Crocodylus mindorensis

Philippine crocodile

By Jamison Law

Geographic Range

Habitat

Physical Description

Development

Reproduction

Lifespan/Longevity

Behavior

Communication and Perception

Food Habits

Predation

Ecosystem Roles

Economic Importance for Humans: Positive

Economic Importance for Humans: Negative

Conservation Status

Other Comments

Contributors

References

Geographic Range

The Phillipine Crocodile, Crocodylus mindorensis, is historically indigenous throughout the Philippine is-
lands including Dalupiri, Luzon, Mindoro, Masbate, Samar, Jolo, Negros, Busuanga and Mindanao. Recent
surveys show it to be limited to northern Luzon and southwestern Mindanao islands. (Oliveros, et al.,
2006; Ortega, 1998; Pontillas, 2000; Ross and Alcala, 1983; Van Weerd and Van der Ploeg, 2003; Van
Weerd, 2010)
Biogeographic Regions oriental native

Other Geographic Terms island endemic

Habitat

Crocodylus mindorensis seems to prefer small wetlands, but has also been found in shallow natural
ponds and marshes, man-made water reservoirs, shallow narrow creeks, littoral creeks and mangrove
areas, and faster-flowing larger rivers in the mountains up to 850 m. They have been observed in both
the Sierra Madre and Cordillera Mountains in fast flowing rivers with rapids and deep pools lined by
limestone cliffs. The cliffs have caves thought to be used as hiding places. The Philippine crocodile has
also been found to make burrows in sandy and clay river banks. (Van Weerd, et al., 2006; Van Weerd,
2010)

Habitat Regions tropical freshwater

Aquatic Biomes lakes and ponds rivers and streams brackish water

Wetlands marsh swamp

Other Habitat Features riparian intertidal or littoral caves

Range elevation

850 (high) m

2788.71 (high) f

Physical Description

Crocodylus mindorensis is a relatively small species of freshwater crocodile. Hatchlings are golden-brown
dorsally with transverse dark stripes, and are white on their ventral side. As they age the brown darkens.
Compared to other crocodiles they have a relatively broad snout and heavy dorsal armor. The record
length is 3.02 m, but most individuals are much smaller. Males mature at about 2.1 m, females at 1.3 m.

They have enlarged post occipital scales ranging from 4 to 6, transverse ventral scale rows ranging from
22 to 25, 12 transverse dorsal midbody scales, palatine-pterygoid sutures that are nearly transverse
(never bisecting the pterygoid), cervical scalation, lateral scales of equal size arranged in longitudinal
rows, and prominent nuchomarginal rows. (Banks, 2005; Hall, 1989; Oliveros, et al., 2006; Ross and Al-
cala, 1983)

Other Physical Features ectothermic heterothermic bilateral symmetry

Sexual Dimorphism male larger

Range length

3.02 (high) m

9.91 (high) f

Average length

2m

6.56 f

Development

Like all crocodilians, C. minodorensis exhibits temperature dependent sex determination. Utilizing artif-
cial incubation, it has been observed that mostly females are produced at 30 to 31°C and mostly males at
33°C. In captivity, egg fertility rates were found to be 56% and 57% in Palawan and Negros,respectively,
and hatching rates of fertile eggs were 45% and 51%. Egg fertility and hatching rates for 10 wild nests
(201 eggs) on Luzon were comparatively higher at 75% and 70%, respectively, but wild egg hatching suc-
cess in the Muleta River was 45.5% in one nest. (Van Weerd, 2010)

Development - Life Cycle temperature sex determination

Reproduction

The mating system of C. mindorensis has not been explicitly investigated, but it is common among croco-
dilians for males and females to have multiple mates. (Britton, 2003)

Mating System polygynandrous (promiscuous)

Captive female and male Philippine crocodiles begin breeding when they are 1.3 meters and 2.1 meters
in length, respectively, and about 15 kilograms. Mating and courtship occur in the dry season from De-
cember to May and egg laying occurs between April and August, peaking at the beginning of the rainy
season in May or June. Philippine crocodiles lay their second clutch 4 to 6 months afer the frst, and can
lay up to three clutches in a year. Clutch sizes vary between 7 and 33 eggs. Incubation periods in the wild
for C. mindorensis are between 65 to 78, and 77 to 85 days in captivity. (Alcala, et al., 1987; Hauswaldt,
et al., 2013; Sibal, et al., 1992; Van Weerd, 2010)

