Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
Behaviour Most populations of this species are fully migratory and travel on a broad front over land and along coasts, some Icelandic and Western European populations remaining close to their breeding grounds1. It breeds from March to August2 in solitarily pairs or in loose colonies1, 2, departing the breeding grounds from June to October, and returning from the wintering grounds again between February and April2. Outside of the breeding season the species forages singly, in small groups1 or occasionally in larger flocks of up to c.1,000 individuals5 especially at roosting sites2 or when feeding on fish1. Habitat Breeding The species breeds on coastal saltmarshes, inland wet grasslands with short swards1 (including cultivated meadows)3, grassy marshes, swampy heathlands1 and swampy moors3. Non-breeding On passage the species may frequent inland flooded grasslands1 and the silty shores of rivers and lakes4, but during the winter it is largely coastal1, occupying rocky, muddy and sandy beaches, saltmarshes, tidal mudflats, saline and freshwater coastal lagoons1, tidal estuaries3, saltworks and sewage farms1. Diet Breeding When breeding its diet consists of insects, spiders and annelid worms1. Non-breeding During the non-breeding season the species takes insects, spiders and annelid worms1, as well as molluscs, crustaceans (especially amphipods e.g. Corophium spp.)1 and occasionally small fish and tadpoles1. Breeding site The nest s a shallow scrape or hollow5 on a hummock or at the base of a tuft4 of grass1, often well hidden by overhanging leaves1. The species usually nests solitarily inland (less than 10 pairs/km2) but in loosely colonial groups (up to 100-300 pairs/km2) on the coast1. Management information Optimal breeding conditions for this species may be provided by creating a mosaic of unflooded grassland, winter-flooded grassland and shallow pools9. Winter flooding of grasslands is beneficial to the species as it helps to keep the sward height short and open and also creates pools which provide a source of aquatic invertebrates in the spring9, 13. Such shallow pools on coastal grazing marshes should be maintained until the end of June16. The number of breeding pairs on improved grassland was successfully increased on a reserve in Wales by the implementation of a two-year rotation of chisel ploughing, as well as a seasonal sheep and cattle grazing regime and a controlled increase in the water-level14. At Lower Lough Erne in Northern Ireland the breeding population of the species increased considerably as a result of cutting rush beds in mid-winter (although the species nested on uncut areas, chicks benefited from the presence of adjacent short, open areas for feeding)15. Low-level grazing of salt marshes (e.g. c.1 cow per hectare) does not appear to affect the species and may even be beneficial to breeding populations19, 20, although cattle should not be put onto the marsh until towards the end of the nesting season (e.g. late-May or early-June) to minimise the risk of nest trampling19. There is also evidence that too heavy grazing can be detrimental18. The species is known to show increased hatching success when ground predators have been excluded by erecting protective fences around nesting areas8, and in the UK there is evidence that the removal of Spartina anglica from tidal mudflats using a herbicide is beneficial for the species18.

Systems
  • Terrestrial
  • Freshwater
  • Marine
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Depth range based on 30 specimens in 1 taxon.
Water temperature and chemistry ranges based on 21 samples.

Environmental ranges
  Depth range (m): 0 - 0
  Temperature range (°C): 8.989 - 12.200
  Nitrate (umol/L): 1.473 - 10.275
  Salinity (PPS): 33.479 - 35.258
  Oxygen (ml/l): 6.221 - 6.596
  Phosphate (umol/l): 0.344 - 0.700
  Silicate (umol/l): 1.720 - 4.619

Graphical representation

Temperature range (°C): 8.989 - 12.200

Nitrate (umol/L): 1.473 - 10.275

Salinity (PPS): 33.479 - 35.258

Oxygen (ml/l): 6.221 - 6.596

Phosphate (umol/l): 0.344 - 0.700

Silicate (umol/l): 1.720 - 4.619
 
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Associations

Known prey organisms

Tringa totanus (Tringa totanus redshank) preys on:
Crangon crangon
Nereis diversicolor
Corophium volutator
Gammarus
Hydrobia ulvae
Littorina saxatilis
Macoma balthica
Chironomidae

