Corylus avellana
Common hazel

Common hazel (Corylus avellana) is a wind-pollinated, deciduous, usually multi-stemmed, small tree native to Europe and western Asia, often found in the understory of mixed deciduous forests. It thrives in a variety of habitats and plays a vital ecological role by providing habitat for wildlife and food during the winter. It contributes to soil stabilization by being an adaptable pioneer species, able to grow in sun and shade. The best growing conditions are on fertile, nutrient-rich soils with mild coastal tempered winters (Rowley et al., 2018). Common hazel is tolerant to different climatic conditions and is even able to withstand frost in the growing season.

Known for its distinctive, serrated leaves and catkin flowers, common hazel has been cultivated worldwide for both its edible nuts and wood. The flexible branches are used in traditional crafts, such as basket weaving and fencing.

in situ genetic conservation unit
ex situ genetic conservation unit
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Acknowledgements

This distribution map has been developed by the European Commission Joint Research Centre (partly based on the EUFORGEN map) and released under Creative Commons Attribution 4.0 International (CC-BY 4.0)


Caudullo, G., Welk, E., San-Miguel-Ayanz, J., 2017. Chorological maps for the main European woody species. Data in Brief 12, 662-666. DOI: https://doi.org/10.1016/j.dib.2017.05.007

The following experts have contributed to the development of the EUFORGEN distribution maps:

