Abstract:The urgency of predicting future impacts of environmental change on vulnerable populations is advancing the development of spatially explicit habitat models. Continental-scale climate and microclimate layers are now widely available. However, most terrestrial organisms exist within microclimate spaces that are very small, relative to the spatial resolution of those layers. We examined the effects of multi-resolution, multi-extent topographic and climate inputs on the accuracy of hourly soil temperature predict… Show more
“…| 1879 be used to define areas where a higher resolution surface should be generated to confirm model predictions and help inform management decisions (Carter et al, 2015). Given the limited data available for O. suteri (i.e.…”
Section: Model Application and Limitationsmentioning
Aim
Predicting the distribution of species relies increasingly on understanding the spatially explicit constraints of environmental conditions on an organism's physiological traits. We combined an empirical model of temperature‐dependent embryonic development with a mechanistic model of soil temperatures to examine potential thermal limitations on the distribution of a nocturnal, oviparous skink, Oligosoma suteri, a range‐restricted endemic.
Location
New Zealand.
Methods
We estimated a thermal requirement for successful embryonic development as 616 degree‐days above a threshold of 13.8°C. We then modelled soil temperatures at representative sites across New Zealand and predicted duration of incubation to map the distribution of potentially viable oviposition sites, given variation in the timing of egg‐laying under even temperature increases.
Results
Successful development of O. suteri embryos is possible in locations outside their current distribution. Increasing temperatures increased the species’ potential range, reducing incubation duration and lengthening the oviposition window. However, due to the disconnected nature of their rocky shore habitat, individuals may not be able to disperse to currently uninhabited sites within that extended range. Additionally, although locations may be thermally suitable for incubation, predation by introduced mammals, competition and habitat modification may prevent successful establishment of populations.
Main conclusions
Our models contribute to understanding fundamental physiological constraints on an important life history stage that will inform conservation management actions, including potential future translocations.
“…| 1879 be used to define areas where a higher resolution surface should be generated to confirm model predictions and help inform management decisions (Carter et al, 2015). Given the limited data available for O. suteri (i.e.…”
Section: Model Application and Limitationsmentioning
Aim
Predicting the distribution of species relies increasingly on understanding the spatially explicit constraints of environmental conditions on an organism's physiological traits. We combined an empirical model of temperature‐dependent embryonic development with a mechanistic model of soil temperatures to examine potential thermal limitations on the distribution of a nocturnal, oviparous skink, Oligosoma suteri, a range‐restricted endemic.
Location
New Zealand.
Methods
We estimated a thermal requirement for successful embryonic development as 616 degree‐days above a threshold of 13.8°C. We then modelled soil temperatures at representative sites across New Zealand and predicted duration of incubation to map the distribution of potentially viable oviposition sites, given variation in the timing of egg‐laying under even temperature increases.
Results
Successful development of O. suteri embryos is possible in locations outside their current distribution. Increasing temperatures increased the species’ potential range, reducing incubation duration and lengthening the oviposition window. However, due to the disconnected nature of their rocky shore habitat, individuals may not be able to disperse to currently uninhabited sites within that extended range. Additionally, although locations may be thermally suitable for incubation, predation by introduced mammals, competition and habitat modification may prevent successful establishment of populations.
Main conclusions
Our models contribute to understanding fundamental physiological constraints on an important life history stage that will inform conservation management actions, including potential future translocations.
