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Review

A Comparison between the Production of Edible Macroalgae Worldwide and in the Mediterranean Sea

by
Gorana Jelić Mrčelić
1,*,
Svjetlana Krstulović Šifner
2 and
Vedrana Nerlović
2
1
Faculty of Maritime Studies, University of Split, Ruđera Boškovića 37, 21000 Split, Croatia
2
Department of Marine Studies, University of Split, Ruđera Boškovića 37, 21000 Split, Croatia
*
Author to whom correspondence should be addressed.
Oceans 2024, 5(3), 442-465; https://doi.org/10.3390/oceans5030026
Submission received: 10 February 2024 / Revised: 11 June 2024 / Accepted: 1 July 2024 / Published: 3 July 2024

Abstract

:
Macroalgae are beneficial for consumers and producers due to their high productivity, their chemical composition and their efficient cultivation without additional feed. Asia dominates global macroalgae production, while European production is still marginal and mainly based on wild harvesting in the North Atlantic. The European Commission has launched initiatives to promote the sustainable production, safe consumption and innovative use of macroalgae products in European regional seas, including the Mediterranean Sea. A variety of coastal and seabed types and a wide range of environmental conditions make the Mediterranean a hotspot of marine biodiversity while providing good conditions for the cultivation of macroalgae. The aim of this paper is to compare the global macroalgae production and macroalgae production in the Mediterranean Sea, focussing on the cultivation of edible macroalgae. The paper also discusses the limitations and possibilities of macroalgae production in the region. Macroalgae production is one of the most promising sectors of the blue economy in the Mediterranean. The production of edible macroalgae suitable for human consumption has great potential, considering future population growth and related food security and health issues, as well as the additional ecosystem benefits of macroalgae production.

1. Introduction

Algae is a common name for a polyphyletic group of taxonomically unrelated organisms. In the broadest sense, algae are a functional group of oxygen-evolving photosynthetic autotrophs that use light to synthesise complex organic compounds from carbon dioxide and water [1,2,3]. Marine macroalgae or seaweeds are macroscopic marine algae that can grow to several metres in length and belong to the domain Eukarya and the kingdoms Plantae (phylum Chlorophyta—green algae and phylum Rhodophyta—red algae) and Chromista (phylum Ochrophyta, class Phaeophyceae—brown algae) [2]. AlgaeBase (http://www.algaebase.org (accessed on 31 December 2023)) currently contains 175,050 species and infraspecific names of algae, and there are about 1800 different species of brown algae, 6200 species of red algae and 1800 species of green algae [2]. As macroalgae require both sufficient light and a fixation point, they mostly inhabit the rocky substrate of coastal areas, with some exceptions that float freely [4].
In addition to their great ecological importance, they are also of great commercial importance as food, food additives, animal feed, fertilisers, nutraceuticals and pharmaceuticals, cosmetics, biofuels and biopackaging [3,5,6,7]. New algae-based products and new uses have yet to be discovered [8]. In recent decades, macroalgae have become interesting for consumers and producers due to their high productivity, their chemical composition and the fact that they can be grown efficiently without additional feed, antibiotics and pesticides [9]. The bioactive substances of macroalgae have a high nutritional, nutraceutical, industrial, agricultural, pharmacological and biomedical value, and are used daily in household and industrial products (in foods such as ice cream, yoghurt, cream, sauces, dressings, jam and cheese, and in hair, skin and oral care products such as shampoo, cream, toothpaste or deodorants, as well as in plastic bags and packaging) [2,6,10,11,12,13,14,15,16,17].
Coastal communities around the world have a long tradition of harvesting and cultivating macroalgae for food, medicine, rituals and coastal defence [18,19]. According to some authors, macroalgae have been used as food and medicine for at least 14,000 years [19] and have been part of the human diet in Japan and China for 2500 years [8]. Macroalgae are of great importance for the development of the human brain, as they contain essential elements for brain development [20,21]. Therefore, they have directly influenced the development of culture and society [22]. In Japan and China, edible macroalgae have been of great importance since ancient times due to the long coastlines and abundance of macroalgae [23], while in the rest of the world the custom of eating macroalgae has only survived in Ireland, Iceland, France (Brittany), Peru and Chile [11]. In Europe, macroalgae have long been used as animal feed and to improve the soil to combat plant diseases and insects [8,24,25]. The custom of eating macroalgae was brought to Europe and other Western countries from the Far East, but in some parts of Europe the consumption of algae was traditionally associated with poverty [10].
Nowadays, the consumption of macroalgae is associated with a healthy diet, as they are a natural food with a high nutritional value and a high content of minerals, vitamins, polysaccharides and a low fat content, which benefits human health [2,14]. As macroalgae are widespread and can be found in all climatic regions of the world, macroalgae gastronomy is experiencing a boom, together with the locavore movement [11].
The cultivation of macroalgae began in East Asia in 1640 [26], or perhaps much earlier [27], while commercial macroalgae cultivation began in the mid-twentieth century [9]. Although macroalgae cultivation has increased significantly in the last two decades, production is very low compared to the global agricultural production of 1.6 trillion tonnes [28]. Nevertheless, it is estimated that 5 million km2 of macroalgae cultivation area could produce the same amount of biomass annually as the entire global agricultural sector [29]. Given the increasing global consumption of seafood and the sustainability of algae cultivation, the sector has great potential to feed the world’s growing population and provide a livelihood for millions of people [7].
Of the approximately 220 commercially used macroalgae species [9], more than 150 species (85%) are used directly for human consumption and indirectly for food products as stabilisers, thickeners, emulsifiers and colourants [6,27]. Between 2000 and 2020, global macroalgae production increased from 10.6 million tonnes to 35 million tonnes, with 97% coming from cultivation mainly for human consumption and for food additives [7]. In 2020, the global production of marine macroalgae accounted for 99.8% of aquatic algae production and 51.4% of global mariculture production [7].
Macroalgae can not only be harvested in nature, but can also be cultivated in onshore, nearshore or offshore macroalgae farms, as well as in integrated multitrophic aquaculture systems (IMTA) or together with wind farms [30]. There are many reasons for integrating macroalgae farms with wind farms, including economic (savings in infrastructure costs by installing macroalgae farm moorings at the same time as wind farm moorings, and the potential for much larger macroalgae farms), social (a reduced occurrence of spatial conflicts through offshore relocation and the integration of human activities) and environmental (an increase in marine biodiversity and associated restorative ecosystem services) benefits [31,32]. Macroalgae farms are usually located on the coasts, while offshore farms are currently too expensive, but will probably be more economically viable in the future [9].
Cultivation techniques are selected according to species and site characteristics, and include line cultivation (with lines close to the seabed, submerged or floating), net cultivation (with floating or slightly submerged nets) and floating (submerged) raft cultivation (lines or nets on a floating or sometimes submerged fixed frame). Tank or pond cultivation consists of cultivation under controlled conditions for sensitive species (Caulerpa spp. or Ulva spp.) that are tied or free-floating), while rock cultivation involves growing macroalgae directly on the seabed or on artificial substrate [33,34]. In IMTA systems, macroalgae are cultivated in proximity to multiple species at different trophic levels, mitigating environmental impacts and producing biomass that can be economically utilised. As dissolved nutrients are an important limiting factor for macroalgae production, the nutrients excreted by fish and molluscs can accelerate macroalgae growth and production [35]. In IMTA systems, waste nutrients are recycled, less nutrients are released into the environment, and the overall productivity of the system is increased [35,36]. Therefore, energy and nutrient losses are minimised, while the efficiency of resource use is maximised by closing the nutrient cycle [37].
Macroalgae farms are a climate-friendly model of aquaculture where the species do not require freshwater, feed or fertiliser, and provide benefits to coastal ecosystems and communities by increasing food security, creating jobs and supporting ocean justice [38,39]. The choice of location for macroalgae harvesting and cultivation in coastal waters is a very important factor, influencing the quantity and quality of macroalgae composition [25] as well as the sustainability of macroalgae production [40]. The response to abiotic stress (temperature, salinity, nutrients, irradiance, desiccation, storms and currents) has implications for algal physiology and biochemical functioning [41]. At low sea temperatures, for example, membrane proteins and lipids can be damaged by the formation of crystals in the cells, which impairs growth [42], while at high temperatures the loss of chlorophyll and other photosynthetic pigments can lead to a partial or complete bleaching of the thalli and the inhibition of growth [43,44]. Abiotic stressors can also promote the transition from growth to the sexual and asexual reproductive phase [45].
The Mediterranean Sea is the largest and deepest enclosed sea, covering 0.8% of the surface and 0.32% of the volume of the world’s oceans [46]. A variety of coastal and seabed types and a wide range of environmental conditions make the Mediterranean a hotspot of marine biodiversity, with more than 1124 macroalgae species (20% endemic) [47], offering good potential for the cultivation of edible macroalgae.
The Mediterranean region has a long and rich history and great cultural importance. It is a densely populated region along the coasts of 21 countries, and almost a third of the Mediterranean population lives in coastal areas [46]. The population of the Mediterranean coastal region will reach 690 million people by 2050 [48]. Population growth and the associated intensification of human activities will increase the risks for the coastal environment, but also for coastal communities. These risks include hazards such as flooding, storms, heat stress, coastal erosion and loss of agricultural land, as well as health problems related to air pollution, lack of water supply, sewage treatment and waste disposal. Nature-based solutions, including regenerative macroalgae cultivation, could help Mediterranean countries to improve their resilience and adaptability to environmental changes (restorative ecosystem services). As macroalgae absorb pollutants (nitrogen, phosphorus and heavy metals), remove carbon dioxide, and produce oxygen, macroalgae cultivation can help to reduce water pollution, oxygen depletion and acidification, and mitigate climate change [49]. In addition to carbon sequestration, there are two other mechanisms by which macroalgae can contribute to climate change mitigation: through carbon offsets (by using macroalgal products to reduce carbon dioxide emissions from the industry) and methane reduction in agriculture (by using algal feed to reduce methane emissions from livestock) [50].
Mediterranean countries are also facing a deficit in food production due to the limited availability of water and agricultural land. Together with population growth and climate change, this will increase dependence on food imports [48]. Another important issue is the increasing obesity in almost all Mediterranean countries since 2012, which is linked to the replacement of the traditional healthy Mediterranean diet with the “Western” diet [48]. The food deficit could be solved by expanding and promoting the cultivation of macroalgae, which can also help to combat unhealthy eating habits and promote the consumption of locally produced, better quality food.
Although macroalgae production has been well analysed at the global level [7,51,52] and in Europe [30,53,54,55,56,57], data on macroalgae production in the Mediterranean are fragmented, incomplete and of low quality [6,58].
Considering all these facts, the aim of this study is to compare the global macroalgae production and the production of macroalgae in the Mediterranean region, with a special focus on the cultivation of edible macroalgae. The paper also discusses the limitations and possibilities of macroalgae production in the Mediterranean region.

2. Macroalgae Fit for Human Consumption

2.1. Global Production

According to the Food and Agriculture Organisation (FAO) data, global algae production (including cultivation and wild harvesting) increased 60-fold from 0.56 million tonnes in 1950 to 35.8 million tonnes (35.7 million tonnes of macroalgae and 56,456 tonnes of microalgae) in 2019 [52].
In 2020, global macroalgae production amounted to 35 million tonnes, worth USD 9.7 billion [59], and 85% of the macroalgae produced were used for human consumption [7]. Some sources have corrected the macroalgae production reported by the FAO to 26.9 million tonnes, as they have calculated that the production of the main producers is six to seven times lower than reported [60].
In 1969, the production of macroalgae from cultivation was, for the first time, as high as the production from wild collection (1.1 million tonnes) [52]. Interestingly, the wild collection of macroalgae has remained at the same level since 1969, while macroalgae production from cultivation has increased rapidly. In 2020, 97% of macroalgae came from cultivation [7].
In the period between 1990 and 2019, the amount of cultivated macroalgae increased significantly, mainly due to the increase in the cultivation of brown macroalgae (from 3.1 million tonnes to 16.4 million tonnes) and red macroalgae (from 1 million tonnes to 18.3 million tonnes), while the cultivation of green macroalgae decreased (from 31,000 tonnes to 17,000 tonnes) [52]. Despite the rapid growth of macroalgae cultivation, it is far from reaching its full potential, which is estimated at up to 100,000 million tonnes [34]. While in Asia, 99.5% of macroalgae were cultivated [36], and outside Asia they were mainly harvested from the wild [34].
In the period between 1976 and 2018, trade in macroalgae increased from USD 65 million to USD 1.3 billion, with Indonesia, Chile and the Republic of Korea being the main exporters, while China, Japan and the United States of America were the main importers [51]. In 2021, world trade in macroalgae and other algae fit for human consumption, fresh, chilled, frozen or dried, totalled USD 895 million, and the main exporters were South Korea, China, Indonesia, Japan, and the USA [61]. The global market for macroalgae was worth USD 8.3 billion in 2023 and is estimated to reach USD 17.8 billion by 2032 [62].
The growth of macroalgae production has been mainly driven by the increasing demand for macroalgae-based food and food additives [30], and the market for macroalgae food will continue to grow with the increasing awareness of healthy and sustainable eating [63].

