Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Ernoul, Lisa
Mesléard, François
and
Béchet, Arnaud
2012.
Diagnostic de l’échec de la contractualisation des mesures agri-environnementales pour réduire les incursions des Flamants dans les rizières de Camargue (France).
VertigO,
Vol. 12-1,
Issue. ,
GILLINGHAM, MARK A. F.
BECHET, ARNAUD
GERACI, JULIA
WATTIER, REMI
DUBREUIL, CHRISTINE
and
CEZILLY, FRANK
2012.
Genetic polymorphism in dopamine receptor D4 is associated with early body condition in a large population of greater flamingos, Phoenicopterus roseus.
Molecular Ecology,
Vol. 21,
Issue. 16,
p.
4024.
Sanz‐Aguilar, Ana
Béchet, Arnaud
Germain, Christophe
Johnson, Alan R.
and
Pradel, Roger
2012.
To leave or not to leave: survival trade‐offs between different migratory strategies in the greater flamingo.
Journal of Animal Ecology,
Vol. 81,
Issue. 6,
p.
1171.
Geraci, Julia
Béchet, Arnaud
Cézilly, Frank
Ficheux, Sébastien
Baccetti, Nicola
Samraoui, Boudjema
and
Wattier, Rémi
2012.
Greater flamingo colonies around the Mediterranean form a single interbreeding population and share a common history.
Journal of Avian Biology,
Vol. 43,
Issue. 4,
p.
341.
Doxa, A.
Besnard, A.
Bechet, A.
Pin, C.
Lebreton, J.‐D.
and
Sadoul, N.
2013.
Inferring dispersal dynamics from local population demographic modelling: the case of the slender‐billed gull inFrance.
Animal Conservation,
Vol. 16,
Issue. 6,
p.
684.
Deville, Anne‐Sophie
Grémillet, David
Gauthier‐Clerc, Michel
Guillemain, Matthieu
Von Houwald, Friederike
Gardelli, Bruno
and
Béchet, Arnaud
2013.
Non‐linear feeding functional responses in the Greater Flamingo (Phoenicopterus roseus) predict immediate negative impact of wetland degradation on this flagship species.
Ecology and Evolution,
Vol. 3,
Issue. 5,
p.
1413.
Tebbs, E.J.
Remedios, J.J.
Avery, S.T.
and
Harper, D.M.
2013.
Remote sensing the hydrological variability of Tanzania's Lake Natron, a vital Lesser Flamingo breeding site under threat.
Ecohydrology & Hydrobiology,
Vol. 13,
Issue. 2,
p.
148.
Yohannes, Elizabeth
Arnaud, Antoine
and
Béchet, Arnaud
2014.
Tracking variations in wetland use by breeding flamingos using stable isotope signatures of feather and blood.
Estuarine, Coastal and Shelf Science,
Vol. 136,
Issue. ,
p.
11.
Katsanevakis, Stelios
Levin, Noam
Coll, Marta
Giakoumi, Sylvaine
Shkedi, Daniel
Mackelworth, Peter
Levy, Ran
Velegrakis, Adonis
Koutsoubas, Drosos
Caric, Hrvoje
Brokovich, Eran
Öztürk, Bayram
and
Kark, Salit
2015.
Marine conservation challenges in an era of economic crisis and geopolitical instability: The case of the Mediterranean Sea.
Marine Policy,
Vol. 51,
Issue. ,
p.
31.
Balkız, Özge
Onmuş, Ortaç
Sıkı, Mehmet
Döndürenc, Ömer
Gül, Orhan
Arnaud, Antoine
Germain, Christophe
İsfendiyaroğlu, Süreyya
Özbek, Melih
Çağlayan, Eray
Araç, Nilüfer
Parmak, Burcu
Özesmi, Uygar
and
Béchet, Arnaud
2015.
Turkey as a crossroad for Greater FlamingosPhoenicopterus roseus: evidence from population trends and ring-resightings (Aves: Phoenicopteridae).
Zoology in the Middle East,
Vol. 61,
Issue. 3,
p.
201.
