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159 results for “pollination interactions”

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zenodo32/100

Figure 3 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem

Figure 3. Landscapes of the study sites S1–S5. (a) a meadow at S1; (b) paddy fields and secondary deciduous forests at S2; (c) a subtropical evergreen forest at S3; (d) a landscape at S4; (e) a valley inhabited by several Impatiens species at S4; (f) an evergreen oak forest near the summit of a mountain at S4; (g) a riverine forest inhabited by Mytilaria laosensis at S4; (h) limestone hills at S5.

opennotspecifiedFeb 2021View details →
zenodo32/100

Figure 11 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem

Figure 11. Flowers visited by lepidopterans. (a) Isodon glaucocalyx visited by papilionid butterfly Papilio polytes; (b) Barleria cristata visited by a papilionid butterfly Papilio protenor; (c) Mussaenda cambodiana visited by a papilionid butterfly Troides helena; (d) Baliospermum montanum visited by a lycaenid butterfly Heliophorus epicles; (e) Lindera tonkinensis visited by a lycaenid butterfly Pithecos corbus; (f) Blumea martiniana visited by a nymphalid butterfly Zemeros flegyas; (g) Lindera tonkinensis visited by a nymphalid butterfly Yptima confusa; (h) Impatiens violaeflora visited by a hesperiid butterfly Onryza siamica; (i) Pottsia laxiflora visited by a pierid butterfly Appias albina; (j) Swertia aungustifolia visited by an arctiid moth and a hovering blue-banded Amegilla bee; (k) Ligustrum indicum visited by an arctiid moth.

opennotspecifiedFeb 2021View details →
zenodo32/100

Figure 16 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem

Figure 16. The observed plant–pollinator network between flowers and eight groups of long-tongued bees. See Table 2 for plant species codes.

opennotspecifiedFeb 2021View details →
zenodo32/100

Figure 15 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem

Figure 15. Flowers of eight observed Impatiens species (Bal1–Bal8): (a) I. chinensis; (b) I. commellinoides; (c) I. ernestii; (d) I. longiloba; (e) I. mengtszeana; (f) I. rubricolor; (g) I. tigrina; (h) I. violaeflora.

opennotspecifiedFeb 2021View details →
zenodo32/100

Figure 18 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem

Figure 18. Comparison of pollination systems among climatic and geographical regions: subalpine forests and meadows at Mt. Kushigata, central Japan (Kato 2000; Kato et al. 1993b), cool temperate deciduous forests at Ashu (Kato et al. 1990), warm temperate evergreen forest ecosystem at Amami Island (Kato 2000), montane evergreen forests in Laos (this paper), tropical monsoon forest ecosystem at lowland Laos (Kato et al. 2008), Bornean tropical rain forests at Lambir Hills National Park in Malaysia (Momose et al. 1998), and a Neotropical rain forest at La Selva (Kress and Beach 1994). The asterisk denotes large bees including long-tongued bees and carpenter bees.

opennotspecifiedFeb 2021View details →
zenodo32/100

Data for: A test of Sensory Drive in plant-pollinator interactions: habitat heterogeneity shapes pollinator preference for a floral visual signal

<p>DATA:</p> <p>FinnKoski_PollData_Final:&nbsp;Pollinator visitation data to floral arrays analyzed</p> <p>Spectra used for vismodels.zip:&nbsp;reflectance spectra of flowers and floral backgrounds, irradiance spectra</p> <p>ColorContrastData: visual contrast data analyzed</p> <p>CODE:&nbsp;</p> <p>vismod_code.R : code used for visual system modeling and calculation of contrast</p> <p>SAS_modelcode.R: SAS code used to analyze pollinator visitation data and color contrast data</p>

opencc-by-4.0Jul 2021View details →
zenodo32/100

FIG. 2 in Interactions between the sexually deceptive orchid Spiculaea ciliata and its wasp pollinator Thynnoturneria sp. (Hymenoptera: Thynninae)

FIG. 2. The number of males contacting an elbow orchid over 5 minute presentations of bait specimens. (Top) Results of 10 trials conducted at Frank Hann National Park in November 1995. DiOEerences in the mean numbers of contacts over the 5 minutes are statistically signi®cant: ANOVA F = 7.6, p &lt;0.001. (Middle) Results of 16 trials at [4,45] Pallarup Rocks Reserve in November 1995. DiOEerences in the mean numbers of contacts over the 5 minutes are statistically signi®cant: ANOVA F = 5.4, p &lt;0.001. (Bottom) [4, 75] Results of 36 trials at Pallarup Rocks Reserve in November 1997. DiOEerences in the mean numbers of contacts over the 5 minutes are statistically signi®cant: ANOVA F = 11.5, p&lt;0.001.

