scholarly journals Using under-ice hyperspectral transmittance to determine land-fast sea-ice algal biomass in Saroma-ko Lagoon, Hokkaido, Japan

2020 ◽  
pp. 1-10
Author(s):  
Pat Wongpan ◽  
Daiki Nomura ◽  
Takenobu Toyota ◽  
Tomonori Tanikawa ◽  
Klaus M. Meiners ◽  
...  

Abstract Sea ice, which forms in polar and nonpolar areas, transmits light to ice-associated (sympagic) algal communities. To noninvasively study the distribution of sea-ice algae, empirical relations to estimate its biomass from under-ice hyperspectral irradiance have been developed in the Arctic and Antarctica but lack for nonpolar regions. This study examines relationships between normalised difference indices (NDI) calculated from hyperspectral transmittance and sympagic algal biomass in the nonpolar Saroma-ko Lagoon. We analysed physico-biogeochemical properties of snow and land-fast sea ice supporting 27 paired bio-optical measurements along three transects covering an area of over 250 m × 250 m in February 2019. Snow depth (0.08 ± 0.01 m) and ice-bottom brine volume fraction (0.21 ± 0.02) showed low (0.06) and high (0.58) correlations with sea-ice core bottom section chlorophyll a (Chl. a), respectively. Spatial analyses unveiled the patch size of sea-ice Chl. a to be ~65 m, which is in the same range reported from previous studies. A selected NDI (669, 596 nm) explained 63% of algal biomass variability. This reflects the bio-optical properties and environmental conditions of the lagoon that favour the wavelength pair in the orange/red part of the spectrum and suggests the necessity of a specific bio-optical relationship for Saroma-ko Lagoon.

Water ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 145
Author(s):  
Jian Liu ◽  
Liyang Zhan ◽  
Qingkai Wang ◽  
Man Wu ◽  
Wangwang Ye ◽  
...  

Nitrous oxide (N2O) is the third most important greenhouse gas in the atmosphere, and the ocean is an important source of N2O. As the Arctic Ocean is strongly affected by global warming, rapid ice melting can have a significant impact on the N2O pattern in the Arctic environment. To better understand this impact, N2O concentration in ice core and underlying seawater (USW) was measured during the seventh Chinese National Arctic Research Expedition (CHINARE2016). The results showed that the average N2O concentration in first-year ice (FYI) was 4.5 ± 1.0 nmol kg−1, and that in multi-year ice (MYI) was 4.8 ± 1.9 nmol kg−1. Under the influence of exchange among atmosphere-sea ice-seawater systems, brine dynamics and possible N2O generation processes at the bottom of sea ice, the FYI showed higher N2O concentrations at the bottom and surface, while lower N2O concentrations were seen inside sea ice. Due to the melting of sea ice and biogeochemical processes, USW presented as the sink of N2O, and the saturation varied from 47.2% to 102.2%. However, the observed N2O concentrations in USW were higher than that of T-N2OUSW due to the sea–air exchange, diffusion process, possible N2O generation mechanism, and the influence of precipitation, and a more detailed mechanism is needed to understand this process in the Arctic Ocean.


2020 ◽  
Author(s):  
Rachael Rhodes ◽  
Xin Yang ◽  
Eric Wolff

<p>It is important to understand the magnitude and rate of past sea ice changes, as well as their timing relative to abrupt shifts in other components of Earth’s climate system. Furthermore, records of past sea ice over the last few centuries are urgently needed to assess the scale of natural (internal) variability over decadal timescales. By continuously recording past atmospheric composition, polar ice cores have the potential to document changing sea ice conditions if atmospheric chemistry is altered.  Sea salt aerosol, specifically sodium (Na), and bromine enrichment (Br<sub>enr</sub>, Br/Na enriched relative to seawater ratio) are two ice core sea ice proxies suggested following this premise.</p><p>Here we aim to move beyond a conceptual understanding of the controls on Na and Br<sub>enr</sub> in ice cores by using process-based modelling to test hypotheses. We present results of experiments using a 3D global chemical transport model (p-TOMCAT) that represents marine aerosol emission, transport and deposition. Critically, the complex atmospheric chemistry of bromine is also included. Three fundamental issues will be examined: 1) the partitioning of Br between gas and aerosol phases, 2) sea salt aerosol production from first-year versus multi-year sea ice, and 3) the impact of increased acidity in the atmosphere due to human activity in the Arctic.</p>