Key Reproductive Features iteroparous seasonal breeding gonochoric/gonochoristic/dioecious (sexes

separate) sexual fertilization oviparous
Breeding interval

Up to three clutches in a year with intervals between 4 and 6 months

Breeding season

Breeding from December to May followed by egg laying between May and August

Range number of offspring

7 to 33

Average number of offspring

25

Range gestation period

4 to 5 months

Average age at sexual or reproductive maturity (female)

10 years

Average age at sexual or reproductive maturity (male)

15 years

Generally, female Philippine crocodiles build either hole nests, mound nests, or a combination of the two
on river or pond banks that are 4 to 21 meters from the edge of the water. Mound nests are built during
the dry season and typically consist of dried leaves, twigs, bamboo leaves, and soil, with a mean height
of 55 cm, length of 2 m and width of 1.7 m (based on 4 nests in Luzon). Afer egg laying males and fe-
males take turns watching the nests, and females routinely visit their nests either early in the morning or
late in the afternoon. Parental care by the female was observed at Silliman University in captivity for
three months afer hatching, but this has yet to be observed in wild Philippine crocodiles. (Hinlo, 2010;
Sibal, et al., 1992; Van Weerd, et al., 2006; Van Weerd, 2010)

Parental Investment male parental care female parental care pre-hatching/birth provisioning male
female protecting female

Lifespan/Longevity

Data on the lifespan of C. mindorensis are lacking but crocodilians are thought to live as long as 70 to 80
years. (Britton, 2003)
Behavior

Philippine crocodiles have been shown to be quite aggressive towards each other in captivity. Juveniles
have displayed intra-specifc aggressiveness in the wild and, according to feld observations in northern
Luzon, establish individual territories through aggressive interactions in their second year. However, in-
tra-specifc aggressiveness has not been observed among adults or between size or age classes, and
sometimes pairs of adult crocodiles are seen basking and swimming together. Crocodiles have also been
shown to use individual sites in larger rivers during the drier season when water levels and currents are
low but congregate in shallow ponds and creeks during the wet season when river currents are high.

Radio telemetry from a breeding pair revealed the maximum daily movement for the male to be 4.3
km/day and 4 km/day for the female. The male travelled longer distances but less frequently. Habitats
favorable to the crocodiles were characterized by waters with average flow velocity, minimum depth and
maximum width. Behavioral studies in Dunoy Lake revealed that average distances among wild C. min-
dorensis, regardless of age, were found to be 20 meters. Areas with lake edge vegetation were found to
be preferred by juveniles and hatchlings whereas areas with open water and large logs to bask were pre-
ferred by adults. (Schreuder, 2006; Tubbs, 2006; Van Weerd, 2010)

Key Behaviors natatorial diurnal motile migratory territorial

Home Range

In northern Luzon home ranges recorded from radio-tagged crocodiles were shown to be over 1 to 6
kilometers of river. (Van Weerd, et al., 2006; Van Weerd, 2010)

Communication and Perception

There has been little study of communication or perception in C. mindorensis so general features applic-
able to crocodilians has been reported here. It is generally true that crocodilians' skin color can change
depending on the environment or the crocodile's mood. Additionally, when the jaw is gaping, bright yel-
low or orange tongue colors may appear as social or warning signs. Crocodilians can achieve complex vo-
calizations by forcing exhaled air through a constriction by varying tensions in the muscles lining the glot-
tis, and by expanding the throat via the hyoid apparatus, amplifcation can be achieved. It is thought that
chemical detection is achieved on land when sensory epithelial cells detect chemicals as air passes
through the sinuses and achieved in the water by the chemoreceptors lining the tongue. Communication
has also been shown to involve pheromones secreted from the chin and paracloacal musk glands. Dome
pressure receptors (DPRs) located on head scales, particularly around the jaws, and integumentary sense
organs (ISOs), located on the caudal margin of body scales, rapidly alert the crocodile to potential prey
by detecting pressure waves created by disturbances of the water surface. Crocodilians can detect fre-
quencies ranging from below 10 Hz to over 10 kHz and, within particular bandwidths, sound pressure
levels below -60 dB can be detected. (Britton, 2003)

