Inside a giant kelp forest, golden stipes and fronds rise through green water toward sunlight breaking through the canopy.

The Logbook · Ocean science

Why some seas are green

The blue guide computed the emptiest water on Earth. Almost nobody dives it. Add the one ingredient the real ocean is never without — life — and the physics acquires a second dial, the colour slides from gyre blue to bloom green, and the light gets shallower. None of that is a defect. Green water is the ocean working.

Published ·8 min read·Photo: BravoGonzalo · Wikimedia Commons ·CC BY-SA 4.0

The desert was the easy case

The blue guide ended on a confession: everything in it was computed for pure water, “the best the ocean can manage”, and real seawater always has something in it. This is the article about the something.

The something is mostly phytoplankton — single-celled algae, the grass of the sea — and its optics are the optics of every leaf on land. Chlorophyll absorbs hardest in the blue and the red and poorly in between: the measured absorption spectrum of ocean phytoplankton has a tall peak near 440 nanometres, a second one near 675, and a valley around 570 where the pigment takes almost nothing. So a sea filling with plankton does not add green, any more than water adds blue. It subtracts. Water eats the red end; life eats the blue end; and green is simply the last part of the spectrum with nobody assigned to eating it.

That is the entire mechanism. What makes it worth an article is that it can be computed — the bio-optics community has spent decades fitting exactly how much each unit of chlorophyll costs each wavelength, and Morel and Maritorena’s Case-1 model turns one number, milligrams of chlorophyll per cubic metre, into the full attenuation spectrum of a living sea. Feed that through the same colour arithmetic as the blue guide and you can dial the ocean from desert to soup and watch what happens.

Seven seas, one dial

The computed colour of seven seas, from ocean desert to bloomSeven colour swatches in a row, computed from chlorophyll concentrations rising from 0.01 to 30 milligrams per cubic metre. The first swatches are deep blue, shifting through teal around 2 milligrams to olive green in a thick bloom. Below each swatch a bar shows the sunlit-zone depth collapsing from 124 metres in the clearest water to 10 metres in the bloom.Ocean desert0.01 mg/m³Jerlov type IClear tropics0.05 mg/m³Jerlov type IARich reef0.1 mg/m³Jerlov type IBTemperate shelf0.5 mg/m³Jerlov type IIGreen coast2 mg/m³Jerlov type IIIBloom10 mg/m³past the bloom lineThick bloom30 mg/m³spring bloom peaksurface124 m98 m85 m55 m34 m17 m10 msunlit zone: 1 % of daylight leftEach swatch is R = 0.33·bb/a under daylight, luminance-matched across the row so only the hue changes.
The colour of the sea, computed from its chlorophyll. Seven waters, from a subtropical gyre at 0.01 mg/m³ to a thick bloom at 30: the reflected colour slides from deep blue to olive green while the sunlit zone collapses from 124 m to 10. Computed with the Case-1 bio-optical model of Morel and Maritorena (2001): reflectance R = 0.33·bb/a under D65, converted through the CIE 1931 colour matching functions.

The swatches are the sea’s own colour — the fraction of daylight the water sends back up, which is what your eye receives from a boat or a mask at the surface — computed across the honest range of the ocean. The subtropical gyres sit near 0.01 mg/m³; oceanographers call them ocean deserts, and their water is the deep violet-blue of the Sargasso, where visibility can reach 60 metres. Temperate shelves run around 0.5 to 2. Past 5 mg/m³ the literature starts calling it a bloom, and a spring bloom in full swing can pass 30. The hue barely moves for the first two rungs — the ladder is logarithmic, and the sea forgives the first traces of life — then swings through teal around 2 mg/m³ and lands in olive.

Underneath the swatches is the price. The sunlit zone — the layer holding one per cent or more of the surface daylight — is 124 metres deep in gyre water and 10 metres in the thick bloom. Nothing about the sun changed; the water simply spent the light faster. Morel and Maritorena’s own cruises measured sunlit depths of 124 to 130 metres in the South Pacific gyre, which is a strange and lovely thought for a diver: in the clearest ocean, the bottom of the light is deeper than double your certification, while in a bloom you can visit it on a single-cylinder no-stop dive. In green coastal water at 3 mg/m³ the one-per-cent line sits near 30 metres (100 feet) — a deep recreational dive in the North Atlantic in June goes to the bottom of the photic zone, which is why it gets so dark down there while the surface still looks like day.

The window walks

Attenuation across the spectrum as chlorophyll risesFour curves of attenuation against wavelength on a logarithmic scale, one per chlorophyll level, above a dashed pure-seawater baseline. In clear gyre water the minimum sits in the blue at 430 nanometres. As chlorophyll rises the blue end lifts by more than a hundredfold while the red end barely moves, and the minimum — the transparency window — walks to 490, 540 and finally 580 nanometres, in the green.Gyre · 0.03 mg/m³window 430 nm, 1% at 241 mShelf · 0.3 mg/m³window 490 nm, 1% at 96 mCoastal water · 3 mg/m³window 540 nm, 1% at 33 mThick bloom · 30 mg/m³window 580 nm, 1% at 13 mdashed: pure seawater400450500550600650700wavelength, nm0.0050.020.10.5attenuation, m⁻¹ (log)Dots mark each water's transparency window. The red end is water's own absorption and hardly moves; life closes the blue end.
The transparency window, closing from the blue end. Attenuation across the spectrum for four chlorophyll levels: the clearest colour walks from 430 nm blue to 580 nm green, and the blue light that reached 239 m in gyre water is finished by 4 m in a bloom. Computed with the Case-1 bio-optical model of Morel and Maritorena (2001): Kd = Kw + χ·Chlᵉ from their Table 2.

