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Brian F. Lantry

Publications and source records attributed to Brian F. Lantry.

At least 55 records · Page 3Linked to original sources

2016 status of the Lake Ontario Lower Trophic levels

Significant Findings for Year 2016: 1) Offshore spring total phosphorus (TP) in 2016 was 6.2 μg/L, higher than 2014 and 2015 (4.0 and 4.2 μg/L); there was no significant decline 2001 - 2016. Offshore soluble reactive phosphorus (SRP) was very low in 2016; Apr/May – Oct mean values were <1 μg/L. SRP has 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 5.2 – 9.9 μg/L). TP and SRP concentrations were significantly higher in nearshore compared to offshore habitats (7.6 μg/L vs 6.0 μg/L, TP; 1.4 μg/L vs 0.8 μg/L, SRP). 2) Chlorophyll-a and Secchi depth values are indicative of oligotrophic conditions in nearshore and offshore habitats. Offshore summer chlorophyll-a declined significantly 2000 - 2016. Nearshore chlorophyll-a increased 1995 - 2004 but then declined 2005 - 2016. Epilimnetic chlorophyll-a averaged between 1.4 and 2.5 μg/L across sites, and offshore and nearshore Apr/May – Oct concentrations were the same (1.9 μg/L). Summer Secchi depth increased significantly in the offshore 2000 - 2016 and showed no trend in the nearshore, 1995 – 2016. Apr/May – Oct Secchi depth ranged from 5.0 m to 13.0 m at individual sites and was significantly higher in the offshore (10.0 m) than nearshore (6.5 m). 3) In 2016, Apr/May – Oct epilimnetic zooplankton density and biomass were not different between the offshore and the nearshore, but calanoid copepod and Limnocalanus biomass were higher in the offshore (4.7 mg/m3 vs 2.6 mg/m3 and 0.7 mg/m3 vs 0.1 mg/m3), and bosminid biomass was higher in the nearshore (1.1 mg/m3 vs 0.3 mg/m3). Zooplankton size was significantly higher in the offshore than the nearshore (0.66 mm vs 0.49 mm). 4) Peak (July) epilimnetic biomass of Cercopagis was 1.0 mg/m3 in the nearshore and 1.4 mg/m3 in the offshore. Peak (October) epilimnetic biomass of Bythotrephes was 1.8 mg/m3 in the nearshore and 0.6 mg/m3 in the offshore. Bythotrephes biomass has increased significantly in the nearshore, 1995 – 2016. Bythotrephes was more abundant in 2016 than in the previous two years and the zooplankton community responded accordingly with a decrease in bosminds and cyclopoids. 5) Summer nearshore zooplankton density and biomass declined significantly 1995 – 2004 and then remained stable 2005 – 2016. The decline was due to reductions in bosminids and cyclopoids. 6) Summer epilimnetic offshore zooplankton density and biomass increased significantly 2005 – 2016. In 2016, offshore summer epilimnetic zooplankton biomass was 22 mg/m3--less than half that observed in 2015--but still slightly higher than the mean from 2005 – 2015 (21 mg/m3). 7) Most offshore zooplankton biomass was found in the metalimnion in July and September, and in the hypolimnion in October. Limnocalanus dominated the metalimnion in July while other calanoids and daphnids comprised most of the biomass in September. Limnocalanus and other calanoids dominated the October hypolimnion. Whole water column samples taken show a stable zooplankton biomass but changing community composition since 2010. Cyclopoids increased 2013 – 2015 and declined in 2016, while the calanoid pattern was the opposite. Daphnids declined 2014 – 2015 but rebounded in 2016.

Lake Ontario↗

Estimates of lake trout ( Salvelinus namaycush ) diet in Lake Ontario using two and three isotope mixing models

