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Status and trends of pelagic prey fish in Lake Huron, 2013

The USGS Great Lakes Science Center (GLSC) conducted acoustic and midwater trawl surveys of Lake Huron during 1997 and annually during 2004-2013. The 2013 survey was conducted during September and October and included transects in Lake Huron’s main basin, Georgian Bay, and North Channel. Pelagic fish density was 1,033 fish/ha in 2013 and increased 62% over the 2012 estimate. Total biomass in 2013 (6.07 kg/ha) was similar to the 2012 estimate (6.97 kg/ha). Mean numeric density of alewife Alosa pseudoharengus was substantially greater in 2013 than in 2012, but the 2013 estimate has low precision. Age-0 rainbow smelt Osmerus mordax abundance increased from 2012, whereas age-1+ rainbow smelt decreased. Age-0 bloater Coregonus hoyi abundance increased over 2012 estimates. Density and biomass of large bloater in 2013 was similar to 2012 levels. Emerald shiner Notropis atherinoides density and biomass increased during 2013. Two adult cisco Coregonus artedi were captured in Georgian Bay. Based on comparable biomass estimates during 2012 and 2013, prey fish availability during 2014 will likely be similar to 2013. Lake Huron has pelagic fish biomass similar to that observed in recent lake-wide acoustic surveys of Lake Michigan and Lake Superior, but species composition differs in the three lakes. There is an increasing gradient of diversity and native species occurrence from Lake Michigan to Lake Superior, with Lake Huron being intermediate in the prevalence of native fish species like coregonines and emerald shiner.

Lake Huron↗

Constraining rates and trends of historical wetland loss, Mississippi River Delta Plain, south-central Louisiana

The timing, magnitude, and rate of wetland loss were described for five wetland-loss hotspots in the Terrebonne Basin of the Mississippi River delta plain. Land and water areas were mapped for 34 dates between 1956 and 2004 from historical National Wetlands Inventory (NWI) datasets, aerial photographs, and Landsat Thematic Mapper (TM) satellite images. Since 1956, the emergent land area at the five study areas in south-central Louisiana has decreased by about 50%. Comparison of the water-area curve derived from the 29 TM images with water-level records from the nearby Grand Isle, Louisiana tide gauge (NOS #8761724) clearly shows that changes in land and water areas fluctuate in response to variations in regional water levels. The magnitude of water-area fluctuations decreased from the 1980s to the 1990s as former areas of wet marsh within and immediately adjacent to the wetland-loss hotspots became permanently submerged. The most rapid wetland loss occurred during the late 1960s and 1970s. Peak wetland-loss rates during this period were two to four times greater than both the pre-1970s background rates and the most recent wetland-loss rates. These results provide constraints on predicting future delta-plain wetland losses and identify Landsat TM imagery as an important source for analyzing land- and water-area changes across the entire delta plain.

Louisiana↗

Status and trends in the Lake Superior fish community, 2014

In 2014, the Lake Superior fish community was sampled with daytime bottom trawls at 73 nearshore and 30 offshore stations. Spring and summer water temperatures were the coldest measured for the period of records for the surveys. In the nearshore zone, a total of 15,372 individuals from 28 species or morphotypes were collected. Nearshore lakewide mean biomass was 6.9 kg/ha, which was higher than that observed in the past few years, but below the long-term average of 9.2 kg/ha. In the offshore zone, a total 12,462 individuals from 11 species were collected lakewide. Offshore lakewide mean biomass was 6.6 kg/ha. The mean of the three previous years was 8.6 kg/ha. We collected larval Coregonus in surface trawls at 94 locations and estimated a lakewide average density of 577 fish/ha with a total lakewide population estimate of 14.2 billion (standard error + 30 million).

