Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition To List the Striped Newt as Threatened, 32911-32929 [2011-13911]

Download as PDF Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules Authority: 49 U.S.C. 31133, 31136, 31151, and 31502; and 49 CFR 1.73. Fish and Wildlife Service 4. Revise § 396.11(b) to read as follows: 50 CFR Part 17 § 396.11 Driver vehicle inspection report(s). [Docket No. FWS–R4–ES–2010–0007; MO 92210–0–0008 B2] * * * * * (b) Report content. (1) The report shall identify the vehicle and list any defect or deficiency discovered by or reported to the driver that would affect the safety of operation of the vehicle or result in its mechanical breakdown. (2) For vehicles other than intermodal equipment tendered by intermodal equipment providers, if no defect or deficiency is discovered by or reported to the driver, the written report shall so indicate. (3) For intermodal equipment tendered by intermodal equipment providers, if no defects or deficiencies are discovered by or reported to the driver, no written report is required. (4) In all instances where a written driver vehicle inspection report is required, the driver shall sign the report. On two-driver operations, only one driver needs to sign, provided both drivers agree as to the defects or deficiencies identified. If a driver operates more than one vehicle during the day, a report shall be prepared for each vehicle operated. * * * * * 5. Revise § 396.12(b)(4) to read as follows: § 396.12 Procedures for intermodal equipment providers to accept reports required by § 390.42 (b) of this chapter. * * * * (b) * * * (4) All damage, defects, or deficiencies of the intermodal equipment must be reported to the equipment provider by the motor carrier or its driver. If no defect or deficiency in the intermodal equipment is discovered by or reported to the driver, no written report is required. * * * * * emcdonald on DSK2BSOYB1PROD with PROPOSALS * Issued on: May 27, 2011. Anne S. Ferro, Administrator, FMCSA. [FR Doc. 2011–13935 Filed 6–6–11; 8:45 am] BILLING CODE 4910–EX–P VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 DEPARTMENT OF THE INTERIOR Endangered and Threatened Wildlife and Plants; 12-Month Finding on a Petition To List the Striped Newt as Threatened Fish and Wildlife Service, Interior. ACTION: Notice of 12-month petition finding. AGENCY: We, the U.S. Fish and Wildlife Service (Service), announce a 12-month finding on a petition to list the striped newt (Notophthalmus perstriatus) as threatened under the Endangered Species Act of 1973, as amended (Act). After review of all available scientific and commercial information, we find that listing the striped newt as endangered or threatened is warranted. Currently, however, listing the striped newt is precluded by higher priority actions to amend the Lists of Endangered and Threatened Wildlife and Plants. Upon publication of this 12-month petition finding, we will add the striped newt to our candidate species list. We will develop a proposed rule to list the striped newt as our priorities allow. We will make any determination on critical habitat during development of the proposed listing rule. During any interim period, we will address the status of the candidate taxon through our annual Candidate Notice of Review (CNOR). DATES: The finding announced in this document was made on June 7, 2011. ADDRESSES: This finding is available on the Internet at http:// www.regulations.gov at Docket Number FWS–R4–ES–2010–0007. Supporting documentation we used in preparing this finding is available for public inspection, by appointment, during normal business hours at the U.S. Fish and Wildlife Service, North Florida Field Office, 7915 Baymeadows Way, Suite 200, Jacksonville, FL 32256. Please submit any new information, materials, comments, or questions concerning this finding to the above street address. FOR FURTHER INFORMATION CONTACT: Dave Hankla, Field Supervisor, North Florida Field Office (see ADDRESSES); by telephone at (904) 731–3336; or by facsimile at (904) 731–3045. If you use a telecommunications device for the SUMMARY: PO 00000 Frm 00034 Fmt 4702 Sfmt 4702 32911 deaf (TDD), please call the Federal Information Relay Service (FIRS) at 800–877–8339. SUPPLEMENTARY INFORMATION: Background Section 4(b)(3)(B) of the Act (16 U.S.C. 1531 et seq.) requires that, for any petition to revise the Federal Lists of Threatened and Endangered Wildlife and Plants that contains substantial scientific or commercial information that listing a species may be warranted, we make a finding within 12 months of the date of receipt of the petition. In this finding, we determine whether the petitioned action is: (a) Not warranted, (b) warranted, or (c) warranted, but immediate proposal of a regulation implementing the petitioned action is precluded by other pending proposals to determine whether species are threatened or endangered, and expeditious progress is being made to add or remove qualified species from the Federal Lists of Endangered and Threatened Wildlife and Plants. Section 4(b)(3)(C) of the Act requires that we treat a petition for which the requested action is found to be warranted but precluded as though resubmitted on the date of such finding, that is, requiring a subsequent finding to be made within 12 months. We must publish these 12month findings in the Federal Register. Previous Federal Actions On July 14, 2008, we received a petition dated July 10, 2008, from Dr. D. Bruce Means, Ryan C. Means, and Rebecca P.M. Means of the Coastal Plains Institute and Land Conservancy (CPI), requesting that the striped newt (Notophthalmus perstriatus) be listed as threatened under the Act. Included in the petition was supporting information regarding the species’ taxonomy, biology, historical and current distribution, and present status, as well as a summary of actual and potential threats. We acknowledged the receipt of the petition in a letter to petitioners dated August 15, 2008. In that letter we also stated that we could not address their petition at that time because responding to existing court orders and settlement agreements for other listing actions required nearly all of our listing funding. Funding became available to begin processing the petition in early 2010. On March 23, 2010, we published a 90day finding (75 FR 13720) that the petition presented substantial information indicating that listing the striped newt may be warranted and that we were initiating a status review, for which we would accept public comments until May 24, 2010. This E:\FR\FM\07JNP1.SGM 07JNP1 32912 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules notice constitutes the 12-month finding on the July 14, 2008, petition to list the striped newt as threatened. emcdonald on DSK2BSOYB1PROD with PROPOSALS Species Information Our 90-day finding summarized much of the current literature regarding the striped newt’s distribution, habitat requirements, and life history, and may be reviewed for detailed information (75 FR 13720, March 23, 2010). Below, we briefly summarize previously presented information, and provide new information that we believe is relevant to understanding our analysis of the factors affecting the striped newt. Taxonomy and Species Description There are three species of Notophthalmus found in North America. These include the eastern red spotted newt (N. viridescens), the blackspotted newt (N. meridionalis), and the striped newt (N. perstriatus). The three species are found in different areas throughout the United States and Mexico (Reilly 1990, p. 51). Reilly (1990, p. 53), in his study of Notophthalmus spp., found that N. perstriatus and N. meridionalis are distinct species that are more similar and phylogenetically more closely related than either is to N. viridescens. In 2008, Zhang et al. (2008, pp. 586 and 592) looked at the phylogenetic relationship (i.e., evolutionary history of an organism) of the family Salamandridae and found that the clade (i.e., group of species that includes all descendents of a common ancestor) containing newts was separate from the clade containing ‘‘true’’ salamanders. The branching order of the clades for newts are: Primitive newts (Echinotriton, Pleurodeles, and Tylototriton), New World newts (Notophthalmus and Taricha), CoriscaSardinia newts (Euproctus), modern European newts (Calotriton, Lissotriton, Mesotriton, Neurergus, Ommatotriton, and Triturus), and modern Asian newts (Cynops, Pachytriton, and Paramesotriton). New World newts, which include Notophthalmus, originally evolved from salamandrids migrating from Europe to North America via the North Atlantic land bridge during the Mid-Late Eocene (Zhang et al. 2008, p. 595). Another genetic study, conducted in 2010, looked at whether populations of Notophthalmus perstriatus that occur in two regions separated by 125 kilometers (km) (78 miles (mi)) exhibit genetic and ecological differentiation showing that these two regions are separate conservation units (Dodd et al. 2005, p. 887; Dodd and LaClaire 1995, p. 42; Franz and Smith 1999, p. 12; Johnson VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 2001, pp. 115–116; May et al. undated, unpublished report). One region consists of populations located in peninsular Florida and southeastern Georgia, and the other region consists of populations located in northwestern Florida and southwestern Georgia (Dodd and LaClaire 1995, p. 42; Franz and Smith 1999, p. 13). May et al. (2010, undated, unpublished report) found that there is gene flow between localities within each region, but none were shared between regions. Johnson (2001, pp. 107, 113–115) found genetic exchange between populations is minimal or nonexistent due to upland habitat fragmentation that has limited long-distance dispersals and restricted gene flow. In 2001, Johnson (2001, p. 115) found there was enough genetic divergence to show that the western region is different than the eastern regions. However, May et al. (2010, unpublished report) did not find that there was sufficient genetic divergence to support splitting eastern and western regions into separate species. May et al. (2010, unpublished report) ran niche-based distribution models that showed that there were significant climatic and environmental differences between the two regions when considering temperature and precipitation. The western region is characterized by lower mean temperatures and more extreme winter cold, coupled with higher variation in temperature and precipitation. These differences in temperatures and precipitation between the regions should be considered if translocation between regions is to be used for conservation of this species. Understanding genetic structure and species ecology will ensure that genetically similar individuals are moved between areas with similar environmental conditions. Life History and Biology Life-history stages of the striped newt are complex, and include the use of both aquatic and terrestrial habitats throughout their life cycle. Striped newts are opportunistic feeders that prey on frog eggs, worms, snails, fairy shrimp, spiders, and insects (adult and larvae) that are of appropriate size (Dodd et al. 2005, p. 889; Christman and Franz 1973, pp. 134–135; Christman and Means 1992, pp. 62–63). Christman and Franz (1973, p. 135) found that newts were attracted to frog eggs by smell. Feeding behavior of newts has only been documented with aquatic adults; little is known of the feeding habits in the terrestrial stage (Dodd et al. 2005, p. 889). PO 00000 Frm 00035 Fmt 4702 Sfmt 4702 Aquatic and breeding adults occur in isolated, temporary ponds associated with well-drained sands. Sexually mature adults migrate to these breeding ponds, which lack predatory fish, and courtship, copulation, and egg-laying take place there. Females lay eggs one at a time and attach them to aquatic vegetation or other objects in the water. It may take one female several months to lay all of her eggs (Johnson 2005, p. 94). Eggs hatch and develop into externally-gilled larvae in the temporary pond environment. Once larvae reach a size suitable for metamorphosis, they may either undergo metamorphosis and exit the pond as immature, terrestrial efts, or remain in the pond and eventually mature into gilled, aquatic adults (paedomorphs) (Petranka 1998, pp. 449– 450; Johnson 2005, p. 94). The immature, terrestrial efts migrate into the uplands where they mature into terrestrial adults. Efts will remain in the uplands until conditions are appropriate (adequate rainfall) to return to the ponds to reproduce. Johnson (2005, p. 94) found that 25 percent of larvae became paedomorphs at his study pond. Paedomorphs will postpone metamorphosis until after they have matured and reproduced. At about a year old, they will reproduce, metamorphose, and migrate into the uplands adjacent to the pond (Johnson 2005, pp. 94–95). Once there are proper conditions (e.g., adequate rainfall) at the ponds, the terrestrial adults will move back to the ponds to court and reproduce. Once they return to the ponds, they are referred to as aquatic adults. Striped newts as well as other Notophthalmus spp. have long lifespans (approximately 12 to 15 years) in order to cope with unfavorable stochastic environmental events (e.g., drought) that can adversely affect reproduction (Dodd 1993b, p. 612; Dodd et al. 2005, p. 889; Wallace et al. 2009, p. 139). Movement of striped newts by both emigration and immigration occurs between ponds and surrounding uplands. Adult newts immigrate into ponds from uplands during the fall and winter months, but some newts also immigrate during the spring and summer months as well, when environmental conditions (e.g., adequate rainfall) are conducive to breeding (Johnson 2005, p. 95). Extended breeding periods allow striped newts to adapt to temporary breeding habitats whose conditions fluctuate within seasons (Johnson 2002, p. 395). Even with suitable water levels in ponds, adults emigrate back into uplands after breeding. There is a E:\FR\FM\07JNP1.SGM 07JNP1 emcdonald on DSK2BSOYB1PROD with PROPOSALS Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules staggered pattern of adult immigration into ponds and eft emigration into uplands due to the required 6 months for larvae to undergo metamorphosis into efts (Johnson 2002, p. 397). Suitability of upland habitat around breeding ponds influences the pattern of immigration and emigration of newts and directional movements (Dodd 1996, p. 46; Dodd and Cade 1998, p. 337; Johnson 2003, p. 16). Dodd and Cade (1998, p. 337) found that striped newts migrated in a direction that favored high pine sandhill habitats. Newts migrate into terrestrial habitats at significant distances from their breeding ponds. Dodd (1996, p. 46) found that 82.9 percent of 12 wetland breeding amphibians (including striped newts) were captured 600 meters (m) (1,969 feet (ft)) from the nearest wetland, and only 28 percent of amphibians were captured less than 400 m (1,300 ft) from the wetland. Johnson (2003, p. 18) found that 16 percent of striped newts in his study migrated more than 500 m (1, 600 ft) from ponds. Dodd and Cade (1998, p. 337) showed that striped newts travelled up to 709 m (2,330 ft) from ponds. These long-distance movements of striped newts from breeding ponds to terrestrial habitats suggest that buffer zones around ponds should be established to protect upland habitats, as well as breeding ponds (Dodd 1996, p. 49; Dodd and Cade 1998, p. 337, Johnson 2003, p. 19; Kirkman et al. 1999, p. 557; Semlitsch and Bodie 2003, p. 1219). Trenham and Shaffer (2005, p. 1166) found that protecting at least 600 m (2,000 ft) of upland habitat would maintain a population with only a 10 percent reduction in mean population size in the California tiger salamander (Ambystoma californiense). Dodd and Cade (1998, p. 337) suggested that terrestrial buffer zones need to consider both distance and direction (migratory patterns) when created. Johnson (2003, p. 19) recommended a protected area extending 1,000 m (3,300 ft) from a breeding site as upland ‘‘core habitat’’ surrounding breeding ponds. Optimal pond hydrology is important for maintaining the complex life-history pathways of striped newts. If there is not enough water in ephemeral ponds, then larvae will not have enough time to reach the minimum size needed for metamorphosis and will die as ponds dry up (Johnson 2002, p. 398). However, permanent ponds could support predatory fish that feed on aquaticbreeding amphibians (Johnson 2005, p. 94; Moler and Franz 1987, p. 235). Variable hydroperiods in breeding ponds over a long time period could result in varying reproductive success. Dodd (1993, p. 610) found a decline in VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 striped newts due to persistent drought conditions. Johnson (2002, p. 399) found that heavy rainfall in the winter of 1997 to spring of 1998 filled ponds to their maximum depth and contributed to the reproductive success at these ponds. At one breeding pond, a minimum hydro-period of 139 days (Dodd 1993, pp. 609–610) was needed for larvae to reach complete metamorphosis. Larvae undergo metamorphosis into efts after a period of 6 months, and in order for larvae to mature into paedomorphs, a breeding pond must hold water for at least a year (Johnson 2005, p. 94). For a paedormorph to successfully reproduce, ponds must hold water for an additional 6 months to allow sufficient time for its larvae to undergo metamorphosis. Striped newts form metapopulations that persist in isolated fragments of longleaf pine-wiregrass ecosystems (Johnson 2001, p. 114; Johnson 2005, p. 95). Within metapopulations, ponds function as focal points for local breeding populations that experience periods of extirpation and recolonization through time (e.g., ‘‘ponds as patches’’) (Johnson 2005, p. 95; Marsh and Trenham 2001, p. 41). Striped newts typically have limited dispersal, which can lead to pond isolation when stochastic events (e.g., drought) affect rates of colonization and extinction (Marsh and Trenham 2001, p. 41). In order for striped newts to recolonize local breeding ponds within the metapopulation, newts must disperse through contiguous upland habitat (Dodd and Johnson 2007, p. 150). Protecting the connectivity between uplands and breeding ponds of diverse hydroperiods is crucial for maintaining metapopulations (Dodd and Johnson 2007, pp. 150–151; Gibbs 1993, p. 25; Johnson 2005, p. 95). Only a few ‘‘stronghold’’ locations exist, where there are multiple breeding ponds with appropriate upland habitat that allow dispersal to occur among the ponds (Johnson 2005, p. 95). These ‘‘stronghold’’ locations represent different metapopulations across the range of the striped newt (Johnson 2005, p. 95). These sites need to be protected and managed to provide long-term protection for newts. In Florida, these include Apalachicola National Forest, Ocala National Forest, Jennings State Forest, Katherine Ordway-Swisher Biological Station, and Camp Blanding Training Site. In Georgia, they are found at Joseph Jones Ecological Research Center and Fort Stewart Military Installation (Johnson 2005, p. 95; Stevenson 2000, p. 4). PO 00000 Frm 00036 Fmt 4702 Sfmt 4702 32913 Habitat Ephemeral ponds are important components of upland habitat in the southeastern United States (LaClaire and Franz 1990, p. 9). Ephemeral ponds tend to be described as small (typically less than 5 hectares (ha) (12.4 acres (ac)), isolated wetlands with a cyclic nature of drying and refilling known as hydroperiods. Ephemeral ponds can hold water at various times throughout a year to allow for reproduction. Precipitation is the most important water source for ephemeral ponds (LaClaire and Franz 1990, p. 12). The cyclical nature of ephemeral ponds prevents predatory fish from inhabiting breeding ponds (Dodd and Charest 1988, pp. 87, 94; LaClaire and Franz 1990, p. 12; Moler and Franz 1987, p. 237). Ephemeral ponds are biologically unique, because they support diverse species that are different than species found in larger, more permanent wetlands or ponds (Moler and Franz 1987, pp. 234, 236; Kirkman et al. 1999, p. 553). The frequency and duration of water in ephemeral ponds creates different zones of vegetation within ponds. One species, maidencane (Panicum hemitomon), has been found at ephemeral ponds where striped newts have been found, and seems be a good indicator of the extent of previous flooding in ponds (LaClaire 1995, p. 88; LaClaire and Franz 1990, p. 10). Persistence of maidencane helps to reduce the rate of oxidation of organic matter, reduce soil moisture loss, and inhibit growth and establishment of upland plant species (LaClaire 1995, p. 94). The center of flooded ponds may contain floating-leaved plants, and is surrounded by vegetation with submerged roots growing along the wet edges. Surrounding the wet areas are tall and short emergents, such as sedges, grasses, and rushes such as sandweed (Hypericum fasciculatum), followed by other grasses such as bluestem grass (Andropogon virginicus) found in the drier margins of ponds. Water-tolerant shrubs or trees are found in some transitional zones between pond and uplands (LaClaire 1995, p. 74; LaClaire and Franz 1990, p. 10). Ephemeral ponds are surrounded by upland habitats of high pine, scrubby flatwoods, and scrub (Christman and Means, 1992, p. 62). Longleaf pineturkey oak stands with intact ground cover containing wiregrass (Aristida beyrichiana) are the preferred upland habitat for striped newts, followed by scrub, then flatwoods (K. Enge, Florida Fish and Wildlife Conservation E:\FR\FM\07JNP1.SGM 07JNP1 32914 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules emcdonald on DSK2BSOYB1PROD with PROPOSALS Commission, personal communication, May 24, 2010). Striped newt habitat is firedependent, and naturally ignited fires and prescribed burning maintain an open canopy and reduce forest floor litter. An open canopy provides sunlight necessary for ground cover growth needed by newts for foraging and sheltering. Fire is also an important factor for wetland vegetation (LaClaire and Franz 1990, p. 10; Means 2008, p. 4). Historically, fire would be naturally ignited in the uplands during the late spring and early summer, and would sweep through the dry pond basins, reducing organic matter and killing encroaching upland plant species (Means 2008, p. 4; Myer 1990, p. 189). Lack of fire in uplands that buffer breeding ponds allows fire-intolerant hardwoods to shade out herbaceous understory needed by striped newts for foraging and sheltering. As a result, fire shadows may form along the upslope wetland and upland boundary. The vegetation in this area contains fireintolerant evergreen shrubs (Ilex spp., Vaccinium spp., Myrica spp., and Ceratiola spp.) and sometimes xeric oak hammock zones (LaClaire and Franz 1990, p. 11). Ponds that are completely burned from the upland margin to the opposite margin lack this vegetation; however, if the ponds are filled with water, fire will burn out at the pond, and allow the invasion of fire-intolerant hardwoods (LaClaire and Franz 1990, p. VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 11). The impacts of fire on these temporary ponds promote species richness of grasses and sedges, especially during droughts (Means 2006, p. 196). To eliminate hardwood encroachment, a prescribed fire regime should be used every 1 to 3 years during May to June, in order to protect striped newt habitat (Means 2006, p. 196). Striped newts use upland habitats that surround breeding ponds to complete their life cycle. Efts move from ponds to uplands where they mature into terrestrial adults. The uplands also provide habitat for the striped newt to forage and burrow during the nonbreeding season (Dodd and Charest 1988, p. 95). Striped newts also use uplands to access alternative ponds that are needed if the original breeding pond is destroyed or the hydroperiod is altered (Means 2006, p. 197). This shows the interdependence between upland and aquatic habitats in the persistence of populations (Semlitsch and Bodie 2003, p. 1219). Semi-aquatic species (such as the striped newt) depend on both aquatic and upland habitats for various parts of their life cycle in order to maintain viable populations (Dodd and Cade 1998, pp. 336–337; Johnson 2001, p. 47; Semlitsch 1998, p. 1116; Semlitsch and Bodie 2003, p. 1219). Distribution The range of the striped newt extends from the Atlantic Coastal Plain of PO 00000 Frm 00037 Fmt 4702 Sfmt 4702 southeastern Georgia to the northcentral peninsula of Florida and through the Florida panhandle into portions of southwest Georgia (Dodd et al. 2005, p. 887). There is a 125-km (78-mi) separation between the western and eastern portions of the striped newt’s range (Dodd et al. 2005, p. 887; Dodd and LaClaire 1995, p. 42; Franz and Smith 1999, p. 12; Johnson 2001, pp. 115–116). The historical range of the striped newt was likely similar to the current range (Dodd et al. 2005, p. 887). However, loss of native longleaf habitat, fire suppression, and the natural patchy distribution of upland habitats used by striped newts have resulted in fragmentation of existing populations (Johnson and Owen 2005, p. 2). In Figure 1, we provide a map illustrating the current and historical ranges of the striped newt on public lands. The dark-shaded areas represent the currently occupied sites documented from 2005 to 2010 surveys of public lands (Enge, FWC, personal communication, 2010; Jensen, Georgia Department of Natural Resources (GDNR), personal communication, 2010). The light-shaded areas represent the historical range where striped newts are now extirpated. There are from 1 to 30 breeding ponds documented within dark shaded areas. However, due to the scale of the map, the specific ponds are not identified. This map represents the best available information used to establish the species’ range. E:\FR\FM\07JNP1.SGM 07JNP1 To determine where there may be additional unsurveyed suitable habitat for striped newts in Florida, Endries et al. (2009, pp. 45–46) developed a striped newt habitat model. The model was developed using Florida Fish and Wildlife Conservation Commission (FWC) 2003 landcover classes. Three classes were identified: (1) Breeding (bay, cypress swamp, freshwater marsh, wet prairie), (2) primary upland (sandhill, xeric oak scrub, sand pine scrub), and (3) secondary upland (hardwood hammocks and forests, pinelands, and shrub and brushlands). Then potential habitat was evaluated for each class. Breeding habitat was limited to patches that were less than 9 ha (22 ac) in size and which were contiguous