Is wall-bound calcium redistributed during the gravireaction of stems and coleoptiles?

We have tested the hypothesis that wall-bound calcium is redistributed from the lower to the upper sides of horizontal stems and coleoptiles during the reaction phase of gravicurvature. We used atomic absorption spectrometry to measure wall-bound calcium in the epidermal and internal layers of sunflower (Helianthus annum L.) hypocotyls and pea (Pisum sativum L.) epicotyls, and total calcium in maize (Zea mays L.) coleoptiles at the time of maximal gravireaction. In every case, we found that there was no measurable redistribution of wall-bound calcium either from the lower to the upper sides, or between epidermal and inner tissues in response to the gravistimulus. These results indicate that a redistribution of wall-bound calcium does not play a role during the gravireaction of stems and coleoptiles.     

Wall extensibility and gravitropic curvature of sunflower hypocotyls: correlation between timing of curvature and changes in extensibility

Abstract. Gravitropic curvature results from unequal growth rates on the upper and lower sides of horizontal stems. These unequal growth rates cold be due to differences in wall extensibility between the two sides. To test this, the time course of curvature of horizontal sunflower ( Helianthus anmus L.) hypocotyls was determined and compared with the time courses of changes in Instron-measured wall extensibility (PEx) of the upper and lower epidermal layers. As gravicurvature developed, so did the difference in PEx between the upper and lower epidermis. The enhanced growth rate on the lower side during the period of maximum increase in curvature was matched by PEx values greater than those of the vertical control, while the inhibited growth rate on the upper side was accompanied by PEx values below that of the control. The close correlation between changes in growth rates and alterations in PEx demonstrates that changes in wall extensibility play a major role in controlling gravicurvature.     

Calcium effect on the mycelial cell walls of Botrytis cinerea

The goal of this study was to determine whether calcium ion, (one of the electrolytes released after plant cell attack), may have a direct effect on fungal growth and chemistry of the fungal cell wall. B. cinerea was grown on Richard's solution containing different amounts of CaCl₂, and the cell walls were extracted from the mycelium after 7 days of growth. Mineral, neutral and aminosugar, protein and uronic acid contents were determined. At 1 g l⁻¹ CaCl₂, only the aminosugar content increased. At 2 g l⁻¹ CaCl₂, neutral sugar synthesis was reduced, whereas the uronic acid content increased. For higher CaCl₂ concentrations, the calcium ion content of the cell wall increased, resulting in reduced protein and neutral sugar contents. Meanwhile, the cell wall proportion of the mycelia increased on a dry weight basis due to an increase in uronic acid, Ca, P, Na and neutral sugar contents of the cell wall with increasing CaCl₂ in the media. The resulting thickening of the fungal cell wall caused by calcium ion may be an important factor in the host-pathogen relationship.     

A Gradient of Endogenous Calcium Forms in Mucilage of Graviresponding Roots of Zea mays

Agar blocks that contacted the upper sides of tips of horizontally-orientedroots of Zea mays contain significantly less calcium (Ca) thanblocks that contacted the lower sides of such roots. This gravity-inducedgradient of Ca forms prior to the onset of gravicurvature, anddoes not form across tips of vertically-oriented roots or rootsof agravitropic mutants. These results indicate that (1) Cacan be collected from mucilage of graviresponding roots, (2)gravity induces a downward movement of endogenous Ca in mucilageoverlying the root tip, (3) this gravity-induced gradient ofCa does not form across tips of agravitropic roots, and (4)formation of a Ca gradient is not a consequence of gravicurvature.These results are consistent with gravity-induced movement ofCa being a trigger for subsequent redistribution of growth effectors(e.g. auxin) that induce differential growth and gravicurvature. Atomic absorption, calcium, corn, gravitropism (root), Zea mays     

The role of ionic calcium in the gravitropic response of a creeping chrysanthemum cultivar

