Ecology and Vulnerability
Black Rail

Image
Black Rail

Photo Credit: Hector Bottai

Scientific name
Laterallus jamaicensis

Profile: Black Rail

Coastal shorebirds, waterbirds, waterfowl, and seabirds face multiple climate change impacts, with increasing evidence for phenological mismatches and changes to habitat availability, quality, and...

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Coastal shorebirds, waterbirds, waterfowl, and seabirds face multiple climate change impacts, with increasing evidence for phenological mismatches and changes to habitat availability, quality, and distribution. Recent studies suggest that the severity of impacts varies with life history traits, phenological plasticity, and type of migration.


Arctic-breeding, long-distance migrant birds such as Pale-bellied Brant (Branta bernicla hrota), Rufa Red Knot (Calidris canutus rufa), and Purple Sandpiper (Calidris maritima) rely on syncing migration with environmental conditions and food resources. The degree of existing or potential phenological mismatch due to climate change depends on the type of migration. For example, long-distance, non-stop migrants such as Pale-bellied Brant, rely on cues at their spring staging areas; these areas may become out of sync with spring onset in the northern breeding areas where warming temperatures are higher (latitude-dependent) and vary regionally (Clausen and Clausen 2013). Short-distance migrants are more likely to remain in sync with seasonal environments because they move across shorter distances with relatively similar conditions (Clausen and Clausen 2013). Species that make migratory stopovers are more likely to acclimate to environmental cues and adjust migratory patterns accordingly (Clausen and Clausen 2013).


Across all taxa, species that are more specialized in resource use will be more vulnerable to changing prey and habitat availability compared to generalists. While not unique to just migratory birds, there are widespread concerns for fitness consequences resulting from phenological mismatches in food resources, particularly during breeding and migration, for many coastal bird species, (Catry et al., 2013, Nightingale et al., 2018, Taillie and Moorman 2019, Tucker et al., 2019, Bratton et al., 2022). Moreover, strong site fidelity during the chick rearing period and a limited radius to hunt for food increases the vulnerability of coastal birds to changes in local environmental conditions and human disturbances including wind energy development, recreation, and fishing (Gibson et al., 2018, USFWS 2020a, Bratton et al., 2022).


Coastal birds are threatened by “coastal squeeze” of habitat from sea level rise, whether that be on their Arctic tundra breeding grounds of Red Knot and Pale-bellied Brant (Clausen and Clausen 2013, Clausen et al., 2013a, Smith et al., 2020), rocky intertidal foraging habitat of Purple Sandpiper (Nightingale et al., 2018), salt marsh and tidal wetland habitat of Eastern Black Rail or Black Skimmer (Adam 2002, Pontee 2013, Hunter et al., 2015, Roach and Barrett 2015, Tallie and Moorman 2019, Tattoni et al., 2020), or sandy beach nesting, foraging, or roosting habitat of Piping Plover, Red Knot, American Oystercatcher, Black Skimmer, Common Tern, or Least Tern (Seavey et al., 2011, Doody 2013, Sims et al., 2013, National Wildlife Federation and Manomet Center for Conservation Sciences 2014, Burger and Niles 2014, Ivajnšič et al., 2017, Maslo et al., 2018, Tattoni et al., 2020). 


Coastal beach habitats that were previously able to migrate across the landscape in response to changes in sea level, are now impeded by coastal modifications and face additional habitat loss and degradation from the direct and indirect effects of climate including erosion, and invasive plants (Taillie and Moorman 2019). Coastal marshes can adapt to rising sea levels through vertical accretion or marsh migration, where conditions allow, but adjacent forests where the saltwater resistance of mature trees limits the pace of migration can lead to net losses, particularly for high marsh habitats (Field et al., 2016, Taillie and Moorman 2019). As sea levels rise at an accelerating rate, these coastal habitats often are narrowing in spatial extent and are at high risk of becoming completely inundated at some locations due to interacting and amplifying climate and non-climate stressors. 