Ernoul, Lisa
and
Wardell-Johnson, Angela
2016.
Representing the Greater Flamingo in Southern France: A semantic analysis of newspaper articles showing change over time.
Ocean & Coastal Management,
Vol. 133,
Issue. ,
p.
105.
Mathevet, Raphaël
Olivier, Anthony
and
Béchet, Arnaud
2018.
Sales bêtes ! Mauvaises herbes !.
p.
173.
Acker, Paul
Francesiaz, Charlotte
Béchet, Arnaud
Sadoul, Nicolas
Lessells, Catherine M.
Pijl, Agata S.
and
Besnard, Aurélien
2018.
Insights on dispersal and recruitment paradigms: sex- and age-dependent variations in a nomadic breeder.
Oecologia,
Vol. 186,
Issue. 1,
p.
85.
Mathevet, Raphaël
Allouche, Aurélien
Nicolas, Laurence
Mitroi, Veronica
Fabricius, Christo
Guerbois, Chloé
and
Anderies, John M.
2018.
A Conceptual Framework for Heuristic Progress in Exploring Management Regime Shifts in Biodiversity Conservation and Climate Change Adaptation of Coastal Areas.
Sustainability,
Vol. 10,
Issue. 11,
p.
4171.
Ernoul, Lisa
Wardell-Johnson, Angela
Willm, Loïc
Béchet, Arnaud
Boutron, Olivier
Mathevet, Raphaël
Arnassant, Stephan
and
Sandoz, Alain
2018.
Participatory mapping: Exploring landscape values associated with an iconic species.
Applied Geography,
Vol. 95,
Issue. ,
p.
71.
Gillingham, Mark Alan Frank
Béchet, Arnaud
Cézilly, Frank
Wilhelm, Kerstin
Rendón-Martos, Manuel
Borghesi, Fabrizio
Nissardi, Sergio
Baccetti, Nicola
Azafzaf, Hichem
Menke, Sebastian
Kayser, Yves
and
Sommer, Simone
2019.
Offspring Microbiomes Differ Across Breeding Sites in a Panmictic Species.
Frontiers in Microbiology,
Vol. 10,
Issue. ,
Martín‐Vélez, Víctor
Sánchez, Marta I.
Shamoun‐Baranes, Judy
Thaxter, Chris B.
Stienen, Eric W. M.
Camphuysen, Kees C. J.
and
Green, Andy J.
2019.
Quantifying nutrient inputs by gulls to a fluctuating lake, aided by movement ecology methods.
Freshwater Biology,
Vol. 64,
Issue. 10,
p.
1821.
De Wit, Rutger
Vincent, Alice
Foulc, Ludovic
Klesczewski, Mario
Scher, Olivier
Loste, Claudine
Thibault, Marc
Poulin, Brigitte
Ernoul, Lisa
and
Boutron, Olivier
2019.
Seventy-year chronology of Salinas in southern France: Coastal surfaces managed for salt production and conservation issues for abandoned sites.
Journal for Nature Conservation,
Vol. 49,
Issue. ,
p.
95.
Gillingham, Mark A.F.
Borghesi, Fabrizio
Montero, B. Karina
Migani, Francesca
Béchet, Arnaud
Rendón-Martos, Manuel
Amat, Juan A.
Dinelli, Enrico
and
Sommer, Simone
2021.
Bioaccumulation of trace elements affects chick body condition and gut microbiome in greater flamingos.
Science of The Total Environment,
Vol. 761,
Issue. ,
p.
143250.
Martín-Vélez, Víctor
Hortas, F.
Taggart, M.A.
Green, A.J.
ÓHanlon, N.J.
and
Sánchez, M.I.
2021.
Spatial variation and biovectoring of metals in gull faeces.
Ecological Indicators,
Vol. 125,
Issue. ,
p.
107534.
