Revision of the family Duboscquellidae with description of Euduboscquella crenulata n. gen., n. sp. (Dinoflagellata, Syndinea), an intracellular parasite of the ciliate Favella panamensis Kofoid & Campbell

Recent recognition that tintinnids are infected by dinophycean as well as syndinean parasites prompts taxonomic revision of dinoflagellate species that parasitize these ciliates. Long overlooked features of the type species Duboscquella tintinnicola are used to emend the genus and family Duboscquellidae, resulting in both taxa being moved from the Syndinea to the Dinophyceae. Syndinean species previously classified as Duboscquella are relocated to Euduboscquella n. gen., with Euduboscquella crenulata n. sp. as the type. As an endoparasitic species, E. crenulata shares with its congeners processes associated with intracellular development and sporogenesis, but differs from closely related species in nuclear and cortical morphology of the trophont, including a distinctively grooved shield (= episome) that imparts a crenulated appearance in optical section. In addition, E. crenulata produces three morphologically distinct spore types, two of which undergo syngamy to form a uninucleate zygote. The zygote undergoes successive division to produce four daughter cells of unequal size, but that resemble the nonmating spore type.     

中华水韭孢子囊发育研究

采用半薄切片法,连续观察了极度濒危级(CR)植物中华水韭大小孢子囊的发育过程,以期从无性生殖的角度,为探讨其濒危原因提供直观可靠的理论根据。结果显示:(1)中华水韭的大小孢子叶相间排列,无混生孢子囊。(2)隔丝为孢子供给营养,其体积直接影响孢子的大小、产量和育性。(3)大小孢子囊都近半数败育,小孢子囊为整齐发育,大孢子囊为不整齐发育。(4)大小孢子囊均无柄,且都不存在开裂结构,只有孢子囊壁腐烂后才能散播孢子。研究认为,中华水韭的濒危与孢子囊的发育特征密切相关,孢子囊的高频率败育、没有开裂结构以及对环境的依赖,是造成中华水韭濒危的重要因素之一;通过与近缘类群孢子囊的比较,发现仅水韭孢子的散播借助外力,对生境要求较高,即验证了水韭古老的系统学地位,同时说明水韭更具有监测生境地区环境指标的能力。     

THE LIFE CYCLE OF BANGIA FUSCOPURPUREA IN CULTURE. I. EFFECTS OF TEMPERATURE AND PHOTOPERIOD ON THE MORPHOLOGY AND REPRODUCTION OF THE BANGIA PHASE12

The Bangia phase of Bangia fuscopurpurea was grown in laboratory culture in a variety of photoperiod and temperature regimes. Plants of the Bangia phase grown from 2 types of asexual spores, monospores and conchospores, exhibited growth differences under similar growing conditions. Plants derived from monospores grew more rapidly and matured earlier than those derived from carpospores. Day length and temperature were found to significantly influence growth rule, maturation, and plant size. Long day lengths resulted in more rapid growth in filament length and diameter and earlier spore formation and spore release. Maximum filament length was observed in a 12/12 hr light-dark cycle at 15 C. Spore formation and release were delayed by decreasing day length or temperature. Temperature and photoperiod were also found to influence the type of spores produced by the Bangia phase. When grown at 22 C, the Bangia phase produced only monospores, which reproduced the Bangia phase. At 9 C, with photoperiods of 11 hr or more of light, the Bangia phase produced carpospores which gave rise to the alternating Conchocelis phase. The conditions under which sporogenesis occurred determined the spore type differentiated.     

