Geographic Range
Marbled orb-weavers (
Araneus marmoreus
) are widespread across the Nearctic and Palearctic regions. Their range extends across
the entirety of Canada and the United States, as far south as Texas and along the
Gulf Coast. They are also found across Europe and the northern half of Asia, particularly
Russia, extending into the Holarctic region.
- Biogeographic Regions
- nearctic
- palearctic
- Other Geographic Terms
- holarctic
Habitat
Marbled orb-weavers live in a large variety of habitats, including deciduous, mountain,
and coniferous forests, as well as meadows, agricultural fields, orchards, peat bogs,
along rivers, and rural and suburban areas. They can usually be found in shrubs and
trees, often along the forest's edge, as well as in man-made structures such as mailboxes.
- Habitat Regions
- temperate
- terrestrial
- Terrestrial Biomes
- savanna or grassland
- forest
- Wetlands
- bog
- Other Habitat Features
- suburban
- agricultural
- riparian
Physical Description
Marbled orb-weavers have an oval-shaped abdomen; this sets them apart from other orb-weaver
spiders. This species exhibits significant sexual dimorphism; females are much larger,
they are 9.0 to 18.0 mm long and 2.3 to 4.5 mm wide, while males are 5.9 to 8.4 mm
long and 2.3 to 3.6 mm wide. Marbled orb-weavers are polymorphic and show a wide variety
of colors and patterns. There are two forms, the 'nominate marmoreus' form and the
'variation pyramidatus' form, which are found primarily in Europe. Both forms have
light brown or orange carapaces and legs, while the ends of their legs are striped
in white, clear, or black. The variation marmoreus form has a white, yellow, or orange
abdomen, patterned in black, grey, and white. This abdominal pattern gives the species
their common name, as they appear "marbled". The variation pyramidatus form has a
paler abdomen, with a large dark brown irregular-shaped spot near the end of their
abdomen. There are also intermediates between these two forms. Marbled orb-weavers
have orange eggs that are about 1.15 mm wide. They can be distinguished from other
members of genus
Araneus
, particularly
shamrock orb-weavers
, by differences in the spines on their tibiae. Spine patterns are mostly consistent
within species. Marbled orb-weavers also have two types of tibial spines. Species
of genus
Araneus
can also be identified by their genital characteristics. The embolus of male marbled
orb-weavers is semi-circular, with flat hook-shaped lamellae. The embolus cap on virgin
males can also be diagnostic of this species. The epigynum of females is also distinct,
with the lamellae visible as large curved folds from the ventral side.
- Other Physical Features
- ectothermic
- heterothermic
- bilateral symmetry
- polymorphic
- Sexual Dimorphism
- female larger
Development
Eggs of marbled orb-weavers hatch in early spring after overwintering in egg sacs.
Juveniles are present from spring to July, during which they molt through several
instars, and eventually molt into reproductive adults. Adults mate in the summer and
can be found from June to September. After mating and laying their egg sacs, adults
die in the fall.
- Development - Life Cycle
- metamorphosis
Reproduction
There is little information about the specific mating habits of marbled orb-weavers.
Females of other
Araneus
species emit pheromones to attract mates; female marbled orb-weavers likely also
emit pheromones. To court their mates, male members of genus
Araneus
spin a "mating-thread" across the female's web. The male moves towards the female
across this thread, plucking and vibrating it, and the female approaches him. The
male touches the front of the female's body with his legs, stroking her, until she
hangs from the mating thread. The courtship habits of marbled orb-weavers are likely
similar. Once courtship is complete, males embrace their female mates and transfer
sperm by inserting their pedipalps. Virgin male marbled orb-weavers have the embolus
on their palps capped. The capped is removed after the first mating. Males mate several
times. Mating takes place in late summer. Other species of orb-weaving spiders exhibit
sexual cannibalism, including
European garden spiders
, which are closely related and live in the same range as marbled orb-weavers. Females
often eat their male mates at any point during the courtship and mating process. It
is possible that marbled orb-weavers also exhibit sexual cannibalism; however, males
mate multiple times and are noted to survive mating, so cannibalism may not be as
significant in this species.