Based on studies in:
Scotland (Estuarine)

This list may not be complete but is based on published studies.
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Known predators

Tringa totanus (Tringa totanus redshank) is prey of:
Himasthla elongata
Cryptocotyle jejuna
Maritrema subdolum
Levinseniella
Apophallus lerouxi
Levinseniella brachysoma
Maritrema humile
Hymenolepis
Spelotrema clariforma

Based on studies in:
Scotland (Estuarine)

This list may not be complete but is based on published studies.
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Life History and Behavior

Life Expectancy

Lifespan, longevity, and ageing

Maximum longevity: 26.9 years (wild) Observations: In the wild, these animals may live up to 26.9 years (http://www.euring.org/data_and_codes/longevity.htm).
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Molecular Biology and Genetics

Molecular Biology

Barcode data: Tringa totanus

The following is a representative barcode sequence, the centroid of all available sequences for this species. 

 
There are 17 barcode sequences available from BOLD and GenBank.  Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.  See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
 
BROM165-06|MKP 2774|Tringa totanus| AACCGATGATTATTCTCAACCAACCACAAAGATATCGGCACCCTATACCTAATCTTCGGAGCATGAGCGGGTATAATCGGAACTGCCCTC---AGCCTTCTCATCCGCGCAGAATTAGGTCAGCCGGGAACTTTACTAGGAGAC---GACCAAATTTACAATGTAATCGTCACCGCCCATGCCTTTGTAATAATCTTCTTCATAGTAATACCAATTATAATTGGTGGCTTCGGAAATTGACTAGTTCCACTCATA---ATCGGCGCCCCCGACATAGCATTCCCCCGTATAAATAACATAAGCTTTTGACTACTCCCCCCATCATTCCTACTACTATTAGCATCCTCAACAGTAGAGGCAGGAGCTGGTACAGGATGAACAGTATATCCTCCTCTCGCCGGTAACCTAGCCCATGCCGGTGCTTCAGTAGATCTA---GCTATCTTCTCTCTCCATTTGGCAGGTGTCTCTTCTATCCTAGGCGCCATCAACTTCATCACAACTGCTATTAACATAAAACCTCCAGCCCTCTCCCAATACCAAACTCCCCTATTTGTATGATCAGTACTTATTACTGCCGTTCTTCTCCTACTCTCCCTTCCAGTTCTCGCTGCC---GGCATCACTATACTTCTAACAGATCGAAACTTAAACACCACATTCTTTGATCCCGCAGGAGGAGGGGACCCAGTCCTATACCAACACCTCTTCTGATTCTTCGGCCACCCAGAAGTTTACATCCTCATTCTACCAGGCTTCGGAATTATCTCCCATGTTGTAGCCTACTATGCAGGTAAAAAA---GAACCATTTGGATATATAGGAATAGTATGAGCTATACTATCCATCGGATTCCTAGGCTTTATTGTATGAGCCCACCACATATTTACAGTAGGA---- 
-- end --

Download FASTA File
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Statistics of barcoding coverage: Tringa totanus

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 17
Species: 21
Species With Barcodes: 1

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Conservation

Conservation Status

Status in Egypt

Regular passage visitor and winter visitor.

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IUCN

Least Concern.

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IUCN Red List Assessment


Red List Category
LC
Least Concern

Red List Criteria

Version
3.1

Year Assessed
2009

Assessor/s
BirdLife International

Reviewer/s
Bird, J., Butchart, S.

Contributor/s

Justification
This species has an extremely large range, and hence does not approach the thresholds for Vulnerable under the range size criterion (Extent of Occurrence <20,000 km2 combined with a declining or fluctuating range size, habitat extent/quality, or population size and a small number of locations or severe fragmentation). The population trend is not known, but the population is not believed to be decreasing sufficiently rapidly to approach the thresholds under the population trend criterion (>30% decline over ten years or three generations). The population size is very large, and hence does not approach the thresholds for Vulnerable under the population size criterion (<10,000 mature individuals with a continuing decline estimated to be >10% in ten years or three generations, or with a specified population structure). For these reasons the species is evaluated as Least Concern.

