Northern lake systems (50°N–80°N) have been subject to an increase in mean annual surface air temperature up to 2.7°C over the last few decades (Box et al., 2019; Meredith et al., 2019; Ballinger et al., 2020). Temperature is one of the key control variable for the mineralization and burial of carbon in lakes, regardless of the origin of carbon (i.e., autochthonous or allochthonous) (Gudasz et al., 2010; Gudasz et al., 2015). Not only is an increase in temperature associated with higher carbon mineralization and burial, but also favors higher turnover of carbon through more in-lake primary production by macrophytes/aquatic plants (Li et al., 2017; Velthuis et al., 2018) and algae (Biskaborn et al., 2022). As a consequence, lake systems can shift from being a net carbon sink to net carbon source and vice versa (Sobek et al., 2014; Heathcote et al., 2015; Denfeld et al., 2018).

Dean and Gorham (1998) estimated that lakes on a global scale accumulate in their sediment about 42 TgC (teragrams of carbon, i.e., one million metric tons of carbon) per year. Based on a new modeling approach, Anderson et al. (2020) approximated that accumulation rates have almost tripled over the past 100 years by about 72 TgC from 0.05 PgC to 0.12 PgC per year. In this model, the authors estimated that lakes in boreal biome contribute the highest (24%) to the global carbon burial rate, while tundra lakes are the lowest at only 2% due to their low carbon burial rate (Anderson et al., 2020). Despite potentially lower carbon burial rates in northern lakes due to current lower temperatures (Gudasz et al., 2010), Sobek et al. (2014) found that Arctic lakes show similar burial efficiencies as other lakes at lower latitudes. In addition, climate change-induced shifts in vegetation (Cramer et al., 2001; Pearson et al., 2013), lake aquatic biomass production (Biskaborn et al., 2023), and increased carbon release from permafrost thawing (Meredith et al., 2019; Schuur et al., 2022) may raise carbon burial rates in Arctic lakes due to the growing availability of carbon within the lakes (Anderson et al., 2020).

Comprehending the complex burial process requires a thorough understanding of how the carbon cycle in a lake responds to temperature fluctuations. Temperature plays a crucial role in shaping the interactions between dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC) in lake ecosystems (Gudasz et al., 2010). DIC comprises carbon in the form of inorganic carbon species, primarily bicarbonate (HCO₃ ⁻), carbonate (CO₃ ⁻²), and dissolved carbon dioxide (CO₂), while DOC refers to the fraction of organic carbon compounds dissolved in water. Higher temperatures can enhance microbial activity, leading to increased breakdown of organic matter and subsequent release of DOC into the lake water (Middelboe and Lundsgaard, 2003; Adams et al., 2010). This process elevates the concentration of DOC in the lake, which influences organic carbon burial rates in lake sediments. Additionally, raised temperatures promote primary production by aquatic plants and algae, which enhances photosynthesis and the uptake of DIC from the water column (Hein, 1997; Hammer et al., 2019). As a result, this process can either increase the outgassing of CO₂ from the lake or promote more carbonate precipitation of carbonated minerals within the lake.

In-lake bioproductivity and carbon accumulation also depend on catchment vegetation and the availability of allochthonous carbon (Roiha et al., 2016). During the Last Glacial Maximum, sparse vegetation and a reduced flux of allochthonous carbon to the lakes prevailed the Arctic due to the severe climatic conditions (Melles et al., 2012). In most areas the lack of nutrients in the underlying permafrost soil prevented further advances of boreal forests (Sundqvist et al., 2014). However, as the climate warmed and glaciers retreated, vegetation types shifted from tundra to boreal forest, which substantially increased the availability of organic carbon (Lozhkin et al., 2007; Lozhkin et al., 2018; Biskaborn et al., 2016; Diekmann et al., 2017).

Nutrient fertilization and atmospheric deposition played a crucial role in the Holocene in enhancing the productivity of the Arctic vegetation (Galloway et al., 2004; Choudhary et al., 2016). A prolonged growing season due to a warmer climate and shorter ice coverage further contributes to an upsurge in carbon turnover within lakes (Walther et al., 2002; Vuglinsky and Valatin, 2018; Sharma et al., 2019; Sharma et al., 2020). However, eutrophication and browning can in turn negate these effects, leading to stable water stratification with anoxic conditions at the bottom of the lake (Bartosiewicz et al., 2019).