Recent development of multi-dimensional stable isotope models for estimating both foraging patterns and niches have presented the analytical tools to further assess the food webs of freshwater populations. One approach to refine predictions from these analyses is to include a third isotope to the more common two-isotope carbon and nitrogen mixing models to increase the power to resolve different prey sources. We compared predictions made with two-isotope carbon and nitrogen mixing models and three-isotope models that also included sulphur ( δ 34 S) for the diets of Lake Ontario lake trout ( Salvelinus namaycush ). We determined the isotopic compositions of lake trout and potential prey fishes sampled from Lake Ontario and then used quantitative estimates of resource use generated by two- and three-isotope Bayesian mixing models (SIAR) to infer feeding patterns of lake trout. Both two- and three-isotope models indicated that alewife ( Alosa pseudoharengus ) and round goby ( Neogobius melanostomus ) were the primary prey items, but the three-isotope models were more consistent with recent measures of prey fish abundances and lake trout diets. The lake trout sampled directly from the hatcheries had isotopic compositions derived from the hatchery food which were distinctively different from those derived from the natural prey sources. Those hatchery signals were retained for months after release, raising the possibility to distinguish hatchery-reared yearlings and similarly sized naturally reproduced lake trout based on isotopic compositions. Addition of a third-isotope resulted in mixing model results that confirmed round goby have become an important component of lake trout diet and may be overtaking alewife as a prey resource.

New York, 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↗

Sea lamprey mark type, marking rate, and parasite-host relationships for lake trout and other species in Lake Ontario

We examined how attack frequency by sea lampreys on fishes in Lake Ontario varied in response to sea lamprey abundance and preferred host abundance (lake trout > 433 mm). For this analysis we used two gill net assessment surveys, one angler creel survey, three salmonid spawning run datasets, one adult sea lamprey assessment, and a bottom trawl assessment of dead lake trout. The frequency of fresh sea lamprey marks observed on lake trout from assessment surveys was strongly related to the frequency of sea lamprey attacks observed on salmon and trout from the creel survey and spawning migrations. Attack frequencies on all salmonids examined were related to the ratio between the abundances of adult sea lampreys and lake trout. Reanalysis of the susceptibility to sea lamprey attack for lake trout strains stocked into Lake Ontario reaffirmed that Lake Superior strain lake trout were among the most and Seneca Lake strain among the least susceptible and that Lewis Lake strain lake trout were even more susceptible than the Superior strain. Seasonal attack frequencies indicated that as the number of observed sea lamprey attacks decreased during June–September, the ratio of healing to fresh marks also decreased. Simulation of the ratios of healing to fresh marks indicated that increased lethality of attacks by growing sea lampreys contributed to the decline in the ratios and supported laboratory studies about wound healing duration.

Lake Ontario↗

Lake Ontario water quality during the 2003 and 2008 intensive field years and comparison with long-term trends

Phosphorus loading declined between the 1970s and the 1990s, leading to oligotrophication of the offshore waters of Lake Ontario during that time period. Using lake-wide data from the intensive field years of 2003 and 2008 and from available long-term data sets on several trophic state indicators (total phosphorus [TP], soluble reactive silica [SRSi], chlorophyll a and Secchi disc transparency [SDT]), we tested the hypothesis that oligotrophication of the offshore waters of Lake Ontario has continued in the 2000s. Significant differences between 2003 and 2008 include higher spring (April) TP, SRSi, and SDT in 2008, lower summer (July–August) SDT in 2008, higher summer chlorophyll a in 2008, and lower fall (September) TP, SRSi, and chlorophyll a in 2008. The decline in SRSi from spring to summer was greater in 2008 than in 2003. Change point and regression analyses on the long-term data revealed no trend in spring TP since 1996, in summer chlorophyll a since 1994, in spring SDT since 1998, in spring SRSi or SRSi decline from spring to summer since 1999, or in summer SDT since 2001. Neither the comparison of the 2003 and 2008 surveys nor the analysis of the long-term data supported our hypothesis of continued oligotrophication of the offshore of Lake Ontario in the 2000s.

Lake Ontario↗

Sea lamprey mark type, wounding rate, and parasite-host preference and abundance relationships for lake trout and other species in Lake Ontario