The stem of the creeping Chrysanthemum morifolium Ramat. cultivar ‘Yuhuajinhua’ responds to a gravitational stimulus by bending. Most of the calcium ion (Ca²⁺) present in the stem cells was concentrated in the cell walls, intercellular space, and vacuoles, with very little in the cytoplasm. An investigation of the effects of supplying exogenous Ca²⁺ or the Ca²⁺ chelator EGTA on the creeping habit and the level of endogenous IAA showed that, for at least 60 min after gravistimulation was initiated, the level of Ca²⁺ present in the epidermis cell walls on the lower side of the stem was maintained at a higher level than in those on the upper side. In the endodermis cells, most of the Ca²⁺ was located in the intercellular space, cell walls, and throughout the vacuole, with only little within the cytoplasm. Endodermis cell Ca²⁺ responded rapidly (within 5 min) to gravistimulation. The level of Ca²⁺ continued to increase within the cytoplasm for at least 30 min into the period of gravistimulation. Exogenously applied calcium chloride (CaCl₂) accentuated gravity-induced bending and the IAA concentration differed between the upper and the lower sides of the gravistimulated bent stem, whereas EGTA decreased these effects. Ca²⁺ appears to play an important role in the gravitropism of the ‘Yuhuajinhua’ creeping stem, not only by changing its distribution in the epidermis cell walls and the endodermis cytoplasm, but also by regulating IAA difference between the upper and lower sides of the creeping stem.     

CALCIUM MOVEMENT,GRAVIRESPONSIVENESS, AND THE STRUCTURE OF COLUMELLA CELLS IN PRIMARY ROOTS OF AMYLOMAIZE MUTANTS OF ZEA MAYS

Primary roots of Zea mays cv. Amylomaize were less graviresponsive than primary roots of the wild-type Calumet cultivar. There were no significant differences in: 1) the partitioning of volume to organelles in columella cells, 2) the size or density of amyloplasts, or 3) rates and overall patterns of organelle redistribution in horizontally-oriented roots of the two cultivars. Amyloplasts and nuclei were the only organelles whose movement correlated positively with the onset of root gravicurvature. However, the onset of gravicurvature was not directly proportional to the average sedimentation rate of amyloplasts, since amyloplasts sedimented at equal rates in columella cells of both cultivars despite their differences in root gravicurvature. The more graviresponsive roots of Calumet seedlings were characterized by a more strongly polar movement of ⁴⁵Ca²⁺ from the upper to lower sides of their root tips than the less graviresponsive roots of Amylomaize seedlings. These results suggest that the decreased graviresponsiveness of horizontally-oriented roots of Amylomaize seedlings may be due to a delay in or decreased ability for polar transport of calcium rather than to smaller, more slowly sedimenting amyloplasts as has been suggested for their less graviresponsive coleoptiles.     

Effects of calcium and kinetin on growth and cell wall composition of pea epicotyls

Kinetin and CaCl₂, in the presence of indoleacetic acid, promoted lateral expansion of epicotyls of decapitated and derooted Alaska pea seedlings (Pisum sativum L.) and inhibited their elongation. This growth response was correlated with the development of cell walls unusually rich in pectic uronic acids. Epicotyls in calcium-auxin solutions continued to enlarge and to add new wall material long after tissues in auxin only had stopped. Longitudinal enlargement, associated with the development of walls poor in pectic uronic acids, was favored by KCl, MgCl₂, and ethylenediaminetetraacetate. The last of these agents promoted the loss of ⁴⁵Ca from the epicotyls. Seedings grown in vermiculite moistened with CaCl₂, KCl, or MgCl₂ solutions did not differ in appearance or in the composition of their walls. They responded similarly to experimental treatment except that the decapitated epicotyls of the MgCl₂-grown plants suffered an absolute loss of pectic uronate when incubated in that salt.     

ACID EFFLUX PATTERNS OF PRIMARY AND LATERAL ROOTS OF PHASEOLUS VULGARIS (FABACEAE)

Graviresponding primary roots of Phaseolus vulgaris were characterized by more acid efflux on the upper (i.e., rapidly growing) side of the root than on the lower side of the root. Acid efflux patterns of the upper and lower sides of horizontally-oriented lateral roots were symmetrical. Addition of sodium orthovanadate (an inhibitor of auxin-induced H⁺ efflux) to the growth medium abolished gravicurvature and development of acid efflux asymmetry in horizontally-oriented roots. These results 1) support the suggestion that auxin redistribution may cause the asymmetry of acid efflux that mediates gravitropism, and 2) indicate that the lack of an auxin-induced asymmetry of acid efflux may be involved in explaining the minimal graviresponsiveness of lateral roots.     

Cytochemical Localization of Calcium in Cap Cells of Primary Roots of Zea mays L.

