scieee AI-readable full text Open interactive document viewer

Assessment of ecosystem services provided by lagoonal seaweeds and seagrasses along the Moroccan coast

Houssa, Rachida; Rezzoum, Nor-Eddine; Chrifi, Ouafa; El Mouttaqui, Sara; El Asri, Fatima; Zidane, Hakima

Abstract

This study assesses the ecosystem services provided by algae and seagrass species structuring the lagoonal ecosystems along the Moroccan Atlantic coast, with a focus on the Oualidia Lagoon. A comprehensive literature review was conducted to identify and evaluate the contributions of key native species (Gracilaria gracilis, Ulva spp., Cystoseira humilis, Fucus spiralis, and Zostera noltei) and the invasive species Sargassum muticum to Marine and Coastal Ecosystem Services (MCES). A semi-quantitative approach was applied to integrate the functional and spatial value of each species into the overall assessment of MCES. Results indicate that 70–85% of potential services are documented, with native species mainly contributing to regulating and supporting services, while S. muticum shows a negative impact on about 43% of them. Current exploitation remains limited, except for agar-agar extraction from Gracilaria, confirming the low use of provisioning services. Overall, 25–30% of potential services are underutilized, aligning with the Ramsar site's emphasis on sustainable use. Promoting native algae cultivation could enhance local economic and ecological outcomes while contributing to multiple SDGs, including food security, climate action, and biodiversity conservation.

Full text

151 Assessment of ecosystem services provided by lagoonal seaweeds and seagrasses along the Moroccan coast Rachida Houssa1, Nor-Eddine Rezzoum1, Ouafa Chrifi2, Sara El Mouttaqui3, Fatima El Asri3, Hakima Zidane1 1 Institut National de Recherche Halieutique (INRH), Casablanca, Morocco 2 Faculty of Sciences and Technologies, Cadi Ayyad University, Marrackech, Morocco 3 Université Hassan II de Casablanca, Laboratoire Biologie et Santé (URAC 34), Casablanca, Morocco Corresponding author: Rachida Houssa ([email protected]) Copyright: © Rachida Houssa et al. This is an open access article distributed under terms of the Creative Commons Attribution License (Attribution 4.0 International – CC BY 4.0). Research Article Abstract This study assesses the ecosystem services provided by algae and seagrass species structuring the lagoonal ecosystems along the Moroccan Atlantic coast, with a focus on the Oualidia Lagoon. A comprehensive literature review was conducted to identify and evaluate the contributions of key native species (Gracilaria gracilis, Ulva spp., Cystoseira humilis, Fucus spiralis, and Zostera noltei) and the invasive species Sargassum muticum to Marine and Coastal Ecosystem Services (MCES). A semi-quantitative approach was applied to integrate the functional and spatial value of each species into the overall assessment of MCES. Results indicate that 70–85% of potential services are documented, with native species mainly contributing to regulating and supporting services, while S. muticum shows a negative impact on about 43% of them. Current exploitation remains limited, except for agar-agar extraction from Gracilaria, confirming the low use of provisioning services. Overall, 25–30% of potential services are underutilized, aligning with the Ramsar site’s emphasis on sustainable use. Promoting native algae cultivation could enhance local economic and ecological outcomes while contributing to multiple SDGs, including food security, climate action, and biodiversity conservation. Key words: Algae, ecosystem services, invasive algae, lagoon ecosystem, Moroccan Coast, seagrass Introduction The 2021 United Nations Food Systems Summit highlighted the need to advance towards healthier, more sustainable, and equitable food systems, as outlined in the 17 Sustainable Development Goals (SDGs) (United Nations 2021; Webb et al. 2023). Achieving these goals requires food systems that contribute less to greenhouse gas (GHG) emissions while meeting the food needs of a continuously growing global population (Von Braun et al. 2021). However, current food systems are estimated to contribute approximately one-third of GHG emissions and negatively impact freshwater resources, biodiversity, and soil quality (Crippa et al. 2021; Webb et al. 2023). One proposed solution is to focus more on water-based food systems, particularly algae, which could Academic editor: Gustavo F. de Carvalho-Souza Received: 31 July 2025 Accepted: 3 December 2025 Published: 11 December 2025 Citation: Houssa R, Rezzoum N-E, Chrifi O, El Mouttaqui S, El Asri F, Zidane H (2025) Assessment of ecosystem services provided by lagoonal seaweeds and seagrasses along the Moroccan coast. Estuarine Management and Technologies 2: 151–184. https://doi.org/10.3897/ emt.2.167289 Estuarine Management and Technologies 2: 151–184 (2025) DOI: 10.3897/emt.2.167289 152 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons represent a transformative change in the global food security equation (Bjerregaard et al. 2016; Webb et al. 2023). As highlighted by Webb et al. (2023) and Msuya et al. (2022), algae could represent a major new crop opportunity for lowand middle-income countries. As for seagrass, they indirectly support food security by providing habitat and nourishment for numerous species targeted by fisheries, while also contributing to carbon sequestration and climate regulation. However, significant gaps remain in understanding the potential benefits of algae and seagrasses within marine and coastal ecosystems. . In a recent study, Webb et al. (2023) demonstrated that in lowand middle-income countries, there are still gaps in the available information and understanding of the potential benefits of algae on nutrition and health, as well as concerns about potential toxic effects and exceeding tolerable upper intake levels for certain nutrients. This is particularly relevant in the North-West African region, including the Moroccan Coast which possesses a natural wealth of algae and seagrasses, yet little is known about their potential to combat food insecurity and reduce the carbon footprint (Webb et al. 2023) . Coastal areas, contribute more than 60% of the total economic value of the biosphere (Costanza et al. 1997; Martínez et al. 2007). Among these coastal areas, lagoons are widely recognized for their biological interest. These delicate and diverse wetland complexes hold ecological, socio-cultural, and economic values (Schuyt and Brander 2004; de Groot et al. 2010). They provide numerous services that contribute to human well-being and poverty reduction (MA 2005; Maresca et al. 2011; Briner et al. 2013; IPBES 2018). Coastal lagoons are typically dominated by seaweeds and seagrass meadows, which are recognized as some of the most valuable ecosystems on our planet due to the numerous functions and ecosystem services they provide (Costanza et al. 2014; Ruiz-Frau et al. 2017; Doo Hwan et al. 2021; Cotas et al. 2023). These ecosystems offer a variety of benefits, including food for human consumption, habitats for marine species, coastal water quality control through nutrient recycling, sediment stabilization, pathogen removal, and oxygen production (Costanza et al. 1997; Nordlund et al. 2016; Lamb et al. 2017; Belondo et al. 2021). However, these ecosystem services are not utilized uniformly across different regions of the world, The lagoon ecosystems in the North-West African region, renowned for their significant biodiversity, are rich in algae and seagrass. Preservation efforts in these areas are fully aligned with the United Nations Sustainable Development Goals (SDGs) for 2030. Unfortunately, there is a lack of exploring the benefits of their marine plant resources. This research contributes to demonstrating the potential of seaweed and seagrass of lagoonal ecosystems for the development of coastal populations in the North-West African region, as well as their role in combating food insecurity and reducing CO2 emissions. We used the Marine and Coastal Ecosystem Services (MCES) classification, adapted from Liquete et al. (2013a), to evaluate the specific contributions of certain species of algae and seagrass commonly found along the North-west African coastlines. The species studied include Gracilaria gracilis (Stackhouse) Steentoft, L.M.Irvine & Farnham, 1995, Ulva Linnaeus, 1753, Cystoseira humilis Schousboe ex Kützing, 1860, Fucus spiralis Linnaeus, 1753, Sargassum muticum (Yendo) Fensholt, 1955 and Zostera noltii Hornemann, 1832. These species, while diverse in habitat 153 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons