|Researched by||Dr Heidi Tillin & Georgina Budd||Refereed by||This information is not refereed.|
A dense turf of foliose red seaweeds (including Plocamium cartilagineum, Cryptopleura ramosa and Delesseria sanguinea) on exposed or moderately exposed lower infralittoral rock, generally at or below the lower limit of the kelp. Most of the red seaweeds are common to the kelp zone above, while the faunal component of the biotope is made up of species that are found either in the kelp zone or the animal-dominated upper circalittoral below. The red seaweed species composition varies considerably and at some sites a single species may dominate (particularly Plocamium cartilagineum or Cryptopleura ramosa) As well as a varied red seaweed component, this biotope may also contain occasional kelp plants and patches of the brown foliose seaweed Dictyota dichotoma. In some areas Dictyota dichotoma may occur at high densities (see EIR.FoR.Dic). Other red seaweed-dominated biotopes occur in less wave-exposed areas (MIR.PolAhn), though they are affected by sand scour and are characterized by seaweeds that are resilient to the scouring. (Information taken from the Marine Biotope Classification for Britain and Ireland, Version 97.06: Connor et al., 1997a, b).
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|Water clarity preferences|
|Limiting Nutrients||Nitrogen (nitrates)|
|Biological zone preferences|
|Tidal strength preferences|
|Wave exposure preferences|
|Other preferences||Wave exposure|
This MarLIN sensitivity assessment has been superseded by the MarESA approach to sensitivity assessment. MarLIN assessments used an approach that has now been modified to reflect the most recent conservation imperatives and terminology and are due to be updated by 2016/17.
|Community Importance||Species name||Common Name|
|Important other||Alcyonium digitatum||Dead man's fingers|
|Important other||Calliostoma zizyphinum||Painted top shell|
|Important other||Clavelina lepadiformis||Light bulb sea squirt|
|Important characterizing||Delesseria sanguinea||Sea beech|
|Important other||Echinus esculentus||Edible sea urchin|
|Important characterizing||Lithophyllum incrustans||Encrusting coralline alga|
|Important other||Nemertesia antennina||Sea beard|
|Important other||Urticina felina||Dahlia anemone|
|Removal of the substratum will result in removal of all the attached species, together with most of the slow mobile faunal species (Crustacea, sea urchins and starfish) and an intolerance of high has been recorded. Recoverability is likely to be high (see additional information below).|
|Species such as Balanus crenatus, Bugulina turbinata and Clavelina lepadiformis were assessed to have a high intolerance to smothering, owing to a combination of small size (zooids of Clavelina lepadiformis typically only grow up to 2 cm in height), inhibition of respiration and prevention of feeding. Fronds of adult Delesseria sanguinea are up to 30cm in height and would survive smothering to a depth of 5cm by sediment. However, algal spores and propagules would be adversely affected by a layer of sediment, which can exclude up to 98 % of light (Vadas et al., 1992). Holme & Wilson (1985) suggested that Urticina felina would survive periodic smothering of up to 5cm of sand, by being able to extend its column to maintain its disc above the sand surface. Smothered Echinus esculentus are unlikely to be able to move through sediment. However, individuals are unlikely to starve within a month. Comely & Ansell (1988) recorded large Echinus esculentus from kelp beds on the west coast of Scotland in which the substratum was seasonally covered with "high levels" of silt. This suggests that Echinus esculentus is unlikely to be killed by smothering, however, smaller specimens and juveniles may be more intolerant. Intolerance has been assessed to be intermediate, whilst germlings of algal species may be killed, adult plants are likely to survive and are perennials, so would recruit the following year. Some populations of faunal species would be degraded. Recoverability has been assessed to be high (see additional information below).|
|Increased suspended sediment may increase sediment scour, especially in winter. Spores and germlings are likely to be highly intolerant of sediment scour (Vadas et al., 1992). Delesseria sanguinea reproduces in winter and increased siltation may interfere with recruitment and long term survival of the population. Significant sediment cover of the middle to lower intertidal in a South Californian shore, resulting from fresh water runoff, caused substantial decline in Corallina spp. cover (Seapy & Littler, 1982). Alcyonium digitatum has been shown to be tolerant of high levels of suspended sediment. Hill et al. (1997) demonstrated that Alcyonium digitatum sloughed off settled particles with a large amount of mucous. Bryozoans are suspension feeding organisms that may be adversely affected by increases in suspended sediment, due to clogging of their feeding apparatus. Similarly increased siltation may clog up the feeding apparatus of Nemertesia spp. requiring energetic expenditure to clear. Intolerance has been assessed to be intermediate as the viability of some faunal species may be affected and in the worst instance recruitment of an important characterizing red algae may be inhibited. On return to prior conditions recoverability has been assessed to be high (see additional information below).|
