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.

Aboveground community and species-specific plant biomass from the Jena Experiment (Dominance Experiment, year 2007)

This data set contains aboveground community plant biomass (Sown plant community, Weed plant community, Dead plant material, and Unidentified plant material; all measured in biomass as dry weight) and species-specific biomass from the sown species of the dominance experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the dominance experiment, 206 grassland plots of 3.5 x 3.5 m were established from a pool of 9 plant species that can be dominant in semi-natural grassland communities of the study region. In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 3, 4, 6, and 9 species). Plots were maintained by bi-annual weeding and mowing. Aboveground community biomass was harvested twice in May and August 2007 on all experimental plots of the dominance experiment. This was done by clipping the vegetation at 3 cm above ground in two rectangles of 0.2 x 0.5 m per experimental plot. The location of these rectangles was assigned by random selection of coordinates within the central area of the plots (excluding an outer edge of 50cm). The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species for the sown plant species, weed plant species (species not sown at the particular plot), detached dead plant material, and remaining plant material that could not be assigned to any category. All biomass was dried to constant weight (70°C, >= 48 h) and weighed. Sown plant community biomass was calculated as the sum of the biomass of the individual sown species. The mean of both samples per plot and the individual measurements are provided in the data file. Overall, analyses of the community biomass data have identified species richness and the presence of particular species as an important driver of a positive biodiversity-productivity relationship.

Aboveground community and species-specific plant biomass from the Jena Experiment (Dominance Experiment, time series since 2002)

This data set comprises a time series of aboveground community plant biomass (Sown plant community, Weed plant community, Dead plant material, and Unidentified plant material; all measured in biomass as dry weight) and species-specific biomass from the sown species of the dominance experiment plots of a large grassland biodiversity experiment (the Jena Experiment; see further details below). In the dominance experiment, 206 grassland plots of 3.5 x 3.5 m were established from a pool of 9 species that can be dominant in semi-natural grassland communities of the study region. In May 2002, varying numbers of plant species from this species pool were sown into the plots to create a gradient of plant species richness (1, 2, 3, 4, 6, and 9 species). Plots were maintained by bi-annual weeding and mowing. Aboveground community biomass was harvested twice a year, generally in May and August (in 2002 only once in September) on all experimental plots of the dominance experiment. This was done by clipping the vegetation at 3 cm above ground in two rectangles of 0.2 x 0.5 m per experimental plot. The location of these rectangles was assigned by random selection of new coordinates every year within the central area of the plots (excluding an outer edge of 50cm). The positions of the rectangles within plots were identical for all plots. The harvested biomass was sorted into categories: individual species for the sown plant species, weed plant species (species not sown at the particular plot), detached dead plant material, and remaining plant material that could not be assigned to any category. Biomass was dried to constant weight (70°C, >= 48 h) and weighed. Sown plant community biomass was calculated as the sum of the biomass of the individual sown species. The mean of both samples per plot and the individual measurements are provided in the data file. Overall, analyses of the community biomass data have identified species richness and the presence of particular species as an important driver of a positive biodiversity-productivity relationship.

Lithology and pollen record of various sediment profiles of postglacial age from Bavaria, Germany

(Einleitung) Im süddeutschen Jungmoränengebiet wurden während der letzten 25 Jahre verschiedene vegetationsgeschichtliche Arbeiten durchgeführt, die der Untersuchung der Späteiszeit galten. Die wichtigsten von ihnen stammen von G. Lang (1952), A. Bertsch (1961), H. Müller (1962) und H. Schmeidl (1971). Ohne Zweifel müssen die dabei gewonnenen Ergebnisse in anderen Landschaften des nördlichen Alpenvorlandes überprüft und verschiedene Probleme weiterhin verfolgt werden, wie z. B. das der Definition und Umgrenzung der Bölling-Zeit und der Älteren Tundrenzeit s. str. und die Abhängigkeit der Vegetationsentwicklung von der Meereshöhe. Die vorliegende Studie ging auch auf die Notwendigkeit zurück, die spätglazialen Ablagerungen bei dem Tonwerk Kolbermoor nahe Rosenheim, einer der klassischen Stätten der Quartärforschung im nördlichen Alpenvorland, einer vegetationsgeschichtlichen Neubearbeitung zu unterziehen. Die Untersuchungen wurden auf benachbarte Seen, den Sims-See und den Hofsrätter See, ausgedehnt, da die Ergebnisse von Kolbermoor faziell beeinflußt schienen (Niedermoore) und an limnischem Material überprüft werden mußten.