and distribution, share overlapping ecological roles, particularly in lagoon and coastal environments. Gracilaria gracilis is a cosmopolitan species found in tropical and temperate seas, commonly observed in the Northeast Atlantic. It thrives in shallow, calm waters (up to 15 m depth) and is highly tolerant of salinity variations, making it a frequent inhabitant of lagoons (Lamare and Verlaque 2022). Similarly, Ulva lactuca, known as sea lettuce, is a globally distributed green algae that colonizes various coastal environments, including lagoons, estuaries, and rocky shores (Hamon et al. 2024). Ulva fasciata, another green algae species, also shares this adaptability to coastal environments. It thrives in tropical and subtropical intertidal and subtidal zones and exhibits a high tolerance to salinity and temperature fluctuations, particularly in the Atlantic Ocean (GBIF 2023). Additionally, Ulva intestinalis, commonly referred to as “Enteromorpha,” is highly adaptable to a variety of coastal habitats, ranging from intertidal zones to estuaries with fresh or brackish water, further linking it to temperate and tropical regions (Sabourin et al. 2022). In contrast, Fucus spiralis is a brown algae primarily found in the upper parts of the intertidal zone on rocky substrates in the Atlantic Ocean, never extending beyond 6 meters in depth (Freitas et al. 2020). Cystoseira humilis, another brown algae, is more commonly associated with rocky areas in the Mediterranean region but also grows along the Atlantic coast, inhabiting shallow waters between 0 and 20 meters deep (Belattmania et al. 2016). Zostera noltei, a marine seagrass, occupies a similar ecological niche, found in shallow coastal areas such as lagoons, estuaries, and bays. It typically grows in muddy or sandy substrates, and is widely distributed along the Atlantic and Mediterranean coasts (Martel et al. 2021). However, the invasive species Sargassum muticum, originally from the Pacific coasts of Asia, presents a contrast. Now widespread in the eastern Atlantic, it colonizes diverse marine habitats, including lagoons, bays, and estuaries, where it often forms dense stands that can disrupt local ecosystems (Hannachi et al. 2020). Together, these species, although differing in taxonomic group and specific ecological preferences, are interconnected by their presence in coastal environments. They play complementary roles in lagoon and estuarine ecosystems, with many of them sharing a resilience to environmental variability, which contributes to their widespread distribution. In this study, we used the Oualidia lagoon along the Atlantic Moroccan coast as a case study to assess the role of lagoonal algae and seagrasses in supporting potential ecosystem services and to compare these contributions with the benefits currently observed. Material and methods Ecosystem Services (ES) classification approach The MCES classification was developed through a critical analysis and integration of various classifications from sources such as MEA (2005); TEEB (2010); Haines-Young and Potschin (2011) and Beaumont et al. (2007). The MCES classification encompasses 14 categories of ES which are summarized in Table 1. For a more comprehensive description, refer to Liquete et al. (2013a, 2013b) and Katsanevakis et al. (2014). 154 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Study area The Oualidia Lagoon, located on the Atlantic coast of Morocco in the Northwest African region (Fig. 1), was chosen as a demonstration site to quantify ecosystem services (ES) provided by algae and seagrass, following the methodology outlined by Liquete et al. (2013a) (Table 1). This lagoon is renowned for its ecological significance and biodiversity and has been protected under the RAMSAR Convention since 2005 (https://rsis.ramsar.org/fr/ris/1474). Historically, it has served as a major site for oyster farming, with a tradition dating back to the 1950s. In addition to oyster farming, various other activities have emerged in the area, including agriculture (primarily focused on cereals and vegetables), pasture (practiced by over 90% of the population), shore fishing (15%), and tourism. However, these activities have expanded without adequate consideration of their environmental impacts on biodiversity and other ecosystem services (Maanan et al. 2014; Houssa et al. 2020). Database The database used to assess the MCES of the Oualidia Lagoon is based on sampling conducted in February 2021 using scuba diving techniques (Rezzoum et al. 2022). Sampling was carried out at 68 stations distributed throughout the lagoon (Fig. 1). The most abundant seaweed and seagrasses include the seagrass Zostera noltei, native algal species such as Gracilaria gracilis, Ulva (Ulva lactuca, Ulva fasciata, and Ulva intestinalis), Cystoseira humilis, Fucus spiralis, and the invasive algal species Sargassum muticum. In terms of Spatial Coverage Rate (SCR) relative to the total area of the main channel within the lagoon, Gracilaria gracilis is the dominant algal species, occupying over 50%, followed by Ulva (17%), Zostera noltei (10%), and finally Fucus spiralis, Cystoseira humilis, and Sargassum muticum, each with 6% coverage (Rezzoum et al. 2022). Ecosystem services: literature review To ensure comprehensive coverage of the literature, searches were conducted across multiple scientific databases including Science-Direct, Scopus, Web of Science, and Google Scholar, as well as widely used academic platforms such as ResearchGate and Academia. We used three combinations of keywords related to different studied species of algae and seagrasses, the 14 categories of MCES classification and the names of studied areas. Boolean operators (AND, OR) were employed to refine the queries, and results were not limited to any date. Table 2 summarizes the databases consulted and the specific search strings used. The PRISMA flowchart in Fig. 2 illustrates, step by step, the process of bibliographic analysis, from identification to use in the manuscript ES Assessment approach To quantify the relative contribution of algae and seagrass species to Marine and Coastal Ecosystem Services (MCES) in the Oualidia Lagoon, a semi-quantitative multi-criteria approach was applied. Following the literature review, each species was evaluated according to its contribution to the different MCES 155 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons categories. A value of +1 was assigned when the species provided a positive contribution, –1 for a negative contribution, and 0 when no measurable effect was observed. This score was then weighted by a factor representing the species’ Spatial Coverage Rate (SCR) relative to the total surface area of the Table 1. Categories of the Marine and Coastal Ecosystem Services (MCES) classification, as adapted from Liquete et al. (2013a). Provisioning services Food provision Supply biomass for human consumption through fishing and aquaculture activities. Water storage and provision The provision of water for human consumption and other uses. Bioactive materials and Biofuels Supply biomass for non-food purposes, including medicinal, ornamental, commercial, and industrial uses. Regulating and maintenance services Water purification Removes wastes and pollutants through biochemical and physicochemical processes like dilution, sedimentation, bioremediation, filtration, and decomposition. Air quality regulation Regulation of atmospheric pollutant concentrations in the lower atmosphere. Coastal protection Protects naturally the coast from flooding and erosion through structures that stabilize sediments and create protective buffers. Climate regulation The ocean acts as a sink for greenhouse gases and climate-active gases. Large perennial algae and higher plants can store carbon for longer periods. Weather regulation Influence on local weather conditions. Ocean nourishment Involved in the natural cycling process leading to the availability of nutrients in seawater for the production of organic matter. Lifecycle maintenance Biological and physical support to facilitate healthy and diverse reproduction of species. Biological regulation Pathogen control Cultural services Symbolic and aesthetic values The exaltation of the senses and emotions by seascapes and the values accorded to coastal natural and cultural sites. Recreation and tourism The opportunities the marine environment provides for relaxation and entertainment (swimming, scuba diving, recreational fishing ...). Cognitive effects Inspiration for arts, research and education Figure 1. Geographic location of Oualidia lagoon and spatial distribution of sampling stations. 