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Biological Journal of the Linnean Society (1994), 51: 25-36. With 6 figures Tidal power and the aquatic environment of La Rance C. RETIERE Museum National D’Histoire Naturelle Laboratoire Maritime, 17 Avenue George V, 35801 Dinard, France The Rance basin, on the northern coast of Brittany, is the only site where a full-scale evaluation of the ecological impact of a tidal power scheme, after 20 years of operation, has been made. The isolation of the estuary, during the construction phase, was particularly damaging to the environment. Gradually, after the scheme was put into service, an increasingly diverse flora and fauna became established. The patterns of distribution of this flora and fauna, their groupings into ecological units and the nature of their interrelationships, indicate a variable degree of biological adjustment to the new environmental conditions. Migratory organisms are able to pass via sluice gates and turbines. However, the new ecological equilibrium, established in the space of 10 years, remains fragile and, being linked to the degree of stability of abiotic conditions, depends to a large extent on the operating conditions of the power station. ADDITIONAL KEY WORDS:-environmental communities - trophic relationships. effects - environmental equilibrium - CONTENTS Introduction . . . . . . . . . . The tidal power installation . . . . . . Effects on the environment . . . . . . Effects of construction . . . . . . Effects of operation . . . . . . . Ecological consequences of operation . . . . Distribution of benthic species and communities Species biology . . . . . . . . Primary and secondary production . . . Movements and migration . . . . . Trophic relationships . . . . . . . Utilization of the basin by overwintering birds Conclusions . . . . . . . . . . References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 26 28 28 28 29 29 32 32 32 33 34 34 34 INTRODUCTION A number of investigators have attempted to predict the effects of various tidal power projects on the marine environment, in various parts of the world, (e.g. Martin, 1970; Gordon & Longhurst, 1979; Shaw, 1980; Larsen & Topinka, 1984). The Rance Basin, on the Armorican seaboard of the Channel, is the only site which offers the opportunity to make a full scale assessment of the ecological impact of a tidal power scheme after 20 years of operation (Retiere, 1989). 0024-4066/94/001025 + 12 $08.00/0 25 0 1994 The Linnean Society of London 26 C. RE’I‘IERE Dinard Tidal Power Station I 19” 30 N t 1 Norman-Breton Gulf . Figure 1. The Norman Breton Gulf and the Rance Estuary. Of the seas of north west Europe, the Western Channel has some of the largest tides: the spring equinox tidal amplitude reaches 15.5 m in the Bay of Mont St Michel and 13.5 m a t the mouth of the Rance river. The latter is a medium-sized river, approximately 100 km in length, with a low discharge (average 7 m3 sec-’). The estuary forms a succession of narrow channels and wide basins, extending approximately 20 kilometres. It is at the mouth of this river, between the towns of Dinard and St Malo, that the tidal power scheme was built. Construction began in 1963 and was completed in 1966, creating a reservoir with a useful capacity of 184 million cubic metres occupying a surface area of 2200 hectares at the 13.50 m level (Fig. 1 ) . + THE TIDAL POWER INSTALLATION The installation is 750 m in length, anchored to granite bedrock 13 m below zero datum level as shown on the marine charts. The structure carries a major road and, from west to east, comprises a lock, the generating station proper with its 24 bulb units, a rockfill dike and a 115 m wide movable dam made up of 6 ~~ Figure 2. The barrage and the tidal power station. sluice gates capable of passing a total flow of 9600 m3 sec-I under a 5 metre head (Fig. 2). I n addition to a 10 MW alternator, each bulb unit incorporates a 4-blade horizontal turbine running at 94 rpm and capable of handling a flow of 275 m3 sec-'. These bulb turbines can handle water flowing in either direction, and are thus able to generate power both during filling and emptying of the basin. This type of operation is referred to as a double action cycle (Fig. 3 ) . 