Silverweed
(Potentilla anserina L., synonyms: Argentina anserina; Dactylophyllum anserine;
Fragaria anserina.)
Family: Rosaceae
[‘RR’ rarity rating, Stace 2010:
254]
 |
|
Silverweed, shown here at the Farlington Marshes,
is easily recognised
by its silver-green tufted leaves
and small
yellow flowers, which bloom betweenJune
and August.
(Farlington Marshes, August 1998)
|
Silverweed
roots are one of the most carbohydrate-rich and palatable of our indigenous
British root-foods. This species is widespread throughout the British Isles,
often observed growing in dense swards on damp grassy areas, waste lands and
sand dunes (for distribution maps see Online Atlas
of the British and IrishFlora). Common in the temperate, alpine and cooler
zones of the northern latitudes of Eurasia and North America, where it has
frequently been reported to be used as food, this plant has an extensive range,
occurring from arctic to almost subtropical latitudes (Rousi 1965, 47). It has
a broad ecological versatility, being tolerant of frost as well as of marine
exposure, and although preferring saltier and wetter environments, it grows on
a range of soil types (Plants
ForA Future [PFAF] database).
The leaves, stems, young shoots and roots of silverweed are edible
although it is the carbohydrate-rich storage roots that have most often been
reported to be eaten. Silverweed, alongside burdock root (Arctium lappa L.), has the highest concentrations of assimilable carbohydrate of any of the wild
British root foods that we have analysed thus far. In fact, silverweed and burdock roots have
greater concentrations of carbohydrate than that of most starch staple foods
consumed in the UK today (e.g. potato, see below) making them both remarkably
sustaining foods.
Distinguishing Features of the Plant
This creeping, hardy
perennial is easily recognised by its silver-green tufted leaves. It has occasional thin red stolons and
small (c. 2 cm.) 5-petalled yellow flowers that
bloom between June and August. In addition to the normal, inedible fibrous
roots, each mature plant produces between one and six starch-rich secondary
roots, which store the plant’s carbohydrate energy reserves.
 |
|
Close-up of the five-petalled floret. (Horseye Level, May 2008) |
The secondary roots
are long and narrow, rarely branching. When fresh they are yellow ochre to dark
brown in colour and a have a transversely wrinkled surface. They typically
measure between three to seven mm in diameter (thickness) and from 15 to 30 cm
long. On rare occasions, the storage
roots are found with thicknesses as great as 10-12mm in diameter, which is most
likely why the silverweed storage root is sometimes incorrectly described as a
tuber[i].
 |
|
Silverweed can form extensive stands such
as in this
sward on the River Medway August 2006.
|
In common with the
secondary root tissue of other dicotyledons, silverweed root is formed of
concentric rings of tissue, the most external being the periderm, followed by a
ring of phloem/parenchyma, internal to which is a cambium band and then the
xylem. Hather (1988; 1993) examined silverweed anatomy under SEM and observed
that parenchyma (storage) cells form the majority of silverweed secondary root
tissue (for more details about the anatomy, see Hather 1993, 50-51).
Nutrient Values
Despite their scrawny appearance, these roots
are highly palatable, raw or cooked.
They have a pleasant nutty taste and crunchy consistency, due to the
rich starch content and absence of stringy fibres. Because of their starch
content, silverweed roots are substantially more digestible if processed with
heat and water, whether by steaming, boiling, light roasting, or made into
"dampers" (a type of unleavened bread made from a flour and water and
baked in the ashes of a fire) after being dried and ground.
 |
|
Individual plants from a
heavily-trodden path. (March 2009)
|
The results of a recent nutrient analysis of
silverweed roots at the King’s College London
Division of Nutrition Sciences (Leeds and
Hillman, unpublished notes[ii])
show that silverweed roots contain exceptional concentrations of assimilable
carbohydrate. With 31g per 100g of edible portion, they provide higher levels
of carbohydrate than most "starch staple foods" presently consumed in
the UK, e.g. cultivated potato (Solanum tuberosum), which has a maximum of 26.5g per 100g FSA 2014). Similar remarkable levels of
carbohydrate are recorded for the roots of other Potentilla species. Pacific silverweed (Potentilla pacifica,
(syn. Argentina egedii and Potentilla
anserina. ssp. pacifica)), a species indigenous to the
Northwest Coast, contains 29.5 g per 100 g of edible portion (Kuhnlein et al.
1982).
