EcoService Models Library (ESML)
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Compare EMs
Which comparison is best for me?EM Variables by Variable Role
One quick way to compare ecological models (EMs) is by comparing their variables. Predictor variables show what kinds of influences a model is able to account for, and what kinds of data it requires. Response variables show what information a model is capable of estimating.
This first comparison shows the names (and units) of each EM’s variables, side-by-side, sorted by variable role. Variable roles in ESML are as follows:
- Predictor Variables
- Time- or Space-Varying Variables
- Constants and Parameters
- Intermediate (Computed) Variables
- Response Variables
- Computed Response Variables
- Measured Response Variables
EM Variables by Category
A second way to use variables to compare EMs is by focusing on the kind of information each variable represents. The top-level categories in the ESML Variable Classification Hierarchy are as follows:
- Policy Regarding Use or Management of Ecosystem Resources
- Land Surface (or Water Body Bed) Cover, Use or Substrate
- Human Demographic Data
- Human-Produced Stressor or Enhancer of Ecosystem Goods and Services Production
- Ecosystem Attributes and Potential Supply of Ecosystem Goods and Services
- Non-monetary Indicators of Human Demand, Use or Benefit of Ecosystem Goods and Services
- Monetary Values
Besides understanding model similarities, sorting the variables for each EM by these 7 categories makes it easier to see if the compared models can be linked using similar variables. For example, if one model estimates an ecosystem attribute (in Category 5), such as water clarity, as a response variable, and a second model uses a similar attribute (also in Category 5) as a predictor of recreational use, the two models can potentially be used in tandem. This comparison makes it easier to spot potential model linkages.
All EM Descriptors
This selection allows a more detailed comparison of EMs by model characteristics other than their variables. The 50-or-so EM descriptors for each model are presented, side-by-side, in the following categories:
- EM Identity and Description
- EM Modeling Approach
- EM Locations, Environments, Ecology
- EM Ecosystem Goods and Services (EGS) potentially modeled, by classification system
EM Descriptors by Modeling Concepts
This feature guides the user through the use of the following seven concepts for comparing and selecting EMs:
- Conceptual Model
- Modeling Objective
- Modeling Context
- Potential for Model Linkage
- Feasibility of Model Use
- Model Certainty
- Model Structural Information
Though presented separately, these concepts are interdependent, and information presented under one concept may have relevance to other concepts as well.
EM Identity and Description
EM ID
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
EM Short Name
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Cultural ES and plant traits, Central French Alps | Pollination ES, Central French Alps | RHyME2, Upper Mississippi River basin, USA | PATCH, western USA | Birds in estuary habitats, Yaquina Estuary, WA, USA | Yasso07 v1.0.1, Switzerland, site level | EnviroAtlas - Restorable wetlands | Grasshopper Sparrow density, CREP, Iowa, USA | Alwife phosphorus flux in lakes, Connecticut, USA | Estuary recreational use, Cape Cod, MA | Gadwall duck recruits, CREP wetlands, Iowa, USA | Seed mix for native plant establishment, IA, USA | Seed mix and mowing in prairie reconstruction, USA | Plant-pollinator networks at reclaimed mine, USA | Recreational fishery index, USA | Valuing environmental ed., New York, New York | Co$ting Nature model method |
EM Full Name
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Cultural ecosystem service estimated from plant functional traits, Central French Alps | Pollination ecosystem service estimated from plant functional traits, Central French Alps | RHyME2 (Regional Hydrologic Modeling for Environmental Evaluation), Upper Mississippi River basin, USA | PATCH (Program to Assist in Tracking Critical Habitat), western USA | Bird use of estuarine habitats, Yaquina Estuary, WA, USA | Yasso07 v1.0.1 forest litter decomposition, Switzerland, site level | US EPA EnviroAtlas - Percent potentially restorable wetlands, USA | Grasshopper Sparrow population density, CREP (Conservation Reserve Enhancement Program) wetlands, Iowa, USA | Net phosphorus flux in freshwater lakes from alewives, Connecticut, USA | Estuary recreational use, Cape Cod, MA | Gadwall duck recruits, CREP (Conservation Reserve Enhancement Program) wetlands, Iowa, USA | Cost-effective seed mix design for native plant establishment, Iowa, USA | Seed mix design and first year management in prairie reconstruction, IA, USA | Restoration of plant-pollinator networks at reclaimed strip mine, Ohio, USA | Recreational fishery index for streams and rivers, USA | Valuing environmental education, Hudson River Park, New York, New York | Co$ting Nature model method |
EM Source or Collection
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EU Biodiversity Action 5 | EU Biodiversity Action 5 | US EPA | US EPA | US EPA | None | US EPA | EnviroAtlas | None | None | US EPA | None | None | None | None | US EPA | None | None |
EM Source Document ID
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260 | 260 | 123 | 2 | 275 | 343 | 262 | 372 | 383 | 387 |
372 ?Comment:Document 373 is a secondary source for this EM. |
394 | 395 | 397 | 414 | 416 | 466 |
Document Author
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Lavorel, S., Grigulis, K., Lamarque, P., Colace, M-P, Garden, D., Girel, J., Pellet, G., and Douzet, R. | Lavorel, S., Grigulis, K., Lamarque, P., Colace, M-P, Garden, D., Girel, J., Pellet, G., and Douzet, R. | Tran, L. T., O’Neill, R. V., Smith, E. R., Bruins, R. J. F. and Harden, C. | Carroll, C, Phillips, M. K. , Lopez-Gonzales, C. A and Schumaker, N. H. | Frazier, M. R., Lamberson, J. O. and Nelson, W. G. | Didion, M., B. Frey, N. Rogiers, and E. Thurig | US EPA Office of Research and Development - National Exposure Research Laboratory | Otis, D. L., W. G. Crumpton, D. Green, A. K. Loan-Wilsey, R. L. McNeely, K. L. Kane, R. Johnson, T. Cooper, and M. Vandever | West, D. C., A. W. Walters, S. Gephard, and D. M. Post | Mulvaney, K K., Atkinson, S.F., Merrill, N.H., Twichell, J.H., and M.J. Mazzotta | Otis, D. L., W. G. Crumpton, D. Green, A. K. Loan-Wilsey, R. L. McNeely, K. L. Kane, R. Johnson, T. Cooper, and M. Vandever | Meissen, J. | Meissen, J. C., A. J. Glidden, M. E. Sherrard, K. J. Elgersma, and L. L. Jackson | Cusser, S. and K. Goodell | Lomnicky. G.A., Hughes, R.M., Peck, D.V., and P.L. Ringold | Hutcheson, W. Hoagland, P., and D. Jin | Mulligan, M. |
Document Year
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2011 | 2011 | 2013 | 2006 | 2014 | 2014 | 2013 | 2010 | 2010 | 2019 | 2010 | 2018 | 2019 | 2013 | 2021 | 2018 | None |
Document Title