Communication Channels visual acoustic chemical

Other Communication Modes pheromones

Perception Channels visual acoustic vibrations chemical

Food Habits

Prey species that were observed for juvenile Philippine crocodiles included snails, shrimps, dragonflies,
and small fsh. Prey species for adults included large fsh, pigs, dogs, "civet cats" (probably Asian palm
civets (Paradoxurus hermaphroditus), possibly Malayan civets (Viverra tangalunga)), snakes and water
birds. True to the crocodile's opportunistic feeding behavior, a variety of prey was taken in captivity in-
cluding marine and freshwater fsh, pork, beef, chicken meat and offal. Smaller prey including shrimp,
mince, and white mice were also taken by juveniles and hatchlings. (Van Weerd, 2010)

Primary Diet carnivore eats terrestrial vertebrates piscivore insectivore

Animal Foods birds mammals reptiles fsh carrion insects mollusks aquatic crustaceans

Predation

Adults of Crocodylus mindorensis have no reported predators other than humans. Larger saltwater croc-
odiles (Crocodylus porosus) might attack them, but the two species have been observed to co-occur in at
least one location on Mindanao. By far the most dangerous predator for this species is Homo sapiens.
People kill these animals for their skins and meat, and to protect their livestock and their own safety.

Eggs and hatchlings are much more vulnerable. Ants, monitor lizards (Varanus), pigs (Sus), dogs (Canis
lupus familiaris), short-tailed mongooses (Herpestes brachyurus), rats (Rattus) and other animals may
eat the eggs from unattended nests. Hatchlings are known to be attacked by rufous night herons (Nycti-
corax caledonicus), probably also large fsh, monitor lizards, and in the past, the now rare and endan-
gered Asian giant sofshell turtle (Pelochelys cantorii).

Parental protection of the nest and hatchlings is an important anti-predator adaptation in this species.
These animals are also cryptically colored. (Britton, 2003; Hinlo, 2010; Van Weerd, 2010)
Anti-predator Adaptations cryptic

Known Predators

monitor lizards (Varanus)

short-tailed mongooses (Herpestes brachyurus)

dogs (Canis lupus familiaris)

ants (Formicidae)

pigs (Sus)

Ecosystem Roles

Very little is known about the ecology of this species, and the surviving wild population is very small. It is
likely to be a top predator in freshwater foodwebs in the Philippines.

Economic Importance for Humans: Positive

Humans have killed Philippine crocodiles for their meat and hide; they were extensively harvested for
the hides from the 1950s to 1970s. Now they are so rare that there is no organized harvesting. (Banks,
2005)

Positive Impacts food body parts are source of valuable material

Economic Importance for Humans: Negative

This species can be a potential threat to livestock, though it is currently too rare to have a significant ef-
fect. It is not considered to be a direct threat to humans. In the Philippines it is ofen confused with the
much larger and more dangerous saltwater crocodile (Crocodylus porosus), which is much more danger-
ous to people. (Banks, 2005; Hauswaldt, et al., 2013; Miranda, et al., 2004)

Conservation Status

The Philippine crocodile is nationally protected by the Republic Act 9147 (the Wildlife Act) since 2001,
and the Protected Areas and Wildlife Bureau (PAWB) of the Department of Environment and Natural Re-
sources (DENR) was made responsible for the protection of crocodiles and conservation of their habitat.
The DENR created the 'Philippine Crocodile National Recovery Team' (PCNRT) under Special Order 2000-
231, which is in charge of recovering C. mindorensis from near extinction. Since the frst breeding facility
at Silliman University Environmental Centre (SUEC), there have been other breeding programs estab-
lished to promote the propagation of the Philippine crocodile including the Palawan Wildlife Rescue and
Conservation Centre (PWRCC). The DENR also has many agreements with zoos in North America, Europe,
and Australia for conservation programs. The Mabuwaya Foundation works through the Crocodile Reha-
bilitation, Observance, and Conservation (CROC) Project to educate the community about C. mindorensis
and encourage its protection by establishing sanctuaries. Additionally, research programs are being im-
plemented with Cagayan Valley Programme on Environment and Development (CVPED) and Dutch and
Filipino students to continue adding to the knowledge base of the species. Public awareness is also
raised by Mabuwaya via information and education (IEC) campaigns, which use passive (e.g. posters), ac-
tive (e.g. lectures), and interactive methods (e.g. Q&A discussions). (Alcala, 1997; Banks, 2005;
Hauswaldt, et al., 2013; Miranda, et al., 2004; Sumiller, 2000; Van Weerd and Van der Ploeg, 2004; Van
Weerd, 2005; Van Weerd, 2010; Van der Ploeg, et al., 2008)

