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RED-SPOTTED
NEWT
Notophthalmus
viridescens
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| INTRODUCTION |
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The red-spotted newt has one of the most complicated life histories
of any pond-breeding amphibian in Rhode Island because it has
four, not three, life stages (egg, aquatic larva, terrestrial
eft, and aquatic adult). Newts eggs are laid in the spring. In
the fall, larvae undergo metamorphosis and transform into a juvenile
terrestrial form referred to as an 'eft '. The terrestrial eft
stage lasts for 2-7 years, then newts undergo a second metamorphoses
-from eft to adult- before returning to ponds to breed. Life history
strategies of this species are highly variable. In some areas,
the eft stage is reproductively active, while in other areas the
eft stage is absent and neotenic newts never leave breeding ponds.
Aquatic larvae and adults are typically found in ponds with relatively
long hydroperiods (Paton and Egan
2001).
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| IDENTIFICATION |
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ADULTS
- Aquatic adults generally have an olive-greenish dorsum
and a yellow venter
with fine black dots.
- They have a flatten tail adapted for swimming.
- Adults have lungs and lack gills.
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Adult newt |
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EFTS
- In Rhode Island, efts generally have a brown to brownish-orange
dorsum and orange venter. At higher elevation sites, and
upland areas, efts are often brilliant orange, this morph
is rare in Rhode Island.
- Efts have rough skin.
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Eft |
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Sexual Dimorphism
- Aquatic males- during the breeding season and late fall-
can be distinguished from females by the presence of black
pads (excrescences) on the digits of their hind feet and
a high tail fin.
- The vent of the male becomes more enlarged than that
of the female (Bishop 1941).
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male newt with excrescences |
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| SIZE |
| AGE / SEX
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SVL (SNOUT
VENT LENGTH) (cm) |
SAMPLE SIZE
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AVERAGE
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RANGE
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Std. Deviation
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ADULT FEMALE
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3.6
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2.5- 4.3 |
0.4
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18
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ADULT MALE
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3.7
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2.5- 4.5 |
3.7
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29
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JUVENILE
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2.7
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1.9- 3.9 |
0.5 |
134
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METAMORPH
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2.1
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1.2- 3.3 |
0.3 |
384
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| AGE / SEX
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TL (TOTAL LENGTH) (cm)
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SAMPLE SIZE
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AVERAGE
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RANGE |
Std. Deviation
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ADULT FEMALE
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7.3
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5.5- 9.4 |
1.1
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18
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ADULT MALE
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7.3
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4.8-
9.4 |
1.0
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29
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JUVENILE
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5.2
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2.9- 8.0 |
1.1
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134
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METAMORPH
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4.1
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2.6- 6.2 |
0.6
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384
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| AGE/ SEX |
MASS (g)
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SAMPLE SIZE
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AVERAGE
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RANGE |
Std. Deviation
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ADULT FEMALE
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1.28
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0.5- 2.0 |
0.5
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18
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ADULT MALE
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1.31
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0.6- 2.2 |
0.4
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29
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JUVENILE
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0.6
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0.1-1.6 |
0.4
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134
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METAMORPH
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0.3
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0.1- 0.8 |
0.1
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384
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| RELATIVE ABUNDANCE |
Rhode Island
Newts are relatively
abundant in rural areas of Rhode Island. Paton
et al. (2000) captured 134 adults immigrating to a 0.16 ha seasonally-flooded
pond in southern Rhode Island at Trustom National Wildlife Refuge.
There is some evidence that they may have been extirpated from urban
areas in the Providence area (Paton
and Egan 2001). |
Regional
Newts are
common to abundant in the region (Klemens
1993; DeGraaf and Yamasaki 2001).
Burne (2000) detected newts in
only 8% of 78 ponds sampled near Concord, Massachusetts. The majority
of the ponds in his study were characterized by longer hydroperiods
and only 9 of these ponds were permanent ponds.
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| DISTRIBUTION |
Rhode Island
Widespread in the state, although
their populations are somewhat localized (Klemens 1993). Paton and Egan
(2001) detected them at 17.6 % of 119 randomly-selected ponds west of
Narragansett Bay, Rhode Island; 30 of the ponds in their study were permanent
ponds.
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Regional
They are found throughout
New England (DeGraaf and Yamasaki 2001) and are one of the more common
species. Klemens (1993) found that they were quite localized along the
coast, but more widespread in upland areas.
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General
Red-spotted newts
are the second most widely distributed salamanders in North America
(Petranka 1998a). They range
from southern Florida west to Texas and north to southern Canada.
