2017
DOI: 10.1111/plb.12644
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Pollination in the Chilean Mediterranean‐type ecosystem: a review of current advances and pending tasks

Abstract: We conducted a systematic review of the scientific literature published on plant-pollinator interactions, from both the plant and pollinator perspective, in the Chilean Mediterranean-type ecosystem (MTE hereafter). Our search identified 69 published papers on 235 native plant species from 62 families. Less than 7.9% of the flowering species inhabiting the Chilean Mediterranean have been studied, and most studies were restricted to only one locality and one reproductive season. The geographic location of the st… Show more

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Cited by 22 publications
(23 citation statements)
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“…This relationship is consistent with their flower morphology (funnelform) and flowering peaks that occur in October and November when pollinator activity increases coupled with the increase in day temperature (Walter, 2008). The high diversity of native bees in the xeric areas of Chile has long been recognized in the literature (Michener, 1979) which are important pollinators in central Chile (Montalva & Ruz, 2010;Medel, González-Browne & Fontúrbel, 2018), some such as Alloscirtetica lanosa Urban, 1971 (Apidae), Diadasia chilensis Spinola, 1851 (Apidae), Xenochilicola diminuta Toro and Moldenke, 1979 (Colletidae) and…”
Section: Pollinator Assemblagessupporting
confidence: 59%
“…This relationship is consistent with their flower morphology (funnelform) and flowering peaks that occur in October and November when pollinator activity increases coupled with the increase in day temperature (Walter, 2008). The high diversity of native bees in the xeric areas of Chile has long been recognized in the literature (Michener, 1979) which are important pollinators in central Chile (Montalva & Ruz, 2010;Medel, González-Browne & Fontúrbel, 2018), some such as Alloscirtetica lanosa Urban, 1971 (Apidae), Diadasia chilensis Spinola, 1851 (Apidae), Xenochilicola diminuta Toro and Moldenke, 1979 (Colletidae) and…”
Section: Pollinator Assemblagessupporting
confidence: 59%
“…For example, Chile has protected ~22% of its territory, but 89% of those protected areas are located in latitudes > 43ºS, resulting in an uneven distribution of the area under protection regime (Armesto et al, 1998), leaving many conservationconcern and highly threatened taxa unprotected (e.g., Duarte et al, 2014). In this example, most of the threatened and endemic species, along with specialized ecological interactions occur in the Mediterranean type-ecosystem of central Chile (Medel et al, 2018), which has the lowest protected area coverage, and also is highly-threatened by the expansion of urban areas, vineyards, and avocado plantations. If we examine this pattern at the global scale, we observe a moderate correspondence of protected areas with biodiversity hotspots (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…This assumption has been critically examined in optimality models that restrict the generality of Stebbins' model to cases where the marginal fitness gain of specialization exceeds the marginal fitness loss of adapting to the many less efficient pollinators [17]. The relatively depauperate Chilean pollinator assemblages (4.25 pollinators per plant species on the average, [18]) offer little gain from evolving generalized flower phenotypes, and, therefore, high marginal fitness loss can be expected relative to specialization on the most effective pollinator.…”
Section: Discussionmentioning
confidence: 99%