Influence of Genotype and Mineral Nutrition on the Distribution of Growth within Plants of Lolium perenne L. grown in Soil

Genotypes of Lolium perenne were grown with two levels of fertilizerapplication. Using exponential growth-rates and parameters derivedfrom them, the rate of growth of each genotype was partitionedinto the rates of initiation of new roots and tillers, and thegrowth of the individual roots and tillers after initiation.The growth of the individual roots was further analysed by measuringchanges in diameter and length of the main root, and the growthin the branches of the main root. The genotypes varied in their response to additional mineralnutrition. The greater the increase in the rate of shoot growthfor a genotype, the greater was its increase in the rate oftiller initiation, the smaller was the increase in the sizeof its tillers, and the greater was the decrease in its rateof root relative to shoot growth. Within a population of genotypes growing with the same levelof mineral nutrition, the greater the rate of shoot growth ofa genotype, the greater was the rate of initiation of new tillersand, at a low level of mineral nutrition, the smaller the sizeof tillers. With a higher level of mineral nutrition, the higherthe rate of tiller production, the smaller or larger was tillersize, depending upon environmental factors other than mineralnutrition. At both levels of mineral nutrition, the greaterthe rate of shoot growth, the smaller was the rate of root growthrelative to shoot growth, due to relatively less growth takingplace in the branches of the main root.     

Invertase Activity, Carbohydrate Metabolism and Cell Expansion in the Stem of Phaseolus vulgaris L.

In the stem of Phaseolus vulgaris L. the specific activity ofacid invertase was highest in the most rapidly elongating internode.Activity of the enzyme was very low in internodes which hadcompleted their elongation, in young internodes before the onsetof rapid elongation, and in the apical bud. From shortly afterits emergence from the apical bud the elongation of internode3 was attributable mainly to cell expansion. Total and specificactivities of acid invertase in this internode rose to a maximumat the time of most rapid elongation and then declined. Transferof plants to complete darkness, or treatment of plants withgibberellic acid (GA₃), increased the rate of internode elongationand final internode length by stimulating cell expansion. Bothtreatments rapidly increased the total and specific activitiesof acid invertase in the responding internodes; peak activitiesof the enzyme occurred at the time of most rapid cell expansion. In light-grown plants, including those treated with GA₃, rapidcell and internode elongation and high specific activities ofacid invertase were associated with high concentrations of hexosesugar and low concentrations of sucrose. As cell growth ratesand invertase activities declined, the concentration of hexosefell and that of sucrose rose. In plants transferred to darkness,stimulated cell elongation was accompanied by a rapid decreasein hexose concentration and the disappearance of sucrose, indicatingrapid utilization of hexose. No sucrose was detected in theapical tissues of light-grown plants. The results are discussed in relation to the role of acid invertasein the provision of carbon substrates for cell growth. Key words: Cell expansion, Acid invertase, Hexose, Sucrose, Phaseolus     

Encystment and Excystment of the Heterotrichous Ciliate Blepharisma stoltei Isquith*

SYNOPSIS. The structure and cytochemistry of encystment and excystment of Blepharisma stoltei Isquith are described. The encystment process may be subdivided into 4 stages: (i) in the precystic stage the buccal apparatus overlaps about the posterior, (ii) in early encystment, the buccal apparatus is resorbed and an ectocyst is secreted, (iii) an interwall space, endocyst, and plug are secreted during late encystment, and (iv) the resting cyst stage typically has disc-like structures on the ectocyst, and a vacuole in the macronucleus. In excystment, 6 distinct stages may be defined: (i) partial kineties are formed in early excystment, (ii) permanent kineties give rise to anlagen of the buccal apparatus during stomatogenesis, (iii) the organism elongates and reforms the vegetative shape in late excystment, (iv) some cysts then divide, (v) the redeveloped organism is liberated thru the plug pore, and (vi) the postcystic stage resembles the vegetative form except for its size and lack of pigmentation. Cortical structures, extracellular membranes, and the macronuclear membrane are composed of protein-lipids. Unbound protein and RNA are found in the cytoplasm thruout the cystic cycle. DNA is present only in the nuclei. Polysaccharides, 1st found in the cytoplasm, are shifted to the plug in encystment. The plug material disappears during excystment, while PAS positive granules appear in the cytoplasm.     

Systematics of Euplotes (Ciliophora, Hypotrichida); Toward Union of the Old and the New

SYNOPSIS. Prior to the general use of methods revealing the silverline system, members of the genus Euplotes were separated on the basis of body shape, sculpturing and arrangement of cirri. Since 1954, species have been separated on the basis of number of dorsolateral cilium rows, dorsal silverline system, number of fronto-ventral cirri, and form of the macronucleus. This paper describes E. charon Müller, 1773, E. quinquecarinatus Gelei, 1950, E. alatus Kahl, 1932, and E. bisulcatus Kahl, 1932, 4 species that are difficult to separate solely on the basis of the latter set of characters. By discussion of characters elucidated by a nigrosin-HgCl₂-formalin method, it is suggested that the following can form a basis for identification of members of this genus: 1) cortical sculpturing, 2) arrangement of all ciliary organelles, including dorsal and endoral cilia, and 3) details of the silverline system. Existing methods are indicated, some far more simple than silver methods, with which these characters can be elucidated.