We examined how the frequency of attacks by Sea Lamprey on fishes in Lake Ontario varied in response to Sea Lamprey abundance and preferred host abundance (Lake Trout >432mm). For this analysis we assembled seven data sets. Two fishery independent surveys for Lake Trout: US Geological Survey (USGS)/New York State Department of Environmental Conservation (NYSDEC) south shore September gillnet assessment of adult Lake Trout (USGS/NYSDEC SGNS)( Lantry and Lantry 2011); and Ontario Ministry of Natural Resources (OMNR) monthly June-November community index gillnetting in northeastern Lake Ontario (OMNR CIS) (Ontario Ministry of Natural Resources 2011). One angler survey: NYSDEC April-September Fishing Boat Survey data collected along the south shore for Chinook and Coho salmon, and Rainbow and Brown trout (NYSDEC FBS) ( Lantry and Eckert 2012). Two spawning run datasets: OMNR north shore data including spring spawning runs of Rainbow Trout in the Ganaraska River and electroshocking data for fall spawning runs of Chinook and Coho salmon in the Credit River (Ontario Ministry of Natural Resources 2011); and NYSDEC data from the Salmon River on the southeastern shore including October spawning runs of Chinook and Coho salmon. One Sea Lamprey spawning survey: Department of Fisheries and Oceans Canada (DFO)/US Fish and Wildlife Service (USFWS) data for spawning-phase Sea Lamprey abundance collected from known spawning streams distributed throughout the Lake Ontario drainage basin (Mullet et al. 2003). One assessment of the abundance of dead Lake Trout: USGS/NYSDEC October-November bottom trawl collection of Lake Trout carcasses (Schneider et al. 1996). Annual patterns in A1, A2 and A3 wound stages did not track well in plots of wounding rates for the USGS/NYSDEC SGNS and correlations between A1 and later stages did not exist. A1 rates were not correlated to either Lake Trout abundance or Sea Lamprey numbers when considered alone, but were strongly correlated to the ratio between Sea Lamprey numbers and Lake Trout abundance (parasite/host ratio). While A2 and A3 rates were correlated to each other, neither was consistently correlated to any of the Lake Trout abundance or Sea Lamprey abundance parameters and sums of A1 to A3 rates did not improve correlations over those for A1 rates considered alone. Our analysis of the strain-specific susceptibility of Lake Trout to attack by Sea Lampreys extended the previous Schneider et al. (1996) analysis of three strains (SUP, CWL, and SEN) and 11 years of data 1982-1992 to an analysis of seven strains (SUP, CWL, SEN, JEN, LEW, ONT, and OXS) and two groups of unmarked fish (1983-1995 and 1996-2010) and included 18 more years of data through 2010. The susceptibility to attack for CWLs and SENs were below SUPs and nearly identical to the earlier values, new values for LEWs were greater than SUPS and values of unmarked Lake Trout prior to 1996 were unexpectedly greater than SUPs. By reexamining the Schneider et al. (1996) regression relationship between A1 wounding on Lake Trout and the incidence of Lake Trout carcasses recovered in fall bottom trawls (including three additional years of data), and substituting A1 wounding rate for total numbers of A1s observed which was used as the independent variable in the previous version, we were able to increase the variance explained by the relationship from an r2 of 0.60 to 0.88. Healing rate of wounds was explored by examining the monthly incidence of A1 and A2 wounds on Lake Trout from the OMNR CIS. Because wounding intensity varied between years and monthly sample size was frequently low, the ratio of A2 to A1s wounds was used to index how wounds accumulated or disappeared from the Lake Trout populations across seasons. The A2/A1 ratio decreased between June/July and October. A simple wounding model for Lake Trout was constructed to simulate the pattern of ratios by inflicting wounds on the population each month according to a predetermined distribution and including parameters for lethality (fixed distribution) and healing rate of A1 and A2 wounds (discretely varied between simulations). The best simulated representation (ratio size and monthly pattern) of the OMNR CIS data came from an A1 healing rate of 0.5 months and an A2 rate of 2 months. To examine whether alternate hosts provided reliable data to index damage caused by Sea Lampreys we compared September values of abundance and A1 wounding rates on Lake Trout, Sea Lamprey abundance, and the parasite/host ratio with NYSDEC Creel data for observations of Sea lampreys attached to sport-caught salmonids and to wounding observations for salmonids sampled in OMNR and NYSDEC spawning run assessments. Attachment frequency on NYSDEC Creel Chinook Salmon, Brown Trout, and Rainbow Trout were strongly correlated to all measures of Lake Trout abundance and wounding and to the parasite/host ratio. Chinook Salmon and Coho Salmon wounding observations for the NYSDEC Salmon River spawning run assessments and Rainbow Trout from the OMNR Ganaraska River spawning run assessment were strongly correlated to wounding measures for nearly all salmonids and to the parasite/host ratio.

