Amblystegium serpens
Common Name: Creeping Feathermoss Conservation Status - Least Concern (Campisi, et. al., 2019)
Previously had one subspecies in the UK, var. salinum, which was smaller and associated with coastal areas, but it has recently been downgraded to just an ecotype (BBIS, n.d.; Blockeel, 2010). Another subspecies, var. juratzkranum, may exist in Europe, however, it is not found in the UK and opinions on whether it should be considered just a subspecies or species in its own right are conflicted (Blockeel, 2014; Meinunger and Schröder 2007; Smith & Smith, 2004).
Appearance and Identification
A. serpens is a mid-dark green, pleurocarpous moss which grows in large, extensive patches of slender shoots, either in loosely intertwined wefts or as rough mats which trail across the ground. Shoots are 1-2cm long with small (0.5mm), irregularly branched leaves which stick out from the shoots, giving a soft, feathery appearance (Blockeel, 2010a; Blockeel, 2014; Campisi et al., 2019; Hill et al., 2017; Smith & Smith, 2004). The leaves themselves have an elongated spearhead shape, rounded and wide at the base before suddenly narrowing about half way up and ending in a finely tapered point. They also have a small nerve which runs up to the mid-point of the leaf, although it can be tricky to see in the field even with a hand lens, and the leaf margins can be entire, toothed, or somewhere in between (Blockeel, 2010a; Smith & Smith, 2004).
A. serpens is autoicous (Blockeel, 2014), meaning that male and female organs will grow on the same plant but on different branches. With the exception of specimens growing in saltmarsh and dune environments, capsules are very common in this species and can be seen from March-August (Blockeel, 2010a; Hill et al., 2017). Capsules are held horizontal rather than upright, and grow to about 2mm long in a curved, cylindrical shape with conical lids and white calyptra (Blockeel, 2010a).
Similar Species
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Anomodon longifolius - Overall this moss has a brighter and more yellow colour with longer shoots (60mm), and a nerve which runs the whole length of the leaf. UK specimens of A. longifolius also do not produce capsules, unlike A. serpens where capsules are abundant during the right months (Hill et al., 2017; Lawley, 2010). Additionally, this species is very rare in Great Britain, occuring in just 6 hectads, and only growing below 250m on hard rocks in either broadleaf deciduous woodland or inland cliffs (Hill et al., 2017).
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Conardia compacta - Leaves are much more irregularly spread which gives the moss a spikier, almost crinkly look. Inspection with a hand lens will also reveal a much longer nerve than found in A. serpens (Blockeel, 2010a; Blockeel; 2010b). The lack of capsules produced by this species in the UK and Ireland can also help to differentiate it from A. serpens (Hill et al., 2017). C. compacta is a lot rarer than A. serpens, it has not been recorded in Wales or Ireland since 1950. It grows almost exclusively in deep shade on inland rock cliffs and outcrops where A. serpens is not found (Hill et al., 2017)
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Cratoneuron filicinum - The most reliable method of differentiation is to view specimens under a microscope and look for patches of orange alar cells, which are present in C. filicinum but not in A. serpens (BIBS, n.d). However, for in the field identification C. filicinum has a more prominent nerve, longer shoots, and only grows capsules in May (A. serpens produces them from March through August) (Blockeel, 2010a; Hill et al., 2017). There are also some habitat differences which can be used to help distinguish these species, C. filicinum but not A. serpens can be found above 580m and in grasslands, bogs and the running waters of streams, while only A. serpens can grow in heathland and horticultural areas (Hill et al., 2017).
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Habrodon perpusillus - Unlike A. serpens, unless they are wet the leaves of H. perpusillus lie overlapping and flat against the stem. They also have no nerve, and are about twice the size of those on A. serpens, making the short, shoots look furry and cylindrical, a bit like a squirrels tail (Blockeel, 2010a; Preston, 2010). This species is also solely epiphytic, restricted to hedgerows and sparsely wooded grassland below 60m elevation, making in very rare in Great Britain and absent in Ireland (Hill, et al., 2017).
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Heterocladium flaccidum - Its leaves have only a very sharp nerve, and end in a sharp acute point, rather than the long, tapered tip characteristic of A. serpens. Its shoots are also about half the length of those in A. serpens, and it does not produce capsules in the UK and Ireland (Blockeel, 2010a; Bosanquet, 2010; Hill et al., 2017). Additionally, any specimens found outside of broadleaf deciduous woodland or inland cliffs, rocks and pavements cannot be H. flaccidum (Hill et al., 2017).