In addition to in-lake primary productivity, other factors can affect the overall carbon balance within a lake, such as sediment resuspension/re-mineralization (Guillemette et al., 2017; Klump et al., 2020), or lake characteristics (e.g., morphology, catchment characteristics, or geographical location) (Ferland et al., 2014; Clow et al., 2015; Denfeld et al., 2018; Zwart et al., 2019). Nevertheless, changes in land use and changing precipitation patterns will in turn affect the distribution and storage of carbon in the Arctic in the future (Tchebakova et al., 2009; Bartsch et al., 2016; Windirsch et al., 2022).

While studies have focused on the carbon balance of lakes in the Holocene (e.g., Anderson et al., 2009; Sobek et al., 2014; Heathcote et al., 2015), investigations into past carbon accumulation rates back to the Late Pleistocene are lacking. Since the burial of organic carbon can react sensitively to temperature changes (Gudasz et al., 2010; Gudasz et al., 2015), a longer observation period with larger temperature differences can reveal new perspectives. To test whether temperature is the key driver in northern high-latitude lakes, we need to consider other influencing factors in our analysis, such as catchment vegetation, underlying permafrost, and lake-specific properties.

The main objective of this paper is to investigate the relationship between temperature and carbon in northern lakes over the past 21,000 years. We estimate the amount of carbon accumulated in 28 lakes since the Late Pleistocene using a combination of measured and newly generated organic carbon and dry bulk density data. To generate new data, we test seven different regression techniques as prediction models and evaluate them against common assessment metrics. We then correlate the obtained accumulation rates with temperature from re-analysis data (TraCE-21ka climate reanalysis dataset) to understand the relationship between these rates and changing temperature. Given the large time span covered by the datasets and the geographic spread of the sediment cores, we further create relationships to permafrost, vegetation, and lake-specific attributes.

To determine the amount of carbon that accumulated over the past 21,000 years, we need to calculate the “organic carbon accumulation rate” (OCAR, in g·m⁻²·yr⁻¹) using the following equation (Eq. 1): O C A R = D B D × T O C 100 × S R (1) where DBD is dry bulk density (in g·cm⁻³), TOC is the total organic carbon content (in weight-%), and SR is the age-depth-model-derived sedimentation rate (in cm·yr^-1). We divided the resulting unit (g·cm⁻²·yr⁻¹) by 0.0001 to get the desired OCAR unit (g·m⁻²·yr⁻¹).

To acquire the necessary data for this project, we conducted a comprehensive data collection process that focused on TOC and DBD measurements. In total, we collected 28 datasets from high latitude lake systems (50°N–80°N—Figure 1) containing TOC, which we standardized following the procedure introduced by Pfalz et al. (2021). In addition to DBD and TOC, our data collection focused on two additional data series: 1) sediment water content (WC) data, and 2) grain size measurements divided into the three subgroups of sand, silt, and clay (in weight-%).

Given the variable data availability of sediment cores with DBD, we divided the sediment cores into two subgroups: “Complete datasets” and “Augmented datasets” (Table 1). “Complete datasets” consist of subsets of sediment cores that contain (C1) DBD, TOC, sand, silt, and WC data, (C2) Wet bulk density, TOC, and WC data, and (C3) both DBD and TOC. On the other hand, “Augmented datasets” refer to datasets that were lacking DBD information but had (A1) grain size and partially WC data available or (A2) neither grain size nor WC data available.

While both C1 and C3 datasets were directly usable for OCAR calculation, in three instances of our data collection (subset C2—“Wet bulk density dataset”—Table 1), we collected values for wet bulk density instead of dry bulk density. Because these datasets also provided data on the water content, we were able to calculate dry bulk density with the following equation (Eq. 2): D B D = 1 − W C 100 × W B D (2) with DBD being dry bulk density (in g·cm⁻³), WC being the water content (in weight-%), and WBD being the wet bulk density (in g·cm⁻³).

As both “augmented datasets” A1 and A2 were lacking DBD measurements, we considered predicting DBD from existing data. A large number of empirically derived pedotransfer functions and techniques for predicting bulk density exist in the literature (e.g., Hollis et al., 2012; Martín et al., 2017; Lu et al., 2021; Palladino et al., 2022; Qin et al., 2022). The majority of these prediction techniques use variations of linear models to predict bulk density. To enable comparison with the existing literature, we decided to use a log-linear model as our base model, which we built in Python using “scikit-learn” and its “LinearRegression” function (Pedregosa et al., 2012).