The distribution of calcium (Ca) in caps of vertically- andhorizontally-oriented roots of Zea mays was monitored to determineits possible role in root graviresponsiveness. A modificationof the antimonate precipitation procedure was used to localizeCa in situ. In vertically-oriented roots, the presumed graviperceptive(i.e., columella) cells were characterized by minimal and symmetricstaining of the plasmalemma and mitochondria. No precipitatewas present in plasmodesmata or cell walls. Within 5 min afterhorizontal reorientation, staining was associated with the portionof the cell wall adjacent to the distal end of the cell. Thisasymmetric staining persisted throughout the onset of gravicurvature.No staining of lateral cell walls of columella cells was observedat any stage of gravicurvature, suggesting that a lateral flowof Ca through the columella tissue of horizontally-orientedroots does not occur. The outermost peripheral cells of rootsoriented horizontally and vertically secrete Ca through plasmodesmata-likestructures in their cell walls. These results are discussedrelative to proposed roles of root-cap Ca in root gravicurvature. Key words: Antimonate, calcium, columella cell, peripheral cell, root gravitropism, Zea mays L.     

Survival and death of Chara internodal cells in electrolyte solutions and calcium release from the cell wall

Abstract. Survival and death of Chara internodal cells were investigated in one of the alkali metal salts KCl, some of the alkali earth metal salts CaCl₂, Ca(NO₃)₂, MgCl₂, Mg(NO₃)₂, SrCl₂, Sr(NO₃)₂, BaCl₂ and Ba(NO₃)₂, potassium phosphate pH buffer solution (pH 7.0), Tris-maleate pH buffer solution (pH 7.0), HEPES (N-2-hydroxyethylpiperazine-N′-2-ethanesulphonic acid)-KOH (pH 7.0) pH buffer solution, calcium buffer solutions, and deionized water. Most of the internodal cells died within a day or a few days in KCl, MgCl₂, Mg(NO₃)₂, BaCl₂ and Ba(NO₃)₂ solutions of higher concentrations, calcium buffer solutions of pCa 6.0, 10.0 mol m^-3 potassium phosphate pH buffer solution and 10.0 mol m^-3 Trismaleate pH buffer solution. However, all of the internodal cells survived more than 10 d in deionized water, 80.0 mol m^-3 CaCl₂, 80.0 mol m^-3 Ca(NO₃)₂, 80.0 mol m^-3 SrCl₂, 80.0 mol m^-3 Sr(NO₃)₂ calcium buffer solutions of pCa 4.0 and pCa 5.0, and 10.0 mol m^-3 HEPES-KOH (pH 7.0) pH buffer solution. Addition of Ca²⁺ or Sr²⁺ to K⁺, Mg²⁺ and Ba²⁺ salt solutions increased the survival rates of the internodal cells. Calcium release from the internodal cell wall was measured in deionized water, KCl, NaCl, MgCl₂, CaCl₂, SrCl₂ and BaCl₂ solutions. Except in deionized water and CaCl₂ solution, most of the calcium binding to the cell wall was released within one or a few hours in respective electrolyte solutions. Thus, survival and death of the internodal cells in the electrolyte solutions tested were interpreted in terms of the calcium release from the cell wall and the cell membrane, and intrinsic ability of Sr²⁺ to maintain the cell membrane normal.     

Loss of capacity for acid-induced wall loosening as the principal cause of the cessation of cell enlargement in light-grown bean leaves

Cell enlargement in primary leaves of bean (Phaseolus vulgaris L.) can be induced, free of cell divisions, by exposure of 10-d-old, red-light-grown seedlings to white light. The absolute rate of leaf expansion increases until day 12, then decreases until the leaves reached mature size on day 18. The cause of the reduction in growth rate following day 12 has been investigated. Turgor calculated from measurements of leaf water and osmotic potential fell from 6.5 to 3.5 bar before day 12, but remained constant thereafter. The decline of growth after day 12 is not caused by a decrease in turgor. On the other hand, Instron-measured cell-wall extensibility decreased in parallel with growth rate after day 12. Two parameters influencing extensibility were examined. Light-induced acidification of cell walls, which has been shown to initiate wall extension, remained constant over the growth period (days 10–18). Furthermore, cells of any age could be stimulated to excrete H⁺ by fusicoccin. However, older tissue was not able to grow in response to fusicoccin or light. Measurements of acid-induced extension on preparations of isolated cell walls showed that as cells matured, the cell walls became less able to extend when acidified. These data indicate that it is a decline in the capacity for acid-induced wall loosening that reduces wall extensibility and thus cell enlargement in maturing leaves.Abbreviations and symbols FC fusicoccin - P turgor pressure - RL red light - WEx wall extensibility - WL white light - P _w leaf water potential - P _s osmotic potential     

