Nano- and micropores (defined as pores less than 10 μm in diameter) are common in carbonate reservoirs as either the sole pore type or in combination (dual pore networks) with matrix macropores and fracture pores. These very fine-scale pores form in limestones and dolostones and in associated organic matter (e.g., solid bitumen). Limestone nano- and micropores occur between crystals that are commonly less than 1 to 9 μm in size in limestone, but in dolostone the crystal size can be much larger. Limestone nano- and micropores commonly originate in three ways, although some inherited original nano- and micropores between mud components are preserved. First, in original lime-mud mixtures of aragonite, Mg–calcite, and calcite, the origin is both depositional and diagenetic as aragonite dissolves and reprecipitates because microrhombic calcite, Mg–calcite transforms to microrhombic calcite, and original calcite grains are generally unaffected. Second, in chalks, nano-and micropores are related to the original depositional fabric as interparticle pores between coccoliths and other pelagic allochems. Third, in sediment originally composed of Mg–calcite-rich allochems, nano-and micropores form by transformation of unstable Mg–calcite allochems to microrhombic calcite. In dolostones, nano-and micropores are associated with extensive dolomitization and the nearly complete occlusion of pores (overdolomitization), whereas another diagenetic origin in dolostones is differential dolomitization at the grain scale. Also, in some dolostones, nano- to micropores pores are inherited from precursor microporous limestone. A late process of nano- and micropore formation is subaerial weathering of both limestones and dolostones resulting in pulverulite. This form of micropores is commonly developed at unconformities as enhanced porosity zones. Organic-matter nano- and micropores in solid bitumen, common in thermally mature organic-rich argillaceous limestone, can also be present in coarser-grained carbonates in which solid-bitumen occurs within macropores. Only in organic-rich limestones do organic-matter pores have potential to form an effective pore system. Because nano- and micropores have multiple origins, their lateral and vertical distribution reflects or depends on their origin; therefore, one must not only describe nano- and micropores, but also define their origin. Recognition of nano- and micropores is important because they form tight carbonate reservoirs and have significant effects on permeability, porosity perseveration with burial, hydrocarbon saturation, hydrocarbon recovery, sweep efficiency, storage, and reserve estimations. Not recognizing nano- and micropore networks can lead to errors relative to the aforementioned measurements and as a result, economic evaluations may be invalid.