156 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons lagoon’s main channel. The overall MCES assessment provided by algae and seagrass species was obtained by summing the weighted scores across the 14 ecosystem service categories described in Table 1. The weighting factor based on the Spatial Coverage Rate (SCR) was defined as follows (Table 3): • 1: SCR ≤ 5% • 2: 5% < SCR ≤ 10% • 3: 10% < SCR ≤ 25% • 4: 25% < SCR ≤ 50% • 5: SCR > 50%. This method integrates both the functional and spatial importance of each species into the overall evaluation of ecosystem services, while accounting for their relative role in the structure and functioning of the lagoon ecosystem. Figure 2. Assessment of Ecosystem Services Provided by Lagoonal Seaweeds and Seagrasses along the Moroccan Coast: A Semi-Quantitative Review. 157 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Results Contribution of the studied algae and seagrass species to marine and coastal ecosystem services Provisioning services Food provision Gracilaria gracilis is commonly harvested for food supply in many countries, especially in Asian countries. It is consumed both fresh and processed (Norziah and Ching 2000; Barsanti and Gualtieri 2006; Pereira 2011). This red seaweed is rich in nutrients and offers several health benefits. It is low in calories and fat while being a good source of dietary fiber. It contains essential vitamins and minerals, including vitamin C, vitamin E, vitamin K, folate, calcium and magnesium. It also contains antioxidants, which help protect the body against oxidative stress (Ortiz et al. 2009; Guerra-Rivas et al. 2010; Pereira 2011; Francavilla et al. 2013; Rasyid et al. 2019). G. gracilis contains a gelling agent called agar, which is extracted from the cell walls of algae. Agar is commonly used in the food industry as a thickening and stabilizing agent. It is used in the production of jellies, puddings, ice creams, sauces and other food products that require a gel-like consistency (Pereira 2011; Francavilla et al. 2013). Table 3. Weighting factor determined by the Spatial Coverage Rate (SCR) in relation to the total area of the main channel within the lagoon: 1 (SCR<= 5%), 2 (5 < SCR <= 10), 3 (10 < SCR <= 25), 4(25 < SCR <= 50) and 5 (SCR > 50). Ecosystem services Native algal species Seagrass invasive algal species Gracilaria gracilis Ulva (U. lactuca, U. fasciata & U. intestinalis) Fucus spiralis Cystoseira humilis Zostera noltei Sargassum muticum Spatial coverage rate (%) 54 17 6 6 10 6 Weighting factor 5 3 2 2 2 2 Table 2. Table of search strings used in the literature review. Combinations Databases Search string (keywords and Boolean operators) Period Combination 1 - Scientific databases (ScienceDirect, Scopus, Web of Science, and Google Scholar) (“algae” OR “macroalgae” OR “seaweed”) AND (“ecosystem services” OR “ecological functions” OR “habitat function”) AND (“lagoon” OR “coastal lagoon”) Any date - Academic databases (ResearchGate and Academia) Combination 2 (Gracilaria gracilis OR Ulva OR Cystoseira humilis OR Fucus spiralis OR Sargassum muticum OR Zostera noltei) AND (Human consumption OR Water storage OR medicinal OR industrial use OR Air quality OR Coastal protection OR Climate regulation OR local weather conditions OR Ocean nourishment OR Lifecycle maintenance OR Pathogen control OR Cultural services) Any date Combination 3 (Gracilaria gracilis OR Ulva OR Cystoseira humilis OR Fucus spiralis OR Sargassum muticum OR Zostera noltei) AND (Human consumption OR Water storage OR medicinal OR industrial use OR Air quality OR Coastal protection OR Climate regulation OR local weather conditions OR Ocean nourishment OR Lifecycle maintenance OR Pathogen control OR Cultural services) AND (Oualidia OR Morocco OR Algeria OR Tunisia OR Mauritania OR Senegal OR Spain OR Portugal OR France OR North west Africa) Any date 158 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons The three Ulva species are promising varieties of green seaweed, each with considerable potential as sustainable food sources, providing distinct nutritional and bioactive profiles. Ulva lactuca is well-documented for its rich content of bioactive compounds, including polysaccharides, phenolic compounds, and essential minerals such as potassium and magnesium, making it a versatile food ingredient with applications in functional foods (Putra et al. 2024). Additionally, U. lactuca is renowned for its high nutritional value, comparable to conventional vegetables, especially when grown under controlled conditions (Roleda et al. 2021). U. fasciata is also rich in essential nutrients, particularly amino acids and fatty acids, which are beneficial for aquaculture, especially in abalone farming, highlighting its role in enhancing the growth and health of marine organisms (Latuihamallo et al. 2016). U. intestinalis, characteristic of arid regions, has been recognized for its rich mineral profile, providing a sustainable food source (Farzanah et al. 2022). Fucus species are not commonly used as food, but their extracts would be useful as dietary supplements (Lopez et al. 2011, 2012, 2013, 2014; Pereira 2011; Ferreres et al. 2012; Andrade et al. 2013). Fucus species are reported to contain polysaccharides mucilage with algin, fucoidan and laminarin; polyphenols, trace elements and minerals, potassium, bromine, chlorine, magnesium, calcium, iron and silicon, mannitol, vitamins and pro-vitamins A and D, ascorbic acid and lipids (glycosylglycerides) (Guiry and Blunden 1991; Holds and Kraan 2011). According to Lopes et al. 2011, F. spiralis is one of the macroalgae species that have been shown to be good sources of bioactive phytosterols that are a good choice for healthy diets, especially for people with high cholesterol levels. However, the freeze-drying process can reduce the bioaccessibility of some antioxidants and polyphenols (Francisco et al. 2020). Cystoseira humilis is not commonly used as food, but recent scientific research has shown that eicosapentaenoic acid (EPA) is a major constituent of the total lipid fraction of C. humilis which also exhibited a low ω-6/ωratio. 3, as well as a high unsaturation index (191.42) and low atherogenicity and thrombogenic indices (Belattmania et al. 2016; Koutsaviti et al. 2018), which can be used as nutritional food supplement in food industries. Concerning Zostera, there has been limited research exploring their promising potential as a source of natural bioactive compounds that can be used as food additives and preservatives in functional food industries. However, some literature confirms that Zostera seeds collected in the spring constituted a significant part of the diet and traditional culture of the Seri Indians living along the Gulf of California (Felger and Moser 1973; Hemminga and Duarte 2000; Nihal et al. 2013). Concerning the benefits for aquaculture, Howarth et al. (2022) reported that shellfish farming can have positive, neutral, and negative effects on seagrass. Few studies have demonstrated the positive interactions that can be generated by the filter-feeding activity of cultivated bivalves. However, more frequently, research studies have reported negative interactions that occur directly under and in the immediate vicinity of shellfish farms and decrease as one moves away from them. Although Sargassum muticum is a traditional food in Korea (Yang et al. 2013), it does not appear to have been commercially exploited as a food source in Western countries (Milledge et al. 2016). A study using Sargassum muticum 159 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons as a dietary supplement found that it led to an increase in natural killer lymphocytes (Park et al. 2015; Milledge et al. 2016). However, this brown algae contains high levels of heavy metals, hence the need to use it with carefulness (Lodeiro et al. 2004; Carro et al. 2015; Ungureanu et al. 2015). Katsanevakis et al. (2014) considered that Sargassum muticum has an indirect negative impact on food supply through fishing and aquaculture because it causes degradation of essential fish habitats and pollutes shellfish farming installations. Water storage and provision The primary negative impact of algae and seagrass on water supply is the clogging of intake pipes in industrial facilities (Katsanevakis et al. 2014). The Oualidia lagoon is particularly renowned for its shellfish farming activities. Currently, no published information exists on the issue of pipe clogging in these facilities due to algae, nor are there any reports on the positive impact native algae and seagrass in the Oualidia lagoon on water supply and