1 With pumping I 7 Single action a t drainage I With pumping 1 Double action Figure 3. Tidal curves compared with the water level variations (single and double actions) in the basin (from Electricit; de France). 28 C. RETIERE Transfer of water from the sea into the basin takes place through the turbine and sluice gate combination and via the turbines alone in the opposite direction. EFFECTS O N T H E ENVIRONMENT Effects of construction Construction was carried out dry inside three cofferdam enclosures. With the exception of small amplitude discharges ( 1 m) a t 2-week intervals, for flushing purposes, the estuary was isolated from the open sea for 3 years between 1963 and 1966 (Rouvillois, 1967). During this period, the conversion of the estuary with a large tidal range into a constant-level basin virtually eradicated the marine fauna and flora; however, some populations of highly euryoecious invertebrate and fish species flourished. Effects of operation The operating constraints of the installation impose highly specific ‘tidal’ conditions on the waters in the basin. Tidal range varies between 4.0 and 5.5 m, depending on whether the turbines are operating in one or both directions. Mean water level is raised by approximately 2.5 m and there is a particularly long high water stand. Reduction in tidal range is correlated with a reduction in the surface area of the intertidal zone. At spring tide, prior to the scheme, this area was estimated at 70% of the total surface of the basin, whilst today the exposed zone accounts for only 50%. Prior to the scheme, the Rance was a ria, with slight haline stratification, along which authors identified a maritime downstream sector followed by a high salinity section giving way to a low salinity sector (Fischer, 1929; Fischer-Piette, 1931, 1933; Marie, 1938; Priou, 1947). Today, only two elements can be identified: the marine reservoir, in which the deepwater salinity remains higher than 30%0, and the estuary proper, upstream (Retiere & Richard, 1980). The junction between ‘brackish’ and ‘marine’ has moved upstream from St Suliac to Port St Jean. The violent sluice and turbine currents have modified the distribution of the sediments, whose origin, nature, texture and distribution had been extensively studied between 1954 and 1959 (Berthois & Berthois, 1954, 1955; Bourcart & Roa Morales, 1957, Bourcart, 1959). Thus, in 1971, Retiere reported that parts of the river bed in proximity to the barrage had become eroded, sandbanks had shifted and the bed was more or less covered with gravel or pebbles (Retiere, 1979). At the same time, the long periods of slack water had promoted deposition of fine particles in the coves and bays (Retiere & Richard, 1980). However, the sedimentary balance appears to reflect a natural evolution of the estuary, influenced by the absence of any large reservoir of suspended material in the coastal waters near the mouth of the Rance (Han, 1982). These changes, which in any event are rather limited in scale, (Laboratoire Central D’hydraulique de France, 1982), were most pronounced during the first few years following startup of the installation (Fig. 4). LA RANCE ENVIRONMENT Figure 4. Sedimentary modifications (from Retiere & Richard, 1980). A, Eroded bottoms, B, Pebbles locally embedded by coarse sands; C, Moved banks; D, Fine particle sedimentation areas; E, Clean heterogenous sands; F, Muddy deposits. ECOLOGICAL CONSEQUENCES OF OPERATION Distribution of benthic species and communities After 20 years of operation, the basin is rich in species: records show no less than 110 species of polychaetes (Retiere, 1979; Lechapt, 1983; Lang, 1986), 47 species of decapod crustaceans (Le Calvez, 1986) and 70 species of fish (Le Mao, 1985). Within the intertidal zone, however, the vertical range of algae is limited to 5-6 m instead of 13 m (Lang, 1986; Herpe, 1986). The irregularity of C. RETIERE 30 m A 13 * 12. 11. 10. 9. 4 3 2 1 January 80 February 80 March 80 April 80 1 I m B 1312 1110. 98- 7. 6. 5- 4. 3. 2. 