2.2. Important Taxa

Of the more than 650 known edible macroalgae species [10], around 150 are used as food [6,27]. The consumption of brown macroalgae predominates (66.5%), compared to the consumption of red (33%) and green (5%) macroalgae [64].
Table 1 shows the annual global production of the eight most important species in relation to the production volume in the years 2000, 2005, 2010, 2015 and 2020 [7].
Some taxa, such as Laminaria spp., Saccharina spp., Undaria spp., Porphyra spp., Eucheuma spp., Gracilaria spp., Macrocystis spp. and Caulerpa spp., are primarily used for human consumption, while their production residues are used for other purposes (feed for abalone culturing) [51]. Gelidum spp. is used for salad and jelly, but also in the production of agar. Gracilaria spp. is mainly used as feed for abalone and for the production of agar, and Eucheuma spp. for the production of carrangeenan [27]. Undaria pinnatifida and Porphyra spp. are among the most consumed macroalgae taxa [67].
Saccharina japonica (kombu) is the most commonly eaten species. It is a brown alga that is restricted to Japan, China, the Pacific coast of Russia, North America and the Mediterranean [68]. Saccharina japonica has been consumed by the Chinese for at least 1500 years, but it was first successfully cultivated on floating rafts in the early 1950s [67]. The species can be easily cultivated by attaching young samples to ropes hanging from the floats. Sites suitable for the cultivation of S. japonica should have a total nitrogen content of over 5 mg/m3, while the optimum temperature is between 5 °C and 10 °C, but growth is still good enough at 20 °C [67]. However, under aquaculture conditions, kelp is grown for one winter [69].
Undaria pinnatifida (wakame) is a brown alga native to Northeast Asia [65]. It occurs in the lower intertidal zone and in shallow, partially sheltered intertidal zones (up to 18 m, but mainly at a depth of 1 to 3 m) [69]. In its natural range, the species prefers average monthly sea surface temperatures of −0.6 °C to 16.8 °C in winter and 23 °C to 29.5 °C in summer [70]. It is an opportunistic species that forms dense kelp forests and can compete with native species for space and light [65]. Wakame has considerable economic importance as a food in Japan, Korea and China [68]. It has been cultivated in Japan since the Nara Period (710–794) [11], but large-scale longline cultivation began in 1957 [11].
Porphyra spp./Pyropia spp. are commonly known as nori, which are used for the preparation of sushi. The biology of Porphyra spp. has been extensively studied for its economic value, but many species have been reclassified as Pyropia. There are currently 53 accepted species names of the genus Porphyra in AlgaeBase, [67], and 79 accepted species names of the genus Pyropia. Porphyra spp. is found on rocky shores worldwide, including some species in the tropics or at the poles, and optimal growth conditions vary. In Wales, traditional laverbread is made by cooking Porphyra umbilicalis in salt, and the Irish counterpart is sleabhac or sloke. The cultivation of Porphyra spp./Pyropia spp. began in the 17th century in Japan, Korea and China, but scientifically based cultivation began in the 1960s [67]. It is a thriving sector of aquaculture, but no dramatic change in overall volume is expected [71]. Several different Porphyra and Pyropia species are cultivated and used for nori preparation (mainly Pyropia yezoensis and Pyropia tenera).

3. Macroalgae Fit for Human Consumption in Europe

3.1. Production

Only a small proportion of the 1700 macroalgae species in European waters [72] are commercially exploited in limited coastal areas [73]. In Europe, interest in macroalgae has increased in recent decades due to the global increase in macroalgae production, the many sustainable uses of macroalgae, and the wide range of macroalgae species [74]. While macroalgae production in Asia has increased significantly over the years, European production has hardly grown at all, as the harvest from the wild has remained at the same level due to overharvesting and weather changes [30,53,54]. In 2015, 296,194 tonnes of macroalgae were produced in Europe and only 0.5% were cultivated [27], while in 2019 only 287,033 tonnes of macroalgae were produced (0.8% of global macroalgae production) and only 3.9% were cultivated (0.03% of global macroalgae cultivation) [52].
European macroalgae production is concentrated in the Atlantic region and is dominated by Spain, France and Ireland in terms of the number of companies, while Norway, France and Ireland dominate in terms of biomass production [56,57,75]. Taking into account the number of companies that produce macroalgae in Europe, wild collection dominates, with 68% compared to cultivation (32% of seaweed production, 76% of which is produced in sea-based facilities and 24% in land-based facilities) [56].
In 2018, the European algae sector had an economic value of EUR 1.7 billion and provided employment for 14,000 people, while macroalgae accounted for EUR 700 million (8% of the global market), with large multinational companies dominating the sector at 80% [8]. The annual growth rate is between 7 and 10%, with a wholesale value of around EUR 24 million and a focus on Alaria esculenta (dabberlocks), Saccharina latissimi (sugar kelp), Porphyra sp., Palmaria palmata (dulse) and Ulva sp. [54,76,77]. The production of edible macroalgae for food is still relatively small, but the market is growing with a variety of food products [54].
The opportunity for an expansion of macroalgae in Europe lies in the poor reputation of Asian producers in the environmentally conscious European market, which demands the best quality of sustainable products [77]. The European macroalgae market could be worth up to EUR 9.3 billion in 2030, with the edible macroalgae sector accounting for a large share (worth up to EUR 1.8 billion), and the remaining share split between animal feed, biostimulants, biopackaging, pharmaceuticals and nutraceuticals, additives, cosmetics and biofuels [30].
European countries were the world’s leading importer of macroalgae products in 2016 with 180,000 tonnes (USD 613 million) [27], and demand for these valuable commodities will continue to rise with the popularity of vegan and plant-based diets and Japanese cuisine in Europe [63]. European exports of seaweed and other algae fit for human consumption, fresh, chilled, frozen or dried, totalled USD 75 million (8% of global exports) in 2021 [61]. Europe is also one of the most innovative regions in the field of food ingredients from macroalgae [6,78].

3.2. Important Taxa and Consumption

More than 650 edible algae species consumed worldwide have entered the EU market, although they are not listed in the EU Novel Food Catalogue (NFC) [10]. A detailed list of algae species consumed as food, food supplements and/or food additives in Europe before and/or after 1997 has been published, together with region/country and source [77]. More than 150 edible algae species have been identified in Europe, including 130 seaweed species, but only 30 species have been authorised by the EU as novel foods [77]. Interestingly, the list of Novel Food Priorities currently contains 104 macroalgae taxa [79].
It is interesting to note that 36% of European macroalgae companies produce macroalgae for direct human consumption and 15% for the production of food additives and supplements, while the remaining percentage is divided between cosmetics and well-being (17%), animal feed (10%), fertilisers and biostimulants (11%), and other applications (11%) including biofuels, bioremediation or biomaterials [56]. Edible macroalgae species are mainly sold fresh or dried for human consumption in France, Iceland, Ireland and Spain [7,11], while in the other European countries the consumption of macroalgae is negligible [56].
In Europe, 60% of the seaweed consumed are Pyropia spp., and are mainly imported from Asia (only 1% comes from Europe) [77]. Palmaria palmata is one of the most popular edible macroalgae species in Europe [11] and has a long tradition of harvesting in France, Iceland and especially in Ireland, where it is considered a delicacy [73]. A total of 90% of the consumed P. palmata is wild harvested in France [77]. The most commonly harvested taxa in Europe are Laminaria spp., Ascophyllum nodosum, P. palmata, Chondrus crispus, Porphyra spp., Ulva spp., Himanthalia elongata, Undaria pinnatifida and Fucus spiralis [56].
The price of edible macroalgae depends on the product (dry products usually have lower prices), on the type of production (harvested macroalgae usually have lower prices) and on the taxa [56]. The macroalgae with the highest average value are as follows: Porphyra spp. (251 EUR/kg dry weight), Codium spp. (155 EUR/kg dry weight), Gracilariopsis longissima (155 EUR/kg dry weight), P. palmata (114 EUR/kg dry weight), U. pinnatifida (108 EUR/kg dry weight), Saccharina latissima (88 EUR/kg dry weight), H. elongata (86 EUR/kg dry weight), C. crispus (72 EUR/kg dry weight), and Fucus spp. (25 EUR/kg dry weight, on the online seaweed market in Spain) [56].
The French Centre d’Etudes et de Valorisation des Algues (CEVA) has revised a seaweed standard for food and cosmetics that includes farmed and wild harvested seaweed and takes into account that the classification of seawater should follow the shellfish regulation. It has also proposed a positive list of (safe) seaweeds (in France): seaweeds (including all major edible seaweed taxa as well as Phymatolithon calcareum and Ulva spp.), [80].

3.3. The Development of Cultivation

The vast majority of macroalgae are wild harvested in Europe (e.g., Palmaria palmata), including all dominant producers: Scotland, Ireland, Iceland, Portugal, Spain, France, the Netherlands, Denmark, Sweden and Norway [58,81]. In Europe, the cultivation of macroalgae began in the mid-1980s [53,54], but has been hampered by a lack of technology, poor infrastructure, complicated management, limited investment and the lack of integration into the value chain [30]. Macroalgae are cultivated in 13 European countries, mainly in near-shore systems [56], while some species (Ulva spp.) are mainly cultivated in land-based systems due to their high growth capacity [74]. In limited European coastal areas, only a few taxa, such as Saccharina latissima, Alaria esculenta and Ulva spp., are cultivated on a larger scale [82].
Europe is the leading region in the number of seaweed start-ups (more than 50% in 2022), but investment in start-ups fell from USD 67 million in 2021 to USD 34 million in 2022 and flowed mainly into downstream companies that process seaweed into products, while cultivation start-ups are the least popular [60]. In the period between 2020 and 2022, USD 70 million was invested in the algae food sector. However, the biggest challenge for seaweed cultivation in Europe is the high cost of cultivated seaweed and the imbalance between the demand for taxa for human consumption, such as Ulva spp., Palmaria spp. and Porphyra spp., and the mainly cultivated taxa, such as Saccharina spp. [60].
As European macroalgae production depends on the harvesting of wild stocks, the demand for certain taxa could jeopardise wild ecosystems [55]. The future expansion of macroalgae cultivation in Europe is expected not only due to the ban on wild collection for some species or the low wild biomass, but also due to the high demand for edible macroalgae and their high commercial value. It is estimated that 30% of demand in the European macroalgae market and around 20% of demand for edible macroalgae could be met by European producers, and that this sector could create 85,000 jobs. However, to reach this target, between 7700 and 26,300 hectares of marine farms, and 300 to 1000 hectares of onshore farms are needed [30].
There are several factors that could promote the increase macroalgae cultivation in Europe, including favourable environmental conditions (nutrient-rich, cold waters suitable for cultivation) in European coastal regions and socio-economic conditions [30,83,84], but also a growing global and European macroalgae market [63]. The socio-economic conditions include the quality of regulation, the efficiency of administration, and the quality of the trading infrastructure, but also a high standard and associated high-calibre customers who are willing to buy high-quality products). According to some authors, the production of species with high market demand, such as P. palmata, Porphyra spp. and Ulva spp., should be expanded [54]. The main macroalgae species cultivated in Europe in 2030 will be Ulva lactuca (sea lettuce) for food, S. latissima for food and feed, and A. esculenta and P. palmata for food and cosmetics [30].

