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BC Conservation Data Centre: Conservation Status Report

Elgaria coerulea
Northern Alligator Lizard


 
Scientific Name: Elgaria coerulea
English Name: Northern Alligator Lizard
   
Provincial Status Summary
Status: S5
Date Status Assigned: March 27, 2025
Date Last Reviewed: March 27, 2025
Reasons: There are many occurrences of Northern Alligator Lizard across southern B.C. with few threats . There are no current data on trends, however local declines have been noted.
 
Range
Range Extent: G = 200,000-2,500,000 square km
Range Extent Estimate (km2): 234,475
Range Extent Comments: Found across southern BC north to Clearwater in the Thompson River valley and to Stuie just east of Bella Coola on the coast. It is also found on Vancouver Island, other islands in the Salish Sea, and the adjacent mainland coast. It is found east to near Yahk, but is absent form the extreme southeastern portion of the province (Matsuda et al. 2006; GBIF; accessed 21 January 2025).
Area of Occupancy (km2): G = 501-2,500
Area of Occupancy Estimate (km2): 3764
Area of Occupancy Comments: Estimate of 3,764 km2 (941 4km2 grid cells) is based on records from GBIF (accessed 21 Jan. 2025).
 
Occurrences & Population
Number of Occurrences: E = > 300
Comments: There are over 1600 observations on GBIF that would translate into over 300 occurrences (GBIF; accessed 21 January 2025).
Number of Occurrences with Good Viability / Ecological Integrity: Rank Factor not assessed
Number of Occurrences Appropriately Protected & Managed: U = Unknown
Comments: Likely some protection within parks.
Population Size: U = Unknown
 
Threats (to population, occurrences, or area affected)
Degree of Threat: D = Low
Comments:

This is a relatively long-lived lizard with low fecundity that faces few serious threats due to the habitat it prefers and a life history that does not include seasonal movements.

The majority of threat categories are thought to have no or negligible impacts on Northern Alligator Lizard populations in British Columbia.

The highest scored threat category is Invasive Non-native species which has an overall impact score of low. Threats from non-native species come from domestic and feral cats, dogs, and Common Wall Lizards (Podarcis muralis). None of these threats are well documented and are based on anecdotal observations. Cats and dogs are both known to prey on Northern Alligator Lizards (D. Fraser, pers. obs.). Common Wall Lizards are suspected of competing with Northern Alligator Lizards for both food and hiding places. Neonate Alligator Lizards are likely eaten by adult Common Wall Lizards. On southern Vancouver Island, where Common Wall Lizards have been established the longest (Engelstoft et al. 2020), anecdotal declines in Alligator Lizards numbers have been suspected but not quantified (D. Fraser, pers. obs; K. Ovaska, pers. obs). Common Wall Lizards have rapidly expanded since they were introduced in 1970 (Bertram 1984) and are expected to continue to do so; as of January 2025 the range extent of Common Wall Lizard in British Columbia using a minimum convex polygon is 26,584 square km. and overlaps with Alligator Lizards. Bertram (1984) identified three study sites that were "unlikely to be colonized" by Wall Lizards on southern Vancouver Island--all of these sites are now occupied by Wall Lizards (D. Fraser, pers. obs.; iNaturalist records). Currently, Wall Lizards are known from Vancouver Island (mostly on the east side of the island from Victoria to Campbell River with some isolated occurrences on the west coast of the island), some of the Gulf Islands (Denman, Hornby, Newcastle, Thetis, Salt Spring, D?Arcy, Sidney and North Pender Islands), the Sunshine Coast, and the Lower Mainland (Richmond, Langely and Chilliwack) (Engelstoft et al 2020, iNaturalist records accessed Dec 2023). There are records of individuals from the Okanagan but these are not known to be established populations. The impact of this threat may increase if the population of Wall Lizards continues to expand at the current rate.

In addition to the threats from vertebrate species, several captive Alligator Lizards died after eating caterpillars of the Cinnabar Moth (Tyria jacobaeae), an introduced pest control agent for controlling poisonous Tansy Ragweed, and there is a possibility that this exotic moth may have adverse effects on Northern Alligator Lizard populations (Nussbaum et al. 1983).

Several potential threats have unknown impact and require more research.

Problematic native species: Anecdotal observations suggest that some avian predators (American Crows, American Kestrels, Northern Pygmy Owls, Great Blue Herons, American Robins, Barred Owls) have increased their reliance on lizards as prey items with the abundance of Common Wall Lizards in habitats along the east side of Vancouver Island. This may increase predation on Northern Alligator Lizards as they are slower and less nimble than Wall Lizards at moderate temperatures (Bertram 2004) and may be easier to catch. Northern Alligator Lizards are thought to be the primary host for the tick, Ixodes pacificus, and heavy tick loads have been recorded on some Northern Alligator Lizards in California (Nieto et al 2009) and the ticks can carry Anaplasma phagocytophilum, a bacterial disease. The impact of the ticks and the bacterial disease on the lizard are not well understood.

