A Method for the Rapid Growth in Culture of Gametophytes of Equisetum arvense with Antheridia

Rapid growth in culture of Equisetum arvense gametophytes wasobtained using Murashige-Skoog's medium plus 3% (w/v) sucroseand continuous illumination. In darkness, growth was reducedand chlorophyll synthesis markedly inhibited. Antheridia formedon the top margin of gametophytes in light and darkness butarchegonia were not observed in either case. ¹Present address: Interdisciplinary Research Institute of EnvironmentalSciences, Higashi-yanagi-cho, Nishi-iru, Shichihon-matsu, Itsutsuji-dori,Kamigyo-ku, Kyoto, 602 Japan. (Received June 5, 1989; Accepted September 12, 1989)     

Accumulation of Pb and Zn in Gametophytes and Sporophytes of the Moss Funaria hygrometrica(Funariales)

Accumulation of lead and zinc was studied in the moss Funariahygrometrica Hedw. collected from mine tailings. Heavy metalaccumulation in gametophytes and sporophytes was quantifiedby graphite furnace atomic absorption spectrometry (GFAAS) andinductively coupled plasma-atomic emission spectrometry (ICP-AES).Pb and Zn accumulation in the placental zone was analysed byx-ray scanning electron microscopy (SEM) and transmission electronmicroscopy (TEM) microanalysis. Spectrometry showed that whilemoss gametophytes accumulated considerable concentrations ofheavy metals, sporophytes accumulated only small concentrationsof metals. X-ray SEM and TEM showed that the two metals accumulatedin placental transfer cells on both the gametophytic and sporophyticsides. To investigate the uptake pattern for both metals undercontrolled conditions, F. hygrometrica plants collected froma non-polluted site were treated in the laboratory with separatesolutions of Pb and Zn at two concentrations (10^-2and 10^-4 M)for 24 or 168 h. Metal accumulation was analysed separatelyin gametophytes and sporophytes using GFAAS and ICP–AES.Each generation had a different accumulation quotient for bothmetals, and gametophytes accumulated significantly more metalthan sporophytes. Concentrations of Zn in sporophytes were alwayshigher than concentrations of Pb. The findings are discussedin relation to the role performed by the gametophyte and theplacenta in the accumulation and sequestration of Pb and Zn.Copyright 2001 Annals of Botany Company Atomic spectroscopy, Funaria hygrometrica, gametophyte, Pb and Zn accumulation, sporophyte, x-ray TEM and SEM microanalysis     

Photosynthetic Rates of Sporophytes and Gametophytes of the Fern, Todea barbara

The photosynthetic rates of intact sporophytes or gametophytes of the fern Todea barbara grown in sterile culture were measured using an infrared gas analyzer. Sporophytes consisted of single whole plants with roots and leaves grown in tubes of agar. Gametophytes were grown as several plants covering the surface of the agar. Sporophytes had photosynthetic rates at light saturation of 8.50 microliters CO₂ per hour per milligram dry weight and 1,300 microliters CO₂ per hour per milligram chlorophyll, whereas rates for gametophytes were lower, 2.36 microliters CO₂ per hour per milligram dry weight and 236 microliters CO₂ per hour per milligram chlorophyll.     

Sterol Composition of the Strobilus of Equisetum arvense L.

“Process whey protein” was prepared by heating bovine milk whey protein isolate solution at neutral pH under salt-free conditions. The process whey protein solution, being clear, was heated at various pHs (2.0 to 11.0) and NaCl concentrations (0 to 200 mM), and the turbidity and gel properties of the products were then examined. For comparison, the properties of the whey protein isolate treated under the same conditions were measured. The whey protein isolate formed a transparent gel or sol below pH 3 and above pH 7 at low NaCl concentration after heating, but the process whey protein formed transparent gels and sols over a wider range of pH and NaCl concentrations than those of the whey protein isolate. More elastic, firmer, and denser gels were obtained from the process whey protein than from the whey protein isolate. The process whey protein provides a novel food material with useful properties.     

Anxiolytic effects of Equisetum arvense Linn. extracts in mice

The petroleum ether (PE), chloroform (CH), ethanol (ETH) and water extracts of E. arvense stems were evaluated for anti-anxiety activity in mice using elevated plus maze model. Ketamine induced hypnosis and actophotometer was used to evaluate sedative effect with various extracts in mice. The results were compared with standard drug diazepam. The ethanolic extract of E. arvense (50 and 100 mg/kg) significantly increased the time-spent and the percentage of the open arm entries in the elevated plus-maze model which was comparable to diazepam. Ethanolic extract (100 mg/kg) prolonged the ketamine-induced total sleeping time and decreased the locomotor activity in mice. The results suggest that the ethanolic extract of E. arvense seems to possess anxiolytic effect with lower sedative activity than that of diazepam. The results could be attributed to the flavonoid content of the ethanolic extract.     

