Research Article |
Corresponding author: José Luis Aguilar-López ( jlal.herp@gmail.com ) Academic editor: Nilton Cáceres
© 2022 Rafael Villegas-Patraca, José Luis Aguilar-López, Julio César Hernández-Hernández, Oscar Muñoz-Jiménez.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Villegas-Patraca R, Aguilar-López JL, Hernández-Hernández JC, Muñoz-Jiménez O (2022) Diversity and conservation of terrestrial vertebrates (birds, mammals, and reptiles) of Sierra Cucapá, Mexicali, Baja California, Mexico. ZooKeys 1088: 17-39. https://doi.org/10.3897/zookeys.1088.76134
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Knowledge about the biodiversity of Baja California has been obtained mainly from natural protected areas (NPAs), while some unprotected natural areas have been poorly studied. The Sierra Cucapá in the northeast of the peninsula is one example. The objectives of this study are 1) to integrate existing knowledge of bird, mammal, and reptile diversity in Cucapá from public databases, citizen science platforms, and information generated from fieldwork, 2) to identify the spatial distribution of records in the study area, 3) to compare the composition of vertebrate species of Cucapá with that of NPAs of northern part of the peninsula, and 4) to assess the biological conservation value of Cucapá. We obtained records of 150 species of native vertebrates (102 birds, 34 mammals, and 14 reptiles) of which 10 species of birds, four mammals, and seven reptiles are included in a risk extinction category. The different sources of information contributed in a complementary way to the species inventories. Large areas in western and northern Cucapá lack records. The total difference in species composition between Cucapá and nearby NPAs ranged between 58 and 69% for birds, 61 and 79% for mammals, and 69 and 87% for reptiles. The species richness of Cucapá, its particular species composition, the presence of species in risk extinction categories, and the number and size of unexplored areas indicate that this area represents an opportunity for biological conservation in the northern part of the Peninsula. This work provides compelling data for the protection of Cucapá.
citizen science, databases, fieldwork, natural protected areas system, species composition
The Baja California Peninsula (hereafter the Peninsula) in northwestern Mexico is a biologically important region with a remarkable species richness and high amount of endemism in various biological groups (
The NPAs system in the northern part of the Peninsula includes eight areas covering two main ecosystems types: arid environments under 100 m above sea level (a.s.l.) in the extreme northeast, and coniferous forests between 1500 and 1900 m a.s.l. in the Sierra de Juárez. Biological information on certain groups of terrestrial vertebrates is available for some of these NPAs under government administration (e.g.
The Sierra Cucapá (hereafter Cucapá) is an unprotected mountainous massif in the northeast of the Peninsula covering 36400 ha and extending approximately 60 km with a northwest–southeast orientation. Cucapá is known to harbor endemic species of flora and fauna (
Here we present the first comprehensive summary of the biological diversity of three groups of terrestrial vertebrates in Cucapá and the first analysis of its complementarity to the NPAs system of the northern Peninsula. Our objectives are 1) to integrate existing knowledge of bird, mammal, and reptile diversity in Cucapá combining information from public databases, citizen science platforms, and information generated from fieldwork, 2) to identify the spatial distribution of records into the study area, 3) to compare the species composition of birds, mammals, and reptiles of Cucapá with that of NPAs of northern part of the Peninsula, and 4) to assess the biological conservation value of Cucapá.
Cucapá is located within the Gulf of Baja California Extensional Province, between the latitudinal and longitudinal ranges of 32°15'–32°39'N, 115°19'–115°47'W, respectively (Fig.
Location of protected natural areas in northern Baja California: government NPAs 1) Parque Nacional Constitucion de 1857, 2) Reserva de la Biosfera Alto Golfo de California y Delta del Río Colorado; Ramsar Sites 3) Humedales del Delta del Río Colorado, 4) Sistema de Humedales Remanentes del Río Colorado, 5) Laguna Hanson; Community NPAs 6) Rancho Rodeo del Rey, 7) El Doctor, and Private NPAs 8) Rancho Rodeo del Rey. * indicates the overlap zone between NPAs 2 and 3, + indicates the overlap zone between NPAs 2 and 4.
