IS 4873 Part 22008AI Search Enabled✦ AI Generated

Methods of laboratory testing of wood preservatives against fungi and borers (powder post beetles) : Part 2 Determination of threshold values of wood preservatives against borers (powder post beetles)

IS 4873 Part 2:2008 specifies the laboratory method to determine the threshold toxicity levels of wood preservatives against borers, specifically powder post beetles such as Lyctus brunneus and Minthea rugicollis. It applies to wood samples treated with various preservative types and evaluates their effectiveness by exposing treated wood to beetle infestation under controlled conditions. This standard is essential for manufacturers, researchers, and quality control professionals involved in wood preservation to assess and compare preservative efficacy against powder post beetle attack.

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What This Standard Covers

IS 4873 Part 2:2008 specifies the laboratory method to determine the threshold toxicity levels of wood preservatives against borers, specifically powder post beetles such as Lyctus brunneus and Minthea rugicollis. It applies to wood samples treated with various preservative types and evaluates their effectiveness by exposing treated wood to beetle infestation under controlled conditions. This standard is essential for manufacturers, researchers, and quality control professionals involved in wood preservation to assess and compare preservative efficacy against powder post beetle attack.

Who Uses This Standard

  • Wood Preservation Specialists
  • Quality Control Engineers in Timber Industry
  • Wood Product Manufacturers
  • Forestry Researchers
  • Laboratory Technicians Testing Wood Preservatives
  • Plywood and Panel Industry Professionals
  • Entomologists specializing in Wood Borers

Key Topics Covered

Preparation and conditioning of wood test samples
Selection of wood species and sample dimensions
Treatment procedures for wood preservatives
Use of powder post beetles for infestation testing
Determination of preservative uptake and retention
Test conditions including temperature and humidity control
Assessment of starch content in wood samples
Exposure duration and beetle culture maintenance
Evaluation criteria for beetle emergence and larval survival
Calculation of threshold toxicity values
Use of control samples treated with solvent only
Reporting and interpretation of test results

Table of Contents

1Scope

IS 4873 Part 2: Scope Summary

  • Scope: Defines methods to determine threshold values of wood preservatives against borers (Powder Post Beetles).
  • Purpose: Establish minimum effective concentrations of preservatives to prevent borer infestation.
  • Application: Used for testing and analyzing wood treated with preservatives.

Key Points:

  • Test Result Rounding: Final values must be rounded per IS 2:1960 rules.
  • Significant Figures: Retain same significant digits as specified values in the standard.

Typical Procedure (Conceptual):

  1. Treat wood samples with varying preservative concentrations.
  2. Expose samples to borers.
  3. Observe infestation levels.
  4. Determine threshold concentration where infestation is inhibited.

No direct formulas or tables are provided in the scope clause, but testing follows statistical analysis of infestation data to identify threshold values.

flowchart LR
    A[Treated Wood Samples] --> B[Exposure to Borers]
    B --> C[Observation of Infestation]
    C --> D[Analysis of Results]
    D --> E[Determine Threshold Preservative Value]

For detailed test methods and values, refer to the full IS 4873 Part 2:2008 document.

2Method of Test

IS 4873 Part 2 — Method of Test: Key Points

  • Rounding Off Results:
    Follow IS 2:1960 for rounding test results. Retain the same number of significant figures as the specified value in the standard.

  • Preparation of Test Samples (Clause 3.2.2):

    • Condition samples for 2 weeks at 25° to 30°C and 70-75% RH to reach ~15% moisture content.
    • Seal end grain with paraffin wax or suitable sealant to prevent preservative penetration through ends.
    • Prepare untreated control blocks similarly sealed.
  • Sample Quantities:

    • 10 samples treated with preservative at each concentration.
    • 5 samples treated with solvent only.
    • 5 untreated control samples.

Summary Table of Sample Requirements

Sample TypeQuantity
Preservative-treated10
Solvent-treated5
Untreated control5

This ensures standardized conditioning and testing for reliable preservative efficacy evaluation.

