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Article

Bio-Optical Properties and Ocean Colour Satellite Retrieval along the Coastal Waters of the Western Iberian Coast (WIC)

by
Luciane Favareto
1,2,*,
Natalia Rudorff
3,
Vanda Brotas
1,2,
Andreia Tracana
1,2,
Carolina Sá
4,
Carla Palma
5 and
Ana C. Brito
1,2
1
MARE—Marine and Environmental Sciences Centre, Faculdade de Ciências, Universidade de Lisboa, Campo Grande 16, 1749-016 Lisbon, Portugal
2
Departamento de Biologia Vegetal, Faculdade de Ciências, Universidade de Lisboa, Campo Grande 16, 1749-016 Lisbon, Portugal
3
INPE—Instituto Nacional de Pesquisas Espaciais, Divisão de Satélites e Sistemas Ambientais, Rod. Presidente Dutra, Cachoeira Paulista 12630-000, SP, Brazil
4
Portugal Space, Estrada das Laranjeiras, 1500-423 Lisboa, Portugal
5
Instituto Hidrográfico, Rua das Trinas 49, 1249-093 Lisboa, Portugal
*
Author to whom correspondence should be addressed.
Remote Sens. 2024, 16(18), 3440; https://doi.org/10.3390/rs16183440
Submission received: 6 August 2024 / Revised: 7 September 2024 / Accepted: 9 September 2024 / Published: 16 September 2024

Abstract

:
Essential Climate Variables (ECVs) like ocean colour provide crucial information on the Optically Active Constituents (OACs) of seawater, such as phytoplankton, non-algal particles, and coloured dissolved organic matter (CDOM). The challenge in estimating these constituents through remote sensing is in accurately distinguishing and quantifying optical and biogeochemical properties, e.g., absorption coefficients and the concentration of chlorophyll a (Chla), especially in complex waters. This study evaluated the temporal and spatial variability of bio-optical properties in the coastal waters of the Western Iberian Coast (WIC), contributing to the assessment of satellite retrievals. In situ data from three oceanographic cruises conducted in 2019–2020 across different seasons were analyzed. Field-measured biogenic light absorption coefficients were compared to satellite estimates from Ocean-Colour Climate Change Initiative (OC-CCI) reflectance data using semi-analytical approaches (QAA, GSM, GIOP). Key findings indicate substantial variability in bio-optical properties across different seasons and regions. New bio-optical coefficients improved satellite data retrieval, reducing uncertainties and providing more reliable phytoplankton absorption estimates. These results highlight the need for region-specific algorithms to accurately capture the unique optical characteristics of coastal waters. Improved comprehension of bio-optical variability and retrieval techniques offers valuable insights for future research and coastal environment monitoring using satellite ocean colour data.

1. Introduction

Ocean colour has been recognized as an Essential Climate Variable (ECV) by the Global Climate Observing System (GCOS, [1,2]). The term “ocean colour” refers to the residual spectrum of incident solar radiation that is constituted by the frequencies that emerge from the upper layer of the ocean after the incident radiation has been scattered and absorbed [3]. Ocean colour is therefore the result of this dispersion and absorption, as light interacts with the water and the materials in it, either particulates or dissolved, namely Optically Active Constituents (OACs). Specifically, in the visible range, passive radiometric sensors provide data on the Apparent Optical Properties (AOPs, e.g., surface reflectance) of the ocean to model the Inherent Optical Properties (IOPs) that depend on the OACs present in a given body of water [4]. The challenge in estimating these constituents through remote sensing is in accurately distinguishing and quantifying their IOPs and biogeochemical properties, e.g., the absorption coefficients of phytoplankton (aph), non-algal particles (NAPs or detritus, ad), coloured dissolved organic matter (CDOM, ag), and the concentration of chlorophyll a (Chla).
After corrections for the atmospheric and unwanted surface effects (i.e., sun and sky glint and whitecaps), the accuracy of the retrieved water properties will depends on the proportion, interaction, type, and vertical distribution of the dissolved (fulvic and humic CDOM) and suspended particulate materials (i.e., organic and inorganic detritus and phytoplankton cells) [5]. Thus, before applying inversion ocean colour algorithms, it is necessary to understand and characterize the IOPs and the physics of the environment, which govern their distribution spatially and temporally. In coastal waters, IOPs and physicochemical properties are more variable on small scales of time and space compared to the open ocean. Freshwater inputs to the system are a source of particulate matter and dissolved organics, often influencing coastal stratification and hydrodynamics. In addition, there may be regions and seasons more subject to the action of wind and wave-induced bottom resuspension and coastal upwelling, where productivity and biological diversity are usually higher [6].
In waters where there is an optical dominance of phytoplankton absorption in the total absorption and where the other constituents, i.e., non-algal particles and CDOM, covary with Chla (i.e., the product of phytoplankton degradation), the estimates of their bio-optical properties tend to be more precise. This is the case for predominantly oceanic waters, where Chla is normally the dominant optical constituent, classified as Case 1 waters [7]. On the other hand, when the optical properties are influenced by the presence of particulate and dissolved materials that do not covary with phytoplankton, Case 2 waters, there is a greater complexity in estimating each of the IOPs [8], and this is when ocean colour algorithms tend to fail or present higher uncertainties.
Biogenic light absorption is a main optical property that can be used to identify phytoplankton based on their spectral characteristics (e.g., [9,10,11,12,13]), which is extremely valuable for addressing several issues like carbon cycling, fisheries management, and climate change [14,15]. Therefore, the characterization of the OACs and IOPs in coastal regions is an important step in determining the appropriate use of ocean-colour bio-optical algorithms, as well as their uncertainties [16] and the need for regional parametrizations of global models [17].
The Western Iberian Coast (WIC) is a highly dynamic region, seasonally influenced by coastal upwelling [18,19], as well as by continental river runoff and occasional storms [20]. The WIC’s primary oceanographic features include the Iberian Poleward Current (IPC), upwelling jet, associated filaments, eddies, and the Western Iberian Buoyant Plume (WIBP). The upwelling system, shaped by the coast’s morphology and wind patterns, exhibits high variability, particularly in the northern WIC (e.g., [19,21,22]). Nutrient inputs from continental sources or intense upwelling support phytoplankton growth, mainly in the northern region (between latitudes 39.5 and 42° N) [22,23]. In contrast, the southern WIC experiences limited phytoplankton growth due to lower nutrient availability, except in the cape of Sagres [24].
The challenge in estimating OACs through remote sensing is in accurately distinguishing and quantifying their optical and biogeochemical properties, especially in complex waters, such as the ones in the Western Iberian Coast (WIC). Thus, the main aim of this study was to evaluate the temporal and spatial variability of bio-optical properties in the coastal waters of Portugal, contributing to the assessment of the best approaches for satellite retrievals. To achieve this, the following specific objectives were considered: (i) analyze the bio-optical composition of the WIC’s coastal waters and classify them according to the general case 1 and case 2 classification scheme; (ii) analyze the temporal and spatial variation of absorption coefficients for phytoplankton, detritus, and CDOM in order to understand their dynamics and sources within the WIC; (iii) investigate the relationships between biogeochemical and bio-optical properties; and (iv) assess the best approaches to deriving bio-optical and biogeochemical properties using ocean colour remote sensing. This study contributes to a better understanding of the bio-optical variability of ocean colour in the coastal shelf off Portugal, providing valuable information for future research and monitoring efforts.