2017 ◽  
Vol 17 (15) ◽  
pp. 9417-9433 ◽  
Author(s):  
Rachael H. Rhodes ◽  
Xin Yang ◽  
Eric W. Wolff ◽  
Joseph R. McConnell ◽  
Markus M. Frey

Abstract. Growing evidence suggests that the sea ice surface is an important source of sea salt aerosol and this has significant implications for polar climate and atmospheric chemistry. It also suggests the potential to use ice core sea salt records as proxies for past sea ice extent. To explore this possibility in the Arctic region, we use a chemical transport model to track the emission, transport, and deposition of sea salt from both the open ocean and the sea ice, allowing us to assess the relative importance of each. Our results confirm the importance of sea ice sea salt (SISS) to the winter Arctic aerosol burden. For the first time, we explicitly simulate the sea salt concentrations of Greenland snow, achieving values within a factor of two of Greenland ice core records. Our simulations suggest that SISS contributes to the winter maxima in sea salt characteristic of ice cores across Greenland. However, a north–south gradient in the contribution of SISS relative to open-ocean sea salt (OOSS) exists across Greenland, with 50 % of winter sea salt being SISS at northern sites such as NEEM (77° N), while only 10 % of winter sea salt is SISS at southern locations such as ACT10C (66° N). Our model shows some skill at reproducing the inter-annual variability in sea salt concentrations for 1991–1999, particularly at Summit where up to 62 % of the variability is explained. Future work will involve constraining what is driving this inter-annual variability and operating the model under different palaeoclimatic conditions.


2016 ◽  
Vol 12 (9) ◽  
pp. 1907-1918 ◽  
Author(s):  
Rasmus A. Pedersen ◽  
Peter L. Langen ◽  
Bo M. Vinther

Abstract. Insolation changes during the Eemian (the last interglacial period, 129 000–116 000 years before present) resulted in warmer than present conditions in the Arctic region. The NEEM ice core record suggests warming of 8 ± 4 K in northwestern Greenland based on stable water isotopes. Here we use general circulation model experiments to investigate the causes of the Eemian warming in Greenland. Simulations of the atmospheric response to combinations of Eemian insolation and preindustrial oceanic conditions and vice versa are used to disentangle the impacts of the insolation change and the related changes in sea surface temperatures and sea ice conditions. The changed oceanic conditions cause warming throughout the year, prolonging the impact of the summertime insolation increase. Consequently, the oceanic conditions cause an annual mean warming of 2 K at the NEEM site, whereas the insolation alone causes an insignificant change. Taking the precipitation changes into account, however, the insolation and oceanic changes cause more comparable increases in the precipitation-weighted temperature, implying that both contributions are important for the ice core record at the NEEM site. The simulated Eemian precipitation-weighted warming of 2.4 K at the NEEM site is low compared to the ice core reconstruction, partially due to missing feedbacks related to ice sheet changes and an extensive sea ice cover. Surface mass balance calculations with an energy balance model further indicate that the combination of temperature and precipitation anomalies leads to potential mass loss in the north and southwestern parts of the ice sheet. The oceanic conditions favor increased accumulation in the southeast, while the insolation appears to be the dominant cause of the expected ice sheet reduction. Consequently, the Eemian is not a suitable analogue for future ice sheet changes.


2015 ◽  
Vol 9 (4) ◽  
pp. 4407-4436 ◽  
Author(s):  
A. Spolaor ◽  
T. Opel ◽  
J. R. McConnell ◽  
O. J. Maselli ◽  
G. Spreen ◽  
...  

