1. Introduction
Spatial patterns in landscapes play a critical role in shaping ecological processes by influencing key functions and providing ecosystem services such as nutrient cycling, energy flow, and biodiversity conservation [
1,
2,
3,
4,
5]. These patterns describe the spatial arrangement, composition, distribution, and configuration of different landscape elements. Understanding the relationships between landscape patterns and ecological processes remains a central challenge in landscape ecology, as these relationships are fundamental for the design and implementation of land use and land cover (LULC) strategies, particularly at the basin scale [
6,
7,
8,
9,
10].
Nutrient cycling is a process particularly sensitive to landscape configuration, especially the export of nutrients from terrestrial ecosystems to aquatic systems. In recent years, the study of landscape configuration and its effect on nutrient transport has gained importance [
11,
12,
13,
14,
15,
16,
17]. The interactions between landscape patterns and topographic features strongly influence runoff, retention, and nutrient delivery to streams [
18,
19,
20,
21]. Moreover, the size, shape, and spatial arrangement of landscape patches affect nutrient retention and mobilization, while LULC classes determine nutrient generation rates. As a result, ecosystem fragmentation and connectivity have major implications for water quality and ecosystem health [
22,
23,
24]. Given this complexity, contemporary analyses should not rely solely on basic LULC data but incorporate multidimensional landscape metrics that integrate information on LULC, soil properties, and topography [
11,
13]. Meng [
13] have highlighted that nitrogen (N) release is associated with landscape configuration in subtropical agricultural basins, where greater dispersion and heterogeneity, and lower shape complexity of landscape patches can increase N release at the watershed level. Similarly, Wu [
15] found that LULC configuration accounts for 23.4–32.2% of spatial variation in N and phosphorous (P) concentrations across different spatial scales, with hydrological regimes further modulating these effects [
15,
16].
However, structural landscape metrics alone may not fully capture functional connectivity, as similar patch arrangements can yield different ecological outcomes [
25]. For this reason, it is crucial to integrate structural information from landscape metrics with measurements of nutrient export. It is also necessary to assess which specific LULC classes and configurations exert the strongest influence on nutrient dynamics. Landscape metrics and indices, combined with controlled landscape experiments, are commonly used to investigate these relationships [
26,
27,
28]. In this context, the development of LULC scenarios allows for the controlled manipulation of spatial configurations, thereby facilitating a better understanding of their effects on ecosystem processes [
25].
Advances in computational tools have facilitated the rapid calculation of multiple landscape metrics [
29,
30], as well as the generation of controlled synthetic scenarios that allow for isolating and analyzing specific aspects of landscape structure [
31,
32,
33]. Combining these three approaches—LULC scenarios, landscape metrics, and nutrient export modeling—offers an effective framework to identify critical spatial patterns and generate evidence-based insights to support land use planning and decision-making.
The main objective of this study is to assess the influence of LULC spatial configuration on nutrient dynamics and export, particularly total phosphorus (TP) and total nitrogen (TN), in the Suquía River Basin (Argentina). This basin is representative of an environment that has been severely impacted by human activities and serves as an ideal setting for evaluating the effect of landscape metrics on nutrient pollution issues. Previous research has documented a clear spatial and temporal gradient of water quality deterioration, with pronounced eutrophication processes in the San Roque reservoir, the region’s main water body [
34,
35]. This degradation is driven by nutrient and contaminant loads from urban and agricultural sources, which are intrinsically linked to changes in land use and land cover [
36,
37]. The problem is further exacerbated by the presence of contaminants of emerging concern, including microplastics and pharmaceuticals, which have been detected in the water column, sediments, and even in the tissues of native fish, evidencing their bioavailability and potential ecotoxicological risk [
38,
39]. Compounding this complex situation is the issue of solid waste management in urban watercourses, which impacts the hydraulics and sustainability of the system [
40,
41]. In this study, we primarily focus on analyzing the current state of the Suquía River Basin as a baseline scenario, through the characterization of landscape ecology metrics at both the basin and LULC class levels to generate synthesized LULC scenarios to calculate nutrient export for TP and TN, evaluating different landscape configurations.
