Varroa Mite Detection Methods

Similar documents
Monitoring it does make a difference by Dewey M. Caron

Spring Management of Honeybees Part 1 Population Dynamics, Varroa

2015 PUB Winter Loss by Dewey M. Caron with statistical assistance of Jenai Fitzpatrick

2015 Southern Oregon (KBBA & SOBA) Winter Loss by Dewey M. Caron with

Varroa mite control what works! By Dewey M. Caron

New Method for American Foulbrood Disease Control. Hossein Yeganehrad Caspian Apiaries

KANAWHA VALLEY BEEKEEPERS ASSOCIATION

Materials and Methods

Introduction to Queen Rearing

Control of Varroa mites in honey bees through the systemic application of essential oils.

Reasonable Expectations

Pest and Disease Treatments Varroa Mites: (Varroa Destructor) Treatments: European Foulbrood: Treatment:

Antioxidants in Wax Cappings of Honey Bee Brood

English Mellifera Sites

Honey Bee Brood Disease, Detection and Management

Guideline on use of oxalic acid for varroa control

Foulbrood Bee Diseases

How to collect raw honeybee pollen from the hive

Honey bee diseases, pests, and disorders

- Determining the Causes - Dr. Diana Cox-Foster Pennsylvania State University

Honeybee Diseases and Parasites Bob Arnold March 5, 2008

2. Identify and distinguish between homogeneous and heterogeneous mixtures.

Kevin Hale

ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS

Washington backyard beekeeper Losses Winter Dewey Caron

The prime directive. The Four Golden Rules of Beekeeping. Maximize the size the adult population

CLEVELAND COUNTY BEEKEEPERS ASSOCIATION

FILTERING HONEY ALMOST EVERY FILTER REMOVES SOME POLLEN

Instructions for using Ferro-Bee

Grow Your Own Queen Bees Recap. Presented By: Kevin Lewis

2. Identify and distinguish between homogeneous and heterogeneous mixtures.

HONEY BEE BIOLOGY Apprentice Level Training Texas Master Beekeeper Program

Pollen Slide Mounting Protocol

Dewey M. Caron UD Emeritus Professor OSU Affiliate Professor

Rhino Clear Sprint Atomizer

Neem Pro Riddance Protection against biting insects for farm animals

Ehlers-Danlos and Medical Marijuana. presented by ellen lenox smith

Ideas for investigations: 1. Prepare slime and investigate its properties. Equipment and consumables. Making the slime

Food Hygiene Guidance For Childminders

Nosema Hidden Killer. Another explanation for bee losses By Mike Sandridge

Patient information. How to use your Fluorouracil 5FU 1% Eye Drops St Paul s Eye Unit PIF 539 V6

INSTRUCTIONS FOR USE HUMIRA 40 MG/0.8 ML, 20 MG/0.4 ML AND 10 MG/0.2 ML SINGLE-USE PREFILLED SYRINGE

Roxanne King. Integrative Nutrition Health Coach The Holistic Mama

Breakthrough Performance

Detailed Instructions with Many Tips and Tricks

Foulbrood Bee Diseases

Laboratory Pesticide Formulations, Labels, and Safety

The EAS Master Beekeeper Program. Part 2. Self-test questions. The oral and written exams

CoaguChek S System. Quick Reference Guide. This is a CLIA-waived System. Coagulation Testing with Fresh Whole Blood

Instructions for Use NITYR (ni-tir) (nitisinone) tablets

Materials and Methods

PATIENT INSTRUCTIONS FOR USE SINGLE- DOSE PREFILLED SYRINGE

To provide you with necessary knowledge and skills to accurately perform 3 HIV rapid tests and to determine HIV status.