The principal carbohydrate in P. anserina root is starch, at 3.3% (per
100g dry weight (Wolfred and Fisher 1944, cited in Lloyd 2011, 129). Although
various analyses of the nutrient profile of Potentilla
spp. have been made, no analysis of specifically the starch content was found
in the literature (a recent analysis of the related North American Pacific
silverweed, Potentilla pacifica (synonym.
Argentina egedii) was inconclusive; Lloyd
2011, 130).
Pacific silverweed also contains remarkably high concentrations
of important essential vitamins and minerals in including Ca, Mg, Fe, Cu, Mn
and Zn (Kuhnlein et al.1982).
 |
|
Starch-rich secondary (storage) roots of P. anserine.
(Weir Wood Reservoir, August 2006)
|
Traditional Food uses of Silverweed roots in the British Isles in recent times
The
19th-century Scottish folklorist Alexander Carmichael (1900) observed that
Silverweed roots were counted as one of the ‘sevenbreads of the Gael’, which up
to the arrival of the potato, were cultivated as well as gathered from the
wild. He also reported that it was claimed in the Outer Hebrides island of
North Uist that silverweed productivity was so great that a man could survive
on the roots from a small plot. The abundance of silverweed in North Uist today
gives credence to Carmichael’s claims (Ray Meares, Pers. Comm. 2011). At Clunie
in Perthshire, people in the late 18th c. consumed silverweed roots as one of
just two caloric staples, the other being the pignut (Conopodium majus) (Darwin and Bewick 1996). Svanberg (2012)
notes their consumption in the Shetlands and Johnson (1862), in his Useful Plants of Great Britain, recorded
the consumption of these roots in times of famine in the Hebrides.
Traditional uses of Silverweed Root in Other Regions within the Northern Hemisphere
Various Silverweed species are reported to for their food uses (or
medicine, see below) for many different societies throughout the Northern
Hemisphere. The roots were eaten, for example, in Iceland
(Svanberg (2012), parts of
Scandinavia, e.g. Norway, the Faroe Islands, eastern Europe, (Łuczaj and Szymański 2007)
and across Asia, particularly among Tibetan pastoralists (Boesi 2014). In his remarkable Geschichte unserer Pflanzennahrung, Maurizio (1927), for example,
describes the roots as a favourite food of the Tanguts of the Tsaidam
Depression in NE Tibet. Hunter-gatherer groups in the Russian Far East, such as
the Chukchi hunter-gatherers in the Russian Far East, also gathered silverweed
roots, which they ate in soups (Strecker 2014).
The most complete ethnobotanies and ethnohistoric descriptions of
silverweed harvesting and processing are for the hunter-gatherer peoples in
north western Canada, particularly the area that is present-day British
Columbia.
Silverweed
Food Uses by Coastal and Interior Plateau Hunter-Gatherers in British Columbia,
Canada
Two Potentilla species were
eaten by Hunter-gatherer peoples in this province: P.
anserina in the interior and P.
pacifica on the coast.
In the relatively arid Southern Interior of the province, P. anserina is common in alkaline soils
around the edges of lakes, ponds, mud flats, marshes and meadows (Turner 1997).
It is one among many wild plants with carbohydrate-rich edible storage organs
that are abundant in the Southern Interior. The Secwepemc, Upper Stl'atl'imx,
Nlaka'pamux and Okanagan First Nations dug the roots in late summer and autumn,
and as with other edible roots, roasted or pit-cooked them before eating
(Turner 1997). In some Southern Interior communities, carbohydrates, primarily
from USOs (plant Underground Storage Organs), comprised more than 50% of the
diet.
Unlike the Interior Plateau, the diet of Coastal First Nations was restricted
to primarily marine foods as sources carbohydrate were less available (Deur 2005).
Therefore, the edible roots of the Pacific silverweed (P. pacifica) and Springbank clover (Trifolium wormskjoldii)) were highly important staple
sources of carbohydrates for coastal First Nations. The most detailed
information on Silverweed harvesting and processing that is found in the
literature is on this species P. pacifica
(see Kuhnlein et al. 1982; Lloyd
2011 Turner 1995; Turner and Kuhnlein
1982).
Also known as Pacific cinquefoil, Pacific silverweed is unique to the
Northwest Coast. It grows in estuarine environments including river tidal
flats, salt marshes, beaches and dunes, from southern Vancouver Island to
Alaska (Turner 1995). From north to south, the Haida, Nuxalk, Kwakwaka'wakw,
Comox, Sechelt, Ditidaht (Nitinaht), Straits Salish, as well the Makah of
Washington are reported to have eaten Pacific silverweed (Turner 1995).
