4.1. Fish Communities as Bioindicators in Lentic Ecosystems
One of the key limitations in developing robust fish-based indices for reservoirs is the predominance of tolerant species with low ecological specialization. These fish are less responsive to environmental pressures, reducing the sensitivity of ecological metrics. In Mediterranean systems, where environmental variability is naturally high, many species are already adapted to harsh conditions, which makes it challenging to detect anthropogenic impacts using traditional biotic indices [
17]. This tolerance often results in a reduced number of reliable metrics, as seen in Blabolil et al. (2016) [
17]. While it is true that many lentic species are generalists, trait-based approaches can still compose meaningful metrics by focusing on functional redundancy and guild shifts rather than species identity alone [
42]. Additionally, the assumed tolerance of lentic fish to stressors may mask subtle sub-lethal effects that are only visible with long-term monitoring or physiological biomarkers (e.g., growth, reproduction, stress proteins, and swimming behavior) [
43].
Several studies have demonstrated that fish biomass and certain species’ CPUE are reliable indicators of eutrophication. For example, total biomass is considered a robust proxy for food web productivity [
44,
45]. Metrics such as the CPUE of planktivores and piscivores are frequently used to signal increased productivity or ecological degradation. However, in Blabolil et al. (2016) [
17], the inclusion of tolerant or recently introduced species like common bream (
Abramis brama) or pikeperch (
Sander lucioperca) may weaken these signals due to differences in behavior and habitat use [
17]. A metric employed by Blabolil et al. (2016) [
17] in the index was the CPUE in gillnets of invertivores/piscivorous fish, with perch (
Perca fluviatilis)/pikeperch (
Sander lucioperca) being the most significant relation. Pikeperch is typical of nutrient-rich lowland waters, and its population grows with increasing eutrophication. The rise in the abundance of perch individuals was also recognized as a factor in increasing ecosystem productivity. However, this may be a meaningless figure due to the difference in size and habitat use of the species. Moreover, the system may not be in a steady state given the recent introduction. In particular, Navarro et al. (2009) [
25] showed that species richness and diversity/evenness indices were not strongly related to water quality, while the CPUE of invasive species like common carp (
Cyprinus carpio) in littoral (electrofishing) and limnetic zones (gillnet) strongly correlated with phosphorus levels and trophic indicators like chlorophyll concentrations. However, the carp is an invasive species widely introduced worldwide, with significant effects on increased water turbidity (nutrient resuspension and macrophyte decline). Argillier et al. (2012) [
26] further supported the use of CPUE and omnivorous species biomass as reliable eutrophication metrics. Degraded conditions benefit opportunistic species like omnivorous feeders due to dietary plasticity, contrasting with specialized feeders [
46]. However, the authors noted that tolerance-based metrics did not correlate well with anthropogenic pressure at large spatial scales, suggesting challenges in defining tolerance thresholds across Europe [
8,
26,
44,
47,
48,
49,
50,
51,
52]. It can be said that while biomass correlates with productivity, it can be non-specific, since it also increases with invasive species or unbalanced food webs. Moreover, CPUE data is highly sensitive to the type of sampling gear selected, with gillnets often underrepresenting smaller-bodied or pelagic species.
