橘黄裸伞子实体个体发育研究

采用石蜡切片法对不同发育时期橘黄裸伞的原基或幼子实体进行个体发育研究。结果表明:橘黄裸伞原基的第一个形态分化是下部边缘菌丝平行排列进行垂直生长,形成菌柄;然后边缘菌丝迅速向外生长,外菌幕形成,菌盖原基生长,在菌盖原基下部观察到菌褶腔,菌褶腔上部连续排列着栅栏细胞;在菌褶形成过程中,囊状体在尖端上聚集,说明菌褶的生长点在与菌盖组织相连的基部而不是尖端;内菌幕由内菌幕原基、菌盖边缘平行向下生长的菌丝和菌柄上部边缘平行向外生长的菌丝共同发育形成,由于内菌幕与菌柄组织的同源性,菌环不易脱落。橘黄裸伞属于半被果型中的双菌幕发育型,发育顺序表明其为菌柄发育型。     

环腺苷酸在灰盖鬼伞子实体发育中的效用研究

通过测试ｃＡＭＰ,子实体浸提液对灰盖鬼伞（Ｃｏｐｒｉｎｕｓ　ｃｉｎｅｒｅｕｓ）双核体菌丝的子实体诱导测试研究及通过用腺苷分别抑制ｃＡＭＰ在子实体发育各阶段的合成,对ｃＡＭＰ在灰盖克伞子实体发育中的影响进行了研究。结果表明：ｃＡＭＰ及子实体浸提液对灰盖鬼伞双核体菌丝的子实体形成并无诱导信号作用,阻止ｃＡＭＰ的合成延缓了子实体原基的发生,菌盖的形成,担孢子梗的形成,也延缓了质配和担孢子的发生,但菌柄的延长,子实体的成熟,担孢子的着色与释放则不受ｃＡＭＰ合成受阻的影响。     

芬娜冬菇子实体发育过程及胞外酶活性

分离并鉴定了采自北京妙峰山的1株野生大型真菌——芬娜冬菇Flammulina fennae,对该菌株进行了子实体发育过程研究,并对其最适生长条件进行了正交实验,测定并分析了菌株液体发酵及子实体生长过程中的酶活变化。结果表明:芬娜冬菇在原基期就完成了菌柄菌盖的分化;正交实验结果显示,不同氮源和p H对菌株生长影响显著,不同碳源则影响不显著;菌株液体发酵过程中未检测到过氧化氢酶和酸性木聚糖酶活性,而子实体发育过程中,漆酶、纤维素酶、超氧化物歧化酶、过氧化氢酶、酸性木聚糖酶活性较高。在原基形成期和子实体发育后期5种酶活性较高,均呈现先升后降的变化趋势,超氧化物歧化酶、过氧化氢酶、纤维素酶活性峰值出现在原基形成期和子实体发育后期,酸性木聚糖酶活性峰值出现在原基发育期,漆酶活性峰值出现在子实体发育后期。     

鬼笔属3种真菌的个体发育及形态观察

为揭示鬼笔属真菌子实体各器官的发育过程和形态特点,采用石蜡切片法对驯化栽培出菇的超短裙竹荪Phallus ultraduplicatus、冬荪P. dongsun和红托竹荪P. rubrovolvatus不同发育阶段的菇蕾进行切片显微观察,结合菌丝、孢子和子实体形态比较3个种的个体发育及形态特点。结果表明：3个种的菌丝和孢子形态差异不明显,超短裙竹荪子实体的菌裙质地较薄、长约4 cm、带有不规则形状的网孔;红托竹荪的菌裙质地较厚、长约7 cm、带有圆形网孔;冬荪仅有1层薄菌幕。3个种的菇蕾内部发育顺序一致,最先发育的都是胶质腔,接着是子实层、菌柄腔、菌盖、菌柄、菌裙（菌幕）;发育过程中菌丝形态经历从疏松到紧密、从交织状到组织状的变化过程;各器官发育完成的时间不同,在菇蕾直径相同的条件下,冬荪发育最快,在菇蕾直径为2 cm时,各器官基本发育完成,红托竹荪在菇蕾直径为3 cm时发育完成,超短裙竹荪的菇蕾发育最慢,在直径达到4 cm时各器官才能发育完成。为鬼笔类真菌的分类研究和亲缘关系探索提供了依据。     

柯夫丝膜菌,中国丝膜菌属一新种(英文)

报道了产自我国云南的丝膜菌属一新种:柯夫丝膜菌Cortinarius korfii。该新种主要特征为菌盖表面橄榄褐色并具小鳞片,菌褶蓝紫色,菌柄表面具绒毛,子实体在紫外光下有显著的荧光反应。详细描述了这一新种,并与其相似种进行了比较。     