3. Results
3.1. The Baseline Scenario
Suquía River Basin serves as the baseline for the generation of synthetic LULC scenarios. The basin is described in terms of diverse metrics at the landscape and LULC class levels. The Suquía River Basin exhibits a highly fragmented configuration, with a high patch density (26.798 patches/100 ha) and edge density (81.221 m/ha). Nevertheless, LULC classes show strong structural cohesion (Patch Cohesion Index = 99.902) and a high level of aggregation (95.924), suggesting that despite their abundance, patches tend to remain clustered. The agriculture class dominates the landscape, covering 55%, containing the largest patch (38% of the landscape), which reduces evenness among LULC classes (Shannon’s Evenness Index = 0.658). Landscape diversity is moderate (Shannon’s Diversity Index = 1.281), with only seven LULC classes present. In terms of configuration, the landscape shows acceptable functional connectivity (Effective Mesh Size = 120,169 ha) and an intermediate level of contagion (61.73), with relatively simple patch shapes (average fractal dimension = 1.267). Overall, this is a highly modified system, where a dominant LULC type coexists with dispersed fragments of other LULC types.
The forest LULC class covers only 9.63% of the landscape. It is a highly fragmented class (26,390 number of patches) and has a high division index (Splitting Index = 2.491), although it maintains good structural cohesion (99.44%) and high aggregation (92.83%). The forest cores still have a considerable extent (average core area = 1.83 ha), but are very scattered. The patch shapes are slightly complex (fractal dimension = 1.382).
The grassland LULC class represents a significant proportion of the landscape (24.27%), but it is highly fragmented, with the highest patch density (6899 patches/100 ha) and a high edge density (53.082 m/ha). Although it shows good cohesion (99.92%) and aggregation (94.51%), the number of patches (45,871) and their separation (Splitting Index = 59.4) indicate a loss of ecological continuity. In addition, the grassland LULC class has somewhat complex shapes (fractal = 1.45) and a good proportion of the core area (19.72% of the landscape), which may reflect extensive livestock use or a mosaic with agriculture.
Agriculture is the dominant class of LULC, accounting for 54.67% of the total area and a highest patch index of 38.49%, revealing extensive and centralized land use. It is the class with the highest functional connectivity (effective mesh = 108,247 ha) and very high cohesion (99.98%). It shows a low level of fragmentation (12,308 patches), high aggregation (98.84%) and relatively simple shapes (fractal = 1.43).
Although it occupies a smaller proportion (4.33%), the urban LULC class presents high structural complexity. Its patches have irregular shapes (fractal = 1.53) and are strongly fragmented (Splitting Index = 1.46). Cohesion remains high (99.77%), suggesting that, although scattered, urbanization maintains some spatial continuity. The interspersion with other LULC classes is also high (interspersion and juxtaposition index = 84.69), indicating that the urban area is integrated into a mixed and possibly peri-urban landscape.
Bare soil and sparse vegetation LULC class covers only 2.41% of the landscape but is extremely fragmented (43,806 patches, splitting index = 2.76), with low cohesion (93.29%) and simple shapes (fractal = 1.51). Although its core is small (0.14 ha on average), its patches are numerous and scattered, which may correspond to degraded or transitional areas. Its low interconnection and marginal distribution reduce its ecological functionality.
Finally, the water bodies LULC class represents a minimal proportion of the landscape (0.36%) and is strongly cohesive (98.41%), with simple shapes (fractal = 1.35) and low fragmentation (splitting index = 201,819). Although structurally marginal, their high interconnection and strategic location may be relevant for ecological connectivity and the provision of key ecosystem services such as nutrient export.
An expanded list of landscape metrics can be found in
Appendix A for the baseline scenario. Class and landscape scope metrics are summarized in
Table A1 and
Table A2, respectively.
3.2. LULC Synthetic Scenarios
To represent a sufficiently broad range of landscape configurations to evaluate how spatial patterns influence nutrient delivery, 10 synthetic LULC scenarios were generated using the rflsgen R package, based on structural parameters derived from the Suquía River Basin’s actual LULC classes. To simulate the different scenarios, the original LULC classes were regrouped and the nutrient contributions were calculated with these new classes. These scenarios were designed to explore how changes in landscape configuration affect nutrient export while keeping LULC class composition constant, considering four LULC classes (forest, grassland, agriculture and urban). The resulting LULC scenarios (
Figure 2), Mean of patch area, Total area, Largest patch index, Percentage of landscape of class, Mean of core area, Landscape division index, Effective Mesh Size, Number of patches, Patch density, Splitting index, Modified Simpson’s diversity index, Patch Richness, Relative patch richness, Shannon’s diversity index, an dShannons’s evenness index, keep constant but vary in configuration metrics such as Mean fractal dimension index, Perimeter-Area Fractal Dimension, Mean perimeter–area ratio, Mean shape index, Mean of core area index, Aggregation index, Patch Cohesion Index, Normalized landscape shape index, Clumpiness index and Modified Simpson’s evenness index. This approach preserved class composition, but introduced variation in patch contiguity, adjacency, and shape complexity.
