Chrysophyceae and Haptophyceae on vertical upper littoral fringe soft rock

Summary

UK and Ireland classification

Description

Chrysophyceae communities form orange, brownish or blackish gelatinous bands at high tide and supralittoral levels on open cliff faces and in caves and tunnels of soft rock. Open cliff-faces and entrances to chalk caves and tunnels at lower supralittoral levels bear a dark brown band comprising an assemblage dominated by Apistonema carterae. During summer this gelatinous growth dries and often peels off. The filamentous green alga Epicladia perforans is often associated with Apistonema, forming a green layer beneath the upper layer of Apistonema. Entodesmus maritima and Thallochrysis litoralis are commonly associated with Apistonema. Associated with this splash zone algal community is an assemblage of animals of terrestrial origin, with red mites, insects and centipedes commonly found. These species descend into the community as the tide falls and retreat as the tide rises. The most common truly marine species is the small winkle Melarhaphe neritoides. (Information taken from the Marine Biotope Classification for Britain and Ireland, Version 97.06: Connor et al., 1997a, b).

Depth range

Upper shore

Additional information

This review is primarily based on detailed studies of the supralittoral algal flora by Anand, (1937a,b, &c) and Tittley & Shaw (1980), to which the reader should refer for further information.  Please note, a recent molecular taxonomic study by Andersen et al. (2014) has synonymized Gloeochrysis litoralis, Gloeochrysis maritima, Apistonema carteri, Thallochrysis litoralis, and Ruttnera litoralis with Chrysotila stipitata (Anand 1936/1937).

Habitat review

Ecology

Ecological and functional relationships

The upper littoral fringe and supralittoral lie above high water springs, and is influenced by wave wash, splash and spray. The mobile fauna will vary with the tide and wave exposure with marine intertidal species further up the shore at high tide and mobile species of terrestrial origin foraging down the shore as the tide recedes only to return to the top of the shore as the tide returns. Other species of terrestrial origin, notably mites (acarids), and some spring tails (Collumbola) seek refuge is cracks and crevices at high tide.

  • Chrysophyceae, Haptophyceae, blue-green algae (Cyanobacteria) and fine filamentous green algae (Chlorophycota) are primary producers, converting sunlight and simple inorganics to biomass.
  • Grazers and browsers feed on unicellular green algae (Chrysophyceae), lichens, and fine filamentous green algae, e.g. the sea slater Ligia oceanica, the bristletail Petrobius maritimus, the small periwinkle Melarhaphne neritoides and some acarid mites (Nicholls, 1931; Joosse, 1976; Roth & Brown, 1976; Pugh & King, 1988; Carefoot & Taylor, 1995; Bücking, 1998).
  • Detritus may accumulate in pits or crevices and is fed on by detritivores such as acarid mites.
  • Predators include mites (acarids), centipedes of terrestrial or intertidal origin (e.g. Strigamia maritima, which may take isopods, amphipods and periwinkles), and terrestrial or maritime spiders (Roth & Brown, 1976; Pugh & King, 1988).
  • The sea slater (Ligia oceanica) may also act as a scavenger (Nicholls, 1931).

Several species are probably more active at night (e.g. Ligia oceanica) to avoid predation by foraging birds. Anand (1937a,b&c) originally described the 'Chrysophyceae' communities of soft chalk cliffs but several species (e.g. Apistonema sp. and Chrysotila sp.) are now described under Haptophyceae (Fowler & Tittley, 1993; van den Hoek et al., 1995), however, the term 'Chrysophyceae' mat or belt is still used.

Seasonal and longer term change

Tittley & Shaw (1980) suggested that Apistonema sp. changed little with the season. In winter, the mucilaginous 'Chrysophyceae' mat may be punctuated by light brown or white patches caused by frost. Chrysotila stipitata (Haptophyceae) community develops in winter but in summer may dry and peel off, being restricted to shaded, moist locations. The primary 'Chrysophyceae' community, dominated by Apistonema carterae is best developed in winter  and present all year round.  Prolonged exposure to sunlight and high temperatures in summer when the seas are calm (low humidity) may result in drying of the mat, which cracks and curls up (Anand, 1937b; Plate IV B). In winter, the mucilaginous mat may be covered by the filamentous growth of Ulothrix sp., and in spring and summer the mat may support numerous species of diatom. Cyanobacteria (e.g. Calothrix sp. and Schizothrix fritschii) are more common in summer. The Rivularia atra belt (see habitat complexity) is best developed in winter but dies back in summer. The growth of the fine green filamentous algae Pseudendoclonium submarinum (previously described by Anand as Endoderma perforans) is favoured in winter (Anand, 1937b; Tittley & Shaw, 1980; Burrows, 1991). No information concerning seasonal changes in the associated fauna was found.

Habitat structure and complexity

This biotope occurs in the upper littoral fringe and supralittoral of soft vertical rock cliffs, above the high water of springs tides, and replaces the Verrucaria maura communities typically found on hard rock substrata. Supralittoral algal communities show a distinct zonation pattern (Anand 1937a,b,&c; Magne, 1974; Tittley & Shaw, 1980). The height of the supralittoral zone and, hence, the height of each individual algal band (or zone) is dependent on moisture and humidity. Moisture or humidity are dependent on the height reached by wave wash, splash and spray and, therefore, on the degree of wave exposure, the porosity of the rock, and the drying forces of wind and sunlight and hence, the north or south aspect of the cliff face. For example, on wave exposed North Atlantic headlands the supralittoral may reach 50-60 ft (ca 15-18m) above mean high water springs tides (MHWS) but only reach 4-5 ft (ca 1-1.5m) above on sheltered shores (Lewis, 1964).
The surface of the soft rock provides complexity to the habitat in the form of pits or crevices that retain moisture and may be punctuated by tunnels and caves. Chrysophyceae and Haptophyceae are single celled (unicellular) microalgae more usually found in planktonic communities. The Chrysophyceae and Haptophyceae found in soft rock communities form a thallus of algal cells bound by mucilage or filaments of mucilage (Anand, 1937a; van den Hoek et al., 1995). Anand (1937a,b&c) described five main communities of Chrysophyceae, Haptophyceae and Cyanobacteria associated with the 'Chrysophyceae' mat.