Fazia Krouchi (Algeria), Hasmik Ghalachyan (Armenia), Thomas Geburek (Austria), Berthold Heinze (Austria), Rudi Litschauer (Austria), Rudolf Litschauer (Austria), Michael Mengl (Austria), Ferdinand Müller (Austria), Franz Starlinger (Austria), Valida Ali-zade (Azerbaijan), Vahid Djalal Hajiyev (Azerbaijan), Karen Cox (Belgium), Bart De Cuyper (Belgium), Olivier Desteucq (Belgium), Patrick Mertens (Belgium), Jos Van Slycken (Belgium), An Vanden Broeck (Belgium), Kristine Vander Mijnsbrugge (Belgium), Dalibor Ballian (Bosnia and Herzegovina), Alexander H. Alexandrov (Bulgaria), Alexander Delkov (Bulgaria), Ivanova Denitsa Pandeva (Bulgaria), Peter Zhelev Stoyanov (Bulgaria), Joso Gracan (Croatia), Marilena Idzojtic (Croatia), Mladen Ivankovic (Croatia), Željka Ivanović (Croatia), Davorin Kajba (Croatia), Hrvoje Marjanovic (Croatia), Sanja Peric (Croatia), Andreas Christou (Cyprus), Xenophon Hadjikyriacou (Cyprus), Václav Buriánek (Czech Republic), Jan Chládek (Czech Republic), Josef Frýdl (Czech Republic), Petr Novotný (Czech Republic), Martin Slovacek (Czech Republic), Zdenek Špišek (Czech Republic), Karel Vancura (Czech Republic), Ulrik Bräuner (Denmark), Bjerne Ditlevsen (Denmark), Jon Kehlet Hansen (Denmark), Jan Svejgaard Jensen (Denmark), Kalev Jðgiste (Estonia), Tiit Maaten (Estonia), Raul Pihu (Estonia), Ülo Tamm (Estonia), Arvo Tullus (Estonia), Aivo Vares (Estonia), Teijo Nikkanen (Finland), Sanna Paanukoski (Finland), Mari Rusanen (Finland), Pekka Vakkari (Finland), Leena Yrjänä (Finland), Daniel Cambon (France), Eric Collin (France), Alexis Ducousso (France), Bruno Fady (France), François Lefèvre (France), Brigitte Musch (France), Sylvie Oddou-Muratorio (France), Luc E. Pâques (France), Julien Saudubray (France), Marc Villar (France), Vlatko Andonovski (FYR Macedonia), Dragi Pop-Stojanov (FYR Macedonia), Merab Machavariani (Georgia), Irina Tvauri (Georgia), Alexander Urushadze (Georgia), Bernd Degen (Germany), Jochen Kleinschmit (Germany), Armin König (Germany), Armin König (Germany), Volker Schneck (Germany), Richard Stephan (Germany), H. H. Kausch-Blecken Von Schmeling (Germany), Georg von Wühlisch (Germany), Iris Wagner (Germany), Heino Wolf (Germany), Paraskevi Alizoti (Greece), Filippos Aravanopoulos (Greece), Andreas Drouzas (Greece), Despina Paitaridou (Greece), Aristotelis C. Papageorgiou (Greece), Kostas Thanos (Greece), Sándor Bordács (Hungary), Csaba Mátyás (Hungary), László Nagy (Hungary), Thröstur Eysteinsson (Iceland), Adalsteinn Sigurgeirsson (Iceland), Halldór Sverrisson (Iceland), John Fennessy (Ireland), Ellen O'Connor (Ireland), Fulvio Ducci (Italy), Silvia Fineschi (Italy), Bartolomeo Schirone (Italy), Marco Cosimo Simeone (Italy), Giovanni Giuseppe Vendramin (Italy), Lorenzo Vietto (Italy), Janis Birgelis (Latvia), Virgilijus Baliuckas (Lithuania), Kestutis Cesnavicius (Lithuania), Darius Danusevicius (Lithuania), Valmantas Kundrotas (Lithuania), Alfas Pliûra (Lithuania), Darius Raudonius (Lithuania), Robert du Fays (Luxembourg), Myriam Heuertz (Luxembourg), Claude Parini (Luxembourg), Fred Trossen (Luxembourg), Frank Wolter (Luxembourg), Joseph Buhagiar (Malta), Eman Calleja (Malta), Ion Palancean (Moldova), Dragos Postolache (Moldova), Gheorghe Postolache (Moldova), Hassan Sbay (Morocco), Tor Myking (Norway), Tore Skrøppa (Norway), Anna Gugala (Poland), Jan Kowalczyk (Poland), Czeslaw Koziol (Poland), Jan Matras (Poland), Zbigniew Sobierajski (Poland), Maria Helena Almeida (Portugal), Filipe Costa e Silva (Portugal), Luís Reis (Portugal), Maria Carolina Varela (Portugal), Ioan Blada (Romania), Alexandru-Lucian Curtu (Romania), Lucian Dinca (Romania), Georgeta Mihai (Romania), Mihai Olaru (Romania), Gheorghe Parnuta (Romania), Natalia Demidova (Russian Federation), Mikhail V. Pridnya (Russian Federation), Andrey Prokazin (Russian Federation), Srdjan Bojovic (Serbia) , Vasilije Isajev (Serbia), Saša Orlovic (Serbia), Rudolf Bruchánik (Slovakia), Roman Longauer (Slovakia), Ladislav Paule (Slovakia), Gregor Bozič (Slovenia), Robert Brus (Slovenia), Katarina Celič (Slovenia), Hojka Kraigher (Slovenia), Andrej Verlič (Slovenia), Marjana Westergren (Slovenia), Ricardo Alía (Spain), Josefa Fernández-López (Spain), Luis Gil Sanchez (Spain), Pablo Gonzalez Goicoechea (Spain), Santiago C. González-Martínez (Spain), Sonia Martin Albertos (Spain), Eduardo Notivol Paino (Spain), María Arantxa Prada (Spain), Alvaro Soto de Viana (Spain), Lennart Ackzell (Sweden), Jonas Bergquist (Sweden), Sanna Black-Samuelsson (Sweden), Jonas Cedergren (Sweden), Gösta Eriksson (Sweden), Markus Bolliger (Switzerland), Felix Gugerli (Switzerland), Rolf Holderegger (Switzerland), Peter Rotach (Switzerland), Marcus Ulber (Switzerland), Sven M.G. de Vries (The Netherlands), Khouja Mohamed Larbi (Tunisia), Murat Alan (Turkey), Gaye Kandemir (Turkey), Gursel Karagöz (Turkey), Zeki Kaya (Turkey), Hasan Özer (Turkey), Hacer Semerci (Turkey), Ferit Toplu (Turkey), Mykola M. Vedmid (Ukraine), Roman T. Volosyanchuk (Ukraine), Stuart A'Hara (United Kingdom), Joan Cottrell (United Kingdom), Colin Edwards (United Kingdom), Michael Frankis (United Kingdom), Jason Hubert (United Kingdom), Karen Russell (United Kingdom), C.J.A. Samuel (United Kingdom).
 

Status of Corylus avellana conservation in Europe

Common hazel has been shown to have the highest level of genetic diversity in Europe compared with other deciduous species such as hawthorn (Crataegus monogyna), ash (Fraxinus excelsior), sessile oak (Quercus petraea), pedunculate oak (Quercus robur), and alder (Alnus glutinosa) (Brown et al., 2016). Its morphology is also highly polymorphic, with previously described species such as filbert hazel (Corylus maxima), pontic hazel (Corylus pontica) and colchian hazel (Corylus colchica) now being included as subspecies of common hazel (Brown et al., 2016).

In Finnish populations 83% of genetic diversity is within populations, and a lack of genetic structure in these populations suggests high gene flow (Tanhuanpää et al., 2019). Natural populations of common hazel in the United Kingdom and Ireland also have high levels of genetic diversity and low levels of population differentiation, indicating high effective gene flow across the populations and low asexual reproduction (Brown et al., 2016). It would be expected that gene flow is low as hazel nuts are heavy so dispersal is limited; however, the nuts can be dispersed far by birds, with nutcrackers (Nucifraga) having been observed to transport seeds up to 22 km, and pollen dispersal is high (Brown et al., 2016). Common hazel has a weak but significant correlation between genetic and geographic distances and absence of population structure, showing genetic uniformity across the recolonized part of the species’ range (Brown et al., 2016).