Native peoples typically managed wild plots of Pacific Silverweed and also
the rhizomatous Springbank clover (a
species that is also unique to the Northwest Coast). These two plants are found
in the same types of habitats and often occur together. Both were managed by Coastal people by weeding,
selective harvesting and replanting. Some communities, most notably the Kingcome Inlet Kwakwaka'wakw
on the central coast and Ditidaht (Nitinaht) of southern Vancouver Island,
created root gardens through by
transplanting and cultivating these plants on purpose-built mounds or terraces (Deur
2005; Lloyd 2011; Kuhnlein et al. 1982; Turner 1995).
Silverweed roots were of such importance that individuals, particularly
chiefs, claimed ownership of the wild and cultivated stands, which were passed
on through inheritance. Both species were also highly valued trade items and
feast foods, and the best specimens were reserved for high-status individuals
and given away at Potlatches (Turner 1995).
Pacific silverweed
roots were not eaten raw because of their inherent bitterness, which is reduced
but not always entirely removed, by steaming (Turner 1995). The roots were gathered in large quantities
in September and October and cooked in steaming pits or bentwood boxes (and in
recent times, kettles). To cook the roots, pit ovens or boxes were lined with
grasses and fuelled by hot rocks placed in the bottom; vegetation, including
leaves and branches, were added in layers, onto which the food to be cooked was
placed; water was then added to create steam and the pits were covered to
retain moisture and heat (Kuhnlein et al. 1982; Lloyd 2011). Among the
vegetation used for steaming Pacific silverweed roots, Kuhnlein et al. (1982, 90) list salal leaves (Gaultheria shallon), red alder branches
(Alnus rubra), and the fronds of the
ferns Polystichum munitum, Droyopteris expansa and sometimes
bracken fern (Pteridium aquilinum).
Detailed
descriptions of Canadian Native uses of these two species can be found in ethnobotany
papers by Deur et al. (2005) Kuhnlein et al. (1982) Lloyd (2011), Turner (1997)
and Turner and Kuhnlein (1982).
Medicinal Uses
Across Eurasia, written and oral histories on
the medicinal uses of Potentilla, for
both internal and external medical applications, have significant time-depth. In
Chinese traditional medicine, particularly on the Tibetan Plateau, it is claimed that P. anserina roots and leaves have been used for
thousands of years to treat a range of
illnesses, including hepatitis-B, certain cancers, diabetes
mellitus infections
as well as external problems such as wounds (Tomczyka and Latte 2009; Zhaoa
et al. 2008).
Several ancient European texts, some dating
from over 1,000 years ago, describe the use of Potentilla. Among these is the Materia
Medica written by Pedanius Dioscorides, a Greek physician and botanist,
which describes a concoction of the roots of a
Potentilla to treat mouth ulcers and facial eczema (Tomczyka and Latte
2009, 185). In Germany, P. anserina has
been employed medicinally since at least medieval times as a tea for treating
menstrual disorders, oral inflammations, diarrhoea and other gastrointestinal
illnesses (Kombal and Glasl 1985). Sami reindeer herders of the Scandinavian
far north are also reported to use a Potentilla
medicinally (Rautio 2014).
On the
Interior Plateau of British Columbia, decoctions of roots, stems, florets
and/or leaves of several Potentilla species
were used to treat both internal and external problems. For example, the
Okanagan-Coleville people drank a
tea from the pounded, fresh or dried plants to treat diarrhoea and applied a
poultice made from various plant parts directly to sores and wounds (Turner
et al. 1980, 126-127).
There is an increasing scientific interest in
the phytochemical and pharmacological properties of Potentilla species. The
results of recent controlled laboratory analyses (Wang et al. 2013; Zhao 2008) demonstrate that the positive medicinal effects of P. anserina are primarily due
to high levels of hydrolysable and condensed tannins, flavonoids and
triterpenes, which are present throughout the plant. It was also found to contain substantial types and amounts of
various steroids, phenolic
acids and coumarin compounds (Kombal
and Glasl 1985). The beneficial medicinal effects include immunity-enhancing, anti-oxidant, anti-inflammatory
anti-fatigue, anti-viral and antimicrobial activities, cardiomyocyte and liver protection (Wang et al. 2013; Tomczyka and Latte 2009).
