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41 Cards in this Set

  • Front
  • Back
Destructive sampling
killing a large amount of species to open up there guts and see what they eat
Gross energy returns
E, what animals want to maximize
Handling time
h, time it takes to pursue, handle and swallow food
Profitabilites
E(gross energy returns)/h(handling time)
Encounter rate
λ, how available the item is
Search time
Ts , total time searching for food
Optimal foraging model
Understand conditions when it is best for an animal to eat both items, or pass up a poorer item and continue searching for a better one
Expected energy reward equation
E = Ts(λ1E1+λ2E2)
Total time requried for foraging
T = Ts + Ts(λ1E1+λ2E2)
Net energy gain per unit time
E(1,2) / T(1,2)
Optimal foraging predictions 1 and 2
1) at greater abundance animals will be more selective, 2) an item should be incledued in the diet based on the abundance of the better item, not considering abundance of worse item
Exploitative resource depression
Animal depletes food supply
Behaviorial resource depression
Animal scares food away
Compression hypothesis
Invading species (predators) will result in a drop of patches from an animals routine. Basically, don’t want to go where they will get eaten
Home range
Where an animal normally frequesnts (every animal has one)
Territory
A defended area, exclusive of other individuals
Feeding territories
Defended exclusively for food
Nesting territories
Small area around nest to protect aggs and young
Multi-purpose territories
Defender sleeps, courts mates, breeds, nests, and feeds offspring
Relative threats hypothesis
The intensity of an owners response to a threat depends on what it stands to lose in fights with neighbors and strangers
The food hypothesis
Animals assess resource availability directly and defend areas containing sufficient quantity of food
The intruder hypothesis
Animals defend as large an area as they can, but this is contrained by competition and neighbors
Lincoln Index
(number of marked individuals, M)/(total number of individuals, N) = (number of recaptured individuals, m)/(total number captured in second visit) N = nM/m
Survivorship
lx = number alive at age x / number alive at birth = nx / n0
Mortality
mx = number of deaths during an age class / number of individuals alive at the start of the age class = (nx− nx+1) / nx
Survival rate
Sx = nx+1 / nx = 1 − mx
Future life expectancy
ex = Tx / nx , how many more years an individual should live on average
Average alive during an age class
Lx = (nx + nx+1) / 2
Sum of average alive during an age class
Tx = Σ (from x=i to ∞) Lx
Three Types of Survivorship Curves
Type 1 = low juvenile mortality, high adult mortality, ex) humans, Type II = constant rate of death, diagnol plot, ex) birds and lizards, Type III = high juvenile mortality, low adult mortality, ex) fish and insects
Fecundity
bx, Fecundity is the number of offspring produced by each breeding female
Realized fecundity
lxbx, The survivorship at each age class multiplied by the fecundity
Net reproductive rate
R0, is the average number of offspring produced by an individual in the population. Thus it is the sum of realized fecundity over all ages: R0 = Σlxbx (x=age i to ∞)
Population
N, where N0 is initial population and Nt is population at a given time
Geometric model of population growth
Nt = N0 R0t , gives us the size of population at time t in the future but not how fast the population is growing. R0 can be substitued with λ, Nt = N0λt
Geometric rate of increase
λ = Nt+1 / Nt ,estimates the rate at which our population is growing
Instantaneous rate of increase
r, r=birth rate (b) − death rate (d)
Exponential growth model
dN/dt = rN, where r, the per capita rate of increase, is constant and N, the size of a population, is the variable. Can be rewritten in computational form: Nt = N0 ert
Density dependent vs. independent factors
Dependent factors are limits on resources such as food and places to live. Independent factors are are hard to predict such as temperature, enviornmental catastrophes, etc.
Carrying capacity
K, the upper limit to population growth
Logistical growth model
dN/dt = r0 N(1−(N/k)) , where 1− (N/k) measures how empty the enviornment is