In contrast to other pedotransfer functions, we included both the depth of a given sample within the sediment core (in cm) and its water content, which gave us the following equation (Eq. 3): ln D B D = α + β 1 × C D e p t h + β 2 × T O C (3) + β 3 × S i l t + β 4 × C l a y + β 5 × W C where DBD is dry bulk density (in g·cm⁻³), CDepth is the composite depth below sediment surface (as mid-point cm), TOC is total organic carbon content (in mg·g⁻¹), Silt and Clay are the silt and clay content from grain size measurements (in weight ratios), WC is the water content (in weight-%), α is the intercept, and β₁ to β₅ are the individual coefficients. We obtained the unit “mg·g⁻¹” for the TOC measurements by multiplying weight percent by factor 10, and unit “weight ratios” for clay and silt data by dividing the weight percent by factor 100.

Considering the significant impact of sediment water content on sediment compaction, we recognized its importance in predicting DBD. However, 11 sediment core datasets (39% of the collected datasets) lacked water content data. To address this limitation and to test whether other regression methods can outperform linear models, we decided to predict WC alongside DBD in several multiple output regression methods in addition to the linear model. We opted for non-linear machine learning techniques to allow for a better comparison with the (non-linear) log-linear model. This includes the following regression methods from the “scikit-learn” and “xgboost” package in Python (Pedregosa et al., 2012; Chen and Guestrin, 2016):

• Random Forest Regression

For training and evaluation purposes, we split the “Full dataset” C1 (Table 1) into a training (80%) and test set (20%), but also used fivefold cross-validation to alleviate potential biases in the splitting process. We scored the individual models by using the following metrics: mean absolute error (MAE), relative absolute error (RAE), mean squared error (MSE), root mean squared error (RMSE), root relative squared error (RRSE), and R ² score. The Supplementary Material contains the equations used for these metrics. We further checked if hyperparameter tuning would improve our results by adding an additional pipeline with the “GridSearchCV” and “RandomizedSearchCV” optimization algorithms from the “scikit-learn” package (Pedregosa et al., 2012).

For subset A1, we used the log-linear model and the regression methods to predict DBD and, where necessary, WC. However, for subset A2 (“Estimate DBD from beta distribution dataset”—Table 1), we only had TOC measurements for 15 sediment cores available for bulk density prediction. We therefore used existing grain size data from eleven sediment cores in the data collection (710 data points) to generate beta distributions for clay and silt. These beta distributions rely on the two parameters α_beta and β_beta, which we individually calculated using the following two equations (Eqs 4, 5): α b e t a = 1 − μ σ 2 − 1 μ × μ 2 (4) β b e t a = α b e t a × 1 μ − 1 (5) with µ and σ² being the mean and the variance of the existing clay or silt data, respectively. After obtaining α_beta and β_beta values for both clay and silt content, we drew 10,000 silt and clay values for each TOC measurement from the newly constructed beta distributions using “random sampling” of the Python package “numpy” (Harris et al., 2020). To reduce overall computing time, we performed random sampling and subsequent prediction of dry bulk density (Eq. 3) in parallel using the “Dask” back-end (Dask Development Team, 2016) and the “joblib” Python package (Joblib Development Team, 2020).

However, we constrained the possible values for clay and silt in two ways before using them in our models to predict dry bulk density ranges. Given that grain size data is compositional data, i.e., the sum of its components should add up to 1% or 100% (Greenacre, 2021), we first removed sums of clay and silt weight ratios that were greater than one. Since grain size data consists of a third component, which is the grain size range for sand, we also considered a lower bound for the sums to account for sand occurrence in the sediment cores. From the given data, we estimated that a maximum of 20% sand in the sediment column would be possible for our data collection. Therefore, we also removed sums of clay and silt weight ratios that were smaller than 0.8.

