Phylogenetic position of the Sphaeropleaceae (Chlorophyta)

 The complete 18S rRNA gene sequences of four Sphaeroplea C.A. Agardh strains (Sphaeropleales, Sphaeropleaceae), two Atractomorpha Hoffman strains (Sphaeropleales, Sphaeropleaceae) and two Ankyra Fott strains (Chlorococcales, Characiaceae) were determined and subjected to phylogenetic analyses. The analyses indicated that all these taxa belong to a monophyletic lineage (Sphaeropleaceae) and are related to a group of chlorophycean algae comprising autosporic taxa and taxa that reproduce by zoospores which are characterized by directly opposed basal bodies. The taxonomic assignment of the Sphaeropleaceae as a family within the Sphaeropleales (Chlorophyta, Chlorophyceae) is discussed. Received December 22, 2000 Accepted September 25, 2001     

MALE GAMETES OF ATRACTOMORPHA ECHINATA HOFFMAN (CHLOROPHYCEAE)1

Many naked gametes are produced in each fusiform, male gametangium of Atractomorpha echinata Hoffman and are liberated through irregularly shaped pores in the gametangial wall. They are typically biflagellate, pyriform or fusiform in shape, 6-11 μm long, and only a few micrometers wide. A mature male gamete is characterized by: (i) a nucleus with condensed chromatin and no nucleoli, (ii) a reduced, starch filled chloroplast occupying a posterior position, and (iii) a cup shaped eyespot consisting of a single layer of plastoglobuli. The flagellar apparatus includes two types of flagellar roots alternating in a cruciate pattern. One type consists of two microtubules, while the other consists of microtubules of varying number, usually eight or nine, but rarely as many as eleven. The paired basal bodies are connected anteriorly by a broad, striated distal fiber; there is no dense apical cap as reported in Sphaeroplea sperm. A unique structure, consisting of three layers of small subunits (6–8 nm diameter) arranged in a paracrystalline array, is positioned beneath each basal body. Based on the structure of its male gametes, Atractomorpha clearly demonstrates affinity with the chlorophycean rather than the ulvaphycean line of evolution. Moreover, if phylogenetic affinities for the Sphaeropleaceae are to be sought among other groups of green algae, the Chlorococcales appears the most promising candidate.     

Identification of novel genes specifically expressed in Chlamydomonas reinhardtii zygotes

The maturation of zygotes formed by the fusion of two gametes is the essential part of the diploid phase of the Chlamydomonas reinhardtii sexual life cycle and results in mature zygotes competent to germinate. To understand the molecular mechanisms underlying zygote maturation and the attainment of competence for germination we isolated genomic clones representing three different genes that are specifically expressed in Chlamydomonas reinhardtii zygotes. Accumulation of the RNAs started more than 24 h after mating, setting these genes apart from genes expressed in young zygotes [9]. Upon light-induced germination of zygotes, the mRNAs disappeared. The patterns of RNA accumulation and disappearance were gene-specific and suggested a function of these genes in maturation and/or in initial steps of germination.     

OBSERVATIONS ON THE FINE STRUCTURE OF OEDOGONIUM. III. MICROTUBULAR ELEMENTS IN THE CHLOROPLASTS OF OE. CARDIACUM12

The expansive, reticulate cliloroplasts of the filamentous green alga Oedogonium tardiacum were found to contain microtubular elements with an outside diameter of about 270 A. These microtubules have been examined in the chloroplast stroma of vegetative cells, zoospores, zoospore germlings, and eggs. They may occur singly or, more commonly, in groups or bundles of 2 to as many as 30. In longitudinal section these microtubules show a regular pattern of slightly oblique cross striations and the margins appear rough. They bear little structural resemblance to the more familiar and slightly smaller microtubules found in the cytoplasm external to the cliloroplasts. Their overall appearance suggests that each is constructed of 2 helically wound, ribbon-like units that are approximately 155-175 A broad and 45-55 A thick. The 2 units of this proposed double helix appear to lie in juxtaposition at a pitch of 17-27 deg. The dimensions of each unit, or helix, are such that it could conceivably be constructed of 3 filamentous subunits similar to those already described in the literature for other microtubular elements.     

