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Fact Sheet: Habitat - Forested Stream and/or Seepage
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Forested stream environments are typically found in the buffer zones between forested land and stream banks, often known as riparian zones. Stream headwaters and seepage areas occur where ground water percolates to the surface through muck, mossy rock, and nettles. It can also be found under rocks, among gravel, or cobble where water has begun to percolate in areas near open water. Breeding grounds are commonly found beneath mosses growing on rocks, on logs, or soil surfaces in these types of seepage areas.
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Fact Sheets
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Fact Sheet: Habitat - Meadows and Marshlands
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Meadows are open grasslands where grass and other non-woody plants are the primary vegetation. With no tree coverage, meadows are typically open, sunny areas that attract flora and fauna that require both ample space and sunlight. These conditions allow for the growth of many wildflowers and are typically important ecosystems for pollinating insects. Marshlands are like meadows in that they typically have no tree coverage and host primarily grasses and woody plants. However, a defining characteristic of marshlands is their wetland features.
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Publications & Outreach
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Fact Sheets
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Fact Sheet: Habitat - Open Woodlands
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Used generally to describe low density forests, open woodland ecosystems contain widely spaced trees whose crowns do not touch, causing for an open canopy, insignificant midstory canopy layer, sparse understory and where groundcover is the most obvious feature of the landscape dominated by diverse flora (grasses, forbes, sedges). Open Woodlands provide habitat for a diverse mix of wildlife species, several of which are of conservation concern, such as Red Headed Woodpecker, Prairie Warbler, Kentucky Warbler, Northern Bobwhite and Eastern Red Bat.
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Publications & Outreach
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Fact Sheets
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Palaeodata-informed modelling of large carbon losses from recent burning of boreal forests
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Wildfires play a key role in the boreal forest carbon cycle(1,2), and models suggest that accelerated burning will increase boreal C emissions in the coming century (3). However, these predictions may be compromised because brief observational records provide limited constraints to model initial conditions (4). We confronted this limitation by using palaeoenvironmental data to drive simulations of long-term C dynamics in the Alaskan bo- real forest. Results show that fire was the dominant control on C cycling over the past millennium, with changes in fire frequency accounting for 84% of C stock variability. A recent rise in fire frequency inferred from the palaeorecord5 led to simulated C losses of 1.4 kg C m?2(12% of ecosystem C stocks) from 1950 to 2006. In stark contrast, a small net C sink of 0.3 kg C m?2 occurred if the past fire regime was assumed to be similar to the modern regime, as is common in models of C dynamics. Although boreal fire regimes are heterogeneous, recent trends6 and future projections (7) point to increasing fire activity in response to climate warming throughout the biome. Thus, predictions (8) that terrestrial C sinks of northern high latitudes will mitigate rising atmospheric CO2 may be over-optimistic.
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Resources
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Climate Science Documents
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Worldwide evidence of a unimodal relationship between productivity and plant species richness
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The search for predictions of species diversity across environmental gradients has challenged ecologists for decades. The humped-back model (HBM) suggests that plant diversity peaks at intermediate productivity; at low productivity few species can tolerate the environmental stresses, and at high productivity a few highly competitive species dominate. Over time the HBM has become increasingly controversial, and recent studies claim to have refuted it. Here, by using data from coordinated surveys conducted throughout grasslands worldwide and comprising a wide range of site productivities, we provide evidence in support of the HBM pattern at both global and regional extents. The relationships described here provide a foundation for further research into the local, landscape, and historical factors that maintain biodiversity.
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Resources
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Climate Science Documents
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Human mining activity across the ages determines the genetic structure of modern brown trout (Salmo trutta L.) populations
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Humans have exploited the earth’s metal resources for thousands of years leaving behind a legacy of toxic metal contamination and poor water quality. The southwest of England provides a well-defined example, with a rich history of metal mining dating to the Bronze Age. Mine water washout continues to negatively impact water quality across the region where brown trout (Salmo trutta L.) populations exist in both metal-impacted and relatively clean rivers. We used micro- satellites to assess the genetic impact of mining practices on trout populations in this region. Our analyses demonstrated that metal-impacted trout populations have low genetic diversity and have experienced severe population declines. Metal-river trout populations are genetically distinct from clean-river populations, and also from one another, despite being geographically proximate. Using approximate Bayesian computation (ABC), we dated the origins of these genetic patterns to periods of intensive mining activity. The historical split of contemporary metal-impacted populations from clean-river fish dated to the Medieval period. Moreover, we observed two distinct genetic populations of trout within a single catchment and dated their divergence to the Industrial Revolution. Our investigation thus provides an evaluation of contemporary population genetics in showing how human-altered landscapes can change the genetic makeup of a species.