Lake Superior↗

Global trends in emerging viral diseases of wildlife origin

Fifty years ago, infectious diseases were rarely considered threats to wildlife populations, and the study of wildlife diseases was largely a neglected endeavor. Furthermore, public health leaders at that time had declared that “it is time to close the book on infectious diseases and the war against pestilence won,” a quote attributed to Dr. William H. Stewart in 1967. There is some debate whether he actually said these words; however, they reflect the widespread belief at that time (Spellberg, 2008). Leap forward to today, and the book on infectious diseases has been dusted off. There is general consensus that the global environment favors the emergence of infectious diseases, and in particular, diseases of wildlife origin (Taylor et al., 2001). Examples of drivers of these infectious diseases include climate and landscape changes, human demographic and behavior changes, global travel and trade, microbial adaptation, and lack of appropriate infrastructure for wildlife disease control and prevention (Daszak et al., 2001). The consequences of these emerging diseases are global and profound with increased burden on the public health system, negative impacts on the global economy and food security, declines and extinctions of wildlife species, and subsequent loss of ecosystem integrity. For example, 35 million people are currently living with HIV infection globally (http://www.who.int/gho/hiv/en); 400 million poultry have been culled since 2003 as a result of efforts to control highly pathogenic H5N1 avian influenza (http://www.fao.org/avianflu/en/index.html), and there are increasing biological and ecological consequences. Examples of health threats to biodiversity include the “spillover” of human diseases to great ape populations (Köndgen et al., 2008), the near-extirpation of the black-footed ferret from canine distemper and sylvatic plague (for a review see Abbott et al., 2012), and threats to Hawaiian forest birds from introduced pathogens such as avian malaria and avian pox (van Riper et al., 1986, 2002). There are also newly discovered pathogens or diseases that have resulted in population declines, and global extinctions of several species. Examples include Batrachochytrium dendrobatidis, which causes a cutaneous fungal infection of amphibians and is linked to declines of amphibians globally (Kriger and Hero, 2009); and recently discovered Pseudogymnoascus (Geomyces) destructans, the etiologic agent of white-nose syndrome (WNS), which has caused precipitous declines of North American bat species (Blehert et al., 2009). Furthermore, there is increasing evidence of the subsequent impacts on human and ecosystem health; for example, increasing risk of exposure to Lyme disease as a consequence of decreased biodiversity (LoGiudice et al., 2003) as well as the economic cost of the loss of bats due to decreased insect control services (Boyles et al., 2011). Figure A12-1 is a timeline of important diseases investigated by the U.S. Geological Survey since the 1970s, which illustrates three factors: 1. The unprecedented emergence of new pathogens and geographic spread of known pathogens since the 1990s; 2. Diseases are increasingly causing large-scale, negative impacts on wildlife populations and spreading over larger geographic areas rather than remaining localized; and 3. Diseases are increasingly of concern for multiple sectors, including public health, agriculture and wildlife management agencies. Of increasing concern are these novel diseases such as WNS as they are hard to anticipate, particularly devastating to human health or wildlife populations, challenging to manage, spread over large geographic areas in short time periods, and may result in ecological ripple effects that are difficult to predict. The following article provides examples of recently emerged viral diseases of wildlife origin. The examples have been selected to illustrate the drivers of emerging viral diseases, both novel pathogens and previously known diseases, the impacts of these diseases, as well as the role of wildlife both as “villains” or reservoirs as well as “victims” of these viral diseases. The article also discusses potential management strategies for emerging viral diseases in wildlife populations and future science directions in wildlife health to prevent, prepare, respond to, and recover from these disease events. Finally, the concept of One Health and its potential role in developing solutions to these issues of mutual concern is discussed.

Conference Paper↗

Climate trends and projections for Guam

The island of Guam experiences a tropical marine climate, which is warm and humid moderated by seasonal tradewinds and a wet and dry season. The dry season lasts from January to June, while the rainy months are from July to December. Annual rainfall totals 84-116 inches (2133-2946 mm), of which two-thirds fall during the rainy season. Seasonal temperatures and precipitation are also affected by the El-Niño Southern Oscillation (ENSO) and tropical cyclones, which cause the largest deviations from average precipitation. An average of three tropical storms and one typhoon pass within 80 nautical miles of Guam each year, and both flooding and drought can impact freshwater supply management and associated infrastructure.

