The webbed foot is a specialized limb with interdigital membranes (webbings) that aids in aquatic locomotion, present in a variety of tetrapod vertebrates. This adaptation is primarily found in semiaquatic species, and has convergently evolved many times across vertebrate taxa.

It likely arose from mutations in developmental genes that normally cause tissue between the digits to apoptose. These mutations were beneficial to many semiaquatic animals because the increased surface area from the webbing allowed for more swimming propulsion and swimming efficiency, especially in surface swimmers. The webbed foot also has enabled other novel behaviors like escape responses and mating behaviors. A webbed foot may also be called a paddle to contrast it from a more hydrofoil-like flipper.

A webbed foot has connecting tissue between the toes of the foot. Several distinct conditions can give rise to webbed feet, including interdigital webbing and syndactyly. The webbing can consist of membrane, skin, or other connective tissue and varies widely in different taxa. This modification significantly increases the surface area of the feet. One of the consequences of this modification in some species, specifically birds, is that the feet are a major location for heat loss. In birds, the legs utilize countercurrent heat exchange so that blood reaching the feet is already cooled by blood returning to the heart to minimize this effect. Webbed feet take on a variety of different shapes; in birds, the webbing can even be discontinuous, as seen in lobate-footed birds like grebes. However, one of the most common is the delta (Δ) or triangular shape seen in most waterfowl and frogs. This delta wing shape is a solution that has convergently evolved in many taxa, and is also used in aircraft to allow for high lift forces at high attack angles. This shape allows for the production of large forces during swimming through both drag-based and lift-based propulsion.

Webbed feet are a compromise between aquatic and terrestrial locomotion. Aquatic control surfaces of non-piscine vertebrates may be paddles or hydrofoils. Paddles generate less lift than hydrofoils, and paddling is associated with drag-based control surfaces. The roughly triangular design of webbed feet, with a broad distal end, is specialized to increase propulsive efficiency by affecting a larger mass of water over generating increased lift. This is in contrast to a more hydrofoil-like flipper of many permanently aquatic animals.

Webbed feet are the result of mutations in genes that normally cause interdigital tissue between the toes to apoptose. Apoptosis, or programmed cell death, in development is mediated by a variety of pathways, and normally causes the creation of digits by death of tissue separating the digits. Different vertebrate species with webbed feet have different mutations that disrupt this process, indicating that the structure arose independently in these lineages.

In humans, syndactyly can arise from as many as nine unique subtypes with their own clinical, morphological, and genetic fingerprints. In addition, the same genetic mutations can underlie different phenotypic expressions of syndactyly. While these conditions are disorders in humans, the variability in genetic cause of webbed digits informs our^[who?] understanding of how this morphological change arose in species where webbed feet were selectively advantageous. These conditions also demonstrate a variety of genetic targets for mutation resulting in webbed feet, which may explain how this homologous structure could have arisen many times over the course of evolutionary history.

One pathway implicated in interdigital necrosis is the bone morphogenetic protein (BMP) signaling pathway. BMP signaling molecules (BMPs) are expressed in the tissue regions between digits during development. In experiments with chickens, mutations to a BMP receptor disrupted the apoptosis of interdigital tissue and caused webbed feet similar to ducks to develop. In ducks, BMPs are not expressed at all. These results indicate that in avian lineages, the disruption of BMP signaling in interdigital tissue caused webbed feet to arise. The magnitude of attenuation in this pathway is correlated with the amount of interdigital tissue preserved. Other genetic changes implicated in webbed feet development in avians include reduction of TGFβ-induced chondrogenesis and reduction of msx-1 and msx-2 gene expression.

Webbed feet could also arise due to being linked to other morphological changes, without a selective advantage. In salamanders, webbed feet have arisen in multiple lineages, but in most do not contribute to increased function. However, in the cave salamander species Chiropterotriton magnipes (bigfoot splayfoot salamander), their webbed feet are morphologically unique from other salamanders and may serve a functional purpose. This demonstrates that webbed feet arise from developmental changes, but do not necessarily correlate with a selective advantage functionally.