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↗

Ecological tracers reveal resource convergence among prey fish species in a large lake ecosystem

1. We measured stable isotopes of carbon (&delta; 13 C) and nitrogen (&delta; 15 N) and fatty acid profiles in Lake Ontario alewife ( Alosa pseudoharengus ), rainbow smelt ( Osmerus mordax ), slimy sculpin ( Cottus cognatus ) and round goby ( Neogobius melanostomus ) collected from 1982 to 2008 to investigate how temporal variability in these ecological tracers can relate to ecosystem-level changes associated with the establishment of highly invasive dreissenid mussels. 2. Prey fish &delta; 15 N values remained relatively constant, with only slimy sculpin exhibiting a temporal increase in &delta; 15 N. In contrast, &delta; 13 C values for alewife, rainbow smelt and, especially, slimy sculpin became less negative over time and were consistent with the benthification of the Lake Ontario food web associated with dreissenids. 3. Principal components analysis revealed higher contributions of 14:0 and 16:1n-7 fatty acids and increasingly negative &delta; 13 C values in older samples in agreement with the greater historical importance of pelagic production for alewife, rainbow smelt and slimy sculpin. 4. Temporal declines in fatty acid unsaturation indices and &Sigma;n-3/&Sigma;n-6 ratios, and also increased 24:0/14:0 ratios for alewife, rainbow smelt and slimy sculpin, indicated the increasing importance of nearshore production pathways for more recently collected fish and resulted in values more similar to those for round goby. 5. These results indicate a temporal convergence of the food niche, whereas food partitioning has historically supported the coexistence of prey fish species in Lake Ontario. This convergence is consistent with changes in food-web processes associated with the invasion of dreissenid mussels.

Lake Ontario↗

Lake trout rehabilitation in Lake Ontario, 2013

Each year we report on the progress toward rehabilitation of the Lake Ontario lake trout ( Salvelinus namaycush ) population, including the results of stocking, annual assessment surveys, creel surveys, and evidence of natural reproduction observed from all standard surveys performed by USGS and NYSDEC. No lake trout from the 2011 year class were stocked into Lake Ontario during October 2011 or May 2012; therefore, no stocked age-2 lake trout were available to bottom trawls during 2013. The catch per unit effort of adult lake trout in gill nets increased each year from 2008-2013, recovering from historic lows recorded during 2005-2007. Adult abundance in 2013 exceeded the level of the 1999-2004 mean which at the time appeared to be the new stable abundance following from the 1993 stocking cuts. The 2013 rate of wounding by sea lamprey ( Petromyzon marinus ) on lake trout caught in gill nets was 2.26 fresh (A1) wounds per 100 lake trout and was slightly above target (2 wounds per 100 lake trout). Estimates from the NYSDEC fishing boat survey indicated 2013 angler catch and harvest rates were the highest estimated in more than 10 years. Adult lake trout condition (indexed from annual length–weight regressions) increased in 2007-2009 from relatively low values observed during 2000-2006, remained nearly constant during 2010-2012 at the highest values observed for the 30 year time-series, but declined in 2013. The low condition values observed for juvenile lake trout during 2010-2012 continued during 2013. Reproductive potential for the adult stock, determined from the annual egg deposition index, rebounded from the 2007-2008 values that were the lowest observed since 1985 and stabilized during 2009-2013 at a mean value of 20.7. In 2013, five age-1 and three age-2 naturally produced lake trout were collected from trawl survey catches providing first evidence of a 2012 year class and continued evidence of a 2011 year class.