The grassland LULC class represents 16.7% of the landscape (PLAND) and is characterized by high fragmentation: it has the highest number of patches of the whole (NP = 106,352) and a very high patch density (PD = 15.99), indicating an extremely dispersed distribution over the territory. This fragmentation is reinforced by high values of the division index (DIVISION = 0.983) and a high SPLIT (58.2), reflecting that patches are subdivided into numerous low units. The average patch size is low (AREA = 1.05 ha), and the average core area (CORE = 0.91 ha) is also very low, indicating that most patches are edge-exposed. Despite this fragmentation, the effective mesh size values (MESH = 111.424 ha) suggest high structural connectivity, possibly due to a regular mosaic-like distribution, where patches are scattered but not isolated.
The forest LULC class represents 24% of the landscape, and appears fragmented and highly subdivided: with a high number of patches (NPs) and a high patch density (PD), this suggests that the forest appears highly dispersed in the landscape. This idea of fragmentation and patches spread over many low fragments is further reinforced by the high partitioning (DIVISION = 0.983) and a SPLIT of almost 60. The average patch size is low (AREA = 3.5) and core area also low (CORE), indicating that patches are small and exposed to the edge. With a moderate LPI (12.8), the largest patch occupies a significant portion of the landscape but is not dominant.
The agriculture LULC class is the dominant class in all scenarios, as it occupies more than 50% of the landscape (PLAND) and its largest patch (LPI = 38.5%) covers a wide proportion of the total. It shows low fragmentation, characterized by few patches (NPs), low patch density (PD) and a low SPLIT (6.14), which indicates aggregation. Large average patch size (29.5 ha) and large core (CORE = 27.9) suggest large and compact patches. High MESH and low DIVISION values indicate that it is well spatially connected.
The urban LULC class is shown to be a marginal but highly dispersed class: although it covers only 4.3% of the landscape, it has a very high number of patches (NPs) and a huge SPLIT (>1400), indicating a hyperdense and fragmented distribution. The DIVISION value (0.99) suggests that almost any urban cell is isolated from the others. The patch size (AREA = 1.88) and reduced core area (CORE) translates into a dispersed and not very compact urban structure, while a low LPI (2.6%) indicates the absence of a consolidated urban core.
Per class landscape metrics for the synthetic scenarios are shown in
Table A3. Landscape scope metrics, scenario-independent, are listed in
Table A4.
The landscape analysis at the basin level reveals a structure dominated by a large patch, reflected in a high LPI (38.49%), indicating that a single LULC class occupies more than one third of the total area (agriculture). In terms of diversity, the index values show moderate diversity. The Modified Simpson’s Diversity Index (MSIDI) reaches 0.948 and the Shannon Diversity Index (SHDI) 1.109, while the equity indices—MSIEI (0.684) and SHEI (0.8)—indicate that the LULC classes are present in balanced proportions, but with some predominance of one or two LULC classes. Finally, Patch Richness (PR) is 4, indicating the presence of four main LULC classes in the landscape, with a very low patch richness density (6.02 × ), suggesting a sparse distribution of LULC classes.
Class scope landscape metrics, scenario-dependent, were plotted in
Figure A1 as line plots. The change in landscape scope metrics, per scenario, are shown in
Figure A2.
3.3. Connectivity Assessment
Regarding functional connectivity, the assessment of the nutrient delivery ratio (NDR
i) across landscape classes reveals distinct patterns of functional connectivity for nutrient transport (
Figure 3). The agricultural class exhibits the highest potential for nutrient delivery, with the maximum NDR
i values. Forest and grassland classes show a significant but secondary role, with NDR
i values. Finally, the urban class, while occupying the smallest spatial extent (<5% of the basin area), displays a measurable NDR
i. The proportional distribution of NDR
i among classes is not directly linear to their areal extent, indicating that other factors beyond mere surface area govern functional connectivity for nutrients in the basin.
