Next Article in Journal
Precautionary Saving and Liquidity Shortage
Next Article in Special Issue
Much More Than Food: The Malaysian Breakfast, a Socio-Cultural Perspective
Previous Article in Journal
Energy Consumption and Environmental Quality in Africa: Does Energy Efficiency Make Any Difference?
Previous Article in Special Issue
Alternative Food Networks, Social Capital, and Public Policy in Mexico City
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Local Food Systems under Global Influence: The Case of Food, Health and Environment in Five Socio-Ecosystems

by
Michael Rapinski
1,*,
Richard Raymond
1,
Damien Davy
2,
Thora Herrmann
3,4,5,
Jean-Philippe Bedell
6,
Abdou Ka
7,
Guillaume Odonne
2,
Laine Chanteloup
8,
Pascal Jean Lopez
9,
Éric Foulquier
10,
Eduardo Ferreira da Silva
11,
Nathalie El Deghel
6,
Gilles Boëtsch
7,
Véronique Coxam
12,
Fabienne Joliet
13,
Anne-Marie Guihard-Costa
14,
Laurence Tibère
15,
Julie-Anne Nazare
16 and
Priscilla Duboz
7
1
UMR 7206 Eco-Anthropologie (CNRS, MNHN, Université Paris-Cité), 75116 Paris, France
2
UAR 3456 LEEISA (CNRS, Université de Guyane, IFFREMER), Cayenne 97300, French Guiana
3
Biodiverse Anthropocenes Profiling Program, History, Culture, and Communication Studies Research Unit, Faculty of Humanities, University of Oulu, Linnanmaa, P.O. Box 1000, FI-90014 Oulu, Finland
4
Helmholtz Centre for Environmental Research—UFZ, Department of Ecosystem Services, Permoserstr. 15, 04318 Leipzig, Germany
5
German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, 04103 Leipzig, Germany
6
Univ Lyon, ENTPE, Université Claude Bernard Lyon 1, CNRS, UMR 5023 LEHNA, 69518 Vaulx-en-Velin, France
7
IRL 3189, Environnement, Santé, Sociétés, Dakar BP15241, Senegal
8
Institute of Geography and Durability—Interdisciplinary Centre for Mountain Research, Université de Lausanne, 1015 Lausanne, Switzerland
9
UMR 8067 BOREA (MNHN/CNRS/Sorbonne Université/IRD/Université de Caen Normandie/Université des Antilles), 75005 Paris, France
10
UMR 6554 LETG-Brest, Université de Bretagne Occidentale, 29238 Brest, France
11
Departamento de Geociências, Universidade de Aveiro, Campus de Santiago, 3810-193 Aveiro, Portugal
12
UMR 1019 Human Nutrition Unit (Université Clermont Auvergne, INRAE), 63000 Clermont-Ferrand, France
13
UMR 6590 ESO, L’Institut Agro, Pôle Paysage, 49045 Angers, France
14
UMR 8045 BABEL, 75014 Paris, France
15
UMR 5044 CERTOP (CNRS, Université Toulouse Jean Jaurès, Université Toulouse III Paul Sabatier), 31058 Toulouse, France
16
Centre de Recherche En Nutrition Humaine Rhône-Alpes, Univ-Lyon, CarMeN Laboratory, Hospices Civils de Lyon, Cens, Université Claude Bernard Lyon1, 69310 Lyon, France
*
Author to whom correspondence should be addressed.
Sustainability 2023, 15(3), 2376; https://doi.org/10.3390/su15032376
Submission received: 12 December 2022 / Revised: 13 January 2023 / Accepted: 18 January 2023 / Published: 28 January 2023

Abstract

:
Globalization is transforming food systems around the world. With few geographical areas spared from nutritional, dietary and epidemiological transitions, chronic diseases have reached pandemic proportions. A question therefore arises as to the sustainability of local food systems. The overall purpose of this article is to put in perspective how local food systems respond to globalization through the assessment of five different case studies stemming from an international research network of Human-Environment Observatories (OHM), namely Nunavik (Québec, Canada), Oyapock (French Guiana, France), Estarreja (Portugal), Téssékéré (Senegal) and Littoral-Caraïbes (Guadeloupe, France). Each region retains aspects of its traditional food system, albeit under different patterns of influence modelled by various factors. These include history, cultural practices, remoteness and accessibility to and integration of globalized ultra-processed foods that induce differential health impacts. Furthermore, increases in the threat of environmental contamination can undermine the benefits of locally sourced foods for the profit of ultra-processed foods. These case studies demonstrate that: (i) the influence of globalization on food systems can be properly understood by integrating sociohistorical trajectories, socioeconomic and sociocultural context, ongoing local environmental issues and health determinants; and (ii) long-term and transverse monitoring is essential to understand the sustainability of local food systems vis-à-vis globalization.

1. Introduction

The globalization of food is old [1]; processes like the exchange of seeds, plants and their cuttings, as well as the circulation of food products in general between human populations have occurred consistently with varying intensity. The novelty today lies in the massiveness of these exchanges and the nature of food that brought about a “monolithic global industrial food system” in the latter half of the 20th century [2]. Globalized food products are cheaper and more available [3]. They have the characteristic of being highly processed and manufactured, thus presenting fattier and sweeter attributes than so-called “traditional” food [2,4,5,6], therefore generating nutritional disruptions with hefty health impacts [3,7]. It is estimated that roughly 24% of total deaths worldwide in 2017 (i.e., 11 million premature deaths) were attributed to unhealthy diets linked with the development of several chronic non-communicable diseases [8]; over 2.8 million deaths annually are related to being obese or overweight alone [9]. This does not include the number of people whose quality of life is greatly impacted by living with such diseases and their comorbidities, e.g., diabetes (463 million individuals in 2019, accounting for 9.3% of the global population [10]), obesity and overweight (671 million and 1.3 billion adults in 2016, respectively [11]), hypertension (1.278 billion adults in 2019 [12]) and cancer (19.3 million new cases in 2020 [13]). Notwithstanding numerous risk factors in the development of a diverse range of cancers, obesity and overweight have been found to contribute a population attributable fraction of over 30% for esophageal adenocarcinoma [14].
Food systems consist of a complex web of activities that involve, among other things, the production, aggregation, processing, transport, consumption and disposal of food products [15]. Major changes to the global food system have resulted from the massification of transport and communication networks that modify the face of the earth like the relations that human societies maintain between themselves and with their environment: they make globalization a “geographical power” [16] (p. 65). This globalization in turn leads to a decrease in planetary geographical diversity that occurs through the process of “geographical opening”, i.e., deep and rapid economic and social transformations of hitherto isolated regions [16] (p. 68). Working hand in hand with the industrialization of food, the global production, manufacturing and distribution of ultra-processed products also leads to excessive use of non-renewable energy and the emission of greenhouse gases that contribute to climate and environmental disruptions, which include biodiversity loss as well as the degradation of soil, water and air quality [3,4,17]. Given the compounding effects of the global food system on human and environmental health, the United Nations (UN) General Assembly has proclaimed a UN Decade of Action on Nutrition from 2016 to 2025, in support of their Sustainable Development Goals [18].
Considering the prevalence of food in the global circulation and trade of goods, almost no geographical area is today spared by its globalization [19]. With more or less intensity, food availability has thus increased over many geographical areas: at local scales, the choice of products and the range of nutritional values are more extensive, while contributing to a global standardized diet [3]. However, availability does not mean consumption because of both the financial resources and the cultural practices of human populations [7,20]. As pointed out by Douglas [21] (p. 146): the principles of selection which guide human beings in the choice of their food resources, in all likelihood, are not physiological but cultural.
In fact, the mechanisms that preside over food syncretism resulting from globalization are diverse, being: (1) ecological (i.e., environmental consequences of sourcing and supply, nutritional composition), (2) technological (i.e., conservation techniques, transportation networks), (3) cultural and symbolic (i.e., acceptability of consumption, ways of preparing, ways of organizing meals, gifts and sharing) and (4) social (i.e., socio-demographic consequences of access and possibility to consume). Food therefore appears as a nexus that integrates many dimensions and that, at the same time, is the expression of a relationship with the singular world. Hubert [22] (p. 34) adds that dietary patterns and ways of eating reflect the values, beliefs and aspirations of a social group, and these patterns, far from representing stable entities, are in constant transformation, just like the society of which they are an expression. Indeed, when new food items are introduced to the food system, these can alter an individual’s cultural (i.e., what foods one has access too) and social (i.e., what interpersonal network one has to access said food) capital standing depending on the values a social group has afforded these new items. Ultimately, this challenges the resilience of the local food system.
Food security occurs when there is physical, social and economic access to available and healthy food that is consumed in sufficient quantity [23,24]. Although it depends on the local supply of food, it is also contingent on global trade [3]. Owing to an increasing dependence on a global food system in many countries and regions [3], a question arises as to the sustainability of local food systems, particularly in connection with environmental and human health. Though large-scale changes to food systems are observed overall, one may be driven to the impression that these are the same everywhere. Yet, to grasp the complexity of transformations of food systems in their diachronic and synchronic dimensions, it is necessary to study their variability and recurrences in differentiated socio-ecosystems.
The overall purpose of this article is to put in perspective how food systems respond to globalization through the assessment of five different case studies centered around an international research network known as the Human-Environment Observatories (OHM). This is achieved by questioning the influence of the global trade of industrialized and ultra-processed food at a local scale through an analysis of consequences and dynamics. Three objectives are defined to accomplish this. First, the nutritional and dietary transitions are presented, which have been extensively studied through the lens of public health issues. Second, the food systems characterizing the socio-ecosystems present within five OHMs and their evolution are described. Third, an attempt is made to describe the impacts of these transformations on the health of human populations based on a One Health perspective that ties environmental health to human health [25].

2. Analytical Approach

First and foremost, this article contextualizes the links between globalization and the evolution of local food systems through the lens of nutrition and food transitions and their impact on the development of chronic diseases. The analytical approach adopted an interdisciplinary synthesis and examination method theoretically rooted in geography, anthropology of food, nutrition, health and environmental sciences. The literature review centered on five regions that are of interest to the interdisciplinary and international OHM research network. Their conception and implementation are thoroughly described by Chenorkian [26].
Briefly, OHMs have been implemented as part of the French government’s “Investing in the Future Program” (Programme d’investissement d’avenir) [26]. Their role is to enable the study of anthropized ecosystems that are susceptible to socio-ecosystemic crises; they have “been designed as a means of stimulating, supporting and organizing the interdisciplinary approach required to deal with the very great complexity of these phenomena” [26] (p. 294). To study the influence of unique disrupting events on the trajectory of local and anthropized socio-ecosystems, they are built on a ternary that consists of: (1) a “socio-ecological framework”, which describes the context of a given place, (2) an anthropogenic “disrupting event”, which disturbs it, and (3) a “focal object”, the product of the first two components [26]. This provides a suitable framework for studying the transformations of local food systems within a globalized context that can be demonstrated through the comparison of five OHMs whose disrupting events can be linked to the process of food globalization at different temporal scales and intensity (Table 1; Figure 1).
These five OHMs were selected for their geographical, social, cultural and environmental diversity within the network. They span four continents (i.e., Africa, Europe, North America and South America), thus including diverse peoples with unique food systems of Indigenous and non-Indigenous heritage. More precisely, they are all characterized by mixed food consumption, between the use of local products and imported industrialized products introduced into family consumption circuits. Furthermore, each region is characterized by a distinct environment with different levels of geographic isolation and integration into the global food trade, therefore justifying their inclusion in a transverse assessment of globalization’s impact on local food systems. A large majority of the authors have been working in the selected OHMs since their creation. Ahead of a concerted effort to document and transversally analyze the evolution of local food systems through a communal protocol, this study provides a perspective based on years of past research and immersion, feedback from experience as well as ongoing research in every socio-ecosystem included herein. Hence, the bibliographic work carried out was not intended to be exhaustive. Instead, it was guided by interdisciplinary research activities conducted in each OHM to mobilize: (i) the scientific and grey literature that they have produced in relation to their concerned food systems and (ii) relevant and complementary literature to facilitate a cross-comparison of each region.