紫萁孢子囊发育中多糖和脂滴的细胞化学观察

采用光镜、透射电镜和细胞化学技术,对紫萁孢子囊发育过程中孢壁的超微结构和孢子囊内多糖和脂滴的分布及其动态变化进行研究,以探讨紫萁孢子囊发育过程中多糖和脂滴的代谢特征,为蕨类孢子发生的研究提供基础资料。结果表明:(1)紫萁孢子囊由1层囊壁细胞、2层绒毡层和产孢组织构成。(2)紫萁孢子壁由发达而分2层的外壁(外壁内层和外壁外层)和薄的不连续的周壁构成,由外壁形成棒状纹饰的轮廓;孢子外壁内层由多糖类物质构成,外壁外层和周壁均含有脂类物质。(3)在紫萁孢原细胞中观察到少量脂滴;随着紫萁孢壁的形成,囊壁细胞中淀粉粒的大小逐渐变小、数目先增加后减少,它们转运到内层绒毡层原生质团并转化为孢粉素前体物质,再穿过原生质团内膜表面进入囊腔,成为孢粉素团块或以小球形式填加到孢子表面形成孢壁。(4)紫萁孢子囊将多糖类营养物质转化为脂类,以脂滴的形式储藏在孢子中。     

Euduboscquella costata n. sp. (Dinoflagellata,Syndinea), an Intracellular Parasite of the Ciliate Schmidingerella arcuata: Morphology,Molecular Phylogeny,Life Cycle,Prevalence, and Infection Intensity

The syndinean dinoflagellate Euduboscquella costata n. sp., an intracellular parasite of the tintinnid ciliate Schmidingerella arcuata, was discovered from Korean coastal water in November of 2013. Euduboscquella costata parasitized in about 62% of the host population, with infection intensity (= number of trophonts in a single host cell) ranging from 1 to 8. Based on morphology and nuclear 18S ribosomal RNA gene sequences, the parasite is new to science. Euduboscquella costata n. sp. had an infection cycle typical of the genus, but had morphological and developmental features that distinguished it from congeneric species. These features include: (1) episome of the trophont with 25–40 grooves converging toward the center of the shield; (2) a narrow, funnel‐shaped lamina pharyngea extending from the margin of the episomal shield to the nucleus; (3) persistence of grooves during extracellular development (sporogenesis); (4) a single food vacuole during sporogenesis; (5) separation of sporocytes early in sporogenesis, regardless of type of spore formed; and (6) dinospore size (ca. 14 μm in length) and shape (bulbous episome with narrower, tapering hyposome). After sporogenesis, E. costata produced four different types of spore that showed completely identical 18S rRNA gene sequences. The gene sequence was completely identical with a previously reported population, Euduboscquella sp. ex S. arcuata, from Assawoman Bay, USA, indicating that the two populations are likely conspecific. Favella ehrenbergii, a widely recorded tintinnid known to host Euduboscquella spp., co‐occurred with S. arcuata, but was not infected by E. costata in field samples or during short‐term, cross‐infection experiments.     

Structural and physiological changes during sporangial development inAchlya intricata beneke

Summary Sporangial development in the zoosporic fungusAchlya intricata has been studied using light microscopy, a plasmolytic technique, KCl-filled microelectrodes and ion-selective microelectrodes. The completion of cleavage (spore delimitation) is accompanied by a change in appearance of the sporangium, loss of turgor and membrane potential, decrease in volume and release of K⁺. The measured loss of K⁺ is in agreement with previous measurements of extracellular ionic currents around developing sporangia ofAchlya using a vibrating probe. The relationship between these changes and the mechanism of spore liberation is discussed.     

Spore emission,sporangium proliferation and spore germination In situ in monosporangia of Acrochaetium virgatulum

Monospore release is effected mainly by an apical tear accompanied by momentary spore distortion, and sometimes with a distinct ‘blow-out’ of the sporangium apex; orientation of the paths of spore release is seen with serially arranged sporangia. Sporangium proliferation is common in cultures, but spore germination in situ is rare. Attempts at experimental induction of the process resulted in some sporangia with early developmental stages coming to resemble tetrasporangia.     

Chemical and Morphological Studies of Bacterial Spore Formation : I. The Formation of Spores in Bacillus cereus

Experimental conditions were developed whereby a culture of Bacillus cereus formed spores with reasonable synchrony following a growth cycle of some 8 hours. The cytology of this metamorphosis was studied by dark phase contrast, bright-field microscopy and electron microscopy of thin sections. Particular attention has been paid to the changes in chromatin patterns and these have been correlated with quantitative chemical estimations of the nucleic acids. The cell commencing sporulation contains two compact chromatin bodies and twice the spore amount of deoxyribonucleic acid. Following fusion of the two chromatin bodies, one-half of this chromatin becomes located at a cell end. A transverse septum growing inwards from, and remaining attached to, the inner surface of the cell wall separates this end-piece of chromatin and some associated cytoplasm from the rest of the cell to form the primordial spore. Although the synthesis of deoxyribonucleic acid ceases during the segregation process, it recommences in this organism and continues at a linear rate as the spore develops. Tracer studies with radioactive phosphorus indicated that this further synthesis is confined to the non-spore portion of the sporangium. Although the net synthesis of ribonucleic acid ceased prior to the onset of sporogenesis, some evidence of a turnover of this fraction during the sporulation process was found.     

