bare patch
Recently Published Documents


TOTAL DOCUMENTS

44
(FIVE YEARS 6)

H-INDEX

14
(FIVE YEARS 0)

2021 ◽  
Vol 36 (6) ◽  
pp. 650-656
Author(s):  
Qiming Yu ◽  
Shaobin Liu ◽  
Zhengyu Huang ◽  
Xiangkun Kong ◽  
Yuehong Hu ◽  
...  

A three-layered transmitting focusing gradient meta-surface (FGMS) has been proposed, which can achieve broadband gain enhancement from 8.2 GHz to 10 GHz. The element of broadband transmitting FGMS has high transmitting efficiencies that over 0.7 and achieve [0, 2π] phase range with a flat and linear trend in the operating band. The FGMS can transform the spherical waves into plane waves. Three patch antennas working at 8.2 GHz, 9.1 GHz, and 10 GHz respectively are placed the focus of broadband FGMS as the spherical-wave source to build a broadband planar lens antenna system. It achieves a simulation gain of 15.44 dBi which is 7.51dB higher than that of the bare patch antenna at 10 GHz with satisfying SLLs and beamwidths. However, it enhanced the gain of the bare patch antenna in a wide operating band. Finally, the FGMS and the patch antenna are fabricated and measured. The measured results are in good agreement with the simulations.


2021 ◽  
Author(s):  
Matthew Back

Abstract Introduction: T. cucumeris is a pathogen with a worldwide distribution and in Japan alone T. cucumeris is reported to infect 35 orders, 52 families, 125 genera and 142 species of plant (Ogoshi, 1996). Yield and economic losses caused by T. cucumeris have not been determined in the majority of crops and environments. The most comprehensive estimates of losses are available for Rhizoctonia bare patch of wheat in Australia, sheath blight of rice in Asia and cotton seedling disease in the USA. The remainder of the reports cited are for only a few crops in selected regions and in selected years.


Plant Disease ◽  
2021 ◽  
Author(s):  
Richard Smiley

Economic loss from Rhizoctonia bare patch, caused by Rhizoctonia solani AG-8, was estimated in two 50-ha fields on a single farm. A winter wheat crop was managed as a conventionally cultivated 2-year wheat/fallow rotation and a spring barley crop was managed as a no-till annual crop. Aerial photographs revealed that patch-affected area was nearly double in barley (17%) compared to wheat (9%). Yield inside patches was reduced by 73% and 68% for wheat and barley, respectively. Grain produced on each field was reduced more for winter wheat (21.6 mt, valued at US$5,080) than spring barley (16.8 mt, valued at US$2,784). More precise estimates of economic damage and more robust management practices for Rhizoctonia bare patch must be developed.


2021 ◽  
pp. 1-18
Author(s):  
Hossein Chegini ◽  
Fernando Beltran ◽  
Aniket Mahanti
Keyword(s):  

2020 ◽  
Vol 12 (24) ◽  
pp. 4121
Author(s):  
Wei Zhang ◽  
Shuhua Yi ◽  
Yu Qin ◽  
Yi Sun ◽  
Donghui Shangguan ◽  
...  

Surface soil moisture (SSM) is a key limiting factor for vegetation growth in alpine meadow on the Qinghai-Tibetan Plateau (QTP). Patches with various sizes and types may cause the redistribution of SSM by changing soil hydrological processes, and then trigger or accelerate alpine grassland degradation. Therefore, it is vital to understand the effects of patchiness on SSM at multi-scales to provide a reference for alpine grassland restoration. However, there is a lack of direct observational evidence concerning the role of the size and type of patches on SSM, and little is known about the effects of patches pattern on SSM at plot scale. Here, we first measured SSM of typical patches with different sizes and types at patch scale and investigated their patterns and SSM spatial distribution through unmanned aerial vehicle (UAV)-mounted multi-type cameras at plot scale. We then analyzed the role of the size and type of patchiness on SSM at both patch and plot scales. Results showed that: (1) in situ measured SSM of typical patches was significantly different (P < 0.01), original vegetation patch (OV) had the highest SSM, followed by isolate vegetation patch (IV), small bare patch (SP), medium bare patch (MP) and large bare patch (LP); (2) the proposed method based on UAV images was able to estimate SSM (0–40 cm) with a satisfactory accuracy (R2 = 0.89, P < 0.001); (3) all landscape indices of OV, with the exception of patch density, were positively correlated with SSM at plot scale, while most of the landscape indices of LP and IV showed negative correlations (P < 0.05). Our results indicated that patchiness intensified the spatial heterogeneity of SSM and potentially accelerated the alpine meadow degradation. Preventing the development of OV into IV and the expansion of LP is a critical task for alpine meadow management and restoration.


