Results 81 to 90 of about 23,163 (285)
5b. MaxEnt output - cumulative
Cumulative data: MaxEnt results (csv) and habitat suitability ascii ...
Sofie te Wierik (3757807)
core +1 more source
Climate change drives shifts in suitable habitats for Eurasian lynx and its prey (hare, roe deer) in Mohe, Daxing'anling Mountains. Under RCP scenarios, moderate warming (RCP4.5) promotes substantial habitat expansion, while high‐emission conditions (RCP8.5) lead to strong expansion in the 2050s but slower gains and partial contraction by the 2070s ...
Binglian Liu +5 more
wiley +1 more source
CarlaBirdy/MaxEnt-habitat-models: MaxEnt-habitat-models
<h1>Habitat suitability maps for Australian flora and fauna under CMIP6 climate scenarios</h1> <p>Authors: Carla Archibald*, David Summers, Erin Graham, Brett Bryan *For inquiries, contact: c.archibald@deakin.edu.au</p> <p> ...
Carla Archibald
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Raw data: MaxEnt results (csv) and haibitat suitability ascii ...
Sofie te Wierik (3757807)
core +1 more source
Read the free Plain Language Summary for this article on the Journal blog. Abstract Climate warming is redistributing insects, but species‐level projections alone rarely show which functional strategies are most exposed or how traits are linked to climatic niche structure.
Facheng Guo +3 more
wiley +1 more source
Description of cross-validated Maxent modeling experiments.
Description of cross-validated Maxent modeling experiments.
Shannon L. J. Bayliss (7059107) +3 more
core +1 more source
Aphelonyx cerricola and the different stages that make this gall colonizable by ants. ABSTRACT Wasps of the family Cynipidae are known to induce galls of a species‐specific morphology, which during senescence provide a refuge for secondary insect fauna, especially ants.
Daniele Giannetti +5 more
wiley +1 more source
Maps of habitat suitability produced by MaxEnt for each species; coordinate system ...
Secondi, Jean +5 more
core +1 more source
Our analysis revealed that while climate strongly influenced species distributions, habitat change drove most observed delays in distribution responses. In terms of community ecology, dispersed communities exhibited shorter time lags than concentrated groups. Analyses of lag duration revealed a 5–6‐year distribution lag effect in high‐altitude ungulate
Lu Wang +6 more
wiley +1 more source