Report↗

Corpus Christi, Nueces, and Aransas Bays: Chapter C in Emergent wetlands status and trends in the northern Gulf of Mexico: 1950-2010

Corpus Christi Bay and Nueces Bay comprise the middle estuarine portion of Texas’ Coastal Bend region (Figure 1; Burgan and Engle, 2006). Aransas Bay is part of the upper estuarine portion of the region. These bays make up part of the Coastal Bend Bays and Estuaries Program, one of the many estuarine areas in the U.S. Environmental Protection Agency’s National Estuary Program (Holt, 1998). The Coastal Bend region is sub-humid and sub-tropical. Summers are long, hot, and humid, and winters are short and mild. The landscape around the estuaries is dominated by row crops, pastures, and brushy rangeland (Handley and others, 2007). The Nueces River, along with other smaller rivers and creeks, provides freshwater inflow - along with essential nutrients and sediment - into Nueces Bay, which feeds into Corpus Christi Bay (Holt, 1998). Freshwater inflow into the Aransas Bay comes from Mission River, Aransas River, and Copano Creek. The region is relatively dry otherwise and prone to droughts. Corpus Christi receives an average of 76.2 cm (30 in) of rain annually; evaporation usually exceeds 177.8 cm (70 in) (Holt, 1998; Handley and others, 2007). The San Antonio-Nueces Coastal Basin drains into Aransas Bay. The Nueces River basin covers 43,253 km 2 (16,700 miles 2 ), from northwest of San Antonio, flowing southeast to where it drains into Nueces and Corpus Christi Bays (Holt, 1998). The Nueces-Rio Grande basin covers approximately 18,648 km 2 (7,200 miles 2 ) and flows partially into Corpus Christi Bay (as well as the upper Laguna Madre). The inflow from Nueces River has declined by approximately 20 percent over the past several decades, partly due to construction of lakes and reservoirs, particularly Lake Corpus Christi and Choke Canyon reservoir. The Corpus Christi Estuary receives approximately 35 percent of the total freshwater inflow of 1,480,178,205 cubic meters (m 3 ) (1.2 million acre-feet) in the region; the Aransas Estuary receives about 53 percent. Tidal range is only 0.46 m (1.5 ft) on the Gulf shoreline and 0.15 m (0.5 ft) in Nueces Bay. Strong winds are the primary force behind water circulation in the Coastal Bend estuaries.

Texas↗

Galveston Bay: Chapter D in Emergent wetlands status and trends in the northern Gulf of Mexico: 1950-2010

The Galveston Bay estuary is located on the upper Texas Gulf coast (Lester and Gonzalez, 2002). It is composed of four major sub-bays - Galveston, Trinity, East, and West Bays. It is Texas’ largest estuary on the Gulf Coast with a total area of 155,399 hectares (384,000 acres) and 1,885 km (1,171 miles) of shoreline (Burgan and Engle, 2006). The volume of the bay has increased over the past 50 years due to subsidence, dredging, and sea level rise. Outside of ship channels, the maximum depth is only 3.7 m (12 ft), with the average depth ranging from 1.2 m (4 ft) to 2.4 m (8 ft) - even shallower in areas with widespread oyster reefs (Lester and Gonzalez, 2002). The tidal range is less than 0.9 m (3 ft), but water levels and circulation are highly influenced by wind. The estuary was formed in a drowned river delta, and its bayous were once channels of the Brazos and Trinity Rivers. Today, the watersheds surrounding the Trinity and San Jacinto Rivers, along with many other smaller bayous, feed into the bay. The entire Galveston Bay watershed is 85,470 km 2 (33,000 miles 2 ) large (Figure 1). Galveston Island, a 5,000 year old sand bar that lies at the western edge of the bay’s opening into the Gulf of Mexico, impedes the freshwater flow of the Trinity and San Jacinto Rivers into the Gulf, the majority of which comes from the Trinity. The Bolivar Peninsula lies at the eastern edge of the bay’s opening into the Gulf. Water flows into the Gulf at Bolivar Roads, 1 U.S. Geological Survey National Wetlands Research Center, 700 Cajundome Blvd., Lafayette, LA 70506 2 Harte Research Institute for Gulf of Mexico Studies, Texas A&M University - Corpus Christi, 6300 Ocean Drive, Unit 5869, Corpus Christi, Texas 78412 2 Galveston Pass, between Galveston Island and Bolivar Peninsula, and at San Luis Pass, between the western side of Galveston Island and Follets Island.