|For a period of one month a decline in the amount of suspended sediment is unlikely to be significant to the biotope. Suspension feeders such as Alcyonium digitatum and Clavelina lepadiformis would suffer a reduced food supply and increased competition, but on return to prior conditions optimal feeding would probably resume rapidly. However, bryozoans turfs are often abundant in clear, fast flowing waters (Moore, 1977a). A decrease in suspended sediment is likely to increase the abundance of bryozoans, including species of Bugula, consequently species richness may increase. Intolerance has been assessed to be low.|
|Not relevant||Not relevant||Not relevant||Not relevant||Not relevant|
|The biotope is sublittoral, desiccation would not be relevant.|
|Not relevant||Not relevant||Not relevant||Not relevant||Not relevant|
|The biotope is sublittoral, changes in the emergence regime would not be relevant.|
|Not sensitive*||Not relevant|
|The biotope is sublittoral, changes in the emergence regime would not be relevant.|
|Typically water flow rates are moderately strong. Increased water flow is likely to reduce the population of large sea urchins. Echinus esculentus was observed to be rolled along the substratum by currents of 2.6 knots or above (Comely & Ansell, 1988). A reduction in grazing by Echinus esculentus would reduce patchiness, possibly allowing fewer species to dominate the biotope (see Vost, 1983) Furthermore, the increased sediment scour (the biotope probably receives a considerable amount of particulate organic matter from the highly productive upper infralittoral kelp biotopes) likely to accompany increased water flow rates may be more damaging. Over the period of a year animal species such as Halichondria panicea, Balanus crenatus and Tubularia indivisa that flourish in fast flowing water are likely to out-compete the algae and become dominant, changing the biotope to a community more like ECR.BalHpan. Intolerance has been assessed to be high. On return to less strong water flows, fast settling algae would again dominate and the abundance of animals decline as natural mortality occurred. Therefore recoverability has been assessed to be high.|
|Water movement is essential for suspension feeders such as hydroids, bryozoans, sponges, amphipods and ascidians to supply adequate food, remove metabolic waste products, prevent accumulation of sediment and disperse larvae or medusae. For instance a decreased water flow rate may impact upon Alcyonium digitatum in that feeding efficiency could decrease as less material (phytoplankton & zooplankton) would be brought into contact with the colonies. Also a lower energy environment favours siltation. However deep growing red algae such as Delesseria sanguinea were observed growing in stagnating water in Kiel Bay, western Baltic Sea (Schwenke, 1960, cited in Kinne, 1971). It is likely therefore that Delesseria sanguinea would be not sensitive to decreased water flow rate. Intolerance has been assessed to be low as the viability of some faunal species may be affected.|
|The tolerance of red algae to temperature changes varies considerably and those of the littoral zone typically have a greater tolerance to both increased and decreased temperature, than those of the sublittoral (see Gessner, 1970, for investigation of the effects of temperature on marine red algae). Sublittoral red algal species, Sphondylothamnion multifidum, Cryptopleura ramosa and Rhodophyllis divaricata were capable of surviving at 27 °C, while other species such as Callophyllis laciniata, Calliblepharis ciliata, Plocamium cartilagineum and Heterosiphonia plumosa died within 12 hours in seawater at 27 °C. However, such a temperature increase exceeds that of the benchmark level. Balanus crenatus is a boreal species, and is intolerant of increases in water temperature. In Queens Dock, Swansea where the water was on average 10 °C higher than average due to the effects of a condenser effluent, Balanus crenatus was replaced by the subtropical barnacle Balanus amphitrite. After the water temperature cooled Balanus crenatus returned (Naylor, 1965). Bishop (1985) noted that gametogenesis of Echinus esculentus proceeded at temperatures between 11 - 19 °C although continued exposure to 19 °C destroyed synchronicity of gametogenesis between individuals. Embryos and larvae developed abnormally after up to 24hr at 15 °C (Tyler & Young, 1998). Bishop (1985) suggested that Echinus esculentus could not tolerate high temperatures for prolonged periods due to increased respiration rate and resultant