4. Macroalgae Fit for Human Consumption in the Mediterranean Region

4.1. Production

Only a few of the 21 Mediterranean countries, including Spain, France, Morocco and Tunisia, harvest or cultivate macroalgae, albeit in very small quantities [28,56], which is mainly due to low natural macroalgae production, the lack of significant tidal fluctuations and inefficient harvesting techniques [6]. Unfortunately, there is a lack of a serious analysis of the algal sector in the Mediterranean, including the edible macroalgae sector, and it is difficult to obtain complete and reliable data on macroalgae production [6,58]. In the European part of the Mediterranean, France and Spain are the largest macroalgae producers [8]. The majority of European macroalgae production is concentrated on the Atlantic coasts due to the larger intertidal zone, wider geographical distribution and greater abundance and size of macroalgae species [56].
Italy reported the production of Gracilaria sp. in the period from 1990 to 2000 with a production between 3000 and 5000 tonnes for the marine waters of the Mediterranean and Black Sea [85]. Since 2016, Morocco has reported the production of Gracilaria gracilis. Production was 8.1 tonnes in 2016, reached a maximum of 272.8 tonnes in 2019, and totalled 174 tonnes in 2022 in the Mediterranean and Black Sea marine waters [85]. Tunisia reported the production of Gracilariopsis longissima in quantities of 50 tonnes in 2019, 20 tonnes in 2020, 30 tonnes in 2021 and 79 tonnes in 2022 for the Mediterranean and Black Sea marine waters [85].
The list of start-ups and scale-ups worldwide involved in macroalgae breeding and propagation, cultivation and harvesting, processing infrastructure and equipment, and monitoring and laboratory analyses is available online [86]. It also contains data on species, production methods, and applications. Of all the listed companies involved in the cultivation and harvesting of macroalgae, only four are located on the Mediterranean coast (one in Spain, one in France and two in Israel) (Table 2).
There is one land-based farm for Ulva spp. and one harvesting site for Ascophyllum nodosum on the Spanish Mediterranean coast, and one land-based farm for Ulva rigida on the French Mediterranean coast [87].
In Italy, most of the macroalgae biomass is imported, and only one out of a total of fifteen companies harvests local macroalgae today [6], although there were several companies in the past that utilised Ulva spp. and Gracilaria spp. from the Venice Lagoon [88]. The lack of macroalgae farms in Italy is explained by the high initial investment and the lack of a supply chain [6]. The coasts of the Adriatic and Ionian Seas offer many suitable sites for the production of macroalgae, but only the production of microalgae has been developed there [89].
It is important to remember that Israel is a pioneer in land-based seaweed cultivation, especially in innovative technologies, since 1982 [90,91,92]. In addition to Israel and Morocco, macroalgae production is still in the pilot phase in Egypt [93] and Tunisia (Gracilaria sp.) [94].
In 2022, the export value of seaweed and other algae fit for human consumption amounted to USD 12.6 million, while imports totalled USD 20.7 million for 15 countries in the Mediterranean region (Figure 1). France, Spain, Israel and Morocco dominated the export value with USD 4.7 million, USD 3.4 million, USD 3.5 million and USD 0.7 million, respectively [61].

4.2. Important Taxa and Their Commercial Potential

Native algal species from the Mediterranean represent only a minority of the total European production [56,74] and are mainly used as food, especially Ulva spp. and Gracilaria sp. [6,77]. Ulva lactuca and Chondracanthus teedei were traditionally consumed fresh by fishermen in the Italian coastal regions, especially in Sicily [77,95].
Table 3 shows the list of edible macroalgae in the Mediterranean Sea [96].
Some of the species listed in Table 3 are non-native species in the Mediterranean Sea, which has the largest number of alien macroalgae of any sea in the world, with more than 60 alien macroalgae [97]. In the coastal areas of the Mediterranean, non-native macroalgae with a high reproduction rate have a high probability of becoming invasive, although their invasion need not be a global phenomenon [97].
For example, Undaria pinnatifida was introduced to the Mediterranean Sea (Thau Lagoon) in 1971 via oyster farming [98]. As an introduced species in many coastal areas worldwide, it has attracted much attention [90,91,92,93,94,95,96,97,98,99,100,101]. Undaria pinnatifida is one of the 100 worst invasive alien species in the world [99,102], and is listed as a species with a negative impact on biodiversity and ecosystem services in European seas and the Mediterranean [100,101]. In Venice, it is considered a pest related to the problem of marine structure fouling [101]. Some authors suggest [70], that U. pinnatifida can be managed as a potentially valuable species that creates new habitats and fisheries. Similar to U. pinnatifida, S. japonica was accidentally introduced via oyster farming in the Thau Lagoon (France, the Mediterranean Sea) in 1984 [103], while according to other sources it was introduced much earlier, in 1976 [66].
Sometimes commercial harvesting is a good option for dealing with alien species (e.g., U. pinnatifida in New Zealand), but under no circumstances should species be introduced into new areas [104,105,106]. Commercial harvesting measures for alien species should be accompanied by commercialisation plans and a risk assessment of commercial use [106].
Of the species listed in Table 3., Ulva spp., C. teedei, Osmundea pinnatifida and Porphyra umbilicalis have a long culinary tradition in Europe.
Chondracanthus teedei is a small red algae that can grow up to 15 cm in size. It is widely distributed in the Atlantic, Mediterranean and Black Seas and has also been introduced in Japan, Brazil and the Indian Ocean [68]. It occurs in intertidal and subtidal zone habitats, in semi-exposed or sheltered areas [107]. Chondracanthus sp. has potential for utilisation due to its importance to the carrageenan and food industries [107]. In Andalusia (Spain), Ulva sp., Gracilaria sp., Gracilariopsis longissima and C. teedei are cultivated in earth ponds [107,108]. The species is used as máru in the traditional cuisine of some Italian regions (Veneto region and the southern regions of Puglia, Sardinia, Sicily and Campania), but this tradition is not widespread [95]. In summer, it is harvested by hand and sold on the street dressed with lemon juice and salt [107].
Osmundea pinnatifida (pepper dulse) is a perennial, abundant, medium-sized red alga (up to 15 cm long). Osmundea pinnatifida is found in the North-East Atlantic, the Atlantic Islands, the Mediterranean and Black Sea, Southwest and East Asia, and South Africa and Australia [109]. It occurs at a sea surface temperature of 5 to 25 °C, a salinity of 30–35 PSU and at a depth of 0 to 30 m on exposed to moderately sheltered rocky shores [109]. It is exposed to fluctuations in low tide, temperature and light, and varies in size and colour depending on its location on the coast [110]. The peak of the vegetation is in summer, and reproduction takes place in spring and summer [109]. Osmundea pinnatifida has a taste and odour similar to a mixture of garlic, pepper and truffle (the truffle of the sea). Information on the cultivation of O. pinnatifida is very scarce [110]. In Spain, 100 kg were produced and marketed fresh/pickled/chopped for flavouring in 2013 [109]. Further studies are needed to develop cultivation methods and potential commercialisation [109].
Porphyra umbilicalis (purple laver, pink laver, laver, nori) is a red alga that occurs under a wide range of conditions in the littoral to splash zone, especially on exposed rocky shores. It is well adapted to desiccation, strong light, extreme and rapid temperature and salinity changes, and can tolerate stronger water movements than most other red algae [111]. The confirmed distribution is currently the North Atlantic, while the global distribution needs to be verified [68]. Of the 133 species of Porphyra sp. (Porphyra sensu lato includes species that are closely related to Porphyra or until recently belonged to the genus Porphyra, such as Pyropia), only six species are usually cultivated, and cultivation requires sophisticated technology and large investments [112]. Porphyra umbilicalis is harvested by hand in France and Spain and cultivated in France, Ireland and Norway (trials) [113]. It is used in the form of leaves and flakes, as a nori substitute, as a laver and as an ingredient in snack mixes. The consumption of P. umbilicalis is associated with many health benefits due to its high protein and low fat content, as well as its high content of mineral salts, trace elements, vitamins, amino acids and polyunsaturated fatty acids, etc. [114].
One of the most promising taxa in the field of macroalgae production in the Mediterranean region is the genus Ulva. There are several pilot projects for the cultivation of Ulva spp. in the Mediterranean region [6]. In the Eastern Mediterranean, the experimental system for the cultivation of Ulva spp. was tested in a shallow coastal area in central Israel, as it is abundant on the Israeli coasts and has high biomass productivity, as shown by its extensive offshore cultivation for biofuel [115]. In this study, the authors used 2 m3 cages with air outlets to test the influence of tumbling, air mixing and external water exchange on the intensification of Ulva sp. growth. The advantage of Ulva spp. is their high abundance and availability in coastal waters around the world [116], their rapid growth under a wide range of environmental conditions, their valuable chemical composition, their high nutrient uptake (bioremediation efficiency) and their diverse applications [115,117]. The genus Ulva often dominates in macroalgae blooms, known as green tide, and can affect coastal ecosystems and associated ecosystem services [118,119].
It has already been mentioned that Ulva lactuca is likely to be the main macroalgae species cultivated for food in Europe in 2030. Ulva spp. are listed in the NFC and the European Union list of Novel Food (ULNF) [120]. The genus Ulva contains a high content of proteins, carbohydrates, polysaccharides, minerals and lipids that make it suitable as food, but the economic viability of large-scale cultivation is still questionable [117]. The major challenge in the cultivation of Ulva spp. is that the genus is not well supported taxonomically, and that species identification based on morphology has led to different species being proposed [116], although genetic analysis does not support the existence of different species [121]. Furthermore, the polymorphism of U. lactuca is largely dependent on environmental conditions (especially salinity) and geographical location [122,123]. The cultivation of Ulva spp. in open systems requires further research, as different environmental conditions influence the quantity and quality of the cultivated organisms [124]. Nitrogen-rich wastewater from fish farms provides optimal conditions for Ulva spp. production [125]. Integrating Ulva spp. into IMTA with species that feed on Ulva spp., and thus reducing not only the nutrient output of the farms but also the need for additional feed for these species, seems to be a promising solution [117].
In contrast to the low commercial harvesting and cultivation of macroalgae in the Mediterranean region, there has been relatively good research and development activity over the last 20 years. In the period between 2002 and 2022, of the 263 publications on the properties and potential applications of 121 macroalgae taxa, 51% concerned red algae (62 taxa), 27% brown algae (34 taxa) and 22% green algae (25 taxa), with Tunisia, Italy and Egypt in the lead [6]. Only 13 publications focused on the potential utilisation of Mediterranean macroalgae species for food purposes, mainly in Egypt and Tunisia. The following 12 species took centre stage: Codium tomentosum, Ulva sp., Ulva intestinalis, U. lactuca, U. rigida, Colpomenia sinuosa, Cystoseira sp., Gracilaria bursa-pastoris, Gracilaria longissimi, Hypnea musciformis, Jania rubens and Pterocladiella capillacea [6].
There is a great opportunity for the use of macroalgae as food, but it is necessary to study which of the species are suitable as food, emphasising their organoleptic properties, and also to develop cultivation techniques and use in gastronomy [107].

4.3. Feasibility of Cultivation

The most important questions related to the expansion of macroalgae cultivation are which species can be produced in which quantities and in which locations [30]. The selection of the most suitable species not only influences the profitability of production, but can also have an impact on biodiversity conservation. To achieve the best results in terms of quantity and quality of production, these species should be native, high-yielding, adapted to low-nutrient conditions, disease-resistant, and resilient to different climate change scenarios [126].
As the cultivation of macroalgae in the Mediterranean is still in its infancy, the physiological screening approach [127] could be applied to the species native to the Mediterranean (with characteristics such as a large size and simple morphology, rapid growth leading to a large biomass, a high photosynthesis/respiration ratio, thermal tolerance to high temperatures, and capacity to store a large nitrogen reserve) to provide a solid scientific base for the development of macroalgae culturing under the expected future environmental conditions in the region. The criteria for the selection of macroalgae in a warmer, more variable climate should include traits that demonstrate the robustness/resilience and adaptability of individuals and populations to the expected future conditions [127]. In addition to climate-related environmental changes, it is also important to identify other causes of possible fluctuations in macroalgae productivity. Strong support for the pilot cultivation projects of the most promising macroalgae species for possible commercial production is also welcome.
The Mediterranean Sea has high water temperatures in summer and generally low productivity (Class III ecosystem—less than 150 g C/m2 year) [46]. Therefore, the most suitable sites for macroalgae production are along the coasts near urban areas and estuaries, where production is high, and in some parts of the Adriatic Sea, where eddies and upwelling increase productivity [46].
The decision whether to cultivate macroalgae on land, in nearshore or in offshore facilities depends on the species, the chosen location and the cultivation facilities. However, the nearshore macroalgae farms have great advantages over the other two options as they help bioremediate nutrient-polluted coastal waters [128] and require less cost and labour [34]. Locations that are sufficiently exposed to waves and currents (semi-exposed sites) are desirable for the cultivation of macroalgae, as they ensure an even supply of nutrients to the cultivated species, but can also reduce the quality of the product due to mechanical damage [118]. The depth range for cultivating macroalgae is between 2 and 50 metres [129], usually up to 27 metres on hard substrate, mostly gravel, but also on sand [118].
The global estimation of ecologically suitable areas for macroalgae cultivation, suitable for 21 commercially farmed macroalgae species based on environmental data on 12 abiotic variables related to macroalgae distribution (depth, distance from land, salinity, sea surface temperature, pH, wave height, dissolved oxygen, nitrate, etc.), revealed some interesting facts [130]. The study concluded that for Tunisia, Slovenia, Croatia, Montenegro and Albania, more than 75% of the area in their Exclusive Economic Zones (EEZs) is ecologically suitable for macroalgae cultivation, while for Greece, Türkiye and Italy, between 50% and 75% of their EEZs is suitable for macroalgae cultivation [130].
As the development of mariculture depends on the availability of sites, the establishment of Allocated Zones for Aquaculture (AZAs) is an important tool for the development of macroalgae farming in combination with IMTA practises. The inclusion of macroalgae cultivation in the IMTA does not require too much space, as macroalgae can grow in a vertical garden near the fish cages [131]. Offshore IMTA can simultaneously solve the problem of competition for coastal sites and the high nutrient content required for macroalgae cultivation, but is logistically more complex and therefore more expensive [6].
Some of the common challenges for macroalgae farms related to environmental factors are as follows: decreasing water quality, nutrient deficiencies, extreme weather events, rising water temperatures, lack of high quality seedlings, natural predators, and low productivity [59]. Climate change is not only associated with extreme weather events and rising water temperatures, but also promotes increased grazing and more frequent and severe disease outbreaks [132].
The suitability of certain areas for macroalgae production depends not only on environmental factors, but also on socio-economic factors (quality of legislation and logistical performance, including administrative efficiency and quality of trade infrastructure) [30]. The socio-economic challenges for macroalgae farms are related to strict policies on cultivation areas, poor access to capital, lack of labour, high labour costs, poor market access and price fluctuations [59].
Additional challenges to the expansion of macroalgae cultivation include competition with other commercial/recreational activities, the negative public perception of extensive farming systems visible from the coast, slow and complicated administration, difficulties in commercialising products, local markets, investment in research and innovation, and low cooperation between countries [133].

