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<p>Abstract Analysis of \&gt;100 surface sediments from across the Barents Sea has shown that the relative abundances of the mono-unsaturated sea ice diatom-derived biomarker \.IP25\ and a tri-unsaturated highly branched isoprenoid (HBI) lipid (HBI III) are characteristic of the overlying surface oceanographic conditions, most notably, the location of the seasonal sea ice edge. Thus, while \.IP25\ is generally limited to locations experiencing seasonal sea ice, with higher abundances found for locations with longer periods of ice cover, \HBI\ \.III\ is found in sediments from all sampling locations, but is significantly enhanced in sediments within the vicinity of the retreating sea ice edge or marginal ice zone (MIZ). The response of \HBI\ \.III\ to this well-defined sea ice scenario also appears to be more selective than that of the more generic phytoplankton biomarker, brassicasterol. The potential for the combined analysis of \.IP25\ and \HBI\ \.III\ to provide more detailed assessments of past sea ice conditions than \.IP25\ alone has been investigated by quantifying both biomarkers in three marine downcore records from locations with contrasting modern sea ice settings. For sediment cores from the western Barents Sea (intermittent seasonal sea ice) and the northern Norwegian Sea (ice-free), high \.IP25\ and low \HBI\ \.III\ during the Younger Dryas (ca. 12.9\textendash11.9 cal. kyr BP) is consistent with extensive sea cover, with relatively short periods of ice-free conditions resulting from late summer retreat. Towards the end of the \YD\ (ca. 11.9\textendash11.5 cal. kyr BP), a general amelioration of conditions resulted in a near winter maximum ice edge scenario for both locations, although this was somewhat variable, and the eventual transition to predominantly ice-free conditions was later for the western Barents Sea site (ca. 9.9 cal. kyr BP) compared to \NW\ Norway (ca. 11.5 cal. kyr BP). For both locations, coeval elevated \HBI\ \.III\ (but absent IP25) potentially provides further evidence for increased Atlantic Water inflow during the early Holocene, but this interpretation requires further investigation. In contrast, \.IP25\ and \HBI\ \.III\ data obtained from a core from the northern Barents Sea demonstrate that seasonal sea ice prevailed throughout the Holocene, but with a gradual shift from winter ice edge conditions during the early Holocene to more sustained ice cover in the Neoglacial; a directional shift that has undergone a reverse in the last ca. 150 yr according to observational records. Our combined surface and downcore datasets suggest that combined analysis of \.IP25\ and \HBI\ \.III\ can provide information on temporal variations in the position of the maximum (winter) Arctic sea ice extent, together with insights into sea ice seasonality by characterisation of the MIZ. Combining \.IP25\ with \HBI\ \.III\ in the form of the previously proposed \PIP25\ index yields similar outcomes to those obtained using brassicasterol as the phytoplankton marker. Importantly, however, some problems associated with use of a variable balance factor employed in the \PIP25\ calculation, are potentially alleviated using \HBI\ III.</p>

Year of Publication
2015
Journal
Earth and Planetary Science Letters
Volume
431
Number of Pages
127-139
ISSN Number
0012-821X
URL
http://www.sciencedirect.com/science/article/pii/S0012821X15005877
DOI
http://dx.doi.org/10.1016/j.epsl.2015.09.020
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