Blabolil et al. (2017) [
18] state that the CZ-FBI clearly defines fish metrics, allowing rapid classification of ecological potential and, when necessary, providing guidance for restoration and fisheries management actions. The authors note that the methodological steps used to develop the new index are transferable to other regions with similar reservoirs and environments that share the same species. The CZ-FBI is based on well-defined indicators, correlating with eutrophication, measured as total phosphorus concentration, as well as in the assessment of fish abundance, community composition, age structure, biomass measures, and species or family-level fish composition. According to the authors, the selected species are widely distributed and constitute a significant part of fish communities across Europe. Additionally, the CZ-FBI reflects the inherent spatial heterogeneity of reservoirs in terms of fish distribution, covering longitudinal and depth gradients in benthic and pelagic habitats. The authors also compared the CWE-FBI with the CZ-FBI, noting that the latter primarily uses single-species indicators, whereas the CWE-FBI relies on functional guilds. It is worth mentioning that, in terms of WFD criteria, the CWE-FBI does not cover age structure. Fish biomass metrics are used in both the CWE-FBI and the CZ-FBI, with the CWE-FBI metric being an integral value for the entire benthic habitat, while pelagic biomass metrics were calculated separately in the reservoir and tributary sections. This approach’s advantage is accounting for the longitudinal productivity gradient present in lentic ecosystems [
18]. Additionally, CZ-FBI development was based on paired correlations with P
total concentration, while CWE-FBI uses hindcast procedures. This advanced hindcast model can reveal causal relationships in large datasets but is generally not applicable to smaller datasets like those used for CZ-FBI. Instead, simpler methods can identify clear patterns in the dataset. Expert assessment was also involved in CZ-FBI development. This subjective approach is appropriate when reference conditions do not exist, and only a limited dataset is available. Despite the different underlying approaches, both indices yield very similar results, confirming either index’s ability to classify reservoirs’ ecological potential across an anthropogenic pressure gradient. Similarly, Launois et al. (2011) [
19] demonstrated that the hindcast approach to fish community-based metrics made it possible to assess lakes’ and reservoirs’ current conditions. A set of metrics, showing significant responses to anthropogenic pressure, was selected and combined into a biotic integrity index for French lakes and reservoirs. In reservoirs, all trophic guilds appeared to relate to anthropogenic pressures, strongly suggesting that a fish community-based index is a relevant eutrophication indicator [
48,
53,
54]. According to the authors [
19], while the FBI (fish-based biotic integrity index) for reservoirs fully meets the set of criteria recommended by Karr et al. (1986) [
55], the FBI developed for natural lakes in France lacks a metric responding to agricultural pressures, possibly due to low agricultural land use in the sampled lake watersheds. Using the hindcast model, the authors assumed that reference conditions were adequately simulated, setting all anthropogenic factors to zero. However, under the WFD, the reference for a given lake corresponds to the “absence of anthropogenic pressures or near-pristine conditions” [
56]. Therefore, the method was even more restrictive in reference assessment than anticipated by the WFD, leading to overestimated FBI values. Although this hindcast method is increasingly popular [
57], users should remember that it includes some subjectivity. However, reproducibility and index precision can be enhanced by adding new fish data. Overall, hindcast approaches are insightful but heavily rely on historical data quality and assumptions about optimal reference conditions, which may not exist for many reservoirs, and indices based on functional guilds (e.g., the CWE-FBI) are often more transferable, while species-based indices (e.g., the CZ-FBI) may be more ecologically precise but regionally restricted [
58].
Regarding biomass-based metrics, Paulovis et al. (2012) [
29] questioned whether they might better reflect ecosystem function than abundance-based ones. Their analysis suggested that while the two types of metrics sometimes diverged (e.g., for omnivores and piscivores), no clear pattern or correlation emerged. Biomass is often skewed by a few large individuals, while abundance may better capture population dynamics, especially of rare or sensitive species. Still, biomass may offer more sensitive insights into community structure and energy flow, especially when assessing the role of dominant species or functional groups. However, combining both (e.g., BPUE + CPUE) provides a fuller picture of ecosystem productivity and structure, which is recommended in recent ecological assessment guidelines [
59].