storage. The negative impact of Sargassum muticum on the clogging of intake pipes in industrial facilities was recorded by Katsanevakis et al. (2014) as direct observation by experts. This is an undesirable effect generally observed in all non-native species. Biotic materials and biofuels While there may not be many patents involving the use of Gracilaria worldwide, recent studies have demonstrated that Gracilaria serves as a source of various natural marine products for diverse biotechnological applications. Gracilaria gracilis is a source of agar and other bioproducts, which are utilized across the pharmaceutical and cosmetic industries. Its bioactive compounds, including polysaccharides and antioxidants, exhibit significant antimicrobial and cytotoxic properties, contributing to its application in healthcare and biorefinery approaches (Martins et al. 2023). Several studies have shown that the green algae Ulva lactuca and Ulva fasciata represent significant resources of antioxidants and antibacterial agents (Chakraborty et al. 2010; Princely and Dhanaraju 2017; Anjali et al. 2019), as well as a rich source of vitamin B, proteins, minerals (calcium, potassium, magnesium, sodium, copper, iron, and iodine), and dietary fibers (Harsha Mohan et al. 2023). Regarding Fucus spiralis, multiple research works have demonstrated its dermo-cosmetic applications due to its antioxidant and anti-enzymatic properties, along with photoprotective attributes, coupled with its role in maintaining skin microbiota homeostasis (Freitas et al. 2020; Grina et al. 2020). Boutjagualt (2022) has shown that Fucus spiralis could be a novel source of natural antitumor agents and may be utilized in the production of promising drugs for cancer treatment. Research on the brown algae Cystoseira humilis has revealed its intriguing antioxidant activities, high degree of total unsaturation, and low atherogenic and thrombogenic indices. Consequently, C. humilis could be regarded as a promising compound for pharmaceutical and cosmetic industries (Belattmania et al. 2016). The bioactive components of algae have also attracted interest in research and development within the aquaculture and agronomy sectors. With the intensification of aquaculture, the emergence of antibiotic-resistant 166 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons and maintenance of the lagoon’s ecosystem health while providing economic benefits to coastal communities. Nevertheless, advanced scientific research and outreach activities to local managers and decision-makers is needed on this subject, taking into account local environmental conditions and specific objectives. Literature review carried out shows the lack of information available on ES of natives seaweed and seagrasses identified in the countries of the North-West African region, including Moroccan coast, especially provisioning services. This finding is confirmed by Web et al. (2023). The majority of the works published concerns the checklist up-to-date, distribution mapping, biomass estimation, biologic cycle and the regulatory role of certain pollutants (Benhissoune et al. 2001, 2002, 2003; De Clerck et al. 2003; John et al. 2004; Givernaud et al. 2005; Gaudry et al. 2007; El Ati-Hellal et al. 2007; Rezzoum et al. 2022; Al Qoh et al. 2022). It is only in the last decade that researchers began to publish on the bioactive components of certain algae for medicinal and cosmetic applications. This research work was carried out particularly on the species Gracilaria gracilis wild or from seaweed farming and this because of the global demand for its agar-agar (Ben Said et al. 2019; Hmani et al. 2021; Belattmania et al. 2021; Yahyaoui et al. 2024) (Table 4). There are also, in the North-West African region, other works of valorization of bioactive components on Fucus spiralis (Andrade et al. 2013; Samri et al. 2019; Grina et al. 2020; Boutjagualt et al. 2022; Baroud et al. 2023), Cystoseira humilis (Belattmania et al. 2016; Grina et al. 2020; Saidani et al. 2022; Farid 2024) and Table 4. Assessment Matrix of MCES for Algae and Seagrass Species in the Oualidia Lagoon: positive impact (+1), negative impact (-1), and Restricted information or lack of information (0). Ecosystem services Native algal species Seagrass species invasive algal species Gracilaria gracilis Ulva (U. lactuca, U. fasciata & U. intestinalis) Fucus spiralis Cystoseira humilis Zostera noltei Sargassum muticum Food provision 1 1 0 0 0 -1 Water storage and provision 0 0 0 0 0 -1 Biotic materials and Biofuels 1 1 1 1 1 1 Total 2 2 1 1 1 -1 Water purification 1 1 1 0 1 1 Air quality regulation 1 1 1 1 1 1 Coastal protection 0 0 0 0 1 -1 Climate regulation 1 1 1 1 1 1 Weather regulation 1 1 1 1 1 1 Ocean nourishment 1 1 1 1 1 0 Lifecycle maintenance 1 1 1 1 1 -1 Biological regulation 1 1 1 1 1 1 Total 7 7 7 6 8 3 Symbolic and aesthetic values 1 1 1 1 1 -1 Recreation and tourism 1 1 1 1 1 -1 Cognitive effects 1 1 1 1 1 1 Total 3 3 3 3 3 1 by species 12 12 11 10 12 3 Weighting factor (see table 3) 5 3 2 2 2 2 by spatial cover by species 60 36 22 20 24 6 167 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Ulva lactuca (Andrade et al. 2013; Oucif et al. 2020; Bouzenad et al. 2024; Brahimi et al. 2024; Ouahabi et al. 2024) (see Table 4). All this research, mostly recent, is still at the analysis and testing stage, and has not yet reached the level of industrialization. Moreover, the introduction of algae into the culinary culture of these countries remains very rare or even completely absent in some countries. The comparison with neighboring countries in Southern Europe as Spain, France and Portugal, shows that the species of Gracilaria gracilis, Ulva lactuca and Fucus spiralis constitute a vital raw material for the food and pharmaceutical industries because of their gelling properties. Agar extracted from Gracilaria is used in food as a thickener and stabilizer, as well as in microbiological and pharmaceutical contexts (Andrade et al. 2013; Filote et al. 2022). France was the first European country to establish a specific regulation concerning the use of seaweeds for human consumption as non-traditional food substances. Currently, 12 macroalgae among which Ulva sp., species of the genus Fucus and Gracilaria are authorized as vegetables and condiment (CEVA 2019). However, the use of algae in the culinary traditions of these Europeen countries is still marginal, often confined to specialized restaurants or regional gastronomic initiatives. Regarding the seagrass species Zostera noltei, all research in Morocco and other countries of the North-West African region has focused on its support and provisioning services (Clavier et al. 2011; Boutahar et al. 2019; El-Hacen et al. 2020; Mosbahi et al. 2020; Bououarour et al. 2021; Sidi Cheikh et al. 2022; Hamza et al. 2024). A similar pattern is observed in Southern European countries (Cabaço et al. 2008; Román et al. 2018; Garmendia et al. 2021), with some rare publications on the valorisation of proactive products, the example of the work of Achamlale et al. (2009), which highlighted the potential of this seagrass as a novel source of zosteric acid (Table 4). This overview of the current consideration of algae and seagrasses in the North-West African region is well illustrated by the case study of the Oualidia Lagoon (Morocco), where the estimation of the potential Marine and Coastal Ecosystem services (MCES) demonstrated a partial exploitation of its ecosystem services, primarily dominated by regulating and maintenance services, while provisioning and cultural services remain almost unexploited (Table 4, Fig. 3). Sargassum muticum, as an invasive species, has negative impacts on the invaded ecosystem by competing with native species. Its assessment in the Oualidia Lagoon shows that this species has a negative impact of 50% of MCES. To mitigate its proliferation and reverse this trend, various research projects have recently been initiated in the North-West African region to explore its potential uses (Ould Abdellahi et al. 2017; Bouzenad et al. 2024; Brahimi et al. 2024), similar to efforts in neighbouring Southern European countries having explored this area several years in advance (Silva et al. 2013, 2019, 2023; Puspita et al. 2017) (Table 5). The World Bank, in its report “Global Seaweed New and Emerging Markets 2023” indicated that in the natural world, the field of seaweed is still untapped, while it could stimulate economic growth and promote greater social equality, while addressing environmental issues. According to the same report, the ecosystem services of seaweed could contribute to the