History
  • 2008
    Least Concern
  • 2004
    Least Concern
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Threats

Threats

Major Threats
The species is threatened by the loss of breeding and wintering habitats through agricultural intensification, wetland drainage, flood control, afforestation, land reclamation, industrial development1, encroachment of Spartina spp. on mudflats1, 18, improvement of marginal grasslands1 (e.g. by drainage, inorganic fertilising and re-seeding)10, coastal barrage construction7, and heavy grazing (e.g. of saltmarshes)17. The species is also threatened by disturbance on intertidal mudflats from construction work (UK)11 and foot-traffic on footpaths12. It is vulnerable to severe cold periods on its Western European wintering grounds1 and suffers from nest predation by introduced predators (e.g. European hedgehog Erinaceus europaeus) on some islands8. The species is also susceptible to avian influenza so may be threatened by future outbreaks of the viurs6.
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Wikipedia

Common Redshank

For the plant called "Redshank", see Persicaria maculosa.

The Common Redshank or simply Redshank (Tringa totanus) is an Eurasian wader in the large family Scolopacidae.

Description and systematics

Bird in flight (Laguna di Venezia, Italy)

Common Redshanks in breeding plumage are a marbled brown color, slightly lighter below. In winter plumage they become somewhat lighter-toned and less patterned, being rather plain greyish-brown above and whitish below. They have red legs and a black-tipped red bill, and show white up the back and on the wings in flight.

The Spotted Redshank (T. erythropus), which breeds in the Arctic, has a longer bill and legs; it is almost entirely black in breeding plumage and very pale in winter. It is not a particularly close relative of the Common Redshank, but rather belongs to a high-latitude lineage of largish shanks. T. totanus on the other hand is closely related to the Marsh Sandpiper (T. stagnatilis), and closer still to the small Wood Sandpiper (T. glareola). The ancestors of the latter and the Common Redshank seem to have diverged around the Miocene-Pliocene boundary, about 5-6 million years ago. These three subarctic- to temperate-region species form a group of smallish shanks with have red or yellowish legs, and in breeding plumage are generally a subdued light brown above with some darker mottling, and have somewhat diffuse small brownish spots on the breast and neck.[1]

Ecology

It is a widespread breeding bird across temperate Eurasia. It is a migratory species, wintering on coasts around the Mediterranean, on the Atlantic coast of Europe from Great Britain southwards, and in South Asia. They are uncommon vagrants outside these areas; on Palau in Micronesia for example, the species was recorded in the mid-1970s and in 2000[2].

Two Redshanks on a stone pillar

They are wary and noisy birds which will alert everything else with their loud piping call. Like most waders, they feed on small invertebrates. Redshanks will nest in any wetland, from damp meadows to saltmarsh, often at high densities. They lay 3-5 eggs.

The Common Redshank is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) applies.

It is widely distributed and quite plentiful in some regions, and thus not considered a threatened species by the IUCN.[3]

Footnotes

  1. ^ Pereira & Baker (2005)
  2. ^ Wiles et al. (2006)
  3. ^ BLI (2008)

References

  • BirdLife International (BLI) (2008). Tringa totanus. In: IUCN 2008. IUCN Red List of Threatened Species. Downloaded on 12 May 2009.
  • Pereira, Sérgio Luiz & Baker, Alan J. (2005): Multiple Gene Evidence for Parallel Evolution and Retention of Ancestral Morphological States in the Shanks (Charadriiformes: Scolopacidae). Condor 107(3): 514–526. DOI:10.1650/0010-5422(2005)107[0514:MGEFPE]2.0.CO;2 PDF fulltext
  • Wiles, Gary J.; Johnson, Nathan C.; de Cruz, Justine B.; Dutson, Guy; Camacho, Vicente A.; Kepler, Angela Kay; Vice, Daniel S.; Garrett, Kimball L.; Kessler, Curt C. & Pratt, H. Douglas (2004): New and Noteworthy Bird Records for Micronesia, 1986–2003. Micronesica 37(1): 69-96. HTML abstract
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