Grown under saline conditions, Suaeda maritima accumulates Na(+) and Cl(-) into its leaves, where individual mesophyll cells behave differently in their compartmentation of these ions. Measurements of ion concentrations within selected subcellular compartments show that freeze-substitution with dry sectioning is a valuable preparative technique for analytical electron microscopy of highly vacuolate plant material. Using this approach, absolute estimates were made of Na(+), K(+) and Cl(-) concentrations in the cytoplasm, cell walls, chloroplasts and vacuoles of leaf mesophyll cells.

SUMMARYSignificant varietal diflFerences were apparent in the survival of seedlings of maize in saline conditions but only at relatively high external concentrations (200 mol m~^ NaCl), where there was a range from 0 to 66 % survival, 25 d after salinization. For the varieties examined there was a strong negative correlation between Na concentrations in the third leaf and survival. Two resistant varieties (Across 8024 and Protador) and one salt-sensitive variety (LGu) were identified. The characteristics of ion accumulation were clearly different in salt-tolerant and salt-sensitive types, the difference becoming more pronounced with plant age.The distribution of ions, particular those of Na, K and Cl, was determined within subcellular compartments of roots cells using X-ray microanalysis of freeze-substituted tissue. Salinity induced a greater increase (about 1-7 times) in cytoplasmic Na concentration in the salt-sensitive variety (LGu) ^^an in resistant varieties (Across 8024 or Protador). The mean K :Na ratio in the cytoplasm of the root cortical cells in the salt-resistant varieties grown for 15 d in saline conditions (100 mol m"^ NaCl) was twice that found for LG^i.Sodium and Cl concentrations in the vacuoles decreased radially inwards from the epidermal cells in salt-treated roots of

SUMMARY Freeze‐substitution is a technique suitable for the preparation of unicellular and multicellular plant and animal specimens for conventional light microscopy, TEM and SEM. It is also widely used as a means of preparing animal and plant tissues for the localization of water soluble substances by analytical electron microscopy, autoradiography or visual detection of precipitates. The technical requirements of preparation, together with an evaluation of the procedures, are presented for various applications. Careful selection and evaluation of freezing technique, substitution solvent and regime are required for meaningful results.

A survey was made of the sweetness and sourness of the fruits of apple cultivars. Measurements of the concentration of sugars and malic acid in ripe fruits were made and the variation between samples of a cultivar, between cultivars, between years and between cultivars and their tetraploid and colour sports was studied and showed a wide range of variation between cultivars but fairly constant values within cultivars.The study of a number of progenies shows that sweetness and sourness are inherited independently. Sweetness shows a quantitative pattern of inheritance and the progeny mean approximates the mid-parent value. Sourness is controlled by a single gene, with medium and high acidity being dominant to very low, superimposed on a quantitative pattern.The mean sugar and acid concentrations of a progeny and the approximate range of variation can be predicted from the sugar and acid concentrations found in the parents.

An attempt has been made to localize glycinebetaine in shoots of Suaeda maritima L. Dum. using a technique based on the formation of an iodoplatinate precipitate. Deposits were largely restricted to the cytoplasm of salt-grown plants and were analysed by transmission analytical electron microscopy. The results are considered to support the hypothesis that glycinebetaine acts as a cytoplasmic osmoticum to balance high vacuolar salt levels in certain halophytes.

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SUMMARY A method, utilizing freeze substitution, is described for the preparation of plant tissue for analytical electron microscopy. The fine structure of the cytoplasm was adequately preserved after freezing leaf tissue in 2‐methylbutane at −170°C. Furthermore, following substitution in ether, losses of sodium and potassium from the tissue were less than 4% of the original ion content and the loss of chloride was less than 1%. The merits of the procedure as a means of tissue preparation for ion localization studies are discussed.