Occurrence of Amoebae on Oak Leaf Lettuce (Lactuca sativa var. crispa) and Boston Lettuce (L. sativa var. capitata)1

The colonization, distribution, population density, and species diversity of amoebae on leaves of Oak Leaf lettuce, Lactuca sativa var. crispa, and Boston lettuce, L. sativa var. capitata, were investigated. The role of soil in the colonization of Oak Leaf lettuce was determined by comparing numbers of amoebae present on basal leaves (those that pass through soil) with numbers on wrapped leaves (those that do not pass through soil). Amoebae were present in ten samples of basal leaves and ranged from 154–1510/g of leaf tissue. Wrapped leaves failed to yield amoebae in seven of ten trials and contained <4 amoebae/g of tissue. Mean values for the population density of amoebae on Oak Leaf basal leaves and Boston lettuce leaves were 484 ± 133 and 453 ± 93, respectively. The distribution of amoebae on green and white parts of leaves from both kinds of lettuce was studied. The occurrence of amoebae on rinsed, unrinsed, visibly clean, and visibly dirty samples of Boston lettuce leaves was established.     

Glugea gasti sp. n., a Microspridan Pathogen of the Boll Weevil Anthonomus grandis1,2,3

SYNOPSIS. Glugea gasti sp. n., a microsporidan pathogen of Anthonomus grandis Boheman (the boll weevil), is described and a probable life cycle presented. The alimentary canal, and probably the mesenteron 1st, is the initial site of infection, altho the disease later becomes generalized thruout most body tissues. Binucleate sporoplasms initiate the 1st schizogonic phase, characterized by mono- and bi-nucleate schizonts. The 2nd schizogonic phase is characterized by mono-, bi- and quadrinucleate schizonts, by prolific multiplication, by the dense compact nuclei early in this phase, and late in this phase by larger schizonts with less dense vesicular nuclei. This phase terminates in formation of diplokarya. The sporogonic phase is characterized by combination of the 2 nuclei in the diplokaryon followed by nuclear divisions in a sequence closely resembling meiosis. Two sporoblasts are produced from each sporont. Mature spores in wet mounts by phase contrast were 4.3 ± 0.3 μ long by 2.3 ± 0.2 μ wide. The polar filament averaged 76 μ long. Mature spores were present about 24 hours after infection. Some observations are presented on an external filament extending from one pole of the spore to host tissue and other events during the process of spore morphogenesis.     

CHROMOSOME COUNTS,CYTOLOGY, AND REPRODUCTION IN THE CACTACEAE

Chromosome counts and observations of reproduction for 55 taxa of Cactaceae indicate that polyploidy is correlated with self-fertility, adventive embryony, profuse branching, and vegetative reproduction. Six genera (Blossfeldia. Cleistocactus, Frailea, Pelecyphora, Rebutia, and Strombocactus) and 35 species or varieties are reported here for the first time. Preliminary observations of pachytene and diplotene indicate that these stages may be more useful in chromosome recognition than mitotic stages. Secondary association at metaphase I and II is interpreted as a retention of homologue association at interphase I and II (interkinesis). During meiosis of certain species, Feulgen negative bodies are present. The production of an abnormal premeiotic division is suggested as a mechanism for polyploid origin.     

GENETIC DIFFERENTIATION AND HYBRIDIZATION BETWEEN CAREX GYNODYNAMA AND C. MENDOCINENSIS (CYPERACEAE) IN CALIFORNIA

Patterns of variation within and between Carex gynodynama and C. mendocinensis were investigated by studying allozyme and chromosome variation in natural populations and structural variation using herbarium specimens. Multivariate analyses of structural data demonstrated that C. gynodynama is clearly distinct from C. mendocinensis, and that sterile specimens similar to C. mendocinensis are intermediate between that species and C. gynodynama. The mean genetic distance between the two species, based on allozyme phenotypes at 17 enzyme-coding loci, was 0.22 ± 0.12. The sterile putative hybrids had the expected heterozygous pattern at three enzyme-coding loci at which the parental species were fixed for different alleles. Chromosome numbers are reported for the first time for both species and their putative hybrid. Carex mendocinensis had a different number in each of the three populations examined with n = 28, n = 29, or n = 30. Chromosome counts from one population of C. gynodynama revealed five plants with n = 25 and one with n = 26. Putative hybrids from this population exhibited irregular pairing at meiosis with 2n = ca. 55–57. Patterns of allozyme variation also suggest that C. mendocinensis has an outcrossing or mixed mating system but that C. gynodynama is an inbreeding species. Carex gynodynama exhibited very little variation in structure, habitat, or at the enzyme-coding loci examined, suggesting that it may have experienced a genetic bottleneck relatively recently. Carex mendocinensis had higher levels of variation both within and between populations at enzyme-coding loci and in structural features. This pattern of variation and a geographic distribution centered in serpentine areas of the Klamath–Siskiyou region, with disjunct smaller populations in serpentine areas farther south, suggest that C. mendocinensis once may have been a more widespread species.     