A comprehensive
review of the phytochemical and pharmacological properties of Potentilla is provided in Tomczyka and Latte
(2009).
The Root Harvest
The best times to
gather Silverweed roots are early spring and early autumn. In the autumn the
plants can be harvested when the leaves have begun to turn a rusty brown, as by
this time of year a new generation of starch-rich roots are available. Although
the roots are edible throughout the winter, until new aboveground shoots appear
in the spring, the plant is impossible to locate after the leaves have died
back in the autumn
In spring, new
shoots sprout from the tops of the last year’s roots. These are best harvested
early, while the silvery new leaves are still barely visible above the soil
surface, and the roots are still sweet, crunchy and highly palatable. However,
the carbohydrate reserves quickly become depleted because they are required to
fuel new growth, including the aboveground stems, leaves and florets, and newly
sprouting belowground roots. The new, thin, white roots (often mauve- or
purple-tinged) sprout from the central stock and develop starch and other
nutrients. Eventually they turn a streaky yellowish-brown, and are fit to eat
again in the autumn.
 |
|
Roots of P. anserina harvested from a
20 X 20 cm plot. (Weir Wood Reservoir,
October 2006)
|
Digging up wild roots
is often hard work, and Silverweed root is no exception, even though the roots
are shallow compared with those of most other USOs. It is especially difficult
on the heavy, sticky clay soils in which inland populations of Silverweed so
often grow, and requires a spade, mattock or digging stick. Turner and Kuhnlein
(1982) reporting on the harvesting of Springbank clover (which is similar to
Pacific silverweed in this regard), estimate that a person might obtain 0.5-1
kg in an hour if digging a productive patch; they further observed that it had
taken a Native colleague as much as five hours to obtain enough clover ‘roots’
for three large servings. Nevertheless, compared with other wild food plants,
particularly those that need detoxifying or grinding, the processing end of the
sequence is significantly less labour-intensive than other wild root
foods.
Archaeological record
Silverweed seeds
(achenes) have been recovered from waterlogged Mesolithic sites in the UK,
Ireland and other European archaeological sites (ASDU 2009), as well as Iron
Age, Roman and Medieval sites but the roots have yet to be found. These finds
verify that Silverweed was widely available,
even though they are not evidence that the roots contributed to local diet.
Given the likelihood
that these roots were consumed in the prehistory of Britain, Ireland and
northern Europe, their absence in the archaeological record is probably due to
preservation problems that are typical of soft plant tissue (see
Colledge and Conolly 2014). The
roots may in future be found preserved in waterlogged contexts or in
sites where they were charred before deposition. However, Hather (1988: 156,
216-8), who described in detail the anatomy of these roots, also subjected them
to charring experiments and found that the central vascular tract typically
disappeared when charred, leaving unidentifiable debris.
Summary and Conclusion
Although the roots of Silverweed roots have yet to be found in Mesolithic
sites, given its edibility and high nutritional composition, it likely played a
role in the diet of the hunter-gatherers in Britain. In the damp conditions of
the Mesolithic Britain there would have been many more inland habitats with
wild meadows suitable for Silverweed. The benefits are that they can be harvested
in quantity, are an extremely palatable energy-packed food, require minimal
processing and cooking and can be eaten raw, and once dried, they can be stored
for long periods. Furthermore, they area functional food that, in addition to
providing starch, energy and significant levels of beneficial vitamins and
mineral, contain phytochemical components that support good health and
disease-prevention.
References Cited
ASDU Archaeology Services Durham University. 2009. Appendix 17: Environmental report.
Clowanstown 1, M3 Motorway Project, Co. Meath, Ireland. Plant macrofossil,
charcoal, cremated bone and mollusc analysis. In Mossop, M. and Mossop, E., M3
Clonee-North of Kells. Contract 2 Dunshaughlin – Navan. Report on the
Archaeological Excavation of Clowanstown 1, Co. Meath. Ministerial Directions
No. A008/011. E3064. ACS Ltd: Unpublished report.
Colledge, S. and
Conolly, J. 2014. Wild plant use in European Neolithic subsistence economies: a
formal assessment of preservation bias in archaeobotanical assemblages and the
implications for understanding changes in plant diet breadth. Quaternary Science Reviews 101: 193-206.
Boesi. A. 2014. Traditional knowledge of wild food
plants in a few Tibetan communities. J.
of Ethnobiology and Ethnomedicine 10. Doi:10.1186/1746-4269-10-75.