柱状田头菇的栽培

柱状田头菇 (Ａｇｒｏｃｙｂｅｃｙｌｉｄｒａｃｅａｅ)又名柳环菌、杨树菇、柱状环锈伞等 ,为粪伞科、田头菇属的木腐生真菌 ,广泛分布于亚洲、欧洲及北美洲的温带地区 ,野生菌各地均有采食。1　生物学特性子实体单生、双生或丛生。菌盖直径 51 0ｃｍ。表面平滑 ,初暗红色 ,后变为褐色或浅土黄褐色 ,边缘淡褐色 ,有浅皱纹。菌肉除表皮和菌柄基部外 ,白色。菌褶白色 ,后变为咖啡色 ,密集 ,近直生 ,菌盖完全开展之后 ,与菌柄分离成箭头状。菌柄长 3 8ｃｍ ,直径 51 2ｃｍ ,中实 ,纤维质、脆、嫩 ,表面有纤维状条纹 ,近白色 ,基部常污褐色。菌…     

中国粪锈伞科锥盖伞属和小鳞伞属的分类

锥盖伞属Conocybe和小鳞伞属Pholiotina界限不明确,在分类上存在混乱。本研究基于中国材料,明确该2属分类学特征,并探索属下等级划分:确认我国锥盖伞属37种,其中白色组sect. Candidae 3种;赭小皮伞组sect. Ochromarasmius 1种;具毛组sect. Pilosellae 10种,含3个中国新记录种,即毛柄锥盖伞Conocybe velutipes、条斑锥盖伞C. moseri和双孢锥盖伞C. bisporigera;锥盖伞组sect. Conocybe 17种,含2个中国新记录种,即刺毛锥盖伞C. echinata、短柄锥盖伞C. brachypodii;混杂组sect. Mixtae 6种。小鳞伞属18种,其中疣孢组sect. Verrucisporae 2种,其中糙孢小鳞伞Pholiotina dasypus为中国新记录;过渡组sect. Intermediae 2种;小鳞伞组sect. Pholiotina 6种;被外菌幕组sect. Vestitae 3种,齿缘小鳞伞Ph. serrata (T. Bau&J. Liu) T. ...     

采自中国西南地区的地锤菌属两新种

基于形态特征和此前发表的DNA序列数据,本文报道了地锤菌属Cudonia的2个新种,它们采自中国东喜马拉雅和横断山的亚高山地区。棒状地锤菌C. claviformis具子实层的部分鲜黄色、棒状,菌柄污白色至淡褐色、光滑。鳞柄地锤菌C. furfuracea具子实层的部分头状、鲜黄色,菌柄被污白色至淡褐色糠麸状鳞片。两种真菌都生长于杜鹃和柳树组成的矮灌丛下苔藓丛中。     

中国甘肃省狭义丝盖伞属二新种

依据形态学和分子系统学研究结果,描述了产自中国甘肃省的狭义丝盖伞属2个新种,即拟黄囊丝盖伞Inocybe muricellatoides和甘肃丝盖伞I. gansuensis。对新种的ITS、LSU和rpb2片段进行了测序和分析,并提供了详细描述、线条图、生态照片及与相似种的区别。拟黄囊丝盖伞以菌盖翘起的鳞片、菌柄纤维状、孢子光滑和厚壁的侧生囊状体为主要识别特征。甘肃丝盖伞具有粗壮的子实体、较大的孢子和厚壁侧生囊状体。基于LSU和rpb2联合数据的分子系统发育分析显示这两个新种隶属于狭义丝盖伞属且分别占据独特的分支。     

松口蘑菌丝体的分离和RAPD-PCR分析

针对松口蘑 [Tricholomamatsutake(S .ItoetImai)Sing .]菌丝体分离培养困难和各种相关分离物目前难以用出菇试验鉴定的现实 ,采用 8种培养基配方 ,对 9个不同来源的松口蘑子实体的不同部位及菌根、菌土进行组织分离 ,计接种试管 81 0多支 ,结果从菌褶部位获得 94支慢生型的菌丝体分离菌株 ,从菌柄部位仅获得 1支快生型的菌丝体分离菌株。以马铃薯葡萄糖土壤滤液培养基 (PDAS)、马铃薯葡萄糖麦麸滤液培养基 (PDAW )、BM培养基、马铃薯葡萄糖琼脂培养基 (PDA)对菌褶进行组织分离 ,获慢生型菌丝体的成功率依次为 74.4%、35.5%、156%和 8.9%。以各分离菌株的来源松口蘑子实体和中日两国松口蘑研究者提供的分离菌株作为DNA参照样品 ,对从供试子实体、菌根、菌土进行组织分离获得的各种相关纯培养物进行亲菌鉴定。采用筛选的 1 7个随机引物介导 2 5个供试松口蘑子实体及其分离菌体的RAPD(RandomAmplifiedPolymorphicDNA) PCR反应 ,全部获得了清晰而稳定的DNA指纹图谱 ,结果一致表明 :每个松口蘑子实体的菌盖 (含菌褶…     