MATURATION OF ALGAL ZYGOTES: ALTERNATIVE EXPERIMENTAL APPROACHES FOR CHLAMYDOMONAS REINHARDTII (CHLOROPHYCEAE)1

Young zygotes from crosses of Chlamydomonas reinhardtii Dang. mutant and wild-type strains were incubated, in the presence or absence of light and/or nitrogen to determine whether continuation of conditions inducing gamete formation permits zygospore formation without loss of viability. Different culture media, continuous illumination vs. dark incubation and various durations of the maturation period were tested, for effect on zygospore germination efficiency, zygospore “burst size” and zoospore viability. Following either the routine maturation procedure of dark incubation on standard minimal medium, or following a new procedure of incubation under continuous illumination on N-free medium, zygospore formation can be ensured and high germination efficiencies obtained within 3 days after mating. Tetrad analysis indicates meiosis occurs normally whether zygotes have been matured in the presence or absence of light or nitrogen. Preliminary data suggest an effect of increased maturation time on the transmission of cytoplasmic genes, if a N-free continuous illumination maturation protocol is followed. Two experimental approaches for the maturation of C. reinhardtii zygotes are suggested and advantages of each are discussed.     

Sphaeromyxa maiyai sp. n. (Protozoa: Myxosporidea), Coelozoic Parasite of the Pacific Tomcod,Microgadus proxiimus*

SYNOPSIS. Sphaeromyxa maiyai sp. n. (Myxosporidea: Myxiidae) is described from the gall bladder of the Pacific tomcod Microgadus proximus Girard, from Newport, Oregon. The plasmodial stage is discoid averaging between 1 and 2 cm. The spore averages 27.6 × 5.6 μm in breadth, with pyriform polar capsules measuring 9.3 × 3.7 μm. Scanning electron microscopy reveals the presence of numerous longitudinal striations.     

SYSTEMATIC ANALYSIS OF SPHAEROPLEA (CHLOROPHYCEAE)1

A systematic investigation of the genus Sphaeroplea was conducted using cladistic analyses of both structural and isozyme characters for the same set of taxa. The structural data were not able to fully resolve some of the taxa while the isozyme data did produce a tree in which all nodes were supported by data. The structural characters were relatively consistent with one another, whereas the isozyme characters were much less internally consistent. Results from independent, cladistic analyses of both data sets support the concept that among those Sphaeroplea species investigated, S. fragilis Buchheim et Hoffman had an early divergence. The two data sets differed primarily in that the structural data support monophyly of the genus Sphaeroplea and the isozyme data do not. The greater relative consistency of the structural data suggests better support for trees inferred from its analysis. Furthermore, searches for character congruence between the two data sets revealed isozyme data which support monophyly of the genus Sphaeroplea, but had been overwhelmed by conflicting isozyme characters.     

Cellulose-synthesizing terminal complexes and microfibril structure in the brown alga Sphacelaria rigidula (Sphacelariales,Phaeophyceae)*

The brown alga Sphacelaria rigidula Kützing synthesizes cellulose microfibrils as determined by CBH I-gold labeling. The cellulose microfibrils are thin, ribbon-like structures with a uniform thickness of about 2.6 nm and a variable width in the range of 2.6-30 nm. Some striations appear along the longitudinal axis of the microfibrils. The developed cell wall in Sphacelaria is composed of three to four layers, and cellulose micro-fibrils are deposited in the third layer from the outside of the wall. A freeze fracture investigation of this alga revealed cellulose-synthesizing terminal complexes (TCs), which are associated with the tip of microfibril impressions in the plasmatic fracture face of the plasma membrane. The TCs consist of subunits arranged in a single linear row. The average diameter of the sub-units is about 6 nm, and the intervals between the neighboring subunits, about 9 nm, are relatively constant. The number of subunits constituting the TC varies between 10 and 100, so that the length of the whole TC varies widely. A model that has been proposed for the assembly of thin, ribbon-like microfibrils was applied to microfibril assembly in Sphacelaria.     