Common names for the Philippine crocodile (Crocodylus mindorensis) include the Philippine freshwater
crocodile, buwaya (general Philippines), bukarot (northern Luzon), and the Mindoro crocodile (as per the
island it was frst discovered on in 1935 by Karl Schmidt).

The species was frst described by Schmidt in 1935, but for decades it was thought to be a subspecies of
the New Guinea crocodile, Crocodylus novaeguineae. Only since Hall's paper in 1989 has it been widely
recognized as a separate species. (Hall, 1989; Hauswaldt, et al., 2013; Ross and Alcala, 1983; Van Weerd,
2010)

Contributors

Jamison Law (author), Indiana University-Purdue University Fort Wayne, Mark Jordan (editor), Indiana
University-Purdue University Fort Wayne.

Glossary

acoustic

uses sound to communicate

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.
brackish water

areas with salty water, usually in coastal marshes and estuaries.

carnivore

an animal that mainly eats meat

carrion

flesh of dead animals.

chemical

uses smells or other chemicals to communicate

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its
natural environment; being difficult to see or otherwise detect.

diurnal

active during the day, 2. lasting for one day.

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate
body temperature

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

food

A substance that provides both nutrients and energy to a living thing.

freshwater

mainly lives in water that is not salty.

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.

insectivore

An animal that eats mainly insects or spiders.

intertidal or littoral

the area of shoreline influenced mainly by the tides, between the highest and lowest reaches of the tide.
An aquatic habitat.

island endemic

animals that live only on an island or set of islands.

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 defnition, survive over multiple
seasons (or periodic condition changes).
male parental care

parental care is carried out by males

marsh

marshes are wetland areas ofen dominated by grasses and reeds.

migratory

makes seasonal movements between breeding and wintering grounds

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

native range

the area in which the animal is naturally found, the region in which it is endemic.

oriental

found in the oriental region of the world. In other words, India and southeast Asia.

World Map

oviparous
reproduction in which eggs are released by the female; development of offspring occurs outside the
mother's body.

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same
species

piscivore

an animal that mainly eats fsh

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several
different females.

riparian

Referring to something living or located adjacent to a waterbody (usually, but not always, a river or
stream).

seasonal breeding

breeding is confned to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

swamp

a wetland area that may be permanently or intermittently covered in water, ofen dominated by woody
vegetation.
territorial

defends an area within the home range, occupied by a single animals or group of animals of the same
species and held through overt defense, display, or advertisement

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

vibrations

movements of a hard surface that are produced by animals as signals to others

visual

uses sight to communicate

References

Alcala, A., C. Ross, E. Alcala. 1987. Observations on reproduction and behaviour of captive Philippine
crocodiles (Crocodylus mindorensis). Silliman Journal, 34 (1-2): 18-28.

Alcala, E. 1997. Silliman University captive breeding program: an institutional report on the status of the
captive breeding project (as of 1994). Sylvatrop, 5: 91-96.

Banks, C. 2005. National recovery plan for the Philippine crocodile, Crocodylus mindorensis, 2005-2008.
Quezon City, Philippines: Department of Environment and Natural Resources- Protected Areas and
Wildlife Bureau (DENR-PAWB) and the Royal Melbourne Zoological Gardens (RMZG). Accessed February
28, 2014 at http://www.chm.ph/index.php?option=com_docman&task=doc_download&gid=8&
Itemid=74.
Britton, A. 2003. Crocodilians (Crocodiles, Alligators, Caimans, and Gharials). Pp. 157-165 in M Hutchins,
A Evans, J Jackson, D Kleiman, J Murphy, D Thoney, eds. Grzimek's Animal Life Encyclopedia, Vol. 7, 2 Edi-
tion. Detroit: Gale.