Analysis of the Growth Response of Air-Grown Rice Coleoptiles to Submergence

The effect of submergence of air-grown rice seedlings (Oryza sativa L. var. Sasanishiki) on coleoptile growth and ultrastructure, extensibility and chemical composition of the cell walls was investigated. The lag-time between start of submergence and the onset of the enhancement of growth was less than 4 h. The growth response was associated with a drastic thinning of the cell walls and an increase in wall extensibility. At the outer epidermal wall of both air-grown and submerged coleoptiles electron-dense (osmiophilic) particles were detected. During submergence, the net accumulation of cellulose and hemicellulose was reduced, but the increase in pectic substances was unaffected. Submergence caused an 80% inhibition of the net accumulation of wall-bound phenolics (ferulic- and diferulic acid) compared with air-grown controls. The osmotic concentration of the tissue saps was not affected by submergence. Our results support the hypothesis that rapid coleoptile elongation under water is caused by an inhibition of the formation of phenolic cross-links between matrix polysaccharides via diferulate, which results in a mechanical stiffening of the cell walls in the air-grown coleoptile.     

Root growth and calcium uptake in relation to calcium concentration

Summary The purpose of the present work has been to investigate the influence of calcium supply on root growth in barley. The plants were grown in pots, in which the upper part was a sand-perlite mixture and the lower part a test solution with varying calcium concentration (10⁻⁶–10⁻² M CaCl₂). The two parts were separated by a peat layer impeding a calcium transport from the upper to the lower part. The growth of the roots in the test media was examined daily by counting the total number of roots and the number of roots with laterals. The development of the number of roots had an exponential course at all calcium concentrations and was enhanced by increased calcium concentration. At harvest it was found that the size of the roots (length and dry weight) decreased with decreasing calcium concentration to a certain extent.     

Pectin immunolocalization and calcium visualization in differentiating derivatives from poplar cambium

Summary Calcium distribution and pectin esterification patterns in the cambial zone of poplar branches were studied with ionic microscopy and immunological tools respectively. Dynamic changes correlating with cell growth and cell differentiation were observed both on the xylem and on the phloem sides. In expanding cell walls of xylem derivatives, unesterified pectins were restricted to cell junctions and middle lamellae, occasionally accompanied by calcium ions. In contrast, in differentiating and mature phloem cells, acidic pectins and Ca²⁺ were present all over the walls leading to early stiffening of the polysaccharide network. Significant labelling was detected with JIM5 antibodies in some dictyosomes suggesting exocytosis of low methylated polymers towards the cell walls. At cell junctions, unesterified pectins might originate from the activity of pectinmethylesterases localized in these areas. Thus un- and deesterified pectins might be located in different cell wall domains whose distribution, varying with cell type, will confer specific extensibility to the wall matrix.Abbreviations BSA bovine serum albumin - DM degree of methylation - FITC fluorescein isothiocyanate - HM highly methylated pectins - LM low methylated pectins - PME pectin methylesterase - SIMS secondary ion mass spectrometry - TBS tris-buffered saline     

Wall extensibility and cell hydraulic conductivity decrease in enlarging stem tissues at low water potentials

