9.2: Chemical and Biochemical Sedimentary Rocks

Chemical and biochemical sedimentary rocks are dominated by mineral components that have been transported as ions in solution (e.g., Na⁺, Ca²⁺, HCO_3^–, etc.). Clastic sedimentary rocks have particles that are cemented together by some of the same materials, but the difference is that in chemical and biochemical rocks, those cementing minerals are the rock, not just “glue.”

Chemical vs. Biochemical

The difference between chemical and biochemical sedimentary rocks is that in biochemical sedimentary rocks, organisms play a role in turning the ions into sediment. This means the presence and nature of biochemical sedimentary rocks are linked to the life requirements of the organisms involved. In chemical sedimentary rocks, the process is inorganic, often resulting from a body of water evaporating and concentrating the ions. It’s possible for one type of sedimentary rock to form through both chemical (inorganic) and biochemical (organically mediated) processes.

Chemical and biochemical sedimentary rocks are classified based on the minerals they contain, and are frequently dominated by a single mineral. It’s true that some clastic sedimentary rocks, such as quartz arenite, can also be dominated by a single mineral, but the reasons are different. A clastic sedimentary rock can contain whatever minerals were present in the parent rock. The minerals the clastic rock ends up containing will depend on how much “processing” the sediments undergo by physical and chemical weathering, and transport, before the sediment was cemented. On the other hand, chemical/biochemical sedimentary rocks are limited largely to those minerals that are highly soluble in water. Because mineral content is a defining characteristic of chemical and biochemical sedimentary rocks, we will use it to organize our discussion of these rocks.

Carbonate Rocks

In carbonate rocks, the dominant mineral contains the carbonate anion (CO₃^2-). The main carbonate minerals are calcite and aragonite. Both minerals have the formula CaCO₃ but they have different crystal structures. A less common carbonate mineral that’s still important for forming carbonate rocks is dolomite, which has the formula CaMg(CO₃)₂. It’s similar to calcite and aragonite, except that some of the calcium is replaced with magnesium. Dolomite is more common as a replacement mineral, which has replaced calcite in carbonate rocks.

Limestone

Limestone is comprised of calcite and aragonite. It can occur as a chemical sedimentary rock, forming inorganically due to precipitation, but most limestone is biochemical in origin. In fact, limestone is by far the most common biochemical sedimentary rock.

Almost all limestone forms in marine (i.e., oceans or salty seas) environments, and most of that forms on the shallow continental shelves, especially in tropical regions with coral reefs. Today continental shelves are relatively narrow zones along the margins of continents, but for large parts of geologic history sea-level was much higher, and large parts of the interiors of continents were flooded.

Reefs are highly productive ecosystems populated by a wide range of organisms, many of which use calcium and bicarbonate ions from seawater to make carbonate minerals (especially calcite) for their shells and other structures. These include corals as well as green and red algae, urchins, sponges, molluscs, and crustaceans. Some of micro-organisms use CaCO₃ to build tiny tests (shells) which accumulate on the ocean floor when these organisms die. Erosion can break all of these carbonate materials apart, scattering fragments throughout surrounding region (Figure 9.8).

Figure 9.8 Various corals and green algae on a reef at Ambergris, Belize. The light-colored sand consists of carbonate fragments eroded from the reef organisms. Source: Steven Earle (2015), CC BY 4.0. View source.

Figure 9.9 shows a cross-section through a typical reef environment in a tropical region (normally between 40 °N and 40 °S). Reefs tend to form near the edges of steep drop-offs because the reef organisms thrive on nutrient-rich upwelling currents. As the reef builds up, waves erode it. Currents carry carbonate sediments into the steep offshore fore-reef area and the shallower inshore back-reef area. Reef-derived sediments are dominated by reef-type carbonate fragments of all sizes, including mud.

Figure 9.9 Cross-section through a typical tropical reef. Source: Steven Earle (2015) CC BY 4.0 view source

In many such areas, carbonate-rich sediments also accumulate in quiet lagoons, where mud and mollusc-shell fragments predominate (Figure 9.10, left) or in offshore areas with strong currents, where either foraminifera tests accumulate (Figure 9.10, middle) or calcite crystallizes inorganically to form ooids–spheres of calcite that form in shallow tropical ocean water with strong currents (Figure 9.10, right).

Figure 9.10 Carbonate rocks and sediments. Left- Mollusc-rich limestone formed in a lagoon area at Ambergris, Belize. Middle- Foraminifera-rich sediment from a submerged carbonate sandbar near to Ambergris, Belize . Right- Ooids from a beach at Joulters Cay, Bahamas. Sources: Left, Middle- Steven Earle (2015), CC BY 4.0. View source. Right- Mark Wilson (2010), Public Domain. View source.

Limestone also accumulates in deeper water, from the steady settling out of the carbonate shells of tiny organisms that lived near the ocean surface. Processes on the ocean floor cause the water in the deepest parts of the ocean to become more acidic. This puts a lower limit on how deep in the ocean calcite and aragonite can accumulate, because they dissolve under acidic conditions.