3Preparation of Test Samples

IS 4873 Part 2: Preparation of Test Samples (Clause 3.2.2)

  • Conditioning:

    • Temperature: 25° to 30°C
    • Relative Humidity: 70 to 75%
    • Duration: 2 weeks
    • Purpose: Achieve equilibrium moisture content ≈ 15%
  • Sample End-Grain Sealing:

    • Use paraffin wax or suitable sealant
    • Prevents undue preservative penetration through ends
  • Sample Quantity per Test:

    Sample TypeNumber of Samples
    Treated with preservative10 (per concentration)
    Treated with solvent only5
    Untreated control (end-coated)5
  • Rounding Off Results:
    Follow IS 2:1960 rules, retaining significant digits equal to the specified values.


Summary Flow for Sample Preparation

flowchart TD
    A[Select Wood Blocks] --> B[Condition 2 weeks at 25-30°C, 70-75% RH]
    B --> C[Seal End Grain with Paraffin Wax]
    C --> D{Sample Type}
    D -->|Preservative Treatment| E[10 Samples per Concentration]
    D -->|Solvent Only| F[5 Samples]
    D -->|Untreated Control| G[5 Samples]

This ensures uniform moisture content and prevents preservative entry through ends, critical for consistent test results.

3.1Principle of the Test

IS 4873 Part 2: Principle of the Test - Key Points

1. Test Sample Preparation (Clause 3.2.2)

  • Conditioning: Samples conditioned for 2 weeks at 25° to 30°C and 70-75% RH to reach ~15% moisture content.
  • Sealing: End grain sealed with paraffin wax or equivalent to prevent preservative penetration through ends.
  • Control Samples: Untreated blocks also sealed similarly.

2. Sample Quantity

Sample TypeQuantity per Test
Treated with preservative10
Treated with solvent only5
Untreated control samples5

3. Rounding Off Results (Method of Test)

  • Final test values rounded per IS 2:1960 rules.
  • Retain significant figures equal to those specified in the standard.

Summary Diagram of Test Preparation

flowchart TD
    A[Start: Select Samples] --> B[Condition at 25-30°C, 70-75% RH for 2 weeks]
    B --> C[Seal end grain with paraffin wax]
    C --> D{Sample Type?}
    D -->|Preservative| E[Treat with preservative (10 samples)]
    D -->|Solvent| F[Treat with solvent only (5 samples)]
    D -->|Control| G[Untreated control (5 samples)]
    E & F & G --> H[Test & Record Results]
    H --> I[Round off as per IS 2:1960]

This ensures uniform moisture content and controlled preservative penetration for reliable, comparable test results.

3.2Test Sample Preparation Details

IS 4873 Part 2: Test Sample Preparation Summary

1. Conditioning of Samples (Clause 3.2.2)

  • Temperature: 25°C to 30°C
  • Relative Humidity: 70% to 75%
  • Duration: 2 weeks
  • Goal: Achieve ~15% equilibrium moisture content
  • End Grain Treatment: Seal with paraffin wax or suitable sealant to prevent preservative penetration through ends.

2. Sample Numbers Required

Sample TypeQuantity
Treated with preservative10 per concentration
Treated with solvent only5
Untreated control5

3. Additional Notes

  • Untreated controls must be end-coated similarly.
  • Results should be rounded per IS 2:1960 rounding rules, maintaining significant figures as per standard.

This ensures uniformity and reliability in preservative treatment testing.

3.3Treatment Procedure

IS 4873 Part 2: Treatment Procedure Summary

Key Steps & Specifications (Clause 3.3)

  • Dilutions: Prepare ≥5 preservative concentrations (weight/weight basis), centered around expected toxic limit.
    • Unknown toxic limit: start with widely spaced geometric series, then finer arithmetic series.
  • Solvent Use:
    • Water-soluble preservatives → freshly prepared aqueous solutions.
    • Insoluble preservatives → dissolve in volatile solvents (e.g., benzene) that leave no toxic residue.
  • Sample Treatment:
    • Immerse 10% concentration test samples for 1 min.
    • Treat from most dilute to most concentrated.
    • Controls: 5 samples treated with solvent/emulsion without toxic ingredients.
  • Post-treatment:
    • Shake off excess, blot, and reweigh samples.
    • Calculate preservative uptake:
      [ \text{Uptake} = (\text{Weight after treatment} - \text{Initial weight}) \times \text{Concentration} ]
    • Select 5 blocks per concentration with uptake variation ≤15%.
    • Dry samples at ≤30°C until control samples return to initial weight.
  • Conditioning (Clause 3.2.2):
    • Condition blocks 2 weeks at 25–30°C, 70–75% RH for ~15% moisture content.
    • Seal end grain with paraffin wax.
  • Sample Numbers:
    • 10 per concentration treated.
    • 5 solvent-only treated controls.
    • 5 untreated controls.