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Using plant functional traits to understand the landscape distribution of multiple ecosystem services | Using plant functional traits to understand the landscape distribution of multiple ecosystem services | Application of hierarchy theory to cross-scale hydrologic modeling of nutrient loads | Defining recovery goals and strategies for endangered species: The wolf as a case study | Intertidal habitat utilization patterns of birds in a Northeast Pacific estuary | Validating tree litter decomposition in the Yasso07 carbon model | EnviroAtlas - National | Assessment of environmental services of CREP wetlands in Iowa and the midwestern corn belt | Nutrient loading by anadromous alewife (Alosa pseudoharengus): contemporary patterns and predictions for restoration efforts | Quantifying Recreational Use of an Estuary: A case study of three bays, Cape Cod, USA | Assessment of environmental services of CREP wetlands in Iowa and the midwestern corn belt | Cost-effective seed mix design and first-year management | Seed mix design and first year management influence multifunctionality and cost-effectiveness in prairie reconstruction | Diversity and distribution of floral resources influence the restoration of plant-pollinator networks on a reclaimed strip mine | Correspondence between a recreational fishery index and ecological condition for U.S.A. streams and rivers. | Valuing environmental education as a cultural ecosystem service at Hudson River Park | Conservation prioritisation and Ecostystem services mapping with Co$ting Nature |
Document Status
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Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed but unpublished (explain in Comment) | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Peer reviewed and published | Other or unclear (explain in Comment) |
Comments on Status
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Published journal manuscript | Published journal manuscript | Published journal manuscript | Published journal manuscript | Published journal manuscript | Published journal manuscript | Published on US EPA EnviroAtlas website | Published report | Published journal manuscript | Draft manuscript-work progressing | Published report | Published report | Published journal manuscript | Published journal manuscript | Published journal manuscript | Published journal manuscript | Web page so cannot tell if documentation is reviewed |
EM ID
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | http://en.ilmatieteenlaitos.fi/yasso-download-and-support | https://www.epa.gov/enviroatlas | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | http://www1.policysupport.org/cgi-bin/ecoengine/start.cgi?project=costingnature&version=3 | |
Contact Name
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Sandra Lavorel | Sandra Lavorel | Liem Tran | Carlos Carroll |
M. R. Frazier ?Comment:Present address: M. R. Frazier National Center for Ecological Analysis and Synthesis, 735 State St. Suite 300, Santa Barbara, CA 93101, USA |
Markus Didion | EnviroAtlas Team | David Otis | Derek C. West | Mulvaney, Kate | David Otis | Justin Meissen | Justin Meissen |
Sarah Cusser ?Comment:Department of Evolution, Ecology, and Organismal Biology, Ohio State University, 318 West 12th Avenue, Columbus, OH 43202, U.S.A. |
Gregg Lomnicky | Walter Hutcheson | Mark Mulligan |
Contact Address
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Laboratoire d’Ecologie Alpine, UMR 5553 CNRS Université Joseph Fourier, BP 53, 38041 Grenoble Cedex 9, France | Laboratoire d’Ecologie Alpine, UMR 5553 CNRS Université Joseph Fourier, BP 53, 38041 Grenoble Cedex 9, France | Department of Geography, University of Tennessee, 1000 Phillip Fulmer Way, Knoxville, TN 37996-0925, USA | Klamath Center for Conservation Research, Orleans, CA 95556 | Western Ecology Division, Office of Research and Development, U.S. Environmental Protection Agency, Pacific coastal Ecology Branch, 2111 SE marine Science Drive, Newport, OR 97365 | Swiss Federal Institute for Forest, Snow and Landscape Research WSL, 8903 Birmensdorf, Switzerland | Not reported | U.S. Geological Survey, Iowa Cooperative Fish and Wildlife Research Unit, Iowa State University | Dept. of Ecology and Evolutionary Biology, Yale University, 165 Prospect Street, New Haven, CT 06511, USA | US EPA, ORD, NHEERL, Atlantic Ecology Division, Narragansett, RI | U.S. Geological Survey, Iowa Cooperative Fish and Wildlife Research Unit, Iowa State University | Tallgrass Prairie Center, University of Northern Iowa | Tallgrass Prairie Center, 2412 West 27th Street, Cedar Falls, IA 50614-0294, USA | Department of Evolution, Ecology, and Behavior, School of Biological Sciences, The University of Texas at Austin, 100 East 24th Street Stop A6500, Austin, TX 78712-1598, U.S.A. | 200 SW 35th St., Corvallis, OR, 97333 | New York University, United States | King's College London, Dept. of Geography |
Contact Email
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sandra.lavorel@ujf-grenoble.fr | sandra.lavorel@ujf-grenoble.fr | ltran1@utk.edu | carlos@cklamathconservation.org | frazier@nceas.ucsb.edu | markus.didion@wsl.ch | enviroatlas@epa.gov | dotis@iastate.edu | derek.west@yale.edu | Mulvaney.Kate@epa.gov | dotis@iastate.edu | Not reported | justin.meissen@uni.edu | sarah.cusser@gmail.com | lomnicky.gregg@epa.gov | wwh235@nyu.edu | mark.mulligan@kcl.uk |
EM ID
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
Summary Description
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ABSTRACT: "Here, we propose a new approach for the analysis, mapping and understanding of multiple ES delivery in landscapes. Spatially explicit single ES models based on plant traits and abiotic characteristics are combined to identify ‘hot’ and ‘cold’ spots of multiple ES delivery, and the land use and biotic determinants of such distributions. We demonstrate the value of this trait-based approach as compared to a pure land-use approach for a pastoral landscape from the central French Alps, and highlight how it improves understanding of ecological constraints to, and opportunities for, the delivery of multiple services." AUTHOR'S DESCRIPTION: "The Cultural ecosystem service map was a simple sum of maps for relevant Ecosystem Properties (produced in related EMs) after scaling to a 0–100 baseline and trimming outliers to the 5–95% quantiles (Venables&Ripley 2002)…Coefficients used for the summing of individual ecosystem properties to cultural ecosystem services were based on stakeholders’ perceptions, given positive or negative contributions." | ABSTRACT: "Here, we propose a new approach for the analysis, mapping and understanding of multiple ES delivery in landscapes. Spatially explicit single ES models based on plant traits and abiotic characteristics are combined to identify ‘hot’ and ‘cold’ spots of multiple ES delivery, and the land use and biotic determinants of such distributions. We demonstrate the value of this trait-based approach as compared to a pure land-use approach for a pastoral landscape from the central French Alps, and highlight how it improves understanding of ecological constraints to, and opportunities for, the delivery of multiple services." AUTHOR'S DESCRIPTION: "The pollination ecosystem service map was a simple sums of maps for relevant Ecosystem Properties (produced in related EMs) after scaling to a 0–100 baseline and trimming outliers to the 5–95% quantiles (Venables&Ripley 2002)…Coefficients used for the summing of individual ecosystem properties to pollination ecosystem services are based on stakeholders’ perceptions, given positive (+1) or negative (-1) contributions." | ABSTRACT: "We describe a framework called Regional Hydrologic Modeling for Environmental Evaluation (RHyME2) for hydrologic modeling across scales. Rooted from hierarchy theory, RHyME2 acknowledges the rate-based hierarchical structure of hydrological systems. Operationally, hierarchical constraints are accounted for and explicitly described in models put together into RHyME2. We illustrate RHyME2with a two-module model to quantify annual nutrient loads in stream networks and watersheds at regional and subregional levels. High values of R2 (>0.95) and the Nash–Sutcliffe model efficiency coefficient (>0.85) and a systematic connection between the two modules show that the hierarchy theory-based RHyME2 framework can be used effectively for developing and connecting hydrologic models to analyze the dynamics of hydrologic systems." Two EMs will be entered in EPF-Library: 1. Regional scale module (Upper Mississippi River Basin) - this entry 2. Subregional scale module (St. Croix River Basin) | **Note: A more recent version of this model exists. See Related EMs below for links to related models/applications.