The presence and dominance of non-native or opportunistic species complicate the use of fish metrics in reservoirs, and their presence can skew index values and undermine attempts to assess native biodiversity health. For those situations, Pieckiel et al. (2024) [
30] propose and test a fish-based index, tailored for assessing the ecological potential of reservoirs in Poland, representing a significant step forward in using fish community metrics to assess water quality under the WFD. The core innovation in this study is the development of a pilot ichthyological indicator called the Cyprinidae/Percidae Index (C/P Index), which reflects the impact of eutrophication on fish communities. This index centers on the relative abundance of two fish families, Cyprinidae and Percidae, as indicators of nutrient load and water quality. The C/P Index draws on the established sensitivity [
26,
60,
61] of Percidae species (like
Lepomis gibbosus—pumpkinseed and
Sander lucioperca—pikeperch) to low nutrient levels, in contrast to the tolerance of Cyprinidae species (such as
Rutilus rutilus—roach and
Cyprinus carpio—common carp) to eutrophic conditions. Essentially, the ratio serves as a proxy for water quality. A higher C/P Index suggests a shift toward nutrient-rich, eutrophic conditions. This pilot index is promising, not only for Poland but for broader European applications, offering a scalable, transferable tool for evaluating ecological potential in various reservoir settings. The use of species-based indicators addresses the need for consistency across regions, since the selected fish families are widely distributed across Europe. The correlation of the C/P Index with TSI values further underscores the practical advantage of combining biological and chemical metrics to assess human impacts in modified water bodies.
Hydrological and morphological features such as waterbody size, depth, and retention time significantly influence fish community structure and water quality, and many fish indices fail to correct for these natural gradients, leading to misclassification of reservoirs with inherently low diversity. Česonienė et al. (2020) [
31] explore the connection between the hydrometric parameters and the ecological status of Lithuanian lakes and ponds. The study emphasizes that larger and deeper water bodies often have better water quality. The key findings reveal that lakes with greater depths generally have lower levels of total phosphorus and nitrogen, which are indicators of higher ecological status, and that fish community indicators, such as the Lithuanian Fish Index (LFI), also correlate with better water quality, suggesting that fish communities can effectively assess water quality. Additionally, the study demonstrates that faster water exchange rates in lakes can positively impact the reduction in nitrogen and phosphorus levels, leading to healthier ecological conditions. Consequently, these findings indicate that fish community characteristics, lake depth, and water exchange rates are reliable hydromorphologic metrics for assessing and enhancing the ecological status of reservoirs.
A recurring theme across studies is the difficulty of standardizing fish metrics across diverse reservoir types, namely, due to differences in sampling protocols, species pools, and pressure gradients. Species-specific, regionally restricted indices (e.g., the CZ-FBI) may not transfer well to other countries or ecoregions without extensive recalibration [
21]. On the other hand, family or guild-level indices (e.g., the C/P Index) may offer broader applicability but with reduced ecological specificity [
30]. Additionally, challenges such as sampling bias, gear selectivity, and lack of reference conditions persist across methodologies and remain barriers to broader adoption. This suggests the use of hybrid indices (guild + species + functional traits) and pressure-specific sub-indices (e.g., eutrophication and hydromorphology) to enhance standardization, aiming for a WFD-defined index for reservoirs.
In fact, Birk et al. (2012) [
62] claim an underrepresentation of fish in WFD assessments, with only 15% of the 297 methods reviewed in their study being related to fish as a biological quality element, making them one of the least-used groups for bioassessment, especially in lakes and transitional waters. This is due in part to practical difficulties with sampling fish at large scales and because it is not required in all water categories under the WFD. There are also concerns that many fish-based methods were developed with insufficient empirical support, making their sensitivity and diagnostic power questionable. This does not mean fish indicators do not possess potential, but, in fact, that they require more robust calibration, long-term datasets, and better integration with physical habitat and hydromorphological data. As agreed in Poikane et al. (2014) [
63], efforts of intercalibration among countries should be encouraged, as they have been marked as valid approaches and can be the key for long-term and effective protection of member state water bodies, in this case, reservoirs.
