This document discusses using measures of evolutionary distinctiveness (ED) and endangerment to prioritize conservation of endangered species. It proposes a new metric called regional evolutionary distinctiveness and endangerment (RED-E) that incorporates both a species' distinctiveness within its region as well as its level of regional endangerment. The document outlines the methodology for calculating RED-E values and applies it to mammals and birds in the continental US, finding RED-E captures similar but not identical priorities as the existing global EDGE metric. It concludes RED-E can be a useful conservation planning tool at regional levels.
Presentation slides from a webinar featuring results from the Climate Change Atlas for New England and northern New York. Part of the New England Climate Change Response Framework (www.forestadaptation.org). Presentation by Louis Iverson, Steve Matthews, and Maria Janowiak.
Presentation slides from a webinar featuring results from the Climate Change Atlas for New England and northern New York. Part of the New England Climate Change Response Framework (www.forestadaptation.org). Presentation by Louis Iverson, Steve Matthews, and Maria Janowiak.
Emerging Issues Presentation Housing Development In Upstatetdilan
Courter, J. R., Surasinghe, T. D., Baldwin, R. F. And Johnson, R. J. (2010). The Impacts of Housing Development on Birds and Amphibians in Upstate South Carolina. Immerging issues along urban rural interfaces, Atlanta, GA.
Emerging Issues Presentation Housing Development In Upstatetdilan
Courter, J. R., Surasinghe, T. D., Baldwin, R. F. And Johnson, R. J. (2010). The Impacts of Housing Development on Birds and Amphibians in Upstate South Carolina. Immerging issues along urban rural interfaces, Atlanta, GA.
Reproduction of Tadorna ferruginea (Pallas, 1764)[Ruddy Shelduck] was studied in the two lakes of Middle Atlas, Morocco namely Afennourir lake and Sidi Ali lake. This water Duck is unusual to build nests at the cedar forests around these lakes. Most nests are placed in the holes in cedar trees (Cedrus atlantica) located at heights varying between 5 and 25m and an average distance of 3km lake. To characterize the nests of Ruddy Shelduck and analyze intrinsic determinants of the choice of type of nest, we conducted a factor analysis of Mixed Data (FAMD) of 13 mesological descriptors studied in 22 nests around the two lakes viz., Afennourir and Sidi Ali. This treatment was performed on the basis of morphometric characters and geomorphological data of the nests.
The classification obtained allowed us to highlight the main nest groups that have similarities and correlations between them. On the whole, the density and composition of the forest around the nesting tree, the age of the nest tree, nesting orientation, the nature of the vegetation cover and the persistence of nesting tree on the soil flux are the most explanatory variables that differ in the grouping of nests. The Ruddy Shelduck mainly uses the following techniques to build the nest: Presence of a dense and diverse forest stands with old cedar forests, soil cover flush with the shaft supporting the nest and Southwest orientation or Southeast opening of nests. This analysis confirms that the cedar forests around the Middle Atlas lakes offer good conditions for the construction of nests for this species.
Authors: Gabriel M. Moulatlet (1), Byron Maza (1,3), Marina Rodes Blanco (1), Karolina Riaño (2)
(1) - Universidad Regional Amazónica Ikiam-ECU
(2) - Cátedra CONACyT, Universidad de Guadalajara-MEX
(3) - Universidad Yachay-ECU
How can we increase our capacity to predict ecosystem responses to environmen...Tano Gutiérrez Cánovas
Chronic stress modifies the structure and function of ecosystems through different processes. Despite that some convergent responses have been found, as changes in community composition and a reduction in diversity, there is unclear how this may affect to the processes explaining changes in beta diversity and ecosystem features. In my research, I used stream macroinvertebrates to explore these questions, as they offer interesting properties to test ecological hypotheses. As these organisms respond to marked environmental habitats, we use natural and anthropogenic stress gradients to see if the degree in which the regional pool of species is adapted to a type of stress, may cause patterns that help to predict responses to ongoing global change. In a first work, I found that natural and anthropogenic stressors reduced species richness and generate contrasting patterns in beta diversity that arise through different mechanisms. While species turnover along natural stress gradients, nested subset of species developed over anthropogenic stress gradients. In a second work, we estimate some functional diversity measures from a multidimensional space composed of axes that represented the variation in biological traits of the aquatic community. Functional measures consisted of mean taxon functional richness (functional variability at taxon level), functional similarity (the percentage of niche overlap between taxon pairs), functional richness (functional variability at community level), functional dispersion (mean departure from community centroid) and functional redundancy (sum of overlapping areas between species pairs). We found similar functional responses to natural and anthropogenic stress, where mean taxon niche and functional similarity augmented with increased stress, while functional richness, dispersion and redundancy decreased when stress intensity augmented. The reduction in functional richness arose from the development of nested subsets of community traits along stress gradient. The results of these studies may have strong conservation implications and may help to predict the ecosystem responses to global change and to elucidate how organisms colonized and evolved in stressful habitats.