achievement of at least nine of the 17 UN Sustainable Development Goals. They can indeed help eliminate hunger, improve health, mitigate climate change, conserve biodiversity and marine life, promote economic growth and create decent jobs. 168 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Conclusion In this study, we examined the ecosystem services provided by algae and seagrass species that dominate the lagoonal ecosystems along the Moroccan Atlantic coast, in northwestern Africa—a region where local research remains limited. Based on a comprehensive literature review, we assessed the contribution of key native species (Gracilaria gracilis, Ulva spp., Cystoseira humilis, Fucus spiralis, and Zostera noltei), as well as the invasive species Sargassum muticum, to Marine and Coastal Ecosystem Services (MCES). A semi-quantitative Table 5. Examples of efforts to valorise seaweeds and seagrasses in the North-western African region, along with a comparison to studies conducted in neighboring Western European countries at later dates. Marine and Coastal Ecosystem Services Species Countries References Provisioning services (Bioactive components) Gracilaria gracilis Tunisia Yahyaoui et al. 2024; Hmani et al. 2021; Ben Said et al. 2019 Morocco Belattmania et al. 2021 Ulva lactuca Algeria Bouzenad et al. 2024; Oucif et al. 2020 Morocco Ouahabi et al. 2024; Brahimi et al. 2024 Portugal Andrade et al. 2013. Fucus spiralis Morocco Baroud et al. 2023; Boutjagualt et al. 2022; Grina et al. 2020; Samri et al. 2019 Portugal Filote et al. 2022; Andrade et al. 2013 Cystoseira humilis Algeria Saidani et al. 2022 Morocco Farid 2024; Grina et al. 2020; Belattmania et al. 2016 Sargassum muticum Algeria Bouzenad et al. 2024 Morocco Brahimi et al. 2024 Mauritania Ould Abdellahi et al. 2017 France Puspita et al. 2017 Spain Baltrusch et al. 2023; Carro et al. 2015; Silva et al. 2023 Portugal Silva et al. 2013; Silva et al. 2019. Zostera noltei France Achamlale et al. 2009a Regulating and maintenance services Zostera noltei Tunisia Mosbahi et al. 2020 Algeria Hamza et al. 2024 Morocco Bououarour et al. 2021; Boutahar et al. 2019 Mauritania Sidi Cheikh et al. 2022; El-Hacen et al. 2020; Clavier et al. 2011 Senegal Sidi Cheikh et al. 2022 Portugal Cabaço et al. 2008 Figure 3. Comparison between potential and current MCES provided by algae and seagrass beds in the Oualidia lagoon. 169 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons approach was then applied to integrate the functional and spatial value of each species into the overall evaluation of MCES, while accounting for their relative importance in the structure and functioning of the lagoon ecosystem. The results from the Oualidia Lagoon indicate that 70–85% of potential ecosystem services are documented, with native algae and seagrass species contributing primarily to regulating and supporting services. In contrast, S. muticum exerts a negative impact on approximately 43% of these services, particularly those related to water retention, coastal protection, and cultural value. An assessment of the current use of ecosystem services shows that, except for the extraction of agar-agar from Gracilaria, none of the studied species are currently exploited for food, medical, cosmetic, or industrial purposes, suggesting minimal provisioning value. Conversely, the lagoon’s high biodiversity, the presence of pollution-sensitive bioindicator species, its role as a nursery for juvenile fish, and its importance as a feeding ground for migratory birds all highlight the dominance of regulating and supporting services. Regarding cultural services, only cognitive benefits were identified as significant, mainly due to the extensive scientific research conducted on the site. A comparison between the theoretical potential and the actual MCES currently utilized reveals an underuse of approximately 25–30% of their potential. This finding aligns with the lagoon’s Ramsar designation, which promotes the sustainable use of natural resources rather than intensive exploitation. In conclusion, strengthening applied research and awareness-raising initiatives is essential to maximize the potential of native species while mitigating the impacts of invasive species such as Sargassum muticum. Bridging current knowledge gaps will not only help reduce ecological pressures but also contribute to the achievement of several United Nations Sustainable Development Goals (SDGs), particularly those related to food security, health, climate action, and biodiversity conservation. Promoting the sustainable use of native species and developing pilot algal aquaculture projects in lagoonal environments could ultimately transform these ecosystems into drivers of blue growth and ecological resilience at the regional scale. Additional information Conflict of interest The authors have declared that no competing interests exist. Ethical statement No ethical statement was reported. Use of AI No use of AI was reported. Funding Rachida HOUSSA, Nor-Eddine REZZOUM, and Hakima ZIDANE are conducting this work within the framework of the Coastal and Marine Habitat Mapping project, funded by the National Institute of Fisheries Research (Institut National de Recherche Halieutique – Morocco), with the scientific collaboration of Ouafa CHRIFI, a professor at Cadi Ayyad University of Marrakech, and the participation of Sara el Mouttaqui and Fatima EL ASRI, two young doctors from Hassan II University. 170 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Author contributions Rachida HOUSSA, Nor-Eddine REZZOUM and Hakima ZIDANE contributed to the study conception and design. Material preparation, data collection and analysis were performed by Nor-Eddine REZZOUM, Hakima ZIDANE, Sara el Mouttaqui, Fatima EL ASRI and Rachida HOUSSA. The first draft of the manuscript was written by Rachida HOUSSA. Ouafa CHRIFI, Nor-Eddine REZZOUM and Hakima ZIDANE commented on previous versions of the manuscript. All authors read and approved the final manuscript. Author ORCIDs Rachida Houssa https://orcid.org/0000-0002-4525-4528 Data availability Data used in this article were published in 2022 by Rezzoum et al. (https://doi. org/10.34874/IMIST.PRSM/fsejournal-v12i1.30614). Fig. 1 satellite image of Oualidia lagoon was generated using open access data from https://earthexplorer.usgs.gov/. References Achamlale S, Rezzonico B, Grignon-Dubois M (2009a) Rosmarinic acid from beach waste: Isolation and HPLC quantification in Zostera detritus from Arcachon lagoon. Food Chemistry 113(4): 878–883. https://doi.org/10.1016/j.foodchem.2008.07.040 Achamlale S, Rezzonico B, Grignon-Dubois M (2009b) Evaluation of Zostera detritus as a potential new source of zosteric acid. Journal of Applied Phycology 21: 347–352. https://doi.org/10.1007/s10811-008-9375-8 Al Qoh S, Fatima L, Bouchra B, Jamal A, Omar A, Samira E (2022) Spatial and temporal variation of physico-chemical parameters of water and its impact on algal distribution in the Oualidia lagoon (Atlantic coast of Morocco). Regional Studies in Marine Science 52: 102326. https://doi.org/10.1016/j.rsma.2022.102326 Andrade PB, Barbosa M, Matos RP, Lopes G, Vinholes J, Mouga T, Valentão P (2013) Valuable compounds in macroalgae extracts. Food Chemistry 138: 1819–1828. https://doi.org/10.1016/j.foodchem.2012.11.081 Anderson RJ, Smit AJ, Levitt GJ (1999) Upwelling and fish-factory waste as nitrogen sources for suspended cultivation of Gracilaria gracilis in Saldanha Bay, South Africa. In Sixteenth International Seaweed Symposium: Proceedings of the Sixteenth International Seaweed Symposium held in Cebu City, Philippines. Springer, Dordrecht, 455–462. https://doi.org/10.1007/978-94-011-4449-0_54 Anjali KP, Sangeetha BM, Devi G, Raghunathan R, Dutta S (2019) Bioprospecting of seaweeds (Ulva lactuca and Stoechospermum marginatum): The compound characterization and functional applications in medicine-a comparative study. Journal of Photochemistry and Photobiology B: Biology 200: 111622. https://doi.org/10.1016/j. jphotobiol.2019.111622 Arnaud-Haond S, Duarte CM, Diaz-Almela E, Marba N, Sintes T, Serrão EA (2012) Implications of extreme life span in clonalorganisms: Millenary clones in meadows of the threatened seagrass Posidonia oceanica. PLoS ONE 7(2): e3045. https://doi. org/10.1371/journal.pone.0030454 Baltrusch K, Flórez-Fernández N, Illera M, Torres MD, López-Mosquera ME, Domínguez H (2023) Potential use of Sargassum muticum as source of plant biostimulants after three different drying methods. Journal of Applied Phycology 35(2): 921–933. https://doi.org/10.1007/s10811-023-02907-2 171 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Baroud