Spores before sporophytes: hypothesizing the origin of sporogenesis at the algal-plant transition

Fossil spores from mid-Ordovician deposits (475 million yr old) are the first indication of plants on land and predate megafossils of plants by 30-50 million yr. Sporopollenin-walled spores distinguish land plants from algae, which typically have heavy-walled zygotes that germinate via meiosis into motile or protonemal cells. All land plants are embryophytes with spores produced by the sporophyte generation. It is generally assumed that retention of the zygote and delay in meiosis led to matrotrophic embryo development and intercalation of the diploid sporophyte before spore production. However, new data on the cell biology of sporogenesis in extant bryophytes suggest that spores were produced directly from zygotes in protoembryophytes. The mechanism of wall transfer from zygote to meiospores was a three-phase heterochrony involving precocious initiation of cytokinesis, acceleration of meiosis, and concomitant delay in wall deposition. In bryophyte sporogenesis, cytokinesis is typically initiated in advance of meiosis, and quadrilobing of the cytoplasm is followed by development of a bizarre quadripolar spindle that assures coordination of nuclear distribution with predetermined spore domains. This concept of the innovation of sporogenesis at the onset of terrestrialization provides a new perspective for interpreting fossil evidence and understanding the evolution of land plants.     

SPORE MORPHOLOGY IN THE CYATHEACEAE. I. THE PERINE AND SPORANGIAL CAPACITY: GENERAL CONSIDERATIONS

The literature on cyatheaceous spore morphology relative to the presence of a perine layer is reviewed, and evidence based on a sodium-hydroxide assay is presented indicating that the outer scultpine layer in certain cyatheaceous spores is perine. Perine so defined characterizes Metaxya, paleotropical and certain neotropical species of Sphaeropteris, nearly all species of Alsophila, all species of Nephelea, and certain species of Trichipteris and Cyathea. It is lacking in Lophosoria, many species of Trichipteris and Cyathea, and all species of Cnemidaria. Two major patterns of spore number per sporangium in the family are reported. Lophosoria, Sphaeropteris, Trichipteris, Cyathea, Cnemidaria, and probably Metaxya are characterized by 64-spored sporangia, whereas most species of Alsophila and all species of Nephelea are characterized by 16-spored sporangia. The congruence of this generic distribution of sporangial-capacity types with Tryon's phyletic arrangement of cyatheaceous genera supports the naturalness of his system. The intrasporangial germination of spores retained in dehisced and dispersed sporangia supports the suggestion that decreased spore number per sporangium in Alsophila and Nephelea may relate to the role of the sporangia as dispersal units. The decreased number of spores per sporangium is associated with a trend toward increase in the number of sporangia per sores, with the highest known count approaching 1000 sporangia per sorus. The Alsophila-Nephelea evolutionary line has probably not been ancestral in the phylogeny of the more advanced groups of ferns.     

OBSERVATIONS ON CHYTRIDIACEOUS PARASITES OF PHANEROGAMS. XIV. PHYSODERMA CALAMI

Physoderma calami, a chytrid (Phycomycetes), has not been studied or apparently even collected in Europe since 1895 and has never been recorded in this hemisphere. Material widely distributed in herbaria indicated it was a Physoderma but no details save color, shape, and size of resting spores were known. A study of living material from Vermont indicates resting spore germination occurs by dehiscence of a lid and production of a sporangium with zoospores. The latter may form either an epibiotic or “ephemeral” sporangial stage and zoospores, or an endobiotic one, with extensive polycentric thallus bearing turbinate cells along the rhizoids, and, as outgrowths of these turbinate cells, straw-colored, thick-walled resting spores. The latter stage produces dark-brown spots on infected parts of the host.     

