Abies cilicica
Cilician fir

Cilician fir (Abies cilicica) is a conifer endemic to the eastern Mediterranean region, found in Lebanon, Syria, and southern Türkiye (Awad et al., 2014). It inhabits mountainous areas, flourishing at elevations of 900 to 2 100 metres. This species thrives best in well-drained, rocky, shallow, and moist calcareous soils in cool mountain climates, often mixing with other conifers and broadleaf trees. Where abundant, the tree’s wood is traded locally and widely utilized in building. It is occasionally used in landscaping and as a Christmas tree due to its attractive form and foliage (Awad et al., 2014).

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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 Abies cilicica conservation in Europe

Genetic diversity and variation

Cilician fir shows considerable variation in morphological traits (Gülsoy, 2022). However, it has low within-population genetic diversity, low allelic richness, and low among-population genetic differentiation compared with other fir (Abies) species (Awad et al., 2014; Sękiewicz et al., 2015). This low diversity could be a result of historical harvesting for timber and current illegal logging and overgrazing causing habitat fragmentation (Awad et al., 2014). Despite this, inbreeding is low and there are no signs of genetic bottlenecking in the species, showing that, despite isolation, long-distance dispersal still takes place and population sizes remain effective (Awad et al., 2014).

Genetic distribution and clustering

Genetic analysis revealed two genetically distinct clusters in the north-east and south-west of Lebanon, with south-western populations being less genetically diverse and more differentiated (Awad et al., 2014). This makes north-eastern populations in Lebanon particularly valuable for genetic conservation of the species (Awad et al., 2014). However, all populations of Cilician fir tend to maintain a high level of genetic diversity considering the species fragmented populations (Sękiewicz et al., 2015), although Lebanese populations may contain less genetic diversity than Turkish populations (Sękiewicz et al., 2015).

Rapid colonization, with both long and short distance seed dispersal, and recent migration along altitudinal gradients to higher altitudes has the result of increased atmospheric aridity during the last glaciation affects the genetic diversity and structure of Cilician fir (Awad et al., 2014; Sękiewicz et al., 2015). Genetic diversity of Cilician fir between populations varies according to altitude and latitude (Gülsoy, 2022). Mountain ranges have also acted as barriers, isolating populations and driving the spatial distribution of genetic variation in the species (Sękiewicz et al., 2015).

 

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

Interspecific taxa dynamics

Cilician fir is closely related to the western-Mediterranean group of firs, which includes Moroccan fir (Abies marocana) and Spanish fir (Abies pinsapo) (Alizoti et al., 2011). It may be divided into two morphologically distinct lineages, an eastern lineage, Abies cilicica subsp. cilicica, in Syria and Lebanon, and a western lineage Abies cilicica subsp. isaurica in Türkiye (Sękiewicz et al., 2015).

 

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

Threats

Overharvesting and illegal logging, overgrazing, prolonged drought, and wildfires are major threats to Mediterranean firs, especially at lower elevations (Sękiewicz et al., 2015). Cilician fir is considered near threatened overall and critically endangered at the national level in Lebanon, making it vulnerable to threats (Awad et al., 2014). Fragmentation has occurred in Cilician fir populations from historic logging and the expansion of agriculture, increasing genetic drift and inbreeding and negatively affecting the genetic diversity of the species’ populations (Sękiewicz et al., 2015). Reduced genetic diversity will have a severe negative impact on the adaptive potential of the species in the face of climate change (Sękiewicz et al., 2015). However, it is difficult to predict the effects of climate change on seed production, natural regeneration, and recruitment or on the risks from insects and pathogens (Alizoti et al., 2011).

Management

Cilician fir is already protected in national parks and nature reserves in Türkiye and Lebanon (Alizoti et al., 2011). Management of conservation units should aim to assist natural regeneration and avoid introducing seeds or seedlings from exotic locations; where this is not possible, artificial regeneration with local genetic material should be used (Alizoti et al., 2011). Cilician fir has sufficient genetic and trait variation to give it potential to adapt to changing climates, meaning assisted migration to locations where future climates will be more suitable could be used to conserve the species’ genetic diversity (Awad et al., 2014; Gülsoy, 2022). The tree is also less water-demanding than species such as silver fir (Abies alba), meaning it could be a useful forestry species where precipitation has declined as a result of climate change (Alizoti et al., 2011). When ex situ conservation is necessary, the focus should be on small populations as they may suffer from insufficient seed production or unsuccessful pollination in their natural environment (Alizoti et al., 2011). Cilician fir has significant economic value in Türkiye; therefore, conservation efforts are focused on monitoring the demography and genetic threats to existing populations to avoid further loss of genetic diversity (Sękiewicz et al., 2015).

 

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

Genetic Characterisation of Abies cilicica and its GCUs

Availability of FRM

FOREMATIS

EUFORGEN’s publications

Technical guidelines for genetic conservation and use

Abies spp - Technical guidelines for genetic conservation and use for Mediterranean firs

Publication Year: 2011
Author: Alizoti, P.G. ; Fady, B.; Prada, M.A.; Vendramin, G.G.

