Wk 1 Journal: Ecological Footprint Update and Course Reflections
Welcome to SCI207! Throughout this course, you will be asked to keep a journal about your
experience in the class. The purpose of this activity is to enable you to reflect on your learning: what
new things you have discovered, what surprises you have encountered, what topics or ideas you
have found particularly challenging, and how the course is going for you. During the five weeks in
which you are participating in the Environmental Footprint Reduction Project, in Week 2 through
Week 4 you will also use this journal as a space for a progress report on your efforts. Your entries
will be evaluated in terms of how well they met the topic and length requirements, and your writing
clarity. Your entries should be a minimum of one typed page each (double-spaced, Times New
Roman, and 12-point font) and will be submitted through Waypoint.
Complete the following:
•
In the first paragraph or two of your first journal entry, please reflect on your previous experiences, if
any with environmental science and environmental issues. What new things do you hope to learn in
this course? What concerns or fears do you have about this class? What strategies to you plan to
put in place to address them?
•
In another one or two paragraphs, share your thoughts about the first week of class. What did you
learn? What experiences stand out for you? What tasks or content did you find difficult or frustrating?
What activities did you find surprising or exciting? Looking ahead, what are your intrigued or
concerned by in the second week of the course?
•
Finally, make a list of at least five lifestyle changes you plan to commit to making for your courselong Ecological Footprint Reduction Project. Once you have recorded them in your journal, you
should begin taking those steps and keeping a weekly journal record of your efforts. You will report
on the results in a class discussion in Week 5.
Ecosystems
1
Moodboard/Thinkstock
Learning Objectives
After studying this chapter, you should be able to:
•
Identify the different terrestrial and aquatic biome types that cover the planet and explain why they
might differ in terms of biodiversity and species richness.
•
Explain how nutrients, such as nitrogen and phosphorous, cycle within ecosystems and how human
activities are altering the flow and location of these nutrients, often with unintended consequences.
•
•
•
•
•
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Describe how energy produced through photosynthesis forms the basis for most life on the planet and
how this energy flows through different trophic levels in an ecosystem.
Understand the difference in life history strategy between different organisms, including those between
r-selected and K-selected species.
Explain the concepts of niche, limiting factor, keystone species, and trophic cascades and how these
relate to the functioning of ecosystems and the species within them.
Discuss how interactions between different species in an ecosystem (such as predators and their prey)
result in evolutionary changes in these organisms and how ecosystem change and succession over time
alters the balance of species present in a given location.
Describe how toxic substances like mercury can find their way into natural environments far from any
source and impact wildlife populations in that area.
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Pre-Test
Pre-Test
1. Which biome would be expected to have the warmest and wettest conditions?
a. Coniferous forest
b. Desert
c. Tropical forest
d. Temperate grassland
2. The major sources of human emissions of the pollutant mercury are
a. disposal of thermometers and hospital waste.
b. car and truck exhaust.
c coal burning and gold mining.
d. agriculture and cattle ranching.
3. Which of the following is NOT an example of an important biogeochemical cycle?
a. The water cycle
b. The phosphorous cycle
c. The solar cycle
d. The carbon cycle
4. The population biology concept that refers to the maximum number of organisms that a
given environment can support is
a. survival rate.
b. reproductive rate.
c. K-selection.
d. carrying capacity.
5. When a top predator is removed from an ecosystem it can have dramatic impacts on the
entire food web. These impacts are referred to as
a. biomagnification.
b. bioaccumulation.
c. trophic cascades.
d. photosynthesis.
6. Which of the following is NOT an example of an avoidance/escape feature used to deter
predators from attacking prey?
a. A panda feeding only on bamboo
b. Fish swimming in a school
c. Wildebeests moving in a herd
d. A moth with false eye spots on its hind wings
7. Because mercury tends to accumulate in an animal’s tissue, we would expect what kinds
of organisms to carry the highest amounts of this toxin?
a. Long-lived predators
b. Primary producers
c. Short-lived predators
d. Detritivores
Answers
1.
2.
3.
4.
5.
6.
7.
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c.
c.
c.
d.
c.
a.
a.
tropical forest. The answer can be found in section 1.1.
coal burning and gold mining. The answer can be found in section 1.2.
the solar cycle. The answer can be found in section 1.3.
carrying capacity. The answer can be found in section 1.4.
trophic cascades. The answer can be found in section 1.5.
a panda bear feeding only on bamboo. The answer can be found in section 1.6.
long-lived predators. The answer can be found in section 1.7.
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INTRODUCTION
Introduction
Anyone who has spent time outdoors in a favorite patch of forest or other natural setting
might gain an appreciation for the complexity of life present in these ecosystems. Though
silent and invisible to us, trees and other plants are busy converting sunlight into stored
energy through photosynthesis. Birds, insects, and other creatures are on the move searching
for food or themselves ending up as food for other organisms. Some of these ecosystems seem
little changed over time while others might undergo rapid and dramatic transformation over
the course of only a few years. For example, mature forests might change little from year to
year, while shallow lakes gradually fill with sediment and slowly morph into swamps. Such
changes to ecosystems move ecologists to investigate the mechanisms that maintain stability
in some systems like the forest, yet promote change in others like the lake. Indeed, ecology is
the study of all natural systems, including the forest and the lake.
Ecologists study the relationships between living organisms and the physical environment.
For example, in an ecosystem, plants compete with one another for sunlight, and some animals eat plants, while others eat plant eaters. Ecologists studying such an ecosystem might
ask questions, such as: What mineral qualities of the soil nourish this particular community
of plants? And, how does competition and predation among all the billions of soil microorganisms affect the nutrient qualities of the soil? Such queries help guide researchers as they
examine the interactions that occur within a particular ecosystem. Furthermore, the knowledge gained from such research helps environmental scientists study the impacts of human
actions on the environment, such as the damage done to a salt marsh by an oil spill or the
impact of air pollution on trees and plants.
This chapter will explore ecology as the study of change and stasis, balance and imbalance, life
and death in all natural systems—rainforests, tundra, grasslands, deserts, rivers, and oceans
that constitute our world. It begins with a review of the concept of biomes, major ecological
communities like forests, deserts, tundra, and oceans. While biomes differ dramatically in
terms of climate and the variety of life present, they all are generally powered by solar energy.
The second section examines how energy enters and flows through different trophic levels in
an ecosystem. The third section considers how nutrients, such as nitrogen and phosphorous,
are cycled within ecosystems. This is followed by an overview of population biology, the study
of how different organisms grow and reproduce in different ways. The fifth section introduces the concepts of niche, limiting factor, keystone species, and trophic cascades, and how
they impact the functioning of various ecosystems. Section 1.6 reviews evolution and natural
selection and how these processes alter the species composition of ecosystems over time. All
of these topics will provide you with a basic foundation in ecology and environmental science
needed to understand the subjects presented in later chapters. To illustrate how the topics
covered in this chapter connect, the final section presents a case history of how mercury contamination is affecting wildlife and ecosystems the world over.
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Earth’s Biomes
1.1
SECTION 1.1
Earth’s Biomes
The diversity of life on Earth is vast. Yet ecologists have found that areas on different continents
that share similar climate conditions tend to have similar ecosystem structures and functions.
As a result, ecologists use the concept of a biome to classify large areas of the planet into a small
number of similar units. Biomes include both terrestrial (land-based) and aquatic (in water)
communities. Biomes display huge differences in the number or diversity of species present and
how these species interact with one another. The following section, which has been excerpted
from Habitable Planet: A Systems Approach to Environmental Science by Annenberg Learner,
discusses the different types of biomes and how they are classified. It will help you gain an appreciation for the incredible variety of ecosystems and natural conditions on the planet, and how
conditions shape the diversity of life found in each area.
The reading points out that scientists have determined that a handful of factors—namely temperature, availability of moisture, abundance of light, and availability of nutrients—are the key
influences on the number and variety of organisms in a given ecosystem. Generally speaking,
tropical regions with their warm temperatures, abundance of moisture, and relatively constant
levels of daylight have the highest number and diversity of organisms. Indeed, tropical, moist forest ecosystems make up the terrestrial biome with the highest productivity and diversity of life.
In contrast, polar regions with their frigid temperatures, low moisture conditions, and months of
the year with little or no natural light tend to have the lowest levels of productivity and diversity.
Scientists study all types of biomes in order to learn about the life cycle and optimal conditions
within different types of climates.
By Annenberg Learner
Geography has a profound impact on ecosystems because global circulation patterns and climate zones set basic physical conditions for the organisms that inhabit a given area. The most
important factors are temperature ranges, moisture availability, light, and nutrient availability, which together determine what types of life are most likely to flourish in specific regions
and what environmental challenges they will face.
Earth is divided into distinct climate zones that are created by global circulation patterns. The
tropics are the warmest, wettest regions of the globe, while subtropical high-pressure zones
create dry zones at about 308 latitude north and south. Temperatures and precipitation are
lowest at the poles. These conditions create biomes—broad geographic zones whose plants
and animals are adapted to different climate patterns. Since temperature and precipitation
vary by latitude, Earth’s major terrestrial biomes are broad zones that stretch around the
globe. Each biome contains many ecosystems (smaller communities) made up of organisms
adapted for life in their specific settings.
Land biomes are typically named for their characteristic types of vegetation, which in turn
influence what kinds of animals will live there. Soil characteristics also vary from one biome
to another, depending on local climate and geology. [. . .]
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SECTION 1.1
Earth’s Biomes
Figure 1.1: Global biomes
Earth’s major biomes result primarily from differences in climate. Each biome contains many
ecosystems made up of species adapted for life in their specific biome.
30° N
Tropic
of Cancer
Equator
Tropic of
Capricorn
30° S
Tropical forest
Savanna
Desert
Temperate
deciduous forest
Temperate
grassland
Coniferous
forest
Chaparral
Oceans
Tundra (arctic
and alpine)
Polar and highmountain ice
Adapted from U.S. Department of Agriculture Natural Resources Conservation Service. Retrieved from http://www.nrcs.usda.gov
/wps/portal/nrcs/detail/soils/use/worldsoils/?cid=nrcs142p2_054013
Aquatic biomes (marine and freshwater) cover three-quarters of the Earth’s surface and
include rivers, lakes, coral reefs, estuaries, and open ocean. Oceans account for almost all of
this area. Large bodies of water (oceans and lakes) are stratified into layers: surface waters
are warmest and contain most of the available light, but depend on mixing to bring up nutrients from deeper levels. The distribution of temperature, light, and nutrients set broad conditions for life in aquatic biomes in much the same way that climate and soils do for land biomes.
Marine and freshwater biomes change daily or seasonally. For example, in the intertidal zone
where the oceans and land meet, areas are submerged and exposed as the tide moves in and
out. During the winter months lakes and ponds can freeze over, and wetlands that are covered
with water in late winter and spring can dry out during the summer months.
There are important differences between marine and freshwater biomes. The oceans occupy
large continuous areas, while freshwater habitats vary in size from small ponds to lakes covering thousands of square kilometers. As a result, organisms that live in isolated and temporary freshwater environments must be adapted to a wide range of conditions and able to
disperse between habitats when their conditions change or disappear.
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Earth’s Biomes
SECTION 1.1
Biomes and Biodiversity
Since biomes represent consistent sets of conditions for life, they will support similar kinds of
organisms wherever they exist, although the species in the communities in different places may not
be taxonomically [the science of classifying animals]
related. For example, large areas of Africa, Australia, South America, and India are covered by savannas (grasslands with scattered trees). The various
grasses, shrubs, and trees that grow on savannas all
are generally adapted to hot climates with distinct
rainy and dry seasons and periodic fires, although
they may also have characteristics that make them
well-suited to specific conditions in the areas where
they appear.
Species are not uniformly spread among Earth’s
biomes. Tropical areas generally have more plant
and animal biodiversity [the diversity of animal and
plant life in a region] than high latitudes, measured
in species richness (the total number of species
present). This pattern, known as the latitudinal biodiversity gradient, exists in marine, freshwater, and
terrestrial ecosystems in both hemispheres. [. . .]
Why is biodiversity distributed in this way? Ecologists have proposed a number of explanations:
•
•
•
•
•
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. luoman/iStock/Thinkstock
Tropical rainforests produce their own
moisture. Scientists believe that as
these ecosystems are cleared through
deforestation—as shown here in the
Amazon—there is a threshold beyond
which they will no longer produce
enough moisture to sustain themselves.
The result could be conversion of
rainforests to drier savannas.
Higher productivity in the tropics allows
for more species;
The tropics were not severely affected by glaciation and thus have had more time for
species to develop and adapt;
Environments are more stable and predictable in the tropics, with fairly constant
temperatures and rainfall levels year-round;
More predators and pathogens limit competition in the tropics, which allows more
species to coexist; and
Disturbances occur in the tropics at frequencies that promote high successional
diversity.
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SECTION 1.2
Energy Flows Through Ecosystems
Of these hypotheses, evidence is strongest
for the proposition that a stable, predictable environment over time tends to produce larger numbers of species. For example, both tropical ecosystems on land and
deep sea marine ecosystems—which are
subject to much less physical fluctuation
than other marine ecosystems, such as
estuaries—have high species diversity.
Predators that seek out specific target
species may also play a role in maintaining species richness in the tropics.
Consider This
Recall that as part of the scientific method
scientists regularly formulate and test
hypotheses about how the world works.
Now, note the language used in the previous paragraph about how “evidence is
strongest . . . ” for one proposition over
the others. What does this tell you about
the scientific method and the kind of language and terminology used by scientists
to describe the natural world?
Excerpted from Weeks, S., Moorcoft, P.R. (2007). Unit 4: Ecosystems. The Habitable Planet: A Systems Approach to
Environmental Science. Retrieved from http://www.learner.org/courses/envsci/unit/text.php?unit=4&secNum
=0. Used with permission of Annenberg Learner.
1.2
Energy Flows Through Ecosystems
Despite the incredible range of conditions that characterize the ecosystems found in different biomes, they all have something in common. With few exceptions, Earth’s ecosystems are
powered by solar energy. Primary producers such as plants and algae use sunlight in a process
known as photosynthesis to convert carbon dioxide and water into glucose (sugars). Glucose
represents a form of stored energy that is used by plants for their own growth and maintenance.
Other organisms can then consume this plant material and use it as a source of energy. Animals,
in turn, can eat the organisms that ate the plants in order to acquire energy. Ecologists use
the concept of trophic levels to study how energy moves through ecosystems. The following
selection adapted from Habitable Planet: A Systems Approach to Environmental Science, by
Annenberg Learner, explains how energy flows through ecosystems and discusses the impact on
the environment. It will introduce you to the critical concept of primary productivity, the basis
for almost all life on the planet.
Trophic levels can be best visualized as a series of steps, with the base made up of large amounts
of primary producers such as plants and algae. These primary producers have the unique ability to transform solar energy from the sun into stored energy in the form of sugars through the
process of photosynthesis. Animals that feed on primary producers are known as primary consumers. An example of a primary consumer is a rabbit that eats grass and then utilizes much of
the energy stored in the grass for its own growth and bodily functions. In order to sustain the
rabbit there must be a huge amount of available grass for it to eat. This is why the trophic level
comprised of primary producers is the largest. However, the animals that eat rabbits and other
primary consumers are fewer in number than rabbits, so their step is smaller than the one below
it that represents plants and algae.
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Energy Flows Through Ecosystems
SECTION 1.2
Ecologists study dynamics between and among trophic levels as well as the concept of primary
productivity to figure out how much energy is available to support the organisms within a particular ecosystem. For example, net primary productivity is the amount of energy available as
plant matter for primary consumers, or the amount left over after plants use some of the energy
from photosynthesis for themselves. The last section made clear that tropical, moist forests are
the most productive of terrestrial biomes. That’s the same as saying that tropical forests have
the highest net primary productivity (NPP). Since it is the NPP of an ecosystem that supports
all life at higher trophic levels, the high NPP in tropical forests helps explain the abundance and
diversity of life in these ecosystems.
One note of clarification regarding the following discussion on bioaccumulation. Bioaccumulation describes an increase, or an accumulation, of a specific pollutant or toxin in an organism
over time. Many toxic substances, such as mercury, are what are known as lipophilic, or having
the tendency to dissolve in fat. Human emissions of mercury from activities like coal burning and
gold mining tend to end up in water bodies. Fish in those water bodies might ingest small amounts
of that mercury, and over time this substance can build up or bioaccumulate in their tissue. When
another organism at a higher trophic level, such as a bear or a fish-eating bird, ingests large numbers of fish, the mercury contained in the fish is transferred higher up the food chain. This process
is known as biomagnification, an increase in the concentration of a pollutant as you move higher
up the food chain. The case history section at the end of this chapter discusses some of the unexpected and troubling ways in which mercury is bioaccumulating in individual organisms, biomagnifying in many food chains, and wreaking havoc on wildlife populations.
By Annenberg Learner
Ecosystems maintain themselves by cycling energy and nutrients obtained from external
sources. At the first trophic level, primary producers (plants, algae, and some bacteria) use
solar energy to produce organic plant material through photosynthesis. Herbivores—animals
that feed solely on plants—make up the second trophic level. Predators that eat herbivores
comprise the third trophic level; if larger predators are present, they represent still higher
trophic levels. Organisms that feed at several trophic levels (for example, grizzly bears that
eat berries and salmon) are classified at the highest of the trophic levels at which they feed.
Decomposers, which include bacteria, fungi, molds, worms, and insects, break down wastes
and dead organisms and return nutrients to the soil.
On average about 10 percent of net energy production at one trophic level is passed on to
the next level. Processes that reduce the energy transferred between trophic levels include
respiration, growth and reproduction, defecation, and nonpredatory death (organisms that
die but are not eaten by consumers). The nutritional quality of material that is consumed also
influences how efficiently energy is transferred, because consumers can convert high-quality
food sources into new living tissue more efficiently than low-quality food sources.
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SECTION 1.2
Energy Flows Through Ecosystems
Figure 1.2: Trophic levels
Energy enters an ecosystem through an external source (the sun) and flows through the progressive
trophic levels of a food chain. On average, about 10 percent of the net energy produced at one trophic
level is passed on to the next level; the rest is lost as heat energy.
Solar energy
Heat
lost
Higher level predator
Predators
(animals that feed on herbivores)
Predators
Herbivores
(animals that feed on plants)
Primary producers
(plants, algae, and some bacteria)
Decomposers
Consider This
It’s estimated that only about 10 percent of
net energy production at one trophic level
is passed to the next level. This pattern can
be used to support an argument for reducing meat consumption by humans and
adopting a more plant-based diet. From
an ecological standpoint (that is, ignoring
ethical or other considerations) why might
this argument make sense?
ben85927_01_c01.indd 31
The low rate of energy transfer between
trophic levels makes decomposers generally more important than producers in
terms of energy flow. Decomposers process large amounts of organic material
and return nutrients to the ecosystem in
inorganic form, which are then taken up
again by primary producers. Energy is
not recycled during decomposition, but
rather is released, mostly as heat (this is
what makes compost piles and fresh garden mulch warm). [. . .]
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Energy Flows Through Ecosystems
SECTION 1.2
Gross and Net Primary Productivity in Ecosystems
An ecosystem’s gross primary productivity (GPP) is the total amount of organic matter that
it produces through photosynthesis. Net primary productivity (NPP) describes the amount
of energy that remains available for plant growth after subtracting the fraction that plants
use for respiration. Productivity in land ecosystems generally rises with temperature up to
about 308C, after which it declines, and is positively correlated [related] with moisture. On
land primary productivity thus is highest in warm, wet zones in the tropics where tropical
forest biomes are located. In contrast, desert scrub ecosystems have the lowest productivity
because their climates are extremely hot and dry.
In the oceans, light and nutrients are important controlling factors for productivity. [. . .]
[L]ight penetrates only into the uppermost level of the oceans, so photosynthesis occurs in
surface and near-surface waters. Marine primary productivity is high near coastlines and
other areas where upwelling brings nutrients to the surface, promoting plankton blooms.
Runoff from land is also a source of nutrients in estuaries and along the continental shelves.
Among aquatic ecosystems, algal beds and coral reefs have the highest net primary production, while the lowest rates occur in the open due to a lack of nutrients in the illuminated
surface layers.
How many trophic levels can an ecosystem support? The answer depends on several factors,
including the amount of energy entering the ecosystem, energy loss between trophic levels,
and the form, structure, and physiology [functioning] of organisms at each level. At higher
trophic levels, predators generally are physically larger and are able to utilize a fraction of the
energy that was produced at the level beneath them, so they have to forage over increasingly
large areas to meet their caloric needs.
Because of these energy losses, most terrestrial ecosystems have no more than five trophic
levels, and marine ecosystems generally have no more than seven. [. . .]
Food Webs and Bioaccumulation
The simplest way to describe the flux of energy through ecosystems is as a food chain in
which energy passes from one trophic level to the next, without factoring in more complex
relationships between individual species. Some very simple ecosystems may consist of a food
chain with only a few trophic levels. For example, the ecosystem of the remote wind-swept
Taylor Valley in Antarctica consists mainly of bacteria and algae that are eaten by nematode
worms. More commonly, however, producers and consumers are connected in intricate food
webs with some consumers feeding at several trophic levels.
An important consequence of the loss of energy between trophic levels is that contaminants
collect in animal tissues—a process called bioaccumulation. As contaminants bioaccumulate
up the food web, organisms at higher trophic levels can be threatened even if the pollutant is
introduced to the environment in very small quantities.
The insecticide DDT, which was widely used in the United States from the 1940s through
the 1960s, is a famous case of bioaccumulation. DDT built up in eagles and other raptors to
levels high enough to affect their reproduction, causing the birds to lay thin-shelled eggs that
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SECTION 1.2
Energy Flows Through Ecosystems
broke in their nests. Fortunately, populations have rebounded over several decades since the
pesticide was banned in the United States. However, problems persist in some developing
countries where toxic bioaccumulating pesticides are still used.
Figure 1.3: Food web
This food web demonstrates how contaminants introduced at lower trophic levels can bioaccumulate
and affect species at higher trophic levels, as was the case with eagles and raptors in the 1940s.
Salmon
Bald Eagles
Rabbits
Snakes
Birds
Mice
Insects
Grass and
Crops
Bioaccumulation can threaten humans as well as animals. For example, in the United States
many federal and state agencies currently warn consumers to avoid or limit their consumption of large predatory fish that contain high levels of mercury, such as shark, swordfish, tilefish, and king mackerel, to avoid risking neurological damage and birth defects.
Excerpted from Weeks, S., Moorcoft, P.R. (2007). Unit 4: Ecosystems. The Habitable Planet: A Systems Approach to
Environmental Science. Retrieved from http://www.learner.org/courses/envsci/unit/text.php?unit=4&secNum
=0. Used with permission of Annenberg Learner.
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Nutrient Cycling in Ecosystems
SECTION 1.3
Apply Your Knowledge
Environmental scientist G. Tyler Miller (1902–1988) once wrote:
Three hundred trout are needed to support one man for a year. The trout, in turn, must
consume 90,000 frogs, that must consume 27 million grasshoppers that live off 1,000
tons of grass (American Chemist, 1971).
This quote illustrates the concept of energy transfer between different trophic levels. For this
activity you should do the following:
Think about an animal that resides at the highest trophic level or at the top of the food web.
Make a list of the kinds of food this animal eats. After that, list the kinds of food eaten
by the animals further down the food chain until you get to the lowest trophic level or
the bottom of the food chain. A simple Internet search like “what do grasshoppers eat”
should turn up enough information.
Create a sketch or diagram of what this food chain might look like as trophic levels
(similar to Figure 1.2) or as a food web (similar to Figure 1.3).
1.3
Nutrient Cycling in Ecosystems
The previous section described how energy tends to flow through ecosystems—entering as sunlight and leaving as heat. In contrast, nutrients such as carbon, nitrogen, and phosphorous tend
to cycle in ecosystems. Ecologists who study this cycle have learned that the same molecule of
carbon that is used by a tree outside your window for photosynthesis may have been exhaled by
a human or animal thousands of years ago. Ecologists also closely study the hydrologic (water)
cycle, and the following excerpt from The Habitable Planet: A Systems Approach to Environmental Science by Annenberg Learner explains why ecologists must have an appre-ciation for
how water and nutrients cycle. Indeed, the study of nutrient cycling through various ecosystems
has made ecologists aware that pollution or contaminants released in one part of an ecosystem
can show up elsewhere in undesirable ways.
The interesting fact about nutrient and water cycles is that we are talking about the same
material cycling over time. In other words, due to conservation of matter—matter can be transformed and combined in different ways but cannot be created, nor destroyed—nutrient and
water cycles are working with a fixed amount of material. Water can be transformed to ice or
mist; it can end up in the ocean only to come down later as rain and soak into the ground to
become groundwater; but it is always water and there is only so much of it. Likewise, a carbon
molecule could be absorbed from the atmosphere by a plant during photosynthesis, transferred
to a rabbit that eats the leaves of the plant, transferred to a fox that eats the rabbit, and then
returned to the atmosphere when the fox exhales carbon dioxide.
This principle of conservation of matter is sometimes described by ecologists as “there is no
away.” When we burn fossil fuels that contain mostly carbon (such as coal or oil), we are moving that carbon from one place, where it had been buried for millions of years, to another. When
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Nutrient Cycling in Ecosystems
SECTION 1.3
we mine phosphate deposits to make fertilizer and some of that fertilizer runs off into streams,
we are moving that phosphorous from one place to another, but it does not go away. This basic
concept of conservation of matter will be a central theme of much of the material in upcoming
chapters. We’ll see that when we release nitrogen and phosphorous from agriculture, carbon
dioxide from fossil fuel combustion, or toxic chemicals from manufacturing, these things don’t
just “go away.” Instead, they can alter ecosystems and organisms in distant locations in unintended ways. A basic understanding of how nutrients cycle through ecosystems will help you see
how that is possible.
By Annenberg Learner
Along with energy, water and several other chemical elements cycle through ecosystems and
influence the rates at which organisms grow and reproduce. About 10 major nutrients and
six trace nutrients are essential to all animals and plants, while others play important roles
for selected species.. The most important biogeochemical cycles [movement of matter, such
as nitrogen, between living and non-living components of an ecosystem] affecting ecosystem
health are the water, carbon, nitrogen, and phosphorus cycles.
As noted earlier, most of the Earth’s area that is covered by water is ocean. In terms of volume,
the oceans dominate further still: nearly all of Earth’s water inventory is contained in the
oceans (about 97 percent) or in ice caps and glaciers (about 2 percent), with the rest divided
among groundwater, lakes, rivers, streams, soils, and the atmosphere. In addition, water
moves very quickly through land ecosystems. These two factors mean that water’s residence
time in land ecosystems is generally short, on average one or two months as soil moisture,
weeks or months in shallow groundwater, or up to six months as snow cover.
But land ecosystems process a lot of water: almost two-thirds of the water that falls on land as
precipitation annually is transpired [conversion of water to water vapor through plant tissue]
back into the atmosphere by plants, with the rest flowing into rivers and then to the oceans.
Because cycling of water is central to the functioning of land ecosystems, changes that affect
the hydrologic cycle are likely to have significant impacts on land ecosystems. [. . .]
Both land and ocean ecosystems are important sinks for carbon, which is taken up by plants
and algae during photosynthesis and fixed as plant tissue. [. . .]
Carbon cycles relatively quickly through land and surface-ocean ecosystems, but may remain
locked up in the deep oceans or in sediments for thousands of years. The average residence
time that a molecule of carbon spends in a terrestrial ecosystem is about 17.5 years, although
this varies widely depending on the type of ecosystem: carbon can be held in old-growth forests for hundreds of years, but its residence time in heavily grazed ecosystems where plants
and soils are repeatedly turned over may be as short as a few months.
Nitrogen and Phosphorous Cycles
Nitrogen and phosphorus are two of the most essential mineral nutrients for all types of ecosystems and often limit growth if they are not available in sufficient quantities. (This is why
the basic ingredients in plant fertilizer are nitrogen, phosphorus, and potassium, commonly
abbreviated as NPK.) [. . .]
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SECTION 1.3
Nutrient Cycling in Ecosystems
Because atmospheric nitrogen (N2) is inert [does not react chemically] and cannot be used
directly by most organisms, microorganisms that convert it into usable forms of nitrogen play
central roles in the nitrogen cycle. So-called nitrogen-fixing bacteria take inert nitrogen (N2)
from the atmosphere and convert it to ammonia (NH4) nitrate (NO3) and another nitrogen
compounds, which in turn are taken up by plants. Some of these bacteria live in mutualistic
relationships [an interaction between two species that benefits both] on the roots of plants,
mainly legumes (peas and beans), and provide nitrogen directly to the plants; farmers often
plant these crops to restore nitrogen to depleted soils. At the back end of the cycle, decomposers break down dead organisms and wastes, converting organic materials to inorganic
nutrients. Other bacteria carry out denitrification, breaking down nitrate to gain oxygen and
returning gaseous nitrogen to the atmosphere.
Figure 1.4: The nitrogen cycle
Nitrogen circulates from the environment to living organisms and back to the environment. This
cycle involves nitrogen-fixing bacteria that convert nitrogen into forms usable by living organisms,
and denitrifying bacteria, which break down nitrogen compounds and return gaseous nitrogen to
the atmosphere.
Atmospheric
Nitrogen
Plant
proteins
eaten
Excretion
Excretion
Nitrogen-fixing
bacteria
“fixation”
Decaying
organic matter
Denitrifying
bacteria
“denitrification”
Ammonia (NH4), nitrate (NO3)
and other nitrogen compounds
“ammonification” and “nitrification”
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SECTION 1.4
Population Biology
Human activities, including fossil fuel combustion, cultivation of nitrogen-fixing crops, and rising use of nitrogen fertilizer, are altering the natural nitrogen cycle. Together these activities
add roughly as much nitrogen to terrestrial ecosystems each year as the amount fixed by natural processes; in other words, anthropogenic [human-caused] inputs are doubling annual nitrogen fixation in land ecosystems. The main effect of this extra nitrogen is over-fertilization of
aquatic ecosystems. Excess nitrogen promotes algal blooms, which then deplete oxygen from
the water when the algae die and decompose. [. . .] Additionally, airborne nitrogen emissions
from fossil fuel combustion promote the formation of ground-level ozone, particulate emissions, and acid rain [forms of pollution discussed in Chapter 9]. [. . .]
Phosphorus, the other major plant nutrient, does not have a gaseous phase like
carbon or nitrogen. As a result it cycles
more slowly through the biosphere. Most
phosphorus in soils occurs in forms that
organisms cannot use directly, such as
calcium and iron phosphate. Usable forms
(mainly orthophosphate, or PO4) are produced mainly by decomposition [disintegration] of organic material, with a small
contribution from weathering [breaking
down] of rocks.
Consider This
As pointed out above, human activities
add roughly as much nitrogen to terrestrial (land-based) ecosystems as natural
processes. If this nitrogen is being added
to terrestrial ecosystems, why is it that the
main effect is over-fertilization of aquatic
(water-based) ecosystems? How does the
nitrogen get from land to water, and since
nitrogen acts as a fertilizer why is this a
bad thing?
Excessive phosphorus can also contribute to over-fertilization and eutrophication [excessive growth of algae] of rivers
and lakes. Human activities that increase
phosphorus concentrations in natural ecosystems include fertilizer use, discharges from
wastewater treatment plants, and use of phosphate detergents. [. . .]
Excerpted from Weeks, S., Moorcoft, P.R. (2007). Unit 4: Ecosystems. The Habitable Planet: A Systems Approach to
Environmental Science. Retrieved from http://www.learner.org/courses/envsci/unit/text.php?unit=4&secNum=0.
Used with permission of Annenberg Learner.
1.4
Population Biology
The excerpted selection below from The Habitable Planet: A Systems Approach to Environmental Science by Annenberg Learner explains that different organisms grow and
reproduce in very different ways. Some organisms are characterized by very short life spans but
high rates of reproduction, whereas others have long life spans and low rates of reproduction.
The difference depends on environmental conditions in a particular area and the organism’s life
history strategy—such as how fast it develops, age of sexual maturity, and number of offspring.
Ecologists study differences in life history strategies to better determine how to manage a species. For example, an insect pest with high rates of reproduction will require one approach to
management whereas an endangered mammal with low rates of reproduction will require a
different approach.
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SECTION 1.4
Population Biology
Since ecosystems vary greatly from each other, organisms must be able to adapt to the conditions
they face in order to survive. Ecologists refer to organisms that reproduce quickly as r-selected
and note that these kinds of species are found in areas that are relatively unstable, such as flood
plains. K-selected species, in contrast, reproduce more slowly and are found in more stable ecosystems such as old-growth forests. Ecologists and resource managers can use their understanding of an organism’s population biology, such as the degree to which it is r-selected or K-selected,
to try to manage a given population. This approach can be utilized for commercial purposes,
such as in the management of wild fish populations.
By Annenberg Learner
Every organism in an ecosystem divides its energy among three competing goals: growing,
surviving, and reproducing. Ecologists refer to an organism’s allocation of energy among these
three ends throughout its lifetime as its life history strategy. There are tradeoffs between these
functions: for example, an organism that spends much of its energy on reproduction early in
life will have lower growth and survival rates, and thus a lower reproductive level later in life.
An optimal life history strategy maximizes the organism’s contribution to population growth.
Understanding how the environment shapes organisms’ life histories is a major question in
ecology. Compare the conditions for survival in an unstable area, such as a flood plain near a
river that frequently overflows its banks, to those in a stable environment, such as a remote
old-growth forest. On the flood plain, there is a higher chance of being killed early in life,
so the organisms that mature and reproduce earlier will be most likely to survive and add
to population growth. Producing many offspring increases the chance that some will survive. Conversely, organisms in the forest will mature later and have lower early reproductive
rates. This allows them to put more
energy into growth and competition
for resources.
Anup Shah/Digital Vision/Thinkstock
As wildlife populations grow toward their carrying
capacity, competition for limited resources such as
food and space increases. Populations that exceed
their carrying capacity experience increased death
rates, reduced birth rates, and sometimes sudden,
catastrophic collapses.
ben85927_01_c01.indd 38
Ecologists refer to organisms at the first
of these two extremes (those adapted
to unstable environments) as r-selected
[able to reproduce quickly]. These
organisms live in settings where population levels are well below the maximum number that the environment can
support—the carrying capacity—so
their numbers are growing exponentially at the maximum rate at which that
population can increase if resources
are not limited (often abbreviated as r).
The other extreme, organisms adapted
to stable environments, are termed
K-selected because they live in environments in which the number of individuals is at or near the environment’s carrying capacity (often abbreviated as K).
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SECTION 1.4
Population Biology
Organisms that are r-selected tend to be small, short-lived, and opportunistic, and to grow
through irregular boom-and-bust population cycles. They include many insects, annual
plants, bacteria, and larger species such as frogs and rats. Species considered pests typically
are r-selected organisms that are capable of rapid growth when environmental conditions are
favorable. In contrast, K-selected species are typically larger, grow more slowly, have fewer
offspring and spend more time parenting them. Examples include large mammals, birds, and
long-lived plants such as redwood trees. K-selected species are more prone to extinction than
r-selected species because they mature later in life and have fewer offspring with longer gestation times.
Consider This
Why are r-selected species most commonly
found in unstable environments while
K-selected species are generally found in
stable environments?
Many organisms fall between these two
extremes and have some characteristics of
both types. As we will see below, ecosystems tend to be dominated by r-selected
species in their early stages with the balance gradually shifting toward K-selected
species.
In a growing population, survival and
reproduction rates will not stay constant
over time. Eventually resource limitations
will reduce one or both of these variables. Populations grow fastest when they are near zero
and the species is uncrowded. A simple mathematical model of population growth implies that
the maximum population growth rate occurs when the population size (N) is at one-half of the
environment’s carrying capacity, K (i.e., at N 5 K/2).
In theory, if a population is harvested at exactly its natural rate of growth, the population will
not change in size, and the harvest (yield) can be sustained at that level. In practice, however, it can be very hard to estimate population sizes and growth rates in the wild accurately
enough to achieve this maximum sustainable yield. [. . .]
Excerpted from Weeks, S., Moorcoft, P.R. (2007). Unit 4: Ecosystems. The Habitable Planet: A Systems Approach to
Environmental Science. Retrieved from http://www.learner.org/courses/envsci/unit/text.php?unit=4&secNum=0.
Used with permission of Annenberg Learner.
Apply Your Knowledge
Ideas and concepts from population biology are often used to develop management plans for
different animal species. In particular, the maximum sustainable yield (MSY) concept is frequently the basis for management of commercially valuable species, such as fish stocks. MSY
is the largest harvest or catch that can be taken from a given population without reducing the
size of that population.
(continued)
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SECTION 1.5
Ecosystem Functions
Apply Your Knowledge (continued)
Assume you were tasked with managing a fish stock of 1,000 individuals and that the rate of
growth (reproduction) of that fish stock was 20 percent or 0.2 annually.
What would the MSY be in that time period?
What would happen to the population of fish if you limited total catch to a lower number
than the MSY?
What would happen to the population of fish if you allowed for a total catch greater than
the MSY?
Using the scientific method, how might you design an experiment to determine what the
MSY might be for a particular fish population?
What kinds of factors might make you cautious or nervous about making use of the MSY
concept as the basis for the management of wildlife populations?
1.5
Ecosystem Functions
An organism’s ability to survive and thrive depends on the availability of resources, including
light, water, and nutrients. Survival also depends on how that organism interacts with other
organisms and what sort of niche it occupies within that ecosystem. Different species compete for limited resources, but generally over time a species will evolve to occupy a particular
niche in an ecosystem. The excerpted selection below from The Habitable Planet: A Systems
Approach to Environmental Science by Annenberg Learner explains how disturbances to ecosystems, often from human activity, can disrupt the availability of resources and alter relationships between species, often with disastrous consequences.
A key concept in understanding how ecosystems work is that of the limiting factor. Consider
that a plant needs sunlight, water, carbon dioxide, and certain essential nutrients to sustain
it. Because a plant needs all of these factors in some combination, increasing one factor, such
as carbon dioxide, may not result in increased plant growth. A more familiar analogy might
be making pancakes, which requires a certain amount of flour, milk, and eggs. Doubling the
amount of flour available will not result in any more pancakes unless you also increase the
amount of milk and eggs.
An impact at one point in an ecosystem can have a ripple effect throughout an entire ecosystem.
For example, phosphorous is often a limiting factor in many aquatic ecosystems. When excess
phosphorous enters an aquatic ecosystem, such as through fertilizer runoff, it can cause an
explosive growth in algae and eventually result in a sharp drop in oxygen levels in that system.
This drop in oxygen can kill or drive off fish species, and this can have ripple effects throughout
the entire food chain. Likewise, ripple effects can begin at higher trophic levels through the
removal of a top predator in a food chain. The removal of that predator can lead to a population explosion at lower trophic levels, known as a trophic cascade. For this reason top predators
are often considered keystone species because their removal can trigger impacts throughout
an ecosystem.
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Ecosystem Functions
SECTION 1.5
Different species in an ecosystem occupy ecological niches or positions within that ecosystem.
Put another way, various species pursue specific survival strategies, make use of particular
resources, occupy different regions, and engage with other species in prescribed ways in order to
meet their survival needs. Because many species will end up competing for the same resources,
their realized niche (positions they actually occupy) will be smaller than their fundamental
niche (the full range of positions they could occupy in the absence of competition). Likewise, species that are specialists that depend on a very narrow range of food sources and conditions will
generally be smaller in number than those species that are generalists that can take advantage
of a wider range of food sources. Specialist species are therefore more prone to ecosystem disturbances, and most endangered species tend to be specialists. An understanding of concepts like
niches, limiting factors, and keystone species helps environmental scientists better understand
how an ecosystem works and predict the impact of a disturbance to that system.
By Annenberg Learner
A key question for ecologists studying growth and productivity in ecosystems is which factors
limit ecosystem activity. Availability of resources, such as light, water, and nutrients, is a key
control on growth and reproduction. Some nutrients are used in specific ratios. For example,
the ratio of nitrogen to phosphorus in the organic tissues of algae is about 16 to 1, so if the
available nitrogen concentration is greater than 16 times the phosphorus concentration, then
phosphorus will be the factor that limits growth; if it is less, then nitrogen will be limiting. To
understand how a specific ecosystem functions, it thus is important to identify what factors
limit ecosystem activity.
Resources influence ecosystem activity differently depending on whether they are essential,
substitutable, or complementary. Essential resources limit growth independently of other
levels: if the minimum quantity needed for growth is not available, then growth does not
occur. In contrast, if two resources are substitutable, then population growth is limited by an
appropriately weighted sum of the two resources in the environment. For example, glucose
and fructose are substitutable food sources for many types of bacteria. Resources may also be
complementary, which means that a small amount of one resource can substitute for a relatively large amount of another, or can be complementary over a specific range of conditions.
Resource availability serves as a so-called “bottom-up” control on an ecosystem: the supply
of energy and nutrients influences ecosystem activities at higher trophic levels by affecting
the amount of energy that moves up the food chain. In some cases, ecosystems may be more
strongly influenced by so-called “top-down” controls—namely, the abundance of organisms
at high trophic levels in the ecosystem. Both types of effects can be at work in an ecosystem at
the same time, but how far bottom-up effects extend in the food web, and the extent to which
the effects of trophic interactions at the top of the food web are felt through lower levels, vary
over space and time and with the structure of the ecosystem.
Trophic Cascades and Keystone Species
Many ecological studies seek to measure whether bottom-up or top-down controls are more
important in specific ecosystems because the answers can influence conservation and environmental protection strategies. For example, a study by Benjamin S. Halpern [a marine ecologist at the Center for Ocean Solutions, University of California—Santa Barbara] and others of food web controls in kelp forest ecosystems off the coast of Southern California found
that variations in predator abundance explained a significant proportion of variations in the
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SECTION 1.5
Ecosystem Functions
abundance of algae and the organisms at higher trophic levels that fed on algae and plankton.
In contrast, they found no significant relationship between primary production by algae and
species abundance at higher trophic levels. The most influential predators included spiny lobster, Kellet’s whelk, rockfish, and sea perch. Based on these findings, the authors concluded
that “[e]fforts to control activities that affect higher trophic levels (such as fishing) will have
far larger impacts on community dynamics than efforts to control, for example, nutrient input,
except when these inputs are so great as to create anoxic (dead) zones.”
Drastic changes at the top of the food
web can trigger trophic cascades, or
domino effects that are felt through
many lower trophic levels. The likelihood of a trophic cascade depends on
the number of trophic levels in the ecosystem and the extent to which predators reduce the abundance of a trophic
level to below their resource-limited
carrying capacity. Some species are so
important to an entire ecosystem that
they are referred to as keystone species, connoting that they occupy an
ecological niche that influences many
other species. Removing or seriously
impacting a keystone species produces major impacts throughout the
ecosystem.
. Nathan Hobbs/iStock/Thinkstock
Reintroducing wolves into Yellowstone National
Park has had a positive effect on the ecosystem.
Many scientists believe that the reintroduction of wolves into Yellowstone National Park in
1995, after they had been eradicated from the park for decades through hunting, has caused
a trophic cascade with results that are generally positive for the ecosystem. Wolves have
sharply reduced the population of elk, allowing willows to grow back in many riparian areas
[the banks of rivers or streams] where the elk had grazed the willows heavily. Healthier willows are attracting birds and small mammals in large numbers.
Consider This
How are the concepts of trophic cascade
and keystone species related? How can
these be used to argue for the protection
and/or reintroduction of top predator species like wolves into areas like Yellowstone
National Park?
Ecological Niches
“Species, like riparian songbirds, insects,
and in particular, rodents, have come back
into these preferred habitat types, and
other species are starting to respond,”
says biologist Robert Crabtree of the Yellowstone Ecological Research Center. “For
example, fox and coyotes are moving into
these areas because there’s more prey for
them. There’s been an erupting trophic
cascade in some of these lush riparian
habitat sites.”
Within ecosystems, different species interact in different ways. These interactions can have
positive, negative, or neutral impacts on the species involved.
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SECTION 1.5
Ecosystem Functions
Each species in an ecosystem occupies a niche, which comprises the sum total of its relationships with the biotic [living] and abiotic [non-living] elements of its environment—more simply, what it needs to survive. In a 1957 address, zoologist George Evelyn Hutchinson framed
the view that most ecologists use today when he defined the niche as the intersection of all
of the ranges of tolerance under which an organism can live. This approach makes ecological
niches easier to quantify and analyze because they can be described as specific ranges of variables like temperature, latitude, and altitude. For example, the African Fish Eagle occupies a
very similar ecological niche to the American Bald Eagle. In practice it is hard to measure all
of the variables that a species needs to survive, so descriptions of an organism’s niche tend to
focus on the most important limiting factors.
The full range of habitat types in which a species can exist and reproduce without any competition from other species is called its fundamental niche. The presence of other species
means that few species live in such conditions. A species’ realized niche can be thought of
as its niche in practice—the range of habitat types from which it is not excluded by competing species. Realized niches are usually smaller than fundamental niches, since competitive
interactions exclude species from at least some conditions under which they would otherwise
grow. Species may occupy different realized niches in various locations if some constraint,
such as a certain predator, is present in one area but not in another.
In a classic set of laboratory experiments, Russian biologist G. F. Gause showed the difference
between fundamental and realized niches. Gause compared how two strains of Paramecium
grew when they were cultured separately in the same type of medium to their growth rates
when cultured together. When cultured separately both strains reproduced rapidly, which
indicated that they were adapted to living and reproducing under the same conditions. But
when they were cultured together, one strain out-competed and eventually eliminated the
other. From this work Gause developed a fundamental concept in community ecology: the
competitive exclusion principle, which states that if two competitors try to occupy the same
realized niche, one species will eliminate the other.
Apply Your Knowledge
A 2006 article in the journal Biological Conservation (Ripple and Beschta, 2006) described in
detail a catastrophic trophic cascade event in Zion National Park in Utah. High visitor numbers
helped drive down the population of cougars in the park, which led to higher populations of
mule deer, which resulted in increased browsing of cottonwood tree seedlings along river and
stream banks. This resulted in higher stream bank erosion and reduced populations of other
terrestrial and aquatic organisms. In this situation:
Which animal was the keystone species?
How did lower cougar numbers help change the mule deer realized niche?
How did higher mule deer numbers help change the realized niche for cottonwood trees?
What kinds of strategies would you recommend the park consider to help address this
problem? What might be some of the limitations or arguments against the strategies you
would recommend?
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Evolution and Natural Selection in Ecosystems
SECTION 1.6
Specialists and Generalists
Many key questions about how species function in ecosystems can be answered by looking
at their niches. Species with narrow niches tend to be specialists, relying on comparatively
few food sources. As a result, they are highly sensitive to changes in key environmental conditions, such as water temperature in aquatic ecosystems. For example, pandas, which only
eat bamboo, have a highly specialized diet. Many endangered species are threatened because
they live or forage in particular habitats that have been lost or converted to other uses. One
well-known case, the northern spotted owl lives in cavities of trees in old-growth forests (forests with trees that are more than 200 years old and have not been cut, pruned, or managed),
but these forests have been heavily logged, reducing the owl’s habitat.
In contrast, species with broad niches are generalists that can adapt to wider ranges of
environmental conditions within their own lifetimes (i.e., not through evolution over generations, but rather through changes in their behavior or physiologic functioning) and survive
on diverse types of prey. Coyotes once were found only on the Great Plains and in the western
United States, but have spread through the eastern states in part because of their flexible
lifestyle. They can kill and eat large, medium, or small prey, from deer to house cats, as well
as other foods such as invertebrates [an animal without a backbone] and fruit, and can live in
a range of habitats, from forests to open landscapes, farmland, and suburban neighborhoods.
Overlap between the niches of two species (more precisely, overlap between their resource
use curves) causes the species to compete if resources are limited. One might expect to see
species constantly dying off as a result, but in many cases competing species can coexist
without either being eliminated. This happens through niche partitioning (also referred to
as resource partitioning), in which two species divide a limiting resource such as light, food
supply, or habitat.
Excerpted from Weeks, S., Moorcoft, P.R. (2007). Unit 4: Ecosystems. The Habitable Planet: A Systems Approach to
Environmental Science. Retrieved from http://www.learner.org/courses/envsci/unit/text.php?unit=4&secNum=0.
Used with permission of Annenberg Learner.
1.6
Evolution and Natural Selection in Ecosystems
Just as the species within an ecosystem change and evolve, ecosystems themselves go through
natural changes in a process known as succession. Successional changes alter conditions for
various species over time, favoring some at the expense of others. For example, a tract of forest
blown over by a hurricane or burned to the ground in a wildfire will usually return to a forested
state given enough time. Initially, r-selected species, those that reproduce quickly and colonize
disturbed areas (see section 1.4), will dominate the site and take advantage of the lack of competition from other species. However, over time K-selected species will move in and the disturbed
ecosystem will move through successional stages to a more diverse and complex system.
It might be tempting to look at an ecosystem, such as a forest, as relatively static and unchanging
over time. However, ecosystems are constantly changing. The theory of evolution, first developed
by Charles Darwin and other 19th-century scientists, suggested that competition between species for scarce resources will favor some species over others. Likewise, natural selection within
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Evolution and Natural Selection in Ecosystems
SECTION 1.6
species is a process where certain individuals in a given population will be better suited for survival and will pass on their genes and traits to future generations.
Competition between species and natural selection within species results in an ongoing process of constant change in order to ensure the survival of a given species. For species that form
a predator–prey relationship—such as bats and insects—ecologists have observed a process
known as coevolution. Coevolution has been compared to an ecological arms race where the
prey species might, over time, develop a defensive mechanism to thwart the predator that then
is overcome by an evolved predator. The adapted section below from The Habitable Planet: A
Systems Approach to Environmental Science by Annenberg Learner explains how constant
species interactions with each other and their environment in a given ecosystem results in a
process of natural selection and evolution.
By Annenberg Learner
As species interact, their relationships with competitors, predators, and prey contribute to
natural selection and thus influence their evolution over many generations. To illustrate this
concept, consider how evolution has
influenced the factors that affect the
foraging efficiency of predators. This
includes the predator’s search time
(how long it takes to find prey), its
handling time (how hard it has to work
to catch and kill it), and its prey profitability (the ratio of energy gained to
energy spent handling prey). Characteristics that help predators to find,
catch, and kill prey will enhance their
chances of surviving and reproducing.
Similarly, prey will profit from attributes that help avoid detection and
make organisms harder to handle or
. Yokpok/iStock/Thinkstock less biologically profitable to eat.
The ability to blend in with, or mimic, its environment
aids the praying mantis in capturing its prey.
•
•
ben85927_01_c01.indd 45
These common goals drive natural
selection for a wide range of traits and
behaviors, including:
Mimicry by either predators or prey. A predator such as a praying mantis that
blends in with surrounding plants is better able to surprise its target. However,
many prey species also engage in mimicry, developing markings similar to those of
unpalatable species so that predators avoid them. For example, harmless viceroy
butterflies have similar coloration to monarch butterflies, which store toxins in their
tissues, so predators avoid viceroy butterflies.
Optimal foraging strategies enable predators to obtain a maximum amount of net
energy per unit of time spent foraging. Predators are more likely to survive and reproduce if they restrict their diets to prey that provide the most energy per unit of handling time and focus on areas that are rich with prey or that are close together. [. . .]
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Evolution and Natural Selection in Ecosystems
•
•
SECTION 1.6
Avoidance/escape features help prey elude predators. These attributes may be behavioral patterns, such as animal herding or fish schooling to make individual organisms
harder to pick out. Markings can confuse and disorient predators: for example, the
automeris moth has false eye spots on its hind wings that misdirect predators.
Features that increase handling time help to discourage predators. Spines serve this
function for many plants and animals, and shells make crustaceans and mollusks
harder to eat. Behaviors can also make prey harder to handle: squid and octopus
emit clouds of ink that distract and confuse attackers, while hedgehogs and porcupines increase the effectiveness of their protective spines by rolling up in a ball to
conceal their vulnerable underbellies.
Some plants and animals emit noxious chemical substances to make themselves less profitable as prey. These protective substances may be bad-tasting, antimicrobial, or toxic. Many
species that use noxious substances as protection have evolved bright coloration that signals
their identity to would-be predators—for example, the black and yellow coloration of bees,
wasps, and yellowjackets. The substances may be generalist defenses that protect against a
range of threats, or specialist compounds developed to ward off one major predator. Sometimes specialized predators are able to overcome these noxious substances: for example, ragwort contains toxins that can poison horses and cattle grazing on it, but it is the exclusive food
of cinnabar moth caterpillars. Ragwort toxin is stored in the caterpillars’ bodies and eventually protects them as moths from being eaten by birds.
Coevolution and Competition
Natural selection based on features that make predators and prey more likely to survive
can generate predator–prey “arms races,” with improvements in prey defenses triggering
counter-improvements in predator attack tools and vice versa over many generations. Many
cases of predator–prey arms races have been identified. One widely known case is bats’ use of
echolocation [the use of echoes to determine the location of something] to find insects. Tiger
moths respond by emitting high-frequency clicks to “jam” bats’ signals, but some bat species
have overcome these measures through new techniques such as flying erratically to confuse
moths or sending echolocation chirps at frequencies that moths cannot detect. This type of
pattern involving two species that interact in important ways and evolve in a series of reciprocal genetic steps is called coevolution and represents an important factor in adaptation
and the evolution of new biological species.
Other types of relationship, such as competition, also affect evolution and the characteristics
of individual species. For example, if a species has an opportunity to move into a vacant niche,
the shift may facilitate evolutionary changes over succeeding generations because the species
plays a different ecological role in the new niche. By the early 20th century, large predators
such as wolves and puma had been largely eliminated from the eastern United States. This has
allowed coyotes, who compete with wolves where they are found together, to spread throughout urban, suburban, and rural habitats in the eastern states, including surprising locations
such as Cape Cod in Massachusetts and Central Park in New York City. Research suggests that
northeastern coyotes are slightly larger than their counterparts in western states, although
it is not yet clear whether this is because the northeastern animals are hybridizing [crossbreeding] with wolves and domestic dogs or because they have adapted genetically to preying
on larger species such as white-tailed deer.
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SECTION 1.6
Evolution and Natural Selection in Ecosystems
Natural Ecosystem Change
Just as relationships between individual species are dynamic, so too is the overall makeup of
ecosystems. The process by which one natural community changes into another over a time
scale of years to centuries is called succession. Common succession patterns include plant
colonization of sand dunes and the regrowth of forests on abandoned farmland. While the
general process is widely recognized, ecologists have offered differing views of what drives
succession and how to define its end point. By analyzing the natural succession process, scientists seek to measure how stable ecosystems are at different stages in their trajectory of
development, and how they respond to disturbances in their physical environment or changes
in the frequency at which they are disturbed.
Figure 1.5: Succession
An example of succession is the change in the type of plants in an area over time. Certain organisms
that initially colonize an area are replaced over time by others, which themselves are later replaced
by other organisms.
e
Tim
Annual
plants
Perennial plants
and grasses
Shrubs
Softwood trees–
Pines
Hardwood trees
In the early 20th century, plant biologist Frederic Clements described two types of succession: primary (referring to colonization of a newly exposed landform, such as sand dunes or
lava flows after a volcanic eruption) and secondary (describing the return of an area to its
natural vegetation following a disturbance such as fire, treefall, or forest harvesting). British
ecologist Arthur Tansley distinguished between autogenic succession—change driven by the
inhabitants of an ecosystem, such as forests regrowing on abandoned agricultural fields—
and allogenic succession, or change driven by new external geophysical conditions such as
rising average temperatures resulting from global climate change.
ben85927_01_c01.indd 47
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Evolution and Natural Selection in Ecosystems
SECTION 1.6
As discussed above, ecologists often group species depending on whether they are better
adapted for survival at low or high population densities (r-selected versus K-selected). Succession represents a natural transition from r- to K-selected species. Ecosystems that have
recently experienced traumatic extinction events such as floods or fires are favorable environments for r-selected species because these organisms, which are generalists and grow
rapidly, can increase their populations in the absence of competition immediately after the
event. Over time, however, they will be out-competed by K-selected species, which often
derive a competitive advantage from the habitat modification that takes place during early
stages of primary succession.
For example, when an abandoned agricultural field transitions back to forest [. . .] sun-tolerant
weeds and herbs appear first, followed by dense shrubs like hawthorn and blackberry. After
about a decade, birches and other small fast-growing trees move in, sprouting wherever the
wind blows their lightweight seeds. In 30 to 40 years, slower-spreading trees like ash, red
maple, and oak take root, followed by shade-tolerant trees such as beech and hemlock.
A common observation is that as ecosystems mature through successional stages, they tend
to become more diverse and complex. The number of organisms and species increases and
niches become narrower as competition for resources increases. Primary production rates
and nutrient cycling may slow as energy moves through a longer sequence of trophic levels.
Many natural disturbances have interrupted the process of ecosystem succession throughout Earth’s history, including
Consider This
natural climate fluctuations, the expansion
For much of the 20th century park manand retreat of glaciers, and local factors
agers in the United States adopted a strict
such as fires and storms. An understandwildfire control and suppression policy,
ing of succession is central for conserving
championed by the iconic Smokey the
and restoring ecosystems because it idenBear. From an ecological perspective, how
tifies conditions that managers must cremight these efforts have been misplaced?
ate to bring an ecosystem back into its natHow might certain disturbances, like fires,
ural state. The Tallgrass Prairie National
be beneficial for biodiversity in certain
Preserve in Kansas, created in 1996 to
locations?
protect 11,000 acres of prairie habitat, is
an example of a conservation project that
seeks to approximate natural ecosystem
succession. A herd of grazing buffalo tramples on tree seedlings and digs up the ground, creating bare patches where new plants can grow,
just as millions of buffalo maintained the grassland prairies that covered North America before
European settlement.
Excerpted from Weeks, S., Moorcoft, P.R. (2007). Unit 4: Ecosystems. The Habitable Planet: A Systems Approach to
Environmental Science. Retrieved from http://www.learner.org/courses/envsci/unit/text.php?unit=4&secNum=0.
Used with permission of Annenberg Learner.
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SECTION 1.6
Evolution and Natural Selection in Ecosystems
Evolution in Action
Public debates and discussions over evolution often center on whether or not such a thing
exists. But for ecologists and other environmental scientists the evidence for evolution is all
around them and constantly presenting itself in new ways. Perhaps part of the problem with
the “debate” over evolution stems from the way scientists refer to evolution as a “theory.”
For many of us a theory is simply a hunch, something we think might be true. For scientists,
however, the term theory means something completely different. Recall from the discussion
of the scientific method in the Introduction that even when an experiment matches up with a
prediction and supports a hypothesis, scientists will continue to make additional predictions
from the knowledge gained and to test these predictions. In this context a scientific theory is
something that’s already well substantiated or supported and based on a large body of evidence developed through repeated observation and experimentation.
Ecologists and environmental scientists are also always seeing new evidence for evolution in
the world around us. Take the case of how some insect populations have responded to the use
of insecticide sprays in agricultural fields. Because insects produce such large numbers of offspring (i.e., they are r-selected) there is a greater chance that some of them will have a genetic
mutation that makes them less susceptible, or resistant, to the pesticide being sprayed. These
individuals may survive pesticide applications and then reproduce, passing on the genetic
mutation that made them resistant to the next generation (see Figure 1.6). This phenomenon
has come to be known as pesticide resistance or the pesticide treadmill since farmers respond
by spraying even more pesticide in a losing battle. The Pesticide Action Network (http://
www.panna.org/issues/pesticides-101-primer) estimates that since 1945 between 500 and
1,000 insect and weed species have evolved to develop resistance to pesticides and herbicides.
Figure 1.6: Pesticide resistance process
Pests can develop resistance to pesticides over time.
Application
of pesticides
in response
to pest
presence.
ben85927_01_c01.indd 49
Some pests
survive
pesticide
application.
Said to be
resistant.
Resistant
pests
reproduce.
Application
of more
pesticide in
response to
continued pest
presence.
Pests
survive,
no longer
affected by
pesticide.
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Case History—Mercury’s Impact on Wildlife
1.7
SECTION 1.7
Case History—Mercury’s Impact on Wildlife
Mercury is a well-known contaminant that is facing increased scrutiny and regulation due to its
impacts on human health. However, it’s less clear how mercury pollution is impacting wildlife
populations around the world. In this article, “Mercury’s Silent Toll on the World’s Wildlife,”
science and environmental journalist Rebecca Kessler describes how scientists are uncovering
disturbing evidence of how even low levels of exposure to mercury can harm a wide variety of
wildlife species. This raises the question of whether efforts to minimize human exposure to mercury will also benefit wildlife populations.
Mercury contamination provides an excellent case study for some of the concepts already
explored in this chapter. Low levels of mercury can exist naturally in many ecosystems, but
certain human activities can increase levels of mercury in the environment significantly. For
example, when coal is burned in a power plant the emissions that enter the atmosphere often
contain trace amounts of mercury. This mercury can travel thousands of miles and get washed
out of the atmosphere, entering streams, lakes, the ocean, and other water bodies. Once in the
water this mercury converts to methylmercury, which is both toxic and easily absorbed by algae
at the base of the aquatic food chain. Small fish consume the algae and in turn are consumed
by larger fish, allowing the mercury to bioaccumulate in their tissue. As mercury-laden fish are
eaten by animals higher up the food chain we can see biomagnification and impacts of mercury
contamination far from the water. Even low levels of exposure to mercury can impact the ability
of some species to reproduce, altering species composition in an ecosystem and possibly triggering trophic cascades.
Another interesting feature of this case history is the example it provides of the scientific method
in action. It describes the results of a research project that fed mercury-contaminated food
to captured ibises (a species of wading bird) and then tracked their breeding behavior. This
research provided new insights into our understanding of mercury contamination, although the
researchers acknowledged that there are possible differences in how mercury enters and moves
through food chains in the wild. Either way, the scientific research discussed in this article makes
clear that low levels of mercury exposure over prolonged periods could be resulting in unexpected and serious impacts on wildlife. As such, regulatory efforts to control mercury emissions
from human activities need to consider these impacts and not just those to human health.
By Rebecca Kessler
This month [January 2013], delegates from over 140 countries gathered in Geneva and finalized the first international treaty to reduce emissions of mercury. The treaty—four years in
the works and scheduled for signing in October—aims to protect human health from this very
serious neurotoxin.
But barely considered during the long deliberations, according to those involved in the treaty
process, was the harm that mercury inflicts on wildlife. While mercury doesn’t kill many animals outright, it can put a deep dent in reproduction, says David Evers, chief scientist at the
Biodiversity Research Institute (BRI), who serves on a scientific committee informing the
process. “It is a bit of a silent threat, where you have to kind of add up what was lost through
studies and demographic models.”
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Case History—Mercury’s Impact on Wildlife
SECTION 1.7
Harmful levels of mercury have turned up in all sorts of animals, from fish and birds living
around the world to pythons invading the Florida Everglades and polar bears roaming far
from any sources of pollution. In recent years, biologists have been tracking mercury’s footprints in unexpected habitats and species. Their research is illuminating the subtle effects of
chronic exposure and is showing that ever-lower levels cause harm.
Coal burning, gold mining, and other
human activities release mercury into
water bodies or the atmosphere, where
it can travel great distances before settling back to Earth. Mercury contamination is ubiquitous and hotspots are
common around the world, with fish
and human hair collected in 14 countries regularly exceeding U.S. Environmental Protection Agency (EPA)
standards, according to a BRI report
released just before the Geneva negotiations. And while mercury emissions are declining in North America
and Europe they are rising quickly in
the developing world, according to
the United Nations Environment Programme, the treaty coordinator.
AP Photo/Esteban Felix
Mining operations—like this illegal one in Peru—
release toxic mercury into the environment. In the
Peruvian state of Madre de Dios alone, 35 metric
tons of mercury is released annually by miners,
slowly poisoning people, plants, animals, and fish.
The new global treaty bans the production, import, and export of certain mercury-containing products,
requires governments to create plans to reduce mercury in small gold mining operations,
and puts some controls on industrial facilities—but some environmental groups warn that it
is too weak. The U.S. is going further. On January 1, an export ban on elemental mercury took
effect, and the EPA is finalizing new limits on coal plant emissions.
“In the end the treaty will reduce mercury that’s being released into the environment. And
I think the question will be, as we move along, ‘Is it enough?’—especially for areas that are
sensitive to mercury input. And then ‘Is it enough for wildlife conservation purposes?’ which
really wasn’t addressed all that well,” Evers says.
Exposed animals have trouble ridding their bodies of mercury, and it accumulates in tissue with every link in the food chain. Long-lived predators tend to carry the heaviest loads.
Research and public attention have largely focused on contaminated fish, the main route of
human exposure. In water, mercury converts quickly to methylmercury, its most toxic and
bioavailable form, so for many years wildlife biologists trained their sights on aquatic, fisheating birds and mammals, says Bill Hopkins, a Virginia Tech physiological ecologist.
Lately, though, Hopkins and others have uncovered mercury in reptiles, amphibians, insects,
spiders, terrestrial songbirds, and a wider variety of mammals than expected. “All these different groups can be exposed to mercury and pass it on to their babies,” says Hopkins.
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Case History—Mercury’s Impact on Wildlife
SECTION 1.7
Mercury is also turning up in strange places, he says. Invertebrate-eating songbirds living in
the floodplain bordering a contaminated Virginia river had as much mercury in their blood
as the river’s fish-eating birds, and sometimes more, showing that mercury pollution doesn’t
stay put in aquatic habitats. Scientists have found mercury-laden food chains in mountainous
forests, and shown that methylmercury forms in the woods, as well as in water. BRI scientists and collaborators discovered high levels in many invertebrate-eating songbird and bat
species living in varied habitats across the U.S. Northeast and Mid-Atlantic states, including
remote uplands. The pollutant has also emerged as a serious problem in the Arctic.
Mercury plays havoc on vertebrates’ development and their neurological and hormonal
systems, and doses too low to kill can cause problems that aren’t always obvious in the
wild, experts say. “Methylmercury is one of most toxic environmental pollutants we’ve ever
come upon,” says Gary Heinz, a recently retired federal wildlife biologist who studied it over
four decades.
In the earliest studies of these sublethal effects in the 1970s, Heinz reported that captive mallards fed mercury-laced food laid fewer eggs than control ducks and laid them outside the
nest. Also, their ducklings didn’t respond well to their calls. Numerous examples have accumulated since. Fish form loose, sloppy schools and are slow to respond to a simulated predator. Several bird species sing different songs. Loons lay smaller eggs, and they incubate their
nests, forage, and feed their chicks less. Salamanders are sluggish and less responsive to prey,
Hopkins and colleagues found. Egret chicks are similarly lethargic and unmotivated to hunt.
Changes like these could be grave for wild animals, says Peter Frederick, a University of Florida ecologist who was part of the egret study. “Getting lunch or a mate depends on milliseconds and millimeters. You have to perform that courtship dance just right. You have to make
the calls just right. You have to stab your prey to within a millimeter. If you’re off by a microsecond, it’s gone,” he says.
Frederick discovered a remarkable example in white ibises from the Everglades. There, mercury levels are low but constant, and ibises seem to nest less and abandon their nests more
often than elsewhere. To see if chronic mercury exposure was responsible, Frederick captured 160 ibis nestlings and fed them food with mercury levels similar to their wild fish prey.
He and his team observed the birds for three years to see if it affected their breeding behavior.
As expected, the dosed birds produced far fewer offspring than undosed controls. There were
the usual reasons: eggs didn’t hatch and chicks died under lousy parenting. But Frederick was
wholly surprised to see widespread homosexual pairing among the dosed males and to find
this caused much of the reproductive deficit. Avian homosexuality usually occurs with stark
sex imbalances—which wasn’t the case here, Frederick says.
No one had ever reported homosexuality as an effect of mercury, or any other contaminant for
that matter, Frederick says. Moreover, the effects appeared in ibises he’d fed as little as 0.05
ppm [parts per million] of mercury in their food—one-tenth of what Heinz fed his mallards.
Further work indicated that hormonal changes wrought by mercury’s effects on the ibises’
endocrine systems were at work. In a 2011 paper, Frederick and a colleague estimated that
out in the Everglades, mercury could cut the number of ibis fledglings by half—easily enough
to curtail the population.
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Case History—Mercury’s Impact on Wildlife
SECTION 1.7
No one has checked wild ibises for poor parental behavior or homosexuality, which might
lay the blame more squarely on mercury, he says. (Different species react to mercury differently, and Frederick stresses that for many reasons his results in no way suggest that mercury
might play a role in human homosexuality.) Nevertheless, the broader implications for chronically exposed wildlife are chilling. “We can be essentially neutering populations by cutting
off reproduction through the endocrine system,” he says. “This could easily be going on in the
wild with many kinds of contaminants. Mercury is not the only endocrine disruptor.”
Like Frederick’s study, much of the research on mercury’s sublethal effects has been conducted on captive animals. In nature, it’s very difficult to get the large sample sizes and control groups needed to identify subtle differences statistically, says Erick Greene, a conservation biologist at the University of Montana.
Studying ospreys living near Montana’s polluted Clark Fork River, Greene and two colleagues
found that about half the eggs laid by high-mercury birds fail to hatch. But they’ve been puzzled as to whether the surviving chicks are affected. In humans, blood levels around .005 ppm
can cause cognitive deficits, Greene says. But his osprey chicks commonly have levels 100—
and even 1,000—times higher. The chicks seem to do fine in the nest, he says. “They may look
all right, but I don’t know if I would recognize a mentally impaired osprey chick.”
Once they’re fledged they soon migrate south, out of sight. Greene suspects they may have
trouble making the demanding migration to Central or South America (where mercury flows
freely in small gold mining operations), or just figuring out how to survive on their own. His
team has begun outfitting fledglings with satellite transmitters to determine how far mercury-loaded birds get compared to their normal peers, and how long they live.
It’s one thing to show that wild animals are exposed to harmful levels of mercury, but solid evidence that whole populations are harmed is harder to come by, experts say. A notable exception is loons. Evers and more than a dozen colleagues amassed an impressive 18-year data
set of nearly 5,500 mercury measurements from loons on 700 lakes across 17 U.S. states and
Canadian provinces. They showed that when mercury in loon blood hits 3 ppm, the number
of young fledged drops by 41 percent—
and that enough loons are affected to set
back some New Hampshire and Maine
populations.
Consider This
Understanding the impacts of mercury
on wildlife is a challenging task, and the
uncertainty surrounding the science can
be used by some to argue against regulation of this contaminant. At what point
do you think there is enough evidence to
take action to address an environmental
problem like this? How can the cautious
approach of scientists “testing hypotheses” be reconciled with political demands
for “scientific proof” before taking action?
ben85927_01_c01.indd 53
In a forthcoming paper, Hopkins and
another researcher go a step further with
a population model they developed based
on four years of field data on American
toads. Toads readily move between small
populations scattered throughout the
landscape. Mercury exposure can kill eggs
and tadpoles, and survivors are often small
and slow to mature. The model revealed
that not only can mercury kill enough tadpoles to wipe out small populations, but
that nearby uncontaminated populations
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Summary & Resources
can also drop or go extinct because there are too few toads around to replenish them if their
numbers happen to dip for other reasons. Hopkins says he thinks the paper will change biologists’ understanding of contaminants. “Contaminant effects in one population can actually affect
adjacent populations that aren’t being exposed to that contaminant,” he says.
Whatever its weaknesses, the new treaty represents a “great step forward,” says Evers, and
the good news is that once local sources are controlled, mercury in nearby wildlife can drop
quickly. The bad news is that mercury from coal burning can travel great distances—for
instance, from China to North America—before settling.
Overall, Evers says the forecast for wildlife is cloudy. When it comes to mercury, “the more we
look the more we find, and the more we find the lower that toxicity level is going,” he says.
“Right now at a global level, mercury is just being released more and more in the system.
Those trend lines are going in the wrong directions.”
Kessler, R. (2013, January 31), “Mercury’s Silent Toll On the World’s Wildlife,” Yale Environment 360. Copyright
© Rebecca Kessler. Reprinted by permission of the author.
Summary & Resources
Chapter Summary
In order to better understand how the natural world works, ecologists and other scientists
study it on very different scales. For example, we started this chapter with the concept of
biomes, which are broad-scale areas of the planet that are characterized by similar climates,
plants, and animals. The biome concept allows ecologists to classify the world into a relatively small number of categories, and then to examine how basic factors such as temperature, moisture, nutrient levels, light, and other physical conditions affect the abundance and
diversity of life in locations with similar characteristics.
Ecosystems are studied on a smaller scale than biomes, and they can be defined as a system
or unit (for example a forest or grassland) and the living (biotic) and non-living (abiotic) components of that system. Ecologists who study ecosystems investigate the way energy enters
the system, usually in the form of sunlight, and how it moves through that system at various
trophic levels. Ecologists also look at how water and nutrients cycle through ecosystems as
well as the impact on the abundance and/or diversity of species based on the availability of
energy (net primary productivity), nutrients, and water.
On an even smaller scale, ecologists study individual species and organisms in specific ecosystems. In order to do this, ecologists focus on concepts of population biology and an organism’s
life history strategy—how it develops and reproduces. In addition, ecologists pay close attention to how different species interact and compete with one another for limited resources in a
given ecosystem. Competition results in species occupying niches within ecosystems and also
helps to drive the process of evolution to ensure the ongoing survival of an individual species.
Throughout all of these stages, ecologists rely on the scientific method to perform their work.
They first observe the natural world and form questions and hypotheses. Next, they acquire
actual data on the system and the question they seek to answer. They examine and analyze
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Summary & Resources
that data against the original hypotheses that drive the research, and finally, they reach a conclusion based on the results. These conclusions are usually disseminated and shared with the
broader scientific community so that the results can be questioned and challenged, and the
original research can be repeated to see if similar results are obtained.
The end result of decades of this sort of work is a generally well-developed understanding
of how our world works, although Earth’s systems are so complex that there are still many
things that we do not understand. Likewise, questions that were once thought to be settled
are sometimes revisited as new information is discovered.
The remainder of this book will focus primarily on how human actions affect the natural
world. Much of the information presented will be based on an understanding first of how an
ecosystem functions and then how human actions—such as the introduction of a pollutant,
removal of a species through over-hunting, or conversion of part of the ecosystem to another
use—alter those systems. Chapter 2 will focus specifically on changes in human population
over time. Indeed, understanding human population is important since, ultimately, it is the
number of people, and the level of material consumption that they engage in, that determine
the scale and scope of the human impact on the environment.
Working Toward Solutions
While the case history reading in Section 1.7 focused on the dangers of mercury to wildlife,
this contaminant can also have serious impacts on human health. Mercury exposure is especially problematic for children and pregnant women because it can interfere with neurological
or brain development and function. As a result, many states issue advisories on how much fish
should be eaten by these groups. Even though individuals are usually not directly related to
mercury emissions, there are things you can do to reduce emissions indirectly as well as limit
your own exposure to mercury pollution.
For a general overview of mercury pollution and how it impacts human health, visit the following pages:
http://www.usgs.gov/mercury/
http://pubs.usgs.gov/fs/1995/fs216-95/
http://www.usgs.gov/themes/factsheet/146-00/
http://www.epa.gov/hg/effects.htm
http://water.epa.gov/scitech/swguidance/standards/criteria/aqlife/methylmercury
/factsheet.cfm
http://www.epa.gov/hg/eco.htm
http://www.stonybrook.edu/commcms/gelfond/fish/fish.html
http://www.oeconline.org/our-work/healthier-lives/pollutioninpeople/solutions
/mercury
http://pubs.usgs.gov/fs/fs095-01/fs095-01.pdf
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(continued)
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Summary & Resources
Working Toward Solutions (continued)
For some discussion of what you can do to help reduce and prevent mercury pollution, visit:
http://www.pca.state.mn.us/index.php/topics/preventing-waste-and-pollution
/p2-pollution-prevention/reducing-toxicity/preventing-mercury-pollution.html
http://www.nrdc.org/health/effects/mercury/reduction.asp
http://www.ec.gc.ca/mercure-mercury/default.asp?lang=En&n=7649B5FA-1
Post-Test
1. Which biome would be expected to have the warmest and wettest conditions?
a. Coniferous forest
b. Desert
c. Tropical forest
d. Temperate grassland
2. The major sources of human emissions of the pollutant mercury are
a. disposal of thermometers and hospital waste.
b. car and truck exhaust.
c. coal burning and gold mining.
d. agriculture and cattle ranching.
3. Which of the following is NOT an example of an important biogeochemical cycle?
a. The water cycle
b. The phosphorous cycle
c. The solar cycle
d. The carbon cycle
4. The population biology concept that refers to the maximum number of organisms
that a given environment can support is
a. survival rate.
b. reproductive rate.
c. K-selection.
d. carrying capacity.
5. When a top predator is removed from an ecosystem it can have dramatic impacts on
the entire food web. These impacts are referred to as
a. biomagnification.
b. bioaccumulation.
c. trophic cascades.
d. photosynthesis.
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Summary & Resources
6. Which of the following is NOT an example of an avoidance/escape feature used to
deter predators from attacking prey?
a. A panda feeding only on bamboo
b. Fish swimming in a school
c. Wildebeests moving in a herd
d. A moth with false eye spots on its hind wings
7. Because mercury tends to accumulate in an animal’s tissue we would expect what
kinds of organisms to carry the highest amounts of this toxin?
a. Long-lived predators
b. Primary producers
c. Short-lived predators
d. Detritivores
8. The latitudinal biodiversity gradient predicts that
a. biodiversity will be highest at high latitudes.
b. biodiversity will be evenly distributed across latitudes.
c. biodiversity will be spread randomly around the planet.
d. biodiversity will be highest in tropical areas at low latitudes.
9. The average rate of energy transfer between one trophic l...
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