metabolic stress. Therefore, although Echinus esculentus would probably have a low intolerance to chronic long term temperature change it is likely to be more intolerant of sudden or short term acute change (e.g. 5 °C for 3 days) in temperature. The British Isles are near the southern limit of range of some species such as Lacuna vincta. Long term increases in temperature may limit the survival of the snail, restricting subsequent distribution. Short term acute temperature increases may cause death. However, other prosobranch species would replace Lacuna vincta, or other northern species, if lost from the biotope. Intolerance has been assessed to be intermediate as some species may be lost. Recoverability has been assessed to be high (see additional information below).|
|The tolerance of red algae to temperature change varies considerably and those of the littoral typically have a greater tolerance to both increased and decreased temperature, than those of the sublittoral. Cold damage usually changes the colour of red algae to a bright yellow orange. Sphondylothamnion multifidum, Cryptopleura ramosa and Rhodophyllis divaricata were partially or completely killed at 5 °C. Callophyllis laciniata, Calliblepharis ciliata, Plocamium cartilagineum and Heterosiphonia plumosa survived -2 °C. Delesseria sanguinea and Phycodrys rubens succumbed at temperatures of -3 °C to -5 °C. During experimental attempts to adapt red algae to cold by maintaining them at -1 °C to + 1 °C for several months, a drop in the lethal temperature tolerance of Delesseria sanguinea and a few other species was detected, in the order of 1 to 2 °C (Gessner, 1970). Although Urticina felina was apparently unaffected by the extremely cold winter of 1962/3 (Crisp, 1964), Gosse (1860) observed that "after the intense and protracted frost of February 1855, the shores of South Devon were strewn with dead and dying anemones, principally of this species". Bearing in mind the equivocal observations from two cold winters, it is suggested that at least some individuals might be killed by extreme cold. Alcyonium digitatum was also reported to be apparently unaffected by the severe winter of 1962-1963 (Crisp, 1964). Evidence suggests that some species (both faunal and floral) would be adversely affected by an acute temperature decrease and intolerance has been assessed to be intermediate. On return to prior conditions recovery is likely and has been assessed to be high.|
|Low||Very high||Very Low||No change||Low|
|Increased turbidity would probably reduce the photosynthetic capability of the algae and reduce the food available for suspension feeders, as phytoplanktonic production is also likely to be inhibited over the period of one year. Intolerance has been assessed to be low as effects of increased turbidity would probably be most significant at the sub lethal level. On return to prior conditions recovery is likely to be rapid.|
|A decrease in turbidity may increase phytoplankton and hence zooplankton productivity and potentially increase food availability. However, increased light penetration may favour the development of a kelp canopy which would change the biotope to one characterized by kelp species. Although the majority of the community would survive as an understorey fauna in the presence of a kelp canopy an intolerance of high has been recorded, as the EIR.FoR biotope may not be recognized. However, if rock is present deeper than the biotope, a decrease in turbidity may allow the biotope to extend downwards, thus shifting the depth band in which the biotope occurs. On return to prior conditions recoverability has been assessed to be high as species would remain in the biotope.|
|The biotope typically occurs in situations that are very exposed to moderately exposed and, at the depth where the biotope occurs, wave action is likely to be a significant environmental factor. For instance, red algae which are characteristic of the biotope, are favoured in wave exposed sites. Delesseria sanguinea occurs on coasts with a wide range of wave exposures, from very exposed to very sheltered and are therefore is likely to be relatively tolerant of increased wave action. Of the animal species, Bugulaspp. produce flexible erect tufts, which are likely to move with the oscillatory flow created by wave action but Nemertesia spp. are intolerant of high wave exposure and so are only found in more sheltered areas. Whilst it might be expected that some important characterizing and key functional species such as Echinus esculentus are likely to be displaced or damaged by strong wave action and alterations in abundance occur, intolerance has been assessed to be low as the biotope would still be recognisable. Recoverability has been assessed to be high (see additional information below).|