Lake Ontario↗

The offshore benthic fish community

Lake Ontario’s offshore benthic fish community includes primarily slimy sculpin, lake whitefish, rainbow smelt, lake trout, burbot, and sea lamprey. Of these, lake trout have been the focus of an international restoration effort for more than three decades (Elrod et al. 1995; Lantry and Lantry 2008). The deepwater sculpin and three species of deepwater ciscoes (Coregonus spp.) that were historically important in the offshore benthic zone became rare or were extirpated by the 1960s (Christie 1973; Owens et al. 2003; Lantry et al. 2007b; Roth et al. 2013). Ecosystem changes continue to influence the offshore benthic fish community, including the effects of dreissenid mussels, the near disappearance of burrowing amphipods (Diporeia spp.) (Dermott et al. 2005; Watkins et al. 2007), and the increased abundance and expanded geographic distribution of round goby (see Nearshore Fish Community chapter) (Lantry et al. 2007b). The fish-community objectives for the offshore benthic fish community, as described by Stewart et al. (1999), are: The offshore benthic fish community will be composed of self-sustaining native fishes characterized by lake trout as the top predator, a population expansion of lake whitefish from northeastern waters to other areas of the lake, and rehabilitated native prey fishes.

New York↗

2013 status of the Lake Ontario lower trophic levels

Phosphorus showed high variation across nearshore (10 m depth) sites but was more stable at offshore (20 m and deeper) stations. In June and July, sites at the mouth of the Niagara River and at Oak Orchard had high phosphorus concentrations (20 – 46 μg/L). Epilimnetic average April-Oct total phosphorus (TP) ranged between 6.9 and 19.9 μg/L in the nearshore and between 5.8 and 10.2 μg/L in the offshore. Average April-Oct soluble reactive phosphorus (SRP) ranged from 0.9 to 7.3 μg/L in the nearshore and 0.8 to 1.4 μg/L in the offshore. TP and SRP were significantly higher in the nearshore than in the offshore. Spring TP has declined in the longer data series (since 1981), but not since 1995. It averaged 8.4 μg/L in the nearshore and 5.0 μg/L in the offshore in 2013—below the 10 μg/L target set by the Great Lakes Water Quality Agreement of 1978 for offshore waters of Lake Ontario. Offshore summer chlorophyll-a declined significantly in both the short- (1995-2013) and long-term (1981-2013) time series at a rate of 3-4% per year. Nearshore chlorophyll-a increased after 2003 but then declined again after 2009. Epilimnetic chlorophyll-aaveraged between 0.5 and 1.3 μg/L across sites with no difference between nearshore and offshore habitats. Average seasonal Secchi disk depth ranged from 4.5 m to 10.6 m and was higher in the offshore (average 8.1 m) than nearshore stations (6.3 m). These values are indicative of oligotrophic conditions in both habitats. In 2013, Apr/May - Oct epilimnetic zooplankton size and total biomass were significantly higher in the offshore than the nearshore. However, with the exception of Limnocalanus (higher in offshore), there were no differences between habitats for any of the zooplankton groups. Most of the zooplankton biomass was in the metalimnion and hypolimnion during the day in 2013. Between 65 and 98% of zooplankton biomass was found below the thermocline throughout the year. The predatory cladoceran Cercopagis continued to be abundant in the summer, peaking at ~7 mg/m3in the offshore. Bythotrephes peaked in October (~0.7 mg/m3), but Bythotrephes biomass was at its lowest biomass in both offshore and nearshore stations since 2005. Summer nearshore zooplankton density and biomass have declined significantly since 1995 at rates of 9-10% per year. Nearshore epilimnetic zooplankton density and biomass have remained stable since 2005 at low levels relative to previous years. Summer offshore zooplankton density and biomass in the epilimnion of Lake Ontario have also declined since 1995 at rates of 10-14% per year, but those declines are marginally significant; density declined significantly in the long-term (since 1981) but has remained at a lower stable level since 2005. Bosminid and cyclopoid copepod biomass declined significantly in nearshore waters. The same pattern occurred in the offshore but declines were significant for bosminids and marginally significant for cyclopoid copepods. Daphnid biomass has also declined significantly in the nearshore. The decline in Daphnid biomass nearshore and Bythotrephes biomass offshore and nearshore is indicative of increased planktivory by alewife. Significant declines in Bosminid and cyclopoid copepod biomass is indicative of increased invertebrate predation by Cercopagis and Bythotrephes in recent years.