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| HABITAT NON BREEDING |
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Efts
The completely terrestrial efts are habitat generalists. They
are usually found in deciduous and coniferous woodlands, but also
use pastures and meadows (Klemens 1993). Healy
(1974a, 1975) tracked postlarval efts from breeding ponds
to upland habitats, and found they require approximately 1 year
to migrate to permanent forest residences. While in the forested
habitat, efts live under leaf litter and other debris during dry
periods and are active during wet periods when temperatures exceed
12° C (Petranka 1998a). They move about the forest floor in
search of food and are frequently observed in groups where food
sources are most abundant, for example, around a decaying log
or mushroom (Petranka 1998a). During the cold months of winter,
they hibernate on land, burrowing under logs and other debris
(Degraaf and Yamasaki 2001).
Gibbs (1998a) found that in
Connecticut newts avoided edges, thus their movements were affected
by forest borders and streambeds. However in Maine, DeMaynadier
and Hunter (1998) found newts were less sensitive than other
species of amphibians to forest edges and suggested they are less
vulnerable to current timber management practices.
Adults
Adult newts remain aquatic all year, unless the pond in which
they live dries up (Petranka 1998a). When ponds do dry up, newts
may remain in the basin of the pond, in the upland close to the
pond, or move to a neighboring pond (Ptingsten and Downs 1989).
By the same token, if the pond is shallow and freezes solid in
the winter, newts leave the pond for the upland or a deeper pond
(Gill 1978a). Morin (1983) found
that in South Carolina newts, avoided desiccation by burrowing
under leaf litter and other debris. Newts return to their home
pond once the pond refills or unfreezes (Ptingsten and Downs 1989).
During fieldwork at Trustom Pond, NWR in Rhode Island (Paton et
al. 2000), we had aquatic adults entering ponds in the spring
and emigrating from ponds in the fall. These individuals were
olive-green, but the tail fin was not as high as some aquatic
adults; they presumably wintered in adjacent upland areas. Gill
(1978a; 1978b) reported similar behavior in his pond in Virginia;
he found that adults migrated to the breeding pond in early spring
(March-April) and emigrated during the fall (August-September).
Aquatic adults are active throughout the winter. They have been
seen swimming under the ice in ponds and streams and have been
observed during the winter in groups of 20-40 (Morgan
and Grierson 1932). As mentioned above, in some areas larval
never undergo metamorphosis to an eft stage. Rather they are neotenic
and spend their entire life in ponds (Lazell
1976). To our knowledge, no neotenic populations exist in
Rhode Island.
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| HABITAT BREEDING |
| Adults newts tend
to breed in permanent or semi-permanent water bodies, including
lakes, large ponds, reservoirs, ditches, swamps, marshes, and slow
moving streams or canals (Bishop 1941; Gates
and Thompson 1982; Petranka 1998a). In southern New England,
they appear to prefer shallow, still water, with an open canopy
and dense aquatic vegetation (e.g., emergent or submergent macrophytes)
(Klemens 1993; Petranka 19998a). It has been our experience that
they are more likely to be found in sites with high densities and
diversity of aquatic invertebrates (C. Heinz, pers. obs.).
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| HYDROLOGY |
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| MOVEMENT CHRONOLOGY |
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In Rhode Island, adults start moving back to temporary ponds
during the first week of March, with most adults at ponds by the
end of March, although some immigrate to ponds as late as mid-April
(Paton and Crouch In press). According to Ptingsten and Downs
(1989), newts in transition from eft to adult typically migrate
back to breeding ponds during August and September (a few return
in the spring).
Young red-spotted newts (efts) are among the last metamorphs
to emerge from ponds in Rhode Island, with the first leaving in
mid-September and some leaving as late as mid- to late November.
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| REPRODUCTION |
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In Rhode Island newts breed during late spring. In contrast,
adults in many northern populations court in both the spring and
fall-though females oviposit only in the spring (Gage 1891; Bishop
1941); whereas, in many southern population, adults breed from
late autumn through early spring (Petranka 1998a). Courtship commences
with males searching the pond looking for sexually active females.
If a female is encountered and responds when the male first approaches,
he performs a brief 'hula' dance or a lateral display involving
body and tail undulations (Petranka 1998a). The interested female
then nudges the males- providing the signal for the intent male
to deposit one or more spermatophores. The female picks up the
spermatophore in her
expanded vent where it remains
until she deposits her eggs (Arnold
1977; Humphries 1955;
Verrell 1982a, 1990a).
If this initial courtship strategy fails, as it does more than 50 %
of the time in laboratory experiments, the male employs a more
aggressive approach (Petranka 1998a). The male will use his strong
back legs to engage the female in amplexus where they can remain
for several hours. During this time the male uses several tactics
to entice the female including waving his tail back and forth
attempting to waft his scent towards the female's nostrils (Petranka
1998a). After some time, the male releases his hold and deposits
one or more spermatophores which hopefully the female will collect
(Petranka 1998a). Gill (1978b)
reported that in some regions females can breed as many as 20-30
times.
