Phylogeny of Schisandraceae based on morphological data: evidence from modern plants and the fossil record

Schisandraceae are traditionally subdivided in two genera, Schisandra and Kadsura, based on differences in the organisation of the floral receptacle, the carpels, and the presence or absence of a ``pseudostigma'. Recently, phylogenetic analyses utilizing ITS sequence data and morphological data resulted in incongruent tree topologies, with the morphological trees suggesting monophyly of the two genera, whereas ITS trees did not resolve Schisandra and Kadsura as monophyletic clades. In the present paper we study seed morphology and leaf epidermal features of 22 species of Schisandraceae in order to provide additional data for a morphological data matrix. Seed morphological characters are highly homoplastic and do not yield further evidence for monophyly of the two genera. Instead, a number of characters appear to support sister group relationships between taxa within the genera, such as, for instance, for K. coccinea and K. scandens, both of which have large seeds along with a multi-layered mesotesta. Considering leaf epidermal characteristics, species of Kadsura were found to be consistently amphistomatic, whereas species of Schisandra are always hypostomatic. Phylogenetic analysis using the extended data matrix resulted in weakly supported Kadsura and Schisandra clades with five and four synapomorphies indicating monophyly of Kadsura and Schisandra, respectively. Fossils ascribed to Schisandraceae date back to the Late Cretaceous. These are tri-and hexacolpate pollen types displaying a combination of features found in modern Schisandraceae and partly also in Illiciaceae. Leaf remains from this period are poorly preserved and difficult to ascribe to Schisandraceae because of the lack of synapomorphies for the family. In the Early Cainozoic, leaf and seed remains from North America and Europe unambiguously belong to the family. Seeds from the Eocene of North America show some similarities to the modern Schisandra glabra from North America, while fossils from Europe show more similarities to modern Asian species.     

Frenelopsis alata and its microsporangiate and ovuliferous reproductive structures from the Cenomanian of Bohemia (Czech Republic, Central Europe)

The conifer, Frenelopsis alata (K. Feistmantel) E. Knobloch (Cheirolepidiaceae), occurring mostly in the Cenomanian of Europe, is revised on the basis of the type material. Its comparison with relevant species of Frenelopsis is discussed.The ovuliferous cone associated with the genus Frenelopsis is recorded for the first time. For the associated ovuliferous cones of Frenelopsis, a new genus, Alvinia, is introduced in a new combination for the type: Alvinia bohemica (Velenovsky) comb. n. Its association with Frenelopsis alata is based on the presence of Classopollis pollen adhering to ovuliferous cone scales, and the same type of pollen found in the microsporangiate cone of F. alata, the same cuticle pattern present on ovuliferous cones, sterile twigs and microsporangiate cones of F. alata, and also the co-occurrence of ovuliferous cones or their scales and sterile twigs of F. alata.Large ovuliferous cones of Alvinia bohemica are formed by helically arranged ovuliferous scales subtended by bracts. Each ovuliferous cone scale displays one or two seeds covered by a covering flap, and three appendages, which form distally a funnel-like structure lined in its inner part by long trichomes. Numerous pollen grains of Classopollis adhere to the trichomes, and the structure is considered to function as a protostigmatic area.The ovuliferous cones of Alvinia differ from similar cones of the Cheirolepidiaceae, Hirmeriella and Tomaxellia, mainly in a high state of unification of the ovuliferous cone scale, reduction of appendages and in a presence of the protostigmatic funnel-like structure.The ovuliferous cones, Alvinia bohemica, rarely occur intact, so it is assumed that they disintegrate when mature. It seems likely that they were not woody. This assumption is supported by the flattened appearance of cones and their cone scales in the sediment, their flexibility and the absence of massive coaly matter known from cones of the Taxodiaceae and Cupressaceae. It is proposed that this type of ovuliferous cone scale indicates a specialized type of pollination. In addition, it is suggested that cone scales enclosing seeds play an important role in propagation.     

Origin and evolution of insect wings and their relation to metamorphosis,as documented by the fossil record

