Liliales

Diversité décrite (Catalogue of Life)

Statut de conservation IUCN (parmi les espèces évaluées)

• LC
  120 (44.8%)
• VU
  44 (16.4%)
• NT
  31 (11.6%)
• EN
  29 (10.8%)
• DD
  23 (8.6%)
• CR
  21 (7.8%)

Distribution biogéographique

• Swedenintroduced3 esp.
• Turkey3 esp.
• Chinanative1 esp.
• China (Hunan)1 esp.
• China (Yunnan)1 esp.
• Cyprus1 esp.
• Distribution and habitat. Gagea khassanovii is endemic to the eastern part of the Fergana Valley, occurring in the middle belt of the Chatkal and Alay Mountain ranges (Fig. 5). The species inhabits gravelly soils and rocky outcrops of mountain spurs, typically within well-drained, xerophytic habitats.1 esp.
• Distribution, habitat and ecology: — Known thus far only from two localities, the old Quito-Santo Domingo Road in Santo Domingo de los Tsachilas Province and the surroundings of Mindo in Pichincha Province (Fig. 3). According to the Ministerio del Ambiente del Ecuador (2013), this area corresponds to the low montane evergreen forest of the Western Cordillera of northern Ecuador (forest type BsBn 04), where the largest number of endemic Ecuadorian species are found (León-Yánez et al. 2011). Field observations show that B. globosa likely climbs only 1 – 2 m on forest vegetation and flowers in shaded areas, making it hard to find. This is likely one of the reasons for the lack of prior collections despite the history of botanical collecting in the area. The new species grows sympatrically with B. pardina Herber (1837: 120).1 esp.
• Greecenative1 esp.
• Greece (Mt. Timfi, Mt. Douskon)1 esp.
• Greece (Samothraki, Mt. Parnassos, N-Peloponissos)1 esp.
• India (Maharashtra)1 esp.
• Irannative1 esp.
• Israelnative1 esp.
• Jordannative1 esp.
• Kazakhstannative1 esp.
• Kazakhstan (Balkhash-Alakol, Dzungarian Alatau)1 esp.
• Kazakhstan (Karatau)1 esp.
• Kyrgyzstan (Talas Alatau)1 esp.
• Lebanonnative1 esp.
• Myanmar (Burma)native1 esp.
• N-Thailand1 esp.
• NC-Thailand1 esp.
• NW-Thailand (Chiang Mai)1 esp.
• NW-Thailand (Lamphun)1 esp.
• S-Brazil (Santa Catarina)1 esp.
• South Africa (W-Cape Prov., N-Cape Prov.)1 esp.
• Sweden1 esp.
• Syrianative1 esp.
• Turkey (Anatolia)1 esp.

Régions biogéographiques agrégées depuis Catalogue of Life Cross-References (distribution par espèce déclarative).

Profil de traits agrégé

• try_woodiness216 esp.
  non-woody176

  woody40
• try_leaf_type213 esp.
  broadleaved213
• try_photosynthetic_pathway189 esp.
  C3189
• try_growth_form176 esp.
  herb175

  shrub1
• try_leaf_compoundness142 esp.
  simple140

  compound2
• fungalroot_name106 esp.
  2637.00à36014.00

  moy 14792.14
• fungalroot_mycorrhiza_type106 esp.
  AM100

  non-mycorrhizal6
• fungalroot_source106 esp.
  10.1890/11-1749.1__Akhmetzhanova, A. A., Soudzilovskaia, N. A., Onipchenko, V. G., Cornwell, W. K., Agafonov, V. A., Selivanov, I. A., & Cornelissen, J. H. (2012). A rediscovered treasure: mycorrhizal intensity database for 3000 vascular plant species across the former Soviet Union. Ecology, 93(3), 689-690.22

  __Maeda, M. (1954). The meaning of mycorrhiza in regard to systematic botany. Kumamoto J. Sci. Ser. B., 3, 57-84.16

  __Merckx V.S.F.T (eds.). 2013. Mycoheterotrophy: The Biology of Plants Living On Fungi. 356 p. Springer, New York. ISBN 9781461452089.12
• fungalroot_am_method106 esp.
  Other76

  McGonigle et al. 1990: RLC (%)23

  Phillips & Hayman 1970: RLC (%)3
• eive_t_position94 esp.
  0.92à9.100-10

  moy 4.75
• eive_m_position92 esp.
  0.33à6.070-10

  moy 3.52
• eive_r_position88 esp.
  2.79à9.730-10

  moy 6.72

Traits agrégés sur les espèces du taxon (matview taxon_traits_best : WoRMS, FishBase, EBird, GBIF, EOL, TRY…).

Taxons enfants directs (10)

• Famille Alstroemeriaceae5
• Famille Campynemataceae2
• Famille Colchicaceae21
• Famille Corsiaceae4
• Famille Liliaceae31
• Famille Melanthiaceae22
• Famille Petermanniaceae1
• Famille Philesiaceae4
• Famille Ripogonaceae2
• Famille Smilacaceae4