Geology ReportsSearch

Geology topics

Russ D. McCullough

Publications and source records attributed to Russ D. McCullough.

4 recordsLinked to original sources

2017 Status of the Lake Ontario Lower Trophic Levels

Significant Findings for Year 2017: 1) Offshore spring total phosphorus (TP) in 2017 was 4.4 µg/L; values remained stable since 2001. Offshore soluble reactive phosphorus (SRP) remained low (1.1 µg/L) in 2017; Apr/May – Oct mean values have been stable in nearshore and offshore habitats since 1998 (range, 0.4 – 3.3 µg/L). Apr/May – Oct mean TP concentrations were low at both nearshore and offshore locations (range, 3.7 – 9.0 µg/L). TP and SRP concentrations were significantly higher in nearshore compared to offshore habitats (7.9 µg/L vs 5.3 µg/L, TP; 1.7 µg/L vs 1.0 µg/L, SRP). 2) Chlorophyll-a and Secchi depth values are indicative of oligotrophic conditions in nearshore and offshore habitats. Offshore summer chlorophyll-a was stable 2000 – 2017. Nearshore chlorophyll-a increased 1995 - 2004 but then declined 2005 – 2015; values were above the long-term mean for 2016 and 2017. In 2017, epilimnetic chlorophyll-a averaged between 1.2 and 2.6 μg/L across sites, and offshore and nearshore Apr/May – Oct concentrations were not significantly different. Summer Secchi depth increased significantly in the offshore 2005 – 2017 and in the nearshore 1995 – 2004. There was no trend in either habitat 1995 – 2017. Apr/May – Oct Secchi depth ranged from 4.4 m to 12.5 m at individual sites and was not significantly different between offshore (8.9 m) and nearshore (5.7 m) locations. 3) In 2017, nearshore summer zooplankton biomass was at an all-time low (10.3 mg/m3). Apr/May – Oct epilimnetic zooplankton density was not different between the offshore and the nearshore, but zooplankton size and biomass were significantly higher in the offshore. (0.7 mm vs 0.52 mm and 14.2 mg/m3 vs 7.7 mg/m3). Daphnid, calanoid copepod, and cyclopoid biomass were all higher in the offshore. 4) Peak (July) epilimnetic biomass of Cercopagis was 2.5 mg/m3 in the nearshore and 1.6 mg/m3 in the offshore. Peak (September/October) epilimnetic biomass of Bythotrephes was 0.9 mg/m3 in the nearshore and 0.5 mg/m3 in the offshore. Bythotrephes biomass has increased significantly in the nearshore, 1995 – 2017. 5) Summer nearshore zooplankton density and biomass declined significantly 1995 – 2004 and then remained stable 2005 – 2017. The decline was due mainly to reductions cyclopoids. 6) Summer epilimnetic offshore zooplankton density and biomass increased significantly 2005 – 2017, due mainly to increases in cyclopoids and daphnids. In 2017, offshore summer epilimnetic zooplankton biomass was 14 mg/m3—well below the mean from 2005 – 2016 (21 mg/m3). 7) Most offshore zooplankton biomass was found in the metalimnion in July and September, and in the hypolimnion in October. Limnocalanus and cyclopoids dominated the metalimnion in July while daphnids and cyclopoids comprised most of the biomass in September. Daphnids dominated the October hypolimnion. Whole water column samples show a declining zooplankton biomass 2015 – 2017. Bythotrephes biomass in whole water column tows is the highest it has been, 2010 – 2017.

Lake Ontario

2015 status of the Lake Ontario lower trophic levels

Offshore spring total phosphorus (TP) in 2015 was 4.2 μ g/L, the same as in 2014; this is lower than 2001 - 2013, but there is no significant time trend 2001 - 2015. Offshore soluble reactive phosphorus (SRP) was very low in 2015; Apr/May - Oct mean values were <1 μ g/L at most sites. SRP has been stable in nearshore and offshore habitats since 1998 (range, 0.4 – 3.3 μ g/L). TP concentrations were low at both nearshore and offshore locations (range 4.2 - 8.1 μ g/L), and TP and SRP concentrations were significantly higher in the nearshore as compared to the offshore (6.8 μ g/L vs 4.8 μ g/L, TP; 1.1 μ g/L vs 0.7 μ g/L, SRP). Chlorophyll- a and Secchi depth values are indicative of oligotrophic conditions in nearshore and offshore habitats. Offshore summer chlorophyll- a declined significantly 2000 - 2015. Nearshore chlorophyll- a increased 1995 - 2004 but then declined 2005 - 2015. Epilimnetic chlorophyll- a averaged between 0.9 and 1.9 1 μg/L across sites, and offshore concentrations (1.4 1 μg/L) were significantly higher than nearshore (1.1 μg/L). Summer Secchi depth increased significantly in the offshore 2000 -2015 and showed no trend in the nearshore, 1995 - 2015. Apr/May - Oct Secchi depth ranged from 5.0 m to 13.0 m at individual sites and was higher in the offshore (9.5 m) than nearshore (6.2 m). In 2015, Apr/May - Oct epilimnetic zooplankton density, size, and biomass were not different between the offshore and the nearshore, but cyclopoid biomass was higher in the offshore (8.3 mg/m 3 vs 2.0 mg/m 3 ) and Bythotrephes biomass was higher in the nearshore (0.17 mg/m 3 vs 0.04 mg/m 3 ). Zooplankton density and biomass peaked in September, an atypical pattern. This coincided with peaks in calanoid copepod, daphnid, and Holopedium Holopedium biomass in the nearshore has increased significantly since 1995. The predatory cladoceran Cercopagis continued to be abundant in summer in the nearshore (3.4 μ g/L) but not in the offshore (0.8 μ g/L). Bythotrephes biomass was very low (<0.3 μ g/L) in both nearshore and offshore habitats. Combined biomass of these predatory cladocerans in the offshore was the lowest recorded since 2001. Summer nearshore zooplankton density and biomass declined significantly 1995 - 2004 and then increased significantly 2005 – 2015. The decline was due to reductions in bosminids and cyclopoids and the increase was due mostly to a rebound in bosminids. Summer offshore zooplankton density and biomass increased significantly 2005 - 2015. The increase was due to an increase in bosminids and cyclopoids. In 2015, offshore summer epilimnetic zooplankton biomass was 52 mg/m 3 (2005 - 2014 mean=18 mg/m 3 ). Most zooplankton biomass was found in the metalimnion in July and in the hypolimnion in September. Cyclopoids and Limnocalanus dominated the metalimnion and Limnocalanus dominated the hypolimnion. Whole water column samples taken show a stable zooplankton biomass but changing community composition since 2010. Cyclopoids increased 2013 - 2015 and daphnids declined 2014 - 2015.