3. Impacts on Human Health: Nutritional and Dietary Transitions

Global trends in the evolution and increasing prevalence of non-communicable diseases were first theorized in 1971 by Omran [28], who posited a model of epidemiological transition whereby patterns of high prevalence of infectious diseases are replaced by high prevalence of chronic and degenerative diseases associated with urban and industrial lifestyles. This is accompanied by a demographic transition, theorized formally in the 1940s by Notestein [29,30], whereby high fertility and mortality rates in societies shift to lower rates of fertility and mortality. The model is further complemented by the notion of nutritional transition, first proposed by Popkin [31] to describe a series of changes in the composition of dietary regimes (i.e., structure and composition of meals) that accompanies the technical development and urbanization of societies. These three models are indissociable from one another, as shifts in diet structures are linked to the nature of diseases, which therefore accompany demographic shifts associated with life expectancy [31,32,33,34].
Overall, nutritional transition describes shifts where “diets high in complex carbohydrates and fiber give way to more varied diets with a higher proportion of fats, saturated fats, and sugars” that have been associated with a higher prevalence of non-communicable diseases like obesity and type 2 diabetes [32] (p. 31). Whereas energy intake is mainly provided initially by complex sugars with an important share of vegetable proteins and lipids, the proportion of food of animal origin increases in diets that have transitioned, thus giving way to a greater contribution of animal protein and lipids to energy intake, and simple sugars take precedence over complex sugars [35]. These changes have been observed in populations from high- to low-income countries under the influence of urbanization, the commodification of food (i.e., transition from self-production to a market economy), the industrialization of the food chain and globalization [7].
Originally developed to describe and predict global trends, the linear patterns and stages of these transitions (i.e., epidemiological, demographic and nutritional) have since been revisited in light of certain countries that do not perfectly fit into these models due to several factors—social, political and economic—that characterize different human populations [7]. In developing the notion of nutrition transition, Popkin [31,33] described five broad dietary patterns (i.e., 1—collecting food, 2—famine, 3—receding famine, 4—degenerative diseases and 5—behavioral change) that are summarized by nutritional, economic and demographic factors and characteristics, as well as levels of food processing. Although they are outlined as historical developments, Popkin noted that “they are not restricted to peculiar periods of human history” and that they “continue to characterize certain geographic and socioeconomic subpopulations” [31] (p. 139). Furthermore, the historical and current dietary patterns of many peoples around the world do not necessarily fit perfectly into these five broad patterns outlined above. For a long time now, the traditional diets of the Inuit and many First Nations people across North America’s arctic and boreal forest regions have been notably characterized by considerable energy intake from animal protein and fat [36,37,38,39]. Although the contribution of foods of plant origin is not negligible, these dietary patterns remain nonetheless far and away from those high in complex carbohydrates and fiber that characterize the starting point of the nutrition transition.
In resolving such incongruities, the nutrition transition, which may best be qualified as many nutrition transitions [20], is frequently employed in a broader fashion to describe dietary changes from “traditional” foods to industrialized, marketed and processed foods through the ever-increasing influence of a globalized food system that drives global shifts and behavior [40]. One of the major global shifts in line with nutrition transitions is the contribution of fat and edible oils to energy intake. Most notably, the consumption of vegetable oils all over the world has seen great changes since the 1940s following a generalized policy of production and subsidies, which has enabled many societies to access diets richer in lipids at income levels much lower than before [32]. This is exacerbated by an acceleration in urbanization rates that allows nutrition transitions to occur in nations with much lower levels of gross national product; documented in South and North America [41,42], Asia [33,43,44,45] and Africa [46,47,48], the shift to high-fat diets is no longer an issue of rich and industrialized nations [32]. In the United States, for example, the percentage of energy intake from fat increased from 32.0% to 33.2% from 1999–2016 [41]. In the Philippines, it increased from 10% to 28% from 1983–2004 [45]. In China, it increased from 23.1% to 35.6% from 1991 to 2015 [44].
A second major global shift is the sweetness of food. Although added sugars from beverage sales decreased by 22% in high-income countries from 2007–2019, they increased up to 40% in middle-income countries, and added sugars from packaged food sales increased by 9% globally [49]. Finally, the contribution of snacking on energy-dense and nutrient-poor foods and beverages towards energy intake has become an increasing cause of concern globally [50,51,52,53]. Global trends in sales of ultra-processed foods and drinks increased from 2002–2016 [54]. Exceptions to this trend in Western Europe, North America and Australasia reveal the efficacy of statutory policies on the marketing of such products in reducing the sale of snack foods [54,55]. Nonetheless, this highlights how marketing is changing the way the world is eating and how big players, namely global agribusinesses, retailers, food manufacturers and large restaurant chains, are turning their attention from high- to low- and middle-income countries in driving food system changes [56,57].
Aside from nutritional changes in diets, these global shifts also demonstrate how the process of food transformation is changing as well. Dubbed by some as the food transition, this notion focuses more on the social processes by which food is produced and consumed [7]. These processes include social differentiation, identity construction and forms of regulation, which have consequences for changes in the origin of food, their modes of acquisition and on the distance they impart to the relationship between eaters and their food [7]. The big players of the global food systems certainly play an important role in changing and structuring this system, such as the importation or on-site manufacturing of processed products, and the behavior of consumers, such as out-of-home eating exemplified by the likes of the fast-food phenomenon [35]. Nonetheless, their success at a local level also depends on the social constructs and representations surrounding pre-existing food systems with which they can integrate, compete, co-exist, or outlast. The notions of food and nutrition transitions are undeniably intertwined, as changing foods implies changing nutrients. They are also inseparable in understanding how food systems evolve locally in different socio-ecosystems. Hence, the stakes involved in changing food systems are multifaceted and are not simply issues affecting nutrition and public health.

4. Food Systems and Their Transformations

Changes in the food systems of different socio-ecosystems are subject to many geographical, economic, cultural, and environmental factors, among others. Access to different categories of food depends on the places and living standards of human populations, as well as on production and distribution systems, which vary from place to place. Throughout the 20th century, all the populations living in the regions concerned by the five OHMs experienced substantial changes to their environment and their food systems linked to their identified disrupting event (Table 1; Figure 1), due in particular to the physical opening up of these territories, a greater connection to a globalized system extending hand in hand with global trade liberalization, as well as environmental degradation (Table 2).

4.1. Regional Examples

4.1.1. Nunavik, Canada

During the 1950s in the Canadian Arctic, governmental policies concerning the sedentarization of Inuit Peoples led to a gradual reduction in self-sufficiency from local country food issued from hunting, fishing and wild harvesting activities that include marine mammals (e.g., beluga (Delphinapterus leucas (Pallas, 1776); Monodontidae), walrus (Odobenus rosmarus (Linnaeus, 1758); Odobenidae) and seals (Phocidae)), fish (e.g., Arctic char (Salvelinus alpinus (Linnaeus, 1758); Salmonidae) and sculpins (Myoxocephalus spp.; Cottidae)), land mammals (e.g., caribou (Rangifer tarandus (Linnaeus, 1758); Cervidae)), wildfowl (e.g., Canada goose (Branta canadensis (Linnaeus, 1758); Anatidae) and ptarmigan (Lagopus spp.; Phasianidae)), as well as rosaceous (cloudberries (Rubus chamaemorus L.)) and ericaceous berries (Vaccinium spp. and crowberries (Empetrum nigrum L.)) [37,58,59,60,61,62,63,64]. In Nunavik, this has led to an increase in the consumption of imported, store-bought food from supermarkets located in each northern village of the region [65,66,67]. By 2011, globalized commercial foods had integrated well into a food system still characterized by local country foods. Yet, Plan Nord promises to intensify changes to the food system, particularly through regional development that will have an impact on access to store-bought and country foods. The share of ultra-processed foods, rich in saturated fats, sugars and additives, remains particularly significant in current dietary practices, while physical exercise is reduced due to an increasingly sedentary lifestyle, even if hunting, fishing and gathering practices maintain a strong identity role even for the younger generation [65,68,69].

4.1.2. Ferlo, Senegal

During the 1970s, the food system of the Fulani herders of the Ferlo in Senegal experienced important transformations due to an episode of intense drought in the Sahel. By the time the Great Green Wall was initiated with the intent of minimizing the expansion of the Sahara Desert, the food system in Téssékéré and its surroundings, located in the Ferlo, had transitioned from almost total dietary self-sufficiency based on livestock (e.g., Bovidae like cattle (Bos taurus indicus Linnaeus, 1758), goats (Capra hircus Linnaeus, 1758) and sheep (Ovis aries Linnaeus, 1758)), dairy products (e.g., butter and curdled milk from livestock, cattle in particular), local fruits (e.g., desert date (Balanites aegyptiaca (L.) Delile; Zygophyllaceae), tamarind (Tamarindus indica L.; Fabaceae) and baobab (Adansonia digitata L.; Malvaceae)), wild dietary plants (e.g., thiaftoki (Leptadenia lancifolia (Schumach. & Thonn.) Decne.; Apocynaceae) and sicklepod (Senna obtusifolia (L.) H.S. Irwin & Barneby; Fabaceae)), local cereals and legumes (e.g., pearl millet (Pennisetum glaucum (L.) R.Br.; Poaceae) and niebe (Vigna unguiculata (L.) Walp.; Fabaceae)) and game (e.g., gazelles (Gazella dorcas (Linnaeus, 1758); Bovidae), ostriches (Struthio camelus Linnaeus, 1758; Struthionidae) and guineafowl eggs (Numida meleagris (Linnaeus, 1758); Numididae)) to a diet increasingly dependent on imported products offered on local weekly markets (e.g., China tea (Camellia sinensis (L.) Kuntze; Theaceae), Asian rice (Oryza sativa L.; Poaceae), sugar, vegetable oils and milk powder) [70,71,72,73,74].

4.1.3. Guadeloupe, France

At the same time in Guadeloupe, the growing containerization of maritime trade contributes to the intensification of trade, particularly regarding perishable goods [75]. As a French overseas department, the Caribbean island has access to the European Economic Area and therefore benefits from trade liberalization with other member states via France. Inevitably, the island population has moved away in part from the Caribbean Creole food model [76,77]. This model is characterized by an important contribution of fish to the diet (e.g., mahi-mahi (Coryphaena hippurus Linnaeus, 1758; Coryphaenidae), bigeye scad (Selar crumenophthalmus (Bloch, 1793)) and snappers (Lutjanus spp.; Lutjanidae)), as well as meat from livestock (e.g., chicken (Gallus gallus domesticus (Linnaeus, 1758)) and goats) and plant-based foods from Creole gardens, both of which hint at Guadeloupe’s colonial past of incorporating several species introduced to the island during that era [76,77,78,79,80]. These gardens include fruits (e.g., bananas (Musa paradisiaca L.; Musaceae), guava (Psidium guajava L.; Myrtaceae), pinneaple (Ananas comosus (L.) Merr.; Bromeliaceae), soursop (Annona muricata L.; Annonaceae), mangoes (Mangifera indica L.; Anacardiaceae), passion fruits (Passiflora edulis Sims; Passifloraceae) and various citruses (Citrus spp.; Rutaceae)), vegetables (e.g., chayote (Sechium edule (Jacq.) Sw.; Cucurbitaceae), avocado (Persea americana Mill.; Lauraceae), gombo (Abelmoschus esculentus (L.) Moench; Malvaceae) and squash (Cucurbita maxima Duchesne; Cucurbitaceae)), legumes (e.g., pigeon pea (Cajanus cajan (L.) Huth; Fabaceae)) and tubers (e.g., yams (Dioscorea spp.; Dioscoreaceae), sweet potatoes (Ipomoea batatas (L.) Lam.; Convolvulaceae), dasheen (Colocasia esculenta (L.) Schott; Araceae), arrowroot (Maranta arundinacea L.; Marantaceae) and cassava (Manihot esculenta Crantz; Euphorbiaceae)) that characterize small family farming or that can be acquired on local markets [79,80,81,82]. Nowadays, the food system increasingly includes products from international trade, such as potatoes (Solanum tuberosum L.; Solanaceae), wheat (Triticum aestivum L., Poaceae)-derived products like pasta as well as poultry, biscuits, sugary drinks and other ultra-processed products [76,77].

4.1.4. French Guiana, France

The status of French Guiana as a French overseas department enables it to access international markets in a similar fashion to Guadeloupe. Nonetheless, it was not until the opening of the road network in the early 2000s that the food systems of the lower course of the Oyapock River, which was only accessible by plane and boat until then, in the department’s eastern region experienced a stark reduction in the contribution of food from self-production [83,84,85]. Due to an important Creole population residing in the region, Creole gardens have played an important role in shaping the local food system, where fruits, vegetables, legumes and tubers, such as those listed for Guadeloupe, are cultivated. The food system is further enriched by Indigenous swidden-fallow models of cultivation that center on cassava crops [83,85,86,87], along with game hunting that includes land mammals (e.g., collared peccary (Pecari tajacu (Linnaeus, 1758); Tayassuidae), brocket deer (Mazama spp.; Cervidae) and agouti (Dasyprocta leporina (Linnaeus, 1758); Dasyproctidae)), wildfowl (e.g., black currasow (Crax alector Linnaeus, 1766; Cracidae) and grey-winged trumpeter (Psophia crepitans Linnaeus, 1758; Psophiidae)) and reptiles (e.g., iguana (Iguana iguana (Linnaeus, 1758); Iguanidae) and tortoises (Chelonoidis spp.; Testudinidae)), as well as fishing (e.g., giant wolf fish (Hoplias aimara (Valenciennes, 1846); Erythrinidae), stripped mullet (Mugil incilis Hancock, 1830; Mugilidae) and banded cichlid (Heros efasciatus Heckel, 1840; Cichlidae)) and wild harvesting of dietary plants (e.g., maripa palm (Attalea maripa (Aubl.) Mart.; Arecaceae), açaí (Euterpe oleracea Mart.; Arecaceae), aymoutabou (Moutabea guianensis Aubl.; Polygalaceae); bagasse (Ambelania acida Aubl.; Apocynaceae)) [84,88,89,90,91,92,93]. Introduced and imported products such as Asian rice are now more consumed than couac (i.e., roasted cassava flour, a staple of the lower Oyapock diet) [84], while chicken and pork from global factory farms have supplanted the consumption of wild game.