** AUTHORS' DESCRIPTION: "PATCH (program to assist in tracking critical habitat), the SEPM used here, is designed for studying territorial vertebrates. It links the survival and fecundity of individual animals to geographic information system (GIS) data on mortality risk and habitat productivity at the scale of an individual or pack territory. Territories are allocated by intersecting the GIS data with an array of hexagonal cells. The different habitat types in the GIS maps are assigned weights based on the relative levels of fecundity and survival expected in those habitat classes. Base survival and reproductive rates, derived from published field studies, are then supplied to the model as a population projection matrix. The model scales these base matrix values using the mean of the habitat weights within each hexagon, with lower means translating into lower survival rates or reproductive output. Each individual in the population is tracked through a yearly cycle of survival, fecundity, and dispersal events. Environmental stochasticity is incorporated by drawing each year’s base population matrix from a randomized set of matrices whose elements were drawn from a beta (survival) or normal (fecundity) distribution. Adult organisms are classified as either territorial or floaters. The movement of territorial individuals is governed by a parameter for site fidelity, but floaters must always search for available breeding sites. As pack size increases, pack members in the model have a greater tendency to disperse and search for new available breeding sites. Movement decisions use a directed random walk that combines varying proportions of randomness, correlation, and attraction to higher-quality habitat (Schumaker 1998)." | AUTHOR'S DESCRIPTION: "To describe bird utilization patterns of intertidal habitats within Yaquina estuary, Oregon, we conducted censuses to obtain bird species and abundance data for the five dominant estuarine intertidal habitats: Zostera marina (eelgrass), Upogebia (mud shrimp)/ mudflat, Neotrypaea (ghost shrimp)/sandflat, Zostera japonica (Japanese eelgrass), and low marsh. EPFs were developed for the following metrics of bird use: standardized species richness; Shannon diversity; and density for the following four groups: all birds, all birds excluding gulls, waterfowl (ducks and geese), and shorebirds." | ABSTRACT: "...We examined the validity of the litter decomposition and soil carbon model Yasso07 in Swiss forests based on data on observed decomposition of (i) foliage and fine root litter from sites along a climatic and altitudinal gradient and (ii) of 588 dead trees from 394 plots of the Swiss National Forest Inventory. Our objectives were to... (ii) analyze the accuracy of Yasso07 for reproducing observed decomposition of litter and dead wood in Swiss forests; and (iii) evaluate the suitability of Yasso07 for regional and national scale applications in Swiss forests." AUTHOR'S DESCRIPTION: "Yasso07 (Tuomi et al., 2011a, 2009) is a litter decomposition model to calculate C stocks and stock changes in mineral soil, litter and deadwood. For estimating stocks of organic C in these pools and their temporal dynamics, Yasso07 (Y07) requires information on C inputs from dead organic matter (e.g., foliage and woody material) and climate (temperature, temperature amplitude and precipitation). DOM decomposition is modelled based on the chemical composition of the C input, size of woody parts and climate (Tuomi et al., 2011 a, b, 2009). In Y07 it is assumed that DOM consists of four compound groups with specific mass loss rates. The mass flows between compounds that are either insoluble (N), soluble in ethanol (E), in water (W) or in acid (A) and to a more stable humus compartment (H), as well as the flux out of the five pools (Fig. 1, Table A.1; Liski et al., 2009) are described by a range of parameters (Tuomi et al., 2011a, 2009)." "The decomposition of below- and aboveground litter was studied over 10 years on five forest sites in Switzerland…" "At the time of this study, three parameter sets have been developed and published:... (3): Rantakari et al., 2012 (henceforth P12)… For the development of P12, Rantakari et al. (2012) obtained a subset of the previously used data which was restricted to European sites." "For this study, we used the Yasso07 release 1.0.1 (cf. project homepage). The Yasso07 Fortran source code was compiled for the Windows7 operating system. The statistical software R (R Core Team, 2013) version 3.0.1 (64 bit) was used for administrating theYasso07 simulations. The decomposition of DOM was simulated with Y07 using the parameter sets P09, P11 and P12 with the purpose of identifying a parameter set that is applicable to conditions in Switzerland. In the simulations we used the value of the maximum a posteriori point estimate (cf. Tuomi et al., 2009) derived from the distribution of parameter values for each set (Table A.1). The simulations were initialized with the C mass contained in (a) one litterbag at the start of the litterbag experiment for foliage and fine root lit-ter (Heim and Frey, 2004) and (b) individual deadwood pieces at the time of the NFI2 for deadwood. The respective mass of C was separated into the four compound groups used by Y07. The simulations were run for the time span of the observed data. The r | DATA FACT SHEET: "This EnviroAtlas national map depicts the percent potentially restorable wetlands within each subwatershed (12-digit HUC) in the U.S. Potentially restorable wetlands are defined as agricultural areas that naturally accumulate water and contain some proportion of poorly-drained soils. The EnviroAtlas Team produced this dataset by combining three data layers - land cover, digital elevation, and soil drainage information." "To map potentially restorable wetlands, 2006 National Land Cover Data (NLCD) classes pasture/hay and cultivated crops were reclassified as potentially suitable and all other landcover classes as unsuitable. Poorly- and very poorly drained soils were identified using Natural Resources Conservation Service (NRCS) Soil Survey information mainly from the higher resolution Soil Survey Geographic (SSURGO) Database. The two poorly drained soil classes, expressed as percentage of a polygon in the soil survey, were combined to create a raster layer. A wetness index or Composite Topographic Index (CTI) was developed to identify areas wet enough to create wetlands. The wetness index grid, calculated from National Elevation Data (NED), relates upstream contributing area and slope to overland flow. Results from previous studies suggested that CTI values ≥ 550 captured the majority of wetlands. The three layers, when combined, resulted in four classes: unsuitable, low, moderate, and high wetland restoration potential. Areas with high potential for restorable