Lake Ontario↗

Changing ecosystem dynamics in the Laurentian Great Lakes: Bottom-up and top-down regulation

Understanding the relative importance of top-down and bottom-up regulation of ecosystem structure is a fundamental ecological question, with implications for fisheries and water-quality management. For the Laurentian Great Lakes, where, since the early 1970s, nutrient inputs have been reduced, whereas top-predator biomass has increased, we describe trends across multiple trophic levels and explore their underlying drivers. Our analyses revealed increasing water clarity and declines in phytoplankton, native invertebrates, and prey fish since 1998 in at least three of the five lakes. Evidence for bottom-up regulation was strongest in Lake Huron, although each lake provided support in at least one pair of trophic levels. Evidence for top-down regulation was rare. Although nonindigenous dreissenid mussels probably have large impacts on nutrient cycling and phytoplankton, their effects on higher trophic levels remain uncertain. We highlight gaps for which monitoring and knowledge should improve the understanding of food-web dynamics and facilitate the implementation of ecosystem-based management.

Illinois, Indiana, Michigan, Minnesota, new York, ↗

Effect of light, prey density, and prey type on the feeding rates of Hemimysis anomala

Hemimysis anomala is a near-shore mysid native to the Ponto-Caspian region that was discovered to have invaded Great Lakes ecosystems in 2006. We investigated feeding rates and prey preferences of adult and juvenile Hemimysis in laboratory experiments to gain insight on the potential for Hemimysis to disrupt food webs. For both age groups (AGs), we measured feeding rates as a function of prey abundance (Bosmina longirostris as prey), prey type (B. longirostris, Daphnia pulex, and Mesocyclops sp.), and light levels (no light and dim light). Mean feeding rates on Bosmina increased with prey density and reached 23 ind. (2 h) −1 for adults and 17 ind. (2 h) −1 for juveniles. Dim light had little effect on prey selection or feeding rate compared to complete darkness. When feeding rates on alternate prey were compared, both AGs fed at higher rates on Bosmina than Daphnia, but only juveniles fed at significantly higher rates on Bosmina relative to Mesocyclops. No significant differences were observed between feeding rates on Mesocyclops and on Daphnia. Hemimysis feeding rates were on the order of 30–60% of their body weight per day, similar to predatory cladocerans that have been implicated in zooplankton declines in Lakes Huron and Ontario.

New York↗

Lake whitefish diet, condition, and energy density in Lake Champlain and the lower four Great Lakes following dreissenid invasions

Lake Whitefish Coregonus clupeaformis support some of the most valuable commercial freshwater fisheries in North America. Recent growth and condition decreases in Lake Whitefish populations in the Great Lakes have been attributed to the invasion of the dreissenid mussels, zebra mussels Dreissena polymorpha and quagga mussels D. bugensis, and the subsequent collapse of the amphipod, Diporeia, a once-abundant high energy prey source. Since 1993, Lake Champlain has also experienced the invasion and proliferation of zebra mussels, but in contrast to the Great Lakes, Diporeia were not historically abundant. We compared the diet, condition, and energy density of Lake Whitefish from Lake Champlain after the dreissenid mussel invasion to values for those of Lake Whitefish from Lakes Michigan, Huron, Erie, and Ontario. Lake Whitefish were collected using gill nets and bottom trawls, and their diets were quantified seasonally. Condition was estimated using Fulton's condition factor (K) and by determining energy density. In contrast to Lake Whitefish from some of the Great Lakes, those from Lake Champlain Lake Whitefish did not show a dietary shift towards dreissenid mussels, but instead fed primarily on fish eggs in spring, Mysis diluviana in summer, and gastropods and sphaeriids in fall and winter. Along with these dietary differences, the condition and energy density of Lake Whitefish from Lake Champlain were high compared with those of Lake Whitefish from Lakes Michigan, Huron, and Ontario after the dreissenid invasion, and were similar to Lake Whitefish from Lake Erie; fish from Lakes Michigan, Huron, and Ontario consumed dreissenids, whereas fish from Lake Erie did not. Our comparisons of Lake Whitefish populations in Lake Champlain to those in the Great Lakes indicate that diet and condition of Lake Champlain Lake Whitefish were not negatively affected by the dreissenid mussel invasion.