Zygote germination in <Emphasis Type="Italic">Pleodorina starrii</Emphasis> (Volvocaceae,Chlorophyta)

Zygote germination of the anisogamous/oogamous colonial green flagellate Pleodorina starrii was observed. After the zygotes were transferred to the usual, illuminated conditions from the dark treatment on the agar plate, they began to germinate. The germinating zygotes gave rise to one or two viable biflagellate gone cells. This type of zygote germination is rare in the colonial Volvocales and may characterize a certain lineage within the anisogamous/oogamous members of the colonial Volvocales. Presented at the International Symposium Biology and Taxonomy of Green Algae V, Smolenice, June 26–29, 2007, Slovakia.     

Urceolaria viridis n. sp., a Ciliate (Peritrichida, Mobilina) with Elongate Symbiotic Green Algae

SYNOPSIS. A new peritrichous ciliate containing elongate symbiotic green algae is described from the marine limpet Acmaea digitalis Eschscholtz (1833). Urceolaria viridis n. sp. is characterized as follows: turban-shaped; diam. 40 μ; diam. striated band 30 μ; diam. corona 23 μ; width of corona 2μ; 16–22 denticles; peristome slightly more than one turn; circlet of delicate cirri adoral to ciliary girdle; macronucleus H-shaped with both ends of side pieces widely separated; diam. micronucleus 4.5 μ, endosome 2.5 μ; cytoplasm containing elongate green algae measuring 2–4 by 8–16 μ.     

Studies on the gill ciliation of the American oyster Crassostrea virginica (Gmelin)

Latero-frontal, para-latero-frontal, and frontal ciliary tracts on the gill filaments of Crassostrea virginica (Gmelin) were studied with light microscopy and scanning electron microscopy. Latero-frontal cirri are complex structures composed of varying numbers of paired cilia. The multiple pairs of cilia which constitute a single cirrus are closely appressed for a portion of their length; they then branch laterally from the central axis in a plume-like fashion. Latero-frontal cirri of adjacent gill filaments create a filtration sieve which should be capable of retaining particles smaller than 1 μm in diameter. Para-latero-frontal cilia are short, closely spaced cilia arranged as a staggered row along the frontal side of each tract of latero-frontal cirri. Latero-frontal cirri and para-latero-frontal cilia occur on ordinary, principal, and transitional gill filaments. Frontal ciliary tracts of ordinary filaments are divided into a central, ventrally directed coarse tract, flanked on either side by a dorsally directed fine ciliary tract. The coarse tract is covered by cirri which are comprised of five to eight cilia, while the fine frontal tracts are made up of individually functioning cilia. The frontal ciliary tracts of principal and transitional filaments bear only dorsally directed fine cilia. The unique direction of effective beat of the coarse frontal cirri of ordinary filaments, in combination with the action of fine frontal cilia and the strategic location of mucus producing cells, is used to describe a possible mechanism for the sorting of filtered particles.     

A giant type I polyketide synthase participates in zygospore maturation in Chlamydomonas reinhardtii