wetlands have suitable landcover (crop/pasture), CTI values ≥ 550, and 80–100% poorly- or very poorly drained soils (PVP). Areas with moderate potential have suitable landcover, CTI values ≥ 550, and 1–79% PVP. Areas with low potential meet the landcover and 80–100% PVP criteria, but do not have CTI values ≥ 550 to corroborate wetness. All other areas were classed as unsuitable. The percentage of total land within each 12-digit HUC that is covered by potentially restorable wetlands was estimated and displayed in five classes for this map." | ABSTRACT: "This final project report is a compendium of 3 previously submitted progress reports and a 4th report for work accomplished from August – December, 2009. Our initial primary objective (Progress Report I) was prediction of environmental services provided by the 27 Iowa Conservation Reserve Enhancement Program (CREP) wetland sites that had been completed by 2007 in the Prairie Pothole Region of northcentral Iowa. The sites contain 102.4 ha of wetlands and 377.4 ha of associated grassland buffers... With respect to wildlife habitat value, USFWS models predicted that the 27 wetlands would provide habitat for 136 pairs of 6 species of ducks, 48 pairs of Canada Geese, and 839 individuals of 5 grassland songbird species of special concern..." AUTHOR'S DESCRIPTION: "The migratory bird benefits of the 27 CREP sites were predicted for Grasshopper Sparrow (Ammodramus savannarum)... Population estimates for these species were calculated using models developed by Quamen (2007) for the Prairie Pothole Region of Iowa (Table 3). The “neighborhood analysis” tool in the spatial analysis extension of ArcGIS (2008) was used to create landscape composition variables (grass400, grass3200, hay400, hay3200, tree400) needed for model input (see Table 3 for variable definitions). Values for the species-specific relative abundance (bbspath) variable were acquired from Diane Granfors, USFWS HAPET office. The equations for each model were used to calculate bird density (birds/ha) for each 15-m2 pixel of the land coverage. Next, the “zonal statistics” tool in the spatial analyst extension of ArcGIS (ESRI 2008) was used to calculate the average bird density for each CREP buffer. A population estimate for each site was then calculated by multiplying the average density by the buffer size." Equation: GRSP density = e (-2.554612 + 0.0246975 * grass400 – 0.1032461 * trees400) | ABSTRACT: "Anadromous alewives (Alosa pseudoharengus) have the potential to alter the nutrient budgets of coastal lakes as they migrate into freshwater as adults and to sea as juveniles. Alewife runs are generally a source of nutrients to the freshwater lakes in which they spawn, but juveniles may export more nutrients than adults import in newly restored populations. A healthy run of alewives in Connecticut imports substantial quantities of phosphorus; mortality of alewives contributes 0.68 g P_fish–1, while surviving fish add 0.18 g P, 67% of which is excretion. Currently, alewives contribute 23% of the annual phosphorus load to Bride Lake, but this input was much greater historically, with larger runs of bigger fish contributing 2.5 times more phosphorus in the 1960s..." AUTHOR'S DESCRIPTION: "Here, we evaluate the patterns of net nutrient loading by alewives over a range of population sizes. We concentrate on phosphorus, as it is generally the nutrient that limits production in the lake ecosystems in which alewives spawn (Schindler 1978). First, we estimate net alewife nutrient loading and parameterize an alewife nutrient loading model using data from an existing run of anadromous alewives in Bride Lake. We then compare the current alewife nutrient load to that in the 1960s when alewives were more numerous and larger. Next, since little is known about the actual patterns of nutrient loading during restoration, we predict the net nutrient loading for a newly restored population across a range of adult escapement… Anadromous fish move nutrients both into and out of freshwater ecosystems, although inputs are typically more obvious and much better studied (Moore and Schindler 2004). Net loading into freshwater ecosystems is fully described as inputs due to adult mortality, gametes, and direct excretion of nutrients minus the removal of nutrients from freshwater ecosystems by juvenile fish when they emigrate… Our research was conducted at Bride Lake and Linsley Pond in Connecticut. Bride Lake contains an anadromous alewife population that we used to both evaluate contemporary and historic net nutrient loading by an alewife population and parameterize our general alewife nutrient loading model." | [ABSTRACT: "Estimates of the types and number of recreational users visiting an estuary are critical data for quantifying the value of recreation and how that value might change with variations in water quality or other management decisions. However, estimates of recreational use are minimal and conventional intercept surveys methods are often infeasible for widespread application to estuaries. Therefore, a practical observational sampling approach was developed to quantify the recreational use of an estuary without the use of surveys. Designed to be simple and fast to allow for replication, the methods involved the use of periodic instantaneous car counts multiplied by extrapolation factors derived from all-day counts. This simple sampling approach can be used to estimate visitation to diverse types of access points on an estuary in a single day as well as across multiple days. Evaluation of this method showed that when periodic counts were taken within a preferred time window (from 11am-4:30pm), the estimates were within 44 percent of actual daily visitation. These methods were applied to the Three Bays estuary system on Cape Cod, USA. The estimated combined use across all its public access sites is similar to the use at a mid-sized coastal beach, demonstrating the value of estuarine systems. Further, this study is the first to quantify the variety and magnitude of recreational uses at several different types of access points throughout the estuary using observational methods. This model focused on the various use by access point type (beaches, landings and way to water, boat use). This work can be transferred to the many small coastal access points used for recreation across New England and beyond." ] | ABSTRACT: "Our initial primary objective (Progress Report I) was prediction of environmental services provided by the 27 Iowa Conservation Reserve Enhancement Program (CREP) wetland sites that had been completed by 2007 in the Prairie Pothole Region of northcentral Iowa. The sites contain 102.4 ha of wetlands and 377.4 ha of associated grassland buffers…" AUTHOR'S DESCRIPTION: "The first phase of the U.S. Fish and Wildlife Service task was to evaluate the contribution of the 27 approved sites to migratory birds breeding in the Prairie Pothole Region of Iowa. To date, evaluation has been completed for 7 species of waterfowl and 5 species of grassland birds. All evaluations were completed using existing models that relate landscape composition to bird populations. As such, the first objective was to develop a current land cover geographic information system (GIS) that reflected current landscape conditions including the incorporation of habitat restored through the CREP program. The second objective was to input landscape variables from our land cover GIS into models to estimate various migratory bird population parameters (i.e. the number of