Zonation (down the shore from the yellow and grey lichen belt)

  • An upper belt (45 cm or more high) of the fine green filamentous algae Pseudendoclonium submarinum (previously described by Anand as Endoderma perforans), filaments of which penetrate the loose rock and give the rock face a green hue. The Pseudendoclonium submarinum belt may reach 8-10 m above high water, more in caves and recesses where the waves break and spray reaches higher.
  • A lower belt of 'Chrysophyceae' communities, forming an orange, light or dark brownish mucilaginous mat. The mucilaginous mat grows over a layer of Pseudendoclonium submarinum that grows endophytically within the 'Chrysophyceae' mat, from which it may protrude. Alternating layers of green algae within the brown Chrysophyceae may form, depending on the season.
  • The 'Chrysophyceae' belt is dominated by Apistonema carterae, commonly with Thallochrysis litoralis and Gloeochrysis maritima. Chrysotila stipitata (Haptophyceae) may form a separate 'Chrysophyceae' community, especially in the winter months.
  • Several species of blue-green algae (Cyanobacteria) live endophytically within the 'Chrysophyceae' mat forming layers of black or dark brown growth within the mucilaginous mat, e.g. the Calothrix sp. community. Schizothrix fritschii (Cyanobacteria), however, may form erect branched bundles of a yellowish or green olive colour on the surface of the mat.
  • A band of Rivularia atra (Cyanobacteria) may occur between the bottom of the 'Chrysophyceae' belt and the top of the Ulva sp. zone (Anand, 1937a,b&c; Tittley & Shaw, 1980; Burrows, 1991).
  • In the winter months, the mucilaginous mat may be covered by the fine, felt like growth of the green algae Ulothrix sp.
  • The lower limit of this biotope is delimited by a band dominated by Ulva sp. (see MLR.Eph).

Caves
The 'Chrysophyceae' belt is found near the entrance but its vertical extent is increased and it may extend for 6-8 m from the floor in well illuminated caves.  The dominant species vary with light intensity and hence, distance into the cave (Anand, 1937b). Pseudendoclonium submarinum (described as Endoderma perforans) penetrates the surface of the mucilaginous mat giving it a green colour. Pseudendoclonium submarinum becomes more prominent in vertical extent in caves than on open cliffs. Anand (1937b) describes three algal communities specific to soft rock caves.

Productivity

The Chrysophyceae, Haptophyceae, the associated Chlorophycota and Cyanobacteria provide primary production within this biotope. However, no further information was found.

Recruitment processes

Chrysophyceae and Haptophyceae reproduce predominantly by asexual reproduction. Flagellate zoospores may also be produced. The Haptophyta Chrysotlia lamellosa is predominately benthic but the motile flagellate part of the life-cycle is an abundant member of the phytoplankton, previously described as Isochrysis maritima. The fine, filamentous green algae found in this biotope produce motile zoospores and swarmers. While Cyanobacteria do not form flagellate cells, they are ubiquitous. Hence, the algae species within this biotope have a high potential for dispersal, depending on local currents.

Therefore, it is likely that recolonization of soft rock cliffs would be relatively rapid, probably occurring within a year. Tittley & Shaw (1980) noted that Apistonema sp. was replaced by Entophysalis sp. (Cyanobacteria) on sea walls and that hard, impervious rock substrata supported different algae communities to those of soft, porous rock substrata. This was probably dependent on the moisture retained by the porous rock surface, e.g. chalk and the ability of algal spores to settle and stick to rough rather than smooth surfaces (Tittley & Shaw, 1980).

Time for community to reach maturity

Little information was found. The 'Chrysophyceae' communities develop in winter, with Cyanobacteria developing in spring and summer, suggesting a seasonal cycle. Therefore, it is likely that the community would reach maturity within a year.

Additional information

With the exception of the studies indicated above, the ecology of soft rock algal communities has received little attention.

Preferences & Distribution

Habitat preferences

Depth Range Upper shore
Water clarity preferencesNot relevant
Limiting Nutrients Nitrogen (nitrates), Phosphorus (phosphates), Silicon (silicates)
Salinity preferences Full (30-40 psu), Variable (18-40 psu)
Physiographic preferences
Biological zone preferences Upper littoral fringe
Substratum/habitat preferences Caves, Chalk
Tidal strength preferences
Wave exposure preferences Moderately exposed
Other preferences Soft porous rock

Additional Information

Soft rocks such as sandstone, limestone (or brick) but especially chalk support diverse algal communities characteristic of this biotope. However, on smooth, impermeable rock surfaces (including artificial substrata such as concrete) the Chrysophyceae and Haptophyceae were replaced by Cyanobacteria (Entophysalis sp.) (Tittley & Shaw, 1980; Fowler & Tittley, 1993).

Several members of this community, especially the fine filamentous algae, Chrysophyceae and Haptophyceae are difficult to identify. Therefore, this biotope and its component species may be under recorded in the British Isles. However, the distribution of this biotope is limited to suitable environmental conditions on suitable rock surfaces (e.g. chalk cliffs) many of which have been affected by the construction of sea defences resulting in loss of this biotope in parts of the UK (see importance; Fowler & Tittley, 1993).

Species composition

Species found especially in this biotope

  • Apistonema carterae
  • Chrysotila lamellosa
  • Chrysotila stipitata
  • Ectocarpus sp.
  • Entocladia viridis
  • Entodesmis litoralis
  • Entodesmis maritima
  • Gleochrysis maritima
  • Kuetzingiella holmesii
  • Petalonia filiformis
  • Pleurocladia lacustris
  • Praisnocladus lubricus
  • Pringsheimiella scutata
  • Pseudendoclonium submarinum
  • Thallochrysis litoralis
  • Trebouxia humicola
  • Ulvella lens

Rare or scarce species associated with this biotope

-

Additional information

The composition of the 'Chrysophyceae' communities and associated species were described in detail by Anand (1937a,b,&c) and in subsequent surveys by Tittley & Shaw (1980) and Tittley (1985; 1988). Anand (1937b) described two main Chrysophyceae communities and three associated Cyanobacteria communities in addition to the Pseudendoclonium submarinum community. In addition, Anand (1937a) recorded two species new to the British Isles and several rare species (see Fowler & Tittley, 1993).

