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L.M. Cowardin

Publications and source records attributed to L.M. Cowardin.

At least 19 recordsLinked to original sources

Indicators of wetland condition for the Prairie Pothole Region of the United States

We describe a study designed to evaluate the performance ofwetland condition indicators of the Prairie Pothole Region (PPR)of the north central United States. Basin and landscape scaleindicators were tested in 1992 and 1993 to determine theirability to discriminate between the influences of grasslanddominated and cropland dominated landscapes in the PPR. Pairedplots were selected from each of the major regions of the PPR.Among the landscape scale indicators tested, those most capableof distinguishing between the two landscapes were: 1) frequencyof drained wetland basins, 2) total length of drainage ditch perplot, 3) amount of exposed soil in the upland subject to erosion,4) indices of change in area of wetland covered by water, and5) number of breeding duck pairs. Basin scale indicators includingsoil phosphorus concentrations and invertebrate taxa richnessshowed some promise; however, plant species richness was the onlystatistically significant basin scale indicator distinguishinggrassland dominated from cropland dominated landscapes. Althoughour study found a number of promising candidate indicators, oneof our conclusions is that basin scale indicators present anumber of implementation problems, including: skill levelrequirements, site access denials, and recession of site accessby landowners. Alternatively, we suggest that the use oflandscape indicators based on remote sensing can be an effectivemeans of assessing wetland integrity.

Environmental Monitoring and Assessment

U.S. Fish and Wildlife Service 1979 wetland classification: A review

In 1979 the US Fish and Wildlife Service published and adopted a classification of wetlands and deepwater habitats of the United States. The system was designed for use in a national inventory of wetlands. It was intended to be ecologically based, to furnish the mapping units needed for the inventory, and to provide national consistency in terminology and definition. We review the performance of the classification after 13 years of use. The definition of wetland is based on national lists of hydric soils and plants that occur in wetlands. Our experience suggests that wetland classifications must facilitate mapping and inventory because these data gathering functions are essential to management and preservation of the wetland resource, but the definitions and taxa must have ecological basis. The most serious problem faced in construction of the classification was lack of data for many of the diverse wetland types. Review of the performance of the classification suggests that, for the most part, it was successful in accomplishing its objectives, but that problem areas should be corrected and modification could strengthen its utility. The classification, at least in concept, could be applied outside the United States. Experience gained in use of the classification can furnish guidance as to pitfalls to be avoided in the wetland classification process.

Vegetatio

How much habitat management is needed to meet mallard production objectives?

We used results from simulation models to demonstrate the benefit-cost ratios of habitat management to increase the number of mallard (Anas platyrhynchos) recruits produced. The models were applied to hypothetical 2-habitat landscapes comprised of managed and unmanaged habitat. Managed habitats were predator barrier fencing and CRP cover; unmanaged habitat was grassland. As the amount of managed cover increased, the production curve rose rapidly and leveled off. If 2 managed habitats are added to a landscape, the cover can compete for available nesting hens, thus negating the benefits of 1 of the covers. After converting benefits and costs to dollars, we determined the point at which maximum net benefit occurs. We present an equation that can be used to determine the maximum net benefit of a management treatment given the size of the breeding population and the values of costs and benefits. Our examples demonstrate that, on local areas, it is inefficient to spend money for habitat management once maximum net benefit has been attained. If desired production can not be attained efficiently on an area, the manager can invest effort on alternative areas with greater management potential. If recruitment is inadequate to maintain a stable population, managers should manage to increase recruitment before attempting to attract additional breeding pairs. If recruitment more than maintains the breeding population, managers should attempt to attract additional breeding pairs to the area.

Wildlife Society Bulletin

Breeding population inventories and measures of recruitment

In this chapter we review the techniques used to measure two important parameters of waterfowl populations, size of breeding population and recruitment. If waterfowl are to be managed toward goals defined in terms of population sizes such as those in the recently signed North American Waterfowl Management Plan (U.S. Fish and Wildlife Service [USFWS] and Canadian Wildlife Service [CWS] 1986), there must be some measure of population size for the various species. Waterfowl managers usually measure population size during the breeding season, although for some species and in some areas winter inventories may be used. Population size is a function of natality and mortality. Other chapters in this volume deal in detail with the biology of those processes. This chapter discusses procedural aspects of measurement and reviews some of the operational systems that have been used to estimate population size and recruitment, especially in North America.