Otherwise, the contributions of TN and TP per LULC scenario and each LULC class are shown in
Figure 4, and the example maps trends in
Figure 5 and
Figure 6. The contribution of different LULC classes to nutrient transport exhibited a highly uneven pattern at the basin scale. For TN (
Figure 4a), agricultural areas accounted for most of the export across all scenarios, while grasslands and natural LULC contributed only marginal amounts. In the case of TP (
Figure 4b), urban and agricultural LULC represented the highest exports, although with a more balanced distribution compared to TN. When comparing nutrient export relative to LULC class area (
Figure 4c), agricultural and urban lands exported a disproportionately higher share than expected based on their extent, indicating high nutrient export intensity. In contrast, natural LULC classes contributed less than expected relative to their area (except for scenario 2), functioning as regulators of diffuse export. These findings show that nutrient export is not only determined by LULC extent, but by hydrological functionality and spatial interactions within the landscape.
The TN and TP aggregated sum for the whole basin, in 10
3 kg/year, is resumed in
Table 4. Scenarios 3, 5 and 10 presented the highest and lowest TN values, respectively. TP export presented the lowest value at scenarios 10 and 2, and the highest at scenario 3.
These minimum and maximum scenarios were selected to plot TN and TP in
Figure 5 and
Figure 6. N export maps, as shown in
Figure 5, showed a pattern with moderate variation between scenarios. The highest N export was observed under scenario 5, with a total basin load of 1087 (
kg/year). In contrast, scenario 10 showed the lowest nitrogen load with a total of 902 ×
kg/year, a reduction of 17% compared to scenario 5. Phosphorus export maps, as shown in
Figure 6, followed a similar trend. The lowest phosphorus load was associated with scenarios 2 and 10 (149 ×
kg/year), while the highest was associated with scenario 3 (184 ×
kg/year), representing a 19% reduction, while other scenarios resulted in intermediate phosphorus exports.
3.4. Correlation: Nutrient Contribution vs. Class Level Metric
Keeping constant structure metrics (area, core and aggregation types) and varying the shape metrics allows one to study the correlations between the latter and the export of TN and TP landscape and LULC class structures. Pearson’s correlations between nutrient contribution and landscape metric per LULC class are shown in
Table 5 and between parenthesis in this paragraph. In all cases, the correlation coefficient was statistically significant, with a 95% confidence interval. Several metrics of grassland LULC class show significant correlations with the TN and TP at basin and class levels. For TN export at the landscape level, strong negative correlations are observed with the COHESION (−0.78) and MESH (−0.72), while significant positive correlations are observed with DIVISION (0.62) and SPLIT (0.63). TP export at the landscape level also shows a strong negative correlation with COHESION (−0.81), MESH (−0.74) and LPI (−0.7), while it shows a positive correlation with DIVISION (0.64) and SPLIT (0.66). TN export at the Grassland class level shows a positive correlation with LPI (0.68) and NLSI (0.7). Finally, TP export at the Grassland class level shows a positive correlation with NLSI (0.68). In the case of forest LULC class, 2 class metrics show correlation (shown between parenthesis) with TN export at landscape level, CLUMPY (0.63) and PAFRAC (−0.64). Agriculture LULC class metrics show correlations (shown between parenthesis) with different TN export and TP export at the landscape level. TN export shows a negative correlation with PAFRAC (−0.67), PARA (−0.63) and SHAPE (−0.63), while it shows a positive correlation with CAI (0.71). TP export also shows a positive correlation with CAI (0.70), and a negative correlation with PARAFRAC (−0.65) and SHAPE (−0.65). Finally, urban LULC class metrics show a positive correlation between TN export at the landscape level and CAI (0.69), CLUMPY (0.66) and COHESION (0.72), while these show a negative correlation with PAFRAC (−0.65). TP export at the landscape level shows a positive correlation with CAI (0.68), CLUMPY (0.64) and COHESION (0.75) while showing a negative correlation with PAFRAC (−0.63).
4. Discussion
The results of this study show how the spatial configuration of the landscape differentially influences nutrient dynamics, particularly for TP and TN in the Suquía River Basin. Diverse metrics to interpret the shape, area, core, aggregation, and connectivity were calculated, at the landscape and LULC class levels, as well as nutrient generation values per LULC class.