2017 ◽  
Vol 107 (11) ◽  
pp. 1284-1297 ◽  
Author(s):  
Daniel Schlatter ◽  
Linda Kinkel ◽  
Linda Thomashow ◽  
David Weller ◽  
Timothy Paulitz

Soils suppressive to soilborne pathogens have been identified worldwide for almost 60 years and attributed mainly to suppressive or antagonistic microorganisms. Rather than identifying, testing and applying potential biocontrol agents in an inundative fashion, research into suppressive soils has attempted to understand how indigenous microbiomes can reduce disease, even in the presence of the pathogen, susceptible host, and favorable environment. Recent advances in next-generation sequencing of microbiomes have provided new tools to reexamine and further characterize the nature of these soils. Two general types of suppression have been described: specific and general suppression, and theories have been developed around these two models. In this review, we will present three examples of currently-studied model systems with features representative of specific and general suppressiveness: suppression to take-all (Gaeumannomyces graminis var. tritici), Rhizoctonia bare patch of wheat (Rhizoctonia solani AG-8), and Streptomyces. To compare and contrast the two models of general versus specific suppression, we propose a number of hypotheses about the nature and ecology of microbial populations and communities of suppressive soils. We outline the potential and limitations of new molecular techniques that can provide novel ways of testing these hypotheses. Finally, we consider how this greater understanding of the phytobiome can facilitate sustainable disease management in agriculture by harnessing the potential of indigenous soil microbes.


2016 ◽  
Vol 106 (5) ◽  
pp. 459-473 ◽  
Author(s):  
Ahmad Kamil Mohd Jaaffar ◽  
Timothy C. Paulitz ◽  
Kurtis L. Schroeder ◽  
Linda S. Thomashow ◽  
David M. Weller

Rhizoctonia root rot and bare patch, caused by Rhizoctonia solani anastomosis group (AG)-8 and R. oryzae, are chronic and important yield-limiting diseases of wheat and barley in the Inland Pacific Northwest (PNW) of the United States. Major gaps remain in our understanding of the epidemiology of these diseases, in part because multiple Rhizoctonia AGs and species can be isolated from the same cereal roots from the field, contributing to the challenge of identifying the causal agents correctly. In this study, a collection totaling 498 isolates of Rhizoctonia was assembled from surveys conducted from 2000 to 2009, 2010, and 2011 over a wide range of cereal production fields throughout Washington State in the PNW. To determine the identity of the isolates, PCR with AG- or species-specific primers and/or DNA sequence analysis of the internal transcribed spacers was performed. R. solani AG-2-1, AG-8, AG-10, AG-3, AG-4, and AG-11 comprised 157 (32%), 70 (14%), 21 (4%), 20 (4%), 1 (0.2%), and 1 (0.2%), respectively, of the total isolates. AG-I-like binucleate Rhizoctonia sp. comprised 44 (9%) of the total; and 53 (11%), 80 (16%), and 51 (10%) were identified as R. oryzae genotypes I, II, and III, respectively. Isolates of AG-2-1, the dominant Rhizoctonia, occurred in all six agronomic zones defined by annual precipitation and temperature within the region sampled. Isolates of AG-8 also were cosmopolitan in their distribution but the frequency of isolation varied among years, and they were most abundant in zones of low and moderate precipitation. R. oryzae was cosmopolitan, and collectively the three genotypes comprised 37% of the isolates. Only isolates of R. solani AG-8 and R. oryzae genotypes II and III (but not genotype I) caused symptoms typically associated with Rhizoctonia root rot and bare patch of wheat. Isolates of AG-2-1 caused only mild root rot and AG-I-like binucleate isolates and members of groups AG-3, AG-4, and AG-11 showed only slight or no discoloration of the roots. However, all isolates of AG-2-1 caused severe damping-off of canola, resulting in 100% mortality. Isolates of Rhizoctonia AG-8, AG-2-1, AG-10, AG-I-like binucleate Rhizoctonia, and R. oryzae genotypes I, II, and III could be distinguished by colony morphology on potato dextrose agar, by PCR with specific primers, or by the type and severity of disease on wheat and canola seedlings, and results of these approaches correlated completely. Based on cultured isolates, we also identified the geographic distribution of all of these Rhizoctonia isolates in cereal-based production systems throughout Washington State.