The conservation of many species depends on sustainable economic activities which shape their habitats. The economic use of these anthropogenic habitats may change quickly due to world trade globalization, market reorientations, price volatility or shifts in subsidy policies (Gauthier et al. Reference Gauthier, Giroux, Reed, Béchet and Belanger2005; Gottschalk et al. Reference Gottschalk, Diekötter, Ekschmitt, Weinmann, Kuhlmann, Purtauf, Dauber and Wolters2007). Recently, the finance crisis has impacted economy worldwide. How this may have affected the use of habitats beneficial to biodiversity has not been documented so far. However, consequences could be particularly acute for species sensitive to climate change while jeopardizing long-term conservation efforts. We illustrate this concern using the case of the greater flamingo Phoenicopterus roseus in the Mediterranean and West Africa.
Flamingos are long-lived colonial waterbirds inhabiting coastal brackish wetlands and salt lakes around the world. Breeding colonies are dependent on both rainfall and availability of undisturbed islands to protect eggs and chicks from terrestrial predators (Simmons Reference Simmons1996; Johnson & Cézilly Reference Johnson and Cézilly2007). Saltpans have been exploited by flamingos because the circulation of brine over extensive areas guarantees favourable water levels and salinities annually (Johnson & Cézilly Reference Johnson and Cézilly2007; Béchet et al. Reference Béchet, Germain, Sandoz, Hirons, Green, Walmsley and Johnson2009).
In the south of the Mediterranean, most colonies of greater flamingos occur in natural wetlands facing the challenge of hydrological stochasticity (Fig. 1). Breeding is intermittent depending on minimum thresholds of precipitation and given scarce rainfall, the average probability of successful breeding in a given year at these sites is only 0.44 (n = 6 colonies; 95% confidence interval (CI): 0.35–0.52). The low rate of successful breeding in the south of the Mediterranean may further decrease in future years due to predicted dryer conditions (Bates et al. Reference Bates, Kundzewicz, Wu and Palutikof2008). This should reduce flooding frequency of favourable wetlands by more episodic rainfall and in turn curtail fewer breeding opportunities for flamingos.
Figure 1 Greater flamingo breeding sites in the Mediterranean and West Africa. Colony sites were classified as active commercial saltpans (□), abandoned saltpans (■) or natural wetlands (○) based on Johnson & Cézilly (Reference Johnson and Cézilly2007). Symbol size is proportional to colony productivity index, calculated as the sum of chicks fledged over the last five years with successful breeding (except in Algeria for which breeding occurred only twice and Tunisia only four times). Chicks were counted from the ground or from aerial photographs depending on sites. In brackets is the average probability of breeding success for a given colony in a given year.
In the north of the Mediterranean, brackish wetlands have often been transformed into saltpans and/or fish farms which buffer hydrological stochasticity. In particular, the Mediterranean coastline comprises >170 saltpans (range 1–12 000 ha) spread over 18 countries (Sadoul et al. Reference Sadoul, Walmsley and Charpentier1998). Throughout this region, most flamingo colonies are located in saltpans which represent 45% of the breeding sites of the Mediterranean and West African population (Fig. 1). The probability of successful breeding in saltpans, 0.83 (n = 7 colonies; 95% CI: 0.66–0.93), is 1.86 ± 0.31 times higher than in natural habitats (logistic GLM, df = 235, p < 0.001). Saltpans contributed to 46% of the chicks fledged in the last five years in the Mediterranean and West Africa.
In 2007, financial changes disrupted the economy of the saltpans of Salin-de-Giraud in the Camargue (Rhône delta, France), the largest commercial saltpans in Europe (12 000 ha), causing flamingos to fail to breed at one of their main colonies in the world. It was the first interruption in annual breeding since 1974. In the 1960s, the Mediterranean population of greater flamingos was only half of what it is today, and breeding occurred at only two sites, the Camargue and Fuente de Piedra (Spain). Poor breeding success was linked to low rainfall in Spain and the lack of suitable nesting sites in the Camargue. In order to solve this latter problem, an artificial island was built in the Fangassier lagoon in the saltpans of Salin-de-Giraud. Flamingos adopted this island in 1974, and bred there annually until 2007.
