ARAGONITE CRYSTALS IN SPIROGYRA SP. (CHLOROPHYTA)

Intracellular crystals of aragonite have been identified by selected area electron diffraction (SAED) in a species of the freshwater filamentous alga Spirogyra from the Thames River, Ontario, Canada. The crystals are 2 to 24 μm in diameter, and characterized by a unique cross-shaped morphology, in which needle-like, or prismatic outgrowths develop from a common axis. Crystals may be dispersed throughout filaments, but tend to cluster as aggregates towards the centre .     

A MOVING MAT: PHOTOTAXIS IN THE FILAMENTOUS GREEN ALGAE SPIROGYRA (CHLOROPHYTA,ZYGNEMATACEAE)1

A blue light– (peak at 470 nm) induced photomovement was observed in the filamentous eukaryotic algae, Spirogyra spp. When Spirogyra filaments were scattered in a water chamber under a unilateral light source, they rapidly aligned toward the light source in 1 h and bound with neighboring filaments to form thicker parallel bundles of filaments. The filaments in the anterior of the bundles curved toward the light first and then those in the posterior began to roll up toward the light, forming an open‐hoop shape. The bundle of filaments then moved toward the light source by repeated rolling and stretching of filaments. When the moving bundle met other filaments, they joined and formed a bigger mat. The coordination of filaments was essential for the photomovement. The average speed of movement ranged between 7.8 and 13.2 μm·s^?1. The movement was induced in irradiance level from 1 to 50 μmol photons·m^?2·s^?1. The filaments of Spirogyra showed random bending and stretching movement under red or far‐red light, but the bundles did not move toward the light source. There was no distinct diurnal rhythm in the photomovement of Spirogyra spp.     

黑龙江省双星藻科新种

三江水绵图1 Spirogyra sanjingensis sp. nov. Celluis vegetativis 104-133μlatis, 142—295μlongis; dissepimentis planis; chromatophoris 9-10(11), anfractibus 1-1.5; conjugations scalari, tubo ex utroque cellula mascula et feminca emisso; cellulis fructiferis cylindricis, levi-     

EFFECTS OF TEMPERATURE AND IRRADIANCE ON THE SEASONAL VARIATION OF A SPIROGYRA (CHLOROPHYTA) POPULATION IN A MIDWESTERN LAKE (U.S.A.)

Although Spirogyra Link (1820) is a common mat‐forming filamentous alga in fresh waters, little is known of its ecology. A 2‐year field study in Surrey Lake, Indiana, showed that it grew primarily in the spring of each year. The population consisted of four morphologically distinct filamentous forms, each exhibiting its own seasonal distribution. A 45‐μm‐wide filament was present from February to late April or early May, a 70‐μm‐wide form was present from late April to mid‐June, a 100‐μm‐wide form was present from February to mid‐June, and a 130‐μm‐wide form appeared only in February of 1 of 2 study years. The 70‐ and 100‐μm‐wide forms contributed to the peak amount of biomass observed in late May and early June. Multiple regression analysis indicated that the presence of the 45‐, 70‐, and 100‐μm‐wide forms was negatively correlated with temperature. Presence of the 130‐μm‐wide form was negatively correlated with irradiance. Isolates of these filament forms were exposed to temperature (15, 25, and 35° C)/irradiance (0, 60, 200, 400, 900, and 1500 μmol·m^?2·s^?1) combinations in the laboratory. Growth rates of the 45‐μm‐wide form were negative at all irradiances at 35° C, suggesting that this form is susceptible to high water temperatures. However, growth rates of the other forms did not vary at the different temperatures or at irradiances of 60 μmol·m^?2·s^?1 or above. Net photosynthesis was negative at 35° C and 1500 μmol·m^?2·s^?1 for the 100‐ and 130‐μm‐wide forms but positive for the 70‐μm‐wide form. All forms lost mat cohesiveness in the dark, and the 100‐ and 130‐μm‐wide forms lost mat cohesiveness under high irradiances and temperature. Thus, the morphological forms differed in their responses to irradiance and temperature. We hypothesize that the rapid disappearance of Spirogyra populations in the field is due to loss of mat cohesiveness under conditions of reduced net photosynthesis, for example, at no to low light for all forms or at high light and high temperatures for the 100‐ and 130‐μm‐wide forms. Low light conditions can occur in the interior of mats as they grow and thicken or under shade produced by other algae.     