opennotspecifiedApr 2000View details →
dryad32/100

Individual flowering phenology shapes plant-pollinator interactions across ecological scales affecting plant reproduction

<p>1. The balance of pollination competition and facilitation amongst co-flowering plants and abiotic resource availability can modify plant species and individual reproduction. Floral resource succession and spatial heterogeneity modulate plant-pollinator interactions across ecological scales (individual plant, local assemblage, interaction network of agroecological infrastructure across the farm). Intraspecific variation in flowering phenology can modulate the precise level of spatio-temporal heterogeneity in floral resources, pollen donor density and pollinator interactions that a plant individual is exposed to, thereby affecting reproduction.</p> <p>2. We tested how abiotic resources and multi-scale plant-pollinator interactions affected individual plant seed set, modulated by intraspecific variation in flowering phenology and spatio-temporal floral heterogeneity arising from agroecological infrastructure. We transplanted two focal insect-pollinated plant species (<em>Cyanus</em> <em>segetum</em> and <em>Centaurea</em> <em>jacea</em>, n = 288) into agroecological infrastructure (10 sown wildflower, 6 legume-grass strips) across a farm-scale experiment (125 ha).</p> <p>3. We applied an individual-based phenologically explicit approach to match precisely the flowering period of plant individuals to the concomitant level of spatio-temporal heterogeneity in plant-pollinator interactions, potential pollen donors, floral resources and abiotic conditions (temperature, water, nitrogen).</p> <p>4. Individual plant attractiveness, assemblage floral density and conspecific pollen donor density (<em>C</em>. <em>jacea</em>) improved seed set. Network linkage density increased focal species' seed set and modified the effect of local assemblage richness and abundance on <em>C</em>. <em>segetum</em>. Mutual dependence on pollinators in networks increased <em>C</em>. <em>segetum</em> seed set, while <em>C</em>. <em>jacea</em> seed set was greatest where both specialization on pollinators and mutual dependence was high. Abiotic conditions were of little or no importance to seed set.</p> <p>5. Intra- and interspecific plant-pollinator interactions respond to spatio-temporal heterogeneity arising from agroecological management affecting wild plant species reproduction. The interplay of pollinator interactions within and between ecological scales affecting seed set implies a co-occurrence of pollinator-mediated facilitative and competitive interactions among plant species and individuals. </p>

opencc-zeroDec 2022View details →
dryad32/100

Data from: Floral volatiles structure plant-pollinator interactions in a diverse community across the growing season

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publicAug 2019View details →
dryad32/100

Habitat loss increases seasonal interaction rewiring in plant-pollinator networks

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publicAug 2022View details →
dryad32/100

Data from: Interaction intensity and pollinator-mediated selection

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publicJan 2018View details →
dryad32/100

Geographical variation in the bill-flower fit in a plant-pollinator interaction in western Mexico

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publicApr 2021View details →
dryad32/100

Data from: Pollinator-mediated interactions between cultivated papaya and co-flowering plant species

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publicDec 2018View details →
dryad32/100

Data from: Asymmetrical nature of the Trollius-Chiastocheta interaction: insights into the evolution of nursery pollination systems

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publicJun 2016View details →
dryad32/100

Data from: Removing interactions, rather than species, casts doubt on the high robustness of pollination networks

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publicOct 2015View details →
dryad32/100

Data from: Quantifying hummingbird preference for floral trait combinations: the role of selection on trait interactions in the evolution of pollination syndromes

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publicMar 2015View details →
dryad32/100

Data from: Species traits and abundances predict metrics of plant–pollinator network structure, but not pairwise interactions

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publicJun 2015View details →
dryad32/100

Data from: Plant interactions shape pollination networks via nonadditive effects

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publicJan 2019View details →
dryad32/100

Data from: Specialization and phenological synchrony of plant–pollinator interactions along an altitudinal gradient

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publicOct 2014View details →
dryad32/100

Data from: Pollinator interactions with yellow starthistle (Centaurea solstitialis) across urban, agricultural, and natural landscapes

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publicOct 2014View details →

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International Brain Laboratory public data

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