In any case, working with modeled values can introduce potential errors that could affect the interpretation of results. The quality and accuracy of the input data play a crucial role in determining the model’s performance and output (Rebba et al., 2006; Huang and Laffan, 2009). Errors during data collection or sample measurement can propagate into the model outputs. We mitigated the risk by relying on original raw data as much as possible and used a database to ensure the values fell within physically plausible ranges (Pfalz et al., 2021). While both Eqs 1, 3 represent simplifications of complex systems, and overly simplistic models can overlook important processes that lead to incorrect results (Andersson et al., 1999; Mathews and Vial, 2017). However, we struck a balance between simplification and computational feasibility, using only publicly available data and ensuring the reproducibility of our results.

We used the LANDO age-depth modeling result from Pfalz et al. (2022) to derive sedimentation rates (SR) for each sediment core. LANDO links five age-depth modeling systems (Bacon, Bchron, clam, hamstr, Undatable) in one multi-language Jupyter Notebook (Haslett and Parnell, 2008; Parnell et al., 2008; Blaauw, 2010; Blaauw and Christen, 2011; Kluyver et al., 2016; Peng et al., 2018; Lougheed and Obrochta, 2019; Dolman, 2022). For all sediment cores, we combined the results from the five modeling systems with standard settings into an ensemble model with two-sigma uncertainty [as described in Pfalz et al. (2022)]. We propagated these sedimentation rate uncertainties into the OCAR calculations (Eq. 1) to obtain OCAR uncertainty ranges.

To understand the temperature development since the Last Glacial Maximum (Clark et al., 2009), we used the TraCE-21ka climate reanalysis dataset (He, 2011), which we will refer to simply as TraCE dataset hereinafter. We divided the timespan covered by the TraCE dataset into the following periods (Walker et al., 2019; Head et al., 2021; Kuang et al., 2021):

• Last Glacial Maximum—22,000 to 18,000 years BP (years before present, i.e., before 1950 CE)

For each core location, we extracted the surface air temperature at reference height (TREFHT) from the nearest grid cell of the TraCE dataset [grid cell resolution: 2.5° × 2.5° (He, 2011; Brown et al., 2020)]. We then converted the temperature from Kelvin (K) to Celsius (°C) by subtracting 273.15 K from each value and then averaging values for the summer months June-July-August (JJA). Following the procedure introduced by Kaufman et al. (2020a), we converted OCAR values to z-score. The z-score measures how many standard deviations each point is away from the mean, and thus normalizes the data. To comprehend how vegetation affects carbon accumulation, we used the vegetation reconstruction by Dallmeyer et al. (2022) (depicted in Figure 2), which incorporates the TraCE dataset into its remodeling.

To determine the correlation between temperature and OCAR, we first had to check for normality of the two variables. For this reason, we visually inspected the data by plotting quantile-quantile plots (Q-Q plots) using the package “statsmodels” (Seabold and Perktold, 2010). We then used both the Shapiro-Wilk as well as the D’Agostino and Pearson’s test from the Python package “scikit-learn” (Pedregosa et al., 2012) for our statistical tests. As both temperature and OCAR did not display normality, we used Spearman’s and Chatterjee’s rank correlation coefficient to check for the correlation between the two variables. In contrast to Chatterjee’s coefficient, Spearman’s coefficient is a well-established, robust correlation metric often used for variables from non-normal distributions (Sadeghi, 2022). However, the Chatterjee’s coefficient showed promising results for testing the non-linear functional correlation between two variables (Chatterjee, 2021; Sadeghi, 2022). In addition to the Spearman and Chatterjee correlation coefficient, we checked the Pearson and Kendall-Tau correlation coefficient on both the untransformed and z-transformed variables. The methods for the more common correlation coefficients came from the Python package “scipy” (Virtanen et al., 2020), while to calculate the Chatterjee coefficient we used the script provided by Chatterjee (2021).

While our data collection yielded 620 data points (Table 1—Complete datasets) containing DBD and TOC which were directly usable for OCAR calculation (Eq. 1), the majority of data points from the augmented datasets (n = 2,236, Table 1—Augmented datasets) required further calculations. In preparation for both A1 and A2, we fitted the log-linear model with training dataset of our subset C1 (Table 1—“Full dataset”) to obtain the following equation to predict dry bulk density using a linear regression: ln D B D = 1.3337 + 0.0001 × C D e p t h − 0.0016 × T O C − 0.3986 × S i l t + 0.353 × C l a y − 0.0267 × W C (6) where DBD is dry bulk density (in g·cm⁻³), CDepth is the composite depth below sediment surface (as mid-point cm), TOC is total organic carbon content (in mg·g⁻¹), Silt and Clay are the silt and clay content from grain size measurements (in weight ratios), WC is the water content (in weight-%).