with upland habitats. The primary upland habitats included in the model were those areas contiguous and within 1,000 m (3,300 ft) of breeding habitat. Secondary upland habitat was included for areas that were contiguous and within 500 m (1,600 ft) of primary uplands and 1,000 m (3,300 ft) of breeding habitat. VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 The GIS analysis found a total of 244,576 ha (604,360 ac) of potential habitat (Endries et al. 2009, p. 45). Of the potential habitat, 122,724 ha (303,257 ac) occurred on 124 sites within public lands, but only 64 of these sites had greater than 40 ha (100 ac) of potential habitat. The remaining habitat was found on privately owned lands in patches that were greater than 79 ha (195 ac) (Endries et al. 2008, pp. 45–46). Of the potential habitat found on public lands, 55 percent occurred on Ocala National Forest (ONF), 8 percent on Camp Blanding Military Installation, 6 percent on Withlacoochee State Forest, 5.3 percent on Apalachicola National Forest (ANF), and 2.9 percent on Jennings State Forest (Enge, FWC, personal communication, 2010). However, no records of striped newt occurrences have been found at Withlacoochee State Forest, even though this appears to be suitable habitat. Ocala National Forest has 67,514 ha (166,831 ac) of potential habitat and 39 occupied ponds, making it the largest ‘‘stronghold’’ for metapopulations for striped newts in PO 00000 Frm 00038 Fmt 4702 Sfmt 4702 32915 Florida (Enge, FWC, personal communication, 2010). Striped newts are also found in ponds throughout Peninsular Florida at Ordway-Swisher Biological Station, Camp Blanding Joint Training Center, Jennings State Forest, Goethe State Forest, Rock Springs State Park, Ft. White Mitigation Park, FaverDykes State Park, and Pumpkin Hill Creek Preserve State Park. Within the panhandle of Florida, striped newts have been found within the Munson Sandhills. This site represents a small physiographic region within the Gulf Coastal Plains in Florida (Means and Means 1998a, p. 3). Striped newts have only been located in the western portion of the Munson Sandhills within the ANF. No newts have been found in the eastern portion of the sandhills since the 1980s, when the area was converted to a dense sand pine (Pinus clausa) plantation (Means and Means 1998a, p. 6). Striped newt distribution continues north of this site to the Tallahassee Red Hills and Tifton Uplands, and finally to the Dougherty Plain in southwestern Georgia. However, the Tallahassee Red Hills no E:\FR\FM\07JNP1.SGM 07JNP1 EP07JN11.009</GPH> emcdonald on DSK2BSOYB1PROD with PROPOSALS Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules 32916 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules emcdonald on DSK2BSOYB1PROD with PROPOSALS longer support the newt. Striped newts were documented once in a breeding pond found in the Red Hills, but this site was dredged, deepened, and stocked with game fish in the 1980s, and no longer supports newts (Means and Means 1998b, pp. 6, 15). The striped newt is currently known to occur in five separate locations in Georgia, including Fort Stewart, Lentile Property, Joseph W. Jones Ecological Research Center (JJERC), Fall Line Sandhills Natural Area, and Ohoopee Dunes Natural Area (J. Jensen, GDNR, personal communication, September 14, 2010; L. Smith, JJERC, personal communication, September 11, 2010; Stevenson 2000, p. 4; Stevenson and Cash 2008, p. 252; Stevenson et al. 2009a, pp. 2–3). Most of these locations are within the Dougherty Plain (Baker Co.), Tifton Uplands (Irwin, Lanier, and Lowndes Counties), and the Barrier Island Sequence (Bryan, Camden, Charlton, Evans, and Long Counties) (Dodd and LaClaire 1995, pp. 40–42). From 1993 to 1994, Dodd and LaClaire (1995, p. 40) found striped newts in one pond each at five sites in Irwin, Baker, and Charlton Counties, and a series of ponds at Ft. Stewart in Bryan and Evans Counties. A pond in Baker County at JJERC was found to be a new location, and extends the known range west of the Flint River approximately 115 km (71 mi) farther from the nearest recorded site (LaClaire et al. 1995, pp. 103–104; Franz and Smith 1999, p. 13). Striped newts were first found on Trail Ridge in 1924 near Okefenokee National Wildlife Refuge (ONWR), but this area has been highly modified since the 1940s (Dodd 1995, p. 44; Dodd and LaClaire 1995, pp. 39–40), and newts are no longer found in this area, except for possibly in the ONWR. In 2008, a new striped newt site was found in Georgia in Camden County, which is the first record for this county since 1953 (Stevenson et al. 2009b, p. 248). Population Status and Trends Surveys have been conducted for striped newts at many sites within Florida and Georgia. These surveys have found that the number of known occupied sites has declined and occupied sites are limited to just a few counties. However, historical information on the location of striped newts is difficult to confirm, as most of these sites underwent substantial land use changes since newts were first collected (Dodd et al. 2005, p. 887). Franz and Smith (1999, p. 8) reviewed 100 records from 20 counties in Florida between 1922 and 1995, and conducted surveys between 1989 and 1995. They found that 4 historical ponds had newts, VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 but also found 34 new ponds containing newts were that were not part of the historical records. All 38 breeding ponds were found on 7 public lands that included ANF, Camp Blanding Military Reservation, Favor-Dykes State Park, Jennings State Forest, Katharine Ordway Preserve-Swisher Memorial Sanctuary, ONF, and Rock Springs State Preserve (Franz and Smith, 1999, pp. 8–9). Johnson and Owen (2005, p. 7) visited 51 sites in 11 counties in Florida from 2000 to 2003 that overlapped with the sites visited by Franz and Smith. They found that of 51 sites visited (totaling 64 ponds), only 26 ponds and adjacent upland habitat had excellent habitat quality (e.g., multiple ephemeral ponds surrounded by fire-maintained native uplands) capable of supporting striped newts. Only 4 of these 26 sites had multiple breeding ponds needed to comprise metapopulations. They were found in Clay, Marion, and Putnam Counties in Camp Blanding Military Reservation (Clay), Jennings State Forest (Clay), Ocala National Forest (Marion), and Katherine Ordway Preserve-Swisher Memorial Sanctuary (Putnam) (Johnson and Owen 2005, p. 7). From 2005 to 2010, Enge (FWC, personal communication, 2010) surveyed ponds in suitable habitat on 32 conservation lands in Florida. He found breeding ponds with newts in 58 ponds on 11 of the 32 conservation lands. He also found that although newts had a wider range in Florida than Georgia, they remained abundant only on public lands in Clay, Marion, and Putnam Counties. This is consistent with the surveys conducted by Franz and Smith (1999, pp. 8–9) and Johnson and Owen (2005, p. 7). He found that there were a total of 49 extant populations known from the peninsula of Florida and 7 populations from the panhandle. An isolated breeding pond farther than 1,000 m (3,300 ft) from the closest other breeding pond represents a separate population (Enge, FWC, personal communication, 2010). The striped newt metapopulations (i.e., multiple breeding ponds with enough upland to allow for dispersal) are now only found on public lands in Clay, Putnam, and Marion Counties. Populations still exist in 10 other counties in Florida, but these counties have fewer than 3 breeding ponds and these populations are considered vulnerable to extirpation (Enge, FWC, personal communication, 2010). The status of the striped newt is unknown on private lands due to the difficulty in accessing these lands; however, Enge (FWC, personal communication, 2010) was able to PO 00000 Frm 00039 Fmt 4702 Sfmt 4702 survey 8 ponds on 2 private lands, and found newts on at least one site. Striped newt breeding ponds at ANF and other areas within the Munson Sandhills region in Leon County, Florida, have seen a decline. ANF was once considered a metapopulation for striped newt (Johnson 2005, p. 95; Johnson and Owen 2005, p. 7; Enge, FWC, personal communication, 2010). However, the western Munson Sandhills in ANF was surveyed from 1995–2007, and researchers were only able to locate 18 breeding ponds (containing larvae or breeding adults) in 265 ephemeral ponds surveyed (Means and Means 1998a, p. 5). Means et al. (2008, p. 6) found only 5 adult striped newts and no larvae in the past 10 years. Since 2000, severe drought conditions were experienced at these ponds, and newts were shown to be declining. Recent surveys conducted in the Munson Sandhills in 2010 were not able to locate any striped newts at any of the breeding ponds (Means, CPI, personal communication, 2010). The precipitous apparent declines now being seen at ANF could occur elsewhere on protected lands within the striped newt’s range, despite the protection of habitat. This indicates that perhaps other threats (e.g., disease and drought) may continue to act on the species at these sites. As mentioned above, striped newts have only been found at five locations in Georgia, and these sites are highly fragmented and isolated (Stevenson 2000, p. 4). An amphibian survey on 196 ephemeral ponds in 17 counties on timber company lands in the Coastal Plain of southeastern Georgia did not locate any striped newts in Georgia; however, striped newts were found in four ponds in Florida (Wigley 1999, pp. 5–10). Stevenson (2000, p. 3) looked at 25 historic striped newt localities in Georgia and was only able to find 2 sites (8 percent) that had multiple breeding ponds and upland habitat that would support striped newt populations. As of 2010, only 2 properties in the State are known to support viable populations: JJERC and Fort Stewart Army Base (Jensen, GDNR, personal communication, 2010; Stevenson et al. 2009a, p. 2). The Fort Stewart population lies within the range of the eastern genetic group on the Atlantic Coastal Plain and was represented by approximately 10 known wetlands. Since 2002, striped newts have been found at only one wetland at Fort Stewart (Stevenson et al. 2009, p. 2). The JJERC population lies within the range of the western genetic group on the Gulf Coastal Plain, and is represented by 5 known wetlands. In E:\FR\FM\07JNP1.SGM 07JNP1 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules emcdonald on DSK2BSOYB1PROD with PROPOSALS annual surveys from 2002 to 2010, researchers confirmed striped newts from only 3 of these 5 known wetlands (Smith, JJERC, personal communication, 2010). Evidence suggests that both the eastern and western striped newt populations in Georgia are rare and declining. Most suitable striped newt habitat in Georgia has been lost to development or converted to pine plantations and silviculture (Dodd and LaClaire 1995, p. 43). Summary of Information Pertaining to the Five Factors Section 4 of the Act (16 U.S.C. 1533) and its implementing regulations (50 CFR 424) set forth procedures for adding species to the Federal Lists of Endangered and Threatened Wildlife and Plants. Under section 4(a)(1) of the Act, a species may be determined to be endangered or threatened based on any of the following five factors: (A) The present or threatened destruction, modification, or curtailment of its habitat or range; (B) Overutilization for commercial, recreational, scientific, or educational purposes; (C) Disease or predation; (D) The inadequacy of existing regulatory mechanisms; or (E) Other natural or manmade factors affecting its continued existence. In making this finding, information pertaining to the striped newt in relation to the five factors provided in section 4(a)(1) of the Act is discussed below. In considering whether a species may warrant listing under any of the five factors, we look beyond the species’ exposure to a potential threat or aggregation of threats under any of the factors, and evaluate whether the species responds to those potential threats in a way that causes actual impact to the species. The identification of threats that might impact a species negatively may not be sufficient to compel a finding that the species warrants listing. The information must include evidence indicating that the threats are operative and, either singly or in aggregation, affect the status of the species. Threats are significant if they drive, or contribute to, the risk of extinction of the species, such that the species warrants listing as endangered or threatened, as those terms are defined in the Act. Factor A. The Present or Threatened Destruction, Modification, or Curtailment of Its Habitat or Range Striped newts have been found to use both aquatic and upland habitats throughout their life cycle. Most of these VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 habitats have been destroyed or modified in the past due to: (1) Conversion of habitat to intensely managed, planted pine plantations or naturally regenerated stands (Dodd 1995b, p. 129; Wear and Greis 2002, p. 46); (2) loss of habitat resulting from urban development (Zwick and Carr 2006, pp. 4–6); (3) degradation of habitat due to fire suppression (Means 2008, pp. 27–28); and (4) degradation of the habitat by the use of off-road vehicles and road construction (Means 1996, p. 2; Means 2001; p. 31, Means 2003 p. 6; Means et al. 1994a., pp. 5–6). Natural Pine Forest Conversion Natural pine forests (i.e., longleaf pine forest) that once were found from southeastern Virginia through eastern Texas have declined to about 13 million ha (33 million ac), and planted pine plantations increased to more than 12 million ha (30 million ac) by 1999 (Dodd 1995b., p. 129; Wear and Greis 2002, p. 46). There are presently about 11 million ha (27 million ac) of managed pine plantations where natural longleaf pines were once found (Frost 2006, p. 36). Within the longleaf pine ecosystem in the South’s coastal plains, only 2.2 percent of the original range exists (Frost 2006, p. 13; Wear and Greis 2002, p. 66). Between 1936 and 1989, longleaf pine forests within the range of the striped newt in Florida decreased from more than 3 million ha (7.6 million ac) to only 384,500 ha (950,000 ac), an 88 percent decrease (Dodd 1995b., p. 129). Longleaf pine forest in Georgia declined 36 percent between 1981 and 1988 (Dodd 1995b., p. 129). Habitat loss from the conversion of natural pine forests to intensely managed, planted pine plantations has greatly disrupted the dispersal of striped newts between breeding ponds and upland habitat. Means and Means (1998a, p. 6) found that striped newt habitat at the Munson Sandhills varied due to differences in silvicultural practice between the eastern and western portions of the Sandhills. In the western portion of the Sandhills found within ANF, native groundcover remains in the second-growth longleaf pine forests, where striped newts spend most of their adult life. However, the eastern portion of the Munson Sandhills has been clear-cut and roller-chopped, and planted in sand pine (Pinus clausa), which is now a closed canopy with little native groundcover. Surveys of ponds located in the eastern Munson Sandhills found no striped newts after the site was converted to sand pine plantations (Means and Means 1998a, p. 4; Means and Means 2005, pp. 58–59; Means 2008, p. 30). PO 00000 Frm 00040 Fmt 4702 Sfmt 4702 32917 Silvicultural practices, including mechanical site preparation, pond ditching, soil disturbance, and the use of fertilizer and herbicides, can interfere with migration and successful reproduction (Dodd 1995b, p. 130; Dodd and LaClaire 1995, pp. 43–44; Means and Means 2005, pp. 59–60; Means 2008, p. 29). Pond ditching, which is used to drain ponds to create ideal conditions for silvicultural operations, is detrimental to striped newts, because it alters pond hydrology and facilitates predatory fish movement into otherwise fishless ponds (Means 2008, p. 30). Ditching creates a shortened hydroperiod, reducing the amount of time striped newts have to undergo metamorphosis, which can eventually decrease the number of reproducing adults (Means 2008, p. 31). Urban Development Alteration of upland habitat to urban development can create habitat fragmentation and loss of metapopulations of striped newts. In 10 coastal Georgia counties, the human population is expected to increase 51 percent by 2030 (Center for Quality Growth and Regional Development 2006, p. 4), but no estimate of impact on native habitats was provided. Striped newts have been found within 5 of these counties in Georgia, including Bryan, Camden, Long, Liberty, and Screven Counties (Franz and Smith 1999, p. 13, Stevenson 2000, pp. 6–7). Zwick and Carr (2006, pp. 4–6) modeled human population growth in Florida, and concluded that 2.8 million ha (7 million ac) of land will be converted to urban use by 2060. Of the 2.8 million ha (7 million ac), they estimated that about 1.1 million ha (2.7 million ac) of native habitat would be destroyed to accommodate urban development (Zwick and Carr 2006, p. 2). It is predicted that more than 800,000 ha (2 million ac) of native habitat in Florida will be developed by 2060 within a mile of public conservation lands (Zwick and Carr 2006, p. 19; FWC 2008, p. 8). Urban sprawl where newts occur will fragment striped newt ponds from upland habitats. This will limit movement of newts between breeding ponds and make them more vulnerable to extinction, as the genetic viability of the newts declines (FWC 2008, p. 8). Powerlines and natural gas rights-ofways impact groundcover associated with longleaf pine adjacent to breeding ponds, creating barriers to dispersal and eventually decreasing populations (Means 2001, pp. 31–32). Striped newt habitat in the Tallahassee Red Hills has been impacted by urban sprawl and land conversion from 1824 to the E:\FR\FM\07JNP1.SGM 07JNP1 32918 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules emcdonald on DSK2BSOYB1PROD with PROPOSALS present, and has resulted in the extirpation of striped newts from this area (Means and Means 1998b, p. 8). Small, isolated wetlands support breeding populations of striped newts. However, small, ephemeral wetlands (less than 0.2 ha (0.5 ac)) receive no protection from development (Johnson 2003, p. 19; Dodd and Cade 1998, p. 337; see discussion under Factor D below). The loss of these small, ephemeral wetlands can potentially increase extinction rates of newts by limiting migration between ponds and corridors, thus decreasing recolonization of local populations (Gibbs 1993, pp. 25–26; LaClaire and Franz 1990, p. 13; Semlitsch and Bodie 1998, pp. 1131–1132). Green (2003, p. 341) concluded that pond-breeding amphibians, like striped newts, that have highly fluctuating populations and high frequencies of local extinctions are likely to be affected rapidly by habitat fragmentation. The loss of breeding ponds due to habitat destruction will reduce corridors and limit migration between the ponds and the uplands. Prescribed Fire Prescribed fire plays an important role in maintaining productive breeding ponds for striped newts (Kirkman et al. 1999, p. 556). Burning in dry ponds is also necessary to maintain the quality of vegetation needed for striped newts (Johnson 2005, p. 97). Fire suppression at many sites with newt breeding ponds has been concurrent with the conversion of uplands to pine plantations (Johnson 2005, p. 97). Lack of fire can result in the succession of natural pine forests converting to fireintolerant species, dominated by hardwoods (Means 2008, pp. 27–28). Wear and Greis (2002, pp. 46–47) found that 3.9 million ha (9.7 million ac) of natural pine forest throughout the Southeast were reclassified to hardwood and natural oak-pine forests. Of the remaining longleaf pine habitat in the southeast, only 0.2 percent is managed with fire and can support native longleaf pine species of plants and animals, including striped newts (Frost 2006, p. 38). The succession of natural pine forest to more shade-tolerant species, such as oaks and hickories, can result in the loss of ground cover, such as wire grass, needed by striped newts for shelter and foraging (Means 2001, p. 31). Frequencies of prescribed burns in these uplands need to take place in a 1to 3-year cycle to provide suitable habitat for striped newts (Johnson and Gjerstad 2006, pp. 287–292). This would also reduce the naturally woody components around the ephemeral ponds, and stimulate flowering of VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 grasses used by the newts along the pond margins (Means 2006, p. 196). In Florida, some public land managers do not currently have the resources to implement effective habitat management programs (Howell et al. 2003, p.10). In a questionnaire to State, Federal, and local land managers throughout Florida, the Service asked what impediments they had in effectively using prescribed fire to manage scrub, a fire-maintained ecosystem. Many respondents indicated that funding, staff, and smoke management issues substantially reduced their ability to burn (Service 2006, Excel spreadsheet; Thomson 2010, p. 12). Less than 25 percent of public land managers had been ranked as having an excellent prescribed burn program (Florida Department of Environmental Protection 2007, p. 1). On most public lands in Florida, striped newt habitat is likely to continue to degrade unless land management funding and staffing increase in the future. Off-Road Vehicles and Road Impacts Means et al. (1994, pp. 6–7; 2008, pp. 11 and 16) found that their study ponds at the Munson Sandhills in ANF offroad vehicle (ORV) use had degraded the littoral zone of the breeding ponds into barren sandy beaches unsuitable for striped newts. The littoral zone provides shallow, warm water where small aquatic invertebrates are concentrated, providing food for newts. ORV use also destroys the grasses and grass-like vegetation around the ponds needed by newts for protection from predators such as wading birds (Means et al. 2008, p. 11). In 1994, 27 of 100 ponds at ANF were found to be damaged by ORV use, including 3 of 18 striped newt ponds (Means et al. 1994, pp. 6–7). By 2006, ORV impacts were documented at nearly every pond at ANF (Means et al. 2008, p. 16). However, by 2010, the ANF closed the Munson Sandhills to ORV use to protect the striped newt ponds (Petrick, USFS, personal communication, 2010; see discussion under Factor D below). Striped newts dispersing from breeding ponds to upland habitat are also impacted by roads and highways. These impacts usually result in direct road mortality; desiccation of small, moist-bodied animals (like newts) on dry asphalt; and increased exposure of these small animals to aerial predation (Means 1996, p. 2). At one study pond in ANF, Means (2003, p. 6) found that most striped newts were emigrating and immigrating to and from the breeding pond across a major highway, U.S. 319. PO 00000 Frm 00041 Fmt 4702 Sfmt 4702 Summary of Factor A We have identified a number of threats to striped newt habitat that have resulted in the destruction and modification of habitat in the past, are continuing to threaten habitat now, and are expected to continue to threaten striped newt habitat in the future. Indications are that the loss of habitat due to conversion of natural pine forests to more intense silvicultural management regimes will continue in interior portions of the range of the striped newt. Striped newt habitat within the species’ range in Florida and Georgia is currently threatened with habitat loss and modification resulting from urban development. Habitat loss and fragmentation due to urban development and road construction is expected to continue in the future. Lack of, or inappropriate use of, prescribed fire is ongoing and likely to continue in the future, and has adverse effects on striped newt habitat and extant populations. On the basis of this analysis, we find that the destruction, modification, or curtailment of the striped newt’s habitat is currently a threat and is expected to persist and possibly escalate in the future. Because this threat is ongoing and we expect it will continue over the coming decades; we consider the threat to be imminent. However, based on the large amount of potential habitat that is currently in public ownership, and fact that most of the known striped newt ponds are on conservation lands, we believe the magnitude of this threat is moderate. Based upon our review of the best commercial and scientific data available, we conclude that the present or threatened destruction, modification, or curtailment of its habitat or range is an imminent threat of moderate magnitude to the striped newt, both now and in the foreseeable future. Factor B. Overutilization for Commercial, Recreational, Scientific, or Educational Purposes The petition provided information that striped newts were collected and sold during the 1970s and 1980s. However, in our 90-day finding (75 FR 13720, March 23, 2010), we determined that there was no evidence to support the existence of any threat under this factor. We obtained no additional information during the status review to indicate that this factor is currently a threat to the species or will become a threat in the foreseeable future. Therefore, based on our review of the best available scientific and commercial information, we conclude that the striped newt is not threatened by E:\FR\FM\07JNP1.SGM 07JNP1 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules emcdonald on DSK2BSOYB1PROD with PROPOSALS overutilization for commercial, recreational, scientific, or educational purposes now or in the foreseeable future. Factor C. Disease or Predation In our 90-day finding (75 FR 13720, March 23, 2010), we found no evidence that predation was a threat to the striped newt, and we obtained no additional information during the status review that would change that finding. As to disease, below we summarize what was previously stated in the 90-day finding (75 FR 13720, March 23, 2010), as well as additional information obtained during the status review. Disease can be difficult to detect in pond-breeding amphibians. In addition, the rarity of striped newts increases the difficulty of documenting mortality in the species. However, there are reasons to believe that disease may be a possible factor in the decline of striped newts. Chytridiomycosis (a disease caused by Batrachochytrium dendrobatidis) is implicated or documented as a causative agent in many New World amphibian declines (Blaustein and Johnson 2003, p. 91). Ouellet et al. (2005, p. 1434) documented the chytrid fungal infections in the eastern