- Mating System
- polygynous
After mating in late summer, female marbled orb-weavers lay their eggs in loose, fluffy
egg sacs constructed from silk. In one report, an egg sac was 13 mm across and held
653 eggs. Eggs overwinter in these sacs and hatch the following spring. By July, the
spiderlings molt into reproductive adults.
- Key Reproductive Features
- semelparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- fertilization
- oviparous
Marbled orb-weavers die after mating, so adults are not present to provide any sort
of care when the spiderlings emerge the following spring. They do provide provisioning
in the eggs, as well as construct an egg sac that likely provides some protection
from the elements.
- Parental Investment
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
Lifespan/Longevity
Since spiderlings emerge from their egg sacs in the spring, mature into adults, and
die in the fall after mating, marbled orb-weavers likely only live about 6 months.
Behavior
To build their orb-webs, marbled orb-weavers use the "second line" technique. A drag
line of silk, produced from two silk glands in their abdomen is created as the spider
descends from a substrate. At some point in the descent, a second line is created
and attached to the main drag line. Farther down, the second line balloons out due
to air currents. Up to several meters of the second line is pulled out from their
spinnerets as they hang motionless. Often, spiders go back up the main drag line,
reel in the second line and begin construction. An orb-web is typically composed of
sticky threads arranged in spirals on non-viscous supporting threads. Marbled orb-weavers
typically spin their web at the top of vegetation, in low shrubs, or tall grasses.
They spin their web in the morning, and typically spend the day resting in a retreat
off to the side of the web, in leaves or moss. During the night, spiders wait in the
middle of the orb web for prey to get snared. Eggs overwinter in egg sacs and most
adults die before winter begins, though some literature reports that marbled orb-weavers
are active during the winter in colder regions, such as Sweden.
Home Range
There is currently very little information available about the home range size of marbled orb-weavers.
Communication and Perception
Marbled orb-weavers have mechanoreceptors in the form of tactile hair sensilla on
their tarsi that can detect not only movement or bending of the hair, but likely also
the direction of the displacement. This allows spiders to perceive the environment
around them through touch; they are also sensitive to air currents.
Orb-spiders
also have chemoreceptors on their tarsi that function in olfaction and chemical detection.
Other spiders in genus
Araneus
use pheromones to attract mates. Female marbled orb-weavers also likely release airborne
pheromones to communicate with and attract their mates. Touch is also used during
mating for many other
orb-weaver
species, as the male courts the female by stroking her body with his legs.
- Other Communication Modes
- pheromones
Food Habits
Marbled orb-weavers prey on many insect species. They construct orb-webs, which have
sticky threads arranged spirally with non-sticky supporting threads. The non-viscous
threads absorb the movement of the prey, while the viscous threads restrain the prey,
which gives the spider time to locate, go to, and attack the prey. They mostly eat
smaller insects, generally ranging from 0 to 4 mm, particularly from orders
Orthoptera
,
Diptera
, and
Hymenoptera
. One study found that a single marbled orb-weaver could catch about 14 prey insects
per day, on average.
- Primary Diet
- carnivore
- Animal Foods
- insects
Predation
Many species of wasps prey on marbled orb-weavers. Some wasp species, including spider
wasps (
Batozonellus lacerticida
) and blue mud daubers (
Chalybion californicum
), catch and paralyze marbled orb-weavers. The paralyzed spiders are placed in a burrow
with a wasp egg, and when the egg hatches and the larvae feed on the available spider
prey. Other wasp species, including organ pipe mud daubers (
Trypoxylon politum
) and white-trimmed black wasp (
Episyron quinquenotatus
), simply catch and feed on marbled orb-weavers. Birds are also predators; one noted
predatory species are penduline tits (
Remiz pendulinus
) in Europe.
Ecosystem Roles
Many species of wasps prey on marbled orb-weavers, feeding as adults or using the
spiders as a food supply for their offspring. Marbled orb-weavers are also prey to
many species of birds. They are a significant insectivore and prey on the many different
insect species caught in their web, particularly
dipterids
and
hymenopterans
.