S, Saida T, Abdelhakim H (2023) Characterization of Three Brown Algae Bifurcaria Bifurcata, Cystoseira Gibraltarica and Fucus Spiralis. International Journal of Life Science and Agriculture Research 2(11): 445–456. https://doi.org/10.55677/ijlsar/ V02I11Y2023-04 Barsanti L, Gualtieri P (2006) Algae and Men, Chapter 7. In: Algae - Anatomy, Biochemistry, and Biotechnology. LLC: CRC Press, Taylor and Francis Group, 251–291. https://doi.org/10.1201/9781003187707 Beaumont NJ, Austen MC, Atkins JP, Burdon D, Degraer S et al. (2007) Identification, definition and quantification of goods and services provided by marine biodiversity: implications for the ecosystem approach. Marine Pollution Bulletin 54: 253–265. https://doi.org/10.1016/j.marpolbul.2006.12.003 Belattmania Z, Engelen AH, Pereira H, Serrão EA, Barakate M, Elatouani S, Sabour B (2016) Potential uses of the brown seaweed Cystoseira humilis biomass: 2-Fatty acid composition, antioxidant and antibacterial activities. Journal of Materials and Environmental Science 7(6): 2074–2081. https://www.jmaterenvironsci.com/Document/ vol7/vol7_N6/222-JMES-2403-Belattmania.pdf Belattmania Z, Bhaby S, Nadri A, Khaya K, Bentiss F, Jama C, Reani A, Vasconcelos V, Sabour B (2021) Gracilaria gracilis (Gracilariales, Rhodophyta) from Dakhla (Southern Moroccan Atlantic Coast) as source of Agar: Content, chemical characteristics, and gelling properties. Marine Drugs 19(12): 672. https://doi.org/10.3390/md19120672 Benhissoune S, Boudouresque CF, Verlaque M (2001) A check-list of marine seaweeds of the Mediterranean and Atlantic coasts of Morocco. I. Chlorophyceae Wille sl. https://doi.org/10.1515/BOT.2001.023 Benhissoune S, Boudouresque C-F, Verlaque M (2002) A Checklist of the Seaweeds of the Mediterranean and Atlantic Coasts of Morocco. II. Phaeophyceae 45(3): 217–230. https://doi.org/10.1515/BOT.2002.021 Benhissoune S, Boudouresque C-F, Perret-Boudouresque M, Verlaque M (2002) “A Checklist of the Seaweeds of the Mediterranean and Atlantic Coasts of Morocco. III. Rhodophyceae (Excluding Ceramiales) 45(5): 391–412. https://doi.org/10.1515/ BOT.2002.041 Benhissoune S, Boudouresque C-F, Perret-Boudouresque M, Verlaque M (2003) “A Checklist of the Seaweeds of the Mediterranean and Atlantic Coasts of Morocco. IV. Rhodophyceae - Ceramiales 46(1): 55–68. https://doi.org/10.1515/BOT.2003.008 Bennouna A, Assobhei O, Berland B, El Attar J (2000) Étude des populations phytoplanctoniques de la lagune de Oualidia (Maroc); dinoflagellés potentiellement nuisibles. Marine Life 10(1–2): 3–18. Ben-Ari T, Neori A, Ben-Ezra D, Shauli L, Odintsov V, Shpigel M (2014) Management of Ulva lactuca as a biofilter of mariculture effluents in IMTA system. Aquaculture 434: 493–498. https://doi.org/10.1016/j.aquaculture.2014.08.034 Ben Jenana RK, Triki MA, Haouala R, Hanachi C, Ben Khedher M, Henchi B (2009) Composted Posidonia, chicken manure and olive mill residues, an alternative to peat as seed germination and seedling growing media in Tunisian nursery. Pakistan Journal of Botany 41(6): 3139–3147. Ben Said R, Nacef E, Marzougui K (2019) Recherche des facteurs les plus influents sur le rendement et la qualité de l’agar-agar de Gracilaria gracilis. Bjerregaard R, Valderrama D, Radulovich R, Diana J, Capron M, Mckinnie CA, .Radulovich R, Valderrama D, Yarish C (2016) Seaweed aquaculture for food security, income generation and environmental health in tropical developing countries (No. 107147, pp. 1–16). The World Bank. 172 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Boström C, Pittman S, Kneib R, Simenstad C (2011) Seascape ecology of coastal biogenic habitats: advances, gaps and challenges. Marine Ecology Progress Series 427: 191–217. https://doi.org/10.3354/meps09051 Bouma TJ, Olenin S, Reise K, Ysebaert T (2009) Ecosystem engineering and biodiversity in coastal sediments: posing hypotheses. Helgoland Marine Research 63: 95–106. https://doi.org/10.1007/s10152-009-0146-y Bououarour O, El Kamcha R, Boutoumit S et al. (2021) Effects of the Zostera noltei meadows on benthic macrofauna in North Atlantic coastal ecosystems of Morocco: spatial and seasonal patterns. Biologia 76: 2263–2275. https://doi.org/10.1007/ s11756-021-00718-9 Boutahar L, Maanan M, Bououarour O, Richir J, Pouzet P, Gobert S, Maanan M, Zourarah B, Benhoussa A, Bazairi H (2019) Biomonitoring environmental status in semi-enclosed coastal ecosystems using Zostera noltei meadows. Ecological Indicators 104: 776–793. https://doi.org/10.1016/j.ecolind.2019.04.039 Boutjagualt I, Laila B, Fouzia H et al. (2022) Chemical characterization, antiproliferative activity and molecular docking of bioactive compounds from brown algae Fucus spiralis. Algal Research 68: 102887. https://doi.org/10.1016/j.algal.2022.102887 Bouzenad N, Ammouchi N, Chaib N, Messaoudi M, Bousabaa W, Bensouici C, Sawicka B, Atanassova M, Ahmad SF, Zahnit W (2024) Exploring Bioactive Components and Assessing Antioxidant and Antibacterial Activities in Five Seaweed Extracts from the Northeastern Coast of Algeria. Marine Drugs 22(6): 273. https://doi.org/10.3390/ md22060273 Brahimi I, EL Boujamaai M, Errachidi F et al. (2024) Biotechnological properties and antifungal activity of lactic acid bacteria isolated from two marine algae Ulva lactuca and Sargassum muticum collected from the Moroccan coast of Sidi Bouzid-El Jadida. Euro-Mediterranean Journal for Environmental Integration 9: 105–113. https://doi. org/10.1007/s41207-023-00448-1 Cabaço S, Machás R, Vieira V, Santos R (2008) Impacts of urban wastewater discharge on seagrass meadows (Zostera noltei). Estuarine, Coastal and Shelf Science 78(1): 1–13. https://doi.org/10.1016/j.ecss.2007.11.005 Capillo G, Savoca S, Costa R, Sanfilippo M, Rizzo C, Lo Giudice A, Albergamo A, Rando R, Bartolomeo G, Span`o N, Faggio C (2018) New insights into the culture method and antibacterial potential of Gracilaria gracilis, Mar. Drugs 16: 492. https://doi. org/10.3390/md16120492 Carro L, Barriada JL, Herrero R, de Vicente MES (2015) Interaction of heavy metals with Ca-pretreated Sargassum muticum algal biomass: characterization as a cation exchange process. Chemical Engineering Journal 264: 181–187. https://doi. org/10.1016/j.cej.2014.11.079 Chakraborty K, Lipton AP, Paulraj R, Chakraborty RD (2010) Guaiane sesquiterpenes from seaweed Ulva fasciata Delile and their antibacterial properties. European Journal of Medicinal Chemistry 45(6): 2237–2244. https://doi.org/10.1016/j.ejmech.2010.01.065 Chan K-Y, Wong K, Ng SL (1982) Growth of Enteromorpha linza in sewage effluent and sewage-effluent seawater mixtures. Hydrobiologia 97: 9–13. https://doi.org/10.1007/ BF00014955 Cheah WY, Show PL, Chang J-S, Ling TC, Juan JC (2015) Biosequestration of atmospheric CO2 and flue gas-containing CO2 by microalgae, Bioresource Technology 184: 190–201. https://doi.org/10.1016/j.biortech.2014.11.026 173 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Çinar ME, Arianoutsou M, Zenetos A, Golani D (2014) Impacts of invasive alien marine species on ecosystem services and biodiversity: a pan-European review. Aquatic Invasions 9(4): 391–423. https://doi.org/10.3391/ai.2014.9.4.01 Clavier J, Chauvaud L, Carlier A, Amice E, Van der Geest M, Labrosse P, Diagne A, Hily C (2011) Aerial and underwater carbon metabolism of a Zostera noltii seagrass bed in the Banc d’Arguin, Mauritania. Aquatic Botany 95(1): 24–30. https://doi. org/10.1016/j.aquabot.2011.03.005 Costa-Domingo G, Critchley M, Vukelic M, Gosling J, Friedrich L (2022) Assessment of ecosystem change, recovery success and ecosystem service change following restoration. AFRIMED, Deliverable 4.3., 56 pp. Crippa M, Solazzo E, Guizzardi D, Monforti-Ferrario F, Tubiello FN, Leip A (2021) Food systems are responsible for a third of global anthropogenic GHG emissions. Nature food 2(3): 198–209. https://doi.org/10.1038/s43016-021-00225-9 De Clerck O, Bolton JJ, John DM (2003) Seaweed diversity patterns in sub-Saharan Africa. Proceedings of te Marine Biodiversity in Sub-Saharan Africa: The Known and the Unknown. Cape Town , South Africa, 229–241. Decker C, Griffith C et al. (Eds). http:// hdl.handle.net/1834/973 Delgard ML, Deflandre B, Deborde J, Richard M, Charbonnier C, Anschutz P (2013) Changes in nutrient biogeochemistry in response to the regression of Zostera noltei meadows in the Arcachon Bay (France). Aquatic Geochemistry 19: 241–259. https:// doi.org/10.1007/s10498-013-9192-9 Deng Y, Liu S, Feng J, Wu Y, Mao C (2021) What drives putative bacterial pathogens removal within seagrass meadows? Marine Pollution Bulletin 166: 112229. Deveau AM, Miller-Hope Z, Lloyd E, Williams BS, Bolduc C, Meader