newts (N. viridescens) in North America. A subspecies of the eastern newt, the central or common newt (N. v. louisanensis), has been found in the same ponds as the striped newt at ANF and other ponds in North Florida (Means 2007, p. 19; Means 2001, pp. 19–21; Means et al. 1994, pp. 9–10 and 30–32). The effect of the disease on striped newts is unknown; however, California newts (Taricha torosa) have tested positive for the pathogen in ponds where a die-off of the species was previously reported (Padgett-Flohr and Longcore 2007, p. 177). Some researchers believe that disease pathogens represent one of the potential causes of decline of the striped newt (Blaustein and Johnson 2003, pp. 87– 92). The presence of chytrid fungal infections could particularly threaten populations of striped newts, as they may not have the resiliency to recover after a population crash caused by this disease (Ouellet et al. 2005, p. 1437). Further, the effect of this disease could be exacerbated by other stressors, such as habitat degradation and climate change (Blaustein and Johnson 2003, p. 91; Ouellet et al. 2005, p. 1432; Rothermel et al. 2008, pp. 3, 13). Daszak et al. (2005, p. 3236) found that the impact of Batrachochytrium dendrobatidis on amphibians can vary among species, and several factors, such as climate (i.e., drought) and life-history traits, can affect the species’ response to VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 the disease. The presence of this disease in the range of the striped newt is not confirmed, but is a potential cause for concern, given the deleterious effect of the disease on other amphibian species. A group of viruses belonging to the genus Ranavirus has been shown to affect some local populations and cause localized die-offs of amphibians (Gray et al. 2009a, p. 244). The Ranavirus could be affecting populations of the striped newt, but it is difficult to detect in less abundant species (Gray et al. 2009a, p. 244), and we do not have confirmation that it is present in striped newt populations. However, Green et al. (2002, p. 334) found that Ranavirus was the most frequent cause of amphibian mortality in at least 10 species, including the spotted salamander (Ambystoma maculatum) and eastern newt, so this virus may be impacting striped newt populations in breeding ponds where other subspecies of eastern newts, such as the central newt (Notophthalmus viridescens louisianensis), are found. There are two reasons for the emergence of Ranavirus in amphibian populations: (1) Reduced amphibian immunity associated with increased occurrence of anthropogenic stressors (e.g. drought), and (2) introduction of Ranavirus strains into amphibian populations by humans (Gray et al. 2009b, p. 2). Another recently described disease, caused by a fungus-like protist (Amphibiocystidium viridescens), has been reported in eastern newt populations (Raffel et al. 2008, p. 204). Specifically, evidence of mortality and morbidity due to infection with this disease, and the potential importance of secondary infections as a source of mortality, were reported (Raffel et al. 2008, p. 204). Also, Cook (2008) found a striped newt in captivity to be infected with a protistan parasite that has caused disease in other species of amphibians. This parasite, currently identified as Demomycoides spp. (Cook 2007, p. 2), caused disease resulting in a complete loss of recruitment of the Mississippi gopher frog population in Harrison County, Mississippi, in 2003. Summary of Factor C We have found that several of the diseases mentioned above have resulted in mortality of species similar to the striped newt, such as the eastern newt (which is in the same genus as the striped newt). Drought conditions are predicted to be more severe and longer in the coming years. As drought (see discussion under Factor E below) and loss of habitat (see discussion under Factor A above) continue to act as stressors, striped newt populations may PO 00000 Frm 00042 Fmt 4702 Sfmt 4702 32919 become more susceptible to disease outbreaks, which could potentially result in some localized population extinctions, as has occurred with similar species. Because, from the best available information, we do not know if disease is currently affecting the striped newt populations, but we believe it is likely that it will in the coming decades, we consider this threat to be nonimminent. Since disease has resulted in loss to similar amphibian species, and additional stressors (e.g., habitat loss, drought, and climate change) might make some populations of striped newts more vulnerable to disease, the magnitude of this threat is moderate. Based upon our review of the best commercial and scientific data available, we conclude that disease is a nonimminent threat of moderate magnitude to the striped newt within the foreseeable future. Factor D. The Inadequacy of Existing Regulatory Mechanisms There is currently little Federal and State protection of isolated wetland habitat and surrounding upland habitats. While many States in the southeastern United States regulate those activities affecting wetlands that are exempt from section 404 of the Federal Clean Water Act (CWA) (33 U.S.C.1251 et seq.), Florida is the only State known to regulate isolated wetlands. In Georgia, there are no State laws that protect isolated wetlands. Lack of protection for upland habitat under wetland statutes can result in loss of recruitment of efts and paedomorphs into the breeding adult population, which would reduce the potential for the population to persist (Semlitsch 1998, p. 1116). Federal Statutes and Regulations The CWA regulates the dredge and fill activities that adversely affect wetlands. Section 404 of CWA regulates the discharge of dredge or fill materials into wetlands. Discharges are commonly associated with projects to create dry land for development sites, watercontrol projects, and land clearing. The U.S. Army Corps of Engineers (COE) and the U.S. Environmental Protection Agency (EPA) share the responsibility for implementing the permitting program under section 404 of the CWA. EPA and COE provided a guidance memorandum for implementing recent court cases addressing jurisdiction over waters of the United States under the CWA, specifically addressing the term ‘‘navigable waters’’ (EPA and COE 2001, pp. 1–7; EPA and COE 2008, pp. 1–13). It is clear from this guidance that isolated wetlands are not considered E:\FR\FM\07JNP1.SGM 07JNP1 emcdonald on DSK2BSOYB1PROD with PROPOSALS 32920 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules waters of the United States under the ‘‘navigable waters’’ definition and thus are not provided protection under the CWA. Further wetland regulations are reviewed by the COE for the development of wetlands less than 1.2 ha (3 ac) under a permit called Nationwide Permit 26 (Kirkman et al. 1999, p. 553; Snodgrass et al. 2000, p. 415). The Department of the Interior, through the Service, administers the National Wildlife Refuge System. The National Wildlife Refuge System Administration Act of 1966 (NWRAA; 16 U.S.C. 668dd–668ee) provides legislation for the administration of a national network of lands and water for the conservation, management, and restoration of fish, wildlife, and plant resources and their habitats for the benefit of the American people. Amendment of the NWRAA in 1997 requires the refuge system to ensure that the biological integrity, diversity, and environmental health of refuges be maintained and requires development and implementation of a comprehensive conservation plan (CCP) for each refuge. The CCP must identify and describe the wildlife and related habitats in the refuge and actions needed to correct significant problems that may adversely affect wildlife populations and habitat (16 U.S.C. 668dd(e)). Striped newt habitat within national wildlife refuges is protected from loss due to urban development. Striped newts have historically been observed at St. Marks National Wildlife Refuge (SMNWR) in Florida and Okefenokee National Wildlife Refuge (ONWR) in Georgia. Striped newts were historically found at ONWR in the 1920s, but the only known breeding pond was last occupied by newts in 1994. Aicher (ONWR, personal communication, September 14, 2010) has not found striped newts at ONWR, even though this breeding pond is still in good condition with well-maintained uplands surrounding it. At SMNWR, surveys conducted in 2002–2005 and again in 2009 were not able to locate any newts at 34 ponds (Enge, FWC, personal communication, 2010; Dodd et al. 2007, p. 29). The last known observation was in 1978, but now the habitat appears to be too degraded to be suitable for striped newts due to the lack of fire. Striped newts may indirectly benefit from fire management programs intended to maintain and restore habitat for species such as the red cockaded woodpecker (Picoides borealis) and gopher tortoise (Gopherus polyphemus), but no systematic monitoring programs are in place to evaluate striped newt responses to land VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 management activities within the refuge system. On military installations, the Department of Defense (DOD) must conserve and maintain native ecosystems, viable wildlife populations, Federal and State listed species, and habitats as vital elements of its natural resource management programs, to the extent these requirements are consistent with the military mission (DOD Instruction 4715.3). Amendments to the Sikes Act (16 U.S.C. 670 et seq.) require each military department to prepare and implement an integrated natural resources management plan (INRMP) for each installation under its jurisdiction. The INRMP must be prepared in cooperation with the Service and State fish and wildlife agencies, and must reflect the mutual agreement of these parties concerning conservation, protection, and management of wildlife resources (16 U.S.C. 670a). Each INRMP must provide for wildlife, land and forest management, wildlife-oriented recreation, wildlife habitat enhancement, wetland protection, sustainable public use of natural resources that are not inconsistent with the needs of wildlife resources, and enforcement of natural resource laws (16 U.S.C 670a). DOD regulations mandate that resources and expertise needed to establish and implement an integrated natural resources management program are maintained (DOD Instruction 4715.3). These regulations further define the INRMP requirements, and mandate that plans be revised every 5 years and that they ensure the military lands suitable for management of wildlife are actually managed to conserve wildlife resources (DOD Instruction 4715.3). The effectiveness of individual INRMPs to protect striped newts vary between and within military departments. Because the striped newt is not a protected species in Florida, the INRMP for Camp Blanding Military Installation does not specifically address management programs for this species. However, management activities that benefit the red-cockaded woodpecker and gopher tortoise, such as prescribed burning, should also benefit the striped newt. The striped newt is listed as threatened by the State of Georgia, so the INRMP for Fort Stewart Range and Garrison does address the specific conservation and management of this species. The Navy does incorporate protective ecosystem management into INRMPs for Naval Air Station Jacksonville (and associated Rodman Bombing Range, Pinecastle Range, and Outlying Landing Field Whitehouse), Naval Station PO 00000 Frm 00043 Fmt 4702 Sfmt 4702 Mayport, and Naval Submarine Base Kings Bay. However, the INRMPs do not include specific management measures for the striped newt. The Forest and Rangeland Renewable Resources Planning Act (16 U.S.C. 36),of 1974, as amended by the National Forest Management Act of 1976 (16 U.S.C. 1600 et seq.), requires that each national forest be managed under a forest plan which must be revised every 10 years. Regulations governing preparation of forest plans are found in 36 CFR 219. The purpose of a forest plan is to provide an integrated framework for analyzing and approving future, sitespecific projects and programs, including conservation of listed species. Identification and implementation of land management and conservation measures to benefit striped newts vary between forests. For example, on the National Forests in Florida, striped newts are not designated as a species for which special management prescriptions are implemented. There are no specific land management objectives for striped newts on the National Forests in Florida. The Land and Resource Management Plan for the National Forests in Florida (U.S. Forest Service 1999, entire) provides for the restoration of longleaf pine forest through various management areas located at Apalachicola National Forest (ANF) and Ocala National Forest (ONF). Metapopulations of striped newts are found at both of these forests. However, a decline of striped newt populations at ANF has occurred over the past 10 years (Means et al. 2008, p. 6). State Statutes and Regulations Generally, State statutes and regulations protect striped newts from take, but the effectiveness and implementation of regulations vary between States. The striped newt is not currently a State-listed species in Florida. However, the ephemeral ponds in Florida have some protection under Florida State regulations. The five Water Management Districts (WMDs) and the Florida Department of Environmental Protection (FDEP) regulate wetland protection. The WMDs include isolated wetlands in the Environmental Resource Permit process, which requires a permit for any activities that would impact a wetland (SJRWMD 2010, p. 1). Under the WMDs permitting process, mitigation for impacts to wetlands below a minimum permitting threshold size of 0.2 ha (0.5 ac) is not addressed unless the wetland supports an endangered or threatened species, is connected by standing or flowing surface water at seasonal high water level to one or more wetlands that total E:\FR\FM\07JNP1.SGM 07JNP1 emcdonald on DSK2BSOYB1PROD with PROPOSALS Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules more than 0.2 ha (0.5 ac), or is of more than minimal value to fish and wildlife (SJRWMD 2010, p. 1). This minimum permitting threshold size was adopted by the WMD, ‘‘based on consensus of scientific and regulatory opinions rather than on biological and hydrological evidence’’ (Hart and Newman 1995, p. 4). However, under Florida Statue Title XXVIII Chapter 371.406, agriculture (which includes silviculture) has exemptions to alter topography unless it is for the sole purpose of impounding or obstructing surface waters. The size of the wetland is primarily how the State of Florida and the COE address wetland regulations. Snodgrass et al. (2000, p. 415) found that wetland values were based on four assumptions: (1) That small wetlands are ephemeral; (2) because wetlands are ephemeral, they support few species; (3) species supported by small wetlands are also found in large wetlands; and (4) populations found in individual wetlands are independent from other wetlands. Snodgrass et al. (2000 p. 219) concluded that these assumptions are not accurate and that there is no relationship between wetland size and species richness. Instead, wetland regulations should include a diversity of hydroperiods and connectedness of wetlands (Snodgrass et al. 2000, p. 219). Protecting these small wetlands will help maintain biodiversity with respect to the number of plant, invertebrate, and vertebrate species, including striped newts (Moler and Franz 1987, pp. 236– 237). The loss of these small, ephemeral wetlands changes the metapopulation dynamics of striped newts by reducing the number of individuals that can disperse and reproduce successfully, and by increasing the dispersal distance among wetlands (Semlitsch and Bodie 1998, p. 1131). The reduction in wetland densities decreases the probability that populations can be recovered by adjacent source populations, due to greater distances between wetlands, which eventually leads to population extinctions (Gibbs 1993, pp. 25–26; Semlitsch and Bodie 1998, pp. 1131–1132). This makes it important to not only consider local and regional wetland distribution in wetland regulations, but also the protection of the surrounding non-breeding uplands, in which the newts complete their metamorphosis from efts to adults, and from which the adults emigrate back to the breeding ponds. In Georgia, a State statute requires that any rule and regulation promulgated for protected species (including the striped newt) shall not affect rights on private property or in public or private streams, nor shall such VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 rules and regulations impede construction of any type (Ga. Code Ann. section 27–3–132(b)). Georgia’s Endangered Wildlife Act of 1973 establishes statutory protection for protected species (Ga. Code Ann. section 27–3–130–133). Georgia Board of Natural Resources Rule (Chapter 391– 4–10) mirrors the statue, but includes permitting for research under a scientific collecting permit (Ga. Code Ann. section 27–2–12). Any implementing regulations are constrained by these statutory requirements, and therefore can only prohibit collection, killing, or selling of individual newts. There are no regulatory or permitting mechanisms in place in Georgia to address habitat destruction or striped newt mortality resulting from development projects on private lands. Consequently, striped newts and their habitat in private ownership in Georgia are vulnerable to ongoing and future habitat loss and mortality. Local Laws and Ordinances Florida’s State Comprehensive Plan and Growth Management Act of 1985 (F.A.C. 163 Part II) requires each county to develop local comprehensive planning documents. Comprehensive plans contain policy statements and natural resource protection objectives, including protection of State and federally listed species, but they are only effective if counties develop, implement, and enforce ordinances. Some Florida county governments have developed protective ordinances for State and federally listed species, but all such ordinances are based on compliance with the State or Federal law, rather than enacting more stringent local laws. Consequently, Florida’s local governments provide no additional protection to striped newts. We are aware of no county or local regulations or ordinances that protect the striped newt beyond existing State law in Georgia. Conservation Efforts To Increase Adequacy of Existing Regulations As we indicated above, the inadequacies of existing regulations are inextricably linked to threats associated with the present or threatened destruction, modification, or curtailment of the striped newt’s habitat or range, explained under Factor A above. However, the U.S. Forest Service (USFS) has now restricted or closed ORV use in sensitive biological communities, such as wetlands (USFS 2010, p. 1), at both ANF and ONF. ORVs have historically been a recurring issue in or around ponds at ANF and ONF. PO 00000 Frm 00044 Fmt 4702 Sfmt 4702 32921 However, recent changes at ANF and ONF have made ORVs off-limits in the Munson Sandhills and the ephemeral ponds in the ONF where striped newt ponds were being affected by ORV use (Petrick, USFS, personal communication, 2006). Summary of Factor D Current Federal, State, and local regulations do not protect the vast majority of striped newts or their habitat on private lands. In Georgia, striped newt populations on private lands are not protected under State regulations, even though the striped newt is listed as threatened in that State. The status of striped newts on private lands is unknown, but is likely threatened by ongoing land uses, such as development and silviculture. Regulatory mechanisms at the local, State, and Federal levels provide varying degrees of protection to wetlands, but do not protect the small, ephemeral wetlands that striped newts use for breeding sites. Many regulations do not address management needs of the striped newt. We find that existing regulatory mechanisms are insufficient to reduce or remove threats to striped newts on public and private lands, including wetlands that may support striped newt populations, and we therefore find that the inadequacy of existing regulatory mechanisms is an imminent threat to this species throughout all of its range, as it is occurring now and not expected to change in the near future. This threat is pervasive throughout the species’ entire range, so the magnitude of this threat is moderate. Therefore, based on our review of the best available scientific and commercial information, we conclude that the inadequacy of existing regulatory mechanisms is an imminent threat of moderate magnitude to the striped newt, both now and in the foreseeable future. Factor E. Other Natural or Manmade Factors Affecting the Species’ Continued Existence The effects of a long-term drought have contributed to the decline of striped newts from breeding ponds at not only the Munson Sandhills of the ANF in Florida, but at breeding sites throughout Florida and Georgia. Droughts normally occur in cycles and amphibian populations fluctuate with drought conditions (Dodd 1992, pp. 138–139). However, droughts lasting several years (more than 4) were found to have affected reproductive success, resulting in population decline (Dodd 1992, p. 139; Dodd and Johnson 2007, p. 150; Petranka 1998, p. 450). Surveys conducted at the Camp Blanding E:\FR\FM\07JNP1.SGM 07JNP1 emcdonald on DSK2BSOYB1PROD with PROPOSALS 32922 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules Training Site in 2000 to 2001, during a drought, did not find any striped newts, due to dry breeding ponds. In previous years, surveys found 7 to 10 sites with newts (Gregory et al. 2006, p. 487). Striped newts will respond to drought conditions in several ways: (1) Temporary extirpation; (2) migration to adjacent areas with better habitat conditions; and (3) survival in upland habitat, with recolonization once water has returned (Dodd 1993, p. 612). Even with the return of water at the Munson Sandhills in ANF, striped newt populations have not recovered (Means, CPI, personal communication, 2010). Although droughts are a naturally occurring event in the ecology of the striped newt, prolonged droughts can worsen threats to already small populations, and exacerbate the degradation and fragmentation of striped newt habitat that is already taking place (discussed under Factor A above), leading to extinction of striped newts in many areas. We expect climate change will result in the loss and degradation of striped newt habitat in the future, particularly in Florida. According to the Intergovernmental Panel on Climate Change Synthesis Report (IPCC 2007, p. 2), warming of the earth’s climate is ‘‘unequivocal,’’ as is now evident from observations of increases in average global air and ocean temperatures, widespread melting of snow and ice, and rising sea level. Temperatures are predicted to rise from 2.0 degrees Celsius (°C) to 5.0 °C (3.6 degrees Fahrenheit (°F) to 9.0 °F) for North America by the end of this century (IPCC 2007, p. 9). The IPCC (2007, pp. 2, 6) report outlines several scenarios that are virtually certain or very likely to occur in the next 50 years, including: (1) Over most land, there will be fewer cold days and nights, and warmer and more frequent hot days and nights; (2) Areas affected by drought will increase; and (3) The frequency of heavy precipitation events over most land areas will likely increase. The Southeastern United States is predicted to experience more severe and longer droughts. Other processes to be affected by this projected warming include rainfall (amount, seasonal timing, and distribution), storms (frequency and intensity), and sea level rise. Indirect impacts are expected due to the relocation of people from floodprone urban areas to inland areas (Ruppert et al. 2008, p. 127), including the relocation of millions of people to currently undeveloped interior natural areas (Stanton and Ackerman 2007, p. 15). Others have proposed implementation of a large-scale VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 systematic translocation of at-risk human populations to interior locations (Gilkey 2008, pp. 9–12). Florida’s interior natural ecological communities will likely be impacted by the increasing need of urban infrastructure to support retreating coastal inhabitants. While available data are not adequately specific to evaluate the potential direct effects of predicted climate changes on the striped newt or provide information on just how much habitat may be lost, any habitat loss related to climate change would be in addition to the 20 percent loss projected to occur by 2060 due solely to people moving into Florida (FWC 2008, p. 2). Summary of Factor E We have identified that long-term droughts have resulted in the loss of striped newt breeding ponds, exacerbating existing population fluctuations and causing local extinctions. This threat is ongoing and is expected to continue in the future, especially because threats to habitat continue to affect existing striped newt populations and may make them more susceptible to potential population extinction. On the basis of this analysis, we find that the natural factor of longterm droughts is currently a threat and is expected to persist, and possibly escalate in the future, as a result of climate change, although climate change itself is not an imminent threat. Because we expect this threat will occur over the coming decades, we consider the threat to be imminent. Throughout the entire range of the striped newt, droughts are predicted to be more severe and longer in duration in the coming years, so we believe the magnitude of this threat is high. Based upon our review of the best commercial and scientific data available, we conclude that other natural or manmade factors affecting the species’ continued existence is an imminent threat of high magnitude to the striped newt, both now and in the foreseeable future. Finding As required by the Act, we conducted a review of the status of the species and considered the five factors in assessing whether the striped newt is endangered or threatened throughout all or a significant portion of its range. We examined the best scientific and commercial information available regarding the past, present, and future threats faced by the striped newt. We reviewed the petition, information available in our files, and other available published and unpublished information, and we consulted with PO 