Green algal films on upper and mid-shore cave walls and ceilings

Summary

UK and Ireland classification

Description

The upper walls and ceilings of upper and mid-shore hard and soft rock (chalk) dominated by a band of green algal films (or 'stains'). Other encrusting algae including the non-calcified Hildenbrandia rubra may be present. In chalk caves, on the east and south-east coasts of England, a distinctive assemblage of species occurs, including the brown alga Pleurocladia lacustris (syn. Pilinia maritima) and the bright green algae Pseudendoclonium submarinum and Entocladia perforans that often covers the cave ceilings. Fauna is generally sparse and limited to limpets such as Patella vulgata and the winkle Littorina saxatilis. The species forming a green algal film that covers upper shore caves in Berwickshire were not identified. More information is required to validate this biotope description. This biotope is situated above the RhoCla or VmucHil zone, extending to cover the upper walls and ceilings of caves. GCv can be found at the entrances to caves and through to the darkest areas at the back and is often found above a zone of RhoPle. In hard rock caves, however, the green and brown algae (RhoPle) or Haptophyceae (ChrHap) occur as separate zones or GCv may occur on its own. (Information from Connor et al., 2004; JNCC, 2015).

Depth range

Upper shore

Additional information

Little information on this biotope was found. The bright green algae Pseudendoclonium submarinum (previously described by Anand (1936, 1937a) as Endoderma perforans) and Entocladia perforans occur on the upper walls and ceilings of caves, especially chalk caves.  The description fits the 'Endoderma' belt described by Anand (1937b&c) that sits above the Chrysophyceae and Haptophyceae belt. However, the two bands may overlap, so that the Chrysophyceae Chrysotila stipitata may grow over the 'Endoderma' belt while the 'Endoderma' belt may extend into the Chrysophyceae belts in periods of drought (Anand, 1937b&c).   Therefore for the purpose of this review, the 'green algal films' are assumed to equate to the 'Endoderma' belt described by Anand (1937b&c) and recorded in chalk and hard rock caves by Norton et al. (1971), Tittley & Shaw (1980), Tittley (1988), Fowler & Tittley (1993).

Listed By

Sensitivity reviewHow is sensitivity assessed?

Sensitivity characteristics of the habitat and relevant characteristic species

This review assumes that the green algal films that characterize this biotope (LRFLR.CvOv.GCv) correspond to the 'Endoderma' belt described by Anand (1937b&c). This biotope may overlap with the Chrysophyceae and Haptophyceae belt (LR.FLR.CvOv.ChrHap) on chalk cliffs and caves, as the 'Endoderma' belt may extend into the 'Chrysophyceae' belt in periods of drought while the Chrysophyceae Chrysotila spp. may grow over the 'Endoderma' belt (Pseudendoclonium submarinum) where adequate sea spray was present.  However, Pseudendoclonium submarinum is also present in the 'Chrysophyceae' belt (the Chrysophyceae-Endoderma-Lyngbya community) and in moist shaded conditions, e.g. during winter, in recesses or on the ceilings of caves and tunnels Pseudendoclonium submarinum 'gains the upper hand (Anand, 1937b) and turns the 'Chrysophyceae' belt green.  Pseudendoclonium submarinum also grows in other conditions, such as on hard rock or artificial substata (e.g. timber, bridge pilings) (Humm & Bert, 1979). Pseudendoclonium submarinum may also occur in communities with blue-green algae e.g. Entophysalis deusta, which can grow over the green algal film (Tittley, 1988). Hildenbrandia rubra is a common species that forms conspicuous patches on stable rock (and stones) on upper littoral cave walls but is also found in the littoral and sublittoral to 12 m (Irvine & Chamberlain, 1994).  The arthropod community of supralittoral rock (red mites, insects, centipedes, and spiders) are mobile species that are found throughout the supralittoral and are not dependent on this biotope. Therefore, the bright green algae Pseudendoclonium submarinum and Entocladia perforans have been used to indicate the sensitivity of this biotope, with reference to detailed studies on the ecology of the chalk cliff and cave algal communities by Anand (1937,b&c), Tittley & Shaw (1980), Tittley (1988), Fowler & Tittley (1993). 