4.4. The Limitations and Possibilities of Production

Despite the strong historical connection between the Mediterranean countries, there is a large gap between the northern and southern Mediterranean countries in terms of natural resources, political context and, above all, the development gap [48]. It is interesting to note that despite the long coastline and strong maritime identity, the Mediterranean region is facing a growing seafood deficit and only six countries (Morocco, Tunisia, Türkiye, Albania, Croatia and Greece) are exporters, while the others rely on imports [133]. Macroalgae production is one of the most promising sectors of the blue economy in the Mediterranean, not only for its environmental and economic benefits, but also for the social benefits of providing a reliable food source and creating new jobs [58]. It represents a valuable nature-based solution to mitigate climate change and restore coastal ecosystems, including protecting the coast from natural and man-made hazards [134].
Macroalgae production fits perfectly with SDG 12: Responsible production and consumption, as macroalgae are abundant, and the fast-growing organisms and the cultivation methods are environmentally friendly, without the need for fertilisers and with low resource requirements (fresh water and space). One of the main advantages of macroalgae cultivation and harvesting is the relatively simple technology and the short time span from start to harvest [27]. As the cultivation of macroalgae is a more sustainable option for wild macroalgae populations than wild harvesting, efforts to promote and commercialise macroalgae production in the Mediterranean should be prioritised over simple harvesting methods. In addition, the large-scale production of macroalgae offers higher quality, product traceability and predictable biomass, providing a solid foundation for any long-term development strategy. As the large-scale expansion of macroalgae cultivation can threaten biodiversity and marine habitats [55], the selection of suitable cultivation areas and species, together with regular monitoring, is crucial to minimise environmental risks.
In the Mediterranean region, the production of macroalgae is marginal compared to global or even European production. There are only a few locations where macroalgae are harvested or cultivated on the Mediterranean coasts, even in countries with a long tradition of macroalgae harvesting on their Atlantic coasts, such as France or Spain, or in Israel, the pioneer of macroalgae cultivation in the Mediterranean. According to some authors [58], the low number of macroalgae producers in the region and the slow transition from pilot projects to the full commercialisation of macroalgae production, especially in the macroalgae farming sector, is held back by the lack of national strategies and incentives to support private small and medium enterprises, and the link between incubators/accelerators and maritime clusters.
The lack of co-operation and support is not the only problem in this sector. On the one hand, there are the higher costs of macroalgae production outside East Asia and, on the other, there is a lack of harvesting and consumption traditions in the Mediterranean region, with a few exceptions. The low production of macroalgae goes hand in hand with the low consumption, which is related to the lack of local supply of macroalgae, the health and safety risks associated with human consumption hazards (microbiological and chemical (excessive iodine, heavy metals, allergens)), legality, and the lack of knowledge of the nutritional properties of macroalgae [21,77]. The consumer’s ambiguous perception of macroalgae is sometimes related to the lack of attractiveness of the sensory properties (appearance, odour, flavour, taste, and texture of foods detectable by human senses) [135,136].
In order to make macroalgae more appealing as a food, the adaptation of products to regional tastes is essential for the development of the macroalgae food market in the Mediterranean [27]. According to the paper on the Italian edible macroalgae market [95], it is a promising sector because Italian consumers want to eat macroalgae, as they are familiar with macroalgae in Asian dishes and in national dishes. Besides a new food design, new marketing strategies are also important to promote the consumption of macroalgae in the Mediterranean region, including publicity campaigns about health and the sustainability effects of macroalgae consumption. An example of good practice to popularise the consumption of seaweed is the Chilean project Here we eat seaweed, which aims to diversify restaurant menus by including new seaweed-based recipes [21].
One of the advantages of macroalgae as a commodity is that it can be certified and promoted as a sustainable, organic, healthy, vegan, macrobiotic and halal food, making it more recognisable on the market. The Marine Stewardship Council and the Aquaculture Stewardship Council published the Seaweed Standard (ASC-MSC Seaweed Standard) in 2017. The joint Seaweed Standard ensures the sustainability of wild harvesting and farming, taking into account the sustainability of wild populations, environmental impact, effective management, social responsibility and community relations [137]. As macroalgae fit well with the green consumption trend and the environmentally friendly lifestyle in Western societies [77,138], the Mediterranean countries could also benefit from the expansion of the European macroalgae market.
Considering all the benefits associated with the production and consumption of macroalgae (SDG 3: Good health and well-being, SDG 12: Responsible production and consumption), macroalgae are an underexploited seafood resource in the Mediterranean. The report of the General Fisheries Commission for the Mediterranean (GFCM) on the status and future of seaweed farming in the Mediterranean and Black Seas points out that an improvement in data quality and close cooperation between all stakeholders, as well as improvements in legislation and funding, are needed to unlock the full potential of seaweed [139]. A multi-stakeholder platform for knowledge exchange and capacity building on the technical, market and regulatory aspects of macroalgae cultivation has been established, working with producers and research institutions to develop best practices and create a regulatory framework for responsible macroalgae cultivation [139].
The important initiative is the COST (European Cooperation in Science and Technology) Action Tomorrow’s Wheat of the Sea: Ulva, a Model for an Innovative Mariculture (SEAWHEAT) CA20106 (https://seawheatcost.haifa.ac.il/ (accessed on 11 June 2024)). It was approved by the European Committee in 2021 with the aim of developing an Ulva-based blue biotech industry in European algaculture and beyond. One of the objectives of this action is to create an efficient network of stakeholders (scientists, producers, end-users, policy makers, NGOs, and the public), dealing with all aspects of Ulva spp.
Mediterranean countries have recognised the importance of the seaweed sector and, in the document Towards a Sustainable Blue Economy in the Mediterranean Region (2021), which deals with governance, research and innovation in the region, the seaweed sector is one of the priorities related to the diversification of mariculture products. The African Mediterranean countries are part of the Blue Belt Initiative, which is an important African instrument to support blue strategies and was launched by Morocco in 2016. One of the strategic objectives for the period 2023–2027 is the development of large-scale seaweed culture, which involves developing and expanding the techniques and diversity of macroalgaculture on open waters, developing the controlled reproduction (sporulation) techniques of seaweed, and supporting the development of land-based marine microalgae farming. One of the most important projects funded by the European Union is the Building the blue biotechnology community in the Mediterranean (B-Blue, 2020–2022) project, funded under the Interreg Mediterranean programme, which aims to create a cluster in the Mediterranean region as well as creating four value chains, including algae production for high-value compounds and sustainable IMTA [140].
In order to develop the edible macroalgae sector in the Mediterranean, it is necessary to invest in research and innovation in the field of cultivation, especially in native species, to avoid wild harvesting due to the risk of overexploitation [141]. Additional efforts should be made to close the identified research gaps in the biology of the Mediterranean macroalgae species (especially Ulva spp.). It is also necessary to enable a continuous flow of funding through structural investments, dedicated tax schemes, grants and loans [58]. Most importantly, strong cooperation and the continuous innovation of production and processing technologies, and capacity building, will make the Mediterranean macroalgae sector viable.

5. Conclusions

This paper gives an overview of the production of edible macroalgae on a global scale, but also in Europe and the Mediterranean, emphasising that data on macroalgae production in the Mediterranean are scarce and fragmented. The most abundant and popular edible macroalgae worldwide are listed, as well as the most promising edible macroalgae suitable for human consumption in the Mediterranean region. The taxon identified as the most promising for future cultivation in the region is Ulva spp. The paper also highlights some of the limitations of macroalgae production in the region, as well as the possible benefits of commercial macroalgae cultivation.
The Mediterranean is the largest and deepest enclosed sea, densely populated along its coasts, with a long and rich history and great cultural significance. The population of the Mediterranean coastal region will grow to 690 million people by 2050. As the population grows, so will human activity and the associated risks to the coastal environment and coastal communities. Mediterranean countries are already struggling with a deficit in food production due to the limited availability of water and agricultural land. In the future, population growth and climate change will further exacerbate the food deficit and dependence on food imports. The expansion of macroalgae cultivation and the popularisation of macroalgae eating habits can also help to combat unhealthy eating habits and promote the consumption of locally produced, better quality food in the Mediterranean region. The expansion of macroalgae production in the region can also contribute to the restoration of coastal ecosystems and associated ecosystem services, while promoting the socio-economic prosperity of vulnerable coastal communities.
Unfortunately, the sector is currently hampered by the lack of a tradition regarding macroalgae production and consumption in the Mediterranean, high production costs and the absence of local supply chains. Other challenges include the lack of national strategies and incentives to support companies, the lack of knowledge about the nutritional properties of macroalgae and sometimes the negative perception of macroalgae products by consumers. The European countries with experience in macroalgae cultivation on their Atlantic coasts (France and Spain), and the North African countries that are investing heavily in scientific research on macroalgae (Israel, Egypt, Tunisia and Morocco), should work together to commercialise the current pilot projects on edible macroalgae cultivation and lead the way for the rest of the region. In addition to the COST Action SEAWHEAT, further joint efforts are needed to address identified research gaps in the biology of Mediterranean macroalgae species (especially Ulva spp.), share information and knowledge from other regions, support capacity building, continuously innovate production and processing technologies, and responsibly manage natural and cultivated macroalgae resources. These efforts should also include customised campaigns to increase the acceptance and attractiveness of macroalgae consumption in the Mediterranean region and open up new potential research avenues in the ever-changing world.
It is obvious that the development of the edible macroalgae sector in the Mediterranean is a complex task with many economic, social and environmental challenges, but at the same time it is a promising sector with an exciting research landscape.

