Mark A. J. Curran

Spatial distribution of dimethylsulfide and dimethylsulfoniopropionate in the Australasian sector of the Southern Ocean

During 1991–1995, seven voyages were made to the Southern Ocean to determine the distribution of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) in seawater and air in the Australasian sector (60°E to 165°E). Measurements of DMSP in sea ice were also made. During the summer months the Subtropical Convergence (STC) and Antarctic Convergence (AC) were identified as important source regions of these sulfur compounds. In the Seasonal Ice zone (SIZ) there were marked longitudinal differences possibly reflecting higher productivity and the extent of the sea ice in this region. Levels of DMSP in sea ice cores were consistent with this regional difference. High and variable concentrations of DMSP also occurred in the Subantarctic Zone (SAZ) (45°-53°S), decreasing to lower levels around 64°S, close to the Antarctic Divergence (AD). Upwelling of deep water around the AD is suggested to have been responsible for the low biological activity and low DMSP levels. While there was generally a good relationship between DMSPp and biomass, there was a marked difference in the DMSPp:chlorophyll a ratio between regions, and between years. DMSP was generally negatively correlated with dissolved nitrate, however, it was unclear if the level of nitrate directly affected DMSP production. DMSw levels were highest in the mixed layer, with lower, yet detectable, levels in the deeper ocean. DMSw was occasionally elevated in Antarctic Bottom Water (AABW), suggesting that ice shelf water transports this substance to deeper waters. DMSP was not found above detection limits below the mixed layer, but some evidence was found that DMSP may be transported to deeper waters, close to the Antarctic continent.

Dimethyl sulfide in the Southern Ocean: Seasonality and flux

The first flux estimate of dimethyl sulfide (DMS) from the Australian sector of the Southern Ocean (63°E to 162°E) has been calculated from seven voyages, which span spring and summer seasons from 1991 to 1995. Increases in seawater DMS and its precursor, dimethyl sulfoniopropionate (DMSP) generally occurred in Southern Ocean surface waters during the transition from spring to summer. DMS flux from the Subantarctic Zone (SAZ), Antarctic Zone (AZ), and Seasonal Ice Zone (SIZ) ranged from 1.7 to 49 μmol/m2/d with a mean value of 9.4 μmol/m2d. These flux calculations are believed to be underestimates, and do not include potential contributions from sea ice. Very high levels of DMSP in sea ice suggest that the SIZ may be a source of DMS to the atmosphere. The different types of vertical DMSP profiles found in sea ice possibly reflect the type of algal assemblage present and the age of the sea ice. Without considering contributions of DMS from sea ice, the overall Southern Ocean DMS emission estimate from this work was 139 Gmol S/yr. The emission estimate for the Antarctic region alone (AZ and SIZ) was 85 Gmol S/yr. This represents 17% of the global emission estimate, from 6% of the ocean surface area. This emission estimate is almost double that of an earlier estimate by Berresheim [1987] of 48 Gmol S/yr, and is likely to be higher when the amount released from the sea ice surrounding Antarctica is more accurately characterized.

The Carrington event not observed in most ice core nitrate records

The Carrington Event of 1859 is considered to be among the largest space weather events of the last 150 years. We show that only one out of 14 well-resolved ice core records from Greenland and Antarctica has a nitrate spike dated to 1859. No sharp spikes are observed in the Antarctic cores studied here. In Greenland numerous spikes are observed in the 40 years surrounding 1859, but where other chemistry was measured, all large spikes have the unequivocal signal, including co-located spikes in ammonium, formate, black carbon and vanillic acid, of biomass burning plumes. It seems certain that most spikes in an earlier core, including that claimed for 1859, are also due to biomass burning plumes, and not to solar energetic particle (SEP) events. We conclude that an event as large as the Carrington Event did not leave an observable, widespread imprint in nitrate in polar ice. Nitrate spikes cannot be used to derive the statistics of SEPs.

