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Erschienen in: Biodiversity and Conservation 3/2011

Open Access 01.03.2011 | Original Paper

Categorizing locally rare plant taxa for conservation status

verfasst von: Benjamin J. Crain, Jeffrey W. White

Erschienen in: Biodiversity and Conservation | Ausgabe 3/2011

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Abstract

Locally rare taxa are those that are rare or uncommon within a local geographical boundary while more common outside of that boundary. In addition to the rare taxa identified by global, national, and state/provincial levels, locally rare taxa are important for the preservation of species diversity and ecological processes, and therefore require effective and recognizable conservation status. Currently, there are no specific local rarity criteria in use to categorize taxa at regional jurisdictional levels. To address this need, we developed criteria for categorizing locally rare plant taxa by using the framework the Natural Heritage Network’s Element Ranking System combined with attributes of the World Conservation Union’s Red List Criteria. We then tested the efficacy of our classification system (called L-ranks) on the flora of Napa County using a geographic information system and available plant distribution data for the State of California. Results indicated that 89 taxa from 34 families met the area of occupancy criteria for local rarity status. Our findings demonstrated that with available geographic data, the proposed criteria for classifying locally rare plants can be usefully applied at the county level to identify significant peripheral plant populations. The proposed L-rank system was specifically designed to be compatible with existing multi-scale conservation programs and will augment the current systems in use by local organizations. By systematically classifying locally rare plants, current regulations that are applicable to locally rare taxa may be used more effectively in conservation planning and prioritizing at the county scale.

Introduction

Unlike globally rare taxa, which are rare with respect to our entire planet, locally rare taxa are those that are rare or uncommon within a local geographical boundary while more common outside of that boundary. Locally rare taxa are frequently composed of peripheral populations located at the edge of the taxon’s overall range. These populations commonly have significant ecological value (Safriel et al. 1994; Lesica and Allendorf 1995; Leppig and White 2006; Thuiller et al. 2008). They often harbor unique genetic and morphological lineages that provide the opportunity for divergence along novel evolutionary paths through the processes of natural selection (Safriel et al. 1994; Lesica and Allendorf 1995; Gaston 2003). Maintenance of genetic variation by locally rare plants increases the probability of overall species survival (Lesica and Allendorf 1992; Lesica and Allendorf 1995) and locales with peripheral populations often act as refugia during catastrophic range contractions (Safriel et al. 1994; Channell and Lomolino 2000). Peripheral plant populations also provide the flexibility required for responding to stochastic environmental events such as global climate change (Safriel et al. 1994; Smith et al. 2001; Leppig and White 2006; Thuiller et al. 2008). Furthermore, many plants, regardless of their rarity status, have intrinsic cultural, economic, and aesthetic value (Ehrlich and Ehrlich 1992; Daily et al. 2000; Gaston 2003). Unfortunately, locally rare taxa are susceptible to the same threats that affect all rare and endangered ecological communities.
Although there is current legislation in the United States designed to protect rare plants within large jurisdictions (e.g. CESA 1970; ESA 1973; CEQA 2005), most conservation efforts and development decisions happen at local and regional scales (Reid 1998; Brooks et al. 2006; Leppig and White 2006). In addition to the rare taxa identified by global, national, and state or provincial agencies, locally rare taxa are important for the preservation of species diversity, and therefore require effective and recognizable conservation status.
Pärtel et al. (2005) conclude that in the case of vascular plants, an analysis of multiple conservation characteristics, including restricted global and local distributions, would provide a powerful and objective tool for conservation planning. They further highlight that “biogeographic reasons” may play an important role in determining local abundance of a species, and that the area of a species distribution is the most common characteristic associated with conservation need. Furthermore, White (2004) demonstrated that area of occupancy, when used with an optimal methodology, significantly reduces experimental error for the estimation of range size, especially for rare taxa. Thus, analysis of area of occupancy criteria is important for plant conservation efforts.
Although Magney (2004) directly applied the Natural Heritage Network Element Ranking System’s (NatureServe 2006) criteria for the sub-national assessment scale to a county jurisdiction (Ventura, California), there are no specific local rarity ranks or criteria presently in use to systematically categorize taxa at the county level. Furthermore, when the absence of a standardized summary system is coupled with a frequent lack of accurate distribution data, locally rare taxa are not well integrated into conservation planning efforts. Regrettably due to such vagueness, repeatable studies are difficult and germane regulations are often not effectively applied to locally rare taxa (Leppig and White 2006). Nevertheless, several programs have been developed using various methods in attempts to identify and protect locally rare plants (see CNPS 2010).
The purpose of this research was to develop and outline a set of criteria for systematically categorizing and assigning conservation ranks to locally rare taxa. The aim was to address the current gap in the available methods for classifying biodiversity at local assessment scales (e.g., counties) in order to catalog locally rare organisms and give them conservation status. After briefly summarizing and analyzing current conservation status criteria, we introduce a proposed set of criteria that are applicable to locally rare taxa and compatible with currently established conservation systems used for larger jurisdictions. We assessed the efficacy of the new criteria by applying them to the flora of Napa County, CA. Our goal is to create a standardized protocol for identifying and categorizing locally rare plant taxa at the local or regional jurisdictional levels.