Author Contributions

All authors contributed to the study conception and design. Conceptualisation (the idea for the article) and writing—original draft preparation: G.J.M., S.K.Š. and V.N. Writing—review and editing (critically revised the work): G.J.M., S.K.Š. and V.N. Resources (the literature search and data analysis): G.J.M., S.K.Š. and V.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Guiry, M.D. How many species of algae are there? J. Phycol. 2012, 48, 1057–1063. [Google Scholar] [CrossRef] [PubMed]
  2. Pereira, L. Macroalgae. Encyclopedia 2021, 1, 177–188. [Google Scholar] [CrossRef]
  3. Braud, L.; McDonnell, K.; Murphy, F. Environmental life cycle assessment of algae systems: Critical review of modelling approaches. Renew. Sustain. Energy Rev. 2023, 179, 113218. [Google Scholar] [CrossRef]
  4. Pereira, L.; Correia, F. Algas Marinhas da Costa Portuguesa—Ecologia, Biodiversidade e Utilizações; Nota de Rodapé Editores: Paris, France, 2015; p. 341. [Google Scholar]
  5. Pereira, L. Macroalgae: Diversity and Conservation. In Life below Water; Leal Filho, W., Azul, A.M., Brandli, L., Lange Salvia, A., Wall, T., Eds.; Encyclopedia of the UN Sustainable Development Goals; Springer: Cham, Switzerland, 2020; pp. 1–13. [Google Scholar]
  6. Armeli Minicante, S.; Bongiorni, L.; De Lazzari, A. Bio-based products from Mediterranean seaweeds: Italian opportunities and challenges for a sustainable blue economy. Sustainability 2022, 14, 5634. [Google Scholar] [CrossRef]
  7. FAO. The State of World Fisheries and Aquaculture 2022. In Towards Blue Transformation; FAO: Rome, Italy, 2022; Available online: https://doi.org/10.4060/cc0461en (accessed on 31 December 2023).
  8. Smith, A.G.; Tredici, M.R.; Boussiba, S.; Verdelho, V.; Cadoret, J.-P.; Davey, M.P.; Huete-Ortega, M.; Acien, F.G.; Schmid-Staiger, U.; Rodriguez, H.; et al. EABA—Position Paper—What Are Algae? EABA: Florence, Italy, 2021. [Google Scholar] [CrossRef]
  9. Ullmann, J.; Grimm, D. Algae and their potential for a future bioeconomy, landless food production, and the socio-economic impact of an algae industry. Org. Agric. 2021, 11, 261–267. [Google Scholar] [CrossRef]
  10. Pereira, L. Edible Seaweeds of the World; CRC Press: Boca Raton, FL, USA; Taylor & Francis Group: Boca Raton, FL, USA, 2016; p. 448. [Google Scholar]
  11. Mouritsen, O.G.; Rhatigan, P.; Pérez-Lloréns, J.L. World cuisine of seaweeds: Science meets gastronomy. Int. J. Gastron. Food Sci. 2018, 14, 55–65. [Google Scholar] [CrossRef]
  12. Pereira, L. Therapeutic and Nutritional Uses of Algae; CRC Press: Boca Raton, FL, USA; Taylor & Francis Group: Boca Raton, FL, USA, 2018; p. 560. [Google Scholar]
  13. Cotas, J.; Leandro, A.; Pacheco, D.; Gonçalves, A.M.M.; Pereira, L. A comprehensive review of the nutraceutical and therapeutic applications of Red Seaweeds (Rhodophyta). Life 2020, 10, 19. [Google Scholar] [CrossRef]
  14. Gaspar, R.; Fonseca, R.; Pereira, L. Illustrated Guide to the Macroalgae of Buarcos Bay, Figueira da Foz, Portugal, 1st ed.; MARE UC, DCV; FCT: Coimbra, Portugal, 2020; p. 128. [Google Scholar] [CrossRef]
  15. Pacheco, D.; García-Poza, S.; Cotas, J.; Gonçalves, A.M.M.; Pereira, L. Fucoidan—A valuable source from the ocean to pharmaceutical. Front. Drug Chem. Clin. Res. 2020, 3, 1–4. [Google Scholar] [CrossRef]
  16. Francezon, N.; Tremblay, A.; Mouget, J.L.; Pasetto, P.; Beaulieu, L. Algae as a source of natural flavors in innovative foods. J. Agric. Food Chem. 2021, 69, 11753–11772. [Google Scholar] [CrossRef]
  17. Mandalka, A.; Cavalcanti, M.I.L.G.; Harb, T.B.; Toyota Fujii, M.; Eisner, P.; Schweiggert-Weisz, U.; Chow, F. Nutritional composition of beach-cast marine algae from the Brazilian coast: Added value for algal biomass considered as waste. Foods 2022, 11, 1201. [Google Scholar] [CrossRef] [PubMed]
  18. Mac Monagail, M.; Cornish, L.; Morrisson, L.; Araújo, R.; Critchley, A.T. Sustainable harvesting of wild seaweed resources. Eur. J. Phycol. 2017, 52, 371–390. [Google Scholar] [CrossRef]
  19. Erlandson, J.M.; Graham, M.H.; Bourque, B.J.; Corbett, D.; Estes, J.A.; Steneck, R.S. The kelp highway hypothesis: Marine ecology, the coastal migration theory, and the peopling of the Americas. J. Isl. Coast. Archaeol. 2007, 2, 161–174. [Google Scholar] [CrossRef]
  20. Cornish, M.L.; Critchley, A.T.; Mouritsen, O.G. A role for dietary macroalgae in the amelioration of certain risk factors associated with cardiovascular disease. Phycologia 2015, 54, 649–666. [Google Scholar] [CrossRef]
  21. Rogel-Castillo, C.; Latorre-Castañeda, M.; Muñoz-Muñoz, C.; Agurto-Muñoz, C. Seaweeds in Food: Current Trends. Plants 2023, 12, 2287. [Google Scholar] [CrossRef]
  22. O’Connor, K. Seaweed: A Global History; Reaktion Books Ltd.: London, UK, 2017; p. 176. [Google Scholar]
  23. Nisizawa, K.; Noda, H.; Kikuchi, R.; Watanabe, T. The main seaweed foods in Japan. Hydrobiologia 1987, 151, 5–29. [Google Scholar] [CrossRef]
  24. Indergaard, M.; Minsaas, J. Animal and Human Nutrition. In Seaweed Resources in Europe: Uses and Potential; Guiry, M.D., Blunden, G., Eds.; John Wiley & Sons: Chichester, UK, 1991; p. 432. [Google Scholar]
  25. Pereira, L.; Bahcevandziev, K.; Joshi, N.H. Seaweeds as Plant Fertilizer, Agricultural Biostimulants and Animal Fodder; CRC Press: Boca Raton, FL, USA; Taylor & Francis Group: Boca Raton, FL, USA, 2019; p. 232. [Google Scholar]
  26. Pulz, O.; Gross, W. Valuable products from biotechnology of microalgae. Appl. Microbiol. Biotechnol. 2004, 65, 635–648. [Google Scholar] [CrossRef] [PubMed]
  27. Ferdouse, F.; Holdt, S.L.; Smith, R.; Murúa, P.; Yang, Z. The global status of seaweed production, trade and utilization. In Globefish Research Programme; FAO: Rome, Italy, 2018; p. 120. Available online: https://backend.orbit.dtu.dk/ws/portalfiles/portal/163078059/FAO_report_Global_seaweed_2018.pdf (accessed on 15 December 2023).
  28. Buschmann, A.H.; Camus, C.; Infante, J.; Neori, A.; Israel, Á.; Hernández-González, M.C.; Pereda, S.V.; Gomez-Pinchetti, J.L.; Golberg, A.; Tadmor-Shalev, N.; et al. Seaweed production: Overview of the global state of exploitation, farming and emerging research activity. Eur. J. Phycol. 2017, 52, 391–406. [Google Scholar] [CrossRef]
  29. Bjerregaard, R.; Valderrama, D.; Radulovich, R.; Diana, J.; Capron, M.; Mckinnie, C.A.; Forster, J. Seaweed Aquaculture for Food Security, Income Generation and Environmental Health in Tropical Developing Countries; The World Bank No. 107147; World Bank: Washington, DC, USA, 2016; p. 16. [Google Scholar]
  30. Vincent, A.; Stanley, A.; Ring, J. Seaweed for Europe—Hidden Champion of the Ocean, Seaweed for Europe; SUN Institute: London, UK, 2021; p. 60. Available online: https://www.seaweedeurope.com/wp-content/uploads/2020/10/Seaweed_for_Europe-Hidden_Champion_of_the_ocean-Report.pdf (accessed on 10 June 2024).
  31. Maar, M.; Holbach, A.; Boderskov, T.; Thomsen, M.; Buck, B.H.; Kotta, J.; Bruhn, A. Multi-use of offshore wind farms with low-trophic aquaculture can help achieve global sustainability goals. Commun. Earth Environ. 2023, 4, 447. [Google Scholar] [CrossRef]
  32. Estridge, P.; Smallman, D. Co-Locating Seaweed Farming alongside Offshore Wind. Available online: https://www.seaweedgeneration.com/education/colocating-seaweed-farm-with-offshore-wind.html (accessed on 28 March 2024).
  33. Radulovich, R.; Neori, A.; Valderrama, D.; Reddy, C.R.K.; Cronin, H.; Forster, J. Farming of seaweeds. In Seaweed Sustainability: Food and Non-Food Applications; Tiwari, B.K., Troy, D.J., Eds.; Academic Press: Cambridge, MA, USA, 2015; pp. 27–59. [Google Scholar] [CrossRef]
  34. García-Poza, S.; Leandro, A.; Cotas, C.; Cotas, J.; Marques, J.C.; Pereira, L.; Gonçalves, A.M.M. The Evolution Road of Seaweed Aquaculture: Cultivation Technologies and the Industry 4.0. Int. J. Environ. Res. Public Health 2020, 17, 6528. [Google Scholar] [CrossRef]
  35. Buck, B.H.; Troell, M.F.; Krause, G.; Angel, D.L.; Grote, B.; Chopin, T. State of the art and challenges for offshore integrated multitrophic aquaculture (IMTA). Front. Mar. Sci. 2018, 5, 165. Available online: https://www.frontiersin.org/articles/10.3389/fmars.2018.00165/full (accessed on 10 June 2024). [CrossRef]
  36. Chopin, T.; Cooper, J.A.; Reid, G.; Cross, S.; Moore, C. Open-water integrated multi-trophic aquaculture: Environmental biomitigation and economic diversification of fed aquaculture by extractive aquaculture. Rev. Aquac. 2012, 4, 209–220. [Google Scholar] [CrossRef]
  37. Nederlof, M.A.J.; Verdegem, M.C.J.; Smaal, A.C.; Jansen, H.M. Nutrient retention efficiencies in integrated multi-trophic aquaculture. Rev Aquac. 2022, 14, 1194–1212. [Google Scholar] [CrossRef]
  38. Nature Conservancy. Available online: https://www.nature.org/en-us/what-we-do/our-insights/perspectives/restorative-aquaculture-for-nature-and-communities/ (accessed on 15 December 2023).
  39. Urban Ocean Lab. Available online: https://urbanoceanlab.org/factsheet/regenerative-ocean-farming (accessed on 15 December 2023).
  40. Visch, W.; Nylund, G.M.; Pavia, H. Growth and biofouling in kelp aquaculture (Saccharina latissima): The effect of location and wave exposure. J. Appl. Phycol. 2020, 32, 3199–3209. [Google Scholar] [CrossRef]
  41. Kaur, M.; Saini, K.C.; Ojah, H. Abiotic stress in algae: Response, signaling and transgenic approaches. J. Appl. Phycol. 2022, 34, 1843–1869. [Google Scholar] [CrossRef]
  42. Kumar, Y.N.; Poong, S.W.; Gachon, C.; Brodie, J.; Sade, A.; Lim, P.E. Impact of elevated temperature on the physiological and biochemical responses of Kappaphycus alvarezii (Rhodophyta). PLoS ONE 2020, 15, e0239097. [Google Scholar] [CrossRef]
  43. Chalanika De Silva, H.C.; Asaeda, T. Effects of heat stress on growth, photosynthetic pigments, oxidative damage and competitive capacity of three submerged macrophytes. J. Plant Interact. 2017, 12, 228–236. [Google Scholar] [CrossRef]
  44. Khan, N.; Sudhakar, K.; Mamat, R. Macroalgae farming for sustainable future: Navigating opportunities and driving innovation. Heliyon 2024, 10, e28208. [Google Scholar] [CrossRef] [PubMed]
  45. Liu, X.; Bogaert, K.; Engelen, A.H.; Leliaert, F.; Roleda, M.Y.; De Clerck, O. Seaweed reproductive biology: Environmental and genetic controls. Bot. Mar. 2017, 60, 89–108. [Google Scholar] [CrossRef]
  46. Aquarone, M.C.; Adams, S. Mifsud, IV-7 Mediterranean Sea: LME 26. In The UNEP Large Marine Ecosystem Report: A Perspective on Changing Conditions in LMEs of the World’s Regional Seas; Sherman, K., Hempel, G., Eds.; UNEP Regional Seas, Report and Studies No. 182; UN Environment Programme; FAO: Rome, Italy, 2008; pp. 189–200. Available online: https://iwlearn.net/resolveuid/4c0aa720-0124-40a3-8689-71757e53e980 (accessed on 10 June 2024).
