The current status of European wetland inventories and classifications

The status of wetland inventory and classification is considered for 44 European countries, as well as for the continent as a whole. Data and information were obtained from questionnaires compiled by the International Waterfowl and Wetland Research Bureau, the MedWet sub-project on inventory and monitoring, and the Ramsar Bureau. Nine European countries have national wetland inventories, and 32 have inventories of sites of international importance listed under the Ramsar Convention. There has been a trend in producing regional or continental inventories for wetlands that are important as waterfowl habitat. There is an urgent need to produce wetland inventories for all European countries. The Ramsar database takes into consideration hydrological and economic wetland values, as well as ecological ones. The Ramsar classification lists a total of 35 wetland types, and is sufficiently flexible that it could be used for classifying European wetlands at the national scale.     

Understorey vegetation change in a Picea mariana chronosequence

Eighteen black spruce (Picea mariana) stands, representing postfire ages of 26 to 120 yr, were surveyed for understorey vegetation and site/microsite characteristics at two spatial scales. This enabled comparison of within- versus among-stand compositional variation.Detrended correspondence analysis (DCA) ordination among the 18 stands revealed a complex age/moisture gradient. DCA ordination among 1 800 quadrats within the stands indicated a similar gradient with much compositional overlap. Quadrats were grouped, using two-way indicator species analysis (TWINSPAN), into 9 classes each representing a phase in understorey vegetation composition. These phases shifted in abundance from young to old stands with a high degree of concordance among replicates in the same age class. Understorey succession is strongly linked to the stages in tree growth, mortality and thinning coupled with the accumulation of site moisture.Abbreviations DCA Detrended Corrospondence Analysis     

To identify impacts in variable systems using anomalous changes: a salt marsh example

A method is proposed to identify impacts of habitat modification in cases where it is difficult to site experimental and control samples. This problem occurs especially in heterogeneous systems, but may pose difficulties in any field experimental situation. The method is relevant to the situation where treated (modified) and untreated sites are spread over a range of habitat types. Types of change are identified and compared to treatments. If a specific change type is associated with a particular treatment then it is likely that the change is causally related to the treatment. There are five stages in the analysis. First, the classes or states of the sample sites, over a period of time, are identified (by numerical classification). Second, for each sample site, the sequence of states is listed. Third, transition matrices are made for each sample site to show the changes which have occurred. Fourth, the transition matrices are classified, to identify types of change. Finally, we use the Chisquared test to indicate whether the treated and untreated sites are associated with particular types of change. As an example, we refer to habitat modification to manage salt-marsh mosquitoes and we evaluate impacts on the environment mainly through changes to the vegetation. We consider that the method has potential to identify changes in heterogeneous systems even though little change was identified in the particular salt marsh studied.     

Book reviews

Editing of community data matrices is complementary to analyzing data by multivariate techniques of classification and ordination in the overall task of data analysis. A computer program, DATAEDIT, is described that can perform numerous editing functions, including data transformation, deletion of certain species or samples, deletion of rare species, deletion of outliers, separation of disjunet sample groups, reordering of the species or samples of a data matrix, and the formation of composite samples or of sample subsets. DATAEDIT can use the information in a nonhierarchical or hierarchical classification, and includes its own internal routine for reciprocal averaging ordination.We appreciate valuable suggestions from the late Robert H. Whittaker, and from Philip Dixon, David Hieks, Laura Huenneke, Linda Olsvig-whittaker, and Mark Wilson. Mark O. Hill kindly supplied a fast subroutine for reciprocal averaging.     

Isorthid AE (Brachiopoda) du dévonien inférieur du massif armoricain

Three species of Isorthidae are described in the Lower Devonian of the Armorican Massif. Two of them were hitherto badly known, being never adequately described nor figured: Isorthis (Protocortezorthis) miloni from the Gahard Formation (Gedinnian) and Isorthis (Protocortezorthis) trigeri from the Saint-Céneré Formation (Gedinnian-Siegenian). Isorthis oehlertiSolle, 1976 is considered as a synonym of Isorthis (Protocortezorthis) trigeri. The geographic distribution of these species allows to corroborate that until the top of the Lower Devonian (top of Le Faou Formation), two provinces with different faunal associations exist in the Armorican Massif.     

