Species distribution modelling

(Redirected from Niche models) Algorithmic prediction of the distribution of a species across geographic space

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Species distribution modelling (SDM), also known as environmental (or ecological) niche modelling (ENM), habitat modelling, predictive habitat distribution modelling, and range mapping uses ecological models to predict the distribution of a species across geographic space and time using environmental data. The environmental data are most often climate data (e.g. temperature, precipitation), but can include other variables such as soil type, water depth, and land cover. SDMs are used in several research areas in conservation biology, ecology and evolution. These models can be used to understand how environmental conditions influence the occurrence or abundance of a species, and for predictive purposes (ecological forecasting). Predictions from an SDM may be of a species’ future distribution under climate change, a species’ past distribution in order to assess evolutionary relationships, or the potential future distribution of an invasive species. Predictions of current and/or future habitat suitability can be useful for management applications (e.g. reintroduction or translocation of vulnerable species, reserve placement in anticipation of climate change).

There are two main types of SDMs. Correlative SDMs, also known as climate envelope models, bioclimatic models, or resource selection function models, model the observed distribution of a species as a function of environmental conditions. Mechanistic SDMs, also known as process-based models or biophysical models, use independently derived information about a species' physiology to develop a model of the environmental conditions under which the species can exist.

The extent to which such modelled data reflect real-world species distributions will depend on a number of factors, including the nature, complexity, and accuracy of the models used and the quality of the available environmental data layers; the availability of sufficient and reliable species distribution data as model input; and the influence of various factors such as barriers to dispersal, geologic history, or biotic interactions, that increase the difference between the realized niche and the fundamental niche. Environmental niche modelling may be considered a part of the discipline of biodiversity informatics.

History

A. F. W. Schimper used geographical and environmental factors to explain plant distributions in his 1898 Pflanzengeographie auf physiologischer Grundlage (Plant Geography Upon a Physiological Basis) and his 1908 work of the same name. Andrew Murray used the environment to explain the distribution of mammals in his 1866 The Geographical Distribution of Mammals. Robert Whittaker's work with plants and Robert MacArthur's work with birds strongly established the role the environment plays in species distributions. Elgene O. Box constructed environmental envelope models to predict the range of tree species. His computer simulations were among the earliest uses of species distribution modelling.

The adoption of more sophisticated generalised linear models (GLMs) made it possible to create more sophisticated and realistic species distribution models. The expansion of remote sensing and the development of GIS-based environmental modelling increase the amount of environmental information available for model-building and made it easier to use.

Correlative vs mechanistic models

Correlative SDMs

SDMs originated as correlative models. Correlative SDMs model the observed distribution of a species as a function of geographically referenced climatic predictor variables using multiple regression approaches. Given a set of geographically referred observed presences of a species and a set of climate maps, a model defines the most likely environmental ranges within which a species lives. Correlative SDMs assume that species are at equilibrium with their environment and that the relevant environmental variables have been adequately sampled. The models allow for interpolation between a limited number of species occurrences.

For these models to be effective, it is required to gather observations not only of species presences, but also of absences, that is, where the species does not live. Records of species absences are typically not as common as records of presences, thus often "random background" or "pseudo-absence" data are used to fit these models. If there are incomplete records of species occurrences, pseudo-absences can introduce bias. Since correlative SDMs are models of a species’ observed distribution, they are models of the realized niche (the environments where a species is found), as opposed to the fundamental niche (the environments where a species can be found, or where the abiotic environment is appropriate for the survival). For a given species, the realized and fundamental niches might be the same, but if a species is geographically confined due to dispersal limitation or species interactions, the realized niche will be smaller than the fundamental niche.

Correlative SDMs are easier and faster to implement than mechanistic SDMs, and can make ready use of available data. Since they are correlative however, they do not provide much information about causal mechanisms and are not good for extrapolation. They will also be inaccurate if the observed species range is not at equilibrium (e.g. if a species has been recently introduced and is actively expanding its range).

Mechanistic SDMs

Mechanistic SDMs are more recently developed. In contrast to correlative models, mechanistic SDMs use physiological information about a species (taken from controlled field or laboratory studies) to determine the range of environmental conditions within which the species can persist. These models aim to directly characterize the fundamental niche, and to project it onto the landscape. A simple model may simply identify threshold values outside of which a species can't survive. A more complex model may consist of several sub-models, e.g. micro-climate conditions given macro-climate conditions, body temperature given micro-climate conditions, fitness or other biological rates (e.g. survival, fecundity) given body temperature (thermal performance curves), resource or energy requirements, and population dynamics. Geographically referenced environmental data are used as model inputs. Because the species distribution predictions are independent of the species’ known range, these models are especially useful for species whose range is actively shifting and not at equilibrium, such as invasive species.

Mechanistic SDMs incorporate causal mechanisms and are better for extrapolation and non-equilibrium situations. However, they are more labor-intensive to create than correlational models and require the collection and validation of a lot of physiological data, which may not be readily available. The models require many assumptions and parameter estimates, and they can become very complicated.