Sensitivity review

Sensitivity characteristics of the habitat and relevant characteristic species

This biotope is characterized by the presence of the mucilaginous mat of Chrysophyceae and Haptophyceae, dominated by Apistonema carterae, growing in association with Pseudendoclonium submarinum (previously described by Anand (1936, 1937a) as Endoderma perforans). The composition of the 'Chrysophyceae and Haptophyceae' communities varies with season, moisture and in caves or tunnels. The arthropod community (red mites, insects, centipedes, and spiders) are mobile species that are found within the supralittoral and are not dependent on this biotope. Therefore, the 'Chrysophyceae and Haptophyceae' communities as a whole have been used to indicate the sensitivity of the biotope and no indicative species were chosen. However, in undertaking this assessment of sensitivity, an account was taken of knowledge of the biology of all characterizing species in the biotope.

Resilience and recovery rates of habitat

Chrysophyceae and Haptophyceae reproduce predominantly by asexual reproduction. Flagellate zoospores may also be produced and 'swarmers' have been identified in Chrysotila spp. (Green & Parke, 1975).  Several members Chrysophyceae and Haptophyceae of the exhibit both a motile flagellated form and a thalloid or tissue-like phase, e.g. Thallocrysis spp  (Van den Hoek et al., 1995). The Haptophyta Chrysotlia lamellosa is predominately benthic but the motile flagellate part of the life-cycle is an abundant member of the phytoplankton, previously described as Isochrysis maritima (Van den Hoek et al., 1995). 

The fine, filamentous green algae found in this biotope produce motile zoospores and swarmers. While Cyanobacteria do not form flagellate cells, they are ubiquitous. Hence, the algae species within this biotope have a high potential for dispersal, depending on local currents. Tittley & Shaw (1980) noted that Apistonema sp. was replaced by Entophysalis sp. (Cyanobacteria) on sea walls and that hard, impervious rock substrata supported different algae communities to those of soft, porous rock substrata. This was probably dependent on the moisture retained by the porous rock surface, e.g. chalk and the ability of algal spores to settle and stick to rough rather than smooth surfaces (Tittley & Shaw, 1980).

The characteristic members of the flora produce swarmers or can occur as motile, flagellate algae in the phytoplankton. Therefore, it is likely that recolonization of soft rock cliffs would be relatively rapid, probably occurring within a year. The 'Chrysophyceae' communities develop in winter, with Cyanobacteria developing in spring and summer, suggesting a seasonal cycle. Therefore, it is likely that the community would reach maturity within a year and resilience is assessed as High, even where the community is removed.

Hydrological Pressures

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ResistanceResilienceSensitivity
Temperature increase (local) [Show more]

Temperature increase (local)

Benchmark. A 5°C increase in temperature for one month, or 2°C for one year. Further detail

Evidence

Anand (1937c) examined the range of temperatures experienced by chalk cliff algal communities. The Pseudendoclonium submarinum belt was exposed to temperatures slightly less than air (since the cliff face heats up slowly) but similar variability in temperature to that of the air. The mucilaginous Chrysophyceae belt was consistently lower in temperature than the air, was least affected by changes in air temperature and showed no marked variation over several hours. Anand (1937c) concluded that its water content and retention acted as a buffer against temperature change. Curiously, in contrast, the Ulva sp. and Fucus sp. belts of the lower shore showed a much greater range of temperatures, especially in bright sunlight. However, Anand (1937b&c) also noted that prolonged exposure to high temperatures during summer in desiccating conditions resulted in death, cracking and peeling off of the 'Chrysophyceae' belt. The mat was seldom seen to crack in areas sheltered from direct sunlight and/or wind.

Sensitivity assessment.  Therefore, an increase in annual temperatures (at the benchmark level) is likely to increase the risk of desiccation and exposure to high temperatures during summer, resulting in loss of the proportion of the population depending on its shelter and aspect. Hence, a resistance of Low has been recorded. Once prior conditions return, recovery is likely to be rapid  and resilience is probably High. Hence, sensitivity is likely to be Low.

Low
High
High
High
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High
Medium
Medium
Medium
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Low
Medium
Medium
Medium
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Temperature decrease (local) [Show more]

Temperature decrease (local)

Benchmark. A 5°C decrease in temperature for one month, or 2°C for one year. Further detail

Evidence

Anand (1937b&c) reported that light brown or white patches appeared in the 'Chrysophyceae' mat during winter due to frost. However, little other information concerning low temperatures was found. A decrease in annual winter temperatures is likely to increase the risk of frost, however, a reduction in average summer temperatures will reduce the risk of desiccation. Since the Chrysophyceae communities are best developed in winter and the associated Cyanobacteria communities develop in spring and summer the biotope as a whole may benefit from a reduction in average summer temperatures. Therefore, resistance is probably High, so that resilience is also High and Not sensitive has been recorded.

High
Medium
Low
Low
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High
High
High
High
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Not sensitive
Medium
Low
Low
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Salinity increase (local) [Show more]

Salinity increase (local)

Benchmark. A increase in one MNCR salinity category above the usual range of the biotope or habitat. Further detail

Evidence

Although not covered by seawater, the upper littoral fringe and supralittoral experience a wide range of salinities due to the evaporation of wave splash and spray, resulting in high salt concentrations, and exposure to rain and freshwater runoff. Anand (1937c) showed that the salt concentration in the 'Chrysophyceae' belt was higher than in the Ulva sp. belt (lower on the shore) but (due to water retention) did not experience as great an increase in salt concentration once the tide fell. However, in the 'Chrysophyceae' belt the salt concentration may be approximately three times that of seawater (Anand, 1937c). Therefore, since soft rock algal communities are also likely to be exposed to freshwater in the form of rain, this biotope is probably resistant to changes in salinity comparable to the benchmark (i.e. >40 PSU).  Therefore, a resistance of High is suggested, so that resilience is also High and Not sensitive is recorded.

