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entomophagous insects
carnivorous insects who feed on other arthropods
high in nitrogen and water compared to other food sources
energetically expensive to capture
parasite
lives at expense of host, without directly killing host
may be vectors for disease and other things that kill host, but feeding does not kill
predator
kills and consumes more than one prey item to reach maturity
parasitoid
symbiont that feeds on host, eventually resulting in host’s death
host death related to development of parasitoid
slavery
primarily in ants
workers take pupa of another species and make them do most of the work in the colony
some enslaved species will neglect the young of their slavemakers in rebellion
phoresy
transport of individuals by another (hitchhiking)
often done by wingless or small insects with low mobility
may lead to predation or parasitism of eggs
Meloe franciscanus phoresy
Meloid beetles lay masses of larvae that emit pheromones of female bees
attracts male bees that the larvae jump onto
when the male bee mates with an actual female, the larvae jump onto the female
beetle larvae are transported to host nest, where they feed
How common are predatory insect?
about 25% of insect species are predatory
monophagous predators
predators that feed exclusively on a single species of prey
highly specialized
oligophagous predators
feeds on a few number of prey species
polyphagous predators
generalist predators that feed on prey based on abundance (prey switching)
seven orders that are exclusively predatory
odonata
mantophasmatodea
mantodea
megaloptera
neuroptera
raphidioptera
mecoptera (adults)
orders with some predatory species
grylloblatodea
thysanoptera
hemiptera
coleoptera
diptera
hymenoptera
etc
general adaptation of predatory insects
larger than other entomophagous insects
larger eyes with good visual detection
raptorial forelegs common
mandibulate or stylet mouthparts
defensive adaptation, like armor that deters counter attacks from prey
well-equipped to travel (decent fliers)
Size as a predatory adaptation
predator size is proportional to prey size (large prey = large predator)
some exceptions, predators that can sting and paralyze prey, or team up against prey, can go after larger things
eyes as a predator adaptation
wider spaced eyes have better binocular perception
good visual detection relative to number of ommatidia and angles
mouthparts as a predator adaptation
neuroptera — mandibles and fused maxillae
hemiptera — stylet-like mandibles and maxillae, all fused
coleoptera — scythe-like mandibles
odonata naiads — hinged and enlarged labium to scoop in prey
extra-oral digestion is common
extra-oral digestion in predators
allows for relatively larger prey items to be consumed
concentrated nutrients can be extracted more quickly
ingested food does not contain any bulky or indigestible items
optimal foraging theory
differences between the costs and benefits associated with strategy are maximized
predators can either maximize energy obtained or minimize time
requires appropriate habitat
benefits of optimal foraging theory
quality and quantity of food
costs of optimal foraging theory
time spent obtaining food (time not spent reproducing)
energy spent obtaining and processing food
exposure to adverse elements
increased risk of being eaten or parasitized
sit and wait/ambush strategy
find suitable habitat and wait for mobile prey to come within striking distance
use camouflage — aggressive mimicry and crypsis
ambushers usually perch on vegetation and make short forays to capture prey (dragonfly adults and robber flies)
aggressive mimicry
mimic another animal in some way to lure prey/host into clsoer proximity
aggressive mimicry of Femme fatale firefly (subfamily Photurinae)
each species of firefly has their own flashing pattern that advertises themselves to mates (mate recognition)
female femme fatale firefly mimics the flashing of another firefly species to lure in males of that species, then eats them
femme fatale firefly sequesters protective chemicals from males because they can’t produce their own
aggressive mimicry of Emesines assassin bugs
Emesines crawl into spiderwebs. movement of web makes spider think there is prey
Emesine can move through silk and eats the spider
aggressive mimicry of flower-mimicking mantis
Mantids that mimic flowers (typically orchids) to lure in predators
crypsis of odonata naiads
aquatic naiads blend into background to avoid detection by prey
trapping
predator foraging strategy
constructing traps to catch prey
trapping of net-spinning caddisflies
spin silken tubes to catch micro arthropods
trapping of antlion
build sand traps that ants fall into
trapping of new Zealand glowworms
glowworms build silken tubes that hang from cave ceilings
glow reflects through silk threads and attracts prey, which gets trapped in silk
Active searching
predator foraging strategy
more energetically expensive than sit & wait/ambush strategies
includes random and directional foraging
random/non-directional foraging
insect moves in a seemingly erratic or exploratory pattern
No directional cues directly leading to food
insect is sampling the environment, often in areas where food might be expected but not immediately detectable.
non-directional foraging of ladybug larvae
ladybug larvae will whip their heads back and forth to locate aphids
directional foraging
a non-random search strategy where an insect moves in a specific direction and follows particular cues to locate prey
stimuli may include chemical, tactile, light, or visual cues
How common are parasitic/parasitoid insects?