Resilience and recovery rates of habitat

Pseudendoclonium submarinum and Entocladia perforans are Ulvales (Chlorophyta).  Anand (1937b) reported that Pseudendoclonium submarinum (as Endoderma perforans)  formed small clusters of cells from which short filaments arise. In moist shaded conditions the filaments are longer and the growth more conspicuous. The filaments grow into chalk, and extend into the algal mat of the Chrysophyceae belt and along the surface of and may aggregate into tooth-like bundles (Anand, 1937b).  In moist conditions, the Pseudendoclonium submarinum turns the upper part of Chrysophyceae belt (the Chrysophyceae-Endoderma-Lyngbya community) green.  Anand (1937b) also noted that Pseudendoclonium submarinum was an early colonizer, that the was overgrown by Chyrsotila spp. to form the Chrysophyceae belt.

Sexual reproduction in Ulvales is isomorphic and diplohaplontic (Van den Hoek et al., 1995), so that the haploid sporophyte and diploid gametophyte are identical in appearance. Both phases produce numerous flagellated gametes.  However, sexual reproduction is not known Pseudendoclonium submarinum, which produces motile zoospores, non-motile aplanospores and dormant resting stages (akinetes) by asexual reproduction (Guiry & Guiry, 2016).  No information on reproduction in Endocladia was found.

Resilience assessment. The characteristic flora produce highly motile zoospores, as well as resting stages. Pseudendoclonium submarinum is probably also widespread and found on a range of substrata.  In California, USA, Seapy & littler (1982) reported that the Endoladia muricata and blue-green algae band on Santa Cruz Island died back but were not lost seasonally in the winter months due to aerial exposure, especially in the presence of hot dry winds. The Endoladia muricata and blue-green algae band recovered from a substantial die back in February 1976, to exceed its formaer abundnace by October 1976 (ca 6 months) only to die back again in February 1977. Although the species differ from the 'Endoderma' band, their life history charactersitcs are probalby similar. Therefore, recruitment and recolonization are probably rapid, within a one or two years, and resilience is probably High even where the entire community is removed. However, no direct evidence of recovery was found and the assessment is based on life history characteristics so that confidence in the assessment is Low.

Hydrological Pressures

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

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 ('Endoderma') 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 (i.e. between 4.9 and 22.6°C in spring and summer).  Anand (1937c) suggested that the 'Endoderma' belt was thin and closed adherent to the substratum so that it benefited from the thermal buffering effect of the rock itself. Chalk also retain moisture. However, the 'Endoderma' belt dominated in shaded and moist environments, such as chalk caves and tunnels walls and ceilings, which are protected from direct sunlight, and probably exhibit a smaller range of temperatures than cliff faces.  Seapy & Littler (1982) reported the seasonal die back of a similar Endocladia and blue-green algal band, on intertidal rock due to desiccation stress in the winter months on Santa Cruz Island, California. The die back was substantial when the intertidal was exposed to dry hot winds 10°C higher than average, in the winter of 1975-76. However, the band exceeded its prior cover within 6 months (Seapy & Littler, 1982). 

Sensitivity assessment.  Therefore, an increase in annual temperature (at the benchmark level) is likely to increase the risk of desiccation and exposure to high temperatures during summer depending on its shelter and aspect. However, populations in caves are likely to be protected from direct sunlight. In addition, Anand (19737c) noted that when the 'Chrysophyceae' belt was cracked and peeling due to desiccation, the 'Endoderma' belt could extend its range. Hence, resistance is assessed as High. Therefore, resilience is High and the biotope is recorded as Not sensitive at the benchmark level.

High
High
High
High
Help
High
High
High
High
Help
Not sensitive
Low
Low
Low
Help
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. Anand (1937b) noted that winter weather with reduced light favoured the Endoderma belt. 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. In addition, caves may gain some protection from frost, depending on their size and aspect.  Therefore, resistance is probably High, so that resilience is also High and Not sensitive has been recorded at the benchmark level.