ULTRASTRUCTURE OF MEIOSIS IN DASYA BAILLOUVIANA (RHODOPHYTA). II. PROMETAPHASE I—TELOPHASE II AND POST-DIVISION NUCLEAR BEHAVIOR1

This is the second of two papers which together are the first comprehensive ultrastructural report of meiosis in a red alga. Many details of the meiotic process in Dasya baillouviana (Gmelin) Montagne are the same as those reported previously for mitotic cells in ceramialian red algae, but several characteristics seem unique to meiotic cells. The nucleus and nucleolus of meiotic cells are larger than those of mitotic cells and large accumulations of smooth ER are often found at the division poles during meiosis 1. The function of the ER accumulations is unknown. Importantly, both interkinesis and a simultaneous division of two separate nuclei during meiosis II was demonstrated. These new observations fail to support earlier speculation on higher red algae for a “uninuclear” meiosis (both nuclear divisions within the same nuclear envelope). However, following meiosis II the four nuclei migrate centripetally and possibly fuse in the center of the tetrasporangium. This post-division nuclear maneuvering is not understood, but our interpretation accounts for the earlier and erroneous impression of “uninuclear” meiosis. Perhaps the most important aspect of meiosis observed in Dasya is its basic adherence to the pattern commonly seen in higher plants and animals. This conservatism of the meiotic process lends further skepticism to the belief that red algae are extremely “primitive” organisms, although they undoubtedly represent a very “ancient” group of eukaryotic plants.     

Growth at 37 degrees C of the EGs strain of the amoeboflagellate Naegleria gruberi containing viruslike particles. I. Nuclear changes

Naegleria gruberi amoebae, EG_s strain, containing viruslike particles (VLP) were grown at temperatures of 21° and 37°C. At 21°C, the amoebae displayed the morphological structures associated with development of the VLP's. At 37°C, however, gross morphological modifications and new structures appeared. When amoebae were at 37°C for less than 12 hr, nuclei were found to have a larger number of VLP's than amoebae at 21°C. Exposure of the amoebae to the higher temperature for 12–24 hr resulted in a scarcity of particles. Large bundles of microtubulelike fibrils were present in the nucleoplasm of amoebae at 37°C, and, in addition, the nuclei showed degenerative modifications. The fibrillar changes were not due to the elevated temperature alone since a substrain of EG_s (=EG_B) not infected with VLP's exhibited no nuclear modifications. It is assumed that the elevated temperature accelerated and enhanced a lytic effect of the VLP's upon the cells.     

Chromosome cycles of the basidiomycete Cyathus stercoreus (Schw.) De Toni

Summary Chromosome cycles of the basidiomycete Cyathus stercoreus (meiosis and mitosis) are described. The fusion of two nuclei of compatible mating type takes place in the developing basidium at the end of telophase of the presynaptic mitosis. Synapsis follows immediately after nuclear fusion. During synapsis the chromosomes elongate, facilitating pairing. Meiosis and mitosis are essentially similar to those processes in higher organisms. Details of divisional stages are described and illustrated with photomicrographs. The presence of centrioles and spindles is demonstrated. The presence of quadrivalents as well as secondary associations of like chromosomes suggests that Cyathus stercoreus may be a tetraploid species.     

Aberrant meiosis and spindle abnormalities in Paspalum paspaloides (Michx.) Scribn (Gramineae)

Meiotic chromosome behaviour was studied in two collections of Paspalum paspaloides (Michx.) Scribn. In one of these chromosome mosaicism, restitution nuclei, multinucleate microsporocytes and multipolar and divergent spindles were observed. Chromosome mosaicism resulted from abnormal cell cleavage. In microsporocytes exhibiting chromosome mosaicism, the number of univalents per cell decreased as the chromosome number per cell increased. The increase in chromosome number brought it close to the euploid number (2n=60). Chromosome mosaicism never involved any increase above the cuploid number. In the other collection, meiosis was relatively normal.The work has been carried out at the Department of Botany, Gorakhpur University.     