00000 Frm 00045 Fmt 4702 Sfmt 4702 striped newt experts and other Federal and State agencies. In considering whether a species may warrant listing under any of the five factors, we look beyond the species’ exposure to a potential threat or aggregation of threats under any of the factors, and evaluate whether the species responds to those potential threats in a way that causes actual impact to the species. The identification of threats that might impact a species negatively may not be sufficient to compel a finding that the species warrants listing. The information must include evidence indicating that the threats are operative and, either singly or in aggregation, affect the status of the species. Threats are significant if they drive, or contribute to, the risk of extinction of the species, such that the species warrants listing as endangered or threatened, as those terms are defined in the Act. This status review identified threats to the striped newt attributable to Factors A, C, D, and E. The primary threats to the striped newt are habitat loss, disease, inadequate regulatory mechanisms, and drought. Habitat destruction and modification (Factor A) in the form of conversion of native longleaf pine forests to intensively managed pine forests and urban development are occurring on private lands throughout the range. Disease (Factor C) is expected to become more problematic for striped newts as additional habitat is lost and fragmentation increases. Stressors such as habitat loss (Factor A) and droughts (Factor E) are expected to elevate risks of diseases in newts because this has been the case with similar species. Regulatory mechanisms are inadequate to prevent further loss of breeding ponds (Factor D) throughout the striped newt’s range. Existing regulations also do not protect striped newts on private lands in Florida and Georgia. Long-term regional droughts in Florida and Georgia (Factor E) have a negative impact on the long-term persistence of striped newts. Since 2000, the striped newt has been monitored at 20 of the best breeding ponds on ANF (Means, CPILC, personal communication, 2010; Means and Means 1998a., pp. 9–25; Means et al. 1994, pp. 14–24; Means et al. 2008, p. 6). Since 2000, severe drought conditions were experienced at these ponds, and newts were shown to be declining. However, despite improving conditions at these ponds, no striped newts were located in 2010. The precipitous apparent declines now being seen at ANF could occur elsewhere on protected lands within the striped newt’s range, despite the E:\FR\FM\07JNP1.SGM 07JNP1 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules emcdonald on DSK2BSOYB1PROD with PROPOSALS protection of habitat. This suggests that perhaps other threats (e.g., disease and drought) may continue to act on the species at these sites. Drought conditions are predicted to be more severe and longer in the coming years. As described under Factor C, drought and other factors continue to act as stressors on existing striped newt populations and may make them more susceptible to disease outbreaks and may result in the population extinction of some metapopulations. There has not been any evidence of disease at other large metapopulations, such as ONF. On the basis of the best scientific and commercial information available, we find that the petitioned action to list the striped newt as endangered or threatened is warranted. We will make a determination on the status of the striped newt as endangered or threatened when we complete a proposed listing determination. However, as explained in more detail below, an immediate proposal of a regulation implementing this action is precluded by higher priority listing actions, and progress is being made to add or remove qualified species from the Lists of Endangered and Threatened Wildlife and Plants. We have reviewed the available information to determine if the existing and foreseeable threats render the species at risk of extinction now such that issuing an emergency regulation temporarily listing the species in accordance with section 4(b)(7) of the Act is warranted. We have determined that issuing an emergency regulation temporarily listing the striped newt is not warranted for this species at this time because there are no impending actions that might result in extinction of the species that would be addressed and alleviated by emergency listing, and the severity and timing of the threats are such that the risk of extinction will not occur over a short duration, or be caused by any one action. However, if at any time we determine that issuing an emergency regulation temporarily listing the striped newt is warranted, we will initiate this action at that time. Listing Priority Number The Service adopted guidelines on September 21, 1983 (48 FR 43098), to establish a rational system for utilizing available resources for the highest priority species when adding species to the Lists of Endangered or Threatened Wildlife and Plants or reclassifying species listed as threatened to endangered status. These guidelines, titled ‘‘Endangered and Threatened Species Listing and Recovery Priority Guidelines,’’ address the immediacy and VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 magnitude of threats, and the level of taxonomic distinctiveness by assigning priority in descending order to monotypic genera (genus with one species), full species, and subspecies (or equivalently, distinct population segments (DPSes) of vertebrates). We assign the striped newt a Listing Priority Number (LPN) of 8, based on our determination that the primary threats are moderate and imminent. These threats include habitat destruction, disease, inadequate regulatory mechanisms, and droughts. Rationale for assigning the striped newt an LPN of 8 is outlined below. Under the Service’s LPN Guidance, the magnitude of threat is the first criterion we look at when establishing a listing priority. The guidance indicates that species with the highest magnitude of threat are those species facing the greatest threats to their continued existence. These species receive the highest listing priority. The primary threats to striped newt (e.g., habitat loss, disease, inadequate regulatory mechanisms, and drought) are occurring in populations throughout the species’ range. For Factor E, we consider the magnitude high because nearly all populations are affected, and this factor may lead to possible extirpation. Also, throughout the entire range of the striped newt, droughts are predicted to be more severe and longer in the coming years, which could have a detrimental effect on the species’ long-term survival. With drought as a possible cause for the decline in the population at ANF, we predict that, with continued drought conditions, declines are likely to occur at other protected lands as well, with possible extirpation in those areas. We consider the magnitude for Factors A and C moderate, as most of the known striped newt metapopulations are on conservation lands, and, although disease has been found in similar species, no known metapopulations of striped newts have shown any evidence of disease. Existing regulatory mechanisms at the local, State, and Federal levels provide varying degrees of protection to wetlands, but do not protect the small, ephemeral wetlands striped newts use for breeding sites. The lack of regulatory protection has not prevented further loss of breeding ponds and adjacent upland habitat throughout the species’ range. We consider this a threat that is moderate in magnitude. In sum, because we find that threats under three factors (A, C, and D) are moderate, we find the overall threats that the striped newt is facing to be moderate in magnitude. Under our LPN Guidance, the second criterion we consider in assigning a PO 00000 Frm 00046 Fmt 4702 Sfmt 4702 32923 listing priority is the immediacy of threats. This criterion is intended to ensure that the species that face actual, identifiable threats are given priority over those for which threats are only potential or that are intrinsically vulnerable but are not known to be presently facing such threats. Factors A, D, and E are considered imminent because they are occurring now and are expected to continue to occur in the future. These actual, identifiable threats are covered in detail under the discussion of Factors A, D, and E of this finding. Because we find that threats under three factors (A, D, and E) are imminent, and the threat under one factor (C) to be nonimminent, we find the overall threats that the striped newt is facing to be imminent. The third criterion in our LPN guidance is intended to devote resources to those species representing highly distinctive or isolated gene pools as reflected by taxonomy. The striped newt is a valid taxon at the species level, and therefore receives a higher priority than subspecies or DPSes, but a lower priority than species in a monotypic genus. The striped newt faces mostly moderate magnitude, largely imminent threats, and is a valid taxon at the species level. Thus, in accordance with our LPN guidance, we have assigned the striped newt an LPN of 8. We will continue to monitor the threats to the striped newt, and the species’ status on an annual basis, and should the magnitude or the imminence of the threats change, we will revisit our assessment of the LPN. Work on a proposed listing determination for the striped newt is precluded by work on higher priority listing actions with absolute statutory, court-ordered, or court-approved deadlines and final listing determinations for those species that were proposed for listing with funds from Fiscal Year 2011. This work includes all the actions listed in the tables below under expeditious progress. Preclusion and Expeditious Progress Preclusion is a function of the listing priority of a species in relation to the resources that are available and the cost and relative priority of competing demands for those resources. Thus, in any given fiscal year (FY), multiple factors dictate whether it will be possible to undertake work on a listing proposal or whether promulgation of such a proposal is precluded by higher priority listing actions. The resources available for listing actions are determined through the E:\FR\FM\07JNP1.SGM 07JNP1 emcdonald on DSK2BSOYB1PROD with PROPOSALS 32924 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules annual Congressional appropriations process. The appropriation for the Listing Program is available to support work involving the following listing actions: Proposed and final listing rules; 90-day and 12-month findings on petitions to add species to the Lists of Endangered and Threatened Wildlife and Plants (Lists) or to change the status of a species from threatened to endangered; annual ‘‘resubmitted’’ petition findings on prior warrantedbut-precluded petition findings as required under section 4(b)(3)(C)(i) of the Act; critical habitat petition findings; proposed and final rules designating critical habitat; and litigation-related, administrative, and program-management functions (including preparing and allocating budgets, responding to Congressional and public inquiries, and conducting public outreach regarding listing and critical habitat). The work involved in preparing various listing documents can be extensive and may include, but is not limited to: Gathering and assessing the best scientific and commercial data available and conducting analyses used as the basis for our decisions; writing and publishing documents; and obtaining, reviewing, and evaluating public comments and peer review comments on proposed rules and incorporating relevant information into final rules. The number of listing actions that we can undertake in a given year also is influenced by the complexity of those listing actions; that is, more complex actions generally are more costly. The median cost for preparing and publishing a 90-day finding is $39,276; for a 12-month finding, $100,690; for a proposed rule with critical habitat, $345,000; and for a final listing rule with critical habitat, $305,000. We cannot spend more than is appropriated for the Listing Program without violating the Anti-Deficiency Act (see 31 U.S.C. 1341(a)(1)(A)). In addition, in FY 1998 and for each fiscal year since then, Congress has placed a statutory cap on funds that may be expended for the Listing Program, equal to the amount expressly appropriated for that purpose in that fiscal year. This cap was designed to prevent funds appropriated for other functions under the Act (for example, recovery funds for removing species from the Lists), or for other Service programs, from being used for Listing Program actions (see House Report 105–163, 105th Congress, 1st Session, July 1, 1997). Since FY 2002, the Service’s budget has included a critical habitat subcap to ensure that some funds are available for other work in the Listing Program (‘‘The VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 critical habitat designation subcap will ensure that some funding is available to address other listing activities’’ (House Report No. 107–103, 107th Congress, 1st Session, June 19, 2001)). In FY 2002 and each year until FY 2006, the Service has had to use virtually the entire critical habitat subcap to address courtmandated designations of critical habitat, and consequently none of the critical habitat subcap funds have been available for other listing activities. In some FYs since 2006, we have been able to use some of the critical habitat subcap funds to fund proposed listing determinations for high-priority candidate species. In other FYs, while we were unable to use any of the critical habitat subcap funds to fund proposed listing determinations, we did use some of this money to fund the critical habitat portion of some proposed listing determinations so that the proposed listing determination and proposed critical habitat designation could be combined into one rule, thereby being more efficient in our work. At this time, for FY 2011, we do not know if we will be able to use some of the critical habitat subcap funds to fund proposed listing determinations. We make our determinations of preclusion on a nationwide basis to ensure that the species most in need of listing will be addressed first and also because we allocate our listing budget on a nationwide basis. Through the listing cap, the critical habitat subcap, and the amount of funds needed to address court-mandated critical habitat designations, Congress and the courts have in effect determined the amount of money available for other listing activities nationwide. Therefore, the funds in the listing cap, other than those needed to address court-mandated critical habitat for already listed species, set the limits on our determinations of preclusion and expeditious progress. Congress identified the availability of resources as the only basis for deferring the initiation of a rulemaking that is warranted. The Conference Report accompanying Public Law 97–304 (Endangered Species Act Amendments of 1982), which established the current statutory deadlines and the warrantedbut-precluded finding, states that the amendments were ‘‘not intended to allow the Secretary to delay commencing the rulemaking process for any reason other than that the existence of pending or imminent proposals to list species subject to a greater degree of threat would make allocation of resources to such a petition [that is, for a lower-ranking species] unwise.’’ Although that statement appeared to refer specifically to the ‘‘to the PO 00000 Frm 00047 Fmt 4702 Sfmt 4702 maximum extent practicable’’ limitation on the 90-day deadline for making a ‘‘substantial information’’ finding (see 16 U.S.C. 1533(b)(3)(A)), that finding is made at the point when the Service is deciding whether or not to commence a status review that will determine the degree of threats facing the species, and therefore the analysis underlying the statement is more relevant to the use of the warranted-but-precluded finding, which is made when the Service has already determined the degree of threats facing the species and is deciding whether or not to commence a rulemaking. In FY 2011, on April 15, 2011, Congress passed the Full-Year Continuing Appropriations Act (Pub. L. 112–10) which provides funding through September 30, 2011. The Service has $22,103,000 for the listing program. Of that, the Service anticipates needing to dedicate $11,632,000 for determinations of critical habitat for already listed species. Also $500,000 is appropriated for foreign species listings under the Act. The Service thus has $9,971,000 available to fund work in the following categories: compliance with court orders and court-approved settlement agreements requiring that petition findings or listing determinations be completed by a specific date; section 4 (of the Act) listing actions with absolute statutory deadlines; essential litigation-related, administrative, and listing programmanagement functions; and highpriority listing actions for some of our candidate species. In FY 2010, the Service received many new petitions and a single petition to list 404 species. The receipt of petitions for a large number of species is consuming the Service’s listing funding that is not dedicated to meeting court-ordered commitments. Absent some ability to balance effort among listing duties under existing funding levels, it is unlikely that the Service will be able to initiate any new listing determinations for candidate species in FY 2011. In 2009, the responsibility for listing foreign species under the Act was transferred from the Division of Scientific Authority, International Affairs Program, to the Endangered Species Program. Therefore, starting in FY 2010, we used a portion of our funding to work on the actions described above for listing actions related to foreign species. In FY 2011, we anticipate using $1,500,000 for work on listing actions for foreign species, which reduces funding available for domestic listing actions; however, currently only $500,000 has been allocated for this function. Although E:\FR\FM\07JNP1.SGM 07JNP1 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules there are no foreign species issues included in our high-priority listing actions at this time, many actions have statutory or court-approved settlement deadlines, thus increasing their priority. The budget allocations for each specific listing action are identified in the Service’s FY 2011 Allocation Table (part of our administrative record). For the above reasons, funding a proposed listing determination for the striped newt is precluded by courtordered and court-approved settlement agreements, listing actions with absolute statutory deadlines, and work on proposed listing determinations for those candidate species with a higher listing priority (i.e., candidate species with LPNs of 1 to 7). Based on our September 21, 1983, guidelines for assigning an LPN for each candidate species (48 FR 43098), we have a significant number of species with a LPN of 2. Using these guidelines, we assign each candidate an LPN of 1 to 12, depending on the magnitude of threats (high or moderate to low), immediacy of threats (imminent or nonimminent), and taxonomic status of the species (in order of priority: monotypic genus (a species that is the sole member of a genus); species; or part of a species (subspecies, distinct population segment, or significant portion of the range)). The lower the listing priority number, the higher the listing priority (that is, a species with an LPN of 1 would have the highest listing priority). Because of the large number of highpriority species, we have further ranked the candidate species with an LPN of 2 by using the following extinction-risk type criteria: International Union for the Conservation of Nature and Natural Resources (IUCN) Red list status/rank; Heritage rank (provided by NatureServe); Heritage threat rank (provided by NatureServe); and species currently with fewer than 50 individuals, or 4 or fewer populations. Those species with the highest IUCN rank (critically endangered); the highest Heritage rank (G1); the highest Heritage threat rank (substantial, imminent threats); and currently with fewer than 50 individuals, or fewer than 4 populations, originally comprised a group of approximately 40 candidate species (‘‘Top 40’’). These 40 candidate species have had the highest priority to receive funding to work on a proposed listing determination. As we work on proposed and final listing rules for those 40 candidates, we apply the ranking criteria to the next group of candidates with an LPN of 2 and 3 to determine the next set of highest priority candidate species. Finally, proposed rules for reclassification of threatened species to endangered are lower priority, because as listed species, they are already afforded the protections of the Act and implementing regulations. However, for efficiency reasons, we may choose to work on a proposed rule to reclassify a species to endangered if we can combine this with work that is subject to a court-determined deadline. With our workload so much bigger than the amount of funds we have to accomplish it, it is important that we be as efficient as possible in our listing process. Therefore, as we work on 32925 proposed rules for the highest priority species in the next several years, we are preparing multi-species proposals when appropriate, and these may include species with lower priority if they overlap geographically or have the same threats as a species with an LPN of 2. In addition, we take into consideration the availability of staff resources when we determine which high-priority species will receive funding to minimize the amount of time and resources required to complete each listing action. As explained above, a determination that listing is warranted but precluded must also demonstrate that expeditious progress is being made to add and remove qualified species to and from the Lists of Endangered and Threatened Wildlife and Plants. As with our ‘‘warranted-but-precluded’’ finding, the evaluation of whether progress in adding qualified species to the Lists has been expeditious is a function of the resources available for listing and the competing demands for those funds. (Although we do not discuss it in detail here, we are also making expeditious progress in removing species from the list under the Recovery program in light of the resource available for delisting, which is funded by a separate line item in the budget of the Endangered Species Program. So far during FY 2011, we have completed one delisting rule; see 76 FR 3029.) Given the limited resources available for listing, we find that we are making expeditious progress in FY 2011. This progress includes preparing and publishing the following determinations: FY 2011 COMPLETED LISTING ACTIONS Publication date Title Actions 10/6/2010 ............... Endangered Status for the Altamaha Spinymussel and Designation of Critical Habitat. 12-Month Finding on a Petition to list the Sacramento Splittail as Endangered or Threatened. Endangered Status and Designation of Critical Habitat for Spikedace and Loach Minnow. 90-Day Finding on a Petition to List the Bay Springs Salamander as Endangered. Determination of Endangered Status for the Georgia Pigtoe Mussel, Interrupted Rocksnail, and Rough Hornsnail and Designation of Critical Habitat. Listing the Rayed Bean and Snuffbox as Endangered. 12-Month Finding on a Petition to List Cirsium wrightii (Wright’s Marsh Thistle) as Endangered or Threatened. Endangered Status for Dunes Sagebrush Lizard Proposed Listing Endangered ............................. 75 FR 61664– 61690 Notice of 12-month petition finding, Not warranted. 75 FR 62070– 62095 Proposed Listing Endangered (uplisting) ............. 75 FR 66481– 66552 75 FR 67341– 67343 75 FR 67511– 67550 12-Month Finding on a Petition to List the North American Wolverine as Endangered or Threatened. Notice of 12-month petition finding, Warranted but precluded. 10/7/2010 ............... 10/28/2010 ............. 11/2/2010 ............... emcdonald on DSK2BSOYB1PROD with PROPOSALS 11/2/2010 ............... 11/2/2010 ............... 11/4/2010 ............... 12/14/2010 ............. 12/14/2010 ............. VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 PO 00000 Frm 00048 Fmt 4702 FR pages Notice of 90-day Petition Finding, Not substantial. Final Listing Endangered ..................................... Proposed Listing Endangered ............................. Notice of 12-month petition finding, Warranted but precluded. Proposed Listing Endangered ............................. Sfmt 4702 E:\FR\FM\07JNP1.SGM 07JNP1 75 FR 67551– 67583 75 FR 67925– 67944 75 FR 77801– 77817 75 FR 78029– 78061 32926 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules FY 2011 COMPLETED LISTING ACTIONS—Continued Publication date Title Actions 12/14/2010 ............. 12-Month Finding on a Petition to List the Sonoran Population of the Desert Tortoise as Endangered or Threatened. 12-Month Finding on a Petition to List Astragalus microcymbus and Astragalus schmolliae as Endangered or Threatened. Listing Seven Brazilian Bird Species as Endangered Throughout Their Range. 90-Day Finding on a Petition to List the Red Knot subspecies Calidris canutus roselaari as Endangered. Endangered Status for the Sheepnose and Spectaclecase Mussels. 12-Month Finding on a Petition to List the Pacific Walrus as Endangered or Threatened. 90-Day Finding on a Petition To List the Sand Verbena Moth as Endangered or Threatened. Determination of Threatened Status for the New Zealand-Australia Distinct Population Segment of the Southern Rockhopper Penguin. 12-Month Finding on a Petition to List Solanum conocarpum (marron bacora) as Endangered. 12-Month Finding on a Petition to List Thorne’s Hairstreak Butterfly as Endangered. 12-Month Finding on a Petition to List Astragalus hamiltonii, Penstemon flowersii, Eriogonum soredium, Lepidium ostleri, and Trifolium friscanum as Endangered or Threatened. 90-Day Finding on a Petition to List the Wild Plains Bison or Each of Four Distinct Population Segments as Threatened. 90-Day Finding on a Petition to List the Unsilvered Fritillary Butterfly as Threatened or Endangered. 12-Month Finding on a Petition to List the Mt. Charleston Blue Butterfly as Endangered or Threatened. 90-Day Finding on a Petition to List the Texas Kangaroo Rat as Endangered or Threatened. Initiation of Status Review for Longfin Smelt ...... Notice of 12-month petition finding, Warranted but precluded. 75 FR 78093– 78146 Notice of 12-month petition finding, Warranted but precluded. 