Book chapter

Premigrational movements and behavior of young mallards and wood ducks in north-central Minnesota

Movements and behavior of 89 young mallards (Anas platyrhynchos) and 48 young wood ducks (Aix sponsa) were monitored on a 932-km2 study area in north-central Minnesota in late summer and fall, 1972-74, with telemetry, visual observation, and aerial surveys. Initial flights of both species were confined to the natal (brood) marsh; first flights away from the natal marsh occurred in the third week after fledging in both species. First flights of young mallards and wood ducks away from their natal marshes were not significantly different between the sexes (mallard, mean = 4.95 km for females and 5.83 km for males; wood ducks, mean = 2.31 km for females and 2.64 km for males). However, flights away from the brood marshes by wood ducks were significantly shorter than for mallards.As young mallards and wood ducks grew, their daytime use of the natal marshes decreased in an irregular pattern as both species began daily flights between day- and night-use areas. Locally reared mallards made longer daily flights between use areas than did wood ducks, but wood ducks changed use areas with greater frequency before 1 October. Despite often extensive movements, most locally reared mallards and wood ducks remained in the vicinity of their brood marshes throughout fall until migration.Movement of young birds to new habitat was not the result of random searching and thus fortuitous discovery of nearby areas. Instead, birds seemed to learn of new habitat and develop movement patterns by associating with other birds; locally reared young always moved in the company of flocks of conspecifics that included adults and older immatures.Differences in movement patterns between the sexes of young birds and between young and adult birds cause them to be differentially distributed by age and sex on and near the breeding grounds. These differences are ultimately reflected in the distribution of the hunter harvest. We have interpreted generalizations about such phenomena, developed from analysis of continent-wide mallard banding data, using our data obtained from individually marked birds. We document (a) greater distances moved by early than by late-hatched young in the postbreeding period before migration, (b) differential movement of age and sex cohorts that explains greater hunting mortality of young than adults and of females than males near natal marshes, (c) differences in length and timing of postbreeding movements of adult male mallards and the postfledging movements of immature male mallards that help explain the northerly continental recovery distribution of young males, and (d) differential timing and rate of movement by birds through harvest areas (early departure of males and some return of females to natal marshes after the beginning of hunting) that explain differences in the timing of hunting season recoveries. Behavioral differences between the age and sex cohorts in the fall waterfowl population on and near their breeding grounds in north-central Minnesota can explain observed differences in survival and recovery rates of adult and young birds.The behaviors observed suggest to us that restrictive harvest regulations such as small-area closure may have little or no local benefits at the breeding grounds because premigratory assemblages of birds make extensive movements. In particular, protection of postbreeding adult females and locally reared young might only occur by closing large areas or scheduling extreme delays in the season opening, neither of which may be compatible with equitably apportioning waterfowl harvest at higher latitudes. Additional research on the local effects of restrictive regulations, and on age- and sex-specific differences in the timing, rate, and direction of fall movements of postbreeding waterfowl is needed.

Fish and Wildlife Research

Applications of a simulation model to decisions in mallard management

A system comprising simulation models and data bases for habitat availability and nest success rates was used to predict results from a mallard (Anas platyrhynchos) management plan and to compare six management methods with a control. Individual treatments in the applications included land purchase for waterfowl production, wetland easement purchase, lease of uplands for waterfowl management, cropland retirement, use of no-till winter wheat, delayed cutting of alfalfa, installation of nest baskets, nesting island construction, and use of predator-resistant fencing.The simulations predicted that implementation of the management plan would increase recruits by 24%. Nest baskets were the most effective treatment, accounting for 20.4% of the recruits. No-till winter wheat was the second most effective, accounting for 5.9% of the recruits. Wetland loss due to drainage would cause an 11% loss of breeding population in 10 years.The models were modified to account for migrational homing. The modification indicated that migrational homing would enhance the effects of management. Nest success rates were critical contributions to individual management methods. The most effective treatments, such as nest baskets, had high success rates and affected a large portion of the breeding population.Economic analyses indicated that nest baskets would be the most economical of the three techniques tested. The applications indicated that the system is a useful tool to aid management decisions, but data are scarce for several important variables. Basic research will be required to adequately model the effect of migrational homing and density dependence on production. The comprehensive nature of predictions desired by managers will also require that production models like the one described here be extended to encompass the entire annual cycle of waterfowl.