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Hygroamblystegium humile - Leaves are sparser and stick out more from the stems, making H. humile look sharp and spiky, in contrast to the soft and feathery appearance of A. serpens, it also rarely produces capsules. H. humile frequents well-lit, waterlogged areas, while A. serpens prefers to be partially shaded with moist but not waterlogged substrate (Blockeel, 2010c, Hill et. al., 2017). Additionally, while A. serpens is widespread, H. humile is absent from most of Northern England, Wales, Ireland, and Scotland (Blockeel, 2010a; Blockeel, 2010c).
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Hygroamblystegium varium - The leaves are larger and wider, with a thicker nerve which extends all the way to the tip of the leaf, and unlike A. serpens it rarely produces capsules. H. varium grows in much less intricate and less dense patches than A. serpens, and can also tolerate waterlogged soils, which A. serpens cannot (Blockeel, 2010a; Blockeel, 2010d; Hill et al., 2017).
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Kandea elodes - At 70mm long the shoots are much loarger, while the leaves are narrower with a longer, more prominent nerve that runs all the way to the leaf tip. It also rarely produces capsules (Blockeel, 2010a; Hill et al., 2017). K. elodes is not only much rarer than A. serpens, but it also grows in quite different habitats. It favours well-lit, waterlogged environments, but cannot grow on rocky substrate or above 365m elevation (Hill et al., 2017).
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Leskea polycarpa - Has sharply pointed leaves which lack the characteristic long, tapered tips of A. serpens leaves. Similarly to A. serpens it frequently produces capsules, although only between May and August, and they are visually quite different, growing upright and straight rather than horizontal and curved (Blockeel, 2010a: Hill et al., 2017).
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Microeurhynchium pumilum - Leaves are shorter, with a more acute, less drawn out tip, and both leaves and branches spread out more than in A. serpens giving it an overall softer, neater, and fluffier look. The differences in leaf shape as easiest to see when examined under a microscope (Blockeel, 2010a; Smith & Smith, 2004). Another way to tell them apart in the field is to look at the timing of when mature capsules are present, for A. serpens they will be visible from March-August, but for M. pumilum they will be visible from November to March (Hill et al., 2017).
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Platydictya jungermannioides - The leaves are nerveless and taper to an even finer point than those of A. serpens, they also sometimes grow purple rhizoids, which do not occur in A. serpens (Blockeel, 2010a; Blockeel, 2010b; Sleath, 2010). Their distribution is much more restricted than A. serpens, they are mostly absent from the South East, South West, and Anglia, and only grow in broadleaf deciduous woodland and inland rocky environments (Hill et al., 2017; Sleath, 2010).
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Rhynchostegiella curvieseta - Leaves have a much narrower base and a less drawn out tip, somewhat resembling a pine needle, in contrast to the wide egg-shaped base and long tip of A. serpens (Blockeel, 2010a). Additionally, R. curvieseta inhabits quite different environments to A. serpens, requiring deep shade and permanently waterlogged substrate below 200m elevation, it is also very rare in the UK (Hill et al., 2017).
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Rhynchostegiella tenella - Has very narrow leaves, which gives the overall moss a distinctive silky appearance. It also frequently produces capsules, but at different times of the year to A. serpens, with mature capsules being most abundant from October to April (Blockeel, 2010a; Hill et al., 2017). Unlike A. serpens, R. tenella needs full shade, and relatively dry, well drained soils in order to grow (Hill et al., 2017).
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Rhynchostegiella teneriffae - Leaves have a much narrower base and a less drawn out tip, somewhat resembling a pine needle, in contrast to the wide egg-shaped base and long tip of A. serpens (Blockeel, 2010a). Also R. teneriffae can only be found near inland water sources, growing in areas which are deeply shaded and permanently water-logged e.g. in streams and bogs (Hill et al., 2017).
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Serpoleskea confervoides -Shoots are generally much shorter, growing to only 10mm, and the leaves do not have any nerves. S. confervoides is also much less common and widespread, it grows specifically on hard rock in deciduous woodland, or occasionally on inland cliffs, and nowhere else (Blockeel, 2010a; Hill et al., 2017).