Tufa and Travertine

Calcite can form chemical sedimentary rocks on land in a number of environments. Tufa forms at springs. The tufa towers in Figure 9.11 formed where spring water discharged into lake water.

Figure 9.11 Tufa towers (made of calcium carbonate) in Mono Lake, California. Evaporation keeps the concentration of ions in the lake very high, allowing the calcium carbonate to precipitate. Source: Brocken Inaglory (2006), CC BY-SA 3.0. View source.

Travertine (which is less porous) forms at hot springs. Similar material precipitates within limestone caves to form speleothems (mineral deposits in caves, Figure 9.12) such as stalactites and stalagmites.

Figure 9.12 Speleothems in Cave Nefza in Tunisia Source: Badreddine Besbes (2015), CC BY-SA 3.0. View source.

Dolostone

Dolostone (also referred to as dolomite) is the carbonate rock made of the mineral dolomite (CaMg(CO₃)₂). Dolostone is quite common (there’s a whole Italian mountain range named after it), which is surprising because marine organisms don’t precipitate dolomite. Dolomite forms through dolomitization, a process thought to involve chemical reactions between magnesium-rich water percolating through rocks, and sediments containing calcite.

Calcite and dolomite can be distinguished from one another by applying a drop of weak acid to the rock; calcite will react with weak acid, whereas dolomite will not. Also, when dolomite weathers, it tends to turn buff (tan) in color, whereas calcite tends toward grey and white.

Chert

Chert is made of silica (SiO₂). It has the same chemical formula as quartz, but is cryptocrystalline, meaning that the quartz crystals comprising chert are so small that it is difficult to see them even under a microscope. Chert can be a chemical sedimentary rock, often forming as beds within limestone (Figure 9.13), or as irregular lenses or blobs (nodules). It can also be biochemical. Some tiny marine organisms (e.g., diatoms and radiolaria) make their tests from silica. When they die their tiny shells settle slowly to the bottom of the lake or ocean, where they accumulate and are transformed into chert.

Figure 9.13 Chert (brown layers) interbedded with limestone, Triassic Quatsino Fm, Quadra Island, BC. All of the layers have been folded, and the chert, being more resistant to weathering than limestone, stands out. Source: Steven Earle (2015), CC BY 4.0. View source.

Banded Iron Formations (BIFs)

Some ancient chert beds—most dating to between 1800 and 2400 Ma—are also part of a rock known as a banded iron formation (BIF). It’s a deep sea-floor deposit of iron oxide that is a common ore of iron. These rocks consist of alternating layers of dark iron oxide minerals (magnetite and hematite) and chert stained red by hematite (Figure 9.14).

Figure 9.14 An example of a banded iron formation with dark iron oxide layers interspersed with chert stained red by hematite. This rock is 2.1 billion years old. Source: Andre Karwath (2005), CC BY-SA. View source.

BIFs formed before Earth’s atmosphere was fully oxygenated. At that time, seawater contained abundant soluble ferrous iron (Fe²⁺). However, once cyanobacteria began releasing oxygen into the atmosphere as a byproduct of photosynthesis, the iron in the seawater reacted with the oxygen, turning it into insoluble ferric iron (Fe³⁺). The result was that iron oxide minerals precipitated and sank to the ocean floor. The prevalence of BIFs in rocks dating from 2400 to 1800 Ma reflects a time when free oxygen was being added to the atmosphere, but removed just as quickly by chemical reactions. After 1800 Ma, little dissolved iron was left in the oceans so no more BIFs formed.

Evaporites

In arid regions, lakes and inland seas typically have no stream outlet, and the water that flows into them is removed only by evaporation. Under these conditions, the water becomes increasingly concentrated with dissolved salts, and eventually some of these salts may reach saturation levels and start to crystallize (Figures 9.15, 9.16).

Figure 9.15 kłlilx’^w (Spotted Lake) near Osoyoos, BC in May. The water was relatively fresh because of winter rains. Source: Steven Earle (2015), CC BY 4.0. View source.

Figure 9.16 kłlilx’^w in mid-August, showing the surface encrusted with salt deposits. Source: Anthropodermic (2011), CC BY-SA 2.0. View source. Note: The lake is a protected cultural heritage site of the Syilx Okanagan People. Anyone wishing to visit should seek permission.

Although all evaporite deposits are unique because of differences in the chemistry of the water, in most cases minor amounts of carbonates start to precipitate when the solution is reduced to about 50% of its original volume. Gypsum (CaSO₄·H₂O) precipitates at about 20% of the original volume, and halite (NaCl) precipitates at 10%. Other important evaporite minerals include sylvite (KCl) and borax (Na₂B₄O₇·10H₂O). Sylvite is mined as potash at numerous locations across Saskatchewan from evaporites that formed during the Devonian (~385 Ma) when an inland sea occupied much of the region.

Practice with Chemical and Biochemical Sedimentary Rocks

Query \(\PageIndex{1}\)

Extra! Detective Work with Evaporite Rocks

Query \(\PageIndex{2}\)