Evaluating bird species diversity based on distribution area and taxonomic un...CIFOR-ICRAF
There are a number of different indicators used to evaluate the biodiversity of an area and its relative importance for protection and conservation – each method produces quite different outcomes. Using Japan as a case study, this presentation examines the different ways of evaluating biodiversity hotspots and proposes an additional methodology using range size and taxonomy that may help decision makers worldwide in determining hotspots for conservation. CIFOR scientist Ken Sugimura gave this presentation at the first Annual World Congress of Biodiversity: Today Eco-civilisation, Tomorrow Happiness, held in Xi’an, China on 25–28 April 2012.
2. Dr. John Withey
Dr. Maureen
Donnelly
Dr. Ken Feeley
Dr. Will Pearse
Florida International
University
Resources For the
Future (RFF)
ACKNOWLEDGEMENTS
3. 27,000 spp/ year
Limited resources
BIODIVERSITY LOSS
Nature Climate Change
6. “phylogenetic diversity of a clade split equally among its
members, taking each branch length for all species into
account”
Correlates with other biodiversity measures
Richness, diversity
ED IMPORTANCE
13. RED-E
Regional, not global
Applicable to any
region
2 Components
Regional Evolutionary
Distinctiveness
RED
Regional
Endangerment
RE
REGIONAL EVOLUTIONARY
DISTINCTIVENESS AND ENDANGERMENT
14. 5 Factors
Damage to or
destruction of a spp’s
habitat
Overutilization of the
spp for commercial, rec,
science, or education
Disease or predation
Inadequacy of existing
protection
Other natural or
manmade factors
ENDANGERED SPECIES ACT (ESA)
16. illegal to "take”
“to harass, harm, pursue,
hunt, shoot, wound, kill,
trap, capture, or collect or
attempt to engage in any
such conduct.”
Critical Habitat
ESA
28. Continental US only
Used drop.tip function
3 mammals trees
Upper
Best
lower
1000 bird trees
Ran ed.calc again
REGIONAL ED
29. IUCN (Global Endangerment)
Least Concern – 0
Near Threatened – 1
Vulnerable – 2
Endangered – 3
Critically Endangered – 4
ESA (Regional Endangerment)
Threatened – 2
Endangered – 4
SAT Species
“threatened due to similar
appearance”
GE AND RE CALCULATION
GE or RE = E * ln(2)
31. EDGE & RED-E calculated from trees with differing branch
numbers
Cannot be directly compared
Used # of std deviations away from the mean
Both have 2 components- ED/RED and GE/RE
Compared relative influence
Regression
STATISTICS
32. Threatened = 0, 1, or 2
Endangered = 1, 2, or 4
Calculated change in rank
SENSITIVITY TO VALUES USED FOR
THREATENED AND ENDANGERED STATUS
33. FWS conservation expenditure reports
2001-2012
Regressed money spend against RED-E value
COST OF PROTECTION
34. Ranked species without CH
Mammals
Birds
RED-E vs EDGE rank change
CH PRIORITY
36. Mammal
Range
7.41 – Utah Prairie Dog
3.33 – West Indian Manatee
Mean – 5.30
Median – 5.33
RED-E
37. Bird
Range
6.27 – Ivory-Billed Woodpecker
3.13 – Roseate Tern
Mean – 5.01
Median – 5.10
RED-E
38. -2.5
-2
-1.5
-1
-0.5
0
0.5
1
1.5
2
2.5
-3 -2 -1 0 1 2 3
EDGE(sdawayfrommean)
RED-E (sd away from mean)
Average rank
change
24 places within
83 species
0.98 deviations
MAMMAL RED-E AND EDGE
Correlation of standardized mammal RED-E and
EDGE scores (R2 = 0.10, p = 0.0029 )
39. MAMMAL RED-E AND EDGE
-4
-3
-2
-1
0
1
2
3
-4 -3 -2 -1 0 1 2
EDGEtoRED-Echange
GE to LE change
A
-4
-3
-2
-1
0
1
2
3
-2 -1 0 1 2 3
EDGEtoRED-Echange
RED to ED change
B
R2 = 0.83 R2 = 0.23
GE to RE change ED to RED change
GE to RE change
40. Average rank
change
13 places within
44 species
1.08 deviations
BIRD RED-E AND EDGE
Correlation of standardized mammal RED-E and
EDGE scores (R2 = 0.022, p = 0.33 )
-2.5
-2
-1.5
-1
-0.5
0
0.5
1
1.5
2
-2 -1 0 1 2 3 4
EDGE(sdawayfrommean)
RED-E (sd away from mean)
41. BIRD RED-E AND EDGE
-4
-3
-2
-1
0
1
2
3
-2 -1 0 1 2 3
EDGEtoRED-Echange
RED to ED change
B
-4
-3
-2
-1
0
1
2
3
-2 -1 0 1 2
EDGEtoRED-Echange
RED to ED change
B
R2 = 0.86 R2 = 0.17
GE to RE change
GE to RE change ED to RED change
42. no difference between (T = 0, E = 1) and (T = 1, E = 2)
(T = 2, E = 4) to (T = 1, E = 2)
No change on extreme ends
Top 5 and bottom 4 remained the same
Threatened species prioritization increased
T/E SENSITIVITY
43. RED-E AND COST OF PROTECTION
0
20
40
60
80
100
120
140
160
180