75 FR 78513– 78556 Final Listing Endangered ..................................... 75 FR 81793– 81815 76 FR 304–311 12/15/2010 ............. 12/28/2010 ............. 1/4/2011 ................. 1/19/2011 ............... 2/10/2011 ............... 2/17/2011 ............... 2/22/2011 ............... 2/22/2011 ............... 2/23/2011 ............... 2/23/2011 ............... 2/24/2011 ............... 2/24/2011 ............... 3/8/2011 ................. 3/8/2011 ................. 3/10/2011 ............... 3/15/2011 ............... 3/22/2011 ............... 4/1/2011 ................. 4/5/2011 ................. 4/5/2011 ................. 4/12/2011 ............... emcdonald on DSK2BSOYB1PROD with PROPOSALS 4/13/2011 ............... 4/14/2011 ............... 4/14/2011 ............... 4/26/2011 ............... VerDate Mar<15>2010 Withdrawal of Proposed Rule to List the Flattailed Horned Lizard as Threatened. 12-Month Finding on a Petition to List the Berry Cave Salamander as Endangered. 90-Day Finding on a Petition to List the Spring Pygmy Sunfish as Endangered. 12-Month Finding on a Petition to List the Bearmouth Mountainsnail, Byrne Resort Mountainsnail, and Meltwater Lednian Stonefly as Endangered or Threatened. 90-Day Finding on a Petition To List the Peary Caribou and Dolphin and Union population of the Barren-ground Caribou as Endangered or Threatened. Proposed Endangered Status for the Three Forks Springsnail and San Bernardino Springsnail, and Proposed Designation of Critical Habitat. 90-Day Finding on a Petition To List Spring Mountains Acastus Checkerspot Butterfly as Endangered. 90-Day Finding on a Petition to List the Prairie Chub as Threatened or Endangered. 12-Month Finding on a Petition to List Hermes Copper Butterfly as Endangered or Threatened. 90-Day Finding on a Petition to List the Arapahoe Snowfly as Endangered or Threatened. 17:26 Jun 06, 2011 Jkt 223001 PO 00000 Frm 00049 Fmt 4702 FR pages Notice of 90-day Petition Finding, Not substantial. Proposed Listing Endangered ............................. 76 FR 3392–3420 Notice of 12-month petition finding, Warranted but precluded. Notice of 90-day Petition Finding, Substantial .... 76 FR 7634–7679 76 FR 9309–9318 Final Listing Threatened ...................................... 76 FR 9681–9692 Notice of 12-month petition finding, Warranted but precluded. Notice of 12-month petition finding, Not warranted. Notice of 12-month petition finding, Warranted but precluded and Not Warranted. 76 FR 9722–9733 Notice of 90-day Petition Finding, Not substantial. 76 FR 10299– 10310 Notice of 90-day Petition Finding, Not substantial. 76 FR 10310– 10319 Notice of 12-month petition finding, Warranted but precluded. 76 FR 12667– 12683 Notice of 90-day Petition Finding, Substantial .... 76 FR 12683– 12690 76 FR 13121– 13122 76 FR 14210– 14268 76 FR 15919– 15932 76 FR 18138– 18143 76 FR 18684– 18701 Notice of Status Review ...................................... Proposed rule withdrawal .................................... Notice of 12-month petition finding, Warranted but precluded. Notice of 90-day Petition Finding, Substantial .... Notice of 12-month petition finding, Not Warranted and Warranted but precluded. 76 FR 991–10003 76 FR 10166– 10203 Notice of 90-day Petition Finding, Substantial .... 76 FR 18701– 18706 Proposed Listing Endangered ............................. 76 FR 20464– 20488 Notice of 90-day Petition Finding, Substantial .... 76 FR 20613– 20622 Notice of 90-day Petition Finding, Substantial .... 76 FR 20911– 20918 76 FR 20918– 20939 Notice of 12-month petition finding, Warranted but precluded. Notice of 90-day Petition Finding, Substantial .... Sfmt 4702 E:\FR\FM\07JNP1.SGM 07JNP1 76 FR 23256– 23265 32927 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules FY 2011 COMPLETED LISTING ACTIONS—Continued Publication date Title Actions 4/26/2011 ............... 90-Day Finding on a Petition to List the SmoothBilled Ani as Threatened or Endangered. Notice of 90-day Petition Finding, Not substantial. Our expeditious progress also includes work on listing actions that we funded in FY 2010 and FY 2011 but have not yet been completed to date. These actions are listed below. Actions in the top section of the table are being conducted under a deadline set by a court. Actions in the middle section of the table are being conducted to meet statutory timelines, that is, timelines required under the Act. Actions in the bottom section of the table are highpriority listing actions. These actions include work primarily on species with an LPN of 2, and, as discussed above, selection of these species is partially based on available staff resources, and when appropriate, include species with FR pages 76 FR 23265– 23271 a lower priority if they overlap geographically or have the same threats as the species with the high priority. Including these species together in the same proposed rule results in considerable savings in time and funding, when compared to preparing separate proposed rules for each of them in the future. ACTIONS FUNDED IN FY 2010 AND FY 2011 BUT NOT YET COMPLETED Species Action Actions Subject to Court Order/Settlement Agreement 4 parrot species (military macaw, yellow-billed parrot, red-crowned parrot, scarlet macaw) 5 ........... 4 parrot species (blue-headed macaw, great green macaw, grey-cheeked parakeet, hyacinth macaw) 5. 4 parrots species (crimson shining parrot, white cockatoo, Philippine cockatoo, yellow-crested cockatoo) 5. Utah prairie dog (uplisting) .................................................................................................................. 12-month petition finding. 12-month petition finding. 12-month petition finding. 90-day petition finding. emcdonald on DSK2BSOYB1PROD with PROPOSALS Actions With Statutory Deadlines Casey’s june beetle ............................................................................................................................. 6 Birds from Eurasia ............................................................................................................................ 5 Bird species from Colombia and Ecuador ....................................................................................... Queen Charlotte goshawk ................................................................................................................... 5 species southeast fish (Cumberland darter, rush darter, yellowcheek darter, chucky madtom, and laurel dace) 4. Ozark hellbender 4 ............................................................................................................................... Altamaha spinymussel 3 ....................................................................................................................... 3 Colorado plants (Ipomopsis polyantha (Pagosa Skyrocket), Penstemon debilis (Parachute Beardtongue), and Phacelia submutica (DeBeque Phacelia)) 4. Salmon crested cockatoo .................................................................................................................... 6 Birds from Peru & Bolivia ................................................................................................................. Loggerhead sea turtle (assist National Marine Fisheries Service) 5 ................................................... 2 mussels (rayed bean (LPN = 2), snuffbox No LPN) 5 ...................................................................... CA golden trout 4 ................................................................................................................................. Black-footed albatross ......................................................................................................................... Mojave fringe-toed lizard 1 ................................................................................................................... Kokanee—Lake Sammamish population 1 .......................................................................................... Cactus ferruginous pygmy-owl 1 .......................................................................................................... Northern leopard frog .......................................................................................................................... Tehachapi slender salamander ........................................................................................................... Coqui Llanero ...................................................................................................................................... Dusky tree vole .................................................................................................................................... 5 WY plants (Abronia ammophila, Agrostis rossiae, Astragalus proimanthus, Boechere (Arabis) pusilla, Penstemon gibbensii) from 206 species petition. Leatherside chub (from 206 species petition) ..................................................................................... Frigid ambersnail (from 206 species petition) 3 ................................................................................... Platte River caddisfly (from 206 species petition) 5 ............................................................................. Gopher tortoise—eastern population ................................................................................................... Grand Canyon scorpion (from 475 species petition) .......................................................................... Anacroneuria wipukupa (a stonefly from 475 species petition) 4 ........................................................ 3 Texas moths (Ursia furtiva, Sphingicampa blanchardi, Agapema galbina) (from 475 species petition). 2 Texas shiners (Cyprinella sp., Cyprinella lepida) (from 475 species petition) ................................ 3 South Arizona plants (Erigeron piscaticus, Astragalus hypoxylus, Amoreuxia gonzalezii) (from 475 species petition). 5 Central Texas mussel species (3 from 475 species petition) .......................................................... 14 parrots (foreign species) ................................................................................................................. Striped Newt 1 ...................................................................................................................................... Fisher—Northern Rocky Mountain Range 1 ........................................................................................ Mohave Ground Squirrel 1 ................................................................................................................... Puerto Rico Harlequin Butterfly 3 ......................................................................................................... VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 PO 00000 Frm 00050 Fmt 4702 Sfmt 4702 Final Final Final Final Final listing listing listing listing listing determination. determination. determination. determination. determination. Final listing determination. Final listing determination. Final listing determination. Final listing determination. Final listing determination. Final listing determination. Final listing determination. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding/Proposed listing. 12-month petition finding. 12-month petition finding. 12-month 12-month 12-month 12-month 12-month 12-month 12-month petition petition petition petition petition petition petition finding. finding. finding. finding. finding. finding. finding. 12-month petition finding. 12-month petition finding. 12-month 12-month 12-month 12-month 12-month 12-month E:\FR\FM\07JNP1.SGM petition petition petition petition petition petition 07JNP1 finding. finding. finding. finding. finding. finding. 32928 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules ACTIONS FUNDED IN FY 2010 AND FY 2011 BUT NOT YET COMPLETED—Continued Species Action Western gull-billed tern ........................................................................................................................ Ozark chinquapin (Castanea pumila var. ozarkensis) 4 ...................................................................... HI yellow-faced bees ........................................................................................................................... Giant Palouse earthworm .................................................................................................................... Whitebark pine ..................................................................................................................................... OK grass pink (Calopogon oklahomensis) 1 ........................................................................................ Ashy storm-petrel 5 .............................................................................................................................. Honduran emerald ............................................................................................................................... Southeastern pop snowy plover & wintering pop. of piping plover 1 .................................................. Eagle Lake trout 1 ................................................................................................................................ 32 Pacific Northwest mollusks species (snails and slugs) 1 ............................................................... 42 snail species (Nevada & Utah) ....................................................................................................... Spring Mountains checkerspot butterfly .............................................................................................. Bay skipper .......................................................................................................................................... Spot-tailed earless lizard ..................................................................................................................... Eastern small-footed bat ...................................................................................................................... Northern long-eared bat ...................................................................................................................... 10 species of Great Basin butterfly ..................................................................................................... 6 sand dune (scarab) beetles .............................................................................................................. Golden-winged warbler 4 ...................................................................................................................... 404 Southeast species ........................................................................................................................ Franklin’s bumble bee 4 ....................................................................................................................... 2 Idaho snowflies (straight snowfly & Idaho snowfly) 4 ....................................................................... American eel 4 ...................................................................................................................................... Gila monster (Utah population) 4 ......................................................................................................... Leona’s little blue 4 ............................................................................................................................... Aztec gilia 5 .......................................................................................................................................... White-tailed ptarmigan 5 ....................................................................................................................... San Bernardino flying squirrel 5 ........................................................................................................... Bicknell’s thrush 5 ................................................................................................................................. Chimpanzee ......................................................................................................................................... Sonoran talussnail 5 ............................................................................................................................. 2 AZ Sky Island plants (Graptopetalum bartrami & Pectis imberbis) 5 ............................................... I’iwi 5 ..................................................................................................................................................... Carolina hemlock ................................................................................................................................. Western glacier stonefly (Zapada glacier) ........................................................................................... Thermophilic ostracod (Potamocypris hunteri) .................................................................................... 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 12-month petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. 90-day petition finding. emcdonald on DSK2BSOYB1PROD with PROPOSALS High-Priority Listing Actions 19 Oahu candidate species 2 (16 plants, 3 damselflies) (15 with LPN = 2, 3 with LPN = 3, 1 with LPN = 9). 19 Maui-Nui candidate species 2 (16 plants, 3 tree snails) (14 with LPN = 2, 2 with LPN = 3, 3 with LPN = 8). Chupadera springsnail 2 (Pyrgulopsis chupaderae (LPN = 2)) ........................................................... 8 Gulf Coast mussels (southern kidneyshell (LPN = 2), round ebonyshell (LPN = 2), Alabama pearlshell (LPN = 2), southern sandshell (LPN = 5), fuzzy pigtoe (LPN = 5), Choctaw bean (LPN = 5), narrow pigtoe (LPN = 5), and tapered pigtoe (LPN = 11)) 4. Umtanum buckwheat (LPN = 2) and white bluffs bladderpod (LPN = 9) 4 ......................................... Grotto sculpin (LPN = 2) 4 ................................................................................................................... 2 Arkansas mussels (Neosho mucket (LPN = 2) & Rabbitsfoot (LPN = 9)) 4 .................................... Diamond darter (LPN = 2) 4 ................................................................................................................. Gunnison sage-grouse (LPN = 2) 4 ..................................................................................................... Coral Pink Sand Dunes Tiger Beetle (LPN = 2) 5 ............................................................................... Miami blue (LPN = 3) 3 ........................................................................................................................ Lesser prairie chicken (LPN = 2) ......................................................................................................... 4 Texas salamanders (Austin blind salamander (LPN = 2), Salado salamander (LPN = 2), Georgetown salamander (LPN = 8), Jollyville Plateau (LPN = 8)) 3. 5 SW aquatics (Gonzales Spring Snail (LPN = 2), Diamond Y springsnail (LPN = 2), Phantom springsnail (LPN = 2), Phantom Cave snail (LPN = 2), Diminutive amphipod (LPN = 2)) 3. 2 Texas plants (Texas golden gladecress (Leavenworthia texana) (LPN = 2), Neches River rosemallow (Hibiscus dasycalyx) (LPN = 2)) 3. 4 AZ plants (Acuna cactus (Echinomastus erectocentrus var. acunensis) (LPN = 3), Fickeisen plains cactus (Pediocactus peeblesianus fickeiseniae) (LPN = 3), Lemmon fleabane (Erigeron lemmonii) (LPN = 8), Gierisch mallow (Sphaeralcea gierischii) (LPN = 2)) 5. FL bonneted bat (LPN = 2) 3 ............................................................................................................... 3 Southern FL plants (Florida semaphore cactus (Consolea corallicola) (LPN = 2), shellmound applecactus (Harrisia (=Cereus) aboriginum (=gracilis)) (LPN = 2), Cape Sable thoroughwort (Chromolaena frustrata) (LPN = 2)) 5. 21 Big Island (HI) species 5 (includes 8 candidate species—6 plants & 2 animals; 4 with LPN = 2, 1 with LPN = 3, 1 with LPN = 4, 2 with LPN = 8). VerDate Mar<15>2010 17:26 Jun 06, 2011 Jkt 223001 PO 00000 Frm 00051 Fmt 4702 Sfmt 4702 Proposed listing. Proposed listing. Proposed listing. Proposed listing. Proposed Proposed Proposed Proposed Proposed Proposed Proposed Proposed Proposed listing. listing. listing. listing. listing. listing. listing. listing. listing. Proposed listing. Proposed listing. Proposed listing. Proposed listing. Proposed listing. Proposed listing. E:\FR\FM\07JNP1.SGM 07JNP1 Federal Register / Vol. 76, No. 109 / Tuesday, June 7, 2011 / Proposed Rules 32929 ACTIONS FUNDED IN FY 2010 AND FY 2011 BUT NOT YET COMPLETED—Continued Species Action 12 Puget Sound prairie species (9 subspecies of pocket gopher (Thomomys mazama ssp.) (LPN = 3), streaked horned lark (LPN = 3), Taylor’s checkerspot (LPN = 3), Mardon skipper (LPN = 8)) 3. 2 TN River mussels (fluted kidneyshell (LPN = 2), slabside pearlymussel (LPN = 2)) 5 .................... Jemez Mountain salamander (LPN = 2) 5 ........................................................................................... Proposed listing. Proposed listing. Proposed listing. 1 Funds for listing actions for these species were provided in previous FYs. funds for these high-priority listing actions were provided in FY 2008 or 2009, due to the complexity of these actions and competing priorities, these actions are still being developed. 3 Partially funded with FY 2010 funds and FY 2011 funds. 4 Funded with FY 2010 funds. 5 Funded with FY 2011 funds. 2 Although We have endeavored to make our listing actions as efficient and timely as possible, given the requirements of the relevant law and regulations, and constraints relating to workload and personnel. We are continually considering ways to streamline processes or achieve economies of scale, such as by batching related actions together. Given our limited budget for implementing section 4 of the Act, these actions described above collectively constitute expeditious progress. The striped newt will be added to the list of candidate species upon publication of this 12-month finding. We will continue to monitor the status of this species as new information becomes available. This review will determine if a change in status is warranted, including the need to make prompt use of emergency listing procedures. We intend that any proposed classification of the striped newt will be as accurate as possible. Therefore, we will continue to accept additional information and comments from all concerned governmental agencies, the scientific community, industry, or any other interested party concerning this finding. References Cited A complete list of references cited is available on the Internet at http:// www.regulations.gov and upon request from the U.S. Fish and Wildlife Service, North Florida Field Office (see ADDRESSES section). emcdonald on DSK2BSOYB1PROD with PROPOSALS Authors The primary authors of this notice are the staff members of the North Florida Field Office. Authority [FR Doc. 2011–13911 Filed 6–6–11; 8:45 am] BILLING CODE 4310–55–P DEPARTMENT OF COMMERCE National Oceanic and Atmospheric Administration 50 CFR Part 665 [Docket No. 100218104–1291–01] RIN 0648–AY27 Western Pacific Pelagic Fisheries; American Samoa Longline Gear Modifications To Reduce Turtle Interactions National Marine Fisheries Service (NMFS), National Oceanic and Atmospheric Administration (NOAA), Commerce. ACTION: Proposed rule; request for comments. AGENCY: This proposed rule would require specific gear configuration for pelagic longline fishing for vessels based in American Samoa, as well as other U.S. longline vessels longer than 40 ft (12.2 m), while fishing south of the Equator in the Pacific Ocean. The requirements include minimum float line and branch line lengths, number of hooks between floats, and distances between floats and adjacent hooks. The rule would also limit the number of swordfish taken. The proposed action is intended to ensure that longline hooks are set at depths of 100 meters (m) or deeper to reduce interactions between longline fishing and Pacific green sea turtles. SUMMARY: Comments on the proposed rule must be received by July 22, 2011. ADDRESSES: Comments on this proposed rule, identified by 0648–AY27, may be sent to either of the following addresses: DATES: The authority for this section is section 4 of the Endangered Species Act of 1973, as amended (16 U.S.C. 1531 et seq.). VerDate Mar<15>2010 Dated: May 3, 2011. Rowan W. Gould, Acting Director, Fish and Wildlife Service. 17:26 Jun 06, 2011 Jkt 223001 PO 00000 Frm 00052 Fmt 4702 Sfmt 4702 • Electronic Submission: Submit all electronic public comments via the Federal e-Rulemaking Portal http:// www.regulations.gov; or • Mail: Michael D. Tosatto, Regional Administrator, NMFS, Pacific Islands Region (PIR), 1601 Kapiolani Blvd., Suite 1110, Honolulu, HI 96814–4700. Instructions: Comments must be submitted to one of the above two addresses to ensure that the comments are received, documented, and considered by NMFS. Comments sent to any other address or individual, or received after the end of the comment period, may not be considered. All comments received are a part of the public record and will generally be posted to http://www.regulations.gov without change. All personal identifying information (e.g., name, address, etc.) submitted voluntarily by the commenter may be publicly accessible. Do not submit confidential business information, or otherwise sensitive or protected information. NMFS will accept anonymous comments (enter ‘‘N/A’’ in the required name and organization fields if you wish to remain anonymous). Attachments to electronic comments will be accepted in Microsoft Word or Excel, WordPerfect, or Adobe PDF file formats only. The Western Pacific Fishery Management Council (Council) prepared Amendment 5 to the Fishery Ecosystem Plan for Pelagic Fisheries of the Western Pacific Region (Pelagics FEP), including an environmental assessment, that presents background information on this proposed rule. The Pelagics FEP and Amendment 5 are available from the Council, 1164 Bishop St., Suite 1400, Honolulu, HI 96813, tel 808–522–8220, fax 808–522–8226, http://www.wpcouncil.org. FOR FURTHER INFORMATION CONTACT: Adam Bailey, Sustainable Fisheries Division, NMFS PIR, 808–944–2248. SUPPLEMENTARY INFORMATION: Longline fishing employs a mainline that is suspended below the surface by floats and float lines that are attached along E:\FR\FM\07JNP1.SGM 07JNP1

