Oligochaetes in full salinity littoral mobile sand

Summary

UK and Ireland classification

Description

A species-poor community of oligochaetes occurring in fully marine conditions on open shores with mobile, medium to fine, usually clean, sand. Oligochaetes, including enchytraeid oligochaetes, constitute the infaunal assemblage. On rare occasions individuals of polychaete or crustacean species may be encountered (e.g. Nephtys spp., Eurydice pulchra, Bathyporeia spp.), though these are not characterising for the biotope and if present in any significant abundance, the area should be classed as AmSco (JNCC, 2015).

Depth range

Upper shore, Mid shore, Lower shore

Additional information

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Listed By

Sensitivity reviewHow is sensitivity assessed?

Sensitivity characteristics of the habitat and relevant characteristic species

The biotope description and characterizing species is taken from (JNCC, 2015). This biotope comprises of a species-poor community of oligochaetes occurring in fully marine conditions. The sediment consists of mobile, medium to fine, usually clean sands. Oligochaetes, including enchytraeid oligochaetes, constitute the infaunal assemblage (these are not recorded to the species level), the sensitivity assessments are thus rather generic and based on Tubificid (largely based on Tubificoides benedii as this species is well studied) and Enchytraeid oligochaetes as most marine species  belong to these families (Giere & Pfannkuche, 1982). Although the evidence base for assessing sensitivity of oligochaetes is limited compared to other taxa, it is clear that there are species-specific responses to environmental factors and perturbations (Rodriguez  & Reynoldson, 2011) and the lack of species information is a key limitation in assessing sensitivity.

The sedimentary habitat and salinity conditions are key factors structuring this habitat and these factors are considered in the sensitivity assessments where the pressure may alter these.

Resilience and recovery rates of habitat

Usually for oligochaetes fertilization is internal and relatively few large eggs are shed directly into a cocoon that is secreted by the worm (Giere & Pfannkuche, 1982).  Asexual reproduction is possible in some species by spontaneous fission (Giere & Pfannkuche, 1982).  The naid oligochaete Panais litoralis can produce asexually producing clones, the rapid rate of increase (18 times pop[ulation abundance in 3 months, Gillett et al., 2007) allows this species (which is sensitive to high temperatures, hypoxia and is exposed to predation due to shallow burial) to repopulate rapidly when conditions are favourable.  However, few Tubificidae and Enchytraeidae produce asexually (Giere & Pfannkuche, 1982).

Tubificid populations tend to be large and to be constant throughout the year, although some studies have noticed seasonal variations (Giere & Pfannkuche, 1982). Many species, including Tubificoides benedii and Baltidrilus costata have a two-year reproductive cycle and only part of the population reproduces each season (Giere & Pfannkuche, 1982). Populations of Tubificoides benedii in the Fourth estuary have not demonstrated clear seasonality in recruitment (Bagheri & McLusky, 1982), although mature Tubificoides benedii (as Peloscolex benedeni) in the Thames Estuary were reported to occur in December with a maximum in late February (Hunter & Arthur, 1978), breeding worms increased from April and maximum cocoon deposition was observed in July (Hunter & Arthur, 1978). Tubificids exhibit many of the traits of opportunistic species. They often reach huge population densities in coastal areas that are enriched in organic matter and are often described as ‘opportunist’ species adapted to rapid environmental fluctuations and stress (Giere, 2006; Bagheri & McLusky, 1982). However, unlike other opportunist species they have a long-lifespan (a few years, Giere, 2006), a prolonged reproductive period from reaching maturity to maximum cocoon deposition and exhibit internal fertilisation, with brooding rather than pelagic dispersal. These factors mean that recolonization is slower than for some opportunistic species such as Capitella capitata and nematodes which may be present in similar habitats.

Bolam and Whomersley (2003) observed faunal recolonization of fine sediments placed on saltmarsh as a beneficial use and disposal of fine grained dredged sediments. They found that tubificid oligochaetes began colonising sediments from the first week following a beneficial use scheme involving the placement of fine-grained dredged material on a salt marsh in southeast England. The abundance of Tubificoides benedii recovered slowly in the recharge stations and required 18 months to match reference sites and those in the recharge stations prior to placement of sediments. The results indicate that some post-juvenile immigration is possible and that an in-situ recovery of abundance is likely to require more than 1 year.  Rapid recolonization has also been observed in the tubificid oligochaete  Baltidrilus costata (Tubifex costatus)  appeared  in upper sediment layer s in experimentally defaunated patches (4m2)  after 3 weeks (Gamenick et al., 1996).

Resilience assessment. In general there was little information found for Tubificoides benedii and other oligochaetes, but, taking into consideration the information above (particularly Bolam & Whomersley, 2003) , this review considers that the recoverability of this species is generally ‘High’, so that recovery from defaunation is suggested to occur within two years and that therefore, recovery from any impact (resistance is ‘None’,  ‘Low’ or ‘Medium’) is assessed as ‘High’.

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

Deeper burrowing oligochaetes are protected from fluctuations in temperature by the overlaying sediments which dampen changes if poorly drained (Giere & Pfannkuche, 1982).  Bamber & Spencer (1984) observed that Tubificoides were dominant species in an area affected by thermal discharge in the River Medway estuary.  Sediments were exposed to the passage of a temperature front of approximately 10oC between heated effluent and estuarine waters during the tidal cycles.

