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DAMAGE AND OVIPOSITION OF TEA MOSQUITO BUG HELOPELTIS ANTONII SIGNORET ON GUAVA, NEEM AND MORINGA.
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- Indian Journal of Entomology, 2024, v. 86, n. 2, p. 554, doi. 10.55446/IJE.2023.816
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Diplodia seriata Isolated from Declining Olive Trees in Salento (Apulia, Italy): Pathogenicity Trials Give a Glimpse That It Is More Virulent to Drought-Stressed Olive Trees and in a Warmth-Conditioned Environment.
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- Plants (2223-7747), 2024, v. 13, n. 16, p. 2245, doi. 10.3390/plants13162245
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Sensitivity of the soil-borne pathogen Phytophthora agathidicida, the causal agent of kauri dieback, to the anti-oomycete fungicides ethaboxam, fluopicolide, mandipropamid, and oxathiapiprolin.
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- New Zealand Plant Protection, 2022, v. 75, p. 14, doi. 10.30843/nzpp.2022.75.11751
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SITE CONDITIONS FOR DECLINE OF ASH STANDS IN EUROPE.
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- ACTA Scientiarum Polonorum Silvarum Colendarum Ratio et Industria Lignaria, 2020, v. 19, n. 2, p. 67, doi. 10.17306/J.AFW.2020.2.7
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Indirect auxiliary organogenesis of Fraxinus excelsior L. as a tool for ash dieback control.
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- New Forests, 2024, v. 55, n. 2, p. 323, doi. 10.1007/s11056-023-09981-x
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Dieback and decline pathogens of olive trees in South Africa.
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- Persoonia, 2020, v. 45, p. 196, doi. 10.3767/persoonia.2020.45.08
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Neighbours matter and the weak succumb: Ash dieback infection is more severe in ash trees with fewer conspecific neighbours and lower prior growth rate.
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- Journal of Ecology, 2023, v. 111, n. 10, p. 2118, doi. 10.1111/1365-2745.14191
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Landscape epidemiology of ash dieback.
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- Journal of Ecology, 2020, v. 108, n. 5, p. 1789, doi. 10.1111/1365-2745.13383
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Role of an opportunistic pathogen in the decline of stressed oak trees.
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- Journal of Ecology, 2006, v. 94, n. 6, p. 1214, doi. 10.1111/j.1365-2745.2006.01173.x
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Distribution of Tracheid Lumen Areas within Annual Rings at Different Heights of Larch Stem under Permafrost Conditions. Crown Dieback.
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- Russian Journal of Ecology, 2021, v. 52, n. 5, p. 391, doi. 10.1134/S1067413621050106
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Chimerism and population dieback alter genetic inference related to invasion pathways and connectivity of biofouling populations on artificial substrata.
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- Ecology & Evolution (20457758), 2019, v. 9, n. 6, p. 3089, doi. 10.1002/ece3.4817
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In Vivo Two-Photon Imaging of Axonal Dieback, Blood Flow, and Calcium Influx with Methylprednisolone Therapy after Spinal Cord Injury.
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- Scientific Reports, 2015, p. 9691, doi. 10.1038/srep09691
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Twig and Shoot Dieback of Citrus, a New Disease Caused by Colletotrichum Species.
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- Cells (2073-4409), 2021, v. 10, n. 2, p. 449, doi. 10.3390/cells10020449
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TREES SURVIVAL EXPOSED TO DIEBACK DISEASE IMPLIES EVOLUTIONARY MODULATION RESISTANCE IN SHISHAM (DALBERGIA SISSOO ROXB .) IN VARIOUS AGRO ECOLOGICAL ZONES OF PUNJAB (PAKISTAN).
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- Pakistan Journal of Phytopathology, 2014, v. 26, n. 2, p. 289
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Canary in the forest?—Tree mortality and canopy dieback of western redcedar linked to drier and warmer summers.
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- Journal of Biogeography, 2024, v. 51, n. 1, p. 103, doi. 10.1111/jbi.14732
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Inheritance of resistance to Pythium dieback in the medicinal plant periwinkle.