  47. Figueroa, F.L.; Flores-Moya, A.; Vergara, J.J.; Korbee, N.; Hernández, I. Autochthonous seaweeds. In The Mediterranean Sea; Goffredo, S., Dubinsky, Z., Eds.; Springer: Dordrecht, The Netherlands, 2014; pp. 123–135. ISBN 978-94-007-6703-4. [Google Scholar]
  48. UNEP/MAP; Plan Bleu. SOED State of the Environment and Development in the Mediterranean; UNEP: Nairobi, Kenya; Plan Bleu Regional Activity Centre: Marseille, France, 2020; p. 342. Available online: https://planbleu.org/wp-content/uploads/2020/11/SoED-Full-Report.pdf (accessed on 10 June 2024).
  49. UNEP. Seaweed Farming: Assessment on the Potential of Sustainable Upscaling for Climate, Communities and the Planet; UNEP: Nairobi, Kenya, 2023; p. 77. Available online: https://wedocs.unep.org/bitstream/handle/20.500.11822/42642/seaweed_farming_climate.pdf?sequence=3&isAllowed=y (accessed on 10 June 2024).
  50. Ross, F.W.R.; Boyd, P.W.; Filbee-Dexter, K.; Watanabe, K.; Ortega, A.; Krause-Jensen, D.; Lovelock, C.; Sondak, C.F.A.; Bach, L.T.; Duarte, C.M.; et al. Potential role of seaweeds in climate change mitigation. Sci. Total Environ. 2023, 885, 163699. [Google Scholar] [CrossRef] [PubMed]
  51. FAO. The State of World Fisheries and Aquaculture 2020. In Sustainability in Action; FAO: Rome, Italy, 2020; Available online: https://doi.org/10.4060/ca9229en (accessed on 31 December 2023).
  52. FAO. Global Seaweeds and Microalgae Production, 1950–2019; FAO: Rome, Italy, 2021; Available online: https://www.fao.org/3/cb4579en/cb4579en.pdf (accessed on 31 December 2023).
  53. Camia, A.; Robert, N.; Jonsson, R.; Pilli, R.; García-Condado, S.; López-Lozano, R.; van der Velde, M.; Ronzon, T.; Gurría, P.; M’Barek, R.; et al. Biomass production, supply, uses and flows in the European Union. In First Results from an Integrated Assessment, EUR 28993 EN; Publications Office of the European Union: Luxembourg, 2018; p. 124. [Google Scholar] [CrossRef]
  54. Barbier, M.; Charrier, B.; Araujo, R.; Holdt, S.; Jacquemin, B.; Rebours, C. PEGASUS—PHYCOMORPH European Guidelines for a Sustainable Aquaculture of Seaweeds; Barbier, M., Charrier, B., Eds.; COST Action FA1406; Station Biologique de Roscoff, CNRS-Sorbonne Université: Roscoff, France, 2019; p. 194. [Google Scholar] [CrossRef]
  55. Campbell, I.; Macleod, A.; Sahlmann, C.; Neves, L.; Funderud, J.; Øverland, M.; Hughes, A.D.; Stanley, M. The environmental risks associated with the development of seaweed farming in Europe—Prioritizing key knowledge gaps. Front. Mar. Sci. 2019, 6, 107. [Google Scholar] [CrossRef]
  56. Araújo, R.; Vázquez Calderón, F.; Sánchez López, J.; Azevedo, I.C.; Bruhn, A.; Fluch, S.; Garcia Tasende, M.; Ghaderiardakani, F.; Ilmjärv, T.; Laurans, M.; et al. Current status of the algae production industry in Europe: An emerging sector of the blue bioeconomy. Front. Mar. Sci. 2021, 7, 626389. [Google Scholar] [CrossRef]
  57. Kuech, A.; Breuer, M.; Popescu, I. Research for PECH Committee—The Future of the EU Algae Sector; Policy Department for Structural and Cohesion Policies: Brussels, Belgium, 2023; p. 47. [Google Scholar]
  58. Mancini, R. The Blue Economy in the Mediterranean Region and Opportunities for the Algae Industry; Istituto Affari Internazionali (IAI): Rome, Italy, 2022; p. 22. Available online: https://www.iai.it/sites/default/files/iaip2222.pdf (accessed on 10 June 2024).
  59. Hatch Innovation Services. Seaweed Insights. Available online: https://seaweedinsights.com/hatch-farm-insights// (accessed on 15 April 2024).
  60. Phyconomy Seaweed State of the Industry. 2023. Available online: https://phyconomy.net/articles/2022-seaweed-review/ (accessed on 25 January 2024).
  61. OEC. The Observatory of Economic Complexity. 2024. Available online: https://oec.world/en/profile/hs/seaweeds-and-other-algae-fit-for-human-consumption-fresh-chilled-frozen-or-dried-whether-or-not-ground (accessed on 15 January 2024).
  62. IMARC. Seaweed Market Report by Environment (Aquaculture, Wild Harvest), Product (Red, Brown, Green), Application (Processed Foods, Direct Human Consumption, Hydrocolloids, Fertilizers, Animal Feed Additives, and Others), and Region 2024–2032. 2023. Available online: https://www.imarcgroup.com/seaweed-market (accessed on 31 December 2023).
  63. Grand View Research. Commercial Seaweed Market Size, Share & Trends Analysis Report by Product (Brown, Red, Green), by Application (Human Consumption, Animal Feed, Agriculture), by Form (Leaf, Powdered, Flakes), by Region, and Segment Forecasts, 2022–2030. Available online: https://www.grandviewresearch.com/industry-analysis/commercial-seaweed-market (accessed on 31 December 2023).
  64. Lorenzo, J.M.; Agregán, R.; Munekata, P.E.S.; Franco, D.; Carballo, J.; Sahin, S.; Lacomba, R.; Barba, F.J. Proximate Composition and Nutritional Value of three macroalgae: Ascophyllum nodosum, Fucus vesiculosus and Bifurcaria bifurcate. Mar. Drugs 2017, 15, 360. [Google Scholar] [CrossRef] [PubMed]
  65. WORMS. Available online: https://www.marinespecies.org (accessed on 31 December 2023).
  66. EASIN. Available online: https://easin.jrc.ec.europa.eu/spexplorer/search/searchpaged (accessed on 31 December 2023).
  67. FAO. Cultivation of Temperate Seaweeds in the Asia Pacific Region. 2023. Available online: https://www.fao.org/3/ab728e/AB728E02.htm (accessed on 31 December 2023).
  68. Guiry, M.D.; Guiry, G.M. AlgaeBase; World-Wide Electronic Publication: Galway, Ireland, 2024; Available online: https://www.algaebase.org (accessed on 16 April 2024).
  69. FAO. Cultured Aquatic Species Information Programme. 2023. Available online: https://www.fao.org/fishery/en/culturedspecies/undaria_pinnatifida/en (accessed on 31 December 2023).
  70. Epstein, G.; Smale, D.A. Undaria pinnatifida: A case study to highlight challenges in marine invasion ecology and management. Ecol Evolut. 2017, 7, 8624–8642. [Google Scholar] [CrossRef] [PubMed]
  71. FAO. Cultured Aquatic Species Fact Sheets Porphyra. 2023. Available online: https://www.fao.org/fishery/docs/DOCUMENT/aquaculture/CulturedSpecies/file/en/en_nori.htm (accessed on 31 December 2023).
  72. Costello, M.J.; Bouchet, P.; Emblow, C.S.; Legakis, A. European marine biodiversity inventory and taxonomic resources: State of the art and gaps in knowledge. Mar. Ecol. Prog. Ser. 2006, 316, 257–268. [Google Scholar] [CrossRef]
  73. Mac Monagail, M.; Morrison, L. The seaweed resources of Ireland: A twenty-first century perspective. J. Appl. Phycol. 2020, 32, 1287–1300. [Google Scholar] [CrossRef]
  74. Limiñana, V.A.; Benoist, T.; Anton Sempere, S.; Maestre Pérez, S.E.; Prats Moya, M.S. Chemical composition of sustainable Mediterranean macroalgae obtained from land-based and sea-based aquaculture systems. Food Biosci. 2023, 54, 102902. [Google Scholar] [CrossRef]
  75. Vazquez Calderon, F.; Sanchez Lopez, J. An overview of the algae industry in Europe. In Producers, Production Systems, Species, Biomass Uses, Other Steps in the Value Chain and Socio-Economic Data; Guillen, J., Avraamides, M., Eds.; JRC130107; Publications Office of the European Union: Luxembourg, 2022. [Google Scholar] [CrossRef]
  76. Bronswijk, L.; Vlottes, M.; Draisma, M.; Brouwers, E.; van Baelen, F.D. Study on Existing Market for Algal Food Applications Part A: Seaweed; North Sea Farm Foundation: The Hague, Amsterdam, 2019; p. 40. Available online: https://www.northseafarmers.org/projects/D4.1.1A_Study-on-the-existing-market-for-seaweed-food-applications.pdf (accessed on 10 June 2024).
  77. Mendes, M.C.; Navalho, S.; Ferreira, A.; Paulino, C.; Figueiredo, D.; Silva, D.; Gao, F.; Gama, F.; Bombo, G.; Jacinto, R.; et al. Algae as Food in Europe: An Overview of Species Diversity and Their Application. Foods 2022, 11, 1871. [Google Scholar] [CrossRef] [PubMed]
  78. Afonso, N.C.; Catarino, M.D.; Silva, A.M.S.; Cardoso, S.M. Brown macroalgae as valuable food ingredients. Antioxidants 2019, 8, 365. [Google Scholar] [CrossRef]
  79. NAFF. New Algae for Food Forum Novel Food Priorities. Available online: https://naff.eaba-association.org/priorities (accessed on 21 May 2024).
  80. CEVA (Centre d’Étude et de Valorisation des Algues). Seaweed Standards for Food and Cosmetics. 2016. Available online: https://media-01.imu.nl/storage/seagriculture.eu/2116/wp/2016/10/2.3-Maud-Benoit-Seaweed-standards-for-food-and-cosmetics.pdf (accessed on 26 January 2024).
  81. Zhang, L.; Liao, W.; Huang, Y.; Wen, Y.; Chu, Y.; Zhao, C. Global seaweed farming and processing in the past 20 years. Food Prod. Process. Nutr. 2022, 4, 23. [Google Scholar] [CrossRef]
  82. Banach, J.L.; Koch, S.J.I.; Hoffmans, Y.; van den Burg, S.W.K. Seaweed Value Chain Stakeholder Perspectives for Food and Environmental Safety Hazards. Foods 2022, 11, 1514. [Google Scholar] [CrossRef]
  83. Froehlich, H.E.; Afflerbach, J.; Frazier, M.; Halpern, B. Blue Growth Potential to Mitigate Climate Change through Seaweed Offsetting. Curr. Biol. 2019, 29, 3087–3093. [Google Scholar] [CrossRef] [PubMed]
  84. Theuerkauf, S.J.; Morris, J.A., Jr.; Waters, T.J.; Wickliffe, L.C.; Alleway, H.K.; Jones, R.C. A global spatial analysis reveals where marine aquaculture can benefit nature and people. PLoS ONE 2019, 14, e0222282. [Google Scholar] [CrossRef] [PubMed]
  85. FishStatJ. Software for Fishery and Aquaculture Statistical Time Series. Available online: https://www.fao.org/fishery/en/statistics/software/fishstatj (accessed on 15 April 2024).
  86. Phyconomy Database. Available online: https://airtable.com/appikoaOp2g37vuOF/shrGYaj6CikiaXEhH/tblZFNBiWgVocM5BA/viwAtxUXazNenKTnu (accessed on 25 January 2024).
  87. European Atlas of the Seas. 2024. Available online: https://ec.europa.eu/maritimeaffairs/atlas/maritime_atlas/#lang=EN;p=w;bkgd=1;theme=321:0.87,638:0.89,242:0.85,717:0.91;c=887823.2177163037,3865863.670161061;z=6 (accessed on 15 January 2024).
  88. Petrocelli, A.; Cecere, E. A 20-year update on the state of seaweed resources in Italy. Bot. Mar. 2019, 62, 249–264. [Google Scholar] [CrossRef]
  89. Trikka, F.; Israel, P.; Koukaras, K.; Argiriou, A. Biochemical characterization of eight Greek algae as candidate species for local seaweed cultivation. Bot. Mar. 2021, 64, 313–326. [Google Scholar] [CrossRef]
  90. Friedlander, M. Israeli R&D activities in seaweed cultivation. Isr. J. Plant Sci. 2008, 56, 15–28. [Google Scholar] [CrossRef]
  91. Neori, A.; Shpigel, M.; Guttman, L.; Israel, A. Development of polyculture and Integrated Multi-Trophic Aquaculture (IMTA) in Israel: A review. IJA 2017, 68, 20874. [Google Scholar] [CrossRef]
  92. Israel, A.; Golberg, A.; Neori, A. The seaweed resources of Israel in the Eastern Mediterranean Sea. Bot. Mar. 2019, 63, 85–95. [Google Scholar] [CrossRef]
  93. Rashad, S.; El-Chaghaby, G.A. Marine Algae in Egypt: Distribution, phytochemical composition and biological uses as bioactive resources (a review). Egypt. J. Aquat. Biol. Fish. 2020, 24, 147–160. Available online: https://ejabf.journals.ekb.eg/article_103630_cfe4e893d2d60bb6b4117f9ddc496875.pdf (accessed on 10 June 2024). [CrossRef]