Increased temperature was found to trigger the onset of reproduction in Baltidrilus costata (studied as Tubifex costatus) in the Thames (Birtwell & Arthur, 1980). This effect was non-lethal and may be beneficial to populations.

Sensitivity assessment. The dominance of Tubificoides spp. when exposed to a heated effluent suggests that this genus would be highly resistant to an increase in temperature at the pressure benchmark. Biotope resistance is therefore assessed as ‘High’ and resilience as ‘High’ (by default), so that the biotope is considered to be ‘Not sensitive’.

High
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Not sensitive
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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

Most littoral oligochaetes, including tubificids and enchytraeids, can survive freezing temperatures and can survive in frozen sediments (Giere & Pfannkuche, 1982). Tubificoides benedii (studied as Peloscolex benedeni) recovered after being frozen for several tides in a mudflat (Linke, 1939).

Sensitivity assessment. Based on freezing tolerances of Tubificoides benedii (Linke, 1939) biotope resistance is assessed as ‘High’ to decreases in temperature. Resilience is assessed as ‘High’ (by default) and the biotope is therefore considered to be ‘Not sensitive’.

High
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Not sensitive
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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

This biotope is present in full (30-35 ppt) salinity habitats (JNCC, 2015), a change at the pressure benchmark, therefore, represents a change from full salinity (30-35 ppt) to hypersalinity (>40 ppt). No evidence was found to support an assessment and this pressure.

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

This biotope is present in full salinity habitats (JNCC, 2015); a change at the pressure benchmark therefore represents a change from full to reduced (18-30 ppt) or variable (18-35 ppt) salinity. The assessed biotope occurs as a sub-biotope of LS.LSa.MoSa.OL., a very similar sub-biotope variant that occurs in variable salinity is also recognised  (LS.LSa.MoSa.Ol.VS)  It is therefore considered that a decrease in salinity at the pressure benchmark would result in biotope reclassification to LS.LSa.MoSa.Ol.VS.  

Sensitivity assessment. A reduction in salinity at the pressure benchmark may lead to species replacement and biotope reclassification to LS.LSa.MoSa.Ol.VS. Biotope resistance is therefore assessed as ‘None’ and resilience as ‘High’ (following a return to usual habitat conditions), so that biotope sensitivity is assessed as ‘Medium’.

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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

This biotope is found in areas where tidal streams are moderately strong (<1.5-3 m/s), (JNCC, 2015).  Increases and decreases in water velocity may lead to increased erosion or deposition. The associated pressures alteration to sediment type and siltation are assessed separately.

 Experimental increases in near-bed current velocity were achieved over intertidal sandflats by placing flumes on the sediment to accelerate water flows (Zuhlke & Reise, 1994). The increased flow led to the erosion of up to 4cm depth of surface sediments.  No significant effect was observed on the abundance of Capitella capitata and numbers of Tubificoides benedii and Tubificoides pseudogaster were unaffected, as they probably avoided suspension by burrowing deeper into sediments. This was demonstrated by the decreased abundance of oligochaetes in the 0-1cm depth layer and increased abundance of oligochaetes deeper in sediments (Zuhlke & Reise, 1994).  A single storm event had a similar result with decreased abundance of oligochaetes in surficial layers, coupled with an increase in deeper sediments (Zuhlke & Reise, 1994). Although Tubificoides spp. can resist short-term disturbances their absence from sediments exposed to higher levels of disturbance indicate that they would be sensitive to longer-term changes in sediment mobility (Zuhlke & Reise, 1994). Birtwell and Arthur (1980) reported seasonal changes in abundance in Baltidrilus costata (as Tubifex costatus) which they attributed to erosion of the upper sediment layers caused by high river flows and wave action.

 Decreases in water flow with increased siltation of fine particles may alter the physical character of this habitat type as it is already found in sheltered areas. Reductions in waterflow occurring through the presence of trestles (for off-bottom oyster cultivation) arranged in parallel rows in the intertidal area (Goulletquer & Héral, 1997) reducing the strength of tidal currents (Nugues et al., 1996) has been observed to limit the dispersal of pseudofaeces and faeces in the water column and thus increase the natural sedimentation process by several orders of magnitude (Ottman & Sornin, 1985, summarised in Bouchet & Sauriau, 2008). As the characterizing oligochaetes can live relatively deeply buried and in depositional environments with low water flows (based on habitat preferences) and low oxygenation they are considered to be not sensitive to decreases in water flow, however deposition and increases in muds is likely to result in biotope reclassification.

Sensitivity assessment. Where increased or decreased water flows alter the sediment type this could lead to sediment reclassification, this change is assessed in the sedimentary change assessment. An increase at the pressure benchmark may lead to increased erosion of sands and disturb the upper layers. Biotope resistance is assessed as ‘Low’ as mobile sands may be present in stronger sands than recorded for this biotope and as particle redistribution may occur during the tidal cycle preventing complete erosion and subsequent loss of the habitat and oligochaetes  (JNCC, 2015). Resilience is assessed as ‘High’ (following restoration of usual conditions) and sensitivity is assessed as ‘Low’. The biotope is also  considered sensitive to decreased flows 9exceedingh the pressure benchmark) as deposition of muds may result in biotope reclassification.