High
High
High
High
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High
High
High
High
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Not sensitive
Medium
Medium
Medium
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Salinity decrease (local) [Show more]

Salinity decrease (local)

Benchmark. A decrease in one MNCR salinity category above the usual range of the biotope or habitat. Further detail

Evidence

Although not covered by seawater, the upper littoral fringe and supralittoral experience a wide range of salinities due to the evaporation of wave splash and spray, resulting in high salt concentrations, and exposure to rain and freshwater runoff. Anand (1937c) showed that the salt concentration in the 'Chrysophyceae' belt was higher than in the Ulva sp. belt (lower on the shore) but (due to water retention) did not experience as great an increase in salt concentration once the tide fell. However, in the 'Chrysophyceae' belt the salt concentration may be approximately three times that of seawater (Anand, 1937c). Therefore, since soft rock algal communities are also likely to be exposed to freshwater in the form of rain, this biotope is probably resistant to changes in salinity comparable to the benchmark (i.e. full to reduced).  Therefore, a resistance of High is suggested, so that resilience is also High and Not sensitive is recorded.

High
High
High
High
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High
High
High
High
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Not sensitive
Medium
Medium
Medium
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Water flow (tidal current) changes (local) [Show more]

Water flow (tidal current) changes (local)

Benchmark. A change in peak mean spring bed flow velocity of between 0.1 m/s to 0.2 m/s for more than one year. Further detail

Evidence

The upper littoral fringe and supralittoral are rarely if ever inundated. Therefore, the biotope is unlikely to be affected by water flow as described by the benchmark. Runoff due to heavy rainfall is possible but is outside the scope of the pressure. Therefore, the pressure is Not relevant.

Not relevant (NR)
NR
NR
NR
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Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
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Emergence regime changes [Show more]

Emergence regime changes

Benchmark.  1) A change in the time covered or not covered by the sea for a period of ≥1 year or 2) an increase in relative sea level or decrease in high water level for ≥1 year. Further detail

Evidence

Anand (1937c) examined the volumes of water and spray received by the littoral fringe and supralittoral on chalk cliffs.  He concluded that the Chrysophyceae belt received occasional spray and rarely very much. In calm weather in summer drought periods the belt was subject to periods of drought of up to three days occasionally separated by brief periods of spray. The Endocladia belt was rarely wetted by spray except in rough weather at spring tides and experienced periods of drought of up to three days and yet still extended to high levels (8-10 m). The Endocladia belts showed more conspicuous growth in tunnels and recesses where waves break and spray reached higher levels (Annand, 1937c). It should be remembered that chalk retains moisture and may offset the desiccation experienced at different shore height.  Anand (1937c) also noted that rainfall contributed to moisture but did not influence zonation (height on the shore) as it affected the entire shore.

A decrease in emergence equivalent would expose the habitat to an increased level of spray. However, decreased emergence will allow the algal communities to colonize further up the shore so that the entire zonation (see habitat complexity) will probably move up the shore.

An increase in emergence will result in a reduction in the height reached by wave splash and spray. Hence, the height of the algal communities in the littoral fringe and supralittoral will also be reduced, resulting in the biotope effectively moving down the shore. Some species particularly abundant in more moist conditions may be lost. Therefore, the extent or abundance of the biotope is likely to be reduced and a resistance of Low has been recorded at the benchmark level.  Once prior conditions return, recovery is likely to be rapid so that resilience is probably High and sensitivity Low.

Low
High
Medium
Medium
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High
Medium
Medium
Medium
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Low
Medium
Low
Low
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Wave exposure changes (local) [Show more]

Wave exposure changes (local)

Benchmark. A change in near shore significant wave height of >3% but <5% for more than one year. Further detail

Evidence

The height and extent of the littoral fringe and supralittoral, and hence the communities they support is dependent on wave wash, splash and spray, and therefore, wave exposure. Anand (1937b&c) noted that the Pseudendoclonium submarinum belt could reach up to 8-10 m above high water but in caves or recesses where waves break and create more spray the algal communities could extend higher up the shore. Similarly, Lewis (1964) noted that the supralittoral could reach 50-60 ft above mean high water springs on wave exposed North Atlantic headlands. Increased wave exposure is likely to increase the overall height of the littoral fringe or supralittoral and increase the height and extent of the associated algal communities. Increased spray may also allow a more diverse community to develop resulting in a rise in species richness. A decrease in wave exposure is likely to reduce the height of the littoral fringe or supralittoral and hence the extent of its associated algal communities. However, as the biotope is typical of moderately wave exposed conditions, a 3-5% change in significant wave height (the benchmark) is unlikely to have a significant effect. Therefore, resistance and resilience are considered High, and the biotope is probably Not sensitive at the benchmark level.

High
Low
NR
NR
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High
High
High
High
Help
Not sensitive
Low
Low
Low
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Chemical Pressures

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ResistanceResilienceSensitivity
Transition elements & organo-metal contamination [Show more]

Transition elements & organo-metal contamination

Benchmark. Exposure of marine species or habitat to one or more relevant contaminants via uncontrolled releases or incidental spills. Further detail

Evidence

This pressure is Not assessed but evidence is presented where available.

Cole et al. (1999) suggested that Pb, Zn, Ni and As were probably very toxic to algae but no direct evidence of the effects on this biotope was found.

Not Assessed (NA)
NR
NR
NR
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Not assessed (NA)
NR
NR
NR
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Not assessed (NA)
NR
NR
NR
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Hydrocarbon & PAH contamination [Show more]

Hydrocarbon & PAH contamination

Benchmark. Exposure of marine species or habitat to one or more relevant contaminants via uncontrolled releases or incidental spills. Further detail

Evidence

This pressure is Not assessed . No evidence concerning the effects of hydrocarbons or oil spills on chalk cliff algal communities was found.

Not Assessed (NA)
NR
NR
NR
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Not assessed (NA)
NR
NR
NR
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Not assessed (NA)
NR
NR
NR
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Synthetic compound contamination [Show more]

Synthetic compound contamination

Benchmark. Exposure of marine species or habitat to one or more relevant contaminants via uncontrolled releases or incidental spills. Further detail

Evidence

This pressure is Not assessed but evidence is presented where available.

