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53 results for “willow species”
Vascular plant species list, by quadrat, for harvests of tussock , wet sedge and dry heath tundra and a toposequence which included "shrub/lupine," "riverside willow" and "footslope Equisetum" communities North Slope Alaska, Arctic LTER 1983-1996.
Vascular plant species list, by quadrat, for harvests of tussock tundra, wet sedge tundra, dry heath tundra, and a toposequence which also included "shrub/lupine," "riverside willow" and "footslope Equisetum" communities. Includes results of long-term nutrient enrichment, increased temperature, and shade houses in selected tundra types.
Photoprotective leaf pigments and chlorophyll fluorescence measurements during a greenhouse drought experiment: An evolutionary perspective on functional diversity in co-occuring willow(salix) species
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by comparing species physiology in a greenhouse.
Phospholipid fatty acids (PFLA) on decomposed litter: An evolutionary perspective on functional diversity in co-occuring willow(salix) species
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by comparing species physiology in a greenhouse.
Gas exchange, dieback, leaf water potential and chlorophyll content during a greenhouse drought experiment: An evolutionary perspective on functional diversity in co-occuring willow(salix) species
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by comparing species physiology in a greenhouse.
Data from: Experimental warming does not change fluctuating asymmetry in three willow species
Open the record for dataset details and reuse information.
Growth, gas exchange and hydraulic conductivity of greenhouse grown willows under pre-drought conditions: Investigating patterns of habitat specialization in fifteen co-occurring willow and poplar species.
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by documenting species distributions in plots across a water availability gradient and comparing species physiology in the field and greenhouse. By taking a phylogenetic approach, I also investigated whether willow communities exhibit phylogenetic community structure and whether there is evidence for environmental filtering.
Functional traits measured in a greenhouse common garden: Investigating patterns of habitat specialization in fifteen co-occurring willow and poplar species.
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by documenting species distributions in plots across a water availability gradient and comparing species physiology in the field and greenhouse. By taking a phylogenetic approach, I also investigated whether willow communities exhibit phylogenetic community structure and whether there is evidence for environmental filtering.
Sequences of the nuclear gene ADH for thirteen species of willows and two poplars: Investigating patterns of habitat specialization in fifteen co-occurring willow and poplar species.
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by documenting species distributions in plots across a water availability gradient and comparing species physiology in the field and greenhouse. By taking a phylogenetic approach, I also investigated whether willow communities exhibit phylogenetic community structure and whether there is evidence for environmental filtering.
Functional traits measured under field conditions in native populations: Investigating patterns of habitat specialization in fifteen co-occurring willow and poplar species.
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by documenting species distributions in plots across a water availability gradient and comparing species physiology in the field and greenhouse. By taking a phylogenetic approach, I also investigated whether willow communities exhibit phylogenetic community structure and whether there is evidence for environmental filtering.
FIGURES 138–151 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). I: Redescriptions of willow-dwelling species from West Tien Shan Mountains
FIGURES 138–151. Macropsis tarbagataica Mitjaev, oscillograms of calling signals of males from different localities. 138– 141, 144–147―Arslanbob, No. 6 on the map; 142, 148–149―environs of Almaty, Southern Kazakhstan; 143, 150– 151―South Urals, Russia. Faster oscillograms of the parts of signals indicated as "144–148" and "150–151" are given under the same numbers.
FIGURES 37–50 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). I: Redescriptions of willow-dwelling species from West Tien Shan Mountains
FIGURES 37–50. Macropsis abdullaevi Dubovskiy, oscillograms of calling signals of males from different localities. 37–38, 45–46―Arslanbob (type locality), No. 6 on the map, 37–38―two parts of the same signal following immediately one after another; 39, 47―Kara-Unkyur River Valley near Kyrgyz-Gava Village, No. 7 on the map; 40–42, 48–49―ca. 5 km North of Karajigach Village, No. 2 on the map, 41–42―two parts of the same signal following immediately one after another; 43–44, 50―Lower Naryn River Valley, Kurpsay Ravine, No. 4 on the map, 43–44―two parts of the same signal following immediately one after another. Faster oscillograms of the parts of signals indicated as "45–50" are given under the same numbers.
FIGURES 2–13 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). I: Redescriptions of willow-dwelling species from West Tien Shan Mountains
FIGURES 2–13. Macropsis abdullaevi Dubovskiy: 2–4―male lateral view; 5–7―female; 8–9― nymph; M. arslanbobica Dlabola: 10–11― holotype labels; M. tarbagataica Mitjaev: 12― male lateral view; 13― female.