Abstract. The role of sea ice in the Earth climate system is still under debate, although it is known to influence albedo, ocean circulation, and atmosphere-ocean heat and gas exchange. Here we present a reconstruction of AD 1950 to 1998 sea ice in the Laptev Sea based on the Akademii Nauk ice core (Severnaya Zemlya, Russian Arctic). The halogens bromine (Br) and iodine (I) are strongly influenced by sea ice processes. Bromine reacts with the sea ice surface in auto-catalyzing "Bromine explosion" events causing an enrichment of the Br / Na ratio and the bromine excess (Brexc) in snow compared to that in seawater. Iodine is emitted from algal communities growing under sea ice. The results suggest a connection between Brexc and spring sea ice area, as well as a connection between iodine concentration and summer sea ice area. These two halogens are therefore good candidates for extended reconstructions of past sea ice changes in the Arctic.


2017 ◽  
Author(s):  
Rachael H. Rhodes ◽  
Xin Yang ◽  
Eric W. Wolff ◽  
Joseph R. McConnell ◽  
Markus M. Frey

Abstract. Growing evidence suggests that the sea ice surface is an important source of sea salt aerosol and this has significant implications for polar climate and atmospheric chemistry. It also offers the opportunity to use ice core sea salt records as proxies for past sea ice extent. To explore this possibility in the Arctic region, we use a chemical transport model to track the emission, transport and deposition of sea salt from both the open ocean and the sea ice, allowing us to assess the relative importance of each. Our results confirm the importance of sea ice sea salt (SISS) to the winter Arctic aerosol burden. For the first time, we explicitly simulate the sea salt concentrations of Greenland snow and find they match high resolution Greenland ice core records to within a factor of two. Our simulations suggest that SISS contributes to the winter maxima in sea salt characteristic of ice cores across Greenland. A north-south gradient in the contribution of SISS relative to open ocean sea salt (OOSS) exists across Greenland, with 50 % of sea salt being SISS at northern sites such as NEEM, while only 10 % of sea salt is SISS at southern locations such as ACT10C. Our model shows some skill at reproducing the inter-annual variability in sea salt concentrations for 1991–1999 AD, particularly at Summit where up to 62 % of the variability is explained. Future work will involve constraining what is driving this inter-annual variability and operating the model under different paleoclimatic conditions.


2020 ◽  
Author(s):  
Abigail G. Hughes ◽  
Tyler R. Jones ◽  
Bo M. Vinther ◽  
Vasileios Gkinis ◽  
C. Max Stevens ◽  
...  

Abstract. An ice core drilled on the Renland Ice Cap in east-central Greenland contains a continuous climate record dating through the last glacial period. The Renland record is valuable because the coastal environment is more likely to reflect regional sea surface conditions, compared to inland Greenland ice cores that capture synoptic variability. Here we present the δ18O water isotope record for the Holocene, in which decadal-scale climate information is retained for the last 8 ka, and the annual water isotope signal is preserved throughout the last 2.6 ka. To investigate regional climate information preserved in the water isotope record, we apply spectral analysis techniques to a 300-year moving window to determine the mean strength of varying frequency bands through time. The strength of interannual frequency bands decays rapidly, but we find that the mean 15–20 year δ18O variability exhibits a millennial-scale cycle in line with the well-known Bond Cycle. Comparison to other North Atlantic proxy records suggests that the 15–20 year variability may reflect fluctuating sea ice conditions throughout the Holocene, driven by changes in the strength of the Atlantic Meridional Overturning Circulation. Additional analysis of the seasonal signal over the last 2.6 ka reveals that the winter δ18O signal has experienced a decreasing trend, while the summer signal has predominantly remained stable. The winter trend likely corresponds to an increase in Arctic sea ice cover, driven by a decrease in total annual insolation. In the context of anthropogenic climate change, the winter trend may have important implications for feedback processes as sea ice retreats in the Arctic.