Increased storm frequency and intensity across the region can create or enhance the early successional beach habitat used by shorebirds and waterbirds for short periods of time (Schulte and Simons 2015 & 2016, Robinson et al., 2019, Walker et al., 2019, Zeigler et al., 2019). In some areas, active management of coastal wetland vegetation and natural disturbance regimes can increase the availability of high-value food or habitat resources, and partially offset reductions in resource availability or increase the carrying capacity of habitats (Clausen et al., 2013a, Livolsi et al., 2021; Maslo et al., 2018 & 2019, Robinson et al., 2019, Walker et al., 2019, USFWS 2020a). However, the cumulative effects of coastal squeeze and increased storm impacts on habitat availability, suitability, and distribution across the geographical ranges of coastal birds is of growing concern. Spatially explicit projections of where coastal squeeze is happening the fastest overlayed with SLR projections are useful to identifying local areas to prioritize actions such as assisted migration and habitat restoration.


Community composition of coastal birds in the Northeast is generally shifting towards warmer-breeding coastal bird species and resulting in declines of breeding habitat availability and increased interspecific competition due to the influx of Arctic- and southern-nesting shorebirds into the area (Anderson et al., 2023). 


Disease and pathogens are another emerging and indirect threat of concern that can result from climate-related increases in storm and precipitation frequency and intensity. For example, heavy rainfall and hurricane events in Tampa Bay, Florida, during the 2016 breeding season for Black Skimmers resulted in repeated sewage overflows into the estuaries adjacent to a breeding colony (Shender et al., 2022). Resulting Salmonellosis killed 39% of the Black Skimmer fledglings in the colony because harmful pathogens persisted in beach sands, allowing the substrate to harbor reservoirs of bacterial pathogens (Whiley et al., 2018, Shender et al., 2022). While this example is outside of the Northeast, it identifies potentially hazardous conditions to monitor in Northeastern habitats as the region continues to experience wetter warmer conditions.

Changes in Population

Models evaluating Black Rail occupancy across marsh to forest gradients suggest increases with greater Cladium jamaicense dominance and closer proximity to the forest-marsh interface where nests are less vulnerable to high water and flooding; however, results were highly uncertain due to low detection probability (Taillie and Moorman 2019). The occupancy of Black Rail and four other marsh bird species was greater in areas where conditions were consistent with the effects of prescribed fire, such as reduced density of herbaceous vegetation and shorter woody vegetation (Taillie and Moorman 2019). Habitat suitability models show impoundments fare better than tidal marshes under sea level rise scenarios (Roach and Barrett 2015). Overall, managing marsh habitat for post-fire conditions and impoundments, larger marsh patch sizes, and higher proportions of marsh within a 200-meter buffer may facilitate vegetation migration and increase habitat availability and quality in the face of sea level rise (Roach and Barrett 2015; Taillie and Moorman 2019). Across their range-wide, high-quality habitat for Black Rail was relatively rare (coastal New Jersey to Texas) and variable at the state level, with the largest proportions of high-quality breeding habitat in North Carolina, South Carolina, and Florida (Stevens and Conway 2021). Average breeding habitat occurred in New Jersey, Delaware, Maryland, and Virginia, with relatively higher quality habitat patches found in New Jersey, Delaware, and Virginia. Highquality breeding habitat was highest on federal and protected lands range-wide, rare in New Jersey and Delaware, and uncommon in Maryland and Virginia (Stevens and Conway 2021). The highest quality patches were rare and unevenly distributed across the range, with 33-42% vulnerable to sea level rise and at increased risk from extreme events (USFWS 2019, Stevens and Conway 2021).

Indirect Effects

Across their range-wide, high-quality habitat for Black Rail was relatively rare (coastal New Jersey to Texas) and variable at the state level, with the largest proportions of high-quality breeding habitat in North Carolina, South Carolina, and Florida (Stevens and Conway 2021). Average breeding habitat occurred in New Jersey, Delaware, Maryland, and Virginia, with relatively higher quality habitat patches found in New Jersey, Delaware, and Virginia. Highquality breeding habitat was highest on federal and protected lands range-wide, rare in New Jersey and Delaware, and uncommon in Maryland and Virginia (Stevens and Conway 2021). The highest quality patches were rare and unevenly distributed across the range, with 33-42% vulnerable to sea level rise and at increased risk from extreme events (USFWS 2019, Stevens and Conway 2021).

 

References

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Anderson, M. G., Clark, M., Olivero, A. P., Barnett, A. R., Hall, K. R., Cornett, M. W., Ahlering, M., Schindel, M., Unnasch, B., Schloss, C., & Cameron, D. R. (2023). A resilient and connected network of sites to sustain biodiversity under a changing climate. Proceedings of the National Academy of Sciences, 120(7), e2204434119.

