Analysis of Weather, Microclimate and Canopy Density … pdf/Day_1_R… · Analysis of Weather,...

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Analysis of Weather, Microclimate and Canopy Density on Sclerotinia Stem Rot Disease in Canola Reanne Pernerowski 1 , Paul Bullock 2 , Dilantha Fernando 3 Sclerotinia stem rot disease (SSR) in an increasingly important disease in the Canadian prairies creating unpredictable yield losses ranging between 5 and 100 percent in Manitoba. Management is extremely important due to the little commercially available resistant canola varieties. Caused by the fungus Sclerotinia sclerotiorum, sclerotinia begins its life cycle as sclerotia in the soil. Under specific environmental conditions sclerotia germinates and eventually releases ascospores into the surrounding atmosphere. Ascospores land on senescing flower tissue of the canola plant and subsequently land on the leaves and stems and begin to kill the entire plant. Canopy density and weather are important factors known to influence disease incidence of SSR as they are capable of modifying the microclimate and creating various environments that affect all levels of the disease cycle. Several researchers have proven that moderate temperatures and moisture is required for sclerotia germination, increasing temperatures and decreasing relative humidity is required for day time release of ascospores and moisture and humidity is required within the canopy for spore germination on petals and for further infection. This study attempts to validate these findings and more accurately depict the specific environmental conditions, and canopy densities most favourable to disease development and incidence. By understanding the environmental requirement for SSR, cost effective management strategies can be implemented based on the findings obtained within this study. More importantly, weather can be used as an indicator of risk in canola crops in Manitoba which can be used to determine appropriate fungicide application rates and timing.

Transcript of Analysis of Weather, Microclimate and Canopy Density … pdf/Day_1_R… · Analysis of Weather,...

Page 1: Analysis of Weather, Microclimate and Canopy Density … pdf/Day_1_R… · Analysis of Weather, Microclimate and Canopy Density on Sclerotinia Stem Rot Disease in Canola . Reanne

Analysis of Weather, Microclimate and Canopy Density on Sclerotinia Stem Rot Disease in Canola

Reanne Pernerowski 1, Paul Bullock 2, Dilantha Fernando 3

Sclerotinia stem rot disease (SSR) in an increasingly important disease in the Canadian prairies creating unpredictable yield losses ranging between 5 and 100 percent in Manitoba. Management is extremely important due to the little commercially available resistant canola varieties. Caused by the fungus Sclerotinia sclerotiorum, sclerotinia begins its life cycle as sclerotia in the soil. Under specific environmental conditions sclerotia germinates and eventually releases ascospores into the surrounding atmosphere. Ascospores land on senescing flower tissue of the canola plant and subsequently land on the leaves and stems and begin to kill the entire plant.

Canopy density and weather are important factors known to influence disease incidence of SSR as they are capable of modifying the microclimate and creating various environments that affect all levels of the disease cycle. Several researchers have proven that moderate temperatures and moisture is required for sclerotia germination, increasing temperatures and decreasing relative humidity is required for day time release of ascospores and moisture and humidity is required within the canopy for spore germination on petals and for further infection. This study attempts to validate these findings and more accurately depict the specific environmental conditions, and canopy densities most favourable to disease development and incidence. By understanding the environmental requirement for SSR, cost effective management strategies can be implemented based on the findings obtained within this study. More importantly, weather can be used as an indicator of risk in canola crops in Manitoba which can be used to determine appropriate fungicide application rates and timing.