SP 131 NONIONIC SPREADER/PENETRANT

Drainage Frequency: PATIENT GUIDE. Dressing Frequency: Every Drainage Weekly Drainage. Physician Contact Information. Dr. Phone:

Activity 4.2 Dissolving a substance in different liquids

Changing Your Two-Piece Disposable Urostomy Appliance

3 To gain experience monitoring a titration with a ph electrode and determining the equivalence point.

Elcometer 138/2. Surface Contamination Kit. Operating Instructions

Disease Complex of the Honey Bee

Research Method Validation

TLC SEPARATION OF AMINO ACIDS

HPLC, CHARM II AND ELISA: ADVANTAGES AND DISADVANTAGES FOR THE ANALYSIS OF TETRACYCLINES IN HONEY

C.16. HONEYBEES - AC UTE ORAL TOXICITY TEST. This acute toxicity test method is a replicate of the OECD TG 213 (1998).

Preliminary report on the use of Viusid vet liquid in the stimulative feeding of bee colonies

Puree Diet. Patient Information Leaflet.

in the heat), heat cramps, and heat exhaustion. You need to seek medical help for heat-related

AMERICAN FOULBROOD CONTROL

BIOL 208: Principles of Ecology and Evolution Lab Week 5, 6, &7. Bioenergetics of Caterpillars

How to Make Topical Cannabis Products. Contents INTRODUCTION... 3 RECIPE # RECIPE # RECIPE # RECIPE # RECIPE #5...

Experimental Procedure

Molecular Gastronomy Lab Lesson Plan: Spherification and Olive Oil Powder For an advanced high school Chemistry class

Product Specifications and Usage Information P4405, P4410, & P4420 Genesys 30 Dosimeter Holder System

nnjbees.org December 2015 NORTHEAST NEW JERSEY BEEKEEPERS ASSOCIATION OF NEW JERSEY A division of New Jersey Beekeepers Association

Lab 6: Cellular Respiration

Giving Medicine by Subcutaneous Injection

Sharps Container (not included) 1 Gather and check supplies. Gather supplies

Instructions for Use HEMLIBRA (hem-lee-bruh) (emicizumab-kxwh) injection, for subcutaneous use

HyProBlack Hexavalent chrome free RoHS and ELV compliant. HyPro System

Who took Jerell s ipod? An organic compound mystery 1

Produced by La Direction des communications du ministère de la Santé et des Services sociaux

Student Nutrition Program. SNP Guidelines. October 2016

Breezhaler. Open to see clear capsule. How do I use my Breezhaler? Care of my Breezhaler

Who took Kaleb s ipod? -- An organic compound mystery

Assessment a New Pollen Supplement Diet for Honey Bee Colonies and Their Effects on some Biological Activities

LeadCare BLOOD LEAD ANALYZER. Quick Reference Guide

1.0 Learning Intentions

Quick Start Guide. Geriatric Tremor Simulator. Product Includes: Safety Instructions

Aac Reagent Set ELISA for the detection of Acidovorax avenae subsp. citrulli Catalog number: SRA 14800

ALTERNATIVE METHOD OF CONTROL OF INFECTIOUS BEE S BROOD DISEASES.

LAB: DIFFUSION ACROSS A SELECTIVELY PERMEABLE MEMBRANE

Exp 03: Avogadro s Number

Fibrlok II 2529 Universal Optical Fiber Splice

Operative dentistry. Lec: 10. Zinc oxide eugenol (ZOE):

C.17. HONEYBEES - AC UTE CONTACT TOXICITY TEST. This acute toxicity test method is a replicate of the OECD TG 214 (1998).

The Hanau Modular Articulator System 194 Fixed 11 cm width, adjustable Radial-Shift Guidances. Illustrated Instruction Manual

Mouse C-Peptide ELISA Kit

Honey Bee Biology. Elina L. Niño Extension Apiculturist

HOME BP USER INSTRUCTIONS

Transcription:

