Recipient Organization
RT SOLUTIONS LLC
32 HERITAGE DRIVE
Geneseo,NY 14454-1188
Performing Department
(N/A)
Non Technical Summary
RT Solutions, LLC (RTS) has built a unique process-controlled "state-of-the-art" earthworm composting facility that process and transforms large volumes of dairy manures into a user friendly and unique plant production product with established horticultural consumers. This environmentally friendly technology known as vermicomposting uses earthworms in an engineered system to consistently produce a little understood class of organic plant production products. There are a multitude of peer-reviewed studies reporting the benefits of vermicompost in agriculture including disease suppression, but to date little has been done to identify the actual mechanisms or how they work. RTS, along with our collaborator Cornell University have preliminary results showing significant suppression of a seedling disease in a laboratory system. The three objectives of this project are to (1) develop an understanding of the mechanism of disease suppression for vermicompost, (2) develop a test that can rapidly predict suppression in vermicompost products and (3) develop a new family of liquid vermicompost extract products for use in commercial applications. RTS was founded to promote professional vermicomposting and develop vermicompost products for use in production agriculture. We are committed to bringing a quality, consistent, and scientifically based product into commercial applications. The information developed in this SBIR project will increase the value of vermicompost products to growers and further develop this environmentally sustainable manure management technology.
Animal Health Component
100%
Research Effort Categories
Basic
(N/A)
Applied
100%
Developmental
(N/A)
Goals / Objectives
The central goal of this project is to develop plant protection products for horticultural production based on earthworm composted dairy manure produced from a uniquely engineered production system. Earthworm composting known as vermicomposting performed by RT Solutions (RTS) produces a new class of microbially active products with verified disease suppressive properties. This project will study and develop materials from (RTS) vermicomposting facility located on a 1,600 head dairy farm that produces commercial quantities of certified organic plant growth products. Materials from this state of the art operation have been proven to suppress the pathogen Pythium Aphanidermatum on cucumber in a model experimental system at Cornell University. This project is designed to (1) explore the mechanisms behind the observed disease suppression (2) develop infrastructure at the vermicomposting facility for production of disease suppressive products (for study at Cornell), (3) examine the ability of the vermicompost to be consistently suppressive, and (4) develop methods to determine if suppressiveness in vermicompost can be assessed in advance. In particular a new extraction system and various methods will be prototyped at the vermicomposting facility to produce a liquid product for testing and development. In the portion of this project devoted to the investigation on mechanisms for disease suppression, work will be performed towards (1) quantifying the disease suppressive capacity of vermicompost, (2) confirming the biological nature of the mediated disease suppression, (3) determine the time frame during which disease suppression occurs, and (4) determine the microbiological mechanism - i.e. are specific bacterial, fungal or oomycete seed-colonizing species associated with suppression.
Project Methods
At the vermicomposting facility, RT Solutions (RTS) will design, test and use an extraction system to produce commercial quantities of a liquid product based on their vermicompost materials. The liquid extract is commonly called a tea, and the end goal is to develop a consistent, quantifiable and reliable disease suppressive product for use in organic agriculture. The tea will be bioassayed in house for phytotoxicity, seed germination rates and seedling growth (biomass). Large scale system design of the extract system will be done and in-house facilities will be constructed. Multiple batches of 200 - 500 gallons of extract will be made to verify product consistency and refine production and handling methods. Extract samples will be sent to commercial labs to determine basic physical and chemical properties. Prior to bioassay and Cornell mechanism studies, the large batches of vermicompost extract will be stored in sealed conditions to replicate holding time between production and use by targeted horticulturalists. An engineering and agronomic analysis will be made of the extract and multiple derivative products from the extracts (seed treatment, soil drench and foliar feed). In particular, soil drench and seed treatment products will be examined, in terms of: (1) equipment needs, (2) production requirements, (3) product registration (biopesticide route). At Cornell University, the Nelson plant pathology lab has developed a disease suppression bioassay that controls for the environmental factors of temperature, light, moisture (including soil matric potential), and inoculums. This experimental system and statistical design will be used to measure the disease suppressive abilities of multiple batches of vermicompost from RTS, as well as a variety of non-aerated vermicompost extracts. Regarding the time frame analysis, previous work in the Nelson Lab has shown that compost mediated suppression can be explained by the presence of a seed-colonizing microbial community that develops only after a certain period of germination in the suppressive media. We will determine this time frame by removing germinating seeds from our known suppressive medium and transplanting them to a sterile medium before challenge with the pathogen in the experimental apparatus. We will take two complimentary approaches to investigating the mechanism of vermicompost-mediated disease suppression. A set of functional assays will determine if the suppressive seed-colonizing microbial consortia are modifying seed exudate in such a way that it no longer serves as an attractant for Pythium zoospores. We will also pursue a taxonomic approach, using molecular techniques to identify taxonomic groups present in the suppressive seed-colonizing microbial community. Based on available information on the groups present, and a comparison with seed-colonizing microbial consortia from materials that do not suppress disease, hypotheses on potential mechanisms can be developed.