Sie sind auf Seite 1von 8

Isopoda

Isopoda is an order of crustaceans that includes woodlice and their


relatives. Isopods live in the sea, in fresh water, or on land. All have Isopoda
rigid, segmented exoskeletons, two pairs of antennae, seven pairs of Temporal range: Carboniferous to
jointed limbs on the thorax, and five pairs of branching appendages Holocene 300–0 Ma
on the abdomen that are used in respiration. Females brood their
young in a pouch under their thorax. PreꞒ Ꞓ O S D C P T J K PgN

Isopods have various feeding methods: some eat dead or decaying


plant and animal matter, others are grazers, or filter feeders, a few
are predators, and some are internal or external parasites, mostly of
fish. Aquatic species mostly live on the seabed or bottom of
freshwater bodies of water, but some taxa can swim for a short
distance. Terrestrial forms move around by crawling and tend to be
found in cool, moist places. Some species are able to roll themselves
into a ball as a defense mechanism or to conserve moisture.
Eurydice pulchra, a carnivorous
There are over 10,000 species of isopod worldwide, with around
isopod found on sandy shores
4,500 species found in marine environments, mostly on the seabed,
500 species in fresh water, and another 5,000 species on land. The Scientific classification
order is divided into eleven suborders. The fossil record of isopods
Kingdom: Animalia
dates back to the Carboniferous period (in the Pennsylvanian
epoch), at least 300 million years ago, when isopods lived in Phylum: Arthropoda
shallow seas. The name Isopoda is derived from the Greek roots
iso- (from ἴσος ísos, meaning "equal") and -pod (from ποδ-, the Subphylum: Crustacea
stem of πούς poús, meaning "foot").[2][3] Class: Malacostraca
Superorder: Peracarida
Order: Isopoda
Contents [1]
Latreille, 1817
Description
Suborders
Diversity and classification
Evolutionary history Asellota
Locomotion Calabozoida
Feeding and nutrition Cymothoida
Reproduction and development Limnoriidea
Terrestrial isopods
Microcerberidea
References
Oniscidea
External links
Phoratopidea
Phreatoicidea
Description Sphaeromatidea
Tainisopidea
Classified within the Valvifera
arthropods, isopods have a
chitinous exoskeleton and
jointed limbs.[4] Isopods are typically flattened dorsoventrally
(broader than they are deep),[5] although many species deviate from
this rule, particularly parasitic forms, and those living in the deep sea
or in ground water habitats. Their colour may vary, from grey to
The woodlouse Oniscus asellus
white,[6] or in some cases red, green, or brown.[7] Isopods vary in
showing the head with eyes and
size, ranging from some Microcerberidae species of just 0.3mm to the
antennae, carapace and relatively
uniform limbs
deep sea Bathynomus spp. of nearly 50 cm (20 in).[3] Isopods lack an
obvious carapace (shell), which is reduced to a "cephalic shield"
covering only the head. This means that the gill-like structures, which
in other related groups are protected by the carapace, are instead found on specialised limbs on the
abdomen.[3][8] The dorsal (upper) surface of the animal is covered by a series of overlapping, articulated plates
which give protection while also providing flexibility. The isopod body plan consists of a head (cephalon), a
thorax (pereon) with eight segments (pereonites), and an abdomen (pleon) with six segments (pleonites), some
of which may be fused.[5] The head is fused with the first segment of the thorax to form the cephalon. There
are two pairs of unbranched antennae, the first pair being vestigial in land-dwelling species. The eyes are
compound and unstalked and the mouthparts include a pair of maxillipeds and a pair of mandibles (jaws) with
palps (segmented appendages with sensory functions) and lacinia mobilis (spine-like movable appendages).[9]

The seven free segments of the thorax each bear a pair of unbranched pereopods (limbs). In most species these
are used for locomotion and are of much the same size, morphology and orientation, giving the order its name
"Isopoda", from the Greek equal foot. In a few species, the front pair are modified into gnathopods with
clawed, gripping terminal segments. The pereopods are not used in respiration, as are the equivalent limbs in
amphipods, but the coxae (first segments) are fused to the tergites (dorsal plates) to form epimera (side plates).
In mature females, some or all of the limbs have appendages known as oostegites which fold underneath the
thorax and form a brood chamber for the eggs. In males, the gonopores (genital openings) are on the ventral
surface of segment eight and in the females, they are in a similar position on segment six.[9]