15% of insects have some parasitic aspect to life history
exclusively parasitic orders
phthiraptera (lice)
siphonaptera (fleas)
strepsiptera (twisted-wing parasites)
orders with some parasitic species
diptera
hymenoptera
hemiptera
coleoptera
strepsiptera hosts
thysanura
blattodea
mantodea
orthoptera
hemiptera
diptera
mostly aculeate (with stingers) hymenoptera
life cycle of strepsiptera
The first instars (triungulins) develop inside the female bee host’s body.
When the host bee visits flowers, the triungulins exit the female and cling to the bee.
triungulin is deposited in the bee’s nest cell when the bee lays her eggs.
it penetrates the bee’s egg and transforms into the second instar, becoming an endoparasite.
The second instar larva feeds on non-vital tissues and fluids of the developing bee.
The parasite pupates within the bee and the pupa protrudes from host’s abdominal segments
Males emerge small (<3 mm), winged, and short-lived. After emerging, they search immediately for females.
Females are reduced to sac of reproductive organs and never leave the pupa embedded in the host. Release sex pheromones to attract males.
The male punctures the female’s pupa to inseminate her. After mating, the male dies.
The female remains inside the host, producing the next generation of triungulins that explode out of her.
ectoparasites
parasites that feed externally
endoparasites
parasites that feed internally
tend to be more specific than ectoparasites
idiobionts
parasites that rapidly consume their host
tend to be ectoparasites
venom keeps host fresh and prevents host from entering metamorphosis
parasite selects fully developed hosts
hosts are either concealed or protected
koinobionts
parasites that interact and feed on host for an extended periods
host typically develops beyond original stage attacked
tend to be endoparasites
venom injection is temporary
younger instars preferred
solitary vs gregarious parasites
Solitary parasites develop as a single individual per host
gregarious parasites allow multiple offspring to develop and share a single host
primary parasitoids
parasitoids attacking phytophagous hosts
hyperparasitoids
parasitoids attacking other parasitoidss
superparasitoidism
if more larvae of the same species than can reach maturity are in one host
general adaptations of ectoparasites
body forms that prevent grooming (flattened body, or claws, hooks, or barbs for attachment)
anesthetizing agents allow for feeding
feeding times are short (idiobionts)
general adaptations of endoparasites
digestion can be typical or nutrients can be directly absorbed
respiration varied
rapid development, hypermetamorphosis, or polyembryony
overcoming host immune response
maternal oviposition
respiratory adaptations for endoparasites
most endoparasites have a closed tracheal system (gas exchange directly through integument)
some perforate host’s tracheal system or integument to access atmospheric air
some use host hemolymph (high O2 concentration)
Encyrtus wasp respiration
endoparasites
tiny, lay eggs into a single scale
larvae live in hole created by mother puncturing scale to oviposit
larvae move to larger tracheal tubes as they grow
hypermetamorphosis
first instars are morphologically and behaviorally different than subsequent molts
1st instars mobile to find target host tissue
2nd instar for feeding
polyembryony
single egg results in 2+ individuals (sometimes 1000s)
found only in parasitic and parasitoid species
possible by totipotent property of early cleavage embryo
Copidosoma floridanum polymebryony
if one egg is laid, one sex emerges (usually female)
if two eggs are laid, both sexes emerge
1st ones to emerge are defender morphs — well-functioning on their own, attack other parasitoids because it lessens competition, and fail to pupate (allows siblings to feed)
2nd ones to emerge are reproductive — emerge, mate, and disperse
female defender morphs attack male reproductive larvae, skews sex ratio (keeps enough males to breed but conserves food for females)
encapsulation host response to endoparasites
endoparasite is surrounded by hemocytes
hemocytes flatten around invader
phagocytosis begins as hemocyte number increases
capsule eventually forms that kills invader
usually observed in non-typical hosts (no coevolution between species)
molecular mimciry
method of circumventing host response by parasites
invader produces something similar to host proteins or insulates itself in a capsule derived of host membranes or tissues
destruction
method of circumventing host response by parasites
invader destroys host hemocytes or tissue
suppresion
method of circumventing host response by parasites
use of viruses to suppress host immune response
Ichneumonidae/Braconidae and viral (PDV) mutualism
ichneumonid and braconid wasps oviposit into larvae and inject secretions containing viruses
PDV viruses replicate in epithelial lining of female’s reproductive tract
resulting eggs are coated in viral particle
viruses prevent encapsulation and host pupating out of 5th instar
hymenoptera parasite ovipositors
suitable length and strength to penetrate host defenses
short ovipositors for penetrating thin tissues (caterpillars, etc)
long for penetrating thick tissues (wood, etc)
ovipositors with chemoreceptors at tip
many with paralytic venom
dipteran parasite oviposition
dipterans lack ovipositors
stick eggs to host bodies