FURTHER STUDIES ON MEIOSIS IN THE MYXOMYCETES

Ross, Ian K. (Yale U., New Haven, Conn.) Further studies on meiosis in the Myxomycetes. Amer. Jour. Bot. 48(3): 244–248. Illus. 1961.—Photomicrographs of meiotic figures in 5 species of Myxomycetes are presented as further evidence of the time and location of meiosis in these organisms. Three members of the Physarales studied differed from species studied previously in that the cleavage of the protoplasm began during the second meiotic division and not after the divisions had been completed. Chromosome numbers were found to be in accord with previous observations and ranged from n = 25 to 90 depending on the species.     

Pattern of DNA synthesis in nuclei of feeding and starving Amoeba proteus : A cytofluorometric study

The DNA content in isolated nuclei of Amoeba proteus was determined for each of the three groups of synchronized amoebae over different intervals after division. Several nuclei of each amoeba group were fixed 1 h after division, before the amoebae were fed. About h after division, some amoebae in each group were given food (Tetrahymena pyriformis), while the rest were left starving. Samples of the nuclei of fed and starved amoebae were fixed 24 h and (in different groups) 42–55 h after division. In each group from 22 to 48% of the fed amoebae had divided prior to the last nuclei fixation. Starved amoebae did not undergo division. In all three amoeba groups the nuclear DNA content of fed cells by the end of interphase had increased to 280–300% the value for 1 h amoebae. The nuclear DNA content of starved amoebae of all three groups was also increased, and in two groups it exceeded the initial level more than two-fold. However, in all three groups, it was lower than that of fed amoebae. In all the groups the nuclear DNA content in fed amoebae grew after 24 h, i.e. during the second half of interphase, the increase accounting for from 11 to 48% of the total increase. The hypothesis is put forward that the increase in the nuclear DNA content during the cell cycle of Amoeba proteus is the result of two processes: (1) one-time replication of the DNA of the whole genome; and (2) repeated replication of some part of the DNA. In amoebae the relation of the pattern of nuclear DNA synthesis to the diet is considered.     

Cytological studies on F1 hybrids of Solanum integrifolium with S. melongena and S. melongena var. insanum

S. integrifolium (2n = 24) can easily be crossed as the pistillate parent with S. melongena (2n = 24) and S. melongena var. insanum (2n = 24). However, crosses in the other direction do not succeed. Both hybrids are vigorous. Chromosome association at diakinesis and metaphase I was studied. Chromosome associations higher than bivalents were observed in the hybrids indicating structural repatterning of chromosomes. The modal chromosome association in hybrids was twelve bivalents per PMC. This is suggestive of the retention of ancestral chromosome homeologies by the taxa concerned. Despite regular meiosis both hybrids were highly pollen-sterile (about 95%), which was attributed to segregational events of the recombined chromosomes.     

DEVELOPMENT OF THE OVULE AND FEMALE GAMETOPHYTE IN EUSTACHYS PETRAEA AND E. GLAUCA (POACEAE)

The unilocular pistil in Eustachys contains a single ovule with lateral placentation. In E. petraea and E. glauca, the mature ovule is bitegmic, tenuinucellate, and amphitropous with the endostomic micropyle oriented toward the base of the locule. A single hypodermal archesporial cell enlarges to form the megasporocyte. The chalazal dyad member is larger than the micropylar one, and meiosis II is nonsynchronized. Two-thirds of the tetrads are linear and one-third T-shaped. The chalazal megaspore is functional. Initially ovoid, the two-nucleate female gametophyte becomes curved as it enlarges. The four-nucleate stage becomes wider at its extremities and constricted in the center. Synchronous mitotic divisions establish the eight-nucleate stage with four nuclei at each pole separated by a large central vacuole. In E. petraea, the maturation sequence begins with antipodal differentiation, followed by differentiation of the egg apparatus, migration of the polar nuclei to the center, and division of the antipodals to produce twelve cells. The sequence in E. glauca begins with migration of the polar nuclei followed by differentiation of the antipodals, egg apparatus, and antipodal replication to six cells. The polar nuclei fuse to form a secondary nucleus appressed to the egg cell in E. glauca and separated from it by a vacuole in E. petraea. T-tests for length measurements for various stages of development indicate that the functional megaspore and two-nucleate female gametophyte are significantly larger in E. glauca than in E. petraea. There is no significant difference in gametophyte length at the four-nucleate stage, and at the eight-nucleate stage, length in E. petraea surpasses that in E. glauca. This gap widens significantly at the mature stage. Nuclear volumes are significantly greater in E. glauca than in E. petraea in the functional megaspore and two-nucleate stage, but the volumes are similar at the four-nucleate stage. Consideration of the differences in structural complexity between the sporophyte and gametophyte generations leads to the conclusion that the female gametophytes of these species are more distinctive than are the sporophytes.     