200
3.0 4.0 5.0 6.0 7.0 8.0
Expenditures(millionsof$)
Mammal RED-E value
0
50
100
150
200
250
300
350
3.0 4.0 5.0 6.0 7.0
Expenditures(millionsof$)
RED-E value
No correlation in birds or mammals
Mammals: R2 = 0.013 p = 0.306
Birds: R2 = 0.0091 p = 0.598
44. RED-E and EDGE correlated in mammals (p = 0.0354)
Not correlated in birds
CRITICAL HABITAT
46. EDGE
Global
Limited use
IUCN Ranking- gold standard
No subspecies or
populations
RED-E
Regional
Region-specific
Blurry lines between T and E
Good for governments or
agencies
Florida Panther
Both
Need complete or almost
complete tree w/ at least
100 spp
Scores can be compared
directly across trees
RED-E VERSUS EDGE
47. T = 2 and E = 4 used for analysis
Other values reduced the impact of RE component
Broke down some of the prioritization already in place
Only extremely distinct T spp should be prioritized over E
T/E SENSITIVITY
48. Expected correlation because RED-E is sensitive to ESA status
E spp more likely to have dedicated conservation plan
7 mammals with most past conservation attention
(>$50million spent) mostly large, charismatic spp, and only 4
listed as endangered
Ocelot
Florida Panther
2 populations of Black Bears
Sea Lions
Manatees
(One species of bat)
COST OF PROTECTION
49. Practical application
Can go into effect immediately
Controversial, but:
Land-use modification
Increases public education in CH areas
Only protection for unoccupied habitats
Spp w/ designation more likely to have actively implemented and
revised recovery plans
CRITICAL HABITAT
50. Closely related spp that are all endangered many be lower on
the list
Reasoning for high prioritization of endangerment level
Trees are based on most likely configurations
This approach is can be updated easily
LIMITATIONS
51. Same analysis on
other species
Biodiversity hotspots
Other countries
categories (ESA)
New Zealand: NZTCS
Australia: EPBC, DEC
Canada: COSEWIC
OTHER APPLICATIONS
53. 1. Identify area for conservation planning
2. Collect phylogenetic trees for global clade chosen
More than 100 spp
No overlapping spp
3. Trim trees
4. Use R, caper, and the ed.calc function to calculate regional
evolutionary distinctiveness for each species.
5. Assign number values to agency conservation status,
preferably from 0-4.
If no agency conservation status is available, IUCN status can be
used.
STEPS
54. 6. Calculate regional evolutionary distinctiveness (RED)
component
RED component =ln1+RED
7. Calculate regional endangerment (RE) component
RE component =RE*ln(2)
8. Add RED and RE to get RED-E score.
9. Order RED-E scores from largest to smallest
Largest score of most concern
STEPS
56. Simple ranking system
for use of limited
resources
Powerful conservation
tool
managers, geneticists, and
the public
With effort from
agencies around the
world, biodiversity loss
can be mitigated
RED-E
58. Bininda-Emonds, O. R., Cardillo, M., Jones, K. E., MacPhee, R. D., Beck, R. M., Grenyer,
R., ... & Purvis, A. (2007). The delayed rise of present -day mammals. Nature, 446(7135),
07-512.
Bennett, P. M., & Owens, I. P. (1997). Variation in extinction risk among birds: chance or
evolutionary predisposition?. Proceedings of the Royal Society of London. Series B:
Biological Sciences, 264(1380), 401-408.
Butchart SHM, Walpole M, Collen B, van Strien A, Scharlemann JPW, et al. (2010) Global
biodiversity: indicators of recent declines. Science 328: 1164{1168.
Cowlishaw, G. (1999). Predicting the pattern of decline of African primate diversity: an
extinction debt from historical deforestation. Conservation Biology, 13(5), 1183-1193.
Department of the Interior, U.S. Fish and Wildlife Services (FWS). (1973). Endangered
Species Act of 1973. Washington, D.C. 20240.
Department of the Interior, U.S. Fish and Wildlife Sevices (FWS). (2015). Endangered
Species. http://www.fws.gov/endangered/
Grelle, C. E. D. V., Fonseca, G. A. B., Fonseca, M. T., & Costa, L. P. (1999). The question
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Isaac NJB, Redding DW, Meredith HM, Sa_ K (2012) Phylogenetically -informed priorities
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International Union for the Conservation of Nature (IUCN). (2014) IUCN Red List of
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