the water-soluble fraction of V. faba mesophyll tissueand distributed approximately equally between the two fractionsin the epidermal tissue. In C. communis Mg was slightly moreabundant in the water-soluble fraction of both mesophyll andepidermis. In both species no statistically significant differences inthe levels of the elements could be detected between epidermaland mesophyll tissues from leaves with open stomata and thesame tissues from leaves with closed stomata, suggesting thatthere was no major flux of ions between mesophyll and epidermisduring stomatal movements. Regardless of whether the stomata were open or closed, therewere considerably more water-soluble inorganic cations thananions present in all tissues of both species with K being themajor cation and Cl being the major anion. In V.faba and C-communis epidermis there was 49–53 per cent and 56%68per cent excess cation respectively. In the mesophyll tissuethe excess cation was 63–75 per cent and 75%78 per centin V.faba and C. communis respectively. When the partitioning of the levels of the elements betweenepidermis and mesophyll of a leaf is considered, except forNO₃-N in both species and Na in V. faba, 20 per cent or lessof each element was present in the epidermis.     

Seasonal Dimorphism in the Mediterranean Cistus incanus L. subsp. incanus

Mediterranean perennial species are described as being sclerophyllous,or summer deciduous, or seasonally dimorphic. Field observationin the coastal maquis of Castelvolturno Nature Reserve, southernItaly, showed thatCistus incanus L. subsp. incanus is a seasonallydimorphic species as it develops brachyblasts with small leavesin summer, and dolichoblasts with large leaves in winter. Fieldbiometric data confirmed that winter shoots were 14-times longerthan those developed in summer and had many more leaves. Thearea of single winter leaves was five-times that of summer leaves.Anatomical leaf structure also changed with the season: winterleaves were flat while summer leaves had a crimped lamina whichwas partially rolled to form crypts in the lower surface. Leaveswere covered by considerably more trichomes in summer than inwinter. Stomata were uniformly distributed along the lower epidermisof winter leaves but were only present in the crypts of summerleaves. In summer leaves, a palisade layer was often found onboth sides of the lamina, the mesophyll cells were generallysmaller and the intercellular spaces were reduced. Winter leaveshad a dorsiventral structure and larger intercellular spaces.Seasonal dimorphism is generally reported to be an adaptationto summer drought. However, the morphology and anatomy of C.incanus L. subsp.incanus showed that the subspecies has notonly developed a strategy to survive summer drought, but hasevolved two different habits, one more xerophytic than the other,to optimize adaptation to the seasonal climatic changes occurringin Mediterranean environments. Copyright 2001 Annals of BotanyCompany Cistus, Cistus incanus L. subsp. incanus, climatic changes, leaf anatomy, leaf dimorphism, Mediterranean shrubs, phenology, seasonal dimorphism     

Flag Leaf Anatomy of Triticum and Aegilops Species in Relation to Photosynthetic Rate

Quantitative anatomical and other measurements were made onfully expanded flag leaves of a series of diploid, tetraploidand hexaploid Triticum and Aegilops species, and photosyntheticrates per unit leaf area were measured at light saturation (P_max). Diploids had the highest P_max, hexaploids the lowest with tetraploidsbeing intermediate. The anatomical features of tetraploids andhexaploids were generally similar, but different from the diploids.The diploids had thinner leaves with less dry matter and chlorophyllper unit area. The surface area of the mesophyll cells per unitvolume of mesophyll tissue was similar for all ploidy levels,as was the ratio mesophyil cell surface area per unit leaf area.It is argued that while these anatomical features are unlikelyto account for the observed variation in Pmax, it is possiblethat other structural factors with which they are correlatedmay causally influence P_max. One such feature is the averagediffusion path length from the plasmalemma at the cell surfaceto the sites of carboxylation. Anatomy, photosynthesis, mesophyll, cell size, Triticum, Aegilops, polyploidy     

Probable mechanical transmission of a virus-like agent from rose rosette disease-infected multiflora rose to Nicotiana species

As part of efforts to identify the causal agent of the rose rosette disease (RRD) of multiflora rose (Rosa multiflora Thunb.), root tip extracts from both symptomatic and nonsymptomatic roses were used to mechanically inoculate leaves of Nicotiana glutinosa. Pale green spots were observed along the margins of the major leaf veins only on leaves inoculated with extracts prepared from symptomatic rose plants. Light microscopy revealed abnormal development of the palisade and spongy mesophyll cells in the symptomatic tissue, although no virus‐like particles (VLPs) were observed by electron microscopy. However, VLPs were observed in cells from tissue adjacent to the leaf veins and bordered by the pale green spots. Inoculation of N. benthamiana with extracts from symptomatic N. glutinosa initially did not result in visible symptoms on N. benthamiana inoculated leaves. However, approximately 4 wk post inoculation, splitting of leaf tissue across and along major leaf veins in expanding leaves occurred. In later stages of leaf expansion some leaves split in regions not associated with veins. Light microscopy of thick sections revealed separation between palisade cells and groups of small dead cells in the mesophyll tissue of expanding systemically infected leaf blades. Electron microscopy revealed crystalline arrays in the cytoplasm of mesophyll cells. No abnormal cellular changes were observed in plants inoculated with extracts prepared from nonsymptomatic rose plants.     