One or more of the abdominal segments, starting with the sixth segment, is fused to the telson (terminal
section) to form a rigid pleotelson.[9][10][11] The first five abdominal segments each bear a pair of biramous
(branching in two) pleopods (lamellar structures which serve the function of gas exchange, and in aquatic
species serve as gills and propulsion),[3][12] and the last segment bears a pair of biramous uropods (posterior
limbs). In males, the second pair of pleopods, and sometimes also the first, are modified for use in transferring
sperm. The endopods (inner branches of the pleopods) are modified into structures with thin, permeable
cuticles (flexible outer coverings) which act as gills for gas exchange.[9] In some terrestrial isopods, these
resemble lungs.[3]

Diversity and classification


Isopods belong to the larger group Peracarida, which are united by the presence of a special chamber under the
thorax for brooding eggs. They have a cosmopolitan distribution and over 10,000 species of isopod, classified
into 11 suborders, have been described worldwide.[3][13] Around 4,500 species are found in marine
environments, mostly on the sea floor. About 500 species are found in fresh water and another 5,000 species
are the terrestrial woodlice, which form the suborder Oniscidea.[14] In the deep sea, members of the suborder
Asellota predominate, to the near exclusion of all other isopods, having undergone a large adaptive radiation in
that environment.[14] The largest isopod is in the genus Bathynomus and some large species are fished
commercially for human food in Mexico, Japan and Hawaii.[15]
Some isopod groups have evolved a parasitic lifestyle, particularly as external
parasites of fish.[9] They can damage or kill their hosts and can cause
significant economic loss to commercial fisheries.[16] In reef aquariums,
parasitic isopods can become a pest, endangering the fish and possibly
injuring the aquarium keeper. Some members of the family Cirolanidae suck
the blood of fish, and others, in the family Aegidae, consume the blood, fins,
tail and flesh and can kill the fish in the process.[17]

The World Marine, Freshwater and Terrestrial Isopod Crustaceans database


subdivides the order into eleven suborders:[1]

Asellota – The suborder containing the majority of freshwater


isopod species, found in both surface and subterranean waters, Numbers of marine Isopoda
along with some deepwater marine species.[9] (except Asellota and
crustacean symbionts) in
Calabozoida – A small suborder consisting of two marine species
biogeographic regions
in the family Calabozoidae and one freshwater species in the
family Brasileirinidae which is found in subterranean locations.[18]
Cymothoida – Chiefly marine isopods[9] with over 2,700
species. Members are mostly carnivorous or parasitic.
Includes the family Gnathiidae, the juveniles of which are
parasitic on fishes.[19] The previously recognised suborder
Epicaridea is included as two superfamilies within this
suborder and Cymothoida now includes part of the formerly
recognised suborder Flabellifera.[20]
Limnoriidea – Mainly tropical isopods, some of which are
herbivorous.[20]
Microcerberidea – Tiny, worm-like isopods that live
between particles on the bed of freshwater and shallow Representative marine isopod forms
marine habitats. [9]

Oniscidea – Semi-terrestrial and terrestrial isopods fully


adapted for life on land.[9] There are over 4,000 species of woodlice inhabiting forests,
mountains, deserts and the littoral zone.[21]
Phoratopidea – A single marine species, Phoratopus remex, which warrants its own suborder
because of its unique characteristics.[20]
Phreatoicidea – Small suborder of freshwater isopods resembling amphipods, limited to South
Africa, India, Australia and New Zealand.[9]
Sphaeromatidea – Benthic isopods mostly from the southern hemisphere with respiratory
pleopods inside a branchial chamber. This suborder now includes part of the formerly
recognised suborder Flabellifera.[20][22]
Tainisopidea – Freshwater isopods in a "relictual environment".[20]
Valvifera – A large group of benthic, marine isopods with respiratory pleopods inside a
branchial chamber under the abdomen.[9]

Evolutionary history
Isopods first appeared in the fossil record during the Carboniferous period of the Paleozoic some 300 million
years ago.[23] They were primitive, short-tailed members of the suborder Phreatoicidea. At that time,
Phreatoicideans were marine organisms with a cosmopolitan distribution. Nowadays, the members of this
formerly widespread suborder form relic populations in freshwater environments in South Africa, India and
Oceania, the greatest number of species being in Tasmania. Other primitive, short-tailed suborders include
Asellota, Microcerberidea, Calabozoidea and the terrestrial Oniscidea.[14]