2016 ◽  
Vol 10 (3) ◽  
pp. 1125-1145 ◽  
Author(s):  
Odile Crabeck ◽  
Ryan Galley ◽  
Bruno Delille ◽  
Brent Else ◽  
Nicolas-Xavier Geilfus ◽  
...  

Abstract. Although the presence of a gas phase in sea ice creates the potential for gas exchange with the atmosphere, the distribution of gas bubbles and transport of gases within the sea ice are still poorly understood. Currently no straightforward technique exists to measure the vertical distribution of air volume fraction in sea ice. Here, we present a new fast and non-destructive X-ray computed tomography technique to quantify the air volume fraction and produce separate images of air volume inclusions in sea ice. The technique was performed on relatively thin (4–22 cm) sea ice collected from an experimental ice tank. While most of the internal layers showed air volume fractions  <  2 %, the ice–air interface (top 2 cm) systematically showed values up to 5 %. We suggest that the air volume fraction is a function of both the bulk ice gas saturation factor and the brine volume fraction. We differentiate micro bubbles (Ø  <  1 mm), large bubbles (1 mm  <  Ø  <  5 mm) and macro bubbles (Ø  >  5 mm). While micro bubbles were the most abundant type of gas bubbles, most of the air porosity observed resulted from the presence of large and macro bubbles. The ice texture (granular and columnar) as well as the permeability state of ice are important factors controlling the air volume fraction. The technique developed is suited for studies related to gas transport and bubble migration.


2005 ◽  
Vol 51 (172) ◽  
pp. 159-166 ◽  
Author(s):  
Dirk Notz ◽  
John S. Wettlaufer ◽  
M. Grae Worster

AbstractWe describe an instrument developed to make in situ measurements of salinity and solid- fraction profiles in growing sea ice. The vertical resolution of the measurements is up to a few millimeters, with a temporal resolution of up to fractions of a second. The technique is based on impedance measurements between platinum wires around which sea ice grows. Data obtained using this instrument in laboratory experiments are in good agreement with theoretical predictions. In a field test in the Arctic, the bulk salinity of growing sea ice has been measured in situ throughout the whole depth of the ice layer. The data are compared with bulk salinities obtained from ice cores, and confirm the general understanding that the bulk salinity in ice-core studies is significantly underestimated in the lower parts of the cores. The approach can also be used in other glaciological applications and for general studies of two-phase, two-component porous media.


2009 ◽  
Vol 55 (189) ◽  
pp. 81-94 ◽  
Author(s):  
Daniel Pringle ◽  
Guy Dubuis ◽  
Hajo Eicken

AbstractWe report impedance measurements of the complex dielectric permittivity ε = ε′ − jε″ of sea ice and laboratory-grown NaCl single crystals using 50 MHz Stevens Water Monitoring Systems Hydra Probes. Temperature cycling of the single-crystal samples shows hydrohalite precipitation, and hysteresis in ε′ and ε″ qualitatively consistent with the expected evolution of brine-inclusion microstructure. Measurements parallel and perpendicular to intra-crystalline brine layers show weak (<10%) anisotropy in ε′ and a 20–40% difference in ε″ due to enhanced d.c. conductivity along the layers. Measurements in landfast, first-year ice near Barrow, Alaska, USA, indicate brine motion in warming ice as the brine volume fraction vb increases above 5%. Plots of vb derived from salinity profiles against ε′ and ε″ for these and previous measurements display too much variability between datasets for unguided inversion of vb. Contributing to this variability are intrinsic microstructural dependence, uncertainties in vb, and sub-representative sample volumes. A standard model of sea-ice permittivity is inverted to derive the apparent brine-inclusion aspect ratio and bulk d.c. conductivity at a spatial scale complementary to previous measurements. We assess Hydra Probe performance in high-salinity environments and conclude that they are not generally suited for autonomous sea-ice salinity measurements, partly due to the range of relevant brine pocket inclusion length scales.


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