Ovular development and morphology in some magnoliaceae species

Floral phenology and ovular development ofLiriodendron tulipifera are described. The ovule primordia are initiated in December, followed by prominent development in March, and the ovules are mature in May. The inner integument is formed as an annular rim on the incurving ovule primordia, but the outer integument develops as a semi-annular rim interrupted on the concave side of the funicle. Later, an outgrowth, which is interpreted here as an obturator, arises on the concave side of the funicle. The funicular outgrowth arises far from the inner integument, while the outer integument is close to the inner. The outer integument and the funicular outgrowth together form an envelope complex. Later the outer integument produces two distal lobes, which disappear at maturity. Mature ovules of the threeMagnolia species examined have similar lobes. It is suggested that the hood-shaped outer integument is primitive in angiosperms.     

Ovular development and morphology of the outer integument of Magnolia grandiflora (Magnoliaceae)

Ovular development of Magnolia grandiflora was examined to determine the morphology of the outer integument. At the time the ovular primordium begins incurving, the outer integument is initiated subdermally, and later the inner integument arises from the dermal layer. Whereas the inner integument is annular, the outer integument is formed as a semiannular rim interrupted on the concave side of the funiculus. Later the outer integument becomes a hood-shaped envelope. The obturator is formed as a transversely elongate outgrowth on the concave side of the funiculus and intervenes in the gap of the outer integument. During further development the inner integument produces several distal lobes, and the outer integument becomes bilobed. The exostome is a transverse slit with a middle notch, formed by the outer integument and the obturator. Presumed wide occurrence of the hood-shaped outer integument in primitive families suggests that it is a primitive state. The outer integument is compared with the ovuliferous sporophylls of the glossopterid and caytonialean seed ferns.     

Some realignments in the dicotyledons

In discussing some ways in which my scheme of classification of dicotyledons differs from more traditional ones, I wish to call attention to McVaugh's principle regarding the delimitation of related larger and smaller groups, and to the fact that makers of general systems should not lose sight of phenetic definability as one of the goals in the organization of affinity–groups into formal taxa.
Daphniphyllum is best considered to form a family and order in the Hamamelidae, remote from the Euphorbiaceae. The Huaceae are best placed in the Violales, and Grubbia in the Ericales. The Surianaceae should be redefined to include Cadellia, Guilfoylia , and Stylobasium , as well as Suriana , and the family moved to the Rosales. Rhabdodendron should form a family in the Rosales. Anisophyllea and its immediate allies (Poga, Polygonanthus , and Combretocarpus) should be removed from the Rhizophoraceae and established as a family in the Rosales. Retzia should form a family in the Asteridae, but its ordinal position is still uncertain; the Gentianales or the Solanales seem more likely than the Lamiales. The Hippuridaceae, Calli–trichaceae, and Hydrostachyaceae should be grouped to form an order Callitrichales in the Asteridae near the Plantaginales.     

Prevention of flower formation in dicotyledons

Prevention of flower formation is important, for example for preventing the spread of transgenes from genetically modified plants or the spread of non-native species, for increasing vegetative growth or preventing the formation of allergenic pollen. The aim of this study was to determine whether flowering of dicotyledonous plants can be prevented by genetic manipulation without harmful effects on vegetative growth. Here we describe isolation of the BpMADS1 gene (similar to SEP3, formerly AGL9) from birch and show that it is expressed only in the inflorescences. In tobacco and Arabidopsis, the expression of BpMADS1::GUS was also virtually inflorescence-specific. Transgenic tobacco and Arabidopsis containing a BpMADS1::BARNASE construct grew well. In one tobacco line the formation of the inflorescence was completely prevented; in several other lines the flowers lacked stamens and carpels and therefore were sterile. The final dry weights of the shoots of the sterile tobacco lines were 140–200% of those of controls. In Arabidopsis, some of the transgenic lines containing the BpMADS1::BARNASE construct formed inflorescences. Some of these lines formed never flowers and some others formed occasionally single fertile flowers. Some other lines did not form inflorescences, but formed up to about one hundred leaves, even in long-day conditions. These results suggest that formation of flowers or inflorescences in widely different dicotyledonous plants could be prevented using the BpMADS1::BARNASE construct and that prevention of flowering may lead to increased vegetative mass.     

