Abstract
Arctic fjords are inherently vulnerable to global warming, particularly because of the substantial freshwater influx resulting from the melting of glaciers. In this study, precipitation, river water, surface ice, and seawater samples from Kongsfjorden were collected to identify the main sources of freshwater. The dual water isotope (δ18O and δD) results and temperature–salinity profiles revealed that between 0% and 7% freshwater contributed to the fjord’s water. Furthermore, different freshwater sources for surface and deep water were identified by the dual water isotope analysis. Turbidity profiles confirmed the alter in particle discharge associated with surface runoff and subglacial discharge. Our study highlighted the sensitivity of water isotope analysis in elucidating the hydrological processes within the fjord system and demonstrated its potential for investigating the impact of meltwater on biological processes in the Arctic.
1 Introduction
The Arctic has warmed nearly four times faster than the global mean (). The rapid melting of glaciers and ice sheets in the Arctic realm has raised significant concerns because the climate system is sensitive to changes in the freshwater budget through deep-water formation and thermohaline circulation (; ; ; ). Arctic fjords serve as channels that link melting glaciers and ice sheets within the Arctic basin (). In this context, the mixing of water masses in fjord systems plays an important role by, facilitating the storage and redistribution of freshwater, heat, and nutrients (; ; ). Therefore, studies on water mass mixing contribute to a better understanding of the freshwater budget and its impact on marine biogeochemical processes ().
Traditionally, temperature–salinity relationships have been used as a viable method for distinguishing water masses (). Nevertheless, this method is limited when used for tracing the mixing of water masses with similar salinities and temperatures in coastal areas (; ). In Arctic fjords, freshwater originates from various sources such as subglacial meltwater, glacier calving, precipitation, and river runoff, which exhibit similar salinity levels; this complicates the determination of their respective contributions. In contrast, dual water isotope analysis (δ18O and δD) is advantageous because the levels of the isotopes differ across various freshwater sources (; ). Variations in the δ18O and δD isotope values in surface seawater are largely controlled by physical processes such as precipitation, evaporation, advection, upwelling, and runoff input (; ). Water isotopes and salinity exhibit similar responses to these physical processes, manifesting lower values in freshwater compared with seawater (). Therefore, the δ18O and δD values in coastal waters decrease with increasing freshwater flushing and precipitation and increase with higher evaporation and seawater intrusion (). Accordingly, different water masses exhibit different δ18O–δD and δ18O–salinity relationships; this is, useful for studying the hydrographic processes in high-latitude oceans, such as the Arctic fjords () and the Southern Ocean ().
The archipelago of Svalbard is one of the rapidly changing regions in the Arctic with increasing water temperatures (), water column stratification (), precipitation (), and retreating glaciers (). Kongsfjorden, an Artic fjord on the Spitsbergen, Svalbard archipelago, is surrounded by glaciers, including Kongsvegen, Kronebreen, Kongsbreen, Conwaybreen, and Blomstrandbreen (Figure 1A). The fjord is between 4 and 10 km wide, ~27 km long, and has a total volume of about 29.4 km3 (; ). Kongsfjorden experiences contributions of subglacial meltwater from five tidewater glaciers, ice calving, and direct discharge (~29 × 106 m3) from the Bayelva River, which receives runoff from two small land-terminating glaciers, Austre and Vestre Brøggerbreen (Figure 1A, ; ). Subglacial discharge strongly impacts the hydrographic dynamics in Kongsfjorden (; ). Furthermore, report that high precipitation during the summer and winter seasons may affect the fjord’s freshwater dynamics (). These on-going transition from tidewater glaciers to land-terminating glaciers do not only impacts the watermass characteristics but also the biogeochemical properties and its ecosystem consequences in Kongsfjorden within a warming Arctic. Freshwater originating from glacial meltwater, precipitation, and river runoff has distinct δ18O and δD values, yet the δ18O–δD relationship remains unexplored. In this study, we present a dataset encompassing dual water isotope values, temperature, and salinity profile results obtained from the water column of the Kongsfjorden in June 2023. The goal of this study is to discern mixing patterns among the different water masses in Kongsfjorden, providing insights into the fjord’s freshwater mixing processes.