Low
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Low
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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

This biotope is found on the lower shore, mid shore and upper shore (JNCC, 2015). As habitats from the sublittoral to the supralittoral are habitable for tubificds and enchytraeid oligochaetes (Giere, 1993) the biotope is not considered sensitive to changes in emergence that alter emergence periods. The characterizing species are found in subtidal biotopes and a change in tidal regime that led to this biotope becoming permanently submerged would result in biotope reclassification to a biotope such as SS.SMu.SMuVS.OlVS (oligochaetes in variable or reduced salinity infralittoral muddy sediment ).

Sensitivity assessment. The biotope based on the biological assemblage is considered to have ‘High’ resistance to changes in emergence and ‘High’ resilience (by default), so that the biotope is considered to be ‘not sensitive to this pressure at the benchmark. 

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Not sensitive
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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

This biotope occurs in habitats where estimated wave exposure ranges from exposed to moderately exposed to sheltered (JNCC, 2015). Disturbance of sediment by waves may reduce oligochaete abundance (Giere, 1977) and oligochaetes may be absent from very wave exposed shores (Giere & Pfannkuche, 1982 and references therein).  As this biotope occurs across a range of wave exposures this is considered to indicate, by proxy, that resistance is ‘High’ and resilience as ‘High’ by default and the biotope is considered to be ‘Not sensitive’. 

High
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High
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Not sensitive
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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.

Contamination at levels exceeding the pressure benchmark may have negative effects. A 2-year microcosm experiment was undertaken to investigate the impact of copper on the benthic fauna of the lower Tyne Estuary (UK) by Hall & Frid (1995). During a 1-year simulated contamination period, 1 mg l−1copper was supplied at 2-weekly 30% water changes, at the end of which the sediment concentrations of copper in contaminated microcosms reached 411 μg g−1. Toxicity effects reduced populations of the four dominant taxa including Tubificoides spp.). When copper dosage was ceased and clean water supplied, sediment copper concentrations fell by 50% in less than 4 days, but faunal recovery took up to 1 year, with the pattern varying between taxa. Since the copper leach rate was so rapid it is concluded that after remediation, contaminated sediments show rapid improvements in chemical concentrations, but faunal recovery may be delayed taking up to a year.

Rygg (1985) classified Tubificoides spp as highly tolerant species, common at the most copper polluted stations (>200 mg Kg-1) in Norwegian fjords.

Not Assessed (NA)
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Not assessed (NA)
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Not assessed (NA)
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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 but evidence is presented where available.

In Finland in oligohaline inland waters near an oil refinery, Baltidrilus costata (as Tubifex costatus) appeared to be sensitive to oil pollution and had completely disappeared from sediments exposed to pollution and did not recolonize during a four year post pollution period (Leppäkoski & Lindström, 1978). Tubificoides benedii appears to be more tolerant and was found in UK waters near oil refineries as the sole surviving member of the macrofauna. Populations were however apparently reduced and the worms were absent from areas of oil discharge and other studies indicate sensitivity to oiling (Giere & Pfannkuche, 1982, references therein).

Not Assessed (NA)
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Not assessed (NA)
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Not assessed (NA)
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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.

Not Assessed (NA)
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Not assessed (NA)
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Not assessed (NA)
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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 for radionuclide uptake by marine oligochaetes.

No evidence (NEv)
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No evidence (NEv)
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No evidence (NEv)
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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)
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Not assessed (NA)
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Not assessed (NA)
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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

Oligochaete species vary in their tolerance of hypoxia and associated high sulphide levels. Most enchytraeids and naidids are sensitive to hydrogen sulphide and hypoxia while tubificids are often more resistant (Giere, 2006).

Tubificoides benedii has a high capacity to tolerate anoxic conditions, its extreme oxygen tolerance  is based on an unusually low respiration rate (Giere et al., 1999).  Respiration rates of Tubificoides benedii measured at various oxygen concentrations showed that aerobic respiration is maintained even at very low oxygen concentrations (Giere et al., 1999). Birtwell & Arthur (1980) showed that Tubificoides benedii could tolerate anoxia in the Thames Estuary (LT50 = 58.8 hours at 20oC, 26.6 hours at 25oC  and 17.8 hours at 30oC in experiments with worms acclimated to 20oC.)

Tolerance experiments by Gamenick et al.  (1996) found that Baltidrilus costata  (as Heterochaeta  costata) was not affected by hypoxic conditions for at least 3 days but the addition of sulphide 91.96 mmol/litre) caused mortality after 1 day (Gamenick et al., 1996)

Sensitivity assessments. As this biotope is found in the intertidal oxygen levels will be recharged during the tidal cycle lowering exposure to this pressure for worms that migrate to surface layers. Based on the reported tolerances for anoxia, biotope resistance is assessed as ‘High’ based on Tubifioides benedii, resilience is assessed as ‘High’ (by default) and the biotope is considered to be ‘Not sensitive’.