2. Materials and Methods

2.1. Sampling Campaigns

Under the framework of the AQUIMAR project (https://aquimar.hidrografico.pt/, accessed on 10 November 2023), four oceanographic campaigns (AQ1 to AQ4) were performed (Table 1), covering five sampling areas (A, B, C, D, and E). See [22] for details of the sampling campaigns. This study uses data from AQ2 to AQ4, as no bio-optical data were collected during AQ1. The AQ2 campaign was carried out within the period between April and May 2019 (spring), AQ3 in October 2019 (autumn), and AQ4 between February and March 2020 (called early spring, given the phytoplankton growing season). A total of 125 bio-optical samples were obtained during these campaigns (Table 1; Figure 1).
Surface seawater was sampled between ~4 and 6 m using Niskin bottles coupled to a rosette system and combined with a multiparametric probe (Ocean Seven 320 Plus WOCE-CTD, IDRONAUT, Brugherio, Italy) equipped with temperature (°C), pressure (dbar), conductivity (mS cm−1), and turbidity (FTU, SEAPOINT OEM) sensors (SEAPOINT, Exeter, NH, USA) (processing details are described in [26]). The dissolved inorganic nitrogen (DIN) was computed as the sum of NO2, NO3, and NH4+ (processing details are described in [22]). The seawater samples for chlorophyll a concentration (and phaeopigments) and light absorption coefficients analyses were kept refrigerated and in dark conditions until further processing, as described below.

2.2. Laboratory Work

2.2.1. Chlorophyll a and Pheopigments

A known volume (±1–3 L) of seawater was filtered through 25 mm glass fibre filter GF/F (0.7 μm pore size). The filter was then placed in aluminium foil, stored in liquid nitrogen, and later transferred to a −80 °C ultra-freezer. The concentrations of chlorophyll a (Chla, mg m−3) and pheopigments (Pheo, the sum of pheophorbide a and pheophytin a, mg m−3) were determined by High-Performance Liquid Chromatography (HPLC), using a Shimadzu Prominence-i LC-2030C 3D instrument (Shimadzu, Kyoto, Japan) with a C8 reversed phase column. Pigments were extracted with 3 mL of 95% cold buffered methanol (2% ammonium acetate) with 0.005 mg L−1 of trans-beta-apo-8′-carotenal. The extracts were filtered (Fluoropore PTFE filter membranes (Merck KGaA, Darmstadt, Germany), nominal pore size 0.2 μm) into the flask with 0.4 mL of ultrapure water to avoid a distortion of their early elution peaks [27] and immediately injected into the HPLC [28,29,30,31]. Chla was defined by the sum of allomers and epimers of divinyl chlorophyll a, chlorophyllide a, and chlorophyll a [32]. TChla includes Chla plus the sum of pheopigments (Pheo). The quality control of the pigment data was performed following the first rule described by [33].

2.2.2. Light Absorption Coefficients

Seawater samples were also analyzed to obtain the light absorption coefficients of coloured dissolved organic matter (CDOM, ag) and particulate matter (ap), which includes phytoplankton (aph) and inorganic particles (detritus, ad).
For the absorption coefficient of the CDOM (ag, m−1), the seawater samples and a blank reference (used to subtract the water’s absorption, using ultrapure water) were filtered through polycarbonate filters with a pore size of 0.2 µm [34]. The residual water was stored in sterile amber glass bottles at 4 °C until laboratory analysis [35]. The absorbance reading of the reference (blank) and samples (in triplicates) was performed using 100 mm acid-cleaned quartz cuvettes in a double-beam spectrophotometer (model Shimatzu 2600 series (Shimadzu, Kyoto, Japan)), from 300 to 800 nm [34]. The ag (λ) (m−1) was determined from the absorbance measurement multiplied by a conversion factor (natural logarithm, 2.303); divided by the cuvette length (m), with an offset correction at 650 nm; and subtracting the water absorption using the blank references of each measurement [34].
For the absorption coefficients of the particulate matter (ap, m−1), a known volume (±1–3 L) of seawater was filtered through 25 mm glass fibre filter GF/F (0.7 μm pore size). The filter was placed in a vial, immediately frozen in liquid nitrogen, and stored in an −80 °C ultra-freezer. The spectral ap, ad, and aph (300–800 nm) were determined using the Transmittance %–Reflectance % (T-R) method described by [36,37], with a dual-beam spectrophotometer (Shimatzu model 2600 series) coupled to an integrating sphere. The ad (λ) was measured after filter depigmentation with NaClO 1% [35]. The absorbance was converted to absorbance in suspension using the pathlength amplification factor of [38] for the T-R method. Finally, ad (λ) was subtracted from ap (λ) to obtain aph (λ). The phytoplankton-specific absorption coefficient (a*ph, m2 mg−1) was obtained by normalizing aph by Chla (N = 122). The sum of the biogenic absorption coefficients (aph, ad and ag) corresponded to at-w, and at to the total absorption coefficient including pure water (aw) [39].
The spectral slope absorption (S) for ag (Sg), ad (Sd), and the sum of these components, namely adg (Sdg), was determined by fitting the absorption coefficients to a single-exponential non-linear curve ([40], S(λ)= ax (λ reference) exp (–S [λ– λ reference]), between wavelengths from 350 nm to 500 nm, with 443 nm as the reference [41,42,43].

2.3. Satellite Data and Derived Products

The approach implemented in this study follows the diagram presented in Figure 2. Chla concentrations and bio-optical properties (absorption coefficients) were derived from OC-CCI reflectance data, as explained below.

2.3.1. Reflectance Data

Daily remote sensing reflectances (Rrs, sr−1 at 412, 443, 510, 560, and 665 nm) elaborated within the scope of the ESA Ocean Colour Climate Change Initiative project (OC-CCI, version 5, level 3 and 1 km spatial resolution) were obtained from the OC-CCI webserver (https://www.oceancolour.org/, accessed on 5 January 2022). This dataset integrates information from several sensors—SeaWiFS, MODIS, MERIS, VIIRS, and OLCI-3—using the unified processing chain described in [44].

2.3.2. Satellite-Derived Chlorophyll a

Chla concentrations were derived from OC-CCI v5, which uses the OC5CCI empirical algorithm for case 1 and case 2 waters [45], developed by IFREMER and PML. The OC5CCI algorithm (from CMEMS webserver https://data.marine.copernicus.eu, CMEMS-OC-QUID-009-034-036-046-047-066 to 069-087 to 092, accessed on 5 January 2022) was chosen based on a CMEMS calibration and sensitivity analysis, which evaluated several algorithms (OC3, OC4ME, OCI, OC5CI, OC5, OC5CCI). This analysis includes an in situ database of 191 samples from the coastal waters of Portugal [46] and has demonstrated its superior performance, with R² values of 0.89 compared to, e.g., OC4Me 0.78, and outperformed the OC’s algorithms using the database from the AQUIMAR project, considering its four oceanographic cruises. Additionally, the Chla concentrations, as one of the products derived from the default semi-analytical GSM algorithm (Garver–Siegel–Maritorena, [47]), presented below were obtained for comparison with the empirical results of the OC5CCI.

2.3.3. Satellite-Derived Absorption Coefficients

Absorption coefficients (at, aph and adg) were also derived from the Rrs of OC-CCI v5 using three semi-analytical approaches: (i) the QAA (Quasi-Analytical Algorithm, [48]) derived from OC-CCI v5; (ii) the default version of the GSM (Garver–Siegel–Maritorena, [47]) algorithm; and (iii) the default version of the GIOP (Generalized Inherent Optical Property) algorithm (from [49]). These approaches, based on radiative transfer equations, relate the spectral distribution of Rrs to the inherent optical properties of water. Such algorithms continue to be used in the provision of standard products by the main projects of space agencies (e.g., the ESA and NASA).
Both the GSM and GIOP approaches were parameterized with coefficients from [50] to ensure consistency. In addition, GIOP was also parameterized with regional coefficients (regional aph). New regional coefficients (named RG) for the relationship between in situ Chla and absorption coefficients (aph) were derived for the coastal waters of Portugal (N = 122). This was implemented following the approach described by [50,51], using the power law function coefficients for the entire spectral range (λ = 400 to 700 nm). See Section 3.3 for details on this regional parameterization.
A relevant difference between the default GIOP and the other approaches is that GIOP needs Chla as an input component. In this case, OC5CCI Chla was used, given the best performance of the algorithm (as presented in Section 3.4). Thus, the GIOP approach was also implemented using two variants: (i) GIOP using OC5CCI-derived Chla as its input, with coefficients from [50] (GIOP-OC5CCI); and (ii) GIOP using OC5CCI-derived Chla as its input and parameterized with regional coefficients (regional aph, GIOP-OC5CCI-RG). In total, 4 different results for satellite-derived absorption coefficients were obtained; three using standard approaches and one using regional coefficients.