Growth of fruit-bodies inFavolus arcularius

The fruiting ofFavolus arcularius in culture is described. When the cultures, which have been pre-incubated in darkness to allow the inoculum mycelia to become thick and white wooly in texture, are exposed to light, fruit-body primordia, 1 mm in height, are formed about 4 days after the start of illumination. The primordium develops into a cylindrical stipe, the growth of which mainly occurs in the final 1 mm of the terminal region. Hyphal elongation in the region within 3 mm of the apex is predominant in the growth of the pileate stipe. With maturation of the stipe, changes in hyphal orientation occur on the periphery of the subapical region, and then the pileus-primordium is formed. The differentiation into the inner layer and the outer layer (pre-hymenial layer) in the pileus tissue is completed at this stage. The early growth of the pileus may be due to rapid elongation of the hyphae on the margin in addition to gradual expansion of the hyphae in the preformed pseudo-tissue. When the pileus has grown to about 3 mm in diameter, the subsequent three to four fold increase in size may be due to parallel expansion of the hyphae constituting the young pileus tissue.     

AXILLARY BUD DEVELOPMENT IN POPULUS DELTOIDES. I. ORIGIN AND EARLY ONTOGENY

Origin and early development of axillary buds on the apical shoot of a young Populus deltoides plant were investigated. The ontogenetic sequence of axillary buds extended from LPI –1 (Leaf Plastochron Index) near the apical bud base to LPI –11, the fifth primordium below the bud apex. Two original bud traces diverged from the central (C) trace of the axillant leaf and developed acropetally. During their acropetal traverse the original bud traces gave rise to three pairs of scale traces. All subsequent scale traces, and later the foliar traces, were derived by divergencies from the first two pairs of scale traces. Just before the bud vascular system separated from that of the main axis, a third pair of traces diverged from the original bud traces to vascularize the adaxial scale. Concomitantly, the original bud traces were inflected toward the main vascular cylinder where they developed acropetally and eventually merged with the left lateral trace of the leaf primordium situated three nodes above the axillant leaf; they did not participate in further vascularization of the bud. During early ontogeny a shell zone formed concurrent with initiation of the original bud traces and lay interjacent to them. The shell zone defined the position of the cleavage plane that formed between the axillary bud and the main axis. The axillary bud apex first appeared in the region bounded laterally by the original bud traces and adaxially by the shell zone. Following divergence of the main prophyll traces from the original bud traces, the apex assumed a new position intermediate to the prophyll traces. Ontogenetic development suggested that the axillary bud apex may have been initiated by the acropetally developing original bud traces under the influence of stimuli arising in more mature vegetative organs below.     

The Mode of Origin of a Leaf Primordium in the Shoot Apex of the Pea (Pisum sativum)

The movement of carbon-particle markers on the surface of acultured pea apex resembled that previously found for the tomatoapex. In the pea the primordium originated lower down on theside of the apical dome than in the tomato, and its generaldirection of growth was more upright. The results accord wellwith existing data on the rates and directions of cell divisionin the pea apex, and show that the primordium is formed by increasedcell division on the flank of the apex in a growth centre (orregion) analagous to that found in the tomato apex. Becauseof the distichous phyllotaxis of the pea it appears that inlongitudinal section two such growth centres at different stagesare visible, whereas in the tomato, which has spiral leaf arrangement,only one is apparent. It is concluded that, while a change indirection of division inevitably occurs in the primordium asit begins to bulge outwards away from the centre of the apex,its initiation can be traced to a local increase in the rateof division some 2 plastochrons before the bulge is well formed.     

DEVELOPMENT AND ORGANIZATION OF THE PRIMARY VASCULAR SYSTEM IN POPULUS DELTOIDES ACCORDING TO PHYLLOTAXY

An actively growing cottonwood bud was embedded in epon-araldite and serially sectioned at 2 μm. The sections were analyzed microscopically with the optical shuttle system of Zimmermann and Tomlinson, and all data were quantitatively recorded relative to the apex and to leaf plastochron index (LPI). Analysis of the sections revealed an acropetally developing procambial system organized according to a precise phyllotaxy. Six procambial strands could be recognized and followed long before the leaf primordia that they would enter were evident at the apex. Origin of these strands coincided with developmental events both in the parent trace and its primordium and in the antecedent leaf on the same orthostichy. Once a primordium and its trace attained a certain stage of development, trace bundles began to develop basipetally from the primordium base. These trace bundles appeared to be the earliest progenitors of wood formation in cottonwood. It was concluded that the concept of residual meristem and its corollary, the hypothesis that acropetally developing procambial strands determine the inception sties of new primordia, apply to the cottonwood apex.     