pairs, individuals, or recruits) for each site. Recruitment for the 27 sites was estimated for Mallards, Blue-winged Teal, Northern Shoveler, Gadwall, and Northern Pintail according to recruitment models presented by Cowardin et al. (1995). Recruitment was not estimated for Canada Geese and Wood Ducks because recruitment models do not exist for these species. Variables used to estimate recruitment included the number of pairs, the composition of the landscape in a 4-square mile area around the CREP wetland, species-specific habitat preferences, and species- and habitat-specific clutch success rates. Recruitment estimates were derived using the following equations: Recruits = 2*R*n where, 2 = constant based on the assumption of equal sex ratio at hatch, n = number of breeding pairs estimated using the pairs equation previously outlined, R = Recruitment rate as defined by Cowardin and Johnson (1979) where, R = H*Z*B/2 where, H = hen success (see Cowardin et al. (1995) for methods used to calculate H, which is related to land cover types in the 4-mile2 landscape around each wetland), Z = proportion of broods that survived to fledge at least 1 recruit (= 0.74 based on Cowardin and Johnson 1979), B = average brood size at fledging (= 4.9 based on Cowardin and Johnson 1979)." ENTERER'S COMMENT: The number of breeding pairs (n) is estimated by a separate submodel from this paper, and as such is also entered as a separate model in ESML (EM 632). | AUTHOR'S DESCRIPTION: "Restoring ecosystem services at scale requires executing conservation programs in a way that is resource and cost efficient as well as ecologically effective…Seed mix design is one of the largest determinants of project cost and ecological outcomes for prairie reconstructions. In particular, grass-to-forb seeding ratio affects cost since forb seed can be much more expensive relative to grass species (Prairie Moon Nursery 2012). Even for seed mixes with the same overall seeding rates, a mix with a low grass-to-forb seeding ratio is considerably more expensive than one with a high grass-to-forb ratio. Seeding rates for different plant functional groups that are too high or low may also adversely affect ecological outcomes…First-year management may also play a role in cost-effective prairie reconstruction. Post-agricultural sites where restoration typically occurs are often quickly dominated by fast-growing annual weeds by the time sown prairie seeds begin germinating (Smith et al. 2010)… Williams and others (2007) showed that prairie seedlings sown into established warm-season grasses were reliant on high light conditions created by frequently mowing tall vegetation in order to survive in subsequent years…Our objective was to compare native plant establishment and cost effectiveness with and without first-year mowing for three different seed mixes that differed in grass to forb ratio and soil type customization. With knowledge of plant establishment, cost effectiveness, and mowing management outcomes, conservation practitioners will be better equipped to restore prairie efficiently and successfully." | ABSTRACT: "Agricultural intensification continues to diminish many ecosystem services in the North American Corn Belt. Conservation programs may be able to combat these losses more efficiently by developing initiatives that attempt to balance multiple ecological benefits. In this study, we examine how seed mix design and first year management influence three ecosystem services commonly provided by tallgrass prairie reconstructions (erosion control, weed resistance, and pollinator resources). We established research plots with three seed mixes, with and without first year mowing. The grass-dominated “Economy” mix had 21 species and a 3:1 grass-to-forb seeding ratio. The forb-dominated “Pollinator”mix had 38 species and a 1:3 grass-to-forb seeding ratio. The grass:forb balanced “Diversity” mix, which was designed to resemble regional prairie remnants, had 71 species and a 1:1 grass-to-forb ratio. To assess ecosystem services, we measured native stem density, cover, inflorescence production, and floral richness from 2015 to 2018. The Economy mix had high native cover and stem density, but produced few inflorescences and had low floral richness. The Pollinator mix had high inflorescence production and floral richness, but also had high bare ground and weed cover. The Diversity mix had high inflorescence production and floral richness (comparable to the Pollinator mix) and high native cover and stem density (comparable to the Economy mix). First year mowing accelerated native plant establishment and inflorescence production, enhancing the provisioning of ecosystem services during the early stages of a reconstruction. Our results indicate that prairie reconstructions with thoughtfully designed seed mixes can effectively address multiple conservation challenges." | ABSTRACT: "Plant–pollinator mutualisms are one of the several functional relationships that must be reinstated to ensure the long-term success of habitat restoration projects. These mutualisms are unlikely to reinstate themselves until all of the resource requirements of pollinators have been met. By meeting these requirements, projects can improve their long-term success. We hypothesized that pollinator assemblage and structure and stability of plant–pollinator networks depend both on aspects of the surrounding landscape and of the restoration effort itself. We predicted that pollinator species diversity and network stability would be negatively associated with distance from remnant habitat, but that local floral diversity might rescue pollinator diversity and network stability in locations distant from the remnant. We created plots of native prairie on a reclaimed strip mine in central Ohio, U.S.A. that ranged in floral diversity and isolation from the remnant habitat. We found that the pollinator diversity declined with distance from the remnant habitat. Furthermore, reduced pollinator diversity in low floral diversity plots far from the remnant habitat was associated with loss of network stability. High floral diversity, however, compensated for losses in pollinator diversity in plots far from the remnant habitat through the attraction of generalist pollinators. Generalist pollinators increased network connectance and plant-niche overlap. Asa result, network robustness of high floral diversity plots was independent of isolation. We conclude that the aspects of the restoration effort itself, such as floral community composition, can be successfully tailored to incorporate the restoration of pollinators and improve success given a particular landscape context." | ABSTRACT: [Sport fishing is an important recreational and economic activity, especially in Australia, Europe and North America, and the condition of sport fish populations is a key ecological indicator of water body condition for millions of anglers and the public. Despite its importance as an ecological indicator representing the status of sport fish populations, an index for measuring this ecosystem service has not been quantified by analyzing actual fish taxa, size and abundance data across the U.S.A. Therefore, we used game fish data collected from 1,561 stream and river sites located throughout the conterminous U.S.A. combined with specific fish species and size dollar weights to calculate site-specific recreational fishery index (RFI) scores. We then regressed those scores against 38 potential site-specific environmental predictor variables, as well as site-specific