2.3.4. Matchup Analysis

The dataset was processed according to the provided quality index, leaving a total of 53 matchups (Figure 1, red circles). As the data acquisition of the sensors (SeaWiFS, MODIS, MERIS, VIIRS and OLCI-3A) used in the OC-CCI product vary between ∼10:00 and ∼13:30 local solar time, the acceptable time window was initially set to ±6 h (following [52]), however, subsequent tests showed a minimal significant effect in accepting in situ samples (N = 7) at any time of the same day. Hence, the time window was set to the same day [9]. To ensure spatial homogeneity, the median of a 3 × 3 window box centred on the sampling site was obtained based on Rrs (sr−1, between bands 412 and 665 nm), with at least 5 valid pixels, a coefficient of variation less than 0.20, and pixels that differ by less than one standard deviation [9,53]. A comparative analysis of the Rrs between OC-CCI and Sentinel-3A (OLCI, N = 22) demonstrated a consistent pattern, with a slope exceeding 0.91 and a coefficient of determination (R²) of 0.65 at 442 nm, 0.85 at 665–670 nm, and over 0.93 for other wavelengths (unpublished data). The 1 km spatial resolution dataset from OC-CCI, utilizing 3 × 3 window values without pixel overlap, could yield more matches and offer valuable insights into variability [44]. Despite Sentinel 3-A’s higher resolution (300 m), OC-CCI’s broader temporal coverage is advantageous for future comprehensive seasonal analyses.
To assess the agreement between in situ observations and the OC-CCI satellite’s ocean colour products, a Type-2 regression least squares fit was applied (lsqfitma.m routine from MBARI, http://www3.mbari.org, accessed on 10 January 2022). Concomitant results (or matchups) were evaluated using regression parameters (coefficient of determination—R2—and linear equation parameters are provided in Supplementary Materials) and error estimations, including the bias (BIAS), mean squared error (RMSE), and mean absolute error (MAE). The BIAS and MAE were applied following [54].
Inherent optical properties (absorption coefficients) were aggregated within ±3 nm of the OC-CCI bands. The 443 nm wavelength was chosen to represent the main variability of the biogenic absorption coefficients and is omitted hereinafter. Moreover, the at (443 nm) was evaluated to minimize the additional uncertainty introduced by partitioning at (443 nm) into its aw, aph, and adg contributions [55].

2.4. Statistics and Data Analysis

The Shapiro–Wilk test was used to confirm the non-normality of the bio-optical parameters, and a Tukey honest significant difference (HSD) was performed to verify if there were mean significant differences between areas and campaigns (p-value < 0.05). Heatmaps of Kendall correlation coefficients (τ, ±0 to 1, pairwise method) and their significance (‘*’, p-value ≤ 0.05) were created using normalized in situ data. In addition, regression analyses were used to describe the relationships between in situ biogeochemical components (e.g., turbidity, Chla concentrations) and absorption coefficients (at, aph, and adg). In order to obtain regional coefficients for the semi-analytical approaches, power law functions were fitted to the data, following [50] and [56]. These relations are presented with their R2, number of samples (N), and the coefficients (“a” and “b”) from a power law fit (a.xb) or polynomial fit (“Poly fit”, a.x + b, when specified).

3. Results

3.1. Case 1 vs. Case 2 Waters

The total non-water absorption coefficient at-w varied between 0.05 and 0.44 m−1 (Table S1; Figure 3 and Figure S1), reaching higher values (>0.22 m−1) during the spring (AQ2) and early spring (AQ4) campaigns. During the spring campaign (AQ2), at-w (average 0.16 m−1) demonstrated strong positive correlations (τ ≥ 0.6 *, Figure S2) with the phytoplankton components (Chla, Pheo, and aph, e.g., in areas A and E), detritus absorption (ad), and turbidity. CDOM absorption (ag), became more strongly correlated to at-w in the autumn campaign (AQ3, average 0.12 m−1), while during the early spring (AQ4, average 0.11 m−1), the detritus and phytoplankton absorption coefficients became again more strongly correlated with at-w (Figure S2, except area D), but were not correlated with each other in the northern areas. The early spring campaign, which occurred during the initial phase of a strong upwelling event [22], was characterized by the highest turbidity (on average up to 1.19 FTU), DIN (up to 2.17 µmol L−1 for areas A, B, and C), and ad (average 0.020 m−1), especially in the northern–central WIC (Figure 4 and Figure S1; Table S1).
Following the [57] classification scheme, Case 1 waters (Figure 4 and Figure S3), dominated by aph (>70% of at-w), represented only 23.2% of the samples and were most frequent in spring (during a phytoplankton bloom) (e.g., AQ2, area A and E) and early spring (AQ4, areas B and D) and had the lowest ag contribution. Case 2 waters (Figure 4) were much more frequent, representing 76.8% of the samples within the WIC; of that, 64% were dominated by aph + ag, 8% by ag, 2.4% by aph + ad, and 2.4% by all three biogenic absorption components. In approximately 58% of the samples, aph contributed between 50 and 70% of the biogenic absorption, mostly during the spring (AQ2) and early spring (AQ4) campaigns. A greater dominance of the CDOM component (38% of samples) was mainly observed during the autumn campaign (AQ3, e.g., area E). The detritus component had a higher contribution (>50%) during the early spring campaign (AQ4), especially in the northern–central WIC (areas B and C).

3.2. Temporal and Spatial Variation of Bio-Optical Properties

The phytoplankton absorption coefficient (aph 443 nm, Figure 5), phytoplankton-specific absorption (a*ph, 443 nm, Figure S4), and Chla ranged from 0.01 to 0.35 m−1, 0.03 to 0.017 m2 mg−1, and 0.10 to 9.38 mg m−3, respectively (Table S1 and Figure S1), within all campaigns. The spring campaign (AQ2), sampled during a weakening upwelling event, was significantly different (p-value < 0.05) from the other campaigns regarding the aph and Chla, associated with a phytoplankton bloom [22]. These differences in aph and Chla were particularly pronounced in areas A, D (next to Cape Carvoeiro), and E, where the highest values were registered (>0.19 m−1 and >4 mg m−3, respectively; Table S1, Figure 5 and Figure S1), concurring with the lowest a*ph values (<0.04 m2 mg−1, e.g., area E, Figure S4). In this period (AQ2) and areas (A, D and E) characterized by enhanced productivity, Pheo values were also higher (>0.4 mg m−3, Table S1), but still representing less than 30% of TChla. In autumn (AQ3) and early spring (AQ4), the maximum of aph, a*ph, Chla, and Pheo did not surpass 0.13 m−1, 0.14 m2 mg−1, 3.34 mg m−3, and 0.31 mg m−3, respectively, excluding only one station in area E (AQ3), where Pheo registered 1.53 mg m−3 (Table S1). This area in the southern WIC (E) had, in contrast, the lowest values of Chla (<1.36 mg m−3) and aph (<0.82 m−1), which were associated with a higher sea surface temperature (AQ3) or higher salinity (AQ4) (Figures S2 and S5I,II). The proportion of Pheo in relation to Chla was greater than ~30% in a few sample stations (N = 6), especially in autumn (Figure S5IV, e.g., AQ3 area E), however, no significant differences were observed between Chla and TChla when considering all sampling data (N = 122).
The detritus’ absorption (ad, m−1) varied between 0.0004 and 0.194 m−1 (Table 1; Figure 5 and Figure S1). The ad was higher near the coastline, displaying a positive correlation (Figure S2) with several parameters related to the OACs during the spring (AQ2) and autumn (AQ3) campaigns. However, during the early spring (AQ4), ad was significantly different, with high values (0.194 and 0.124 m−1) in areas B and C. During this campaign in particular (AQ4), the correlation between ad and turbidity became stronger. On the other hand, a reduction in the correlation power between ad and phytoplankton was observed, except for in area D.
The absorption coefficient of the CDOM (ag m−1, Table 1; Figure 5 and Figure S1) ranged from 0.008 to 0.127 m−1. The average values of ag were similar between the spring (AQ2) and autumn (AQ3) campaigns, with a higher ag (>0.09 m−1) in area E, especially during autumn. The ag (Figure 5) sampled during the strong upwelling in early spring (AQ4), was significantly different from the other campaigns, which showed a much lower ag (<0.04 m−1), especially in areas B, D, and E. This contrasts with the highest turbidity and DIN values also recorded in this campaign (AQ4) (northern areas) and the lowest salinities in area B, near the Mondego estuary (Figure S1 and Table S1).