Evaluation (Clause 3.6)

  • Record:
    • Number of samples with exit holes.
    • Treated samples without exit holes but with live larvae.
  • Toxic limit: Interval between highest concentration with beetle emergence/live larvae and next higher concentration with no emergence/all larvae dead.
  • Express concentrations in kg/m³ of wood.

Quick Reference Table: Sample Preparation & Testing

StepDetails
Conditioning25–30°C, 70–75% RH, 2 weeks
End grain sealingParaffin wax or suitable sealant
Number of samples10 per concentration, 5 solvent controls, 5 untreated controls
Treatment duration1 minute immersion
Dry
3.4Test Insects

IS 4873 Part 2: Test Insects for Powder Post Beetle Attack

Key Specifications (Clauses 3.1, 3.4, 3.5, 3.6)

  • Test Insects: Adults of Lyctus brunneus or Minthia rugicollis from lab cultures.
  • Culture Initiation: Use naturally infested wood + untreated feeder wood (semul/mango/rubber/bahera/tapioca chips with starch).
  • Test Setup:
    • Samples stored singly in glass containers with cambric covers.
    • Each sample exposed to 4 pairs of beetles or infested material.
    • Conditions: 25–30°C, 70–75% RH.
  • Duration: Until all beetles die; emergence of adults monitored (6-8 months).
  • Examination: Check for exit holes; split samples to detect live/dead larvae or tunnels.

Evaluation (Clause 3.6)

  • Threshold Value (Toxic Limit):
    Interval between:

    • Highest concentration where adults/larvae emerge, and
    • Next higher concentration with no adult emergence and all larvae dead.
  • Units: Kilogrammes per cubic metre (kg/m³) of wood.

  • Reporting:

    • Concentration of preservative solution used.
    • Diluents used.
    • Time between treatment and insect exposure.

Visual Starch Test (Annex A)

  • Starch presence essential for larval development.
  • Visual test to confirm starch content before testing.

Summary Table: Test Setup Parameters

ParameterSpecification
Test insectsLyctus brunneus, Minthia rugicollis (adults)
Exposure4 pairs per sample
Temperature25–30°C
Relative Humidity70–75%
Sample containersGlass with cambric cover
Control Samples5 untreated + 5 solvent-treated
Test durationUntil adult emergence (~6-8 months)

flowchart TD
    A[Obtain naturally infested wood] --> B[Maintain lab culture of beetles]
    B --> C[Prepare test samples with
3.5Examination of Test Samples

IS 4873 Part 2: Examination of Test Samples — Key Points

Sample Preparation (Clause 3.2 & 3.2.1)

  • Wood species: Semul, rubber, or mango.
  • Sample size:
    • Length = 100 mm
    • Width = 40 mm
    • Thickness = 12.5 mm
  • Orientation: Long axis parallel to grain; wide face tangential to growth rings.
  • Condition:
    • Open-piled and air-dried in a well-ventilated room (no kiln or heating).
    • Use heartwood only, free from knots, abnormalities, or irregular growth.
  • Rejection criteria: Samples with inadequate starch content (tested per Annex A) must be discarded.

Rounding Off (IS 2:1960)

  • Final test values are rounded to the same number of significant digits as the specified value.

Summary Table: Sample Dimensions

DimensionSize (mm)Orientation
Length100Parallel to grain
Width40Tangential to growth rings
Thickness12.5

flowchart LR
    A[Select timber (semul/rubber/mango)] --> B[Cut samples 100x40x12.5 mm]
    B --> C[Align long axis with grain]
    C --> D[Open-pile dry in ventilated room]
    D --> E{Test starch content}
    E -- Adequate --> F[Use sample for testing]
    E -- Inadequate --> G[Reject sample]

This ensures consistency and reliability in test results per IS 4873 Part 2.