Background

Two leading international conservation organizations, The Natural Heritage Network (NatureServe) and the World Conservation Union (IUCN), have developed and implemented criteria for categorizing rare species by using combinations of quantitative and qualitative measures. Criteria are based on geographic, demographic, and ecological characteristics such as range sizes (using various methods), number of occurrences, population sizes, threat levels, and/or extinction probabilities (see IUCN 2001; NatureServe 2006 for complete descriptions). While these systems are not designed to classify locally rare taxa, they serve as excellent models for the development of a new system designed specifically to accomplish this task.
NatureServe employs a series of criteria to classify taxa into five “Element Ranks” based on their level of rarity, threat level, and population/range size trends, and uses three prefix letters (G, N, and S) to designate the geographic assessment level (Global, National, and Sub-national) of the assigned rank (NatureServe 2006; Master et al. 2009). Benefits of NatureServe’s methods include specific numerical criteria for identifying rarity by range size, population size, and number of element occurrences, as well as their applicability to multiple geographic scales and taxonomic levels. Recent updates to this system assign higher weightings to threats and trends, and thus create ranks that are closer to measuring actual vulnerability (Master et al. 2009). Overall clarity and descriptiveness of category nomenclature is also a positive attribute of the NatureServe system.
The IUCN uses its own system to categorize rare taxa on its RED List which includes specific criteria based on geographic range size, population decline, overall population size, and probability of extinction (IUCN 2001). The IUCN system categorizes species into three threat categories: Critically Endangered, Endangered, and Vulnerable. It should be noted that many of the IUCN’s criteria for individual categories, including those for area of occupancy and population numbers, do not operate alone. For example, a taxon may need to meet specific area of occupancy criteria as well as specific thresholds for two other criteria, such as extreme fragmentation and population decline, to be included in a given threat category. Additionally, many of the criteria have optional temporal components to them, such as probability of extinction within a given time frame.
In both the NatureServe and IUCN systems, their criteria for area of occupancy provide the most concrete thresholds that are readily measurable at any given time and are compatible with current data sets and tools for geographic analysis. Area of occupancy criteria for local scales has become the preferred method in which geographical data is quantified, summarized, and used for comparative analyses (Williams et al. 1996; White 1999; Draper et al. 2003). Therefore, we focus specifically on these geographic measures to develop our proposed local rarity ranking system.