3.3. Relationships between Biogeochemical Components and Bio-Optical Properties

The aph coefficients tended to increase (and the a*ph coefficients tended to decrease, Figure S5V–VIII) with increasing Chla (or TChla) in a power law function. For wavelengths from λ = 400 to 700 nm, new regional coefficients (named RG) were calculated using the relationship between in situ Chla and aph (λ) for the coastal waters of Portugal (N = 122). As an example, Figure 6 presents the relationship between Chla and aph for the specific wavelength of 443 nm. The relationship obtained herein was closer to that reported in B04 [58] and L10 [56] than in B98 [50] and B10 [42] (Figure 6 and Figure S6). This could be related to an overestimation of the Chla by the fluorimetric measurements included in the B98 and [51] global fits, as discussed by [42]. Inverting the relation, the aph (443 nm) vs. Chla derived from our dataset (Figure 6II, Table S2) was closer to the relation used in the Algal 2 (A2) algorithm for the North Sea [59,60] than the regional relation obtained by S15 [52] for the WIC. Both relations, that between Chla vs. aph (443 nm) and vice versa (Table S2), show a better agreement in the spring (AQ2) and autumn campaigns (AQ3) compared to the early spring campaign (AQ4). The highest errors were, in general, related to stations with a higher a*ph (e.g., area D in AQ2) and a higher proportion of Pheo in relation to Chla (>30%).
Despite the slightly stronger correlation between ad and Chla during spring (AQ2) (R2 = 0.42, Table S3), most samples were scattered and, in general, positioned below the fit obtained by B10 for oceanic waters (Figure 7I and Table S3, except some samples in AQ4). The relationship between ad and turbidity (FTU) was described through a power law equation (Figure 7II) which showed a high covariation (R2 = 0.92), with higher deviations related to lower ad values, especially in the autumn (AQ3) campaign (Table S3). Figure S7 shows a negative relationship between ad and temperature, as well as a more scattered pattern with salinity. The spectral slope Sd (nm−1) had a relatively strong negative relation with ad (Figure 7IV), with higher deviations in some stations with lower ad (<~0.005 m−1).
In general, CDOM’s relationships with the other parameters were very scattered (Figure 7 and Figure S8; Table S4), suggesting great variability in its origin and state, which is confirmed by its weak (τ < 0.3) and non-significant correlations with most parameters (Figure S2). Each campaign showed a different behaviour concerning ag variability. The ag was significantly correlated (Figure S2) with Chla, turbidity, and DC in spring (AQ2); with salinity, detritus, turbidity, Pheo, and DC in autumn (AQ3); and with only DIN in the early spring (AQ4). The Sg (nm−1) and Sdg (nm−1) had a strong negative relation with ag and adg, respectively (Figure 7V,VI).

3.4. Evaluation of Semi-Analytical Approaches to Deriving Bio-Optical Properties from Ocean Colour

The Chla retrievals with OC5CCI and GSM algorithms were evaluated to determine the optimal input for the GIOP algorithm. In this study, the Chla retrieved with the empirical OC5CCI algorithm (Figure 8I, N = 53) yielded good statistical results (R2 = 0.77) which were superior to those obtained by the standard GSM (R2 = 0.50, Figure 8II), but still with some degree of underestimation for most cases (BIAS 0.87; Figure 8I). According to [54], a BIAS < 1.0 indicates underestimations.
The comparison between the in situ absorption coefficients (at, aph, and adg, N = 53) and their corresponding retrievals obtained by the standard semi-analytical algorithms QAA, GSM, and GIOP (with Chla OC5CCI as input) are presented in Figure 9. All standard semi-analytical algorithms underestimated the total absorption retrievals (at, BIAS ~ 0.69 to 0.75) and exhibited a mean absolute error (MAE) ranging from 1.45 to 1.53 (Figure 9I,IV,VII; Table S5).
The aph retrievals were even more underestimated (BIAS 0.41 to 0.66), especially for three cases in spring with highly underestimated values (AQ2, Figure 9II,V,VIII, green diamond—area D; Table S5). The GIOP algorithm, utilizing Chla retrievals from OC5CCI as its input, achieved the smallest underestimation in aph retrievals, yielding the best statistical outcomes (MAE = 1.63, R2 = 0.47, and S = 0.66). In contrast, the QAA and GSM’s (using B98 coefficients) retrievals exhibited substantial underestimations, with BIAS values of 0.41 and 0.52, respectively.
For the adg retrievals, on the other hand, the QAA yielded better results (R2 = 0.22 and slope of 0.94), especially due to its improved estimate of the highest adg value in early spring (AQ4, Figure 9III, blue cross—in area B, where only one station exhibited the highest ad values; Table S5). For all algorithm retrievals, including that of the QAA, significant underestimations were observed in cases with a higher ag contribution in autumn (AQ3, Figure 9III,VI,IX, the yellow ones mostly in area E). The adg statistical results for the GSM and GIOP algorithms (MAE = 1.7 and 1.66, BIAS = 0.86 and 0.83, R2 = 0.09 and 0.13, and both S = 0.46) were not significantly different.
Considering the results obtained with the standard GIOP algorithm for at and aph, the subsequent phase involved the use of the regional parameterization (RG) obtained for the power law relation between the in situ Chla and aph (λ) instead of the B98 coefficients for the aph estimation [49] (Figure S6).
As expected, the results obtained with the regional coefficients (GIOP-OC5CCI-RG, Figure 10) were better than the standard GIOP version in terms of the at and aph coefficients. This was mainly related to a significant improvement in the aph retrievals, which consequently led to an improvement mostly in the slope results for at (0.78). The adg retrievals from the GIOP’s regional version (Figure 10) were close to its standard results (Figure 9). The stations with the highest biases (3 for aph and 7 for adg) remained with high underestimations, even for the GIOP-RG.

