Pollen record of sediment core MD95-2043
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PANGAEA
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| Autores principales: | , |
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| Formato: | Dataset Open Access |
| Lenguaje: | en |
| Publicado: |
PANGAEA
2008
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| _version_ | 1867169956290887680 |
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| author | Fletcher, William J Sanchez Goñi, Maria Fernanda |
| author_facet | Fletcher, William J Sanchez Goñi, Maria Fernanda |
| collection | Datos científicos de ciencias marinas y ambientales |
| contents | High-resolution pollen analysis of Alborán Sea core MD95-2043 provides a 48-ka continuous vegetation record that can be directly correlated with sea surface and deep-water changes. The reliability of this record is supported by comparison with that of Padul (Sierra Nevada, Spain). Marine Isotope Stage (MIS) 3 was characterised by fluctuations in Quercus forest cover in response to Dansgaard-Oeschger climate variability. MIS 2 was characterised by the dominance of semi-desert vegetation. Despite overall dry and cold conditions during MIS 2, Heinrich events (HEs) 2 and 1 were distinguished from the last glacial maximum by more intensely arid conditions. Taxon-specific vegetation responses to a tripartite climatic structure within the HEs are observed. In MIS 1, the Bölling-Allerød was marked by rapid afforestation, while a re-expansion of semi-desert environments occurred during the Younger Dryas. The maximum development of mixed Quercus forest occurred between 11.7 and 5.4 cal ka BP, with forest decline since 5.4 cal ka BP. On orbital timescales, a long-term expansion of semi-desert vegetation from MIS 3 into MIS 2 reflects global ice-volume trends, while Holocene arboreal decline reflects summer insolation decrease. The influence of precession on the amplitude of forest development and vegetation composition is also detected. |
| format | Dataset Open Access |
| id | pangaea_https___doi_org_10_1594_PANGAEA_711649 |
| institution | PANGAEA |
| language | en |
| publishDate | 2008 |
| publisher | PANGAEA |
| record_format | pangaea |
| spellingShingle | Pollen record of sediment core MD95-2043 Fletcher, William J Sanchez Goñi, Maria Fernanda Abies; Acer; AGE; Alboran Sea; Alisma-type; Alnus; Ambrosia-type; Anogramma leptophylla; Anthemis-type; Apiaceae; Arceuthobium; Artemisia; Asphodelus; Aster-type; Betula; Boraginaceae; Botrychium-type; Brassicaceae; Bupleurum-type; Buxus; Calluna; CALYPSO; Calypso Corer; Campanulaceae; Carpinus; Caryophyllaceae; Cedrus; Centaurea nigra-type; Centaurea scabiosa-type; Centaurium; Cerealia-type; Chenopodiaceae; Cirsium-type; Cistus; Concentricystes; Coriaria myrtifolia; Corylus; Counting, palynology; Crassulaceae; Cryptogramma; Cupressaceae; Cyperaceae; DEPTH, sediment/rock; Echinops; Ephedra distachya-type; Ephedra fragilis-type; Ericaceae; Erodium; Euphorbia; Fabaceae; Filipendula; Fraxinus excelsior-type; Galium-type; Gentianaceae; Geranium; Halimium; Hedera helix; Helianthemum; Hippophae; IMAGES; IMAGES I; Indeterminable: broken; Indeterminable: corroded; Indeterminable: crumpled; Indeterminable: hidden; Indeterminable: unknown; International Marine Global Change Study; Isoetes; Lamiaceae; Lemna; Liliaceae; Linum; Lygeum spartum; Lythrum; Marion Dufresne (1995); Marker, added; Marker, found; MD101__Campaign; MD952043; MD95-2043; Mentha-type; Mercurialis-type; Myrica; Olea; Ophioglossum lusitanicum; Pedicularis; Phillyrea; Picea; Pilularia globulifera; Pinus; Pistacia; Plantago; Plantago lanceolata-type; Plumbaginaceae; Poaceae; Pollen, main; Pollen, main concentration; Pollen, temperate Mediterranean forest; Pollen, total; Pollen and spores; Polygonum aviculare-type; Polygonum persicaria-type; Polypodium vulgare-type; Populus; Potamogeton; Primulaceae; Quercus, deciduous-type; Quercus evergreen-type; Quercus suber-type; Ranunculaceae; Rhamnus-type; Rosaceae; Rumex; Salix; Sample