geography of communities

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Page 1: Geography of Communities

Geography of Communities

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image source: www.dmr.nd.gov/ndfossil

Page 2: Geography of Communities

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Geography of Communities

Page 3: Geography of Communities

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Species rarely occur alone but instead coexist with other species in communities. 1) Describe biogeoclimatic zones (or ecoregions) and biomes, globally and

regionally

2) Explore the role that energetics and productivity have in assembly of communities

3) Understand perspectives of whether species distributions are independent or dependent on other species within communities

4) Examine how communities change over space and time

5) Discuss whether communities are random collections of species that are co-distributed more by historical accident than determinism

Geography of Communities

Page 4: Geography of Communities

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Species exist in communities

By Sten Porse (Image:Vegetation) [CC-BY-SA-3.0 (www.creativecommons.org/licenses/by-sa/3.0)], via Wikimedia Commons

Biogeoclimatic Zones

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Species exist in communities Biogeoclimatic zones of BC (British Columbia Forest Service) after dominant tree species:

Coastal Western Hemlock

Biogeoclimatic Zones

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Species exist in communities Biogeoclimatic zones, ecoregions, and biomes are defined by: 1. precipitation 2. humidity 3. temperature 4. soil characteristics 5. microbial life 6. flora 7. fauna

Biomes: regions defined on the basis of distinct abiotic and biotic characteristics involving climatic and soil conditions and assemblage of plant and animal species.

Biogeoclimatic Zones

Page 7: Geography of Communities

Terrestrial Biomes

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Major Terrestrial Biomes:

Our most productive terrestrial biomes are in places that are hot and wet

Least productive terrestrial biomes are

cold and dry

Page 8: Geography of Communities

Terrestrial Biomes

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Major Terrestrial Climatic Patterns:

(From Lomolino et al. 2010)

Page 9: Geography of Communities

Terrestrial Biomes

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Major Terrestrial Biomes:

(From Lomolino et al. 2010)

Page 10: Geography of Communities

Terrestrial Biomes

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Matching Terrestrial Patterns in Soil Type:

(From Lomolino et al. 2010)

Page 11: Geography of Communities

Aquatic Biomes

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Marine

northern temperate

subarctic

arctic

northern subtropical

tropical

southern subtropical

southern temperate

subantarctic

antarctic

Page 12: Geography of Communities

Aquatic Biomes

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Marine

photic

aphotic

(From Lomolino et al. 2010)

Page 13: Geography of Communities

Aquatic Biomes

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Freshwater Basic division between flowing lotic environments (streams, rivers) and standing water lentic environments (lakes, ponds, swamps) Freshwater environment is profoundly influenced by surrounding terrestrial environment

(From Lomolino et al. 2010)

Dep

th (

m)

Page 14: Geography of Communities

Biome Comparisons

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(From Lomolino et al. 2010)

Total NPP (Net Primary Productivity) Total Surface Area

Only the open ocean has both high surface area and high NPP Only Tropical and Temperate forest have low surface area and high NPP

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Community assemblage depends, in part, on energetics and productivity

Energetics and Communities

Two basic characteristics affect energy use: body mass and trophic level Let’s look at trophic level first:

http://picasaweb.google.com/lh/photo/PifWR9JmBZcrm-7nihofCA

Organisms use stored energy to move, grow and reproduce When energy stores are used, most (> 90%) energy is dissipated as heat Most organisms can only incorporate 1-10% of energy into tissue Producers harness 1% of sunlight resources

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Energetics and Communities

http://universe-review.ca/R10-35-metabolic.htm

Body mass scales with metabolic rate as a power function (note the log scale) between 2/3 and 3/4 This means that bigger animals have higher (whole organism) metabolic rates and need more energy to meet their energetic demands

MR = c M3/4

Mass (g, log scale)

Met

abo

lic r

ate

(kca

l/h

, lo

g sc

ale)

Community assemblage depends, in part, on energetics and productivity

Two basic characteristics affect energy use: body mass and trophic level

Page 17: Geography of Communities

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Energetics and Communities

Tertiary consumers tend to be large bodied and numerically rare in communities: they have the largest energetic demands and receive the lowest amount of energy compared to lower trophic levels

http://universe-review.ca/R10-35-metabolic.htm http://picasaweb.google.com/lh/photo/PifWR9JmBZcrm-7nihofCA

Community assemblage depends, in part, on energetics and productivity

MR = c M3/4

Mass (g, log scale)

Met

abo

lic r

ate

(kca

l/h

, lo

g sc

ale)

Page 18: Geography of Communities

18 (From Currie 1991)

Energetics and Communities

Recall where the productive terrestrial biomes are: we should have more species represented at all trophic levels in these biomes

Community assemblage depends, in part, on energetics and productivity

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By Sten Porse (Image:Vegetation) [CC-BY-SA-3.0 (www.creativecommons.org/licenses/by-sa/3.0)], via Wikimedia Commons

Energetics and Communities

Community assemblage depends, in part, on energetics and productivity

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Interdependence of species in communities

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One of the longest standing themes in community ecology is the definition of an ecological community How do we define communities of coexisting species? What “boundaries” separate one community from another? To what extent are coexisting species interdependent? The classic views: cohesive-unit and individualistic communities The expanding view: Ricklefs’ communities should not be defined