4. Discussion

4.1. Case 1 vs. Case 2 Waters

The Western Iberian Coast (WIC), located in an Eastern Boundary Upwelling System (EBUS), is characterized by dynamic coastal upwelling, with interactions between oceanographic features (e.g., capes and canyons) and continental river runoff. The interaction of the oceanic water masses with freshwater inputs governs the spatial distributions of the temperature, salinity, and nutrients, which in turn influence the optical properties of the surface waters. In the WIC, salinity shows a clear north–south gradient, with the lowest values (<35) in the northern region (e.g., areas A, B, and C) more influenced by continental runoff compared to the southern region (this study, [19,26,61]). Sea surface salinity, temperature, and the distance from the coastlines had weak but significant correlations (<0.4) with the OACs, denoting the high variability in the OACs’ distribution at each coastal site and between different seasons.
The spring (AQ2) and early spring (AQ4) campaigns occurred during coastal upwelling events, but at different stages; the first at the end of this event, with a phytoplankton bloom on course, and the second in the initial phase, with a lower phytoplankton biomass but high nutrients [22], and a significant increase in turbidity and detritus, especially in the northern region of the WIC. Both the spring and early spring campaigns thus had the highest at-w values recorded, but with different contributions from OACs. For the spring campaign, aph (and Chla) had a high correlation with ad, denoting the main autochthonous source of the detritus, which was tightly linked to the phytoplankton bloom. The early spring campaign, on the other hand, had a lower aph contribution and higher ad contribution to at-w, which covariates with turbidity but was not significant with Chla. Hence, the non-algal particles in this case were not only regulated by the phytoplankton community (its growth and decay) but also associated with external sources linked to other coastal processes, such as seasonal sedimentary dynamics. This is similar to the observations made by [62] for coastal waters in the Eastern English Channel. Higher coastal water turbidity in the WIC was also observed by [63] in the winter and early spring months, associated with more intense wave action, resuspending bottom sediments, especially across the wider northern shelf (during winter) added to initiating coastal upwelling events in the early spring, as sampled during AQ4. Moreover, [64] has previously reported the importance of internal waves in the resuspension of sediments and bottom currents near the Nazaré Canyon (next to area C). Winter is also the rainy season in Portugal [19], and river runoff was also likely a source of the higher ad and turbidity values observed, especially at the coastal stations nearest to Porto city (area A), the Mondego River (area B), and Cape Carvoeiro (area C), during the following early spring season (AQ4). In fact, [65] identified seasonal variations in water type classification using satellite imagery. During winter and spring, the waters of the WIC were predominantly classified as Case 2 waters (complex waters), which exhibited higher CDOM per Chla ratios compared to typical Case 1 waters. Case 1 waters were primarily observed in the southern and offshore regions during the autumn and summer seasons. In our case, due to the phytoplankton bloom, most Case 1 waters were found in the spring campaign. Sá [65] attributed the higher CDOM in Case 2 waters to biogenic material resulting from the degradation of phytoplankton blooms in spring and from riverine inputs in winter.
The autumn campaign had lower surface water turbidity, but similar at-w values compared to the early spring, in most stations. In this case, CDOM together with phytoplankton were the dominant optical constituents contributing to at-w. CDOM, however, had no correlation with Chla, especially during the autumn and early spring campaigns. Only the spring campaign showed some correlation between CDOM and Chla (0.3), which coincided with a phytoplankton bloom. Sá [65] reported a higher dominance of CDOM during the spring season in the Nazaré Canyon area, though the mean phytoplankton absorption value was lower than that observed in our study for the same period (0.033 m−1 and 0.098 m−1, respectively). In our case, we also found a higher CDOM contribution in the southern WIC (area E), which is characterized by a lower contribution of river runoff and a narrower shelf [19]. Besides the contribution of continental runoff to the coastal waters of the WIC, another possible source that may explain the higher CDOM absorption and its relative contribution to at-w during the autumn campaign may be the degradation products released during the decay of phytoplankton blooms associated with coastal upwelling events. Hence, even if they are produced by autochthonous sources, the possible lag between phytoplankton growth and CDOM production, especially during and post-bloom decay phase, could maybe explain the temporal disconnection between CDOM and Chla in highly dynamic coastal areas such as the WIC. In fact, the stations with the highest CDOM absorption contributions had also higher contributions of Chla degradation products, i.e., Pheo. Less CDOM photobleaching processes, associated with the lower incident solar irradiance during the autumn months, may also partly contribute to the higher CDOM contribution in this season. Unfortunately, in this study, it was not possible to further investigate the possible sources of CDOM due to limited spectral ag information and auxiliary data. Further studies using more spectrally resolved ag (220–700 nm) [66] and carbon pool measurements are encouraged to verify the sources of CDOM in the WIC, as well as their spatial and temporal variability.
Following [57]’s optical classification scheme, the majority (74%) of the samples collected during this study in the coastal waters of Portugal were classified as Case 2 waters (Case 1 corresponded to 23.2%), and most of the samples were dominated by aph + ag. The autumn and early spring seasons, under non-bloom conditions, are especially characterized by more complex Case 2 optical water types, with higher detritus and CDOM contributions to the at-w. The present results are consistent with the findings obtained by [65] for similar areas of the Portuguese coast and those of [67] in the Sagres region (the west area, E), which identified a majority of aph optically dominated waters, but also with an important contribution of ag, varying between 33 and 60% of at-w during bloom and non-bloom conditions, respectively.

4.2. Temporal and Spatial Variation of Bio-Optical Properties

As discussed in the previous section, the WIC presents high temporal and spatial bio-optical variability, regulated by highly dynamic coastal processes and some regional site-specific characteristics. Chla and aph had high spatial variability, especially during the spring campaign (AQ2), which occurred during the end of a strong upwelling event [22]. Phytoplankton blooms (e.g., Chla > ~5 mg m−3, see [22]), dominated by microphytoplankton groups (diatoms and dinoflagellates, [68]), in response to coastal upwelling events (e.g., AQ2) are a common feature in the spring and summer months (April to September), along the west coast of Portugal, especially in the northern region [19,67,68,69,70,71], as well as around the Carvoeiro and Sagres capes (areas D and E, respectively), as shown in the present study. The a*ph spectra were mostly flattened during the spring and had lower values, especially at the stations with the highest Chla (areas A and E). These areas also had high concentrations of fucoxanthin and peridinin (unpublished data), suggesting the dominance of phytoplankton groups with larger cells (e.g., diatoms and dinoflagellates), with a higher packaging effect [72]. The overall power law relation between aph (443) and Chla, and the negative relation between a*ph (443) and Chla, denotes the effects of intracellular pigment self-shading and the increase in accessory pigments observed in other studies [58].
Moita [69] examined the temporal and spatial variations of phytoplankton assemblages in the WIC and observed that phytoplankton’s biomass and diversity varied seasonally and spatially in response to the dominant oceanographic processes, with diatoms being the dominant group during spring and early summer, when northerly winds and upwelling conditions were prevalent, followed by dinoflagellates during late summer and autumn, when more stratified conditions in the water column developed. The study reported high concentrations of Chla during the upwelling season in the WIC, with Chla concentrations reaching up to 6 mg m−3. Goela et al. [67] also investigated the contribution of phytoplankton to the optical properties of the southwest coast of Portugal and found that the a*ph varied according to the taxonomic composition of the phytoplankton assemblages, with diatoms having a lower a*ph than other phytoplankton groups. The authors also reported a negative correlation between a*ph and Chla, with the highest values of Chla seen during the upwelling season in the WIC, as observed in this study.
Brito et al. [17], on the other hand, reported a high specific absorption coefficient (an a*ph up to 0.17 m2 mg−1) associated with pico/nanophytoplankton cells during the summer months (August–September) in the western and southern coastal waters of Portugal (e.g., areas B, D, and E). A high a*ph (up to 0.17 m2 mg−1) was also observed in the present study in some offshore stations during the spring campaign (AQ2, at areas B and D), which may indicate a low packing effect associated with the dominance of smaller picophytoplankton cells [42]. This is supported by the higher presence of photoprotective pigments such as alloxanthin and zeaxanthin in these areas (unpublished data), suggesting the presence of cryptophytes (offshore of area D) and cyanobacteria (offshore of area B). In general, the a*ph values obtained in our study (except the highest values in areas B and D in AQ2) are close to the range of coefficients reported by [16] (0.02 to 0.12 m2 mg−1 at 440 nm) for the Sagres cape (area E). Further analysis of a*ph variability and phytoplankton composition will be part of future work.
The early spring season was characterized by lower phytoplankton absorption and Chla and higher detritus absorption, which was correlated to turbidity, suggesting the contribution of other sources rather than just phytoplankton degradation products, such as continental runoff, the bottom resuspension of sediments, and strong upwelling, as discussed in the previous section. CDOM absorption was higher in the autumn season along most of the inner shore stations within the WIC, which is probably attributed to post-bloom degradation products, in addition to continental runoff and resuspension, as previously discussed.

