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#immigration rates

8 public questions tagged with this topic.

Increase in island distance primarily affects:

“Immigration rate” for increase in island distance primarily affects. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. Larger islands usually support more habitats and larger populations, lowering extinction risk; less isolated islands receive colonists more readily and may experience rescue effects. These mechanisms also apply to habitat fragments that function as ecological islands. The remaining alternatives—“Extinction rate”, “Resource availability”, “Genetic drift”—refer to different states, processes, or scales and therefore do not express the same causal relationship. At equilibrium, species identities can continue to turn over even when richness is approximately stable. The model predicts a balance of rates, not an absence of colonization or extinction. Field observations could test this account by measuring the proposed driver and the demographic or ecosystem response while controlling plausible confounding factors. This distinction matters because similar surface patterns can arise through different mechanisms, whereas ecological prediction depends on identifying the mechanism that actually changes rates.

Ref: Biogeography, Lomolino et al., 5th Ed., Ch. 5-8

Immigration rates are primarily influenced by island:

“Distance from mainland” for immigration rates are primarily influenced by island. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. Island biogeography explains species richness as a dynamic balance between immigration and extinction. Immigration generally declines as an island fills with species, whereas extinction rises as more species divide finite area and maintain smaller populations. The remaining alternatives—“Vegetation type”, “Altitude”, “Climate”—refer to different states, processes, or scales and therefore do not express the same causal relationship. Larger islands usually support more habitats and larger populations, lowering extinction risk; less isolated islands receive colonists more readily and may experience rescue effects. These mechanisms also apply to habitat fragments that function as ecological islands. Linking the wording to measurable consequences for fitness, abundance, or flux gives the conclusion its scientific meaning and prevents a purely mnemonic interpretation.

Ref: Biogeography, Lomolino et al., 5th Ed., Ch. 5-8

What happens to immigration rates as the island's distance from the mainland increases?

“Decrease” for what happens to immigration rates as the island's distance from the mainland increases. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. At equilibrium, species identities can continue to turn over even when richness is approximately stable. The model predicts a balance of rates, not an absence of colonization or extinction. The remaining alternatives—“Increase”, “Remain constant”, “Initially increase then decrease”—refer to different states, processes, or scales and therefore do not express the same causal relationship. Island biogeography explains species richness as a dynamic balance between immigration and extinction. Immigration generally declines as an island fills with species, whereas extinction rises as more species divide finite area and maintain smaller populations. Linking the wording to measurable consequences for fitness, abundance, or flux gives the conclusion its scientific meaning and prevents a purely mnemonic interpretation.

Ref: Biogeography, Lomolino et al., 5th Ed., Ch. 5-8

Which island typically has the highest immigration rates?

“Large, near mainland” for which island typically has the highest immigration rates. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. Larger islands usually support more habitats and larger populations, lowering extinction risk; less isolated islands receive colonists more readily and may experience rescue effects. These mechanisms also apply to habitat fragments that function as ecological islands. The remaining alternatives—“Large, far from mainland”, “Small, near mainland”, “Small, far from mainland”—refer to different states, processes, or scales and therefore do not express the same causal relationship. At equilibrium, species identities can continue to turn over even when richness is approximately stable. The model predicts a balance of rates, not an absence of colonization or extinction. Field observations could test this account by measuring the proposed driver and the demographic or ecosystem response while controlling plausible confounding factors.

Ref: Biogeography, Lomolino et al., 5th Ed., Ch. 5-8

At equilibrium, the rate of species immigration is:

“Equal to extinction rate” for at equilibrium, the rate of species immigration is. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. Larger islands usually support more habitats and larger populations, lowering extinction risk; less isolated islands receive colonists more readily and may experience rescue effects. These mechanisms also apply to habitat fragments that function as ecological islands. The remaining alternatives—“Greater than extinction rate”, “Less than extinction rate”, “Unrelated to extinction rate”—refer to different states, processes, or scales and therefore do not express the same causal relationship. At equilibrium, species identities can continue to turn over even when richness is approximately stable. The model predicts a balance of rates, not an absence of colonization or extinction. This distinction matters because similar surface patterns can arise through different mechanisms, whereas ecological prediction depends on identifying the mechanism that actually changes rates.

Ref: Biogeography, Lomolino et al., 5th Ed., Ch. 1-4

As species accumulate on an island, immigration rates generally:

“Decrease” for as species accumulate on an island, immigration rates generally. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. Island biogeography explains species richness as a dynamic balance between immigration and extinction. Immigration generally declines as an island fills with species, whereas extinction rises as more species divide finite area and maintain smaller populations. The remaining alternatives—“Increase”, “Remain constant”, “Fluctuate randomly”—refer to different states, processes, or scales and therefore do not express the same causal relationship. Larger islands usually support more habitats and larger populations, lowering extinction risk; less isolated islands receive colonists more readily and may experience rescue effects. These mechanisms also apply to habitat fragments that function as ecological islands. The cited framing is therefore most useful when treated as a conditional biological claim, with assumptions about scale and environmental context kept explicit.

Ref: Biogeography, Lomolino et al., 5th Ed., Ch. 1-4

Immigration rates are highest on islands:

“Near and large” for immigration rates are highest on islands. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. Island biogeography explains species richness as a dynamic balance between immigration and extinction. Immigration generally declines as an island fills with species, whereas extinction rises as more species divide finite area and maintain smaller populations. The remaining alternatives—“Distant and large”, “Near and small”, “Distant and small”—refer to different states, processes, or scales and therefore do not express the same causal relationship. Larger islands usually support more habitats and larger populations, lowering extinction risk; less isolated islands receive colonists more readily and may experience rescue effects. These mechanisms also apply to habitat fragments that function as ecological islands. The cited framing is therefore most useful when treated as a conditional biological claim, with assumptions about scale and environmental context kept explicit.

Ref: Biogeography, Lomolino et al., 5th Ed., Ch. 1-4

Factors primarily influencing colonization rates on islands:

“Distance from mainland” for factors primarily influencing colonization rates on islands. This relationship follows from the ecological mechanism represented by the terms in the item, not merely from an association between their names. Larger islands usually support more habitats and larger populations, lowering extinction risk; less isolated islands receive colonists more readily and may experience rescue effects. These mechanisms also apply to habitat fragments that function as ecological islands. The remaining alternatives—“Island shape”, “Island vegetation”, “Island altitude”—refer to different states, processes, or scales and therefore do not express the same causal relationship. At equilibrium, species identities can continue to turn over even when richness is approximately stable. The model predicts a balance of rates, not an absence of colonization or extinction. This distinction matters because similar surface patterns can arise through different mechanisms, whereas ecological prediction depends on identifying the mechanism that actually changes rates. The cited framing is therefore most useful when treated as a conditional biological claim, with assumptions about scale and environmental context kept explicit.

Ref: The Theory of Island Biogeography, MacArthur & Wilson, Ch. 2-4