Agencies

[Federal Register Volume 76, Number 109 (Tuesday, June 7, 2011)]
[Proposed Rules]
[Pages 32911-32929]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-13911]


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DEPARTMENT OF THE INTERIOR

Fish and Wildlife Service

50 CFR Part 17

[Docket No. FWS-R4-ES-2010-0007; MO 92210-0-0008 B2]


Endangered and Threatened Wildlife and Plants; 12-Month Finding 
on a Petition To List the Striped Newt as Threatened

AGENCY: Fish and Wildlife Service, Interior.

ACTION: Notice of 12-month petition finding.

-----------------------------------------------------------------------

SUMMARY: We, the U.S. Fish and Wildlife Service (Service), announce a 
12-month finding on a petition to list the striped newt (Notophthalmus 
perstriatus) as threatened under the Endangered Species Act of 1973, as 
amended (Act). After review of all available scientific and commercial 
information, we find that listing the striped newt as endangered or 
threatened is warranted. Currently, however, listing the striped newt 
is precluded by higher priority actions to amend the Lists of 
Endangered and Threatened Wildlife and Plants. Upon publication of this 
12-month petition finding, we will add the striped newt to our 
candidate species list. We will develop a proposed rule to list the 
striped newt as our priorities allow. We will make any determination on 
critical habitat during development of the proposed listing rule. 
During any interim period, we will address the status of the candidate 
taxon through our annual Candidate Notice of Review (CNOR).

DATES: The finding announced in this document was made on June 7, 2011.

ADDRESSES: This finding is available on the Internet at http://www.regulations.gov at Docket Number FWS-R4-ES-2010-0007. Supporting 
documentation we used in preparing this finding is available for public 
inspection, by appointment, during normal business hours at the U.S. 
Fish and Wildlife Service, North Florida Field Office, 7915 Baymeadows 
Way, Suite 200, Jacksonville, FL 32256. Please submit any new 
information, materials, comments, or questions concerning this finding 
to the above street address.

FOR FURTHER INFORMATION CONTACT: Dave Hankla, Field Supervisor, North 
Florida Field Office (see ADDRESSES); by telephone at (904) 731-3336; 
or by facsimile at (904) 731-3045. If you use a telecommunications 
device for the deaf (TDD), please call the Federal Information Relay 
Service (FIRS) at 800-877-8339.

SUPPLEMENTARY INFORMATION: 

Background

    Section 4(b)(3)(B) of the Act (16 U.S.C. 1531 et seq.) requires 
that, for any petition to revise the Federal Lists of Threatened and 
Endangered Wildlife and Plants that contains substantial scientific or 
commercial information that listing a species may be warranted, we make 
a finding within 12 months of the date of receipt of the petition. In 
this finding, we determine whether the petitioned action is: (a) Not 
warranted, (b) warranted, or (c) warranted, but immediate proposal of a 
regulation implementing the petitioned action is precluded by other 
pending proposals to determine whether species are threatened or 
endangered, and expeditious progress is being made to add or remove 
qualified species from the Federal Lists of Endangered and Threatened 
Wildlife and Plants. Section 4(b)(3)(C) of the Act requires that we 
treat a petition for which the requested action is found to be 
warranted but precluded as though resubmitted on the date of such 
finding, that is, requiring a subsequent finding to be made within 12 
months. We must publish these 12-month findings in the Federal 
Register.

Previous Federal Actions

    On July 14, 2008, we received a petition dated July 10, 2008, from 
Dr. D. Bruce Means, Ryan C. Means, and Rebecca P.M. Means of the 
Coastal Plains Institute and Land Conservancy (CPI), requesting that 
the striped newt (Notophthalmus perstriatus) be listed as threatened 
under the Act. Included in the petition was supporting information 
regarding the species' taxonomy, biology, historical and current 
distribution, and present status, as well as a summary of actual and 
potential threats. We acknowledged the receipt of the petition in a 
letter to petitioners dated August 15, 2008. In that letter we also 
stated that we could not address their petition at that time because 
responding to existing court orders and settlement agreements for other 
listing actions required nearly all of our listing funding.
    Funding became available to begin processing the petition in early 
2010. On March 23, 2010, we published a 90-day finding (75 FR 13720) 
that the petition presented substantial information indicating that 
listing the striped newt may be warranted and that we were initiating a 
status review, for which we would accept public comments until May 24, 
2010. This

[[Page 32912]]

notice constitutes the 12-month finding on the July 14, 2008, petition 
to list the striped newt as threatened.

Species Information

    Our 90-day finding summarized much of the current literature 
regarding the striped newt's distribution, habitat requirements, and 
life history, and may be reviewed for detailed information (75 FR 
13720, March 23, 2010). Below, we briefly summarize previously 
presented information, and provide new information that we believe is 
relevant to understanding our analysis of the factors affecting the 
striped newt.

Taxonomy and Species Description

    There are three species of Notophthalmus found in North America. 
These include the eastern red spotted newt (N. viridescens), the black-
spotted newt (N. meridionalis), and the striped newt (N. perstriatus). 
The three species are found in different areas throughout the United 
States and Mexico (Reilly 1990, p. 51). Reilly (1990, p. 53), in his 
study of Notophthalmus spp., found that N. perstriatus and N. 
meridionalis are distinct species that are more similar and 
phylogenetically more closely related than either is to N. viridescens. 
In 2008, Zhang et al. (2008, pp. 586 and 592) looked at the 
phylogenetic relationship (i.e., evolutionary history of an organism) 
of the family Salamandridae and found that the clade (i.e., group of 
species that includes all descendents of a common ancestor) containing 
newts was separate from the clade containing ``true'' salamanders. The 
branching order of the clades for newts are: Primitive newts 
(Echinotriton, Pleurodeles, and Tylototriton), New World newts 
(Notophthalmus and Taricha), Corisca-Sardinia newts (Euproctus), modern 
European newts (Calotriton, Lissotriton, Mesotriton, Neurergus, 
Ommatotriton, and Triturus), and modern Asian newts (Cynops, 
Pachytriton, and Paramesotriton). New World newts, which include 
Notophthalmus, originally evolved from salamandrids migrating from 
Europe to North America via the North Atlantic land bridge during the 
Mid-Late Eocene (Zhang et al. 2008, p. 595).
    Another genetic study, conducted in 2010, looked at whether 
populations of Notophthalmus perstriatus that occur in two regions 
separated by 125 kilometers (km) (78 miles (mi)) exhibit genetic and 
ecological differentiation showing that these two regions are separate 
conservation units (Dodd et al. 2005, p. 887; Dodd and LaClaire 1995, 
p. 42; Franz and Smith 1999, p. 12; Johnson 2001, pp. 115-116; May et 
al. undated, unpublished report). One region consists of populations 
located in peninsular Florida and southeastern Georgia, and the other 
region consists of populations located in northwestern Florida and 
southwestern Georgia (Dodd and LaClaire 1995, p. 42; Franz and Smith 
1999, p. 13). May et al. (2010, undated, unpublished report) found that 
there is gene flow between localities within each region, but none were 
shared between regions. Johnson (2001, pp. 107, 113-115) found genetic 
exchange between populations is minimal or nonexistent due to upland 
habitat fragmentation that has limited long-distance dispersals and 
restricted gene flow. In 2001, Johnson (2001, p. 115) found there was 
enough genetic divergence to show that the western region is different 
than the eastern regions. However, May et al. (2010, unpublished 
report) did not find that there was sufficient genetic divergence to 
support splitting eastern and western regions into separate species.
    May et al. (2010, unpublished report) ran niche-based distribution 
models that showed that there were significant climatic and 
environmental differences between the two regions when considering 
temperature and precipitation. The western region is characterized by 
lower mean temperatures and more extreme winter cold, coupled with 
higher variation in temperature and precipitation. These differences in 
temperatures and precipitation between the regions should be considered 
if translocation between regions is to be used for conservation of this 
species. Understanding genetic structure and species ecology will 
ensure that genetically similar individuals are moved between areas 
with similar environmental conditions.

Life History and Biology

    Life-history stages of the striped newt are complex, and include 
the use of both aquatic and terrestrial habitats throughout their life 
cycle. Striped newts are opportunistic feeders that prey on frog eggs, 
worms, snails, fairy shrimp, spiders, and insects (adult and larvae) 
that are of appropriate size (Dodd et al. 2005, p. 889; Christman and 
Franz 1973, pp. 134-135; Christman and Means 1992, pp. 62-63). 
Christman and Franz (1973, p. 135) found that newts were attracted to 
frog eggs by smell. Feeding behavior of newts has only been documented 
with aquatic adults; little is known of the feeding habits in the 
terrestrial stage (Dodd et al. 2005, p. 889).
    Aquatic and breeding adults occur in isolated, temporary ponds 
associated with well-drained sands. Sexually mature adults migrate to 
these breeding ponds, which lack predatory fish, and courtship, 
copulation, and egg-laying take place there. Females lay eggs one at a 
time and attach them to aquatic vegetation or other objects in the 
water. It may take one female several months to lay all of her eggs 
(Johnson 2005, p. 94). Eggs hatch and develop into externally-gilled 
larvae in the temporary pond environment.
    Once larvae reach a size suitable for metamorphosis, they may 
either undergo metamorphosis and exit the pond as immature, terrestrial 
efts, or remain in the pond and eventually mature into gilled, aquatic 
adults (paedomorphs) (Petranka 1998, pp. 449-450; Johnson 2005, p. 94). 
The immature, terrestrial efts migrate into the uplands where they 
mature into terrestrial adults. Efts will remain in the uplands until 
conditions are appropriate (adequate rainfall) to return to the ponds 
to reproduce. Johnson (2005, p. 94) found that 25 percent of larvae 
became paedomorphs at his study pond. Paedomorphs will postpone 
metamorphosis until after they have matured and reproduced. At about a 
year old, they will reproduce, metamorphose, and migrate into the 
uplands adjacent to the pond (Johnson 2005, pp. 94-95). Once there are 
proper conditions (e.g., adequate rainfall) at the ponds, the 
terrestrial adults will move back to the ponds to court and reproduce. 
Once they return to the ponds, they are referred to as aquatic adults.
    Striped newts as well as other Notophthalmus spp. have long 
lifespans (approximately 12 to 15 years) in order to cope with 
unfavorable stochastic environmental events (e.g., drought) that can 
adversely affect reproduction (Dodd 1993b, p. 612; Dodd et al. 2005, p. 
889; Wallace et al. 2009, p. 139).
    Movement of striped newts by both emigration and immigration occurs 
between ponds and surrounding uplands. Adult newts immigrate into ponds 
from uplands during the fall and winter months, but some newts also 
immigrate during the spring and summer months as well, when 
environmental conditions (e.g., adequate rainfall) are conducive to 
breeding (Johnson 2005, p. 95). Extended breeding periods allow striped 
newts to adapt to temporary breeding habitats whose conditions 
fluctuate within seasons (Johnson 2002, p. 395). Even with suitable 
water levels in ponds, adults emigrate back into uplands after 
breeding. There is a

[[Page 32913]]

staggered pattern of adult immigration into ponds and eft emigration 
into uplands due to the required 6 months for larvae to undergo 
metamorphosis into efts (Johnson 2002, p. 397).
    Suitability of upland habitat around breeding ponds influences the 
pattern of immigration and emigration of newts and directional 
movements (Dodd 1996, p. 46; Dodd and Cade 1998, p. 337; Johnson 2003, 
p. 16). Dodd and Cade (1998, p. 337) found that striped newts migrated 
in a direction that favored high pine sandhill habitats. Newts migrate 
into terrestrial habitats at significant distances from their breeding 
ponds. Dodd (1996, p. 46) found that 82.9 percent of 12 wetland 
breeding amphibians (including striped newts) were captured 600 meters 
(m) (1,969 feet (ft)) from the nearest wetland, and only 28 percent of 
amphibians were captured less than 400 m (1,300 ft) from the wetland. 
Johnson (2003, p. 18) found that 16 percent of striped newts in his 
study migrated more than 500 m (1, 600 ft) from ponds. Dodd and Cade 
(1998, p. 337) showed that striped newts travelled up to 709 m (2,330 
ft) from ponds. These long-distance movements of striped newts from 
breeding ponds to terrestrial habitats suggest that buffer zones around 
ponds should be established to protect upland habitats, as well as 
breeding ponds (Dodd 1996, p. 49; Dodd and Cade 1998, p. 337, Johnson 
2003, p. 19; Kirkman et al. 1999, p. 557; Semlitsch and Bodie 2003, p. 
1219). Trenham and Shaffer (2005, p. 1166) found that protecting at 
least 600 m (2,000 ft) of upland habitat would maintain a population 
with only a 10 percent reduction in mean population size in the 
California tiger salamander (Ambystoma californiense). Dodd and Cade 
(1998, p. 337) suggested that terrestrial buffer zones need to consider 
both distance and direction (migratory patterns) when created. Johnson 
(2003, p. 19) recommended a protected area extending 1,000 m (3,300 ft) 
from a breeding site as upland ``core habitat'' surrounding breeding 
ponds.
    Optimal pond hydrology is important for maintaining the complex 
life-history pathways of striped newts. If there is not enough water in 
ephemeral ponds, then larvae will not have enough time to reach the 
minimum size needed for metamorphosis and will die as ponds dry up 
(Johnson 2002, p. 398). However, permanent ponds could support 
predatory fish that feed on aquatic-breeding amphibians (Johnson 2005, 
p. 94; Moler and Franz 1987, p. 235). Variable hydroperiods in breeding 
ponds over a long time period could result in varying reproductive 
success. Dodd (1993, p. 610) found a decline in striped newts due to 
persistent drought conditions. Johnson (2002, p. 399) found that heavy 
rainfall in the winter of 1997 to spring of 1998 filled ponds to their 
maximum depth and contributed to the reproductive success at these 
ponds. At one breeding pond, a minimum hydro-period of 139 days (Dodd 
1993, pp. 609-610) was needed for larvae to reach complete 
metamorphosis. Larvae undergo metamorphosis into efts after a period of 
6 months, and in order for larvae to mature into paedomorphs, a 
breeding pond must hold water for at least a year (Johnson 2005, p. 
94). For a paedormorph to successfully reproduce, ponds must hold water 
for an additional 6 months to allow sufficient time for its larvae to 
undergo metamorphosis.
    Striped newts form metapopulations that persist in isolated 
fragments of longleaf pine-wiregrass ecosystems (Johnson 2001, p. 114; 
Johnson 2005, p. 95). Within metapopulations, ponds function as focal 
points for local breeding populations that experience periods of 
extirpation and recolonization through time (e.g., ``ponds as 
patches'') (Johnson 2005, p. 95; Marsh and Trenham 2001, p. 41). 
Striped newts typically have limited dispersal, which can lead to pond 
isolation when stochastic events (e.g., drought) affect rates of 
colonization and extinction (Marsh and Trenham 2001, p. 41). In order 
for striped newts to recolonize local breeding ponds within the 
metapopulation, newts must disperse through contiguous upland habitat 
(Dodd and Johnson 2007, p. 150). Protecting the connectivity between 
uplands and breeding ponds of diverse hydroperiods is crucial for 
maintaining metapopulations (Dodd and Johnson 2007, pp. 150-151; Gibbs 
1993, p. 25; Johnson 2005, p. 95). Only a few ``stronghold'' locations 
exist, where there are multiple breeding ponds with appropriate upland 
habitat that allow dispersal to occur among the ponds (Johnson 2005, p. 
95). These ``stronghold'' locations represent different metapopulations 
across the range of the striped newt (Johnson 2005, p. 95). These sites 
need to be protected and managed to provide long-term protection for 
newts. In Florida, these include Apalachicola National Forest, Ocala 
National Forest, Jennings State Forest, Katherine Ordway-Swisher 
Biological Station, and Camp Blanding Training Site. In Georgia, they 
are found at Joseph Jones Ecological Research Center and Fort Stewart 
Military Installation (Johnson 2005, p. 95; Stevenson 2000, p. 4).