Common hazel can reproduce vegetatively, allowing it to create clonal individuals, which typically reduces overall genetic diversity, but vegetative reproduction appears to be rare in wild populations of common hazel (Brown et al., 2016).

 

The bibliographic review was conducted by James Chaplin of the EUFORGEN Secretariat in August 2024.

Glacial biogeography evolution

Pollen records suggest common hazel was one of the first species to recolonize Europe after the last ice age, replacing earlier colonizers such as birch (Betula) and then becoming an understory species, with its most northern populations in Fennoscandia (Brown et al., 2016). The recolonization of northern Europe by common hazel likely came from southwestern refugia, with Italian and Balkan refugial populations remaining in situ (Brown et al., 2016).

Cultivation and human intervention

Common hazel is diploid, monoecious, hermaphroditic, and self-incompatible, and has dichogamy and sporophytic incompatibility to avoid self-fertilization, making it strictly cross-pollinated. This also makes intraspecific hybridization common and means it is typically clonally propagated in cultivation (Brown et al., 2016; Helmstetter et al., 2020).

Its current distribution is heavily influenced by human-mediated dispersal, with Mesolithic tribes likely spreading the species even if they did not cultivate it (Helmstetter et al., 2020). Genetic and archaeological data suggest common hazel was domesticated multiple times (Brown et al., 2016). Common hazel is now the sixth most economically important tree nut crop worldwide. Italy produces roughly 15% of the world’s hazel nuts, and Türkiye producing as much as 80% (Helmstetter et al., 2020). Therefore, there is interest in breeding for commercially valuable cultivars and varieties resistant to disease and fungus such as Eastern filbert blight (Anisogramma anomola) (Rowley et al., 2018). Common hazel is the first genetically sequenced plant in the order Fagales (Rowley et al., 2018).

Domestication and selective breeding often cause bottlenecking and reduce genetic diversity. However, this may not be the case for perennial species such as hazelnut, as similar levels of heterozygosity were found in cultivated and wild individuals in Türkiye (Helmstetter et al., 2020). However, cultivated populations in Türkiye show more structuring and clustering than wild common hazel, with cultivars assigned to groups based on morphology such as nut shape (Helmstetter et al., 2020). There is evidence of past gene flow between wild and domesticated common hazel as well as among different cultivars. This can be problematic as gene flow between wild and cultivated varieties can lead to extinction of the wild species or poorer yields of cultivated varieties (Helmstetter et al., 2020).

 

The bibliographic review was conducted by James Chaplin of the EUFORGEN Secretariat in August 2024.

Threats to genetic diversity and gene flow of common hazel include habitat loss due to urbanization, land-use change, climate change, and diseases and fungus such as Eastern filbert blight (Brown et al., 2016). Additionally, the introduction of non-native species poses a risk of genetic pollution through hybridization. Recently a new powdery mildew disease has emerged affecting trees in the Black Sea region threatening Türkiye’s hazelnut production while also threatening American cultivars (Helmstetter et al., 2020). Therefore, controlled management of domestic common hazel varieties to reduce genetic pollution or the spread of diseases may be prudent. However, there is a lack of research on the conservation of common hazel genetic variation or the management of genetic conservation units.

 

The bibliographic review was conducted by James Chaplin of the EUFORGEN Secretariat in August 2024.

Genetic Characterisation of Corylus avellana and its GCUs

Availability of FRM

FOREMATIS

Contacts of experts

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Further reading

Beltramo, C., Valentini, N., Portis, E., Torello Marinoni, D., Boccacci, P., Sandoval Prando, M.A., and Botta, R. 2016. Genetic mapping and QTL analysis in European hazelnut (Corylus avellana L.). Molecular Breeding, 36: 27. https://doi.org/10.1007/s11032-016-0450-6

References

Brown, J.A., Beatty, G.E., Montgomery, W.I., and Provan, J. 2016. Broad-scale genetic homogeneity in natural populations of common hazel (Corylus avellana) in Ireland. Tree Genetics & Genomes, 12: 122. https://doi.org/10.1007/s11295-016-1079-7

Helmstetter, A.J., Oztolan‐Erol, N., Lucas, S.J., and Buggs, R.J. 2020. Genetic diversity and domestication of hazelnut (Corylus avellana L.) in Turkey. Plants, People, Planet, 2(4): 326–339.

Rowley, E.R., VanBuren, R., Bryant, D.W., Priest, H.D., Mehlenbacher, S.A., and Mockler, T.C. 2018. A draft genome and high-density genetic map of European hazelnut (Corylus avellana L.). BioRXiv, 469015. https://doi.org/10.1101/469015

Tanhuanpää, P., Heinonen, M., Bitz, L., and Rokka, V.M. 2019. Genetic diversity and structure in the northern populations of European hazelnut (Corylus avellana L.). Genome, 62(8): 537–548.