No information on the effects of synthetic chemicals on soft rock algal communities was found. However, 1µg/l TBT was shown to significantly reduce growth of the diatoms Pavlova lutheri and Dunaliella tertiolecta and Skeletonema costatum would not grow at 100 ng/l TBT. All species died at 5 µg/l TBT (Beaumont & Newman, 1986; Bryan & Gibbs, 1991). Bryan & Gibbs (1991) reported that TBT suppressed growth of the Skeletonema costatum (EC50 350ng/l) and Thalassiosira pseudonana (EC50 1.15 µg/l). Cole et al. (1999) reported that TBT impaired the development of motile spores of green macroalgae (5 day EC50 of 1 ng/l TBT), which were considered the most intolerant phase of their life cycle. In addition, Cole et al. (1999) suggested that the herbicides Atrazine, Simazine, Diuron, Linuron and the insecticide Dimethoate were probably very toxic to algae.

Therefore, it is probable that soft rock algal communities are intolerant of synthetic chemicals, in particular, herbicides that may be contained in runoff (during heavy rains) from adjacent agricultural land.

Not Assessed (NA)
NR
NR
NR
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Not assessed (NA)
NR
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NR
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Not assessed (NA)
NR
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NR
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Radionuclide contamination [Show more]

Radionuclide contamination

Benchmark. An increase in 10µGy/h above background levels. Further detail

Evidence

No evidence was found.

Not relevant (NR)
NR
NR
NR
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Not relevant (NR)
NR
NR
NR
Help
No evidence (NEv)
NR
NR
NR
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Introduction of other substances [Show more]

Introduction of other substances

Benchmark. Exposure of marine species or habitat to one or more relevant contaminants via uncontrolled releases or incidental spills. Further detail

Evidence

This pressure is Not assessed.

Not Assessed (NA)
NR
NR
NR
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Not assessed (NA)
NR
NR
NR
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Not assessed (NA)
NR
NR
NR
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De-oxygenation [Show more]

De-oxygenation

Benchmark. Exposure to dissolved oxygen concentration of less than or equal to 2 mg/l for one week (a change from WFD poor status to bad status). Further detail

Evidence

The littoral fringe and supralittoral are rarely inundated and are, therefore, permanently exposed to the air. The biotope is unlikely to be exposed to deoxygenated conditions.

Not relevant (NR)
NR
NR
NR
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Not relevant (NR)
NR
NR
NR
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Not relevant (NR)
NR
NR
NR
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Nutrient enrichment [Show more]

Nutrient enrichment

Benchmark. Compliance with WFD criteria for good status. Further detail

Evidence

Maritime cliff plant and algae communities are probably nutrient poor, i.e. lack nutrients. An increase in nutrients in the form of runoff from adjacent agricultural land may benefit the communities. However, the opportunistic filamentous algae such as Ulothrix sp. and Urospora sp. and even Pseudendoclonium submarinum may overgrow the 'Chrysophyceae' belt, resulting in the dominance of a few species at the expense of a more diverse community. However, no evidence concerning the effects of nutrient enrichment on these communities was found.

Not relevant (NR)
NR
NR
NR
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Not relevant (NR)
NR
NR
NR
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No evidence (NEv)
NR
NR
NR
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Organic enrichment [Show more]

Organic enrichment

Benchmark. A deposit of 100 gC/m2/yr. Further detail

Evidence

Maritime cliff plant and algae communities are probably nutrient poor, i.e. lack nutrients. An increase in nutrients in the form of runoff from adjacent agricultural land may benefit the communities. However, the opportunistic filamentous algae such as Ulothrix sp. and Urospora sp. and even Pseudendoclonium submarinum may overgrow the 'Chrysophyceae' belt, resulting in the dominance of a few species at the expense of a more diverse community. However, no evidence concerning the effects of nutrient enrichment on these communities was found.

Not relevant (NR)
NR
NR
NR
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Not relevant (NR)
NR
NR
NR
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No evidence (NEv)
NR
NR
NR
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Physical Pressures

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ResistanceResilienceSensitivity
Physical loss (to land or freshwater habitat) [Show more]

Physical loss (to land or freshwater habitat)

Benchmark. A permanent loss of existing saline habitat within the site. Further detail

Evidence

Urban and industrial development in south east UK, resulted in a need for coastal defence works to stabilise cliffs and reduce coastal erosion. The construction of sea walls at the base of cliffs cuts off caves and tunnels from the inundation by the sea and prevents sea wash or spray reaching the cliff face. The cliff face may also be scarped and straightened to reduce falls and gullies torn down, resulting in loss of substratum (Fowler & Tittley, 1993). The resultant sea walls do not support the 'Chrysophyceae' algal communities, although limestone and brick structures support similar communities but with a reduced range of chalk species and communities (Tittley & Shaw, 1980; Fowler & Tittley, 1993). Tittley et al. (1998) surveyed chalk cliffs throughout England and revealed that 56% of coastal chalk in Kent and 33% in Sussex had been modified by coastal defence and other works. On the Isle of Thanet, this increased to 74% and had resulted in the loss of a wide range of microhabitats on the upper shore and the removal of splash-zone communities. Elsewhere in England, coastal chalk remains in a largely natural state (Anon, 1999e, Tittley et al., 1998). Fowler & Tittley (1993) noted that the brown algae Kuetzingiella holmesii, characteristic of cave communities and Pleurocladia lacustris had not been re-recorded since the 1930s.

All marine habitats and benthic species are considered to have a resistance of ‘None’ to this pressure and to be unable to recover from a permanent loss of habitat (resilience is ‘Very Low’).  Sensitivity within the direct spatial footprint of this pressure is, therefore ‘High’.  Although no specific evidence is described confidence in this assessment is ‘High’, due to the incontrovertible nature of this pressure.

None
High
High
High
Help
Very Low
High
High
High
Help
High
High
High
High
Help
Physical change (to another seabed type) [Show more]

Physical change (to another seabed type)

Benchmark. Permanent change from sedimentary or soft rock substrata to hard rock or artificial substrata or vice-versa. Further detail

Evidence

Soft rock, such as chalk, is liable to split and wave action and frost can result in loss of the surface of the rock, and localised landslides. However, this would free up new substratum for colonization, and the biotope would probably recover quickly.  It is unlikely that chalk cliffs would be replaced by sedimentary substrata. But the replacement of soft chalk with man-made structures, e.g. of concrete or hard rock has resulted in the loss of the chalk cliff algal communities.