High
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High
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Not sensitive
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Nutrient enrichment [Show more]

Nutrient enrichment

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

Evidence

In nutrient enriched tidal sediments oligochaetes can dominate assemblages (Gray, 1971; Leppäkoski, 1975; Birtwell & Arthur, 1980). Green algae such as Ulva spp. may form mats on the surface of the mud during the summer months, particularly if nutrient enrichment occurs.

Sensitivity assessment. As the benchmark is relatively protective and would not lead to blooms of Ulva spp. (although green algae may be present on the surface layers of sediments in the summer), biotope resistance is assessed as ‘High’, resilience is assessed as ‘High’ and the biotopeis considered to be ‘Not sensitive’.

High
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Not sensitive
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Organic enrichment [Show more]

Organic enrichment

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

Evidence

Tubificoides benedii and Baltidrilus costatus are both very tolerant of high levels of organic enrichment and often dominate sediments where sewage has been discharged or other forms of organic enrichment have occurred (Pearson & Rosenberg, 1978; Gray, 1971; McLusky et al., 1980). Their tolerance for organic enrichment is attributed to their adaptation to live in and feed on enriched organic deposits (Pearson & Rosenberg, 1978) and their high population densities in such areas is enhanced by the lack of predation and competition. Tubificoides benedii are abundant in mussel beds (mussel relaying may be the source of smothering) which  has been attributed to their tolerance of organically rich deoxygenated sediment (Commito & Boncavage, 1989). Tubificoides benedii has also been found in elevated abundances in areas of organic enrichment around fish farms (Haskoning, 2006).

Sensitivity assessment. Based on the high tolerance of the characterizing species Tubificoides benedii for organic enrichment, biotope resistance is assessed as ‘High’ and resilience as ‘High’, so that the biotope is considered to be Not sensitive’.

High
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Not sensitive
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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

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
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Very Low
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High
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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

A change to an artificial or natural hard substratum would significantly alter the habitat type. The oligochaetes, nemerteans and nematodes that characterize this biotope are infaunal species living within sediment. If the changed habitat contained pockets of sediment these species may still be present but the habitat will be unsuitable overall and the biotope will be reclassified. The presence of hard substratum is likely to support colonization by filamentous green and red algae tolerant of variable salinity.

Sensitivity assessment. Based on the loss of the biotope, resistance is assessed as ‘None’, recovery is assessed as ‘Very low’ (as the change at the pressure benchmark is permanent) and sensitivity is assessed as ‘High’.

None
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Very Low
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High
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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

This biotope is characterterized by mobile clean sands (JNCC, 2015). The sediment type present reflects the habitats in which this biotope occurs where wave action removes finer particles. Oligochaete dominated biotopes occur in a range of sedimentary habitats. Although the lack of identification to species level has hampered understanding of species preferences (and the species that typically occur in this biotope) it is clear that at least some species exhibit strong p[references for sediment type. Tubificoides heterochaetusfor example, sampled in South Carolina salt marsh and tidal inlets was found in significantly greater abundances in coarser sediments where silt and clay fractions were lower (Gillett et al., 2007).

A change in sediment type (without a change in salinity) may therefore lead to species replacement, although an oligochaete dominated biotope may remain. Tubificoides benedii (studied as Peloscolex benedeni) are found in a range of substratum types from sandy mixed habitats, fine sands and coarse sands (Giere & Pfannkuche, 1982). Similarly, Baltidrilus costata (asTubifex costatus) is found in mud/silts (Giere & Pfannkuche,1982). Giere & Pfannkuche (1982) suggest that factors that correlate to substratum types such as organic matter availability, size and shape of the intertstitial space between grains, the level of sediment disturbance and water content, rather than the sediment type alone are the key factors influencing distribution.

Sensitivity assessment.  A change in sediment type is likely to result in biotope reclassification (although a similar infaunal assemblage may be present). Based on the loss of the biotope as classified, resistance is assessed as ‘None’ and resilience as ‘Very Low’ (as the change at the pressure benchmark is permanent). Sensitivity is therefore assessed as ‘High’.

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Very Low
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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

Sedimentary communities are likely to be highly intolerant of substratum removal, which will lead to partial or complete defaunation, expose underlying sediment which may be anoxic and/or of a different character or bedrock and lead to changes in the topography of the area (Dernie et al., 2003). Any remaining species, given their new position at the sediment / water interface, may be exposed to conditions to which they are not suited, Removal of 30 cm of surface sediment will remove the oligochaete community and other species present in the biotope. Recovery of the biological assemblage may take place before the original topography is restored, if the exposed, underlying sediments are similar to those that were removed. Hydrodynamics and sedimentology (mobility and supply) influence the recovery of soft sediment habitats (Van Hoey et al. 2008).

Sensitivity assessment. Extraction of 30 cm of sediment will remove the characterizing biological component of the biotope. Resistance is assessed as ‘None’ and biotope resilience is assessed as ’High’.  Biotope sensitivity is therefore ‘Medium’. 

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Medium
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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

Tubificoides benedii can be relatively deeply buried and could avoid direct exposure to abrasion although sediment disturbance and compaction could damage these soft-bodied species and oligochaetes in general are not found in high abundances in sediments with high levels of disturbance from wave action.