3.6Evaluation and Reporting of Results

IS 4873 Part 2 - Clause 3.6: Evaluation and Reporting of Results

  • Data to Record:

    • Number of treated and untreated samples with exit holes.
    • Number of treated samples without exit holes but containing live larvae.
  • Threshold Value (Toxic Limit):

    • Defined as the interval between:
      • The highest concentration where adult beetles emerge or live larvae are found.
      • The next highest concentration where no adults emerge and all larvae are dead.
    • Expressed in kg/m³ of wood.
  • Additional Reporting:

    • Concentration of the treating solution used.
    • Type of diluents employed.
    • Time interval between impregnation and exposure to infestation.

Summary Table for Reporting

ParameterDescription
Exit holes (treated & untreated)Count of samples showing exit holes
Live larvae in treated samplesCount of samples without exit holes but live larvae present
Toxic limit concentrationInterval between highest emergence conc. and next highest no emergence conc. (kg/m³)
Treating solution concentrationConcentration used in impregnation
Diluents usedType of solvent or carrier
Exposure intervalTime between impregnation and infestation exposure

Notes on Rounding (IS 2:1960)

  • Final test values must be rounded off matching the significant figures of the specified value.

flowchart LR
    A[Prepare Samples] --> B[Impregnate with Treatment]
    B --> C[Expose to Infestation]
    C --> D{Check Samples}
    D -->|Exit Holes Present| E[Record Number]
    D -->|No Exit Holes| F{Live Larvae?}
    F -->|Yes| G[Record Number]
    F -->|No| H[Record as Treated & Safe]
    E & G --> I[Determine Toxic Limit]
    I --> J[Report Concentration, Diluents, Interval]

This process ensures consistent and standardized evaluation of wood treatment efficacy against beetle infestation per IS 4873 Part 2.

Annex AMethod of Testing for Starch Content

IS 4873 Part 2: Method of Testing for Starch Content (Annex A & Clauses 3.2, 3.6)

Sample Preparation (Clause 3.2.1)

  • Sample size: 100 mm × 40 mm × 12.5 mm
  • Orientation: Long axis parallel to grain; wide face tangential to growth rings
  • Wood species: Semul, rubber, or mango
  • Condition: Open-piled, air-dried (no kiln or heat drying)
  • Quality: Clean, bright, knot-free, heartwood with no structural abnormalities

Starch Content Test (Annex A)

  • Purpose: Visual test to assess starch adequacy for Lyctus/Minthea larvae development
  • Procedure: Test each prepared sample visually for starch presence
  • Outcome: Reject samples with inadequate starch content

Evaluation and Reporting (Clause 3.6)

  • Record:
    • Number of samples with exit holes (treated & untreated)
    • Number of treated samples without exit holes but with live larvae
  • Define threshold (toxic) limit as the concentration interval between:
    • Highest concentration with beetle emergence or live larvae
    • Next higher concentration with no emergence and all larvae dead
  • Express concentrations in kg/m³ of wood
  • Report:
    • Concentration of treatment solution required
    • Diluents used
    • Time interval between impregnation and infestation exposure

Summary Table: Sample Dimensions & Conditions

ParameterSpecification
Size100 mm × 40 mm × 12.5 mm
Grain OrientationLong axis parallel to grain
Face OrientationWide face tangential to rings
Wood SpeciesSemul, Rubber, Mango
Drying MethodAir-dried, no kiln/heat
QualityHeartwood, clean, knot-free

flowchart TD
    A[Wood Selection] --> B[Cut Samples (100x40x12.5 mm)]
    B --> C[Orientation: Grain & Growth Rings]
    C --> D[Air Dry Samples (No Heat)]
    D --> E[Visual Starch Test]
    E -->|Adequate Starch| F[Sample Accepted]
    E
Annex BCommittee Composition

IS 4873 Part 2: Committee Composition & Key Specifications

Committee Composition (Annex B)

  • The Timber and Timber Stores Sectional Committee, CED 9 is responsible for this standard.
  • Members include representatives from:
    • Government bodies (Forest Departments, Directorate Generals)
    • Research Institutes (Forest Research Institute, Indian Plywood Industries, Institute of Wood Science & Technology)
    • Industry (Bamboo Society, Plywood Industry Federation)
    • Other organizations (Ministry of Defence, Rubber Board, Timber Development Association)
  • Chairman: Shri Shyam Sunder (Personal capacity, Bangalore)
  • Convener (Subcommittee on Timber Terminology, etc.): Dr. R. V. Rao (Institute of Wood Science & Technology)