Classifying local rarity

Based on our review of NatureServe’s and the IUCN’s systems, we establish a new local assessment level (L-rank) for categorizing locally rare taxa within local jurisdictions and geographic regions. Under this proposed system, a taxon will be considered locally rare if it meets minimum area of occupancy levels using grids composed of 1 km × 1 km (1 km2) cells. Although grids composed of 2 km × 2 km cells are commonly used in factoring the G, N, and S ranks, data were available at a 1 km2 scale. Cells of this size create a more accurate picture and thereby alleviate some of the problems associated with models based on larger cell sizes (Thuiller et al. 2008). At the same time, 1 km2 cells are compatible with other commonly used metric grids (e.g., 1 ha or 100 km2 cells), thus simplifying conversion of data to other scales. Moreover, unlike global, national, or sub-national assessments, it is less prohibitive to collect local data at the 1 km2 scale within a reasonable amount of time and level of effort. Accordingly, the L-rank category is an incorporation and modification of aspects of the NatureServe and IUCN systems and is specifically designed to be used in conjunction with NatureServe’s original geographic assessment scales.
To identify and classify locally rare taxa through geographic analysis, we outline specific area of occupancy criteria to designate different levels of rarity at the local scale. While we lend our support to the IUCN’s explicit area of occupancy criteria for larger scales, the same numbers cannot be logically applied to local assessment levels due to the fact that many local jurisdictions are relatively small and have an overall area of <2,000 km2, the maximum range to be considered for conservation status (IUCN 2001). If the IUCN’s area of occupancy criteria were applied to these small jurisdictions, taxa distributed throughout the entire county would still meet the minimum criteria for conservation status at the local assessment level. Therefore, we created new area of occupancy criteria specifically for the local assessment level (Table 1). Numerical criteria were chosen qualitatively based upon analysis of criteria used by other systems, available information on average county sizes in the United States, and reviews of research showing the effects of range size on susceptibility to environmental and biological stressors. The “Critically Imperiled” range size criteria of 10 km2 used in our system is based directly on the IUCN criteria for “Critically Endangered” as it is a good measure of extreme rarity and vulnerability. The criteria in our system for “Imperiled” and “Vulnerable to Threat or Extinction” increase exponentially from the criteria for “Critically Imperiled” in a manner similar to the IUCN system but were downscaled to a more appropriate size for county level assessments.
Table 1
Criteria for proposed L-rank system based on area of occupancy using km2 raster grid cells
L-rank categories
Criteria
X = Presumed extinct
Not located despite extensive searches and virtually no likelihood of rediscovery
H = Possibly extinct
Missing; known from only historical occurrences but still some hope of rediscovery
1 = Critically imperiled
Area < 10 km2 (or fewer then ten 1 km2 cells)
2 = Imperiled
Area < 50 km2 (or fewer then fifty 1 km2 cells)
3 = Vulnerable to threat or extinction
Area < 250 km2 (or fewer then two hundred fifty 1 km2 cells)
4 = Apparently secure
Uncommon but not rare, some cause for long-term concern due to declines or other factors
5 = Demonstrably widespread, abundant, and secure
Common; widespread and abundant
In sum, the unique features included in our proposed system for categorizing locally rare taxa are (1) scaling of the geographic assessment level to correspond with local rarity, the L-rank, and (2) inclusion of defined area of occupancy criteria for L-ranks 1, 2, and 3 (Table 1). Thus, a taxon that meets “Critically Imperiled” criteria at all geographical assessment levels could now be labeled G1N1S1L1, representing critical imperilment at global, national, sub-national, and local levels. Likewise, a taxon that is common at the global, national, and sub-national levels, but rare in a given county, could be labeled G5N5S5L1 and thus receive conservation status within the local jurisdiction. These examples demonstrate how the proposed L-rank system is intended to be viewed as an extension of the NatureServe and IUCN systems that enables local jurisdictions to identify and manage locally rare species.