We compiled records of bird, mammal, and reptile species in Cucapá from three sources 1) the Global Biodiversity Information Facility database (GBIF; https://www.gbif.org), 2) citizen science platforms iNaturalist (https://www.inaturalist.org), and eBird (https://www.ebird.org/), and 3) fieldwork.
Both citizen science platforms were accessed between May and June 2020 and, in the case of iNaturalist, we only considered records tagged as having research quality that were accompanied with photographs in which species identity could be verified. We conducted fieldwork in four different periods (9–24 October 2017, 26 February–12 March 2018, 21 February–4 March 2019, 4 March– 8 June 2019), and, when a method involved captures (see below), all individuals were released after being measured, weighed, photographed, and identified to species.
During three seasons (autumn, winter, and spring), we obtained visual and acoustic records of birds along 43 linear transects of variable distance (
We sampled small mammal diversity at 15 sites. At each site, we placed four parallel lines 10 m apart with five Sherman traps each. We baited the traps with a mixture of oats and vanilla, placed them at sunset (18:00 h) and checked them at dawn (06:00 h), for a total sampling effort of 1200 trap-nights. We recorded medium and large mammal species (i.e. > 500 g,
We recorded the vocal signature of bats along six 2.5-km transects using a Song Meter SM2BAT (Wildlife Acoustics, Inc.; sampling frequency 384 kHz) coupled with an ultrasonic microphone SMX-U1. At each transect we recorded for 90 min starting at sunset (18:00 h), for a total sampling effort of 540 min of recordings. We analyzed the recordings with Batsound 3.1.0 (Pettersson Elektronik AB, Uppsala, Sweden), and identified species comparing the obtained sonograms with those in the literature (
We established 55 plots (500 × 10 m) to sample reptile diversity. At each plot, one person searched for reptiles using the time-constrained technique (
We compiled records from all sources in a database that we updated according to recent taxonomic changes. We only included records identified to the species level that also included its precise location (i.e. geographic coordinates). We checked the currently known geographic distribution of each species in the database and filtered out those records that did not overlap with it. We consulted taxonomic information and geographic distribution ranges on specialized platforms (http://www.reptile-database.org/,
We obtained the conservation status of species from the list of species at risk of extinction (NOM-059-SEMARNAT-2010) published by the Ministry of the Environment and Natural Resources of Mexico (
We compiled records of bird, mammal, and reptile species in eight NPAs located in the north part of Baja California state, within a 63 km radius from Cucapá (Fig.
where a is the number of species shared between two sites, b the number of unique species from the poorest site, and c the number of unique species at the richest site. The total dissimilarity value ranges from 0 (when all species are shared) to 1 (when there are no shared species). The analysis was carried out using the language and environment for statistical computing R version 3.1.3 (Core Team 2015) and the betapart package (
We recorded a total of 150 species of vertebrates for Cucapá: 102 species of birds, taxonomically grouped in 15 orders, 38 families and 83 genera; 34 species of mammals, grouped into six orders, 14 families and 26 genera, and 14 species of reptiles, belonging to one order, five families and 12 genera (Tables
List of species and conservation status of birds, mammals and reptiles of Cucapá. The source of record: 1 = GBIF with collected specimens, 2 = iNaturalist and eBird observations (the second, only for birds), 3 = fieldwork. The risk extinction categories from NOM-059-SEMARNAT-2010 are A = Threatened, Pr = Subject to Special Protection, P = Endangered, E = Probably Extinct in the Wild. The risk extinction categories from the IUCN Red List are: LC = Least Concern, NT = Near Threatened, VU = Vulnerable. * = exotic species.
