Chloroplast ultrastructure, pigment content, and composition were investigated during growth of 'Puma' rye at warm and cold-hardening temperatures. Cytological characteristics of leaf mesophyll cells were altered upon growth at cold-hardening temperatures as indicated by an apparent increase in the amount of cytoplasm. Univacuolate and multivacuolate mesophyll cells were found in leaves from cold-hardened plants, but only univacuolate mesophyll cells were found in leaves from warm-grown plants. Chloroplast ultrastructure was affected by growth at low temperature as indicated by a higher frequency of smaller granal stacks. However, there was no significant difference in the number of grana per chloroplast in mesophyll cells from either warm- or cold-grown plants. Chlorophyll per plastid increased by a factor of 1.67 upon growth at cold-hardening temperatures, as did β-carotene and the xanthophylls. However, there was no significant difference in photosynthetic unit size based on P700 measurements between chloroplasts from warm- or cold-grown tissue. Analysis of freeze-fractured thylakoid membranes indicated a loss in the bimodal nature of particle size distribution on the exoplasmic fracture face and a general increase in particle size on the protoplasmic fracture face upon growth and development at cold temperatures. However, particle densities on the exoplasmic and protoplasmic fracture faces were not significantly different in thylakoids from plastids developed at either warm or cold temperatures. It is concluded that chloroplast ultrastructure and pigment content but not composition are altered upon growth and development at cold-hardening temperatures.

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Chlorophyll–protein complexes of thylakoid membranes from rye plants (Secale cereale L. cv. Puma) grown at warm and cold-hardening temperatures were investigated by gel electrophoresis. Complex IV from cold-grown tissue was detectable in the presence of dodecyl sulfate if and only if solubilization and electrophoresis were performed at 4 °C, whereas complex IV from warm-grown material was detectable if membrane solubilization and electrophoresis were performed at either 4 or 23 °C in the presence of dodecyl sulfate. In the presence of octyl-β-D-glucopyranoside, the chlorophyll–protein complexes from cold-grown tissue were less stable at 23 °C than those from warm-grown tissue. Regardless of the detergent used, there was always more oligomer of the light-harvesting complex present in samples prepared from thylakoid membranes of warm-grown tissue than those from membranes of cold-grown tissue. It is concluded that the pigment–protein interaction in those complexes associated with photosystem II and the light-harvesting chlorophyll a/b – protein complex has been altered upon growth and development at cold-hardening temperatures.

Chloroplasts isolated from rye (Secale cereale L. cv Puma) grown at 5°C (RH) accumulated 260% more plastoquinone A (PQA) per plastid than chloroplasts isolated from rye grown at 20°C (RNH). The number of plastoglobuli increased by 270% in RH chloroplasts compared with RNH plastids. When RH plastids were lysed and washed, the number of plastoglobuli associated with thylakoid membranes decreased significantly, yet the PQA levels remained high. Room temperature fluorescence induction indicated that (a) there is no change in the size of the PQA pool immediately available for photochemistry in RNH and RH thylakoids and (b)

The green algal genus Nannochloris Naumann was originally described as having a simple binary division mechanism and lacking autosporulation and a parental cell wall. An initial observation of autosporulation in one isolate ascribed to this genus encouraged a broader investigation to determine whether or not autosporulation is restricted to only certain forms or is the reproductive mechanism used in the genus as a whole. Five cultures were examined; all had typically chlorophycean ultrastructure and both chlorophylls a and b. Nannochloris atomus differed from the other forms (two Nannochloris spp., Nannochloris bacillaris, and Nannochloris maculants) in having a pyrenoid and different wall structure and other ultrastructural features. However, reproduction in all five was by autosporulation with a thin, yet clearly defined, parental wall surrounding the two–four daughter cells in electron micrographs. These and related findings of other workers point to the need for a redefinition of the genus.