The Parker transects revisited: long-term herbaceous vegetation trends on Yellowstone's northern winter range
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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).
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.
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.
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.
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.
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.
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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.
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.
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.
No abstract available.
Nonparametric regression analysis of historic flow and rainfall data was used to estimate declining flows in a river draining a large spring complex in northern Florida, USA. The analysis indicated that flow declined by an estimated 23 percent from 1900 to 2009. The rate of decline appeared to increase over time, from about 0.8 cubic foot per second per year during the period from 1930-1970, to about 1.1 cubic feet per second per year over the period from 1970-2009. The estimated decline for the period prior to 1980 is consistent with evidence indicating groundwater withdrawals to the east of the study area have diverted groundwater that formerly flowed toward the Ichetucknee River under predevelopment conditions.
Hydrographs of ground-water levels in Wisconsin display fluctuations in the potentiometric surface of confined and unconfined aquifers. The graphs are plotted from periodic (weekly or monthly) measurements and from continuous recording gage records. Two hundred and ten hydrographs having periods of record of at least 5 years between 1934 and 1981 are included. The water-level changes shown represent both natural fluctuations reflecting climatic control and declines or recovery brought about by pumping or cessation of pumping of ground water.
The water supplies of Wisconsin are the State's most valuable natural resource. Although the State has abundant water supplies to maintain the perennial flow of most streams, and to sustain large increases in municipal, agricultural, and industrial use in many areas, the available supply is not distributed equally throughout the State, either areally or in time. Intelligent development of all water resources depends on knowledge of the occurrence, distribution and movement of water, the amount of discharge to and from a region, the interrelationship of ground and surface water, and the quantity and quality of the water available.
The USGS Great Lakes Science Center (GLSC) conducted acoustic/midwater trawl surveys of Lake Huron during 1997 and annually during 2004-2012. The 2012 survey was conducted during September and October, and included transects in Lake Huron’s Main Basin, Georgian Bay, and North Channel. Pelagic fish density (638 fish/ha) was lower in 2012 compared to 2011, with density in 2012 only 34% of 2011. Total biomass in 2012 was 74% of the 2011 value. Alewife Alosa pseudoharengus remained nearly absent, and only one cisco Coregonus artedi was captured. Rainbow smelt Osmerus mordax density was only 31% of the 2011 density. Bloater Coregonus hoyi density was less than half the 2011 density, mostly as a result of lower density of small bloater. Density and biomass of large bloater in 2012 were similar to 2011 levels. During 2012 we observed significantly higher fish biomass in North Channel than in the Main Basin or Georgian Bay. Prey availability during 2013 will likely be similar to 2012. Lake Huron now has pelagic fish biomass similar to that observed in recent lakewide acoustic surveys of Lake Michigan and Lake Superior, but species composition differs in the three lakes. There is an increasing diversity and prevalence of native species gradient from Lake Michigan to Lake Superior, with Lake Huron being intermediate in the prevalence of native fish species like coregonines and emerald shiner Notropis atherinoides.
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 2013 fall bottom trawl survey was carried out between 25 October – 21 November 2013 and included all U.S. ports as well as Goderich, ON. The 2013 main basin prey fish biomass estimate for Lake Huron was 47 kilotonnes, less than half of the estimate in 2012 (97 Kt), and approximately 13 percent of the maximum estimate in the time series. The biomass etimate for YAO alewife in 2013 was lower than in 2012, remained much lower than levels observed before the crash in 2004, and populations were dominated by small fish. Estimated biomass of rainbow smelt also decreased and was the second lowest observed in the time series. Estimated YAO bloater biomass in Lake Huron was also reduced compared to 2012. YOY alewife, rainbow smelt, and bloater abundance and biomass increased over 2012. Biomass estimates for deepwater and slimy sculpins, trout-perch, ninespine stickleback, and round goby in 2013 were lower than in 2012 and remained low compared to historic estimates. Wild juvenile lake trout were captured again in 2013, suggesting that natural reproduction by lake trout continues to occur.
The Great Lakes Science Center (GLSC) 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 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 2008. 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 2008 was estimated at 8.27 kilotonnes (kt) (1 kt = 1000 metric tons), which was the smallest biomass estimate in the entire time series and 29% lower than the 2007 estimate. Lake-wide biomass of bloater in 2008 was estimated at 3.33 kt, which was the lowest estimate since 1977 and 38% lower than the 2007 estimate. Rainbow smelt lake-wide biomass equaled 0.89 kt, which was only 0.01 kt higher than 2007, which is the lowest estimate in the time series. Deepwater sculpin lake-wide biomass equaled 5.23 kt, which is the fourth straight year of declining biomass. The 2008 estimate is the second smallest in the time series, and 39% lower than the 2007 estimate. Slimy sculpin lake-wide biomass remained relatively high in 2008 (2.75 kt), increasing 25% over 2007. Ninespine stickleback lake-wide biomass equaled only 0.50 kt in 2008, which was 79% lower than the 2007 estimate. The final prey fish, exotic round goby, increased two orders of magnitude between 2007 and 2008, from 0.02 to 4.65 kt. Round gobies now represent 18% of the prey fish biomass. Burbot lake-wide biomass (0.91 kt in 2008) has remained fairly constant since 2002. Numeric density of age-0 yellow perch (i.e., < 100 mm) equaled 0.7 fish per ha, which is indicative of a relatively poor year-class. Lake-wide biomass of dreissenid mussels dropped precipitously in 2008, down to 9.47 kt, and a 96% decline from the 2007 biomass estimate. 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 2008 was 25.62 kt, which was the lowest observed since the survey began in 1973.