TEMPERATURE AND IRRADIANCE EFFECTS ON GROWTH OF PITHOPHORA OEDOGONIA (CHLOROPHYCEAE) AND SPIROGYRA SP. (CHAROPHYCEAE)1

Growth responses of Pithophora oedogonia (Mont.) Wittr. and Spirogyra sp. to nine combinations of temperature (15°, 25°, and 35°C) and photon flux rate (50, 100, and 500 μmol·m^?2·s^?1) were determined using a three-factorial design. Maximum growth rates were measured at 35°C and 500 pmol·m^?2·s^?1 for P. oedogonia (0.247 d^?1) and 25°C and 500 μmol·m^?2·s^?1 for Spirogyra sp. (0.224 d^?1). Growth rates of P. oedogonia were strongly inhibited at 15°C (average decrease= 89%of maximum rate), indicating that this species is warm stenothermal. Growth rates of Spirogyra sp. were only moderately inhibited at 15° and 35°C (average decrease = 36 and 30%, respectively), suggesting that this species is eurythermal over the temperature range employed. Photon flux rate had a greater influence on growth of Spirogyra sp. (31% reduction at 50 pmol·m^?2·s^?1 and 25°C) than it did on growth of P. oedogonia (16% reduction at 50 μmol·m^?2·s^?1 and 35°C). Spirogyra sp. also exhibited much greater adjustments to its content of chlorophyll a (0.22–3.34 μg·mg fwt^?1) than did P. oedogonia (1.35–3.08 μg·mg fwt^?1). The chlorophyll a content of Spirogyra sp. increased in response to both reductions in photon flux rate and high temperatures (35°C). Observed species differences are discussed with respect to in situ patterns of seasonal abundance in Surrey Lake, Indiana, the effect of algal mat anatomy on the internal light environment, and the process of acclimation to changes in temperature and irradiance conditions.     

A POLYPLOID SPECIES COMPLEX OF SPIROGYRA COMMUNIS (CHLOROPHYTA) OCCURRING IN NATURE 1

Investigations were conducted to determine whether ploidal changes found in laboratory cultures of Spirogyra also occur in nature. In an earlier study filament types identifiable as three different species (Spirogyra singu-laris Nordstedt, S. communis (Hassall)Kütz., S. fragilis Jao) arose from an original clonal culture through vegetative growth and sexual reproduction. These three “species” or filament groups differed in filament width, chloroplast number, zygospore size, and chromosome number. The differences in chromosome number represented a polyploid series of diploid (S. communis), triploid (S. fragilis), and tetraploid (S. singularis) forms in which width increased with ploidal level. The three width groups constituted a “species complex.” Five years after isolation of the original strain in this species complex, filaments corresponding to two of the width groups (S. singularis and S. communis) were found at the original collection site in the Santa Catalina Mountains in southern Arizona. The two field-collected groups were indistinguishable from the laboratory species complex in morphology and chromosome number. Homothallic conjugation within the two field width groups yielded progeny similar to those from homothallic conjugation of groups in the laboratory species complex. Filament widths of progeny were generally within the width limits of respective parental groups. The four possible intergroup crosses between the two laboratory and two field width groups yielded progeny similar to the wider parent (S. singularis) or the parent of intermediate width (S. fragilis). Progeny characteristics were determined by the width groups of parents, regardless of whether parents came from the laboratory or field. The similarities in morphology, chromosome numbers, and reproductive behavior of laboratory and field width groups imply that the laboratory species complex of S. communis has a natural counterpart in the field.     