4.1.5. Aveiro, Portugal

Finally, the situation of the Aveiro district is different. As a member of the European Economic Area, Portugal benefits from trade liberalization with other member states. However, modifications to the food system there are old, notably due to the country’s historically close contacts and exchanges with other continents (Africa and the Americas in particular). Therefore, transformations linked to globalization can hardly be interpreted in the same way as in other socio-ecosystems. The appearance of supermarkets in this area is relatively recent (2000s), and industrial foodstuffs from the globalized food system are increasingly accessible and therefore more present despite the presence of local markets that continue to offer locally produced and harvested food. Small-scale farming and self-production from kitchen gardens (e.g., tomatoes (Solanum lycopersicum L.; Solanaceae), cabbage (Brassica oleracea L.; Brassicaceae), maize (Zea mays L., Poaceae), potatoes [94,95,96,97]), livestock (e.g., cattle (Bos taurus taurus Linnaeus, 1758; Bovidae), pigs (Sus domesticus Erxleben, 1777; Suidae), poultry [98]) and milk production from cattle [98], along with shellfish harvesting (e.g., European cockle (Cerastoderma edule (Linnaeus, 1758); Cardiidae), peppery furrow shell (Scobicularia plana (da Costa, 1778)); Semelidae) [99,100]) and fishing (e.g., European bass (Dicentrarchus labrax (Linnaeus, 1758); Moronidae), sea lamprey (Petromyzon marinus Linnaeus, 1758; Petromyzontidae), European eel (Anguilla anguilla (Linnaeus, 1758); Anguillidae) [100,101]) remain important and valued. These activities of self-sufficiency are coupled with commercial activities in a constantly changing foodscape. The production of rice, for example, once played an important economic role in the region, but its cultivation is now practiced on a considerably reduced scale [98]. Furthermore, the presence of a polluting chemical complex (CQE) in the municipality of Estarreja has long brought attention to health risks associated with exogenous contamination linked to this industrial activity [94,95,96,97,102,103,104]. Despite the adoption of virtuous practices within the CQE, there is an increased sensitivity regarding different sources of pollution and an apprehension regarding industrial pollution. This appears to reflect the last pattern of Popkin’s model of the nutrition transition that corresponds to behavioral changes [31]. This resonates with the region’s disrupting event (Table 1, Figure 1); promoting virtuous industrial practices in accordance with Portugal’s public health policies potentially favors the preservation and emergence of short food circuits centered on local production so that the local population can integrate healthy food products into their diet to promote the reduction of chronic non-communicable diseases.

4.2. Food Profiles and Typologies

As Fumey [105] (p. 74) points out, modifications to food systems take place over the long term, and the societies concerned, far from making a clean sweep of the past, integrate new products by adapting them to their needs built from past consumption, which are themselves based on dietetics and religions, tools and techniques, availability and exchanges, desires or rejections. Thus, and in most of the socio-ecosystems included herein, several food system profiles co-exist.
Several food profiles distinguished in French Guiana and Guadeloupe reflect populational distinctions as well as similarities due to increasing exposure to a globalized food system [76,77,106]. Along French Guiana’s Oyapock River, the Indigenous food profile is characteristically based on the cultivation and consumption of cassava along with meat and fish from hunting and fishing, complemented with plant-based products from wild harvesting [76,89]. This coexists with an Amazonian Creole food profile that, despite the historical influence of Indigenous food systems, shares some similarities with the Caribbean Creole model from Guadeloupe; both are characterized by a predominance of rice over cassava, as well as high consumption of fish, fruits, vegetables and tubers. All three typologies are inevitably low in products processed by the food industry and fast food, yet they are changing rapidly, such as through the reduction of hunting, one of the features distinguishing the Amazonian Creole food profile from its Caribbean counterparts, and agricultural practices.
In French Guiana, both typologies described undeniably have influenced and continue to influence one another. Although geographical isolation has historically facilitated the preservation of the food system on the Oyapock River, proximity to Brazil has always enabled exchanges, and more recently, the introduction of ultra-processed foods. Nonetheless, food systems in both French Guiana and Guadeloupe have consistently been under the influence of imported food items and practices attributed to French populations from the European territory of France, along with evolutions to their associated food system. In Guadeloupe, not only has this led to a profile, characterized by a low proportion of fatty and sugary products with a high proportion of fruits, vegetables, legumes, cereals and dairy products, that mirrors the nutritional recommendations of the French National Health Nutrition Program (Programme national nutrition santé—PNNS), but has also led to one characterized by large consumption of processed products at the other extreme. Méjean et al. [76] identified a fourth profile in Guadeloupe that mixes agro-industrial foods and so-called “traditional” foods, hybridized and dubbed “in transition”, which analyses from nutritional surveys corroborate as ongoing [107,108]. Although this pertains to Guadeloupe, this may very well apply to both French overseas territories that are increasingly being opened up.
Just as Méjean et al. [76] described the nutrition transition towards globalized foodstuff in the Caribbean to be advanced, a similar trend is described in Arctic Canada [39,109,110]. This trend dichotomizes two different typologies that are ascribed to Inuit food systems in Nunavik, namely one characterized by traditional Inuit food and another characterized by introduced market foods [111,112]. Despite important changes to Inuit lifestyles, hunted and wild-harvested foods are still stored in community freezers that are made available to village residents, thus supporting two key elements of Inuit culture: hunting and sharing [113]. Although imported and purchased foods are increasingly taking hold of the local food system, Inuit people maintain a strong link with the practice of traditional and subsistence activities [59,65,69], and the local food system can be more accurately described as hybrid. In keeping with this notion of hybridization, greenhouse projects that are being implemented in Nunavik reveal that these are being appropriated as a new practice of cultivation through the connection between gardening and berry picking, though local production of fruits and vegetables by these means is still limited and virtually inaccessible in most villages [66,67,114].
What the cases of Nunavik, French Guiana and Guadeloupe tell us is that typologies are not mutually exclusive. As the term “transition” implies, they exist on a spectrum and involve a process that is inevitably navigated by individuals and groups of people. The geographical opening of territories by infrastructure development (i.e., Plan Nord in Nunavik, port development in Guadeloupe and road access on the Oyapock) has and will likely continue to facilitate the importation of globalized ultra-processed and industrialized foods into local food systems. This implies a transition into an increasingly globalized food system that supposes a convergence towards homogeneity. Yet, this premise does not account for interactions between co-existing food systems, as is the case in French Guiana (e.g., Indigenous and Creole typologies), the possible divergence of paths as testified in Guadeloupe (i.e., typologies reflecting the French National Health Nutrition Program as opposed to processed foods) or active attempts at reappropriating the evolving food system on the premise of self-determination and increasing food security, as observed in Nunavik.
Both Estarreja and Téssékéré present cases where it is very difficult to say that several typologies co-exist. Indeed, the composition of meals is relatively stable, though the external offering is high in the former and low in the latter. Possibilities for local supply in both regions have both been undermined by environmental degradation in the past. Industrial pollution has been a source of contamination to locally produced food near Estarreja, but agriculture remains an important sector, just as households continue to grow vegetables and raise poultry despite the presence of supermarkets and large fast-food brands that offer alternatives [115,116]. In Téssékéré, desertification has led to the disappearance of winter crops and dairy resources; the Fulani food system therefore relies heavily on the weekly market for fresh produce and the village grocery stores, which is very clearly reflected in the discourse of the local population [117]. As opposed to Nunavik, French Guiana and Guadeloupe, which are experiencing rapid changes in recent times, the reason for the relative stability of the Estarreja food system may in part lie in the fact that it has evolved and changed slowly over time, modulated by a process of food globalization to which Portugal has contributed since the Colombian exchange. In Téssékéré, the attachment to Fulani culture and way of life remains linked to a few dietary traits, such as a central consumption of milk, but the latter is now imported and mainly purchased in powdered form [71,72]. Despite the population’s limited financial means [117,118,119,120], junk foods (e.g., carbonated soft drinks and chips) are available, and their consumption is also restrained in part by their cultural and social representations [73,121]. One might argue that the relative stability of the Fulani food system is in part due to a low exposure to imported ultra-processed foodstuffs. However, local markets provided a point of entry for these products into a system whose resilience is rendered vulnerable by climate change, and is therefore susceptible to experiencing increasingly rapid changes.