High
Medium
Low
Low
Help
High
High
High
High
Help
Not sensitive
Low
Low
Low
Help
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. For example, 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. The 'Chrysophyceae' belt the salt concentration may be approximately three times that of seawater (Anand, 1937c). Pseudendoclonium submarinum (as Endoderma perforans) is a constant part of the 'Chrysophyceae' belt, growing within the belt and is, therefore, exposed to similar salinity conditions.  However, Anand (1937c) was unable to test the salinity range within the 'Endoderma' belt directly but noted that the 'Endoderma' was rarely wetted by spray except in rough weather, so that is was probably less exposed to 'salt' than the Chrysophyceae' belt (Anand, 1937b&c). In addition, caves are likely to retain moisture and be more humid than cliff faces as they are protected from wind and sunlight and direct rainfall, although rainwater could potentially percolate through soft rock.  Therefore, 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
Medium
High
Help
High
High
High
High
Help
Not sensitive
High
Medium
High
Help
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. For example, 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. The 'Chrysophyceae' belt the salt concentration may be approximately three times that of seawater (Anand, 1937c). Pseudendoclonium submarinum (as Endoderma perforans) is a constant part of the 'Chrysophyceae' belt, growing within the belt and is, therefore, exposed to similar salinity conditions.  However, Anand (1937c) was unable to test the salinity range within the 'Endoderma' belt directly but noted that the 'Endoderma' was rarely wetted by spray except in rough weather, so that is was probably less exposed to 'salt' than the Chrysophyceae' belt (Anand, 1937b&c). In addition, caves are likely to retain moisture and be more humid than cliff faces as they are protected from wind and sunlight and direct rainfall, although rainwater could potentially percolate through soft rock.  Therefore, 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 at the benchmark level.

High
High
Medium
High
Help
High
High
High
High
Help
Not sensitive
High
Medium
High
Help
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. Tidal influence in mid-littoral to supralittoral caves is probably is probably limited to the floor and sides of the caves, and the upper walls and ceilings only receive spray and splash. Therefore, the biotope is unlikely to be affected by water flow as described by the benchmark.  Therefore, the pressure is Not relevant.

Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
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 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' belt 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, although caves may be protected from direct rainfall (depending on aspect) and only receive freshwater via percolation.  Caves (and tunnels) retains moisture and are therefore dependent on wave action for spray and splash and rainfall to maintain the humidity of the atmosphere.

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. Anand (1937c) noted that in caves and tunnels where waves break  and spray reaches high levels, the 'Endoderma' belt showed more conspicuous growth. 

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, although mitigated by the humid cave environment,  and a resistance of Medium has been recorded.  Once prior conditions return, recovery is likely to be rapid so that resilience is probably High and sensitivity Low.

Medium
High
Medium
Medium
Help
High
Low
NR
NR
Help
Low
Low
Low
Low
Help
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.  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 or wave sheltered 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
Help
High
High
High
High
Help
Not sensitive
Low
Low
Low
Help

Chemical Pressures

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

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. However, this biotope is considered to be This pressure is Not assessed but evidence is presented where available.

Not Assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
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 or cave green algal communities was found.

Not Assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
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 or hard rock algal film 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 or hard rock algal film 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
Help
Not assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
Radionuclide contamination [Show more]

Radionuclide contamination

Benchmark. An increase in 10µGy/h above background levels. 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 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
Help
Not assessed (NA)
NR
NR
NR
Help
Not assessed (NA)
NR
NR
NR
Help
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, and cave ceilings 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
Help
Not relevant (NR)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
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. may overgrow the 'Endoderma' or 'Chrysophyceae' belts, but  Pseudendoclonium submarinum may benefit from nutrient enrichment,  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.

No evidence (NEv)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
No evidence (NEv)
NR
NR
NR
Help
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. may overgrow the 'Endoderma' or 'Chrysophyceae' belts, but  Pseudendoclonium submarinum may benefit from nutrient enrichment,  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.

No evidence (NEv)
NR
NR
NR
Help
Not relevant (NR)
NR
NR
NR
Help
No evidence (NEv)
NR
NR
NR
Help

Physical Pressures

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

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).  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., 1988). 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.  The resultant sea walls do not support the 'Chrysophyceae' algal communities, but the 'Endoderma' belt grew on both chalk and seawalls (Tittley & Shaw, 1980, Figure 11; Fowler & Tittley, 1993).  Titlley (1988) reported that Pseudendoclonium submarinum grew on chalk and hard chalk, sea walls, limestone, hard rock and flint in crevices and cracks. Nevertheless, coastal defence works also resulted in loss of caves or cut caves off from the influence of the sea (Fowler & Tittley, 1993).