Economic Importance for Humans: Positive
There are no known positive effects of marbled orb-weavers on humans.
Economic Importance for Humans: Negative
There are no known adverse effects of marbled orb-weavers on humans.
Conservation Status
Marbled orb-weavers have no special conservation status.
Additional Links
Contributors
Angela Miner (author), Animal Diversity Web Staff, Leila Siciliano Martina (editor), Texas State University.
- Nearctic
-
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
- Palearctic
-
living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.
- holarctic
-
a distribution that more or less circles the Arctic, so occurring in both the Nearctic and Palearctic biogeographic regions.
Found in northern North America and northern Europe or Asia.
- temperate
-
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
- terrestrial
-
Living on the ground.
- tropical savanna and grassland
-
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
- savanna
-
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
- temperate grassland
-
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- bog
-
a wetland area rich in accumulated plant material and with acidic soils surrounding a body of open water. Bogs have a flora dominated by sedges, heaths, and sphagnum.
- suburban
-
living in residential areas on the outskirts of large cities or towns.
- agricultural
-
living in landscapes dominated by human agriculture.
- riparian
-
Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).
- ectothermic
-
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
- heterothermic
-
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
- bilateral symmetry
-
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
- polymorphic
-
"many forms." A species is polymorphic if its individuals can be divided into two or more easily recognized groups, based on structure, color, or other similar characteristics. The term only applies when the distinct groups can be found in the same area; graded or clinal variation throughout the range of a species (e.g. a north-to-south decrease in size) is not polymorphism. Polymorphic characteristics may be inherited because the differences have a genetic basis, or they may be the result of environmental influences. We do not consider sexual differences (i.e. sexual dimorphism), seasonal changes (e.g. change in fur color), or age-related changes to be polymorphic. Polymorphism in a local population can be an adaptation to prevent density-dependent predation, where predators preferentially prey on the most common morph.
- metamorphosis
-
A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.
- polygynous
-
having more than one female as a mate at one time
- semelparous
-
offspring are all produced in a single group (litter, clutch, etc.), after which the parent usually dies. Semelparous organisms often only live through a single season/year (or other periodic change in conditions) but may live for many seasons. In both cases reproduction occurs as a single investment of energy in offspring, with no future chance for investment in reproduction.
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- fertilization
-
union of egg and spermatozoan
- internal fertilization
-
fertilization takes place within the female's body
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- nocturnal
-
active during the night
- motile
-
having the capacity to move from one place to another.
- solitary
-
lives alone
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- chemical
-
uses smells or other chemicals to communicate
- pheromones
-
chemicals released into air or water that are detected by and responded to by other animals of the same species
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- chemical
-
uses smells or other chemicals to communicate
- carnivore
-
an animal that mainly eats meat
- insectivore
-
An animal that eats mainly insects or spiders.
References
Carmichael, L. 1973. Correlation Between Segment Length and Spine Counts in Two Spider Species of Araneus ( Araneae : Araneidae ). Psyche , 80: 62-69.
Eberhard, W. 1987. How spiders initiate airborne lines. Journal of Arachnology , 15/1: 1-9.
Edwards, R., E. Edwards. 1997. Society Behavior and Niche Selection by Mailbox Spiders. Journal of Arachnology , 25/1: 20-30.
Elgar, M., D. Nash. 1988. Sexual cannibalism in the garden spider Araneus diadematus . Animal Behaviour , 36/5: 1511-1517.
Enders, F. 1974. Vertical Stratification in Orb-Web Spiders ( Araneidae , Araneae ) and a Consideration of Other Methods of Coexistence. Ecology , 55/2: 317-328.
Endo, T., A. Endo. 1994. Prey selection by a spider wasp, Batozonellus lacerticida ( Hymenoptera : Pompilidae ) - Effects of seasonal-variation in prey species, size, and density. Ecological Research , 9/2: 225-235.
Esyunin, S., A. Ermakov, Y. Mikhailov. 2013. Remarks on the Ural spider fauna ( Arachnida : Aranei ), 14. On the spider fauna of the Kytlym plexus of mountains (the North Urals). Arthropoda Selecta , 22/1: 75-82.