The short-tailed isopods have a short pleotelson and terminal, stylus-like uropods and have a sedentary lifestyle
on or under the sediment on the seabed. The long-tailed isopods have a long pleotelson and broad lateral
uropods which can be used in swimming. They are much more active and can launch themselves off the
seabed and swim for short distances. The more advanced long-tailed isopods are mostly endemic to the
southern hemisphere and may have radiated on the ancient supercontinent of Gondwana soon after it broke
away from Laurasia 200 million years ago. The short-tailed forms may have been driven from the shallow seas
in which they lived by increased predatory pressure from marine fish, their main predators. The development
of the long-tailed forms may also have provided competition that helped force the short-tailed forms into
refugia. The latter are now restricted to environments such as the deep sea, freshwater, groundwater and dry
land. Isopods in the suborder Asellota are by far the most species-rich group of deep sea isopods.[14]

Locomotion
Unlike the amphipods, marine and freshwater isopods are entirely benthic. This gives them little chance to
disperse to new regions and may explain why so many species are endemic to restricted ranges. Crawling is
the primary means of locomotion, and some species bore into the seabed, the ground or timber structures.
Some members of the Flabellifera can swim to a limited extent and have their front three pairs of pleopods
modified for this purpose, with their respiratory structures limited to the hind pleopods. Most terrestrial species
are slow-moving and conceal themselves under objects or hide in crevices or under bark. The semi-terrestrial
sea slaters (Ligia spp.) can run rapidly on land and many terrestrial species can roll themselves into a ball when
threatened, a feature that has evolved independently in different groups and also in the marine
sphaeromatids.[9]

Feeding and nutrition


Isopods have a simple gut which lacks a midgut section; instead there
are caeca connected to the back of the stomach in which absorption
takes place. Food is sucked into the esophagus, a process enhanced in
the blood-sucking parasitic species, and passed by peristalsis into the
stomach, where the material is processed and filtered. The structure of
the stomach varies, but in many species there is a dorsal groove into
which indigestible material is channelled and a ventral part connected
to the caeca where intracellular digestion and absorption take place.
Anilocra (Cymothoidae) parasitising Indigestible material passes on through the hindgut and is eliminated
the fish Spicara maena, Italy through the anus, which is on the pleotelson.[9]

Isopods are detritivores, browsers, carnivores (including predators and


scavengers), parasites, and filter feeders, and may occupy one or more of these feeding niches. Only aquatic
and marine species are known to be parasites or filter feeders.[24][25] Some exhibit coprophagia and will also
consume their own fecal pellets.[25] Terrestrial species are in general herbivorous, with woodlice feeding on
moss, bark, algae, fungi and decaying material. In marine isopods that feed on wood, cellulose is digested by
enzymes secreted in the caeca. Limnoria lignorum, for example, bores into wood and additionally feeds on the
mycelia of fungi attacking the timber, thus increasing the nitrogen in its diet. Land-based wood-borers mostly
house symbiotic bacteria in the hindgut which aid in digesting cellulose. There are numerous adaptations to
this simple gut, but these are mostly correlated with diet rather than by taxonomic group.[9]
Parasitic species are mostly external parasites of fish or crustaceans and feed on blood. The larvae of the
Gnathiidae family and adult cymothoidids have piercing and sucking mouthparts and clawed limbs adapted for
clinging onto their hosts. In general, isopod parasites have diverse lifestyles and include Cancricepon elegans,
found in the gill chambers of crabs; Athelges tenuicaudis, attached to the abdomen of hermit crabs;
Crinoniscus equitans living inside the barnacle Balanus perforatus; cyproniscids, living inside ostracods and
free-living isopods; bopyrids, living in the gill chambers or on the carapace of shrimps and crabs and causing a
characteristic bulge which is even recognisable in some fossil crustaceans; and entoniscidae living inside some
species of crab and shrimp.[9][26] Cymothoa exigua is a parasite of the spotted rose snapper Lutjanus guttatus
in the Gulf of California; it causes the tongue of the fish to atrophy and takes its place in what is believed to be
the first instance discovered of a parasite functionally replacing a host structure in animals.[27]

Reproduction and development


In most species, the sexes are separate and there is little sexual dimorphism, but a few species are
hermaphroditic and some parasitic forms show large differences between the sexes.[9] Some Cymothoidans are
protandrous hermaphrodites, starting life as males and later changing sex, and some Anthuroideans are the
reverse, being protogynous hermaphrodites that are born female. Some Gnathiidans males are sessile and live
with a group of females.[24] Males have a pair of penises, which may be fused in some species. The sperm is
transferred to the female by the modified second pleopod which receives it from the penis and which is then
inserted into a female gonopore. The sperm is stored in a special receptacle, a swelling on the oviduct close to
the gonopore. Fertilisation only takes place when the eggs are shed soon after a moult, at which time a
connection is established between the semen receptacle and the oviduct.[9]