ACCUMULATION AND REDUCTION OF ARSENATE BY THE FRESHWATER GREEN ALGA CHLORELLA SP. (CHLOROPHYTA)

Arsenate accumulation and reduction kinetics at both high and low phosphate concentrations were investigated in the green alga Chlorella sp, isolated from the arsenic-contaminated Upper Mystic Lake near Boston, MA. Growth rate, accumulated cellular arsenic, and release of As(III) were determined over a range of arsenate concentrations. Arsenate inhibited growth and reduced final cell yield at high phosphate concentration. However, growth rate, final cell yield, and cellular arsenic content were all enhanced by higher arsenate concentrations in cultures grown at a low concentration of phosphate. The traditional view that phosphate-limited cells are necessarily more sensitive to As(V) toxicity may not be correct. The reduction rates of As(V) by Chlorella sp. obtained in our laboratory were similar to net reduction rates measured in epilimnetic water from the Upper Mystic Lake, demonstrating the importance of phytoplankton in arsenic reduction in freshwater.     

PHYLOGENY OF SPIROGYRA AND SIROGONIUM (ZYGNEMATOPHYCEAE) BASED ON RBCL SEQUENCE DATA1

DNA sequence data were obtained for the gene encoding the large subunit of RUBISCO (rbcL) from 26 strains of Spirogyra and seven of Sirogonium, using as outgroups 10 genera in the Zygnematales and Desmidiales (Closterium, Cosmarium, Cylindrocystis, Gonatozygon, Mesotaenium, Netrium, Penium, Zygnema, Zygnemopsis, Zygogonium). Sequence data were analyzed using maximum parsimony (MP), maximum likelihood (ML), and Bayesian inference (BI), with bootstrap replication (MP, ML) and posterior probabilities (BI) as measures of support. MP, ML, and BI analyses of the rbcL data strongly support a single clade containing Spirogyra and Sirogonium. The Spirogyra taxa are monophyletic, with the exception of Spirogyra maxima (Hassall) Wittrock, which is nested within a clade with Sirogonium and shares with them the characters of loosely spiraled chloroplasts (<1 complete turn per cell) and anisogamy of gametangial cells; S. maxima differs from Sirogonium in displaying well‐defined conjugation tubes rather than a tubeless connection involving bending (genuflection) of filaments. The ML and BI analyses place this Sirogonium/Spirogyra maxima clade sister to the remaining Spirogyra. Morphological differences among strains of Spirogyra grouped together on the basis of rbcL data, including laboratory strains derived from clonal cultures (Spirogyra communis, S. pratensis), indicate that some characters (filament width, chloroplast number) used in the traditional taxonomy of this group are poor measures of species identity. However, some characters such as replicate end walls and loose spiraling of chloroplasts may be synapomorphies for Spirogyra clades.     

PHYSIOLOGICAL RESPONSES TO TEMPERATURE AND IRRADIANCE IN SPIROGYRA (ZYGNEMATALES, CHAROPHYCEAE)1

Spirogyra Link (1820) is an anabranched filamentous green alga that forms free-floating mats in shallow waters. It occurs widely in static waters such as ponds and ditches, sheltered littoral areas of lakes, and stow-flowing streams. Field observations of its seasonal distribution suggest that the 70-μm-wide filament form of Spirogyra should have a cool temperature and high irradiance optimum for net photosynthesis. Measurements of net photosynthesis and respiration were marie at 58 combinations of tight and temperature in a controlled environment facility. Optimum conditions were 25°C and 1500 μmol photons m⁻² s⁻¹, at which net photosynthesis averaged 75.7 mg O₂ gdm⁻¹ h⁻¹. Net photosynthesis was positive at temperatures from 5° to 35°C at most irradiances except at combinations of extremely low irradiances and high temperatures (7 and 23 μmol photons m⁻² s⁻¹ at 30°C and 7, 23, and 35 μmol photons m⁻² s⁻¹ at 35°C). Respiration rates increased with both temperature and prior irradiance. Light-enhanced respiration rates were significantly greater than dark respiration rates following irradiances of 750 μmol photons m⁻² s⁻¹ or greater. Polynomials were fitted to the data to generate response surfaces; such response surfaces can be used to represent net photosynthesis and respiration in ecological models. The data indicate that the alga can tolerate the cool water and high irradiances characteristic of early spring but cannot maintain positive net photosynthesis under conditions of high temperature and low light (e.g. when exposed to self-shading ).     

