Animalia > Chordata > Aves > Passeriformes > Fringillidae > Fringilla > Fringilla coelebs

Fringilla coelebs (Common Chaffinch)

Wikipedia Abstract

The common chaffinch (Fringilla coelebs), usually known simply as the chaffinch, is a common and widespread small passerine bird in the finch family. The male is brightly coloured with a blue-grey cap and rust-red underparts. The female is much duller in colouring but both sexes have two contrasting white wings-bars and white sides to the tail. The male bird has a strong voice and sings from exposed perches to attract a mate.
View Wikipedia Record: Fringilla coelebs

Infraspecies

EDGE Analysis

Uniqueness Scale: Similiar (0) 
5
 Unique (100)
Uniqueness & Vulnerability Scale: Similiar & Secure (0) 
27
 Unique & Vulnerable (100)
ED Score: 11.6636
EDGE Score: 2.53873

Attributes

Adult Weight [1]  22 grams
Birth Weight [2]  2.2 grams
Female Weight [1]  21 grams
Male Weight [1]  24 grams
Weight Dimorphism [1]  14.3 %
Diet [3]  Carnivore (Invertebrates), Granivore, Herbivore
Diet - Invertibrates [3]  60 %
Diet - Plants [3]  20 %
Diet - Seeds [3]  20 %
Forages - Mid-High [3]  30 %
Forages - Understory [3]  30 %
Forages - Ground [3]  40 %
Clutch Size [7]  5
Clutches / Year [6]  1
Fledging [4]  14 days
Incubation [6]  12 days
Mating Display [2]  Ground display
Mating System [2]  Monogamy
Maximum Longevity [5]  29 years
Speed [8]  28.633 MPH (12.8 m/s)
Wing Span [8]  10 inches (.26 m)
Female Maturity [5]  1 year
Male Maturity [5]  1 year

Ecoregions

Protected Areas

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Ecosystems

Important Bird Areas

Biodiversity Hotspots

Name Location Endemic Species Website
Caucasus Armenia, Azerbaijan, Georgia, Iran, Russia, Turkey No
Irano-Anatolian Armenia, Azerbaijan, Georgia, Iran, Iraq, Turkey, Turkmenistan No
Japan Japan No
Mediterranean Basin Algeria, Egypt, France, Greece, Israel, Jordan, Lebanon, Libya, Portugal, Spain, Syria, Tunisia, Turkey No
Mountains of Central Asia Afghanistan, China, Kazakhstan, Kyrgyzstan, Tajikistan, Uzbekistan No

Prey / Diet

Prey / Diet Overlap

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Predators

Providers

Shelter 
Abies clanbrassiliana (Norway spruce)[9]

Consumers

External References

Audio

Play / PauseVolume
Provided by Xeno-canto under a Creative Commons BY-NC-ND 2.5 License Author: Paolo Almeida

Citations

Attributes / relations provided by
1Storchová, Lenka; Hořák, David (2018), Data from: Life-history characteristics of European birds, Dryad, Dataset, https://doi.org/10.5061/dryad.n6k3n
2Terje Lislevand, Jordi Figuerola, and Tamás Székely. 2007. Avian body sizes in relation to fecundity, mating system, display behavior, and resource sharing. Ecology 88:1605
3Hamish Wilman, Jonathan Belmaker, Jennifer Simpson, Carolina de la Rosa, Marcelo M. Rivadeneira, and Walter Jetz. 2014. EltonTraits 1.0: Species-level foraging attributes of the world's birds and mammals. Ecology 95:2027
4Nathan P. Myhrvold, Elita Baldridge, Benjamin Chan, Dhileep Sivam, Daniel L. Freeman, and S. K. Morgan Ernest. 2015. An amniote life-history database to perform comparative analyses with birds, mammals, and reptiles. Ecology 96:3109
5de Magalhaes, J. P., and Costa, J. (2009) A database of vertebrate longevity records and their relation to other life-history traits. Journal of Evolutionary Biology 22(8):1770-1774
6British Trust for Ornithology
7Jetz W, Sekercioglu CH, Böhning-Gaese K (2008) The Worldwide Variation in Avian Clutch Size across Species and Space PLoS Biol 6(12): e303. doi:10.1371/journal.pbio.0060303
8Alerstam T, Rosén M, Bäckman J, Ericson PGP, Hellgren O (2007) Flight Speeds among Bird Species: Allometric and Phylogenetic Effects. PLoS Biol 5(8): e197. doi:10.1371/journal.pbio.0050197
9Ecology of Commanster
10Predators, parasitoids and pathogens: species richness, trophic generality and body sizes in a natural food web J. Memmott N.D. Martinez J.E. Cohen Journal of Animal Ecology Volume 69, Issue 1 January 2000 Pages 1-15
11Jorrit H. Poelen, James D. Simons and Chris J. Mungall. (2014). Global Biotic Interactions: An open infrastructure to share and analyze species-interaction datasets. Ecological Informatics.
12O'Donnell, Colin F J and Dilks, Peter J, Foods and Foraging of Forest Birds in Temperate Rainforest, South. Westland, New Zealand, NZ J Ecology 18(2) (1994) pp. 87-107
13Recruitment of a Mast-Fruiting, Bird-Dispersed Tree: Bridging Frugivore Activity and Seedling Establishment, Carlos M. Herrera, Pedro Jordano, Luis López-Soria, Juan A. Amat, Ecological Monographs, 64(3), 1994, pp. 315-344
14Farwig, Nina; Schabo, Dana G.; Albrecht, Jörg (2017), Data from: Trait-associated loss of frugivores in fragmented forest does not affect seed removal rates, Dryad, Dataset, https://doi.org/10.5061/dryad.2784g
15Food habits of Zamenis longissimus (Laurenti, 1768) (Reptilia: Serpentes: Colubridae) in Bieszczady (south-eastern Poland), BARTŁOMIEJ NAJBAR, Vertebrate Zoology 57 (1) 2007, 73-77
16Gibson, D. I., Bray, R. A., & Harris, E. A. (Compilers) (2005). Host-Parasite Database of the Natural History Museum, London
17International Flea Database
Ecoregions provided by World Wide Fund For Nature (WWF). WildFinder: Online database of species distributions, ver. 01.06 Wildfinder Database
Biodiversity Hotspots provided by Critical Ecosystem Partnership Fund
Abstract provided by DBpedia licensed under a Creative Commons License
Audio software provided by SoundManager 2
Species taxanomy provided by GBIF Secretariat (2022). GBIF Backbone Taxonomy. Checklist dataset https://doi.org/10.15468/39omei accessed via GBIF.org on 2023-06-13; License: CC BY 4.0