4.3. Relationships between Biogeochemical Components and Bio-Optical Properties

The relationship between aph (443 nm) and Chla (and TChla) obtained in the present study (N = 122) was similar to that found by [58] and [56] for global oceanic and coastal waters. Some minor deviations are likely attributed to local and regional phytoplankton species and ecophysiological conditions, with different proportions of photosynthetic and photoprotective pigments and packaging effects. The global relation proposed by Bricaud et al. [50,51] was somewhat offset, as also noticed by Bricaud et al. [42,58], who discussed the major differences as being related to the fluorimetric Chla measurements which composed most of the previous global datasets, instead using only HPLC. This has important implications for ocean colour retrievals since standard default versions of the GIOP semi-analytical model are still presented with Bricaud et al.’s [50,51] global fit to derive the aph* eigenvectors. Our results contrast with the findings obtained by [41] using a dataset from the Atlantic Ocean and the Mediterranean Sea, where a better agreement was obtained with [51]. In addition to the regional variability of the phytoplankton communities in coastal waters, regional departures from the average global parameterization are expected even for Case 1 waters, as discussed by [50,51], but they may occur more often in coastal waters [41].
The relationship between the aph (443 nm) and Chla derived from our dataset was also close to the relation used in the Algal 2 algorithm derived from the MERMAID dataset (Meris Matchup in situ Database [60]). The regional relation found by [52,65] for the coastal waters of Portugal, sampled during the beginning of the spring season (30 March to 12 April 2011), was closer to the relation found in the autumn (AQ3) campaign in our study, probably due to the lower aph (443 nm, <0.1 m−1) and Chla (<2 mg m−3) of both datasets. Higher deviations in the aph (443) and Chla (and TChla) relationships were observed for the early spring campaign (AQ4), likely due to changes in the phytoplankton assemblage [41,42].
The large variability observed around the ag (443) versus Chla relationships is a common feature [73,74]. Even in the open ocean, the part of the variance in ag explained by algal biomass is generally rather low (e.g., [40,75]). CDOM exhibits significant variability due to biological processes (e.g., microbial and planktonic), photobleaching, inputs of CDOM, and nutrients from deep waters through vertical mixing, upwelling, or terrestrial sources. Regarding biological processes, this can also be attributed to the temporal decoupling between CDOM production and algal biomass growth [74], as previously discussed. Therefore, the CDOM’s quantity may be reflecting the biological productivity of a previous bloom event, since CDOM tends to be a long-lived product of phytoplankton degradation. When the origin of CDOM is not local, for example, from the degradation of phytoplankton cells and other organic particles [76], it can be used as an indicator of the freshwater input into the system and riverine/estuarine discharge [77], as well as indicating sediment resuspension events in coastal waters. However, due to the non-significant (AQ2 and AQ4) or non-strong (AQ3) correlation between CDOM and salinity, this may not be the most of case for the WIC.
Regarding the relationship between ad and Chla, despite its scattered pattern, a better correlation (R2 = 0.42) was achieved only during the period of higher phytoplankton biomass (AQ2), which closely resembled the relationship found by [42]. Nonetheless, regardless of the sampled period, turbidity displayed a strong correlation with detritus, suggesting its potential utility for the satellite-based estimation of detritus from turbidity data for the coastal waters of Portugal.

4.4. Semi-Analytical Approaches to Deriving Bio-Optical Properties from Ocean Colour

The Chla concentration estimated through the empirical OC5CCI algorithm [9] from OC-CCI data yielded better results than semi-analytical algorithms (GSM) for the WIC in the North Atlantic. The OC5CCI is an empirical approach adapted specifically to retrieving Chla in coastal waters under the influence of suspended sediments from different sources [78], such as the WIC, and it proved to be a reasonable approach, at least for most cases. Sá et al. [52] also found that empirical algorithms adapted to coastal waters perform better than standard global approaches (e.g., OC4, [79]) within the WIC.
Nonetheless, the retrieval of a bulk set of IOPs using semi-analytical algorithms remains a challenge. The new regional coefficients (RG) from the in situ relation of Chla and aph, used in the GIOP algorithm (GIOP-OC5CCI-RG) instead of the B98 coefficients, helped to improve the aph and at retrievals. Further improved results for phytoplankton absorption could be achieved using empirical relationships by directly applying the RG coefficients over Chla OC5CCI (aph RG-OC5CCI, Figure 11), compared to the semi-analytical algorithms, due to the additional uncertainty introduced by partitioning at (443 nm) into its aw, aph, and adg contributions [55]. Nevertheless, empirical algorithms still do not resolve complex cases, such as variations in the average aph vs. Chla relation, with higher aph* values seen for three stations in AQ2 (area D), which caused aph to have a higher underestimation for all approaches tested. Such variations may be linked to site-specific changes in the phytoplankton assemblage, as well as photoadaptation processes. Other factors that depart from average behaviours, such as one case in area B during spring (AQ2), which had a high overestimation, may be associated with higher turbidity, as empirical approaches tend to fail even with the OC5, which aims to determine the Chla and suspended sediment in more complex coastal waters.
The QAA exhibited good results for higher ad values, as expected in optically complex waters [80,81]. However, this algorithm, as well as the others tested, was not able to improve its estimates in the presence of high concentrations of CDOM. In the case of the GIOP, the default Sdg used to estimate the adg is a fixed value of 0.018 m−1, higher than the average 0.014 m−1 found in the present study. Nonetheless, recent works have shown that the uncertainties in this algorithm have been more closely linked to the low performance in estimating the bbp slope (η) [55]. Despite the fact that the GIOP algorithm uses the QAA method to estimate the bbp spectral slope (band ratio Rrs 443 nm/Rrs 560 nm, step 4, as described in [48]), a low correlation (R2 = 0.12) between this band ratio and turbidity (commonly related to bbp and η) was observed in this study. While GIOP and GSM are more suitable for Case 1 waters, they could eventually yield better results with regionalized parametrizations [82]. Considering the greater flexibility of the GIOP in applying different parameterization methods, it could be a strong candidate for regional parameterizations to improve algorithm performance in coastal environments. However, a robust database for coastal waters is still necessary to support these modifications [49,83].
Another source of uncertainty that was not analyzed in the present work due to the absence of in situ radiometric data, but which also affects the performance of bio-optical retrievals, is the accuracy of the satellite’s CCI Rrs product. This product aggregates the Rrs from different sensors, including OLCI, VIIRS, and MODIS, for our study period, using the Polymer (v4.12) atmospheric correction. It is, however, known that atmospheric correction is challenging, especially in coastal environments, which have continental aerosols, optically complex waters, and continental adjacency effects. Several works have been dedicated to evaluating the accuracy of satellite Rrs products, including the CCI project [9], but this is an ongoing and continuous effort which needs to be included in future works within the WIC and elsewhere.
It is evident that the continuous adaptation and validation of these algorithms are necessary to ensure accuracy in coastal waters [49]. The development of regional parameterizations and the improvement of calibration and atmospheric correction procedures are fundamental steps to enhancing the accuracy of the inherent optical property (IOP) estimates for coastal waters provided by the QAA, GSM, and GIOP algorithms [84,85,86,87,88].