Pollen records and lithology of profiles from Lobsigensee, Switzerland

Lobsigensee is a small kettle hole lake 15 km north-west of Bern on the Swiss Plateau, at an altitude of 514 m asl. Its surface is 2ha today, its maximum depth 2.7 m; it has no inlet and the overflow functions mainly during snow melting. The area was covered by Rhone ice during the Last Glaciation (map in Fig.2). Local geology, climate and vegetation are summarized in Figure 3A-C, the history of settlement in Figures 5-7. In order to reconstruct the vegetational and environmental history of the lake and its surroundings pollen analysis and other bio- and isotope stratigraphies were applied to twelve profiles cored across the basin with modified Livingstone corers (Fig.3 D). (1) The standard diagram: The central core LQ-90 is described as the standard pollen diagram (Chapter 3) with 10 local pollen assemblage zones of the Late-Glacial (local PAZ Ll to Ll0, from about 16'000(7) to 10'000 years BP) and 20 PAZ of the Holocene (local PAZ L11 to L30), see Figs. 8-10 and 20-24. Local PAZ L 1 to L3 are in the Late-Glacial clay and record the vegetational development after the ice retreat: L1 shows very low pollen concentration and high Pinus percentages due to long-distance transport and reworking; the latter mechanism is corroborated by the findings of thermophilous and pre-Quaternary taxa. Local PAZ L2 has a high di versi ty of non-arboreal pollen (NAP) and reflects the Late-Glacial steppe rich in heliophilous species. Local PAZ L3 is similar but additionally rich in Betula nana and Sal1x, thus reflecting a "shrub tundra". The PAZ L1 to L3 belong to the Oldest Dryas biozone. Local PAZ L4 to L 10 are found in the gyttja of the profundal or in the lake marl of the littoral and record the Late-Glacial forests. L4 is the shrub phase of reforestation with very high Junlperus and rapidly increasing Betula percentages. L5 is the PAZ with a first, L7 with a second dominance of tree-birches, separated by L6 showing a depression in the Betula curve. L4 to L7 can be assigned to the Balling biozone. Possible correlation of the Betula depression to the Older Dryas biozone is discussed. In local PAZ L8 Plnus immigrates and expands. L9 shows a facies difference in that Plnus dominates over Betula in littoral but not in profundal spectra. L8 and L9 belong to the Allerod biozone. In its youngest part the volcanic ash from Laach/Eifel is regularly found (11,000 BP). The local PAZ Ll0 corresponds to the Younger Dryas blozone. The merely slight increase of the NAP indicates that the pine forests of the lowland were not strongly affected by a cooler climate. In order to evaluate the significance of the littoral accumulation of coniferous pollen the littoral profile LQ-150 is compared to the profundal. Radiocarbon stratigraphies derived from different materials are presented in Figures 13 and 14 and in Tables 2 and 3. The hard-water errors in the gyttja samples and the carbonate samples are similar. The samples of terrestrial plant macrofossils are not affected by hard-water errors. Two plateaux of constant age appear in the age-depth relationship; their consequence for biostratigraphy as well as pollen concentration and influx diagrams are discussed. Radiocarbon ages of the Late-Glacial pollen zones are shown in Table 10. The Holocene vegetational history is recorded in the local PAZ L 11 to L30. After a Preboreal (PAZ L11) dominated by pine and birch the expansions of Corylus, Ulmus and Quercus are very rapid. Among these taxa Corylus dominates dur ing the Boreal (PAZ L 12 and L 1 3), whereas the components of the mixed oak forest dominate in the Older Atlantic (PAZ L14 to L16). In the Younger Atlantic (PAZ L 17 to L 19) Fagus and Alnus play an increasing, the mixed oak forest a decreasing role. During the period of local PAZ L19 Neolithic settlers lived on the shore of Lobsigensee. During the Subboreal (PAZ L20 and L21) and the Older Subatlantic (L22 to L25) strong fluctuations of Fagus and often antagonistic peaks of NAP, Alnus, Betula and Corylus can be interpreted as signs of human impact on vegetation. L23 is characterized not only by high values of NAP (especially apophytes and anthropochorous species) but also by the appearance of Juglans, Castanea and Secale which point to the Roman colonization of the area. For a certain period during the Younger Subatlantic (PAZ L26 to L30) the lake was used for retting hemp (Cannabis). Later the dominance of Quercus pollen indicates the importance of wood pastures. The youngest sediments reflect the wide-spread agricultural grass lands and the plantation of Pinus and Picea. Radiocarbon dates for the Holocene are given in Figure 23 and Table 4, the extrapolated ages of the Holocene pollen zones in Table 15. (2) The cross sections: Figures 25 and 26 give a summary of the litho- and palynostratigraphy of the two cross sections. Based on 