Habitat

    Ephemeral ponds are important components of upland habitat in the 
southeastern United States (LaClaire and Franz 1990, p. 9). Ephemeral 
ponds tend to be described as small (typically less than 5 hectares 
(ha) (12.4 acres (ac)), isolated wetlands with a cyclic nature of 
drying and refilling known as hydroperiods. Ephemeral ponds can hold 
water at various times throughout a year to allow for reproduction. 
Precipitation is the most important water source for ephemeral ponds 
(LaClaire and Franz 1990, p. 12). The cyclical nature of ephemeral 
ponds prevents predatory fish from inhabiting breeding ponds (Dodd and 
Charest 1988, pp. 87, 94; LaClaire and Franz 1990, p. 12; Moler and 
Franz 1987, p. 237). Ephemeral ponds are biologically unique, because 
they support diverse species that are different than species found in 
larger, more permanent wetlands or ponds (Moler and Franz 1987, pp. 
234, 236; Kirkman et al. 1999, p. 553).
    The frequency and duration of water in ephemeral ponds creates 
different zones of vegetation within ponds. One species, maidencane 
(Panicum hemitomon), has been found at ephemeral ponds where striped 
newts have been found, and seems be a good indicator of the extent of 
previous flooding in ponds (LaClaire 1995, p. 88; LaClaire and Franz 
1990, p. 10). Persistence of maidencane helps to reduce the rate of 
oxidation of organic matter, reduce soil moisture loss, and inhibit 
growth and establishment of upland plant species (LaClaire 1995, p. 
94). The center of flooded ponds may contain floating-leaved plants, 
and is surrounded by vegetation with submerged roots growing along the 
wet edges. Surrounding the wet areas are tall and short emergents, such 
as sedges, grasses, and rushes such as sandweed (Hypericum 
fasciculatum), followed by other grasses such as bluestem grass 
(Andropogon virginicus) found in the drier margins of ponds. Water-
tolerant shrubs or trees are found in some transitional zones between 
pond and uplands (LaClaire 1995, p. 74; LaClaire and Franz 1990, p. 
10).
    Ephemeral ponds are surrounded by upland habitats of high pine, 
scrubby flatwoods, and scrub (Christman and Means, 1992, p. 62). 
Longleaf pine-turkey oak stands with intact ground cover containing 
wiregrass (Aristida beyrichiana) are the preferred upland habitat for 
striped newts, followed by scrub, then flatwoods (K. Enge, Florida Fish 
and Wildlife Conservation

[[Page 32914]]

Commission, personal communication, May 24, 2010).
    Striped newt habitat is fire-dependent, and naturally ignited fires 
and prescribed burning maintain an open canopy and reduce forest floor 
litter. An open canopy provides sunlight necessary for ground cover 
growth needed by newts for foraging and sheltering. Fire is also an 
important factor for wetland vegetation (LaClaire and Franz 1990, p. 
10; Means 2008, p. 4). Historically, fire would be naturally ignited in 
the uplands during the late spring and early summer, and would sweep 
through the dry pond basins, reducing organic matter and killing 
encroaching upland plant species (Means 2008, p. 4; Myer 1990, p. 189). 
Lack of fire in uplands that buffer breeding ponds allows fire-
intolerant hardwoods to shade out herbaceous understory needed by 
striped newts for foraging and sheltering. As a result, fire shadows 
may form along the upslope wetland and upland boundary. The vegetation 
in this area contains fire-intolerant evergreen shrubs (Ilex spp., 
Vaccinium spp., Myrica spp., and Ceratiola spp.) and sometimes xeric 
oak hammock zones (LaClaire and Franz 1990, p. 11). Ponds that are 
completely burned from the upland margin to the opposite margin lack 
this vegetation; however, if the ponds are filled with water, fire will 
burn out at the pond, and allow the invasion of fire-intolerant 
hardwoods (LaClaire and Franz 1990, p. 11). The impacts of fire on 
these temporary ponds promote species richness of grasses and sedges, 
especially during droughts (Means 2006, p. 196). To eliminate hardwood 
encroachment, a prescribed fire regime should be used every 1 to 3 
years during May to June, in order to protect striped newt habitat 
(Means 2006, p. 196).
    Striped newts use upland habitats that surround breeding ponds to 
complete their life cycle. Efts move from ponds to uplands where they 
mature into terrestrial adults. The uplands also provide habitat for 
the striped newt to forage and burrow during the non-breeding season 
(Dodd and Charest 1988, p. 95). Striped newts also use uplands to 
access alternative ponds that are needed if the original breeding pond 
is destroyed or the hydroperiod is altered (Means 2006, p. 197). This 
shows the interdependence between upland and aquatic habitats in the 
persistence of populations (Semlitsch and Bodie 2003, p. 1219). Semi-
aquatic species (such as the striped newt) depend on both aquatic and 
upland habitats for various parts of their life cycle in order to 
maintain viable populations (Dodd and Cade 1998, pp. 336-337; Johnson 
2001, p. 47; Semlitsch 1998, p. 1116; Semlitsch and Bodie 2003, p. 
1219).

Distribution

    The range of the striped newt extends from the Atlantic Coastal 
Plain of southeastern Georgia to the north-central peninsula of Florida 
and through the Florida panhandle into portions of southwest Georgia 
(Dodd et al. 2005, p. 887). There is a 125-km (78-mi) separation 
between the western and eastern portions of the striped newt's range 
(Dodd et al. 2005, p. 887; Dodd and LaClaire 1995, p. 42; Franz and 
Smith 1999, p. 12; Johnson 2001, pp. 115-116). The historical range of 
the striped newt was likely similar to the current range (Dodd et al. 
2005, p. 887). However, loss of native longleaf habitat, fire 
suppression, and the natural patchy distribution of upland habitats 
used by striped newts have resulted in fragmentation of existing 
populations (Johnson and Owen 2005, p. 2).
    In Figure 1, we provide a map illustrating the current and 
historical ranges of the striped newt on public lands. The dark-shaded 
areas represent the currently occupied sites documented from 2005 to 
2010 surveys of public lands (Enge, FWC, personal communication, 2010; 
Jensen, Georgia Department of Natural Resources (GDNR), personal 
communication, 2010). The light-shaded areas represent the historical 
range where striped newts are now extirpated. There are from 1 to 30 
breeding ponds documented within dark shaded areas. However, due to the 
scale of the map, the specific ponds are not identified. This map 
represents the best available information used to establish the 
species' range.

[[Page 32915]]

[GRAPHIC] [TIFF OMITTED] TP07JN11.009

    To determine where there may be additional unsurveyed suitable 
habitat for striped newts in Florida, Endries et al. (2009, pp. 45-46) 
developed a striped newt habitat model. The model was developed using 
Florida Fish and Wildlife Conservation Commission (FWC) 2003 landcover 
classes. Three classes were identified: (1) Breeding (bay, cypress 
swamp, freshwater marsh, wet prairie), (2) primary upland (sandhill, 
xeric oak scrub, sand pine scrub), and (3) secondary upland (hardwood 
hammocks and forests, pinelands, and shrub and brushlands). Then 
potential habitat was evaluated for each class. Breeding habitat was 
limited to patches that were less than 9 ha (22 ac) in size and which 
were contiguous with upland habitats. The primary upland habitats 
included in the model were those areas contiguous and within 1,000 m 
(3,300 ft) of breeding habitat. Secondary upland habitat was included 
for areas that were contiguous and within 500 m (1,600 ft) of primary 
uplands and 1,000 m (3,300 ft) of breeding habitat.
    The GIS analysis found a total of 244,576 ha (604,360 ac) of 
potential habitat (Endries et al. 2009, p. 45). Of the potential 
habitat, 122,724 ha (303,257 ac) occurred on 124 sites within public 
lands, but only 64 of these sites had greater than 40 ha (100 ac) of 
potential habitat. The remaining habitat was found on privately owned 
lands in patches that were greater than 79 ha (195 ac) (Endries et al. 
2008, pp. 45-46). Of the potential habitat found on public lands, 55 
percent occurred on Ocala National Forest (ONF), 8 percent on Camp 
Blanding Military Installation, 6 percent on Withlacoochee State 
Forest, 5.3 percent on Apalachicola National Forest (ANF), and 2.9 
percent on Jennings State Forest (Enge, FWC, personal communication, 
2010). However, no records of striped newt occurrences have been found 
at Withlacoochee State Forest, even though this appears to be suitable 
habitat. Ocala National Forest has 67,514 ha (166,831 ac) of potential 
habitat and 39 occupied ponds, making it the largest ``stronghold'' for 
metapopulations for striped newts in Florida (Enge, FWC, personal 
communication, 2010). Striped newts are also found in ponds throughout 
Peninsular Florida at Ordway-Swisher Biological Station, Camp Blanding 
Joint Training Center, Jennings State Forest, Goethe State Forest, Rock 
Springs State Park, Ft. White Mitigation Park, Faver-Dykes State Park, 
and Pumpkin Hill Creek Preserve State Park.
    Within the panhandle of Florida, striped newts have been found 
within the Munson Sandhills. This site represents a small physiographic 
region within the Gulf Coastal Plains in Florida (Means and Means 
1998a, p. 3). Striped newts have only been located in the western 
portion of the Munson Sandhills within the ANF. No newts have been 
found in the eastern portion of the sandhills since the 1980s, when the 
area was converted to a dense sand pine (Pinus clausa) plantation 
(Means and Means 1998a, p. 6). Striped newt distribution continues 
north of this site to the Tallahassee Red Hills and Tifton Uplands, and 
finally to the Dougherty Plain in southwestern Georgia. However, the 
Tallahassee Red Hills no

[[Page 32916]]

longer support the newt. Striped newts were documented once in a 
breeding pond found in the Red Hills, but this site was dredged, 
deepened, and stocked with game fish in the 1980s, and no longer 
supports newts (Means and Means 1998b, pp. 6, 15).
    The striped newt is currently known to occur in five separate 
locations in Georgia, including Fort Stewart, Lentile Property, Joseph 
W. Jones Ecological Research Center (JJERC), Fall Line Sandhills 
Natural Area, and Ohoopee Dunes Natural Area (J. Jensen, GDNR, personal 
communication, September 14, 2010; L. Smith, JJERC, personal 
communication, September 11, 2010; Stevenson 2000, p. 4; Stevenson and 
Cash 2008, p. 252; Stevenson et al. 2009a, pp. 2-3). Most of these 
locations are within the Dougherty Plain (Baker Co.), Tifton Uplands 
(Irwin, Lanier, and Lowndes Counties), and the Barrier Island Sequence 
(Bryan, Camden, Charlton, Evans, and Long Counties) (Dodd and LaClaire 
1995, pp. 40-42). From 1993 to 1994, Dodd and LaClaire (1995, p. 40) 
found striped newts in one pond each at five sites in Irwin, Baker, and 
Charlton Counties, and a series of ponds at Ft. Stewart in Bryan and 
Evans Counties. A pond in Baker County at JJERC was found to be a new 
location, and extends the known range west of the Flint River 
approximately 115 km (71 mi) farther from the nearest recorded site 
(LaClaire et al. 1995, pp. 103-104; Franz and Smith 1999, p. 13). 
Striped newts were first found on Trail Ridge in 1924 near Okefenokee 
National Wildlife Refuge (ONWR), but this area has been highly modified 
since the 1940s (Dodd 1995, p. 44; Dodd and LaClaire 1995, pp. 39-40), 
and newts are no longer found in this area, except for possibly in the 
ONWR. In 2008, a new striped newt site was found in Georgia in Camden 
County, which is the first record for this county since 1953 (Stevenson 
et al. 2009b, p. 248).

Population Status and Trends

    Surveys have been conducted for striped newts at many sites within 
Florida and Georgia. These surveys have found that the number of known 
occupied sites has declined and occupied sites are limited to just a 
few counties. However, historical information on the location of 
striped newts is difficult to confirm, as most of these sites underwent 
substantial land use changes since newts were first collected (Dodd et 
al. 2005, p. 887).
    Franz and Smith (1999, p. 8) reviewed 100 records from 20 counties 
in Florida between 1922 and 1995, and conducted surveys between 1989 
and 1995. They found that 4 historical ponds had newts, but also found 
34 new ponds containing newts were that were not part of the historical 
records. All 38 breeding ponds were found on 7 public lands that 
included ANF, Camp Blanding Military Reservation, Favor-Dykes State 
Park, Jennings State Forest, Katharine Ordway Preserve-Swisher Memorial 
Sanctuary, ONF, and Rock Springs State Preserve (Franz and Smith, 1999, 
pp. 8-9).
    Johnson and Owen (2005, p. 7) visited 51 sites in 11 counties in 
Florida from 2000 to 2003 that overlapped with the sites visited by 
Franz and Smith. They found that of 51 sites visited (totaling 64 
ponds), only 26 ponds and adjacent upland habitat had excellent habitat 
quality (e.g., multiple ephemeral ponds surrounded by fire-maintained 
native uplands) capable of supporting striped newts. Only 4 of these 26 
sites had multiple breeding ponds needed to comprise metapopulations. 
They were found in Clay, Marion, and Putnam Counties in Camp Blanding 
Military Reservation (Clay), Jennings State Forest (Clay), Ocala 
National Forest (Marion), and Katherine Ordway Preserve-Swisher 
Memorial Sanctuary (Putnam) (Johnson and Owen 2005, p. 7).
    From 2005 to 2010, Enge (FWC, personal communication, 2010) 
surveyed ponds in suitable habitat on 32 conservation lands in Florida. 
He found breeding ponds with newts in 58 ponds on 11 of the 32 
conservation lands. He also found that although newts had a wider range 
in Florida than Georgia, they remained abundant only on public lands in 
Clay, Marion, and Putnam Counties. This is consistent with the surveys 
conducted by Franz and Smith (1999, pp. 8-9) and Johnson and Owen 
(2005, p. 7). He found that there were a total of 49 extant populations 
known from the peninsula of Florida and 7 populations from the 
panhandle. An isolated breeding pond farther than 1,000 m (3,300 ft) 
from the closest other breeding pond represents a separate population 
(Enge, FWC, personal communication, 2010). The striped newt 
metapopulations (i.e., multiple breeding ponds with enough upland to 
allow for dispersal) are now only found on public lands in Clay, 
Putnam, and Marion Counties. Populations still exist in 10 other 
counties in Florida, but these counties have fewer than 3 breeding 
ponds and these populations are considered vulnerable to extirpation 
(Enge, FWC, personal communication, 2010).
    The status of the striped newt is unknown on private lands due to 
the difficulty in accessing these lands; however, Enge (FWC, personal 
communication, 2010) was able to survey 8 ponds on 2 private lands, and 
found newts on at least one site.
    Striped newt breeding ponds at ANF and other areas within the 
Munson Sandhills region in Leon County, Florida, have seen a decline. 
ANF was once considered a metapopulation for striped newt (Johnson 
2005, p. 95; Johnson and Owen 2005, p. 7; Enge, FWC, personal 
communication, 2010). However, the western Munson Sandhills in ANF was 
surveyed from 1995-2007, and researchers were only able to locate 18 
breeding ponds (containing larvae or breeding adults) in 265 ephemeral 
ponds surveyed (Means and Means 1998a, p. 5). Means et al. (2008, p. 6) 
found only 5 adult striped newts and no larvae in the past 10 years. 
Since 2000, severe drought conditions were experienced at these ponds, 
and newts were shown to be declining. Recent surveys conducted in the 
Munson Sandhills in 2010 were not able to locate any striped newts at 
any of the breeding ponds (Means, CPI, personal communication, 2010). 
The precipitous apparent declines now being seen at ANF could occur 
elsewhere on protected lands within the striped newt's range, despite 
the protection of habitat. This indicates that perhaps other threats 
(e.g., disease and drought) may continue to act on the species at these 
sites.
    As mentioned above, striped newts have only been found at five 
locations in Georgia, and these sites are highly fragmented and 
isolated (Stevenson 2000, p. 4). An amphibian survey on 196 ephemeral 
ponds in 17 counties on timber company lands in the Coastal Plain of 
southeastern Georgia did not locate any striped newts in Georgia; 
however, striped newts were found in four ponds in Florida (Wigley 
1999, pp. 5-10). Stevenson (2000, p. 3) looked at 25 historic striped 
newt localities in Georgia and was only able to find 2 sites (8 
percent) that had multiple breeding ponds and upland habitat that would 
support striped newt populations. As of 2010, only 2 properties in the 
State are known to support viable populations: JJERC and Fort Stewart 
Army Base (Jensen, GDNR, personal communication, 2010; Stevenson et al. 
2009a, p. 2). The Fort Stewart population lies within the range of the 
eastern genetic group on the Atlantic Coastal Plain and was represented 
by approximately 10 known wetlands. Since 2002, striped newts have been 
found at only one wetland at Fort Stewart (Stevenson et al. 2009, p. 
2). The JJERC population lies within the range of the western genetic 
group on the Gulf Coastal Plain, and is represented by 5 known 
wetlands. In

[[Page 32917]]

annual surveys from 2002 to 2010, researchers confirmed striped newts 
from only 3 of these 5 known wetlands (Smith, JJERC, personal 
communication, 2010). Evidence suggests that both the eastern and 
western striped newt populations in Georgia are rare and declining. 
Most suitable striped newt habitat in Georgia has been lost to 
development or converted to pine plantations and silviculture (Dodd and 
LaClaire 1995, p. 43).

Summary of Information Pertaining to the Five Factors

    Section 4 of the Act (16 U.S.C. 1533) and its implementing 
regulations (50 CFR 424) set forth procedures for adding species to the 
Federal Lists of Endangered and Threatened Wildlife and Plants. Under 
section 4(a)(1) of the Act, a species may be determined to be 
endangered or threatened based on any of the following five factors:
    (A) The present or threatened destruction, modification, or 
curtailment of its habitat or range;
    (B) Overutilization for commercial, recreational, scientific, or 
educational purposes;
    (C) Disease or predation;
    (D) The inadequacy of existing regulatory mechanisms; or
    (E) Other natural or manmade factors affecting its continued 
existence.
    In making this finding, information pertaining to the striped newt 
in relation to the five factors provided in section 4(a)(1) of the Act 
is discussed below.
    In considering whether a species may warrant listing under any of 
the five factors, we look beyond the species' exposure to a potential 
threat or aggregation of threats under any of the factors, and evaluate 
whether the species responds to those potential threats in a way that 
causes actual impact to the species. The identification of threats that 
might impact a species negatively may not be sufficient to compel a 
finding that the species warrants listing. The information must include 
evidence indicating that the threats are operative and, either singly 
or in aggregation, affect the status of the species. Threats are 
significant if they drive, or contribute to, the risk of extinction of 
the species, such that the species warrants listing as endangered or 
threatened, as those terms are defined in the Act.

Factor A. The Present or Threatened Destruction, Modification, or 
Curtailment of Its Habitat or Range

    Striped newts have been found to use both aquatic and upland 
habitats throughout their life cycle. Most of these habitats have been 
destroyed or modified in the past due to: (1) Conversion of habitat to 
intensely managed, planted pine plantations or naturally regenerated 
stands (Dodd 1995b, p. 129; Wear and Greis 2002, p. 46); (2) loss of 
habitat resulting from urban development (Zwick and Carr 2006, pp. 4-
6); (3) degradation of habitat due to fire suppression (Means 2008, pp. 
27-28); and (4) degradation of the habitat by the use of off-road 
vehicles and road construction (Means 1996, p. 2; Means 2001; p. 31, 
Means 2003 p. 6; Means et al. 1994a., pp. 5-6).
Natural Pine Forest Conversion
    Natural pine forests (i.e., longleaf pine forest) that once were 
found from southeastern Virginia through eastern Texas have declined to 
about 13 million ha (33 million ac), and planted pine plantations 
increased to more than 12 million ha (30 million ac) by 1999 (Dodd 
1995b., p. 129; Wear and Greis 2002, p. 46). There are presently about 
11 million ha (27 million ac) of managed pine plantations where natural 
longleaf pines were once found (Frost 2006, p. 36). Within the longleaf 
pine ecosystem in the South's coastal plains, only 2.2 percent of the 
original range exists (Frost 2006, p. 13; Wear and Greis 2002, p. 66). 
Between 1936 and 1989, longleaf pine forests within the range of the 
striped newt in Florida decreased from more than 3 million ha (7.6 
million ac) to only 384,500 ha (950,000 ac), an 88 percent decrease 
(Dodd 1995b., p. 129). Longleaf pine forest in Georgia declined 36 
percent between 1981 and 1988 (Dodd 1995b., p. 129).
    Habitat loss from the conversion of natural pine forests to 
intensely managed, planted pine plantations has greatly disrupted the 
dispersal of striped newts between breeding ponds and upland habitat. 
Means and Means (1998a, p. 6) found that striped newt habitat at the 
Munson Sandhills varied due to differences in silvicultural practice 
between the eastern and western portions of the Sandhills. In the 
western portion of the Sandhills found within ANF, native groundcover 
remains in the second-growth longleaf pine forests, where striped newts 
spend most of their adult life. However, the eastern portion of the 
Munson Sandhills has been clear-cut and roller-chopped, and planted in 
sand pine (Pinus clausa), which is now a closed canopy with little 
native groundcover. Surveys of ponds located in the eastern Munson 
Sandhills found no striped newts after the site was converted to sand 
pine plantations (Means and Means 1998a, p. 4; Means and Means 2005, 
pp. 58-59; Means 2008, p. 30).
    Silvicultural practices, including mechanical site preparation, 
pond ditching, soil disturbance, and the use of fertilizer and 
herbicides, can interfere with migration and successful reproduction 
(Dodd 1995b, p. 130; Dodd and LaClaire 1995, pp. 43-44; Means and Means 
2005, pp. 59-60; Means 2008, p. 29). Pond ditching, which is used to 
drain ponds to create ideal conditions for silvicultural operations, is 
detrimental to striped newts, because it alters pond hydrology and 
facilitates predatory fish movement into otherwise fishless ponds 
(Means 2008, p. 30). Ditching creates a shortened hydroperiod, reducing 
the amount of time striped newts have to undergo metamorphosis, which 
can eventually decrease the number of reproducing adults (Means 2008, 
p. 31).
Urban Development
    Alteration of upland habitat to urban development can create 
habitat fragmentation and loss of metapopulations of striped newts. In 
10 coastal Georgia counties, the human population is expected to 
increase 51 percent by 2030 (Center for Quality Growth and Regional 
Development 2006, p. 4), but no estimate of impact on native habitats 
was provided. Striped newts have been found within 5 of these counties 
in Georgia, including Bryan, Camden, Long, Liberty, and Screven 
Counties (Franz and Smith 1999, p. 13, Stevenson 2000, pp. 6-7). Zwick 
and Carr (2006, pp. 4-6) modeled human population growth in Florida, 
and concluded that 2.8 million ha (7 million ac) of land will be 
converted to urban use by 2060. Of the 2.8 million ha (7 million ac), 
they estimated that about 1.1 million ha (2.7 million ac) of native 
habitat would be destroyed to accommodate urban development (Zwick and 
Carr 2006, p. 2). It is predicted that more than 800,000 ha (2 million 
ac) of native habitat in Florida will be developed by 2060 within a 
mile of public conservation lands (Zwick and Carr 2006, p. 19; FWC 
2008, p. 8). Urban sprawl where newts occur will fragment striped newt 
ponds from upland habitats. This will limit movement of newts between 
breeding ponds and make them more vulnerable to extinction, as the 
genetic viability of the newts declines (FWC 2008, p. 8). Powerlines 
and natural gas rights-of-ways impact groundcover associated with 
longleaf pine adjacent to breeding ponds, creating barriers to 
dispersal and eventually decreasing populations (Means 2001, pp. 31-
32). Striped newt habitat in the Tallahassee Red Hills has been 
impacted by urban sprawl and land conversion from 1824 to the