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Reanne Pernerowski Dr. Paul Bullock, Dr. W.G Dilantha Fernando University of Manitoba

Analysis of Weather, Microclimate and Canopy Density on Sclerotinia Stem Rot

Disease in Canola

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Sclerotinia Stem Rot (SSR) Canadian Prairies

• Fungus Sclerotinia sclerotiorum

• Economically important disease of canola

• Reduce yields by 0.4 to 0.5 times the percentage of

infection (Manitoba Agriculture)

• Losses ranging from 5-100%

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3

Disease cycle of Sclerotinia

Apothecia germination Windborne ascospores

Lesions spread on stem Sclerotia form in stem Leaf infection

Petal infection

Infection stage

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Management of SSR • Crop rotations (4 years) with non host crops

– Limitations • Genetic Resistance

– Cultivar availability

• Fungicide applications – Costly, timing

• Biological control agents • Tillage • Seeding rates and row spacing • Disease forecasting

Presenter
Presentation Notes
Not many non host crops, long rotation periods
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Objectives 1. Impact of microclimatic conditions in varying

canopy densities on S. sclerotiorum 2. Assess risk of SSR disease on canola based on

standard weather conditions 3. Impact of a disease infected field containing a non-

host wheat crop on sclerotinia disease development and spread by spore dispersal

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Study Sites and Layout

• Carman – 2011 – 2012

• Winnipeg – 2011 – 2012

• 3 treatments of high, medium and low seeding rates and fertilizers treatments

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Field Setup • Even Inoculation

– Canola, Wheat

• Weather station – Wind, RH, temperature, solar

radiation, rainfall

• Microclimate stations – RH, temperature, soil moisture

and temperature, leaf wetness

• Misting • Rotorods

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Carman 2012 Carman Flowering 2011

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Effects of Canopy Density and Misting on Microclimate and

Disease

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Seeding Rate – Crop Density

1

1.5

2

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3

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June 30, 2011 July 5, 2011 July 12, 2011 July 21, 2011

WINNIPEG CARMAN 2011

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July 8, 2011 July 11, 2011 July 19, 2011 July 27, 2011 August 3, 2011

2011

LOW MEDIUM HIGH

Presenter
Presentation Notes
Blue: high Green: medium Red: low Significance bw high and low seeding rates for both fields in 2011
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Hourly Relative Humidity among Canopy Densities

30

40

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100

110

2011/07/02 12:00 2011/07/04 0:00 2011/07/05 12:00 2011/07/07 0:00

Rela

tive

Hum

idity

(%)

0% to 30% flowering

High Medium

Low

• Winnipeg 2011

FLOWERING PERIOD Average RH: significant differences among all plot densities

Presenter
Presentation Notes
A high, medium and low density plots indicated by the arrows Significant impacts are shown by the density differences on relative humidities with higher RH at higher density plots Similar trend throughout flowering period Makes sense due to large differences in LAI density differences
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Hourly Temperature among Canopy Densities

• Winnipeg 2011

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2011/07/02 0:00 2011/07/04 0:00 2011/07/06 0:00 2011/07/08 0:00

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pera

ture

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rees

Ce

lsiu

s)

0% to 30% flowering

FLOWERING PERIOD Average Temperature: significant differences among all plots densities

High

Medium

Low

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Total Daily Mean Ascospore Concentrations (ascospores/m3)

WINNIPEG 2011 WINNIPEG 2012

CARMAN 2011 CARMAN 2012

R² = 0.0033

R² = 0.0005

R² = 0.257

R² = 0.1507

400

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spor

e Co

ncen

trat

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(asc

ospo

res/

m3 )

LAI

R² = 0.0217 R² = 0.0087

R² = 0.2206

R² = 0.0001

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Asco

spor

e Co

ncen

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plants/m3

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Percentage of Infection

R² = 0.2856

R² = 0.0679 0

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enta

ge o

f Inf

ectio

n (%

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LAI

R² = 0.0686

R² = 0.3383

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f Inf

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n (%

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WINNIPEG 2011 WINNIPEG 2012

CARMAN 2011 CARMAN 2012

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Misting (2011)

Winnipeg 2011 Misted Non-Misted

Leaf Area Index 3.2 3.0

Plant Counts (plants/m3) 133.1 148.3

Relative Humidity (%)* 78.2 76.6

Leaf Wetness* 32.9 24.4

Air Temperature (°C)* 20.6 20.8

Soil Temperature (°C)* 20.4 20.4

Ascospore Concentration (ascospores/m3) 628 705

Percentage of Infection (%) 6 14

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Potential Relationships between Weather Variables and Ascospore Dispersal