|The moderately strong to weak tidal currents typical of this biotope are probably more important for water movement than wave induced oscillatory flow. Therefore, a decrease in wave action may allow more delicate species, such as Nemertesia ramosa, ascidians and sponges to increase in abundance. Decreased wave action may allow the biotope to extend into shallower water. However, reduced wave action may result in an increase in sea urchin predation and hence increased patchiness and species richness (Sebens, 1985; Hartnoll, 1998), but excessive grazing may create an urchin barren, in which case the biotope would be lost. Overall, a decrease in wave action may not adversely affect the biotope while the moderately strong currents maintain adequate water flow, and although some species in the biotope may change, important characterizing species of the biotope will probably survive. Therefore, an intolerance of low has been recorded.|
|Tolerant||Not relevant||Not relevant||No change||Moderate|
|Species within the biotope are likely to be not sensitive to noise at the benchmark level.|
|Tolerant||Not relevant||Not relevant||No change||Moderate|
|Species within the biotope are likely to be not sensitive to the visual presence of objects as described in the benchmark.|
|The growth form of Delesseria sanguinea and other foliose red algae suggests that its lamina would probably be damaged by abrasion but not removed. However, a passing scallop dredge would probably tear off a large proportion of the macroalgae and remove any associated species with them. Mobile species, such as isopods would probably avoid damage. Similarly, individuals in crevices or overhangs would probably be unaffected. Bradshaw et al. (2000) suggested that fragile species such a urchins (e.g. Echinus esculentus), suffered badly from impact with a passing scallop dredge. Other sessile faunal species such as Clavelina lepadiformis have relatively delicate growth forms and are likely to be damaged or removed by a passing dredge. Intolerance has been assessed to be intermediate as populations of species may be partially destroyed but the biotope would still be recognized. Recoverability has been assessed to be high (see additional information below).|
|Red algae are permanently attached to the substratum, as are many faunal species. If displaced re-attachment is not possible. Red algae characterize the biotope, in their absence the biotope would not be recognized and intolerance has been assessed to be high. If populations of important characterizing species remain in the vicinity of the denuded substratum recruitment is likely to occur and recoverability has been assessed to be high (see additional information below).|
|O'Brien & Dixon (1976) report that red algae are effective indicators of detergent damage since they undergo colour changes when exposed to relatively low concentrations. Smith (1968) reported that 10 ppm of the oil dispersive detergent BP 1002 killed the majority of specimens in 24hrs in toxicity tests. However, the effects take several days to manifest; when killed the algae turn bright orange. Smith (1968) also demonstrated that 0.5 -1ppm of the detergent BP1002 resulted in developmental abnormalities in echinopluteus larvae of Echinus esculentus. Echinus esculentus populations in the vicinity of an oil terminal in La Coruna Bay, Spain, showed developmental abnormalities in the skeleton. Hoare & Hiscock (1974) reported that red algae (e.g. Lithothamnia spp., Corallina officinalis, Polyides rotundus, Dilsea carnosa, Rhodymenia palmata and Desmarestia aculeata), echinoderms, Polyzoa and amphipod crustaceans appeared to be particularly intolerant of the reduction in water quality associated with the effluent discharged (containing free halogens, HCL & H2SO4) from a bromine extraction works into Amlwch Bay, Anglesey. Red algal species and the urchin Echinus esculentus are likely to be affected by synthetic chemicals, so intolerance has been assessed to be high. Recoverability has been assessed to be moderate as populations may not remain in the immediate vicinity of the biotope so that recruits are not readily available.|
|Uptake of heavy metals from solution by seaweed is influenced by factors such as light, algal nitrogen content, frond age, length of emersion, temperature, salinity, season of the year and presence of other pollutants in the surrounding water (see Lobban & Harrison, 1997) and consequently seaweeds may not accurately reflect metal concentrations in the surrounding water. The order of metal toxicity to algae varies with the algal species and the experimental conditions, but generally the order is Hg>Cu>Cd>Ag>Pb>Zn (Rice et al., 1973; Rai et al., 1981), however insufficient information was available to comment further on the particular intolerance of algal species within the biotope. Kinne (1984) reported developmental disturbances in Echinus esculentus exposed to waters containing 25 µg / l of copper (Cu) and reduced species viability would result in the long term as the species fail to successfully recruit. The information available is patchy but there would appear to be some intolerance of species within the biotope to heavy metals and intolerance has been reported to be intermediate. Recovery should be rapid as heavy metals would not be accumulated in the substratum (as occurs with sediments) and most species in the biotope either have planktonic propagules or are likely to migrate into the area.|