Urban and industrial development in south east UK, resulted in a need for coastal defence works to stabilise cliffs and reduce coastal erosion. The construction of sea walls at the base of cliffs cuts off caves and tunnels from the inundation by the sea and prevents sea wash or spray reaching the cliff face. The cliff face may also be scarped and straightened to reduce falls and gullies torn down, resulting in loss of substratum (Fowler & Tittley, 1993). The resultant sea walls do not support the 'Chrysophyceae' algal communities, although limestone and brick structures support similar communities but with a reduced range of chalk species and communities (Tittley & Shaw, 1980; Fowler & Tittley, 1993). Tittley et al. (1998) surveyed chalk cliffs throughout England and revealed that 56% of coastal chalk in Kent and 33% in Sussex had been modified by coastal defence and other works. On the Isle of Thanet, this increased to 74% and had resulted in the loss of a wide range of microhabitats on the upper shore and the removal of splash-zone communities. Elsewhere in England, coastal chalk remains in a largely natural state (Anon, 1999e, Tittley et al., 1998). Fowler & Tittley (1993) noted that the brown algae Kuetzingiella holmesii, characteristic of cave communities and Pleurocladia lacustris had not been re-recorded since the 1930s.

Sensitivity assessment. Therefore, the resistance is assessed as None, resilience as Very low (as it is a permanent change) and sensitivity as High.

None
High
High
High
Help
Very Low
High
High
High
Help
High
High
High
High
Help
Physical change (to another sediment type) [Show more]

Physical change (to another sediment type)

Benchmark. Permanent change in one Folk class (based on UK SeaMap simplified classification). Further detail

Evidence

It is unlikely that chalk would be replaced by sediment in the littoral fringe or supralittoral.  Therefore, this pressure is Not relevant. However, change in substratum type is address above.
 

Not relevant (NR)
NR
NR
NR
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Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Habitat structure changes - removal of substratum (extraction) [Show more]

Habitat structure changes - removal of substratum (extraction)

Benchmark. The extraction of substratum to 30 cm (where substratum includes sediments and soft rock but excludes hard bedrock). Further detail

Evidence

Extraction of sediment, as described under this pressure, is not relevant in soft rock habitats. However, soft rocks could suffer extraction due to tunnelling, mining or construction. Therefore, removal of chalk from the cliff would remove the surface Chrysophyceae and Haptophyceae belt, resulting in loss of the biotope. Resistance would, therefore, be None. But if the existing substratum (chalk) remains in the same habitat (upper littoral fringe to supralittoral) then the biotope would recover rapidly and resilience is probably High, therefore, sensitivity to extraction is probably Medium.

None
Low
NR
NR
Help
High
Medium
Medium
Medium
Help
Medium
Low
Low
Low
Help
Abrasion / disturbance of the surface of the substratum or seabed [Show more]

Abrasion / disturbance of the surface of the substratum or seabed

Benchmark. Damage to surface features (e.g. species and physical structures within the habitat). Further detail

Evidence

The 'Chrysophyceae' mat is very thin (a few millimetres) and the Pseudendoclonium submarinum belt exists as a thin coating of the rock. These algal communities are likely to be removed as a result of any abrasion, e.g. from vessel grounding or recreational access and trampling, especially where the friable rock surface is removed.  Therefore, resistance is probably Low (depending on the scale of the impact). However, recovery is likely to be rapid if suitable substratum remains so that resilience is probably High and sensitivity is probably Low.

Low
Low
NR
NR
Help
High
Medium
Medium
Medium
Help
Low
Low
Low
Low
Help
Penetration or disturbance of the substratum subsurface [Show more]

Penetration or disturbance of the substratum subsurface

Benchmark. Damage to sub-surface features (e.g. species and physical structures within the habitat). Further detail

Evidence

Penetration by mobile fishing gear is unlikely to occur on vertical chalk cliffs. However, soft rock, by definition, can be damaged by other penetrative activities, for example during construction.  The 'Chrysophyceae' mat is very thin (a few millimetres) and the Pseudendoclonium submarinum belt exists as a thin coating of the rock. These algal communities are likely to be removed as a result of any abrasion or penetration,  especially where the friable rock surface is removed.  Therefore, resistance is probably Low (depending on the scale of the impact). However, recovery is likely to be rapid if suitable substratum remains so that resilience is probably High and sensitivity is probably Low.

Low
Low
NR
NR
Help
High
Medium
Medium
Medium
Help
Low
Low
Low
Low
Help
Changes in suspended solids (water clarity) [Show more]

Changes in suspended solids (water clarity)

Benchmark. A change in one rank on the WFD (Water Framework Directive) scale e.g. from clear to intermediate for one year. Further detail

Evidence

The upper littoral fringe or supralittoral are rarely inundated. It is, therefore, unlikely to be exposed to changes in water clarity due to changes in suspended sediment.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Smothering and siltation rate changes (light) [Show more]

Smothering and siltation rate changes (light)

Benchmark. ‘Light’ deposition of up to 5 cm of fine material added to the seabed in a single discrete event. Further detail

Evidence

Smothering could occur as a result of rainwater runoff of silt and soil from the tops of the cliffs. However, the slope of the cliff would preclude the build up of significant deposits (except on crevices and pits) sufficient to block the algal communities access to sunlight. Therefore, the factor is probably Not relevant at the level of the benchmark. Smothering by impermeable materials or by other hard construction materials, however, would result in loss of the biotope (see physical loss above).

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Smothering and siltation rate changes (heavy) [Show more]

Smothering and siltation rate changes (heavy)

Benchmark. ‘Heavy’ deposition of up to 30 cm of fine material added to the seabed in a single discrete event. Further detail

Evidence

Smothering could occur as a result of rainwater runoff of silt and soil from the tops of the cliffs. However, the slope of the cliff would preclude the build up of significant deposits (except on crevices and pits) sufficient to block the algal communities access to sunlight. Therefore, the factor is probably Not relevant at the level of the benchmark. Smothering by impermeable materials or by other hard construction materials, however, would result in loss of the biotope (see physical loss above).

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Litter [Show more]

Litter

Benchmark. The introduction of man-made objects able to cause physical harm (surface, water column, seafloor or strandline). Further detail

Evidence

Not assessed.

