Study area
The study was conducted at the Research and Development Center of the Abra State Institute of Sciences and Technology (ASIST) in Lagangilang, Abra, Philippines, from April 2024 to April 2025. The site is situated in a tropical monsoon climate zone, characterized by mean annual temperatures ranging from 26°C to 32°C and relative humidity levels between 65% and 85%. These conditions are conducive to year-round
Tetragonula biroi activity and colony development. All apiaries used in the study were situated within a 2-km radius to ensure comparable environmental exposure, forage availability and landscape conditions across treatments.
Experimental design
A controlled-comparative experimental design with replication was employed to evaluate the Hose Method relative to traditional colony propagation. Thirty healthy, queenright colonies of
Tetragonula biroi of comparable population size and resource stores were selected. Colonies were randomly assigned to two treatments:
1. Traditional propagation method (n = 15).
2. Hose method propagation (n = 15).
To reduce selection bias, colonies were stratified by initial population strength (weak, moderate, strong) prior to randomization. Each treatment was subdivided into three replicates of five colonies, resulting in a total of six experimental blocks. The experiment ran for 12 months to capture the dynamics of colony growth during the dry season, transition and wet season.
Traditional propagation procedure
Traditional colony propagation followed widely practiced meliponiculture techniques. Colonies were opened manually and brood combs containing late-stage larvae and pupae were removed and transferred into newly prepared hive boxes. Adult workers were encouraged to migrate into the new hive through scent placement, positioning near the mother colony and gradual hive separation over 3–5 days. All handling followed standardized protocols to minimize brood damage and queen disturbance. The conventional brood transfer and colony splitting process used in the study is presented in Plate 1.
Hose method propagation procedure
The hose method utilized a flexible, food-grade polyethylene hose (diameter: 1.0-1.2 cm; length: 50-75 cm). The procedure involved the following steps:
Hive preparation
New empty colonies were prepared with standardized internal structures (brood chamber, resin lining, cerumen starter discs).
Colony connection
A hole was drilled into the mother colony and the receiving hive. The hose was inserted and sealed using propolis-resin mixtures to prevent light leakage and external intrusions.
Colony migration
The receiving colony was placed 20-30 cm away from the mother colony. Worker bees freely moved through the hose, initiating nest construction in the new hive. Queens were not forced to migrate; instead, workers gradually established brood zones in the receiving hive and the queen would voluntarily relocate, a process monitored daily.
Separation protocol
Once egg-laying commenced in the receiving hive (usually within 7-14 days), the hose was gradually constricted until complete detachment was achieved.
This method reduced direct handling of brood and minimized exposure of nest structures to the environment. The physical setup and actual colony connection using the hose conduit are shown in Plate 2.
Data collection
Data were collected monthly for 12 months using standardized measurement protocols.
Colony establishment success
A colony was considered successfully established if:
• The queen relocated to the new hive.
• New brood cells were observed.
• Colony population growth was positive for ≥60 consecutive days.
Colony health indicators
•
Brood cell counts
Total number of capped and uncapped brood cells, measured through photographic grid analysis.
•
Queen performance
Egg-laying regularity based on the presence of brood in at least two brood layers.
•
Adult population strength
Semi-quantitative scoring (weak, moderate, strong) based on entrance activity and internal comb occupancy.
Productivity measures
•
Honey production (grams)
Extracted using non-destructive sampling at 3-month intervals.
•
Pollen stores (grams)
Measured through digital estimation of pollen pot volumes using calibrated photographic analysis.
Practicality metrics
•
Labor input: Number of people required per propagation event.
•
Time requirement: Time (hours) from initiation to colony independence.
•
Cost analysis: Materials, equipment and labor cost per colony (in Philippine pesos).
Sustainability indicators
•
Colony survival rate: Percentage of colonies alive at month 12.
•
Long-term productivity: Average honey and brood production post-establishment.
•
Beekeeper satisfaction: Assessed using a 5-point Likert scale.
Research instruments
• Colony assessment sheets for monthly brood, honey and pollen measurements.
• Digital image analysis software (ImageJ) for quantifying brood and resource stores.
• Entrance activity counter for semi-quantitative worker flow estimation.
• Beekeeper perception surveys for sustainability parameters.
Instrument reliability was validated through pilot testing on five non-experimental colonies.
Statistical analysis
Quantitative analyses were performed using SPSS v.27. Significance was set at p<0.05.
Chi-square test
Used to compare colony establishment success between propagation methods.
Independent samples t-test
Applied to compare:
• Brood cell counts.
• Honey and pollen production.
• Time, labor and cost efficiency.
• Beekeeper satisfaction scores.
Repeated measures ANOVA
Used to evaluate changes in colony health and productivity across time.
Effect size calculations
• Cohen’s
d for mean differences.
• Eta squared (η
2) for ANOVA effects.
Effect sizes were interpreted following conventional thresholds (small = 0.2, medium = 0.5, large = 0.8).
Assumptions testing
Normality and homogeneity of variance were assessed using:
• Shapiro-Wilk test.
• Levene’s test.
Non-parametric alternatives (Mann-Whitney U) were used when assumptions were violated.
Ethical and safety considerations
All procedures adhered to ASIST’s environmental and research ethics policies. Only healthy colonies were used. No harmful chemicals or invasive procedures were employed. Colony disturbance was minimized to ensure animal welfare. No human subjects were involved; hence, human ethics approval was not required.