Polyketide synthases (PKSs) occur in many bacteria, fungi and plants. They are highly versatile enzymes involved in the biosynthesis of a large variety of compounds including antimicrobial agents, polymers associated with bacterial cell walls and plant pigments. While harmful algae are known to produce polyketide toxins, sequences of the genomes of non‐toxic algae, including those of many green algal species, have surprisingly revealed the presence of genes encoding type I PKSs. The genome of the model alga Chlamydomonas reinhardtii (Chlorophyta) contains a single type I PKS gene, designated PKS1 (Cre10.g449750), which encodes a giant PKS with a predicted mass of 2.3 MDa. Here, we show that PKS1 is induced in 2‐day‐old zygotes and is required for their development into zygospores, the dormant stage of the zygote. Wild‐type zygospores contain knob‐like structures (~50 nm diameter) that form at the cell surface and develop a central cell wall layer; both of these structures are absent from homozygous pks1 mutants. Additionally, in contrast to wild‐type zygotes, chlorophyll degradation is delayed in homozygous pks1 mutant zygotes, indicating a disruption in zygospore development. In agreement with the role of the PKS in the formation of the highly resistant zygospore wall, mutant zygotes have lost the formidable desiccation tolerance of wild‐type zygotes. Together, our results represent functional analyses of a PKS mutant in a photosynthetic eukaryotic microorganism, revealing a central function for polyketides in the sexual cycle and survival under stressful environmental conditions.     

ATRACTOMORPHA ECHINATA GEN. ET SP. NOV., A NEW ANISOGAMOUS MEMBER OF THE SPHAEROPLEACEAE (CHLOROPHYCEAE)1,2

Atractomorpha echinata gen. et sp. nov. is described from isolates derived from zygotes present in a dry soil sample obtained from Texas. The new genus is distinguished from Sphaeroplea primarily by its pattern of vegetative growth. While Sphaeroplea is distinctly filamentous with numerous coenocytic cells uniseriately arranged, Atractomorpha grows as individual, multinucleate, spindle-shaped cells with sharply pointed extremities. Such cells may vary considerably in length (25–6000 μm, or more) and normally lack septa. In young, rapidly growing cultures the cells often attain lengths of 300–500 μm, but rarely exceed 1800 μm. The new species is further characterized by: (1) the regular formation of biflagellate zoospores in asexual reproduction, (2)anisogamy (occasionally oogamy) and (3) the size and ornamentation of its zygotes. Variations in vegetative morphology are discussed as are conditions for obtaining gametogenesis.     

Poly(a)+ rna during vegetative development ofacetabularia peniculus

Summary In the juvenile stage, the diploid giant-celled green algae Acetabularia spp. are differentiated into an upright stalk and an irregularly branched rhizoid. Early amputation and grafting experiments as well as biochemical and molecular analyses have shown that mRNA (as poly(A)⁺ RNA) is continuously supplied from the primary nucleus in the rhizoid and accumulates in the stalk apex. In the present study, localization of poly(A)⁺ RNA in the juvenile stage of theAcetabularia peniculus was investigated by fluorescent in situ hybridization using oligo(dT) as a probe. The signal was localized in the apical cytoplasm and, in addition, multiple longitudinal striations throughout the stalk and rhizoid cytoplasm. A large portion of the poly(A)⁺ RNA striations exhibited structural polarity, broadened at one end and gradually thinned toward the other end. Some of the striations in the rhizoid cytoplasm were continuous with a zone of signal in the area of the perinuclear rim. The poly(A)⁺ RNA striations were associated with thick bands of longitudinal actin bundles which run through the entire length of the stalk. Cytochalasin D caused fragmentation of the actin bundles and irregular distribution of the fluorescent signal. We suggest that the poly(A)⁺ RNA striations constitute a hitherto unknown form of packaged mRNA that is transported over large distances along the actin cytoskeleton to be stored and expressed in the growing apex.     

Redefinition of the Urostylidae (Ciliophora,Hypotrichida) on the Basis of Morphogenetic Characters*

SYNOPSIS Examination of stained specimens (protargol and nigrosinbutanol) of hypotrich ciliates during division allows understanding of morphogenesis of buccal structures and cirri. Midventral, frontal, and transverse cirri in both proter and opisthe of Urostyla marina differentiate from a longitudinal series of numerous oblique ciliary streaks in a manner similar to that of Bakuella, Holosticha, Keronopsii. Pseudourostyla, and Uroleptus. This pattern differs markedly from that in Amphisiella, Kahliella, Paraholosticha, and Paraurostyla, in which the fronto-ventral and transverse cirri arise from a series of fewer (2–5) ciliary streaks in a longitudinal or fan-like array. Rows of marginal cirri in U. marina arise independently, as in Urostyla grandis. On the basis of comparisons of both structural and morphogenetic features of this and other hypotrichs, the family Urostylidae is redefined to contain Urostyla (type), Bakuella, Holosticha, Keronopsis, Pseudourostyla, and Uroleptus. Other genera formerly contained in the families Holostichidae and Urostylidae are placed in synonymy, assigned to other families, or held in uncertain familial relationship pending their rediscovery and further investigation.     