Some synchorological aspects of basiphilous pine forests in Fennoscandia

Basiphilous pine forests and related birch forests are herb-and grass-rich forests on calcareous substrate. These forests are complex communities with floristic/ecological elements from different vegetation types occurring in a subtle micromosaic. These elements are e.g. species from acidophilous conifer forests, thermophilous forest-rim communities, calcareous shallow-soil and steppe communities, eutrophic wet meadows and fens, and in northern Fennoscandia also species from alpine Dryas heaths. Four associations are recognized in Fennoscandia: Convallario-Pinetum, Melico-Piceetum pinetosum, Peucedano-Pinetum and Epipacto atrorubentis-Betuletum. The main association is the Convallario-Pinetum, a widespread community in Fennoscandia and Estonia with a considerable floristic variation between the different regions. Examples of the floristic variation along west-east profiles and south-north profiles in Fennoscandia are presented. The basiphilous pine forest complex can be divided into a number of ecological types along the moisture and nutritional gradients. A further subdivision into geographical types (races) is presented.Nomenclature follows Lid (1974) for vascular plants, Nyholm (1954–1969) for musci and Dahl & Krog (1973) for lichens.     

The chorologic pattern of European Nardus-rich communities

Two types of Nardus-rich communities may be distinguished in Europe according to their geographic pattern:I. Communities of high mountains showing discontinuous variation. Different florogenesis in island-like high mountains results in a number of alliances characteristic for particular mountain systems: Trifolion humilis Quézel 57 (Atlas, N Africa), Plantaginion thalackeri Quézel 53 (Sierra Nevada), Campanulo-Nardion Rivaz-Martinez 63 (mountains of the central Iberian peninsula), Nardion Br.-Bl. 26 (from Pyrenees, Auvergne to W and E Carpathians), Potentillo ternatae-Nardion Simon 58 (S Carpathians, Pirin, Rila), Jasionion orbiculatae Lakui 66 (Dinarids), Trifolion parnassi Quézel 64 (S Greece), Nardo-Caricion rigidae Nordhagen 37 (Iceland, Scotland, Scandinavia, W Sudeten).II. Communities at lower altitudes with continuous variation, where particular syntaxa are difficult to distinguish. Along the climatic gradient from a subatlantic to a subcontinental climate, a cline in floristic composition of the communities under discussion is found. Towards the eastern borderline, the communities are poorer in characteristic species. Here only one alliance is considered-Violion caninae Schwickerath 44. A Similar situation occurs along the altitudinal gradient in mountains. Only in mountains with a belt of alpine communities the montane Nardeta are saturated with alpine species. This thpe of communities was described as Nardo-Agrostion tenuis by Sillinger (1933).     

On the variability of “flexion creases” in the distal plantar areas of newborns

The plantae of 83 male and 95 female healthy, full-term Caucasian newborns from Austria (gestational age 235–301 days) were photographed and the flexion creases in the distal part were examined. Analysis of the creases was done under four different aspects, the main evaluation based on a scheme of nine creases introduced by Schenk and Patzer (1959). Two transversal (No. 1 and No. 9) and three longitudinal (Nos. 3, 6, and 7) creases are always or predominantly present, a finding corresponding with the data of Schenk on 52 male and 48 female newborns from Germany. In addition, the nine plantar creases were evaluated according to six degrees of expression, and some typical crease combinations are shown. Bilateral and bisexual similarity prevails. The results of this study might serve investigations of different populations and of medical disorders.     

周口店地区仓鼠材料的重新观察

经重新鉴定,周口店地区第四纪期间共有4属7种仓鼠,包括大型种类Allocricetus ehiki、A. teilhardi sp. nov. 及Cricetinus varians和小型种类Cricetulus longicaudatus, C. barabensis griseus, C. b. obscurus, C. cf. migratorius, Phodopus sp.其中A. ehiki-A. teilhardi sp. nov.,C. varians-现生种“C.”triton及小型仓鼠可能分别和中国新第三纪晚期的Sinocricetus, Kowalskia等有较密切的亲缘关系。