MITOSIS IN THE ALGA VACUOLARIA VIRESCENS

Details of mitosis in the chloromonadophycean alga Vacuolaria virescens Cienk. have been studied with the light microscope. The chromosomes are relatively large (up to μ in length at metaphase) and so mitotic stages are readily distinguishable. Chromosomes can be recognized in interphase nuclei as fine strands of chromatin. Contraction of these chromosomes marks the beginning of mitosis and continues progressively until the transition from metaphase to anaphase. Disintegration of nucleoli is complete by late prophase and nucleolar reformation begins in telophase. Some chromosomes exhibit less densely stained regions; centromeres are also present as indicated by their differential staining and by the behavior of chromosomes at metaphase and anaphase. At anaphase progeny chromosomes move apart parallel to the division axis of the nucleus. As anaphase progresses the chromosomes fuse at the polar surface of the progeny chromosome groups. This process continues in telophase and the chromosome groups become more spherical. By the end of telophase nucleolar reformation has begun and the chromosomes have relaxed to their interphase condition.     

EFFECT OF BLUE-GREEN LIGHT ON PHOTOSYNTHETIC PIGMENTS AND CHLOROPLAST STRUCTURE IN THE MARINE DIATOM STEPHANOPYXIS TURRIS1

Blue-green light increased the chlorophyll concentration and chloroplast number of cells of Stephanopyxis turris (Grev.) Ralfs, compared to white light controls. Light fields for growth were 400 μW·cm^?2 (12:12 LD cycles). Chlorophyll increased up to 100%/cell, but no change in the ratio of chlorophylls to major carotenoids occurred. The effect was, therefore, not that of complementary chromatic adaptation. At the same time, blue-green light enhanced the photosynthetic fixation of CO₂. At the ultrastructure level, an increase in, and rearrangement of, the thylakoid system occurred.     

MITOSIS AND CYTOKINESIS IN THE CHLOROMONADOPHYCEAN ALGA GONYOSTOMUM SEMEN1

Mitosis and cytokinesis in Gonyostomum semen (Ehrenberg) Diesing have been investigated with the light microscope. During prophase nucleoli disappear and the chromatid structure of the chromosomes becomes apparent. Separation of chromatids at anaphase is accompanied by progressive fusion of the progeny chromosomes. This process continues into telophase by which stage the progeny nuclei consist of dense masses of chromatin with occasional chromosomes extending from their equatorial surfaces. By the end of telophase, nucleoli are reforming and the interphase nuclear morphology is reestablished. Mitosis is followed by cytokinesis, which is a relatively lengthy phase. In early cytokinesis the 2 interphase nuclei are present, and there is no indication of the forthcoming division of the cytoplasm. Later in cytokinesis a membrane is formed between the 2 nuclei. Final separation of the progeny individuals is accomplished by vigorous movements of swimming cells or, in the case of palmelloid cells, by the deposition of a mucilaginous layer.     

PHYCOBILIPROTEIN COMPOSITION AND CHLOROPLAST STRUCTURE IN THE FRESHWATER RED ALGA COMPSOPOGON COERULEUS (RHODOPHYTA)1

Serial sections of uncorticated axial cells of Compsopogon coeruleus revealed a single interconnected parietal chloroplast. Phycobilisomes in such chloroplasts were hemidiscoidal in shape with a broad-face diameter of ca. 25–30 nm. The molar ratio of phycobiliproteins in whole cell extracts was IPE:3PC:1APC, similar to isolated phycobilisomes. Two spectrally distinct C-phycocyanin forms (A618 nm, F648 nm and A630 nm, F652 nm) were resolved in dissociated phycobilisomes along with B-phycoerythrin and allophycocyanin.     

CHLOROPLAST STRUCTURE AND PIGMENT COMPOSITION IN THE RED ALGA GRIFFITHSIA PACIFICA: REGULATION BY LIGHT INTENSITY1

The ratio of accessory phycobiliproteins to chlorophyll a is controlled by light intensity in the marine red alga Griffithsia pacifica. The greatest changes in pigment ratios are observed below 300 ft-c; above 300 ft-c the response approaches saturation. Ultrastructural examination of chloroplasts of plants grown at different intensities reveals that the number of phycobilisomes per unit of photosynthetic thylakoid changes in direct proportion to the pigment ratios and in inverse proportion to the light intensity.     