Morphology,morphogenesis, and molecular phylogeny of a novel saline soil ciliate,Heterourosomoida sinica n. sp. (Ciliophora,Hypotrichia)

The living morphology, infraciliature, morphogenesis and phylogenetic position of a new hypotrichous ciliate, Heterourosomoida sinica n. sp., discovered in saline soil in Northwest of China, were investigated. Heterourosomoida sinica n. sp. is characterized as follows: body size about 70–95 × 20–30 μm in vivo, ellipsoid or elongate; cortical granules dark green, 0.5 μm across, arranged around dorsal cilia and in short irregular rows on ventral side; consistently 18 frontoventral-transverse cirri; left and right marginal rows composed of 17–24 and 13–21 cirri, respectively; two macronuclear nodules and one or two micronuclei. The detailed morphogenesis of a species of Heterourosomoida is reported for the first time. The ontogenesis on dorsal side is basically similar to that in Urosomoida-species and the process on ventral side is characterized by: 18 frontoventral-transverse cirri develop from six anlagen with the anlagen V and VI formed in the primary mode. Phylogenetic analyses based on SSU rDNA sequence data reveal that Heterourosomoida sinica n. sp. clusters with Kleinstyla dorsicirrata and forms a clade with the type species H. lanceolata.     

Pleurotricha indica n. sp., a New Hypotrich Ciliate from the Indian Subcontinent1

A new species, Pleurotricha indica n. sp., is described, characterized by an average size of 220 × 119 μm, a firm and inflexible body, six rows of dorsal kineties, one left and two right rows of marginal cirri, and an “Oxytricha-like” pattern of ventral cirri. The parts of the macronucleus are variable in shape and number. The comparison with other members of the genus shows that P. indica differs from other congeneric species in the combination of these characters.     

Comparison of the Giemsa C-banded karyotypes of the three subspecies ofPsathyrostachys fragilis,subspp.villosus (2x),secaliformis (2x, 4x), andfragilis (2x) (Poaceae), with notes on chromosome pairing

The karyotypes of diploidP. fragilis subsp.villosus (2n = 2x = 14) and tetraploid subsp.secaliformis (2n = 4x = 28) were studied by Giemsa C- and N-banding, and AgNO₃ staining and compared with the karyotype of subsp.fragilis (2x). The complements of subsp.villosus and subsp.fragilis were similar, with 8 metacentric and 6 SAT-chromosomes, one metacentric and two submetacentric pairs, with small to minute, polymorphic, heterochromatic satellites. The complement of subsp.secaliformis on the whole agreed with a doubling of the complement of diploidP. fragilis, suggesting autopolyploidy. Only the presence of 12 nucleoli in interphases identified 6 SAT-chromosome pairs. In subsp.villosus one or two extra micronucleoli indicated a chromosome pair with very low nucleolusforming activity, bringing the number of SAT-chromosome pairs to 4. This number may be a characteristc ofPsathyrostachys. Besides very small, inconsistently observed bands, the C-banding pattern consisted of 0–3 small bands per chromosome at intercalary and terminal locations, and at NORs. The level of banding pattern polymorphism was low, but enough to indicate that the taxa are outbreeders. Similarities in chromosome morphology and C-banding patterns identified homology of all chromosomes of subsp.villosus, but for 12 pairs only in subsp.secaliformis. Between plants, reliable identification of homology and homoeology (subsp.secaliformis) was possible only for the SAT-chromosomes and the shortest metacentrics. Chromocentres were very small and the amount of constitutive heterochromatin was low. N-banding stained chromosomes uniformly. The basic karyotypes of theP. fragilis taxa were similar to those ofP. juncea, P. lanuginosa, andP. stoloniformis supporting a close relationship and the presence of a common genome, N. NORs had different nucleolus-forming activities. Meiotic analysis demonstrated a high level of bivalent pairing in the three taxa. A chromosomal rearrangement was suggested in subsp.villosus. The low multivalent frequency in subsp.secaliformis indicates the presence of a pairing regulation mechanism. The majority of chiasmata were interstitial. Pollen grain size discriminated between diploid and tetraploid taxa. The existence of a diploid cytotype of subsp.secaliformis is supported by pollen measurements of herbarium material.     

