Brook Stickleback

Culaea inconstans

Gasterosteidae · freshwater water fish

11 minute read · Species guide

Brook Stickleback field guide illustration

About Brook Stickleback

The brook stickleback (Culaea inconstans) is a small freshwater fish that is distributed across the US and Canada. It grows to a length of about 2 inches. It occupies the northern part of the eastern United States, as well as the southern half of Canada. Small populations are scattered throughout the Mississippi-Great Lakes basin extending to Colorado, New Mexico, Kentucky, Tennessee, etc., though some of these areas are not native to the species. This small fish inhabits clear, cool streams and lakes. They eat small Invertebrates, algae, insect larvae, and occasionally their own eggs. They are also preyed upon by smallmouth bass and northern pike. Feeding time is usually dawn and sunset. The brook stickleback does have active competition mostly from minnows, but feeding times are different, along with diet. Spawning occurs in midsummer. Males secure a territory, build a nest, and mate with females. Males provide protection for the eggs, ward off predators, and usually die later in the season. The nests are built out of aquatic grasses. This is considered an annual species. Though the brook stickleback is not considered a threatened species, deforesting and changing waters are altering ecosystems of the species. Harvesting of trees around riparian environments is having a large effect of the stream ecosystem where the brook stickleback resides.

Taxonomy

The brook stickleback was first formally described as Gasterosteus inconstans in 1840 by the American naturalist Jared Potter Kirtland with its type locality given as Trumbull County, Ohio. In 1876 David Starr Jordan proposed the monospecific genus Eucalia for the brook stickleback but Jordan's name was invalid because it was preoccupied in Lepidoptera. Culaea was then proposed as the replacement name in 1950 by Gilbert Percy Whitley. The brook stickleback is the only species in the genus Culaea which is classified within the stickleback family, Gasterosteidae. Culea is a near anagram of Eucalia which is a combination of eu, meaning "well"and calia, meaning"nested", and allusion to the sticklebacks' building of nests. The specific name inconstans means "variable" and is a reference to the variable number of dorsal spines and fin rays in the dorsal and anal fins.

Description

The brook stickleback has a tapered body with a slim caudal peduncle and a fan-shaped tail. It very much resembles the ninespine stickleback (Pungitius pungitius) but only has five, or occasionally six, dorsal spines. It also lacks lateral bony plates. Most of the year the colouring is grayish or olive green with a varying amount of indistinct mottling, but during the spawning season, males are nearly black and females have darker and lighter patches. This species grows to a maximum length of 3 to 5 cm (1.2 to 2.0 in).

Geographic distribution of species

Culaea inconstans occurs throughout the southern half of Canada and the northern part of the eastern United States. It is one of the smallest fishes in the region. Brackish water populations are uncommon but certainly exist. It extends down to the southern reaches of the Mississippi River – Great Lakes drainage basins. Populations also exist in Colorado and Nebraska to the west, and in Alberta, Saskatchewan, Manitoba, and the Northwest Territories to the north. Though these are typically the native ranges of the brook stickleback, the species has been introduced to Alabama, Kentucky, Tennessee, northwestern Colorado, Wyoming, northeastern Utah and California, and even in parts of South Dakota and Washington State. Certain geographical distribution studies have found that certain populations may have been native in New Mexico and still exist today. Nebraska does have brook stickleback populations, but they are generally found in small streams in the northern portion of the state. The fish have been found in Nebraska since the early part of the nineteen hundreds. River drainages that sustain brook stickleback populations are the Loup, Middle Platt, Niobrara, and smaller distributions in the Lower Platte, Missouri River tributaries, North Platte, and South Platte. Though the species appears to have an abundant distribution across North America, the Nature Conservancy has declared the species to be a S3 (vulnerable) level. Reasons for the level of vulnerability could be due to increased dam construction, especially in the eastern United States. This can lead to a destruction of habitat, increase in silted waterways, alteration of stream nutrient transport, and damaged breeding grounds. Alteration of stream dynamics could also lead to a change in predator frequency, thus exposing the brook stickleback to unforeseen predators.

Introduction in Europe

The brook stickleback was introduced in upper drainage of the River Inn in Bavaria. And in the 1960s was accidentally introduced alongside Micropterus species to Lake Lohjanjarvi in southern Finland, where it has become established.

Ecology

As with a large geographical distribution, this species also lives in a wide range of flowing water habitats. Waterways such as rivers, streams, floodwater streams and drainages, lakes, ponds, potholes, hot springs, sinkholes, and seasonal melt water or spring fed ponds are all viable brook stickleback territories. Though the species can thrive in these habitats, primary spawning, breeding, and rearing grounds are located in shallow (< 1.5m) near shore environments with high vegetation cover and low velocity water. The species has a wide elevation range with specimens identified from sea level to ~ 2,400m.