  94. Ktari, L.; Chebil Ajjabi, L.; De Clerck, O.; Gómez Pinchetti, J.L.; Rebours, C. Seaweeds as a promising resource for blue economy development in Tunisia: Current state, opportunities, and challenges. J. Appl. Phycol. 2021, 34, 489–505. [Google Scholar] [CrossRef]
  95. Palmieri, N.; Forleo, M.B. The potential of edible seaweed within the western diet. A segmentation of Italian consumers. Int. J. Gastron. Food Sci. 2020, 20, 100202. [Google Scholar] [CrossRef]
  96. Pereira, L. Seaweed Flora of the European North Atlantic and Mediterranean. In Springer Handbook of Marine Biotechnology; Springer Handbooks; Kim, S.K., Ed.; Springer: Berlin/Heidelberg, Germany, 2015; pp. 65–178. [Google Scholar] [CrossRef]
  97. Otero, M.M.; Cebrian, E.; Francour, P.; Galil, B.; Savini, D. Monitoring Marine Invasive Species in Mediterranean Marine Protected Areas (MPAs): A Strategy and Practical Guide for Managers; IUCN: Malaga, Spain, 2013; p. 136. [Google Scholar]
  98. Floc’h, J.Y.; Pajot, R.; Wallentinus, I. The Japanese brown alga Undaria pinnatifida on the coast of France and its possible establishment in European waters. ICES J. Mar. Sci. 1991, 47, 379–390. [Google Scholar] [CrossRef]
  99. Lowe, S.; Browne, M.; Boudjelas, S.; De Poorter, M. 100 of the World’s Worst Invasive Alien Species: A Selection from the Global Invasive Species Database; The Invasive Species Specialist Group (ISSG): Auckland, New Zealand; A Specialist Group of the Species Survival Commission (SSC) of the World Conservation Union (IUCN): Auckland, New Zealand; IUCN: Auckland, New Zealand, 2000; p. 12. [Google Scholar]
  100. Katsanevakis, S.; Wallentinus, I.; Zenetos, A.; Leppäkoski, E.; Çinar, M.E.; Oztürk, B.; Grabowski, M.; Golani, D.; Cardoso, A.C. Impacts of invasive alien marine species on ecosystem services and biodiversity: A pan-European review. Aquat. Invasions 2014, 9, 391–423. [Google Scholar] [CrossRef]
  101. Tsirintanis, K.; Azzurro, E.; Crocetta, F.; Dimiza, M.; Froglia, C.; Gerovasileiou, V.; Langeneck, J.; Mancinelli, G.; Rosso, A.; Stern, N.; et al. Bioinvasion impacts on biodiversity, ecosystem services, and human health in the Mediterranean Sea. Aquat. Invasions 2022, 17, 308–352. [Google Scholar] [CrossRef]
  102. Streftaris, N.; Zenetos, A. Alien Marine Species in the Mediterranean—The 100 ‘WorstInvasives’ and their Impact. Mediterr. Mar. Sci. 2006, 7, 87–118. [Google Scholar] [CrossRef]
  103. Cormaci, M.; Furnari, G.; Catra, M.; Alongi, G.; Giaccone, G. Flora marina bentonica del Mediterraneo: Phaeophyceae. Boll. Dell’Accad. Gioenia Sci. Nat. Catania 2012, 45, 1–508. Available online: https://www.gioenia.unict.it/bollettino/bollettino2012-n375/full_papers/Erratum.pdf (accessed on 31 December 2023).
  104. Ministry of Agriculture and Forestry New Zeland. Review of the Undaria Commercial Harvest Policy. 2009. Available online: https://www.mpi.govt.nz/dmsdocument/19880-Commercial-harvest-of-Undaria-discussion (accessed on 15 January 2024).
  105. Pereira, A.G.; Fraga-Corral, M.; Garcia-Oliveira, P.; Lourenço-Lopes, C.; Carpena, M.; Prieto, M.A.; Simal-Gandara, J. The Use of Invasive Algae Species as a Source of Secondary Metabolites and Biological Activities: Spain as Case-Study. Mar. Drugs 2021, 19, 178. [Google Scholar] [CrossRef] [PubMed]
  106. NIMPIS. National Introduced Marine Pest Information System. Available online: https://nimpis.marinepests.gov.au/species/species/53 (accessed on 15 January 2024).
  107. Pereira, L.; Silva, P. A concise review of the red macroalgae Chondracanthus teedei (Mertens ex Roth) Kützing and Chondracanthus teedei var. lusitanicus (J.E. De Mesquita Rodrigues) Bárbara Cremades. J. Appl. Phycol. 2021, 33, 111–131. [Google Scholar] [CrossRef]
  108. Bermejo, R.; Cara, C.L.; Macías, M.; Sánchez-García, J.; Hernández, I. Growth rates of Gracilariopsis longissima, Gracilaria bursapastoris and Chondracanthus teedei (Rhodophyta) cultured in ropes: Implication for N biomitigation in Cadiz Bay (Southern Spain). J. Appl. Phycol. 2020, 32, 879–1891. [Google Scholar] [CrossRef]
  109. Silva, P.; Pereira, L. Concise review of Osmundea pinnatifida (Hudson) Stackhouse. J. Appl. Phycol. 2020, 32, 2761–2771. [Google Scholar] [CrossRef]
  110. Biancacci, C.; Abell, R.; McDougall, G.J. Annual compositional variation in wild Osmundea pinnatifida (Hudson) Stackhouse from the west coast of Scotland. J. Appl. Phycol. 2022, 34, 1661–1675. [Google Scholar] [CrossRef]
  111. Royer, C. Advancing Development of Porphyra umbilicalis as a Red Algal Model System and Aquaculture Crop. Master’s Thesis, University of Maine, Orono, ME, USA, 2017; p. 2683. Available online: http://digitalcommons.library.umaine.edu/etd/2683 (accessed on 10 June 2024).
  112. Fleurence, J.; Levine, I. Seaweed in Health and Disease Prevention; Academic Press: Cambridge, MA, USA, 2016; p. 458. [Google Scholar] [CrossRef]
  113. Netalgae EU. Seaweed Industry in Europe. Available online: https://www.seaweed.ie/irish_seaweed_contacts/doc/Filieres_12p_UK.pdf (accessed on 16 April 2024).
  114. Un Mondo Ecosostenibile. Available online: https://antropocene.it/en (accessed on 15 April 2024).
  115. Chemodanov, A.; Robin, A.; Jinjikhashvily, G.; Yitzhak, D.; Liberzon, A.; Israel, A.; Golberg, A. Feasibility study of Ulva sp. (Chlorophyta) intensive cultivation in a coastal area of the Eastern Mediterranean Sea. Biofuels Bioprod. Biorefining 2019, 13, 864–877. [Google Scholar] [CrossRef]
  116. Wichard, T.; Charrier, B.; Mineur, F.; Bothwell, J.H.; Clerck, O.D.; Coates, J.C. The green seaweed Ulva: A model system to study morphogenesis. Front. Plant Sci. 2015, 6, 72–82. [Google Scholar] [CrossRef] [PubMed]
  117. Simon, C.; McHale, M.; Sulpice, R. Applications of Ulva Biomass and Strategies to Improve Its Yield and Composition: A Perspective for Ulva Aquaculture. Biology 2022, 11, 1593. [Google Scholar] [CrossRef] [PubMed]
  118. Franzen, D.; Nathaniel, H.; Lingegård, S.; Gröndahl, F. Macroalgae Production Manual Production, Challenges & Pathways; KTH Royal Institute of Technology: Stockholm, Sweden, 2022; p. 23. [Google Scholar]
  119. Dominguez, H.; Loret, E.P. Ulva lactuca, a Source of Troubles and Potential Riches. Mar Drugs. 2019, 17, 357. [Google Scholar] [CrossRef]
  120. Araujo, R.; Peteiro, C. Algae as Food and Food Supplements in Europe; EUR 30779 EN; JRC125913; Publications Office of the European Union: Luxembourg, 2021; ISBN 978-92-76-40548-1. [Google Scholar] [CrossRef]
  121. Hayden, H.S.; Blomster, J.; Maggs, C.A.; Silva, P.C.; Stanhope, M.J.; Waaland, J.R. Linnaeus was right all along: Ulva and Enteromorpha are not distinct genera. Eur. J. Phycol. 2003, 38, 277–294. [Google Scholar] [CrossRef]
  122. Rybak, A. Species of Ulva (Ulvophyceae, Chlorophyta) as indicators of salinity. Ecol. Indic. 2018, 85, 253–261. [Google Scholar] [CrossRef]
  123. Steinhagen, S.; Karez, R.; Weinberger, F. Cryptic, alien and lost species: Molecular diversity of Ulva sensu lato along the German coasts of the North and Baltic Seas. Eur. J. Phycol. 2020, 54, 466–483. [Google Scholar] [CrossRef]
  124. Zertuche-González, J.A.; Sandoval-Gil, J.M.; Rangel-Mendoza, L.K.; Gálvez-Palazuelos, A.I.; Guzmán-Calderón, J.M.; Yarish, C. Seasonal and Interannual Production of Sea Lettuce (Ulva sp.) in Outdoor Cultures Based on Commercial Size Ponds. J. World Aquac. Soc. 2021, 52, 1047–1058. [Google Scholar] [CrossRef]
  125. Sebok, S.; Hanelt, D. Cultivation of the brackish-water macroalga Ulva lactuca in wastewater from land-based fish and shrimp aquacultures in Germany. Aquaculture 2023, 571, 739463. [Google Scholar] [CrossRef]
  126. Augyte, S.; Kim, J.K.; Yarish, C. Seaweed aquaculture—From historic trends to current innovation. J. World Aquac. Soc. 2021, 52, 1004–1008. [Google Scholar] [CrossRef]
  127. Kübler, J.E.; Dudgeon, S.; Bush, D. Climate change challenges and opportunities for seaweed aquaculture in California, USA. J. World Aquac. Soc. 2021, 52, 1069–1080. [Google Scholar] [CrossRef]
  128. Zheng, Y.; Jin, R.; Zhang, X.; Wang, Q.; Wu, J. The considerable environmental benefits of seaweed aquaculture in China. Stoch. Environ. Res. Risk Assess. 2019, 33, 1203–1221. Available online: https://www.researchgate.net/publication/333413291_The_considerable_environmental_benefits_of_seaweed_aquaculture_in_China (accessed on 10 June 2024). [CrossRef]
  129. Weinberger, F.; Paalme, T.; Wikström, S.A. Seaweed resources of the Baltic Sea, Kattegat and German and Danish North Sea coasts. Bot. Mar. 2020, 63, 61–72. [Google Scholar] [CrossRef]
  130. Liu, Y.; Cao, L.; Cheung, W.; Sumaila, R. Global estimates of suitable areas for marine algae farming. Environ. Res. Lett. 2023, 18, 064028. [Google Scholar] [CrossRef]
  131. REMEDIA (Remediation of Marine Environment and Development of Innovative Aquaculture: Exploitation of Edible/Not Edible Biomass). Available online: https://remedialife.eu/wp-content/uploads/2023/08/5.-REPLICABILITY-PLAN.pdf (accessed on 12 April 2024).
  132. Cai, J.; Lovatelli, A.; Aguilar-Manjarrez, J.; Cornish, L.; Dabbadie, L.; Desrochers, A.; Diffey, S.; Garrido Gamarro, E.; Geehan, J.; Hurtado, A.; et al. Seaweeds and Microalgae: An Overview for Unlocking their Potential in Global Aquaculture Development; FAO Fisheries and Aquaculture Circular No. 1229; FAO: Rome, Italy, 2021; p. 37. [Google Scholar] [CrossRef]
  133. UMF (Union for the Mediterranean). Towards a Sustainable Blue Economy in the Mediterranean Region. 2021. Available online: https://ufmsecretariat.org/wp-content/uploads/2021/07/21.7.19-2021UfM.studydefEN-web.pdf (accessed on 21 January 2024).
  134. Lecerf, M.; Herr, D.; Thomas, T.; Elverum, C.; Delrieu, E.; Picourt, L. Coastal and Marine Ecosystems as Nature-Based Solutions in New or Updated Nationally Determined Contributions, Ocean & Climate Platform, Conservation International, IUCN, GIZ, Rare, the Nature Conservancy and WWF. 2021, p. 26. Available online: https://ocean-climate.org/wp-content/uploads/2021/06/coastal-and-marine-ecosystem-2806.pdf (accessed on 10 June 2024).
  135. Lyon, B.G.; Lyon, C.E. Meat quality: Sensory and instrumental evaluations. In Poultry Meat Processing; Sams, A.R., Ed.; CRC Press: New York, NY, USA, 2001; pp. 97–120. [Google Scholar]
  136. Plantinga, G. The Perception of Consumers about Algae as Alternative Protein Source: A Systematic Literature Review. Bachelor’s Thesis, WUR, Wageningen, The Netherlands, 2020; p. 36. Available online: https://edepot.wur.nl/520803 (accessed on 10 June 2024).
  137. ASC-MSC Seaweed Standard. 2017. Available online: https://www.asc-aqua.org/wp-content/uploads/2017/11/ASC-MSC-Seaweed-Standard.pdf (accessed on 26 January 2024).