The blue guide’s central image was a window: water is transparent at the blue end and opaque at the red end, so blue is what survives. Chlorophyll closes that window from the blue side — its 440-nanometre peak lands almost exactly on pure water’s point of greatest transparency, which is either a coincidence or four billion years of natural selection aiming the antenna at the light that penetrates. As the concentration rises, the transparency window walks: 430 nanometres in gyre water, 490 on the shelf, 540 in coastal water, 580 in a bloom — out of the blue and into the green.

The numbers underneath are brutal for the blue. Light at 440 nanometres that reached 239 metres at the chart’s cleanest rung is down to its one per cent by 4 metres in a thick bloom — a demotion of nearly sixtyfold — while green at 560 still manages 11. Meanwhile the red end of the chart barely moves, because red never depended on the plankton: water itself eats it, exactly as before. Which resolves a thing divers notice and rarely name: in green water the colour rules change at both ends. Red still dies in the first metres — the parent guide’s grid applies unchanged — but now blue dies young too, and the ambient light converges on a green-grey that flattens everything. Photographs get worse faster; the fix is the same and more so. A torch is not an accessory in green water; it is the only red and blue on the dive.

A strobe-lit cabezon rests on rocks in the foreground while the kelp forest behind it fades into green-blue water.
A cabezon in the Monterey Bay sanctuary: warm reds where the strobe reaches, and the sanctuary's green water everywhere it does not.Photo: Chad King, NOAA ·Wikimedia Commons ·Public domain

Tea, not soup

Not all green-brown water is alive. The second ingredient is dissolved — coloured dissolved organic matter, gelbstoff, the tannins and humic acids of decayed vegetation — and it is optically the mirror image of water itself: an absorption that rises exponentially toward the blue, with a canonical slope that doubles the absorption every 50 nanometres. At the blue peak it absorbs some twenty times harder than at the red end. Water passes blue and eats red; tea passes red and eats blue; mix them and very little of anything gets through, which is why heavily stained water is not green but brown-dark.

Divers meet the pure form of this in fresh water — the tannin lakes and blackwater rivers the freshwater guide visits, where the Rio Negro’s water is, in Wikipedia’s phrase, the colour of strong tea. The saltwater form has made two of diving’s strangest places. At Milford Sound, rain running off the fiord walls floats a permanent tea-stained freshwater lid, centimetres to ten metres thick, over the sea — and the twilight it casts pulls deep-water species like black coral up into recreational depths: an entire dark-water ecosystem built by CDOM. And the brackish Baltic, fed by rivers and ringed by farmland, runs dark and blooms hard — a 2010 satellite pass measured a single algal bloom covering 377,000 square kilometres — so its wreck dives, like the 1771 Vrouw Maria, are torch dives at depths that would still be daylit in the Caribbean. (The Baltic’s famous preservation of wooden ships is its own separate gift of chemistry and shipworm-free brackish water; the darkness just sets the mood.)

The bio-optics trade keeps these cases in separate ledgers: Case 1 waters, where phytoplankton and everything that covaries with it set the optics and one chlorophyll number rules the model above; and Case 2, where river-borne CDOM and stirred sediment answer to nobody’s chlorophyll. Most temperate shore diving is somewhere between the two — which is why the ladder in our charts is a spine to reason along, not a promise about your local quarry.

Green means food

Here is the reframe the brochures never make. The chlorophyll dial is a productivity dial: those swatches are, left to right, a desert becoming a farm. The green upwelling systems — the Benguela, the California Current, the Humboldt, the Canary, the Somali — cover about 5 per cent of the ocean and land roughly 25 per cent of the world’s marine fish catch; coastal upwelling zones account for around half of all marine productivity. Every link in the chain that divers cross oceans for is bolted to that green: the sardine run is green-water economics in motion, a temperate shoal following cool, plankton-rich water up a subtropical coast; the kelp cathedrals of False Bay, Monterey and La Jolla stand in upwelling water; Manta Alley’s mantas hold station precisely where cold, nutrient-rich water funnels through and blooms; Punta Vicente Roca’s molas ride the Cromwell Current’s upwelling; and Djibouti’s juvenile whale sharks arrive for a winter plankton bloom. When the visibility briefing says “green water, stay close”, it is describing the same fact as the wildlife briefing that says “everything is here this month”. You generally do not get mantas and gin-clear blue on the same dive, and the physics is why.