lay eggs in suitable habitat and 1st instars locate host
sit and wait parasites
many parasites wingless and with reduced mobility and vision
adults locate host
do not emerge until host cues are detected (vibration, rise in temperature, increased CO2)
active searching parasites
more energetically expensive than sit and wait parasite strategies
limited to directional foraging
usually in response to host stimulus (pheromones, sound, etc)
pheromone detection of active searching parasites
detect pheromones in host frass
detect pheromones produced by other species for mate recognition
detect chemicals produced by plants in response to herbivory
sound detection of active searching parasites examples
Corethrella flies find treefrog hosts by following frog calls
Tachinid flies have specialized “Ears” to hear male cricket calls
thanatosis
host counter-adaptation
feigning death in chrysomelid beetles
osmeterium
Y-shaped, forked organ found on swallowtail caterpillars that they can extend from their head when threatened
emits chemicals to deter parasites
Cleptoparasites
lay their eggs in the nests of other species
parasite’s offspring directly or indirectly (via competition) kill the host’s offspring
Common in cuckoo leafcutter bees
social parasites
females enter another’s nest and takes over role as queen (inquilines)
ex) cuckoo bumblebees
integument
basis for exoskeleton
largest organ system
determines form and size of insect (forces ecdysis)
integument functions
barrier to water loss
barrier to disease and chemicals
resists attack by predators, conceals, and aposematically warns
nervous system connected to specialized regions
layers of integument
cuticle
epidermis
basement membrane
cuticle
made of multiple specialized layers
secreted by epidermis
noncellular
epicuticle
outermost layer of cuticle
thin but multilayered (thinness provides flexibility)
has sites for muscle attachment
one of outermost layers is a wax layer (prevents water loss)
procuticle
2nd layer of cuticle
includes exocuticle and endocuticle
composed of protein and chitin
exocuticle has thicker protein structure and is responsible for rigidity of exoskeleton
endocuticle is more flexible and allows for movement
where sclerotization takes place (not all areas are sclerotized)
proteins in procuticle
10-100 different types of proteins in procuticle
harder exoskeletons have more protein diversity
includes arthropodin (predominant protein, provides rigidity) and resilin (flexible)
types of proteins vary with life stages; larvae have less than adults
chitin in procuticle
60% of the dry weight of an insect’s cuticle
chitin chains are bundled together
sclerotization
process of crosslinking the proteins in exocuticle
fixing chitin tubules to each other in an organized way
enzymes transform proteins into stable molecular structure
chitin molecules dehydrate, hydrogen bond with adjacent chains and become linked with other proteins
each layer of chitin is twisted slightly, provides structural integrity
epidermis
single layer of cells beneath cuticle
basement membrane
beneath epidermis, anchors connective tissue
spines
immobile cuticular extensions
multicellular with undifferentiated epidermal cells
spurs
mobile cuticular extensions
multicellular with undifferentiated epidermal cells
setae
multicellular cuticular extensions with specialized cells
hairs, bristles, scales, etc
acanthae
unicellular cuticular extensions
provide ridges
Microtrichia
subcellular cuticular extensions
multiple extensions per cell
production of color
color is typically independent of sclerotization
majority of coloration due to properties of cuticle
structural colors
selective reflection of light by physical structure
interference or scattering of light
interference
structural colors caused by air bubbles or distortions in the cuticle, or helicoidal arrangement of chitin fibrils
how do air bubbles cause interference?
both the upper and lower surface of air bubbles reflect light
light from lower surface travels a longer distance than light from the upper surface
lights waves become out of phase
reflections cancel each other out and the only colors visible are those in phase
colors seen by observer changes with their point of view
interference caused by chitin fibrils
chitin fibers arranged helicoidally
requires a particular spacing and arrangement of layers with respect to one another
act like different films
can also polarize light; may be used in insect communication
scattering of light
not dependent on angle of observer
caused by small particles or waxy secretions
Tyndall blue caused by particles that selectively reflect blue (appears green in most due to presence of yellow pigments as well)
larger granules reflect all wavelengths and produce structural white
pigments
wider range of colors but not metallic or iridescent
frequently excretory products
may be absorbed from food
melanin
excretory pigments
ex) pieridae pigments derived from uric acid (yellow)
ex) reddish-yellow pigments produced from a meamorphosis byproduct
diet-based pigments
ex) carotenoids
deposited into epidermis or fat cells
deposited in different areas = patterns
melanin
results in black, brown, or dark yellow
synthesis poorly understood, but includes oxidation with tyrosine in hemolymph
melanogenesis
production of melanin
influenced by temperature; lower temps increase the process