Fish and Wildlife Technical Report

Some considerations in modeling the mallard life cycle

We outline a population model proposed to accommodate the full life cycle of the mallard (Anas platyrhynchos}. Events during the breeding season are better understood than events at other times of the year, but recent findings suggest the importance of phenomena away from the breeding grounds. Several processes are discussed relative to mallard population dynamics. Compensatory mortality is a poorly understood concept, but one that can overwhelm many other components of a population model. Diseases and environmental contaminants can inflict indirect as well as direct mortality and can reduce reproduction. They interact with numerous other variables in complex and yet unknown ways. Recent evidence of a wintering-ground effect on subsequent recruitment provides one avenue for modeling phenomena occurring at different times of the year. Finally, the role of heterogeneity among individuals is widely acknowledged but not fully appreciated. We illustrate with an example the importance of heterogenicity to population processes, including compensatory mortality.

Book chapter

Some considerations in modeling the mallard life cycle

We outline a population model proposed to accommodate the full life cycle of the mallard (Anas platyrhynchos). Events during the breeding season are better understood than events at other times of the year, but recent findings suggest the importance of phenomena away from the breeding grounds. Several processes are discussed relative to mallard population dynamics. Compensatory mortality is a poorly understood concept, but one that can overwhelm many other components of a population model. Diseases and environmental contaminants can inflict indirect as well as direct mortality and can reduce reproduction. They interact with numerous other variables in complex and yet unknown ways. Recent evidence of a wintering-ground effect on subsequent recruitment provides one avenue for modeling phenomena occurring at different times of the year. Finally, the role of heterogeneity among individuals is widely acknowledged but not fully appreciated. We illustrate with an example the importance of heterogeneity to population processes, including compensatory mortality.

Book chapter

Evaluation of a mallard productivity model

A stochastic model of mallard (Anas platyrhynchos) productivity has been developed over a 10-year period and successfully applied to several management questions. Here we review the model and describe some recent uses and improvements that increase its realism and applicability, including naturally occurring changes in wetland habitat, catastrophic weather events, and the migrational homing of mallards. The amount of wetland habitat influenced productivity primarily by affecting the renesting rate. Late snowstorms severely reduced productivity, whereas the loss of nests due to flooding was largely compensated for by increased renesting, often in habitats where hatching rates were better. Migrational homing was shown to be an important phenomenon in population modeling and should be considered when evaluating management plans.

Book chapter

Improving waterfowl production estimates: Results of a test in the prairie pothole region

The U.S. Fish and Wildlife Service in an effort to improve and standardize methods for estimating waterfowl production tested a new technique in the four-county Arrowwood Wetland Management District (WMD) for three years (1982-1984). On 14 randomly selected 10.36 km2 plots, upland and wetland habitat was mapped, classified, and digitized. Waterfowl breeding pairs were counted twice each year and the proportion of wetland basins containing water was determined. Pair numbers and habitat conditions were entered into a computer model developed by Northern Prairie Wildlife Research Center. That model estimates production on small federally owned wildlife tracts, federal wetland easements, and private land. Results indicate that production estimates were most accurate for mallards (Anas platyrhynchos), the species for which the computer model and data base were originally designed. Predictions for the pintail (Anas acuta), gadwall (A. strepa), blue-winged teal (A. discors), and northern shoveler (A. clypeata) were believed to be less accurate. Modeling breeding period dynamics of a waterfowl species and making credible production estimates for a geographic area are possible if the data used in the model are adequate. The process of modeling the breeding period of a species aids in locating areas of insufficient biological knowledge. This process will help direct future research efforts and permit more efficient gathering of field data.