Chromosome or chromatin condensation leads to meiosis or apoptosis in stationary yeast (Saccharomyces cerevisiae) cells

When starved of essential nutrients, yeast cells cease mitotic division and enter an alternative state called the 'stationary phase'. In this paper, we report that stationary cells enter two major pathways: meiosis and apoptosis. Using transmission electron microscopy, five types of cell were identified in the stationary phase: (1) cells with chromosome condensed nuclei; (2) cells with normal, homogeneously stained nuclei; (3) sporulated cells; (4) apoptotic cells, in which chromatin, but not individual chromosomes, was condensed; and (5) dead cells, in which nuclei and cytoplasm were degraded. Further evidence using live cell imaging and mutation analysis suggested that cells with condensed chromosomes underwent meiosis, whereas chromatin condensed cells underwent apoptotic cell death. Cells with homogeneous nuclei are believed to be in the true resting state and undergo cell death when starvation continues. Chromosome or chromatin condensation may serve as a hallmark of life or death for stationary cells.     

The pattern of zygotene and pachytene pairing in allotetraploid Aegilops species sharing the D genome

Chromosome pairing behaviour of the allotetraploid Aegilops species sharing the D genome, Ae. crassa (DDMM), Ae. cylindrica (DDCC) and Ae. ventricosa (DDNN), was analyzed by electron microscopy in surfacespread prophase-I nuclei. Synaptonemal-complex analysis at zygotene and pachytene revealed that synapsis in the allotetraploids was mostly between homologous chromosomes, although a few multivalents were also formed. Only homologous bivalents were observed at metaphase-I. It is concluded that the mechanism controlling bivalent formation in these species acts mainly at zygotene by restricting pairing to homologous chromosomes, but also acts at pachytene by preventing chiasma formation in homoeologous associations. These observations are discussed in relation to mechanisms of diploidization of polyploid meiosis.     

Evidence for Meiosis in the Testate Amoeba Arcella

ABSTRACT. Electron microscopic studies of Arcella vulgaris have revealed a sexual process occurring in cysts. The evidence includes: I) synaplonemal complexes in prophasic nuclei. 2) two consecutive divisions different from vegetative mitosis, 3) degeneration of certain products of these nuclear divisions, and 4) fusion of nuclei indicating karyogamy. The process is apparently autogamy preceded by a two-division meiosis. The testate amoebae can no longer be considered asexual.     

Nuclear transfer in cattle using in vivo-derived vs. in vitro-produced donor embryos: Effect of developmental stage

To determine the best developmental stage of donor embryos for yielding the highest number of clones per embryo, we compared the efficiencies of nuclear transfer when using blastomeres from morulae or morulae at cavitation, or when using inner-cell-mass cells of blastocysts as nuclear donors. This comparison was done both on in vivo-derived and in vitro-produced donor embryos. In experiment 1, with in vivo-derived donor embryos, nuclei from morulae at cavitation supported the development of nuclear transfer embryos to the blastocyst stage (36%) at a rate similar to that of nuclei from morulae (27%), blastomeres from morulae at cavitation being superior (P < 0.05) to inner-cell-mass cells from blastocysts (21%). The number of blastocysts per donor embryo was significantly (P < 0.05) higher when using nuclei from morulae at cavitation (15.7 ± 4.1) rather than nuclei from morulae (9.8 ± 5.5) or blastocysts (6.3 ± 3.3). With in vitro-produced donor embryos (experiment 2), nuclei from morulae yielded slightly more blastocysts (32%) than nuclei from morulae at cavitation (29%), both stages being superior to nuclei from blastocysts (15% development to the blastocyst stage). Morulae at cavitation yielded a higher number of cloned blastocysts per donor embryo (11.5 ± 5.9) than did morulae (9.3 ± 3.2) and blastocysts (3.3 ± 1.4). Transfer of cloned embryos originating from in vivo-derived morulae, morulae at cavitation, and blastocysts resulted in four pregnancies (10%), three pregnancies (7%), and one (17%) pregnancy on day 45. The corresponding numbers of calves born were 3 (4%), 3 (7%), and 0, respectively. After transfer of blastocysts derived from in vitro nuclear donor morulae (n = 16) and morulae at cavitation (n = 7), two (20%) and two (50%) recipients, respectively, were pregnant on day 45. However, transfer of seven cloned embryos from in vitro donor blastocysts to three recipients did not result in a pregnancy. Using in vitro-produced donor embryos, calves were only obtained from morula-stage donors (13%). Our results indicate that the developmental stage of donor embryos affects the efficiency of nuclear transfer, with morulae at cavitation yielding a high number of cloned blastocysts. © 1996 Wiley-Liss, Inc.     