PARTIAL CHARACTERIZATION OF THE CHLOROPLAST GENOME FROM THE CHROMOPHYTIC ALGA SYNURA PETERSENII (SYNUROPHYCEAE)1

Hoechst dye 33258-CsCl density gradients were used to isolate two satellite DNA species from Synura petersenii Korsh. sensu lato, a member of the Synurophyceae. One satellite DNA was identified as the chloroplast genome. The chloroplast genome is the smallest (91.5 kb) published for any chromophyte and approximates the size of the smallest functional chlorophyte chloroplast genome (Codium fragile, 89 kb). The second satellite DNA was small (34.5 kb), and its origin is undetermined. The potential of using the S. petersenii chloroplast genome in comparative studies for evaluating organellar evolution and algal systematics is discussed.     

CARBONIC ANHYDRASE IN THE CHLOROPLAST OF A COCCOLITHOPHORID (PRYMNESIOPHYCEAE)1

The activity and subcellular distribution of carbonic anhydrase in a coccolithophorid alga, CCMP 299, was examined. The enzyme could not be detected in crude cell homogenates but was present at high specific activity (27.5 unit·mg^?1 protein) in chloroplasts (density, 1.14 g·cm^?3) isolated in a sucrose gradient. The carbonic anhydrase activity was sensitive to known inhibitors. Inhibition at 50% (I₅₀) was obtained with concentrations of 4.60 mM and 2.65 mM for acetazolamide and NaN₃, respectively. These levels are more consistent with patterns of inhibition previously observed for chloroplastic (as compared to periplasmic) carbonic anhydrase. In this organism, carbonic anhydrase was localized in the chloroplast stroma. These findings are discussed in terms of the relationship among dissolved inorganic carbon interconversions, photosynthesis, and calcification.     

A GREEN DINOFLAGELLATE WITH CHLOROPHYLLS a and b: MORPHOLOGY,FINE STRUCTURE OF THE CHLOROPLAST AND CHLOROPHYLL COMPOSITION1

A green-colored marine unicell has been grown in unialgal culture and its morphology, chloroplast fine structure, and chlorophyll composition investigated. The organism is typical of dinoflagellates in its shape, flagellation, nucleus, mitochondria, and trichocysts. It is similar to Gymnodinium but possesses fine body scales. Chloroplasts and two kinds of vesicles bounded by double membranes, but no organelles obviously identifiable as nuclei or mitochondria, are associated in ribosome-dense cytoplasm separated by a double membrane from the dinophycean cytoplasm. The chloroplasts are unlike any previously reported for dinoflagellates. Each is enclosed by an envelope consisting of a double membrane. Chloroplast lamellae consist of three appressed thylakoids. Interlamellar pyrenoids are present. Pigment analysis reveals chlorophylls a and b but not chlorophyll c. It seems likely that the organism is an undescribed dinoflagellate containing an endosymbiont with chlorophylls a and b and that the reduction of the endosymbiont nucleus and mitochondria has permitted a more initmate symbiosis.     

CHLOROPLAST STRUCTURAL CHANGES INDUCED BY WHITE LIGHT IN THE MARINE DIATOM STEPHANOPYXIS TURRIS1,2

The intensity of white tight used for growing Stephanopyxis Turris (Grev.) Ralfs affects the structure of the chloroplasts. In particular, the conformation of the thylakoids, within the bands is altered by increasing the intensity. At low light (100 μW.cm^-2, 12:12 LD cycles) the thylakoids are generally parallel, whereas at 500 μW.cm^-2 the thylakoids tend to be twisted and out of plane. The possible significance of these conformational changes is discussed.     

DIVISION APPARATUS OF THE CHLOROPLAST IN NANNOCHLORIS BACILLARIS (CHLOROPHYTA)1

Chloroplast division in Nannochloris bacillaris Naumann (Chlorophyta) was examined by electron microscopy after preparation of samples by freeze-substitution. A pair of belts appeared on the surface of the outer and inner envelope membranes at the middle of the chloroplast. These belts seemed to be constructed of thin fibrils that run parallel to the longitudinal direction of the belts. The outer fibrillar belt increased in width as the constriction of the chloroplast advanced. It appears that the fibrillar belt is the division apparatus of the chloroplast. It encircles the chloroplast and finally divides the chloroplast in two as the diameter of the belt decreases.     