[[Page 32918]]

present, and has resulted in the extirpation of striped newts from this 
area (Means and Means 1998b, p. 8).
    Small, isolated wetlands support breeding populations of striped 
newts. However, small, ephemeral wetlands (less than 0.2 ha (0.5 ac)) 
receive no protection from development (Johnson 2003, p. 19; Dodd and 
Cade 1998, p. 337; see discussion under Factor D below). The loss of 
these small, ephemeral wetlands can potentially increase extinction 
rates of newts by limiting migration between ponds and corridors, thus 
decreasing recolonization of local populations (Gibbs 1993, pp. 25-26; 
LaClaire and Franz 1990, p. 13; Semlitsch and Bodie 1998, pp. 1131-
1132). Green (2003, p. 341) concluded that pond-breeding amphibians, 
like striped newts, that have highly fluctuating populations and high 
frequencies of local extinctions are likely to be affected rapidly by 
habitat fragmentation. The loss of breeding ponds due to habitat 
destruction will reduce corridors and limit migration between the ponds 
and the uplands.
Prescribed Fire
    Prescribed fire plays an important role in maintaining productive 
breeding ponds for striped newts (Kirkman et al. 1999, p. 556). Burning 
in dry ponds is also necessary to maintain the quality of vegetation 
needed for striped newts (Johnson 2005, p. 97). Fire suppression at 
many sites with newt breeding ponds has been concurrent with the 
conversion of uplands to pine plantations (Johnson 2005, p. 97). Lack 
of fire can result in the succession of natural pine forests converting 
to fire-intolerant species, dominated by hardwoods (Means 2008, pp. 27-
28). Wear and Greis (2002, pp. 46-47) found that 3.9 million ha (9.7 
million ac) of natural pine forest throughout the Southeast were 
reclassified to hardwood and natural oak-pine forests. Of the remaining 
longleaf pine habitat in the southeast, only 0.2 percent is managed 
with fire and can support native longleaf pine species of plants and 
animals, including striped newts (Frost 2006, p. 38). The succession of 
natural pine forest to more shade-tolerant species, such as oaks and 
hickories, can result in the loss of ground cover, such as wire grass, 
needed by striped newts for shelter and foraging (Means 2001, p. 31). 
Frequencies of prescribed burns in these uplands need to take place in 
a 1- to 3-year cycle to provide suitable habitat for striped newts 
(Johnson and Gjerstad 2006, pp. 287-292). This would also reduce the 
naturally woody components around the ephemeral ponds, and stimulate 
flowering of grasses used by the newts along the pond margins (Means 
2006, p. 196).
    In Florida, some public land managers do not currently have the 
resources to implement effective habitat management programs (Howell et 
al. 2003, p.10). In a questionnaire to State, Federal, and local land 
managers throughout Florida, the Service asked what impediments they 
had in effectively using prescribed fire to manage scrub, a fire-
maintained ecosystem. Many respondents indicated that funding, staff, 
and smoke management issues substantially reduced their ability to burn 
(Service 2006, Excel spreadsheet; Thomson 2010, p. 12). Less than 25 
percent of public land managers had been ranked as having an excellent 
prescribed burn program (Florida Department of Environmental Protection 
2007, p. 1). On most public lands in Florida, striped newt habitat is 
likely to continue to degrade unless land management funding and 
staffing increase in the future.
Off-Road Vehicles and Road Impacts
    Means et al. (1994, pp. 6-7; 2008, pp. 11 and 16) found that their 
study ponds at the Munson Sandhills in ANF off-road vehicle (ORV) use 
had degraded the littoral zone of the breeding ponds into barren sandy 
beaches unsuitable for striped newts. The littoral zone provides 
shallow, warm water where small aquatic invertebrates are concentrated, 
providing food for newts. ORV use also destroys the grasses and grass-
like vegetation around the ponds needed by newts for protection from 
predators such as wading birds (Means et al. 2008, p. 11). In 1994, 27 
of 100 ponds at ANF were found to be damaged by ORV use, including 3 of 
18 striped newt ponds (Means et al. 1994, pp. 6-7). By 2006, ORV 
impacts were documented at nearly every pond at ANF (Means et al. 2008, 
p. 16). However, by 2010, the ANF closed the Munson Sandhills to ORV 
use to protect the striped newt ponds (Petrick, USFS, personal 
communication, 2010; see discussion under Factor D below).
    Striped newts dispersing from breeding ponds to upland habitat are 
also impacted by roads and highways. These impacts usually result in 
direct road mortality; desiccation of small, moist-bodied animals (like 
newts) on dry asphalt; and increased exposure of these small animals to 
aerial predation (Means 1996, p. 2). At one study pond in ANF, Means 
(2003, p. 6) found that most striped newts were emigrating and 
immigrating to and from the breeding pond across a major highway, U.S. 
319.
Summary of Factor A
    We have identified a number of threats to striped newt habitat that 
have resulted in the destruction and modification of habitat in the 
past, are continuing to threaten habitat now, and are expected to 
continue to threaten striped newt habitat in the future. Indications 
are that the loss of habitat due to conversion of natural pine forests 
to more intense silvicultural management regimes will continue in 
interior portions of the range of the striped newt. Striped newt 
habitat within the species' range in Florida and Georgia is currently 
threatened with habitat loss and modification resulting from urban 
development. Habitat loss and fragmentation due to urban development 
and road construction is expected to continue in the future. Lack of, 
or inappropriate use of, prescribed fire is ongoing and likely to 
continue in the future, and has adverse effects on striped newt habitat 
and extant populations. On the basis of this analysis, we find that the 
destruction, modification, or curtailment of the striped newt's habitat 
is currently a threat and is expected to persist and possibly escalate 
in the future. Because this threat is ongoing and we expect it will 
continue over the coming decades; we consider the threat to be 
imminent. However, based on the large amount of potential habitat that 
is currently in public ownership, and fact that most of the known 
striped newt ponds are on conservation lands, we believe the magnitude 
of this threat is moderate. Based upon our review of the best 
commercial and scientific data available, we conclude that the present 
or threatened destruction, modification, or curtailment of its habitat 
or range is an imminent threat of moderate magnitude to the striped 
newt, both now and in the foreseeable future.

Factor B. Overutilization for Commercial, Recreational, Scientific, or 
Educational Purposes

    The petition provided information that striped newts were collected 
and sold during the 1970s and 1980s. However, in our 90-day finding (75 
FR 13720, March 23, 2010), we determined that there was no evidence to 
support the existence of any threat under this factor. We obtained no 
additional information during the status review to indicate that this 
factor is currently a threat to the species or will become a threat in 
the foreseeable future. Therefore, based on our review of the best 
available scientific and commercial information, we conclude that the 
striped newt is not threatened by

[[Page 32919]]

overutilization for commercial, recreational, scientific, or 
educational purposes now or in the foreseeable future.

Factor C. Disease or Predation

    In our 90-day finding (75 FR 13720, March 23, 2010), we found no 
evidence that predation was a threat to the striped newt, and we 
obtained no additional information during the status review that would 
change that finding. As to disease, below we summarize what was 
previously stated in the 90-day finding (75 FR 13720, March 23, 2010), 
as well as additional information obtained during the status review.
    Disease can be difficult to detect in pond-breeding amphibians. In 
addition, the rarity of striped newts increases the difficulty of 
documenting mortality in the species. However, there are reasons to 
believe that disease may be a possible factor in the decline of striped 
newts. Chytridiomycosis (a disease caused by Batrachochytrium 
dendrobatidis) is implicated or documented as a causative agent in many 
New World amphibian declines (Blaustein and Johnson 2003, p. 91). 
Ouellet et al. (2005, p. 1434) documented the chytrid fungal infections 
in the eastern newts (N. viridescens) in North America. A subspecies of 
the eastern newt, the central or common newt (N. v. louisanensis), has 
been found in the same ponds as the striped newt at ANF and other ponds 
in North Florida (Means 2007, p. 19; Means 2001, pp. 19-21; Means et 
al. 1994, pp. 9-10 and 30-32). The effect of the disease on striped 
newts is unknown; however, California newts (Taricha torosa) have 
tested positive for the pathogen in ponds where a die-off of the 
species was previously reported (Padgett-Flohr and Longcore 2007, p. 
177).
    Some researchers believe that disease pathogens represent one of 
the potential causes of decline of the striped newt (Blaustein and 
Johnson 2003, pp. 87-92). The presence of chytrid fungal infections 
could particularly threaten populations of striped newts, as they may 
not have the resiliency to recover after a population crash caused by 
this disease (Ouellet et al. 2005, p. 1437). Further, the effect of 
this disease could be exacerbated by other stressors, such as habitat 
degradation and climate change (Blaustein and Johnson 2003, p. 91; 
Ouellet et al. 2005, p. 1432; Rothermel et al. 2008, pp. 3, 13). Daszak 
et al. (2005, p. 3236) found that the impact of Batrachochytrium 
dendrobatidis on amphibians can vary among species, and several 
factors, such as climate (i.e., drought) and life-history traits, can 
affect the species' response to the disease. The presence of this 
disease in the range of the striped newt is not confirmed, but is a 
potential cause for concern, given the deleterious effect of the 
disease on other amphibian species.
    A group of viruses belonging to the genus Ranavirus has been shown 
to affect some local populations and cause localized die-offs of 
amphibians (Gray et al. 2009a, p. 244). The Ranavirus could be 
affecting populations of the striped newt, but it is difficult to 
detect in less abundant species (Gray et al. 2009a, p. 244), and we do 
not have confirmation that it is present in striped newt populations. 
However, Green et al. (2002, p. 334) found that Ranavirus was the most 
frequent cause of amphibian mortality in at least 10 species, including 
the spotted salamander (Ambystoma maculatum) and eastern newt, so this 
virus may be impacting striped newt populations in breeding ponds where 
other subspecies of eastern newts, such as the central newt 
(Notophthalmus viridescens louisianensis), are found. There are two 
reasons for the emergence of Ranavirus in amphibian populations: (1) 
Reduced amphibian immunity associated with increased occurrence of 
anthropogenic stressors (e.g. drought), and (2) introduction of 
Ranavirus strains into amphibian populations by humans (Gray et al. 
2009b, p. 2).
    Another recently described disease, caused by a fungus-like protist 
(Amphibiocystidium viridescens), has been reported in eastern newt 
populations (Raffel et al. 2008, p. 204). Specifically, evidence of 
mortality and morbidity due to infection with this disease, and the 
potential importance of secondary infections as a source of mortality, 
were reported (Raffel et al. 2008, p. 204). Also, Cook (2008) found a 
striped newt in captivity to be infected with a protistan parasite that 
has caused disease in other species of amphibians. This parasite, 
currently identified as Demomycoides spp. (Cook 2007, p. 2), caused 
disease resulting in a complete loss of recruitment of the Mississippi 
gopher frog population in Harrison County, Mississippi, in 2003.
Summary of Factor C
    We have found that several of the diseases mentioned above have 
resulted in mortality of species similar to the striped newt, such as 
the eastern newt (which is in the same genus as the striped newt). 
Drought conditions are predicted to be more severe and longer in the 
coming years. As drought (see discussion under Factor E below) and loss 
of habitat (see discussion under Factor A above) continue to act as 
stressors, striped newt populations may become more susceptible to 
disease outbreaks, which could potentially result in some localized 
population extinctions, as has occurred with similar species. Because, 
from the best available information, we do not know if disease is 
currently affecting the striped newt populations, but we believe it is 
likely that it will in the coming decades, we consider this threat to 
be nonimminent. Since disease has resulted in loss to similar amphibian 
species, and additional stressors (e.g., habitat loss, drought, and 
climate change) might make some populations of striped newts more 
vulnerable to disease, the magnitude of this threat is moderate. Based 
upon our review of the best commercial and scientific data available, 
we conclude that disease is a nonimminent threat of moderate magnitude 
to the striped newt within the foreseeable future.

Factor D. The Inadequacy of Existing Regulatory Mechanisms

    There is currently little Federal and State protection of isolated 
wetland habitat and surrounding upland habitats. While many States in 
the southeastern United States regulate those activities affecting 
wetlands that are exempt from section 404 of the Federal Clean Water 
Act (CWA) (33 U.S.C.1251 et seq.), Florida is the only State known to 
regulate isolated wetlands. In Georgia, there are no State laws that 
protect isolated wetlands. Lack of protection for upland habitat under 
wetland statutes can result in loss of recruitment of efts and 
paedomorphs into the breeding adult population, which would reduce the 
potential for the population to persist (Semlitsch 1998, p. 1116).
Federal Statutes and Regulations
    The CWA regulates the dredge and fill activities that adversely 
affect wetlands. Section 404 of CWA regulates the discharge of dredge 
or fill materials into wetlands. Discharges are commonly associated 
with projects to create dry land for development sites, water-control 
projects, and land clearing. The U.S. Army Corps of Engineers (COE) and 
the U.S. Environmental Protection Agency (EPA) share the responsibility 
for implementing the permitting program under section 404 of the CWA. 
EPA and COE provided a guidance memorandum for implementing recent 
court cases addressing jurisdiction over waters of the United States 
under the CWA, specifically addressing the term ``navigable waters'' 
(EPA and COE 2001, pp. 1-7; EPA and COE 2008, pp. 1-13). It is clear 
from this guidance that isolated wetlands are not considered

[[Page 32920]]

waters of the United States under the ``navigable waters'' definition 
and thus are not provided protection under the CWA. Further wetland 
regulations are reviewed by the COE for the development of wetlands 
less than 1.2 ha (3 ac) under a permit called Nationwide Permit 26 
(Kirkman et al. 1999, p. 553; Snodgrass et al. 2000, p. 415).
    The Department of the Interior, through the Service, administers 
the National Wildlife Refuge System. The National Wildlife Refuge 
System Administration Act of 1966 (NWRAA; 16 U.S.C. 668dd-668ee) 
provides legislation for the administration of a national network of 
lands and water for the conservation, management, and restoration of 
fish, wildlife, and plant resources and their habitats for the benefit 
of the American people. Amendment of the NWRAA in 1997 requires the 
refuge system to ensure that the biological integrity, diversity, and 
environmental health of refuges be maintained and requires development 
and implementation of a comprehensive conservation plan (CCP) for each 
refuge. The CCP must identify and describe the wildlife and related 
habitats in the refuge and actions needed to correct significant 
problems that may adversely affect wildlife populations and habitat (16 
U.S.C. 668dd(e)). Striped newt habitat within national wildlife refuges 
is protected from loss due to urban development. Striped newts have 
historically been observed at St. Marks National Wildlife Refuge 
(SMNWR) in Florida and Okefenokee National Wildlife Refuge (ONWR) in 
Georgia. Striped newts were historically found at ONWR in the 1920s, 
but the only known breeding pond was last occupied by newts in 1994. 
Aicher (ONWR, personal communication, September 14, 2010) has not found 
striped newts at ONWR, even though this breeding pond is still in good 
condition with well-maintained uplands surrounding it. At SMNWR, 
surveys conducted in 2002-2005 and again in 2009 were not able to 
locate any newts at 34 ponds (Enge, FWC, personal communication, 2010; 
Dodd et al. 2007, p. 29). The last known observation was in 1978, but 
now the habitat appears to be too degraded to be suitable for striped 
newts due to the lack of fire. Striped newts may indirectly benefit 
from fire management programs intended to maintain and restore habitat 
for species such as the red cockaded woodpecker (Picoides borealis) and 
gopher tortoise (Gopherus polyphemus), but no systematic monitoring 
programs are in place to evaluate striped newt responses to land 
management activities within the refuge system.
    On military installations, the Department of Defense (DOD) must 
conserve and maintain native ecosystems, viable wildlife populations, 
Federal and State listed species, and habitats as vital elements of its 
natural resource management programs, to the extent these requirements 
are consistent with the military mission (DOD Instruction 4715.3). 
Amendments to the Sikes Act (16 U.S.C. 670 et seq.) require each 
military department to prepare and implement an integrated natural 
resources management plan (INRMP) for each installation under its 
jurisdiction. The INRMP must be prepared in cooperation with the 
Service and State fish and wildlife agencies, and must reflect the 
mutual agreement of these parties concerning conservation, protection, 
and management of wildlife resources (16 U.S.C. 670a). Each INRMP must 
provide for wildlife, land and forest management, wildlife-oriented 
recreation, wildlife habitat enhancement, wetland protection, 
sustainable public use of natural resources that are not inconsistent 
with the needs of wildlife resources, and enforcement of natural 
resource laws (16 U.S.C 670a). DOD regulations mandate that resources 
and expertise needed to establish and implement an integrated natural 
resources management program are maintained (DOD Instruction 4715.3). 
These regulations further define the INRMP requirements, and mandate 
that plans be revised every 5 years and that they ensure the military 
lands suitable for management of wildlife are actually managed to 
conserve wildlife resources (DOD Instruction 4715.3).
    The effectiveness of individual INRMPs to protect striped newts 
vary between and within military departments. Because the striped newt 
is not a protected species in Florida, the INRMP for Camp Blanding 
Military Installation does not specifically address management programs 
for this species. However, management activities that benefit the red-
cockaded woodpecker and gopher tortoise, such as prescribed burning, 
should also benefit the striped newt. The striped newt is listed as 
threatened by the State of Georgia, so the INRMP for Fort Stewart Range 
and Garrison does address the specific conservation and management of 
this species.
    The Navy does incorporate protective ecosystem management into 
INRMPs for Naval Air Station Jacksonville (and associated Rodman 
Bombing Range, Pinecastle Range, and Outlying Landing Field 
Whitehouse), Naval Station Mayport, and Naval Submarine Base Kings Bay. 
However, the INRMPs do not include specific management measures for the 
striped newt.
    The Forest and Rangeland Renewable Resources Planning Act (16 
U.S.C. 36),of 1974, as amended by the National Forest Management Act of 
1976 (16 U.S.C. 1600 et seq.), requires that each national forest be 
managed under a forest plan which must be revised every 10 years. 
Regulations governing preparation of forest plans are found in 36 CFR 
219. The purpose of a forest plan is to provide an integrated framework 
for analyzing and approving future, site-specific projects and 
programs, including conservation of listed species. Identification and 
implementation of land management and conservation measures to benefit 
striped newts vary between forests. For example, on the National 
Forests in Florida, striped newts are not designated as a species for 
which special management prescriptions are implemented. There are no 
specific land management objectives for striped newts on the National 
Forests in Florida. The Land and Resource Management Plan for the 
National Forests in Florida (U.S. Forest Service 1999, entire) provides 
for the restoration of longleaf pine forest through various management 
areas located at Apalachicola National Forest (ANF) and Ocala National 
Forest (ONF). Metapopulations of striped newts are found at both of 
these forests. However, a decline of striped newt populations at ANF 
has occurred over the past 10 years (Means et al. 2008, p. 6).
State Statutes and Regulations
    Generally, State statutes and regulations protect striped newts 
from take, but the effectiveness and implementation of regulations vary 
between States. The striped newt is not currently a State-listed 
species in Florida. However, the ephemeral ponds in Florida have some 
protection under Florida State regulations. The five Water Management 
Districts (WMDs) and the Florida Department of Environmental Protection 
(FDEP) regulate wetland protection. The WMDs include isolated wetlands 
in the Environmental Resource Permit process, which requires a permit 
for any activities that would impact a wetland (SJRWMD 2010, p. 1). 
Under the WMDs permitting process, mitigation for impacts to wetlands 
below a minimum permitting threshold size of 0.2 ha (0.5 ac) is not 
addressed unless the wetland supports an endangered or threatened 
species, is connected by standing or flowing surface water at seasonal 
high water level to one or more wetlands that total

[[Page 32921]]

more than 0.2 ha (0.5 ac), or is of more than minimal value to f