5. Health Outcomes of the Nutrition and Dietary Transitions in the Five OHMs’ Socio-Ecosystems

Nutrition and food transitions make it possible to set the framework for a comparison between the socio-ecosystems dealt with in this article. It appears that in Senegal, in the area concerned by the OHM Téssékéré, recovery from the consequences of the 1970s’ drought would situate it in the pattern of receding famine, according to Popkin’s model of nutrition transition [31]. Unlike the regions concerned by the other OHMs, the Ferlo region has not experienced the same level of reduction in the friction of the terrain, that is, the constantly increasing capacity to lower transport costs and delays that allows greater state control of these areas and thereby facilitates global food upheavals, constrained or not [122]. In the early 1980s, the Fulani diet was associated with a caloric intake in line with WHO recommendations, but not very diversified [74]. Forty years later, the diet characterizing the population of the rural commune of Téssékéré is a little more diversified, particularly in terms of manufactured and ultra-processed foods, and quantitatively a little more important than in the 1980s [70,71]. Acute malnutrition nevertheless remains a characteristic of the populations of the area [120]. The consumption of processed products from industry and brought to Ferlo is rare due to the lack of financial means, of course, but also due to the still-significant isolation of the region. On the other hand, the consumption of vegetable oil has increased considerably [71,73]. Nonetheless, if the presence of diseases associated with dietary imbalances is any indication, this would indicate that populations in Ferlo are gearing towards Popkin’s fourth pattern of nutrition transition (i.e., degenerative diseases [31]); in 2015, the prevalence of diabetes was 4.2% [118], whereas those of overweight and obesity were 13.2% and 3%, respectively [119] (Table 3).
In the regions concerned by the other four OHMs, however, the prevalence of non-communicable chronic diseases, namely diabetes, overweight and obesity, bears witness to Popkin’s fourth pattern of nutrition transition (Table 3). The cases of French Guiana, Guadeloupe and Nunavik underscore notable health disparities and inequities when compared to their associated states, namely France and Canada (Table 3). Such disparities are well illustrated in French Guiana, where there is a lower density of liberal and mixed health professionals [107]. Diabetes, obesity and hypertension, whose prevalence was estimated at 18% in 2011 [129], are considered the most common chronic pathologies [130]. Furthermore, this region has a younger diabetic population than the European territory of France [131]. Adjusted for age, the prevalence of diabetes was 1.6 times higher than the national rate in 2015 [128] (Table 3). Furthermore, Richard et al. [125] estimated that more than half of the French Guianese population (52%) were overweight and obese (i.e., body mass index (BMI) ≥ 25 kg/m2) compared to 41% in the European territory of France and that these disparities were greater in obese people, for which the rate in France was two-thirds of that in French Guiana (Table 3). Moreover, Delocalized Centers for Prevention and Care (Centres Délocalisés de Prévention et de Soins) of the Andrée Rosemon Hospital Center (Centre Hospitalier de Cayenne Andrée Rosemon) recorded the largest number of treated diabetic patients in Saint-Georges de l’Oyapock on the Oyapock River [132]. This reality was expressed through the discourse of Saint-Georges’ residents who identified diabetes as one of the main health problems among the population [133]. Indigenous populations of the region, such as the Palikur, have been particularly concerned by diabetes for several decades. As one resident pointed out:
“There has been a big change in Saint-Georges since the 2000s; diabetes has doubled since the change in diet, the meals eaten now are not at all the meals eaten before because there was no freezing. To keep, it was only the things you could smoke, salt...”
[84].
In Guadeloupe, the distribution of dietary profiles created in the wake of such a dietary and nutrition transition were marked by a generational effect: older populations adopted a so-called “traditional” profile, whereas younger populations had a so-called “modern” profile, transformed and more caloric [77]. The consequences of this nutritional transformation are significant, as the first cause of mortality in Guadeloupe is attributed to the development of chronic diseases [134]. In 2014, nearly half of the population was overweight or obese (Table 3), and these conditions are accompanied by an increased risk of many cardio-metabolic pathologies. For example, diabetes-related mortality, which is higher in Guadeloupe than in the European territory of France [135], increased between 2010 and 2015 [136]. To deal with these health problems, many public policies are undertaken to promote a transition towards a more sustainable agri-food system [137]. In Canada, however, various public health policies have failed to curb the incidence of pathologies associated with weight and diabetes. Among Inuit women, abdominal obesity was observed in nearly 71% of the group, while 15% were affected by hyperinsulinemia [138]. Consumer preferences are partly influenced by socio-economic characteristics, as ultra-processed foods (i.e., chips, sweets, sodas, etc.) appear more affordable and more nutritious when compared to unprocessed store-bought produces like fruits, vegetables and meat, all of which remain expensive [139]. The economic dimension of processed food is compounded by elevated costs associated with hunting (i.e., snowmobiles, boats, gas, guns and ammunitions), which can widen inequality and decrease food security by hindering access to country foods among financially precarious families [66,67,140,141]. According to the Health Quebec survey, such foods accounted for “16% of energy intake in 2004, compared to 21% in 1992” [142] (p. 2).
In contrast to French Guiana, Guadeloupe and Nunavik, Estarreja does not demonstrate the same level of geographical health disparities, as the prevalence of diabetes, overweight and obesity was similar to national rates (Table 3). Although the prevalence of diabetics in Portugal is comparable to that of French Guiana and Guadeloupe, the ratio of the overweight and obese population to diabetics is noticeably smaller than that observed for France and the two overseas departments included here (Table 3). This is alarming for the French territories, as the high rate of overweight and obesity, which remain the strongest modifiable risk factors associated with the development of diabetes [10,143], suggests that the number of diabetics will likely increase in those regions. This is also true for Canada, and even more so for Nunavik where the ratio of the overweight and obese population to diabetics reveals an even greater gap (Table 3). For Estarreja and Portugal, on the other hand, this could be an indicator that they are well on their way out of the fourth pattern of the nutrition transition described by Popkin [31] (i.e., degenerative diseases) and heading into the fifth (i.e., behavioral changes).
The fifth pattern of Popkin’s nutritional transition lies in part in adopting behaviors promoting the consumption of healthier food [31]. Very often, short food circuits are perceived as being the best source from which to acquire healthy food. However, in the regions of four of the five OHMs herein, local products appear to be contaminated. Concerns over the impact of organic and inorganic contamination in food on human health remain elevated in Estarreja due to chemical industries (CQE) near the Aveiro Lagoon (Table 1; Figure 1). Geochemical studies have shown an evolution over time in the distribution of inorganic pollutants: (i) progressive confinement of certain trace metals (e.g., mercury) in the immediate environment of the chemical complex and (ii) continuous extension of water and soil contamination by other trace metals (e.g., arsenic) [103]. Several studies have shown such metals as the contaminants presenting the most cancerous and non-cancerous risks for the exposed population, particularly in three localities of the municipality of Estarreja: Veiros, Beduído and Pardilhó [94,102,104]. Furthermore, the content of trace metals (e.g., arsenic, mercury, copper and zinc) in soil and vegetables harvested in family gardens near the chemical complex indicates that 46%, 15% and 11.5% of soils, respectively, presented concentrations of arsenic, copper and mercury higher than the thresholds established by Canadian legislation [144]; while cabbage leaves concentrated arsenic, mercury and zinc, tomatoes concentrated copper [95,96,97]. Risk perceptions by individuals of Estarreja’s population presented differences according to the environments frequented and the professional activities they have developed throughout life. More precisely, the greater the relationship with industrial activity (i.e., has worked or is working, has family members who have worked or are working) and the closer the activities are in the territory (e.g., subsistence agriculture, livestock farming), the greater the notion and visualization of the risk by the people interviewed [104]. On the other hand, a moderate presence of avoidance behaviors has been identified. Although 30% of the population declared that they did not consume local products, they did not express fears linked to contamination, and 10% declared they consume water from wells [104]. Despite this, the question as to whether or not fishing and local agricultural production activities present a health risk in the diet of local populations due to contamination persists. Among all factors presented herein, contamination undeniably presents itself as another influencing factor of transformation in the food system (Table 2). Moreover, how does this undermine efforts to tackle the incidence of chronic diseases like diabetes and obesity when the alternative that is increasingly presented is the “safe haven” of the global food system?
This conundrum is particularly relevant to Nunavik, French Guiana and Guadeloupe which are bearing the brunt of the nutrition and dietary transition in terms of health outcomes. In French Guiana, gold mining is a concerning source of environmental degradation. Such activities have led to mercury contamination in fish caught in the Oyapock River [145,146,147]. Furthermore, high lead levels detected in blood have been associated with the consumption of couac and other products derived from cassava, as well as big game [148,149], though the origin of this environmental contaminant has yet to be determined. Concerns associated with lead poisoning are particularly real among the inhabitants of the villages of the Oyapock [149,150], who still partially depend on hunting and fishing products, as well as cassava-derived products. This is all the truer for the Palikur, who also depend on these modes of subsistence and whose cultivation and consumption of cassava still define their identity [89]. In Guadeloupe, the banana plantation system has long been a source chlordecone input into the ecosystem, persisting in the soil and accumulating in root vegetables grown in family gardens [107,137]. Adding to this, Sargassum spp. (Phaeophyceae) seaweed blooms that act as sources of exogenous arsenic to the local socio-ecosystem have plagued the coast of Guadeloupe, and the Caribbean, since the beginning of the 2010s [151]. Notwithstanding threats to environmental health, this has increasingly become an international public health concern, let alone exposure to toxic gases produced by Sargassum decomposition [152]. In Nunavik, there is also an increasing concern regarding the contamination of local country foods by organic (e.g., polychlorinated biphenyls—PCBs [153,154,155], perfluoroalkyl acids—PFAAs [156]) and inorganic (e.g., lead [155,157], mercury and its organometallic counterpart methylmercury [37,154,157]) pollutants in fish and marine mammals, as well as the presence of zoonotic pathogens, such as Toxoplasma gondii, linked with the consumption of marine mammals and feathered game [158]. These situations that exacerbate food insecurity contribute to the social and psychological malaise of Inuit people residing in Nunavik, where country foods are associated with Inuit identity, are integrated with spiritual beliefs and play a role in health and well-being as an integral part of Inuit medicines [69,159,160].
Environmental contaminations in these regions are not isolated, nor are they issues that simply concern local food systems. While there are no known anthropogenic sources of mercury in the arctic region of Nunavik, the safety of local country foods is of great concern, as they bioaccumulate high concentrations of environmental contaminants [37]. Inorganic mercury emissions that are released from coal burning and artisanal gold mining in East and Southeast Asia, for instance, accumulate at the poles following long-range atmospheric, oceanic and river transport [37]. Moreover, many semi-volatile and persistent environmental contaminants that include PCBs are transported from warmer regions of the earth to colder regions by global distillation [161]. This geochemical process thus implies that few places on the planet can escape these pollutants, as they travel far from their source of emission, either anthropogenically or facilitated by climate change [161], and accumulate at the poles. While the decline in the consumption of marine country foods in Nunavik has been identified as the most important factor associated with decreasing levels of mercury and PCB contamination in individuals, it is inversely related with a shift towards an increased consumption of store-bought food [154]. With this in mind, the globalization of food takes a new meaning, one that extends beyond the capacity to transport industrialized and processed foods to all corners of the world but includes the health of environments that produce food. Transitioning between local food systems and the global food system ironically presents itself as a double-edged sword, both figuratively and literally, with favorable and unfavorable human health consequences in either direction, or more appropriately: a catch-22.

6. Conclusions: Interrogating the Relationship between Food Systems, the Environment and Health through the Lens of Populations

In the context of an increasingly globalized food system and increasingly contaminated local food supplies, consumers are left with choices that they may justify through a multitude of ways. Public health policies in a number of countries worldwide strive to act as beacons to guide societies out of the plunge into chronic and non-communicable diseases by attempting to change and influence diets based on the current state of knowledge in nutrition and dietetics: this is the etic perspective viewed through the lens of research and researchers. This is exemplified by the existence of a multitude of front-of-pack and back-of-pack labelling systems. Based on a meta-analysis of the efficacy of front-of-pack labelling, however, Ikonen et al. [162] (p. 1) argued that the ability of such labels “to nudge consumers toward healthier choices is more limited” because such labels may lead to a halo effect by positively influencing consumer health perceptions of both “good” and “bad” foods [162]. Furthermore, recent crises, such as the COVID-19 pandemic, and global food shortages due to 2022′s extreme drought in Europe and the conflict in Ukraine, continue to underscore vulnerabilities in the global food system. One of the outcomes of the COVID-19 pandemic, for example, has been the valorization (or revalorization) of smaller food supply chains and local produce in Guadeloupe based on the premise of solidarity towards local producers and the wish to eat healthily [163], despite general concerns of environmental degradation by chlordecone and contamination of local food supplies. The evolution of eating habits is based on long-, medium- and short-term events that may have a lasting or ephemeral impact on how certain foods are perceived and preferences justified: this is the emic perspective viewed through the lens of populations and their people. Thus, dietary habits, preferences and values given to the cultural capital of foods (e.g., traditional vs. exotic food; local vs. imported food; natural vs. processed food; non-contaminated vs. contaminated food; healthy vs. non-healthy food) play an important role in maintaining, improving or deteriorating the state of health, as well as driving changes to food systems in general.
Despite the pervasive nature of food globalization, all five regions presented here hang on to the particularities of their traditional food system. In Guadeloupe, French Guiana and Nunavik, this has led, in part, to the creation of different food typologies characterized by indigenous and introduced foods, for example, that interact with one another and may hybridize. The presence of industrialized and ultra-processed foods is imposing on these food systems in full transition, and their consequence on health, leading to relatively high prevalences of chronic diseases is in keeping with Popkin’s model of the nutrition transition. Despite its relatively stable food system, the Ferlo (Senegal) appears as the most vulnerable one. Recovering from an historically important famine, the diversification of foodstuffs from global trade could spell the beginning of a shift towards an increasing incidence of chronic diseases. In Portugal, on the other hand, the current food system appears to cope well with globalization. However, to suggest that it has entered the last pattern of the nutrition transition (i.e., behavioral changes) does not shield it from change, nor from further succumbing to food globalization and the health impacts it carries.
Indeed, the notion of food systems makes it possible to consider the complexity of structures of which food is a reflection [164]. Herein lies one of the limits of this study: it is difficult to make broad generalizations regarding the evolution of food systems due to the complexity of local situations. Despite attempting an in-depth assessment of several case studies, these can be called into question when the influence of lifestyles that have not been considered or overlooked is appraised (e.g., Brazilian populations in French Guiana, Indian populations along with Creole populations from other Caribbean Islands in Guadeloupe, Wolof populations in the Senegalese Ferlo or simply the effect of any population migrating back and forth from a specific location, and in and out of a specific food system). To account for the composition and the overall functioning food systems, as well as manners by which they evolve and transform, the adoption of an interdisciplinary approach is essential. This is reinforced when attention is paid to consequences on health, both in humans and, more generally, ecosystems, which are both mutually influenced. The integrative notion of the One Health concept therefore takes on its full extent [165]. In keeping with this approach, OHMs provide an appropriate tool for the transversal and long-term analysis of food systems and their transformations. The strength of this research network lies in the diversity of socio-ecosystems where observations made in the long term can contribute to the development of detailed local knowledge and an understanding of the dynamics of change at a global scale. More precisely, such long-term monitoring can enable the observation of how the speed of change along with the nature of the implicated factors influence the sustainability and trajectory of evolving local food systems in a globalized world. Such results, including those presented here, can benefit (1) political decision-makers in adjusting local dietary policies or (2) local organizations implicated in indirect actions (i.e., promotion of culture, valorization of knowledge), in order to reinforce local food systems or insert desired social developments into local cultural contexts. The focus on socio-ecosystems and human-environment interactions promptly fosters interdisciplinary research conducted through multiple lens and perspectives, namely etic and emic, for a holistic understanding of food systems under influence.

Author Contributions

M.R. and P.D. wrote and prepared the original draft. The following authors contributed to writing the synthesis and providing resources for the presentation of the OHM with which they are associated: D.D. and G.O. for OHM-Oyapock; R.R., P.J.L. and É.F. for OHM-Littoral Caraïbes; T.H., L.C., V.C. and F.J. for OHM-Nunavik; J.-P.B., E.F.d.S., N.E.D. and A.-M.G.-C. for OHM-Estarreja; A.K., G.B., L.T. and P.D. for OHM-Téssékéré. All authors, including L.T. and J.-A.N., were implicated in the review and editing process, as well as in contributing ideas to the conceptualization and the development of all sections from the introduction to the conclusion. All authors have read and agreed to the published version of the manuscript.

Funding

This work was carried out within the framework of the OHM-Téssékéré, OHM-Nunavik, OHM-Estarreja, OHM-Oyapock and OHM-Littoral Caraïbes and benefited from state funding managed by the National Research Agency under the LabEx DRIIHM “Investing in the Future Program” (reference # ANR-11-LABX-0010).

