Geographic Range
Bipes biporus
(Mexican Mole Lizards) are found solely on the Baja California Peninsula of Mexico.
Their range extends throughout the southern half of the Baja California peninsula,
west of the Peninsula Ranges. They can be found as far south as Cabo San Lucas and
north to the northwest edge of the VizcaÃno Desert.
- Biogeographic Regions
- nearctic
- neotropical
Habitat
The distribution of
Bipes biporus
reflects the type of environment it inhabits. The range is widest in the VizcaÃno
Desert and the Magdalena Plain because the soil is loose and dry. The climate is seasonably
cool in these areas. Mexican Mole Lizards build intricate burrowing systems that
run horizontally right below the surface of the soil. The systems usually emerge
to the surface under rocks or logs. Because
Bipes biporus
is a burrowing species, data are difficult to collect regarding the depths that they
are found, and the average and maximum depths in the soil that they inhabit is unknown.
However, Papenfuss (1982), found
B. biporus
from 2.5 cm to 15 cm deep, with most being found at 4 cm.
- Habitat Regions
- terrestrial
- Terrestrial Biomes
- desert or dune
Physical Description
Bipes biporus
can be identified by its small, ossified head, a cylindrical body covered with scales
in a pattern of vertical rings (annuli), and two preanal pores. Juveniles are mainly
pink in color, turning white as they mature. Mexican Mole Lizards do not exhibit
sexual dimorphism, so sexual identity can only be determined by looking at the gonads.
The species within the family Bipedidae differ from other Amphisbaenians in that they
have forelimbs. All other members of this group are completely legless. The three
species of Bipedidae have small, powerful forelimbs that are specialized for burrowing.
Bipes biporus
is the only member of the family with five clawed digits on each forelimb. When
compared to the other two species in the family,
B. canaliculutus
and
B. triductylus
,
B. biporus
has the shortest average tail length. All species in the family Bipedidae exhibit
tail autotomy, but they are unable to regenerate their tails. In
B. biporus
, tail autotomy occurs between caudal annuli 6 and 10. There is a positive correlation
between tail autotomy and body size. Since the larger specimens are usually older,
it can be inferred that older specimens are more likely to be tailless than younger
specimens. This is due to the higher likelihood of older animals coming into contact
with a predator at some point in their lives.
- Other Physical Features
- ectothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes alike
Development
In the close relative
Bipes canuliculutus
, hatchlings (less than 1 year of age), juveniles (greater than one year of age but
not yet sexual mature), and adults can easily be distinguished by a size range: those
90 to 130 mm in length are considered hatchlings, 130 to 185 mm are considered juveniles,
and greater than 185 mm are considered adults and sexually mature. In
B. biporus
, however, hatchlings and juveniles cannot be reliably distinguished from one another
by size, so size can only be used for identifying adults (greater than 185 mm long).
Due to the burrowing lifestyle of
B. biporus
and difficulty in obtaining specimens, information on sex determination is unavailable.
Reproduction
No studies have been done to determine the type of mating system that
Bipes biporus
may use. Of the 2719 specimens collected in the extensive study done by Papenfuss
(1982), the ratio of adults to hatchlings stayed relatively constant throughout the
study. This suggests that reproductive success remains somewhat stable from year
to year and does not depend on the annual rainfall as previously thought, because
the study took place during a time of drought. Papenfuss (1982) also found that,
on average, larger females tended to lay more eggs than smaller females. Almost twice
the number of female adult and juvenile specimens were collected compared to the number
of males, although the difference was not statistically significant. Whether or not
this difference was due to sampling bias or if the primary sex ratio was actually
skewed could not be determined.
Bipes biporus
is an oviparous species. Females lay from 1 to 4 eggs per clutch, with an average
of 2 eggs per clutch. The eggs take roughly 2 months to hatch, but there is no mention
in the literature on whether the females guard the eggs or display any type of parental
care once the eggs are hatched. The eggs are generally laid at the end of June to
the beginning of July and begin hatching in late September. Females reach sexual maturity
at about 45 months of age. At 45 months, most females are 185 mm or longer, and this
length is considered the start of the adult stage in
B. biporus
. Once sexually mature, females only reproduce, at most, once every other year. Late
sexual maturity, small clutch size, and a biennial breeding interval makes the reproductive
potential of this species much lower than in most lizards.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
No data has been collected regarding the extent, if any, of parental care performed by Bipes biporus .
Lifespan/Longevity
Due to its secretive lifestyle, there has been little research done on the average
lifespan of
B. biporus
. Because females do not reach sexual maturity until roughly 45 months of age and
only reproduce every other year, average life expectancy must exceed this point. A
captive specimen, captured as an adult, lived for 3 years and 3 months.
