When were the straits between the Baltic Sea and the Kattegat inundated by the sea during the Holocene?

Boreas ◽  
2021 ◽  
Author(s):  
Ole Bennike ◽  
Jørn Bo Jensen ◽  
Niels Nørgaard‐Pedersen ◽  
Katrine Juul Andresen ◽  
Marit‐Solveig Seidenkrantz ◽  
...  
2014 ◽  
Vol 35 (4) ◽  
pp. 413-424 ◽  
Author(s):  
Carolin Kindler ◽  
Carolin Kindler ◽  
Henrik Bringsøe ◽  
Carolin Kindler ◽  
Henrik Bringsøe ◽  
...  

We show that Fennoscandia was invaded in the Holocene by three distinct mitochondrial lineages of Natrix natrix. Two of these lineages arrived from the south, and one from the east. One of the ‘southern lineages’ is confined to Gotland, where also the second ‘southern lineage’ is found. The latter is widely distributed in the southwestern Baltic region, western Fennoscandia and on the Åland Islands, while the other lineage present on Gotland is only known from a few sites in the Baltic region. In addition, we recorded a third mitochondrial lineage in southern continental Finland, which was previously unknown from Fennoscandia. This lineage also occurs in the southeastern Baltic region and further east, suggesting that southern Finland was colonized from the east. Thus, the phylogeography of N. natrix matches a general paradigm for Fennoscandia, with Holocene invasions from the south and east.


Author(s):  
Jan Harff ◽  
Hauke Jöns ◽  
Alar Rosentau

The correlation of climate variability; the change environment, in particular the change of coastlines; and the development of human societies during the last millennia can be studied exemplarily in the Baltic area. The retreat of the Scandinavian ice-sheet vertical crustal movement (glacio-isostatic adjustment), together with climatically controlled sea-level rise and a continuously warming atmosphere, determine a dramatic competition between different forcings of the environment that advancing humans are occupying step by step after the glaciation. These spatially and temporally changing life conditions require a stepwise adjustment of survival strategies. Changes in the natural environment can be reconstructed from sedimentary, biological proxy data and archaeological information. According to these reconstructions, the main shift in the Baltic area’s environment happened about 8,500 years before present (BP) when the Baltic Sea became permanently connected to the Atlantic Ocean via the Danish straits and the Sound, and changed the environment from lacustrine to brackish-marine conditions. Human reaction to environmental changes in prehistoric times is mainly reconstructed from remains of ancient settlements—onshore in the uplifting North and underwater in the South dominated by sea-level rise. According to the available data, the human response to environmental change was mainly passive before the successful establishment of agriculture. But it became increasingly active after people settled down and the socioeconomic system changed from hunter-gatherer to farming communities. This change, mainly triggered by the climatic change from the Holocene cool phase to the warming period, is clearly visible in Baltic basin sediment cores as a regime shift 6,000 years (BP). But the archaeological findings prove that the relatively abrupt environmental shift is reflected in the socioeconomic system by a period of transition when hunter-gatherer and farming societies lived in parallel for several centuries. After the Holocene warming, the permanent regression in the Northern Baltic Sea and the transgression in the South did affect the socioeconomic response of the Baltic coastal societies, who migrated downslope at the regressive coast and upslope at the transgressive coast. The following cooling phases, in particular the Late Antique Little Ice Age (LALIA) and the Little Ice Age (LIA), are directly connected with migration and severe changes of the socioeconomic system. After millennia of passive reaction to climate and environmental changes, the Industrial Revolution finally enabled humans to influence and protect actively the environment, and in particular the Baltic Sea shore, by coastal constructions. On the other hand, this ability also affected climate and environment negatively because of the disturbance of the natural balance between climate, geosystem, and ecosystem.


2018 ◽  
Vol 65 (2) ◽  
pp. 109-122
Author(s):  
Ekaterina N. Badyukova ◽  
Leonid A. Zindarev ◽  
Svetlana A. Lukyanova ◽  
Galina D. Solovieva

AbstractThis article addresses the southern sector of the Curonian Spit, the largest coastal barrier of the Baltic Sea. A comparative analysis of the deposits that make up parts of the Curonian and Vistula Spits is given. The detailed analysis of the geological and geomorphological structure of the southern part of the Curonian Spit suggests that, within this sector, it is not a sedimentary barrier created by wave action and Aeolian processes in the Holocene, but a part of a pre-Holocene fluvioglacial plain. Field work has shown that the ancient alluvial or fluvioglacial plain is in the lagoon shore of the Vistula Spit.