Figure 1
2 Materials and methods
2.1 Sampling
Sampling was conducted in Kongsfjorden in June 2023 (Figure 1A; Supplementary Table S1). A total of 22 seawater samples were collected at each of the 10 stations from three nominal water depths (surface, 100 m, and bottom depth) using 10 L Niskin bottles on board of MS Teisten. Station 1 in the inner fjord was the closest accessible sampling location from the Kronebreen for the safety region. Seawater samples for dual water isotope analyses were filtered through acetate membranes (0.45 μm pore size) to prevent the effect of bioprocesses on water isotopes after sampling in the vial. The filtrate was transferred to a glass vial (Labco, 12 mL borosilicate vial, non-evacuated) that was pre-baked at 450°C and wrapped with parafilm (PM-996, Amcor, Switzerland) to reduce biological effects and avoid isotopic fractionation through evaporation, and then stored at 4°C before analysis.
Hydrographic data at each station included salinity, conductivity, temperature, fluorescence and turbidity obtained with CTD (SD204, SAIV A/S, Norway). To distinguish between different freshwater sources, freshwater end-members from the region were also sampled (Figure 1A). Two ice samples from Station 1 and 2 (Ice-1 and Ice-2) were collected using a bucket; one Bayelva River water sample and two precipitation samples (Snow-1 and Snow-2) samples were also obtained. Ice and snow samples were collected in zipper−closed plastic bags and transported to the Kings Bay Marine Laboratory in Svalbard. The samples were immediately melted at room temperature and treated in the same method as seawater.
2.2 Stable water isotopes
Dual water isotope analysis determines the ratios of the stable isotopes of oxygen (i.e., 18O and 16O) and hydrogen (i.e., 2H and 1H). The ratios are reported in per mil (‰) deviations from the Vienna Standard Mean Ocean Water (V-SMOW), denoted as δ18O and δD, as follows:
where Rsample and RV-SMOW indicate the 18O/16O and 2H/1H ratios in the sample and V-SMOW, respectively.
The dual water isotope analyses were performed using a Picarro water isotope analyzer (L2140-I, Picarro, USA) at the Shaanxi Key Laboratory of Earth Surface System and Environmental Carrying Capacity. Five standards were used for the calibration curve including USFS53 (USGS RSIL, USA), GBW04458, GBW04459, GBW04460 and GBW04461 (National Institute of Metrology, China). Results have been reported in the standard delta notation as δ18O and δD relative to the V-SMOW. The precision of the Picarro analyzer was ±0.2‰ and ±0.5‰ for the δ18O and δD, respectively. The reproducibility of the δ18O and δD of this study’s samples were ±0.1‰ and ±0.2‰, with an average relative standard deviation (RSD) of 9% and 6.5%, respectively, based on duplicate analyses of four samples.
The deuterium excess (d-excess), defined as d = δD – 8 × δ18O, has long been used as a diagnostic tool for analyzing moisture sources, hydrological cycles, and local climate conditions (
2.3 Mixing model
A simplified two end-member mixing model was used to determine the δ18O and δD values of freshwater input based on the isotopic mass balance as follows:
where Ss, δ18Os, and δDs represent the salinity, δ18O, and δD of the samples, respectively, Ssw, δ18Osw, and δDsw represent the salinity, δ18O, and δD of the open sea water, respectively, and Ff is the fraction of freshwater. Equation 3, 4 can be expressed as follows:
Accordingly, the intercept of the linear correlation between the water isotopes and salinity in fjord water is the water isotope signal for the freshwater discharge.
To better quantify the surface discharge and subglacial meltwater contribution, here we also separate freshwater source into surface freshwater (sf) and deep freshwater (df), representative to surface discharge and subglacial meltwater. A three end-member mixing model is implied:
3 Results
3.1 Hydrological properties
Water masses within Kongsfjroden are composed of warm and saline Atlantic Water (AW; T > 1°C, S > 34.9), transformed AW, fresh meltwater, winter cold water, and surface water (Figure 1B,
In the inner fjord at deeper depths, the temperature and salinity fall below the mixing line between transformed AW and cold subglacial meltwater, indicating the involvement of winter cold water. Surface temperature and salinity are influenced by mixing processes involving transformed AW, runoff, and warm surface water. Cross-sectional profile of salinity reveals a surface meltwater contribution down to a depth of 15 m, while temperature suggests a cold water source at depth of 15–30 m in front of tidewater glacier (Figures 2A, B).