Class/order/suborder/family/species | Source | NOM-059 | IUCN |
---|---|---|---|
Class AVES | |||
Order Anseriformes | |||
Anatidae | |||
Anas platyrhynchos | 3 | A | LC |
Spatula discors | 3 | LC | |
Order Galliformes | |||
Odontophoridae | |||
Callipepla gambelii | 1,2,3 | LC | |
Phasianidae | |||
Phasianus colchicus* | 2,3 | LC | |
Order Columbiformes | |||
Columbidae | |||
Columbina inca | 2 | LC | |
Columba livia* | 2,3 | LC | |
Streptopelia decaocto* | 2,3 | LC | |
Zenaida asiatica | 2,3 | LC | |
Zenaida macroura | 2,3 | LC | |
Order Cuculiformes | |||
Cuculidae | |||
Geococcyx californianus | 2,3 | LC | |
Order Caprimulgiformes | |||
Caprimulgidae | |||
Chordeiles acutipennis | 1,2,3 | LC | |
Phalaenoptilus nuttallii | 2 | LC | |
Order Apodiformes | |||
Apodidae | |||
Aeronautes saxatalis | 3 | LC | |
Trochilidae | |||
Calypte anna | 2,3 | LC | |
Calypte costae | 2,3 | LC | |
Selasphorus rufus | 2,3 | NT | |
Order Gruiformes | |||
Rallidae | |||
Fulica americana | 3 | LC | |
Gallinula galeata | 3 | LC | |
Porzana carolina | 2,3 | LC | |
Order Charadriiformes | |||
Recurvirostridae | |||
Himantopus mexicanus | 2 | LC | |
Charadriidae | |||
Charadrius vociferus | 2,3 | LC | |
Scolopacidae | |||
Calidris mauri | 2 | LC | |
Calidris minutilla | 2,3 | LC | |
Limnodromus scolopaceus | 2 | LC | |
Numenius americanus | 3 | LC | |
Tringa melanoleuca | 2 | LC | |
Laridae | |||
Larus argentatus | 2 | LC | |
Larus californicus | 2 | LC | |
Larus delawarensis | 2,3 | LC | |
Larus fuscus | 2 | LC | |
Larus glaucescens | 2 | LC | |
Order Pelecaniformes | |||
Ardeidae | |||
Ardea alba | 2,3 | ||
Ardea herodias | 2,3 | LC | |
Bubulcus ibis* | 2,3 | LC | |
Egretta thula | 3 | LC | |
Threskiornithidae | |||
Plegadis chihi | 2,3 | LC | |
Order Cathartiformes | |||
Cathartidae | |||
Cathartes aura | 2,3 | LC | |
Order Accipitriformes | |||
Accipitridae | |||
Accipiter cooperii | 2,3 | Pr | LC |
Accipiter striatus | 2,3 | Pr | LC |
Buteo jamaicensis | 2,3 | Pr | LC |
Buteo lineatus | 3 | Pr | LC |
Buteo regalis | 2 | Pr | LC |
Circus hudsonius | 2,3 | LC | |
Elanus leucurus | 2 | LC | |
Parabuteo unicinctus | 1 | Pr | LC |
Order Strigiformes | |||
Tytonidae | |||
Tyto alba | 2,3 | LC | |
Strigidae | |||
Athene cunicularia | 2,3 | Pr | LC |
Order Piciformes | |||
Picidae | |||
Colaptes auratus | 2,3 | E | LC |
Dryobates scalaris | 2 | LC | |
Melanerpes uropygialis | 1 | LC | |
Order Falconiformes | |||
Falconidae | |||
Caracara cheriway | 1 | LC | |
Falco mexicanus | 2,3 | A | LC |
Falco sparverius | 2,3 | LC | |
Order Passeriformes | |||
Tyrannidae | |||
Contopus sordidulus | 3 | LC | |
Myiarchus cinerascens | 1,2,3 | LC | |
Pyrocephalus rubinus | 2,3 | LC | |
Tyrannus verticalis | 2 | LC | |
Sayornis nigricans | 2,3 | LC | |
Sayornis saya | 2,3 | LC | |
Laniidae | |||
Lanius ludovicianus | 1,2,3 | NT | |