4.2. Case Study—Aguieira Reservoir
Building on the broader issues discussed above, case in point, the use of fish communities as indicators of water quality, it becomes important to provide a relevant real case to examine how fish-based indices perform in practice. The Aguieira Reservoir was chosen as a case study for this reason, being the only case in Portugal included in the intercalibration exercise of the WFD for defining elements to be assessed in reservoirs. The ecological classification of this ecosystem has consistently been poor [
40,
64], a pattern also observed in this study, based on the quantified physical, chemical, and biological results (
Table 7). The application of the F-IBIP in a Portuguese reservoir characterized by the dominance of tolerant and invasive species offers a way to test and illustrate some of the methodological constraints identified in the literature, including sampling bias, index sensitivity, and the adequacy of standardized metrics in lentic settings. This case study was not intended to serve as a comprehensive ecological characterization of the reservoir but rather as a practical demonstration of how the limitations highlighted in the previous sections may manifest in real-scenario applications of fish-based indices, providing a representative example of the difficulties faced when assessing ecological potential in such systems under the Water Framework Directive.
Regarding the fish specimens found in Aguieira, it is important to highlight that the use of multi-mesh gillnets alone may introduce sampling bias and limit the representation of small species. Different sampling methodologies ought to be employed together, as explored in Mueller et al. (2017) [
22]. Despite this limitation, gillnets remain useful for detecting dominant or larger-bodied species, which, in the case of highly disturbed or simplified fish communities, can still provide relevant information about ecological condition and potential. As sampling was limited to a standardized multi-mesh gillnet protocol [
18] at three representative sites, this small sample size constrains representativeness. However, it allows the index’s sensitivity to be tested in a highly disturbed system and illustrates the methodological constraints of fish-based bioassessment in reservoirs, as reported by Blabolil et al. (2016) [
17], Blabolil et al. (2017) [
18], and Mueller et al. (2017) [
22]. The shad is native to Portuguese rivers, and its abundance has drastically decreased, especially in the rivers Tagus, Sado, Guadiana, and Douro, with the latter facing a serious reduction [
65,
66]. However, significant shad populations still exist in the Mondego, Lima, and Minho Rivers, where fishing for this species is economically important for fishing communities [
66]. In addition to migratory populations, there are land-locked populations, particularly in reservoirs, such as Castelo do Bode (Tagus River) and Aguieira (Mondego River), where they remained after the construction of dams [
66]. This species primarily feeds on crustaceans and filamentous algae by filtering water, while in brackish water, it feeds almost exclusively on crustaceans [
66].
The barbel (
Luciobarbus bocagei) is an endemic cyprinid of the Iberian Peninsula with a wide distribution across most river basins in mainland Portugal, except for the Guadiana, Mira, and Algarve Rivers, and the Minho River [
66]. It is highly adaptable to various freshwater systems, occupying a broad spectrum of lotic and lentic ecosystems, preferring areas with weak-to-moderate currents while avoiding cold waters. These traits often correspond to the middle and lower sections of water courses. This species is well-adapted and is present in a significant percentage of reservoirs [
67]. The common barbel (
Barbus barbus) is a bottom-feeding, omnivorous, and opportunistic species, feeding on plant material (aquatic macrophytes and filamentous algae), insects, and crustaceans [
67]. The introduction of some exotic species has also contributed to the barbel population decline on the Iberian Peninsula, mainly due to competition for resources (e.g., food and habitats) and predation, particularly of juveniles, by introduced piscivorous species, such as the largemouth bass (
Micropterus salmoides), northern pike (
Esox lucius), and pikeperch (
Sander lucioperca) [
67].