|O'Brien & Dixon (1976) concluded that red algae were the most sensitive group of algae to hydrocarbon or dispersant contamination, possibly attributable to the susceptibility of the photosynthetic pigment phycoerythrin to chemical damage. Following a series of laboratory and field experiments Grandy (1984) reported Delesseria sanguinea, Cryptopleura ramosa, Phycodrys rubens and Plocamium cartilagineum to be sensitive to oil/dispersant mixtures; Cryptopleura ramosa and Plocamium cartilagineum were the most sensitive and Phycodrys rubens the least sensitive. In toxicity experiments, Smith (1968) found Delesseria sanguinea to be particularly intolerant of the oil dispersant BP 1002; 10 ppm of BP 1002 was lethal to the species. Heavy mortality of Delesseria sanguinea was also observed down to a depth of 12 m after the Torrey Canyon oil spill (Drew et al., 1967). However, experience during the Torrey Canyon oil spill seems to be exceptional. As after the Esso Bernicia spill in 1978 in the Sullom Voe and heavy use of dispersants on significant quantities of oil, practically no damage to shallow (< 5 m) red algae could be found in Martins Haven (K. Hiscock, pers. comm.). Following the Sea Empress oil spill the most dramatic effect on the seaweeds was the marked bleaching of the encrusting coralline algae Lithothamnion incrustans and Phymatolithon purpureum. Corallina officinalis, Chondrus crispus and Mastocarpus stellatus also showed signs of bleaching. The encrusting corallines, however, recovered quickly, suggesting that the damage had been restricted to the surface layers (Y. Chamberlain, pers. comm. to Crump et al., 1999). At the depth at which this biotope occurs, only in the most severe conditions would damage probably occur to the characterizing species, and intolerance has been assessed to be intermediate. Recoverability has been assessed to be high assuming deterioration of contaminants (see additional information below).|
|No information||Not relevant||No information||Not relevant||Not relevant|
|Delesseria sanguinea can grow new blades in darkness by drawing on reserves held in the frond midrib and stipe (Lüning, 1990), suggesting that nutrients are subject to 'luxury' accumulation in the winter months. Delesseria sanguinea is likely to tolerate low nutrient levels, during spring and summer. An increase in abundance of red algae, including Delesseria sanguinea, was associated with eutrophication in the Skagerrak area, Sweden, especially in areas with the most wave exposure or water exchange (Johansson et al., 1998). However, where eutrophication resulted in high siltation rates, the delicate foliose red algae such as Delesseria sanguinea were replaced by tougher, erect red algae (Johansson et al., 1998). Lundäve (1990) reported the effects of a serious plankton bloom of Chrysochromulina polyepis in May-June 1998 on rocky-subtidal communities of the Swedish west coast. A site at 4.5 m depth contained small populations of ascidians, sponges and echinoderms in addition to the more dominant red algae, including Delesseria sanguinea and Corallina officinalis. In addition to almost total mortality of the faunal population, the site also showed severe damage to several of the algal species, by early June plants of Delesseria sanguinea lost all pigmentation. Whilst moderate nutrient may be beneficial, e.g. addition of nutrients may encourage the growth of ephemeral and epiphytic algae and therefore increase the food available to sea-urchin populations, severe nutrient enrichment is likely to cause the loss of important characterizing species. At the benchmark level intolerance has been assessed to be intermediate. On return to prior to prior conditions, recoverability has been assessed to be moderate. Lundäve (1990) observed significant changes in the rocky-subtidal community composition after the phytoplankton bloom, regeneration of Delesseria sanguinea was not observed, so following more severe episodes of nutrient enrichment the biotope may not recover.|
|Not relevant||Not relevant||Not relevant||Not relevant||Not relevant|
|The biotope occurs in locations of full salinity.|