Figure 2

Cross-sectional distributions of (A) salinity, (B) temperature, (C) δ18O, (D) δD, (E) fluorescence, (F) turbidity, and (G) estimated freshwater content. Station numbers are indicated above each panel, and sampling locations and depths for (C) δ18O and (D) δD values are indicated with black dots.
3.2 Spatial variability in the δ18O and δD values
The lowest dual water isotope values were observed in the glacier calving ice samples collected at Stations 1 and 2, with an average δ18O and δD of –14.0‰ and –101.7‰, respectively (Table 1). Slightly higher δ18O and δD values were observed in fresh snow and precipitation, remaining relatively constant at –12.2‰ and –92.0‰, for the δ18O and δD, respectively. These values were closely aligned with the ones for Bayelva River water, where similar isotope values of –12.9‰ and –91.7‰ were observed for δ18O and δD, respectively. The δ18O and δD values of all seawater samples spanned between –0.85‰ and 0.41‰ and –5.6‰ and 2.5‰, respectively.
Table 1
| Sources | δ18O (‰) | δD (‰) | Reference |
|---|---|---|---|
| Linear regression intercept | –18.8 ± 1.9 | –133.4 ± 13.8 | This study |
| Ice (Glacier calving) | –14.0 | –101.7 | This study |
| –18.0 to –14.6 | ND | ||
| Snow/precipitation | –12.2 | –92.0 | This study |
| River | –12.9 | –91.7 | This study |
| Ice cores (Average) | –20.3 | 7.68× δ18O + 4.5 | Averaged value |
| -Kangerlugssaq | –26.5 | ND | |
| -Austfonna | –18.2 | ND | |
| -Lomonosovfonna | –15.7 | –116.1 | |
| Open sea water | 0.3 ± 0.1 (n=7) | 1.7 ± 0.7 (n=7) | This study* |
Sources of freshwater input and their respective water isotope ratios.
*Averaged values collected from stations 6 and 7.
The cross-sectional profiles of the δ18O exhibit spatial patterns similar to those in salinity (Figures 2A, C). The δ18O of surface water increased with the distance from the glacier in the fjord system, showing particularly low values in the inner fjord. In general, the δ18O values were lower in surface water compared with bottom water. A similar trend was observed in the δD values; however, there was larger variability. Additionally, the cross-sectional profiles of the δ18O and δD values demonstrated that the intrusion of freshwater extended to a depth between 15–30 m (Figures 2C, D), in contrast, a difference was difficult to differentiate in the salinity profiles.
3.3 Spatial variability in fluorescence and turbidity
The fluorescence data were obtained using a CTD fluorometer to observe relative variations among stations. Lower fluorescence was observed in the inner fjord (Stations 1–4), with values ranging between nearly 0 and <2 μg/L (Figure 2E). The cross-section of fluorescence demonstrated higher fluorescence concentrations in the outer fjord (Stations 5 and 6) with a subsurface peak at depths of between 30–50 m. In addition, a slight decrease in fluorescence (peaked at 7.5 μg/L) was observed at Station 7.
In contrast, elevated turbidity was determined in the inner fjord (Station 1–4), exhibiting a gradual decrease towards the outer fjord stations. The highest values were retrieved from the subsurface water (10–30 m) in front of the glacier, indicating a subglacial discharge (Figure 2F). This suggests that particulate matter could be delivered from subglacial meltwater and penetrated to deeper depths by fast deposition. Furthermore, highest turbidity was observed in the surface water at Station 8 near the coast.
4 Discussion
4.1 Factors affecting water isotope values in Kongsfjorden
The δ18O and δD values of all the seawater samples were within the range bounded by the Arctic meteoric water line (
Figure 3

(A) δD–δ18O relationship for water samples in Kongsfjorden. The inner and outer fjord samples are indicated with solid and open dots, respectively. The global ocean water line (GOWL; solid line), global metric water line (GMWL; dashed line), and local metric water line (LMWL; dotted line) from Arctic metric water are shown. (B) The d-excess with δ18O for all the seawater samples. Samples collected at bottom depths of each station are shown in triangles. (C) The δ18O and (D) δD–salinity mixing line. Linear regression is indicated by a red line with a 95% confidence band.