A case study of local rarity

Using the flora of Napa County, California as a case study system, we tested the efficacy of the proposed L-rank criteria to classify and catalog the locally rare plant populations of the region. We chose Napa County for our case study due to its high level of plant diversity (Stebbins and Major 1965; Parisi 2003; Crain and White unpublished data) and due to the large number of plant taxa who reach the edge of their range in Napa (Thorne et al. 2004). Furthermore, Napa is rich with geographical and floristic data (Stoms et al. 2005).
Although numerous botanical surveys have been conducted in Napa County (Major unpublished data, Stebbins and Major 1965; Jepson Flora Project 2005; CCH 2010) resulting in large databases of plant collection records, no checklist or flora has been published specifically for the region. Therefore, we developed a comprehensive plant checklist for Napa County (Crain and White unpublished data), making both this and future research possible. We compiled all vouchered records for native plant taxa listed on the Jepson Herbaria Online Inventory for California Floristics SMASCH database and the Consortium of California Herbaria (Jepson Flora Project 2005; CCH 2010), Calflora (2000), the California Native Plant Society’s Inventory of Rare and Endangered Plants (2005), with personal observations from 2005 to 2007. These sources were chosen due to their representation of significant local and regional herbaria. Although there are likely to be some data gaps in these collections as a result of variable sampling efforts or techniques, these data sources remain highly significant as they represent the most comprehensive collection of plant diversity for the area that is based on decades of primary research. Each available record was screened for nomenclatural errors and updates using Fred Hrusa’s Crosswalk (2005). The resulting checklist (available upon request) included 1,418 native plant taxa for Napa County.
For our initial geographical analysis, we used the CaprICE Plant Species Distribution Map Browser (available at http://​cain.​ice.​ucdavis.​edu/​cgi-bin/​mapserv?​map=​.​.​/​html/​cain/​plants_​animals/​plants/​caprice/​capricemap.​map&​mode=​browse&​layer=​county) which allows online access to a plant distribution map series based on the CalJep Geodatabase (Viers et al. 2006). This database is developed from distributional information available from the Jepson Flora Project and the Calflora database. The CalJep Geodatabase maps show statewide plant distributions in California using 1 km × 1 km grid cells (Viers et al. 2006). We used these maps to visually identify several hundred native plant taxa in Napa County as candidates for local rarity status (LH, L1, L2, and L3) based on our proposed area of occupancy criteria (Table 1). All native plant taxa listed for Napa County that did not currently meet the criteria for one of the threat categories at the global, national, or state assessment levels (CNDDB 2007), and with distributions estimated to be less than 50% of Napa’s overall area of ≈2,052 km2 (United States Census Bureau 2000) were considered candidates for local conservation status. For all candidate taxa, Allan Hollander of the Information Center for the Environment and the Department of Environmental Science and Policy at the University of California-Davis, provided geographic data layers from the CalJep spatial distribution database. Each layer showed the statewide distribution of an individual candidate taxon based on 1 km × 1 km raster grid cells. Layers were generated by intersecting distribution data (elevation, presence in subecoregions, and subcounty distributions) from the Jepson Manual and its online counterpart, the Jepson Online Interchange, as well as from Calflora circa 2000 (Viers et al. 2006). In these databases distribution information was generated from collection records and expert observations, however, the Jepson Online Interchange is more restricted to collection records and was therefore considered the foremost authority when discrepancies occurred (Viers et al. 2006).
We imported all statewide layers into Arc GIS 9.1 (ESRI 2005) for more detailed analysis. Each data layer was reclassified with Spatial Analyst to create new layers with a binary code indicating presence or absence of the taxon in each 1 km2 raster cell in California. A mask layer for Napa County was created by reclassifying our layer for the State of California to create a new layer with a binary code distinguishing Napa from the rest of the state. We multiplied the statewide distribution layers for individual taxa with the Napa County mask layer to create new layers isolating plant distributions within Napa County (cells with a product of one). We queried the attribute tables in the resulting layers and then classified those taxa with distributions meeting the minimum area of occupancy criteria for local rarity (<250 km2) into one of the three threat categories (L1, L2, L3) or the LH category.