(Abair, 2020)
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Distribution
A. serpens is incredibly widespread, found on all continents across both the North and South hemispheres (Vanderpoorten, 2015). This includes the UK, Ireland, and all of mainland Europe, minus a small strip of land along the border of Norway and Sweden. The species is also present in the Arctic circle, it is considered a Boreo-temperate species, so the northern reaches of its range stretch all the way to Arctic Russia, Iceland, and Svalbard (Blockeel, 2014; Campisi, et al., 2019; Ignatov, 2006). It is also common across North Asia, spreading into the eastern tips of Russia, as well as into northern India, Pakistan, and Tibet, although it has yet to be recorded in Uzbekistan (Blockeel, 2014; Ignatov, 2006; Smith & Smith, 2004). Other places it can be found are the islands of Sardinia, Sicilia, Crete, the Canaries, and the Azores, as well as Ecuador and Peru (South America), Mexico, Algeria, Kenya and Uganda (Africa), Australia, Tasmania, and New Zealand (Oceania) (Blockeel, 2014; Campisi et al., 2019; Smith & Smith, 2004). Its primary habitat consists of Boreal and Temperate forest, and Mediterranean shrubland, with secondary use of artificial habitats such as pastures, plantations, and urban areas. It can be found anywhere between 0-1300m above sea level. Within Europe there are no major threats, and the species is abundant with stable populations. As a result, there are no countries in Europe where A. serpens is considered regionally threatened, although it does become slightly rarer as you reach the edges of its range (Campisi, et al., 2019).
Within her notes Jan remarked that this species is very common in Kent, which matches its distribution across the rest of the UK and Ireland, where it is considered widespread and abundant throughout. Although, it is absent from parts of central Scotland and Ireland. This probably at least partly due to the fact that A. serpens can survive in an incredibly wide range of substrates and environments (Blockeel, 2014).

UK Altitudinal Range: 10-625m (Blockeel, 2014).
Habitat and Ecology
A. serpens is mostly a perennial species, although may sometimes resort to an annual lifestyle instead. This means it can generally be seen throughout the year, however, because its capsules are a key identifying feature it might be best to look for this species between March and August when mature capsules are present (Hill et al., 2017).
A. serpens is considered a semi-shade plant, so while it cannot tolerate full light it is still usually found in places with more than 10% relative illumination. In terms of substrate conditions, it favours moist but not waterlogged soils of varying pH which are fertile and nitrogen rich.It also prefers sheltered over more exposed conditions, but will still grow under both circumstances (Blockeel, 2014; Hill et al., 2017). A. serpens is not picky when it comes to type of substrate or environment, it will grow on almost any substrate which retains sufficient amounts of moisture, and can even tolerate moderate levels of salinity. Common substrates include the wood and roots of soft barked trees, e.g. Elder and Willow, soil near streams and rivers, and dunes in the upper salt marsh zone (Blockeel, 2014; Hill et al., 2017). The complete list of substrates A. serpens has been recorded on in the UK is; rock (hard, soft, and worked), soil, gravel and sand, and wood (dead, rotting, or alive). It has also been observed in the following habitats; intertidal saltmarshes, coastal dunes, shores and cliffs, the shores of inland water sources, temperate scrub, riverine fen, scrubland, hedgerows, broadleaved deciduous wood, coniferous wood, cultivated parks, buildings (rural and urban), field walls, and finally extractive industry sites such as quarries (Hill et al., 2017).
Associated species: Jan's notes mention that A. serpens often grows alongside other mosses, and it is known to form part of an agricultural assemblage of mosses found in late successional fields which includes, Brachythecium rutabulum, Calliergonella cuspidata, Kindbergia praelonga, and Oxyrrhynchium hians (Preston et al., 2013).
Regional Threat Level
British Red List: A. serpens is currently listed as Least Concern in the UK, with no evidence of historical or current declines. It is incredibly widespread, occupying at least 2048 hectads across the UK and Ireland meaning it is neither Nationally Rare or Scarce (Callaghan, 2022; Pescott, 2016).
Irish Red List: A. serpens is also considered Least Concern in Ireland (Hodgetts & Lockhart, 2025), and because it occupies around 220 hectads is neither Nationally Rare or Scarce (Hill et al., 2017; Hodgetts & Lockhart, 2013).
References
Abair, A. (2020). Creeping feather-moss (Amblystegium serpens) in the United States [Graphic]. https://www.inaturalist.org/photos/59258317. https://commons.wikimedia.org/wiki/File:Amblystegium_serpens_59258317.jpg
BIBS. (n.d.). Cratoneuron filicinum. British and Irish Bryological Society. Retrieved 6 October 2026, from https://www.bibsbryology.org/learning/species-finder/cratoneuron-filicinum/
Blockeel, T. J. (2010b). Amblystegium confervoides. In I. Atherton, S. D. S. Bosanquet, & M. Lawley (Eds), Mosses and liverworts of Britain and Ireland: A field guide (p. 705). British Bryological Society.
