A pond is not simply “water with organisms in it.” It is a structured, dynamic ecosystem shaped by spatial heterogeneity, nutrient availability, oxygen gradients, and trophic interactions. Even a small volume of pond water can contain primary producers (algae and photosynthetic protists), primary consumers (protozoa, rotifers, microcrustaceans), predators, decomposers, and detritus.
These organisms are not evenly distributed. Many associate with sediment, algal mats, plant fragments, or specific microhabitats within the water column. Over short periods of time, changes in light, nutrient availability, and oxygen can alter community composition.
In this lab, you will construct a small pond microecosystem, systematically sample it, document its biodiversity, and evaluate how that biodiversity changes over one week.
Your goal is not simply to observe organisms, but to collect semi-quantitative diversity data using a standardized sampling method.
Pond water sample
Beaker, sample bag, or small clear container
Permanent marker (for labeling)
Compound light microscope
Glass slides (minimum 5–6)
Coverslips
Transfer pipettes
Lens paper
Paper towels or Kimwipes
Identification key (provided)
Phone or camera for photomicrography
Gently swirl the source pond water to suspend organisms.
Transfer approximately 150–250 mL into a beaker, sample bag, or container.
Include:
A small amount of bottom sediment (recommended)
Visible algae or plant fragments if present
Leave air space at the top for oxygen exchange.
Label the container with group name and date.
Place the ecosystem in the designated lab area under ambient light (not direct sunlight).
Do not disturb the container except when sampling.
You will examine 5 wet mounts.
Each wet mount must contain two drops of sample.
Total sampling effort = 10 drops.
How to Sample
Before each slide:
Gently swirl the container once.
Sample from different microhabitats:
Just above sediment
Near algae or plant material
Mid-water column
Surface layer
Avoid vigorous shaking.
Slide Preparation
Place two drops on a clean slide.
Lower the coverslip at an angle to minimize air bubbles.
Scan under 40× to locate organisms.
Observe under 100× and 400× for identification.
Examine each slide carefully before moving to the next.
Using the provided identification key:
Identify each distinct organism type observed.
Take at least one clear photo of each organism type.
Count total individuals across all 5 slides.
Assign an abundance category:
Rare: 0–2 individuals total
Uncommon: 3–10 individuals total
Common: More than 10 individuals total
Record results in a data table including:
Organism name
Abundance category
Trophic role (producer, consumer, decomposer)
Be systematic. Count cumulatively across all slides before assigning abundance.
After one week:
Repeat the same 5-slide sampling protocol.
Use the same abundance criteria.
Record all organisms observed.
Compare Week 2 data to Week 1.
Genus Navicula
Genus Nitzchia
Genus Pinnularia
Genus Epithemia
Genus Gomphonema
Genus Cymbella
Genus Gyrosigma
Genus Amphora
Genus Craticula
Carpenter's Rule Diatom
Bacillaria Paxillifera
Genus Fragilaria
Genus Surirella
Phylum Urocentrum
Genus Halteria
Genus Euplotes
Paramecium bursaria
Genus Stylonychia
Genus Paramecium
Genus Stentor
Swan Tear
Lacrymaria olor
Genus Loxodes
Genus Vorticella
Genus Coleps
Genus Euglena
Genus Phacus
Genus Ceratium
Class Globoalamea
Genus Synura
Genus Pediastrum
Genus Volvox
Genus Eudorina
Genus Desmodesmus
Genus Monactinus
Water Net
Hydrodictyon reticulatum
Genus Tetradesmus
Genus Gonium
Genus Spirogyra
Genus Zygnema
Genus Staurastrum
Genus Closterium
Genus Micrasterias
Genus Cosmarium
Genus Amoeba
Genus Centropyxis
Genus Arcella
Copepods
Daphnia (Water Flea)
Ostracods (Seed Shrimp)
Freshwater Annelid
Mosquito Larvae
Amphipods
Nematodes
Rotifers
Gastrotrich
Water Mite