FIGURE 1 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). I: Redescriptions of willow-dwelling species from West Tien Shan Mountains
FIGURE 1. Map of localities in West Tien Shan Mts. where the materials examined were collected. 1―Chatkal Mtn. Range, Sary-Chelekskiy Biosphere Nature Reserve, the ravine of Khodzha-Ata River in the environs of Arkyt Village; 2―foothills of Chatkal Mtn. Range, ca. 5 km north of Karajigach; 3―foothills of Chatkal Mtn. Range, Kara-Suu River Valley near Ak-Jol Village; 4―Kurpsay Ravine on the right bank of Lower Naryn River Valley, ca. 30 km downstream from Kara-Kul'; 5―Bekechal Ravine on the left bank of Lower Naryn River Valley, ca. 40 km downstream from Kara-Kul'; 6―Ferghana Mtn. Range, Arslanbob Town; 7―foothills of Ferghana Mtn. Range, Kara-Unkyur River Valley in the environs of Kyrghyz-Gava Village.
FIGURES 101–113 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). I: Redescriptions of willow-dwelling species from West Tien Shan Mountains
FIGURES 101–113. Macropsis asiatica Dubovskiy, oscillograms of calling signals of males from different localities. 101– 103, 107–109―Kara-Suu River Valley near Ak-Jol Village (5 km South-East from type locality), No. 3 on the map; 104–106, 110–113―Bekechal Ravine on the left bank of Lower Naryn River Valley, No. 5 on the map. Faster oscillograms of the parts of signals indicated as "107–113" are given under the same numbers.
FIGURES 72–83 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). I: Redescriptions of willow-dwelling species from West Tien Shan Mountains
FIGURES 72–83. Macropsis ibragimovi Dubovskiy, oscillograms of calling signals of males from different localities. 72–74, 78–80―Arslanbob (type locality), No. 6 on the map; 75–76, 81–82―the ravine of Khodzha-Ata River in the environs of Arkyt, No. 1 on the map; 77, 83―Lower Naryn River Valley, Kurpsay Ravine, No. 4 on the map. Faster oscillograms of the parts of signals indicated as "78–83" are given under the same numbers.
FIGURES 155–168. 155–163 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). II: Redescriptions of poorly known species, new synonyms, and description of a new willow-dwelling species
FIGURES 155–168. 155–163―Macropsis tienschanica sp. n., oscillograms of male calling signals; 164–168―M. elaeagnicola Dubovsky, same. Faster oscillograms of the parts of signals indicated as "159–163" and "166–168" are given under the same numbers.
FIGURES 72–85 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). II: Redescriptions of poorly known species, new synonyms, and description of a new willow-dwelling species
FIGURES 72–85. Macropsis vicina (Horvath), oscillograms of calling signals of males from different localities, 72–81―simple form of calling signal, 82–85―complex form. 72–73, 77–78, 82, 84―Arslanbob (type locality of M. populicola Dubovsky, 1966), No. 6 on the map; 74, 79―Arkyt, No. 1 on the map; 75, 80, 83, 85―environs of Anapa, Black Sea Coast of Northern Caucasus, Russia; 76, 81―Volgograd Area (Lower Volga Region, Russia). Faster oscillograms of the parts of signals indicated as "77–81" and "84–85" are given under the same numbers.
FIGURES 112–124 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). II: Redescriptions of poorly known species, new synonyms, and description of a new willow-dwelling species
FIGURES 112–124. Macropsis iliensis Mityaev, oscillograms of calling signals of males from different localities. 112–113, 115–117, 120–122―Jumgal River Valley, No. 8 on the map; 114, 118–119, 123–124―South Urals, Russia. Faster oscillograms of the parts of signals indicated as "115", "117–118" and "120–124" are given under the same numbers.
FIGURES 37–46 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). II: Redescriptions of poorly known species, new synonyms, and description of a new willow-dwelling species
FIGURES 37–46. Macropsis validiuscula Dubovsky, oscillograms of male calling signals. 37–38, 40–42―simple form of calling signal, 39, 43–46―complex form. Faster oscillograms of the parts of signals indicated as "40–46" are given under the same numbers.
FIGURES 2–16 in Taxonomic study of Central Asian species of the genus Macropsis Lewis, 1836 (Homoptera: Auchenorrhyncha: Cicadellidae: Macropsinae). II: Redescriptions of poorly known species, new synonyms, and description of a new willow-dwelling species
FIGURES 2–16. Macropsis validiuscula Dubovsky: 2–4―female lateral view; 5–6―male; 7—nymph; M. vicina (Horvath): 8―female lateral view; 9–10―male; M. iliensis Mityaev: 11―male lateral view; 12―nymph; M. tienschanica sp. n.: 13―male lateral view; 14―nymph; M. elaeagnicola Dubovsky: 15―male lateral view; 16―nymph.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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