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Journal articles on the topic 'Fumana procumbens'

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1

Tóth, Sándor, and Ágnes Révay. "Oncopodium lidiae sp. nov. (Hyphomycetes) on Fumana procumbens from Hungary." Mycologia Balcanica 8 (December 13, 2011): 89–91. https://doi.org/10.5281/zenodo.2550418.

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<em>Oncopodium lidiae</em> sp. nov. is described and illustrated from the cortex of <em>Fumana procumbens</em> (<em>Cistaceae</em>) collected in Hungary. This species has been collected several times and from different localities in Hungary exclusively from dry twigs of <em>Fumana procumbens.</em> A key of <em>Oncopodium</em> species is presented.
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2

Laštůvka, Aleš, and Zdeněk Laštůvka. "Parafomoria fumanae sp. n., a new stem miner on Fumana procumbens (Lepidoptera: Nepticulidae)." Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis 53, no. 1 (2005): 15–18. http://dx.doi.org/10.11118/actaun200553010015.

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Parafomoria fumanae sp. n. is described from southern France. The new species is similar to Parafomoria ladaniphila (Mendes, 1910), but very close to P. cistivora (Peyerimhoff, 1871) and P. helianthemella (Herrich-Schäffer, 1860) after its genital morphology. It differs especially by the characters on valvae, tegumen, uncus and aedeagus. Its larva is a stem miner of Fumana procumbens (Dunal) Gr. et Godr., the species is the first stem miner in the genus Parafomoria van Nieukerken, 1983.
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3

Gürbüz, Perihan, and Şengül Dilem Doğan. "Biflavonoids from Fumana procumbens (Dunal) Gren. & Godr." Biochemical Systematics and Ecology 74 (October 2017): 57–59. http://dx.doi.org/10.1016/j.bse.2017.09.004.

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4

Emerce, Esra, Perihan Gürbüz, Şengül Dilem Doğan, Ela Kadioglu, and Ipek Süntar. "Cytotoxic Activity-Guided Isolation Studies on Fumana procumbens (Dunal) Gren. & Godr." Records of Natural Products 13, no. 3 (2019): 189–98. http://dx.doi.org/10.25135/rnp.98.18.07.331.

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5

Shevchenko, Svitlana, and M. GAPHAROVA. "Some embryology features of the Fumana procumbens (Dun.) Gren. et Godr. (fam. Cistaceae)." Chornomorski Botanical Journal 8, no. 4 (2012): 379–85. http://dx.doi.org/10.14255/2308-9628/12.84/4.

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6

Güemes, Jaime, Christian Raynaud, and Trad C. Raynaud. "Fumana ericoidess.l. etFumana procumbens(Dunal) Gren. et Godr. (Cistaceae) en Afrique du Nord." Bulletin de la Société Botanique de France. Lettres Botaniques 138, no. 2 (1991): 167–76. http://dx.doi.org/10.1080/01811797.1991.10824918.

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7

Labuda, Roman, Pavol Eliáš, Hacer Sert, and Katja Sterflinger. "Alternaria jesenskae sp. nov., a new species from Slovakia on Fumana procumbens (Cistaceae)." Microbiological Research 163, no. 2 (2008): 208–14. http://dx.doi.org/10.1016/j.micres.2006.05.004.

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8

Barth, Uwe, and Andreas König. "Projekt „Erhaltungskulturen von bedrohten Pflanzen in Hessen“." Der Palmengarten 82, no. 2 (2019): 5–16. http://dx.doi.org/10.21248/palmengarten.474.

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Im Rahmen eines von der KfW Stiftung geförderten Artenschutzprojektes wurden Samen von 15 vom Aussterben bedrohten Pflanzenarten gesammelt und im Botanischen Garten der Stadt Frankfurt vermehrt. In Zusammenarbeit mit den zuständigen Naturschutzbehörden und lokalen Vertretern von Naturschutzverbänden wurden dokumentierte Wiederansiedlungsmaßnahmen durchgeführt. Bei den 15 gefährdeten Arten handelt es sich um Allium strictum, Festuca albensis (syn. F. tomanii, F. duvalii p.p.), Fumana procumbens, Iris spuria, Jurinea cyanoides, Mibora minima, Moenchia erecta, Nigella arvensis, Poa badensis, Scleranthus verticillatus, Sedum villosum, Spergula pentandra, Ventenata dubia, Veronica acinifolia, Vicia orobus. Alle 15 Arten sind als „Verantwortungsarten“ Bestandteil der hessischen Biodiversitätsstrategie. Zwei dieser Arten, Mibora minima (Sand-Zwerggras) und Nigella arvensis (Acker-Schwarzkümmel) werden näher vorgestellt. Der Beitrag gibt anhand von Beispielen einen Einblick in die praktische Durchführung der Samensammlung, Kultivierung und Wiederausbringung heimischer Wildpflanzen.
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9

Bengtsson, Karin. "Fumana Procumbens on Oland--Population Dynamics of a Disjunct Species at the Northern Limit of its Range." Journal of Ecology 81, no. 4 (1993): 745. http://dx.doi.org/10.2307/2261672.