Diet

The brook stickleback is an omnivore, with primary feeding tendencies toward aquatic insect larvae, adult terrestrial insects, crustaceans, fish eggs and larvae, snails, oligochaetes, nematodes, rotifers, and mites. However, brook stickleback feed on vascular plant material, as well as algae. Newly hatched stickleback larvae and planktonic crustaceans from both streams and ponds. Juveniles eat small organisms due to mouth size restrictions, and adults eat both large and small organisms.

Predators

Certain large invertebrates, birds, mammals, and fish all prey on the brook stickleback. With its small size, this species of stickleback has evolved piercing spines and protective plates to hinder predators. With this protection, as well as advanced anti-predator behavior, the brook stickleback is only a minor prey item. In a lab study, adult water bugs (Lethocerus americanus) and dragonfly nymphs (Aeschna spp.) both successfully preyed on the stickleback, but only in a night setting. Fish have been observed to be the most successful predator of the brook stickleback. Examples of these fish predators include yellow perch (Perca flavescens), rock bass (Ambloplites rupestris), creek chub (Semotilus atromaculatus), burbot (Lota lota), central mudminnow (Umbra limi), smallmouth bass (Micropterus dolomieu), largemouth bass (Micropterus salmoides), northern pike (Esox lucius), brook trout (Salvelinus fontinalis), rainbow trout (Oncorhynchus mykiss) and round goby (Neogobius melanostomus). Brook stickleback eggs can be cannibalized, as well as consumed by rainbow trout (O. mykiss). Competition among the ninespine stickleback exists. However, ninespine stickleback habitat exists in the pelagic zone, while the brook stickleback occupies the littoral zone. In the presence of fathead minnows (Pimephales promelas), the brook stickleback has a more diverse diet since the fathead is a more generalist feeder.

Life history

For this particular species, spawning occurs in mid-summer. Brook sticklebacks migrate annually up affluent streams and creeks of rivers and lakes during the spring to spawn in weedy areas. Spawning occurs as males secure a protected territory and construct a nest. These nests are constructed using algae, roots, and aquatic vegetation. There is one entrance with no exit. When the female enters, she deposits her eggs by shaking violently. Each shake allows more eggs to be deposited. Once all the eggs have been placed, the female must push her way through the wall of the nest to exit. During this process, studies have shown that the female makes acoustic noises, which is thought to advertise to sneaker males, as this can increase the proportion of eggs fertilized. After spawning, the male assumes protection of the eggs which hatch in 7–11 days. New hatched stickleback can wander from the nest, but the male gathers them into his mouth to deposit them back in the protective nest. Spawning usually ends around mid-July due to swift temperature changes in the water. The newly fertilized eggs are vulnerable to slight temperature changes. These fish grow rapidly during their first summer and typically reach sexual maturity by spring of the next year. Most adults die within the spawning season or shortly after causing them to be deemed an annual species.

Conservation

Although the Nature Conservancy has listed the brook stickleback as level S3 (vulnerable), the numbers of this species aren't threatened. The species is observed to be migrating westward and is seen as an invasive species in Wyoming. The strength of this species' success in its natural environment is seen in the amount of locations it has successfully colonized after the last ice age with the northern retreat of the glacial caps.

However, there is a potential for the population of the brook stickleback to decrease. The spawning season for this species is relatively short with high sensitivity to temperature changes. Global temperature changes are at an unprecedented rise, which could eventually lead to a global shift in water temperature. This could highly affect the spawning season for the brook stickleback species. Protecting the habitats is key to preserving the integrity of local ecosystems, as well as the integrity of the species. It is found that stable habitats allow brook stickleback to have a longer lifespan. The brook stickleback can be found from the northern parts of the Canadian interior all the way down to southern reaches of the United States.

Protection of this species should be on high priority because this species has led scientist in significant breakthroughs in sympatric and allopathic speciation. Tracking their progress in increasing or declining numbers would help conservationists categorize specific threats for that region.

Article text: Wikipedia contributors, Brook stickleback (source revision). Licensed under CC BY-SA 4.0. Retrieved 2026-10-11.

Diet and feeding

The FishTraits compilation records these diet categories for this species: algae or phytoplankton; invertebrates or larval fish; fish or frog eggs. These are broad categories, not a claim that every individual consumes every example in a category.

Reported feeding positions include bottom feeding and surface or water-column feeding. The compilation combines published observations; diets can vary with age, locality, and available food.

Habitat preferences

Reported habitat associations include medium to large rivers, streams and small rivers, creeks, still-water habitats, springs or subterranean waters.

The source records associations with muck, clay or silt, sand, gravel, cobble, boulders. An association indicates reported use, rather than an exclusive requirement.

Reproduction and parental care

The compilation reports a representative maturity age of 1 years. Its maturity field summarizes mean, median, or modal estimates, usually for females; male estimates can be used when female data are unavailable. It is not a fixed age at which every fish first breeds.

Recorded spawning months are Apr, May, Jun for the source’s reporting region (WI). This is a regional calendar, not a range-wide schedule.