An important element of Kongsfjorden hydrological cycling is the subsurface discharge of meltwater (
4.2 Identifying isotopic signature of freshwater sources
The δ18O values were strongly correlated with salinity in the inner fjord samples (R2 = 0.88, n = 14, Figure 3C), with a slope of 0.54 and an intercept of –18.8 ± 1.9‰, which is consistent with the previously reported δ18O–salinity relationship in Kongsfjorden (δ18O = 0.54 × salinity – 18.42,
The offset between the results of studies is likely caused by the depth of water sampling. In
Figure 4

Distribution of the dual water isotope (δ18O and δD) values. The cross demonstrates the intercept of the δ18O–salinity and δD–salinity regressions. Snowpit sample values were taken from
Similarly, the δD is positively correlated with salinity (R2 = 0.88, n = 14, Figure 3D), featuring an intercept of –133.4 ± 13.8‰, which is close to the estimated value based on Arctic precipitation water (–139.9‰). In addition, this intercept was significantly lower than the intercept when considering the surface samples only (–102‰). All end-members did not fully cover the water isotope depleted sources, since a higher δD was observed in surface floating ice (–101.7‰), precipitation/snow (–92.0‰), and river water (–91.7‰) in Kongsfjorden (Table 1). The δD record from ice cores in Svalbard is limited, with only one value reported from the Lomonosovfonna ice core (average δD value of –116.1‰,
For evaluating the freshwater distribution, we employed freshwater isotope signals from the linear regressions (δ18O and δD; –18.8 ± 1.9‰ and –133.4 ± 13.8‰, respectively). The estimations from the sample’s water isotopes and salinity results were tightly correlated (R2 = 0.88). However, the fractions obtained based on the salinity were generally slightly lower (a slope > 1; Supplementary Figure S2), possibly due to uncertainty of freshwater source that we implied. The freshwater distribution in Kongsfjorden was estimated by combining the δ18O, δD, and salinity values, and ranged between near 0% and 7% in the fjord. The averaged distribution of freshwater based on all indicators in the fjord is shown in Figure 2F, there was no obvious subglacial meltwater plume observed deeper than 15 m (see Section 4.1). Nevertheless, a detailed in-depth profile was constrained by the lack of a high-resolution water isotope dataset.
We hypothesized that the surface freshwater mainly originated from precipitation, river, glacier calving, and supraglacial runoff, while the subsurface freshwater is mainly from subglacial meltwater. Sampling for end-members was limited in this study. Therefore, previously reported water isotope values were adapted (Figure 4). Precipitation/snow samples vary with elevation and season, therefore, this study utilized the δ18O and δD values reported by
The intercept of the δ18O–salinity and δD–salinity regression for all fjord samples (represented as a red cross) and only surface samples (grey square) were indicated on the Figure 4. Water isotope signal of freshwater throughout the water column is lower than the snowpit’s water isotope values but within the range of the glacier ice. In addition, the intercept of the δ18O–salinity and δD–salinity regression based on surface water is identical to that of the out floating ice samples. Since the calved ice originally containly similar water isotope values with glacier ice core, the enrichment in δ18O and δD from freshwater in surface is likely caused by other sources such as river discharge, precipitation, and melting snow. Although this study’s water isotope dataset did not record the subglacial meltwater directly, the estimated water isotopes of the freshwater sources confirmed that different freshwater sources contributed to Kongsfjorden.
Three end-member mixing model also implied to quantify the contribution of surface discharge and subglacial meltwater contribution (Method section 2.3). Mixing model indicates the subglacial meltwater contribute significantly to the Kongsfjorden freshwater (Figure 5) and the model estimated δ18O values of subglacial meltwater is ranged from –41.2 to –19.7‰ with a median of –21.2‰. These values are closely aligned with the previous reported ice core values (Figure 4, Table 1).
Figure 5

Mixing model results: Fraction of (A) seawater, (B) surface discharge, and (C) subglacial meltwater. (D) The model estimated δ18O of subglacial meltwater. Bars represent the 1-sigma range, with mean and median values indicated by the dot and line in the middle, respective. The error bar indicates the 2-sigma range.
4.3 Particles delivered by surface runoff and subglacial meltwater
Glacier discharge influences the availability of light and nutrients. The changes in turbidity with changes in temperature and salinity were plotted across all sampling stations (Figure 6); two distinctive particle sources, fresh and warm (~2°C) surface source and fresh and cold (<0°C) subsurface source, were identified (Figure 6A). Unfortunately, the water isotope analysis results did not aid in identifying the two distinct sources, possibly due to lack of samples (Figure 6B).
