Jan 28, 2025
Version 4
Measurement of biogenic silica from plankton V.4
- Ying-Yu Hu1,
- Nuwanthi Samarasinghe1,
- Zoe V. Finkel1
- 1Dalhousie University
- Marine Microbial Macroecology LabTech. support email: [email protected]
Protocol Citation: Ying-Yu Hu, Nuwanthi Samarasinghe, Zoe V. Finkel 2025. Measurement of biogenic silica from plankton. protocols.io https://dx.doi.org/10.17504/protocols.io.8epv5jjzjl1b/v4Version created by Ying-Yu Hu
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: January 03, 2025
Last Modified: January 28, 2025
Protocol Integer ID: 117649
Keywords: biogenic silica, dissolution, silicomolybdic acid, measuring biogenic silica, biogenic silica from plankton, biogenic silica, amorphous silica, molybdate measurement technique, plankton, diatomaceous earth, sodium carbonate, accuracy of the measurement, production of monosilicic acid
Funders Acknowledgements:
Simons Foundation
Grant ID: 549937
Simons Foundation
Grant ID: 723789
Abstract
Here, we present a method for measuring biogenic silica from plankton. Biogenic silica is digested using a wet-alkaline method, in which 2 M sodium carbonate is used to hydrate and depolymerize amorphous silica, resulting in the production of monosilicic acid. The molybdate measurement technique is based on the method described by Shemesh et al. (1988) and follows the JGOFS protocols outlined by UNESCO (1994).
To ensure the accuracy of the measurement, Celite S diatomaceous earth is used as a check standard for the recovery of biogenic silica. Our method yields a recovery rate of 85% to 90%.
Citation
LINK
Protocol materials
Celite S diatomaceous earthMerck MilliporeSigma (Sigma-Aldrich)Catalog #06858
Ammonium molybdateMerck MilliporeSigma (Sigma-Aldrich)Catalog #09878-100G
Oxalic acid dihydrateVWR International (Avantor)Catalog #BDH4556-500G
Sodium hexafluorosilicateMerck MilliporeSigma (Sigma-Aldrich)Catalog #250171
4-(methylamino)phenol hemisulfate saltMerck MilliporeSigma (Sigma-Aldrich)Catalog #320013
Sodium sulfiteFisher ScientificCatalog #S430-500
Methyl orangeMerck MilliporeSigma (Sigma-Aldrich)Catalog #1013230250
Troubleshooting
Sample collection
Estimation:
The low limit of detection is approximately 0.6 uM silicate in the molybdate method. For siliceous plankton, sample requires no less than 4 ug PON (particulate organic nitrogen) per filter when using a 50 mL volumetric flask, or 2 ug PON per filter when using a 25 mL volumetric flask. The sampling volume for biogenic silica samples is approximately 10% of the PON sample volume. For seawater samples, the sampling volume for biogenic silica samples should be determined based on the community composition.
Filter blank media (without cells, same volume as plankton samples) through polycarbonate filter as blank
Transfer filter into 2 mL cryogenic vial
Flash freeze and store at -20 °C
Filter plankton sample in liquid media onto polycarbonate filters, using gentle vacuum pressure (130 mmHg)
Equipment
Filter forceps
NAME
blunt end, stainless steel
TYPE
Millipore
BRAND
XX6200006P
SKU
Rinse filter funnel with filtered artificial seawater without macronutrients
Fold the filter with two tweezers:
(1) Fold in half along its diameter, creating a semicircular shape;
(2) Fold once more in the same direction, resulting in a long strip;
(3) Fold once more, halving its length, so that sample is secured.
Transfer filter with sample into 2 mL cryogenic vial
Flash freeze and store at -20 °C
Transfer sample to 50 mL falcon tube with clean filter forceps (rinsed by 95% ethanol and air-dried), dry at 85 °C in the airforce oven. Prior to transferring:
(1) For filters folded into half-strip, unfold once to return to a strip.