Behavior
Bipes biporus
is unique among the other members of the Bipedidae in that it has an enhanced capacity
for thermoregulation. Because Mexican Mole Lizards are ectotherms, they attain their
body temperature from the soil of their environment.
B. biporus
can regulate its body temperature by moving deeper underground or closer to the surface
through its underground tunnels. Typically, Mexican Mole Lizards spend the cooler
morning hours near the surface of the ground, and as the temperature of the surroundings
rise throughout the day, they retreat deeper into the soil. The capacity for thermoregulation
and inhabiting a reliably warm climate enables year-round activity in Mexican Mole
Lizards; they appear to lack a regular period of hibernation.
In terms of locomotion,
B. biporus
exhibits concertina locomotion. This motion, used by many elongate burrowing animals,
occurs when one part of the body anchors in one spot while the anterior portion extends
forward while pushing against the anchored spot. Then the anchored portion moves forward
and the body anchors at a different spot. While this process has been found to be
energetically expensive in snakes,
Bipes
may use it more economically, because they seem to move entirely using aerobic respiration.
When constructing and extending the underground tunnels,
B. biporus
flexes and extends its forelimbs for clearing of the soil and for stabilizing and
forward propulsion of its body.
Communication and Perception
In contrast to the middle ear structure of most amphisbaenians, the stapes and cartilaginous
extracolumella of
Bipes biporus
are connected by fibrous tissue to a deep fold on the skin of the neck, apparently
making
B. biporus
more efficient at receiving sounds. This structure is likely most effective at intercepting
air-borne sounds. The importance of this highly specialized structure is not completely
understood for this otherwise rather primitive species. However, this unique ear
structure may be important for locating prey above the surface.
- Other Communication Modes
- vibrations
- Perception Channels
- tactile
- acoustic
- vibrations
Food Habits
Bipes biporus
can be described as an opportunistic carnivore. Mexican Mole Lizards will target
a variety of prey including ants, ant eggs and pupae, cockroaches, termites, beetle
larvae and other insect larvae, and most other small invertebrates. They are considered
generalist predators because they will seize anything of suitable size that they contact.
If they encounter a large number of ants, they will eat enough to fill up their stomachs,
while their next meal may be a single adult cockroach. The one characteristic that
remains the same for all prey is the practice of
B. biporus
to capture their prey and then retreat underground to consume it. As is true of many
squamates, their teeth are attached to the sides of the jaws in a pleurodont manner.
- Primary Diet
-
carnivore
- eats eggs
- insectivore
- eats non-insect arthropods
- vermivore
- Animal Foods
- eggs
- insects
- terrestrial non-insect arthropods
- terrestrial worms
Predation
Due to its burrowing lifestyle,
B. biporus
avoids many reptile-eating predators such as birds. Nocturnal mammals, such as badgers
and skunks, that often prey on burrowing animals may be unable to find and dig up
B. biporus
because the latter usually burrows deeper at night. The most likely predators of
Mexican Mole Lizards are snakes; snakes are easily able to enter the burrow systems
constructed by
Bipes
. However, all species of
Bipes
are able to autotomize (drop) their tails as a defense mechanism; it is thought that
the autotomized tail may distract the predator or even block the burrow while the
Mole Lizard escapes. However, Mole Lizards cannot regenerate the lost tail for future
encounters with predators.
Ecosystem Roles
Bipes biporus
plays a role in the ecosystem as a predator on terrestrial or burrowing invertebrates.
Mexican Mole Lizards may act as a control on certain pest population by consuming
numbers of mites, insects, and their larvae. In turn,
B. biporus
represents a food source (prey) for slender, burrowing snakes, such as
Phyllorhynchus decurtatus
, on the Baja California Peninsula.
- Ecosystem Impact
- soil aeration
Economic Importance for Humans: Positive
Due to the large number of insects and other small invertebrates that
Bipes biporus
feeds on, Mexican Mole Lizards undoubtedly play a role in controlling the populations
of their prey. Whether they are ever abundant enough to have a significant economic
impact is currently unknown.
- Positive Impacts
- controls pest population
Economic Importance for Humans: Negative
Bipes biporus
does no harm to humans or human economic interests; however, people sometimes kill
them due to their intimidating appearance. Many people believe them to be snakes,
so if they are dug up during agricultural activities, they are often unnecessarily
killed out of fear.
Conservation Status
Despite their low reproductive potential, Mexican Mole Lizards are considered a relatively
stable species, with no immediate concern of endangerment or extinction. These lizards
would seem to have at least some ability to adapt to changing environments. If the
habitat of
B. biporus
is disturbed by excavation, they appear to respond largely by digging deeper into
the soil or burrowing in a new area. The Mexican Mole Lizard is a secretive species
that stays hidden underground most of the time, thus limiting its exposure to predation
and negative human interactions. They occur in some protected areas and are considered
protected wildlife under Mexican law (catagory Pr).