Measurements with a guillotine psychrometer (H Nonami, JS Boyer [1990] Plant Physiol 94: 1601-1609) indicate that the inhibition of stem growth at low water potentials (low ψ_w) is accompanied by decreases in cell wall extensibility and tissue hydraulic conductance to water that eventually limit growth rate in soybean (Glycine max L. Merr.). To check this conclusion, we measured cell wall properties and cell hydraulic conductivities with independent techniques in soybean seedlings grown and treated the same way, i.e. grown in the dark and exposed to low ψ_w by transplanting dark grown seedlings to vermiculite of low water content. Wall properties were measured with an extensiometer modified for intact plants, and conductances were measured with a cell pressure probe in intact plants. Theory was developed to relate the wall measurements to those with the psychrometer. In the elongation zone, the plastic deformability of the walls decreased when measured with the extensiometer while growth was inhibited at low ψ_w. It increased during a modest growth recovery. This behavior was the same as that for the wall extensibility observed previously with the psychrometer. Tissue that was killed before measurement with the extensiometer also showed a similar response, indicating that changes in wall extensibility represented changes in wall physical properties and not rates of wall biosynthesis. The elastic compliance (reciprocal of bulk elastic modulus) did not change in the elongating or mature tissue. The hydraulic conductivity of cortical cells decreased in the elongating tissue and increased slightly during growth recovery in a response similar to that observed with the psychrometer. We conclude that the plastic properties of the cell walls and the conductance of the cells to water were decreased at low ψ_w but that the elastic properties of the walls were of little consequence in this response.     

Cell wall-bound malate dehydrogenase from horseradish

Isolated cell walls from horseradish contain NAD-specific malate dehydrogenase which is not released on treatment with 2 M NaCl. This enzyme catalyses a rapid reduction of oxalacetate. Its physiological role, however, is assumed to be the oxidation of malate, thus providing NADH as electron donor in the formation of H₂O₂, by a wall-bound peroxidase. In the presence of malate, NAD and Mn²⁺ ions, cell walls catalyse the synthesis of H₂O₂ which might be utilized in lignin formation. In analogy to the known malate-oxalacetate shuttles, the possibility is discussed that this cell wall-associated malate dehydrogenase is involved in the transport of cytoplasmic reducing equivalents through the plasmalemma into the cell wall.     

Sequence of key events in shoot gravitropism

It has recently been shown that asymmetric acid efflux is closely correlated with the gravitropic curvature of plant shoots and roots. The research reported here addresses whether auxin (IAA) redistribution in shoots is the cause or result of asymmetric acid efflux.

When abraded sunflower (Helianthus annuus cv Mammoth) hypocotyls are submerged in 20 millimolar neutral buffer, gravicurvature is greatly retarded relative to 0.2 millimolar controls. Nevertheless, in both buffer systems there is a similar redistribution of [³H]IAA toward the lower surface of gravistimulated sunflower hypocotyls. These results suggest that graviperception initiates IAA redistribution, which in turn results in auxin-induced asymmetric H⁺ efflux across the shoot. This interpretation is reinforced by data showing the effects of removal of the epidermal layers (peeling), osmotic shock, and morphactin treatment on gravicurvature and [³H]IAA redistribution. Peeling and osmotic shock inhibit gravicurvature but not redistribution. Morphactin inhibits both processes but does not inhibit hypocotyl straight growth.

     

On the role of calcium in indole-3-acetic acid movement and graviresponse in etiolated pea epicotyls

To determine whether Ca²⁺ plays a special role in the early graviresponse of shoots, as has been reported for roots, we treated etiolated pea epicotyls with substances known to antagonize Ca²⁺ (La³⁺), to remove Ca²⁺ from the wall (spermidine, EGTA), to inhibit calmodulin mediated reactions (chlorpromazine), or to inhibit IAA transport (TIBA). We studied the effect of these substances on IAA and Ca²⁺ uptake into 7 mm long subapical 3rd internode etiolated pea epicotyl sections and pea leaf protoplasts, on pea epicotyl growth, and graviresponse and on lateral IAA redistribution during gravistimulation.Our results support the view that adequate Ca²⁺ in the apoplast is required for normal IAA uptake, transport and graviresponse. Experiments with protoplasts indicate that Ca²⁺ may be controlling a labile membrane porter, possibly located on the external surface of cell membrane, while inhibitor experiments suggest that calmodulin is also implicated in both the movement of IAA and graviresponse. Since a major transfer of Ca²⁺ through free space during graviresponse has not yet been demonstrated, and since inhibition of calcium channels does not affect IAA redistribution (Migliaccio and Galston, 1987, Plant Physiology 85:542), we conclude that no clear evidence links prior Ca²⁺ movement with IAA redistribution during graviresponse in stems.Abbreviations IAA indole-3-acetic acid - CPZ chlorpromazine - EGTA ethylene glycol bis-(aminoethyl ether) N, N, N¹, N¹-tetracetic acid - G C gravicurvature The research was supported by NASA grant NSG-7290 to AWG.     