(2) For filters folded into quarter-circles, unfold once to return to a half-circle shape, then fold once along the dimension to form a strip.
(2) For filters haphazardly into a compact mass, carefully unfold with two tweezers (avoiding losing biomass), fold once into a half-cricle shape, then fold once more along the dimension to form a strip
Equipment
Forced air oven
NAME
VWR
BRAND
89511-410
SKU
Equipment
Falcon® Centrifuge Tubes
NAME
Polypropylene, Sterile, 50 mL
TYPE
Corning®
BRAND
352070
SKU
Standard primary solution and reagents
Molybdate reagent stock solution
Note
Require 100 uL per sample
Ammonium molybdateMerck MilliporeSigma (Sigma-Aldrich)Catalog #09878-100G
Ammonium paramolybdate:
[(NH4)6Mo7O24.4H2O]
CAS: 12054-85-2
Add 1.6 g ammonium paramolybdate into a 125 mL plastic bottle and top to 100 g with MilliQ.
Store out of direct sunlight. Discard if white precipitation forms.
HCl stock solution
Note
Require 100 uL per sample
Use graduated cylinder, measure 95 mL MilliQ and transfer into a 125 mL plastic bottle.
In the fume hood, add 5 mL 12 N HCl into the bottle, mix well.
Metol-sulfite solution
Note
Require 100 uL per sample
4-(methylamino)phenol hemisulfate saltMerck MilliporeSigma (Sigma-Aldrich)Catalog #320013
Sodium sulfiteFisher ScientificCatalog #S430-500
Require:
(1) 50 mL syringe
(2) Syringe filter
Equipment
Syringe filter
NAME
0.2 um PES
TYPE
VWR
BRAND
28145-501
SKU
In a 100 to 250 mL plastic beaker, add 0.6 g sodium sulphite.
Add 1 g 4-(methyl amino)phenol hemisulfate.
Top to 50 g with MilliQ water.
Fill syringe with Metol-sulfite solution, filter through the syringe filter, collect filtrate into four 15 mL falcon tubes wrapped with foil, keep at room temperature.
Prepare fresh every month.
Oxalic acid solution
Note
Require 100 uL per sample.
Oxalic acid dihydrateVWR International (Avantor)Catalog #BDH4556-500G
In a 125 mL plastic bottle, add 6 g oxalic acid and top to 100 g.
Let the solution stand at room temperature overnight.
Decant the solution from the crystals into a plastic bottle.
Keep at room temperature.
Sulphuric acid (30%)
Note
Require 100 uL per sample
Mix 3 part concentrated sulphuric acid into 7 part of MilliQ
Cool down to room temperature
Note
This can be prepared on Day 2 prior to molybdate reaction
Primary silica standard solution (~ 1 mM Si)
Sodium hexafluorosilicateMerck MilliporeSigma (Sigma-Aldrich)Catalog #250171
Transfer 1 g sodium fluorosilicate in a plastic vial
Keep the vial in a vacuum desiccator overnight to remove excess water (do not heat or fuse)
In a one litre plastic volumetric flask, dissolve ~0.1881 g (log the actual mass) of dry sodium fluorosilicate in MilliQ water and top to 1 L with MilliQ water.
It takes about 30 min to complete the dissolution. This cannot be rushed.
Store in a plastic bottle at room temperature.
Day 1: Dissolution
2 Mass Percent Na2CO3 (18.69%)
Note
Need to be freshly prepared.
The old reagent can yield high blank possibly by leaching silicate from plastic material.
Each sample requires 10 mL 2 M Na2CO3
Weigh 186.9 g Na2CO3 in a weighing dish.
(CAS: 497-19-8, FW 105.99)
Tare a 1 L plastic erlenmeyer flask
Transfer Na2CO3 into the flask
Top to 1000 g with MilliQ and shake until all salt is completely dissolved.
Aliquot the solution into four 250 mL plastic bottles.
Turn on airforce oven to 85 °C
In the fume hood, transfer diatomaceous into a 5 mL plastic tube for weighing convenience (the original package is 1 kg).