Acknowledgments

Many thanks to Jean-Pierre Poulain for providing insight on this manuscript.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Food: A Culinary History from Antiquity to the Present; Flandrin, J.L.; Montanari, M.; Sonnenfeld, A. (Eds.) Columbia University Press: New York, NY, USA, 1999. [Google Scholar]
  2. Monteiro, C.A.; Cannon, G.; Levy, R.; Moubarac, J.-C.; Jaime, P.; Paula Martins, A.; Canella, D.; Louzada, M.; Parra, D. NOVA. The Star Shines Bright. World Nutr. 2016, 7, 28–38. [Google Scholar]
  3. Benton, T.G. Using Scenario Analyses to Address the Future of Food. EFSA J. 2019, 17, e170703. [Google Scholar] [CrossRef] [PubMed]
  4. Monteiro, C.A.; Cannon, G.; Moubarac, J.-C.; Levy, R.B.; Louzada, M.L.C.; Jaime, P.C. The UN Decade of Nutrition, the NOVA Food Classification and the Trouble with Ultra-Processing. Public Health Nutr. 2018, 21, 5–17. [Google Scholar] [CrossRef] [Green Version]
  5. Monteiro, C.A.; Cannon, G.; Lawrence, M.; Da Costa Louzada, M.L.; Pereira Machado, P. Ultra-Processed Foods, Diet Quality, and Health Using the NOVA Classification System; FAO: Rome, Italy, 2019; ISBN 978-92-5-131701-3. [Google Scholar]
  6. Combris, P. 8.3. Les Transitions Nutritionnelles et Leurs Déterminants. In L’alimentation à Découvert; Esnouf, C., Fioramonti, J., Laurioux, B., Eds.; CNRS Éditions: Paris, France, 2015; pp. 277–278. [Google Scholar]
  7. Poulain, J.-P. Food in Transition: The Place of Food in the Theories of Transition. Sociol. Rev. 2021, 69, 702–724. [Google Scholar] [CrossRef]
  8. Wang, D.D.; Li, Y.; Afshin, A.; Springmann, M.; Mozaffarian, D.; Stampfer, M.J.; Hu, F.B.; Murray, C.J.L.; Willett, W.C. Global Improvement in Dietary Quality Could Lead to Substantial Reduction in Premature Death. J. Nutr. 2019, 149, 1065–1074. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. WHO. Obesity. Available online: https://www.who.int/news-room/facts-in-pictures/detail/6-facts-on-obesity (accessed on 8 June 2021).
  10. Saeedi, P.; Petersohn, I.; Salpea, P.; Malanda, B.; Karuranga, S.; Unwin, N.; Colagiuri, S.; Guariguata, L.; Motala, A.A.; Ogurtsova, K.; et al. Global and Regional Diabetes Prevalence Estimates for 2019 and Projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th Edition. Diabetes Res. Clin. Pract. 2019, 157, 107843. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Bentham, J.; Di Cesare, M.; Bilano, V.; Bixby, H.; Zhou, B.; Stevens, G.A.; Riley, L.M.; Taddei, C.; Hajifathalian, K.; Lu, Y.; et al. Worldwide Trends in Body-Mass Index, Underweight, Overweight, and Obesity from 1975 to 2016: A Pooled Analysis of 2416 Population-Based Measurement Studies in 128·9 Million Children, Adolescents, and Adults. Lancet 2017, 390, 2627–2642. [Google Scholar] [CrossRef] [Green Version]
  12. Zhou, B.; Carrillo-Larco, R.M.; Danaei, G.; Riley, L.M.; Paciorek, C.J.; Stevens, G.A.; Gregg, E.W.; Bennett, J.E.; Solomon, B.; Singleton, R.K.; et al. Worldwide Trends in Hypertension Prevalence and Progress in Treatment and Control from 1990 to 2019: A Pooled Analysis of 1201 Population-Representative Studies with 104 Million Participants. Lancet 2021, 398, 957–980. [Google Scholar] [CrossRef]
  13. Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef]
  14. Whiteman, D.C.; Wilson, L.F. The Fractions of Cancer Attributable to Modifiable Factors: A Global Review. Cancer Epidemiol. 2016, 44, 203–221. [Google Scholar] [CrossRef]
  15. FAO. Sustainable Food Systems. Concept and Framework; FAO: Rome, Italy, 2018. [Google Scholar]
  16. Grenier, C. From the Geography of Globalization to Geographic Globalization. Ann. Georgr. 2019, 726, 58–80. [Google Scholar] [CrossRef]
  17. NRDC. Food Miles. How Far Your Food Travels Has Serious Consequences for Your Health and the Climate; Natural Resources Defense Council: New York, NY, USA, 2007. [Google Scholar]
  18. FAO. UN General Assembly Proclaims Decade of Action on Nutrition. Available online: https://www.fao.org/news/story/en/item/408970/icode/ (accessed on 1 January 2021).
  19. Dictionnaire Critique de La Mondialisation, 2nd ed.; Ghorra-Gobin, C. (Ed.) Armand Colin: Paris, France, 2012. [Google Scholar]
  20. Delisle, H. Transition Nutritionnelle. In Dictionnaire des Cultures Alimentaires; Poulain, J.-P., Ed.; PUF: Paris, France, 2018; pp. 1449–1453. [Google Scholar]
  21. Douglas, M. Les Structures Du Culinaire. Communications 1979, 31, 145–170. [Google Scholar] [CrossRef] [Green Version]
  22. Hubert, A. L’anthropologie Nutritionnelle: Aspects Socio-Culturels de l’alimentation. Cah. D’études Rech. Francoph. Santé 1991, 1, 165–168. [Google Scholar]
  23. Council of Canadian Academies. Aboriginal Food Security in Northern Canada: An Assessment of the State of Knowledge; The Expert Panel on the State of Knowledge of Food Security in Northern Canada, Council of Canadian Academies: Ottawa, ON, Canada, 2014. [Google Scholar]
  24. Giudice, F.; Caferra, R.; Morone, P. COVID-19, the Food System and the Circular Economy: Challenges and Opportunities. Sustainability 2020, 12, 7939. [Google Scholar] [CrossRef]
  25. Destoumieux-Garzón, D.; Mavingui, P.; Boetsch, G.; Boissier, J.; Darriet, F.; Duboz, P.; Fritsch, C.; Giraudoux, P.; Le Roux, F.; Morand, S.; et al. The One Health Concept: 10 Years Old and a Long Road Ahead. Front. Vet. Sci. 2018, 5, 14. [Google Scholar] [CrossRef] [Green Version]
  26. Chenorkian, R. Conception and Implementation of Interdisciplinarity in the Human-Environment Observatories (OHM, CNRS). Nat. Sci. Sociétés 2020, 28, 292–305. [Google Scholar] [CrossRef]
  27. Beck, H.E.; Zimmermann, N.E.; McVicar, T.R.; Vergopolan, N.; Berg, A.; Wood, E.F. Present and Future Köppen-Geiger Climate Classification Maps at 1-Km Resolution. Sci. Data 2018, 5, 180214. [Google Scholar] [CrossRef] [Green Version]
  28. Omran, A.R. The Epidemiologic Transition: A Theory of the Epidemiology of Population Change. Milbank Mem. Fund Q. 1971, 49, 509–538. [Google Scholar] [CrossRef]
  29. Notestein, F.W. Summary of the Demographic Background of Problems of Undeveloped Areas. Milbank Mem. Fund Q. 1948, 26, 249–255. [Google Scholar] [CrossRef]
  30. Notestein, F.W. Problems of Policy in Relation to Areas of Heavy Population Pressure. Milbank Mem. Fund Q. 1944, 22, 424–444. [Google Scholar] [CrossRef]
  31. Popkin, B.M. Nutritional Patterns and Transitions. Popul. Dev. Rev. 1993, 19, 138–157. [Google Scholar] [CrossRef]
  32. Drewnowski, A.; Popkin, B.M. The Nutrition Transition: New Trends in the Global Diet. Nutr. Rev. 1997, 55, 31–43. [Google Scholar] [CrossRef] [PubMed]
  33. Popkin, B.M. The Nutrition Transition in Low-Income Countries: An Emerging Crisis. Nutr. Rev. 1994, 52, 285–298. [Google Scholar] [CrossRef]
  34. Popkin, B.M. Nutrition in Transition: The Changing Global Nutrition Challenge. Asia Pac. J. Clin. Nutr. 2001, 10, S13–S18. [Google Scholar] [CrossRef]
  35. Maire, B.; Lioret, S.; Gartner, A.; Delpeuch, F. Nutritional Transition and Non-Communicable Diet-Related Chronic Diseases in Developing Countries. Cah. D’études Rech. Francoph. Santé 2002, 12, 45–55. [Google Scholar]
  36. Kuhnlein, H.V.; Soueida, R.; Receveur, O. Dietary Nutrient Profiles of Canadian Baffin Island Inuit Differ by Food Source, Season, and Age. J. Am. Diet. Assoc. 1996, 96, 155–162. [Google Scholar] [CrossRef] [PubMed]
  37. Lemire, M.; Kwan, M.; Laouan-Sidi, A.E.; Muckle, G.; Pirkle, C.; Ayotte, P.; Dewailly, E. Local Country Food Sources of Methylmercury, Selenium and Omega-3 Fatty Acids in Nunavik, Northern Quebec. Sci. Total Environ. 2015, 509, 248–259. [Google Scholar] [CrossRef] [Green Version]
  38. Schuster, R.C.; Wein, E.E.; Dickson, C.; Chan, H.M. Importance of Traditional Foods for the Food Security of Two First Nations Communities in the Yukon, Canada. Int. J. Circumpolar Health 2011, 70, 286–300. [Google Scholar] [CrossRef] [PubMed]
  39. Kuhnlein, H.V.; Receveur, O. Local Cultural Animal Food Contributes High Levels of Nutrients for Arctic Canadian Indigenous Adults and Children. J. Nutr. 2007, 137, 1110–1114. [Google Scholar] [CrossRef] [Green Version]
  40. Popkin, B.M.; Adair, L.S.; Ng, S.W. Global Nutrition Transition and the Pandemic of Obesity in Developing Countries. Nutr. Rev. 2012, 70, 3–21. [Google Scholar] [CrossRef] [Green Version]
  41. Shan, Z.; Rehm, C.D.; Rogers, G.; Ruan, M.; Wang, D.D.; Hu, F.B.; Mozaffarian, D.; Zhang, F.F.; Bhupathiraju, S.N. Trends in Dietary Carbohydrate, Protein, and Fat Intake and Diet Quality Among US Adults, 1999–2016. JAMA 2019, 322, 1178. [Google Scholar] [CrossRef] [Green Version]
  42. Kovalskys, I.; Fisberg, M.; Gómez, G.; Pareja, R.G.; Yépez García, M.C.; Cortés Sanabria, L.Y.; Herrera-Cuenca, M.; Rigotti, A.; Guajardo, V.; Zalcman Zimberg, I.; et al. Energy Intake and Food Sources of Eight Latin American Countries: Results from the Latin American Study of Nutrition and Health (ELANS). Public Health Nutr. 2018, 21, 2535–2547. [Google Scholar] [CrossRef] [Green Version]
  43. Saito, A.; Imai, S.; Htun, N.C.; Okada, E.; Yoshita, K.; Yoshiike, N.; Takimoto, H. The Trends in Total Energy, Macronutrients and Sodium Intake among Japanese: Findings from the 1995–2016 National Health and Nutrition Survey. Br. J. Nutr. 2018, 120, 424–434. [Google Scholar] [CrossRef] [PubMed]
  44. Wang, L.; Wang, H.; Zhang, B.; Popkin, B.M.; Du, S. Elevated Fat Intake Increases Body Weight and the Risk of Overweight and Obesity among Chinese Adults: 1991–2015 Trends. Nutrients 2020, 12, 3272. [Google Scholar] [CrossRef] [PubMed]
  45. Lipoeto, N.I.; Geok Lin, K.; Angeles-Agdeppa, I. Food Consumption Patterns and Nutrition Transition in South-East Asia. Public Health Nutr. 2013, 16, 1637–1643. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Galal, O.M. The Nutrition Transition in Egypt: Obesity, Undernutrition and the Food Consumption Context. Public Health Nutr. 2002, 5, 141–148. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Wentzel-Viljoen, E.; Laubscher, R.; Vorster, H.H. Changes in Food Intake from 2005 to 2010 by a Cohort of Black Rural and Urban African Men and Women in the North West Province of South Africa: The PURE-NWP-SA Study. Public Health Nutr. 2018, 21, 2941–2958. [Google Scholar] [CrossRef] [PubMed]
  48. Vorster, H.H.; Kruger, A.; Margetts, B.M. The Nutrition Transition in Africa: Can It Be Steered into a More Positive Direction? Nutrients 2011, 3, 429–441. [Google Scholar] [CrossRef] [Green Version]
  49. Russell, C.; Baker, P.; Grimes, C.; Lindberg, R.; Lawrence, M.A. Global Trends in Added Sugars and Non-Nutritive Sweetener Use in the Packaged Food Supply: Drivers and Implications for Public Health. Public Health Nutr. 2022, 1–39. [Google Scholar] [CrossRef]
  50. Jensen, M.L.; Corvalán, C.; Reyes, M.; Popkin, B.M.; Taillie, L.S. Snacking Patterns among Chilean Children and Adolescents: Is There Potential for Improvement? Public Health Nutr. 2019, 22, 2803–2812. [Google Scholar] [CrossRef]