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Climate Science Documents
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Bird Richness and Abundance in Response to Urban Form in a Latin American City
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There is mounting evidence that urban areas influence biodiversity. Generalizations how- ever require that multiple urban areas on multiple continents be examined. Here we evaluated the role of urban areas on avian diversity for a South American city, allowing us to examine the effects of urban features common worldwide, using the city of Valdivia, Chile as case study. We assessed the number of birds and their relative abundance in 152 grid cells of equal size (250 m2) distributed across the city. We estimated nine independent variables: land cover diversity (DC), building density (BD), impervious surface (IS),municipal green space (MG),non-municipal green space (NG), domestic garden space (DG), distance to the periphery (DP), social welfare index (SW), and vegetation diversity (RV). Impervious surface represent 41.8% of the study area, while municipal green, non-municipal green and domestic garden represent 11.6%, 23.6% and 16% of the non- man made surface. Exotic vegetation species represent 74.6% of the total species identified across the city. We found 32 bird species, all native with the exception of House Sparrow and Rock Pigeon. The most common species were House Sparrow and Chilean Swallow. Total bird richness responds negatively to IS and MG, while native bird richness responds positively to NG and negatively to BD, IS DG and, RV. Total abundance increase in areas with higher values of DC and BD, and decrease in areas of higher values of IS, SW and VR. Native bird abundance responds positively to NG and negatively to BD, IS MG, DG and RV. Our results suggest that not all the general patterns described in previous studies, conducted mainly in the USA, Europe, and Australia, can be applied to Latin American cities, having important implications for urban planning. Conservation efforts should focus on non-municipal areas, which harbor higher bird diversity, while municipal green areas need to be improved to include elements that can enhance habitat quality for birds and other species. These findings are relevant for urban planning in where both types of green space need to be considered, especially non-municipal green areas, which includes wetlands, today critically threatened by urban development.
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Climate Science Documents
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Protected areas in Borneo may fail to conserve tropical forest biodiversity under climate change
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Protected areas (PAs) are key for conserving rainforest species, but many PAs are becoming increasingly
isolated within agricultural landscapes, which may have detrimental consequences for the forest biota
they contain. We examined the vulnerability of PA networks to climate change by examining connectivity
of PAs along elevation gradients. We used the PA network on Borneo as a model system, and examined
changes in the spatial distribution of climate conditions in future. A large proportion of PAs will not
contain analogous climates in future (based on temperature projections for 2061–2080), potentially
requiring organisms to move to cooler PAs at higher elevation, if they are to track climate changes. For
the highest warming scenario (RCP8.5), few (11–12.5%; 27–30/240) PAs were sufficiently topographically
diverse for analogous climate conditions (present-day equivalent or cooler) to remain in situ. For the
remaining 87.5–89% (210–213/240) of PAs, which were often situated at low elevation, analogous climate
will only be available in higher elevation PAs. However, over half (60–82%) of all PAs on Borneo are too
isolated for poor dispersers (<1 km per generation) to reach cooler PAs, because there is a lack of connecting
forest habitat. Even under the lowest warming scenario (RCP2.6), analogous climate conditions will
disappear from 61% (146/240) of PAs, and a large proportion of these are too isolated for poor dispersers
to reach cooler PAs. Our results suggest that low elevation PAs are particularly vulnerable to climate
change, and management to improve linkage of PAs along elevation gradients should be a conservation
priority
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Climate Science Documents
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A drought-induced pervasive increase in tree mortality across Canada’s boreal forests
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Drought-induced tree mortality is expected to increase worldwide under projected future climate changes (1–4). The Canadian boreal forests, which occupy about 30% of the boreal forests worldwide and 77% of Canada’s total forested land, play a critical role in the albedo of Earth’s surface (5) and in its global carbon budget (6). Many of the previously reported regional-scale impacts of drought on tree mortality have affected low- and middle-latitude tropical regions (2) and the temperate forests of the western United States (3), but no study has examined high-latitude boreal regions with multiple species at a regional scale using long-term forest permanent sampling plots (7–9). Here, we estimated tree mortality in natural stands throughout Canada’s boreal forests using data from the permanent sampling plots and statistical models. We found that tree mortality rates increased by an overall average of 4.7%yr−1 from 1963 to 2008, with higher mortality rate increases in western regions than in eastern regions (about 4.9 and 1.9% yr−1 ,respectively).The water stress created by regional drought may be the dominant contributor to these widespread increases in tree mortality rates across tree species, sizes, elevations, longitudes and latitudes. Western Canada seems to have been more sensitive to drought than eastern Canada.
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Climate Science Documents
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South-Central Interior Small Stream and Riparian Habitat
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This habitat was assessed in both the Cumberland - Southern Appalachian subregion and the Interior Low Plateau subregion. Results are in the first two tabs of the spreadsheet. A description of the habitat, and a list of associated species, is included in the description tab. The remaining tabs describe the individual factors and their definitions. These results are in the review stage. Please send comments to lesley_sneddon@natureserve.org.
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Phase II: Vulnerability Assessments
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Habitat Vulnerability Assessments