Note
- Diatomaceous is used as a check standard for the recovery of biogenic silica
- Diatomaceous is hygroscopic, it needs to be stored in the vacuum desiccator
Safety information
Diatomaceous:
Upper respiratory irritant. May cause coughing or throat irritation. Breathing dust containing crystalline silica over a long period may cause lung damage.
Celite S diatomaceous earthMerck MilliporeSigma (Sigma-Aldrich)Catalog #06858
Weigh 100~200 ug diatomaceous into 50 mL falcon tube, in triplicate. Log the actual weight.
Safety information
Do not open the container until the static charge of diatomaceous powder has been neutralized by ionization blower.
Note
Less than 100 ug sample might introduce more error amongst the replicates in recovery.
Prepare one empty 50 mL falcon tube as the reagent blank for diatomaceous.
Add 10 mL 2 M Na2CO3 to each tube, including:
- reagent blank for check standards
- check standards
- blank for samples
- samples
Vortex
Loose the caps and place all tubes into the airforce oven overnight (for example, from 5 pm to 9 am).
16h
Day 2: Acidification
Volume of 12 N HCl required:
about 3.5 mL X N
Transfer 12 N HCl into a 50 mL Falcon tube in the fume hood.
Work on one tube at a time, and leave other tubes in the oven.
In the fume hood, add 30 µL Methyl orange into the tube. Methyl orangeMerck MilliporeSigma (Sigma-Aldrich)Catalog #1013230250
Add MilliQ until the volume of solution in the falcon tube is 10 mL.
Note
The original volume of Na2CO3 is reduced due to evaporation of water during 20-h dissolution.
Dropwise add 3 mL 12 N HCl by using 1000 uL pipet.
Safety information
Do it slowly. Swirl the tube until reaction stops and then add the next drop. The most vigorous reaction is at about 3 mL 12 N HCl.
Switch to a 100 uL pipette, add 100 uL at a time. Near the equivalence point, when the colour starts to change to pink more markedly but after mixing the orange colour returns, it is necessary to add HCl drop by drop. The first drop that causes a permanent colour change to pink determines the equivalence point. Stop adding HCl.
Note
We have found that the optimal pH for the reaction between silicate and molybdate to form silicomolybdic acid is 3 to 4. Too low or too high pH decreases recovery of biogenic silica.
The acidified solution yields pH at 2 to 3. It is diluted to 10% in the molybdate assay, which gives pH at 3 to 4.
Transfer resulted solution from falcon tube to 25 or 50 mL polypropylene volumetric flask.
If the color of solution change back to orange, add more drops of HCl until the color turns to permanent pink again.
Note
Be careful while transferring the solution and ensure that the filter does not fall out of the tube, which spills the solution and causes sample loss.
Use MilliQ to rinse the tube three times and transfer all samples into the volumetric flask.
Note
If a 50 mL volumetric flask is used, rinse the falcon tube with 5 mL of MilliQ at a time.
If a 25 mL volumetric flask is used, rinse the falcon tube with 1 mL of MilliQ at a time.
Use transfer pipet, top final volume to 25 or 50 mL with Milli-Q.
Shake and thoroughly mix the solution.
Note
Before mixing, check the cap to avoid leaking
Transfer solution from volumetric flask to a clean and labelled Falcon tube.
Day 2: Molybdate reaction
3h
Secondary standard solution (Freshly prepared prior to the assay)
50 uL primary stock solution
450 uL MilliQ
Standard working solutions (Freshly prepared prior to the assay)
| Standards | Secondary (uL) | MilliQ (uL) | Conc. (uM) | |
| S1 | 0 | 500 | 0 | |
| S2 | 5 | 495 | 1 | |
| S3 | 10 | 490 | 2 | |
| S4 | 20 | 480 | 4 | |
| S5 | 40 | 460 | 8 | |
| S6 | 60 | 440 | 12 | |
| S7 | 80 | 420 | 16 | |
| S8 | 100 | 400 | 20 |
Sample dilution
Vortex and then transfer 50 µL from the following solutions to labelled 2 mL microtubes.
