Análisis de comunidades vegetales de Montecaseros (Gral. San Martín, Mendoza) en áreas naturales fragmentadas por la agricultura

El área estudiada abarca 250 has en el distrito de Montecaseros, Departamento de Gral. San Martín, Mendoza; enclavada en la llanura norte (Travesía de Guanacache) y su vegetación natural pertenece a la provincia fitogeográfica del Monte. El principal uso del suelo es la agricultura, aunque no ha logrado modificar todo el territorio. Se observan, en una matriz dominada por áreas cultivadas, parches de vegetación natural característicos de un área fragmentada. El objetivo de esta tesis es el análisis de las comunidades vegetales naturales de un sector de la llanura mendocina, fragmentadas por la actividad agrícola. En Montecaseros no hay antecedentes sobre estudios de las comunidades vegetales. Mediante el método fitosociológico se caracterizaron las comunidades presentes en el área de estudio y su diversidad a nivel específico. Se seleccionaron sitios representativos de cada comunidad y se efectuaron los análisis de suelo pertinentes en cada una. Finalmente se elaboró el listado florístico de la zona estudiada, con 108 especies. Se diferenciaron seis comunidades vegetales a lo largo de un gradiente, desde la máxima modificación en 1) las parcelas cultivadas, hasta la vegetación prácticamente sin evidencias de alteración: 2) médanos, 3) matorral, 4) chañaral y 5) algarrobal, incluyendo parcelas desmontadas, cultivadas y luego abandonadas identificadas como 6) parcela en recuperación. La fisonomía dominante en la zona es la del matorral con especies de los géneros Larrea, Atriplex y Lycium. Los bosquecillos de Prosopis flexuosa son de escasa extensión (abiertos, semi cerrados o cerrados) localizados donde pueden usufructuar la capa freática. En las áreas con suelo de textura más fina, al pie de médanos o en zonas deprimidas se desarrollan bosquecillos de Geoffroea decorticans var. decorticans. En los médanos la vegetación psamófila está bien representada con especies como Portulaca grandiflora, Ibicella parodii, Mimosa ephedroides, Larrea divaricata y Panicum urvilleanum. En áreas cultivadas se hallan especies adventicias dependientes de un buen aporte hídrico como Melilotus albus o Taraxacum officinale y aquellas capaces de sobrevivir y reproducirse en condiciones menos favorables como Flaveria bidentis o Wedelia glauca. En la parcela en recuperación, el desmonte, el laboreo y el posterior abandono de los cultivos hace 25 años generaron nuevas condiciones edáficas y la revegetación natural resulta en comunidades con composición florística diferente de la inicial. En este sector, el matorral original se ha transformado en una estepa de arbustos, halófilos en parte, y gramíneas junto con árboles jóvenes de pequeño porte. Se concluye que las limitaciones edáficas existentes naturalmente en el terreno se ven agravadas por el laboreo y el abandono del cultivo, situación que dificulta el reingreso a la parcela de varias de las especies presentes en los alrededores, aún siendo éstas halófilas. Con los resultados obtenidos se aporta información sobre las comunidades vegetales presentes en sitios fragmentados por la actividad agrícola en la zona este de Mendoza. Además, se demuestra la necesidad de aplicar etodologías de evaluación previas al desmonte, que permitan el reconocimiento y valoración de las especies indicadoras de las limitaciones edáficas. Esto es particularmente importante dado que estas últimas dificultan o encarecen el establecimiento de determinados cultivos y afectan su productividad. Asimismo el trabajo realizado pone en valor la conservación de comunidades naturales en áreas fragmentadas privadas.

Pollen records and age determination of site Bokanjacko Blato

In summary, one may conclude that human influence in the Bokanjac area started in the Eneolithic or Earlier Bronze Age - the third to second millennia Cal. BC. Traces of agriculture are weak or missing in the pollen diagram but grazing is indicated. Chestnut and walnut were introduced by humans to the area in classical times. These findings are in general agreement with the results of earlier studies at coastal sites north-west and south-east of Bokanjacko Blato.

Planktonic foraminifera in ODP Hole 112-688A (Table 1)

Species of Globorotalia are among the most dissolution-resistant planktonic foraminifers in sediments of the inner wall of the Middle America Trench; parts of their Phylogenetic history have been recognized in sediments of Leg 107 (Glacon and Bourgois, 1985). These species can be integrated into the biostratigraphic scheme on the basis of calcareous and siliceous nannoplankton and calibrated on the basis of paleomagnetism (Keller, 1980, 1981; Keller et al., 1982; Barron and Keller, 1982). Data compiled for this data report extend to the southern area of occurrence of Globorotalia species. About 250 sediment samples were collected on board JOIDES Resolution and examined as follows: 20-cm**3 samples were dried for 8 hr at 60°C, weighed, and then washed through sieves of 0.5, 0.2, 0.125, and 0.063 mm mesh size. The residues were dried and reweighed. The abundance of planktonic foraminifers counted is reported as numbers of specimens per weight of the original sample.