Regarding the invasive species captured, we found pikeperch (
Sander lucioperca), which inhabits deep, calm areas with rocky bottoms and turbid waters, though it can also be found in the water column. Its distribution includes the Azores, the Ermal and Aguieira Reservoirs, the Mondego River and its tributaries, and Lamas de Olo (Vila Real) [
66]. Adults feed exclusively on fish (bleak, barbel, nase, and crayfish, which can be their primary food source during certain times of the year), while juveniles feed on crustaceans (e.g.,
Daphnia) [
68]. Carps (
Cyprinus carpio) prefer lentic habitats with fine substrate, abundant aquatic vegetation, and warmer waters. They are found in reservoirs and are highly resistant to low dissolved oxygen levels and poor water quality [
11], a fact recorded in this ecosystem regarding physical, chemical, and biological parameters (
Table 7). During winter, they remain near the bottom, sometimes burying themselves in sandy/muddy substrate, limiting their activity until spring arrives. Spawning occurs in May/June in shallow areas with abundant vegetation to which the eggs adhere and follow an omnivorous feeding regime (vegetable detritus, insects, crustaceans, and fry of other fish) [
11]. Like carp, the goldfish (
Carassius auratus) prefers lentic habitats with fine substrate and abundant aquatic vegetation, often found near the shore in calm zones [
13]. It is also present in reservoirs and is highly resistant to low dissolved oxygen levels and poor water quality (
Table 7). Spawning occurs between May and June, in shallow areas with abundant vegetation to which the eggs adhere, with an omnivorous diet [
13]. Pumpkinseed (
Lepomis gibbosus) is also a lentic species found in reservoirs and shallow watercourses with low current speed, aquatic vegetation, and warmer temperatures. Like most non-native species, it is resistant to deteriorating environmental conditions [
69]. Reproduction occurs between May and July, during which they build nests (small depressions in sandy or gravelly substrate) defended by males, who display strong territorial behavior. Most individuals primarily feed on insects, though they may also prey on eggs, larvae, and small fish [
69]. These species occupy similar habitats and share identical ecological characteristics, making them unsuitable for distinguishing the quality of aquatic ecosystems.
The results obtained for fish communities showed low representativeness and diversity, regarding the capture method used (multi-mesh gillnets), and future efforts ought to include complementary methods (e.g., seine nets) and increase temporal coverage to account for diel activity of species. According to Mueller et al. (2017) [
22], while electrofishing is inefficient in lakes and reservoirs, other capture methods, such as seine nets and gillnets, are more effective and less selective, resulting in broader representativeness and diversity of fish species. The authors also noted that repeating capture methods with seine nets, electrofishing, and lift nets with bait should be considered to increase capture efficiency and representativeness, although this study was conducted in the backwaters (lentic systems) of a river. Mueller et al. (2017) [
22] also advocate using capture methods at different times of the day (day, night, dusk, and dawn) for a more realistic assessment of fish communities. The higher capture rates of certain species at night, dusk, and dawn may be explained by species-specific behavioral differences, such as preferred hunting times during dusk and dawn (e.g.,
Sander lucioperca). In addition to the low representativeness of fish species recorded, the high percentage of invasive species was noted as a parameter with known negative effects on water quality evaluation [
27]. Although the physical and chemical results indicated poor water quality (
Table 7), invasive species are known to easily adapt to eutrophic environments and contribute to water quality deterioration [
27]. Conversely, some exotic species (e.g., pikeperch—
Sander lucioperca and
Micropterus salmoides—largemouth bass) prey on native species (e.g., barbel—
Luciobarbus bocagei) [
68], decreasing water quality classification, as most fish indices use native species as a parameter for the ecological assessment of the ecosystem.
The ichthyofauna of the Aguieira Reservoir has been studied since 1999, and it was evaluated and characterized through sampling using gillnets, electrofishing, surveys, and data from previous studies [
70]. Thirteen species were recorded: shad—
Alosa sapidissima, eel—
Anguilla anguilla, common barbel—
Barbus barbus, goldfish—
Carassius auratus, Iberian nase
—Pseudochondrostoma polylepis, goby—
Gobio lozanoi, carp—
Cyprinus carpio, northern chub
—Leuciscus carolitertii, ruivaco—
Achondrostoma oligolepis, spined loach—
Cobitis taenia, pumpkinseed—
Lepomis gibbosus, largemouth bass—
Micropterus salmoides, and trout—
Oncorhynchus mykiss. The community showed low diversity, with about 42% comprising introduced species, with some very common, such as pumpkinseed (
Lepomis gibbosus) and largemouth bass (
Micropterus salmoides). The disappearance or decline of several migratory species (lamprey—
Petromyzon marinus, shad—
Alosa sapidissima, twaite shad—
Alosa fallax, eel—
Anguilla anguilla) is a clear indication of the artificialization of the ecosystem due to dam construction [
70]. There is no reference to the presence of lamprey (
Petromyzon marinus) in the reservoir, and the presence of twaite shad (
Alosa fallax) was indicated only by local sport fishers. However, fishers sometimes call smaller shad (
Alosa sapidissima) specimens “twaite shad” due to morphological similarities between the two species [
70].