JM, Weiss F, Burkholder KM (2016) Antimicrobial activity of extracts from macroalgae Ulva lactuca against clinically important Staphylococci is impacted by lunar phase of macroalgae harvest. Letters in Applied Microbiology 62(5): 363–371. https://doi.org/10.1111/lam.12563 Dion P, Le Bozec S (1999) Contenu tissulaire des ulves en azote et phosphore comme facteurs limitants de leur croissance en baie de Douarnenez. Actes de colloques-IFREMER, 77–85. https://archimer.ifremer.fr/doc/00716/82812/87634.pdf#page=78 Dirhamsyah (2007) An economic valuation of seagrass ecosystems in east Bintan, Riau Archipelago, Indonesia. Oseanologidan Limnologi di Indonesia 33: 257–270. Doumeizel V (2022) La révolution des algues. éd. des Équateurs. Duarte CM, Chiscano CL (1999) Seagrass biomass and production: a reassessment. Aquatic Botany 65(1–4): 159–174. https://doi.org/10.1016/S0304-3770(99)00038-8 Duarte CM, Middelburg JJ, Caraco N (2005) Major role of marine vegetation on the oceanic carbon cycle. Biogeosciences 2(1): 1–8. https://doi.org/10.5194/bg-2-1-2005 Duarte CM, Marba N, Gacia E, Fourqurean JW, Beggins J, Barron C et al. (2010) Seagrass community metabolism: Assessing thecarbon sink capacity of seagrass meadows. Global Biogeochemical Cycles 24: GB4032. https://doi.org/10.1029/2010GB003793 Duarte CM, Kennedy H, Marbà N, Hendriks I (2013) Assessing the capacity of seagrass meadows for carbon burial: current limitations and future strategies Ocean Coast. Manage 83: 32–38. https://doi.org/10.1016/j.ocecoaman.2011.09.001 El Ati-Hellal M, Hedhili A, Dachraoui M (2007) Contents of Trace Metals in Water and Macroalgae along the Mediterranean Coast of Tunisia. Bulletin of Environmental Contamination and Toxicology 78: 33–37. https://doi.org/10.1007/s00128-007-9000-6 El-Hacen EHM, Cheikh MAS, Bouma TJ, Olff H, Piersma T (2020) Long-term changes in seagrass and benthos at Banc d’Arguin, Mauritania, the premier intertidal system 174 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons along the East Atlantic Flyway. Global Ecology and Conservation 24: e01364. https:// doi.org/10.1016/j.gecco.2020.e01364 El Hamoumi R, El Malki S, Abdeslam R, Fahmi A, Dakki M (2022) The Sidi Moussa-Oualidia wetland complex A Bird Paradise between land and sea. Frontiers in Science and Engineering, [S.l.], 12(1): 1–11. https://doi.org/10.34874/IMIST.PRSM/fsejournal-v12i1.31633 El-Sayed HS, Elshobary ME, Barakat KM, Khairy HM, El-Sheikh MA, Czaja R, Allam B, Senousy HH (2022) Ocean acidification induced changes in Ulva fasciata biochemistry may improve Dicentrarchus labrax aquaculture via enhanced antimicrobial activity. Aquaculture 560: 738474. https://doi.org/10.1016/j.aquaculture.2022.738474 Farrelly DJ, Everard CD, Fagan CC, McDonnell KP (2013) Carbon sequestration and the role of biological carbon mitigation: A review, Renewable and Sustainable Energy Reviews 21: 712–727. https://doi.org/10.1016/j.rser.2012.12.038 Farid Y, Etahiri S, Assobhei O (2009) Activité antimicrobienne des algues marines de la lagune d’Oualidia (Maroc): Criblage et optimisation de la période de la récolte. Applied Biosciences 24: 1543–1552. https://www.m.elewa.org/JABS/2009/24/8.pdf Farid Y, Chennaoui M, Assobhei O, Etahiri S (2012) Screening des algues marines d’oualidia à la recherche d’activités antimicrobienne et antiinflammatoire. Revue de Microbiologie Industrielle, Sanitaire, et Environnementale 6(2): 192–209. Farid Y, Chennaoui M, Assobhei O, Etahiri S (2020) Evaluation de l’effet du lieu de récoltes des algues marines des côtes atlantiques marocaines sur l’activité antibactérienne anti-inflammatoire. Éditions universitaires européennes. Farid Y (2024) Exploration of Antimicrobial Potential in Oualidia Algae-Unveiling Cystoseira Humilis as a Promising Source of Bioactive Molecules. Ecological Engineering & Environmental Technology 25. https://doi.org/10.12912/27197050/175119 Farzanah R, Clausen MP, Arnspang EC, Schmidt JE, Bastidas-Oyanedel JR (2022) Feasibility of United Arab Emirates native seaweed Ulva intestinalis as a food source: study of nutritional and mineral compositions. Phycology 2(1). https://doi.org/10.3390/ phycology2010008 Fei XG (2004) Solving the coastal eutrophication problem by large scale seaweed cultivation. Hydrobiologia 512: 145–151. https://doi.org/10.1007/978-94-007-0944-7_19 Felger R, Moser MB (1973) Eelgrass (Zostera marina L.) in the Gulf of California: discovery of its nutritional value by the Seri Indians. Science 181(4097): 355–356. https:// doi.org/10.1126/science.181.4097.355 Ferreres F, Lopes G, Izquierdo AG, Andrade PB, Sousa C, Mouga T, Valentão P (2012) Phlorotannins extracts from Fucales characterized by HPLC-DAD-ESI-MSn: Approaches to hyaloronidase innibitory capacity and antioxidant properties. Mar. Drugs 10: 2766–2781. https://doi.org/10.3390/md10122766 Filote C, Lanez E, Popa VI, Lanez T, Volf I (2022) Characterization and bioactivity of polysaccharides separated through a (sequential) biorefinery process from Fucus spiralis brown macroalgae. Polymers 14(19): 4106. https://doi.org/10.3390/polym14194106 Florez-Fernandez N, Illera M, Sanchez M, Lodeiro P, Torres MD, López-Mosquera ME, Dominguez H (2021) Integrated valorization of Sargassum muticum in biorefineries. Chemical Engineering Journal 404: 125635. https://doi.org/10.1016/j. cej.2020.125635 Fourqurean JW, Duarte CM, Kennedy H, Marbà N, Holmer M, Mateo MA et al. (2012) Seagrass ecosystems as a globally significant carbon stock. Nature Geoscience 5(7): 505–509. https://doi.org/10.1038/NGEO1477 175 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Francavilla M, Franchi M, Monteleone M, Caroppo C (2013) The red seaweed Gracilaria gracilis as a multi products source. Marine Drugs 11(10): 3754–3776. https://doi. org/10.3390/md11103754 Francisco J, Horta A, Pedrosa R, Afonso C, Cardoso C, Bandarra NM, Gil MM (2020) Bioaccessibility of antioxidants and fatty acids from Fucus spiralis. Foods 9(4): 440. https://doi.org/10.3390/foods9040440 Freitas R, Martins A, Silva J et al. (2020) Highlighting the biological potential of the brown seaweed Fucus spiralis for skin applications. Antioxidants 9(7): 611. https:// doi.org/10.3390/antiox9070611 Gaudry A, Zeroual S, Gaie-Levrel F et al. (2007) Heavy Metals Pollution of the Atlantic Marine Environment by the Moroccan Phosphate Industry, as Observed through their Bioaccumulation in Ulva Lactuca. Water Air Soil Pollut 178: 267–285. https://doi. org/10.1007/s11270-006-9196-9 GBIF Secretariat (2023) Ulva fasciata Delile in GBIF Backbone Taxonomy. https://doi. org/10.15468/39omei [accessed via GBIF.org on 2024-09-24] Givernaud T, Sqali N, Barbaroux O, Orbi A, Semmaoui Y, Rezzoum NE, Mouradi A, Kaas R (2005) Mapping and biomass estimation for a harvested population of Gelidium sesquipedale (Rhodophyta, Gelidiales) along the Atlantic coast of Morocco. Phycologia 44(1): 66–71. https://doi.org/10.2216/0031-8884(2005)44[66:MABEFA]2.0.CO;2 Grina F, Ullah Z, Kaplaner E, Moujahid A, Eddoha R, Nasser et al. (2020) In vitro enzyme inhibitory properties, antioxidant activities, and phytochemical fingerprints of five Moroccan seaweeds. South African Journal of Botany 128: 152–160. https://doi. org/10.1016/j.sajb.2019.10.021 Guerra-Rivas G, Gómez-Gutiérrez CM, Alarcón-Arteaga G, Soria-Mercado IE, Ayala-Sánchez NE (2010) Screening for anticoagulant activity in marine algae from the Northwest Mexican Pacific coast. Journal of Applied Phycology 23: 495–503. https://doi. org/10.1007/s10811-010-9618-3 Guiry MD, Blunden G (1991) Seaweed Resources in Europe: Uses and Potential. New York: John Wiley and Sons Ltd. Haglund K, Pedersén M (1993) Outdoor pond cultivation of the subtropical marine red alga Gracilaria tenuistipitata in brackish water in Sweden. Growth, nutrient uptake, co-cultivation with rainbow trout and epiphyte control. Journal of Applied Phycology 5: 271–284. https://doi.org/10.1007/BF02186230 Haines-Young R, Potschin M (2011) Common International Classification of Ecosystem Services (CICES): 2011 Update. Nottingham: Report to the European Environmental Agency. Hamon F, Camille N, Michel B, Jean LC, Noël Pierre FEY (2024) Ulva lactuca Linnaeus, 1753, https://doris.ffessm.fr/ref/specie/808 Hamza H, De Wit R, Mammeria AB (2024) Spatiotemporal variation of seagrass meadow and associated bivalves in Mediterranean lagoon (El Mellah-Algeria). ARPHA Preprints. Hannachi Y, Hafidh A (2020) Biosorption potential of Sargassum muticum algal biomass for methylene blue and lead removal from aqueous medium. International Journal of Environmental Science and Technology 17: 3875–3890. https://doi.org/10.1007/ s13762-020-02742-9 Harsha ME, Madhusudan