Overview

Distribution

Range Description

This species is endemic to the southeast of the United States. Its range encompasses the Coastal Plain from Virginia to southern Florida, and west to Alabama, and also the piedmont of the Carolinas and Georgia (Mount 1975, Tennant 1984, Mitchell 1994, Palmer and Braswell 1995, Ernst and Ernst 2003).
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Geographic Range

Brown water snakes are found in southeastern North America, along the Coastal Plain from Virginia south through the lowlands of the Carolinas, most of Georgia, all of Florida and southern Alabama.

Biogeographic Regions: nearctic (Native )

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endemic to a single nation

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National Distribution

United States

Origin: Native

Regularity: Regularly occurring

Currently: Present

Confidence: Confident

Type of Residency: Year-round

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Global Range: (200,000-2,500,000 square km (about 80,000-1,000,000 square miles)) The range encompasses the Coastal Plain from Virginia to southern Florida, and west to Alabama, and also the piedmont of the Carolinas and Georgia (Mount 1975, Tennant 1984, Mitchell 1994, Palmer and Braswell 1995, Ernst and Ernst 2003).

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Continent: North-America
Distribution: USA (Florida, SE Alabama, Georgia, South Carolina, E North Carolina, W Virginia)
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Physical Description

Morphology

Physical Description

Nerodia taxispilota ranges in length from 28 to 69 inches (71.1cm-175.3 cm). The record length is 69.5" (176.6 cm). Females are larger; males do not reach the size of the largest females. Brown Water Snakes are relatively heavy-bodied, and have a large head distinctly wider than the neck. This produces a heart- or diamond-headed appearance (if viewed from above) that makes this species easy to confuse with venomous snakes in the Viperidae family (such as cottonmouths (Agkistrodon piscivorous) and rattlesnakes. Nerodia taxispilota is brown to dark brown in color (indicated by its common name). The most distinctive mark is the separation between its large brown (usually light-edged), squarish vertebral blotches that occur along the lengths of its body. These blotches alternate with a row of similar blotches on each side of the body. Many specimens are exceptionally dark, being a deep chocolate brown in gross appearance and with blotches only a little darker than ground color. The belly of -N. taxispilota- is yellow to brown and boldly marked with brown splotches and black crescents. These markings are often arranged in broken rows along its sides. The dorsal scales of Nerodia taxispilota are strongly keeled in 25-33 midbody rows, and its anal plate is divided. The tail tapers abruptly, and its eyes are high and set forward towards the nose.

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Size

Length: 175 cm

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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
This snake inhabits rivers, large creeks, lakes, ponds, reservoirs, swamps, and marshes, including brackish tidal waters in some areas; it often climbs into woody vegetation overhanging the water, and it also perches on fallen trees, jetties, duck blinds, debris or other object along shorelines (Ernst and Ernst 2003, Gibbons and Dorcas 2004). In South Carolina, it was significantly associated with the steep-banked outer bends of the river and with areas having good perch-site availability; only large individuals crossed a 100 m wide river (Mills et al. 1995).

Systems
  • Freshwater
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Habitat

Nerodia taxispilota is most common in and around clear, quiet waters, on fallen trees, or even bushes suitable for basking. The species has been collected in lakes, rivers, streams, cypress swamps and waterways, canals, drainage ditches, and ponds, especially where overhanging vegetation is present. It is also common around hardwood hammocks of wet materials, sawgrass prairies, bottomland forests, and near tree-bordered margins of brackish tidal marshes.

Terrestrial Biomes: forest

Aquatic Biomes: lakes and ponds; rivers and streams

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Comments: This snake inhabits rivers, large creeks, lakes, ponds, reservoirs, swamps, and marshes, including brackish tidal waters in some areas; it often climbs into woody vegetation overhanging the water, and it also perches on fallen trees, jetties, duck blinds, debris or other object along shorelines (Ernst and Ernst 2003, Gibbons and Dorcas 2004). In South Carolina, is was significantly associated with the steep-banked outer bends of the river and with areas having good perch-site availability; only large individuals crossed a 100-meter-wide river (Mills et al. 1995).

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Migration

Non-Migrant: Yes. At least some populations of this species do not make significant seasonal migrations. Juvenile dispersal is not considered a migration.

Locally Migrant: No. No populations of this species make local extended movements (generally less than 200 km) at particular times of the year (e.g., to breeding or wintering grounds, to hibernation sites).

Locally Migrant: No. No populations of this species make annual migrations of over 200 km.

In South Carolina, seasonal movements may have occurred; relatively large movements were recorded in late summer-early fall (Mills et al. 1995).

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Trophic Strategy

Food Habits

Nerodia taxispilota is piscivorous, preying primarily benthic-feeding fish (mostly minnows, some juvenile catfish), and on frogs. Fetal brown water snakes are nourished by fat yolks deposited within their membranous egg shrouds. Thus female Nerodia taxispilota must acquire lipid reserves well in advance of pregnancies. Gravid females are limited in their hunting strategies (because of their weight) and may rely on scavenging.