11 Late-Glacial and 9 Holocene pollen diagrams (in addition to the standard ones), the consistency of the criteria for the definition of the pollen zones is examined in Tables 7 and 8 for the Late-Glacial and in Tables 11 to 14 for the Holocene. Sediment thicknesses across the basin for each pollen zone are presented in these tables as well as in Figures 43 to 45 for the Late-Glacial and in Figures 59 to 65 for the Holocene. Sediment focusing can explain differences between the gyttja cores of the profundal. Focusing is more than compensated for through "stretching" by carbonate precipitation on the littoral terrace. Pollen influx to the cross section are discussed (Chapters 4.1.5. and 4.2.3.). (3) The regional pollen zones: Based on some selected sites between Lake Geneva and Lake Constance regional pollen zones are proposed (Table 16, 17 and 19). (4) Paleoecology: Climatic change in the Late-Glacial can be inferred from Coleoptera, Trichoptera, Chironomidae and d18O of carbonates: a distinct warming is recorded around 12' 600 BP and around 10' 000 BP. The Younger Dryas biozone (10'700-10'000 BP) was the only cooling found in the Late-Glacial. The Betula depression often correlated wi th the Older Dryas biozone was possibl not colder but dryer than the previous period. During the Holocene the lowland site is not very sensitive to the minor climatic changes. Table 22 summarizes climatic and trophic changes before 8'000 BP as deduced from various biostratigraphies studied by a number of authors. Ostracods, Chironomids and fossil pigments indicate that anoxic conditions prevailed during the BoIling (possibly meromixis). Changes in the lake level are illustrated in Figure 74. A first lake-level lowering occurred in the early Holocene (10'000 to 9'000 BP), a second during the Atlantic (about 6'800 to 5'200 BP). The first "shrinking" of the lake volume resulted in a eutrophication recorded by laminations in the profundal and by pigments of Cyanophyceae. The second fall in water level corresponds to an increase of Nymphaeaceae. Human impact can be inferred in three ways: eutrophication of the lake (since the Neolithic), changes of terrestrial vegetation by deforestations (cyclicity of Fagus, see Figures 78 to 80), and enhanced erosion (increasing sedimentation rates by inwashed clay, particularly since the Roman Colonization, see Figures 49 and 81). Summary: This paper was planned as the final report on Lobsigensee. However, a number of issues are not answered but can only be asked more precisely, for example: (1) For the two periods with the highest rates of change, Le. the Bolling and the Preboreal biozones, pollen influx may reflect vegetation dynamics. Detailed investigations of these periods in annually laminated sediments are planned. (2) Biostratigraphies other than palynostratigraphy are needed to estimate the degree of linkage or independence in the development of terrestrial and lacustrine ecosystems. Often our sampling intervals were not identical, thus influencing our temporal resolution. (3) 6180- and 14C-stratigraPhies with high resolution will elucidate the leads and lags of these dynamic periods. Plateaux of constant age in the age-depth relationship have a strong bearing on both biological and geophysical understanding of Late-Glacial and early Holocene developments. (4) Numerical methods applied to the pollen diagrams of the cross section will help to quantify the significance of similari ties and dissimilarities across a single basin (with Prof. Birks). (5) Numerical methods applied to different sites on the Swiss Plateau and on the transect across the Alps will be helpful in evaluating the influence of different environmental factors (with Prof. Birks). (6) A new map 1: 1000 with 50cm-contour lines prov ided by Prof. Zurbuchen will be combined with a grid of cores sampling the transition from lake marl to peat enabling us to calculate paleo-volumes of the lake. This is interesting for the two "shrinking periods" (in Fig. 74A numbers 2-6 and 7-10), both accompanied by eutrophication. The pal eo-volume during the Neoli thic set tlement of the Cortaillod culture linked wi th an est l.mate of trophic change derived from diatoms (Prof. Smol in prep.) could possibly give an indication of the size of the human population of this period. (7) For the period with the antagonism between Fagus peaks and ABC-peaks close collaboration between palynologists, geochemists and archeologists should enable us to determine the influence of prehistoric and historic people on vegetation (collaboration with Prof. Stockli and Prof. Herzig). (8) The core LL-75 taken with a "cold letter box" will be analysed for major and trace elements by Dr. Sturm for 210pb and 137Cs by Prof.von Gunten and for pollen. We will see if our local PAZ L30 really corresponds to the surface sediment and if the small seepage lake reflects modern pollution.