Varroa Mite Detection Methods Apiculture Bulletin # 222 Updated: 10/15 Effective mite control is dependent on frequent and reliable mite detection. Varroa mites spread rapidly between hives and apiaries due to drifting, robbing and hive movement. Mite levels rise rapidly in late summer and early fall. In heavily infested areas, individual colony infestations can grow from being undetectable to life-threatening levels within a few months. It is important to monitor mite levels regularly by sampling all or most colonies. Larger beekeepers should sample at least 10% of the colonies in each yard in the spring and the fall. Unusually large or small colonies and those at the end of rows should be tested. How Often To Monitor The Varroa mite have become an endemic pest in British Columbia. Its high virulence demands frequent monitoring throughout the beekeeping season. It is recommended to start with an early spring mite test, followed by a test every 3-4 weeks. There are different detection methods available, some more sensitive than others. High-sensitivity tests are labor intensive and more costly, while less sensitive tests may be quicker to apply and cheaper. To compensate for lower accuracy, these tests can be applied more frequently. To optimize the value of the test methodology chosen, it is recommended to, To ensure consistency of test results, use the same testing method through the entire season. Keep a record of each test result. While the actual number of counted mites is important, equally important is to observe any trend of mite numbers which may project future population rises. Common detection methods and required equipment include: Drone Brood sampling decapping fork. Alcohol Wash Method windshield wiper fluid, sieve, bucket, cheese cloth Icing Sugar Method 1 Icing sugar, sticky board Icing Sugar Method 2 Icing sugar, screened containers. 24-hour Strip / Sticky Board Method Sticky Boards Some detection tests require the use of Sticky Boards that are commercially available or can be easily prepared by the beekeeper:

Commercial Boards: Commercial sticky boards are covered with a super sticky film of Tanglefoot. These boards require the installation of a 8-gauge screen on top of the sticky surface to prevent bees getting stuck. Home-made Boards: white sheet of thick paper, cardboard or corrugated plastic (eg. Tenplast), cut to cover most of the hive bottom surface (40 x 30 cm / 16 x 12 in). Spray one side of the board with a thin coating of PAM vegetable oil, or apply a coating of a 1:1 mixture of cooking oil and petroleum jelly. No cover screen is required. Install the sticky board for 24 hours only. When left longer, debris will make it difficult to count mites. After mites have been counted, wipe the board clean with a squeegee. Note: Sticky boards are recommended for use in combination with any of the miticide strips or formic acid. The installation of a sticky board by itself relies on natural mite drop which doesn t offer an accurate measure of mite infestation levels. Drone Brood Sampling Method Up to 85% of the mites in a colony are in capped brood cells and not visually detectable. Varroa mites are more attracted to drone brood than worker brood, so look there first. Sample about 100 cells. Locate a patch of drone cells in the purple-eye pupal stage. Slide the prongs of a de-capping fork along the comb face and into the protruding drone cappings. Pry upward and remove the pupae. Carefully examine the bodies and the interior of the cells for mites. This method is easy to apply frequently but only offers an approximate indication of low or high mite levels.

Alcohol Wash Method This method is simple, quick and quite accurate when applied to a larger number of colonies in the apiary. It doesn t require a second visit after 24 hours. The test is carried out as follows: Use a wide-mouth glass jar and scoop about 300 bees (~ 1 cup) from the brood area. Make sure that the queen is NOT included! Add 50 ml (~ 2 oz) of windshield wiper fluid (or diluted methyl hydrate, or rubbing alcohol) to the jar and shake for several minutes. Remove the lid and pour contents into a container covered with light metal wire-mesh screen (8 mesh/in) or a coarse sieve. Repeat. Pour alcohol solution into a second container covered with cheesecloth or fine sieve. Count number of mites. Mite Level Determination: With a bee sample size of 300, every three mites count for 1% infestation increase. At nine (9) mites, infestation level is 3% when colony damage can be expected. At 15 mites (5% infestation level) immediate treatment is recommended. Icing Sugar Method (1) This is a very easy, quick and cheap method to detect mites and determine level of infestation. Install sticky board on the bottom board. Sprinkle a cupful of icing sugar at the top of spaces between brood frames of the single box colonies, or onto the second brood chamber of two boxed colonies. Colonies with honey supers, remove honey supers, apply icing sugar to the top of the second brood chamber, and reinstall honey supers. Remove sticky board after 24 hours. Icing Sugar Method (2) This mite testing method is the same as the Alcohol Wash Method except Icing Sugar is used instead of alcohol. Collect approximately 300 bees in a jar. Add about 100 ml of icing sugar. Gently shake the container with bees for about 2 minutes. Pour contents over a sieve that allows the icing sugar and mites to pass through but not the bees. Spread the mite-containing icing sugar on a flat dark surface and count mites. 24-Hour Strip & Sticky Board Method This testing method offers the highest level of accuracy in determining Varroa mite infestation levels in the colony. It requires the use of one of the three registered strip formulations for 24 hours in combination with a sticky board. For details about the three strip formulations, see below. To determine mite levels, install one strip per nucleus or two strips for a standard two-supered hive, where the strips are placed between frames in the central brood area. Daytime temperatures should be 10 degrees C or higher. Strips and sticky board should be removed after 24 hours. For treatment purposes, follow label instructions.