5. Conclusions

This study provided a comprehensive overview of the optical component variability in the WIC, representing an unprecedented investigation for this region, covering the entire coast and different seasons, including partitioned biogenic absorption coefficients and biogeochemical properties. Significant seasonal variability in bio-optical properties i.e., phytoplankton (Chla), detritus, and CDOM absorption, was found due to factors associated with the changes in environmental conditions (e.g., upwelling and bottom resuspension) at each site. Furthermore, based on this robust in situ dataset, empirical relationships were established and are provided herein. This is a valuable contribution to the development of ocean colour algorithms. An overall validation was conducted using multi-sensor OC-CCI products for the estimation of absorption coefficients and Chla in the WIC, involving a direct comparison between in situ reference measurements and retrievals from standard and regionally parametrized semi-analytical algorithms. A set of relevant outcomes and conclusions were obtained:
  • A strong power law relation between turbidity and detritus suggests the potential for using satellite-based turbidity data to estimate detritus in coastal waters.
  • In terms of the performance and limitations of algorithms, semi-analytical algorithms (QAA, GSM, GIOP) tended to underestimate the absorption coefficients, a common issue in coastal waters.
  • The WIC regional coefficients (RG), derived from the relationship between in situ Chla and aph, improved the results of the semi-analytical algorithm GIOP for aph (λ). Additionally, the RG coefficients improved the empirical results when applied directly to Chla values obtained from the OC5CCI algorithm.
  • These observations highlight the importance of regional-specific studies and the development of tailored algorithms to improve the accuracy of ocean colour remote sensing in diverse and dynamic coastal environments, especially for the analysis of the phytoplankton community’s composition.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/rs16183440/s1.

Author Contributions

Conceptualization, L.F., N.R. and A.C.B.; methodology, L.F., N.R. and A.C.B.; software, L.F.; validation, L.F.; formal analysis, L.F.; investigation, L.F.; resources, L.F., V.B., C.P. and A.C.B.; data curation, L.F. and A.T.; writing—original draft preparation, L.F., N.R. and A.C.B.; writing—review and editing, L.F., N.R., V.B., C.S., A.T., C.P. and A.C.B.; visualization, L.F., N.R. and A.C.B.; supervision, A.C.B., V.B. and N.R.; project administration, C.P. and A.C.B.; funding acquisition, C.P. and A.C.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the AQUIMAR-Marine knowledge supporting aquaculture Project through the Operational Programme MAR2020 (MAR-02.01.01-FEAMP-0107) and by the European Union’s Horizon 2020 Research and Innovation Programme under grant agreement N 810139: Project Portugal Twinning for Innovation and Excellence in Marine Science and Earth Observation–PORTWIMS. This work benefited from the Infrastructure CoastNet—Portuguese Coastal Monitoring Network (http://geoportal.coastnet.pt, accessed on 7 August 2024), funded by the Foundation for Science and Technology (FCT) and the European Regional Development Fund (FEDER) through LISBOA2020 and ALENTEJO2020 regional operational programmes, in the framework of the National Roadmap of Research Infrastructures of strategic relevance (PINFRA/22128/2016). This study received further support from the FCT (https://doi.org/10.54499/UIDB/04292/2020, accessed on 5 August 2024, https://doi.org/10.54499/UIDB/00006/2020, accessed on 7 August 2024) awarded to the MARE-Marine and Environmental Sciences Centre through the Associate Laboratory ARNET (https://doi.org/10.54499/LA/P/0069/2020, accessed on 7 August 2024). L.F. received support from the National Council for Scientific and Technological Development (CNPq) Brazil (200589/2019-9). A.C.B. was also partially funded by the Scientific Stimulus Programme (CEECIND/00095/2017) of the FCT.

Data Availability Statement

The data presented in this study, collected under the scope of the AQUIMAR project (https://aquimar.hidrografico.pt/, accessed on 7 August 2024), are described in the SeaDataNet database of Pan-European infrastructure for ocean and marine data management at https://www.seadatanet.org/Metadata/CSR-Cruises (accessed on 7 August 2024), reference numbers 21025541, 21025539, 21025536, and 21025538. Access to the database is subject to request.

Acknowledgments

The authors are also indebted to the ESA Ocean Colour-Climate Change Initiative (OC-CCI) project (https://climate.esa.int/en/projects/ocean-colour and https://www.oceancolour.org, accessed on 5 August 2024).

