THE EFFECT OF ENVIRONMENT ON CHEMOTYPE OF WILD DRUG CANNABIS SATIVA L. OVER MULTIPLE GENERATIONS
Ok I've started an experiment some of you might fine interesting. Unfortunately the results will only be able to be measured through subjective bioassay and no objective method of measuring potency and chemotype is available to me yet. Hopefully by the time this experiment is finished I will have access to a gas chromatagraph . Also I have a concern about males pollinating flowers that are not part of this experiment so selections will be made outdoors cuttings will be made then the males will be culled.
The goal of this experiment is to see if a strain of wild malawi plants can retain chemotype and potency over multiple generations of selection based purely on size early fertility vigorous growth and reproductive success in a temperate climate. Unfortunately the methods of selection will be fairly subjective also and I will try to make my selections based on their overall reproductive success in the temperate climate I live and will try to slightly exagerate this to speed up the process and simulate a more northern climate. 50 seeds picked directly from wild plants in malawi were germinated in february and kept in a cold frame until this week. The plants are placed in holes of a standard size supplemented with lime high quality compost 3 year old chicken manure and slow release organic nutrient rock phosphate and greensand. Supplemental nutrient and water will only be provided the continued success of the experiment is in danger because of a lack of water or nutrient. Supplemental nutrient beyond what was put in the holes is probably unnecesarry as the nutrient and requirements of the wild malawi are very low. Only what is neccessarry to allow the experiment to continue and if provided at all will be provided evenly to each specimen. No insect prevention will be used. Animal prevention will be provided through a perimeter of blood meal around the plants and bottles filled with coton and coyote urine will be placed near the plants. After sexing cuttings will be taken off of the most successful males. The males will then be culled. The cuttings will be taken to another location. Pollen from one cutting of each plant will be mixed together then applied to the most successful females that have no health or insect problems. Pollen will be applied from the very earliest stages of flowering to select for plants that show early fertility and allow the plants that show early fertility to produce a larger portion of seeds. If drought occurs during seed production plants will be allowed to wilt to select for plants that can protect seeds from drought since rain and humidity tend to be less frequent in temperate climate though my climate is still fairly humid. After harvest unseeded flowers will be sampled and stored for later generational comparison. Seeded flowers will be dried using a standardized method sieved using a standardized method using an equal weight of flowers for an equal amount of time at an equal temperature and humidity in a tumbler. Resin yield and physical characteristics will be noted. It will be sampled then will be vacuum sealed and stored frozen for future comparison. Leaves will be taken from a standard location on each plant on the same dates and maturity stages every year and will be analyzed with a refractometer. Results will be noted. On predetermined dates and maturity stages samples of floral clusters will be taken from a standardized location on each plant. Trichome height density and gland head size will be noted.
Any of you guys have any suggestions on things I should do differently? Any advice or reasons why this experiment might not produce usable results will be welcomed.
Ok I've started an experiment some of you might fine interesting. Unfortunately the results will only be able to be measured through subjective bioassay and no objective method of measuring potency and chemotype is available to me yet. Hopefully by the time this experiment is finished I will have access to a gas chromatagraph . Also I have a concern about males pollinating flowers that are not part of this experiment so selections will be made outdoors cuttings will be made then the males will be culled.
The goal of this experiment is to see if a strain of wild malawi plants can retain chemotype and potency over multiple generations of selection based purely on size early fertility vigorous growth and reproductive success in a temperate climate. Unfortunately the methods of selection will be fairly subjective also and I will try to make my selections based on their overall reproductive success in the temperate climate I live and will try to slightly exagerate this to speed up the process and simulate a more northern climate. 50 seeds picked directly from wild plants in malawi were germinated in february and kept in a cold frame until this week. The plants are placed in holes of a standard size supplemented with lime high quality compost 3 year old chicken manure and slow release organic nutrient rock phosphate and greensand. Supplemental nutrient and water will only be provided the continued success of the experiment is in danger because of a lack of water or nutrient. Supplemental nutrient beyond what was put in the holes is probably unnecesarry as the nutrient and requirements of the wild malawi are very low. Only what is neccessarry to allow the experiment to continue and if provided at all will be provided evenly to each specimen. No insect prevention will be used. Animal prevention will be provided through a perimeter of blood meal around the plants and bottles filled with coton and coyote urine will be placed near the plants. After sexing cuttings will be taken off of the most successful males. The males will then be culled. The cuttings will be taken to another location. Pollen from one cutting of each plant will be mixed together then applied to the most successful females that have no health or insect problems. Pollen will be applied from the very earliest stages of flowering to select for plants that show early fertility and allow the plants that show early fertility to produce a larger portion of seeds. If drought occurs during seed production plants will be allowed to wilt to select for plants that can protect seeds from drought since rain and humidity tend to be less frequent in temperate climate though my climate is still fairly humid. After harvest unseeded flowers will be sampled and stored for later generational comparison. Seeded flowers will be dried using a standardized method sieved using a standardized method using an equal weight of flowers for an equal amount of time at an equal temperature and humidity in a tumbler. Resin yield and physical characteristics will be noted. It will be sampled then will be vacuum sealed and stored frozen for future comparison. Leaves will be taken from a standard location on each plant on the same dates and maturity stages every year and will be analyzed with a refractometer. Results will be noted. On predetermined dates and maturity stages samples of floral clusters will be taken from a standardized location on each plant. Trichome height density and gland head size will be noted.
Any of you guys have any suggestions on things I should do differently? Any advice or reasons why this experiment might not produce usable results will be welcomed.