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10

Dudagova, Elsa, Marjan Astamirova, Musa Taisumov, and Elina Baybatyrova. "Analysis of the flora species distribution along the altitudinal zones of the Argun river basin." Sustainable Development of Mountain Territories 16, no. 2 (2024): 630–41. http://dx.doi.org/10.21177/1998-4502-2024-16-2-630-641.

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The Argun River is the largest river in the Sunzha basin. It originates on the Main Caucasian Ridge near the Chokismta-Matura peak (3189.7 m) in Georgia (historical region of Khevsureti). Before crossing the Lateral Ridge, it receives a large right tributary of the Andaki River (31 km long), whose sources are also on the Main Ridge near the Mal. Barbalo peak (3136 m). The length of the Argun River is 148 km, the total area of the basin is 3390 km2, it flows into the Sunzha River, a right tributary of the Terek River. In the upper reaches before the confluence with the right tributary, the Sharo-Argun River is historically called Chanty-Argun. Materials and methods. Materials and methods of research. Flora species and floristic complexes with different habitats within the Argun River basin were selected as the object of study. The material for the study was obtained during expeditionary trips for observations and herbarium collections in the period 2020–2023 in various altitudinal zones of the Argun River basin. Results and discussion. As a result of the research carried out in the Argun. Results. River basin, we recorded three groups of floras in the study area: plain-foothill, mid-mountain and high-mountain, the uneven distribution of floristic complexes in which made it possible to distinguish 6 floristic regions; More than half of the flora territory is located in the protected area system (2 reserves of republican significance, one of federal significance), 116 species are listed in the Red Books of the federal and regional levels, and another 16 species are proposed for protection. Discussion. The presence of narrow-local endemics in the flora also emphasizes its originality. It is advisable to include the entire Itum-Kalinsky floristic region in the territory of the Sovetsky biological reserve. Thus, many “Red Book” species, most of which are found only in this area, will be taken under real protection. These are Astracantha denudata, Berberis vulgaris, Сeltis glabrata, Cerasus incana, Cladochaeta candidissima Clenmatis integrifolia, Colutea orientalis, Cotynus coggygria, Crambe grandiflora, Dianthus daghestanicus, Ephedra procera, Fumana procumbens, Galanthus caucasicus, Gentiana grossheimii, Hippophaer hamnoides, Iris pumila, Gladiolus tenuis, Juniperus oblonga, Mandenovia komarovii, Medicago daghestanica, Notholaena maranthae, Omphalodes rupestris, Scabiosa rotata, Stipa caucasica, S. pennata, S. pulcherrima, Xanthobrychys majorovii. Conclusions. The total number of flora elements is significantly greater than the number of species in this area, since many of them are ecologically flexible and can be found in two or three vegetation zones, less often in four. Most species are confined to the steppe and forest zones, where the highest percentage of ruderal-segetal and alien species is observed, i.e. the quantitative composition is associated with anthropogenic impact on natural phytocenoses. The least number of species is in the subnival zone, where only petrophytes live, mostly endemics and subendemics.
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11

Crous, P. W., A. J. Carnegie, M. J. Wingfield, et al. "Fungal Planet description sheets: 868–950." Persoonia - Molecular Phylogeny and Evolution of Fungi 42, no. 1 (2019): 291–473. http://dx.doi.org/10.3767/persoonia.2019.42.11.