Lake Ontario

2014 status of the Lake Ontario lower trophic levels

Soluble reactive phosphorus (SRP) concentrations have been stable in nearshore and offshore habitats since 1998 (0.4 – 3.3 μg/L). SRP concentrations were low in 2014; Apr/May – Oct mean values were <1 μg/L at most sites. Spring TP concentrations at individual sites exceeded 10 μg/L on occasion, but spring means were below the 10 μg/L target set by the Great Lakes Water Quality Agreement of 1978 for offshore waters of Lake Ontario. TP concentrations were low at both nearshore and offshore locations; Apr/May – Oct mean values from individual sites ranged from 4.6 – 9.1 μg/L. Spring TP has declined significantly in the longer data series (since 1981), but not since 1995 indicating stable nutrient loading into Lake Ontario for nearly two decades. It averaged 7.8 μg/L in the nearshore and 5.6 μg/L in the offshore in 2014. Chlorophyll-a and secchi depth values are indicative of oligotrophic conditions in nearshore and offshore habitats. Offshore summer chlorophyll-a declined significantly in both the short- (2000-2014) and long-term (1981-2014) time series at a rate of 4-6% per year. Nearshore chlorophyll-a increased after 2003 but then declined again after 2009. Epilimnetic chlorophyll-a averaged between 0.6 and 1.6 μg/L across sites with no difference between nearshore and offshore habitats. Apr/May – Oct Secchi depth ranged from 4.0 m to 10.8 m at individual sites and was higher in the offshore (average 9.1 m) than nearshore (5.9 m). In 2014, Apr/May – Oct epilimnetic zooplankton density, size, and biomass were not different between the offshore and the nearshore, and there were no differences in epilimnetic biomass between offshore and nearshore areas for any of the zooplankton groups. Zooplankton density and biomass peaked in September, an atypical pattern. This coincided with peaks in calanoid copepod, daphnid, and Holopedium biomass. Holopedium biomass in the nearshore increased significantly since 1995. The predatory cladoceran Cercopagis continued to be abundant in the summer, peaking at ~10 mg/m3in the offshore. Bythotrephes biomass was at its lowest level since 2005 in both offshore and nearshore habitats. Summer nearshore zooplankton density and biomass have declined significantly since 1995 at rates of 9-10% per year but have remained stable since 2005. However, bosminids and daphnids increased in 2013 and 2014. Summer offshore zooplankton density and biomass declined significantly in the long-term (since 1981), but remained at a lower stable level 2000 – 2014. A positive change point in 2013 is due to increases in bosminids, cyclopoid copepods, and daphnids. The observed decline in zooplankton biomass may be due in part to redistribution of zooplankton throughout the water column. Most of the zooplankton biomass was in the metalimnion and hypolimnion during the stratified period in 2014. By October, the bulk of the biomass was in the epilimnion.

Lake Ontario

Double-crested Cormorant studies at Little Galloo Island, Lake Ontario in 2013: Diet composition, fish consumption and the efficacy of management activities in reducing fish predation

For almost two decades Little Galloo Island (LGI) has supported a large colony of Double-crested Cormorants ( Phalacrocorax auritus ) in the eastern basin of Lake Ontario. Cormorant nest counts on the island since the early 1990's have averaged 4,297 per year. However, less than 2,000 pairs have nested on the island in three of the past five years. The highest count was reached in 1996 with 8,410 nesting pairs on the island. Johnson et al. (2013) estimated that cormorants from LGI alone have consumed 504 million fish since 1992. The proliferation of cormorants in the eastern basin of Lake Ontario coincided with declines in two important recreational fish species, smallmouth bass ( Micropterus dolemieu ) and yellow perch ( Perca falvescens ). Lantry et al. (2002) and Burnett et al. (2002) provide convincing evidence linking cormorant population increases to declining eastern basin smallmouth bass and yellow perch stocks. Decline of these fish stocks was evident only in the eastern basin, suggesting a localized problem, which is consistent with the halo effect where large piscivorous waterbird colonies may deplete local fish stocks (Birt et al. 1987). The year 2013 marked the twenty second consecutive year of study of the food habits and fish consumption of LGI cormorants and the fifteenth consecutive year evaluating the efficacy of management activities to control the reproductive success of cormorants nesting at LGI. The program consists mainly of spraying cormorant eggs with food grade vegetable oil as well as the culling of adult and immature birds. This paper reports the findings of work carried out in 2013 at LGI.

New York