Mite Level Determination: Same as Alcohol Wash Method. Note: Strips that are only used for detection purposes may be re-used 10 times for 24-hour tests before disposal. Make sure that the strips are not exposed to sunlight. When not in use, store in a marked container in a cool, dry and dark place. Note: The development of mite resistance to Apistan and CheckMite+ in parts of the province, has made it important to determine the efficacy of these products. For efficacy testing, refer to Bulletin #223. Apivar strips (Amitraz) Amitraz is the active ingredient of Apivar, a plastic strip formulation applied to the colony. Apivar strips are specifically formulated for use in beehives as it is wax-soluble, reducing the risk of residues. Apivar strips should not be substituted with other amitraz formulations used in livestock production to control ticks and fleas because they are water soluble. Apistan strips (10% fluvalinate) Fluvalinate is a contact miticide and is applied in plastic strips under the trade name Apistan. It does not affect mites developing in capped (bee) brood cells. In some parts of British Columbia, Varroa mites have developed resistance to Apistan. Apistan may not provide the same accuracy of determining mite infestation levels compared to other strip formulations. To determine efficacy of Apistan, repeat 24 hour test with Apivar or CheckMite+ and examine sticky board for additional mite drops. CheckMite+ (Coumaphos) Coumaphos is applied in plastic strips under the trade name CheckMite+. Coumaphos does not kill mites in sealed brood cells. When there is no brood in the colony, the mite count on a sticky board will accurately reflect the colony's infestation level. Formic Acid Formic acid is used to control both Varroa and tracheal mites. Several application methods have been developed. It is important to remember that efficacy of formic acid is influenced by colony size, weather, condition and behavior of the colony, etc. Notwithstanding its variable efficacy, formic acid is recommended as part of an overall mite control strategy. For detection purposes, apply 40 ml (1.5 oz) of 65% formic acid liquid onto several layers of paper towels placed on the top bars of the upper brood chamber. Use enough paper towels to prevent acid from dripping. Install a sticky board and check after 24 hrs. Mite Level Determination: Multiply the number of mites on the board by 6. Note: There are various application methods, including soak-pads (used in packaged meats) or formic acid dispensers such MiteGone and Neissenheider. All methods involve the evaporation of formic acid.

Note: Do not apply Apivar, Coumaphos, Apistan, formic acid or other chemicals to a hive for detection purposes when honey supers are in place. Use the Alcohol Wash or Icing Sugar methods instead. When to Treat? After determining the estimated mite infestation level, one must decide when to treat. In general, treatment should be applied when 10-15 mites or more are counted. Full-length treatments can be applied in the spring and fall but may be difficult when honey supers are in place. When mite controls must be applied during the honey season, remove honey supers and treat the colony with formic acid for 24 hours with sticky board, and then reinstall honey supers. Repeat one week or two weeks later. For more information on Varroa Control Methods, refer to Bulletin #221. Plant & Animal Health Branch 1767 Angus Campbell Road Abbotsford, BC V3G 2M3 Toll Free: 1-800-661-9903 Phone: 604-556-3003 Fax: 604-556-3010