  51. Almoraie, N.M.; Saqaan, R.; Alharthi, R.; Alamoudi, A.; Badh, L.; Shatwan, I.M. Snacking Patterns throughout the Life Span: Potential Implications on Health. Nutr. Res. 2021, 91, 81–94. [Google Scholar] [CrossRef] [PubMed]
  52. Mattes, R.D. Snacking: A Cause for Concern. Physiol. Behav. 2018, 193, 279–283. [Google Scholar] [CrossRef]
  53. Taillie, L.S.; Afeiche, M.C.; Eldridge, A.L.; Popkin, B.M. Increased Snacking and Eating Occasions Are Associated with Higher Energy Intake among Mexican Children Aged 2–13 Years. J. Nutr. 2015, 145, 2570–2577. [Google Scholar] [CrossRef] [PubMed]
  54. Vandevijvere, S.; Jaacks, L.M.; Monteiro, C.A.; Moubarac, J.; Girling-Butcher, M.; Lee, A.C.; Pan, A.; Bentham, J.; Swinburn, B. Global Trends in Ultraprocessed Food and Drink Product Sales and Their Association with Adult Body Mass Index Trajectories. Obes. Rev. 2019, 20, 10–19. [Google Scholar] [CrossRef] [Green Version]
  55. Kovic, Y.; Noel, J.K.; Ungemack, J.A.; Burleson, J.A. The Impact of Junk Food Marketing Regulations on Food Sales: An Ecological Study. Obes. Rev. 2018, 19, 761–769. [Google Scholar] [CrossRef]
  56. Popkin, B.M. Nutrition, Agriculture and the Global Food System in Low and Middle Income Countries. Food Policy 2014, 47, 91–96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Zhou, Y.; Du, S.; Su, C.; Zhang, B.; Wang, H.; Popkin, B.M. The Food Retail Revolution in China and Its Association with Diet and Health. Food Policy 2015, 55, 92–100. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Cuerrier, A.; Elders of Kangiqsualujjuaq. The Zoological Knowledge of the Inuit of Kangiqsualujjuaq, Nunavik; Avataq Cultural Institute: Inukjuak, QC, Canada, 2012. [Google Scholar]
  59. Rapinski, M.; Cuerrier, A.; Harris, C.S.; Elders of Ivujivik; Elders of Kangiqsujuaq; Lemire, M. Our Sea, Our Health; Avataq Cultural Institute: Westmount, QC, Canada, 2021. [Google Scholar]
  60. Cuerrier, A.; Elders of Kangiqsualujjuaq. The Botanical Knowledge of the Inuit of Kangiqsualujjuaq, Nunavik; Avataq Cultural Institute: Inukjuak, QC, Canada, 2011. [Google Scholar]
  61. Cuerrier, A.; Elders of Kangiqsujuaq. The Botanical Knowledge of the Inuit of Kangiqsujuaq; Avataq Cultural Institute: Inukjuak, QC, Canada, 2011. [Google Scholar]
  62. Cuerrier, A.; Elders of Umiujaq; Elders of Kuujjuarapik. The Botanical Knowledge of the Inuit of Umiujaq and Kuujjuarapik, Nunavik; Avataq Cultural Institute: Inukjuak, QC, Canada, 2011. [Google Scholar]
  63. Labrèche, Y. Terres Habitées, Interactions et Changement Au Temps de La. In Le Nord: Habitants et Mutations; Duhaime, G., Ed.; Les Presses de l’Université Laval (coll. «Atlas historique du Québec»): Québec, QC, Canada, 2001; pp. 7–22. ISBN 2763778046. [Google Scholar]
  64. Saladin d’Anglure, B. Les Inuits Du Nunavik. In Le Nord: Habitants et Mutations; Duhaime, G., Ed.; Les Presses de l’Université Laval (coll. «Atlas historique du Québec»): Québec, QC, Canada, 2001; pp. 85–102. [Google Scholar]
  65. Lamalice, A. Géographie Du Système Alimentaire Des Inuit Du Nunavik: Du Territoire Nourricier Au Supermarché. Ph.D. thesis, Université Montpellier et Université de Montréal, Montpellier, France, Montréal, QC, Canada, 2019. [Google Scholar]
  66. Lamalice, A.; Haillot, D.; Lamontagne, M.-A.; Herrmann, T.M.; Gibout, S.; Blangy, S.; Martin, J.-L.; Coxam, V.; Arsenault, J.; Munro, L.; et al. Building Food Security in the Canadian Arctic through the Development of Sustainable Community Greenhouses and Gardening. Écoscience 2018, 25, 325–341. [Google Scholar] [CrossRef]
  67. Lamalice, A.; Avard, E.; Coxam, V.; Herrmann, T.; Desbiens, C.; Wittrant, Y.; Blangy, S. Supporting Food Security in the Far North: Community Greenhouse Projects in Nunavik and Nunavut. Études/Inuit/Studies 2016, 40, 147–169. [Google Scholar] [CrossRef] [Green Version]
  68. Blanchet, C.; Rochette, L. Nutrition and Food Consumption among the Inuit of Nunavik. Nunavik Inuit Health Survey 2004, Qanuippitaa? How Are We? Institut National de Santé Publique du Québec (INSPQ) & Nunavik Regional Board of Health and Social Services (NRBHSS): Québec, QC, Canada, 2008. [Google Scholar]
  69. Rapinski, M.; Cuerrier, A.; Harris, C.; Ivujivik, E.; Kangiqsujuaq, E.; Lemire, M. Inuit Perception of Marine Organisms: From Folk Classification to Food Harvest. J. Ethnobiol. 2018, 38, 333–355. [Google Scholar] [CrossRef] [Green Version]
  70. Ka, A. Eating in Ferlo (Senegal). Anthropol. Sociétés 2020, 44, 241–258. [Google Scholar] [CrossRef]
  71. Macia, E.; Tibère, L.; Ka, A.; Seksik, P.; Faye, B.; Boëtsch, G.; Duboz, P. The Diet of the Fulani of Senegal; Comparison between Rural and Urban Contexts around Emblematic Elements. Anthropol. Food 2021, 1–18. [Google Scholar] [CrossRef]
  72. Ka, A.; Boëtsch, G.; Macia, E. The Feeding of the Fulani Pastoralists in Sahel. Cah. Nutr. Diététique 2020, 55, 47–52. [Google Scholar] [CrossRef]
  73. Ka, A. Manger à Widou Thiengoly (Nord-Sénégal). De l’abondance Remémorée à La Dépendance Au Marché. Ph.D. Thesis, Université Cheikh Anta Diop de Dakar, Dakar, Senegal, 2016. [Google Scholar]
  74. Bénéfice, E.; Chevassus-Agnès, S.; Barral, H. Nutritional Situation and Seasonal Variations for Pastoralist Populations of the Sahel (Senegalese Ferlo). Ecol. Food Nutr. 1984, 14, 229–247. [Google Scholar] [CrossRef]
  75. Foulquier, É. Transport Maritime Sous Régime de Froid. Mondialisation Des Circulations Des Marchandises Périssables. Le Déméter 2016. Econ. Strat. Agric. 2015, 22, 261–279. [Google Scholar]
  76. Food and Nutrition in the Overseas Departments and Regions; Méjean, C.; Debussche, X.; Martin-Prével, Y.; Réquillart, V.; Soler, L.-G.; Tibère, L. (Eds.) IRD Éditions (coll. «Expertise Collective»): Marseille, France, 2020. [Google Scholar]
  77. Colombet, Z.; Lamani, V.; Allès, B.; Terrieux, P.; Ducrot, A.; Drogué, S.; Méjean, C. The French West Indian Nutrition Transition Determinants. Cah. Nutr. Diététique 2022, 57, 37–58. [Google Scholar] [CrossRef]
  78. Weiss, J.; Duchêne, J.; Le Blond, S.; Guyader, O.; Demanèche, S.; Berthou, P.; Le Roy, E.; Leblond, E. Synthèse Des Pêcheries de Guadeloupe 2017. Ifremer-sih-2020.01; 2020. [Google Scholar]
  79. Stehlé, H. Les Associations Végétales de La Guadeloupe et Leur Intérêt Dans La Valorisation Rationnelle. Rev. Bot. Appliquée D’agriculture Colon. 1937, 17, 98–109. [Google Scholar] [CrossRef]
  80. Rasse, C.; Andrieu, N.; Diman, J.-L.; Fanchone, A.; Chia, E. Use of Agroecological Practices and Performances of Small Family Farming: The Case of Guadeloupe. Cah. Agric. 2018, 27, 55002. [Google Scholar] [CrossRef]
  81. Farani, M. Le Machinisme Agricole et Les Plantes à Tubercules. In Proceedings of the Caribbean Food Crops Society 31st Annual Meeting, Dover, Barbados, 10–14 July 1995; pp. 320–323. [Google Scholar]
  82. Guyot, H. Évolution de La Production et de La Technologie Fruitières En Guadeloupe. Fruits 1971, 26, 115–126. [Google Scholar]
  83. Davy, D.; Boudoux d’Hautefeuille, M.; Nicole, S.; Grenand, F. Du Manioc et Un Pont: Un Observatoire Hommes/Milieux Sur La Frontière Franco-Brésilienne. In Reformatações Fronteiriças no Platô das Guianas: (Re)territorialidades de Cooperações em Construção; Porto, J., Doff Sotta, E., Eds.; Publit Soluções Editoriais: Rio de Janeiro, Brazil, 2011; pp. 91–118. [Google Scholar]
  84. Vincent, N. De l’étranger Dans Le Quotidien... Évolutions et Adaptations de l’alimentation à Saint-Georges de l’Oyapock. Master 2 thesis, École des Hautes Études en Sciences Sociales, Toulouse, France,, 2013. [Google Scholar]
  85. Ouhoud-Renoux, F. Le Cas Palikur: Un Combat Pour Une Adaption à Des Contraintes Fortes. In Les Peuples des Forêts Tropicales Aujourd’hui, Vol. IV: Région Caraïbes; Grenand, P., Ed.; APFT: Bruxelles, Belgium, 2000; pp. 162–193. [Google Scholar]
  86. Grenand, P. Agriculture Sur Brûlis et Changements Culturels: Le Cas Des Indiens Wayapi et Palikur de Guyane. J. D’agriculture Tradit. Bot. Appliquée 1981, 28, 23–31. [Google Scholar] [CrossRef]
  87. Capiberibe, A.; Cristinoi, A.; Grenand, P. Un Peuple Arawak: Les Palikur. In Encyclopédies Palikur Wayana Wayãpi: Langue, Milieu et Histoire; Grenand, F., Ed.; Éditions du Comité des Travaux Historiques et Scientifiques & Presses Universitaires d’Orléans: Orléans, France, 2009; pp. 32–57. ISBN 9782735506927. [Google Scholar]
  88. Hansen, E.; Richard-Hansen, C. Faune de Guyane. Guide Des Principales Espèces Soumises à Réglementation; Éditions Roger Le Guen: L’Estéou, France, 2007. [Google Scholar]
  89. Rapinski, M. Ethnobiologie et Ethnomédecine Des Peuples Premiers d’Amérique (Cris d’Eeyou Istchee, Parikwene et Pekuakamilnuatsh): L’impact de l’alimentation et Des Médecines Locales Sur La Santé et Le Bien-Être Des Diabétiques. Ph.D. thesis, Université de Montréal et Université de Guyane, Montréal, QC, Canada, Cayenne, French Guiana, 2021. [Google Scholar]
  90. Berton, M.-È. Les Plantes Médicinales Chez Les Amérindiens Palikurs de St-Georges de l’Oyapock et Macouria (Guyane Française). Master thesis, Université de Paris VII, Paris, France, 1997. [Google Scholar]
  91. Iaparrá, M.; Martiniano, N.; Felício, J.A.; Orlando, A.; Green, H.; Green, D. Kinetihwa Kabayntiwa Ariku Parantunka Ariku Parikwaki. Comunique-Se Bem Na Lingua Palikur e Na Lingua Portuguesa; Sociedade Internacional de Linguística: Macapá, Brazil, 2017. [Google Scholar]
  92. de Granville, J.-J.; Gayot, M. Guide Palmiers de Guyane; ONF: Guyane, France, 2014. [Google Scholar]
  93. Grenand, P.; Moretti, C.; Jacquemin, H.; Prévost, M.-F. Pharmacopées Traditionnelles En Guyane: Créoles, Palikur, Wayapi.; IRD Éditions: Paris, France, 2004. [Google Scholar]
  94. Cabral-Pinto, M.M.S.; Inácio, M.; Neves, O.; Almeida, A.A.; Pinto, E.; Oliveiros, B.; Ferreira da Silva, E.A. Human Health Risk Assessment Due to Agricultural Activities and Crop Consumption in the Surroundings of an Industrial Area. Expo. Health 2020, 12, 629–640. [Google Scholar] [CrossRef]
  95. Inácio, M.; Neves, O.; Pereira, V.; Ferreira Da Silva, E.; Veiga, N. Heavy Metals Accumulation in Forage Plants and Crops Growing in Podzols of a Portuguese Industrial Site. Comun. Geológicas 2014, 101, 1019–1022. [Google Scholar]
  96. Inácio, M.; Neves, O.; Pereira, V.; Ferreira da Silva, E. Levels of Selected Potential Harmful Elements (PHEs) in Soils and Vegetables Used in Diet of the Population Living in the Surroundings of the Estarreja Chemical Complex (Portugal). Appl. Geochem. 2014, 44, 38–44. [Google Scholar] [CrossRef]
  97. Inácio, M.; Neves, O.; Pereira, V.; Silva, E. Concentration of As, Cu, Hg and Zn in Soil and Agricultural Products (Brassica Oleracea L., Lycopersicon Esculentum Mill and Zea Mays L.) in an Industrial Area in NW of Portugal. Rev. Ciências Agrárias 2013, 36, 229–237. [Google Scholar]