Hall, P. 1989. Variation in Geographic Isolates of the New Guinea Crocodile (Crocodylus novaeguineae
Schmidt) Compared with the Similar, Allopatric, Philippine Crocodile (C. mindorensis Schmidt). Copeia, 1:
71-80. Accessed March 09, 2014 at http://www.jstor.org/stable/1445607.

Hauswaldt, S., M. Vences, E. Louis, R. Brennemann, T. Ziegler. 2013. Genetic Screening of Captive Philip-
pine Crocodiles (Crocodylus mindorensis) as Prerequisite for Starting a Conservation Breeding Program in
Europe. Herpetological Conservation and Biology, 8/1: 75-87. Accessed February 28, 2014 at http://
herpconbio.org/Volume_8/Issue_1/Hauswaldt_etal_2013.pdf.

Hinlo, M. 2010. Population genetics and conservation of the Philippine crocodile : a thesis presented in
partial fulflment of the requirements for the degree of Master of Science in Conservation Biology at
Massey University, Manawatu, New Zealand. Manawatu, New Zealand: Massey University. Accessed
March 06, 2014 at http://mro.massey.ac.nz/bitstream/handle/10179/2054/02_whole.pdf?sequence=3.

Miranda, J., M. Van Weerd, J. Van der Ploeg. 2004. Devolving crocodile conservation to the local level:
the case of the Philippine crocodile conservation in the municipality of San Mariano. Northeast Luzon,
the Philippines. 17th Working Meeting of the Crocodile Specialist Group, Gland Switzerland and Cam-
bridge, UK: 309-316. Accessed May 15, 2014 at http://www.iucncsg.org/365_docs/attachments/
protarea/17th-fd70721f.pdf.

Oliveros, C., S. Telan, M. Van Weerd. 2006. "Crocodile Surveys On Dalupiri and Fuga" (On-line pdf). Croc-
odile Specialist Group. Accessed March 09, 2014 at http://iucncsg.org/365_docs/attachments/protarea/
dalu-11c95805.pdf.

Ortega, V. 1998. Philippine crocodile conservation. Comprehensive report. Proceedings of the 14th
Working Meeting of the IUCN-SSC Crocodile Specialist Group: 101-134.
Pontillas, F. 2000. New breeding sites for the Philippine crocodile. Crocodile Specialist Group Newsletter,
19: 7-12. Accessed March 09, 2014 at http://www.iucncsg.org/365_docs/attachments/protarea/CSG
%20-b3308c69.pdf.

Ross, C., A. Alcala. 1983. Distribution and status of the Philippine crocodile (Crocodylus mindorensis). Ka-
likasan: Philippine Journal of Biology, 12/1-2: 169-173.

Schreuder, I. 2006. The behavior and ecology of the Philippine crocodile (Crocodylus mindorensis) in its
natural habitat. Leiden University and College of Forestry: CVPED. Institute of Environmental Sciences:
Cagayan Valley Programme on Environment and Development (CVPED).

Sibal, M., I. Sarsagat, Y. Satake. 1992. Captive breeding of C. mindorensis and C. porosus. Workshop on
the prospects and future strategy of crocodile conservation of the two species (C. mindorensis and C.
porosus) occurring in the Philippines, Puerto Princesa, Philippines: 36-44.

Sumiller, R. 2000. Captive breeding of Crocodylus mindorensis and Crocodylus porosus at the Crocodile
Farming Institute. CFI Research Bulletin, 1: 3-8.

Tubbs, N. 2006. Movements and home ranges of the VHF radio-tracked Philippine crocodile (Crocodylus
mindorensis) in Northeast Luzon, the Philippines. Student Report Number 216. Cabagan, Philippines:
CVPED and Leiden University.

Van Weerd, M. 2005. Monitoring program crocodile rehabilitation, observance and conservation (CROC)
project. Proceedings of the National Biodiversity Monitoring Workshop: 1-11.

Van Weerd, M. 2010. Crocodiles: Status Survey and Conservation Action Plan. Pp. 71-78 in S Manolis, C
Stevenson, eds. Philippine Crocodile Crocodylus mindorensis. Gland, Switzerland: Crocodile Specialist
Group. Accessed February 28, 2014 at http://www.iucncsg.org/365_docs/attachments/protarea/13_C-
511712ed.pdf.
Van Weerd, M., J. Van der Ploeg. 2004. Devolution of natural resource management and crocodile con-
servation: the case of San Mariano, Isabela. Philippine Studies, 52 (3): 346-383.