The spores of Pteris cretica complex (Pteridaceae-Pteridophyta) in America

Spore morphology in the Pteris cretica complex, including Pteris brasiliensis, P. ciliaris, P. cretica, P. denticulata var. denticulata, P. denticulata var. tristicula, P. ensiformis, P. multifida and P. mutilata was examined using light and scanning electron microscope. The spores are trilete, triangular to circular in shape, with an equatorial thickening (= cingulum). Equatorial diameter ranges from 29 to 69 μm, and polar diameter from 18 to 53 μm. Exospore is proximally verrucate and distally rugate, with the exception of Pteris ensiformis, which has cones on both polar faces. Perispore is generally less than 1 μm thick, apparently single-layered in section, and translucent under light microscope. Spheroids were frequently observed on the surfaces of both perispore and exospore. Hyaline spores lacking cingulum were found in all specimens. Pteris brasiliensis, P. cretica and P. denticulata exhibit pronounced polymorphism and, in addition to trilete spores these taxa also produce atypical spores such as tetralete, monolete and intermediate types.     

Musculature in polychaetes: comparison of Myrianida prolifera (Syllidae) and Sphaerodoropsis sp. (Sphaerodoridae)

Abstract. The relationship of the polychaete taxa Syllidae and Sphaerodoridae within Phyllodocida is still unresolved: phylogenetic analyses either show them as sister groups or more widely separated. The present article aims to provide information about the structure of the muscular system that could be essential for understanding their relationship. A crucial point is whether the body wall contains circular muscles, which has recently been shown to be absent in more taxa than previously known. The F-actin filaments in members of Myrianida prolifera (Syllidae) and Sphaerodoropsis sp. (Sphaerodoridae) were labeled with phalloidin and their three-dimensional relationships reconstructed by means of confocal laser scanning microscopy. Among the noteworthy differences that emerged between the species are (1) members of M. prolifera possess four, those of Sphaerodoropsis sp. eight, longitudinal muscle strands; (2) the body wall in M. prolifera contains transverse fibers in a typical, supralongitudinal position, while in Sphaerodoropsis sp., corresponding fibers lie beneath the longitudinal strands; (3) pro- and peristomium in M. prolifera have no distinct F-actin fibers, while five longitudinal pairs and three single transverse muscular fibers shape the anterior end in Sphaerodoropsis sp.; (4) the proventricle of M. prolifera comprises primarily radial muscle fibers arranged in distinct rows, while in Sphaerodoropsis sp. the axial proboscis consists of longitudinal and circular fibers and radial fibers are lacking; (5) in M. prolifera, the proximal and distal sections of the two anteriormost pairs of dorsal cirri possess longitudinal myofilaments, which are separate from the body wall musculature; by contrast, all appendages in Sphaerodoropsis sp. do not; (6) both species have bracing muscles: in M. prolifera they are positioned above the longitudinal fibers, whereas in Sphaerodoropsis sp. they are uniquely positioned between longitudinal and sublongitudinal transverse fibers. These results do not support a sister-group relationship of Syllidae and Sphaerodoridae. In addition, Sphaerodoropsis sp. is yet another example in the list of polychaetes lacking typical circular muscles in the body wall.