Corvidae | |||
Corvus brachyrhynchos | 3 | LC | |
Corvus corax | 2,3 | LC | |
Alaudidae | |||
Eremophila alpestris | 3 | LC | |
Hirundinidae | |||
Stelgidopteryx serripennis | 2,3 | LC | |
Hirundo rustica | 3 | LC | |
Petrochelidon pyrrhonota | 2,3 | LC | |
Tachycineta bicolor | 2,3 | LC | |
Remizidae | |||
Auriparus flaviceps | 1,2,3 | LC | |
Troglodytidae | |||
Campylorhynchus brunneicapillus | 1,2,3 | LC | |
Cistothorus palustris | 2,3 | LC | |
Salpinctes obsoletus | 1,2,3 | LC | |
Thryomanes bewickii | 2,3 | LC | |
Troglodytes aedon | 3 | LC | |
Polioptilidae | |||
Polioptila caerulea | 2,3 | LC | |
Polioptila melanura | 1,2,3 | LC | |
Regulidae | |||
Regulus calendula | 2,3 | LC | |
Turdidae | |||
Catharus guttatus | 2 | LC | |
Catharus ustulatus | 3 | LC | |
Mimidae | |||
Mimus polyglottos | 1,2,3 | LC | |
Toxostoma crissale | 1 | LC | |
Sturnidae | |||
Sturnus vulgaris* | 2,3 | LC | |
Ptiliogonatidae | |||
Phainopepla nitens | 1,2,3 | LC | |
Passeridae | |||
Passer domesticus* | 2 | LC | |
Motacillidae | |||
Anthus rubescens | 2 | LC | |
Fringillidae | |||
Haemorhous mexicanus | 1,2,3 | LC | |
Spinus psaltria | 2,3 | LC | |
Passerellidae | |||
Amphispiza bilineata | 1,2,3 | LC | |
Artemisiospiza belli | 3 | LC | |
Chondestes grammacus | 2,3 | LC | |
Junco hyemalis | 1 | LC | |
Melospiza lincolnii | 3 | LC | |
Melospiza melodia | 2,3 | LC | |
Melozone aberti | 1,2,3 | LC | |
Pooecetes gramineus | 2 | LC | |
Spizella passerina | 1,3 | LC | |
Spizella breweri | 1,2,3 | LC | |
Zonotrichia leucophrys | 2,3 | LC | |
Icteridae | |||
Agelaius phoeniceus | 1,2,3 | LC | |
Icterus bullockii | 3 | LC | |
Molothrus ater | 1,2,3 | LC | |
Quiscalus mexicanus | 2,3 | LC | |
Sturnella neglecta | 2,3 | LC | |
Xanthocephalus xanthocephalus | 3 | LC | |
Parulidae | |||
Geothlypis trichas | 2,3 | LC | |
Leiothlypis celata | 2 | LC | |
Leiothlypis ruficapilla | 3 | LC | |
Setophaga coronata | 1,2,3 | LC | |
Cardinalidae | |||
Passerina caerulea | 3 | LC | |
Class Mammalia | |||
Order Didelphimorphia | |||
Didelphidae | |||
Didelphis virginiana | 3 | LC | |
Order Lagomorpha | |||
Leporidae | |||
Sylvilagus audubonii | 3 | LC | |
Lepus californicus | 2,3 | LC | |
Order Rodentia | |||
Cricetidae | |||
Neotoma lepida | 2,3 | LC | |
Peromyscus eremicus | 1,2 | LC | |
Peromyscus maniculatus | 2,3 | LC | |
Peromyscus crinitus | 1,2,3 | LC | |
Geomyidae | |||
Thomomys bottae | 3 | LC | |
Sciuridae | |||
Ammospermophilus leucurus | 1,3 | LC | |
Xerospermophilus tereticaudus | 3 | LC | |
Heteromyidae | |||
Dipodomys deserti | 1 | LC | |
Dipodomys merriami | 1,2,3 | LC | |
Chaetodipus baileyi | 1 | LC | |
Chaetodipus formosus | 2,3 | LC | |
Chaetodipus penicillatus | 1,3 | LC | |
Chaetodipus spinatus | 1,2,3 | LC | |
Perognathus longimembris | 3 | LC | |
Ondatra zibethicus | 3 | A | LC |