High-precision dating of volcanic events (A.D. 1301–1995) using ice cores from Law Dome, Antarctica

A record of volcanic activity over the period A.D. 1301–1995 has been extracted from three Law Dome ice cores (East Antarctica). The record dating is unambiguous at the annual level from A.D. 1807 to 1995 and has an uncertainty of ±1 year at A.D. 1301. Signals from 20 eruptions are preserved in the record, including those of two unknown eruptions with acid deposition beginning in A.D. 1810.8 and A.D. 1685.8. The beginning of the ice core signal from the A.D. 1815 Tambora eruption is observed in the austral summer of A.D. 1816/1817. The mean observed stratospheric transport and deposition time to Law Dome from the eruption site is 1.5 years (σ = 0.6 years) from 11 well-dated eruptions. The largest eruption observed in the Law Dome record has its maximum in A.D. 1460 with volcanic sulfate deposition beginning in the austral winter of A.D. 1459. This event is also observed in other ice core records and is attributed to the volcano Kuwae, with an eruption date in the range A.D. 1455.9–1459.9 if all sources of error are considered. This is at least three years later than the date previously ascribed by dendrochronological and historical studies.

Deglacial and Holocene changes in accumulation at Law Dome, East Antarctica

Abstract Dating constraints have been combined with an ice-flow model to estimate surface accumulation rates at Law Dome, East Antarctica, to approximately 80 kyr BP. Results indicate that the present high-accumulation regime (~0.7ma–1 ice equivalent) was established some time after ~7 kyr BP, following an increase of approximately 80% from early to mid-Holocene. The accumulation rate at the Last Glacial Maximum is estimated at less than ~10% of the modern value. The record reveals an approximately linear dependence between temperature (inferred from isotope ratio) and accumulation rate through the glacial period. This dependence breaks down in the early Holocene, and this is interpreted as a change to a mode in which moisture-transport changes have a stronger influence on accumulation than temperature (via absolute humidity). The changes in accumulation, including the large change in the early to mid-Holocene, are accompanied by changes in sea-salt concentrations which support the hypothesis that Law Dome climate has shifted from a glacial climate, more like that of the present-day Antarctic Plateau, to its current Antarctic maritime climate. The change between these two modes occurred progressively through the early Holocene, possibly reflecting insolation-driven changes in atmospheric moisture content and circulation.

Influence of different water masses and biological activity on dimethylsulphide and dimethylsulphoniopropionate in the subantarctic zone of the Southern Ocean during ACE 1

Measurements of salinity, temperature, phytoplankton biomass and speciation, dissolved nitrate, dimethylsulfide (DMS) in seawater and air, and dimethylsulfoniopropionate (DMSP), were made in the subantarctic zone of the Southern Ocean from 40°-54°S, and 140°-153°E during the southern hemisphere marine First Aerosol Characterization Experiment (ACE 1). DMSP concentrations were highest in subtropical convergence zone (STCZ) waters, intermediate in subantarctic waters, and lowest in polar waters. DMSP appeared to decrease at frontal regions between these major water masses. In subantarctic waters, high levels of DMSP were generally associated with an increase in dinoflagellate biomass and low microzooplankton grazing rates. Lower DMSP concentrations occurred in polar waters when the diatom biomass and grazing rates were high. DMS levels measured on Southern Surveyor ranged from not detectable (nd) to 5.6 nM (mean 1.7 nM), with below average levels in subantarctic waters (mean 1.25 nM), and above average levels (mean = 1.93 nM) in polar waters. Pulses of DMS occurred as Southern Surveyor traveled south into polar waters, with a large pulse (mean = 2.3 nM) highlighted as the vessel traveled back into subantarctic waters (46°-47°S, 148°-151°E) in early December. By using the dissolved DMSP (DMSPd) to DMS ratio as an index of the bacterial conversion of DMSPd to DMS some evidence was found that, in polar waters, increased microzooplankton (MZP) grazing in diatom dominated waters, may lead to above average concentrations of DMS. This does not appear to be the case when the biomass was dominated by dinoflagellates in subantarctic waters.

A Millennial Proxy Record of ENSO and Eastern Australian Rainfall from the Law Dome Ice Core, East Antarctica