  98. Sousa, L.P.; Lillebø, A.I.; Soares, J.A.; Alves, F.L. The Management Story of Ria de Aveiro. In Coastal Lagoons in Europe: Integrated Water Resource Strategies; Lillebø, A.I., Stålnacke, P., Gooch, G.D., Eds.; IWA Publishing: London, UK, 2015; pp. 31–38. ISBN 9781780406299. [Google Scholar]
  99. Braga, H.O.; Azeiteiro, U.M.; Magalhães, L. A Case Study of Local Ecological Knowledge of Shellfishers about Edible Cockle (Cerastoderma Edule) in the Ria de Aveiro Lagoon, Western Iberia. J. Ethnobiol. Ethnomed. 2022, 18, 11. [Google Scholar] [CrossRef]
  100. Pereira, M.E.; Lillebø, A.I.; Pato, P.; Válega, M.; Coelho, J.P.; Lopes, C.B.; Rodrigues, S.; Cachada, A.; Otero, M.; Pardal, M.A.; et al. Mercury Pollution in Ria de Aveiro (Portugal): A Review of the System Assessment. Environ. Monit. Assess. 2009, 155, 39–49. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  101. Lillebø, A.I.; Ameixa, O.M.C.C.; Sousa, L.P.; Sousa, A.I.; Soares, J.A.; Dolbeth, M.; Alves, F.L. The Physio-Geographical Background and Ecology of Ria de Aveiro. In Coastal Lagoons in Europe: Integrated Water Resource StrategiesLagoons in Europe: Integrated Water Resource Strategies; Lillebø, A.I., Stålnacke, P., Gooch, G.D., Eds.; IWA Publishing: London, UK, 2015; pp. 21–29. ISBN 9781780406299. [Google Scholar]
  102. Cabral-Pinto, M.M.S.; Ordens, C.M.; Condesso de Melo, M.T.; Inácio, M.; Almeida, A.; Pinto, E.; Ferreira da Silva, E.A. An Inter-Disciplinary Approach to Evaluate Human Health Risks Due to Long-Term Exposure to Contaminated Groundwater Near a Chemical Complex. Expo. Health 2020, 12, 199–214. [Google Scholar] [CrossRef]
  103. Inácio, M.; Ferreira da Silva, E.; Perreira, V.; Guihard-Costa, A.-M.; Valente, S. Evaluation of Urinary Arsenic in Children and Their Mothers Living near an Industrial Complex (Estarreja, Portugal). In Proceedings of the GeoMed2011-4th International Conference on Medical Geology, Bari, Italy, 20–25 September 2011; Volume 408. [Google Scholar]
  104. Bento, S.; Gramaglia, C.; Fernandes, L.; Erdlenbruch, K.; Levasseur, P.; Condesso de Melo, M.T. Contaminação de Solos e Água Em Estarreja (Portugal): Que Efeitos Na Vida Dos Habitantes? CAPTAR 2021, 10, 11. [Google Scholar]
  105. Fumey, G. La Mondialisation de l’alimentation. Inf. Geogr. 2007, 71, 71–82. [Google Scholar] [CrossRef]
  106. Pitot, S.; Cornély, V. Typologie Des Comportements Alimentaires En Guadeloupe; Basse-Terre: Guadeloupe, France, 2012. [Google Scholar]
  107. Barrau, M.; Godard, E.; Suivant, C.; Ledrans, M. Common Base Methods for the Four Components of the Kannari Study on Health, Nutrition and Exposure to Chlordecone in the French West Indies, 2011–2018; Santé Publique France: Saint-Maurice, France, 2020. [Google Scholar]
  108. ORSAG. Présentation et Synthèse de l’enquête En Guadeloupe; Basse-Terre: Guadeloupe, France, 2012. [Google Scholar]
  109. Kuhnlein, H.V.; Receveur, O.; Soueida, R.; Egeland, G.M. Arctic Indigenous Peoples Experience the Nutrition Transition with Changing Dietary Patterns and Obesity. J. Nutr. 2004, 134, 1447–1453. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  110. Egeland, G.M.; Johnson-Down, L.; Cao, Z.R.; Sheikh, N.; Weiler, H. Food Insecurity and Nutrition Transition Combine to Affect Nutrient Intakes in Canadian Arctic Communities. J. Nutr. 2011, 141, 1746–1753. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  111. Gagné, D.; Blanchet, R.; Lauzière, J.; Vaissière, É.; Vézina, C.; Ayotte, P.; Déry, S.; Turgeon O’Brien, H. Traditional Food Consumption Is Associated with Higher Nutrient Intakes in Inuit Children Attending Childcare Centres in Nunavik. Int. J. Circumpolar Health 2012, 71, 18401. [Google Scholar] [CrossRef] [PubMed]
  112. Proust, F.; Lucas, M.; Dewailly, E. Fatty Acid Profiles among the Inuit of Nunavik: Current Status and Temporal Change. Prostaglandins. Leukot. Essent. Fatty Acids 2014, 90, 159–167. [Google Scholar] [CrossRef] [PubMed]
  113. Martin, T. Reflexive Modernity in Nunavik. Globe 2005, 8, 175–206. [Google Scholar] [CrossRef] [Green Version]
  114. Avard, E. Northern Greenhouses: An Alternative Local Food Provisioning Strategy for Nunavik. Ph.D. Thesis, Université Laval, Québec, QC, Canada, 2015. [Google Scholar]
  115. Pinto, C.M.T.M.Q. Atitudes e Perceções Dos Adolescentes Face à Alimentação: Estudo Exploratório Nos Agrupamentos de Escolas Do Município de Estarreja. Master thesis, Universidade Aberta, Lisbon, Portugal, 2013. [Google Scholar]
  116. Ribeiro, C.; Coelho, C. The Development of Agriculture and Industry in Estarreja (Portugal) and Its Relationship with the Environment: Documentary Information and Agent View. InterfacEHS Saúde Meio Ambient. Sustentabilidade 2015, 10, 42–52. [Google Scholar]
  117. Diallo, A.H. Marchés Hebdomadaires et Mutations Du Système de Production Pastoral Au Ferlo (Sahel Sénégalais). Ph.D. thesis, Université Cheikh Anta Diop de Dakar, Dakar, Senegal, 2020. [Google Scholar]
  118. Duboz, P.; Boëtsch, G.; Gueye, L.; Macia, E. Type 2 Diabetes in a Senegalese Rural Area. World J. Diabetes 2017, 8, 351–357. [Google Scholar] [CrossRef]
  119. Duboz, P.; Boëtsch, G.; Gueye, L.; Macia, E. Hypertension in the Ferlo (Northern Senegal): Prevalence, Awareness, Treatment and Control. Pan Afr. Med. J. 2016, 25, 177. [Google Scholar] [CrossRef]
  120. Sougou, N.; Boëtsch, G. Diet and Growth of Young Fulani Children in Widou Thiengoly (Ferlo, Sénégal). Bull. Mem. Soc. Anthropol. Paris 2016, 28, 145–154. [Google Scholar] [CrossRef]
  121. Brunone, L. The Influence of the Great Green Wall Development Project on Food in Widou Thiengoly (Ferlo, Senegal). Master Thesis, Université Toulous-Jean Jaurès, Toulouse, France, 2022. [Google Scholar]
  122. Scott, J.C. The Art of Not Being Governed: An Anarchist History of Upland Southeast Asia; Yale University Press: New Haven, CT, USA, 2009; ISBN 9780300152289. [Google Scholar]
  123. Dewailly, É.; Chateau-Degat, M.-L.; Ékoé, J.-M.; Ladouceur, R.; Rochette, L. Nunavik Inuit Health Survey 2004. Qanuippitaa? How Are We? Status of Cardiovascular Disease and Diabetes in Nunavik; Institut National de Santé Publique du Québec (INSPQ) & Nunavik Regional Board of Health and Social Services (NRBHSS): Québec, QC, Canada, 2007. [Google Scholar]
  124. Mongeau, L.; Audet, N.; Aubin, J.; Baraldi, R. L’Excès de Poids dans la Population Québecoise de 1987 à 2003; Institut National de Santé Publique du Québec (INSPQ): Québec, QC, Canada, 2005. [Google Scholar]
  125. Richard, J.-B.; Koivogui, A.; Carbunar, A.; Sasson, F.; Duplan, H.; Marrien, N.; Lacapère, F.; Pradines, N.; Beck, F. Premiers Résultat Du Baromètre Santé DOM 2014-Guyane; Santé Publique France: Saint-Maurice, France, 2015. [Google Scholar]
  126. Richard, J.-B.; Pitot, S.; Cornely, V.; Pradines, N.; Beck, F. Premiers Résultats Du Baromètre Santé DOM 2014-Guadeloupe; Santé Publique France: Saint-Maurice, France, 2015. [Google Scholar]
  127. Logframe. Diagnóstico Social Do Concelho de Estarreja 2019; Câmara Municipal de Estarreja: Estarreja, Portugal, 2019. [Google Scholar]
  128. Mandereau-Bruno, L.; Fosse-Edorh, S. Prévalence Du Diabète Traité Pharmacologiquement (Tous Types) En France En 2015. Disparités Territoriales et Socio-Économiques. Bull. Épidémiologique Hebd. 2017, 27–28, 586–591. [Google Scholar]
  129. Inamo, J.; Daigre, J.-L.; Boissin, J.-L.; Kangambega, P.; Larifla, L.; Chevallier, H.; Balkau, B.; Smadja, D.; Atallah, A. High Blood Pressure and Obesity. J. Hypertens. 2011, 29, 1494–1501. [Google Scholar] [CrossRef] [PubMed]
  130. Glenisson, J. Un Tiers Des Guyanais Ont Retardé Ou Renoncé à Un Soin Médical En 2019. Insee Anal. Guyane 2021, 52, 1–4. [Google Scholar]
  131. Ndong, J.-R.; Romon, I.; Druet, C.; Prévot, L.; Hubert-Brierre, R.; Pascolini, E.; Thomasset, J.-P.; Cheungkin, R.; Bravo, A.; Chantry, M.; et al. Characteristics, Vascular Risk, Complications and Quality of Health Care in People with Diabetes in French Overseas Departments and Comparison with Metropolitan France: ENTRED 2007–2010, France. Bull. Épidémiologique Hebd. 2010, 42–43, 432–436. [Google Scholar]
  132. Guarmit, B.; Brousse, P.; Mosnier, E.; Martin, E.; Desrousseaux, G.; Fradin, S.; Verbanis, M.; Beauson, M.; Planes, L.; Lutin, Y.; et al. Bilan D’activité Des Centres Délocalisés de Prévention et de Soins (C.D.P.S.) de Guyane; Centre Hospitalier André Rosemon: Cayenne, French Guiana, 2017. [Google Scholar]
  133. Van Gastel, B.; Peiter, P.; Morel, V.; Roux, E.; Da Cruz Franco, V.; Mendes, A.P.; Coelho Eugenio, N.C.; Gomes, M. Frontières, Territoires de Santé et Réseaux de Soins. Accès Aux Soins, Prévention Des Maladies Vectorielles et Coopération Transfrontalière En Santé: Une Analyse Qualitative à La Frontière Brésilienne. In Maillages, Interfaces, Réseaux Transfrontaliers, de Nouveaux Enjeux Territoriaux de la Santé; Moullé, F., Reitel, B., Eds.; Presses Universitaires de Bordeaux: Pessac, France, 2021; pp. 111–127. [Google Scholar] [CrossRef]
  134. ORSAG. Surcharge Pondérale et Obésité Abdominale En Guadeloupe En 2013, KANNARI, Santé, Nutrition et Exposition Au Chlordécone Aux Antilles; Basse-Terre: Guadeloupe, France, 2016. [Google Scholar]
  135. Yacou, C.; Cornély, V. Données Sur Le Diabète en Guadeloupe; Observatoire Régional de la Santé de Guadeloupe: Baie-Mahault, Guadeloupe, 2015. [Google Scholar]
  136. ORSAG. Maladie Chronique: Diabète En Guadeloupe; Basse-Terre: Guadeloupe, France, 2021. [Google Scholar]
  137. DEAL; DAAF. Diagnostic Du Système Alimentaire Guadeloupéen-Rapport DIAG’Alim 2021; Direction de l’Environnement, de l’Aménagement et du Logement (DEAL) Guadeloupe: Basse-Terre, Guadeloupe, 2021. [Google Scholar]
  138. Dewailly, É.; Chateau-Degat, L.; Ékoé, J.-M.; Ladouceur, R.; Rochette, L. Enquête de Santé Auprès Des Inuits Du Nunavik 2004: État Des Maladies Cardiovasculaires et Du Diabète Au Nunavik; Institut National de Santé Publique du Québec (INSPQ) & Nunavik Regional Board of Health and Social Services (NRBHSS): Québec, QC, Canada, 2008. [Google Scholar]
  139. Duhaime, G.; Chabot, M.; Gaudreault, M. Food Consumption Patterns and Socioeconomic Factors among the Inuit of Nunavik. Ecol. Food Nutr. 2002, 41, 91–118. [Google Scholar] [CrossRef]
  140. Furgal, C.; Seguin, J. Climate Change, Health, and Vulnerability in Canadian Northern Aboriginal Communities. Environ. Health Perspect. 2006, 114, 1964–1970. [Google Scholar] [CrossRef] [Green Version]
  141. Huet, C.; Rosol, R.; Egeland, G.M. The Prevalence of Food Insecurity Is High and the Diet Quality Poor in Inuit Communities. J. Nutr. 2012, 142, 541–547. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  142. Couturier, C.; Lévesque, C. Les Contaminants et Leurs Impacts Sur La Santé Au Nunavik; Commission d’Enquête sur les Relations Entre les Autochtones et Certains Services Publics: Québec, QC, Canada, 2019. [Google Scholar]