Additional Links
Contributors
Morgan Casanova (author), Michigan State University, James Harding (editor), Michigan State University, Tanya Dewey (editor), University of Michigan-Ann Arbor.
- 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.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- Neotropical
-
living in the southern part of the New World. In other words, Central and South America.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- terrestrial
-
Living on the ground.
- desert or dunes
-
in deserts low (less than 30 cm per year) and unpredictable rainfall results in landscapes dominated by plants and animals adapted to aridity. Vegetation is typically sparse, though spectacular blooms may occur following rain. Deserts can be cold or warm and daily temperates typically fluctuate. In dune areas vegetation is also sparse and conditions are dry. This is because sand does not hold water well so little is available to plants. In dunes near seas and oceans this is compounded by the influence of salt in the air and soil. Salt limits the ability of plants to take up water through their roots.
- ectothermic
-
animals which must use heat acquired from the environment and behavioral adaptations to regulate 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.
- iteroparous
-
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
- 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
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- fossorial
-
Referring to a burrowing life-style or behavior, specialized for digging or burrowing.
- diurnal
-
- active during the day, 2. lasting for one day.
- sedentary
-
remains in the same area
- vibrations
-
movements of a hard surface that are produced by animals as signals to others
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- vibrations
-
movements of a hard surface that are produced by animals as signals to others
- soil aeration
-
digs and breaks up soil so air and water can get in
- carnivore
-
an animal that mainly eats meat
- insectivore
-
An animal that eats mainly insects or spiders.
References
Dial, B., R. Gatten, S. Kamel. 1987. Energetics of Concertina Locomotion in Bipes biporus (Reptilia: Amphisbaenia). Copeia , 1987 (2): 470-477. Accessed December 18, 2016 at http://www.jstor.org.proxy1.cl.msu.edu/stable/1445785?Search=yes&resultItemClick=true&searchText=bipes&searchText=biporus&searchUri=%2Faction%2FdoBasicSearch%3Famp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26wc%3Don%26prq%3Dbipes%2Bbiporus%2Breproduction%26hp%3D25%26fc%3Doff%26Query%3Dbipes%2Bbiporus%2B%26so%3Drel%26acc%3Don&seq=5#page_scan_tab_contents .
Grismer, L. 1955. Amphibians and Reptiles of Baja California, Including Its Pacific Islands and the Islands in the Sea of Cortés . Berkeley, California: University of California Press. Accessed December 19, 2016 at https://web-b-ebscohost-com.proxy2.cl.msu.edu/ehost/ebookviewer/ebook/ZTAwMHhuYV9fOTA0NjVfX0FO0?sid=57d8e672-136f-4dba-9fc5-6b9e504d7851@sessionmgr105&vid=0&format=EB&lpid=lp_254&rid=0 .
Hollingsworth, B., D. Frost. 2007. "Bipes biporus" (On-line). International Union for Conservation of Nature and Natural Resources. Accessed December 16, 2016 at http://www.iucnredlist.org/details/63723/0 .
Kearney, M. 2003. Diet in the Amphisbaenian Bipes biporus. Journal of Herpetology , 37: (2): 404-408. Accessed December 16, 2016 at http://www.jstor.org.proxy2.cl.msu.edu/stable/pdf/1566161.pdf .
Papenfuss, T. 1982. The Ecology and Systematics of the Amphisbaenian Genus Bipes. Occasional Papers of the California Academy of Sciences , 136: 1-42. Accessed December 18, 2016 at http://s3.amazonaws.com/academia.edu.documents/34858036/Bipes.pdf?AWSAccessKeyId=AKIAJ56TQJRTWSMTNPEA&Expires=1482205672&Signature=%2Bf8f%2BBZbZX5qfZrKmbpCaANDj6k%3D&response-content-disposition=inline%3B%20filename%3DOCCASIONAL_PAPERS_The_Ecology_and_System.pdf .
Slavens, F., K. Slavens. 1999. Reptiles and Amphibians in Captivity: Breeding— Longevity and Inventory Current January 1, 1998 . Seattle, Washington: Slaveware.
Wever, E., C. Gans. 1972. The Ear and Hearing in Bipes biporus. Proceedings of the National Academy of Sciences of the United States of America , 69 (9): 2714-2716. Accessed December 17, 2016 at http://www.jstor.org.proxy1.cl.msu.edu/stable/61851?Search=yes&resultItemClick=true&searchText=bipes&searchText=biporus&searchUri=%2Faction%2FdoBasicSearch%3FQuery%3Dbipes%2Bbiporus%2B%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26amp%3D%26acc%3Don%26fc%3Doff%26hp%3D25%26so%3Drel%26wc%3Don%26resultsServiceName%3DdoBackToBasicResults%26prq%3Dbipes%2Bbiporus%2Breproduction&seq=1#page_scan_tab_contents .