Key Specifications for Test Samples (Clause 3.2.2)

  • Conditioning: 2 weeks at 25–30°C & 70–75% RH to reach ~15% moisture content.
  • End grain sealing: Seal with paraffin wax or suitable sealant to prevent preservative penetration.
  • Sample numbers per test:
    • 10 treated with preservative per concentration
    • 5 treated with solvent only
    • 5 untreated controls

Summary Table: Sample Preparation

StepCondition/Quantity
Conditioning2 weeks, 25–30°C, 70–75% RH
Moisture Content~15% equilibrium moisture
End Grain SealingParaffin wax or suitable sealant
Samples per test10 preservative-treated per concentration
5 solvent-only treated
5 untreated controls

If you need specific formulas or test procedures, please specify the clause or test type.

Popular Questions About IS 4873 Part 2

?What wood species and sample sizes are specified for testing?

According to IS 4873 Part 2, the specifications for wood species and sample sizes for testing are:

  • Wood Species: Semul, Rubber, or Mango.
  • Sample Size: 100 mm (length) × 40 mm (width) × 12.5 mm (thickness).
  • Orientation: Long axis parallel to grain; wide face tangential to growth rings.
  • Quality: Heartwood, clean, bright, knot-free, normal structure and growth rate.
  • Preparation:
    • Open-piled, air-dried in a well-ventilated room (no kiln drying).
    • Conditioned for 2 weeks at 25–30°C and 70–75% RH to ~15% moisture content.
    • Ends sealed with paraffin wax or similar before preservative treatment.
  • Testing Samples Required:
    • 10 samples per preservative concentration.
    • 5 solvent-only treated samples.
    • 5 untreated control samples.

This ensures uniformity and reliability in preservative efficacy testing against powder post beetles.

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?How are wood preservatives applied and at what concentrations?

Wood Preservative Application & Concentrations (IS 4873 Part 2)

  • Preparation of Solutions:

    • Prepare ≥5 concentrations around the expected toxic limit (weight/weight basis).
    • Unknown toxic limit: use widely spaced geometric series initially, then finer arithmetic series.
  • Treatment Procedure:

    • Test samples (10% concentration) are weighed, end grains sealed with paraffin.
    • Completely immerse blocks for 1 minute in preservative solution, starting from the most dilute.
    • Control samples treated with solvent or oil-in-water emulsion without toxic ingredients.
  • Post-Treatment:

    • Shake off excess liquid, blot ends, reweigh to calculate preservative uptake:
      [ \text{Preservative uptake} = (\text{Weight after} - \text{Initial weight}) \times \text{Concentration} ]
    • Dry samples with air ≤30°C until control samples return to initial weight.
    • Stack samples at room temperature for ≥1 month before testing.
  • Concentration Expression:

    • Expressed as kg/m³ of exposed wood block.
  • Sample Conditioning:

    • Condition samples for 2 weeks at 25–30°C, 70–75% RH to ~15% moisture content before treatment.

This method applies to tar-oil, water-borne, and organic solvent preservatives, ensuring consistent comparison despite different preservative mechanisms.

?Which powder post beetle species are used for infestation tests?

According to IS 4873 Part 2 (Clause 3.4), the powder post beetle species used for infestation tests are:

  • Lyctus brunneus
  • Minthia rugicollis

Key points for testing:

  • Adults of these beetles are obtained from laboratory cultures initiated from naturally infested wood.
  • Untreated timber (e.g., semul, mango, rubber) or dry tapioca chips act as feeders to maintain beetle cultures.
  • Test samples are exposed to four pairs of adult beetles individually in glass containers.
  • Conditions maintained: 25° to 30°C temperature and 70 to 75% relative humidity.
  • Beetles are removed once all are dead to conclude the test.

This method evaluates the toxicity of wood preservatives against these borers by simulating natural infestation in controlled lab conditions.

?How is the threshold toxicity value of a preservative determined?