Experimental studies on crab-tiling impacts have found that densities of Tubificoides benedii and Tubificoides pseudogaster were higher in non-trampled plots (Sheehan et al. 2010), indicating that these oligochaetes have some sensitivity to trampling. Whomersley et al., (2010) conducted experimental raking on intertidal mudflats at two sites (Creeksea- Crouch estuary England and Blackness- lower Forth estuary, Scotland), where Tubificoides benedii were dominant species. For each treatment 1 m2 plots were raked twice to a depth of 4cm (using a garden rake). Plots were subject to either low intensity treatments (raking every four weeks) or high (raking every two weeks). The experiment was carried out for 10 months at Creeksea and a year at Blackness. The high and low raking treatments appeared to have little effect on Tubificoides benedii (Whomersley et al., 2010)

Sensitivity assessment. The experiments by Whomersley et al. (2010), suggest that disturbance of the surficial layers has little effect on Tubificoides benedii. Many individuals are likely to be buried more deeply and can migrate to the surface following disturbance, so that little impact is observed through sampling. Abrasion with associated compaction (as in trampling) may have a greater impact. Resistance is therefore assessed as ‘medium’ and resilience as ‘High’ (by default) so that sensitivity is assessed as ‘Low’.

Medium
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Low
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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

Tubificoides benedii can be relatively deeply buried and could avoid direct exposure to penetration and disturbance of upper sediment layers although sediment disturbance and compaction could damage these soft-bodied species and oligochaetes in general are not found in high abundances in sediments with high levels of disturbance from wave action.

Whomersley et al., (2010) conducted experimental raking on intertidal mudflats at two sites (Creeksea- Crouch estuary England and Blackness- lower Forth estuary, Scotland), where Tubificoides benedii were dominant species. For each treatment 1 m2 plots were raked twice to a depth of 4cm (using a garden rake). Plots were subject to either low intensity treatments (raking every four weeks) or high (raking every two weeks). The experiment was carried out for 10 months at Creeksea and a year at Blackness. The high and low raking treatments appeared to have little effect on Tubificoides benedii (Whomersley et al., 2010). These results are supported by observations that two experimental passes of an oyster dredge that removed the sediment to a depth of between 15-20 cm did not significantly affect Tubifcoides benedii (EMU, 1992).

Sensitivity assessment. The experiments by Whomersley et al., (2010) and EMU (1992), suggest that penetration and disturbance of the upper surface  has little effect on Tubificoides benedii. Many individuals are likely to be buried more deeply and can migrate to the surface following disturbance, so that little impact is observed through sampling. Resistance is therefore assessed as ‘Medium’ and resilience as ‘High’ so that sensitivity is assessed as ‘Low’.

Medium
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High
High
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Low
High
High
High
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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 biological assemblage characterizing this biotope is infaunal and consists of sub-surface deposit feeders. Increased suspended solids are unlikely to have an impact and resistance is assessed as ‘High’ and resilience as ‘High’, so that the biotope is considered to be ‘not sensitive’. A reduction in suspended solids may reduce deposition and supply of organic matter, resistance to a decrease is therefore assessed as ‘Medium’ as a shift between deposition and erosion could result in the net loss of surficial sediments. A reduction in organic matter as suspended solids could also reduce production within this biotope. Resistance is assessed as ‘Medium’ as over a year the impact may be relatively small and resistance is assessed as ‘High’, following restoration of usual conditions. Biotope sensitivity is therefore assessed as ‘Low’. 

Medium
Low
NR
NR
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High
High
Low
High
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Low
Low
Low
Low
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

This biotope occurs in areas of mobile sediments and it is likely that the assemblage present undergoes periodic burial as sedimentsshift following increased wave action or water flow. Oligochaete dominated biotopes may occur in sheltered accreting environments such as intertidal mudflats, where deposition rather than erosion is the dominant process, this means that the assemblages present (primarily deposit feeders) are adapted to natural levels of siltation through life history traits and can withstand burial (by repositioning in sediment or similarly extending tubes or feeding and respiration structures above the sediment surface). At low levels of siltation the high bioturbatory nature of mudflat organisms decreases sensitivity to effects (Elliott et al. 1998) as sediment turnover rates are relatively rapid. Tubificoides live relatively deeply buried and can tolerate periods of low oxygen that may occur following the deposition of a fine layer of sediment. In addition the presence of this species in areas experiencing deposition, such as estuaries, indicate that this species is likely to have a high tolerance to siltation events. Tubificoides spp. showed some recovery through vertical migration following the placement of a sediment overburden 6cm thick on top of sediments (Bolam, 2011).

Whomersley et al., (2010) experimentally buried plots on intertidal mudflats at two sites (Creeksea- Crouch Estuary, England and Blackness- lower Forth Estuary, Scotland), where Tubificoides benedii were dominant species. For each treatment anoxic mud was spread evenly to a depth of 4cm on top of each treatment plot. The mud was taken from areas adjacent to the plots, and was obtained by scraping off the surface oxic layer and digging up the underlying mud from approximately 20cm depth. Plots were subject to either low intensity treatments (burial every four weeks) or high (burial every two weeks). The experiment was carried out for 10 months at Creeksea and a year at Blackness. At Creeksea numbers of Tubificoides benedii increased in both burial treatments until the third month (high burial) and sixth month (low burial). At Blackness increased numbers of Tubificoides benedii  were found in both burial treatments after one month (Whomersley et al., 2010). 