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.

Lithology, age determination and pollen records of five profiles for nothern Bavaria, Germany

Palynological investigations in northeastern Bavaria (Bavarian Vogtland, Fichtelgebirge, Steinwald) reveal the Late Glacial and Postglacial history of the regional vegetation. Radiocarbon data in comparison with those from the neighbouring regions (Rhön, Oberpfälzer Wald, Bavarian Forests) show a time lag in the development of the arboreal vegetation due to migration processes. The Fichtelgebirge is the southernmost part ofnortheastern Bavaria where the early Alleröd period (pollen zone IIa) is characterised by a dominance of birch forests. Hazel reached maximal values around 8000 BP in the area from the Fichtelgebirge to the Bavarian Forests, e.g. about 600 years earlier than in the more northern Rhön mountains. For spruce there is a considerable time lag between the Bavarian Forests and the Fichtelgebirge. Spruce spreading started in the Fichtelgebirge during the older part of the Atlantic period (pollen zone VI). At the same time, spruce already was the dominant tree in the Bavarian Forests. During the younger part of the Atlantic period (pollen zone VII) spruce and mixed oak forest tree species frequently occurred in the Fichtelgebirge. At the end of pollen zone VI, spruce came to dominance. At the same time, the immigration of beech started. During the Subboreal period (pollen zone VIII), spruce remained being a dominant member in the forests and at the end of pollen zone VIII, fir began to spread rapidly. During the first part of the Subatlantic period (pollen zone IX) spruce, beech, fir and pine formed the mountainous forests in the Fichtelgebirge. In the area of the Bavarian Vogtland, however, fir was a dominant forest tree during pollen zone IX, while spruce and beech played a less important role. During the 12th century, human colonisation started in the area of the Fichtelgebirge. This is 400 years later as in the area of the Rhön mountains. Indicators for earlier forest clearances are rare or absent.

Lithology and palynology of profiles from three low mountain ranges in northern Germany

Im Fichtelgebirge, im Harz und in der Rhön wurden die spätglazialen und frühpostglazialen Ablagerungen von vier Mooren in 625-805 m Meereshöhe pollenanalytisch hinsichtlich von Makrofossilien (Samen, Früchte) und stratigraphisch untersucht. 1. Nur im Fichtelgebirge konnte in 625 m Höhe ein vollständiger Spätglazialablauf aufgedeckt werden. Es handelt sich dabei um einen ehemaligen kleinen See südlich Fichtelberg, der wahrscheinlich durch Tieftauen eines begrabenen Firn- oder Schneefeldes entstand. Betula pubescens wurde kontinuierlich vom Ende der Älteren Tundrenzeit bis zum Boreal nachgewiesen. Auf nahe Vorkommen von Kiefern darf man seit IIb (Jüngere Allerödzeit) schließen, sie wurden aber durch die Jüngere Tundrenzeit, während der es noch zu Solifluktionserscheinungen kam, von ihren höher gelegenen Standorten wieder verdrängt. Die allerödzeitlichen Birken- bzw. Birkenkiefernwälder müssen in diesen Höhen noch licht oder parkartig gewesen sein. Verbreitet waren Rasengesellschaften, die hauptsächlich aus Gramineen und Artemisia bestanden. Auch Beutla nana und Pollen von Ephedra cf. distachya wurden nachgewiesen. In der Seelohe (770-780 m) ist nur der Ausklang einer waldarmen Zeit, offensichtlich der Jüngeren Tundrenzeit, erfaßt. Großreste von Bäumen fehlen. 2. Im Oberharz (Radauer Born, 800 m) wurde nur ein kurzes Stück der Jüngeren Tundrenzeit aufgedeckt. Großreste von Bäumen fehlen hier ebenfalls. Aus dem Praeboreal stammt der erst fossile Nachweis von Betuala nana im Oberharz. Die Zwergbirke wächst auf dem Moor noch heute und gilt hier als Eiszeitrelikt. 3. Eine Datierung der spätglazialen Ablagerungen vom Roten Moor in der Rhön ist zur Zeit nur mit Vorbehalt möglich. Zwar wurde hier der Laacher Bimstuff gefunden, er ist jedoch umgelagert und unmittelbar über dem Tuffhorizont befindet sich eine Schichtlücke. Wahrscheinlich zeigt die Bimsstuffschicht aber doch noch den Allerödhorizont an. 4. Während der Jüngeren Tundrenzeit dürfte im Fichtelgebirge die Waldgrenze bei etwas 600 m gelegen haben. Das bedeutet gegenüber der heutigen Waldgrenze eine Erniedrigung um rund 700 m. Am Schluß der Älteren Tundrenzeit lag die Waldgrenze wahrscheinlich wie in der Allerödzeit höher als 600-650 m, aber unter 800 m. 5. Pollenkörner der Ericalen sind in den Ablagerungen aus dem Harz wesentlich häufiger als in den anderene Gebieten. Häufungen von Ericalen-pollen sind besonders für Spätglazialablagerungen solcher Gebiete charakteristisch, die heute im subozeanischen oder ozeanischen Klimabereich liegen (Niederlande, Irland). 6. Während sich die Bodengegensätze in der heutigen Vegetation der drei Untersuchungsgebiete sehr deutlich bemerkbar machen, wurden keine nennenswerten Unterschiede im spätglazialen Pollenniederschlag der drei Mittelgebirge gefunden. Vermutlich erfolgte die Auswaschung der Nährstoffe aus den an sich nährstoffkräftigen Granitverwitterungsböden während der Späteiszeit nicht so rasch, wie es heute der Fall ist. Die Niederschlagsmengen dürften geringer und das Klima weniger humid gewesen sein. 7. In der Liste der spätglazialen Pflanzen überwiegen die Arten mit borealzirkumpolarer Verbreitung. Arktisch-alpine Arten treten zurück. Kontinentale und subatlantische bzw. subozeanische Arten sind etwa gleich stark vertreten.