  138. Griskevicius, V.; Tybur, J.M.; Van den Bergh, B. Going green to be seen: Status, reputation, and conspicuous conservation. J. Personal. Soc. Psychol. 2010, 98, 392–404. [Google Scholar] [CrossRef]
  139. GFCM (General Fisheries Commission for the Mediterranean). Report of the Workshop on the Status and Future of Seaweed Farming in the Mediterranean and the Black Sea. 2021. Available online: https://www.fao.org/gfcm/technical-meetings/detail/en/c/1442598/ (accessed on 25 January 2024).
  140. B-Blue. Available online: https://keep.eu/projects/25082/Building-the-blue-biotechno-EN/ (accessed on 25 January 2023).
  141. Cebrian, E.; Tamburello, L.; Verdura, J.; Guarnieri, G.; Medrano, A.; Linares, C.; Hereu, B.; Garrabou, J.; Cerrano, C.; Galobart, C.; et al. A Roadmap for the restoration of Mediterranean macroalgal forests. Front. Mar. Sci. 2021, 8, 709219. [Google Scholar] [CrossRef]
Figure 1. Export and import values (in thousands of USD) of seaweed and other algae fit for human consumption, fresh, chilled, frozen or dried, whether ground or not, for 15 Mediterranean countries in 2022 [61].
Figure 1. Export and import values (in thousands of USD) of seaweed and other algae fit for human consumption, fresh, chilled, frozen or dried, whether ground or not, for 15 Mediterranean countries in 2022 [61].
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Table 1. The annual global production (in thousand tons, live weight) of the eight most important macroalgae species in relation to the production volume in the years 2000, 2005, 2010, 2015 and 2020 [7,65,66].
Table 1. The annual global production (in thousand tons, live weight) of the eight most important macroalgae species in relation to the production volume in the years 2000, 2005, 2010, 2015 and 2020 [7,65,66].
SpeciesThe Global Annual Production (in Thousand Tons, Live Weight)
20002005201020152020Total (%) in 2020
Saccharina japonica
Royal Kombu, Sea tangle or Japanese kelp
5380.95699.16525.610,313.712,469.835.5
Eucheuma spp.214.3983.93472.610,182.18129.423.2
Gracilaria spp.55.5933.21657.13767.05180.414.8
Undaria pinnatifida
Wakame, Sea mustard
311.12439.71505.12215.62810.68.0
Porphyra spp./Pyropia spp.
Nori, Laver
424.9703.11040.71109.92220.26.3
Kappaphycus alvarezii
Elkhorn sea moss
649.51283.51884.21751.81604.14.6
Sargassum fusiforme
Fusiform sargassum
12.1115.697.0209.3292.90.8
Eucheuma denticulatum
Spiny eucheuma
85.3174.5265.5280.8154.10.4
Subtotal of eight important species in total aquatic algae production (%)67.383.281.596.093.793.7
Total aquatic algae production10,595.614,831.320,174.331,073.535,077.6100
Table 2. Production process, annual production (in tonnes, wet weight) and application of macroalgae species in Mediterranean countries (Spain, France, Morocco and Israel) [86].
Table 2. Production process, annual production (in tonnes, wet weight) and application of macroalgae species in Mediterranean countries (Spain, France, Morocco and Israel) [86].
CountrySpeciesProduction ProcessAnnual Production (Wet Weight/Tonnes)Application
Spain (Mediterranean)Ulva sp.Onshore aquaculture0–10Food, personal care, plant and soil nutrition
SpainSaccharina sp.,Wild harvesting0–10Food
SpainHimanthalia elongata, Undaria sp.Wild harvesting0–10Food
SpainLaminaria ochroleuca, Palmaria palmata, Saccharina latissimaWild harvesting0–10Food
SpainGracilaria sp., Ulva sp.Aquaculture10–100Food
SpainCodium sp., Gracilaria sp., Ulva sp.Wild harvesting10–100Food
SpainCodium sp., Himanthalia elongata, Porphyra sp., Ulva sp., Undaria sp.Wild harvesting10–100Food
SpainChondrus crispus, Codium sp., Gigartina pistillata, Himanthalia elongata, Laminaria ochroleuca, Mastocarpus stellatus, Porphyra sp., Saccharina latissima, Ulva sp., Undaria sp.Wild harvesting100–1000-
SpainCodium sp., Ulva sp., Undaria sp.Wild harvesting and aquaculture100–1000Food
Spain-Wild harvesting10,000–100,000Hydrocolloids
FranceAlaria esculenta, Saccharina latissima, Undaria sp.Offshore aquaculture10–100Food, personal care
France-Wild harvesting and aquaculture10–100Feed
FranceAlaria sp., Chondrus crispus, Fucus sp., Himanthalia elongata, Palmaria palmata, Phymatolithon calcareum, Porphyra sp., Saccharina latissima, Ulva sp., Undaria sp. Porphyra sp., Undaria pinnatifidaWild harvesting10–100-
France-Wild harvesting10–100Food
FranceAlaria sp., Himanthalia elongata, Palmaria palmataWild harvesting10–100Food
FranceLaminaria digitata, Palmaria palmataWild harvesting10–100Plant and soil nutrition
France
(Mediterranean)
Ulva rigidaAquaculture and wild harvesting100–1000Bioplastics
FranceSaccharina latissima, Palmaria palmataAquaculture, IMTA100–10,000-
FranceHimanthalia elongata, Palmaria palmata, Porphyra sp., Ulva sp., Undaria sp.Wild harvesting100–10,000Food
FranceHimanthalia elongata, Palmaria palmata, Porphyra sp., Saccharina latissima, Ulva sp., Undaria sp.Wild harvesting100–10,000-
FranceHimanthalia elongata, Palmaria palmata, Porphyra umbilicalis, Saccharina latissima, Ulva sp., Undaria sp.Wild harvesting100–10,000Food
FranceHimanthalia elongata, Palmara palmata, Porphyra sp., Saccharina latissima, Ulva sp., Undaria pinnatifidaWild harvesting100–10,000Food
FranceLaminaria sp., Palmaria sp., Himanthalia elongata, Ascophyllum nodosumAquaculture and wild harvesting1000–10,000-
FranceGracilaria sp., Gelidium corneum, Kappaphycus alvarezii, Eucheuma denticulatumWild harvesting and aquaculture1000–10,000Hydrocolloids
FranceUlva sp.Wild harvesting1000–10,000-
FranceSargassum sp., Solieria sp., Ulva sp.Wild harvesting1000–10,000-
FranceSargassum sp.Wild harvesting10,000–100,000-
FranceSolieria sp., Ulva sp.Wild harvesting and aquaculture100,000–1,000,000Plant and soil nutrition, feed
MoroccoUlva lactuca, Gelidium corneum, Gracilaria sp., Gigartina sp., Laminaria sp.-0–10-
MoroccoGelidium corneumWild harvesting1000–10,000Hydrocolloids
IsraelGracilaria sp.Onshore aquaculture0–10Personal care, pharmaceuticals
IsraelUlva sp., Gracilaria sp.Onshore aquaculture10–100Nutraceuticals, food, personal care
Table 3. Edible macroalgae in the Mediterranean Sea [96].
Table 3. Edible macroalgae in the Mediterranean Sea [96].
SpeciesCommon NameHabitatUsed as Food
Green algae
Caulerpa racemosa
alien
sea grape, green caviar, grape caulerpatide pools, reef flatspeppery flavour, common in Polynesian, Asian and Island cuisines in salad
Ulva clathrataAonorirocks and stones, from mid-littoral to
sublittoral
commonly eaten fresh as a sea vegetable or dried, particularly with eggs
Ulva compressaGreen nori, plat darmwiermarine and estuarine, rock pools and
sandy rocks, varying salinities
very popular due to fine texture and lovely fresh taste (Hawaii)
Ulva intestinalisGut weedsheltered and exposed locations, natural and artificial structure, also epiphytically, from the upper littoral pools into the sublittoralyes
Ulva lactucaSea lettuce, green laverintertidal to shallow infra-littoral, often in tide pools, quick colonizer, blooms in the presence of nutrient run-off and fresh water inputdelicate with mild flavour fresh and dried, in flakes, powders, used as a seasoning in soups and salads
Ulva linzaBreed darmwier, bright grass kelp, welded green norirocks or rock pools, usually in marine water sometimes in brackishin many cultures, due to high nutrient content and silky texture
Ulva proliferaGreen ribbon planton rocks or other algae, on open coasts, estuaries and harbours, mixed with other species of the same genusyes
Ulva rigidaGreen laverepilithic, in the entire littoral zone to the sublittoralused as a fresh sea vegetable by many island cultures due to high nutrient content and fresh taste
Red algae
Amphiroa cryptarthrodia on rocks in sheltered waters, tide pools, forms large lawnsused on functional foods
Amphiroa fragilissima up to 10 m depth, in seagrass meadows and rock hollowsused on functional foods
Chondracanthusteedei habitats in the intertidal and subtidal zone, semi-exposed or sheltered areasused for salads (máru) in parts of Italy
Gracilaria bursa-pastoris epilithic, calm water of the upper sublittoralyes
Grateloupia filicina on rocks in pools, mid-littoral to shallow
sublittoral, sporadic
yes
Grateloupia turuturu
alien
epilithic, shallow tide pools, sand covered
rocks near coast
commonly used in Japan as a sea vegetable, rich in dietary fibre
Hypnea spinella
alien
lower intertidal to 7 m, attached to small shells or rubble, in seagrass bedscommonly eaten (boiled in coconut milk) in the Pacific and Asia
Nemalion elminthoides exposed rocky shores, generally on barnacles and limpetsyes
Osmundea pinnatifidaPepper dulseperennial, intertidal and sublittoral, on exposed rocks, generally distributed, abundantaromatic seaweed, a pepper- or curry-flavoured spice in Scotland, Ireland, and Portugal
Plocamium cartilagineumCock’s comb, kammtang, kamwier, red comb weeddepths from 2 to 26 m, strong to moderate wave action, on
other algae
yes
Porphyra umbilicalisPurple laver, pink laver, laver, norion rocks, mussels, in the littoral to splash zone, especially on exposed coastsin flaked and whole leaf form, as a nori substitute, as laver, as an ingredient in snack mixes
Brown algae
Colpomenia sinuosa Epiphytic, hard surfaces
lower intertidal up to 15 m deep
yes
Dictyopteris plagiogrammaLimu lipoaon hard substrates, often attached to coral fragments or scattered rocks on deep sand plains from 9 to 55 m deepyes
Hydroclathrus clathratusPerforated brown seaweedmid-littoral, wave-exposed rocksin traditional Asian cuisine for centuries
Petalonia fascia on rock in the mid intertidal
to shallow sublittoral, protected or semi-exposed
yes
Scytosiphon lomentariaSausage weedLittoral, wave-exposed
shores and rock pools
yes
Treptacantha abies-marina wave-exposed sublittoral zoneyes
Undaria pinnatifida
alien
Wakameshallow sublittoral zonesweet flavour and slippery texture, dried and fresh, a delicacy in East Asian countries, miso soup and salads
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Jelić Mrčelić, G.; Krstulović Šifner, S.; Nerlović, V. A Comparison between the Production of Edible Macroalgae Worldwide and in the Mediterranean Sea. Oceans 2024, 5, 442-465. https://doi.org/10.3390/oceans5030026

AMA Style

Jelić Mrčelić G, Krstulović Šifner S, Nerlović V. A Comparison between the Production of Edible Macroalgae Worldwide and in the Mediterranean Sea. Oceans. 2024; 5(3):442-465. https://doi.org/10.3390/oceans5030026

Chicago/Turabian Style

Jelić Mrčelić, Gorana, Svjetlana Krstulović Šifner, and Vedrana Nerlović. 2024. "A Comparison between the Production of Edible Macroalgae Worldwide and in the Mediterranean Sea" Oceans 5, no. 3: 442-465. https://doi.org/10.3390/oceans5030026

APA Style

Jelić Mrčelić, G., Krstulović Šifner, S., & Nerlović, V. (2024). A Comparison between the Production of Edible Macroalgae Worldwide and in the Mediterranean Sea. Oceans, 5(3), 442-465. https://doi.org/10.3390/oceans5030026

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