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Novel species of fungi described in this study include those from various countries as follows: Australia, Chaetomella pseudocircinoseta and Coniella pseudodiospyri on Eucalyptus microcorys leaves, Cladophialophora eucalypti, Teratosphaeria dunnii and Vermiculariopsiella dunnii on Eucalyptus dunnii leaves, Cylindrium grande and Hypsotheca eucalyptorum on Eucalyptus grandis leaves, Elsinoe salignae on Eucalyptus saligna leaves, Marasmius lebeliae on litter of regenerating subtropical rainforest, Phialoseptomonium eucalypti (incl. Phialoseptomonium gen. nov.) on Eucalyptus grandis × camaldulensis leaves, Phlogicylindrium pawpawense on Eucalyptus tereticornis leaves, Phyllosticta longicauda as an endophyte from healthy Eustrephus latifolius leaves, Pseudosydowia eucalyptorum on Eucalyptus sp. leaves, Saitozyma wallum on Banksia aemula leaves, Teratosphaeria henryi on Corymbia henryi leaves. Brazil, Aspergillus bezerrae, Backusella azygospora, Mariannaea terricola and Talaromyces pernambucoensis from soil, Calonectria matogrossensis on Eucalyptus urophylla leaves, Calvatia brasiliensis on soil, Carcinomyces nordestinensis on Bromelia antiacantha leaves, Dendryphiella stromaticola on small branches of an unidentified plant, Nigrospora brasiliensis on Nopalea cochenillifera leaves, Penicillium alagoense as a leaf endophyte on a Miconia sp., Podosordaria nigrobrunnea on dung, Spegazzinia bromeliacearum as a leaf endophyte on Tilandsia catimbauensis, Xylobolus brasiliensis on decaying wood. Bulgaria, Kazachstania molopis from the gut of the beetle Molops piceus. Croatia, Mollisia endocrystallina from a fallen decorticated Picea abies tree trunk. Ecuador, Hygrocybe rodomaculata on soil. Hungary, Alfoldia vorosii (incl.Alfoldia gen. nov.) from Juniperus communis roots, Kiskunsagia ubrizsyi (incl. Kiskunsagia gen. nov.) from Fumana procumbens roots. India, Aureobasidium tremulum as laboratory contaminant, Leucosporidium himalayensis and Naganishia indica from windblown dust on glaciers. Italy, Neodevriesia cycadicola on Cycas sp. leaves, Pseudocercospora pseudomyrticola on Myrtus communis leaves, Ramularia pistaciae on Pistacia lentiscus leaves, Neognomoniopsis quercina (incl. Neognomoniopsis gen. nov.) on Quercus ilex leaves. Japan, Diaporthe fructicola on Passiflora edulis × P. edulis f. flavicarpa fruit, Entoloma nipponicum on leaf litter in a mixed Cryptomeria japonica and Acer spp. forest. Macedonia, Astraeus macedonicus on soil. Malaysia, Fusicladium eucalyptigenum on Eucalyptus sp. twigs, Neoacrodontiella eucalypti (incl. Neoacrodontiella gen. nov.) on Eucalyptus urophylla leaves. Mozambique, Meliola gorongosensis on dead Philenoptera violacea leaflets. Nepal, Coniochaeta dendrobiicola from Dendriobium lognicornu roots. New Zealand, Neodevriesia sexualis and Thozetella neonivea on Archontophoenix cunninghamiana leaves. Norway, Calophoma sandfjordenica from a piece of board on a rocky shoreline, Clavaria parvispora on soil, Didymella finnmarkica from a piece of Pinus sylvestris driftwood. Poland, Sugiyamaella trypani from soil. Portugal, Colletotrichum feijoicola from Acca sellowiana. Russia, Crepidotus tobolensis on Populus tremula debris, Entoloma ekaterinae, Entoloma erhardii and Suillus gastroflavus on soil, Nakazawaea ambrosiae from the galleries of Ips typographus under the bark of Picea abies. Slovenia, Pluteus ludwigii on twigs of broadleaved trees. South Africa, Anungitiomyces stellenboschiensis (incl. Anungitiomyces gen. nov.) and Niesslia stellenboschiana on Eucalyptus sp. leaves, Beltraniella pseudoportoricensis on Podocarpus falcatus leaf litter, Corynespora encephalarti on Encephalartos sp. leaves, Cytospora pavettae on Pavetta revoluta leaves, Helminthosporium erythrinicola on Erythrina humeana leaves, Helminthosporium syzygii on a Syzygium sp. barkcanker, Libertasomyces aloeticus on Aloe sp. leaves, Penicillium lunae from Musa sp. fruit, Phyllosticta lauridiae on Lauridia tetragona leaves, Pseudotruncatella bolusanthi (incl. Pseudotruncatellaceae fam. nov.) and Dactylella bolusanthi on Bolusanthus speciosus leaves. Spain, Apenidiella foetida on submerged plant debris, Inocybe grammatoides on Quercus ilex subsp. ilex forest humus, Ossicaulis salomii on soil, Phialemonium guarroi from soil. Thailand, Pantospora chromolaenae on Chromolaena odorata leaves. Ukraine, Cadophora helianthi from Helianthus annuus stems. USA, Boletus pseudopinophilus on soil under slash pine, Botryotrichum foricae, Penicillium americanum and Penicillium minnesotense from air. Vietnam, Lycoperdon vietnamense on soil. Morphological and culture characteristics are supported by DNA barcodes.
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12

TAISUMOV, Musa, Marjan ASTAMIROVA, and Elsa Dudagova. "Protection and use of the flora gene of the Argun River basin." Sustainable Development of Mountain Territories 15, no. 4 (2023): 842–52. http://dx.doi.org/10.21177/1998-4502-2023-15-4-842-852.