2001 ◽  
Vol 177 (3-4) ◽  
pp. 221-242 ◽  
Author(s):  
G Sohlenius ◽  
K.-C Emeis ◽  
E Andrén ◽  
T Andrén ◽  
A Kohly

2017 ◽  
Vol 14 (24) ◽  
pp. 5789-5804 ◽  
Author(s):  
Martina Sollai ◽  
Ellen C. Hopmans ◽  
Nicole J. Bale ◽  
Anchelique Mets ◽  
Lisa Warden ◽  
...  

Abstract. Heterocyst glycolipids (HGs) are lipids exclusively produced by heterocystous dinitrogen-fixing cyanobacteria. The Baltic Sea is an ideal environment to study the distribution of HGs and test their potential as biomarkers because of its recurring summer phytoplankton blooms, dominated by a few heterocystous cyanobacterial species of the genera Nodularia and Aphanizomenon. A multi-core and a gravity core from the Gotland Basin were analyzed to determine the abundance and distribution of a suite of selected HGs at a high resolution to investigate the changes in past cyanobacterial communities during the Holocene. The HG distribution of the sediments deposited during the Modern Warm Period (MoWP) was compared with those of cultivated heterocystous cyanobacteria, including those isolated from Baltic Sea waters, revealing high similarity. However, the abundance of HGs dropped substantially with depth, and this may be caused by either a decrease in the occurrence of the cyanobacterial blooms or diagenesis, resulting in partial destruction of the HGs. The record also shows that the HG distribution has remained stable since the Baltic turned into a brackish semi-enclosed basin ∼ 7200 cal. yr BP. This suggests that the heterocystous cyanobacterial species composition remained relatively stable as well. During the earlier freshwater phase of the Baltic (i.e., the Ancylus Lake and Yoldia Sea phases), the distribution of the HGs varied much more than in the subsequent brackish phase, and the absolute abundance of HGs was much lower than during the brackish phase. This suggests that the cyanobacterial community adjusted to the different environmental conditions in the basin. Our results confirm the potential of HGs as a specific biomarker of heterocystous cyanobacteria in paleo-environmental studies.


2016 ◽  
Vol 102 ◽  
pp. 30-44 ◽  
Author(s):  
Lisa Warden ◽  
Marcel T.J. van der Meer ◽  
Matthias Moros ◽  
Jaap S. Sinninghe Damsté

2017 ◽  
Author(s):  
Martina Sollai ◽  
Ellen C. Hopmans ◽  
Nicole J. Bale ◽  
Anchelique Mets ◽  
Matthias Moros ◽  
...  

Abstract. Heterocyst glycolipids (HGs) are lipids exclusively produced by heterocystous dinitrogen-fixing cyanobacteria. The Baltic Sea is an ideal environment to study the distribution of HGs and test their potential as biomarkers because of its recurring summer phytoplankton blooms, dominated by a few heterocystous cyanobacterial species. A multicore and a gravity core from the Gotland basin were analyzed to determine the abundance and distribution of HGs at high resolution to investigate the changes in past cyanobacterial communities during the Holocene. The HG distribution of the sediments deposited during the Modern Warm Period (MoWP) was compared with those of cultivated heterocystous cyanobacteria, revealing high similarity. However, the abundance of HGs dropped substantially with depth and this may be caused by either a decrease of the cyanobacterial blooms or diagenesis, resulting in partial destruction of the HGs. The record also shows that the HGs distribution has remained stable since the Baltic has turned into a brackish semi-enclosed basin ~ 7200 yrs BP. This suggests that the heterocystous cyanobacterial species composition remained relatively stable as well. During the earlier freshwater phase of the Baltic (i.e. the Ancylus Lake phase) the distribution of the HGs varied much more than in the subsequent brackish phase and the absolute abundance of HGs was much lower than during the brackish phase. This suggests that the cyanobacterial community adjusted to the different environmental conditions in the basin. Our results confirm the potential of HGs as specific biomarker of heterocystous cyanobacteria in paleo-environmental studies.


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