Results

Our results indicated that 89 taxa from 34 families met the area of occupancy criteria for local rarity ranks 1, 2, 3, and H in Napa County, CA (Table 2). Figure 1 shows examples of the distributions of three L-ranked plants (categories 1, 2, and 3) based on analysis using 1 km2 grid cells. Although each of these taxa exhibits a relatively large distribution in California, they are all rare to some degree in Napa County. A post-hoc analysis of the distributions of the locally rare taxa identified in this study revealed that these plants are distributed in an average of 20 counties in California. This indicates that they are relatively widespread in the state and would fail to meet criteria for conservation status at state or global levels but could be given status at the local level via the L-rank system.
Table 2
Native locally rare plant taxa distributed in Napa County
L-rank
Taxon
Family
L1
Lomatiumdasycarpum (Torr. & A. Gray) J.M. Coult. & Rose ssp. tomentosum (Benth.) Theob.
Apiaceae
L1
Silenelemmonii S. Watson
Caryophyllaceae
L1
Carexbrainerdii Mack.
Cyperaceae
L1
Chimaphilamenziesii (D. Don) Spreng.
Ericaceae
L1
Phaceliamutabilis Greene
Hydrophyllaceae
L1
Calochortusvenustus Benth.
Liliaceae
L1
Bromusgrandis (Shear) Hitchc.
Poaceae
L1
Elymusglaucus Buckley ssp. jepsonii (Burtt Davy) Gould
Poaceae
L1
Ceanothusprostratus Benth.
Rhamnaceae
L2
Eryngiumarmatum (S. Watson) J.M. Coult. & Rose
Apiaceae
L2
Gnaphaliumbicolor Bioletti
Asteraceae
L2
Gnaphaliumcanescens DC. ssp. microcephalum (Nutt.) Stebb. & D.J. Keil
Asteraceae
L2
Heterothecasessiliflora (Nutt.) Shinn. ssp. bolanderi (A. Gray) Semple
Asteraceae
L2
Barbareaorthoceras Ledeb.
Brassicaceae
L2
Dudleyacaespitosa (Haw.) Britton & Rose
Crassulaceae
L2
Juncuslesueurii Bol.
Juncaceae
L2
Juncusoccidentalis (Coville) Wiegand
Juncaceae
L2
Juncusphaeocephalus Engelm. var. phaeocephalus
Juncaceae
L2
Forestierapubescens Nutt.
Oleaceae
L2
Limoniumcalifornicum (Boiss.) A. Heller
Plumbaginaceae
L2
Ceanothusdentatus Torr. & A. Gray
Rhamnaceae
L2
Penstemonnewberryi A. Gray var. sonomensis
Scrophulariaceae
L3
Angelicatomentosa S. Watson
Apiaceae
L3
Bowlesiaincana Ruiz & Pav.
Apiaceae
L3
Lomatiumvaginatum (M.E. Jones) J. Coulter & Rose
Apiaceae
L3
Erigeronreductus (Cronq.) G.L. Nesom var. ruductus
Asteraceae
L3
Erigeronreductus (Cronq.) G.L. Nesom var. angustatus (A. Gray) G.L. Nesom
Asteraceae
L3
Grindeliastricta DC. var. angustifolia (A. Gray) M.A. Lane
Asteraceae
L3
Jaumeacarnosa (Less.) A. Gray
Asteraceae
L3
Plagiobothryscanescens Benth.
Boraginaceae
L3
Idahoascapigera (Hook.) A. Nelson & J.F. Macbr.
Brassicaceae
L3
Streptanthusbrachiatus F.W. Hoffmann ssp. brachiatus
Brassicaceae
L3
Paxistimamyrsinites (Pursh) Raf.
Celastraceae
L3
Dichondradonelliana Tharp & M.C. Johnst.
Convolvulaceae
L3
Bergiatexana (Hook.) Seub.
Elatinaceae
L3
Lotuspinnatus Hook.
Fabaceae
L3
Garryaflavescens S. Watson
Garryaceae
L3
Geraniumbicknellii Britton
Geraniaceae
L3
Hydrophyllumoccidentale (S. Watson) A. Gray
Hydrophyllaceae
L3
Triglochinmaritima L.
Juncaginaceae
L3
Monardellasheltonii Torr.
Lamiaceae
L3
Alliumlacunosum S. Watson var. Lacunosum
Liliaceae
L3
Epilobiumhalleanum Hausskn.
Onagraceae
L3
Elymuselymoides (Raf.) Swezey
Poaceae
L3
Leptochloafascicularis (Lam.) A. Gray
Poaceae
L3
Spartinafoliosa Trin.
Poaceae
L3
Collomiagrandiflora Lindl.
Polemoniaceae
L3
Navarretiadivaricata (A. Gray) Greene ssp. vividior (Jeps. & V.L. Bailey) H. Mason
Polemoniaceae
L3
Cheilanthescovillei Maxon
Pteridaceae
L3
Ceanothuspumilus Greene
Rhamnaceae
L3
Acaenapinnatifida Ruiz & Pav.var. californica (Bitter) Jeps.
Rosaceae
L3
Potentillaanserina L. ssp. Anserina
Rosaceae
L3
Potentillaanserina L. ssp. pacifica (Howell) Rousi
Rosaceae
L3
Collinsiatinctoria Benth.
Scrophulariaceae
L3
Cordylanthusmollis A. Gray ssp. mollis
Scrophulariaceae
L3
Cordylanthuspringlei A. Gray
Scrophulariaceae
LH
Eryngiumvaseyi J.M. Coult. & Rose
Apiaceae
LH
Lomatiumcaruifolium (Hook. & Arn.) J.M. Coult. & Rose var. denticulatum Jeps.