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Introduction. The Russian Federation has adopted a Strategy for the conservation of rare and endangered species of animals, plants and fungi for the period until 2030 (Order of the Government of the Russian Federation dated February 17, 2014 No. 212), developed in accordance with the principles and norms of international law, the Fundamentals of State Policy in the field of environmental development of the Russian Federation for the period until 2030 and other regulatory legal acts. The goal of the Strategy is to ensure on a long-term basis the conservation and restoration of rare and endangered species of animals, plants and fungi in the interests of sustainable development of the Russian Federation. Purpose of the study: to analyze the species of flora of the Argun River basin and develop recommendations for expanding the list of plants to be protected. Materials and methods of research. Rare and protected species and floristic complexes with different habitats within the Argun River basin were selected as the object of study. The material for the study was obtained during expeditionary trips for observations and herbarium collections in the period 2018-2022. in various parts of this territory. Results and its discussion. As a result of our research in the Argun River basin, we identified 132 species (or 8.5% of the total flora) that are subject to protection. Almost half are species of categories I and II, i.e. local endemics and subendemics, constituting 47.0% of all protected taxa. This is the most important part of the gene pool, of which species of the first category require special attention - local endemics - carriers of a unique gene pool that are subject to priority protection. Conclusion. The presence of narrowly local endemics in the flora also emphasizes its originality. It is advisable to include the entire Itum-Kalinsky floristic region in the territory of the Sovetsky biological reserve. Thus, many “Red Book” species, most of which are found only in this area, will be taken under real protection. These are Astracantha denudata, Berberis vulgaris, Сeltis glabrata, Cerasus incana, Cladochaeta candidissima Clenmatis integrifolia, Colutea orientalis, Cotynus coggygria, Crambe grandiflora, Dianthus daghestanicus, Ephedra procera, Fumana procumbens, Galanthus caucasicus, Gentiana grossheimii, Hippophae rhamnoides, Iris pumila, Gladiolus tenuis , Juniperus oblonga, Mandenovia komarovii, Medicago daghestanica, Notholaena maranthae, Omphalodes rupestris, Scabiosa rotata, Stipa caucasica, S. pennata, S. pulcherrima, Xanthobrychys majorovii. Resume. The article provides information about protected and recommended plant species in the Argun River basin. It has been established that almost half of the species include species of categories I and II, i.e. local endemics and subendemics, constituting 47.0% of all protected taxa. It has been determined that for all species it is necessary to comply with the requirements of maintaining the Red Book. It was revealed that for the first time for the Argun River basin, an inventory of the flora was carried out and its comprehensive analysis was carried out. Plant species in need of protection have been identified and prospects for the economic use of flora have been determined. Phytosozological data can be used in maintaining the regional Red Book and as a project for amending it. Information of a utilitarian nature can be used in the economic sphere of the population, and the scientific component can be used in the educational process of regional universities as disciplines with botanical content.
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13

Skrzyczyńska, Janina, and Teresa Skrajna. "The segetal flora of the Kałuszyn Upland." Acta Agrobotanica 52, no. 1-2 (2013): 183–202. http://dx.doi.org/10.5586/aa.1999.019.

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In the paper a state of preservation and the characteristics of flora of the cultivated fields of the Kaluszyńska Upland is given. The flora of agrocenosis of the Kałuszyńska Upland is rich. The presence of 278 vascular plant species was noted in the study area. It is mainly the diversity of habitats and human activity that affected its species abundance. More than a half of a number of taxa (166 species - 59,6%) belong to the group of rare, 40 of them are endangered extinction. Among the most threatened species there are 14 taxa e.g.: &lt;em&gt;Fumaria schleicheri, Euphorbia exigua, Illecebrum verticillatum, Asperugo procumbens, Polycnemum arvense, Radiola linoides, Camelina sativa&lt;/em&gt;.
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14

Kirpluk, Izabella, and Anna Bomanowska. "Rare, endangered and protected plant species of synanthropic flora of the Kampinos National Park (Central Poland)." Biodiversity: Research and Conservation, no. 11-12 (December 30, 2008): 71–80. http://dx.doi.org/10.14746/biorc.2008.11-12.10.

