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. Author manuscript; available in PMC: 2019 Sep 22.
Published in final edited form as: Sci Total Environ. 2017 Sep 28;615:123–130. doi: 10.1016/j.scitotenv.2017.09.232

Table 4.

Quantification of positive signals for FIB, human- and gull-associated and pathogen markers detected in single feces and cloacae samples from five individual gulls tracked with radio telemetry traveling between waste sites and beaches.

Mean positive signal concentration (DNA copies/unit)
EC23S857 Entero1 GenBac3 HF183 Gull4 Camp2 Faecalis1 Faecium1
Gull feces (1 g)
aGHCB to CL & GHCB to MWMb 1.8 × 103 6.5 × 104 6.5 × 102 < LOQ 8.9 × 107 3.8 × 106 < LOQ < LOQ
Gull cloacae (1 ml)
GHCB to CL & GHCB to MWMb 2.0 × 103 1.1 × 104 1.8 × 102 6.3 × 101 7.0 × 103 < LOQ < LOQ < LOQ
GHCB to CL 8.3 × 102 4.5 × 103 < LOQ < LOQ 2.3 × 105 1.2 × 106 < LOQ < LOQ
GHCB to MWM & GHCB to ML 9.7 × 102 4.2 × 104 < LOQ < LOQ 3.4 × 106 3.7 × 104 < LOQ < LOQ
GHCB to CL 1.3 × 103 2.9 × 104 < LOQ 5.8 × 101 9.0 × 105 < LOQ 6.7 × 104 < LOQ
GHCB to CL 1.3 × 103 7.4 × 105 < LOQ < LOQ 4.0 × 104 8.8 × 104 3.2 × 106 < LOQ

< LOQ, below limit of quantification. LOQs and range of amplification efficiency for each qPCR are noted in Table S1.

a

Flight path, gulls were tracked flying from site A to B using radio telemetry technology where GHCB to CL is Grand Haven City Beach to Coopersville Landfill; GHCB to MWM is Grand Haven City Beach to Muskegon Wastewater Management lagoon; GHCB to ML is Grand Haven City Beach to Muskegon Landfill.

b

Feces and cloacae samples were collected from the same gull.