volume; Sanguisorba minor; Sanguisorba officinalis; Scabiosa; Scrophulariaceae; Selaginella denticulata; Serratula-type; Spergularia-type; Spores, monolete ornamented; Spores, monolete psilate; Spores, trilete ornamented; Spores, trilete psilate; Spores, trilete reworked; Tamarix; Taraxacum; Taxa analyzed; Taxus; Thalictrum; Tilia; Typha; Ulex-type; Ulmus; Urtica; Valerianaceae; Veronica-type; Vicia-type; Vitis High-resolution pollen analysis of Alborán Sea core MD95-2043 provides a 48-ka continuous vegetation record that can be directly correlated with sea surface and deep-water changes. The reliability of this record is supported by comparison with that of Padul (Sierra Nevada, Spain). Marine Isotope Stage (MIS) 3 was characterised by fluctuations in Quercus forest cover in response to Dansgaard-Oeschger climate variability. MIS 2 was characterised by the dominance of semi-desert vegetation. Despite overall dry and cold conditions during MIS 2, Heinrich events (HEs) 2 and 1 were distinguished from the last glacial maximum by more intensely arid conditions. Taxon-specific vegetation responses to a tripartite climatic structure within the HEs are observed. In MIS 1, the Bölling-Allerød was marked by rapid afforestation, while a re-expansion of semi-desert environments occurred during the Younger Dryas. The maximum development of mixed Quercus forest occurred between 11.7 and 5.4 cal ka BP, with forest decline since 5.4 cal ka BP. On orbital timescales, a long-term expansion of semi-desert vegetation from MIS 3 into MIS 2 reflects global ice-volume trends, while Holocene arboreal decline reflects summer insolation decrease. The influence of precession on the amplitude of forest development and vegetation composition is also detected. |
| title | Pollen record of sediment core MD95-2043 |
| topic | Abies; Acer; AGE; Alboran Sea; Alisma-type; Alnus; Ambrosia-type; Anogramma leptophylla; Anthemis-type; Apiaceae; Arceuthobium; Artemisia; Asphodelus; Aster-type; Betula; Boraginaceae; Botrychium-type; Brassicaceae; Bupleurum-type; Buxus; Calluna; CALYPSO; Calypso Corer; Campanulaceae; Carpinus; Caryophyllaceae; Cedrus; Centaurea nigra-type; Centaurea scabiosa-type; Centaurium; Cerealia-type; Chenopodiaceae; Cirsium-type; Cistus; Concentricystes; Coriaria myrtifolia; Corylus; Counting, palynology; Crassulaceae; Cryptogramma; Cupressaceae; Cyperaceae; DEPTH, sediment/rock; Echinops; Ephedra distachya-type; Ephedra fragilis-type; Ericaceae; Erodium; Euphorbia; Fabaceae; Filipendula; Fraxinus excelsior-type; Galium-type; Gentianaceae; Geranium; Halimium; Hedera helix; Helianthemum; Hippophae; IMAGES; IMAGES I; Indeterminable: broken; Indeterminable: corroded; Indeterminable: crumpled; Indeterminable: hidden; Indeterminable: unknown; International Marine Global Change Study; Isoetes; Lamiaceae; Lemna; Liliaceae; Linum; Lygeum spartum; Lythrum; Marion Dufresne (1995); Marker, added; Marker, found; MD101__Campaign; MD952043; MD95-2043; Mentha-type; Mercurialis-type; Myrica; Olea; Ophioglossum lusitanicum; Pedicularis; Phillyrea; Picea; Pilularia globulifera; Pinus; Pistacia; Plantago; Plantago lanceolata-type; Plumbaginaceae; Poaceae; Pollen, main; Pollen, main concentration; Pollen, temperate Mediterranean forest; Pollen, total; Pollen and spores; Polygonum aviculare-type; Polygonum persicaria-type; Polypodium vulgare-type; Populus; Potamogeton; Primulaceae; Quercus, deciduous-type; Quercus evergreen-type; Quercus suber-type; Ranunculaceae; Rhamnus-type; Rosaceae; Rumex; Salix; Sample volume; Sanguisorba minor; Sanguisorba officinalis; Scabiosa; Scrophulariaceae; Selaginella denticulata; Serratula-type; Spergularia-type; Spores, monolete ornamented; Spores, monolete psilate; Spores, trilete ornamented; Spores, trilete psilate; Spores, trilete reworked; Tamarix; Taraxacum; Taxa analyzed; Taxus; Thalictrum; Tilia; Typha; Ulex-type; Ulmus; Urtica; Valerianaceae; Veronica-type; Vicia-type; Vitis |
| url | https://doi.org/10.1594/PANGAEA.711649 |