Page 21: Geography of Communities

21 21 Environmental gradient

Spec

ies

Ab

un

dan

ce

(From Whittaker 1975)

Interdependence of species in communities

Whittaker describes a classic and comprehensive view of the delineation of communities and distribution of species within those communities

Page 22: Geography of Communities

22 22 Environmental gradient

Spec

ies

Ab

un

dan

ce

(From Whittaker 1975)

Interdependence of species in communities

The “individualistic” hypothesis, proposed by Gleason, states that species do not occur in definable communities

Whittaker describes a classic and comprehensive view of the delineation of communities and distribution of species within those communities

Page 23: Geography of Communities

23 23 Environmental gradient

Spec

ies

Ab

un

dan

ce

(From Whittaker 1975)

Interdependence of species in communities

Clements proposed that co-occurring species occur as definable units ...species within communities were interdependent and coevolved

Whittaker describes a classic and comprehensive view of the delineation of communities and distribution of species within those communities

Page 24: Geography of Communities

24 24 Environmental gradient

Spec

ies

Ab

un

dan

ce

(From Whittaker 1975)

Interdependence of species in communities

Whittaker combines both individualistic and community-unit scenarios including biotic processes (also competitive interactions and species replacements

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Interdependence of species in communities

An expanding view of communities describes coexisting species as a fluid and undefined assembly of species, where a larger regional “pool” of species (beyond a local community) underlies the composition of species over space and time.

“Disintegration of the Ecological Community” “...the seemingly indestructible concept of the community as a local, interacting assemblage of species has hindered progress toward understanding species richness at local to regional scales...The local community is an epiphenomenon that has relatively little explanatory power in ecology and evolutionary biology” -- Robert Ricklefs

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Five tree species: - black spruce - white spruce - blue spuce - red spruce - Engelmann spruce

(from www.conifers.org)

Three bird species: -white-throated sparrow -ruby-crowned kinglet -golden-crowned kinglet

(from avibase.bsc-eoc.org)

Four mammal species: - moose - northern red-backed vole - southern red-backed vole - western red-backed vole

(from gis.wwfus.org/wildfinder)

Northern forest (spruce-moose) community: Coincident distribution of 12 species from distantly-related taxa. Is it random?

Interdependence of species in communities

Page 27: Geography of Communities

Continental Divide

Pacific slope (strong rainshadow effect)

Caribbean slope

Bird survey point

Protected Area

Dry, seasonal forest

Cloud forest

Change in bird community composition with elevation in Costa Rica. What processes structure these communities?

Communities Over Space and Time

Tilarán Mountains, Costa Rica: 1100-1800m

Page 28: Geography of Communities

28 (Jankowski et al. 2009)

Example: Bird communities change quickly along the rainshadow elevational gradient in Costa Rica

Cloud Forest Rainshadow forest

Communities Over Space and Time

Bird Species

Spec

ies

Ab

un

dan

ce

1600-1700m

1500-1600m

1400-1500m

1300-1400m

1200-1300m

1100-1200m

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Dissimilarity index : 0.93

Jankowski et al. 2009, J. Anim. Ecol.

Bird Species

1100 -1200 m

1600 -1700 m

Communities Over Space and Time Sp

ecie

s A

bu

nd

ance

In 500m elevation, nearly 100% turnover in species...

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Primary succession: succession "from scratch", i.e. from a place devoid of life and the soil on which it depends. Imagine a volcano or glacier that destroys all life, leaving bare rock or till. Secondary succession: succession when the soil is left after a disturbance (e.g., flood or fire).

Assemblages of species in a location change over long periods of time

Communities Over Space and Time

Succession: progressive change in community structure, composition, and function with time

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Biomes of western North America at 0, 6000 and 18,000 14C yr BP reconstructed from pollen and packrat midden data. Pollen sites are represented by a circle, midden sites by a triangle.

Communities Over Space and Time

Assemblages of species in a location change over long periods of time

Thompson & Anderson 2000

0 yr BP 6000 yr BP 18,000 yr BP

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Communities Over Space and Time Assemblages of species in a location change over long periods of time

Nu

mb

er o

f Fa

mili

es

Geologic Time (106 yrs)

Geologic Time (106 yrs)

Page 33: Geography of Communities

References for this section:

Currie, D.J. 1991. Energy and large-scale patterns of animal- and plant-species richness. American Naturalist 137: 27-49.

Jankowski, J.E., et al. 2009. Beta diversity along environmental gradients: implications of habitat specialization in tropical montane landscapes. Journal of Animal Ecology 78: 315-327.

Jankowski, J.E., S.K. Robinson, & D.J. Levey. 2010. Squeezed at the top: Interspecific aggression may constrain elevational ranges in tropical birds. Ecology 91: 1877-1884.

Lomolino, M.V., B.R. Riddle, R.J. Whittaker, & J.A. Brown. 2010. Biogeography (4th ed., Chapter 2). Sinauer Associates, Inc., Sunderland, Mass.

Ricklefs, R.E. 2008. Disintegration of the ecological community. American Naturalist 172: 741-750

Thompson, R.S., and K.H. Anderson. 2000. Biomes of western North America at 18,000, 6000 and 0 14C yr BP reconstructed from pollenand packrat midden data. J. Biogeography 27: 555–584.

Whittaker, R.H. 1975. Communities and Ecosystems. 2nd ed. New York: MacMillan.

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Geography of Communities