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Barrie Creeks, Lovers Creek, and Hewitt's Creek Subwatershed Plan

Barrie Creeks, Lovers Creek, and Hewitt's Creek Subwatershed Plan

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The <strong>Barrie</strong> <strong><strong>Creek</strong>s</strong>, <strong>Lovers</strong> <strong>Creek</strong> <strong>and</strong> Hewitt’s <strong>Creek</strong> <strong>Subwatershed</strong> <strong>Plan</strong><br />

The most common forest types in the <strong>Barrie</strong> <strong><strong>Creek</strong>s</strong> subwatershed are cultural woodl<strong>and</strong>s<br />

(which refers to young or early successional forests, often dominated by species such as<br />

trembling aspen, eastern white cedar, or red cedar), <strong>and</strong> deciduous <strong>and</strong> mixed forests. Similarly,<br />

the most common woodl<strong>and</strong>s in the <strong>Lovers</strong> <strong>Creek</strong> subwatershed are deciduous <strong>and</strong> mixed<br />

forests, <strong>and</strong> in the Hewitt’s <strong>Creek</strong> subwatershed are deciduous forests (Table 6-1). Deciduous<br />

<strong>and</strong> mixed forests are found typically on well drained s<strong>and</strong>y loam sites. Deciduous forests are<br />

found more typically on relatively flat ground around the crest of the glacial meltwater valley<br />

extending from the tip of Kempenfelt Bay (Figure 2-22, Chapter 2 – Study Area), while mixed<br />

forests are more common on areas with steeper slopes (including ravines, <strong>and</strong> the side of that<br />

glacial valley) which have slightly cooler microclimates (Figure 6-3).<br />

Relatively uncommon in these subwatersheds are coniferous woodl<strong>and</strong>s (including forests,<br />

swamps, <strong>and</strong> plantations), which account for only 17% of the total woodl<strong>and</strong>. These uncommon<br />

forest types provide habitat for unique wildlife communities, particularly those which prefer<br />

coniferous woodl<strong>and</strong>s, such as pine warbler (Dendroica pinus), Cooper’s hawk (Accipiter<br />

cooperii), <strong>and</strong> blue jay (Cyanocitta cristata) (Bird Studies Canada et al., 2008).<br />

Structural diversity of habitat is a key driver of biodiversity. In woodl<strong>and</strong>s, habitat niches can<br />

range from microhabitats such as the surfaces of fissured trunks, leaves, <strong>and</strong> rotting logs to<br />

macrohabitat features such as the horizontal layers within the woodl<strong>and</strong> (e.g. supercanopy,<br />

canopy, subcanopy). In addition, woodl<strong>and</strong>s are present in a wide variety of topographic<br />

settings <strong>and</strong> soil <strong>and</strong> moisture regimes. For all of these reasons it is not surprising that many<br />

woodl<strong>and</strong> species are obligates (i.e. they are only found in woodl<strong>and</strong>s), or that woodl<strong>and</strong>s<br />

provide habitat for a wide range of flora <strong>and</strong> fauna. They form important building blocks of the<br />

natural heritage system.<br />

The summary statistics reflecting the percentage of the watershed under forested cover cannot<br />

address these more detailed issues related to the diversity <strong>and</strong> ecological integrity of individual<br />

forest patches. These issues relate typically to factors such as forest size, forest age, proximity<br />

to other natural areas, topographic heterogeneity, <strong>and</strong> structural diversity within the forest.<br />

Policy 6.48 of the LSPP requires the MNR (in collaboration with the LSRCA, First Nations, <strong>and</strong><br />

Métis communities) to map <strong>and</strong> identify `high quality` natural areas in the Lake Simcoe<br />

watershed. When this policy has been developed <strong>and</strong> mapping complete, more could be said<br />

about the distribution of these site-specific quality measures in this study area.<br />

Although the total extent of forest cover in a subwatershed is the primary driver for many forestdependent<br />

ecological processes, some species are also sensitive to the size of remnant forest<br />

patches (Robbins et al., 1989; Lee et al., 2002), the amount of ‘interior’ forest habitat (Burke <strong>and</strong><br />

Nol, 1998a; Burke <strong>and</strong> Nol, 2000), <strong>and</strong> the proximity or connectivity between remnant forest<br />

patches (Nupp <strong>and</strong> Swihart, 2000).<br />

Contiguous woodl<strong>and</strong> areas have been calculated <strong>and</strong> the distributions of woodl<strong>and</strong> patch sizes<br />

are displayed in Figure 6-4, Figure 6-5, <strong>and</strong> Figure 6-6. While the total area of woodl<strong>and</strong><br />

represents the amount of forest completely within the subwatershed, the number of patches<br />

also includes any patches touching the subwatershed boundary. This methodology was used to<br />

avoid underestimating the number of large patches. If only patches within the subwatershed<br />

boundaries were considered, the number of large patches would be underestimated.<br />

The <strong>Barrie</strong> <strong><strong>Creek</strong>s</strong> subwatershed is characterized by a large number of small forest patches<br />

(Figure 6-3, Figure 6-4). There are a total of 117 separate patches of woodl<strong>and</strong> in this<br />

subwatershed, 90% of which are small (less than 10 ha in size). Despite their small size,<br />

collectively these small fragments represent half of the subwatershed’s total forest cover. The<br />

Chapter 6: Terrestrial Natural Heritage 268

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