Peach Crop Protection in Sustainable Agriculture

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    PEACHCROPPROTECTIONINSUSTAINABLEAGRICULTURE

    CONDITIONSINSMALLANDMEDIUMFARMS

    VasileJINGA1,CarmenLUPU

    1,RoxanaDUDOIU1,AndreeaPETCU

    2,Gigel-GabrielLUPU3

    1Research-DevelopmentInstituteforPlantProtectionBucharest,

    8IonIonescudelaBradBlvd.,District1,71592,Bucharest,Romania2ResearchandDevelopmentStationforFruitTreeGrowing-Baneasa,

    4IonIonescudelaBradBlvd,District1,Bucharest,Romania3UniversityofAgronomicSciencesandVeterinaryMedicineofBucharest,

    59MarastiBlvd.,Bucharest,Romania

    Correspondingauthoremail:[email protected]

    Abstract

    Scientific work aims topromote disease management systems offruit trees stone group (peach), using chemicaltreatmentmethodswith low impacton theenvironmentandhumanhealth, whichcontribute to increasecropqualityandquantity.ResearchhasbeenconductedonpeachspeciescultivatedinResearchandDevelopmentStationforFruitTreeGrowing-Baneasa, Bucharest, intheclimaticconditionsoftheyear2012.Stigminacarpophilawasthepathogenfor which measures have been takenfor itsprevention and control. Treatments againstpathogen were applied atwarning, depending onthebiologicalreserveofthevegetationperiodandtheclimateevolutioninthatyear.Among thefivefungicidesused, thebestresultswereobtainedwiththeproductsScore250EC andSysthaneC PU.

    Keywords: peachorchard, diseasecontrol, ARM software.

    INTRODUCTION

    PrunuspersicaL. culturehasahigheconomic

    value on national as well as on internationallevel. Production and fruits marketing is the

    goalofan intensemodern trade. Annually, the

    trees suffer from attacksof variouspathogens

    causingcropdiseaseswhichdevelopdependent

    totheclimateconditionsoftheyearandtothe

    cultivatedvariety(Ivascu,2002; Delian,2006).

    Longtermuseofpesticidesinpomicultureand

    ignoring its side effects, have had negative

    consequences towards the environment (Hoza

    etal.,2000; Burzoetal.,2005). Nowdays, the

    more severe requirements regarding the

    environmentprotectionandhealthorchardsled

    to the development of ecological selective

    methods (Toncea, 2001) specifically for the

    crops pest control (Jinga et al., 2008). The

    treatmentsappliedduringthevegetationperiod

    determine the improvement of the yields

    qualityandquantity(Delianetal.,2012).

    MATERIALSANDMETHODS

    The evaluation of several plant protectionproducts efficacy against the main studied

    pathogensforthepeachculturewasdeveloped

    during several visits at the Research and

    Development Station for FruitTreeGrowing-

    Baneasa. Therewere takenbiological samples(plantswithpathogen attack symptoms) from

    this orchard and therewere isolated themain

    pathogen agents. The isolatedpathogenswere

    usedinlaboratoryexperimentsfortestingthese

    newplantprotectionproductsproposed in the

    technology. After the laboratory trials, there

    were also performed field treatments, during

    thespringseason,inthevegetationperiod,with

    fungicides, followed by establishing the

    efficacy of the testedproducts. In thePrunus

    persica L. orchard there were carried outtreatments in order toprevent and control the

    attackofthemainfruitspathogens. Theattack

    ratewas calculatedwith the formulas RA%=

    F*I/100,F%-frequencyof theattackedorgans,

    I intensity of the organ attack. The tested

    peachvarietywasVictoria,whichisasensitive

    one. Duringthelaboratorytrialswastestedthe

    biological action of the following products:

    Dithane M45, Bravo Folicur Solo 250EW,

    Score250ECandSysthaneCPU. Itwasused

    amethodbasedon the inclusionof the testedfungicide into thePDAmedium, in5different

    concentrations. The medium was poured in

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    Scientific Papers. Series B, Horticulture. Vol. LVII, 2013Print ISSN 2285-5653, CD-ROM ISSN 2285-5661, Online ISSN 2286-1580, ISSN-L 2285-5653

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    Petridishes, thepathogenic fungiwereplaced

    onthemedium,anditwasobservedthegrowth

    of the colonies compared to control fungi,

    growthonmediumwithoutfungicide(Baicuet

    al., 1996; Severin et al., 2001). For each

    fungicide concentration was calculated the

    inhibition percent of the mycelium growth(Alexandri,1982; Geamanu,2006).