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Comments: Eats mainly fishes, sometimes frogs (Mount 1975; Mills and Hudson 1995, Herpetol. Rev. 26:149).

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Population Biology

Number of Occurrences

Note: For many non-migratory species, occurrences are roughly equivalent to populations.

Estimated Number of Occurrences: 81 to >300

Comments: This species is represented by a large number of occurrences (subpopulations). Palmer and Braswell (1995) maped well over 100 collection sites in North Carolina alone.

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Global Abundance

100,000 - 1,000,000 individuals

Comments: Adult population size is unknown but presumably exceeds 100,000. This snake is often locally common to abundant in suitable habitat (Gibbons and Dorcas 2004).

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General Ecology

In South Carolina, density was estimated at 43 individuals per km of river habitat; most individuals were found within 250 m of their previous capture location, but a few moved more than 1 km (Mills et al. 1995).

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Life History and Behavior

Cyclicity

Comments: Mostly diurnal though sometimes active at night.

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Life Expectancy

Lifespan/Longevity

Average lifespan

Status: captivity:
6.1 years.

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Lifespan, longevity, and ageing

Maximum longevity: 6.1 years (captivity) Observations: Considering the longevity of similar species, maximum longevity in this species could be significantly underestimated.
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Reproduction

Reproduction

This species breeds between late February and early May, with neonates appearing between June and October. Snakes don't have set gestation periods because pregnancy is initiated by the females' ovulation, not by deposition of semen. Viable sperm may be stored for months or even years within the cloaca of inseminated but not-yet-fertilized females. Female Nerodia taxispilota must increase their body's store of lipids by some 50% in order to become pregnant. They give live birth to as many as 60 offspring at once. These offspring range from 7 to 11 inches in length, and their coloring is much brighter than that of their parents.

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Gives birth to about 14-45 young in summer and early fall. Larger females have larger litters. In central Georgia, courtship occurred in late April-early May; young were born in late August-early September; males were sexually mature in 2.5 years, females in 3.5 years (Herrington 1989).

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Molecular Biology and Genetics

Molecular Biology

Barcode data: Nerodia taxispilota

The following is a representative barcode sequence, the centroid of all available sequences for this species. 

 
There is 1 barcode sequence available from BOLD and GenBank.   Below is the sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.  See the BOLD taxonomy browser for more complete information about this specimen.  Other sequences that do not yet meet barcode criteria may also be available.
 
GBGCR026-10|GQ279082|Nerodia taxispilota| ------------------------------------GGAACCCTATACCTACTATTTGGGGCCTGATCCGGACTAATCGGGGCCTGCCTC---AGCATGCTAATACGAATAGAACTGACGCAACCCGGGTCCTTATTCGGAAGC---GACCAAATCTTCAACGTCCTAGTCACAGCCCACGCATTCATCATAATCTTCTTCATAGTAATACCAATTATAATCGGCGGTTTTGGAAACTGATTAATCCCACTTATA---ATCGGAGCCCCAGACATAGCCTTCCCGCGTATAAACAATATAAGCTTCTGACTACTTCCACCAGCACTTCTCCTGCTTCTATCCTCCTCTTATGTAGAAGCCGGTGCCGGCACCGGCTGAACAGTTTACCCGCCACTCTCGGGGAACCTGGTACACTCAGGCCCCTCGGTAGACCTA---GCAATCTTCTCCCTACACCTAGCAGGAGCCTCGTCCATCCTGGGAGCAATCAACTTTATCACGACATGTGTCAACATAAAACCAAAATCCATGCCAATATTTAACATCCCATTGTTTGTTTGGTCAGTCTTAATTACCGCCATTATACTACTGTTAGCCCTACCAGTACTAGCGGCA---GCGATTACCATACTACTAACTGACCGAAACATCAACACCTCGTTCTTCGACCCT-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------  
-- end --

Download FASTA File
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Statistics of barcoding coverage: Nerodia taxispilota

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 1
Species: 1
Species With Barcodes: 1

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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
LC
Least Concern

Red List Criteria

Version
3.1

Year Assessed
2007

Assessor/s
Hammerson, G.A.

Reviewer/s
Cox, N., Chanson, J.S. & Stuart, S.N. (Global Reptile Assessment Coordinating Team)

Justification
Listed as Least Concern in view of its wide distribution, tolerance of a degree of habitat modification, presumed large population, and because it is unlikely to be declining fast enough to qualify for listing in a more threatened category.
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Conservation Status

Nerodia taxispilota is fairly abundant (so much so that in favorable habitats, 12 or more can be seen in the same area in a small amount of time).