裸伞属的的两个新种

本文报道了广东地区裸伞属(Gymnopilus Karsten)的7个种,其中2个新种,除近缘裸伞外,其余为国内新纪录。并附分种检索表。     

COMPARATIVE STUDY ON EARLY ONTOGENY OF COMPOUND LEAVES IN LARDIZABALACEAE

The early ontogeny of the pinnately, palmately, and ternately compound leaves in the Lardizabalaceae was studied by SEM. The leaf primordium of each of the three leaf types emerges as an identical short protrusion on the shoot apex; the leaf primordium produces the first leaflet initials laterally on its margin. Successive acropetal growth of the leaf axis and the following inception of the leaflet primordia are responsible for the pinnately compound leaf, whereas short basipetal growth accompanied with initiation of two or more pairs of leaflet initials results in a palmately compound leaf. If no elongation of the leaf axis nor additional inception of leaflet primordia occur during early ontogeny, a ternate leaf ensues.     

FOLIAR ONTOGENY AND HISTOGENESIS IN MAGNOLIA GRANDIFLORA L. I. APICAL ORGANIZATION AND EARLY DEVELOPMENT

Foliar ontogeny of Magnolia grandiflora was studied to elucidate possible unique features of evergreen leaves and their development. The apex of Magnolia grandiflora is composed of a biseriate or triseriate tunica overlying a central initial zone, a peripheral zone and a pith rib meristem. Leaf primordia are initiated by periclinal divisions on the apical flank of the tunica in its second layer. This initiation and expansion is seasonal just as in related deciduous magnolias. Following leaf initiation, a foliar buttress is formed and the leaf base gradually extends around the apex. As growth continues, separation of the leaf blade primordium from the stipule proceeds by intensified anticlinal divisions in the surface and subsurface layers near the base. Marginal growth begins in the blade primordium when it reaches approximately 200 μm in height and results in the formation of two wing-like extensions, the lamina. This young blade remains in a conduplicately folded position next to the stipule until bud break.     

CHANGE IN EPILOBIUM PHYLLOTAXY DURING REPRODUCTIVE TRANSITION

The ontogeny of Epilobium hirsutum grown under natural summer photoperiod in a glasshouse was divided into vegetative, early transitional, transitional, and floral stages. Bijugate phyllotaxy, common to both the vegetative and early transitional stages, is transformed into spiral phyllotaxy during the transitional stage by an initial change in the divergence angle of a single primordium inserted at a unique level on the shoot. Leaf primordia subsequently are inserted in a spiral arrangement in the indeterminate floral shoot apex. The early transitional shoot apical meristem is about 1.5 times the volume of the vegetative meristem but expands at about two-thirds the relative plastochron rate of volume increment of the vegetative meristem. There are progressive decreases in the plastochron and relative plastochron rates of radial and vertical shoot growth through ontogeny. Relative chronological rates of shoot growth, however, are not altered during ontogeny. Spiral transformation results from changes in the relative points of insertion of leaf primordia on the shoot meristem. These changes are accompanied by an increased rate of primordia initiation on a more circular shoot meristem. The change in phyllotaxy during ontogeny is similar to that which was artificially induced by chemical modification of auxin concentration gradients in the shoot apex, with the additional feature that there is an initial increase in the volume of the shoot meristem prior to the natural spiral transformation. Size of the shoot apical meristem, however, appears to have little influence on Epilobium phyllotaxy; but the geometric shape of the meristem is well correlated with bijugate to spiral transformations. This suggests that geometric parameters of the shoot meristem should be considered in theoretical models of phyllotaxy.     

Flower primordium formation at the Arabidopsis shoot apex: quantitative analysis of surface geometry and growth

Geometry changes, especially surface expansion, accompanying flower primordium formation are investigated at the reproductive shoot apex of Arabidopsis with the aid of a non-invasive replica method and a 3-D reconstruction algorithm. The observed changes are characteristic enough to differentiate the early development of flower primordium in Arabidopsis into distinct stages. Primordium formation starts from the fast and anisotropic growth at the periphery of the shoot apical meristem, with the maximum extension in the meridional direction. Surprisingly, the primordium first becomes a shallow crease, and it is only later that this shape changes into a bulge. The bulge is formed from the shallow crease due to slower and less anisotropic growth than at the onset of primordium formation. It is proposed that the shallow crease is the first axil, i.e. the axil of a putative rudimentary bract subtending the flower primordium proper, while the flower primordium proper is the bulge formed at the bottom of this axil. At the adaxial side of the bulge, the second axil (a narrow and deep crease) is formed setting the boundary between the flower primordium proper and the shoot apical meristem. Surface growth, leading to the formation of the second axil, is slow and anisotropic. This is similar to the previously described growth pattern at the boundary of the leaf primordium in Anagallis.