The Presence of Keratin-like Substance in Spore Coat of Bacillus subtilis

Unique crystalline structures were found by X-ray diffractometry to be present in spore coats of Bacillus subtilis. By crystallographical and chemical studies of the purified spore coats it was found that these crystalline structures of the spore coats were essentially similar to those of α- and β-keratin, and that the spore coats were composed of keratin-like substance (or keratin). This keratin-like substance was found to be synthesized during sporogenesis from sulfur-containing water-soluble substances in the cells.     

STRUCTURE AND HISTOGENESIS OF THE EMBRYO OF ACER SACCHARINUM. I. EMBRYO SAC AND PROEMBRYO

Structure of the embryo sac and development of the proembryo of Acer saccharinum L. are described from paraffin sections. The embryo sac is monosporic and identical to the 8-nucleate Polygonum type in all respects. Cell, nuclear, and nucleolar sizes are constant within a narrow range and sharply distinctive for all components of the mature sac. Polar nuclei fuse before double fertilization. The longitudinal axis of symmetry of the egg, zygote, and proembryo is variously oriented with respect to the longitudinal axis of the embryo sac and is determined by the point of attachment of the presumptive egg cell to the sac wall. Subsequent development of the young embryo is responsive to aligning factors within the embryo sac and is collateral with the longitudinal axis of the sac. The first segmentation is transverse to the longitudinal axis of the zygote; the second and third are transverse in the basal cell and longitudinal in the apical cell. Descendants of ci form a short irregular suspensor; ca and m give rise to the apical and basal halves respectively of the embryo proper. The contribution of the proembryonic tiers to the older embryo differs in embryos of different initial orientation. Distribution and orientation of mitosis in the proembryo are shown in two accumulation maps.     

Development of ovarioles and nurse-cell cytoskeleton in <Emphasis Type="Italic">Calliphora erythrocephala</Emphasis> Mg (Diptera: Calliphoridae)

We have examined ovariole morphology and their development in Calliphora erythrocephala Mg. (Diptera: Calliphoridae). It has been shown that several regions can be distinguished in C. erythrocephala germarium. In these regions, cyst morphogenesis subsequently continues until the separation of the formed egg chamber. The germarium has variously branching fusomes. Two egg chambers develop in the C. erythrocephala vitellarium. The distribution of actin filaments and the formation of ring canals was studied in C. erythrocephala nurse cells. The diameter of the ring canal increases in the germarium zone from 1.5 μm to 14.7 μm during the third and fourth studies of oogenesis. A scheme is presented that illustrates the irregular stretching of actin rollers, which are formed during middle and late oogenesis around ring canals, which joins the proximal and neighboring parts and dramatically increases the size of nurse cells.     

Allomyces neo-moniliformis gametogenesis

Summary InAllomyces neo-moniliformis meiosis takes place during resting sporangium germination. The meiospores are characteristically binucleate and biflagellate as described byEmerson (1938) andTeter (1944). A variation in the number of nuclei and flagella per meiospore from two is correlated with germination of the resting sporangia under reduced oxygen tension. The meiospores are extremely poor swimmers and are typically amoeboid. At encystment the gamma bodies of the cell are mobilized and appear involved in cyst wall synthesis. A single mitotic division of each nucleus gives rise to four nuclei. Gamete cleavage is as described for spore cleavage inBlastocladiella (Lessie andLovett 1968). The assembly of the nuclear cap and side body complex of the spore are extremely late processes in gametogenesis. The gametes are released when the single papilla dissolves. The gametes fuse in pairs and after zygote formation the cell is uninucleate with two flagella. The biflagellate zygote is an active swimming cell. The presence of homothallism or hetero-thallism inA. neo-moniliformis is discussed.     