Regarding LULC scenarios and metric analysis, since each LULC class in the ten scenarios has exactly the same amount of surface area, number of patches, and average size, it is possible to separate composition (which classes there are and how much space they occupy) from configuration (how they are arranged in space). Metrics such as LPI, SHDI, SHDI, and PD have constant values, indicating that LULC scenarios maintain certain invariant structural properties. These findings are in accordance with the work of Chen, W. et al (2022) [
54], who found that landscape metrics such as PD, LSI, aggregation index, and SHDI are effective and critical indicators to reflect landscape composition, structure, shape, and fragmentation, and diversity, respectively. Also, Chen J. et al. (2023) [
3] used landscape metrics such as PD, PLAND, LSI and SHDI to assess the impact of landscape patterns on the provision of different ecosystem services, describing the general key role of the most abundant land type in a landscape in this impact.
In our study, some of the most significant correlations occurred with other metrics with a variable value throughout the scenarios. In this regard, in line with the work of Arora et al. (2021) [
55] and Keeley et al. (2021) [
56], there is no single metric or standard that can explain nutrient input, the distinctive characteristics of a landscape structure and the selected ecosystem services to study, requiring the selection of specific metrics to optimize the analysis. For example, Duarte and collaborators (2018) [
1] also found that metrics such as cohesion, clumpyness and aggregation index can describe landscape connectivity, while metrics such as number of patches, edge density and splitting can be useful to describe landscape fragmentation.
Our analysis shows that the spatial configurations of different LULC classes have a differential impact on the nutrient dynamics, both in terms of production scale and the type of nutrient involved. In accordance with Zhou et al, (2025), who found similar results for Fujiang river basin in China [
57], in the Suquía River Basin, agriculture LULC class predominates, with high functional connectivity and cohesion —characterized by large, compact patches with low fragmentation, accompanied by high functional connectivity (NDR
i)—while natural LULC classes, such as forest, are fragmented. Moreover, it was found that the nutrient concentrations (TN and TP) in Argentine shadow lakes whose basins are used for agricultural activities tended to be higher than those influenced by cities, despite these lakes receiving sewage waste sporadically or permanently [
58].
The spatial configuration of the agricultural LULC class was found to be a primary driver of nutrient export, in accordance with previous studies [
59,
60]. Higher loads of TP and TN were strongly associated with larger, more compact, and geometrically simpler field patches (indicated by high CAI, low PAFRAC, and low SHAPE values). This configuration, characteristic of modern industrial agriculture, maximizes the hydrological efficiency of the landscape: large, rectangular fields minimize edge effects and internal retention capacity, effectively funneling runoff from vast areas directly into the drainage network. This process minimizes nutrient retention and maximizes transport from fields to watercourses. Our findings align with Duarte et al. (2018), who observed that the most significant improvement in water quality was linked to an increase in non-crop areas, as our results suggest that the converse—large, contiguous, and simplified crop areas—act as engines for nutrient export [
1].
The grassland LULC class functioned as a significant nutrient sink, with its spatial configuration being a critical determinant of its retention capacity. Landscapes with cohesive, well-connected grassland patches (high COHESION, low DIVISION/SPLIT) and a large, dominant patch (high LPI) were consistently associated with lower TN and TP exports. This configuration supports larger core areas, minimizing edge effects and maximizing the potential for nutrient infiltration, sedimentation, and biogeochemical processing. Conversely, grassland fragmentation (high DIVISION, high SPLIT, low MESH) disrupts this hydrological function, transforming these areas from functional sinks into passive conduits, as documented in other studies [
61,
62]. The notable outlier in scenario 2, where TN export from grasslands increased disproportionately, provides a critical insight into the limits of this sink function. We hypothesize that this specific configuration may represent a ‘tipping point’ where extreme fragmentation, potentially combined with a spatial position that increases hydrological connectivity to the stream network (e.g., on steeper slopes or directly contributing to drainage lines), overwhelms the retention capacity of the remaining grassland patches. This suggests that the nutrient sink function of grasslands is non-linear and can collapse under specific configurations of disaggregation and high connectivity, a mechanism that warrants further investigation at the sub-basin scale.