The eggs, which may number up to several hundred, are brooded by the female in the marsupium, a chamber
formed by flat plates known as oostegites under the thorax. This is filled with water even in terrestrial
species.[9] The eggs hatch as mancae, a post-larval stage which resembles the adult except for the absence of
the last pair of pereopods. The lack of a swimming phase in the life cycle is a limiting factor in isopod
dispersal, and may be responsible for the high levels of endemism in the order.[14] As adults, isopods differ
from other crustaceans in that moulting occurs in two stages known as "biphasic moulting".[3] First they shed
the exoskeleton from the posterior part of their body and later shed the anterior part. The giant Antarctic isopod
Glyptonotus antarcticus is an exception, and moults in a single process.[28]

Terrestrial isopods
The majority of crustaceans are aquatic and the isopods are one of the few groups of which some members
now live on land.[29][30] The only other crustaceans which include a small number of terrestrial species are
amphipods (like sandhoppers) and decapods (crabs, shrimp, etc.).[29] Terrestrial isopods play an important role
in many tropical and temperate ecosystems by aiding in the decomposition of plant material through
mechanical and chemical means, and by enhancing the activity of microbes.[31] Macro-detritivores, including
terrestrial isopods, are absent from arctic and sub-arctic regions, but have the potential to expand their range
with increased temperatures in high latitudes.[32]

The woodlice, suborder Oniscidea, are the most successful group of terrestrial crustaceans[9] and show various
adaptations for life on land. They are subject to evaporation, especially from their ventral area, and as they do
not have a waxy cuticle, they need to conserve water, often living in a humid environment and sheltering
under stones, bark, debris or leaf litter. Desert species are usually nocturnal, spending the day in a burrow and
emerging at night. Moisture is achieved through food sources or by drinking, and some species can form their
paired uropodal appendages into a tube and funnel water from dewdrops onto their pleopods. In many taxa,
the respiratory structures on the endopods are internal, with a spiracle and pseudotrachaea, which resemble
lungs. In others, the endopod is folded inside the adjoining exopod (outer
branch of the pleopod). Both these arrangements help to prevent
evaporation from the respiratory surfaces.[9]

Many species can roll themselves into a ball, a behaviour used in defence
that also conserves moisture. Members of the families Ligiidae and
Tylidae, commonly known as rock lice or sea slaters, are the least
specialised of the woodlice for life on land. They inhabit the splash zone
on rocky shores, jetties and pilings, may hide under debris washed up on
the shore and can swim if immersed in water.[9] Armadillidium vulgare on the
move ...