S, Revathy B (2023) The sea lettuce Ulva sensu lato: Future food with health-promoting bioactives, Algal Research 71: 103069. https://doi. org/10.1016/j.algal.2023.103069 182 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Sabourin N, Huet S, Lamare V, Verlaque M (2022) Ulva sp. groupe intestinalis Linnaeus 1753. https://doris.ffessm.fr/ref/specie/3093 Saidani K, González-Peña D, Giménez L, Touati N, Bedjou F, de Ancos B, Sánchez-Moreno C (2022) Bioactive compounds identification, antioxidant and antibacterial activities of Algerian marine algae extracts. Current Bioactive Compounds 18(8): 81–93. https://doi.org/10.2174/1573407218666220310100414 Salomidi M, Katsanevakis S, Borja A, Braeckman U, Damalas D, Galparsoro I, Mifsud R, Mirto S, Pascual M, Pipitone C, Rabaut M, Todorova V, Vassilopoulou V, Vega Fernandez T (2012) Assessment of goods and services, vulnerability, and conservation status of European seabed biotopes: a stepping stone towards ecosystem-based marine spatial management. Mediterranean Marine Science 13(1): 49–88. https:// doi.org/10.12681/mms.23 Samri N, Hsaine L, El Kafhi S, Khlifi S, Etahiri S (2019) Radical scavenging activity and phenolic contents of brown seaweeds harvested from the coast of Sidi Bouzid (El Jadida, Morocco). International Journal of Pharmaceutical Sciences Review and Research 54(21): 116–122. Shams El DNG, El-Sherif ZM (2013) Nutritional value of Cymodocea nodosa and Posidonia oceanica along the western Egyptian Mediterranean coast. The Egyptian Journal of Aquatic Research 39(3): 153–165. https://doi.org/10.1016/j.ejar.2013.10.001 Sharma Mona Sandeep KM, Neha S, Bansal D, Arivalagan P, Smita SK (2021) Towards sustainable agriculture with carbon sequestration, and greenhouse gas mitigation using algal biochar. Chemosphere 275: 129856. https://doi.org/10.1016/j.chemosphere.2021.129856 Shpigel M, Shauli L, Odintsov V, Ashkenazi N, Ben-Ezra D (2018) Ulva lactuca biofilter from a land-based integrated multi trophic aquaculture (IMTA) system as a sole food source for the tropical sea urchin Tripneustes gratilla elatensis. Aquaculture 496: 221–231. https://doi.org/10.1016/j.aquaculture.2018.06.038 Shpigel M, Guttman L, Shauli L, Odintsov V, Ben-Ezra D, Harpaz S (2017) Ulva lactuca from an integrated multi-trophic aquaculture (IMTA) biofilter system as a protein supplement in gilthead seabream (Sparus aurata) diet. Aquaculture 481: 112–118. https://doi.org/10.1016/j.aquaculture.2017.08.006 Shpigel M, Guttman L, Ben-Ezra D, Yu J, Chen S (2019) Is Ulva sp. able to be an efficient biofilter for mariculture effluents? Journal of Applied Phycology 31: 2449–2459. https://doi.org/10.1007/s10811-019-1748-7 Sidi C, Mohamed A, Bandeira S, Soumah S, Diouf G, Diouf EM, Sanneh O, Cardoso N, Kujabie A, Ndure M, John L, Moreira L, Radwan Z, Santos I, Ceesay A, Vinaccia M, Potouroglou M (2022) Seagrasses of West Africa: New discoveries, distribution limits and prospects for management. Diversity 15(1): 5. https://doi.org/10.3390/d15010005 Silkina A, Bazes A, Vouve F, Le Tilly V, Douzenel P, Mouget JL, Bourgougnon N (2009) Antifouling activity of macroalgal extracts on Fragilaria pinnata (Bacillariophyceae): a comparison with Diuron. Aquatic Toxicology 94: 245–254. https://doi.org/10.1016/j. aquatox.2009.07.004 Silva J, Alves C, Pinteus S, Horta A, Pedrosa R (2013) High antioxidant activity of Sargassum muticum and Padina pavonica collected from Peniche coast (Portugal). Current Opinion in Biotechnology 24: S116. https://doi.org/10.1016/j.copbio.2013.05.361 Silva LD, Bahcevandziev K, Pereira L (2019) Production of bio-fertilizer from Ascophyllum nodosum and Sargassum muticum (Phaeophyceae). Journal of Oceanology and Limnology 37: 918–927. https://doi.org/10.1007/s00343-019-8109-x 183 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Silva A, Soares C, Carpena M, Oliveira PG, Echave J, Chamorro F, Donn P, Mansour SS, Barroso MF, Prieto MA (2023) Assessment of Nutritional Profile of Sargassum muticum Alga from the Spanish Coastline. In Biology and Life Sciences Forum 26(1): 94. https://doi.org/10.3390/Foods2023-15028 Sogard S, Able KW (1991) A comparison of eelgrass, sea lettuce macroalgae, and marsh creeks as habitats for epibenthic fishes and decapods. Estuarine, Coastal and Shelf Science 33: 501–519. https://doi.org/10.1016/0272-7714(91)90087-R Spanò N, Di Paola D, Albano M, Manganaro A, Sanfilippo M, D’Iglio C et al. (2022) Growth performance and bioremediation potential of Gracilaria gracilis (Steentoft, LM Irvine & Farnham, 1995). International Journal of Environmental Studies 79(4): 748–760. https://doi.org/10.1080/00207233.2021.1954775 Tasdemir D, Silvia S, Caroline U-T, Timo J, Martina B, Arlette W-S, Claudia W, Vivien AE (2024) Epiphytic and endophytic microbiome of the seagrass Zostera marina: Do they contribute to pathogen reduction in seawater? Science of The Total Environment 908: 168422. https://doi.org/10.1016/j.scitotenv.2023.168422 TEEB (2010) The Economics of Ecosystems and Biodiversity: ecological and economic foundation. Kumar P, editor London and Washington: Earthscan. Thibaut T, Blanfune A, Markovic L, Verlaque M, Boudouresque CF, Perret-Boudouresque M, Macic V, Bottin L (2014) Unexpected abundance and longterm relative stability of the brown alga Cystoseira amentacea, hitherto regardedas a threatened species, in the north-western Mediterranean Sea. Marine Pollution Bulletin 89: 305e323. https:// doi.org/10.1016/j.marpolbul.2014.09.043 Ungureanu G, Santos S, Boaventura R, Botelho C (2015) Biosorption of antimony by brown algae S. muticum and A. nodosum. Environmental Engineering and Management Journal 14: 455–463. https://doi.org/10.30638/eemj.2015.047 United Nations (2021) United Nations Food Systems Summit. https://www.un.org/en/ food-systems-summit/vision-principles Von Braun J, Afsana K, Fresco LO, Hassan MHA (2023) Science and innovations for food systems transformation. Springer Nature, 948 pp. https://doi.org/10.1007/9783-031-15703-5 Webb P, Natalie K, Somers S, Thilsted H (2023) Seaweed’s contribution to food security in lowand middle-income countries: Benefits from production, processing and trade. Global Food Security 37: 100686. https://doi.org/10.1016/j.gfs.2023.100686 Wilson KA, Able KW, Heck Jr KL (1990) Predation rates on juvenile blue crabs in estuarine nursery habitats: evidence for the importance of macroalgae (Ulva lactuca). Marine Ecology Progress Series 58(3): 243–251. https://doi.org/10.3354/ meps058243 Yahyaoui K, Traikia M, Rihouey C, Picton L, Gardarin C, Ksouri WM, Laroche C (2024) Chemical characterization of polysaccharides from Gracilaria gracilis from Bizerte (Tunisia). International Journal of Biological Macromolecules 266: 131127. https:// doi.org/10.1016/j.ijbiomac.2024.131127 Yang EJ, Ham YM, Lee WJ, Lee NH, Hyun CG (2013) Antiinflammatory effects of apo-90-fucoxanthinone from the brown alga, Sargassum muticum. DARU Journal of Pharmaceutical Sciences 21: 62. https://doi.org/10.1186/2008-2231-21-62 Yang YF, Fei XG, Song JM, Hu HY, Wang GC, Chung IK (2006) Growth of Gracilaria lemaneiformis under different cultivation conditions and its effects on nutrient removal in Chinese coastal waters. Aquaculture 254: 248–255. https://doi.org/10.1016/j. aquaculture.2005.08.029 184 Estuarine Management and Technologies 2: 151–184 (2025), DOI: 10.3897/emt.2.167289 Rachida Houssa et al.: Seaweed and seagrass services in Moroccan lagoons Yang Y, Chai Z, Wang Q, Chen W, He Z, Jiang S (2015) Cultivation of seaweed Gracilaria in Chinese coastal waters and its contribution to environmental improvements. Algal research 9: 236–244. https://doi.org/10.1016/j.algal.2015.03.017 Zerrifi S, El Khalloufi F, Oudra B, Vasconcelos V (2018) Seaweed bioactive compounds against pathogens and microalgae: potential uses on pharmacology and harmful algae bloom control. Marine Drugs 16(2): 55. https://doi.org/10.3390/md16020055 Zhang Y, Han JY, Mu J, Feng Y, Gu XJ, Ji YX (2013) Bioactivity and constituents of several common. Seaweeds. Chinese Science Bulletin 58(19): 2282–2289. https://doi. org/10.1007/s11434-013-5745-y Zhao F, Liu F, Liu J, Ang PO, Duan D (2008) Genetic structure analysis of natural Sargassum muticum (Fucales, Phaeophyta) populations using RAPD and ISSR markers. Journal of Applied Phycology 20: 191–198. https://doi.org/10.1007/s10811-0079207-2 Zidane H, Houssa R, El asri F, El hajli N, Elillouchi M, CharoukIN, Rezzoum N (2022) Spatio-Temporal distribution of the endobenthic fauna community in the Oualidia lagoon (2013 and 2019). Frontiers in Science and Engineering, [S.l.], 12(1): 1–15. https://doi. org/10.34874/IMIST.PRSM/fsejournal-v12i1.30767