[Accessed on line January 27, 2018]
Carmichael, A. 1900. Carmina Gadelica, 1. Norman Macleod,
Edinburgh.
Darwin, T. and Bewick T. 1996. The
Scots Herbal: Plant Lore of Scotland. 1st edition.
Mercat Press, United Kingdom.
Deur,
Douglas E. 2005. Tending the Garden,
Making the Soil, Northwest Coast Estuarine Gardens as Engineered Environments.
In Keeping it Living, Traditions of Plant use and Cultivation on
the Northwest Coast of North America, eds. Deur, D.E. and Turner, N J., pp.
296‐327. University of Washington Press; UBC
Press, Seattle, WA; Vancouver, BC.
FSA (Food Standards Agency).
2002.
McCance and Widdowson's The Composition of Foods,
Seventh Summary
edition. Royal Society of Chemistry, Cambridge. Johnson, C.P. 1826. Useful Plants of Great
Britain. London, Robert Hardwicke.
Kuhnlein,
H.V., Turner, N.J. & Kluckner, P.D.1982.
Nutritional significance of two important root foods (springbank clover and
pacific silverweed) used by native people on the coast of British Columbia. Ecology of Food and Nutrition, 12:
89-95.
Liu, Z.J., Bai, Y., Guo, L. and Wang, S. 2015
Research progresses on chemical constituents of the root of Potentilla anserina L. and its
pharmacological activities. Journal of Food Safety and
Quality 6: 3569-3574.
Łuczaj, L. and Szymański, W.M. 2007. Wild vascular plants gathered for consumption
in the Polish countryside: a
review. Journal of Ethnobiology and Ethnomedicine 3 doi:10.1186/1746-4269-3-17.
[Accessed 26 January, 2018].
Maurizio, A. 1927. Die Geschichte unserer Pflanzennahrung, Parey, Berlin.
Plants For A
Future (PFAF). 1996-2012. http://www.pfaf.org/ [accessed Jan 15, 2018].
Ratio, A.M. 2014. People-Plant Interralationships: Historical Plant-Use in Native Sami
Societies. Unpublished Doctoral Thesis, Swedish University of Agricultural
Science, Umeå, Sweden.
Rousi, A. (1965).
Biosystematic studies on the species aggregate Potentilla anserina L. Annales Botanici Fennici, 2:
47-112.
Strecker, L. They know all
about their plants: Georg W. Steller (1709-1746) and the first ethnobotanical
study in Kamchatka. In Pioneers of
European Ethnobiology, eds. Svanberg, I. and Łuczaj,
L., 51-72. Uppsala University. Uppsala.
Svanberg, I. 2012 The use
of wild plants as food in pre-industrial Sweden. Acta Societatis Botanicorum Poloniae 81:
317-327. DOI: 10.5586/asbp.2012.039. [Accessed Jan 27, 2018].
Turner,
N. J., Bouchard, R. and Kennedy, D.1980. Ethnobotany
of the Okanagan-Colville Indians of British Columbia and Washington.
Occasional Papers of the British Columbia Provincial Museum, Victoria.
Turner N.J. and Kuhnlein, H.V. 1982. Two
important "root" foods of the Northwest Coast Indians: springbank
clover (Trifolium wormskioldii) and
Pacific silverweed (Potentilla Anserina
ssp. pacifica). Economic Botany 36:411-432
Wang, J., Zhang, J., Zhao, B., Wang, X.,
Wu, Y., & Yao, J. (2010). A comparison study on microwave-assisted extraction
of Potentilla anserina L.
polysaccharides with conventional method: Molecule weight and antioxidant
activities evaluation. Carbohydrate
Polymers, 80, 84–93 doi:10.1016/j.carbpol.2009.10.073 [Accessed January 26,
2018].
Zhao, Y.-L., Cai, G.-M., Hong, X., Shan,
L.-M., Xiao, X.-H., 2008. Anti-hepatitis B virus activities of triterpenoid
saponin compound from Potentilla anserine
L. Phytomedicine 15 253–258.
[i] Some readers may find the
distinction of "root" from "tuber" to be merely semantics, but
recognising the anatomical differences between root and tuber tissue are
critical steps in archaeological identification.
[ii] Anthony Leeds is now a Visiting Senior Fellow in the Faculty of Health
and Medical Sciences, Surrey University.