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- Plant Breeding, 2003, v. 122, n. 2, p. 184, doi. 10.1046/j.1439-0523.2003.00837.x
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Valsalnicola oxystoma (Rehm) D.M. Walker & Rossman - primary biotic agent responsible for the dieback and high mortality of green alder in Călimani and Rodnei Mountains (North-Eastern Romania).
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- Annals of Forest Research (1844-8135), 2023, v. 66, n. 2, p. 69, doi. 10.15287/afr.2023.3225
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Etiology and management of shisham die-back disease in Pakistan forests.
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- Pakistan Journal of Agricultural Sciences, 2023, v. 60, n. 3, p. 407, doi. 10.21162/PAKJAS/23.103
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Assessment of the distribution, incidence, and severity of Shisham (Dalbergia sissoo) dieback disease in Pakistan.
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- Pakistan Journal of Agricultural Sciences, 2021, v. 58, n. 6, p. 1819, doi. 10.21162/PAKJAS/21.132
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Synergism of citrus nematode (Tylenchulus semipenetrans Cobb.) and Colletotrichum gloeosporioides plays a major role in citrus dieback.
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- Pakistan Journal of Agricultural Sciences, 2021, v. 58, n. 4, p. 1291, doi. 10.21162/PAKJAS/21.399
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UNVEILING THE Fusarium proliferatum ASSOCIATION WITH FICUS DIEBACK FROM PUNJAB, PAKISTAN.
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- Pakistan Journal of Agricultural Sciences, 2020, v. 57, n. 5, p. 1337, doi. 10.21162/PAKJAS/20.643
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Integrated System for Cashew Disease Management and Yield.
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- Cameroon Journal of Experimental Biology, 2019, v. 13, n. 1, p. 40, doi. 10.4314/cajeb.v13i1.6
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Sea Minerals Reduce Dysbiosis, Improve Pasture Productivity and Plant Morphometrics in Pasture Dieback Affected Soils.
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- Sustainability (2071-1050), 2022, v. 14, n. 22, p. 14873, doi. 10.3390/su142214873
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Relationship between the application dosage of PP<sub>333</sub> and the incidence of twig dieback in Chinese bayberry.
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- Phytoparasitica, 2019, v. 47, n. 5, p. 711, doi. 10.1007/s12600-019-00761-y
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Characterization of Colletotrichum gloeosporioides, as the main causal agent of citrus anthracnose, and C. karstii as species preferentially associated with lemon twig dieback in Portugal.
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- Phytoparasitica, 2016, v. 44, n. 4, p. 549, doi. 10.1007/s12600-016-0537-y
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Phylogeny of Paecilomyces, the causal agent of pistachio and some other trees dieback disease in Iran.
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- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0200794
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Analysis of ecological thresholds in a temperate forest undergoing dieback.
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- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189578
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Comparison of Variability in Leaves and Roots Nutrient Contents of Persian Oak (Quercus brantii Lindl.) in Drought Affected Declining Forests.
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- BioResources, 2023, v. 18, n. 2, p. 3885, doi. 10.15376/biores.18.2.3885-3894
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The Influence of Abiotic Factors on the Occurrence of Jackfruit Dieback Disease.
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- Pertanika Journal of Science & Technology, 2023, v. 31, n. 5, p. 2487, doi. 10.47836/pjst.31.5.24
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Drops in needle production are early-warning signals of drought-triggered dieback in Scots pine.
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- Trees: Structure & Function, 2023, v. 37, n. 4, p. 1137, doi. 10.1007/s00468-023-02412-6
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Taxonomic and structural diversity indices predict soil carbon storage better than functional diversity indices along a dieback intensity gradient in semi-arid oak forests.
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- Trees: Structure & Function, 2022, v. 36, n. 2, p. 537, doi. 10.1007/s00468-021-02227-3
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The role of morpho-physiological traits in frost tolerance of neotropical savanna trees.
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- Trees: Structure & Function, 2021, v. 35, n. 5, p. 1687, doi. 10.1007/s00468-021-02150-7
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Do soil properties and ecophysiological responses of oak (Quercus brantii Lindl.) correlate with the rate of dieback?
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- Trees: Structure & Function, 2021, v. 35, n. 5, p. 1639, doi. 10.1007/s00468-021-02142-7
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Evidence of climate-induced stress of Norway spruce along elevation gradient preceding the current dieback in Central Europe.