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The aim of this paper is to present the rare, endangered and protected plant taxons growing in the synanthropic habitats of the Kampinos National Park. The research was conducted on agricultural fields (still maintained) and in ruderal habitats in over a dozen abandoned villages in the Kampinos Forest. Among species considered to be endangered are: Agrostemma githago, Asperugo procumbens, Atriplex rosea, Camelina microcarpa, Centunculus minimus, Filago arvensis, Fumaria officinalis, Gagea pratensis, Holosteum umbellatum, Myosurus minimus, Pulicaria vulgaris and Radiola linoides. To the category of rare plant species belong: Anthemis ruthenica, Arabis glabra, Arnoseris minima, Chenopodium ficifolium, Ch. pedunculare and Euphorbia peplus. Species protected by law, found during the study, include: Epipactis helleborine, Jovibarba sobolifera and Helichrysum arenarium. According to our observations some of the segetal plant species, for example Filago arvensis, Centaurea cyanus and Papaver rhoeas, have tendencies to habitat change. These plant species move from agricultural fields to ruderal habitats. In the Kampinos Forest’s synanthropic habitats the species from seminatural non-forest habitats such as Sedum sexangulare, Eryngium planum, Cerastium semidecandrum, find their place.
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15

Beránek, Ábel, Csaba Molnár, Attila Molnár, et al. "Apró közlemények." Kitaibelia 24, no. 1 (2019). http://dx.doi.org/10.17542/kit.24.106.

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1. Kiegészítések a Fumana procumbens északi-középhegységbeli elterjedéséhez&#x0D; 2. A henye kunkor (Heliotropium supinum) jelentős állományai a Pentezugi Vadlórezervátumban (Hortobágy)&#x0D; 3. A Rochel-törpezanót (Chamaecytisus rochelii) két új előfordulása az Alföldön&#x0D; 4. A Daphne laureola spontán megjelenése városi parkokban&#x0D; 5. Lindernia procumbens és L. dubia előfordulása Budapesten&#x0D; 6. A Moneses uniflora előfordulásának megerősítése a kőszegi Alsóerdőben
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16

Özaslan, Cumali, and Esmanur Pekcan Kaçar. "Weed Flora of Vineyards in Diyarbakır Province, Turkey." Agricultural Science Digest - A Research Journal, OF (August 24, 2020). http://dx.doi.org/10.18805/ag.d-259.

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Background: Viticulture occupies an important place in agricultural production of Diyarbakır province, Turkey. However, weeds significantly impair the productivity of vineyards in the province. The knowledge of weed flora of a particular region is crucial to develop region-specific weed management strategies. Methods: This study was carried out to determine the weed species, their densities and frequency of occurrence in 78 vineyards of 13 districts in Diyarbakır province. Exploratory surveys were conducted to record the occurrence, density and coverage area of weed species. A 1×1 m quadrate was used, which was randomly placed in vineyards and weed species falling within the quadrate were noted. Result: A total 165 weed species and 128 taxa belonging to 35 botanical families (1 parasitic, 16 monocotyledons and 18 dicotyledons) were identified from the surveyed area. The weed species’ density over the whole province was 91 weeds m-2. Avena sterilis L. was the most widespread weed with the highest density (9.93 plants m-2) in the surveyed area followed by Fumaria asepale Boiss. (7.18), Galium tricornutum (4.85), Ranunculus arvensis (3.82), Silene aegyptiaca (3.70), Bromus sterilis (3.64) Lamium purpureum (3.58), Hordeum spontaneum (3.35), Anthemis sp. (3.07), Crepis alpina (2.94), Thlaspi perfoliatum (2.91), Alopecurus myosuroides (2.81), Bongardia chrysogonum (2.80), Scandix pecten-veneris (2.24), Cynodon dactylon (1.71), Hypecoum procumbens (1.69), Lolium perenne (1.41), Sorghum halepense (1.33), Sinapis arvensis (1.24), Buglossoides arvense (1.22), Daucus carota (1.21), Trifolium nigrescens (1.21), Vicia hybrida (1.05), Senecio vernalis (1.04) and Ornithogalum narbonense (1.02). The most prevalent weed were L. purpureum (66.68%), Papaver sp. (66.49%), S. vernalis (65.82%), Anthemis sp. (65.10%), A. sterilis (63.07%), R. arvensis (60.44%), Convolvulus arvensis (56.76%), Carduus pycnocephalus (55.79%), G. tricornutum (55.43%), Fumaria asepale (55.05%), Crepis alpina (54.08%), Thlaspi perfoliatum (51.95%) and S. arvensis (51.04%).
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