Pollen records of profile Krumbach from southern Germany

Some years ago a fossil lake basin was found in the northeastern part of the former Rhine-pied- mont-glacier, situated between the endmoraine system ofthe elassical Riß- andWürm glacia- tions, respectively. The lacustrine sediments contain the pollenflora ofthe Eemian interglacial. They are intensively thrusted. These sediments are eovered by a loam-layer, rieh in elasts. The thickness of this loam-layer varies between at least 170 and 400 cm. It consists in its major part of loess-loam and solifluction material. Yet just on top of the lake sediments mentioned an in- tensively compressed loam, characterized by quarzgrains with all features of glacially pressed material, together with striated elasts is met with. It strongly resembles atil!. Ifthis is true, the stratigraphie division ofthe last glaciation strongly deviates from the hitherto accepted scheme, incorporating an early glacier advance, long before the elassical young-endmoraine systems of the Würm glaciation were formed.

Radiolarians of the Celebes Sea

Two sites were drilled in the Celebes Sea as part of Ocean Drilling Program Leg 124; Site 767 and Site 770. Radiolarians are preserved in Paleogene pelagic claystones with minor occurrences in certain Neogene successions. The brown clays that immediately overlie basalt at both sites contain radiolarians of the late middle Eocene Podocyrtis chalara Zone. Late Eocene radiolarians are not found, due to dissolution and probable hiatus. The Oligocene is represented by the Theocyrtis tuberosa and Dorcadospyris ateuchus Zones. Oligocene sediments are strongly dominated by abundant and diverse radiolarians of the TristylospyrislDorcadospyris lineage. Preservation of Paleogene radiolarian assemblages ranges from good to very poor. Late Miocene radiolarians of the Didymocyrtis antepenultima Zone are found only in Site 770. Other Neogene sediments are barren of radiolarian remains, with the exception of latest Pleistocene and Holocene sediments.

Pollen record and dating of a sediment profile from Lake Voulkaria, Greece

A palynological investigation of a Holocene profile from Lake Voulkaria, western Greece, was carried out as a contribution to the environmental history of the coastal area of northwestern Acarnania and the Classical city of Palairos. It shows that deciduous oaks dominated the natural vegetation of the area throughout the Holocene. Until ca. 7000 B.C. Pistacia occurred abundantly, while other evergreen woody taxa were rare. At ca. 6300 B.C. an expansion of Carpinus orientalis/Ostrya can be observed. Around ca. 5300 B.C. spreading of Erica indicates a change to a drier climate and/or first human impact. Since ca. 3500 B.C. an increase of evergreen shrubs now clearly indicates land-use. The foundation of the Classical city of Palairos led to a temporary expansion of Phillyrea maquis. Within this period, molluscs of brackish water indicate the use of the lake as a harbour after the construction of a connection to the sea. The deciduous Quercus woodland recovered when human impact decreased in the area, and lasted until modern times.