Methods
For CA-GAP, we identified vegetation types by one to three overstory
species, each contributing greater than 20% of relative canopy cover.
The 20% cover criterion, which we selected to be consistent with
the California Vegetation Type Mapping (VTM) survey (Wieslander
1946; see Colwell 1988, for overview), is lower than typically applied
to define canopy dominance. For example, the CALVEG classification
defines dominant as > 50% (Parker and Matyas 1981). Paysen et
al. (1980) define Series based on a single dominant overstory species
or genus. The ongoing California Native Plant Society Community
Inventory is identifying Series primarily based on a single, overstory
dominant, although a few series are based on two co-dominant species,
and others are defined by environment (e.g., Alpine Series) (Sawyer
and Keeler-Wolf 1995). For our purposes and at our 1:100,000 mapping
scale, we found that use of single canopy dominants to type vegetation
produced an unacceptable simplification of vegetation composition
and pattern. For example, much of the chaparral vegetation in the
Southwestern California Region would be mapped as Chamise or Scrub
oak chaparral, masking systematic, regional variation in community
composition. By using the 20% cover threshold, we retained information
on one to three canopy species that are dominant or co-dominant
over several-to-many hectares. This area is much larger than plot
sizes used in traditional vegetation studies. To avoid confusing
these vegetation types with Series or Associations as defined by
other systems, we refer to these combinations as Species Assemblages.
In the field, species in an assemblage may be uniformly mixed or
in a fine mosaic of patches, depending on the scale at which the
pattern is observed. This means that in practice, species assemblages
in our database can be a series recognized by existing classification
systems, a combination of two or three recognized series, or previously
unrecognized species combinations.
A map of actual vegetation was produced using summer 1990 Landsat
Thematic Mapper (TM) satellite imagery, 1990 high altitude color
infrared photography (1:58,000 scale), VTM maps based on field surveys
conducted between 1928 and 1940, and miscellaneous recent vegetation
maps and ground surveys. Details of the mapping process are provided
in Davis et al. (1995), and are only summarized here.
We did not have the resources to map individual stands of homogeneous
vegetation. Instead, we have attempted to delimit "landscapes,"
which we defined as areas of one to many square kilometers in extent
with uniform climate, physiography, substrate and disturbance regime,
and covered by a single species assemblage or by a mosaic of a few
species assemblages associated with different sites (e.g., riparian
zones, mesic slopes, xeric slopes). Landscape boundaries were mapped
subjectively by photointerpretation of patterns in the satellite
imagery. Final delineation of a landscape unit was an iterative
process based on evidence from the satellite imagery, 1990 air photos,
existing vegetation maps and field reconnaissance. The map was produced
using a minimum mapping unit of 100 ha (1 km�). The state was mapped
into greater than 21,000 landscape units, or polygons, with a mean
size of approximately 1,950 ha.
TM imagery was resampled to the Albers equal-area projection with
100 meter resolution (i.e. 1 hectare pixels), and a false color
composite of red, near-infrared and mid-infrared reflectance images
was displayed on a video monitor. Obvious landscape boundaries were
digitally drafted over the imagery based on image tone and texture.
Ancillary information, especially air photos and VTM maps, was used
to capture additional compositional changes in vegetation that were
not visually obvious in the TM imagery. VTM maps were used to position
landscape boundaries on vegetation gradients where no obvious break
was visible on either the satellite imagery or in air photos. Two
hundred and thirty polygons (excluding urban and agricultural areas)
were checked in the field, primarily by roadside reconnaissance.
Using these various sources, a large amount of information was
collected for each landscape unit (Table 2-1). Based on our concept
of landscape, we recorded a primary species assemblage, which was
the most widespread vegetation type or land use/land cover type
in the polygon, a secondary and tertiary type, and the fraction
of the landscape covered by each type. We also recorded the most
widespread wetland assemblage, which was usually riparian vegetation.
Each species assemblage was defined by up to three dominant species.
We also recorded the occurrence of minor overstory species of special
conservation concern (e.g., Juglans californica, Quercus
engelmanii, Cupressus forbesii).
Species data were derived from field survey, air photos or from
the VTM and other detailed maps. VTM information was used for areas
where air photos provided no evidence of recent disturbance, based
on the assumption that canopy dominants observed by VTM field crews
have not changed over the past 50-60 years. We realize this is a
tenuous assumption. We found during our field surveys that the assumption
is usually valid for forest and hard chaparral types. Although the
relative dominance of species may have changed over the interval,
species that were mapped as co-dominants by VTM crews in the 1930s
are usually still canopy dominants across the same landscape. The
composition of shrubland and grassland types is not as stable over
the same interval, and we made special efforts to view these types
in the field or to find more current maps. Our landscape units are
many square kilometers in extent, and canopy composition can vary
greatly from site to site within a landscape. Thus the species assemblages
that we have mapped record those species that most frequently dominate
most sites in that landscape.
Table 2-1. Landscape attributes for CA-GAP land-cover
map units.
Polygon ID Number
Primary Vegetation
Dominant Species 1
Codominant Species 2
Codominant Species 3
Canopy Closure (4 classes)
Fraction of polygon occupied by primary type (10% intervals)
CNDDB Community type
WHR habitat type
Secondary Vegetation
Dominant Species 1
Co-dominant Species 2
Codominant Species 3
Canopy Closure
Fraction of polygon occupied by type
CNDDB Community type
WHR habitat type
Tertiary Vegetation
Dominant Species 1
Co-dominant Species 2
Codominant Species 3
Canopy Closure
Fraction of polygon occupied by type
CNDDB Community type
WHR habitat type
Presence/Absence of 9 wetland habitat types (CA WHR types)
Primary Wetland Vegetation
Dominant Species 1
Codominant Species 2
Codominant Species 3
Presence of canopy species of special status (narrow endemics,
RTE species)
We have tried to account for fire dynamics by recording recent
burns and by retaining information on the pre-burn dominants (e.g.,
an area of recently burned chamise chaparral that is presently dominated
by herbs would be recorded as sparse chamise canopy co-dominated
by annual herbs).
Rather than a multi-colored vegetation map, the information we
have developed is better treated as a vegetation database linked
to a set of areas. One can retrieve distribution data on individual
species, unique combinations of species, or vegetation types defined
by physiognomy and/or composition (Stoms et al. 1992, Davis et al.
1995). Although the database approach provides a more flexible framework
for representing vegetational variation than the traditional vegetation
map, it does not eliminate the need for classification in order
to simplify and communicate results. We recorded many thousands
of unique species (or species/landuse) combinations in over 21,000
polygons. Many unusual species combinations occurred at the margins
of regions in transitional environments. We summarize distribution
data for individual dominant species and based on plant communities
as defined in the California NDDB (Holland 1986), which we derived
from the database by an equivalence table assigning each species
combination to a unique NDDB community. The criteria for class assignment
in the NDDB classification system are qualitative and often not
explicitly based on dominant overstory species. Where ambiguities
existed, we assigned species combinations to more general types.
For example, Holland (1986) identified several pinyon and/or juniper
community types in the Mojave Desert region that we aggregated into
a single type at his next higher level of classification.
Several procedures were implemented to ensure quality in the final
map. The distribution of each dominant plant species in the coverage
was compared to the documented distribution recorded in the CalFlora
database (see http://s27w007.pswfs.gov/calflora/) which was derived
from the Munz flora and revised with some more current data. Apparent
outlying locations of species in the GAP database were re-examined
to either confirm that the location was documented in the data source
or to change the species code if it appeared to be an incorrect
interpretation or a data input error. A similar comparison was made
for each community type with the written description in Holland
(1986).