问荆中三个新的酚甙化合物

从问荆（Equisetum arvense L.)营养茎的水溶性成分中分离到１２个化合物。经波谱解析和化学方法鉴定。其中３个新的酚甙化合物分别命名为equisetumosideA(3-methoxy-11,12-dihydroxy-phenylhexane-9-one-4-O-β－Ｄglucopyra-noside)、equisetumoside B(3-methoxy-4,11-dihdroxy-phenylhexane-9-one-12-O-β－Ｄ－glucopyranoside)和equisetumosideＣ（cis-ferulic acid potassium salt 4-O-β－Ｄ－glucopyranoside);其他成分鉴定为尿甙、次黄甙、２′－脱氧次黄甙、２′－脱氧胞甙、色氨酸、胸甙、５－羟基－２′－脱氧尿甙、松柏甙和莰非醇－３－O-β－Ｄ－槐糖基 －７－O-β－Ｄ－吡喃葡萄糖甙。这些化合物均为首次从该植物中分离得到。     

Direct production of sporophytic plants from spores of Equisetum arvense

Spores of Equisetum arvense were cultured in Murashige and Skoog liquid medium with or without cytokinin. Without cytokinin, spores germinated 2–3 days after sowing and developed into normal young gametophytes. These gametophytes were composed of well-vacuolated cells. On the other hand, germinated spores in the medium with cytokinin formed globular cell masses that were composed of small and dense cells. These cell masses developed into sporophytic plants after further culture. This revised version was published online in June 2006 with corrections to the Cover Date.     

蕨类植物问荆DEAD-box RNA解旋酶基因的克隆与分析

DEAD-box RNA解旋酶参与RNA多方面的代谢,在植物生长发育和逆境反应中起重要作用。本研究从蕨类植物问荆（Equisetum arvense）中克隆到一条DEAD-box RNA解旋酶c DNA全长序列,命名为EaRH1,并在Gen Bank注册登记（KJ734026）。序列分析显示：该c DNA全长3 230 bp,包含一个从487 bp到2 799 bp编码770个氨基酸的开放读码框,其对应的蛋白序列包含9个保守模块结构。EaRH1与其它物种DEAD-box RNA解旋酶蛋白序列比对结果显示：模块Ⅰa、Ⅱ和Ⅲ序列几乎完全相同,模块Q、Ⅰ和Ⅳ序列存在一些差异。EaRH1与江南卷柏（Selaginella moellendorffii）基因组一条假定序列相似度高达69%,其中相似度最高的区域集中在包含9个保守模块的结构域。系统进化树分析显示：EaRH1与拟南芥（Arabidopsis thaliana）DEAD-box RNA解旋酶At3g22320在氨基酸序列上有相对较高的同源性。序列结构比较和进化分析可推测出EaRH1可能参与植物体生长发育、miRNA生物合成、与RNA结合蛋白的相互作用和非生物胁迫应答。本文的研究为探索问荆DEAD-box RNA解旋酶的进一步功能提供参考。     

Arrangement of microtubules during spore formation in Equisetum arvense (Equisetaceae)

The arrangement of cortical microtubules (MTs) during spore formation in Equisetum arvense was examined by immunofluorescence microscopy. The arrangement of MTs was observed to change during sporoderm formation. During exospore formation, the cortical MTs of the tapetum appeared along the tapetal plasma membrane that enclosed each developing spore cell. After exospore formation, the arrangement of the cortical MTs changed into one of separate bands of MTs arranged spirally (spiral bands of MTs). The spiral bands of MTs were superimposed on the developing elaters. This new pattern corresponded to the pattern of cellulose microfibrils deposited in the inner layer of the elater, suggesting that these spiral bands are involved in the deposition of the cellulose microfibrils in the elater. We conclude that the spiral bands of MTs are functionally equivalent to cortical MTs in secondary wall formation.     

Autofluorescence of intact Equisetum arvense L. spores during their development

The autofluorescence of horsetail Equisetum arvense spores excited with UV-light of 360-380 nm was studied by microspectrofluorimetry during their development from an individual cell to the formation of a multicellular thallus with the generative organs. The investigation involved the registration of the fluorescence spectra of individual intact developing cells and the measurement of the ratio of cell fluorescence intensities in the blue and red regions of the spectrum. Dry blue-fluorescing microspores showed the maxima at 460 and 530 nm and a small maximum at 680 nm. Thirty minutes after moistening in water, red-fluorescing cells arose among blue-fluorescing microspores, indicating the onset of development. Red fluorescence with a maximum at 680 nm enhanced as cells put off their cover, which brightly fluoresced in the blue region of the spectrum with the main maximum at 460 nm. By estimating the ratio of autofluorescence intensities in the blue region of the spectrum to red lightening of microspores at the first stages of development up to 24 h (in particular, their first division, the formation of nonfluorescencing rhizoid, etc.), nonviable (only blue-lightening) cells were distinguished from viable cells, in which red fluorescence began to prevail. After 25-40 days of development, the gametophyte fluorescing mainly at 680 nm formed male organs, antheridia, with blue-green-fluorescing spermatozoids. Then female generative organs archegonia with the egg cell appeared, which fluoresced blue, whereas the surrounding cells fluoresced red. It was supposed that the lightening in the blue and green regions of the spectrum is due to the presence of phenols, terpenoids, and azulenes, whereas the emission in the red region is associated with the presence of chlorophyll and azulenes. The observation of autofluorescence makes it possible to easily distinguish generative cells without additional staining.     