Since we wanted to test whether other regression methods could outperform the log-linear model, we had to ensure that there were no calibration and validation issues. Figure 3 and Table 2 provide an overview of the train and test performance with five-fold cross-validation of each regression methods we used to predict DBD (first column) and WC (second column). Ensemble methods such as AdaBoost, Random Forest, Gradient Boosting, and Extreme Gradient Boosting achieved the highest R ² score and lowest error across all error scores. The Random Forest regression performed best for both DBD and WC with an R ² score of 0.8551 and 0.8662, respectively. However, all regression methods yielded a high mean absolute error for WC between 3.9758 (Random Forest Regression) and 6.6296 (Linear Regression), which translated to a deviation from true water content percentages, i.e. 3.98%–6.63%. Hyperparameter tuning using grid search and randomized search did not yield any improvement of these results.

During the first predictions for DBD with the subset A1, we used the mean error between predicted WC versus measured WC as an additional measure of quality for all prediction methods. Table 3 summarizes the results across all prediction methods. In contrast to the previous test and training performance, Linear Regression performed with the smallest error (9.70%), while Random Forest Regression had the highest error (12.13%) amongst the methods.

Before we could predict DBD for A2, we required a clay-silt pair for each of the 1790 data points in A2. Figure 4 shows the beta distributions for clay and silt based on the existing data across all datasets (Table 4). Clay content peaks between 10 and 20 percent, while silt content has its highpoint between 70 and 80 percent. We used random samples from these beta distributions with the subset A2 (Table 1) to estimate dry bulk density for all regression methods. To verify that model results were within a reasonable range and to allow comparison with the literature, we compared TOC values with measured and predicted DBD values. In Figure 5 we summarize the results obtained from the model predictions for Random Forest regression, Support Vector regression, and Linear Regression as well as measured values of TOC and dry bulk density. For completion, we show the results of the remaining four methods in the Supplementary Material (see Supplementary Figure S1).

In Figure 5A, the random forest regression displays a step-like curve with a plateau between about 20 and 150 mg·g⁻¹ TOC. Predicted values of dry bulk density ranged from 0.18 to 1.21 g·cm⁻³. We associated this pattern with potential overfitting, as the method ignores other measured values. Support Vector regression (Figure 5B) predicted values follow the measured values with a shallow increase from 300 to 500 mg·g⁻¹ TOC. DBD values for this method varied between 0.18 and 1.25 g·cm⁻³. The curve within Figure 5C (Linear regression) shows a similar log curve as presented in the literature, however, it exceeds the level of possible values [linear regression method maximum value: 4.06 g·cm⁻³; maximum physically possible value: 2.65 g·cm⁻³ (Avnimelech et al., 2001)]. The minimum value of this method was 0.07 g·cm⁻³. The exceeding values (n = 27) corresponded to deep level samples of core PG1341 (deeper than 15 m) where compactions plays a greater role than the method can reflect. To allow comparison with the literature, we excluded the values above 2.65 g·cm⁻³ from the linear model and continued with linear model further.

Figure 6 contains the comparison between mean OCAR and the temperature data from TraCE dataset for the 28 sediment cores. Some temperature data showed similarities as the core-drilling locations were in the same TraCE grid cell, e.g., EN18208 (Core No. 4—Lake Ilirney) and EN18218 (Core No. 5—Lake Rauchuvagytgyn), or PG2133 (Core No. 25—Lake Bolshoe Toko) and PG2208 (Core No. 27—Lake Bolshoe Toko). However, temperature ranges strongly varied within the dataset depending on the core location. For instance, for sediment core Tel 2006 (Core No. 28—Lake Teletskoye) we saw temperatures ranged from a minimum of −22.61°C to a maximum of 17.88°C, while temperatures for EN18218 (Core No. 5—Lake Rauchuvagytgyn) only spanned from −8.06°C to 2.60°C. Regarding OCAR values, we obtained the lowest overall values for PG1351 (Core No. 15—Lake El’gygytgyn) with a mean of 0.286 g·m⁻²·yr⁻¹ (uncertainty range max: 6.131 g·m⁻²·yr⁻¹, uncertainty range min: 0.008 g·m⁻²·yr⁻¹). We saw the highest OCAR value in ESM-1 (Core No. 6—East Sayan Mountains Lake) with 278 g·m⁻²·yr⁻¹, however, this value came with a large uncertainty range (min: 8.78 g·m⁻²·yr⁻¹, max: 3018.625 g·m⁻²·yr⁻¹). We calculated a mean OCAR of 24.615 g·m⁻²·yr⁻¹ for all collected sediment cores in our dataset.