Pollen profiles from three former lakes in the Lake Garda area

1. Late glacial and postglacial sediments from three former lakes in the Lake Garda area (Southern Alps) were investigated. 2. The pollen diagram from Bondone (1550 m) shows an older phase rich in NAP. A younger one corresponds with the Younger Dryas time according to two radiocarbon determinations. In the Preboreal no climatic deterioration could be found. 3. At first plants, which are nowadays typical for snow-ground, pioneer and dwarf shrub associations, immigrated into the surroundings of Bondone. In Alleröd times larch and pine appeared as the first trees. At the beginning of the Preboreal dense forest existed in that region. During the Alleröd timber line was at about 1500 m. 4. In the pollen diagrams from Saltarino (194 m) and Fiavè (654 m) an oldest period rich in NAP is followed by two stadial and two interstadial phases. Tree birches and larches immigrated during the oldest interstadial phase. 5. In the case of Saltarino and Fiavè only a preliminary dating could be made. A correlation seems to be possible with diagrams published by Zoller as well as with the diagram of Bondone. Discrepances in dating, which arise then, are discussed. According to the two possibilities of dating the youngest stadial is synchronous either with the so-called Piottino stadial or the Younger Dryas time. Consequently the oldest interstadial phase of Saltarino corresponds either with the Bölling or with a pre-Bölling interstadial. The last possibility seems to be more probable. 6. In the southern part of the Lake Garda area reforestation was preceded by a long shrub phase mainly with Juniperus. At about 650 m there was a period with Pinus mugo and only with a small amount of Juniperus before reforestation. A phase with Betula nana well known from areas north of the Alps could nowhere be found. 7. In the area under study larch appeared as the first tree. Lateron it has been the most important constituent of the forests near timber line. Birch, which plays an important role as a pioneer tree in Denmark - for instance at the transition of the pollen zones III/IV - as well as in Southern Germany during Bölling time, was of less importance at the southern border of the Alps. In that area the spreading of Pinus occurred very early causing dense forests. 8. During the last stadial phase (probably Younger Dryas time) dense forests with Pinus and Larix existed at 650 m. In the lower part of the Lake Garda area, however, both thermophilous trees as Quercus and herbs frequently occurred. This leads to the conclusion that during this time tree growth was limited by dryness in lower altitudes of the border of the Southern Alps. Pinus and Juniperus, however, do not show higher values in this period, a fact which cannot yet be explained. 9. A list of plants, which were found in the sediments, is compiled. Helodium lanatum, Dictamnus albus, Mercurialis cf. ovata, Buxus, Cerinthe cf. minor, Onosma, Anthericum and Asphodelus albus are findings, which are of special interest for the history of the flora of that region.

Age determination and pollen profile of sediment core Voulkaria 1966, Greece

Lake Voulkaria is situated in northwestern Greece in the Prefecture of Etoloakarnania, 6 km SW of the city of Vonitsa and 10 km east of the northern tip of the island of Levkás (Leukás, Lefkada). The lake is separated from the Ionian Sea on the West by a narrow limestone ridge ca 10 m high and has a size of 940 ha. An almost continuous fringe of Phragmites surrounds the open water. This reed bank is up to 500 m wide along the southern shore of the lake. Water depth is low, predominantly less than 2 m. In the south-eastern part of the lake a maximum depth of 3.1 m was measured in September 1997.

Abundance and biomass of in- and epibenthic invertebrate macrofauna in the German Bight from 1969 to 2000

In order to examine the long-term development of offshore macrozoobenthic soft-bottom communities of the German Bight, four representative permanent stations (MZB-SSd, -FSd, -Slt, -WB) have been sampled continuously since 1969. Inter-annual variability and possible long-term trends were analysed based on spring-time samples from 1969 until 2000. This is part of the ecological long-term series of the AWI and is supplemented by periodic large-scale mapping of the benthos. The main factors influencing the development of the benthic communities are biological interactions, climate, food supply (eutrophication) and the disturbance regime. The most frequent disturbances are sediment relocations during strong storms or by bottom trawling, while occasional oxygen deficiencies and extremely cold winters are important disturbance events working on a much larger scale. Benthic communities at the sampling stations show a large inter-annual variability combined with a variation on a roughly decadal scale. In accordance with large-scale system shifts reported for the North Sea, benthic community transitions occurred between roughly the 1970ies, 80ies and 90ies. The transitions between periods are not distinctly marked by strong changes but rather reflected in gradual changes of the species composition and dominance structure.