1~ I I 1 Figure 5. Tidal curves ( A ) and variations of high and low water levels in the basin ( B ) (from Lang, 1986). fluctuations in water level (Fig. 5) has resulted in the establishment of a unique community in the littoral zone, within which the belts described for the true intertidal range are not clearly manifested. LA RANGE ENVIRONMENT 31 Melinna palmata Figure 6 . Benthic communities (from Retiere, 1979). A, Spisula elliplica - S. ovalis - Saccocirrus papillocercus coarse sand community; B, Abra alba - Melinna palmata muddy fine sand community. C, Impoverished facies of the Abra alba - Melinna palmata community; D, Epifaunal hard bottom community; E, Neph&s cirrosa clean sand community. Subtidally, in 1971, Retiere identified four major benthic communities (Fig. 6). A period of 5 years had been, therefore, sufficient for the establishment, albeit in limited diversity and on certain substrata formerly occupied by intertidal fauna, of the subtidal communities present at the periphery of the Normand-Breton gulf (Retiere, 1976; 1979). Species maps prepared 5 years apart (1971/1976) showed clearly that the stability of the abiotic factors was reflected in the spatial distribution of the organisms (Retiere & Richard, 1980: Lechapt, 1983). Between 1972 and 1982, monitoring of the principal infaunal components of the Melinna palmata facies of the Abra alba-Corbula gibba community indicated that a period of increase in species richness and density (up to 1976) was followed by a period of stabilization (Clavier et al., 1983). Throughout the 32 C. RElIERE observation period, six populations of polychaetes alone accounted for 80% of the infaunal abundance and 90% of its biomass, thus largely controlling the community dynamics. Study of these populations (Retiere, 1976, 1979; Clavier, 198I; Rivain, 1983; Lechapt, 1983) clearly indicated that recolonization followed recruitment from populations closest to the estuary, irrespective of the lifespan of the species or the length of the pelagic phase within their life-cycle. Passive transport of adults also made a significant contribution to their establishment in the Rance Basin. Despite rapid stabilization of environmental conditions once the installation was commissioned, it took 10 years (1966-1976) to establish a new community balance. This has subsequently evolved via the natural mechanisms of intra and inter specific rela tionships, unrelated to the initial disturbance, with the long-lifespan species imposing the general trend. Species biology Reproduction and growth of organisms do not appear to have been affected by the new conditions. The Rance is a spawning ground for some fish such as Clupea harengus and a nursery ground for others (Pollachius pollachius). Catadromous eels (Anguilla anguilla, Conger conger) enter as larvae and leave to breed. Not less than 30 fish species are confirmed breeders in the area. Studies on the biology of many species of fish (Le Mao, 1985), suggest that the reproduction and growth of organisms within the basin have not been affected by the barrage. As another example, the ormer, Haliotis tuberculata is present at high densities in northern Brittany (Gaillard, 1958) and compared with populations living on the coast, those in the Rance had a more extended period of laying but not significantly different growth rates (Clavier & Richard, 1985). Primary and secondary production Primary production is higher in the upstream regions (Lacaze et al., 1976) particularly in spring. Even in the lower Rance, however, figures are higher than in the adjoining sea (Grall, 1972). Secondary production and biomass fluctuate from year to year, but mean annual biomass of the subtidal Abra alba-Corbula gibba community in the Rance (15-18 gm-2 (Retiere, 1979) is double that of intertidal flats (8.5 gm-'y) (Clavier, 1981) and of subtidal areas outside (9.5 grnp2y) (Dauvin, 1984). Production (P) and production to biomass (P/B) ratios of Nephgs hombergii (P = 6 grnp2y, P/B = 1.2) (Retiere, 1976) and Ampharete acutifons ( P = 1.5-9.0 gm-*y; P/B = 2.5-6.0) (Clavier, 1981) in the Rance are, however, similar to measured values for the same species in the Lynher River, Britain (Price & Warwick, 1980). Movements and migration Being transition zones between coastal and fresh waterways, estuaries normally provide essential lines of passage for numerous species. Movements vary in scope and affect one or more phases of their life cycle. To what extent does the presence of a barrage and the operation of