Plant Disease ◽  
2016 ◽  
Vol 100 (3) ◽  
pp. 640-644
Author(s):  
Patricia A. Okubara ◽  
Natalie Leston ◽  
Ute Micknass ◽  
Karl-Heinz Kogel ◽  
Jafargholi Imani

Rhizoctonia solani AG8, causal agent of Rhizoctonia root rot and bare patch in dryland cereal production systems of the Pacific Northwest United States and Australia, reduces yields in a wide range of crops. Disease is not consistently controlled by available management practices, so genetic resistance would be a desirable resource for growers. In this report, we describe three rapid and low-cost assays for R. solani AG8 resistance in wheat and barley, with the view of facilitating screens for genetic resistance in these hosts. The first assay uses 50-ml conical centrifuge tubes containing soil infested with R. solani AG8 on a substrate of ground oats. The second assay uses roots of 3-day-old seedlings directly coated with infested ground oats, followed by incubation in plastic dishes. The third assay, suitable for barley, uses whole infested oat kernels in 50-ml tubes. Symptoms are quantified on the bases of root fresh weight and total root length at 7 and 3 days for the tube and coating assays, respectively. Each of the assays show the same disease differential between susceptible and partially resistant wheat genotypes. The assays can be conducted in the laboratory, growth chamber, or greenhouse.


2014 ◽  
Vol 104 (7) ◽  
pp. 683-691 ◽  
Author(s):  
Patricia A. Okubara ◽  
Kurtis L. Schroeder ◽  
John T. Abatzoglou ◽  
Timothy C. Paulitz

The necrotrophic soilborne fungal pathogens Rhizoctonia solani AG8 and R. oryzae are principal causal agents of Rhizoctonia root rot and bare patch of wheat in dryland cropping systems of the Pacific Northwest. A 3-year survey of 33 parcels at 11 growers' sites and 60 trial plots at 12 Washington State University cereal variety test locations was undertaken to understand the distribution of these pathogens. Pathogen DNA concentrations in soils, quantified using real-time polymerase chain reaction, were correlated with precipitation, temperature maxima and minima, and soil texture factors in a pathogen-specific manner. Specifically, R. solani AG8 DNA concentration was negatively correlated with precipitation and not correlated with temperature minima, whereas R. oryzae concentration was correlated with temperature minima but not with precipitation. However, both pathogens were more abundant in soils with higher sand and lower clay content. Principal component analysis also indicated that unique groups of meteorological and soil factors were associated with each pathogen. Furthermore, tillage did not affect R. oryzae but affected R. solani AG8 at P = 0.06. Lower soil concentrations of R. solani AG8 but not R. oryzae occurred when the previously planted crop was a broadleaf (P < 0.05). Our findings showed that R. solani AG8 concentrations were consistent with the general distribution of bare patch symptoms, based on field observations and surveys of other pathogens, but was present at many sites in which bare patch symptoms were not evident. Management of Rhizoctonia root rot and bare patch should account for the likelihood that each pathogen is affected by a unique group of agroecological variables.


Sign in / Sign up

Export Citation Format

Share Document