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20 results for “evergreen montane forest”
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021). in Floristic, Vegetation And Climate Assessment Of The Early/Middle Miocene Parschlug Flora Indicates A Distinctly Seasonal Climate
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021).
Data from: Montane regions shape patterns of diversification in small mammals and reptiles from Madagascar’s moist evergreen forest
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Figure 14. A in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 14. A relationship between fore wing length and tongue length of the observed bees and syrphid flies.
Figure 13. A in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 13. A scatter chart of non-metric multidimensional scaling (NMDS) ordination of flower-visitor assemblages (stress value = 0.22). Pearson and Kendall correlations of 13 guilds with ordination axes are shown in red arrows.
Figure 17 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 17. Comparison of pollination systems among different habits of the plants observed in the montane forests in Laos.
Figure 9 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 9. Flowers visited by dipterans. (a) Curculigo crassifolia visited by a syrphid fly; (b) Lindera tonkinensis visited by a muscid fly; (c) Flueggea virosa visited by a mosquito; (d) Breynia retusa visited by a cecidomyiid midge; (e) Isodon coetsa visited by a syrphid fly; (f) Arisaema balansae visited by a mycetophilid midge (spathe dissected); (g, h) Alocasia odora visited by a drosophilid fly; (i) Maesa sp. visited by a sciarid midge.
Figure 7 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 7. Flowers visited by long-tongued bees and flies. (a) Derris scandens visited by Bombus sp.; (b) Amalocalyx microlobus visited by Bombus trifasciatus; (c) Zingiber zerumbet visited by B. trifasciatus; (d, e) Myrioneuron faberi visited by Elaphropoda; (f) Alpinia kwangsiensis visited by Xylocopa caerulea; (g) Phlogacanthus sp. visited by long-tongued syrphid fly.
Figure 5 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 5. Seasonal changes in numbers of bees observed on flowers: (a) honeybees of subgenera Megapis and Apis; (b) honeybees of subgenus Micrapis and stingless bees; (c) bumblebees; (d) Anthophorini; (e) Xylocopini, Ctenoplectini and Megachilidae; (f) Halictidae, Colletidae and Melittidae.
Figure 4 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 4. Seasonal changes in the number of observed flowering plant species at the study sites in Laos. The letter 'n' in the graph denotes a lack of data.
Figure 12 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 12. Flowers visited by thrips and bugs. (a, b) Chloranthus nervosus visited by thrips; (c) Mytilaria laosensis visited by thrips; (d, e) Dioscorea bulbifera visited by thrips; (f) Maesa sp., visited by a mecopteran; (g) Elatostema involucratum visited by a mirid bug; (h) Elatostema balansae visited by a mirid bug.
Figure 10 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 10. Flowers visited by beetles. (a, b) Fissistigma cupreonitens visited by chrysomelid beetles, an inner petal removed to show the inner chamber in (b); (c) Gentiana zollingeri visited by a scarabaeid beetle; (d) Melastoma malabathrica visited by scarabaeid beetles; (e) Photinia prunifolia visited by a scarabaeid beetle; (f) Lithocarpus elegans visited by a cerambycid beetle; (g) Euodia lepta visited by cerambycid beetles; (h) Photinia prunifolia visited by a cerambycid beetle; (i) Melastoma malabathrica visited by a meloid beetle, Mylabris phalerata; (j) Lithocarpus mucronata visited by a dermatid beetle; (k) Vitex leptobotrys visited by a curculionid beetle.
Figure 8 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 8. Flowers visited by small bees and wasps. (a) Embelia ribes visited by a stingless bee; (b) Thladiantha sp. visited by Ctenoplectra cornuta (visitor not in the photo); (c) Uncaria scandens visited by a halictid bee; (d) Sterculia henryi visited by a halictid bee; (e) Ludwigia hyssopifolia visited by a halictid bee; (f) Lysimachia siamensis visited by a Macropis orientalis bee; (g) Baliospermum montanum visited by a scoliid wasp; (h) Euphorbia lathyris visited by an ant; (i) Euodia lepta visited by an eumenid wasp; (j) Cynoglossum zeylanicum visited by an eumenid wasp; (k) Photinia prunifolia visited by an eumenid wasp.
Figure 2 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 2. Seasonal changes in monthly temperature (averages of monthly maximum, mean and minimum) and rainfall at Xam Neua near S4.
Figure 6 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 6. Flowers visited by honeybees: A. laboriosa (a–c), A. dorsata (d–f), Apis cerana (g–k) and A. florea (l). (a) Castanopsis diversifolia; (b) Castanopsis diversifolia; (c) Rubus multibracteatus; (d) Stachytarpheta jamaicensis; (E) Symplocos ramosissima; (f) Pogostemon nelsonii; (g) Ageratum houstonianum; (h) Photinia prunifolia; (i) Rubus obcordatus; (j) Bidens pilosa var. radiata; (k) Ixeris gracilis; (l) Photinia prunifolia.
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.
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.
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.
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.
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.
Figure 1 in Community-level plant-pollinator interactions in a Palaeotropical montane evergreen oak forest ecosystem
Figure 1. Map of study sites S1–S5 in Laos. See Table 1 for details of the sites.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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