turbines impede such movements? This problem has been analysed by Le Mao (1985) who, in addition to fish, focused attention on two invertebrates of economic interest, one LA RANCE ENVIRONMENT 33 a creeping spider crab, Maia squinado, and the other a swimming cuttlefish, Sepia oficinalis. Immature M . squinado occupy the basin throughout the year, but adults arrive in the spring in sufficient numbers to provide a fishery (De Kergariou, 1971). For them, the barrage is no real obstacle. Sepia oficinalis also provides a seasonal fishery. I n 1982, between April and June, Le Mao (1985) estimated production at 25-35 tonnes, and in good years this can rise to 40 tonnes. Similarly, the abundance of migratory fish suggests that passage through the turbines is effective. Le Mao (1985) concluded that the passage of both fish and cephalopods through the turbines takes place without major problems because of their large diameter and low rotational speed (but see Dadswell & Rulifson, 1994). A degree of indirect mortality is, however, detectable: crossing the structures throws shoals into disarray, providing the opportunity for predation by fish-eating birds such as gulls, cormorants and auks. Trophic relationships Le Mao (1985) discussed the food webs within the Rance basin. Within the pelagic communities, dominant plankton-feeders were the fish Sprattus sprattus, Sardina pilchardus, Atherina presbyter and Clupea harengus. Feeding on these were squid, Loligo vulgaris, L. forbesi, and larger fish Scomber scombrus, Trachurus trachurus. Benthic fish communities on hard substrate included herbivores (Spondyliosoma centharus, juvenile Blennius gattorugine) , species which feed off the sessile zoobenthos (Blenniuspholis) or vagile zoobenthos (Ciliata mustela, Trisopterus luscus, Symphodus melops) and fish-eating species, which also feed on decapod crustaceans, (Pollachius pollachius, Dicentrarchus labrax, Enophrys bubalis) . O n soft sediments, some fish feed preferentially on the permanent (Gobius niger) or temporary meiobenthos (juvenile Solea vulgaris and Pleuronectes platessa) , whilst adult plaice and Callionymus bra prefer to feed off the macrobenthic infauna Vagile decapod crustaceans form a significant proportion of the prey base and diet of Dicentrarchus labrax, Anguilla anguilla and Platichthys Jesus. The cuttlefish, Sepia oficinalis heads the food-chain on soft sediments. This chain has a more hierarchical structure in the marine sector than in the estuarine sector where crustaceans and benthic fish occupy the same trophic level. It is important to consider whether the links established between the various ecological compartments of the Rance basin are liable to be affected by the operating practices of the power station. I n this respect, the consequences of the abrupt level variations, recorded in June 1983 following the changeover from single to double action operation and causing periodic exposure of otherwise constantly submerged mudflats, are very revealing. The abundance of young plaice, Pleuronectes platessa, declined by around 80% at a critical time-since recruitment ceases in July. Many young plaice were found stranded on the mud or having succumbed to the rise in temperature of the water in the puddles where they had sought refuge, and invariably exposing themselves to predation by birds. Colonization by gobies Pomatoschistus minutus followed the high mortality. Le Mao (1986) also noted an increase in the vacuity coefficient of surviving plaice which could not be attributed to prey depletion since, by the 34 C. RETIERE following month, the incidence of Ampharete acutzfrons was increased in the gut contents of gobies. Even a brief destabilization of environmental conditions, following a change in the operating pattern of the station, is liable to have lasting repercussions on the functioning of the ecosystem. Utilization of the basin by overwintering birds Every year, the Rance receives an influx of several thousand wintering birds. Surveys by LF Mao el al. (1986) and Schricke & Bourgault (1982) have indicated that the larger surface area of permanent water favours diving ducks and grebes, especially Podiceps nigricollis. Since 1970, the numbers of overwintering shelduck, Tadorna tadorna, and brent