CELL WALL STRUCTURE AND IRON DISTRIBUTION IN THE GREEN ALGA STAURASTRUM LUETKEMUELLERI (DESMIDIACEAE)1

The cell wall of Staurastrum luetkemuelleri Donnat & Ruttner was examined with scanning electron microscope (SEM) using whole cells, in thin sections with transmission electron microscope (TEM), and in air dried whole cells and unstained thin sections with X-ray microanalysis in the scanning-transmission electron microscope (STEM). The cell wall was ornamented with spines and wartlike structures. Spines were solid structures, consisting of deposits of cell wall material between two main cell wall layers. The wart-like structures were pore organs extending through the cell wall and the mucilaginous layer outside the cell wall. The pore cylinder was surrounded by deposits of cell wall material similar to the ones in the spines. X-ray microanalysis of selected areas on whole cells from a natural population showed iron accumulation in discrete locations on the cell extensions of S. luetkemuelleri. In the unstained thin sections iron was found only in the cell wall deposits in the spines. Cells grown in laboratory cultures failed to show iron accumulation regardless of readdition of iron-EDTA (Fe-EDTA) to the culture medium.     

WALL STRUCTURE AND LATERAL FORMATION IN THE ALGA BRYOPSIS

Green , Paul B. (U. Pennsylvania, Philadelphia.) Wall structure and lateral formation in the alga Bryopsis. Amer. Jour. Bot. 47(6) : 476–481. Illus. 1960.—The large multinucleate cells of Bryopsis pennata regularly produce laterals at the apical tip. Cells were freed of protoplasm and the remaining cell wall was flattened and studied in polarized light and interference microscopes. Both the cylindrical main axis and the cylindrical laterals are negatively birefringent and thus apparently have generally a transverse arrangement of microfibrils. Lateral formation is first seen in the formation of round fields of concentric microfibrils on the main axis which persist as lateral-bases. The center of a field protrudes, making a small out-pouching of the main axis. The thin-walled protrusion increases first mostly in diameter and then in length to make a lateral. There is a definite correlation between wall structure (optical anisotropy) and cell shape in Bryopsis.     

ULTRASTRUCTURE OF THE GREEN ALGA DICHOTOMOSIPHON TUBEROSUS WITH SPECIAL REFERENCE TO THE OCCURRENCE OF STRIATED TUBULES IN THE CHLOROPLAST1

The ultrastructure of the siphonous green alga Dichotomosiphon tuberosus (A. Br.) Ernst is compared with that of other siphonous plants. There is a characteristic association between the Golgi bodies and endoplasmic reticulum, but. the mitochondria are not involved in the association as they are in Vaucheria and the phycomycete Saprolegnia. An unusual structure and arrangement of the chloroplasts is described as well as a previously unreported type of “striated tubule” which occurs in most if not all chloroplasts, and amyloplasts. The structure of these tubules is compared with that of other tubules recently found in green algae and higher plants. In addition, cytoplasmic microtubules arranged in the longitudinal direction of the siphon suggest a function in cytoplasmic streaming.     

SEXUAL REPRODUCTION AND GENETIC VARIATION IN THE SUBAERIAL ALGA CEPHALEUROS VIRESCENS (ULVOPHYCEAE,CHLOROPHYTA)

Cephaleuros virescens is a pantropical subaerial green alga with no known long‐range dispersal mechanisms. Sexual reproduction is relatively rare and may involve intragametangial fusion of identical, mitotically produced gametes. This situation may be a consequence of adaptation to the subaerial habitat. Genetic variation among populations of C. virescens may be very low and might be positively correlated to the distance (hence, time) separating populations. Thus, assessing the global biogeography of C. virescens requires analysis of what might be low levels of variation. Because C. virescens occurs on literally hundreds of different host species, the question of host‐races must also be considered. Preliminary analysis of local populations of C. virescens, originally obtained as field collections from three different host species and subsequently raised in culture, is the first step in addressing the biogeography of this alga. We are using the AFLP plant mapping protocol by PE Applied Biosystems to detect genetic variability in the three isolates of C. virescens. AFLP is a PCR‐based DNA fingerprinting technique that detects the presence or absence of restriction fragments rather than fragment length differences. Because the number of restriction fragments that can be detected with the AFLP technique is “virtually unlimited,” it is a very powerful tool for assessing the degree of relatedness or variability among cultivars or isolates. AFLP techniques have been used successfully to distinguish morphologically identical bacteria, determine relatedness among soybean accessions, reveal genetic variability within bee samples, and identifyfall armyworm strains and hybrids.     