Texas↗

Status and trends of prey fish populations in Lake Michigan, 2013

The U.S. Geological Survey Great Lakes Science Center has conducted lake-wide surveys of the fish community in Lake Michigan each fall since 1973 using standard 12-m bottom trawls towed along contour at depths of 9 to 110 m at each of seven index transects. The resulting data on relative abundance, size and age structure, and condition of individual fishes are used to estimate various population parameters that are in turn used by state and tribal agencies in managing Lake Michigan fish stocks. All seven established index transects of the survey were completed in 2013. The survey provides relative abundance and biomass estimates between the 5-m and 114-m depth contours of the lake (herein, lake-wide) for prey fish populations, as well as burbot, yellow perch, and the introduced dreissenid mussels. Lake-wide biomass of alewives in 2013 was estimated at 29 kilotonnes (kt, 1 kt = 1000 metric tonnes), which was more than three times the 2012 estimate. However, the unusually high standard error associated with the 2013 estimate indicated no significant increase in lake-wide biomass between 2012 and 2013. Moreover, the age distribution of alewives remained truncated with no alewife exceeding an age of 5. The population of age-1 and older alewives was dominated (i.e., 88%) by the 2010 and 2012 year-classes. Record low biomass was observed for deepwater sculpin (1.3 kt) and ninespine stickleback (0.004 kt) in 2013, while bloater (1.6 kt) and rainbow smelt (0.2 kt) biomasses remained at low levels. Slimy sculpin lake-wide biomass was 0.32 kt in 2013, marking the fourth consecutive year of a decline. The 2013 biomass of round goby was estimated at 10.9 kt, which represented the peak estimate to date. Burbot lake-wide biomass (0.4 kt in 2013) has remained below 3 kt since 2001. Numeric density of age-0 yellow perch (i.e., < 100 mm) was only 1 fish per ha, which is indicative of a relatively poor year-class. Lake-wide biomass estimate of dreissenid mussels in 2013 was 23.2 kt. Overall, the total lake-wide prey fish biomass estimate (sum of alewife, bloater, rainbow smelt, deepwater sculpin, slimy sculpin, round goby, and ninespine stickleback) in 2013 was 43 kt, with alewives and round gobies constituting 92% of this total.

Lake Michigan↗

Trends in fishery agency assessments of black bass tournaments in the southeastern United States

Studies conducted during the last 30 years have identified benefits and adverse impacts and have documented increased frequency of fishing tournaments. This study used information provided by state fisheries management agency administrators to measure the frequency of black bass (Micropterus spp.) tournaments in southeastern states and assessed how reported changes in tournament frequency have impacted fisheries management. The average annual number of black bass tournaments reported by 14 southeastern states for 2009-2011 was 41,939, which was a 124% increase from the average annual number of tournaments for all freshwater species reported by southeastern states for 2002-2004. Despite this considerable increase, agencies reported that tournaments were generally beneficial. The highest ranking benefit factors (developed from factor analysis of 21 potential benefits) were unchanged from the same survey administered in 2005 and included the benefits of promotion of fishing, specific fisheries, and agency programs. Similarly, the highest ranking adverse-impact factors developed from 29 potential problems (resource overuse and user-group conflicts) were also consistent with the 2005 survey. Black bass tournaments offer benefits to fisheries management that could be better realized. The persistence and consistently high impact ratings of resource overuse and user-group conflicts along with generally low incidence of monitoring tournaments suggests that the negative impacts have become part of contemporary recreational fishing and are not problems that require management solutions.