Order Carnivora | |||
Mephitidae | |||
Mephitis mephitis | 2 | LC | |
Canidae | |||
Canis latrans | 2,3 | LC | |
Urocyon cinereoargenteus | 3 | LC | |
Vulpes macrotis | 3 | A | LC |
Procyonidae | |||
Procyon lotor | 3 | LC | |
Felidae | |||
Lynx rufus | 3 | LC | |
Order Artiodactyla | |||
Bovidae | |||
Ovis canadensis | 1,2,3 | Pr | LC |
Cervidae | |||
Odocoileus hemionus | 2,3 | LC | |
Order Chiroptera | |||
Molossidae | |||
Tadarida brasiliensis | 1,3 | LC | |
Eumops perotis | 1,3 | LC | |
Vespertilionidae | |||
Eptesicus fuscus | 1 | LC | |
Macrotus californicus | 1 | LC | |
Myotis californicus | 3 | LC | |
Myotis vivesi | 1 | P | VU |
Myotis yumanensis | 3 | LC | |
Parastrellus hesperus | 1,3 | A | LC |
Class Reptilia | |||
Order Squamata | |||
Suborder Lacertilia | |||
Phrynosomatidae | |||
Callisaurus draconoides | 1,2,3 | LC | |
Crotaphytus grismeri | 1,3 | LC | |
Dipsosaurus dorsalis | 3 | LC | |
Phrynosoma platyrhinos | 3 | LC | |
Sauromalus ater | 3 | Pr | LC |
Sceloporus magister | 1,3 | LC | |
Urosaurus graciosus | 3 | LC | |
Urosaurus ornatus | 3 | LC | |
Uta stansburiana | 1,2,3 | A | LC |
Teiidae | |||
Aspidoscelis tigris | 1,2,3 | LC | |
Suborder Serpentes | |||
Colubridae | |||
Masticophis flagellum | 1 | A | LC |
Natricidae | |||
Thamnophis marcianus | 1 | A | LC |
Viperidae | |||
Crotalus cerastes | 1,2 | Pr | LC |
Crotalus mitchellii | 1 | Pr | LC |
In general, data sources contributed with multiple overlapping species (i.e. same species reported in two or more data sources), but each source also contributed with unique species (Table
In terms of number of records and locations, birds are the best represented group in the study area, followed by mammals, while reptiles are the group with the fewest records. The records are located mainly in the south, southeast, and central-west parts of the study area, covering the entire elevation range of Cucapá, while wide high areas with rugged terrain in the western portion, the northern area, and some low and flat areas to the east lack records (Fig.
According to
Bird species richness in Cucapá (102 spp.) is higher than richness in community NPA Rancho Rodeo del Rey (90 spp.), but lower than in the rest of the NPAs. Mammal species richness in Cucapá (34 spp.) is higher than in HDRC (30 spp.) and SHRRC (24 spp.), but lower than in the rest of the NPAs. For reptiles, species richness in Cucapá (14 spp.) was lower than for all NPAs (Table
Number of orders, families, genera, and species of birds, mammals and reptiles recorded in Sierra Cucapá and six NPAs of northern Baja California: Parque Nacional Constitución de 1857, Reserva de la Biosfera del Alto Golfo de California (RBAGC), Humedales Remanentes del Río Colorado (HDRC), Sistema de Humedales Remanentes del Río Colorado (SHRRC), Laguna Hanson, Rodeo del Rey (community).