Sensitivity assessment. The characterizing species Tubificoides benedii is considered to be able to survive under a deposit of fine grained sediment up to 5cm thick and to burrow and reposition within this. The assessment is supported by the burial experiments conducted by Whomersley et al. (2010). Although fine sediments are cohesive, water flows within the biotope may remove the deposit mitigating the effects.

High
High
High
High
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High
High
High
High
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Not sensitive
High
High
High
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

The pressure benchmark (30 cm deposit) represents a significant burial event and the deposit may be rapifdle removed by water flows and wave action, mitigating effects, or may remain for some time in upper shore examples that are submerged for only short periods. Some impacts on Tubificoides benedii and other characterizing oligochaetes may occur and it is considered unlikely that signficiant numbers of the population could reposition, based on (Bolam, 2011). Placement of the deposit will therefore result in a defaunated habitat until the deposit is recolonized. Biotope resistance is therefore assessed as 'Low' as some removal of deposit and vertical migration through the deposit may occur. Resilience is assessed as 'High' as migration and recolonization of oligochaetes is likely to occur within two years, biotope sensitivity is therefore assessed as 'Low'.

Low
High
Low
NR
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High
High
Low
High
Help
Low
High
Low
Low
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
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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

A number of studies have investigated the effects of electromagnetic fields on terrestrial oligochaetes, notable earthworms. Some negative effects have been observed e.g. Tkalec et al., 2013. However no evidence was found to support an assessment at the pressure benchmark for the marine oligochaetes that characterize this biotope.

No evidence (NEv)
NR
NR
NR
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No evidence (NEv)
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.

Not relevant (NR)
NR
NR
NR
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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

No evidence was found to assess this pressure. Studentowicz (1936) found that the enchytraeid oligochaete  Enchytraeus albidus, retracted from light, although the worms accumulated at the surface even when illuminated to avoid low oxygen and hydrogen sulpfide.  Giere and Pfannkuche (1982) considered that other enchytraeids and tubificids are likely to react in the same way. As the biological assemblage occurs within the sediment and can be deeply buried (to 10cm or more) this pressure is considered ‘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
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

As the tubificid oligochaetes that characterize this biotope have benthic dispersal strategies (via egg cocoons laid on the surface, Giere & Pfannkuche, 1982), water transport is not a key method of dispersal over wide distances, as it is for some marine invertebrates that produce pelagic larvae.  The biotope (based on the biological assemblage) is therefore considered to have ‘High’ resistance to the presence of barriers that lead to a reduction in tidal excursion, resilience is assessed as ‘High’ (by default) and the biotope is considered to be ‘not sensitive’.

High
Low
NR
NR
Help
High
High
High
High
Help
Not sensitive
Low
Low
Low
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

Not relevant’ to seabed habitats.  NB. Collision by grounding vessels is addressed under ‘surface abrasion.

Not relevant (NR)
NR
NR
NR
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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

Most aquatic oligochaetes have no eyes although a few have simple ocelli (eyspots) which are light receptors. Visual disturbance is not considered relevant to this biotope.

Not relevant (NR)
NR
NR
NR
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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

Key characterizing species within this biotope are not cultivated or translocated. This pressure is therefore considered ‘Not relevant’ to this biotope group.

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

The mobility of the sediment, coupled with the variable salinity may prevent colonization by most non-indigenous species. No examples were found. The polychaete Marenzellaria viridis has become established in estuaries in Europe but a recent paper on its impacts where Tubificoides were abundant did not report on oligochaete impacts (Delefosse et al., 2012).

Sensitivity assessment. As the biotope characteristics are likely to limit colonization of this biotope, resistance is assessed as 'High', resilience as 'High' and the biotope is conisdered to be be 'Not sensitive'. This assessment may need revising based on future surveys or new species colonizing the UK.

High
Low
NR
NR
Help
High
High
High
High
Help
Not sensitive
Low
Low
Low
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

Marine oligochaetes host numerous protozoan parasites without apparent pathogenic effects even at high infestation levels  (Giere & Pfannkuche, 1982 and references therein)

Sensitivity assessment. Based on the lack of evidence for mass mortalities in oligochaetes from microbial pathogens resistance is assessed as ‘High’ and resilience as ‘High’, by default, so that the biotope is assessed as ‘Not sensitive’.

High
High
High
Low
Help
High
High
High
High
Help
Not sensitive
High
High
Low
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

No species within the biotope are targeted by commercial or recreational fishers or harvesters. This pressure is therefore considered ‘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
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 characterizing species would alter the character of the biotope and the delivery of ecosystem services such as secondary production and bioturbation. Populations of oligochaetes provide food for macroinvertebrates fish and birds. For example up to 67% of flounder and plaice stomachs examined from the Medway estuary (UK) (Van den Broek, 1978) contained the remains of Tubificoides benedii ​(studied as Peloscolex benedeni) and shrimps which in turn support higher trophic levels (predatory birds and fish). For some migratory birds the characterizing species Tubificoides benedii can form an important part of the diet during winter (Bagheri & McLusky, 1984). Polychaetes and crustaceans are also predators of oligochaetes and may significantly reduce numbers (Giere & Pfannkuche, 1982 and references therein). The loss of the oligochaete population could, therefore,  impact other trophic levels.