The role of extracellular free-calcium gradients in gravitropic signalling in maize roots

Gravitropism in roots has been proposed to depend on a downward redistribution of calcium across the root cap. However, because of the many calcium-binding sites in the apoplast, redistribution might not result in a physiologically effective change in the apoplasmic calcium activity. To test whether there is such a change, we measured the effect of gravistimulation on the calcium activity of statocyte cell walls with calcium-specific microelectrodes. Such a measurement must be made on a tissue with gravity sensing cells at the surface. To obtain such a tissue, decapped maize roots (Zea mays L. cv. Golden Cross Bantam) were grown for 31 h to regenerate gravitropic sensitivity, but not root caps. The calcium activity in the apoplasm surrounding the gravity-sensing cells could then be measured. The initial pCa was 2.60 ± 0.28 (approx 2.5 mM). The calcium activity on the upper side of the root tip remained constant for 10 min after gravistimulation, then decreased 1.7-fold. On the lower side, after a similar lag the calcium activity increased 1.6-fold. Control roots, which were decapped but measured before recovering gravisensitivity (19 h), showed no change in calcium activity. To test whether this gradient is necessary for gravitropic curvature, we eliminated the calcium activity gradient during gravitropism by applying a mobile calcium-binding site (di-nitro-BAPTA; 1,2-bis(2-amino-5-nitro-phenoxy)ethane-N,N,N,N-tetraacetic acid) to the root cap; this treatment eliminated gravicurvature. A calcium gradient may be formed by proton-induced calcium desorption if there is a proton gradient. Preventing the formation of apoplastic pH gradients, using 10 and 50 mM 2-(N-morpholino)ethanesulfonic acid (Mes) buffer or 10 mM fusicoccin to stimulate proton excretion maximally, did not inhibit curvature; therefore the calcium gradient is not a secondary effect of a proton gradient. We have found a distinct and rapid differential in the apoplasmic calcium activity between the upper and lower sides of gravistimulated maize root tips which is necessary for gravitropism.Abbreviations BAPTA 1,2-bis(2-aminophenoxy)ethane-N,N,N,N-tetraacetic acid - FC fusicoccin - Mes 2-(N-morpholino)ethanesulfonic acid The authors thank Phyllis Woolwine for drawing Fig. 1, Dr. Sarbjit Virk for assistance with total calcium measurements, Dr. Paul Sampson for statistical advice, and Michael Newton for developing the EM algorithm to analyze the time-series data. This work was supported by NASA grant NAGW-1394 and by a NASA Research Associateship to T.B. through NASA grant NAGW-70.     

Galvanic Stimulation of Volvox globator II. Mechanism of Galvanic Response, an Effect of Calcium Displacement

Slight increases or decreases in calcium ions in solutions which supported the growth of Volvox globator colonies caused the colonies to fall to the bottoms of their containers. High speed cinematography (600 frames/sec) showed that the flagella beat normally (21/sec) in balanced electrolyte solutions which have calcium concentrations between 0.5 and 1.0 mM. When colonies were placed in 10.0 or 0.0 mM CaCl₂ solutions, flagellar beating disappeared within 1 hr. The cessation of flagellar beating was reversible when colonies were replaced in the balanced solution. The Volvox cell wall has been shown to be a fairly good cation-exchanger with calcium ions acting as the counterion to the fixed negative change. Colonies that were photopositive and gave a cathodal galvanotaxis responded to DC electrical potentials by producing solution patterns that were indicators of colony electronegativity. Colony resistance to electroosmotic flow was compared in potassium and calcium solutions. When colonies were placed in darkness for 24 hr and stimulated by DC electrical potentials, their cation-exchange properties became reduced and the cell walls appeared thinner. Application of a high DC electrical potential to dark-adapted colonies caused the colonies to shrink on their anode sides (anodal contraction). Other workers have found that the flagella on the anodal sides of dark-adapted colonies ceased beating during DC electrical stimulation. It is hypothesized that the electric current caused an increase of calcium ions on the anodal side of the colony that inhibited the flagellar mechanism of beating on that side. It is also hypothesized that the galvanotaxis associated with light-adapted (photopositive) colonies was due to calcium displacements in the colony cell walls that affected the flagellar beating on both sides of the colony.