... and rolled into a ball

References
1. "Isopoda" (http://www.marinespecies.org/aphia.php?p=taxdetails&id=1131). WoRMS. World
Register of Marine Species. 2014. Retrieved 8 May 2014.
2. "Isopod" (http://www.merriam-webster.com/dictionary/isopod). Merriam-Webster. Encyclopædia
Britannica. Retrieved 27 June 2014.
3. Schotte, M.; Boyko, C. B.; Bruce, N. L.; Markham, J.; Poore, G. C. B.; Taiti, S.; Wilson, G. D. F.
"World List of Marine, Freshwater and Terrestrial Isopod Crustaceans" (http://www.marinespeci
es.org/isopoda/index.php). World Register of Marine Species. Retrieved 4 June 2014.
4. Valentine, J. W. (2004). On the Origin of Phyla (https://books.google.com/?id=DMBkmHm5fe4C
&dq=arthropod+synapomorphy). University of Chicago Press. p. 33. ISBN 978-0-226-84548-7.
5. Naylor, E. (1978). British Marine Isopods: Keys and Notes for the Identification of the Species (h
ttps://archive.org/details/britishmarineiso0000nayl/page/2) (2nd ed.). Academic Press. p. 2 (http
s://archive.org/details/britishmarineiso0000nayl/page/2). ISBN 978-0-12-515150-4.
6. "Isopod, Pillbug, Sow Bug Information" (https://web.archive.org/web/20140923101009/http://ins
ected.arizona.edu/isoinfo.htm). University of Arizona. 1997. Archived from the original (http://ins
ected.arizona.edu/isoinfo.htm) on 23 September 2014. Retrieved 21 August 2014.
7. Lee, Welton L. (1966). "Color change and the ecology of the marine isopod Idothea
(Pentidotea) montereyensis Maloney, 1933". Ecology. 47 (6): 930–941. doi:10.2307/1935640
(https://doi.org/10.2307%2F1935640). JSTOR 1935640 (https://www.jstor.org/stable/1935640).
8. Keable, S. J.; Poore, G. C. B.; Wilson, G. D. F. (2 October 2002). "Australian Isopoda: Families"
(https://web.archive.org/web/20181010185506/http://www.crustacea.net/crustace/isopoda/inde
x.htm). Australian Museum. Archived from the original (http://www.crustacea.net/crustace/isopo
da/index.htm) on 10 October 2018. Retrieved 5 June 2014.
9. Ruppert, Edward E.; Fox, Richard, S.; Barnes, Robert D. (2004). Invertebrate Zoology (7th ed.).
Cengage Learning. pp. 661–667. ISBN 978-81-315-0104-7.
10. Wilson, G. D. F. (1989). "A systematic revision of the deep-sea subfamily Lipomerinae of the
isopod crustacean family Munnopsidae" (https://escholarship.org/uc/item/5nm8z7td). Bulletin of
the Scripps Institution of Oceanography. 27: 1–138.
11. Wilson, G. D. F. (2009). "The road to the Janiroidea: Comparative morphology and evolution of
the asellote isopod crustaceans". Journal of Zoological Systematics and Evolutionary
Research. 25 (4): 257–280. doi:10.1111/j.1439-0469.1987.tb00608.x (https://doi.org/10.1111%
2Fj.1439-0469.1987.tb00608.x).
12. Wilson, George D. F. (1991). "Functional morphology and evolution of isopod genitalia". In
Bauer, Raymond T.; Martin, Joel W. (eds.). Crustacean Sexual Biology. Columbia University
Press. pp. 228–245. ISBN 978-0-231-06880-2.
13. Martin, Joel W.; Davis, George E. (2001). An Updated Classification of the Recent Crustacea (h
ttp://atiniui.nhm.org/pdfs/3839/3839.pdf) (PDF). Natural History Museum of Los Angeles
County. p. 132.
14. Brusca, Richard (6 August 1997). "Isopoda" (http://tolweb.org/Isopoda/6320/1997.08.06). Tree
of Life Web Project. Retrieved 5 June 2014.
15. Williams, Ernest H. Jr. (2000). Keynote Address: Isopods as parasites or associates of fishes.
Parasitology 2000: One Eye on the Future, One Eye on the Past. Southeastern Society of
Parasitologists. pp. 9–10.
16. Ravichandran, S.; Rameshkumar, G.; Balasubramanian, T. (2010). "Infestation of isopod
parasites in commercial marine fishes" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC308173
3). Journal of Parasitic Diseases. 34 (2): 97–98. doi:10.1007/s12639-010-0014-3 (https://doi.or
g/10.1007%2Fs12639-010-0014-3). PMC 3081733 (https://www.ncbi.nlm.nih.gov/pmc/articles/
PMC3081733). PMID 21966129 (https://pubmed.ncbi.nlm.nih.gov/21966129).
17. Shimek, Ronald L. (2002). "Pills, parasites, and predators; isopods in the reef aquarium" (http://
reefkeeping.com/issues/2002-05/rs/index.php). Reefkeeping. Vol. 1 no. 4.
18. "Calabozoidea" (http://www.marinespecies.org/aphia.php?p=taxdetails&id=244442). WoRMS.
World Register of Marine Species. 2014. Retrieved 5 June 2014.
19. Srour, Marc (13 July 2012). "Tongue Biters and Deep Sea Giants: The Cymothoida (Crustacea:
Isopoda)" (https://web.archive.org/web/20140606205614/http://bioteaching.com/tongue-biters-a
