Modified Rapid Phytolith Methods

Kali R Wade

Published: 2023-06-26 DOI: 10.17504/protocols.io.3byl4qerzvo5/v1

Abstract

Processing procedures here are modified from those outlined in Katz et al 2010. Samples can be processed in this way and, following completion, rinsed with deionized water and dried to a stable state for storage and to make extra slides for morphological IDs.

Before start

Follow the "fail-safe" practices outlined here, in addition to any other health and safety paperwork or contamination recommendations from your organization.

Steps

Fail-Safe Practices

1.

Wiping down all equipment, surfaces, and tools used with soap and water followed by acetone (beginning and end of every day of the project).

2.

Checking and adjusting the density of sodium polytungstate (SPT) to conform to the protocol being used (normally between 2.3 and 2.5 g/ml).

3.

Plating one slide of each hydrocloric acid (HCl) SPT, and the mounting agent (likely Cargille Immersion Oil, Type B) and viewing them under microscopy to ensure no contamination.

4.

Calibrating analytical balances.

Sample Preparation

5.

If necessary, place samples in desiccator overnight, set to 30°C.

6.

Label 1.5 ml centrifuge tubes (2 per sample being processed) with sample ID.

7.

Sieve samples through 0.5 mm mesh, rinsing mesh between each sample with soap and water, acetone, then deionized water.

8.

Weigh 30-80 mg of sediment into 1.5 ml centrifuge tube. Ensure balance is tared following the weight of the tube, prior to weighing sediment, with balances' scale and lab doors closed.

Organic and Carbonate Removal

9.

Add 50μl of 6N HCl, waiting for bubbling to cease (give the samples a few minutes). Shake tube to ensure chemical gets through all of the sample

10.

Add 450μl of 2.5 g/ml SPT

Breaking up Soil Aggregates & Creating Pellet

11.

Vortex for 3 sec, sonicate for 10 min, vortex 3 sec

12.

Centrifuge for 10 min at 6rpm

Plating Slides

13.

Remove supernatant to clean 1.5ml test tube. Be mindful of proper labels.

14.

Vortex supernatant for 3sec

15.

Pipette 50μl of supernatant onto a labelled microscope slide and cover with a coverslip. Seal with nail polish. Slides last between 6-12 hours before crystallization

18.

Inventory samples.

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