Southeastern states↗

Status and trends of the Lake Huron offshore demersal fish community, 1976-2012

The USGS Great Lakes Science Center has conducted trawl surveys to assess annual changes in the offshore demersal fish community of Lake Huron since 1973. Sample sites include five ports in U.S. waters with less frequent sampling near Goderich, Ontario. The 2012 fall bottom trawl survey was carried out between 20 October – 5 November 2012 and included all U.S. ports as well as Goderich, ON. The 2012 main basin prey fish biomass estimate for Lake Huron was 97 kilotonnes, higher than the estimate in 2011 (63.2 Kt), approximately one third of the maximum estimate in the time series, and nearly 6 times higher than the minimum estimate in 2009. The biomass estimates for adult alewife in 2012 were higher than 2011, but remained much lower than observed before the crash in 2004, and populations were dominated by small fish. Estimated biomass of rainbow smelt also increased and was the highest observed since 2005. Estimated adult bloater biomass in Lake Huron has been increasing in recent years, and the 2012 biomass estimate was the third highest ever observed in the survey. Biomass estimates for trout-perch and ninespine stickleback were higher than in 2011 but still remained low compared to historic estimates. The estimated biomass of deepwater and slimy sculpins increased over 2011, and slimy sculpin in particular seem to be increasing in abundance. The 2012 biomass estimate for round goby was similar to that in 2011 and was the highest observed in the survey. Substantial numbers of wild juvenile lake trout were captured again in 2012, suggesting that natural reproduction by lake trout continues to occur. The 2012 Lake Huron bottom trawl survey results suggest that several species of offshore demersal fish are beginning to increase in abundance.

Michigan↗

Temporal and basin-specific population trends of quagga mussels on soft sediment of a multi-basin reservoir

Invasive quagga (Dreissena bugnesis) and zebra (Dreissena ploymorpha) mussels have rapidly spread throughout North America. Understanding the relationships between environmental variables and quagga mussels during the early stages of invasion will help management strategies and allow researchers to predict patterns of future invasions. Quagga mussels were detected in Lake Mead, NV/AZ in 2007, we monitored early invasion dynamics in 3 basins (Boulder Basin, Las Vegas Bay, Overton Arm) bi-annually from 2008-2011. Mean quagga density increased over time during the first year of monitoring and stabilized for the subsequent two years at the whole-lake scale (8 to 132 individuals·m-2, geometric mean), in Boulder Basin (73 to 875 individuals·m-2), and in Overton Arm(2 to 126 individuals·m-2). In Las Vegas Bay, quagga mussel density was low (9 to 44 individuals·m-2), which was correlated with high sediment metal concentrations and warmer (> 30°C) water temperatures associated with that basin. Carbon content in the sediment increased with depth in Lake Mead and during some sampling periods quagga density was also positively correlated with depth, but more research is required to determine the significance of this interaction. Laboratory growth experiments suggested that food quantity may limit quagga growth in Boulder Basin, indicating an opportunity for population expansion in this basin if primary productivity were to increase, but was not the case in Overton Arm. Overall quagga mussel density in Lake Mead is highly variable and patchy, suggesting that temperature, sediment size, and sediment metal concentrations, and sediment carbon content all contribute to mussel distribution patterns. Quagga mussel density in the soft sediment of Lake Mead expanded during initial colonization, and began to stabilize approximately 3 years after the initial invasion.

Book chapter↗