In 2007, Salins Group, the owner of the lagoon, decided to decrease salt production by 60%, reduce its employees by 50% and sell 20% of its estate, including the Fangassier lagoon. This decision triggered a social conflict and a strike that prevented the traditional flooding of the lagoon. In the absence of water, the birds did not breed. The decision to reduce salt production resulted from cascading events of acquisitions and sales, moving the capital from managers of industry to financial investors. Salins Group was bought out twice between 1997 and 2000, and returned to its original managers through two successive leverage buy outs (LBO), in 2000 and 2004. LBOs are financial operations facilitating the purchase of firms by financial groups, financing an important share of the cost of acquisition by debt. Typically, LBOs increase the debt by 5–8 times, and the firm's turnover is used to reimburse this debt. As a result, there are layoffs and reductions in mid-term investments to rapidly reimburse high-interest loans (Bruton et al. Reference Bruton, Keels and Scifres1999; World Economic Forum 2008; Nielsen Reference Nielsen2008; Hall Reference Hall2008). In 2006, the chemical company Arkema, who purchased 40% of the Salins Group's annual production, breached its contract following a technical innovation disposing of its need for salt. This imperilled the reimbursement of Salins Group's debt, causing financial distress and triggering land sales. In 2009, following the 2008 world financial crisis, Salins Group put 9000 ha of saltpans up for sale and announced a new dismissal plan.
The closure of 45% of the Mediterranean saltpans in the 1990 s was restricted to small-scale entities (Paracuellos et al. Reference Paracuellos, Castro, Nevado, Ona, Matamala, García and Salas2002), but this is no longer the case. Even the largest saltpans are sensitive to global financial conditions. Since saltpans provide up to 50% of flamingos foraging requirements during the breeding season (Béchet et al. Reference Béchet, Germain, Sandoz, Hirons, Green, Walmsley and Johnson2009), this species will obviously be affected by such economically-driven changes. Saltpans buffer rainfall variability, thus allowing annual reproduction of flamingos (Béchet & Johnson Reference Béchet and Johnson2008; Béchet et al. Reference Béchet, Germain, Sandoz, Hirons, Green, Walmsley and Johnson2009). The closure of saltpans may thus enhance the adverse effects on flamingos and other waterbirds of predicted reductions in precipitation (Bates et al. Reference Bates, Kundzewicz, Wu and Palutikof2008) by limiting the availability of alternative nesting sites. As flamingos of the Mediterranean belong to a metapopulation, local changes could affect the species at a much larger scale (Balkız et al. Reference Balkız, Béchet, Rouan, Choquet, Germain, Amat, Rendón-Martos, Baccetti, Nissardi, Özesmi and Pradel2010). Finally, the sea level rise predicted for the Mediterranean (Bates et al. Reference Bates, Kundzewicz, Wu and Palutikof2008) may constitute an additional threat, flooding existing breeding sites (for example the submersion of the Ebro delta; Rovira & Ibàñez Reference Rovira and Ibàñez2007).
Increasingly, global economy stochasticity directly affects land use, with important negative consequences for wildlife (Robertson & Van Schaik Reference Robertson and Van Schaik2001; Gauthier et al. Reference Gauthier, Giroux, Reed, Béchet and Belanger2005; Gottschalk et al. Reference Gottschalk, Diekötter, Ekschmitt, Weinmann, Kuhlmann, Purtauf, Dauber and Wolters2007). Here, we additionally show that financial agendas can disrupt a conservation success story, which relied on pursuing a sustainable economic industry: solar saltpans. Global finance could thus exacerbate negative effects of climate change by affecting anthopogenic habitats acting as biodiversity refuges. We call for large-scale monitoring of the effects on species conservation of this new type of stochasticity imposed by financial volatility in the global economy. This requires multi-case analyses by interdisciplinary teams, including economists and ecologists. Fighting for regulations that would divert financial volatility from sustainable economic activities, thus favouring long-term stable sources of funding for such activities, should become a top-ranking priority of conservation agendas.
Acknowledgements
We thank the Greater Flamingo Network for providing counts and Salins Group for granting access to Salin-de-Giraud. From 2005, flamingo data from the Camargue are property of Salins Group, Tour du Valat and Réserve Nationale de Camargue.