THE FINE STRUCTURE OF MITOSIS AND CELL DIVISION IN THE CHRYSOPHYCEAN ALGA OCHROMONAS DANICA1

At the ultrastructural level, cell division in Ochromonas danica exhibits several unusual features. During interphase, the basal bodies of the 2 flagella replicate and the chloroplast divides by constriction between its 2 lobes. The rhizoplast, which is a fibrous striated root attached to the basal body of the long flagellum, extends under the Golgi body to the surface of the nucleus in interphase cells. During proprophase, the Golgi body replicates, apparently by division, and a daughter rhizoplast, appears. During prophase, the 2 pairs of flagellar basal bodies, each with their accompanying rhizoplast and Golgi body, begin to separate. Three or 4 flagella are already present at this stage. At the same time, there is a proliferation of microtubules outside the nuclear envelope. Gaps then appear in the nuclear envelope, admitting the microtubules into the nucleus, where they form a spindle. A unique feature of mitosis in O. danica is that the 2 rhizoplasts form the poles of the spindle, spindle microtubules inserting directly onto the rhizoplasts. Some of the spindle microtubules extend from pole to pole; others appear to attach to the chromosomes. Kinetochores, however, are not present. The nuclear envelope breaks down, except, in the regions adjacent, to the chloroplasts; chloroplast ER remains intact throughout mitosis. At late anaphase the chromosomes come to lie against part of the chloroplast ER. This segment of the chloroplast ER appears to be incorporated as part of the reforming nuclear envelope, thus reestablishing the characteristic nuclear envelope—chloroplast ER association of the interphase cell.     

THE ULTRASTRUCTURE OF GALLS ON THE RED ALGA GRACILARIA EPIHIPPISORA1

A strain of Gracilaria epihippisora Hoyle produces gall-like cell proliferations in culture. These growths can be excised and grown separately, where they retain an undifferentiated morphology and reach 5mm in diameter. The gall tissue consists of a single morphological cell type without any differentiation between surface and internal cells as is characteristic of normal thallus tissue. Gall cells are typically 20–40 μm in diameter and contain the usual complement of organelles and a prominent vacuole, although there are several distinct features. The large multilobed plastids have an extensive proliferation of thylakoid membranes, which form an arrangement of loops and spirals. The thallus outer cell wall layer is highly reduced. The gall growths contain intracellular virus-like particles (ca. 80 nm in diameter) that occur in discrete groups.     

THE CHLOROPLAST STRUCTURE OF IOJAP MAIZE

The ultrastructure of the plastids from the genetically caused but maternally transmitted mutant iojap of maize was studied at four stages of development. The plastids of green and potentially green tissue were normal at all stages studied. The plastids of the white tissue were aberrant at all stages studied and lacked the normal grana-fretwork system as well as a normal prolamellar body. DNA-like fibrils were present in aberrant plastids, but ribosomes were absent. This indicates that chloroplast ribosomes are important in chloroplast membrane formation. Aberrant plastids fail to develop normally and are not a degeneration of normal plastids. Aberrant and normal plastids occur in single cells in green tissue, but only aberrant plastids have been found in white tissue.     

THE FINE STRUCTURE OF SPOROGENESIS IN THE XANTHOPHYCEAN ALGA PSEUDOBUMILLERIOPSIS PYRENOIDOSA1,2

The fine structure of vegetative cells, sporogenesis, and zoospores of the xanthophycean alga Pseudo-bumilleriopsis pyrenoidosa is described. Cleavage in sporogenesis closely resembles that of certain aquatic fungi.