Chloroplast Doublets and Differential Staining of the Cell Walls in Photosynthetic Tissues of Amaranthus dubius Mart

Ultrastructural studies of the leaves of Amaranthus dubius revealpresence of chloroplast doublets in mature leaf tissues. Theyalso highlight the difference in the structural organisationof the bundle sheath and the mesophyll cell walls, a featurewhich may have functional significance. Amaranthus dubius Mart., Calaloo, mesophyll, bundle sheath, chloroplast doublets, plastid fusion, plastid division, differential staining of the cell walls     

Monomeric and Dimeric Forms and the Mechanism-Based Inactivation of 1-Aminocyclopropane-1-Carboxylate Synthase

The molecular mass of 1-aminocyclopropane-1-carboxylate (ACC)synthase from a variety of sources was examined by both high-performancegel-filtration chromatography and polyacryl-amide gel electrophoresisin the presence of sodium dodecylsulfate. Enzymes used wereprepared from wounded or non-wounded pericarp of ripe tomatofruits and wounded mesocarp of winter squash fruits, as wellas from cells of E. coli that had been transformed with cDNAsfor the wound-induced or ripening-induced ACC synthases of tomatoand the wound-induced or auxininduced enzymes from winter squash.The enzymes from tomato fruit tissues were isolated in a monomericform, whereas the enzymes synthesized in E. coli from cDNAsfor tomato ACC synthase were isolated in a dimeric form. ACCsynthases of winter squash obtained either from fruit tissuesor from transformed E. coli cells were isolated in dimeric forms.ACC synthase in the monomeric form was less sensitive to theinactivation that is associated with the catalytic reaction(the mechanism-based inactivation) than the enzyme in the dimericform. A plausible mechanism relating the difference in molecularform to sensitivity to the mechanism-based inactivation of tomatoACC synthase is discussed. (Received February 1, 1993; Accepted May 17, 1993)     

Stomata and Mesophyll Characteristics of Barley Leaf as Affected by Light: Stereological Analysis

The anatomical structure of the second leaf blade of barley{Hordeum vulgare L. cv. Koral) was studied in plants exposedto a photosynthetic photon flux density (PPFD) of 200 µmolm^–2 s^–1 compared with those grown under 25µmolm^–2–11. Design-based stereological methods wereused for the estimation of various leaf anatomical characteristicssuch as mesophyll volume, proportion of intercellular spaces,number of mesophyll cells, mean mesophyll cell volume, and internalleaf surface area. The structure of the mesophyll was more affectedby different levels of PPFD than were the stomatal characteristics.Increased PPFD produced thicker leaves with a larger mesophyllvolume having a higher number of less elongated mesophyll cellsand a larger internal leaf surface area. Key words: Hordeum vulgare, light effect, mesophyll, stereology, stomata     

Ultrastructural Changes in Leaves of Cichorium during Somatic Embryogenesis

A detailed electron microscopy study of early cellular eventsduring somatic embryogenesis in leaves of Cichorium is described.Leaves on in-vitro grown plantlets were sectioned and put at35°C, in darkness, in an agitated liquid induction medium.No sign of embryogenic predetermination, such as thick cellwall, dense cytoplasm and enlarged nucleus, could be seen inany cell before treatment. Perivascular cells were the firstto react. Addition of glycerol (330 mM) allowed the arrest ofembryogenic cells at an activated stage. The main events werea thickening of the wall, with extracellular secretion and anaccumulation of Ca²⁺ in the vacuole, demonstrated by an antimonateprocedure. After 5 d, leaves were transferred to glycerol-freemedium where multicellular proembryos could be observed. Theyshowed reduced vacuoles, cortical microtubules, numerous multivesicularbodies and lipid globules. The embryoid cells were lined alongthe mesophyll lacunae by an extracellular secretion with a tubularstructure; histochemical tests proved its complex lipo-glyco-proteicnature.Copyright 1993, 1999 Academic Press Cichorium, extracellular tubular protein, somatic embryogenesis, vacuolar calcium     

Leaf Characteristics and Net Gas Exchange of Diploid and Autotetraploid Citrus

The effect of tetraploidy on leaf characteristics and net gasexchange was studied in diploid (2x ) and autotetraploid (4x) ‘Valencia’ sweet orange (Citrus sinensis (L.)Osb.) and ‘Femminello’ lemon (Citrus limon (L.)Burm. f.) leaves. Comparisons between ploidy levels were madeunder high irradiance (I) in a growth chamber or low total Iin a glasshouse. Tetraploids of both species had thicker leaves,larger mesophyll cell volume and lower light transmittance thandiploids regardless of growth I. Mesophyll surface area perunit leaf area of 2x leaves was 5–15% greater than on4x leaves. Leaf thickness and mesophyll cell volume were greaterin high I leaves than low I leaves. In high I, average leafarea was similar for 2x and 4x leaves, whereas in low I it was30% greater in 4x than in 2x leaves. Nitrogen and chlorophyllconcentration per cell increased with ploidy level in both growthconditions. The ratio of chlorophyll a:b was 25% greater in2x than in 4x leaves. When net CO₂assimilation rate (A_CO2) wasbased on leaf area, 4x orange leaves had 24–35% lowerA_CO2than their diploids. There were no significant differencesin A_CO2between 2x and 4x orange or lemon leaves when expressedon a per cell basis. Overall, lower A_CO2per unit leaf area oftetraploids was related to increase in leaf thickness, largermesophyll cell volume, the decrease in mesophyll area exposedto internal air spaces, and the lower ratio between cell surfaceto cell volume. Such changes probably increased the resistanceto CO₂diffusion to the site of carboyxlation in the chloroplasts. Cell volume; chlorophyll; irradiance; leaf thickness; nitrogen; photosynthesis; ploidy; Citrus limon ; C. sinensis ; ‘Valencia’ sweet orange; ‘Femminello’ lemon