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Mean Daily Ascospore Concentrations Carman and Winnipeg Overlay (2011)

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12-J

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pore

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cent

ratio

ns

(Asc

ospo

re/m

3)

Date

CarmanWinnipeg

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Precipitation on Ascospore Concentrations

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-Jul

07-Ju

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l

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l

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ug

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ug

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Tota

l Dai

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ainf

all (

mm

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n D

aily

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ospo

re C

once

ntra

tion

(Asc

ospo

res/

m3 )

CARMAN – 2011

• Qandah and Mendoza (2011): ascospore release during elevated periods of RH followed by rapidly decreasing RH

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Analysis of Spore Release Dispersal from a Non-Host Wheat Crop

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684 604 727

682

723 673

659 662

707

748 603 640

Wind on Mean Ascospore Concentrations (ascospores/m3)

DOMINANT WIND DIRECTION

CA

NO

LA

WH

EAT

N

E S

W CARMAN 2011 57

7 a/

m3

- 19

%

622

a/m

3 - 3

0 %

655

a/m

3 - 1

6 %

Presenter
Presentation Notes
Wheat not biggest contributing factor to ascospore concentrations and disease incidence in neighbouring canola field Higher concentrations in bar soil closer to canola compared to wheat in both carman fields (2011 and 2012)
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Interpretation –Canopy density and misting –Crop rotations –Weather forecasting and fungicide use

Brenleigh Ramm Samantha Erichsen Ives Nikiema

Presenter
Presentation Notes
Additional data analysis required to determine exactly what is influencing the pathogen, we know so far that canopy density plot treatments alone do not influence the spread of ascospores or the onset of disease it may however have an influence on the germination of sclerotia at the beginning of the life cycle of the disease, however this is not studied here spore dispersal needs to be observed over time and compared with other microclimate and weather factors also a more in depth analysis of individual plots needs to be completed, due to possibility of weeds/ other factors affecting these results analysis of spore dispersal in neighbouring wheet field to see if we can quantify the distance travelled by these spores and the effects of non host crops The insignificant results can be interpreted in many ways ascospore release and dispersal may be more sporadic than we think ascospores can also be spread further than the plot limitations disease incidences not coordinating with plot densities may be linked to the nature of spore dispersal within the plots it may be possible that spore dispersal and disease is not influenced by factors affected by canopy desnity such as RH and Temperature, there may be more significant underlying factors affecting disease development
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Acknowledgements

• Canola Council of Canada • Advisors, Drs. Paul Bullock and W.G. Dilantha

Fernando • Technicians Paula Parks, Tim Stem, Bo Pan and

Besrat Demoz • Summer students (Michael Chiasson, Jennifer

Ellis, Brenleigh Ramm, Michelle Lacroix, Samantha Erichsen, Ives Nikiema and Todd Pernerowski)

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Fungicides Used

• Lance • Vertisan • Astound • Iprodione • Proline • Quadris • Serenade • Biological control agent: Contans

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Petal Sampling 2011 • Rose Bengal Agar • Sampled twice

– 30% bloom – 70% bloom

2012

• Semi- selective media • Sampled 3 times

– 20% bloom – 30% bloom – 70% bloom

Presenter
Presentation Notes
2011 Identification: sclerotia bodies forming, white mycelium, agar turns clear -results: no patterns, sclerotinia identified in a couple plots only on certain petals in both years 2012 identification: blue to greenish yellow, sclerotia bodies and white mycelia
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Wind Speed on Ascospore Concentration

CARMAN 2011

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age

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eed

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n Da

ily A

scos

pore

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ncen

trat

ion

(asc

ospo

res/

m3 )

WINNIPEG 2011

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eed

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)

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n D

aily

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ospo

re

Conc

entr

atio

n (a

scos

pore

s/m

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Wind Speed on Ascospore Concentration CARMAN 2012

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