    The field trialsof the fungicidesselectedafter

    the laboratory tests were made in the 2012

    spring season. Therewere used the following

    variants:

    V1= untreatedcontrol

    V2= DithaneM450.2% concentration

    V3= Bravo500SC0.15% concentration

    V4= FolicurSolo250EW0.1% conc

    V5= SysthaneCPU0.1% concentrationV6= Score250EC0.02% concentration

    Weatherconditionsduringapplication:

    Table1. 1sttreatment04-04-2012

    Temperatureofair 19.2C

    Relativehumidity 54%Windspeed 0.8Winddirection NCloudcover(%) 0

    Rainfallwith1weekbeforeofspraying 0.4mmRainfallwith2weeksafterspraying 0mmFirstrainfallaftersprayinganditsamount 15-05-2012

    Table2. 2ndtreatment06-05-2012

    Temperatureofair 13.9C

    Relativehumidity 72%Windspeed 0.5Winddirection NECloudcover(%) 0Rainfallwith1weekbeforeofspraying 0.4mmRainfallwith2weeksafterspraying 3.4mm

    Firstrainfallaftersprayinganditsamount 19-05-2012

    Table3. 3rdtreatment09-06-2012

    Temperatureofair 19.6C

    Relativehumidity 64%Windspeed 0.7Winddirection NCloudcover(%) 0Rainfallwith1weekbeforeofspraying 0mmRainfallwith2weeksafterspraying 0mmFirstrainfallaftersprayinganditsamount 24-06-2012

    There were applied 3 treatments on the 4th

    April,6thMayand9thJune,inaccordancewith

    the meteorological conditions, and the

    observations took place 8 days after each

    treatment, taking into account the frequency

    (PESING) and the intensity (PESSEV) of the

    attack. Theobservations targeted theStigminacarpophilapathogenwhichproduces the shot

    holedisease(Figure1).

    The treatments were carried out using the

    SOLOatomizerpump(Figure2).Studies regarding the experimentalmodels of

    the proposed technology took place in an 8

    yearsPrunuspersica L. orchard, at Researchand Development Station for Fruit Tree

    Growing-Baneasa,inordertoestablishtherate

    ofinfectiousloadfromthisarea.

    Itwasused theclassical testingmethodwhich

    consist in 6 variants in 4 replicationswith 5

    treespereachvariantinrandomdisposal.

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    Figure1. ShotholeandfruitstainproducedbyStigminacarpophila

    Figure2. Treatmentsinvegetationperiod

    RESULTSANDDISCUSSIONSThebiologicalactionofsomefungicidesonthe

    development of Stigmina carpophila funguscolonies on leaves and fruits is presented inTable4.

    Table4. BiologicalactionofsomefungicidesonthedevelopmentoffunguscoloniesStigminacarpophila

    ProductColonydiameter(mm)atconc.% Inhibitionpercentatconc.%

    0,2 0,1 0,05 0,025 0,015 0,2 0,1 0,05 0,025 0,015DithaneM45 0 7 10 16 20 98,6 70,0 65,0 37,1 11,5Bravo500SC 0 8 20 25 41 100 80,5 70,5 20,0 14,8FolicurSolo250EW 0 0 8 10,5 15 100 91,4 88,6 75,0 50,1SysthaneCPU 0 0 8 19 31 100 100 78,5 58,6 42,5Score250EC 0 0 0 0 0 100 100 100 87,1 51,5Control 70mm

    Based on the datapresented in Table 4were

    selected the products and their optimal con-

    centrationwhichwillfurtherbeusedduringthe

    field trials in order to control the fungus

    Stigminacarpophila.Theproductswithverygoodbiologicalaction

    were: Folicur Solo 250 EW in 0.1% concen-

    tration,SysthaneCPUin0.05%concentration,

    Score 250 EC in 0.02% concentration, Bravo

    500SCin0.2%concentration,DithaneM45in

    0.2%concentration.

    During theexperiments therewere taking into

    account the 100% fungi inhibition in accor-

    dancewith the various factors acting towards

    plants.

    The results obtained in field during the vege-

    tationperiodarepresentedinTables5and6.

    Table5. ThefrequencyandintensityoftheStigminacarpophilaattack

    TreatmentproductnamePESINC

    %PESSEV

    %

    PESINC%

    PESSEV%

    PESINC%

    PESSEV%

    04.04.2012 09.05.2012 12.06.2012

    Variant 1

    R1 27.0 12.0 39.0 12.0 52.0 16.0R2 19.0 10.0 27.0 16.0 43.0 20.0R3 28.0 9.0 34.0 14.0 48.0 23.0R4 31.0 12.0 31.0 16.0 51.0 20.0

    Average 26.3 10.8 32.8 14.5 48.5 19.8

    Variant 2

    R1 16.0 6.0 20.0 11.0 21.0 13.0R2 12.0 4.0 18.0 12.0 31.0 21.0R3 17.0 5.0 15.0 6.0 24.0 14.0R4 14.0 4.0 21.0 10.0 28.0 12.0

    Average 14.8 4.8 18.5 9.8 26.0 15.0Variant 3 R1 17.0 5.0 17.0 15.0 20.0 9.0

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    R2 11.0 4.0 15.0 7.0 22.0 10.0R3 16.0 4.0 16.0 5.0 17.0 8.0R4 9.0 5.0 12.0 8.0 21.0 10.0

