This map of Local connectedness measures how impaired the
structural connections are between natural ecosystems within a local landscape.
Roads, development, noise, exposed areas, dams, and other structures all
directly alter processes and create resistance to species movement by
increasing the risk (or perceived risk) of harm. This dataset is an important
component of resilience because it indicates whether a process is likely to be
disrupted or how much access a species has to the microclimates within its
given neighborhood.
The method used to map local connectedness for the region
was resistant kernel analysis, developed and run by Brad Compton using software
developed by the UMASS CAPS program (Compton et al. 2007,
http://www.umasscaps.org). Connectedness refers to the connectivity of a focal
cell to its ecological neighborhood when it is viewed as a source; in other
words, it asks the question: to what extent are ecological flows outward from
that cell impeded or facilitated by the surroundinglandscape? Specifically,
each cell is coded with a resistance value base on land cover and roads, which
are in turn assigned resistance weights by the user. The theoretical spread of
a species or process outward from a focal cell is a function of the resistance
values of the neighboring cells and their distance from the focal cell out to a
maximum distance of three kilometers.
To calculate this metric, resistance weights were assigned
to the elements of a land cover/road map. A variety of methods have been
developed for determining resistance weights, in particular metrics of
ecological similarity in community types (e.g. oak forest to oak forest assumed
to be more connected than oak forest to spruce forest) have been used to good
effect (B. Compton personal communication 2009, Compton et al. 2007). However,
our weighting scheme was intentionally more generalized, such that any natural
cover adjacent to other natural cover was scored as highly connected. We did
not differentiate between forest types, and only slightly between open wetland
and upland habitats (Table 1). Our assumption was that the requirements for
movement and flows through natural landscape were less specific than the
requirements for breeding, and that physical landscapes are naturally composed
of an interacting mosaic of different ecosystems. Our goal was to locate areas
where these arrays occur in such a way as o maintain their natural
relationships and the connections between all types of flows, both material
processes and species movements, not to maximize permeability for a single
species (Hunter and Sulzer 2002, Ferrari and Ferrarini 2008, Forman and Godron
1986).
The resistance grid i was based on a 90-meter classified
land use map with roads embedded in the grid. The source data was the 2001 NLCD
for United States and NALC 2005 for Canada that identify each grid cell as one
of 16 classes of land cover (NALCMS 2005). We used 90-meter grid cells to make
a reasonable processing time because the CAPS software program is
computationally intense.
The final result was a grid of 90-meter cells for the entire
region where each cell was scored with a local connectivity value from 0 (least
connected) to 100 (most connected).