Dispersal, biotic interactions, and evolutionary processes present challenges, as they aren’t usually incorporated into either correlative or mechanistic models.

Correlational and mechanistic models can be used in combination to gain additional insights. For example, a mechanistic model could be used to identify areas that are clearly outside the species’ fundamental niche, and these areas can be marked as absences or excluded from analysis. See for a comparison between mechanistic and correlative models.

Niche models (correlative)

There are a variety of mathematical methods that can be used for fitting, selecting, and evaluating correlative SDMs. Models include "profile" methods, which are simple statistical techniques that use e.g. environmental distance to known sites of occurrence such as BIOCLIM and DOMAIN; "regression" methods (e.g. forms of generalized linear models); and "machine learning" methods such as maximum entropy (MAXENT). Ten machine learning techiniques used in SDM can be seen in. An incomplete list of models that have been used for niche modelling includes:

Profile techniques

Regression-based techniques

Generalized linear model (GLM)
Generalized additive model (GAM)
Multivariate adaptive regression splines (MARS)
Maxlike
Favourability Function (FF)

Machine learning techniques

MAXENT
Artificial neural networks (ANN)
Genetic Algorithm for Rule Set Production (GARP)
Boosted regression trees (BRT)/gradient boosting machines (GBM)
Random forest (RF)
Support vector machines (SVM)
XGBoost (XGB)

Furthermore, ensemble models can be created from several model outputs to create a model that captures components of each. Often the mean or median value across several models is used as an ensemble. Similarly, consensus models are models that fall closest to some measure of central tendency of all models—consensus models can be individual model runs or ensembles of several models.

Niche modelling software (correlative)

SPACES is an online Environmental niche modeling platform that allows users to design and run dozens of the most prominent methods in a high performance, multi-platform, browser-based environment.

MaxEnt is the most widely used method/software uses presence only data and performs well when there are few presence records available.

ModEco implements various methods.

DIVA-GIS has an easy to use (and good for educational use) implementation of BIOCLIM

The Biodiversity and Climate Change Virtual Laboratory (BCCVL) is a "one stop modelling shop" that simplifies the process of biodiversity and climate impact modelling. It connects the research community to Australia's national computational infrastructure by integrating a suite of tools in a coherent online environment. Users can access global climate and environmental datasets or upload their own data, perform data analysis across six different experiment types with a suite of 17 different methods, and easily visualize, interpret and evaluate the results of the models. Experiments types include: Species Distribution Model, Multispecies Distribution Model, Species Trait Model (currently under development), Climate Change Projection, Biodiverse Analysis and Ensemble Analysis. Example of BCCVL SDM outputs can be found here

Another example is Ecocrop, which is used to determine the suitability of a crop to a specific environment. This database system can also project crop yields and evaluate the impact of environmental factors such as climate change on plant growth and suitability.

Most niche modelling methods are available in the R packages 'dismo', 'biomod2' and 'mopa'..

Software developers may want to build on the openModeller project.

The Collaboratory for Adaptation to Climate Change adapt.nd.edu Archived 2012-08-06 at the Wayback Machine has implemented an online version of openModeller that allows users to design and run openModeller in a high-performance, browser-based environment to allow for multiple parallel experiments without the limitations of local processor power.

References

^ Elith, Jane; Leathwick, John R. (2009-02-06). "Species Distribution Models: Ecological Explanation and Prediction Across Space and Time". Annual Review of Ecology, Evolution, and Systematics. 40 (1): 677–697. doi:10.1146/annurev.ecolsys.110308.120159. ISSN 1543-592X. S2CID 86460963.
^ Kearney, Michael; Porter, Warren (2009). "Mechanistic niche modelling: combining physiological and spatial data to predict species' ranges". Ecology Letters. 12 (4): 334–350. doi:10.1111/j.1461-0248.2008.01277.x. ISSN 1461-0248. PMID 19292794.
A. F. W. Schimper (1908), Pflanzen-Geographie auf physiologischer Grundlage (in German) (2nd ed.), Jena: Gustav Fischer Verlag, doi:10.5962/BHL.TITLE.46243, OCLC 12120623, OL 24353101M, Wikidata Q117084350
Murray, Andrew, 1812-1878 (1866), The geographical distribution of mammals, London: Day and Son, limited, doi:10.5962/BHL.TITLE.15762, LCCN 04035567, OCLC 8680065, OL 16272962M, Wikidata Q51421963{{citation}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
Box, Elgene O. (1981-05-01). "Predicting physiognomic vegetation types with climate variables". Vegetatio. 45 (2): 127–139. doi:10.1007/BF00119222. ISSN 1573-5052. S2CID 25941018.
Morin, X.; Thuiller (2009). "Comparing niche- and process-based models to reduce prediction uncertainty in species range shifts under climate change". Ecology. 90 (5): 1301–13. doi:10.1890/08-0134.1. PMID 19537550.
Nix HA (1986). "BIOCLIM — a Bioclimatic Analysis and Prediction System". Research Report, CSIRO Division of Water and Land Resources. 1983–1985: 59–60.
Nix HA (1986). "A biogeographic analysis of Australian elapid snakes". In Longmore (ed.). Atlas of Elapid Snakes of Australia. Australian Flora and Fauna Series 7. Bureau of Flora and Fauna, Canberra. pp. 4–15.
Effrosynidis, Dimitrios; Tsikliras, Athanassios; Arampatzis, Avi; Sylaios, Georgios (2020-12-13). "Species Distribution Modelling via Feature Engineering and Machine Learning for Pelagic Fishes in the Mediterranean Sea". Applied Sciences. 10 (24): 8900. doi:10.3390/app10248900.
Real, Raimundo; Barbosa, A. Márcia; Vargas, J. Mario (2006). "Obtaining Environmental Favourability Functions from Logistic Regression". Environmental and Ecological Statistics. 13 (2): 237–245. doi:10.1007/s10651-005-0003-3. hdl:10174/20244. S2CID 34887643.
"FAO Ecocrop". ECHOcommunity. Retrieved 2019-08-19.
Rosenstock, Todd S.; Nowak, Andreea; Girvetz, Evan (2018). The Climate-Smart Agriculture Papers: Investigating the Business of a Productive, Resilient and Low Emission Future. Cham, Switzerland: Springer. p. 41. ISBN 9783319927978.