fish assemblage condition (multimetric index; MMI) scores based on entire fish assemblages, to determine the factors most associated with the RFI scores. We found weak correlations between RFI and MMI scores and weak to moderate correlations with environmental variables, which varied in importance with each of 9 ecoregions. We conclude that the RFI is a useful indicator of a stream ecosystem service, which should be of greater interest to the U.S.A. public and traditional fishery management agencies than are MMIs, which tend to be more useful for ecologists, environmentalists and environmental quality agencies.] | ABSTRACT: " The Hudson River and its estuary is once again an ecologically, economically, and culturally functional component of New York City’s natural environment. The estuary’s cultural significance may derive largely from environmental education, including marine science programs for the public. These programs are understood as ‘‘cultural” ecosystem services but are rarely evaluated in economic terms. We estimated the economic value of the Hudson River Park’s environmental education programs. We compiled data on visits by schools and summer camps from 32 New York City school districts to the Park during the years 2014 and 2015. A ‘‘travel cost” approach was adapted from the field of environmental economics to estimate the value of education in this context. A small—but conservative—estimate of the Park’s annual education program benefits ranged between $7500 and 25,500, implying an average capitalized value on the order of $0.6 million. Importantly, organizations in districts with high proportions of minority students or English language learners were found to be more likely to participate in the Park’s programs. The results provide an optimistic view of the benefits of environmental education focused on urban estuaries, through which a growing understanding of ecological systems could lead to future environmental improvements. " | ABSTRACT: " Co$tingNature is a sophisticated web-based spatial policy support system for natural capital accounting and analysing the ecosystem services provided by natural environments (i.e. nature's benefits), identifying the beneficiaries of these services and assessing the impacts of human interventions. This PSS is a testbed for the development and implementation of conservation strategies focused on sustaining and improving ecosystem services. It also focused on enabling the intended and unintended consequences of development actions on ecosystem service provision to be tested in silico before they are tested in vivo . The PSS incorporates detailed spatial datasets at 1-square km and 1 hectare resolution for the entire World, spatial models for biophysical and socioeconomic processes along with scenarios for climate and land use. The PSS calculates a baseline for current ecosystem service provision and allows a series of interventions (policy options) or scenarios of change to be used to understand their impact on ecosystem service delivery. We do not focus on valuing nature (how much someone is willing to pay for it) but rather costing it (understanding the resource e.g. land area and opportunity cost of nature being protected to produce the ecosystem services that we need and value). " |
Specific Policy or Decision Context Cited
em.detail.policyDecisionContextHelp
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None identified | None identified | Not reported | AUTHOR DESCRIPTION: "Comprehensive habitat and viability assessments. . . [more rigoursly defined] can clarify debate of goals for recovery of large carnivores"; Endangered Species Act and related litigation | None identified | None identified | None Identified | None identified | Restoration and management of diadromous fish runs in coastal New England | None identified | None identified | Seed mix design and management practices for native plant restoration | None identified | None identified | None identified | None identified | Conservation priorities |
Biophysical Context
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Elevations ranging from 1552 m to 2442 m, on predominantly south-facing slopes | Elevations ranging from 1552 m to 2442 m, on predominantly south-facing slopes | No additional description provided | Great Plains to Pacific Coast, northern Rocky Mountains, Pacific Northwest | Estuarine intertidal, eelgrass, mudflat, sandflat and low marsh | Different forest types dominated by Norway Spruce (Picea abies), European Beech (Fagus sylvatica) and Sweet Chestnut (Castanea sativa). | No additional description provided | Prairie pothole region of north-central Iowa | Bride Lake is 28.7 ha and linked to Long Island Sound by the 3.3 km Bride Brook. | None identified | Prairie Pothole Region of Iowa | The soils underlying the study site are primarily poorly drained Clyde clay loams, with a minor component of somewhat poorly drained Floyd loams in the northwest (NRCS 2016). Topographically, the study site is level, and slopes do not exceed 5% grade. Land use prior to this experiment was agricultural, with corn and soybeans consistently grown in rotation at the site. | The site, located at the Iowa State University Northeast Research and Demonstration Farm near Nashua, Iowa, is relatively level with slopes not exceeding a 5% grade. Soil composition is primarily poorly drained Clyde clay loams with a minor component of somewhat poorly drained Floyd loams. Sub-surface tile drains exist on site and are spaced approximately 18–24m apart. The land was used for corn and soybean production prior to site establishment in 2015. | The site was surface mined for coal until the mid-1980s and soon after recontoured and seeded with a low diversity of non-native grasses and forbes. The property is grassland in a state of arrested succession, unable to support tree growth because of shallow, infertile soils. | None | N/A | Woldwide coverage |
EM Scenario Drivers
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No scenarios presented | No scenarios presented | No scenarios presented | Population growth, road development (density) on public vs private land | No scenarios presented | No scenarios presented | No scenarios presented | No scenarios presented | current and historical run size | N/A | No scenarios presented | No scenarios presented | Seed mix design | No scenarios presented | N/A | N?A | Policy decisions affecting future land use |
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
Method Only, Application of Method or Model Run
em.detail.methodOrAppHelp
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Method + Application | Method + Application | Method + Application | Method + Application (multiple runs exist) View EM Runs | Method + Application |
Method + Application (multiple runs exist) View EM Runs ?Comment:Model runs are for different sites (Beatenberg, Vordemwald, Bettlachstock, Schanis, and Novaggio) differentiated by climate and forest types dominated by Norway Spruce (Picea abies), European Beech (Fagus sylvatica) and Sweet Chestnut (Castanea sativa). |
Method + Application | Method + Application | Method + Application (multiple runs exist) View EM Runs | Method + Application (multiple runs exist) View EM Runs | Method + Application | Method + Application (multiple runs exist) View EM Runs | Method + Application (multiple runs exist) View EM Runs | Method + Application (multiple runs exist) View EM Runs | Method + Application | Method + Application | Method Only |
New or Pre-existing EM?
