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Jana R. Lantry

Publications and source records attributed to Jana R. Lantry.

9 recordsLinked to original sources

Balancing prey availability and predator consumption: A multispecies stock assessment for Lake Ontario

Trophic interactions are drivers of ecosystem change and stability, yet are often excluded from fishery assessment models, despite their potential capacity to improve estimates of species dynamics and future fishery sustainability. In Lake Ontario, recreational salmonine fisheries, including Chinook salmon ( Oncorhynchus tshawytscha ) and lake trout ( Salvelinus namaycush ), depend on a single prey species, alewife ( Alosa pseudoharengus ). To accommodate strong trophic interactions among species, we developed a multispecies statistical catch-at-age assessment (MSCAA) model that links the dynamics of the salmonine fisheries and alewife via prey consumption and predator growth. We found that prey availability had declined since 2015 due to decreased alewife recruitment and increased Chinook salmon biomass, leading to higher alewife mortality rates and lower predator growth rates. Forward projections of predator–prey dynamics suggest that Chinook salmon stocking reductions may improve the probability for alewife population growth, but could be counteracted by increased natural Chinook salmon recruitment. Combined with predator- and prey-monitoring efforts, multispecies assessments show promise as models of intermediate complexity to support a transition to ecosystem-based approaches to fisheries management.

Lake Ontario

Deepwater sculpin status and recovery in Lake Ontario

Deepwater sculpin are important in oligotrophic lakes as one of the few fishes that use deep profundal habitats and link invertebrates in those habitats to piscivores. In Lake Ontario the species was once abundant, however drastic declines in the mid-1900s led some to suggest the species had been extirpated and ultimately led Canadian and U.S. agencies to elevate the species' conservation status. Following two decades of surveys with no captures, deepwater sculpin were first caught in low numbers in 1996 and by the early 2000s there were indications of population recovery. We updated the status of Lake Ontario deepwater sculpin through 2016 to inform resource management and conservation. Our data set was comprised of 8431 bottom trawls sampled from 1996 to 2016, in U.S. and Canadian waters spanning depths from 5 to 225 m. Annual density estimates generally increased from 1996 through 2016, and an exponential model estimated the rate of population increase was ~ 59% per year. The mean total length and the proportion of fish greater than the estimated length at maturation (~ 116 mm) generally increased until a peak in 2013. In addition, the mean length of all deepwater sculpin captured in a trawl significantly increased with depth. Across all years examined, deepwater sculpin densities generally increased with depth, increasing sharply at depths > 150 m. Bottom trawl observations suggest the Lake Ontario deepwater sculpin population has recovered and current densities and biomass densities may now be similar to the other Great Lakes.

Journal of Great Lakes Research

Nearshore fish community

Lake Ontario’s nearshore fish community consists of a diverse assemblage of warm- and cool-water species. The “nearshore zone,” loosely separated from the “offshore zones” by the 15-m depth contour, consists of complex habitats spanning a gamut from vast open-coastal areas to sheltered embayments and wetlands. Lake Ontario’s nearshore habitat has been affected to varying degrees by human activities. Although many areas are relatively unimpaired, some are severely degraded and have been designated as Areas of Concern (AOCs) (http://www.ec.gc.ca/raps-pas/; http://www2.epa.gov/great-lakes-aocs).