Sporogenesis in Eusporangiate Ferns: II. Polyplastidic Meiosis in Ophioglossum (Ophioglossales)

Ophioglossum petiolatum . Unlike Angiopteris (Marattiales), which is monoplastidic, Ophioglossum undergoes polyplastidic meiosis like members of the fern-seed plant clade. The meiotic spindle is distinctly multipolar in origin and is consolidated into a bipolar spindle that is variously twisted and curved to accommodate the large number of chromosomes. Although a phragmoplast forms after first meiosis, no wall is deposited. Instead, an organelle band consisting of intermingled plastids and mitochondria is formed in the equatorial region between the dyad domains. Following second meiosis, a complex of phragmoplasts forms among sister and non-sister nuclei. Cell plates are deposited first between sister nuclei and then in the region of the organelle band resulting in a tetrad of spores each with a equal allotment of organelles. Received 30 January 2001/ Accepted in revised form 24 April 2001     

PLOIDAL CHANGES IN CLONAL CULTURES OF SPIROGYRA COMMUNIS AND IMPLICATIONS FOR SPECIES DEFINITION

A clonal culture of Spirogyra filaments of initially uniform width produced filaments of three additional significantly different widths. Group I filaments of the original clone were 30.9 ± 0.7 μm wide (mean ± SD, N = 50). Group I filaments produced Group II filaments (22.0 ± 1.1 μm) through vegetative growth and sexual reproduction. Zygospores from homothallic Group I filaments produced germlings representative of Groups I and II; zygospores from homothallic Group II filaments produced germlings representative of Group II only. Germlings of Groups III (27.7 ± 1.0 μm) and IV (44.9 ± 0.8 μm) were produced in the cross of I × II. Viable zygospores from homothallic Group III filaments were obtained. Cells of Group IV filaments were initially binucleate and did not conjugate. Of the six intergroup crosses possible, four resulted in conjugation-tube formation only; two crosses yielded zygospores (I × II and III × IV). Germlings from the successful cross of Groups III and IV produced filaments of all four groups. Chromosome counts were: Group I (24), Group II (12), Group III (18), and Group IV (24, one nucleus). Relative nuclear fluorescence values of mithramycin-stained DNA were (mean ± SD, N ≥ 30): Group I (11.1 ± 1.4), Group II (5.7 ± 0.7), Group III (8.8 ± 1.3), and Group IV (10.0 ± 0.9, one nucleus). Cytologically, Group II appears to be a diploid (2x), Group I a tetraploid (4x), and Group III a triploid (3x). Systematically, Groups I, II, and III key out to Spirogyra singularis, S. communis, and S. fragilis, respectively, using Transeau's mongraph of the family Zygnemataceae. These species are interpreted to represent a species complex of S. communis (whose name has priority) with the ancestral haploid (x = 6) missing.     

Mitosis in the protostelidPlanoprotostelium aurantium

Summary Mitosis in the protostelidPlanoprotostelium aurantium Olive andStoianovich is characterized by an open, centric spindle. The nuclear envelope breaks down prior to metaphase, begins to reform during late anaphase, and is complete by telophase. Centrioles are present at the poles throughout mitosis and are devoid of rootlet microtubules from metaphase to late anaphase. Chromosomes are small and numerous and are attached to single kinetochore microtubules during metaphase and early anaphase. Chromosome separation takes place by a presumed shortening of the chromosome to pole spindle followed by a lengthening of the interzonal spindle. Mitosis inP. aurantium is similar to that of certain other protostelid amoebae and to myxomycete amoebae, but it is considerably different from that of dictyostelid amoebae. The phylogenetic significance of this is discussed.This research represents part of a Ph.D. dissertation presented to the University of North Carolina.