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New or revised model | New or revised model | New or revised model | New or revised model | New or revised model | Application of existing model | New or revised model |
Application of existing model ?Comment:Models developed by Quamen (2007). |
New or revised model | New or revised model | New or revised model | New or revised model | New or revised model | New or revised model | New or revised model | New or revised model | New or revised model |
Related EMs (for example, other versions or derivations of this EM) described in ESML
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
Document ID for related EM
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None | Doc-260 | Doc-123 | Doc-328 | Doc-337 | None | Doc-342 | Doc-343 | None | Doc-372 | None | None | Doc-372 | Doc-373 | Doc-395 | Doc-394 | None | None | None | None |
EM ID for related EM
em.detail.relatedEmEmIdHelp
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EM-65 | EM-66 | EM-68 | EM-69 | EM-70 | EM-71 | EM-79 | EM-80 | EM-82 | EM-83 | EM-65 | EM-66 | EM-68 | EM-69 | EM-70 | EM-71 | EM-79 | EM-80 | EM-81 | EM-83 | None | EM-403 | EM-422 | None | EM-466 | EM-467 | EM-469 | EM-480 | None | EM-652 | EM-651 | EM-650 | EM-648 | EM-667 | EM-672 | EM-674 | EM-673 | EM-682 | EM-684 | EM-685 | EM-705 | EM-704 | EM-702 | EM-701 | EM-700 | EM-632 | EM-728 | EM-719 | None | None | None | None |
EM Modeling Approach
EM ID
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
EM Temporal Extent
em.detail.tempExtentHelp
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Not reported | Not reported | 1987-1997 | 2000-2025 | December 2007 - November 2008 | 2000-2010 | 2006-2013 | 2002-2007 | 1960"s and early 2000's | Summer 2017 | 1987-2007 | 2015-2017 | 2015-2018 | 2009-2010 | 2013-2014 | 2015 | Not applicable |
EM Time Dependence
em.detail.timeDependencyHelp
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time-stationary | time-stationary | time-stationary | time-dependent | time-stationary | time-dependent | time-stationary | time-stationary | time-stationary | time-dependent | time-stationary | time-dependent | time-dependent | time-stationary | time-dependent | time-stationary | time-dependent |
EM Time Reference (Future/Past)
em.detail.futurePastHelp
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Not applicable | Not applicable | Not applicable | future time | Not applicable | future time | Not applicable | Not applicable | Not applicable | past time | Not applicable | Not applicable | Not applicable | Not applicable | past time | Not applicable | Not applicable |
EM Time Continuity
em.detail.continueDiscreteHelp
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Not applicable | Not applicable | Not applicable | discrete | Not applicable | discrete | Not applicable | Not applicable | Not applicable | discrete | Not applicable | discrete | discrete | Not applicable | discrete | Not applicable | Not applicable |
EM Temporal Grain Size Value
em.detail.tempGrainSizeHelp
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Not applicable | Not applicable | Not applicable | 1 | Not applicable | 1 | Not applicable | Not applicable | Not applicable | 1 | Not applicable | 1 | 1 | Not applicable | 1 | Not applicable | Not applicable |
EM Temporal Grain Size Unit
em.detail.tempGrainSizeUnitHelp
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Not applicable | Not applicable | Not applicable | Year | Not applicable | Year | Not applicable | Not applicable | Not applicable | Day | Not applicable | Year | Year | Not applicable | Year | Not applicable | Not applicable |
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
Bounding Type
em.detail.boundingTypeHelp
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Physiographic or Ecological | Physiographic or Ecological | Watershed/Catchment/HUC | Physiographic or ecological | Physiographic or ecological | Geopolitical | Geopolitical | Multiple unrelated locations (e.g., meta-analysis) | Watershed/Catchment/HUC | Physiographic or ecological | Multiple unrelated locations (e.g., meta-analysis) | Other | Other | Physiographic or ecological | Geopolitical | Geopolitical | Not applicable |
Spatial Extent Name
em.detail.extentNameHelp
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Central French Alps | Central French Alps | Upper Mississippi River basin; St. Croix River Watershed | Western United States | Yaquina Estuary (intertidal), Oregon, USA | Switzerland | conterminous United States | CREP (Conservation Reserve Enhancement Program) wetland sites | Bride Lake and Linsley Pond | Three Bays, Cape Cod | CREP (Conservation Reserve Enhancement Program | Iowa State University Northeast Research and Demonstration Farm | Iowa State University Northeast Research and Demonstration Farm near Nashua, Iowa | The Wilds | United States | Hudson River Park | Not applicable |
Spatial Extent Area (Magnitude)
em.detail.extentAreaHelp
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10-100 km^2 | 10-100 km^2 | 100,000-1,000,000 km^2 | >1,000,000 km^2 | 1-10 km^2 | 10,000-100,000 km^2 | >1,000,000 km^2 | 1-10 km^2 | 10-100 ha | 1000-10,000 km^2. | 10,000-100,000 km^2 | <1 ha | <1 ha | 1-10 km^2 | >1,000,000 km^2 | 10-100 ha | Not applicable |
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
EM Spatial Distribution
em.detail.distributeLumpHelp
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spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially lumped (in all cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially lumped (in all cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially distributed (in at least some cases) | spatially lumped (in all cases) | spatially lumped (in all cases) |
Spatial Grain Type
em.detail.spGrainTypeHelp
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area, for pixel or radial feature | area, for pixel or radial feature | NHDplus v1 | area, for pixel or radial feature | other (habitat type) | Not applicable | other (specify), for irregular (e.g., stream reach, lake basin) | other (specify), for irregular (e.g., stream reach, lake basin) | Not applicable | length, for linear feature (e.g., stream mile) | other (specify), for irregular (e.g., stream reach, lake basin) | area, for pixel or radial feature | area, for pixel or radial feature | area, for pixel or radial feature | length, for linear feature (e.g., stream mile) | Not applicable | Not applicable |
Spatial Grain Size
em.detail.spGrainSizeHelp
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20 m x 20 m | 20 m x 20 m | NHDplus v1 | 504 km^2 | 0.87-104.29 ha | Not applicable | irregular | multiple, individual, irregular shaped sites | Not applicable | beach length | multiple, individual, irregular sites | 20 ft x 28 ft | 6.1 m x 8.53 m | 10 m radius | stream reach (site) | Not applicable | Not applicable |
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
EM Computational Approach
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Analytic | Analytic | Numeric | Numeric | Analytic | Numeric | Analytic | Analytic | Analytic | Numeric | Analytic | Analytic | Analytic | Analytic | Analytic | Numeric | Analytic |
EM Determinism
em.detail.deterStochHelp
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deterministic | deterministic | deterministic | stochastic | deterministic | stochastic | deterministic | deterministic | deterministic | deterministic | deterministic | stochastic | stochastic | deterministic | deterministic | deterministic | deterministic |
Statistical Estimation of EM
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EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
Model Calibration Reported?
em.detail.calibrationHelp
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No | No | Yes | Unclear | Unclear | No | No | Unclear | Yes | Yes | Unclear | Not applicable | Not applicable | Not applicable | No | No | Not applicable |
Model Goodness of Fit Reported?
em.detail.goodnessFitHelp
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No | No | Yes | No | No | No | No | No | No | No | No | Not applicable | No | Not applicable | No | No | Not applicable |
Goodness of Fit (metric| value | unit)
em.detail.goodnessFitValuesHelp
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None | None |
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None | None | None | None | None | None | None | None | None | None | None | None | None | None |
Model Operational Validation Reported?