Paleobotanical evidence on the early radiation of nonmagnoliid dicotyledons

Paleobotanical studies indicate that several isolated and systematically depauperate groups of extant woody dicotyledons originated in the Mid Cretaceous. TheChloranthaceae had probably differentiated into insect-pollinated (Chloranthus andSarcandra) and wind-pollinated (Ascarina andHedyosmum) forms by the end of the Albian, and leaves referable to theTrochodendrales are known from the Albian and Cenomanian. In the latest Cretaceous and Early Tertiary, extinct representatives of theTrochodendrales includedNordenskioldia and theJoffrea-Nyssidium complex. ThePlatanaceae also differentiated before the end of the Albian and initially had insect-pollinated, unisexual flowers with five carpels or stamens. Some of these features persisted in the platanoid lineage until the Early Tertiary, and during the Paleocene and Eocene thePlatanaceae included forms with elliptical, palmate and pinnate foliage. The history of thePlatanaceae suggests that several features of the reproductive morphology of extant taxa may have arisen in association with a trend toward wind pollination. In the Mid Cretaceous, platanoid foliage partially intergrades with pinnateSapindopsis and pedateDebeya-Dewalquea leaves suggesting a close relationship betweenPlatanaceae andRosidae andFagaceae respectively. TheChloranthaceae, Trochodendrales, andPlatanaceae all occupy a somewhat intermediate position between theMagnoliidae andHamamelidae and are of considerable interest with respect to their role in the initial radiation of nonmagnoliid (higher) dicotyledons.     

On pollen shape in some groups of dicotyledons

Shape change of pollen grains under different conditions are discussed for some families of dicotyledons. Reversibility of pollen form in relation to age and humidity are described. A technique for stabilizing shape is discussed.     

The trilobite family Nileidae: morphology and classification

Species of genera currently referred to Nileidae are reviewed, and those of Hemibarrandia , Lakaspis , Peraspis and Symphysurina are excluded from the family. Nileidae are united in having a distinctive form of the hypostome, the glabellar organ, in the shallowness or absence of external furrows on the axial and pleural regions, and in the development of strong ventral ridges on the axial region. It is contended that the glabellar organ of nileids and illaenids may not be homologous with the glabellar tubercle of asaphids, that the median ventral suture is not exclusively a character of Asaphina, and doubt is cast on the identification of an asaphoid protaspis as being that of Nileus . These arguments provide a case for allying Nileidae with the Illaenidae, rather than with the Asaphina.     

大螺旋藻的形态观察和培养试验

蓝藻—螺旋藻(Spirulina)作为大规模工业化培养的对象,以其高的蛋白质含量和合理的氨基酸组成,极大地吸引了国内外生物学工作者的注意,他们对原产于非洲的钝顶螺旋藻(S.platensis)或墨西哥的极大螺旋藻(S.maxima)进行了广泛的研究3-6。笔者在我国广州珠江河畔一个小池塘里发现采集了一种螺旋藻——大螺旋藻(Spirulina major)1,2,进行了分离和单种培养。       

红褐斑腿蝗血细胞的形态与分类

利用光学显微镜和显微数码拍照系统,对红褐斑腿蝗Catantops pinguis(Stal)血细胞的形态进行观察和分类。结果在红褐斑腿蝗血淋巴中观察到5种血细胞,分别是原血胞、浆血胞、粒血胞、珠血胞和囊血胞。原血胞为小型圆形细胞,边缘圆滑、清晰,核质比例很大。粒血胞多为中型,形状不规则,边缘凹突不平,内含较大的异质性溶酶体颗粒。浆血胞多为中型,刚离体时形状较规则,常呈圆形、卵圆形。浆血胞内缺乏大的颗粒,细胞核大而圆形,细胞质内具许多小型颗粒状物质。浆血胞离体后形状变化较多,常发展出伪足,呈丝状、短芒状、钩状或片状伪足。珠血胞多为大、中型,外形大体呈圆形,但边缘由于大小不等的珠形内含物突出,呈花瓣状。囊血胞多为中型,圆形或椭圆形,细胞质内具有大小不一的带有折光性的颗粒或块状物,细胞边缘比较光滑。