International Congress of Game Biologists

Classification of wetlands and deepwater habitats of the United States

This classification, to be used in a new inventory of wetlands and deepwater habitats of the United States, is intended to describe ecological taxa, arrange them in a system useful to resource managers, furnish units for mapping, and provide uniformity of concepts and terms. Wetlands are defined by plants (hydrophytes), soils (hydric soils), and frequency of flooding. Ecologically related areas of deep water, traditionally not considered wetlands, are included in the classification as deepwater habitats.Systems form the highest level of the classification hierarchy; five are defined-Marine, Estuarine, Riverine, Lacustrine, and Palustrine. Marine and Estuarine Systems each have two Subsystems, Subtidal and Intertidal; the Riverine System has four Subsystems, Tidal, Lower Perennial, Upper Perennial, and Intermittent; the Lacustrine has two, Littoral and Limnetic; and the Palustrine has no Subsystems.Within the Subsystems, Classes are based on substrate material and flooding regime, or on vegetative life form. The same Classes may appear under one or more of the Systems or Subsystems. Six Classes are based on substrate and flooding regime: (1) Rock Bottom with a substrate of bedrock, boulders, or stones; (2) Unconsolidated Bottom with a substrate of cobbles, gravel, sand, mud, or organic material; (3) Rocky Shore with the same substrates as Rock Bottom; (4) Unconsolidated Shore with the same substrates as Unconsolidated Bottom; (5) Streambed with any of the substrates; and (6) Reef with a substrate composed of the living and dead remains of invertebrates (corals, mollusks, or worms). The bottom Classes, (1) and (2) above, are flooded all or most of the time and the shore Classes, (3) and (4), are exposed most of the time. The Class Streambed is restricted to channels of intermittent streams and tidal channels that are dewatered at low tide. The life form of the dominant vegetation defines the five Classes based on vegetative form: (1) Aquatic Bed, dominated by plants that grow principally on or below the surface of the water; (2) Moss-Lichen Wetland, dominated by mosses or lichens; (3) Emergent Wetland, dominated by emergent herbaceous angiosperms; (4) Scrub-Shrub Wetland, dominated by shrubs or small trees; and (5) Forested Wetland, dominated by large trees.The Dominance Type, which is named for the dominant plant or animal forms, is the lowest level of the classification hierarchy. Only examples are provided for this level; Dominance Types must be developed by individual users of the classification.Modifying terms applied to the Classes or Subclasses are essential for use of the system. In tidal areas, the type and duration of flooding are described by four Water Regime Modifiers: subtidal, irregularly exposed, regularly flooded, and irregularly flooded. In nontidal areas, eight Regimes are used: permanently flooded, intermittently exposed, semipermanently flooded, seasonally flooded, saturated, temporarily flooded, intermittently flooded, and artificially flooded. A hierarchical system of Water Chemistry Modifiers, adapted from the Venice System, is used to describe the salinity of the water. Fresh waters are further divided on the basis of pH. Use of a hierarchical system of soil modifiers taken directly from U.S. soil taxonomy is also required. Special modifiers are used where appropriate: excavated, impounded, diked, partly drained, farmed, and artificial.Regional differences important to wetland ecology are described through a regionalization that combines a system developed for inland areas by R. G. Bailey in 1976 with our Marine and Estuarine provinces.The structure of the classification allows it to be used at any of several hierarchical levels. Special data required for detailed application of the system are frequently unavailable, and thus data gathering may be prerequisite to classification. Development of rules by the user will be required for specific map scales. Dominance Types and relationships of plant and anima

FWS/OBS

Characteristics of central North Dakota wetlands determined from sample aerial photographs and ground study

Wetland characteristics were assessed from a systematic sample of 66 plots, 3.22 km2 each, drawn from a 10,041-km2 study area in central North Dakota. Each plot was visited once and 8 sets of aerial photographs were obtained in 3 years. Density of wetland basins was 11.00 ha/km2, and area averaged 9.7 ha/km2. Seasonal and temporary wetlands were most abundant; semipermanent wetlands occupied the greatest area. Basin size was positively correlated with water permanence. Discriminant function analysis based on size and an index to wetness derived from photographs misclassified 33% of the wetland basins. Forty percent of the wetlands were tilled. Photography of sample plots is potentially useful for determining number of basins and wetland area, but precise classification of plant communities in this region would require ground study.

Wildlife Society Bulletin

Mathematics and mallard management

Waterfowl managers can effectively use simple population models to aid in making management decisions. We present a basic model of the change in population size as related to survival and recruitment. A management technique designed to increase survival of mallards (Anas platyrhynchos) by limiting harvest on the Chippewa National Forest, Minnesota, is used to illustrate the application of models in decision making. The analysis suggests that the management technique would be of limited effectiveness. In a 2nd example, the change in mallard population in central North Dakota is related to implementing programs to create dense nesting cover with or without supplementary predator control. The analysis suggests that large tracts of land would be required to achieve a hypothetical management objective of increasing harvest by 50% while maintaining a stable population. Less land would be required if predator reduction were used in combination with cover management, but questions about effectiveness and ecological implications of large scale predator reduction remain unresolved. The use of models as a guide to planning research responsive to the needs of management is illustrated.

Journal of Wildlife Management