External links

Climate Envelope Modeling Working Group - Online gathering place for scientists, practitioners, managers, and developers to discuss, support, and develop climate Environmental Niche Modeling tools and platforms
BioVeL Ecological Niche Modeling (ENM) - online tool with workflows to generate ecological niche models
EUBrazilOpenBio SpeciesLab Virtual Research Environment - online working environment to support the production of ecological niche modeling by (i) simplifying access to occurrence points and environmental parameters and (ii) offering a powerful version of openModeller benefitting from a distributed computing infrastructure;
openModeller - open source niche modelling library
Lifemapper 2.0 - video of presentation by Aimee Stewart, Kansas University, at O'Reilly Where 2.0 Conference 2008
AquaMaps - global predictive maps for marine species
Ecological Modelling - International Journal on Ecological Modelling and Systems Ecology

Scholia has a profile for environmental niche modelling (Q5381340).

v t e Ecology: Modelling ecosystems: Trophic components
General	Abiotic component Abiotic stress Behaviour Biogeochemical cycle Biomass Biotic component Biotic stress Carrying capacity Competition Ecosystem Ecosystem ecology Ecosystem model Green world hypothesis Keystone species List of feeding behaviours Metabolic theory of ecology Productivity Resource Restoration
Producers	Autotrophs Chemosynthesis Chemotrophs Foundation species Kinetotrophs Mixotrophs Myco-heterotrophy Mycotroph Organotrophs Photoheterotrophs Photosynthesis Photosynthetic efficiency Phototrophs Primary nutritional groups Primary production
Consumers	Apex predator Bacterivore Carnivores Chemoorganotroph Foraging Generalist and specialist species Intraguild predation Herbivores Heterotroph Heterotrophic nutrition Insectivore Mesopredators Mesopredator release hypothesis Omnivores Optimal foraging theory Planktivore Predation Prey switching
Decomposers	Chemoorganoheterotrophy Decomposition Detritivores Detritus
Microorganisms	Archaea Bacteriophage Lithoautotroph Lithotrophy Marine Microbial cooperation Microbial ecology Microbial food web Microbial intelligence Microbial loop Microbial mat Microbial metabolism Phage ecology
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Example webs	Lakes Rivers Soil Tritrophic interactions in plant defense Marine food webs cold seeps hydrothermal vents intertidal kelp forests North Pacific Gyre San Francisco Estuary tide pool
Processes	Ascendency Bioaccumulation Cascade effect Climax community Competitive exclusion principle Consumer–resource interactions Copiotrophs Dominance Ecological network Ecological succession Energy quality Energy systems language f-ratio Feed conversion ratio Feeding frenzy Mesotrophic soil Nutrient cycle Oligotroph Paradox of the plankton Trophic cascade Trophic mutualism Trophic state index
Defense, counter	Animal coloration Anti-predator adaptations Camouflage Deimatic behaviour Herbivore adaptations to plant defense Mimicry Plant defense against herbivory Predator avoidance in schooling fish

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Species interaction	Antibiosis Biological interaction Commensalism Community ecology Ecological facilitation Interspecific competition Mutualism Parasitism Storage effect Symbiosis
Spatial ecology	Biogeography Cross-boundary subsidy Ecocline Ecotone Ecotype Disturbance Edge effects Foster's rule Habitat fragmentation Ideal free distribution Intermediate disturbance hypothesis Insular biogeography Land change modeling Landscape ecology Landscape epidemiology Landscape limnology Metapopulation Patch dynamics r/K selection theory Resource selection function Source–sink dynamics
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