Due to the threats, endemism and geographically scattered distribution, the conservation of Mediterranean firs and their genetic resources is a major challenge.

The genetic resources of the firs are currently conserved in various protected areas that have rarely been established for this purpose. Due to their evolutionary history and specific adaptation, the fir forests harbour unique genetic resources that are important beyond the Mediterranean. Thus, the establishment of conservation units for the firs that meet pan-European minimum requirements for dynamic gene conservation is of crucial importance.

At present, several of the species and their genetic resources are protected either in situ (national parks, nature reserves and gene conservation units) or ex situ (conservation seed orchards and stands). The critically endangered A. nebrodensis is conserved in situ in the Madonie Regional Park in Sicily, but the reinforcement of the species has been problematic mainly due to soil degradation in its natural habitat. A. nebrodensis is also conserved ex situ in a seed orchard (with grafts of the 29 remaining individuals of the species) in Arezzo, in botanical gardens (40 000 plants in the Botanical Garden of Palermo), arboreta and in private properties in the Madonie Mountains close to the natural habitat. A. borisiiregis and A. cephalonica are protected in situ in various protected areas in Greece. Genetic material, representing almost the whole natural distribution of the fir species, is included in provenance trials established in Greece and France. A. cilicica is protected in national parks, nature reserves and seed stands in ten areas in Turkey and in Lebanon while in Syria it is considered as an endangered species. A. equi-trojani is conserved in situ in the Kazdagi Goknari nature reserve in Turkey. A. nordmanniana is also covered by protected areas in Turkey and several provenances are growing ex situ in test sites, plantations and arboreta in Denmark and France. The A. pinsapo forests are included in three protected areas in Spain. A. numidica is protected in the Djebel Barbor nature reserve located in the Petite Kabylia Mountain range of Algeria and the same provenance is reportedly also conserved in ex situ stands. At present A. marocana is conserved in a nature reserve in Morocco and seven ex situ stands have also been established for the species.

Climate change will have an impact on the current in situ conservation efforts but it is difficult to predict its effect on seed production, natural regeneration and recruitment of the firs as well as on the risks from insects and pathogens. The dynamic gene conservation units should be monitored in order to ensure that the populations are not seriously affected and that they retain their evolutionary potential and regenerate naturally. Management of the units should aim mainly at assisting natural regeneration and when this is not possible, the area should be artificially regenerated with local genetic material. Management of natural forests should also safeguard genetic resources by allowing natural selection to occur on regeneration in a variety of situations. Ex situ conservation efforts should focus on small populations that have an endangered status, insufficient seed production or unsuccessful pollination in their natural environment. This approach is useful especially in case of rare species or species with limited or scattered distribution as ex situ stands with a sufficient number of genotypes form new interbreeding populations that will produce seeds with a potentially high genetic diversity.

Mediterranean firs offers an opportunity to tackle the predicted forest decline in southern Europe as a result of climate change. A. nordmanniana has already been used for reforestation in Europe. Other Mediterranean firs (particularly A. cephalonica, A. bornmuelleriana and A. cilicica) are far less water demanding and could represent an alternative for silver fir (A. alba) in Europe. Fir provenance tests in the Mediterranean include material that has demonstrated good growth, adaptation to drought and late bud burst in spring. Such provenances of Mediterranean firs could be of interest for the European forestry.

Due to the threats, endemism and geographically scattered distribution, the conservation of Mediterranean firs and their genetic resources is a major challenge.

The genetic resources of the firs are currently conserved in various protected areas that have rarely been established for this purpose. Due to their evolutionary history and specific adaptation, the fir forests harbour...

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References

Alizoti, P.G., Fady, B., Prada, M.A., and Vendramin, G.G. 2011. EUFORGEN Technical Guidelines for genetic conservation and use of Mediterranean firs (Abies spp.). Rome, Bioversity International. 6 pp.

Awad, L., Fady, B., Khater, C., Roig, A., and Cheddadi, R. 2014. Genetic structure and diversity of the endangered fir tree of Lebanon (Abies cilicica Carr.): implications for conservation. PLoS One, 9(2): e90086. https://doi.org/10.1371/journal.pone.0090086

Gülsoy, A.M. 2022. Genetic variation pattern among Abies cilicica (Pinaceae) populations: Adaptive seed and seedling traits. PhD Thesis. Ankara, Middle East Technical University.

Sękiewicz, K., Dering, M., Sękiewicz, M., Boratyńska, K., Iszkuło, G., Litkowiec, M., Ok, T., Dagher-Kharrat, M.B., and Boratyński, A. 2015. Effect of geographic range discontinuity on species differentiation – East-Mediterranean Abies cilicica: a case study. Tree Genetics & Genomes, 11: 810. https://doi.org/10.1007/s11295-014-0810-5