nd-deep-sea-giants-the-cymothoida-crustacea-isopoda/). Teaching Biology. Archived from the
original (http://bioteaching.com/tongue-biters-and-deep-sea-giants-the-cymothoida-crustacea-is
opoda/) on 6 June 2014. Retrieved 8 May 2014.
20. Brandt, Angelika; Poore, Gary C. B. (2003). "Higher classification of the flabelliferan and
related Isopoda based on a reappraisal of relationships". Invertebrate Systematics. 17 (6): 893–
923. doi:10.1071/IS02032 (https://doi.org/10.1071%2FIS02032).
21. Brusca, Richard; Coelho, Vania R.; Taiti, Stefano (2001). "Suborder Oniscidea (Terrestrial
Isopods)" (http://tolweb.org/notes/?note_id=4179). Tree of Life Web Project. Retrieved 8 May
2014.
22. "Flabellifera" (http://www.marinespecies.org/aphia.php?p=taxdetails&id=13796). WoRMS.
World Register of Marine Species. 2014. Retrieved 12 June 2014.
23. Schram, Frederick R. (1970). "Isopod from the Pennsylvanian of Illinois". Science. 169 (3948):
854–855. doi:10.1126/science.169.3948.854 (https://doi.org/10.1126%2Fscience.169.3948.85
4). PMID 5432581 (https://pubmed.ncbi.nlm.nih.gov/5432581).
24. Poore, G. C.; Bruce, N. L. (2012). "Global diversity of marine isopods (except Asellota and
crustacean symbionts)" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432053). PLOS ONE.
7 (8): e43529. doi:10.1371/journal.pone.0043529 (https://doi.org/10.1371%2Fjournal.pone.004
3529). PMC 3432053 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432053).
PMID 22952700 (https://pubmed.ncbi.nlm.nih.gov/22952700).
25. Warburg, M. R. (1987). Isopods and their terrestrial environment. Advances in Ecological
Research. 17. pp. 187–242. doi:10.1016/S0065-2504(08)60246-9 (https://doi.org/10.1016%2F
S0065-2504%2808%2960246-9). ISBN 9780120139170.
26. Shields, Jeffrey. "Epicaridea: The parasitic isopods of Crustacea" (http://www.vims.edu/researc
h/departments/eaah/programs/crustacean/research/parasitic_isopods/index.php). Virginia
Institute of Marine Science. Retrieved 23 March 2014.
27. Brusca, R. C.; Gilligan, M. R. (1983). "Tongue replacement in a marine fish (Lutjanus guttatus)
by a parasitic isopod (Crustacea: Isopoda)". Copeia. 1983 (3): 813–816. doi:10.2307/1444352
(https://doi.org/10.2307%2F1444352). JSTOR 1444352 (https://www.jstor.org/stable/1444352).
28. George, Robert Y. (1972). "Biphasic moulting in Isopod Crustacea and the finding of an
unusual mode of moulting in the antarctic genus Glyptonotus". Journal of Natural History. 6 (6):
651–656. doi:10.1080/00222937200770591
(https://doi.org/10.1080%2F00222937200770591).
29. Broly, Pierre; Deville, Pascal; Maillet, Sébastien (2012). "The origin of terrestrial isopods
(Crustacea: Isopoda: Oniscidea)". Evolutionary Ecology. 27 (3): 461–476. doi:10.1007/s10682-
012-9625-8 (https://doi.org/10.1007%2Fs10682-012-9625-8).
30. "Benthic animals" (https://web.archive.org/web/20140511155231/http://www.fisheries.is/ecosys
tem/marine-life/benthic-animals/). Icelandic Ministry of Fisheries and Agriculture. Archived from
the original (http://www.fisheries.is/ecosystem/marine-life/benthic-animals/) on 11 May 2014.
Retrieved 4 June 2014.
31. Zimmer, M. (2002). "Nutrition in terrestrial isopods (Isopoda: Oniscidea): an evolutionary-
ecological approach". Biological Reviews of the Cambridge Philosophical Society. 77 (4):
455–493. doi:10.1017/S1464793102005912 (https://doi.org/10.1017%2FS146479310200591
2). PMID 12475050 (https://pubmed.ncbi.nlm.nih.gov/12475050).
32. Geffen, Koert G.; Berg, Matty P.; Aerts, Rien (2011). "Potential macro-detritivore range
expansion into the subarctic stimulates litter decomposition: a new positive feedback
mechanism to climate change?" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213348).
Oecologia. 167 (4): 1163–1175. doi:10.1007/s00442-011-2051-8 (https://doi.org/10.1007%2Fs
00442-011-2051-8). PMC 3213348 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213348).
PMID 21735203 (https://pubmed.ncbi.nlm.nih.gov/21735203).

External links
Media related to Isopoda at Wikimedia Commons
Data related to Isopoda at Wikispecies

Retrieved from "https://en.wikipedia.org/w/index.php?title=Isopoda&oldid=974253710"

This page was last edited on 21 August 2020, at 23:30 (UTC).

Text is available under the Creative Commons Attribution-ShareAlike License; additional terms may apply. By using this
site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia
Foundation, Inc., a non-profit organization.

Das könnte Ihnen auch gefallen