As in other basins, the shad (
Alosa sapidissima) maintains a resident population in Aguieira, whose migration was hindered by the physical barrier (dam). These individuals have adopted a completely different lifestyle from their anadromous migrating counterparts, a phenomenon known as “land-locked populations” [
70]. Studies by Pedroso (1997) [
71] and Sales-Luís (1998) [
72] using electrofishing in this reservoir reported pumpkinseed—
Lepomis gibbosus as the dominant species, with a significant presence of largemouth bass—
Micropterus salmoides, goldfish—
Carassius auratus, common barbel—
Barbus barbus, Iberian nase—
Pseudochondrostoma polylepis, eel—
Anguilla anguilla, and shad—
Alosa sapidissima [
70]. Surveys from fishing clubs corroborate these results, indicating pumpkinseed—
Lepomis gibbosus as the predominant species, while largemouth bass—
Micropterus salmoides, common barbel—
Barbus barbus, Iberian nase—
Pseudochondrostoma polylepis, and carp—
Cyprinus carpio are also common in this reservoir. The latter species can reach large sizes, according to local sport fishers (e.g., total length: 70 cm; total weight: 6 kg). In general, the information collected indicates a decline in
Pseudochondrostoma polylepis – Iberian nase,
Carassius auratus—goldfish, and
Squalius carolitertii—northern chub populations, coinciding with the proliferation of introduced species [
70]. In the littoral zone, mainly sedentary species adapted to lentic waters, such as pumpkinseed—
Lepomis gibbosus and largemouth bass—
Micropterus salmoides, were found. The pelagic zone (surface and deep) is primarily inhabited by exotic limnophilic cyprinids like the common carp (
Cyprinus carpio) and goldfish (
Carassius auratus), and native cyprinids, particularly potamodromous species like
Pseudochondrostoma polylepis—Iberian nase, and
Barbus barbus—common barbel [
70].
The classification of “poor” water quality from the F-IBIP highlights the challenges and opportunities in using fish-based metrics to evaluate reservoir water quality, which, despite representing only a preliminary exploratory study, is in agreement with WFD metrics (
Table 7). In this assessment, a “poor” ecological potential indicates that the biological (ichthyofauna) quality of the aquatic ecosystem is severely degraded. This classification is characterized by low native fish diversity, a high prevalence of invasive species, and disruptions to natural ecological balance. These issues reflect broader challenges in bioassessment, such as the difficulty in distinguishing natural variability from anthropogenic impacts and the need for region-specific indices. Moreover, the fish community structure in Aguieira Reservoir points to environmental stressors, including pollution, habitat alteration, and the loss of natural stream features, factors that particularly impact sensitive species and reduce overall biodiversity.
The case study of Aguieira Reservoir reflects the same key patterns identified in the literature review, particularly the low representation of native fish species and the dominance of invasive taxa [
27,
32]. These findings are consistent with the challenges commonly reported across European reservoirs, including limitations in sampling methodologies [
22,
26] and the sensitivity of fish-based indices to anthropogenic pressures and artificialized ecosystems [
17,
26]. The prevalence of tolerant, non-native species and the reduced ecological quality, as indicated by the F-IBIP classification, emphasize broader concerns about biodiversity loss and the need for improved monitoring strategies within the Water Framework Directive context. The F-IBIP output needs to be carefully evaluated, given its original application in river systems, although Česonienė et al. (2020) [
31] applied the LFI in reservoirs, which is also used in rivers [
73], and this approach provides a comparative basis and a starting point for the development of a reservoir-specific index.