In contemporary entomology the morphological characters of insects are not always treated according to their phylogenetic rank. Fossil evidence often gives clues for different interpretations. All primitive Paleozoic pterygote nymphs are now known to have had articulated, freely movable wings reinforced by tubular veins. This suggests that the wings of early Pterygota were engaged in flapping movements, that the immobilized, fixed, veinless wing pads of Recent nymphs have resulted from a later adaptation affecting only juveniles, and that the paranotal theory of wing origin is not valid. The wings of Paleozoic nymphs were curved backwards in Paleoptera and were flexed backwards at will in Neoptera, in both to reduce resistance during forward movement. Therefore, the fixed oblique-backwards position of wing pads in all modern nymphs is secondary and is not homologous in Paleoptera and Neoptera. Primitive Paleozoic nymphs had articulated and movable prothoracic wings which became in some modern insects transformed into prothoracic lobes and shields. The nine pairs of abdominal gillplates of Paleozoic mayfly nymphs have a venation pattern, position, and development comparable to that in thoracic wings, to which they are serially homologous. Vestigial equivalents of wings and legs were present in the abdomen of all primitive Paleoptera and primitive Neoptera. The ontogenetic development of Paleozoic nymphs was confluent, with many nymphal and subimaginal instars, and the metamorphic instar was missing. The metamorphic instar originated by the merging together of several instars of old nymphs; it occurred in most orders only after the Paleozoic, separately and in parallel in all modern major lineages (at least twice in Paleoptera, in Ephemeroptera and Odonata; separately in hemipteroid, blattoid, orthopteroid, and plecopteroid lineages of exopterygote Neoptera; and once only in Endopterygota). Endopterygota evolved from ametabolous, not from hemimetabolous, exopterygote Neoptera. The full primitive wing venation consists of six symmetrical pairs of veins; in each pair, the first branch is always convex and the second always concave; therefore costa, subcosta, radius, media, cubitus, and anal are all primitively composed of two separate branches. Each pair arises from a single veinal base formed from a sclerotized blood sinus. In the most primitive wings the circulatory system was as follows: the costa did not encircle the wing, the axillary cord was missing, and the blood pulsed in and out of each of the six primary, convex-concave vein pair systems through the six basal blood sinuses. This type of circulation is found as an archaic feature in modern mayflies. Wing corrugation first appeared in preflight wings, and hence is considered primitive for early (paleopterous) Pterygota. Somewhat leveled corrugation of the central wing veins is primitive for Neoptera. Leveled corrugation in some modern Ephemeroptera, as well as accentuated corrugation in higher Neoptera, are both derived characters. The wing tracheation of Recent Ephemeroptera is not fully homologous to that of other insects and represents a more primitive, segmental stage of tracheal system. Morphology of an ancient articular region in Palaeodictyoptera shows that the primitive pterygote wing hinge in its simplest form was straight and composed of two separate but adjoining morphological units: the tergal, formed by the tegula and axillaries; and the alar, formed by six sclerotized blood sinuses, the basivenales. The tergal sclerites were derived from the tergum as follows: the lateral part of the tergum became incised into five lobes; the prealare, suralare, median lobe, postmedian lobe and posterior notal wing process. From the tips of these lobes, five slanted tergal sclerites separated along the deep paranotal sulcus: the tegula, first axillary, second axillary, median sclerite, and third axillary. Primitively, all pteralia were arranged in two parallel series on both sides of the hinge. In Paleoptera, the series stayed more or less straight; in Neoptera, the series became V-shaped. Pteralia in Paleoptera and Neoptera have been homologized on the basis of the fossil record. A differential diagnosis between Paleoptera and Neoptera is given. Fossil evidence indicates that the major steps in evolution, which led to the origin first of Pterygota, then of Neoptera and Endopterygota, were triggered by the origin and the diversification of flight apparatus. It is believed here that all above mentioned major events in pterygote evolution occurred first in the immature stages.     

植物Nramp基因及其与金属离子转运的关系

概述了植物Nramp基因家族及其序列结构分析;在金属离子转运方面的作用机制;表达调控及亚细胞定位;与植物乙烯信号转导途径的核心组分EIN2基因之间的关系等;对今后的研究重点和应用也做了展望。     

Genetic diversity of six arable plants in relation to their Red List status

In Central Germany and throughout Europe, arable plants count among some of the most endangered plant species. Over the last few decades, the number and size of populations have been in sharp decline due to modern land use techniques, including the application of fertilizers, herbicide use and seed cleaning procedures. As arable plant species are underrepresented in population genetic studies, it is unknown whether agricultural intensification has affected the extant populations, and whether genetic structure varies among species with differing vulnerability in respect of their Red List status. We sampled 53 populations from 6 arable plant species throughout Central Germany. Random amplified polymorphic DNA analyses (RAPD) were applied to calculate measures of genetic diversity at the population level and genetic differentiation. Genetic diversity was found to be lowest in Bupleurum rotundifolium and Anagallis foemina, and highest in Consolida regalis and Nigella arvensis. The highest levels of genetic differentiation were observed among populations of An. foemina and B. rotundifolium but within populations in all other species. Φ_ST values differed strongly ranging between 0.116 for C. regalis and 0.679 for An. foemina. Patterns of genetic structure were related to the Red List status for all the species studied except An. foemina, for which it should consequently be raised. Our data confirm that even relatively recent threats are accompanied by detrimental genetic structure. As losses of populations and increased fragmentation have occurred in all common and uncommon species, the situation for arable plants could change for the worse in the following decades, highlighting the need for consistent monitoring.     

Salmonella choleraesuis proteins and their relation to proteins from bacteria of heterologous sero-groups.