“…We modelled substrate temperatures for Takapourewa (also referred to as Stephens Island), New Zealand [40°40 0 00″ S 174°00 0 00″ E], a 150-ha offshore island that supports a population of 30,000+ tuatara (Newman, 1987). We used a localized version of the NicheMapR mechanistic microclimate model, which solves heat-mass balance equations for up to ten soil depths (Carter et al, 2015;Kearney & Porter, 2016) (Figure 1). We parameterized the model using local, daily climate data downloaded from the NIWA CliFlo database (see Data accessibility) (Station nos 26169, 12430; http://www.cliflo.…”
Section: Microclimate Componentmentioning
confidence: 99%
“…niwa.co.nz), generating hourly soil temperatures for three climate scenarios: (1) a 'current climate' scenario, using in situ weather station data from the year 2000; (2) a 'minimum warming' scenario predicted for the next century, in which minimum and maximum air temperatures were increased by the predicted range of 0.3-0.9°C, with an increase of 0.3°C in the meteorological austral spring, a 0.6°C increase in autumn and winter, and an increase of 0.9°C in summer; and (3) a 'maximum warming' scenario, in which minimum and maximum temperatures were increased by the predicted range of 4.8-5.6°C, with an increase of 4.8°C in the austral spring, a 5.0°C increase in autumn and winter, and a 5.6°C increase in summer over the next 100 years (Ministry for the Environment (MFE) (New Zealand), 2008). Available shade was simulated as 95% for forested microsites and 0% otherwise, with sites classed as 'forest' or 'nonforest' according to a spatially explicit vegetation map (Carter et al, 2015). The model under-predicted substrate temperatures, compared with measured values (Carter et al, 2015), so modelled soil F I G U R E 1 Flow chart summarizing the procedure for predicting offspring sex ratios for tuatara, using modelled hourly soil temperatures.…”
Section: Microclimate Componentmentioning
confidence: 99%
“…Available shade was simulated as 95% for forested microsites and 0% otherwise, with sites classed as 'forest' or 'nonforest' according to a spatially explicit vegetation map (Carter et al, 2015). The model under-predicted substrate temperatures, compared with measured values (Carter et al, 2015), so modelled soil F I G U R E 1 Flow chart summarizing the procedure for predicting offspring sex ratios for tuatara, using modelled hourly soil temperatures. Semi-enclosed rectangles designate model inputs, enclosed rectangles are model algorithms, parallelograms are outputs, and the diamonds are optional modifications.…”
Section: Microclimate Componentmentioning
confidence: 99%
“…For example, examining species' responses to environmental extremes (Kearney, Matzelle, & Helmuth, 2012) or at range edges requires finer-resolution predictions of microclimate conditions than can be attained by simply modelling distributional limits within available environments. In addition, the coarser the spatial resolution of a predictive surface, the more within-pixel variation is masked and, as a result, model uncertainty increased (Carter et al, 2015). For example, if a population is bounded within an area of 1 km 2 , a model built using 1-km 2 -gridded climate variables (very high resolution on a continental scale) could not capture effects of environmental heterogeneity on that population.…”
Aim
Recognition that statistical models do not always reliably predict habitat suitability under future climate scenarios is leading increasingly to explicit incorporation of the physiological constraints that underlie species’ distributions into spatially explicit predictions. However, computational intensity constrains the use of high‐resolution, process‐explicit models. We examined whether geostatistical analysis can effectively interpolate a biophysical model, reducing the computational investment typically required for using mechanistic methods to inform physiological predictions.
Location
New Zealand [40°40′00″ S 174°00′00″ E].
Methods
We used a spatially explicit, mechanistic microclimate model to predict hourly temperatures at five soil depths under two scenarios of climate warming. Using the predicted soil temperatures as input to a biophysical model of temperature‐dependent embryonic development, we estimated incubation temperatures and corresponding hatchling sex ratios for tuatara, a reptile with temperature‐dependent sex determination, at a submetre horizontal spatial resolution. We then applied ordinary kriging, a robust method of geostatistical interpolation, to estimate predictions throughout the full extent of our study location, an additional 480,000+ microsites, and validated the interpolation against an independent set of predictions.
Results
Ordinary kriging accurately predicted spatial variability in incubation temperatures. Mean predictions were similar between methods, and error in the geospatial model generally decreased with increasing soil depth. Error was higher for the geospatial model of the ‘maximum warming’, compared with the ‘minimum warming’, scenario of climate change.
Main conclusions
Our results show that ordinary kriging can be a reliable method for interpolating variability in high‐resolution predictions. However, the effects of error on the accuracy of interpolated predictions will become more severe as values approach a physiological threshold, such as the minimum and maximum incubation temperatures that result in extreme sex ratio bias. For distribution models, the widths of geographic areas predicted to be suitable for, in this case, maintaining balanced sex ratios, compared to those predicted to be unsuitable, may be narrower than in reality.
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