|Gessner & Schramm (1971) give a summary of the effects of salinity changes on marine algae. Most sublittoral red algae cannot withstand salinities below 15 psu. Echinoderms are generally unable to tolerate low salinity (stenohaline) and possess no osmoregulatory organ (Boolootian, 1966). The distribution of, and the depth at which Alcyonium digitatum occurs suggest that it is unlikely to survive significant dilution. Clavelina lepadiformis is tolerant of a wide range of salinities; Fish & Fish (1996) found that the ascidian could tolerate salinities as low as 14 psu. Braber & Borghouts (1977) found that Urticina felina (as Tealia felina) penetrated to about the 11ppt Chlorinity (about 20psu) isohaline at mid tide during average water discharge in the Westerschelde estuary suggesting that, during high river flow, it would be tolerant of reduced salinity conditions. Intertidal and rock pool individuals will also be subject to variations in salinity because of precipitation on the shore; albeit for short periods on the lower shore. Therefore, the species seems to have a high tolerance to reduction in salinity but may have to retract tentacles and suffer reduced opportunity to feed. The community is likely to tolerate a decrease in one salinity category of the MNCR salinity scale for one year, although some faunal species may decline in abundance as a result of intolerance or migration. A reduction in grazing pressure by Echinus esculentus may allow some algal species to dominate the biotope and species richness may decline. However, the biotope would still be recognized despite being impoverished so intolerance has been assessed to be intermediate and recoverability high on return to prior conditions (see additional information below).|
|The effects of deoxygenation in plants has been little studied. However, a study of the effects of anaerobiosis on some marine algae reported Delesseria sanguinea to be very intolerant of anaerobic conditions; at 15 °C death occurred within 24hrs and no recovery took place, some specimens however survived at 5 °C. (Hammer, 1972). Under hypoxic conditions echinoderms become less mobile and stop feeding. Death of a bloom of the phytoplankton Gyrodinium aureolum in Mounts Bay, Penzance in 1978 produced a layer of brown slime on the sea bottom. This resulted in the death of fish and invertebrates, including Echinus esculentus, presumably due to anoxia caused by the decay of the dead dinoflagellates (Griffiths et al. 1979). Alcyonium digitatum mainly inhabits environments in which the oxygen concentration usually exceeds 5 ml per litre and respiration is aerobic. Assimilation of oxygen occurs simply by diffusion through the epidermis of exposed tissues and transport to tissues is facilitated by hydroplasmic flow and ciliary activity (Hickson, 1901). It is likely that Alcyonium digitatum would be highly intolerant of a period of hypoxia. Delesseria sanguinea is an important characterizing species in its absence the biotope would not be recognized. Death of Delesseria sanguinea was recorded within 24 hours (see above) so it unlikely to survive anoxic conditions for a period on one week, unless temperatures are very low. Furthermore, sessile faunal species would probably be lost and mobile species are likely to migrate to avoid adverse conditions, so species richness would decline. On return to prior conditions recoverability has been assessed to be high if populations of important characterizing species are in the vicinity of the denuded substratum (see additional information below).|
|No information||Not relevant||No information||Not relevant||Not relevant|
|In Rhodophyta, viruses have been identified by means of electron microscopy (Lee, 1971) and it is obvious that they are widespread. However, nothing is known of their effects on growth or reproduction in red algae and experimental transfer from an infected to an uninfected specimen has not been achieved (Dixon & Irvine, 1977). Echinus esculentus is susceptible to 'Bald-sea-urchin disease', which causes lesions, loss of spines, tube feet, pedicellariae, destruction of the upper layer of skeletal tissue and death (Bower, 1996). It is thought to be caused by the bacteria Vibrio anguillarum and Aeromonas salmonicida. Bald sea-urchin disease was recorded from Echinus esculentus on the Brittany Coast. However, no evidence of mass mortalities of Echinus esculentus associated with disease have been recorded in Britain and Ireland.|
|No information||Not relevant||No information||Not relevant||Not relevant|
|There are currently no known non-native species that occur in, and, might adversely affect this biotope.|
|The collection of Echinus esculentus for the curio trade was studied by Nichols (1984). He concluded that the majority of divers collected only large specimens that are seen quickly and often missed individuals covered by seaweed or under rocks, especially if small. As a result, a significant proportion of the population remains. He suggested that exploited populations should not be allowed to fall below 0.2 individuals per square metre. Echinus esculentus has been identified as a key functional species, owing to its grazing which may prevent dominance of the biotope by a few species (see Vost, 1983). Intolerance has been assessed to be intermediate and recovery high via migration from adjacent biotopes. We have no evidence for the indirect effects of extraction of other species on this biotope.|
|Not relevant||Not relevant||Not relevant||Not relevant||Not relevant|
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Last Updated: 30/05/2002