Hurlbert (1970b) found that efts
returning to the ponds as adults for the first time breed later
than older adults.
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| EGG MASS |
| Females oviposit eggs singly
under leaves (both dead and alive), stems of aquatic plants or on
other debris where they are often covered by bits of vegetation
(Petranka 1998a). Newly deposited eggs are about 1.5 mm (0.06 inches)
in diameter, are light to dark brown in color, and are surrounded
by three elliptical envelopes (Petranka 1998a). Females deposit
6-10 eggs per day (Ptingsten and Downs 1989) and scattered them
widely through out the aquatic habitat. 80-450 eggs are deposited
annually (Albert and Albert-Knoop
1999); thus, the process may take several weeks to complete
(Petranka 1998a). The eggs, as well as the larvae, the eft, and
the adult, are toxic (Ptingsten and Downs 1989). |
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| LARVAE |
| Hatching is temperature dependent
and usually takes 3-5 weeks. (Ptingsten and Downs 1989; Petranka
1998a). Larvae are approximately 6 mm in length and are light
green in color (Ptingsten and Downs 1989). Newt larvae have
a black line extending through their eye; a characteristic
which aids in separating them from the larvae of spotted salamanders
(Ambystoma maculatum). |

Red-spotted newt larva
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| METAMORPHS |
| As discussed in previous sections, the newt
metamorph is referred to as a red eft or simply an eft. We
do not have red efts in southern Rhode Island, but efts which
have brown dorsums and orangish bellies. The eft is terrestrial
and will not return to the pond to breed for 2-7 years. Not
all populations of newts produce the eft - a phenomenon that
is still a mystery (Albert and Albert-Knoop 1999). Newts that
skip the eft stage are referred to as neotenes. These individuals
do not leave the pond. They mature to adults in 2 years, growing
much faster than their terrestrial counterparts because they
are able to feed throughout the year; efts generally forage
only during the warmer months. |
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| JUVENILES |
| Estimates of the length
of the juvenile stage terrestrial 'eft' are highly variable. Bishop (1941)
reported that efts became sexually mature after 2-3 years and re-entered
water then. However, Healy (1974) reported that efts in interior sites
in Massachusetts remained on land for 3-7 years before immigrating back
to aquatic habitats. In either case, once the transformation is complete
adults reproduce for the first time the following spring (Ptingsten and
Downs 1989). |
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| FOOD |
Adults
Adults prey on insects (their
preferred prey), leeches, ostracods, copepods, snails, finger clams,
beetle larva, mosquitoes, worms, mosquitoes, water mites, spiders,
tiny mollusks, crustaceans, young amphibians and anuran/caudata
eggs (Conant and Collins 1991;
Petranka 1998a), |
Larvae
Larval mainly feed on invertebrates (Petranka 1998a). They also will
ingest molted skin (DeGraaf and Yamasaki 2001). One beneficial characteristic
of newts is that they feed on midge and mosquito larvae, thus reducing
the numbers of these human pests (Albert and Albert-Knoop 1999).
Efts
Efts consume diet of worms, grubs and small insects. In wet years
efts forage more and thus grow faster (Ptingsten and Downs 1989).
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| PREDATION |
Adults
Adults and efts have
few predators as their skin is toxic. Brightly colored adults tend
to be more toxic than brownish efts, which is an example of batesian
mimicry (Petranka 1998a). Gill (1978c) reported that adult newts
in some area are severely attacked by amphibian blood leeches; he
found that the newts will exit the ponds temporality during the
summer to rid themselves of the leeches.
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Larvae
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| CONSERVATION CONCERNS |
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According to Petranka (1998a) newts were one of the few species whose
population may have increased as a result of European colonization.
Newts thrive in heavily vegetated farm ponds, which apparently provides
cover from predatory fish. Farm ponds increased dramatically with increased
colonization; therefore, presumably newt populations increased as well.
However, as southern New England has reforested with the abandonment
of extensive agricultural fields, newt habitat has seemingly declined.
In Maine, where large areas of forest are clear-cutted, newts
appear to be less sensitive than other amphibian species to forest
fragmentation (DeMaynadier and Hunter 1998). However, our ongoing
research suggests that they may be extirpated from urban areas
in the state (Paton and Egan 2001). Presumably, habitat fragmentation
and roads have a negative impact on these species, as the eft
stage is so critical to maintaining metapopulations (Gill 1978).
These anthropogenic habitat changes may provide significant dispersal
barriers that prevent dispersal among breeding ponds and to eventual
extirpation from isolated breeding ponds. Klemens (1993) felt
that newt populations in eastern Connecticut were threatened by
increased suburbanization of the region.
In another study, Robinson (1993)
found newts to be less stressed by acid rain than other amphibians,
apparently because they can regulate their sodium balance.
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