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Location of in situ sampling stations (black dots, N = 125) and their matches with OC-CCI data (red circle, N = 53) in the five regions (A, B, C, D, and E). The AQ2 campaign was carried out in April/May 2019 (spring), AQ3 in October 2019 (autumn), and AQ4 in February/March 2020 (early spring). The main capes (Carvoeiro, Espichel, Sines, and São Vicente-Sagres; black lines) and the main points of freshwater entrance (from north to south: Minho, Lima, Ave, Douro, Ria de Aveiro, Mondego, Tagus, Sado, Mira, Odiáxere, Arade, Quarteira, Ria Formosa, Gilão, and Guadiana; blue dots) are identified on the map. Isobaths of 100, 200, and 1000 m (m) were obtained from GEBCO [25].
Figure 1. Location of in situ sampling stations (black dots, N = 125) and their matches with OC-CCI data (red circle, N = 53) in the five regions (A, B, C, D, and E). The AQ2 campaign was carried out in April/May 2019 (spring), AQ3 in October 2019 (autumn), and AQ4 in February/March 2020 (early spring). The main capes (Carvoeiro, Espichel, Sines, and São Vicente-Sagres; black lines) and the main points of freshwater entrance (from north to south: Minho, Lima, Ave, Douro, Ria de Aveiro, Mondego, Tagus, Sado, Mira, Odiáxere, Arade, Quarteira, Ria Formosa, Gilão, and Guadiana; blue dots) are identified on the map. Isobaths of 100, 200, and 1000 m (m) were obtained from GEBCO [25].
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Figure 2. Schematic representation of the satellite data processing routine implemented to derive Chla concentrations and bio-optical properties (aph and adg).
Figure 2. Schematic representation of the satellite data processing routine implemented to derive Chla concentrations and bio-optical properties (aph and adg).
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Figure 3. Distribution map of the total in situ absorption coefficients (at-w m−1, without the sum of water absorption, N = 125) at wavelength (λ) 443 nm and their respective spectra (λ = 350 to 700 nm) by area (A to E) and oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 3. Distribution map of the total in situ absorption coefficients (at-w m−1, without the sum of water absorption, N = 125) at wavelength (λ) 443 nm and their respective spectra (λ = 350 to 700 nm) by area (A to E) and oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Figure 4. Triangular diagram (I to V) representing the contribution of the in situ absorption coefficients of phytoplankton (aph at 443 nm, m−1), non-algal particles (NAPs, at 443 nm, m−1), and coloured dissolved organic matter (CDOM, ag at 443 nm, m−1) by sampled area (A to E) and oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring). The bar graph (VI) shows the percentage (%) number of samples by area and campaign for each type of water [57], named according to the contribution of their components: aph + ag, aph, ag, aph + ad, and aph + ag + ad.
Figure 4. Triangular diagram (I to V) representing the contribution of the in situ absorption coefficients of phytoplankton (aph at 443 nm, m−1), non-algal particles (NAPs, at 443 nm, m−1), and coloured dissolved organic matter (CDOM, ag at 443 nm, m−1) by sampled area (A to E) and oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring). The bar graph (VI) shows the percentage (%) number of samples by area and campaign for each type of water [57], named according to the contribution of their components: aph + ag, aph, ag, aph + ad, and aph + ag + ad.
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Figure 5. Spatial variation of phytoplankton absorption coefficient (aph, m−1), non-algal particles or detritus (ad, m−1), and CDOM (ag, m−1), at wavelength (λ) 443 nm and their respective spectra (λ = 350 to 700 nm) by area (A to E) and oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 5. Spatial variation of phytoplankton absorption coefficient (aph, m−1), non-algal particles or detritus (ad, m−1), and CDOM (ag, m−1), at wavelength (λ) 443 nm and their respective spectra (λ = 350 to 700 nm) by area (A to E) and oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Figure 6. (I) Relationships between the in situ Chla (mg m−3) and phytoplankton absorption coefficient (aph at 443 nm, m−1) obtained by fitting a power law function (“Fit”, with coefficients “a” and “b”, r-squared: R2, and the number of samples: N). The relationship between Chla and aph was compared to the results obtained by Bricaud et al. [42,50,58] (B98, B04, and B10, respectively) and Loisel et al. [56] (L10). (II) aph versus Chla, which was compared to the results obtained by Sá et al. [52] (S15) and the Algal 2 (A2) algorithm [60]. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 6. (I) Relationships between the in situ Chla (mg m−3) and phytoplankton absorption coefficient (aph at 443 nm, m−1) obtained by fitting a power law function (“Fit”, with coefficients “a” and “b”, r-squared: R2, and the number of samples: N). The relationship between Chla and aph was compared to the results obtained by Bricaud et al. [42,50,58] (B98, B04, and B10, respectively) and Loisel et al. [56] (L10). (II) aph versus Chla, which was compared to the results obtained by Sá et al. [52] (S15) and the Algal 2 (A2) algorithm [60]. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Figure 7. Relationships between (I) in situ absorption coefficient of non-algal particles (ad, m−1) and in situ Chla (mg m−3); (II) in situ absorption coefficient of non-algal particles (ad, m−1) and turbidity (Turb, FTU); (III) in situ absorption coefficient of coloured dissolved organic matter or gelbstoff (ag, m−1) and in situ Chla (mg m−3); (IV) spectral slope of detritus (Sd, nm−1) and the absorption coefficient of non-algal particles (ad, m−1); (V) spectral slope of CDOM (Sg, nm−1) and the absorption coefficient of CDOM (ag, m−1); and (VI) spectral slope of detritus + CDOM (Sdg, nm−1) and the absorption coefficient of detritus + CDOM (adg, m−1). The fit curve was obtained by a power law function (“Fit”, with coefficients “a” and “b”, r-squared: R2, and number of samples: N). Comparisons with the curves obtained by B10 [42] are also presented. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 7. Relationships between (I) in situ absorption coefficient of non-algal particles (ad, m−1) and in situ Chla (mg m−3); (II) in situ absorption coefficient of non-algal particles (ad, m−1) and turbidity (Turb, FTU); (III) in situ absorption coefficient of coloured dissolved organic matter or gelbstoff (ag, m−1) and in situ Chla (mg m−3); (IV) spectral slope of detritus (Sd, nm−1) and the absorption coefficient of non-algal particles (ad, m−1); (V) spectral slope of CDOM (Sg, nm−1) and the absorption coefficient of CDOM (ag, m−1); and (VI) spectral slope of detritus + CDOM (Sdg, nm−1) and the absorption coefficient of detritus + CDOM (adg, m−1). The fit curve was obtained by a power law function (“Fit”, with coefficients “a” and “b”, r-squared: R2, and number of samples: N). Comparisons with the curves obtained by B10 [42] are also presented. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Figure 8. Comparison between in situ Chla (mg m−3) and its corresponding retrievals using the (I) OC5CCI algorithm (OC-CCI) [9] and (II) Garver–Siegel–Maritorena—the GSM algorithm [57]. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 8. Comparison between in situ Chla (mg m−3) and its corresponding retrievals using the (I) OC5CCI algorithm (OC-CCI) [9] and (II) Garver–Siegel–Maritorena—the GSM algorithm [57]. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Figure 9. Comparison between in situ absorption coefficients (at, aph, and adg at 443 nm, m−1) and their corresponding retrievals, obtained by default algorithms—the QAA from OC-CCI v5 ((I)–(III)), GSM ((IV)–(VI)), and GIOP—using Chla OC5CCI retrievals as their input (GIOP-OC5CCI; VIIIX). The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 9. Comparison between in situ absorption coefficients (at, aph, and adg at 443 nm, m−1) and their corresponding retrievals, obtained by default algorithms—the QAA from OC-CCI v5 ((I)–(III)), GSM ((IV)–(VI)), and GIOP—using Chla OC5CCI retrievals as their input (GIOP-OC5CCI; VIIIX). The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Figure 10. Comparison between in situ absorption coefficients (at, aph, and adg at 443 nm, m−1) (IIII) and the GIOP, with Chla OC5CCI retrievals as the input and using the RG coefficients (regional, Figure S5), namely the GIOP-OC5CCI-RG. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 10. Comparison between in situ absorption coefficients (at, aph, and adg at 443 nm, m−1) (IIII) and the GIOP, with Chla OC5CCI retrievals as the input and using the RG coefficients (regional, Figure S5), namely the GIOP-OC5CCI-RG. The symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Figure 11. Comparison between in situ aph at 443 nm (m−1) and the retrievals from the OC5CCI using the RG coefficients at 443 nm (Chla vs. aph). The dotted line is the 1:1 line, symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
Figure 11. Comparison between in situ aph at 443 nm (m−1) and the retrievals from the OC5CCI using the RG coefficients at 443 nm (Chla vs. aph). The dotted line is the 1:1 line, symbols correspond to different sampled areas (A to E), with different colours representing each oceanographic campaign (AQ2—spring, AQ3—autumn, and AQ4—early spring).
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Table 1. Details and number (N) of bio-optical (absorption) samples collected during the oceanographic campaigns of AQUIMAR (AQ1 to AQ4) in five areas (A, B, C, D and E).
Table 1. Details and number (N) of bio-optical (absorption) samples collected during the oceanographic campaigns of AQUIMAR (AQ1 to AQ4) in five areas (A, B, C, D and E).
Autumn (AQ1)
October 2018
Spring (AQ2)
April/May 2019
Autumn (AQ3)
October 2019
Early Spring (AQ4)
February/March 2020
No absorption dataAreaStart dateEnd dateNAreaStart dateEnd dateNAreaStart dateEnd dateN
E18/0422/0411E10/1013/1011C24/0225/026
D29/0430/049B21/1023/109D27/0228/029
B02/0505/059A24/1026/109E29/0202/0310
A05/0506/056C28/1029/107B10/0315/037
C11/0512/056D30/1031/109A17/0319/037
Total18/0412/0541Total10/1031/1045Total24/0219/0339
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Favareto, L.; Rudorff, N.; Brotas, V.; Tracana, A.; Sá, C.; Palma, C.; Brito, A.C. Bio-Optical Properties and Ocean Colour Satellite Retrieval along the Coastal Waters of the Western Iberian Coast (WIC). Remote Sens. 2024, 16, 3440. https://doi.org/10.3390/rs16183440

AMA Style

Favareto L, Rudorff N, Brotas V, Tracana A, Sá C, Palma C, Brito AC. Bio-Optical Properties and Ocean Colour Satellite Retrieval along the Coastal Waters of the Western Iberian Coast (WIC). Remote Sensing. 2024; 16(18):3440. https://doi.org/10.3390/rs16183440

Chicago/Turabian Style

Favareto, Luciane, Natalia Rudorff, Vanda Brotas, Andreia Tracana, Carolina Sá, Carla Palma, and Ana C. Brito. 2024. "Bio-Optical Properties and Ocean Colour Satellite Retrieval along the Coastal Waters of the Western Iberian Coast (WIC)" Remote Sensing 16, no. 18: 3440. https://doi.org/10.3390/rs16183440

APA Style

Favareto, L., Rudorff, N., Brotas, V., Tracana, A., Sá, C., Palma, C., & Brito, A. C. (2024). Bio-Optical Properties and Ocean Colour Satellite Retrieval along the Coastal Waters of the Western Iberian Coast (WIC). Remote Sensing, 16(18), 3440. https://doi.org/10.3390/rs16183440

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