Determination of Threshold Toxicity Value of a Preservative (IS 4873 Part 2)

  1. Prepare Dilutions:

    • Make at least 5 preservative concentrations (w/w), centered around the expected toxic limit.
    • If unknown, start with widely spaced geometric series; refine with arithmetic series later.
  2. Sample Treatment:

    • Immerse wood blocks (10% concentration) for 1 minute starting from the most dilute.
    • Use solvent controls (aqueous, benzene, or oil-in-water emulsion without toxic ingredients) treated similarly.
  3. Post-Treatment Handling:

    • Shake off excess liquid, blot ends, and weigh blocks immediately.
    • Calculate preservative uptake:
      [ \text{Preservative uptake} = (\text{Weight after treatment} - \text{Initial weight}) \times \text{Concentration} ]
    • Select 5 blocks per concentration with absorption variation ≤ 15%.
  4. Drying & Aging:

    • Dry samples at ≤30°C until control samples return to initial weight.
    • Stack samples openly at room temperature for ≥1 month.
  5. Result:

    • The lowest concentration that effectively controls powder post beetles without excessive toxicity is the threshold toxicity value, expressed in kg/m³ of wood.

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This method ensures consistent, comparable toxicity thresholds for wood preservatives against powder post beetles.

?What environmental conditions are maintained during the test?

According to IS 4873 Part 2, the environmental conditions maintained during the test are:

  • Temperature: 25°C to 30°C
  • Relative Humidity: 70% to 75%

These conditions apply during:

  • Conditioning of test samples before treatment (for 2 weeks to reach ~15% moisture content).
  • Exposure of test samples to powder post beetles during the bioassay until all beetles die.

Samples are stored individually in covered glass containers to prevent mite infestation, ensuring consistent test environment.


Summary of Environmental Conditions

ParameterValue
Temperature25°C to 30°C
Relative Humidity70% to 75%
Conditioning Time2 weeks before treatment

This controlled environment ensures reliable insect activity and preservative efficacy results.

?How is starch content in wood samples assessed and why is it important?

Assessment of Starch Content in Wood (IS 4873 Part 2)

  • Importance:
    Starch presence is critical for the development of larvae of powder post beetles (Lyctus spp. and Minthia rugicollis). Without adequate starch, larvae cannot survive, making starch content a key factor in wood susceptibility to infestation.

  • Method (Annex A):

    1. Use test samples from semul, rubber, or mango wood sized 100 mm × 40 mm × 12.5 mm, with grain direction along the long axis.
    2. Samples must be clean, bright, knot-free, and heartwood only.
    3. Dry samples in a well-ventilated room (no kiln or heating).
    4. Perform a visual starch test (specific visual method details are in Annex A, typically iodine staining to detect starch presence).
    5. Reject samples with inadequate starch content before testing for beetle resistance.
  • Why:
    Ensuring sufficient starch confirms the wood is a valid substrate for testing beetle attack and preservative efficacy.


Summary Table

ParameterDetails
Sample size100 × 40 × 12.5 mm
Wood typeSemul, rubber, mango (heartwood)
Drying methodAir-dried (no kiln)
Starch testVisual (e.g., iodine staining)
PurposeConfirm susceptibility to beetles
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This ensures reliable evaluation of wood preservative effectiveness against powder post beetles.

?What controls are used to validate the test results?

Validation Controls in IS 4873 Part 2 (Clause 3.6 & related clauses):

  • Sample Controls: Use five untreated control samples and five solvent-only treated samples alongside treated samples to compare infestation results.
  • Test Insects: Use lab-cultured adults of Lyctus brunneus or Minthia rugicollis obtained from naturally infested wood.
  • Environmental Conditions: Maintain 25°-30°C temperature and 70%-75% relative humidity during testing.
  • Observation Metrics:
    • Record number of samples (treated & untreated) with exit holes.
    • Count treated samples without exit holes but with live larvae.
  • Threshold (Toxic Limit): Defined as the interval between:
    • Highest concentration where adults or live larvae are found.
    • Next higher concentration with no adult emergence and all larvae dead.
  • Reporting: State concentration of treatment (kg/m³), diluents used, and time between impregnation and infestation exposure.

This systematic control ensures test reliability by comparing treated, untreated, and solvent-only samples under controlled conditions.

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