Figure 7 contains two comparisons: on the left, a direct comparison between mean OCAR values and JJA temperature data across all sediment cores, while on the right is a comparison of z-transformed OCAR values over time. We obtained mean OCAR values for Last Glacial Maximum (9.47 g·m⁻²·yr⁻¹) and Last Deglaciation (10.53 g·m⁻²·yr⁻¹) at the lowest mean temperatures −12.75°C (range: −24.14°C to −0.51°C) and −10.62°C (range: −20.58°C to 2.12°C), respectively. We observed the highest temperature ranges in the Late Holocene with a mean temperature of 3.37°C (range: −12.69°C to 14.76°C), but only with a mean OCAR of 21.8 g·m⁻²·yr⁻¹. The highest OCAR values occurred in Bølling Allerød (38.07 g·m⁻²·yr⁻¹) and Early Holocene (40.68 g·m⁻²·yr⁻¹), where temperature ranged from −14.51°C to 1.69°C (mean value: −4.28°C) and −12.02°C to 8.20°C (mean value: −1.65°C), respectively.

However, when comparing the normalized data over time, we found that Mid-Holocene (mean z-score: 0.126, median z-score: −0.015) and Late Holocene (mean z-score: 0.089, median z-score: −0.055) were among the higher z-transformed OCAR values. Both Mid-Holocene and Late Holocene showed the highest temperature ranges, as shown on the left side of Figure 7. Periods that displayed a lower temperature range, i.e., Last Glacial Maximum, Last Deglaciation, and Younger Dryas, also revealed lower z-transformed OCAR values. Mean z-scores were −0.643, −0.402, and −0.616, while their median z-scores were −0.735, −0.429, and −0.577 for Last Glacial Maximum, Last Deglaciation, and Younger Dryas, respectively.

To check for correlation between temperature and OCAR, we first had to inspect visually Q-Q plots of those variables to check for normality (see Supplementary Figure S2). The visual inspection of the Q-Q plots, however, showed that variables were non-normal distributed. D'Agostino’s K² and Shapiro-Wilk test (Table 5) confirmed this numerically. We then determined the appropriate correlation coefficients for both variables untransformed, both variables z-transformed, and one where only OCAR was z-transformed while temperature was untransformed. Table 6 shows the correlation coefficients for Pearson, Spearman, Kendall-Tau, and Chatterjee, their p-value, and their statistical significance for the above cases. Except for Pearson correlation coefficient for both untransformed variables, all coefficient showed a statistical significance for the relationship between temperature and OCAR. Chatterjee coefficient displayed in all three cases a positive significance. Spearman’s rho value denoted a weak negative relationship (−0.06367) for untransformed values, while for z-transformed values it saw a weak positive relationship between temperature and OCAR (0.2394 and 0.0863).

The purpose of the study was to determine whether there is connection between carbon accumulation in northern lakes and temperature changes that have occurred over the past 21,000 years. We found a slightly positive relationship between OCAR and temperature among our data collection, for which we generated more data using our log-linear model that superseded other data science techniques. While our dataset was diverse in terms of location, age of the sediment, permafrost areas, lake parameters, and catchment vegetation, we generally saw the highest OCAR values occurring during Bølling Allerød (14,300 to 12,700 years BP—38.07 g·m⁻²·yr⁻¹) and the Early Holocene (11,700–8,200 years BP—40.68 g·m⁻²·yr⁻¹). This could indicate that rapid warming events lead to high levels of carbon accumulation in lakes. As warming progresses, this effect appears to change with lower accumulation rates, presumably due to increased microbial activity triggering carbon dioxide and methane outgassing. While we achieved promising results with data from 28 sediment cores, more data from northern lakes would help us to build a greater level of confidence and accuracy on the matter.