Satellite view of the Baltic Sea with green phytoplankton bloom swirls curling through dark water between Sweden and the Baltic states.
A July bloom curling through the Baltic, photographed by NASA's Terra satellite. Ocean-colour instruments read chlorophyll from exactly the blue-to-green shift this article computes.Photo: Jeff Schmaltz, MODIS Land Rapid Response Team, NASA GSFC ·Wikimedia Commons ·Public domain

The green is even how we know where the food is. Satellite ocean-colour instruments estimate chlorophyll from the blue-to-green ratio of the light the sea reflects — the working premise, in NASA’s phrasing, being that the more phytoplankton in the water, the greener it is. The idea was first demonstrated in 1970 from an aircraft over Georges Bank, and it is this article’s arithmetic run backwards: we computed colour from chlorophyll; the satellites read chlorophyll from colour, bloom by bloom, for the whole planet. They have also noticed something at the decadal scale: analyses of twenty years of ocean-colour data report the low-latitude ocean measurably greening — the palette above is not just a map, it is a trend line. And for the diver who wants to meet the soup itself, there is a genre for that: the open-ocean blackwater night dives at Kona drift you through the plankton in the dark, when its daily vertical migration brings the animals up to torch depth.

Where the water is alive

Green-water diving from our records — upwelling coasts, kelp forests, plankton grounds and one tea-stained fiord — every one a place where the colour of the water is the reason to go
SiteDepthLevelBest months
Milford Sound (Piopiotahi)
Fiordland · New Zealand
to 40 mAdvancedDec–Feb
Port St Johns
Wild Coast Sardine Run · South Africa
to 10 mAdvancedJun–Jul
Coffee Bay
Wild Coast Sardine Run · South Africa
to 10 mAdvancedJun–Jul
Tacoma wreck
Dakar & Ngor · Senegal
13–14 mIntermediateOct–Nov
Miller's Point
Cape Peninsula Kelp Forests · South Africa
to 8 mIntermediateNov–Jun
Point Lobos — Whalers Cove
Monterey Bay · United States
9–21 mIntermediateSep–Oct
La Jolla Cove
La Jolla Cove & Canyon · United States
to 14 mBeginnerJul–Oct
Keystone Jetty
Puget Sound · United States
to 21 mAdvancedOct–Feb
Punta Vicente Roca
Galápagos West (Isabela & Fernandina) · Ecuador
12–27 mAdvancedJan–Apr
Manta Alley
Komodo · Indonesia
10–25 mAdvancedJun–Oct
Manta Sandy
Raja Ampat · Indonesia
8–15 mBeginnerNov–Mar
Arta Beach Whale Shark Grounds
Djibouti · Djibouti
to 5 mBeginnerNov–Feb
Kona Blackwater Dive
Kona · United States
to 15 mAdvancedDec–Apr
Vrouw Maria
Gulf of Finland · Finland
to 41 mAdvancedJun–Aug
Den Osse
Zeeland · Netherlands
to 30 mIntermediateApr–Jun

Milford sound marine reserve (Piopiotahi) dive · Zachary Penman on YouTube

Milford Sound, Fiordland: diving under a permanent tannin-stained freshwater lid that turns midday into dusk — dissolved colour building an ecosystem.Milford Sound (Piopiotahi) →

The pure-water half of this physics — why the empty ocean is blue and what the missing red does to your photographs — is in the parent guide; the tannin lakes are in freshwater diving; and the animals the green water feeds have guides of their own, from mantas to whale sharks.

Sources

  1. Bio-optical properties of oceanic waters: A reappraisal — Morel & Maritorena, Journal of Geophysical Research
  2. Phytoplankton — Ocean Optics Web Book
  3. Colored Dissolved Organic Matter — Ocean Optics Web Book
  4. Classification Schemes — Ocean Optics Web Book
  5. Reflectances — Ocean Optics Web Book
  6. Ocean color — Wikipedia
  7. Photic zone — Wikipedia
  8. Upwelling — Wikipedia
  9. Colored dissolved organic matter — Wikipedia
  10. Chlorophyll — Wikipedia
  11. Water clarity — Wikipedia
  12. Blackwater river — Wikipedia

Destinations in this guide

Australia & New Zealand

Fiordland

New Zealand

Tannin-darkened water tricks deep-water black coral into growing at diveable depths.

8–16°C · vis 15madvanced

Africa

Bronze whalers and common dolphins tear through sardine baitballs in open water.

16–24°C · vis 20madvanced

Atlantic

Snapper shoals and barracuda swirl over basalt at Africa's westernmost point

17–28°C · vis 20mintermediate

Africa

Cape fur seals and sevengill sharks weave through towering kelp canopies.

8–20°C · vis 15mintermediate

North America

Monterey Bay

United States

Exceptional nudibranch diversity in cold-water kelp forests off Monastery Beach.

9–16°C · vis 15mintermediate

North America

Market squid spawn in their millions over the sand on winter nights

13–22°C · vis 15mbeginner

Cold Water

Puget Sound

United States

Giant Pacific octopus over 4 m across, and wolf eels paired in rock dens

7–13°C · vis 25madvanced

And 6 more — browse all destinations.

More from The Logbook

All in Ocean science →