ENSO causes climate extremes across and beyond the Pacific basin; however, evidence of ENSO at high southern latitudes is generally restricted to the South Pacific and West Antarctica. Here, the authors report astatisticallysignificantlinkbetweenENSOandseasaltdepositionduringsummerfromtheLawDome(LD) ice core in East Antarctica. ENSO-related atmospheric anomaliesfrom the central-western equatorialPacific (CWEP) propagate to the South Pacific and the circumpolar high latitudes. These anomalies modulate high- latitude zonal winds, with El Nino (La Nina) conditions causing reduced (enhanced) zonal wind speeds and subsequent reduced (enhanced) summer sea salt deposition at LD. Over the last 1010 yr, the LD summer sea salt(LDSSS)recordhasexhibitedtwobelow-average(ElNino-like)epochs,1000-1260 ADand1920-2009 AD, and a longer above-average (La Nina-like) epoch from 1260 to 1860 AD. Spectral analysis shows the below- average epochs are associated with enhanced ENSO-like variability around 2-5 yr, while the above-average epoch is associated more with variability around 6-7 yr. The LDSSS record is also significantly correlated with annual rainfall in eastern mainland Australia. While the correlation displays decadal-scale variability similar to changes in the interdecadal Pacific oscillation (IPO), the LDSSS record suggests rainfall in the modern instrumental era (1910-2009 AD) is below the long-term average. In addition, recent rainfall declines in some regions of eastern and southeastern Australia appear to be mirrored by a downward trend in the LDSSS record, suggesting current rainfall regimes are unusual though not unknown over the last millennium.

Antarctic-wide array of high-resolution ice core records reveals pervasive lead pollution began in 1889 and persists today

Interior Antarctica is among the most remote places on Earth and was thought to be beyond the reach of human impacts when Amundsen and Scott raced to the South Pole in 1911. Here we show detailed measurements from an extensive array of 16 ice cores quantifying substantial toxic heavy metal lead pollution at South Pole and throughout Antarctica by 1889 – beating polar explorers by more than 22 years. Unlike the Arctic where lead pollution peaked in the 1970s, lead pollution in Antarctica was as high in the early 20th century as at any time since industrialization. The similar timing and magnitude of changes in lead deposition across Antarctica, as well as the characteristic isotopic signature of Broken Hill lead found throughout the continent, suggest that this single emission source in southern Australia was responsible for the introduction of lead pollution into Antarctica at the end of the 19th century and remains a significant source today. An estimated 660 t of industrial lead have been deposited over Antarctica during the past 130 years as a result of mid-latitude industrial emissions, with regional-to-global scale circulation likely modulating aerosol concentrations. Despite abatement efforts, significant lead pollution in Antarctica persists into the 21st century.

A 700 year record of Southern Hemisphere extratropical climate variability

Abstract Annually dated ice cores from West and East Antarctica provide proxies for past changes in atmospheric circulation over Antarctica and portions of the Southern Ocean, temperature in coastal West and East Antarctica, and the frequency of South Polar penetration of El Niño events. During the period AD 1700–1850, atmospheric circulation over the Antarctic and at least portions of the Southern Hemisphere underwent a mode switch departing from the out-of-phase alternation of multi-decadal long phases of EOF1 and EOF2 modes of the 850 hPa field over the Southern Hemisphere (as defined in the recent record by Thompson and Wallace, 2000; Thompson and Solomon, 2002) that characterizes the remainder of the 700 year long record. From AD 1700 to 1850, lower-tropospheric circulation was replaced by in-phase behavior of the Amundsen Sea Low component of EOF2 and the East Antarctic High component of EOF1. During the first phase of the mode switch, both West and East Antarctic temperatures declined, potentially in response to the increased extent of sea ice surrounding both regions. At the end of the mode switch, West Antarctic coastal temperatures rose and East Antarctic coastal temperatures fell, respectively, to their second highest and lowest of the record. Polar penetration of El Niño events increased during the mode switch. The onset of the AD 1700–1850 mode switch coincides with the extreme state of the Maunder Minimum in solar variability. Late 20th-century West Antarctic coastal temperatures are the highest in the record period, and East Antarctic coastal temperatures close to the lowest. Since AD 1700, extratropical regions of the Southern Hemisphere have experienced significant climate variability coincident with changes in both solar variability and greenhouse gases.

Suppressed ion chromatography methods for the routine determination of ultra low level anions and cations in ice cores

The concentration of trace ionic species in snow and ice samples was determined using suppressed ion chromatography (IC) with conductivity detection and ultra-clean sample preparation techniques. Trace anion species were determined in a single 24-min run by combining sample preconcentration with gradient elution using Na2B4O7 eluent. The detection limits (ranging from 0.001 to 0.006 microM) are the lowest reported in the literature. Cation species were analysed by direct injection of 0.25 ml and isocratic elution with a H2SO4 eluent. The clean preparation techniques showed no evidence of a difference (Students t-test) between Milli-Q water samples analysed directly and processed Milli-Q ice samples. These robust, ultra-clean IC methods were routinely applied to the analysis of large number of samples to produce a high-resolution trace ion ice core record from Law Dome, East Antarctica.