    Average 13.3 4.5 15.0 8.8 20.0 9.3

    Variant 4

    R1 10.0 3.0 16.0 7.0 17.0 6.0R2 12.0 5.0 10.0 4.0 19.0 7.0R3 9.0 4.0 12.0 6.0 21.0 8.0

    R4 11.0 6.0 14.0 3.0 14.0 7.0Average 10.5 4.5 13.0 5.0 17.8 7.0

    TreatmentproductnamePESINC

    %PESSEV

    %

    PESINC%

    PESSEV%

    PESINC%

    PESSEV%

    04.04.2012 09.05.2012 12.06.2012

    Variant 5

    R1 14.0 7.0 11.0 4.0 11.0 7.0R2 12.0 4.0 12.0 6.0 16.0 5.0R3 16.0 4.0 14.0 5.0 14.0 8.0R4 10.0 5.0 13.0 6.0 16.0 4.0

    Average 13.0 5.0 12.5 5.3 14.3 6.0

    Variant 6

    R1 10.0 5.0 7.0 5.0 11.0 6.0R2 12.0 4.0 10.0 4.0 12.0 5.0R3 9.0 4.0 12.0 3.0 9.0 4.0R4 8.0 3.0 11.0 3.0 10.0 3.0

    Average 9.8 4.0 10.0 3.8 10.5 4.5

    Table6. Processingofdatafromthethreetreatmentsappliedinthevegetationperiod

    VariantTreatment

    ProductName

    PESINC%

    PESSEV%

    PESINC%

    PESSEV%

    PESINC%

    PESSEV%

    04.04.2012 09.05.2012 12.06.2012

    1 Variant1 26.3a 10.8b 32.8a 14.5a 48.5a 19.8a2 Variant2 14.8b 4.8b 18.5b 9.8b 26.0b 15.0b3 Variant3 13.3b 4.5b 15.0bc 8.8b 20.0c 9.3c4 Variant4 10.5b 4.5b 13.0c 5.0bc 17.8c 7.0cd

    5 Variant5 13.0b 5.0b 12.5c 5.3bc 14.3cd6.0cd

    6 Variant6 9.8b 4.0b 10.0c 3.8c 10.5d 4.5dLSD(P=.05) 4.56 1.59 4.32 3.57 4.85 3.41StandardDeviation 3.02 1.05 2.87 2.37 3.22 2.27CV 20.74 18.88 16.91 30.27 14.09 22.1Bartlett'sX2 6.773 3.184 5.618 8.991 4.713 10.298P(Bartlett'sX2) 0.238 0.672 0.345 0.109 0.452 0.067ReplicateF 1.270 2.050 1.114 1.166 0.462 1.136ReplicateProb(F) 0.3204 0.1501 0.3746 0.3555 0.7131 0.3662TreatmentF 15.787 23.460 33.049 11.431 71.803 27.351TreatmentProb(F) 0.0001 0.0001 0.0001 0.0001 0.0001 0.0001*Meansfollowedbysameletterdonotsignificantlydiffer(P=0.05,Student-Newman-Keuls)MeancomparisonsperformedonlywhenAOVTreatmentP(F)issignificantatmeancomparisonOSL.

    The data processed using ARM 8 software

    (ARM is a recognized and respected standard

    throughout the plant production, used by

    thousands of researchers around the world),

    concludes, that after the first treatment (April

    4) all 5 fungicides showed significant effects

    (b) in fungus control. After the 2nd treatment

    (May 9) the results are significant (b) in

    variants2and3andsignificantdistinct(bc)in

    variants4and5andverysignificantinvariant

    6. The results obtained after the 3rd treatment

    (June 12) are from distinct significant in

    variants3and5uptoverysignificantinvariant

    6.

    It results that the following contact fungicides

    Bravo500SCandDithaneM45(V2andV3)

    have a good efficacy, and the systemic ones

    (V3-V6) present a high efficacy. The best

    results were obtained with V6, the fungicide

    Score250EC.

    CONCLUSIONSDuringthelaboratorytrialstherewereselected

    theproducts with thebestbiological activity

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    against the development of the studied fungi.

    Theproductswith the highestbiological acti-

    vityagainstthedevelopmentoffunguscolonies

    ofStigminacarpophilawere:FolicurSolo250EW in0.1% concentration,SysthaneCPU in

    0.05% concentration, Score 250EC in 0.02%

    concentration,Bravo500SC in0.2% concen-tration,DithaneM 45 in 0.2% concentration.

    Laboratory resultsenable the selectionof fun-

    gicides showing high inhibitionpercentage in

    order to establish a treatment chart for the

    vegetationperiod, regarding the controlof the

    majordiseasesspecifictothepeach.

    Thephytosanitary treatmentswillbemade at

    warning,accordingtotheevolutionofenviron-

    mental conditions and pathogenic organisms,

    pursuanttotheproposedtechnology.

    It results that the following contact fungicides

    Bravo500SCandDithaneM45(V2andV3)

    have a good efficacy, and the systemic ones

    (V3-V6) present a high efficacy. The best

    results were obtained with V6, the fungicide

    Score250EC.

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