(1) blank for check standards,
(2) check standards,
(3) blank for samples,
(4) samples
Add 450 µL MilliQ into each tube to obtain a 10% dilution.
Molybdate working solution
Note
Require 200 uL per sample
1 part Molybdate stock reagent
1 part HCl stock reagent
Safety information
The addition of reagent must be operated in the fume hood. Acidified sodium fluorosilicate may contain some hydrofluoric acid.
Add 200 µL Molybdate reagent into each tube.
Vortex each tube and then shake at Room temperature for 00:15:00 for the formation of silicomolybdic acid.
15m
Reducing solution
Note
Require 300 uL per sample
1 part Metol-sulfite solution
1 part oxalic acid solution
1 part sulphuric acid solution
Add 300 µL reducing solution into each tube.
Vortex each tube and then shake at Room temperature for 03:00:00
3h
....Measure pH of each sample (in the Falcon tube)
| Sample code (example) | Sample code | pH | |
| Blank for check standards | |||
| Check standard 1 | |||
| Check standard 2 | |||
| Check standard 3 | |||
| Blank for samples | |||
| Sample 1 | |||
| Sample 2 | |||
| ... |
Day 2: Colorimetric measurement
3h
In the fume hood, vortex each tube and then load 250 µL of the sample into one well of the microplate. Vortex again and load the same sample into another well of the microplate as replicate.
Equipment
96-Well Microplates, Polystyrene, Clear,
NAME
Greiner Bio-One
BRAND
655101
SKU
Setup the layout.
Setup the program
| A | B | |
| Shake duration | 00:00:05 | |
| Shaking type | Continuous | |
| Shaking force | High | |
| Shaking speed [rpm] | 600 | |
| Wavelength [nm] | 812 | |
| Use transmittance | No | |
| Pathlength correction | No | |
| Measurement Time [ms] | 100 |
Equipment
Varioskan LUX Multimode Microplate Reader
NAME
Thermo Fisher
BRAND
VL0L00D0
SKU
Read the samples.
Export data sheet to excel.
Waste disposal
3h
Collect all solution with paramethylaminophenol sulphate and sodium fluorosilicate into the waste container.
Rinse microtubes and microplate with tap water, dispose in blue recycling bin.
Day 2: Calculation
3h
Subtract the average absorbance at 812 nm of the blank standard replicates from the absorbance at 812 nm of all other standard working solutions.
Subtract the average absorbance at 812 nm of the blank sample (i.e. blank filter) replicates from the absorbance at 812 nm of all other individual samples.
Prepare a standard curve by plotting the average blank-corrected 812 nm absorbance for each standard working solution versus its concentration in uM.
Use the standard curve to determine the silicate concentration of each unknown sample by using its blank-corrected 812 nm absorbance.
Si per sample = Si X V X (0.001) X DF
| Variable | Unit | Definition | |
| Si per sample | umol | element Si in the sample collected | |
| Si | uM | silicate concentration calculated from the standard curve | |
| V | mL | volume of volumetric flask | |
| DF | From volumetric flask to the microtube, DF=10 |
% Diatomaceous recovery = 100 X Si X V X (0.001) X MW X DF /(M_ug X Purity X 0.01)
| Variable | Unit | Definition | |
| % Diatomaceous recovery | percentage recovery of diatomaceous | ||
| Si | uM | silicate concentration calculated from the standard curve | |
| V | mL | volume of volumetric flask | |
| MW | ug/umol | molecular mass of SiO2, i.e. 60.08 | |
| DF | From volumetric flask to the microtube, DF=10 | ||
| M | ug | actual mass of diatomaceous | |
| Purity | purity of SiO2 in Celite S diatomaceous earth (06858) is 90.2% |
Note
The recovery should be around 85 to 90%.