NPA/region | Taxonomic group | Orders | Families | Genera | Species |
---|---|---|---|---|---|
Sierra Cucapá | Birds | 15 | 38 | 83 | 102 |
Mammals | 6 | 14 | 26 | 34 | |
Reptiles | 1 | 5 | 12 | 14 | |
Constitución 1857 | Birds | 18 | 45 | 116 | 174 |
Mammals | 8 | 19 | 41 | 63 | |
Reptiles | 1 | 15 | 30 | 48 | |
RBAGC | Birds | 22 | 58 | 174 | 320 |
Mammals | 8 | 21 | 42 | 58 | |
Reptiles | 2 | 13 | 32 | 46 | |
HDRC | Birds | 20 | 50 | 139 | 217 |
Mammals | 7 | 13 | 26 | 30 | |
Reptiles | 2 | 10 | 17 | 21 | |
SHRRC | Birds | 20 | 49 | 145 | 241 |
Mammals | 6 | 10 | 18 | 24 | |
Reptiles | 1 | 12 | 25 | 28 | |
Laguna Hanson | Birds | 18 | 44 | 110 | 165 |
Mammals | 7 | 15 | 26 | 39 | |
Reptiles | 1 | 12 | 20 | 31 | |
Rodeo del Rey (C) | Birds | 15 | 36 | 68 | 90 |
Total differences in species composition (βjac) between Cucapá and the NPAs ranged between 0.58–0.69 for birds (Table
Differences in species composition between pairs of sites. A birds B mammals C reptiles. The values outside the parentheses correspond to the total difference in species composition (βjac), the first value inside the parentheses indicates the difference due to species turnover (βjtu) and the second value indicates the proportion due to nestedness (βjne).
Sierra Cucapá | Laguna Hanson | HDRC | SHRRC | Const. 1857 | RBAGC | |
---|---|---|---|---|---|---|
A) | ||||||
Laguna Hanson | 0.68 (0.55+0.13) | |||||
HDRC | 0.63 (0.28+0.35) | 0.62 (0.53+0.09) | ||||
SHRRC | 0.60 (0.09+0.51) | 0.59 (0.44+0.15) | 0.31 (0.25+0.06) | |||
Const. 1857 | 0.69 (0.53+0.16) | 0.08 (0.02+0.06) | 0.61 (0.54+0.07) | 0.56 (0.44+0.13) | ||
RBAGC | 0.69 (0.06+0.63) | 0.61 (0.29+0.32) | 0.33 (0.02+0.31) | 0.33(0.12+0.21) | 0.60 (0.31+0.29) | |
Rodeo del Rey | 0.58 (0.54+0.04) | 0.72 (0.55+0.17) | 0.58 (0.02+0.56) | 0.64 (0.08+0.56) | 0.72 (0.53+0.19) | 0.72 (0.02+0.70) |
B) | ||||||
Laguna Hanson | 0.75 (0.62+0.13) | |||||
HDRC | 0.79 (0.74+0.05) | 0.81 (0.78+0.03) | ||||
SHRRC | 0.61 (0.58+0.03) | 0.79 (0.70+0.09) | 0.65 (0.59+0.06) | |||
Const. 1857 | 0.72 (0.24+0.48) | 0.42 (0.05+0.37) | 0.76 (0.57+0.19) | 0.72 (0.34+0.38) | ||
RBAGC | 0.69 (0.24+0.45) | 0.78 (0.70+0.08) | 0.54 (0.12+0.42) | 0.64 (0.15+0.49) | 0.59 (0.56+0.03) | |
C) | ||||||
Laguna Hanson | 0.87 (0.78+0.09) | |||||
HDRC | 0.74 (0.67+0.07) | 0.89 (0.86+0.03) | ||||
SHRRC | 0.69 (0.44+0.24) | 0.77 (0.75+0.02) | 0.63 (0.52+0.11) | |||
Const. 1857 | 0.85 (0.60+0.25) | 0.34 (0+0.34) | 0.84 (0.71+0.13) | 0.63 (0.44+0.19) | ||
RBAGC | 0.76 (0.25+0.51) | 0.83 (0.78+0.05) | 0.64 (0.18+0.46) | 0.62 (0.40+0.22) | 0.70 (0.69+0.01) |
Differences in species composition between Cucapá and the NPAs A birds B mammals C reptiles. Total difference in species composition (βjac; complete bar), proportion of the difference due to species turnover (βjtu; black portion of bar) and proportion of the difference due to nestedness (βjne; gray portion of bar).