CALCIUM OXALATE CRYSTALS IN THE GREEN ALGA SPIROGYRA SP. (ZYGNEMATALES, CHLOROPHYTA)

Specimens of an unidentified species of the freshwater green alga Spirogyra were found to have abundant cruciate cellular inclusions up to 34 micrometers long. A crystalline nature was shown by birefringence in polarized light. Despite their large size and complex shape, these inclusions did not occur free in the large central vacuole. Instead, they were associated with cytoplasmic strands that spanned the space between gyres of the parietal spiral chloroplasts and with strands that suspended the nucleus in a cytoplasmic embayment of the central vacuole. Some crystals moved directionally along the cytoplasmic strands, and their movement was arrested by cytochalasin B, suggesting that actin microfilaments had a role in crystal movement. Solubility tests showed that the inclusions were composed of calcium oxalate; they dissolved rapidly in weak hydrochloric acid without effervescence, but they were not soluble in concentrated acetic acid or sodium hypochlorite. A colorimetric enzymatic test for oxalate was used to demonstrate microscopically the presence of oxalate and to quantify the amounts. The calcium oxalate crystals were surrounded by a water-soluble organic matrix that retained the shape of the crystal even after demineralization. Scanning electron microscopy was used to examine the morphology of isolated crystals.     

A POLYPLOID SPECIES COMPLEX IN SPIROGYRA MAXIMA (CHLOROPHYTA,ZYGNEMATACEAE), A SPECIES WITH LARGE CHROMOSOMES1

A species complex in Spirogyra consists of the series of filament morphotypes of various ploidal levels arising from an original morphotype within a clonal culture or in nature. A clonal culture of filaments identified as Spirogyra maxima (Hassall) Kützing produced several morphotypes, i.e. filament types of distinctly different widths and ploidal levels. Banding patterns and satellites were visible on chromosomes stained at mitotic prophase and metaphase. The original culture of S. maxima contained filaments averaging 127 μ wide. Vegetative cells of the original culture contained six large chromosomes (>4 μ long), identifiable as three distinct pairs based on banding patterns and presence of satellites: (1) one pair of short chromosomes (ca. 5.0 μ); (2) one pair of long chromosomes (ca. 8.0 μm); and (3) a second pair of long chromosomes (ca. 9.0 μm) including a nucleolar organizing region and satellite. A larger morphotype averaging 175 μm in width contained 12 chromosomes, with two pairs of short chromosomes and four pairs of long chromosomes (satellites were usually indistinct). Aneuploid chromosome numbers ranging from 5 to 13 were observed in a few cells. Binucleate and trinucleate cells were also observed. A twobanded chromosome fragment was observed in a few cells with 6 chromosomes and a few cells with 12 chromosomes. The variety of morphotypes derived in this study could be identified as four different species of Spirogyra by conventional taxonomic criteria. The banding patterns and satellites on chromosomes suggest that three pairs of homologous chromosomes are present in filaments of the original clonal culture and that these filaments are themselves autopolyploid (diploid) descendants of ancestral form with a base chromosome number of x = 3.     

SNOW ALGAE OF THE WINDMILL ISLANDS, CONTINENTAL ANTARCTICA: DESMOTETRA AUREOSPORA, SP. NOV. AND D. ANTARCTICA, COMB. NOV. (CHLOROPHYTA)

Two cryophilic Desmotetra species, D. aureospora , sp. nov., and D. antarctica (Fritsch) Ling appear to be unique to the southern hemisphere snow ecosystem, or at least to the Windmill Island region, Antarctica. They have not been encountered in previous extensive studies of the Arctic and northern alpine regions. Also unusual are the higher pH (6.8 and 7.8) and conductivities of 279 μS·cm⁻¹ and 426 μS·cm⁻¹ for habitat conditions of D. antarctica that can be attributed to the influence of penguin guano. Both species are characterized by cells enveloped in individual mucilage layers, 1–3 contractile vacuoles, and a cup-shaped chloroplast containing a diffuse pyrenoid. The cells divided in three planes to form cubical loosely aggregated green cell packages embedded in mucilage. Vegetative cells of the two species cannot be distinguished with certainty; however, their zygospores are very different. Desmotetra aureospora has spherical, smooth-walled, golden zygospores, whereas D. antarctica has pale, yellow green, aereolate zygospores. Mucilage stalk morphology of cells in stationary-phase cultures can also be used to separate the two species. Zygospores of D. antarctica have previously been identified as the snow alga Trochiscia antarctica Fritsch. Both species are currently maintained in culture at the Australian Antarctic Division. The cultures did not grow at temperatures above 15° C. The two species are compared with the soil alga D. stigmatica (Deason) Deason et Floyd, the only other species in the genus, and also with Chlorosarcina stigmatica Deason strain T105. Results show that the three Desmotetra species form a natural group and that the absence or presence of a wall on the zoospore is of dubious value in classifications of green algal taxa above the species level.     