geese, Branta bernicula, have increased and the concentrations of small waders have remained high. Development of the estuary as a tidal power scheme has not had any adverse effect on the avifauna. CONCLUSIONS It is possible to draw a number of general scientific conclusions from the investigations conducted in the Rance basin (Retiere, 1984): ( 1) T h e tidal power installation is, to varying degrees, biologically permeable: it permits recolonization of a modified environment and normal exchanges between estuarine and coastal waters. (2) A new balance is attained after about 10 years; the system then functions on the basis of intra and inter-specific relationships, independently of the initial disturbance. (3) This new balance is entirely dependent upon the mode of operation of the installation; a regular pattern stabilizes abiotic conditions. (4) Sudden variations in environmental factors (associated with production requirements or maintenance of the installations), albeit of short duration, may have severe ecological effects at various levels in both space and time. ( 5 ) T h e success of a tidal power scheme depends upon striking the correct balance, which it is possible to define, between operational constraints and biological equilibrium. REFERENCES Berthois L, Berthois C. 1954. Etude de la skdimentation dans I'estuaire de la Rance. I. Granulomktrie des skdiments. Bulletin du Laboratoire Maritime de Dinard 40: 4-15. Berthois L, Berthois C. 1955. Etude de la skdimentation dans I'estuaire de la Rance. 11. Minkralogie des skdirnents. Bulletin du Laboratoire Maritime de Dinard 41: 3-18. Bourcart J. 1959. Carte de La Rance. In: Cows de Pe'trographie sddimentaire: les roches sddimentaires el leur ghkse. Centre de Documentation Universitaire, Paris: 102 pp. Bourcart J, Roa M o d e s P. 1957. Les dkpbts vaseux de La Rance maritime et du Mont Saint-Michel. Bulletin de la Socidtd Ge'ologique de France 7 (4-5): 345-352. Clavier J. 1981. Ecologie descriptive et fonctionnelle du peuplement des sables fins vaseux dans le bassin maritime de La Rance. Thkse de Doctorat de 3""' Cycle de 1'Universitk Paris VI, France: 232 pp. Clavier J, Lechapt JP, Retiere C, Rivain V. 1983. Effets a long terme du fonctionnement de I'usine maremotrice sur I'Cvolution du peuplement des sable fins vaseux de La Rance. Oceanologica Acta, Actes du 17'"' Qmposium Europe'en de Biologie Marine, B r a t , France: 75-79. LA RANCE ENVIRONMENT 35 Clavier J, Richard 0. 1985. Etudes sur Ics ormeaux d a m la rkgion de Saint-Malo. Rapport &Etude de I‘Association pour la Mise en Valeur du Littoral de la Co’te d’Emeraude: 285 pp. Dadswell MJ, Rulifson RA. 1994. Macrotidal estuaries: a region of collision between migratory marine animals and tidal power development. Biological Journal of the Linnean Sociely 51: 93-1 13 Dauvin JC. 1984. Dynamique d’ecosysthes macrobenthiques des fonds sedimentaires de la baie de Morlaix et leur perturbation par les hydrocarbures de I’Amoco Cadiz. These de Doctorat d’Etat, Sciences Naturelles, annexes 139 pp. UniversitP Pierre et Marie Curie, France: 468 p p De Kergariou G. 1971. L’araignke de mer Maia squinado L. sur le littoral de Bretagne. Sciences et Ptches 205: + 11-19, Fischer E. 1929. Recherches de bionomie et d’ockanographie littorales sur La Rance et le littoral de La Manche. Annales de l’lnstitut Ocdanographique de Monaco, Nouuelle S h i e 5 (3): 205-249. Fischer-Piette E. 1931. Sur la penetration de diverses espkces sessiles dans les estuaires et sa limitation par de Monaco, .,Vouuelle Se‘rie 10 (8): 21 7-243. Seau douce. Annales de I’InJlitut ~c~anographique Fischer-Piette E. 1933. Nouvelles observations sur I’ordrc d’euryhalinite des especes littorales. Bulletin de l’lnstilut Oce‘anographique de Monaco 619: 1-16, Gaillard JM. 1958. Haliotis tuberculata Linne. Systtmatique et distribution. Bulletin du Laboratoire Maritime de Dinard 44: 7- I I . Gordon DC, Longhurst AR. 1979. The environmental aspects of a tidal project in the upper reaches of the Bay of Fundy. Marine Pollution Bulletin 1 0 47-5 1. Grall JR.1972. Recherches quantitatives sur la production primaire du phytoplancton dans les parages de Roscoff. Thkse de Doctorat d’Etat, Sciences Naturelles, Universitk dc Paris: 247 pp. Han SJ. 1982. Conditions skdimentologiques comparkes pour deux sites d’usine markmotrice: La Baie de Garolim, Republique de Coree; La Rance, Bretagne, France. These de 3“”‘ Cycle, Universitk de Paris Sud: 182 pp. Herpe E. 1986. La vegetation algale d e La Rance: ses modifications depuis la construction d u barrage. Sociitk Scientijque de Bretagne 58 (1-4): 19-33. Laboratoire Central d’hydraulique de France 1982. Etude skdimentologique dc La Rance. Rapport ge‘ne‘fal: 21 PP. Lacaze JC, Le Pemp X, Villedon de Naide 0. 