Exploitation of the molecular potential of plants:Equisetum arvense (EQUISETACEAE)

After a search of the literature including computerized data bases on the economic potential of various plants, experiments designed to improve the extraction of silica from the horsetailEquisetum arvense L. were carried out. Improved yields of colloidal silica were obtained by sonication in a shorter time than by conventional extraction with boiling distilled water. However we conclude that commercial exploitation of silica (colloidal or solid) fromEquisetum arvense is not feasible at present because: growing conditions of this plant species are not yet well defined; the disappearance of the plant during the winter months limits its period of exploitation; the silica content of the plant can vary over a six-fold range depending on weather and soil conditions, and so its economic potential is unpredictable.     

Influence of shade timing on an Equisetum arvense L. population

Equisetum arvense L. is a perennial pteridophyte that grows in open sites. In Tokyo, the plant has photosynthetic shoots from late March to November. However, in some populations, these shoots are lost before summer because of shading by taller plants. To investigate the contribution of shoots that remain on the plant for a certain duration, in terms of the maintenance of the E.arvense population, tubers were cultivated under different light conditions and the dry weight of growth, photosynthetic rates and respiration rates were measured. Individual growth was simulated on the basis of matter production and its partitioning. Biomass at the start of the next growing season (the initial size) was seriously decreased by shading before July. However, shading after July had little effect on the initial size of the next season plants. Thus, E.arvense can maintain its population if its shoots are retained until summer.     

Tubers and rhizome fragments as propagules: competence for vegetative reproduction in Equisetum arvense

Rhizome fragments (referred to as “fragments”) and tubers of Equisetum arvense L. were cultured in order to investigate their competence with respect to vegetative reproduction. The starch concentration of the fragments was lower than that of the tubers, but the initial growth of new individuals from these fragments was superior to that from tubers obtained from the same dry mass. This superior growth was due to the large number of buds (grown from nodes) and aerial shoots on the fragments. The competence for vegetative reproduction depended on the relationship between the stored starch and the number of buds.     

The nucleotide sequence of the cytoplasmic 5S rRNA from the horsetail, Equisetum arvense

Using 3'- and 5'-end labelling sequencing techniques, the following sequence for the cytoplasmic 5S rRNA of the horsetail Equisetum arvense could be determined: (sequence in text). This sequence exhibits all features expected for higher plant cytoplasmic 5S rRNAs, and can be fitted to the secondary structure model for 5S rRNA proposed by De Wachter et al. (15).     

Enhancement of the Division of Equisetum arvense Protoplasts in Culture by Activated Charcoal and Their Further Development

Protoplasts were isolated from subcultured gametophytes of Equisetumarvense by treatment with Driselase and then cultured in vitro.Addition of activated charcoal (AC) to the culture medium enhancedthe rate of cell division, as well as the survival of both protoplastsand regenerated protoplasts. However, subsequent division ofcells was not observed after one or two cycles of replicationin cultures supplemented with AC. When regenerated protoplastswere transferred to fresh medium without AC 3 to 5 weeks afterthe first plating, the transferred cells formed rhizoids anddeveloped into small, young gametophytes without the prior formationof cell clusters or calluses. Furthermore, sprophytic shootsdifferentiated from the protoplast-derived gametophytes whenthey were cultured on medium supplemented with 6-benzylaminopurine(BA). (Received April 5, 1990; Accepted July 30, 1990)     

Genetic diversity and population structure in the outcrossing populations of Equisetum arvense and E. hyemale (Equisetaceae)

An allozyme examination was conducted to study the mating systems and genetic differentiation of populations of Equisetum arvense and E. hyemale. The study revealed that the rate of intragametophytic selfing in these homosporous pteridophytes is very low, i.e., on average 0.020 and 0.019, respectively, despite the potential hermaproditism and selfing of the gametophytes. Most populations consisted of numerous genotypes, and the average heterozygosities of E. arvense and E. hyemale equalled 0.092 and 0.134, respectively. The commonly observed excess of the heterozygote genotypes indicates that there are interclonal differences in the frequency of vegetative reproduction. The level of genetic divergence among populations was considerable even within a limited geographic area. It is suggested that the life history of Equisetum, characterized by the inefficiency of spore germination and gametophyte reproduction in noncolonizing situations, limits the level of gene flow and leads to a great genetic divergence between populations.