Our analysis underscores the critical role of forest spatial configuration in regulating TN dynamics at the basin scale. While forests contributed minimally to nutrient generation, their arrangement significantly influenced TN export. We found that landscapes with highly aggregated (high CLUMPY) and simply shaped (low PAFRAC) forest patches were associated with significantly lower TN export. This specific configuration—large, contiguous patches with regular shapes—maximizes the interior core habitat while minimizing edge effects. This structure enhances the forest’s collective capacity for internal nutrient processing and retention, acting as an effective landscape-scale sink. Consequently, the fragmentation of forests into disaggregated, complex patches compromises this regulatory function, facilitating increased TN transport to aquatic systems. This emphasis on patch configuration provides a basin-scale perspective that complements the findings of Walton et al. (2020) [
63]. While their work effectively highlights the paramount importance of the presence of riparian forest buffers for filtering overland flow at the local scale, our results reveal a distinct mechanism at the basin scale. Here, the aggregation and simplicity of the entire forest network, including upland areas, promote nutrient retention through processes like denitrification and uptake in large core areas, rather than solely through edge-of-field filtration. This distinction does not contradict but rather enriches the understanding of forest functions, illustrating that the mechanism of nutrient retention is scale-dependent [
64,
65,
66,
67]. Other studies which contribute to water quality also mention the valuable effect of forested buffers to mitigate the nutrient pollution and contribute to water quality [
68,
69,
70]. Consequently, effective management requires a dual strategy: protecting local riparian buffers and maintaining well-connected, contiguous forest patches throughout the broader catchment to mitigate nitrogen loads at multiple scales.
Despite its limited areal extent, the urban LULC class exerted a strong influence on nutrient export, functioning as a highly efficient conduit rather than a retention landscape. Nutrient loads were highest when urban areas exhibited high structural connectivity (high COHESION), strong aggregation (high CLUMPY), and simple geometric shapes (low PAFRAC). This configuration—characteristic of consolidated impervious surfaces—minimizes infiltration and retention while maximizing the hydraulic efficiency of runoff conveyance. Unlike the nutrient-sink behavior observed in grasslands, this urban fabric creates a rapid-transport network that effectively funnels pollutants from impervious surfaces directly into the drainage network. Our findings align with previous studies [
54,
71,
72] that attribute degraded water quality in urbanizing areas to enhanced runoff generation and efficient pollutant conveyance, underscoring that the spatial configuration of urbanization can exacerbate its hydrological impact beyond what would be expected from its areal contribution alone. This relates to the possibility that, once urbanization surpasses a certain threshold, fragmentation of the built-up landscape can enhance water quality by reducing connectivity of impermeable surfaces, as indicated by Duo et al. (2024) [
73].
This study presents a methodology that links landscape configuration to nutrient export. Although powerful, this approach has limitations, including its computational intensity and the use of retention parameters and biophysical coefficients that require field calibration. This means that our quantitative estimates should be interpreted as relative rather than absolute. These limitations define clear pathways for future work, including securing greater computational capacity, expanding LULC class detail and gathering field data on nutrient loads (biophysical parameters inputs) to empirically validate and calibrate the model.
5. Conclusions
The integration and synergy between the rflsgen R package and landscape metrics for the simulation and analysis of land use patterns, together with the NDR InVEST module for the modeling of nutrient flows, represents a novel and relevant methodological combination that allows for evaluating complex ecological relations and for the design of reproducible spatial experiments.
This study shows that the spatial configuration of land use is a key driver of nutrient export in the Suquía River basin. While some landscape metrics, such as LPI, SHDI, SHDI, and PD have constant values, revealing structural invariability between scenarios, the results highlight that agriculture and urban areas, through their spatial arrangement, play the most critical roles in nutrient export. Agriculture organized in small, compact, and large patches significantly increases nitrogen and phosphorus export. Urban areas, despite their limited extent and low total area contribution, exert a disproportionate influence due to their moderate functional connectivity (NDRi) with highly spatially connected structure, facilitating rapid runoff and timely release of nutrients. Also, nutrient export is significantly higher when the urban surface is highly connected, aggregated, and has simple patch shapes (low edge complexity).
The analysis and integration of landscape metrics with nutrient delivery modeling in Suquía River basin can contribute to evidence-based decision-making aimed at mitigating eutrophication risks and improve ecosystem health in this highly impacted basin. Moreover, it is expected that the proposed methodology and the relationships or interactions found can be extrapolated to other basins with similar characteristics, both regionally and globally.