Sensitivity assessment. Removal of the characterizing species would alter the character of the biotope. Resistance is, therefore, assessed as ‘Low’ and resilience as ‘High’ so that sensitivity is categorised as ‘Low’.

Low
Low
NR
NR
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High
High
Low
High
Help
Low
Low
Low
Low
Help

Bibliography

  1. Bagheri, E. & McLusky, D., 1982. Population dynamics of oligochaetes and small polychaetes in the polluted forth estury ecosystem. Netherlands Journal of Sea Research, 16, 55-66.

  2. Bagheri, E.A. & McLusky, D.S., 1984. The oxygen consumption of Tubificoides benedeni (Udekem) in relation to temperature and its application to production biology. Journal of Experimental Marine Biology and Ecology, 78, 187-197.

  3. Bamber, R.N. & Spencer, J.F. 1984. The benthos of a coastal power station thermal discharge canal. Journal of the Marine Biological Association of the United Kingdom, 64, 603-623.

  4. Birtwell, I.K. & Arthur, D.R., 1980. The ecology of tubificids in the Thames Estuary with particular reference to Tubifex costatus (Claparède). In Proceedings of the first international symposium on aquatic oligochaete biology, Sydney, British Colombia, Canada, May 1-4, 1979. Aquatic oligochaete biology (ed. R.O. Brinkhurst & D.G. Cook), pp. 331-382. New York: Plenum Press

  5. Bolam, S. & Whomersley, P., 2003. Invertebrate recolonization of fine-grained beneficial use schemes: An example from the southeast coast of England. Journal of Coastal Conservation, 9 (2), 159-169.

  6. Bolam, S.G., 2011. Burial survival of benthic macrofauna following deposition of simulated dredged material. Environmental Monitoring and Assessment, 181 (1-4), 13-27.

  7. Bouchet, V.M. & Sauriau, P.-G., 2008. Influence of oyster culture practices and environmental conditions on the ecological status of intertidal mudflats in the Pertuis Charentais (SW France): A multi-index approach. Marine Pollution Bulletin, 56 (11), 1898-1912.

  8. Brinkhurst, R. & Kennedy, C., 1962. Some aquatic Oligochaeta from the Isle of Man with special reference to the Silver Burn Estuary. Archive fur Hydrobiologie, 58 (3), 367-766.

  9. Commito, J.A. & Boncavage, E.M., 1989. Suspension-feeders and coexisting infauna: an enhancement counterexample. Journal of Experimental Marine Biology and Ecology, 125 (1), 33-42.

  10. Commito, J.A., 1987. Adult-larval interactions: predictions, mussels and cocoons. Estuarine, Coastal and Shelf Science, 25, 599-606.

  11. Delefosse, M., Banta, G.T., Canal-Vergés, P., Penha-Lopes, G., Quintana, C.O., Valdemarsen, T. & Kristensen, E., 2012. Macrobenthic community response to the Marenzelleria viridis (Polychaeta) invasion of a Danish estuary. Marine Ecology Progress Series, 461, 83-94.

  12. Dernie, K.M., Kaiser, M.J., Richardson, E.A. & Warwick, R.M., 2003. Recovery of soft sediment communities and habitats following physical disturbance. Journal of Experimental Marine Biology and Ecology, 285-286, 415-434.

  13. Elliot, M., Nedwell, S., Jones, N.V., Read, S.J., Cutts, N.D. & Hemingway, K.L., 1998. Intertidal sand and mudflats & subtidal mobile sandbanks (Vol. II). An overview of dynamic and sensitivity for conservation management of marine SACs. Prepared by the Scottish Association for Marine Science for the UK Marine SACs Project. Available from: http://ukmpa.marinebiodiversity.org/uk_sacs/pdfs/sandmud.pdf

  14. EMU, 1992. An experimental study on the impact of clam dredging on soft sediment macro invertebrates. English Nature Research Reports. No 13.

  15. Gamenick, I., Jahn, A., Vopel, K. & Giere, O., 1996. Hypoxia and sulphide as structuring factors in a macrozoobenthic community on the Baltic Sea shore: Colonization studies and tolerance experiments. Marine Ecology Progress Series, 144, 73-85. DOI https://doi.org/10.3354/meps144073

  16. Giere, O., 1977. An ecophysiological approach to the microdistribution of meiobenthic Oligochaeta. I. Phallodrilus monospermathecus (Knöllner)(Tubificidae) from a subtropical beach at Bermuda. Biology of benthic organisms. Pergamon Press New York, 285-296.

  17. Giere, O., 2006. Ecology and biology of marine oligochaeta–an inventory rather than another review. Hydrobiologia, 564 (1), 103-116.

  18. Giere, O. & Pfannkuche, O., 1982. Biology and ecology of marine Oligochaeta, a review. Oceanography and Marine Biology, 20, 173-309.

  19. Giere, O., Preusse, J. & Dubilier, N. 1999. Tubificoides benedii (Tubificidae, Oligochaeta) - a pioneer in hypoxic and sulfide environments. An overview of adaptive pathways. Hydrobiologia, 406, 235-241.