Blockeel, T. J. (2010a). Amblystegium serpens. In M. Lawley, I. Atherton, & S. Bosanquet (Eds), Mosses and liverworts of Britain and Ireland: A field guide (First Edition, p. 702). British Bryological Society.
Blockeel, T. J. (2014). Amblystegium serpens. In T. J. Blockeel, S. D. S. Bosanquet, M. O. Hill, & C. D. Preston (Eds), Atlas of British and Irish Bryophytes (Vol. 2, p. 435). Pisces Publications.
Blockeel, T. L. (2010c). Amblystegium humile. In M. Lawley, I. Atherton, & S. Bosanquet (Eds), Mosses and liverworts of Britain and Ireland: A field guide (First Edition, p. 704). British Bryological Society.
Blockeel, T. L. (2010d). Amblystegium varium. In M. Lawley, I. Atherton, & S. Bosanquet (Eds), Mosses and liverworts of Britain and Ireland: A field guide (First Edition, p. 703). British Bryological Society.
Bosanquet, S. D. S. (2010). Heterocladium heteropterum/flaccidum. In I. Atherton, S. D. S. Bosanquet, & M. Lawley (Eds), Mosses and liverworts of Britain and Ireland: A field guide (p. 687). British Bryological Society.
Callaghan, D. A. (2022). A new IUCN Red List of the bryophytes of Britain, 2023. Journal of Bryology, 44(4), 271–389. https://doi.org/10.1080/03736687.2023.2185393
Campisi, P., Cogoni, A., Garcia, C., Hodgetts, N., Kucera, J., Lara, F., Lüth, M. & Schröck, C. 2019. Amblystegium serpens (Europe assessment). The IUCN Red List of Threatened Species 2019: e.T84375671A87766856. Accessed on 08 October 2026.
Hodgetts, N. G., & Lockhart, N. (2013). Rare and Scarce Bryophytes of Ireland. 110, 12–26.
Hodgetts, N., & Lockhart, N. (2020). Checklist and country status of European bryophytes – update 2020. National Parks and Wildlife Service.
Hodgetts, N., & Lockhart, N. (2025). Bryophytes (Mosses, Liverworts & Hornworts). Ireland Red List No. 14. National Parks and Wildlife Service, Department of Housing, Local Government and Heritage.
Ignatov, M., Afonina, O., & Ignatova, E. (2006). Checklist of mosses of East Europe and North Asia. Arctoa, 15, 1–130. https://doi.org/10.15298/arctoa.15.01
Lawley, M. (2010). Anomodon longifolius. In M. Lawley, I. Atherton, & S. Bosanquet (Eds), Mosses and liverworts of Britain and Ireland: A field guide (First Edition, p. 693). British Bryological Society.
Meinunger, L., & Schröder, W. (2007). Verbreitungsatlas der Moose Deutschlands—Band 3. Oliver Dürhammer für die Regensburgische Botanische Gesellschaft.
Pescott, O. (2016). Revised lists of nationally rare and scarce bryophytes for Britain. 115, 22–30.
Preston, C. D. (2010). Habrodon purpusillus. In I. Atherton, S. D. S. Bosanquet, & M. Lawley (Eds), Mosses and liverworts of Britain and Ireland: A field guide (p. 686). British Bryological Society.
Preston, C., Hill, M., Porley, R., & Bosanquet, S. (2013). Survey of the bryophytes of arable land in Britain and Ireland 1: A classification of arable field assemblages. Journal of Bryology, 32, 61–79. https://doi.org/10.1179/037366810X12578498135959
Sleath, Jonathon. (2010). Platydicta jungermannioides. In I. Atherton, S. D. S. Bosanquet, & M. Lawley (Eds), Mosses and liverworts of Britain and Ireland: A field guide (p. 778). British Bryological Society.
Smith, A. J. E., & Smith, R. (2004). The Moss Flora of Britain and Ireland (2nd edn). Cambridge University Press. https://doi.org/10.1017/CBO9780511541858
Vanderpoorten, A. 2015. Amblystegium. Flora of North America Editorial Committee, eds. 1993+. Flora of North America North of Mexico. 20+ vols. Vol. 3, pp. 356-357. New York and Oxford.
Written By: Lucy Hudson. Last Updated: 8th October 2026.