Not Assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
Electromagnetic changes [Show more]

Electromagnetic changes

Benchmark. A local electric field of 1 V/m or a local magnetic field of 10 µT. Further detail

Evidence

No evidence was found.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
No evidence (NEv)
NR
NR
NR
Help
Underwater noise changes [Show more]

Underwater noise changes

Benchmark. MSFD indicator levels (SEL or peak SPL) exceeded for 20% of days in a calendar year. Further detail

Evidence

Not relevant.  The biotope is rarely underwater and microalgae are not known to respond to noise.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Introduction of light or shading [Show more]

Introduction of light or shading

Benchmark. A change in incident light via anthropogenic means. Further detail

Evidence

An increase in artificial light might be beneficial but shading is likely to result in loss of the biotope.  Anand (1937b&c) reported that the Chrysophyceae belt was restricted to the entrance and mouth of caves and out-competed in tunnels.  In the two caves examined, the Chrysophyceae belt was restricted to the 9m from the cave mouth where light intensity was reduced to 10% of incident light. In caves where light could not penetrate, the Chrysophyceae belt was replaced in shaded areas.  Resistance to shading is probably Low.  However, the Chrysophyceae belt would probably recover rapidly once the shading activity is removed, and resilience is probably High. Therefore, the sensitivity to change in light is probably Low.

Low
High
High
High
Help
High
Medium
Medium
Medium
Help
Low
Medium
Medium
Medium
Help
Barrier to species movement [Show more]

Barrier to species movement

Benchmark. A permanent or temporary barrier to species movement over ≥50% of water body width or a 10% change in tidal excursion. Further detail

Evidence

Not relevant. This pressure is considered applicable to mobile species, e.g. fish and marine mammals rather than seabed habitats. Physical and hydrographic barriers may limit the dispersal of spores. But spore dispersal is not considered under the pressure definition and benchmark.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Death or injury by collision [Show more]

Death or injury by collision

Benchmark. Injury or mortality from collisions of biota with both static or moving structures due to 0.1% of tidal volume on an average tide, passing through an artificial structure. Further detail

Evidence

The pressure definition is not directly applicable to the littoral fringe so Not relevant has been recorded.  Collision via ship groundings or terrestrial vehicles is possible but the effects are probably similar to those of abrasion above.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Visual disturbance [Show more]

Visual disturbance

Benchmark. The daily duration of transient visual cues exceeds 10% of the period of site occupancy by the feature. Further detail

Evidence

Not relevant. Microalgae respond to light intensity but are unlikely to respond to 'visual' cues.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help

Biological Pressures

Use [show more] / [show less] to open/close text displayed

ResistanceResilienceSensitivity
Genetic modification & translocation of indigenous species [Show more]

Genetic modification & translocation of indigenous species

Benchmark. Translocation of indigenous species or the introduction of genetically modified or genetically different populations of indigenous species that may result in changes in the genetic structure of local populations, hybridization, or change in community structure. Further detail

Evidence

No evidence was found to suggest that the Chrysophyceae and Haptophyceae that characterize the green algal mats in this biotope were subject to translocation, nor that they were subject to genetic modification or hybridization with other similar species.  Several species of Chrysophyceae and Haptophyceae may be cultured as a food source or for research but no evidence was found to suggest that genetically modified or laboratory stocks were released into the wild.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
No evidence (NEv)
NR
NR
NR
Help
Introduction or spread of invasive non-indigenous species [Show more]

Introduction or spread of invasive non-indigenous species

Benchmark. The introduction of one or more invasive non-indigenous species (INIS). Further detail

Evidence

No evidence was found.

No evidence (NEv)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
No evidence (NEv)
NR
NR
NR
Help
Introduction of microbial pathogens [Show more]

Introduction of microbial pathogens

Benchmark. The introduction of relevant microbial pathogens or metazoan disease vectors to an area where they are currently not present (e.g. Martelia refringens and Bonamia, Avian influenza virus, viral Haemorrhagic Septicaemia virus). Further detail

Evidence

Viruses are thought to play a part in the control of phytoplankton populations (Brussaard, 2004). However, no evidence specific to these chalk cliff communities was found.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
No evidence (NEv)
NR
NR
NR
Help
Removal of target species [Show more]

Removal of target species

Benchmark. Removal of species targeted by fishery, shellfishery or harvesting at a commercial or recreational scale. Further detail

Evidence

Soft-rock algal communities are unlikely to be targetted by any commercial or recreational fishery or harvest.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Removal of non-target species [Show more]

Removal of non-target species

Benchmark. Removal of features or incidental non-targeted catch (by-catch) through targeted fishery, shellfishery or harvesting at a commercial or recreational scale. Further detail

Evidence

Incidental removal of the Chrysophyceae and Haptophyceae 'belt' would probably remove the entire belt rather than specific characteristic species. The Cyanobacteria probably depend on the mucilaginous 'belt' for substratum but are otherwise not closely associated with any other species. Similarly, the mobile invertebrate fauna are probably not entirely dependent on the 'belt' for food or habitat and would forage elsewhere. 

However, soft-rock communities are unlikely to be targetted by any commercial or recreational fishery or harvest. Accidental physical disturbance due to access (e.g. trampling) or grounding is examined under abrasion above.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help

Bibliography

  1. Anand, P.L., 1937a. A taxonomic study of the algae of British Chalk-cliffs. Journal of Botany, 75 (Supplement II), 1-51.

  2. Anand, P.L., 1937b. An ecological study of the algae of the British chalk cliffs. Part I. Journal of Ecology, 25, 153-188.

  3. Anand, P.L., 1937c. An ecological study of the algae of the British chalk cliffs. Part II. Journal of Ecology, 25, 344-367.

  4. Andersen, R.A., Kim, J.I., Tittley, I. & Yoon, H.S., 2014. A re-investigation of Chrysotila (Prymnesiophyceae) using material collected from the type locality. Phycologia, 53 (5), 463-473.

  5. Anonymous, 1999e. Littoral and sublittoral chalk. http://www.ukbap.org.uk/ukplans.aspx?id=31, 2001-09-26

  6. Beaumont, A.R. & Newman, P.B., 1986. Low levels of tributyl tin reduce growth of marine micro-algae. Marine Pollution Bulletin, 17, 457-461.

  7. Brussaard, C.P.D., 2004. Viral Control of Phytoplankton Populations — a Review. Journal of Eukaryotic Microbiology, 51(2), 125-138.