Bratton, R. M., Legett, H. D., Shannon, P., Yakola, K. C., Gerson, A. R., & Staudinger, M. D. (2022). Pre-breeding foraging ecology of three tern species nesting in the Gulf of Maine. Avian Conservation & Biology, 17(1).

Burger, J., & Niles, L. (2014). Effects on five species of shorebirds of experimental closure of a beach in New Jersey: Implications for severe storms and sea-level rise. Journal of Toxicology and Environmental Health, Part A: Current Issues, 77(18), 1102–1113.

Catry, T., Ramos, J. A., Catry, I., Monticelli, D., & Granadeiro, J. P. (2013). Inter-annual variability in the breeding performance of six tropical seabird species: Influence of lifehistory traits and relationship with oceanographic parameters. Marine Biology, 2013(160), 1189–1201.


Clausen, K. K., & Clausen, P. (2013). Earlier Arctic springs cause phenological mismatch in long-distance migrants. Oecologia, 173, 1101–1112.

Doody, J. P. (2013). Coastal squeeze and managed realignment in southeast England, does it tell us anything about the future? Ocean and Coastal Management, 79, 34–41.

Field, C. R., Gjerdrum, C., & Elphick, C. S. (2016). Forest resistance to sea-level rise prevents landward migration of tidal marsh. Biological Conservation, 201, 363–369.

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Ivajnšič, D., Lipej, L., Škornik, I., & Kaligarič, M. (2017). The sea level rise impact on four seashore breeding birds: The key study of Sečovlje Salina Nature Park. Climatic Change, 140, 549–562.

Maslo, B., Leu, K., Pover, T., Weston, M. A., & Schlacher, T. A. (2018). Managing birds of conservation concern on sandy shores: How much room for future conservation actions is there? Ecology and Evolution, 8, 10976–10988.

National Wildlife Federation, 2014

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Pontee, N. (2013). Defining coastal squeeze: A discussion. Ocean and Coastal Management, 84, 204–207.


Roach, N.S., and Barrett, K. 2015. Managed habitats increase occupancy of Black Rails (Laterallus jamaicensis) and may buffer impacts from sea level rise. Wetlands 6(35):1065-1076. 

Robinson, S. G., Fraser, J., Catlin, D., Karpanty, S. M., Altman, J., Boettcher, R., Holcomb, K., Huber, C., Hunt, K., & Wilke, A. (2019). Irruptions: Evidence for breeding season habitat 160 limitation in Piping Plover (Charadrius melodus). Avian Conservation and Ecology, 14(1).

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Shender, L. A., Cody, T., Ruder, M., Fenton, H., Nideringhaus, K. D., Blanton, J., Motes, J., Schmedes, S., & Forys, E. (2022). Heavy rainfall, sewer overflows, and salmonellosis in black skimmers (Rynchops niger). EcoHealth, 19, 203–215.

Sims, S. A., Seavey, J. R., & Curtin, C. G. (2013). Room to move? Threatened shorebird habitat in the path of sea level rise sea level rise– dynamic beaches, multiple users, and mixed ownership: A case study from Rhode Island, USA. Journal of Coastal Conservation, 17, 339–350.


Stevens, B.S., and Conway, C.J. 2021. Mapping habitat quality and threats for Eastern Black Rails (Laterallus jamaicensis jamaicensis). Waterbirds 2(44):245-256.

Taillie, P.J., and Moorman, C.E. 2019. Marsh bird occupancy along the shoreline-to-forest gradient as marshes migrate from rising sea level. Ecosphere 1(10): e02555.

Tattoni, D. J., Mordecai, E. A., & Stantial, M. L. (2020). Spatial and temporal changes in nesting behavior by black skimmers (Rynchops niger) New Jersey, USA, from 1976-2019. Waterbirds, 43(4), 307–313.

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USFWS. 2019. Species status assessment report for the Eastern Black Rail (Laterallus jamaicensis jamaicensis), v. 1.3. U.S. Fish and Wildlife Service, Atlanta, Georgia.

Walker, K. M., Fraser, J. D., Catlin, D. H., Ritter, S. J., Robinson, S. G., Bellman, H. A., DeRose-Wilson, A., Karpanty, S. M., & Papa, S. T. (2019). Hurricane Sandy and engineered response created habitat for a threatened shorebird. Ecosphere, 10(6).

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