The reproductive-guild classification includes guarding eggs or young at a spawning substrate or nest.

Size and recorded longevity

FishTraits reports a maximum total length of 8.7 centimetres. Some entries use an estimated asymptotic length; this value should not be treated as a certified record catch.

Recorded longevity in the compilation is 2.5 years. Wild observations were preferred, but captive records were accepted where wild records were unavailable, and unspecified records were assumed wild. The value is not a guaranteed wild lifespan or an aquarium life expectancy.

Native range

Atlantic and Arctic drainages from Nova Scotia to Northwest Territories; Great Lakes-Mississippi River basins south to southern Ohio and New Brunswick, and west to Manitoba and eastern British Columbia (Page and Burr 1991). Whittier collected it in the St. Johns drainage in Maine and determined it was native there (T. Whittier, pers. comm.).

Introduction history

Many introductions have been attributed to bait bucket releases. According to Smith-Vaniz (1968), the Alabama record was based on a single specimen, and was likely the result of an escape or release from a minnow hatchery located several miles downstream. Holding tanks at the hatchery contained stickleback, and the species was frequently observed in shipments of commercial bait minnows brought to Alabama from Wisconsin. Nelson (1969) also reported the species as commonly found with Pimephales promelas in baitfish shipments from Minnesota and Wisconsin. In certain southwestern localities, the species may have been introduced accidentally as a contaminant in stockings of sport fishes. For instance, Hatch (1985, cited by Sublette et al. 1990) believed that the presence of this species in New Mexico was the result of baitbucket introductions or introduced incidental to stocking of salmonids. He based his conclusions on the fact that this stickleback had not been found in New Mexico prior to 1954 and that headwaters of the Canadian River drainage are popular with trout anglers. Zuckerman and Behnke (1986) suggested that the Colorado Division of Wildlife may have accidentally introduced the species into the Rio Grande drainage of Colorado waters along with northern pike brought in from Minnesota. Pigg et al. (1993) discovered Brook Stickleback in a bait shipment of fathead minnows from Minnesota and suggested a possible link between its introduction into Oklahoma and the bait fish industry. A much earlier report in Oklahoma is apparently based on observations of this species in bait tanks near Ft. Gibson Reservoir in Wagoner County (Heard 1959). The owner of the bait establishment said the minnows were imported from Minnesota. The retailer had noticed the dace mixed in the primarily fathead minnow bait shipments that he had been purchasing and re-selling for over a year. Although, there are no verified records from open waters, at least some individuals were likely introduced through discarded or escaped bait. Bait bucket release is also thought to be the source of the introduced populations in Montana (Fredenberg, personal communication). It was introduced to two sites in Utah in 1983 (Sigler and Sigler 1987), possibly intentional stockings as forage. The species was first discovered in California in 1991, but the means of introduction remains unknown (Dill and Cordone 1997). Denoncourt et al. (1975c) were uncertain as to the origin of this species in the Susquehanna River drainage of Pennsylvania; they stated that the populations may be natural or the result of accidental introductions.

Ecological impacts

Largely unknown. Woodling (1985) stated that the species is pugnacious and preys on eggs. As such, he said that its use as a bait fish is discouraged so as to prevent accidental range expansion.

Range

Where it lives

Share of 4,610 GBIF observation records with a state location, across 28 states. The orange dots are USGS stream-survey sites where this species was caught.
0%
26.9%
Share of 4,610 GBIF observation records with a state location, across 28 states. The orange dots are USGS stream-survey sites where this species was caught.

A blank area on the dot layer usually means nobody sampled there, not that the fish is absent. Turn on “every survey site” to see where the survey looked.

The USGS stream survey caught it at 1,732 of its sites, in 17 states. That survey and the GBIF records are two different counts of two different things, so the site keeps them apart.

Habitat

Water and movement

Water
WoRMS records this species in fresh water.
USGS NAS habitat
Freshwater
US status
Native transplant — native to part of the United States, moved to other waters inside it.
Migration
Undetermined
Pattern
Disagreement
3 published references do not agree on the pattern: Non-migratory, Potamodromous. The site shows every assignment rather than picking one.

Classification

Taxonomy

Kingdom
Animalia
Phylum
Chordata
Superclass
Actinopterygii
Class
Teleostei
Order
Gasterosteiformes
Genus
Culaea
Species
Culaea inconstans
ITIS TSN
166399
WoRMS AphiaID
567530
GBIF key
2356556
Outside the US
ITIS also files it in Canada.

Common questions about Brook Stickleback

What is the scientific name of Brook Stickleback?
The scientific name is Culaea inconstans, in the family Gasterosteidae. Classification follows ITIS.
Does Brook Stickleback live in fresh water or salt water?
WoRMS records this species in fresh water.
Where has Brook Stickleback been recorded in the United States?
GBIF has observations in 28 states, with the most records in Minnesota, Michigan, Wisconsin. The map shows observation records, which do not establish the complete natural range.

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