  8. Bryan, G.W. & Gibbs, P.E., 1991. Impact of low concentrations of tributyltin (TBT) on marine organisms: a review. In: Metal ecotoxicology: concepts and applications (ed. M.C. Newman & A.W. McIntosh), pp. 323-361. Boston: Lewis Publishers Inc.

  9. Bücking, J., 1998. Investigations on the feeding habits of the rocky shore mite Hyadesia fusca (Acari: Astigmata: Hyadesiidae): diet range, food preference, food quality, and the implications for distribution patterns. Helgolander Meersuntersuchungen, 52, 159-177.

  10. Burrows, E.M., 1991. Seaweeds of the British Isles. Volume 2. Chlorophyta. London: British Museum (Natural History).

  11. Carefoot, T.H. & Taylor, B.E., 1995. Ligia: a prototypal terrestrial isopod. In Terrestrial isopod biology (ed. M.A. Alikhan), pp. 47-60. Rotterdam: A.A. Balkema. [Crustacean Issues 9.]

  12. Cheng, L. (ed.), 1976. Marine insects. Amsterdam: North-Holland Publishing Company.

  13. Cole, S., Codling, I.D., Parr, W. & Zabel, T., 1999. Guidelines for managing water quality impacts within UK European Marine sites. Natura 2000 report prepared for the UK Marine SACs Project. 441 pp., Swindon: Water Research Council on behalf of EN, SNH, CCW, JNCC, SAMS and EHS. [UK Marine SACs Project.]. Available from: http://ukmpa.marinebiodiversity.org/uk_sacs/pdfs/water_quality.pdf

  14. Connor, D.W., Brazier, D.P., Hill, T.O., & Northen, K.O., 1997b. Marine biotope classification for Britain and Ireland. Vol. 1. Littoral biotopes. Joint Nature Conservation Committee, Peterborough, JNCC Report no. 229, Version 97.06., Joint Nature Conservation Committee, Peterborough, JNCC Report No. 230, Version 97.06.

  15. Davies, C.E. & Moss, D., 1998. European Union Nature Information System (EUNIS) Habitat Classification. Report to European Topic Centre on Nature Conservation from the Institute of Terrestrial Ecology, Monks Wood, Cambridgeshire. [Final draft with further revisions to marine habitats.], Brussels: European Environment Agency.

  16. Fletcher, R.L., 1987. Seaweeds of the British Isles vol. 3. Fucophyceae (Phaeophyceae) Part 1. London: British Museum (Natural History).

  17. Fowler, S.L. & Tittley, I., 1993. The marine nature conservation importance of British coastal chalk cliff habitats. English Nature Research Reports, no. 32.

  18. Green, J.C. & Parke, M., 1975. New observations upon members of the genus Chrysotila Anand, with remarks upon their relationships within the Haptophyceae. Journal of the Marine Biological Association of the United Kingdom, 55, 109-121.

  19. JNCC (Joint Nature Conservation Committee), 2022.  The Marine Habitat Classification for Britain and Ireland Version 22.04. [Date accessed]. Available from: https://mhc.jncc.gov.uk/

  20. JNCC (Joint Nature Conservation Committee), 1999. Marine Environment Resource Mapping And Information Database (MERMAID): Marine Nature Conservation Review Survey Database. [on-line] http://www.jncc.gov.uk/mermaid

  21. Joosse, E.N.G., 1976. Littoral apterygotes (Collembola and Thysanura). In Marine insects (ed. L. Cheng), pp. 151-186. Amsterdam: North-Holland Publishing Company.

  22. Lewis, J.R., 1964. The Ecology of Rocky Shores. London: English Universities Press.

  23. Magne, F., 1974. Peuplement d'un substrat calcaire dans la zone intercotidale. Bulletin. Société phycologique de France. Paris, 19, 121-128.

  24. Nicholls, A.G., 1931. Studies on Ligia oceanica. Part II. The process of feeding, digestion and absorption, with a description of the structure of the foregut. Journal of the Marine Biological Association of the United Kingdom, 17, 675-705.

  25. Pugh, P.J.A. & King, P.E., 1988. Acari of the British Isles. Journal of Natural History, 22, 107-122.

  26. Roth, V.D. & Brown, W.L., 1976. Other intertidal air-breathing arthropods. In Marine insects (ed. L. Cheng), pp. 119-150.

  27. Tittley, I. & Shaw, K.M., 1980. Numerical and field methods in the study of the marine flora of chalk cliffs. In The shore environment, vol. 1: methods (ed. J.H. Price, D.E.G. Irvine & W.F. Farnham), pp. 213-240. London & New York: Academic Press. [Systematics Association Special Volume, no. 17(a).]

  28. Tittley, I., 1985. Chalk cliff algal communities of Kent and Sussex, Southeast England. Nature Conservancy Council, Contract Reports, no. 200., Peterborough: Nature Conservancy Council.

  29. Tittley, I., 1988. Chalk cliff algal communities: 2. Outside south eastern England. Nature Conservancy Council, Contract Reports, no. 878., London: British Museum (Natural History).

  30. Tittley, I., Spurrier, C.J.H., Chimonides, P.J., George, J.D., Moore, J.A., Evans, N.J. & Muir, A.I., 1998. Survey of chalk cave, cliff, intertidal and subtidal reef biotopes in the Thanet coast cSAC. Report to English Nature., London: Natural History Museum.

  31. Van den Hoek, C., Mann, D.G. & Jahns, H.M., 1995. Algae: an introduction to phycology: Cambridge University Press.

Citation

This review can be cited as:

Tyler-Walters, H., 2016. Chrysophyceae and Haptophyceae on vertical upper littoral fringe soft rock. In Tyler-Walters H. and Hiscock K. (eds) Marine Life Information Network: Biology and Sensitivity Key Information Reviews, [on-line]. Plymouth: Marine Biological Association of the United Kingdom. [cited 09-10-2024]. Available from: https://www.marlin.ac.uk/habitat/detail/121

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Last Updated: 29/01/2016

  1. green algae
  2. blue green algae
  3. soft rock
  4. chalk
  5. splash zone
  6. vertical
  7. cliff
  8. supralittoral