Apiaceae
LH
Lomatiumdissectum (Torr. & A. Gray) Mathias & Constance var. dissectum
Apiaceae
LH
Lemnatrisulca L.
Araceae
LH
Balsamorhizamacrolepis W.M. Sharp var. platylepis (W.M. Sharp) Ferris
Asteraceae
LH
Erigeronfoliosus Nutt. var. Foliosus
Asteraceae
LH
Gutierreziasarothrae (Pursh) Britton & Rusby
Asteraceae
LH
Pyrrocomaracemosa (Nutt.) Torr. & A. Gray var. paniculata (Nutt.) Kartesz & Gandhi
Asteraceae
LH
Seneciointegerrimus Nutt. var. exaltatus (Nutt.) Cronq.
Asteraceae
LH
Stephanomeriavirgata Benth. ssp. virgata
Asteraceae
LH
Wyethiamollis A. Gray
Asteraceae
LH
Plagiobothryscusickii (Greene) I.M. Johnst.
Boraginaceae
LH
Arabissparsiflora Torr. & A. Gray var. arcuata (Nutt) Rollins
Brassicaceae
LH
Calystegiamalacophylla (Greene) Munz ssp. malacophylla
Convolvulaceae
LH
Arctostaphylosviscida Parry ssp. viscida
Ericaceae
LH
Lupinusalbicaulis Hook.
Fabaceae
LH
Isoetesorcuttii A.A. Eaton
Isoetaceae
LH
Juncusorthophyllus Coville
Juncaceae
LH
Juncusphaeocephalus Engelm. var. paniculatus Engelm.
Juncaceae
LH
Triteleiaixioides (S. Watson) Greene ssp. scabra (Greene) L. Lenz
Liliaceae
LH
Zigadenuspaniculatus (Nutt.) S. Watson
Liliaceae
LH
Camissonialuciae P.H. Raven
Onagraceae
LH
Clarkiabottae (Spach) F.H. Lewis & M.R. Lewis
Onagraceae
LH
Gauracoccinea Pursh
Onagraceae
LH
Mimulusalsinoides Benth.
Phrymaceae
LH
Achnatherumcoronatum (Thurb.) Barkworth
Poaceae
LH
Allophyllumgilioides (Benth.) A.D. Grant & V.E. Grant ssp. violaceum (A. Heller) A.G. Day
Polemoniaceae
LH
Calyptridiumroseum S. Watson
Portulacaceae
LH
Galiumandrewsii A. Gray ssp. intermedium Dempster & Stebb.
Rubiaceae
LH
Galiumangustifolium Nutt. ssp. angustifolium
Rubiaceae
LH
Salixmelanopsis Nutt.
Salicaceae
LH
Castillejalacera (Benth.) Chuang & Heckard
Scrophulariaceae
LH
Veronicaserpyllifolia L. ssp. humifusa (Dicks.) Syme
Scrophulariaceae
L-ranks are based strictly on area of occupancy criteria outlined in Table 1
The number of locally rare plants identified using the proposed criteria equated to a total of 6.3% of Napa’s 1,418 native plant taxa (Crain & White unpublished data). Of these L-ranked plants, nine taxa from eight families met the criteria for L-rank 1, equating to 0.63% of Napa’s native flora. Another 13 taxa from nine families met the criteria for L-rank 2, equating to 0.91% of Napa’s native flora. Furthermore, 34 taxa from 21 families met the criteria for L-rank 3, equating to 2.39% of Napa’s native flora. The remaining 33 taxa, representing 19 families and 2.32% of Napa’s native flora, met the criteria for the L-rank H according to available distribution data. Although the geographic data published by Viers et al. (2006) includes no evidence that these 33 taxa are present in Napa County, it is possible that the taxa are present and actually meet criteria for L-rank 1, 2, or 3 as each of them are documented in Napa County through collection records or observations by a botanical expert. However, the distribution data for these taxa stems from information included on Calflora and the Jepson Manual/Online Interchange (Viers et al. 2006; Calflora 2000; Jepson Flora Project 2005; CCH 2010) and does not entirely correspond with available collection data. Additionally, Calflora includes records from multiple sources that are of variable degrees of reliability (Calflora 2000). To be conservative, listings from Calflora that were not represented by a collection record, documented by an expert on site, or corroborated through another source (e.g., Jepson Flora Project 2005; CNPS 2005; or CCH 2010) were not included in this analysis. Nevertheless, few plant checklists are 100% accurate and when multiple datasets are combined or compared there is often conflicting information due to variation in collecting efforts, taxonomic updates, synonymy, and timing. Therefore, due to these minor inconsistencies between the collection records and the available distribution data, the L-rank “H?” was assigned to these taxa, thus maintaining the integrity of the methodology.