1976. Recherches hydrobiologiques likes B la realisation dc pollutions experimentales a une grande Cchelle dans I’estuaire de La Rance. Production primaire en relation avec certains parametres physicwchimiqucs. Bulletin du Museum National #Histoire Naturelle 386 (32): 71-106. Lang F. 1986. Peuplements des fonds durs du bassin maritime de La Rance: r61e fonctionnel de Eupolymnia nebulosa (Annelide Polychete). These de Doctorat de I’Universitk de Rennes 1, France: 240 pp. Larsen PF, Topinka JA (Eds) 1984. F u n 4 tidal power deuelopment. Preliminary evaluations o f its enuironmental consequences to Maine. Technical Report no. 35, Bigelow Laboratory for Ocean Sciences, West Boothbay Harbor, Maine, U.S.A.: 136 pp. Le Calvez JC. 1986. Les crustacts decapodes dans Ie bassin maritime de La Rance; cas particulier du crabe vert Carcinus maenas L.: rBle trophique et impact sur les communautks de substrat meuble. ‘I‘hkse de Doctorat de I’Universite de Rennes 1, France: 223 pp. Lechapt JP. 1983. Contribution i I’etude des anntlides polychttcs de substrat meuble en Rance maritime. These de 3‘”‘ Cycle de I’Universitk de Rcnnes 1, France: 129 pp. Le Mao P. 1985. Peuplements piscicole et teuthologique du bassin maritime de La Ranee; impact de I’amenagement markmoteur. Thtse de Docteur-Inginieur, Ecole Nationale Suptrieure Agronomique de Rennes, France: 125 pp. Le Mao P. 1986. Feeding relationships between the benthic Fauna and the dominant benthic fish of the Rance Estuary (France). Journal of the Marine Biological Association, U.K. 66: 391-401, Le Mao P., Le Calvez JC, Lang F, Fouche M. 1986. Utilisation du bassin de retenuc de I’usine maremotrice d r La Rance par les oiseaux aquatiques hivcrnants. L’oiseau et la Revue Frangaise d‘Ornithologie 56 (2): 171-191. Marie P. 1938. Sur la faune des forarniniferes de La Rance. Bulletin du Laboratoire Maritime de Dinard 20: 68-85. Martin WR. 1970. Predicted effects of proposed tidal power structures on groundfish catches in Charlotte County, N.B. Journal of Fisheries Research Board Canada 17 (2): 169-173. Priou ML. 1947. La repartition des alques dans La Rance. DiplBme d’Etudes Suptrieures, UniversitP de Rennes, France: 58 pp. Retiere C. 1976. Dktermination des classes d’bges des populations de Nephtys hombergii (Annklide Polychtte) par lecture dcs michoircs en microscopie electronique a balayage. Structure des populations en Rance maritime. Comptes rendus de I’Acaddmie des Sciences, Paris 282 1553-1556. Retiere C. 1979. Contribution a la connaissance des peuplements benthiques du golfe normanno-breton. Thtsc dc Doctorat d’Etat, Sciences Naturelles, Universitk de Rennes 1, France: 431 pp. Retiere C. 1984. Energie maremotrice: aspects liGs B I’environment aquatique. La Houille Blanche 8: 583-589. Retiere C. 1989. Energie martmotrice et environment aqautique. La Houille Blanche 2: 133-147. Retiere C, Richard 0. 1980. Consequences Pcologiques de 10 anntes de fonctionnement de I’usine markmotrice de La Rance. Rapport Electricit6 de France et Laboratoire Maritime de Dinard: 71 pp. Rivain V. 1983. Contribution a I’etude dynamique et fonctionnelle des peuplements de sables fins du golfe normano-breton. These de Doctorat de 3””<Cycle, Cniversite de Paris VI, France: 166 pp. 36 C. RETIERE Rouvilfois A. 1967. Observations morphologiques sedimentaires e t tcologiques sur la plage de La Ville-Ger, dans I’estuaire de La Rance. Cahiers Ocbnographiques 19 (5): 375-387. Shaw, TL (Ed.). 1980. An environmental appraisal of tidal power stations with particular reference to the Severn barrage. Boston-London-Melbourne: Pitman Advanced Publishing Program, 220 pp. Schricke V, Bourgault Y. 1982. Hivernage des oiseaux d’eau dans l’estuaire de La Rance, 1971-1982. La Sauuagine et sa Chasse 219: 16-18.