  20. Gillett, D.J., Holland, A.F. & Sanger, D.M., 2007. On the ecology of oligochaetes: monthly variation of community composition and environmental characteristics in two South Carolina tidal creeks. Estuaries and Coasts, 30 (2), 238-252.

  21. Goulletquer, P. & Heral, M., 1997. Marine molluscan production trends in France: from fisheries to aquaculture. NOAA Tech. Rep. NMFS, 129.

  22. Gray, J.S., 1971. The effects of pollution on sand meiofauna communities. Thalassia Jugoslovica, 7, 76-86.

  23. Hall, J.A. & Frid, C.L.J., 1995. Response of estuarine benthic macrofauna in copper-contaminated sediments to remediation of sediment quality. Marine Pollution Bulletin, 30 (11), 694-700. DOI https://doi.org/10.1016/0025-326x(95)00051-n

  24. Haskoning UK Ltd. 2006. Investigation into the impact of marine fish farm deposition on maerl beds. Scottish Natural Heritage Commissioned Report No. 213 (ROAME No. AHLA10020348).

  25. Hunter, J., & Arthur, D.R., 1978. Some aspects of the ecology of Peloscolex benedeni Udekem (Oligochaeta: Tubificidae) in the Thames estuary. Estuarine and Coastal Marine Science, 6, 197-208.

  26. 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/

  27. 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/

  28. Leppäkoski, E. & Lindström, L., 1978. Recovery of benthic macrofauna from chronic pollution in the sea area off a refinery plant, southwest Finland. Journal of the Fisheries Board of Canada, 35 (5), 766-775.

  29. Leppäkoski, E., 1975. Assessment of degree of pollution on the basis of macrozoobenthos in marine and brackish water environments. Acta Academiae Åboensis, Series B, 35, 1-90.

  30. Linke, O., 1939. Die Biota des Jadebusenwatts. Helgolander Wissenschaftliche Meeresuntersuchungen, 1, 201-348.

  31. McLusky, D.S., 1982. The impact of petrochemical effluent on the fauna of an intertidal estuarine mudflat. Estuarine, Coastal and Shelf Science, 14, 489-499.

  32. McLusky, D.S., Teare, M. & Phizachlea, P., 1980. Effects of domestic and industrial pollution on distribution and abundance of aquatic oligochaetes in the Forth estuary. Helgolander Wissenschaftliche Meeresuntersuchungen, 33, 384-392.

  33. Nugues, M., Kaiser, M., Spencer, B. & Edwards, D., 1996. Benthic community changes associated with intertidal oyster cultivation. Aquaculture Research, 27 (12), 913-924.

  34. Parr, W., Clarke, S.J., Van Dijk, P., Morgan, N., 1998. Turbidity in English and Welsh tidal waters. Report No. CO 4301/1 to English Nature.

  35. Pearson, T.H. & Rosenberg, R., 1978. Macrobenthic succession in relation to organic enrichment and pollution of the marine environment. Oceanography and Marine Biology: an Annual Review, 16, 229-311.

  36. Rygg, B., 1985. Effect of sediment copper on benthic fauna. Marine Ecology Progress Series, 25, 83-89.

  37. Sheehan, E., Coleman, R., Thompson, R. & Attrill, M., 2010. Crab-tiling reduces the diversity of estuarine infauna. Marine Ecology Progress Series, 411, 137-148.

  38. Studentowicz, J., 1936. Der Einfluss des Lichtes auf das Verhalten des Oligochaeten Enchytraeus albidus Henle: Bulletin International Academy of Polish Science Letters, Series B. .

  39. Tang, M. & Kristensen, E., 2010. Associations between macrobenthos and invasive cordgrass, Spartina anglica, in the Danish Wadden Sea. Helgoland Marine Research, 64 (4), 321-329.

  40. Van den Broek, W., 1978. Dietary habits of fish populations in the Lower Medway Estuary. Journal of Fish Biology, 13 (5), 645-654.

  41. Van Hoey, G., Guilini, K., Rabaut, M., Vincx, M. & Degraer, S., 2008. Ecological implications of the presence of the tube-building polychaete Lanice conchilega on soft-bottom benthic ecosystems. Marine Biology, 154 (6), 1009-1019.

  42. Verdonschot, P., Smies, M. & Sepers, A., 1982. The distribution of aquatic oligochaetes in brackish inland waters in the SW Netherlands. Hydrobiologia, 89 (1), 29-38.

  43. Whomersley, P., Huxham, M., Bolam, S., Schratzberger, M., Augley, J. & Ridland, D., 2010. Response of intertidal macrofauna to multiple disturbance types and intensities – an experimental approach. Marine Environmental Research, 69 (5), 297-308.

  44. Zühlke, R. & Reise, K., 1994. Response of macrofauna to drifting tidal sediments. Helgoländer Meeresuntersuchungen, 48 (2-3), 277-289.

Citation

This review can be cited as:

Tillin, H.M. 2016. Oligochaetes in full salinity littoral mobile sand. In Tyler-Walters H. and Hiscock K. Marine Life Information Network: Biology and Sensitivity Key Information Reviews, [on-line]. Plymouth: Marine Biological Association of the United Kingdom. [cited 28-03-2024]. Available from: https://www.marlin.ac.uk/habitat/detail/1098

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Last Updated: 01/06/2016