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- Trees: Structure & Function, 2021, v. 35, n. 1, p. 103, doi. 10.1007/s00468-020-02022-6
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Modulation of antioxidant enzymes in Juniperus procera needles in relation to habitat environment and dieback incidence.
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- Trees: Structure & Function, 2016, v. 30, n. 5, p. 1669, doi. 10.1007/s00468-016-1399-0
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Topography influences the distribution of autumn frost damage on trees in a Mediterranean-type Eucalyptus forest.
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- Trees: Structure & Function, 2014, v. 28, n. 5, p. 1449, doi. 10.1007/s00468-014-1048-4
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Strong hydraulic segmentation and leaf senescence due to dehydration may trigger die-back in Nothofagus dombeyi under severe droughts: a comparison with the co-occurring Austrocedrus chilensis.
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- Trees: Structure & Function, 2014, v. 28, n. 5, p. 1475, doi. 10.1007/s00468-014-1050-x
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- Article
Differential occurrence of suberized sheaths in canes of grapevines suffering from black dead arm, esca or Eutypa dieback.
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- Trees: Structure & Function, 2013, v. 27, n. 4, p. 1087, doi. 10.1007/s00468-013-0859-z
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Association Between Fusarium spp. on Spartina alterniflora and Dieback Sites in Connecticut and Massachusetts.
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- Estuaries & Coasts, 2012, v. 35, n. 2, p. 436, doi. 10.1007/s12237-011-9448-9
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Stem Borer Frequency and Composition in Healthy Spartina alterniflora (smooth cordgrass) and Dieback Zones in a Southern Atlantic Coast Salt Marsh.
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- Estuaries & Coasts, 2011, v. 34, n. 5, p. 1078, doi. 10.1007/s12237-010-9359-1
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Pomegranate dieback and fruit rot caused by Coniella granati recorded in Croatia.
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- Journal of Central European Agriculture, 2023, v. 24, n. 3, p. 689, doi. 10.5513/JCEA01/24.3.3932
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Fungi associated with canker diseases on olive in Istria (Croatia)maslini u Istri (Hrvatska).
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- Journal of Central European Agriculture, 2023, v. 24, n. 2, p. 470, doi. 10.5513/JCEA01/24.2.3795
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Distinctive expansion of gene families associated with plant cell wall degradation, secondary metabolism, and nutrient uptake in the genomes of grapevine trunk pathogens.
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- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1624-z
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Reconstructing extreme climatic and geochemical conditions during the largest natural mangrove dieback on record.
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- Biogeosciences, 2020, v. 17, n. 18, p. 4707, doi. 10.5194/bg-17-4707-2020
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Biology of Leptoypha hospita (Hemiptera: Tingidae), a Potential Biological Control Agent of Chinese Privet.
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- Annals of the Entomological Society of America, 2011, v. 104, n. 6, p. 1327, doi. 10.1603/AN11042
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Drought resistance in two populations of invasive Tamarix compared using multiple methods.
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- Tree Physiology, 2024, v. 44, n. 1, p. 1, doi. 10.1093/treephys/tpad140
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Within- versus between-species size effects on drought-induced dieback and mortality.
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- Tree Physiology, 2021, v. 41, n. 5, p. 679, doi. 10.1093/treephys/tpaa167
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Amplifying feedback loop between growth and wood anatomical characteristics of Fraxinus excelsior explains size-related susceptibility to ash dieback.
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- Tree Physiology, 2021, v. 41, n. 5, p. 683, doi. 10.1093/treephys/tpaa091
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Isolation and Identification of Pennogenin Tetraglycoside from Cestrum nocturnum (Solanaceae) and Its Antifungal Activity against Fusarium kuroshium , Causal Agent of Fusarium Dieback.
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- Molecules, 2022, v. 27, n. 6, p. 1860, doi. 10.3390/molecules27061860
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A novel mitovirus detected in Diaporthe rudis, a fungus associated with Phomopsis dieback on grapevines.
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- Archives of Virology, 2020, v. 165, n. 10, p. 2405, doi. 10.1007/s00705-020-04755-8
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