Discussion

Although Magney (2004) argues that NatureServe’s Element Ranking System can be applied to county scales in some instances, in most cases, all criteria used by NatureServe cannot be logically and effectively applied to local jurisdictions due to size constraints. In short, because of variation in jurisdictional areas, NatureServe’s exact criteria should not be used as the entire basis for setting local rarity criteria. The Element Ranking System is a valuable system at larger scales however, and it provided the framework for classifying local rarity.
The IUCN Red List was also a valuable model for developing the L-rank system but again, their criteria cannot be applied directly to local jurisdictions. IUCN Red List criteria, such as those for population decline or probability of extinction, can be valuable tools for assigning conservation priority to threatened taxa. Nevertheless, these are measures that are dynamic over time and distinguishing taxa that meet these criteria can require long-term analysis (10 years or more) in situations where available time and data are quite limited.
The inclusion of a local rarity rank into a recognized system is meant to enhance existing methods used by local governments and organizations by providing them with a standardized system for local level analysis. The proposed L-rank system is specifically designed to be compatible with broad scale conservation programs, specifically NatureServe’s Element Ranking System and the IUCN Red List. Therefore, it is important to realize that using the proposed system will not significantly affect overall assessment outcomes at the sub-national, national, or global levels. Rather, the proposed local rarity criteria will provide a useful tool for comparative analysis at the local level and significantly augment the current systems in use.
Through the analysis of the distributions of globally common plants in Napa County, we identified several locally rare plant taxa using the proposed L-rank criteria. The results presented here indicate that with available geographical data, our criteria for classifying locally rare plants can be usefully applied at the county level to identify significant peripheral or ‘edge of range’ plant populations. Much as the S-rank can be applied to state or provincial boundaries, we encourage the use of the L-rank system in other local jurisdictional areas that are similar in size to a typical county, e.g., national parks, watersheds, or municipalities, when applicable. Individual jurisdictions are geographically unique in size and shape however, and these factors should be considered when applying this system to any area.
Many biologically significant locally rare plant populations highlighted in this analysis are not currently considered for conservation status by global and national conservation policies. These unique organisms deserve conservation status and county agencies should manage them accordingly. Additionally, similar research needs to be conducted in other local jurisdictions to enhance our understanding of the ecological factors affecting the distributions of locally rare plant taxa.
Without an explicit set of criteria for identifying and classifying locally rare taxa, they cannot be effectively protected. The proposed L-rank system provides an effective and systematic tool to address this issue. We suggest that the ecological significance and conservation status of the locally rare plants identified in this study be further evaluated. Use of the L-rank system at local levels will allow researchers to fill the data gap concerning locally rare peripheral plant populations and help to highlight their significance in regards to the global environment.

Acknowledgments

We thank the members of the Biodiversity Research and Education Laboratory at Humboldt State University for their assistance with this manuscript. We also give special thanks to S. Steinberg at the Humboldt State University Institute for Spatial Analysis for his invaluable assistance with the GIS portions of this research and A. Hollander at the Information Center for the Environment at University of California-Davis for providing us with distribution data. We greatly appreciate the insightful and extremely useful comments provided by two anonymous reviewers. Finally, and most importantly, we thank our families and our friends, A. Allard, G. Leppig and S. Calderón, for their support during this research.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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Metadaten
Titel
Categorizing locally rare plant taxa for conservation status
verfasst von
Benjamin J. Crain
Jeffrey W. White
Publikationsdatum
01.03.2011
Verlag
Springer Netherlands
Erschienen in
Biodiversity and Conservation / Ausgabe 3/2011
Print ISSN: 0960-3115
Elektronische ISSN: 1572-9710
DOI
https://doi.org/10.1007/s10531-010-9929-3

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