US Federal List: no special status

CITES: no special status

IUCN Red List of Threatened Species: least concern

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National NatureServe Conservation Status

United States

Rounded National Status Rank: N5 - Secure

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NatureServe Conservation Status

Rounded Global Status Rank: G5 - Secure

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Population

Population
This species is represented by a large number of occurrences (subpopulations). Palmer and Braswell (1995) mapped well over 100 collection sites in North Carolina alone. The adult population size is unknown but presumably exceeds 100,000. This snake is often locally common to abundant in suitable habitat (Gibbons and Dorcas 2004). No major declines have been recorded, aside from local reductions in limited portions of the range. Currently, extent of occurrence, area of occupancy, number of subpopulations, and population size are probably relatively stable.

Population Trend
Stable
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Global Short Term Trend: Relatively stable (=10% change)

Comments: Currently, extent of occurrence, area of occupancy, number of subpopulations, and population size probably are relatively stable.

Global Long Term Trend: Increase of 10-25% to decline of 30%

Comments: No major declines have been recorded, aside from local reductions in limited portions of the range.

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Threats

Threats

Major Threats
No major threats are known. Declines may have occurred at the periphery of the range and in areas subject to intense urbanization or pollution (Gibbons and Dorcas 2004). Many watersnakes are killed by people who fear that the snakes are venomous (Mitchell 1994). However, in most areas, this species apparently faces no significant threats.
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Comments: No major threats are known. Declines may have occurred at the periphery of the range and in areas subject to intense urbanization or pollution (Gibbons and Dorcas 2004). Many watersnakes are killed by people who fear that the snakes are venomous (Mitchell 1994). However, in most areas, this species apparently faces no significant threats.

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Management

Conservation Actions

Conservation Actions
Many occurrrences are in protected areas.
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Global Protection: Very many (>40) occurrences appropriately protected and managed

Comments: Many occurrrences are in protected areas.

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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

Nerodia taxispilota has no economic importance (positive or negative) for humans.

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Economic Importance for Humans: Positive

Nerodia taxispilota has no economic importance (positive or negative) for humans.

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Wikipedia

Brown Water Snake

The brown water snake (Nerodia taxispilota) is a large species of Natricine snake found in the southeast United States.

Lycodonomorphus rufulus is sometimes also called the brown water snake, but L. rufulus is found in South Africa.

Contents

Common Names

Brown water snake, water-pilot[1], aspic, false moccasin, great water snake, pied water snake, southern water snake, water rattle, water rattler.[2].

Geographic Range

Found in lower coastal regions from southeastern Virginia, through the Carolinas and Georgia, to Northern and western Florida (Gulf Coast), then west through Alabama and Mississippi, to Louisiana, normally from sea level to 500 ft. (150 m) elevation.[3]

Description

The brown water snake is very heavy-bodied, and its neck is distinctly narrower than its head. Dorsally it is brown or rusty brown with a row of about 25 black or dark brown square blotches down its back. Smaller similar blotches alternate on the sides. Ventrally it is yellow heavily marked with black or dark brown[4]. Dorsal scales are in 27-33 rows (more than any other North American water snake), and it has 2-4 anterior temporals (usually 1 in others)[5]. Adults measure 30-60 in. (76-152 cm) in total length; record 69 in. (175 cm)[6].

Habitat

It is found in swamps and streams and is often mistaken for a venomous snake.

Reproduction

Nerodia taxispilota is ovoviviparous. Mating takes place in the spring on land or on tree branches. On average adult females are larger than adult males. The young are born alive, usually in August, in broods of 14-58, more commonly 30-40. The newborns are 7-10¾ in. (18-27 cm) long, with males longer than females, opposite of adults.[7]

Source

Holbrook, J.E. 1842. North American Herpetology; or, a Description of the Reptiles Inhabiting the United States, Vol. IV. Dobson. Philadelphia. Plate VIII & pp. 35-36.

  1. ^ Stejneger, L. and Barbour, T. 1917. A Check List of North American Amphibians and Reptiles.Harvard University Press. Cambridge.
  2. ^ Wright, A.H. and A.A. Wright. 1957. Handbook of Snakes of the United States and Canada. Comstock. Ithaca and London.
  3. ^ Wright, A.H. and A.A. Wright. 1957. Handbook of Snakes of the United States and Canada. Comstock. Ithaca and London.
  4. ^ Schmidt, K.P. and D.D. Davis. 1941. Field Book of Snakes of the United States and Canada. G.P. Putnam's Sons. New York.
  5. ^ Smith, H.M. and E.D. Brodie, Jr. 1982. A Guide to Field Identification Reptiles of North America. Golden Press. New York.
  6. ^ Conant, Roger. 1975. A Field Guide to Reptiles and Amphibians of Eastern and Central North America. Houghton Mifflin. Boston.
  7. ^ Wright, A.H. and A.A. Wright. 1957. Handbook of Snakes of the United States and Canada. Comstock. Ithaca and London.

Featured Herp: Brown Water Snake (Nerodia taxispilota)

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Names and Taxonomy

Taxonomy

Comments: Formerly included in genus Natrix.

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