Nevertheless, the application of the F-IBIP to Aguieira highlights several limitations of the index itself, many of which are reflected in the literature. This index still does not account for population parameters such as age, gender, or biomass/catch unit effort, which have been previously indicated by other authors [
17,
18,
25,
29] as important and sensitive markers in demonstrating water quality and ecosystem disruption, nor reproductive metrics, which are critical in reservoirs affected by long-term stressors. Moreover, its reliance on taxonomic metrics alone may overlook functional changes in the community, such as the rise of opportunistic feeders or shifts in trophic dynamics. Compared to hybrid or trait-based indices, such as the CZ-FBI or the C/P Index, the F-IBIP appears less sensitive to the nuanced ecological degradation seen in Aguieira. A trait-based approach might have captured functional homogenization within the fish community or better reflected the dominance of stress-tolerant, invasive species, as discussed in the previous section. Another key limitation is the calibration of the index itself. Since it was originally developed for lotic systems, its application to reservoirs may require adjustment or recalibration, particularly in accounting for lentic-specific dynamics such as depth gradients, water retention time, and pelagic vs. benthic species distributions. These limitations are consistent with the broader concerns raised in
Section 4.1, as shown in, e.g., Launois et al. (2011) [
19], that used different metrics (% of lithophilic species biomass, omnivorous species biomass, herbivorous species count, % piscivorous species, strictly lithophilic species %, and BPUE) to define a specific index for French lentic systems due to the lack of adequate FBIs for these scenarios. This reinforces the need for regionally calibrated, functionally inclusive indices to ensure meaningful ecological assessments in Mediterranean reservoirs.
This case study also provides a concrete illustration of the key challenges highlighted in the literature review. The limited sample size and reliance on a single sampling gear also highlight a key methodological challenge in reservoir bioassessment of balancing the need for standardized, WFD-compliant approaches with the representativeness required for robust community assessment. As reported by Blabolil et al. (2016) [
17], Blabolil et al. (2017) [
18], and Launois et al. (2011) [
19], fish-based indices originally developed for rivers often show reduced sensitivity when applied to reservoirs, particularly in systems dominated by tolerant, generalist, or invasive
taxa, a pattern that emerged clearly in Aguieira, where 62.5% of the captured individuals were non-native species, and native assemblages were strongly underrepresented. The poor F-IBIP classification reflects this imbalance and underscores the limitation of relying solely on taxonomic metrics without incorporating functional traits, biomass-based measures (e.g., BPUE and CPUE), or pressure-specific indicators, such as the Cyprinidae/Percidae ratio proposed by Pieckiel et al. (2024) [
30]. Thus, the Aguieira results not only confirm but exemplify the gaps identified in the literature, supporting the call for regionally calibrated, hybrid indices that integrate species, guild, and functional metrics to improve ecological potential assessments in Mediterranean reservoirs.
This underscores a key challenge. Fish metrics must account for multiple stressors and their interactions to provide accurate water quality assessments. However, these challenges also present opportunities. Advancements in fish-based bioindicators, coupled with improved monitoring techniques and adaptive management strategies, could enhance the reliability of these assessments. Due to data limitations, no statistical correlations between fish metrics and environmental variables could be conducted. Future studies should, therefore, expand sampling effort and integrate complementary gears (e.g., seine nets and baited traps) to overcome these limitations and support the development of hybrid, functionally inclusive indices for reservoirs. Future applications should incorporate multivariate approaches (e.g., RDA and PCA) to better understand the environmental drivers shaping fish community composition and improve the ecological interpretation of index responses. By improving fish indices and integrating them with complementary ecological data, such as hydromorphological and physical and chemical parameters, water managers can develop more effective conservation and restoration strategies for reservoir ecosystems.