Figure 6

Variations in turbidity (Formazin Turbidity Units, FTU) with (A) temperature and salinity, and with (B) temperature and δ18O (‰) across all stations. (C) Variations in turbidity with depth (m); inner fjord (Stations 1 and 2), coastal (Station 8), outer fjord (Station 7). (D) Variations in fluorescence (μg/L) with turbidity and salinity across all stations.
According to
The low fluorescence values in front of the glaciers confirmed this light limitation was due to particles discharge (
In Greenlandic fjords, subglacial discharge from tidewater glaciers sustains high phytoplankton productivity (
Figure 7

Schematic graph illustrating different sources contribution to freshwater and particles in the fjord. Snowpit sample values were taken from
While subglacial meltwater predominated the freshwater supply in Kongsfjorden during our sampling time, the substantial presence of particles restricted the biological production within the inner fjord because of reduced light availability. Similarly, the turbidity profiles revealed two sources of particulate matter within the fjord: surface particles transported laterally and fine sediments originating from subglacial discharge, that exerted an influence on the biological productivity within the inner fjord. Overcoming these knowledge gaps, future investigations will aim to enhance the knowledge of the roles played by surface glacier calving and subglacial meltwater by determining high-resolution water isotope profiles throughout the year.
5 Conclusion
Kongsfjorden, Svalbard is a suitable region for studying the impacts of climate change on water mass mixing in fjord systems and subsequent ecosystem dynamics. Dual water isotopes and temperature–salinity profiles were used to distinguish between freshwater sources in surface and deep waters. Turbidity profiles confirmed variations in particle discharge from surface runoff and subglacial discharge. Freshwater distribution in Kongsfjorden was estimated between 0% and 7%, with a three end-member mixing model indicating that subglacial meltwater is a significant freshwater source. This study emphasized the effectiveness of water isotope analysis in understanding the fjord’s hydrological processes and its potential for studying the influence of meltwater on Arctic biological processes. This method has potential for further investigating the effects of meltwater on biological processes in the Arctic, highlighting broader implications of climate change on these ecosystems.
Statements
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Author contributions
LF: Methodology, Writing – original draft. EY: Funding acquisition, Supervision, Writing – review & editing. JY: Data curation, Methodology, Writing – original draft. MK: Conceptualization, Project administration, Supervision, Writing – review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The research was supported by the Korea Polar Research Institute (KOPRI) grant funded by the Ministry of Oceans and Fisheries (KOPRI PE24900). FL was supported by the National Natural Science Foundation of China (Grant No. 41971088) and the Shaanxi Nature Science Research Fund (Grant No. 2022JQ-246). MK was partly supported by the Global-Learning & Academic research institution for Master’s·PhD students, and Postdocs (LAMP) Program of the National Research Foundation of Korea (NRF) grant funded by the Ministry of Education (No. RS-2023-00301914).
Acknowledgments
The authors thank the Kings Bay Marine Laboratory staff for their assistance, and the captain of the MS Teisten and Sunmin Oh for helping with the water sampling. Water isotope analyses were supported by Huan Zhang from the Department of Urban and Environmental Sciences, Northwest University, China. The authors declare no conflicts of interest relevant to this study. We also would like to thank the reviewers for their comments and construction suggestions.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmars.2024.1426793/full#supplementary-material
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Summary
Keywords
stable water isotopes, meltwater, turbidity, terrestrial particle discharge, Arctic fjord, Kongsfjorden
Citation
Fang L, Yang EJ, Yoo J and Kim M (2024) Tracing freshwater sources and particle discharge in Kongsfjorden: insights from a water isotope approach. Front. Mar. Sci. 11:1426793. doi: 10.3389/fmars.2024.1426793
Received
02 May 2024
Accepted
16 October 2024
Published
04 November 2024
Volume
11 - 2024
Edited by
Manuel Dall´Osto, Spanish National Research Council (CSIC), Spain
Reviewed by
Daiki Nomura, Hokkaido University, Japan
Haiyan Jin, Ministry of Natural Resources, China
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Copyright
© 2024 Fang, Yang, Yoo and Kim.
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*Correspondence: Minkyoung Kim, minkyoung@knu.ac.kr
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