Esyunin, S., A. Laetin. 2009. More on the spider fauna ( Arachnida , Aranei ) of the lower reaches of Ob River and South Yamal, Russia. Arthropoda Selecta , 18/1-2: 87-94.
Fasola, M., F. Mogavero. 1995. Structure and habitat use in a webâbuilding spider community in northern Italy. Bolletino di zoologia , 62/2: 159-166.
Foelix, R., I. Chuwang. 1973. Morphology of spider sensilla i. mechanoreceptors. Tissue & Cell , 5/3: 451-460.
Gunnarsson, B. 1985. Interspecific predation as a mortality factor among overwintering spiders. Oecologia , 65: 498-502.
Hoffman, R. 1982. A Note on Some Supposed Texan Localities for Some Araneus Species ( Araneae , Araneidae ). Journal of Arachnology , 10/1: 93-95.
Japyassu, H., R. Caires. 2008. Hunting Tactics in a Cobweb Spider ( Araneae - Theridiidae ) and the Evolution of Behavioral Plasticity. Journal of Insect Behavior , 21: 258-284.
Kristofik, J., P. Masan, Z. Sustek, P. Gajdos. 1993. Arthropods in the nest of the Penduline Tit ( Remiz pendulinus ). Biologia , 48/5: 493-505.
Kurczewski, F., E. Kurczewski. 1968. Host Records for Some North American Pompilidae ( Hymenoptera ) with a Discussion of Factors in Prey Selection. Journal of the Kansas Entomological Society , 41/1: 1-33.
Landes, D., M. Obin, A. Cady, J. Hunt. 1987. Seasonal and latitudinal variation in spider prey of the mud dauber Chalybion californicum ( Hymenoptera , Sphecidae ). Journal of Arachnology , 15/2: 249-256.
Levi, H. 1971. The Diadematus group of the orb-weaver genus Araneus north of Mexico Araneae Araneidae . Bulletin of the Museum of Comparative Zoology , 141/4: 131-179.
Olive, C. 1982. Sex pheromones in two orbweaving spiders ( Araneae , Araneidae ) : An experimental field study. Journal of Arachnology , 10: 241-245.
Opell, B., A. Tran, S. Karinshak. 2011. Adhesive Compatibility of Cribellar and Viscous Prey Capture Threads and its Implication for the Evolution of Orb-Weaving Spiders. Journal of Experimental Zoology , 315: 376-384.
Opell, B., J. Bond. 2001. Changes in the mechanical properties of capture threads and the evolution of modern orb-weaving spiders. Evolutionary Ecology Research , 3: 567-581.
Opell, B., M. Hendricks. 2007. Adhesive recruitment by the viscous capture threads of araneoid orb-weaving spiders. Journal of Experimental Biology , 210: 553-560.
Opell, B., M. Hendricks. 2009. The adhesive delivery system of viscous capture threads spun by orb-weaving spiders. Journal of Experimental biology , 212: 3026-3034.
Pasquet, A. 1984. Prey and predatory strategies of 2 orb-weaving spiders - Argiope bruennichi and Araneus marmoreus . Entomologia Experimentalis et Applicata , 36/2: 177-184.
Pekar, S. 1999. Effect of IPM practices and conventional spraying on spider population dynamics in an apple orchard. Agriculture, Ecosystems & Environment , 73/2: 155-166.
Rehnberg, B. 1987. Selection of spider prey by Trypoxylon politum (Say) ( Hymenoptera , Sphecidae ). Canadian Entomologist , 119/2: 189-194.
Roberts, M. 1985. The Spiders of Great Britain and Ireland Vol. 1 . England: Harley Books.
Roggenbuck, H., S. Pekar, J. Schneider. 2011. Sexual cannibalism in the European garden spider Araneus diadematus : the roles of female hunger and mate size dimorphism. Animal Behaviour , 81/4: 749-755.
Svaton, J., R. Pridavka. 2000. Spiders ( Araneae ) of the peatbog national nature reserve Vihrovske Raelinisko (Slovakia). Ekologia , 19/4: 97-104.