ENDOPHYTIC ALGAE OF CHONDRUS CRISPUS (RHODOHYTA). II. ACROCHAETE HETEROCLADA SP. NOV., A. OPERCULATA SP. NOV., AND PHAEOPHILA DENDROIDES (CHLOROPHYTA)1

The occurrence of three endophytic green algae within Chondrus crispus Stackh. is reported. Two of them are new to science and are described as Acrochaete heteroclada Correa and Nielsen sp. nov. and A. operculata Correa and Nielsen sp. nov. The algae were studied in unialgal culture and in association with the host following infection of C. crispus under laboratory conditions. The experimental infection showed A. heteroclada to be initially epiphytic, with endophytic filaments growing into the cortex of the host during late infection. A. operculata is entirely endophytic when associated with the host. Phaeophila dendroides (Crouan frat.) Batters behaves as an epiphyte at 15 and 24°C but penetrates the host tissues at 20°C. For all three species, a close physical association with the host is established only when zoospores settle and germinate on the surface of C. crispus.     

STRUCTURE OF EXTRACELLULAR POLYSACCHARIDES PRODUCED BY A SOIL CRYPTOMONAS SP. (CRYPTOPHYCEAE)1

The Hindak strain of a Cryptomonas species (Cryptophyceae) produces extracellular polysaccharides. Because there is no information on the structure of these compounds in the Cryptophyceae we conducted structural studies. Gas–liquid chromatographic analyses showed that the polysaccharide is composed of fucose, rhamnose, xylose, mannose, glucose, galactose, galacturonic acid, glucuronic acid, and traces of 3-O-methyl galactose. The polysaccharide was separated into two subtractions by ion-exchange chromatography. Fraction A consisted mainly of 1,3-linked galactose units and 1,4-linked galacturonic acid. Unlike fraction B, fraction A did not have xylose, 3-O-methyl galactose, or glucuronic acid. Also, its degree of branching was low compared to that of fraction B. Only traces of sulfate were present infraction A, but fraction B was 10–15% sulfated. Protein was approximately 1% in both fractions. These polysaccharides appear to be a novel type of polymer in algae.     

LIGHT MICROSCOPY AND ELECTRON MICROSCOPY OF NEPHROSELMIS SPINOSA SP. NOV. (PRASINOPHYCEAE,CHLOROPHYTA)1

Nephroselmis spinosa Suda sp. nov. is described based on LM and EM observations. Two strains of N. spinosa (S222 and SD959‐3) were isolated from sand samples collected from the northwest coast of western Australia. The cells were remarkably right–left flattened and appeared ellipse or bean‐shaped when viewed from their right or left side. A single, parietal, crescent chloroplast was pale green to yellowish green and contained one conspicuous eyespot in its anterior ventral edge near the base of the short flagellum. A pyrenoid with three starch plates was located at the dorsal of the chloroplast. The cells divided by transverse binary cell division, as is common in other species of this genus. This alga possessed four types of body scales, and three scale types were similar to N. olivacea Stein and N. astigmatica Inouye & Pienaar. However, the fourth and outermost scale type was distinctive because although it was a spiny stellate scale with nine spines, one of them extended about 1 μm and was slightly curved with a hook at the end. This scale morphology, an important taxonomic characteristic, has never been described for the genus Nephroselmis. The cell's morphology, pyrenoid structure, hair scales, and cell size were distinctive from previously described Nephroselmis species, and its unique scale characteristic led me to name this newly proposed species “spinosa,” meaning spiny.     