  143. Carbone, S.; Del Buono, M.G.; Ozemek, C.; Lavie, C.J. Obesity, Risk of Diabetes and Role of Physical Activity, Exercise Training and Cardiorespiratory Fitness. Prog. Cardiovasc. Dis. 2019, 62, 327–333. [Google Scholar] [CrossRef] [PubMed]
  144. CCME. Canada Council of Ministers of the Environment (Updated 1999, 2001, 2011). Canadian Soil Quality Guidelines for the Protection of Environmental and Human Health; Canadian Council of Ministers of the Environment: Winnipeg, MB, Canada, 2011. [Google Scholar]
  145. Maury-Brachet, R.; Durrieu, G.; Dominique, Y.; Boudou, A. Mercury Distribution in Fish Organs and Food Regimes: Significant Relationships from Twelve Species Collected in French Guiana (Amazonian Basin). Sci. Total Environ. 2006, 368, 262–270. [Google Scholar] [CrossRef]
  146. Brousse, P.; Mosnier, E.; Guarmit, B.; Nacher, M.; Ville, M. Prise En Charge Des Populations Vivant En Forêt et Le Long Des Fleuves En Guyane. Actual. Doss. Santé Publique 2015, 91, 40–42. [Google Scholar]
  147. Maury-Brachet, R.; Gentes, S.; Dassié, E.P.; Feurtet-Mazel, A.; Vigouroux, R.; Laperche, V.; Gonzalez, P.; Hanquiez, V.; Mesmer-Dudons, N.; Durrieu, G.; et al. Mercury Contamination Levels in the Bioindicator Piscivorous Fish Hoplias Aïmara in French Guiana Rivers: Mapping for Risk Assessment. Environ. Sci. Pollut. Res. 2020, 27, 3624–3636. [Google Scholar] [CrossRef] [PubMed]
  148. Rimbaud, D.; Restrepo, M.; Louison, A.; Boukhari, R.; Ardillon, V.; Carles, G.; Lambert, V.; Jolivet, A. Blood Lead Levels and Risk Factors for Lead Exposure among Pregnant Women in Western French Guiana: The Role of Manioc Consumption. J. Toxicol. Environ. Health Part A 2017, 80, 382–393. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  149. Maurice, L.; Barraza, F.; Blondet, I.; Ho-A-Chuck, M.; Tablon, J.; Brousse, P.; Demar, M.; Schreck, E. Childhood Lead Exposure of Amerindian Communities in French Guiana: An Isotopic Approach to Tracing Sources. Environ. Geochem. Health 2021. [Google Scholar] [CrossRef] [PubMed]
  150. Mosnier, E. Epidémiologie Des Maladies Infectieuses et Épidémiques En Milieu Isolé Amazonien. Ph.D. thesis, Université de Guyane, Cayenne, French Guiana, 2017. [Google Scholar]
  151. Devault, D.A.; Massat, F.; Lambourdière, J.; Maridakis, C.; Dupuy, L.; Péné-Annette, A.; Dolique, F. Micropollutant Content of Sargassum Drifted Ashore: Arsenic and Chlordecone Threat Assessment and Management Recommendations for the Caribbean. Environ. Sci. Pollut. Res. 2022, 29, 66315–66334. [Google Scholar] [CrossRef] [PubMed]
  152. Resiere, D.; Valentino, R.; Nevière, R.; Banydeen, R.; Gueye, P.; Florentin, J.; Cabié, A.; Lebrun, T.; Mégarbane, B.; Guerrier, G.; et al. Sargassum Seaweed on Caribbean Islands: An International Public Health Concern. Lancet 2018, 392, 2691. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  153. Dewailly, E.; Nantel, A.; Weber, J.-P.; Meyer, F. High Levels of PCBs in Breast Milk of Inuit Women from Arctic Quebec. Bull. Environ. Contam. Toxicol. 1989, 43, 641–646. [Google Scholar] [CrossRef] [PubMed]
  154. Adamou, T.Y.; Riva, M.; Muckle, G.; Laouan Sidi, E.A.; Lemire, M.; Ayotte, P. Blood Mercury and Plasma Polychlorinated Biphenyls Concentrations in Pregnant Inuit Women from Nunavik: Temporal Trends, 1992–2017. Sci. Total Environ. 2020, 743, 140495. [Google Scholar] [CrossRef]
  155. Boucher, O.; Muckle, G.; Ayotte, P.; Dewailly, E.; Jacobson, S.W.; Jacobson, J.L. Altered Fine Motor Function at School Age in Inuit Children Exposed to PCBs, Methylmercury, and Lead. Environ. Int. 2016, 95, 144–151. [Google Scholar] [CrossRef] [Green Version]
  156. Caron-Beaudoin, É.; Ayotte, P.; Blanchette, C.; Muckle, G.; Avard, E.; Ricard, S.; Lemire, M. Perfluoroalkyl Acids in Pregnant Women from Nunavik (Quebec, Canada): Trends in Exposure and Associations with Country Foods Consumption. Environ. Int. 2020, 145, 106169. [Google Scholar] [CrossRef]
  157. Couture, A.; Levesque, B.; Dewailly, É.; Muckle, G.; Déry, S.; Proulx, J.-F. Lead Exposure in Nunavik: From Research to Action. Int. J. Circumpolar Health 2012, 71, 18591. [Google Scholar] [CrossRef]
  158. Messier, V.; Lévesque, B.; Proulx, J.-F.; Rochette, L.; Libman, M.D.; Ward, B.J.; Serhir, B.; Couillard, M.; Ogden, N.H.; Dewailly, É.; et al. Seroprevalence of Toxoplasma Gondii Among Nunavik Inuit (Canada). Zoonoses Public Health 2009, 56, 188–197. [Google Scholar] [CrossRef]
  159. Bradette-Laplante, M.; Courtemanche, Y.; Desrochers-Couture, M.; Forget-Dubois, N.; Bélanger, R.E.; Ayotte, P.; Jacobson, J.L.; Jacobson, S.W.; Muckle, G. Food Insecurity and Psychological Distress in Inuit Adolescents of Nunavik. Public Health Nutr. 2020, 23, 2615–2625. [Google Scholar] [CrossRef]
  160. Lamoureux-Tremblay, V.; Muckle, G.; Maheu, F.; Jacobson, S.W.; Jacobson, J.L.; Ayotte, P.; Bélanger, R.E.; Saint-Amour, D. Risk Factors Associated with Developing Anxiety in Inuit Adolescents from Nunavik. Neurotoxicol. Teratol. 2020, 81, 106903. [Google Scholar] [CrossRef] [PubMed]
  161. Sadler, R.; Connell, D. Global Distillation in an Era of Climate Change. In Organic Pollutants Ten Years After the Stockholm Convention-Environmental and Analytical Update; Puzyn, T., Ed.; InTech: London, UK, 2012; pp. 191–216. ISBN 978-953-307-917-2. [Google Scholar]
  162. Ikonen, I.; Sotgiu, F.; Aydinli, A.; Verlegh, P.W.J. Consumer Effects of Front-of-Package Nutrition Labeling: An Interdisciplinary Meta-Analysis. J. Acad. Mark. Sci. 2020, 48, 360–383. [Google Scholar] [CrossRef]
  163. Biabiany, O.; Mandonnet, N.; Bolo, A.; Alexandre, G.; Chia, E. Family Farmers and Consumers in Guadeloupe Facing the COVID-19. Études Caribéennes 2021. [Google Scholar] [CrossRef]
  164. Malassis, L. Food Systems Analysis; University of California: Berkeley, CA, USA, 1983. [Google Scholar]
  165. Institute of Medicine. Improving Food Safety Through a One Health Approach: Workshop Summary; The National Academies Press: Washington, DC, USA, 2012; ISBN 978-0-309-25933-0. [Google Scholar]
Figure 1. Description of the regions impacted by the disrupting event identified by each OHM, i.e., the focal object [26].
Figure 1. Description of the regions impacted by the disrupting event identified by each OHM, i.e., the focal object [26].
Sustainability 15 02376 g001
Table 1. Description of the social-ecological framework, the disrupting event and the climate that describes the location of each OHM.
Table 1. Description of the social-ecological framework, the disrupting event and the climate that describes the location of each OHM.
OHMSocial-Ecological FrameworkDisrupting Event (Date)Climate 1
Téssékéré
Senegal
Desertification of the Sahel regionGreat Green Wall (2008)Hot semi-arid (arid, steppe and hot; BSh)
Oyapock
French Guiana, France
Opening of the Franco-Brazilian cross-border region by road accessOyapock River Bridge (2017)Tropical rainforest (Af) to tropical monsoon (Am)
Littoral Caraïbes
Guadeloupe, France
Development of an urban port complex in an island contextTransformation and acceleration of maritime trade (from the 1970s)Tropical rainforest (Af)
Nunavik
Québec, Canada
Sedentarization, urbanization and economic development of Québec’s arctic regionPlan Nord, i.e., Plan North (2011)Tundra (polar tundra; ET) to subarctic (cold, without dry season and cold summers; Dfc)
Estarreja
Portugal
Environmental pollution linked to a complex of chemical industries (CQE) near the Aveiro LagoonAdoption of virtuous practices within the CQE (1990)Warm-summer Mediterranean (temperate, dry and warm summers; Csb)
1 Based on the most recent maps of the Köppen-Geiger climate classification [27].
Table 2. Summary of factors influencing the food systems of regions concerned by one or more OHMs.
Table 2. Summary of factors influencing the food systems of regions concerned by one or more OHMs.
Factors of InfluenceExamples
  • Socioeconomic
Purchasing power of individuals and households
  • Environmental
Climate change, industrial pollution
  • Geographical
Level of isolation and connectivity, proximity to markets
  • Globalization
Supermarket chains, containerization, trade liberalization
  • Governmental policy
Economic, geographical and industrial development, trade liberalization
  • Historical
Colonization, sedentarization, assimilation
  • Identity and cultural
Customs, practices, values, both shared and individual
  • Industrial
Massification of crops, transformation and distribution of food products
  • Sanitary
Food contamination (e.g., pollutants), consumption of “good” and “bad” food
Table 3. Summary of the prevalences of diet-related non-communicable illnesses in each OHM. Prevalences in percentage (%) for each region are presented with the national average in parentheses. References are in brackets. ND = not determined.
Table 3. Summary of the prevalences of diet-related non-communicable illnesses in each OHM. Prevalences in percentage (%) for each region are presented with the national average in parentheses. References are in brackets. ND = not determined.
IllnessNunavik
(Canada)
French Guiana
(France)
Guadeloupe
(France)
Estarreja 1
(Portugal)
Téssékéré
(Senegal)
Overweight
(30 < BMI ≥ 25 kg/m2)
29.8 (34) [123,124] 34 (29) [125]31 (29) [126]6.0 (6.4) [127]13.2 (ND) [119]
Obesity
(BMI ≥ 30 kg/m2)
28.3 (15) [123,124] 18 (12) [125]17 (12) [126] 10.1 (8.0) [127]3.00 (ND) [119]
Diabetes4.8 (4.8) [123]8.08 (5) [128]9.12 (5) [128]8.3 (7.8) [127]4.2 (ND) [118]
Ratio
(Overweight+Obesity): Diabetes
12 (10)6.4 (8)5.3 (8)1.9 (1.8)3.9 (ND)
1 Percentage of diagnosed cases in the region of Baixo Vouga where Estarreja is located.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Rapinski, M.; Raymond, R.; Davy, D.; Herrmann, T.; Bedell, J.-P.; Ka, A.; Odonne, G.; Chanteloup, L.; Lopez, P.J.; Foulquier, É.; et al. Local Food Systems under Global Influence: The Case of Food, Health and Environment in Five Socio-Ecosystems. Sustainability 2023, 15, 2376. https://doi.org/10.3390/su15032376

AMA Style

Rapinski M, Raymond R, Davy D, Herrmann T, Bedell J-P, Ka A, Odonne G, Chanteloup L, Lopez PJ, Foulquier É, et al. Local Food Systems under Global Influence: The Case of Food, Health and Environment in Five Socio-Ecosystems. Sustainability. 2023; 15(3):2376. https://doi.org/10.3390/su15032376

Chicago/Turabian Style

Rapinski, Michael, Richard Raymond, Damien Davy, Thora Herrmann, Jean-Philippe Bedell, Abdou Ka, Guillaume Odonne, Laine Chanteloup, Pascal Jean Lopez, Éric Foulquier, and et al. 2023. "Local Food Systems under Global Influence: The Case of Food, Health and Environment in Five Socio-Ecosystems" Sustainability 15, no. 3: 2376. https://doi.org/10.3390/su15032376

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop