Table 1.1. Ecological Surprises Caused by Complex Interactions
Voluntary or involuntary introductions or deletions of species often trigger unexpected alterations in the normal provision of ecosystem services by terrestrial, freshwater, and marine ecosystems. In all cases, the community and ecosystem alterations have been the consequence of indirect interactions among three or more species (C11, Table 11.2).
Study Case |
Nature of the Interaction Involved |
Ecosystem Service Consequences |
Introductions |
Top predators |
Introduction of brown trout (Salmo trutta) in New Zealand for angling |
trophic cascade, predator increased primary producers by decreasing herbivores |
negative— increased eutrophication |
Introduction of bass (Cichla ocellaris) in Gatun Lake, Panama |
trophic cascade, top predator decreased control by predators of mosquito larvae |
negative— decreased control of malaria vector |
IIntroduction of pine marten (Martes martes) in the Balearic Islands, Spain |
predator of frugivorous lizards (main seed dipersers) |
negative— decreased diversity of frugivorous lizards due to extinction of native lizards on some islands; changes in dominant shrub (Cneorum tricoccon) distribution because marten replaced the frugivorous-dispersing role |
Intraguild predators |
Egg parasitoid (Anastatus kashmirensis) to control gypsy moth (Lymantria dispar) |
hyperparasitism (parasitoids that use parasitoids as hosts) |
negative— disruption of biological control of pests; introduced parasitoid poses risk of hyperparasitism to other pest-regulating native parasitoids |
Gambusia and Lepomis fish in rice fields to combat mosquitoes |
intraguild predator (adult fish feed on juveniles as well as on mosquito larvae) |
opposed to goal— decreased control of disease vector (mosquito) |
Intraguild preys |
Opossum shrimp (Mysis relicta) in Canadian lakes to increase fish production |
intraguild prey depletes shared zooplankton prey |
opposed to goal— decreased salmonid fish production |
Apparent competitors |
Rats (Rattus spp) and cats (Felis catus) in Steward Island, New Zealand |
rats induced high cat densities and increased predation on endangered flightless parrot (Strigops habroptilus) |
negative— reduced diversity |
Herbivores |
Zebra mussel (Dreissena polymorpha) in Great Lakes, United States |
zebra mussel reduced phytoplankton and outcompeted native bivalves |
negative— reduced diversity
positive— increased water quality |
Mutualists |
Myna bird (Acridotheres tristis) for worm pest control in Hawaiian sugarcane plantations |
myna engaged in the dispersal of the exotic woody weed Lantana camara |
negative— increased invasion by Lantana produced impenetrable thorny thickets; reduced agricultural crops and pasture carrying capacity and sometimes increased fire risk; displaced habitat of native birds |
Ecosystem engineers |
Earthworm (Pontoscolex corethrurus)in Amazonian tropical forests converted to pasture |
dramatically reduces soil macroporosity and gas exchange capacity |
negative— reduces soil macrofaunal diversity and increases soil methane emissions |
C4 perennial grasses Schizachyrium condesatum, Melinis minutiflora in Hawaii for pasture improvement |
increased fuel loads, fuel distribution, and flammability |
negative— increases fire frequency, affecting fire-sensitive plants; reduced plant diversity; positive feedback for further invasion of flammable exotic species on burned areas |
Nitrogen-fixing firetree (Myrica faya) in Hawaii |
increases soil nitrogen levels in newly formed nitrogen-poor volcanic soils |
negative— increased fertility, increased invasion by other exotics, reduced regeneration of native Metrosideros tree, alteration of successional patterns |
Deletions/Harvesting |
Top predators |
Selective harvesting of piscivorous fishes in Canadian lakes |
piscivorus fishes promote Daphnia that effectively suppresses primary (algal) production |
negative— shifts from net carbon sinks in piscivorous-dominated to equilibrium or net carbon sources in planktivorous-dominated lake |
Sea otter (Enhydra lutris) harvesting near extinction in southern California |
cascading effects produced reductions of kelp forests and the kelp-dependent community |
negative— loss of biodiversity of kelp habitat users |
Pollution-induced reductions in predators of nematodes in forest soils |
heavy metal bioaccumulation produced reductions nematophagous predators and increased herbivorous nematodes |
negative— disruption of forest soil food webs; increases in belowground herbivory; decrease in forest productivity |
Intraguild predators |
Declining populations of coyote (Canis latrans) in southern California |
releases in raccoons (Procyon lotor) and feral house cats |
negative— threat to native bird populations |
Overhavesting of seals and sea lions in Alaska |
diet shifts of killer whales increased predation on sea otters |
negative— conflict with other restoration programs; failure of reintroduction of sea otters to restore kelp forest ecosystems |
Keystone predators |
Harvesting of triggerfish (Balistaphus) in Kenyan coral reefs |
triggerfish declines release sea urchins, which outcompete herbivorous fish |
negative— increased bioerosion of coral substrates; reduced calcium carbonate deposition |
Herbivores |
Voluntary removal of sheep and cattle in Santa Cruz Island, United States, for restoration |
release of the exotic plant component from top-down control |
opposite to goal— explosive increases in exotic herbs and forbs and little recovery of native plant species |
Overhavesting of seals and sea lions in Alaska |
lack of fish grazers allowed macroalgae to outcompete coral following disturbances |
negative— coral cover was reduced from 52% to 3%, and macroalgae increased from 4% to 92% |
Ecosystem engineers |
Voluntary removal of exotic tamarisk (Tamariscus sp.) for restoration of riparian habitats in Mediterranean deserts |
long-established tamarisk has replaced riparian vegetation and serves as habitat to endangered birds |
opposite to goal— reduction in biodiversity; structural changes in riparian habitats |
Source:
Millennium Ecosystem Assessment
Ecosystems and Human Well-being: Biodiversity Synthesis
(2005), p.26-27
Related publication:
Other Figures & Tables on this publication:
Direct cross-links to the Global Assessment Reports of the Millennium Assessment
Box 1. Biodiversity and Its Loss— Avoiding Conceptual Pitfalls
Box 1.1. Linkages among Biodiversity, Ecosystem Services, and Human Well-being
Box 1.2. Measuring and Estimating Biodiversity: More than Species Richness
Box 1.3. Ecological Indicators and Biodiversity
Box 1.4. Criteria for Effective Ecological Indicators
Box 2. MA Scenarios
Box 2.1. Social Consequences of Biodiversity Degradation (SG-SAfMA)
Box 2.2. Economic Costs and Benefits of Ecosystem Conversion
Box 2.3. Concepts and Measures of Poverty
Box 2.4. Conflicts Between the Mining Sector and Local Communities in Chile
Box 3.1. Direct Drivers: Example from Southern African Sub-global Assessment
Box 4.1. An Outline of the Four MA Scenarios
Box 5.1. Key Factors of Successful Responses to Biodiversity Loss
Figure 3.3. Species Extinction Rates
Figure 1.1. Estimates of Proportions and Numbers of Named Species in Groups of Eukaryote Species and Estimates of Proportions of the Total Number of Species in Groups of Eukaryotes
Figure 1.2. Comparisons for the 14 Terrestrial Biomes of the World in Terms of Species Richness, Family Richness, and Endemic Species
Figure 1.3. The 8 Biogeographical Realms and 14 Biomes Used in the MA
Figure 1.4. Biodiversity, Ecosystem Functioning, and Ecosystem Services
Figure 2. How Much Biodiversity Will Remain a Century from Now under Different Value Frameworks?
Figure 2.1. Efficiency Frontier Analysis of Species Persistence and Economic Returns
Figure 3. Main Direct Drivers
Figure 3.1. Percentage Change 1950–90 in Land Area of Biogeographic Realms Remaining in Natural Condition or under Cultivation and Pasture
Figure 3.2. Relationship between Native Habitat Loss by 1950 and Additional Losses between 1950 and 1990
Figure 3.3. Species Extinction Rates
Figure 3.4. Red List Indices for Birds, 1988–2004, in Different Biogeographic Realms
Figure 3.5. Density Distribution Map of Globally Threatened Bird Species Mapped at a Resolution of Quarter-degree Grid Cell
Figure 3.6. Threatened Vertebrates in the 14 Biomes, Ranked by the Amount of Their Habitat Converted by 1950
Figure 3.7. The Living Planet Index, 1970–2000
Figure 3.8. Illustration of Feedbacks and Interaction between Drivers in Portugal Sub-global Assessment
Figure 3.9. Summary of Interactions among Drivers Associated with the Overexploitation of Natural Resources
Figure 3.10. Main Direct Drivers
Figure 3.11. Effect of Increasing Land Use Intensity on the Fraction of Inferred Population 300 Years Ago of Different Taxa that Remain
Figure 3.12. Extent of Cultivated Systems, 2000
Figure 3.13. Decline in Trophic Level of Fisheries Catch since 1950
Figure 3.14. Estimated Global Marine Fish Catch, 1950–2001
Figure 3.15. Estimates of Forest Fragmentation due to Anthropogenic Causes
Figure 3.15. Estimates of Forest Fragmentation due to Anthropogenic Causes
Figure 3.15. Estimates of Forest Fragmentation due to Anthropogenic Causes
Figure 3.15. Estimates of Forest Fragmentation due to Anthropogenic Causes
Figure 3.15. Estimates of Forest Fragmentation due to Anthropogenic Causes
Figure 3.15. Estimates of Forest Fragmentation due to Anthropogenic Causes
Figure 3.16. Fragmentation and Flow in Major Rivers
Figure 3.17 Trends in Global Use of Nitrogen Fertilizer, 1961–2001 (million tons)
Figure 3.18 Trends in Global Use of Phosphate Fertilizer, 1961–2001 (million tons)
Figure 3.19. Estimated Total Reactive Nitrogen Deposition from the Atmosphere (Wet and Dry)
in 1860, Early 1990s, and Projected for 2050
Figure 3.20. Historical and Projected Variations in Earth’s Surface Temperature
Figure 4. Trade-offs between Biodiversity and Human Well-being under the Four MA Scenarios
Figure 4.1. Losses of Habitat as a Result of Land Use Change between 1970 and 2050 and Reduction in the Equilibrium Number of Vascular Plant Species under the MA Scenarios
Figure 4.2. Relative Loss of Biodiversity of Vascular Plants between 1970 and 2050 as a Result of Land Use Change for Different Biomes and Realms in the Order from Strength Scenario
Figure 4.3. Land-cover Map for the Year 2000
Figure 4.4. Conversion of Terrestrial Biomes
Figure 4.5. Forest and Cropland/Pasture in Industrial and Developing Regions under the MA Scenarios
Figure 4.6. Changes in Annual Water Availability in Global Orchestration Scenario by 2100
Figure 4.7. Changes in Human Well-being and Socioecological Indicators by 2050 under the MA Scenarios
Figure 6.1. How Much Biodiversity Will Remain a Century from Now under Different Value Frameworks?
Figure 6.2. Trade-offs between Biodiversity and Human Well-being under the Four MA Scenarios
Table 1.1. Ecological Surprises Caused by Complex Interactions
Table 2.1. Percentage of Households Dependent on Indigenous Plant-based Coping Mechanisms at Kenyan and Tanzanian Site
Table 2.2. Trends in the Human Use of Ecosystem Services and Enhancement or Degradation of the Service Around the Year 2000 - Provisioning services
Table 2.2. Trends in the Human Use of Ecosystem Services and Enhancement or Degradation of the Service Around the Year 2000 - Regulating services
Table 2.2. Trends in the Human Use of Ecosystem Services and Enhancement or Degradation of the Service Around the Year 2000 - Cultural services
Table 2.2. Trends in the Human Use of Ecosystem Services and Enhancement or Degradation of the Service Around the Year 2000 - Supporting services
Table 6.1. Prospects for Attaining the 2010 Sub-targets Agreed to under the Convention on Biological Diversity