Impacts of wildfires are also an unknown but

 
Trend (in population, range, area occupied, and/or condition of occurrences)
Short-Term Trend: U = Unknown
Comments: The overall population is likely relatively stable in extent of occurrence, however abundance is unknown and anecdotally there are local declines noted.
Long-Term Trend: U = Unknown
Comments: Likely relatively stable in extent of occurrence, however there likely have been decline in area of occupancy and abundance based on long term loss of habitat and threats.
 
Other Factors
Intrinsic Vulnerability: B=Moderately vulnerable
Environmental Specificity: CD = Moderate to broad.
Other Rank Considerations:
 
Information Gaps
Research Needs:
Inventory Needs:
 
Stewardship
Protection:
Management:
 
Version
Author: Ramsay, L. (2025), Gelling, L. (2011)
Date: January 21, 2025
 
References

Bertram, N. 2004a. Ecology of the introduced European wall lizard, Podarcis muralis, near Victoria, British Columbia. M.Sc. Thesis. University of Victoria. 100 pp.

Englestoft, C. , J. Robinson, D. Fraser and G. Hanke. 2020. Recent Rapid Expansion of Common Wall Lizards (Podarcis muralis) in British Columbia, Canada. Northwestern Naturalist, 101(1):50-55.

GBIF.org. 2025h. GBIF. Occurrence download for Elgaria coerulea. Accessed 21 January 2025.
Hooven, E. F. 1973. A wildlife brief for the clearcut logging of Douglas-fir. Journal of Forestry, v. 71, no. 4, p. 211-214.
Lais, P. M. 1976. Gerrhonotus coeruleus. Catalogue of American Amphibians and Reptiles 178.1-178.4.
Maxell, B.A., P. Hendricks, M.T. Gates, and S. Lenard. 2009. Montana amphibian and reptile status assessment, literature review, and conservation plan. Montana Natural Heritage Program, Helena, MT and Montana Cooperative Wildlife Research Unit and Wildlife Biology Program, University of Montana, Missoula, MT. 642 p.
Nieto, N. C., J.E. Foley, J. Bettaso, and R.S. Lane. 2009. Reptile Infection with Anaplasma phagocytophilum, the Causative Agent of Granulocytic Anaplasmosis. The Journal of Parasitology,95(5), 1165?1170.
Ramsay, L. Personal communication. Program zoologist. BC Conservation Data Centre, Ministry of Environment. Victoria, BC.
Rochester, C. J., Brehme, C. S., Clark, D. R., Stokes, D. C., Hathaway, S. A., & R.N. Fisher. 2010. Reptile and Amphibian Responses to Large-Scale Wildfires in Southern California. Journal of Herpetology,44(3), 333?351.
Rutherford, P. L. and P. T. Gregory. 2003. Habitat use and movement patterns of northern alligator lizards (Elgaria coerulea) and western skinks (Eumeces skiltonianus) in southeastern British Columbia. Journal of Herpetology 37: 98-106.
Sadoway, K.L. 1986. Effects of intensive forest management on amphibians and reptiles of Vancouver Island: problem analysis. IWIFR-23. Ministry of Forests, Victoria, B.C. 30 pp.
Stewart, J.R. 1985. Growth and survivorship in a California population of Gerrhonotus coerulens, with comments on intraspecific variation in adult female size. American Midland Naturalist 113: 30-44.
Telemeco R.S.,and E.A.Addis, 2014. Temperature has species-specific effects on corticosterone in alligator lizards. Gen Comp Endocrinol. 2014 Sep 15;206:184-92.
Telemenco, R.S. 2014. There be dragons: Functional analyses of thermal adaptation and biogeography of reptiles in a changing world. Ph D. dissertation. Iowa State University.258 pp.
Vitt, L. J. 1973. Reproductive Biology of the Anguid Lizard, Gerrhonotus Coerulens Principis. Herpetologica 29:176-184.
 

Please visit the website Conservation Status Ranks for information on how the CDC determines conservation status ranks. For global conservation status reports and ranks, please visit the NatureServe website http://www.natureserve.org/.

Suggested Citation:

B.C. Conservation Data Centre. 2025. Conservation Status Report: Elgaria coerulea. B.C. Minist. of Environment. Available: https://a100.gov.bc.ca/pub/eswp/ (accessed Apr 17, 2026).