em.detail.validationHelp
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No | No | No | No | No | Yes | No | Unclear | No | No | No | No | No | Yes | No | No | Not applicable |
Model Uncertainty Analysis Reported?
em.detail.uncertaintyAnalysisHelp
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No | No | No | No | No | Yes | No | No | No | No | No | Not applicable | No | Yes | No | No | Not applicable |
Model Sensitivity Analysis Reported?
em.detail.sensAnalysisHelp
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No | No |
No ?Comment:Some model coefficients serve, by their magnitude, to indicate the proportional impact on the final result of variation in the parameters they modify. |
Yes ?Comment:No results reported. Just a general statement was made about PATCH sensitivity and that demographic parameters are more sensitive that variation in other parameters such as dispersadistance . Reference made to another publication Carroll et al. 2003. Use of population viability analysis and reserve slelection algorithms in regional conservation plans. Ecol. App. 13:1773-1789. |
No | No | No | No | Yes | No | No | Not applicable | No | No | No | No | Not applicable |
Model Sensitivity Analysis Include Interactions?
em.detail.interactionConsiderHelp
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Not applicable | Not applicable | Not applicable | Unclear | Not applicable | Not applicable | Not applicable | Not applicable | Unclear | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable | Not applicable |
EM Locations, Environments, Ecology
Terrestrial location (Classification hierarchy: Continent > Country > U.S. State [United States only])
EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
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None |
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None |
Marine location (Classification hierarchy: Realm > Region > Province > Ecoregion)
EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
None | None | None | None |
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None | None | None | None |
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None | None | None | None | None | None | None |
Centroid Lat/Long (Decimal Degree)
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
Centroid Latitude
em.detail.ddLatHelp
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45.05 | 45.05 | 42.5 | 39.88 | 44.62 | 46.82 | 39.5 | 42.62 | 41.33 | 41.62 | 42.62 | 42.93 | 42.93 | 39.82 | 36.21 | 40.73 | Not applicable |
Centroid Longitude
em.detail.ddLongHelp
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6.4 | 6.4 | -90.63 | -113.81 | -124.06 | 8.23 | -98.35 | -93.84 | -72.24 | -70.42 | -93.84 | -92.57 | -92.57 | -81.75 | -113.76 | -74.01 | Not applicable |
Centroid Datum
em.detail.datumHelp
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WGS84 | WGS84 | WGS84 | WGS84 | None provided | WGS84 | WGS84 | WGS84 | WGS84 | WGS84 | WGS84 | WGS84 | WGS84 | WGS84 | WGS84 | WGS84 | Not applicable |
Centroid Coordinates Status
em.detail.coordinateStatusHelp
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Provided | Provided | Estimated | Estimated | Provided | Estimated | Estimated | Estimated | Estimated | Estimated | Estimated | Provided | Provided | Provided | Estimated | Estimated | Not applicable |
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
EM Environmental Sub-Class
em.detail.emEnvironmentalSubclassHelp
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Agroecosystems | Grasslands | Agroecosystems | Grasslands | Aquatic Environment (sub-classes not fully specified) | Rivers and Streams | Inland Wetlands | Terrestrial Environment (sub-classes not fully specified) | Agroecosystems | Atmosphere | Terrestrial Environment (sub-classes not fully specified) | Near Coastal Marine and Estuarine | Forests | Agroecosystems | Inland Wetlands | Agroecosystems | Grasslands | Rivers and Streams | Lakes and Ponds | Near Coastal Marine and Estuarine | Inland Wetlands | Agroecosystems | Grasslands | Agroecosystems | Grasslands | Agroecosystems | Grasslands | Grasslands | Rivers and Streams | Created Greenspace | Terrestrial Environment (sub-classes not fully specified) |
Specific Environment Type
em.detail.specificEnvTypeHelp
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Subalpine terraces, grasslands, and meadows. | Subalpine terraces, grasslands, and meadows. | None | Not reported | Estuarine intertidal | forests | Terrestrial | Grassland buffering inland wetlands set in agricultural land | Coastal lakes and ponds and associated streams | Beaches | Wetlands buffered by grassland within agroecosystems | Research farm in historic grassland | prairie/grassland reconstruction at demonstration farm site | Grassland | reach | Park | Non urban |
EM Ecological Scale
em.detail.ecoScaleHelp
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Ecological scale is coarser than that of the Environmental Sub-class | Ecological scale is coarser than that of the Environmental Sub-class | Ecosystem | Ecological scale corresponds to the Environmental Sub-class | Ecological scale is finer than that of the Environmental Sub-class | Ecological scale corresponds to the Environmental Sub-class | Ecological scale is finer than that of the Environmental Sub-class | Ecological scale corresponds to the Environmental Sub-class | Ecological scale corresponds to the Environmental Sub-class | Ecological scale is finer than that of the Environmental Sub-class | Ecological scale corresponds to the Environmental Sub-class | Ecological scale corresponds to the Environmental Sub-class | Ecological scale corresponds to the Environmental Sub-class | Ecological scale corresponds to the Environmental Sub-class | Ecological scale is finer than that of the Environmental Sub-class | Ecological scale is finer than that of the Environmental Sub-class | Ecological scale is finer than that of the Environmental Sub-class |
Scale of differentiation of organisms modeled
EM ID
em.detail.idHelp
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EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
EM Organismal Scale
em.detail.orgScaleHelp
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Community | Community | Not applicable | Species | Guild or Assemblage | Community | Not applicable | Species | Individual or population, within a species | Not applicable | Individual or population, within a species | Community | Community | Species | Guild or Assemblage | Not applicable | Not applicable |
Taxonomic level and name of organisms or groups identified
EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
None Available | None Available | None Available |
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None Available | None Available |
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None Available |
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None Available | None Available |
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None Available | None Available | None Available |
EnviroAtlas URL
EM Ecosystem Goods and Services (EGS) potentially modeled, by classification system
CICES v 4.3 - Common International Classification of Ecosystem Services (Section > Division > Group > Class)
EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
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None |
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<a target="_blank" rel="noopener noreferrer" href="https://www.epa.gov/eco-research/national-ecosystem-services-classification-system-nescs-plus">National Ecosystem Services Classification System (NESCS) Plus</a>
(Environmental Subclass > Ecological End-Product (EEP) > EEP Subclass > EEP Modifier)
EM-81 | EM-82 | EM-91 |
EM-98 ![]() |
EM-103 |
EM-485 ![]() |
EM-492 | EM-649 |
EM-661 ![]() |
EM-686 ![]() |
EM-703 |
EM-719 ![]() |
EM-728 ![]() |
EM-774 ![]() |
EM-862 | EM-875 | EM-996 |
None | None | None |
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None | None |
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None |
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None | None |
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