Van Weerd, M., J. Van der Ploeg. 2003. A new future for the Philippine crocodile, Crocodylus mindoren-
sis. Sylvatrop, The Technical Journal of Philippine Ecosystems and Natural Resources, 13/1-2: 31-50. Ac-
cessed February 28, 2014 at http://www.researchgate.net/publication/235800476_A_new_future_for_
the_Philippine_crocodile_Crocodylus_mindorensis/fle/9fcfd5139f795a09df.pdf.

Van Weerd, M., J. Van der Ploeg, D. Rodriguez, J. Guerrero, B. Tarun, S. Telan, J. De Jonge. 2006. Philip-
pine crocodile conservation in Northeast Luzon: an update of population status and new insights into
Crocodylus mindorensis ecology. Proceedings of the 18th working meeting of the Crocodile Specialist
Group.: 306-321. Accessed March 09, 2014 at http://www.vantienhovenfoundation.com/uploads/Van
%20Weerd%20et%20al.%20(2006).pdf.

Van der Ploeg, J., D. Rodriguez, B. Tarun, J. Guerrero, M. Balbas, S. Telan, A. Masipiquena, M. Van Weerd.
2008. "Crocodile Rehabilitation, Observance and Conservation (CROC) project: the conservation of the
critically endangered Philippine crocodile (Crocodylus mindorensis) in Northeast Luzon, the Philippines"
(On-line pdf). Accessed February 28, 2014 at https://openaccess.leidenuniv.nl/bitstream/handle/1887/
13055/Final%20report%20CROC%20BPCP%20consolidation%20award%202008.pdf?sequence=1.

ADW Pocket Guides on the iOS App Store!

The Animal Diversity Web team is excited to announce ADW Pocket Guides!

Read more...

Connect with us

Help us improve the site by taking our survey.

Facebook Twitter Pinterest Search

Enter search text

Search ADW

Search

Search in feature

Explore Data @ Quaardvark

Search Guide

Navigation Links

Information

Pictures

Classifcation

Classifcation

Kingdom

Animalia

animals

Animalia: information (1) Animalia: pictures (20673) Animalia: specimens (7109) Animalia: sounds (722)
Animalia: maps (42)

Phylum

Chordata

chordates

Chordata: information (1) Chordata: pictures (15057) Chordata: specimens (6829) Chordata: sounds
(709)

Subphylum

Vertebrata

vertebrates

Vertebrata: information (1) Vertebrata: pictures (15020) Vertebrata: specimens (6827) Vertebrata:
sounds (709)

Class
Reptilia

turtles, snakes, lizards, and relatives

Reptilia: information (1) Reptilia: pictures (8805) Reptilia: specimens (170) Reptilia: sounds (676)

Order

Crocodylia

Crocodylia: information (1) Crocodylia: pictures (169) Crocodylia: specimens (7)

Family

Crocodylidae

Crocodylidae: pictures (169) Crocodylidae: specimens (7)

Genus

Crocodylus

Crocodylus: pictures (68) Crocodylus: specimens (2)

Species

Crocodylus mindorensis

Philippine crocodile

Crocodylus mindorensis: information (1) Crocodylus mindorensis: pictures (2)

To cite this page: Law, J. 2015. "Crocodylus mindorensis" (On-line), Animal Diversity Web. Accessed
September 06, 2019 at https://animaldiversity.org/accounts/Crocodylus_mindorensis/

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college
students. ADW doesn't cover all species in the world, nor does it include all the latest scientifc
information about organisms we describe. Though we edit our accounts for accuracy, we cannot
guarantee all information in those accounts. While ADW staff and contributors provide references to
books and websites that we believe are reputable, we cannot necessarily endorse the contents of
references beyond our control.

U-M Gateway | U-M Museum of Zoology

U-M Ecology and Evolutionary Biology

© 2014 Regents of the University of Michigan

Report Error / Comment

This material is based upon work supported by the National Science Foundation Grants DRL 0089283,
DRL 0628151, DUE 0633095, DRL 0918590, and DUE 1122742. Additional support has come from the
Marisla Foundation, UM College of Literature, Science, and the Arts, Museum of Zoology, and
Information and Technology Services.

The ADW Team gratefully acknowledges their support.