The role of the follicular epithelium in growing eggs of a dipteran insect during late oogenesis and cleavage

The gall midge Heteropeza pygmaea can reproduce by means of paedogenesis (i.e., larval parthenogenesis). In that process, follicles are produced that develop while floating in the hemocoele of the mother larva. A chorion is not formed at the end of oogenesis, and the growing embryos remain enveloped by the follicular epithelium. To investigate possible adaptations of the follicular epithelium to this unusual egg development, its ultrastructure has been studied during late oogenesis and cleavage. Earlier investigations had shown that the follicle cells are provided with a specifically arranged microtubular frame, which may be responsible for the anisometric growth of the egg. The present work shows that the follicle cells are always joined by desmosomes and septate junctions. During development, the septate junctions increase their surface and change their orientation to become parallel to the longitudinal egg axis, thus increasing the resistance of the follicle cells to being torn apart by growth tensions. The total surface of the follicular epithelium increases during development. Well-developed nucleoli in the nuclei and numerous ribosomes in the cytoplasm of follicle cells indicate a high level of synthetic activity. This activity may be required to support the increase in the membrane surface and the establishment of the microtubular frame. Lipid droplets, glycogen, and different inclusions in the follicle cells may represent nutrient and energy reserves. Structures indicating a quantitative significant transfer of nutrients from the follicle cells to the egg were not found.     

Effects of embryo energy,egg size,and larval food supply on the development of asteroid echinoderms

Organisms have limited resources available to invest in reproduction, causing a trade‐off between the number and size of offspring. One consequence of this trade‐off is the evolution of disparate egg sizes and, by extension, developmental modes. In particular, echinoid echinoderms (sea urchins and sand dollars) have been widely used to experimentally manipulate how changes in egg size affect development. Here, we test the generality of the echinoid results by (a) using laser ablations of blastomeres to experimentally reduce embryo energy in the asteroid echinoderms (sea stars), Pisaster ochraceus and Asterias forbesi and (b) comparing naturally produced, variably sized eggs (1.7‐fold volume difference between large and small eggs) in A. forbesi. In P. ochraceus and A. forbesi, there were no significant differences between juveniles from both experimentally reduced embryos and naturally produced eggs of variable size. However, in both embryo reduction and egg size variation experiments, simultaneous reductions in larval food had a significant and large effect on larval and juvenile development. These results indicate that (a) food levels are more important than embryo energy or egg size in determining larval and juvenile quality in sea stars and (b) the relative importance of embryo energy or egg size to fundamental life history parameters (time to and size at metamorphosis) does not appear to be consistent within echinoderms.     

Systematics of the genus Ceratopteris Brongn. (Parkeriaceae) II. Taxonomy

A revision of the genusCeratopteris is presented based on comparative morphology and geographical distribution. Four species are recognized:C. thalictroides, C. cornuta, C. pteridoides, andC. richardii. Characteristics of taxonomic importance include frond length, shape, and dissection; stipe width; insertion of basal pinnae; bud development; habit; annulus cell number; spore number per sporangium; spore size; and spore surface features. Evolution within species and putative hybridization between species are discussed.     

Induction of Accelerated Sporangial Lysis by Basic Peptide Antibiotics. A Novel Method of Preparation of Free Spores of Bacilli

An accelerated release of free spores from sporangia of Bacillus cereus NCIB-8122 and Bacillus subtilis SMYW was induced by the addition of the basic peptide antibiotics, polymyxin B or colistin (100 μg/ml), to sporangia formed in liquid Bactopeptone medium. Destruction of sporangial cell walls of B. cereus prelabelled with ³H-4-diaminopimelic acid commenced shortly after the addition of either antibiotic, the label being gradually released into the medium. Normal free spores were released following the addition of antibiotics to sporangia containing refractile spores (stages IV-V of sporogenesis). Earlier additions induced the lysis of both compartments of the sporangium, accompanied by the release of already-synthesized dipicolinic acid and alreadyaccumulated ⁴⁵calcium. The heat resistance and germination ability of spores released in the presence of the antibiotics were the same as those of control spores released by long-term spontaneous lysis of sporangia. Similar effects of the antibiotics were observed with B. subtilis SMYW. Results obtained were used firstly for fast preparation of relatively clean free spores and secondly for the characterization of the developmental stage of sporogenesis at which the spore becomes independent of the maternal cell. It reaches this property at the end of stage IV and during stage V.