Report

Nutrients, phytoplankton, zooplankton, and macrobenthos

Lower trophic levels support the prey fish on which most sport fish depend. Therefore, understanding the production potential of lower trophic levels is integral to the management of Lake Ontario’s fishery resources. Lower trophic-level productivity differs among offshore and nearshore waters. In the offshore, there is concern about the ability of the lake to support Alewife (Table 1) production due to a perceived decline in productivity of phytoplankton and zooplankton whereas, in the nearshore, there is a concern about excessive attached algal production (e.g., Cladophora) associated with higher nutrient concentrations—the oligotrophication of the offshore and the eutrophication of the nearshore (Mills et al. 2003; Holeck et al. 2008; Dove 2009; Koops et al. 2015; Stewart et al. 2016). Even though the collapse of the Alewife population in Lake Huron in 2003 (and the associated decline in the Chinook Salmon fishery) may have been precipitated by a cold winter (Dunlop and Riley 2013), Alewife had not returned to high abundances in Lake Huron as of 2014 (Roseman et al. 2015). Failure of the Alewife population to recover from collapse has been attributed to declines in lower trophic-level production (Barbiero et al. 2011; Bunnell et al. 2014; but see He et al. 2015). In Lake Michigan, concerns of a similar Alewife collapse led to a decrease in the number of Chinook Salmon stocked. If lower trophic-level production declines in Lake Ontario, a similar management action could be considered. On the other hand, in Lake Erie, which supplies most of the water in Lake Ontario, eutrophication is increasing and so are harmful algal blooms. Thus, there is also a concern that nutrient levels and algal blooms could increase in Lake Ontario, especially in the nearshore. Solutions to the two processes of concern—eutrophication in the nearshore and oligotrophication in the offshore—may be mutually exclusive. In either circumstance, fisheries management needs information on the productivity of lower trophic levels in Lake Ontario. In this chapter, we review the status of lower trophic levels in Lake Ontario with special attention to the current (2008-2013) and previous (2003-2007) reporting periods. During the two reporting periods, three whole-lake surveys of lower trophic levels were conducted: the Lower Trophic Level Assessment (LOLA) in 2003 and 2008 (Makarewicz and Howell 2012; Munawar et al. 2015b) and the Cooperative Science and Management Initiative (CSMI) in 2013. Analyses of the CSMI data are ongoing. In addition to the three one-year sources of information on lower trophic levels, several multi-year sources of information are available, including data from the surveillance program conducted since 1965 by Environment Canada (EC) (Dove 2009), monitoring conducted since 1980 by the U.S. Environmental Protection Agency’s (EPA) Great Lakes National Program Office (GLNPO) (Barbiero et al. 2014; Reavie et al. 2014), sampling for a Bioindex Program at two stations, one offshore and one in the Eastern Basin, assessments of Mysis diluviana (formerly Mysis relicta) conducted since 1980 by Fisheries and Oceans Canada (Johannsson et al. 1998, 2011) and the Ontario Ministry of Natural Resources and Forestry (OMNRF), and monitoring conducted since 1995 by the Biomonitoring Program (BMP) on the New York side of the lake (Holeck et al. 2015b). The BMP is a collaboration of the New York State Department of Environmental Conservation (DEC), U.S. Fish and Wildlife Service, U.S. Geological Survey (USGS), and Cornell University.

Special Publication

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

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

Population dynamics of Lake Ontario lake trout during 1985-2007

Lake trout Salvelinus namaycush were extirpated from Lake Ontario circa 1950 owing to commercial and recreational fishing, predation by sea lampreys Petromyzon marinus , and habitat degradation. Since the 1970s, substantial efforts have been devoted to reestablishing a self-sustaining population through stocking, sea lamprey control, and harvest reduction. Although a stocking-supported population has been established, only limited natural reproduction has been detected. Since the 1990s, surveys have indicated a continuing decline in overall abundance despite fairly static stocking levels. We constructed a statistical catch-at-age model to describe the dynamics of Lake Ontario lake trout from 1985 to 2007 and explore what factor(s) could be causing the declines in abundance. Model estimates indicated that abundance had declined by approximately 76% since 1985. The factor that appeared most responsible for this was an increase in age-1 natural mortality rates from approximately 0.9 to 2.5 between 1985 and 2002. The largest source of mortality for age-2 and older fish was sea lamprey predation, followed by natural and recreational fishing mortality. Exploitation was low, harvest levels being uncertain and categorized by length rather than age. Accurate predictions of fishery harvest and survey catch per unit effort were obtained despite low harvest levels by using atypical data (e.g., numbers stocked as an absolute measure of recruitment) and a flexible modeling approach. Flexible approaches such as this might allow similar assessments for a wide range of lightly exploited stocks. The mechanisms responsible for declining age-1 lake trout survival are unknown, but the declines were coincident with an increase in the proportion of stocked fish that were of the Seneca strain and a decrease in the overall stocking rate. It is possible that earlier studies suggesting that Seneca strain lake trout would be successful in Lake Ontario are no longer applicable given the large ecosystem changes that have occurred subsequent to invasion by dreissenid mussels.

North American Journal of Fisheries Management

Mysid and fish zooplanktivory in Lake Ontario: quantification of direct and indirect effects

Mysis relicta and planktivorous fish feed on zooplankton in Lake Ontario and form a trophic triangle that includes intraguild predation by fish on mysids. Thus, fish affect zooplankton both directly and indirectly. To evaluate the importance of alewife (Alosa pseudoharengus), rainbow smelt (Osmerus mordax), and mysids as zooplanktivores in Lake Ontario, we measured abundances and distributions, assessed diets, and computed mysid and fish consumption rates based on bioenergetics models. We further estimated indirect effects by comparing clearance rates given observed and potential mysid distributions. Estimated consumption rates varied widely with season and water depth and ranged between 2.6 x 10-3 and 1.3 gm-2day-1 for mysids and between 1.4 x 10-3 and 0.5 gm-2day-1 for fish, representing a daily removal of zooplankton of up to 10.2%-day-1 and 2.0%-day-1 by mysids and fish, respectively. Mysid planktivory exceeded fish planktivory in May and August, but fish planktivory dominated in October. Estimated mysid planktivory rates were 2- to 90-fold lower than the potential rate if mysids moved to temperatures that maximized their predation rates, suggesting an indirect positive effect of fish on zooplankton.

Canadian Journal of Fisheries and Aquatic Sciences