A diversity of proteins was identified in the material isolated from S. choleraesuis with the help of sera prepared in rabbits with this material. The sera displayed, in agar-gel diffusions, numerous superimposed precipitation lines against proteins from: Salmonellae, Shigellae and E. coli. In contrast to proteins from S. paratyphi C, sharing identical identical 'O' 'factors, the serological activity of the S. choleraesuis proteins was impaired by heating. The immunochemical analysis of the sera before and after exhaustive absorptions with heterologous proteins exhibited a stronger relation of S. choleraesuis with S. thyphimiurium and S. Newport than with S. paratyphi C. The antibodies induced against free proteins with S. paratyphi C specificity, present in the mosaic of proteins isolated from S. choleraesuis, were removed by the respective absorption without substantial modifications of the homologous precipitation. In contrast, the absorption of the serum with proteins from either S. newport or S. typhimurium removed almost all the homologous induced antibodies. The strong relations found among species belonging to different serogroups underline the non-conformity of the empirical established serofactors.     

Some properties of pea enation mosaic virus isolated from field pea and broad bean plants in Bohemia

Pea enation mosaic virus (PEMV) was isolated from disea sed field pea (Pisum sativum L.ssp. arvense A.Gr.) and broad bean (Faba vulgaris Moench) plants grown as filed crops at Bohumilice in Bohemia. The virus proved to be pathogenic for the following plant species:Pisum sativum L. cv. Raman,Faba vulgaris Moench,Lens culinaris Med.,Vicia sativa L.,Lathyrus odoratus L.,Glycine soja L.,Phaseolus vulgaris L.,Chenopodium amaranticolor Coste andReyn,Nicotiana clevelandi Gray,Trifolium incarnatum L. The dilution end point of the isolate was higher in pea plants (10^?4) than in broad bean plants (10^?2). The thermal inactivation point was 65–68° and the longevityin vitro between 10 and 14 days. According to the host range, symptoms on pea plants and physical properties the virus isolate studied resembles some isolates described in the U.S.A. and represents a PEMV strain different from those reported so far in Czechoslovakia.     

Germination ecology of three endangered river corridor plants in relation to their preferred occurrence

As a contribution to conservation, we investigated germination requirements of three perennial, endangered river corridor plants of Central European lowlands coexisting in subcontinental flood meadows, but preferring particular zones of decreasing flooding frequency and duration along the elevational gradient of the banks. It was hypothesized that the species have specific germination requirements to respond successfully to open patch creation depending on their occurrence along the gradient of spring flooding in the field. This study involved controlled experiments and phenological studies.     

The fungal flora of loganberries in relation to storage and spoilage

Botrytis cinerea, Cladosporium spp., Penicillium spp., Aureobasidium pullulans, Mucor mucedo, Phoma state of Didymella applanata, Cryptococcus laurentii var. laurentii, C. albidus var. albidus, Candida sake and Sporobolo-myces roseus were consistently present on freshly harvested loganberries. Botrytis cinerea was the main spoilage organism with Mucor mucedo of minor importance. The importance of benomyl-resistant strains of B. cinerea is discussed.     

Portal circulations and their relation to counter-current systems.

We have reviewed the distribution of portal circulations throughout the animal body; they are commoner than is generally supposed. Most portal circulations consist of two serial capillary beds connected by one or more larger vessels. We have called these 'convergent' portal circulations: examples are hepatic portal, placental, hypophysial, renal, ovarian and testicular circulations, as are parts of the lymphatic circulation. A second type of portal circulation, which is less common, consists of two serial capillary beds that are not connected by larger vessels. These we have called 'continuous' portal circulations: adrenal and pancreatic circulations are examples of this type. When a countercurrent concentrating mechanism exists in the body it is always part of the primary or secondary bed of a convergent portal circulation, though some convergent portal circulations are not associated with countercurrent mechanisms.     

Navassa Island and its flora. 2. Checklist of the vascular plants

A revised checklist of the vascular plants of Navassa Island, a U.S. possession in the Caribbean, is presented. This is the first update since the original list was published by Ekman in 1929. A recent expedition to the island resulted in the addition of 35 taxa. Eight pteridophytes and 139 angiosperms are recorded from the island.     

Evolution of oxygen by plants in relation to biosphere evolution.

The process of water decomposition by plants is discussed in connection with biosphere evolution. This process consists of two parts: water oxidation and oxygen evolution. The origin of the water oxidation process took place after the synthesis of chlorine-type pigments, the structure of which corresponds to a more oxidized state than the bacteriochlorophyll type. The ability of plants to evolve oxygen is the result of a long evolution process. The capability of decomposing water in the lung wave length spectral region by algae and higher plants, which can be only seen under anaerobic conditions was discovered. This mechanism was suggested to be a reflection of a relict form of plant apparatus having operated under ancient, strictly anaerobic, conditions.