Great Lakes;Lake Champlain↗

Laboratory-derived temperature preference and effect on the feeding rate and survival of juvenile Hemimysis anomala

Hemimysis anomala is a warm-water mysid that invaded the Great Lakes region in 2006 and has since rapidly spread throughout the basin. We conducted three laboratory experiments to better define the temperature preference, tolerance limits, and temperature effects on feeding rates of juvenile Hemimysis, using individuals acclimated to mid (16 °C) and upper (22 °C) preferred temperature values previously reported for the species. For temperature preference, we fit a two-parameter Gaussian (μ, σ) function to the experimental data, and found that the peak values (μ, interpreted as the preference temperature) were 22.0 °C (SE 0.25) when acclimated to 16 and 21.9 °C (SE 0.38) when acclimated to 22 °C, with the σ-values of the curves at 2.6 and 2.5 °C, respectively. No mysids were observed in temperatures below 10 or above 28 °C in these preference experiments. In short-term tolerance experiments for temperatures between 4 and 32 °C, all mysids died within 8 h at 30.2 °C for 16 °C acclimated mysids, and at 31.8 °C for 22 °C acclimated mysids. No lower lethal limit was found. Feeding rates increased with temperature from an average of 4 Bosmina eaten per hour at 5 °C to 19 Bosmina eaten per hour at 27 °C. The results of our experiments indicate an optimal temperature for Hemimysis between 21 and 27 °C, which corresponds with temperatures during periods of high population growth in the field. These results contribute a better understanding of this species' biological response to temperature that will help guide field studies and inform bioenergetics modeling.

New York↗

Long-term impacts of invasive species on a native top predator in a large lake system

1. Declining abundances of forage fish and the introduction and establishment of non-indigenous species have the potential to substantially alter resource and habitat exploitation by top predators in large lakes. 2. We measured stable isotopes of carbon (δ 13 C) and nitrogen (δ 15 N) in field-collected and archived samples of Lake Ontario lake trout ( Salvelinus namaycush ) and five species of prey fish and compared current trophic relationships of this top predator with historical samples. 3. Relationships between δ 15 N and lake trout age were temporally consistent throughout Lake Ontario and confirmed the role of lake trout as a top predator in this food web. However, δ 13 C values for age classes of lake trout collected in 2008 ranged from 1.0 to 3.9‰ higher than those reported for the population sampled in 1992. 4. Isotope mixing models predicted that these changes in resource assimilation were owing to the replacement of rainbow smelt ( Osmerus mordax ) by round goby ( Neogobius melanostomus ) in lake trout diet and increased reliance on carbon resources derived from nearshore production. This contrasts with the historical situation in Lake Ontario where δ 13 C values of the lake trout population were dominated by a reliance on offshore carbon production. 5. These results indicate a reduced capacity of the Lake Ontario offshore food web to support the energetic requirements of lake trout and that this top predator has become increasingly reliant on prey resources that are derived from nearshore carbon pathways.

Freshwater Biology↗

Age-specific light preferences and vertical migration patterns of a Great Lakes invasive invertebrate, Hemimysis anomala

We use a combination of spectral sensitivity analyses, laboratory behavioral observations and field distributions of a vertically migrating invertebrate, Hemimysis anomala (a recent invasive species to the Laurentian Great Lakes of North America), to determine if light preference and timing of emergence has an ontogenetic component. Juvenile Hemimysis (< 4.5 mm) preferred light levels between 10 −3.4 and 10 −2.4 mylux— a Hemimysis -specific unit of brightness derived from visual pigment analyses (wavelength of maximum absorbance = 500 nm; 1 mylux ~ 159 lx). These preferred light levels are equivalent to those present during nautical twilight on the Earth's surface and were several orders of magnitude brighter than those most preferred by adults (> 4.5 mm) in the laboratory (10 −6.4 to 10 −7.4 mylux). Both size classes completely avoided light levels of 10 −0.4 mylux and greater, which are representative of daytime light levels at the Earth's surface. Net hauls taken at ~ 20-min intervals from sunset to the end of nautical twilight on two sampling occasions on Seneca Lake, New York (sampling depth = 2 m) revealed that juveniles emerged into the water column during civil twilight. Adult Hemimysis emerged later during nautical twilight when juveniles had already reached their maximum abundance in the water column. Laboratory-derived light preferences successfully predicted the timing of emergence and time of maximal abundance of both size classes on both sampling occasions. This study is one of the first to demonstrate that Hemimysis diel vertical migration has an ontogenetic component and to report the specific light levels likely to initiate and limit vertical movements.

Great Lakes↗