OBSERVATIONS ON LICHENIZED AND FREE-LIVING PHYSOLINUM (CHLOROPHYTA,TRENTEPOHLIACEAE)1

Lichenized Physolinum Printz and free-living Physolinum from a dimly lit cave were studied from fresh collections and cultures, preserved specimens fixed in situ, and cultures that had persisted for 5 years in an environmental chamber. The branched filamentous association consists of a phycobiont and a characteristic ascomycetous mycobiont of one layer that completely ensheathes the algal partner. Epiphytic blue-green algae commonly occur attached to the mycobiont. The phycobiont, Physolinum monilia (De Wildem.) Printz, produces thick-walled, green spiny cells, some of which enlarge and contact the sheathing mycobiont cells; the phycobiont and mycobiont may then develop into new lichenized filaments. The hyaline mycobiont cells extend haustoria bound by the fungus wall deeply into the phycobiont chloroplasts. The epiphytes, Synechocystis-like colonies, are firmly attached to the outer walls of the mycobiont and are associated with several-celled extensions of the fungus beyond the apical phycobiont cells. Free-living Physolinum monilia filaments are branched and moniliform; the search-containing uninucleate cells are spherical to pyriform and have walls of cellulose. Each cell has a single massive chloroplast with plastoglobuli among tightly packed thylakoids. Except for their larger cells, P. monilia filaments appear to be identical to the phycobiont of lichenized Physolinum.     

ISOLATION OF A NUCLEUS-ASSOCIATED MICROTUBULE SCAFFOLD FROM SPIROGYRA (ZYGNEMATALES, CHAROPHYCEAE)

A phragmosome-like perinuclear scaffold attaches to helical chloroplast bands in the peripheral cytoplasm of Spirogyra crassa Kützing by rigid, stalk-like cytoplasmic strands. Balanced integration of forces within this scaffold by microfilament-based tension conveyed along stabilized microtubules (MTs) within the stalks controls transverse centering of the lenticular nucleus in the cylindrical cell prior to mitosis. Nuclei with their associated scaffolds were released from rapidly frozen, shattered cells upon thawing in a MT-stabilizing buffer and could be purified by a procedure combining filtration, differential centrifugation, and isopyknic centrifugation in a linear density gradient. In the osmotically indifferent gradient medium Nycodenz™, nuclei with adhering scaffolds attained a buoyant density of 1.26–1.27 g·cm⁻³. The nuclei maintained their energetically unfavorable, lenticular shape in vitro and appeared structurally preserved as judged by video-enhanced differential interference contrast and by fluorescent staining of DNA with 4'-6'-diamidino-2-phenylindole. The stalks of the scaffold, though still radiating from the nuclear rim, lost their straightness and were often severed during the isolation process. The distal ends of many unsevered stalks and of stalk fragments were still associated with chloroplast fragments. Persistent flexural rigidity of the scaffold stalks and indirect immunofluorescence indicated preservation of MTs. In addition to tubulin, both actin and an intermediate filament antigen of M _r ≈ 68 kDa were detected in the isolated nuclei with associated scaffolds by immunoblot with monoclonal antibodies.     

ETIOLOGY AND DEVELOPMENT OF HYPERPLASIA INDUCED BY STREBLONEMA SP. (PHAEOPHYTA) ON MEMBERS OF THE LAMINARIALES (PHAEOPHYTA)1

Filaments of Streblonema sp. isolated from hyperplasia (galls) on Nereocystis luetkeana (Mert.) Post. et Rupr. induced similar gall growths when inoculated on young sporophytes of Nereocystis luetkeana, Macrocystis integrifolia Bory, and Laminaria japonica Aresch. Filaments were irregularly branched and uniseriate with cells 5–8 μm in diameter and 10–30 μm long. Growth under varied cultured conditions produced unilocular sporangia. Zoospores released from the sporangia germinated into identical filaments which also formed unilocular sporangia. Gall tissue originated from the innermost cells of the epidermal meristematic zone. When infected these cells divided in an irregular and unorganized manner. The resulting structure was a pronounced departure from normal morphology.