ManaKai – Prototype: Getting Started Guide

 

 

 

 

🌱 ManaKai Prototype: Getting Started Guide

Goal: Build a basic ManaKai seed prototype for under £500 to test frequency response, UV conversion, and growth patterns.

⚠️ Before You Start

This guide is for controlled laboratory testing only. Do not release into the environment. ManaKai is designed with built-in decay mechanisms, but untested biological systems require careful containment.

💰 Equipment Cost Breakdown

 

🔬 ESSENTIAL EQUIPMENT

Fungal Culture Setup

  • Pleurotus ostreatus or Ganoderma lucidum culture: £15-25
  • Autoclaved volcanic substrate (pumice, basalt sand): £20-30
  • Growth containers with humidity control: £30-50
  • Basic microscope (400x minimum): £80-150

Subtotal: £145-255

 

📡 Frequency & UV System

 

Signal Generation

  • Function generator (432/528 Hz capable): £60-100
  • UV-A/UV-B LED panel (2.5 µW/cm²+): £40-80
  • Frequency amplifier/speakers: £30-60
  • EM field meter (optional): £50-100

Subtotal: £180-340

 

🧪 Measurement & Analysis

 

Data Collection

  • Digital camera with macro lens: £100-200
  • pH/EC meter: £30-60
  • Thermal hygrometer: £20-40
  • UV light meter: £40-80

Subtotal: £190-380

 

🎯 MINIMUM VIABLE PROTOTYPE

Essential Equipment Only: £325-595

With basic measurement tools: £515-975

 

🛠️ Step-by-Step Construction

 

 

Step 1: Prepare the Mycelial Matrix (Week 1)

Inoculate fungal spawn into sterilized volcanic substrate. Maintain 20-25°C, high humidity, darkness for 5-10 days.

 

Success indicator: White mycelial growth visible throughout substrate

 

 

 

Step 2: Form the Seed Matrix (Week 2)

Harvest mycelial layer, dehydrate, and compress into 3-7cm discs. Apply mineral coating (basalt/granite fines).

 

Key: Mineral interface must be evenly distributed for resonance testing

 

Step 3: Set Up Test Environment (Week 3)

Prepare controlled chamber with: 8-12% substrate moisture, frequency generator at 432 Hz, UV-A/B lighting ≥2.5 µW/cm².

 

Critical: All parameters must be measurable and loggable

 

Step 4: Activation Testing (Week 4)

Place seed in test environment. Apply frequency input ≥3 hours/day. Monitor for growth initiation (should see within 7-14 days if conditions met).

 

Document: Time to first visible growth, growth rate, any fluorescence

Step 5: Fatigue & Decay Testing (Weeks 6-8)

Remove frequency/UV inputs. Monitor for propagation decay and dormancy as predicted by your equation.

 

Validation: System should self-limit without reinforcement

 

📊 What Success Looks Like

✅ Positive Results

  • Frequency Response: Growth rate significantly higher at 432/528 Hz vs control
  • UV Conversion: Measurable fluorescence and enhanced growth under UV
  • Self-Limiting: Growth decay when reinforcement removed
  • Mineral Response: Growth patterns vary with substrate composition

 

❌ Negative Results (Still Valid)

  • No frequency response → frequency mechanism needs revision
  • No UV effect → wavelength-shifting hypothesis incorrect
  • No self-limiting → decay equation parameters need adjustment

Either way, you get data to refine the model

 

🚀 Scaling Up (If Basic Tests Succeed)

Phase 2: Controlled Environment Farming

Larger growth chambers, multiple seed matrices, environmental monitoring systems

Additional Cost: £2,000-5,000

Phase 3: Field Trials

Greenhouse deployment, soil testing, nutrient analysis, harvest validation

Additional Cost: £10,000-25,000

 

🔬 Safety & Ethics Protocol

  • Containment: All tests in controlled environment only
  • Monitoring: Daily observation for unexpected behavior
  • Disposal: Autoclave or incinerate all biological material
  • Documentation: Full lab notes, photos, measurements
  • Open Source: Share all results (positive and negative)

 

💡 Bottom Line

Starting cost: £325-595 for a basic prototype that can validate your core hypotheses.

This is absolutely doable as a serious research project. You're not asking for millions in funding — you're asking for the cost of a decent laptop to test whether your mathematical models translate to biological reality.

Next steps:

  1. Secure small grant or crowdfunding for equipment
  2. Partner with university lab for access to microscope/measurement tools
  3. Document everything and publish results open-source
  4. Iterate based on data

 

"The simulations demonstrate mathematical consistency. Now let's see if nature agrees."