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’), in this case, loss of caves themselves. 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 (Tittley et al., 1988; Fowler & Tittley, 1993). The resultant sea walls did not support the 'Chrysophyceae' algal communities, but the 'Endoderma' belt grew on both chalk and sea walls (Tittley & Shaw, 1980, Figure 11; Fowler & Tittley, 1993).  Anand (1937b) reported that the 'Endoderma' belt was replaced on embankments by a dark coloured band of the blue-green alga Pleurocapsa entophysaloides, the ChlorophyteTrebouxia humicola and Pseudendoclonium submarinum (as Endoderma perforans).  Titlley (1988) reported that Pseudendoclonium submarinum grew on chalk and hard chalk, sea walls, limestone, hard rock and flint in crevices and cracks.  Humm & Belt (1975) also recorded Pseudendoclonium submarinum from artificial substrata such as timber and bridge pilings.

Sensitivity assessment. Therefore, the 'Endoderma' belt that characterizes this biotope could grow on a range of soft or hard rock substrata. However, a change to sedimentary substrata, however unlikely, would result in the permanent loss of the biotope.  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
Help
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 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 'Endoderma' belts, 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 Pseudendoclonium submarinum ('Endoderma') 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
Low
NR
NR
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 in caves. or on vertical chalk cliffs. However, soft rock, by definition, can be damaged by other penetrative activities, for example during construction.  The Pseudendoclonium submarinum (Endoderma) 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
Low
NR
NR
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. Similarly, smothering of vertical walls and ceilings of caves is unlikely. 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. Similarly, smothering of vertical walls and ceilings of caves is unlikely. 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. Litter is unlikely to accumulate on vertical or steep slopes or cave ceilings.

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

Anand (1937b&c) reported that the Pseudendoclonium submarinum (as Endoderma perforans) was favoured within the Chrysophyceae belt, during diffuse light or short duration in winter.  Incident light in tunnels was considerably less than on cliff faces (Anand, 1937c) and the 'Endoderma' belt was more extensive in tunnels  than on cliff faces  Anand (1937b&c) noted that the Endoderma belt became very prominent and extended to the roof in well-illuminated caves, while the 'Chrysophyceae' belt was restricted to the entrance. The Chrysophyceae-Endoderma-Lyngbya community was also restricted to the entrance of caves but did not exhibit its usual brown colour, as it was green due to the growth of Pseudendoclonium submarinum.  Therefore, an increase in shading may benefit the 'Endoderma' belt, depending on intensity, as a complete lack of light would be detrimental for all algae. Resistance to shading is probably Medium. Hence, resilience is probably High and the sensitivity to change in light is probably Low.

Medium
Medium
Medium
Medium
Help
High
Low
NR
NR
Help
Low
Low
Low
Low
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 benchmarks, 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, supralittoral or caves 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 microalgae 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  Chlorophyceae 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.

No evidence (NEv)
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 or cave communities was found.

No evidence (NEv)
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

The microalgal communities characteristic of this biotope 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 'Endoderma' belt would probably remove the entire belt rather than specific characteristic species. Where present, mobile invertebrate fauna are probably not entirely dependent on the 'belt' for food or habitat and would forage elsewhere.  However, soft-rock and cave 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. Humm, H.J. & Bert, T.M., 1979. The Benthic Marine Algae of Timbalier Bay, Louisiana. Rice Institute Pamphlet-Rice University Studies, 65 (4), 379-399.

  20. Irvine, L. M. & Chamberlain, Y. M., 1994. Seaweeds of the British Isles, vol. 1. Rhodophyta, Part 2B Corallinales, Hildenbrandiales. London: Her Majesty's Stationery Office.

  21. 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/

  22. 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

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

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

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

  26. 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.

  27. Norton, T.A., Ebling, F.J. & Kitching, J.A., 1971. Light and the distribution of organisms in a sea cave. In Fourth European Marine Biology Symposium (ed. D.J. Crisp), pp.409-432. Cambridge: Cambridge University Press

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

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

  30. Seapy , R.R. & Littler, M.M., 1982. Population and Species Diversity Fluctuations in a Rocky Intertidal Community Relative to Severe Aerial Exposure and Sediment Burial. Marine Biology, 71, 87-96.

  31. 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).]

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

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

  34. 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.

  35. 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. Green algal films on upper and mid-shore cave walls and ceilings. In Tyler-Walters H. 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/1070

 Download PDF version


Last Updated: 08/03/2016

  1. Endoderma