To our knowledge, this is the first study that integrates information on the diversity of terrestrial vertebrates that inhabit Cucapá and analyzes its conservation value. Our results indicate that Cucapá is home to a considerable number of bird, mammal, and reptile species. The number of species recorded in Cucapá represent 22% of the 473 bird species (
The geographic distribution of bird, mammal, and reptile records available through GBIF, iNaturalist, and eBird indicates that large areas of Cucapá remain unexplored. Furthermore, some nearby NPAs (e.g. Parque Nacional Constitución de 1857 and Laguna Hanson) hold greater richness in considerably smaller areas. Thus, we consider that species richness of terrestrial vertebrates in Cucapá might actually be higher than what we report here, especially considering that at least 41, five, and 14 additional species of birds, mammals, and reptiles respectively have been recorded in nearby locations (
The inclusion of records from three different data sources provided complementary contributions to the inventory of Cucapá. The high percentage of bird, mammal, and reptile species recorded during fieldwork (78%, 79%, and 71%, respectively) and the percentage of species recorded exclusively by this method (20% for birds, 35% for mammals, and 35.7% for reptiles) indicate the importance of field sampling efforts to the species inventory for this relatively unexplored area. It also suggests the need for further fieldwork in areas that still lack information, but seasonal variations in species composition and overall activity should be considered. In the case of birds, for instance, seasonal changes are particularly marked due to migratory processes (
The number of species listed in the NOM-059 (Table
The diversity of vertebrates and the number of species under risk categories reported in this study suggest that Cucapá represents an important conservation region and an opportunity for biological conservation in the northern Peninsula. Currently, Cucapá is not under any legal protection scheme and is therefore not within the NPAs system, not even within the priority terrestrial regions of the state of Baja California (
For the three groups of vertebrates evaluated here, species richness in Cucapá is not higher than in the nearby NPAs with biological information (Table
Several studies have evaluated the role that the NPAs system in the northern Peninsula has for the conservation of biodiversity in the state of Baja California (
The current situation of Cucapá should draw attention of the urgent need to implement strategies for the conservation of its biodiversity. Among the activities that have been effective at slowing the deterioration of other unprotected areas with high biological diversity are the establishment of NPAs under non-government administration. Some examples include the Wildlife Management and Sustainable Use Units (UMA from its name in Spanish;
We found that Cucapá harbors high bird, mammal, and reptile species richness. Considering the number and size of unexplored areas, as well as the cryptic behavior and generally low detection probabilities of some species or groups (e.g. reptiles), species richness could be even higher than what we report here. The Cucapá Sierra has a particular species composition of the three groups of vertebrates, with high species turnover with three or more NPAs, and it harbors several species in risk extinction categories as well as endemic species. Taken together, these characteristics indicate that Cucapá has a complementary conservation value to the NPAs system of a region that has been severely transformed by various human activities. The lack of records in certain areas indicates the need to carry out further fieldwork to complement the species inventory reported here. In terms of conservation, we recommend the urgent establishment of strategies for the protection of Cucapá and its biodiversity.
We thank the technical staff of Unidad de Servicios Altamente Especializados del Instituto de Ecología, A.C. for help with fieldwork. Thanks are extended to Paulina García for producing the map. Milton Díaz Toribio, Rosaura Valdez and Sergio Cabrera provided helpful suggestions that improved this manuscript. Margaret Schroeder revised the English of the manuscript. The authors have no funding, and no conflicts of interest to report.