| set |
group |
trait |
id |
type |
n.states |
units |
source |
trait.dfn |
| Core |
Vegetative: whole plant |
Growth form |
1 |
nominal |
20 |
NA |
Cornelissen et al. 2003 |
Growth form, mainly determined by canopy structure and height |
| Core |
Vegetative: whole plant |
Life form |
2 |
nominal |
7 |
NA |
Raunkiaer (1934) as in Cornelissen et al 2003 |
Type of plant form defined by the relation of the perennating
tissue to the ground surface |
| Core |
Vegetative: whole plant |
Plant habit |
4 |
nominal |
6 |
NA |
TJM2 |
Characteristic mode of growth, general form, or shape of a
plant |
| Core |
Vegetative: whole plant |
Maximum height (d) |
5 |
ordered discrete |
8 |
NA |
Cornelissen et al. 2003 |
Shortest distance between upper boundary of the main
photosynthetic tissues on a plant at reproductive
maturity and the ground level |
| Core |
Vegetative: leaves |
Leaf type |
13 |
nominal |
5 |
NA |
TJM2 |
Leaf type or shape of the whole leaf |
| Core |
Vegetative: leaves |
Compound leaf type |
14 |
nominal |
5 |
NA |
TJM2 |
type of compound leaf |
| Core |
Vegetative: leaves |
Blade morphology |
15 |
nominal |
9 |
NA |
TJM2 |
Shape of the lamina or leaflet if compound leaf |
| Core |
Vegetative: leaves |
Blade length (d) |
16 |
ordered discrete |
7 |
NA |
EFBI |
Blade is leaflet if compound leaf |
| Core |
Vegetative: leaves |
Blade width (d) |
17 |
ordered discrete |
6 |
NA |
EFBI |
Blade is leaflet if compound leaf |
| Core |
Vegetative: leaves |
Compound leaf length (d) |
20 |
ordered discrete |
7 |
NA |
|
Only for compound leaves |
| Core |
Vegetative: leaves |
Compound leaf width (d) |
21 |
ordered discrete |
7 |
NA |
|
Only for compound leaves |
| Core |
Vegetative: leaves |
Raunkiaer leaf size |
27 |
ordered discrete |
6 |
NA |
Raunkiaer 1934 |
Leaf size classes define by leaf areas in mm2 (close to
Cornelissen flammability 5) |
| Core |
Vegetative: leaves |
Blade margin |
28 |
nominal |
7 |
NA |
TJM2 |
Outline of leaflets if leaves are compound |
| Core |
Vegetative: leaves |
Leaf texture |
39 |
nominal |
3 |
NA |
Sampson? |
Definitions based on authorsÕ field use of the term. |
| Core |
Vegetative: leaves |
Leaf habit |
54 |
nominal |
4 |
NA |
|
|
| Core |
Vegetative: stems/defenses |
Green/photosynthetic stems |
59 |
nominal |
2 |
NA |
|
|
| Core |
Vegetative: stems/defenses |
Stem succulence |
60 |
nominal |
3 |
NA |
TJM2 |
Thick and juicy; fleshy (e.g. Sesuvium verrucosum) |
| Core |
Vegetative: stems/defenses |
Spinescence (density) |
64 |
ordered discrete |
6 |
NA |
Cornelissen et al 2003 |
Size/density of spine equivalents (spines, thorns, prickles) |
| Core |
Life history and regeneration |
Seed length |
80 |
ordered discrete |
7 |
NA |
LEDA |
The longest dimension of the seed, no matter if it is
equivalent to the morphological length |
| Core |
Life history and regeneration |
Seed width |
81 |
ordered discrete |
7 |
NA |
LEDA |
The widest axis perpendicular to the length axis of the seed |
| Core |
Life history and regeneration |
Dispersal mode |
86 |
nominal |
9 |
NA |
Cornelissen et al 2003 |
Mode of dispersal (record all categories assumed to give
significant potential dispersal in order of
decreasing importance) |
| Core |
Life history and regeneration |
Diaspore type |
87 |
nominal |
3 |
NA |
LEDA |
Indicates if the dispersule is vegetative or generative and if
it is single-seeded or multi-seeded |
| Core |
Life history and regeneration |
Fruit morphology |
89 |
nominal |
9 |
NA |
TJM2 |
|
| Core |
Life history and regeneration |
Dehiscent fruit |
90 |
nominal |
2 |
NA |
TJM2 |
|
| Core |
Life history and regeneration |
Simple fruit |
91 |
nominal |
2 |
NA |
TJM2 |
|
| Core |
Life history and regeneration |
Fleshy fruit |
92 |
nominal |
2 |
NA |
TJM2 |
|
| Core |
Life history and regeneration |
Longevity |
96 |
ordered discrete |
4 |
NA |
EFBI |
General longevity of an individual plant (not ramet) |
| Core |
Life history and regeneration |
Reproductive episodes |
97 |
nominal |
2 |
NA |
|
Reproductive behavior in relation to frequency of reproductive
episodes (semelparous or iteroparous) |
| Core |
Life history and regeneration |
Minimum age at reproductive maturity |
98 |
ordered discrete |
5 |
NA |
EFBI; LEDA |
|
| Core |
Life history and regeneration |
Clonality |
99 |
nominal |
8 |
NA |
Cornelissen et al 2003 |
Category of clonal behavior |
| Core |
Life history and regeneration |
Resprouting behavior |
100 |
nominal |
5 |
NA |
|
|
| Core |
Life history and regeneration |
Resprouting factors |
101 |
nominal |
4 |
NA |
|
Factors that cue a resprouting response. |
| Core |
Reproductive morphology and phenology |
Pollen vector |
102 |
nominal |
10 |
NA |
BiolFlor |
Pollen vector or type of pollen transfer |
| Core |
Reproductive morphology and phenology |
Floral rewards |
104 |
nominal |
4 |
NA |
BiolFlor |
Provided by flowers to attract insects |
| Core |
Reproductive morphology and phenology |
Flower size |
105 |
ordered discrete |
8 |
NA |
TJM2 |
Corolla/inflorescence length (or diameter?) |
| Core |
Reproductive morphology and phenology |
Flower tube length |
106 |
continuous |
NA |
mm |
|
The length of the corolla or group of corollas functioning as
a flower (distance from the base to the opening of
the corolla) |
| Core |
Reproductive morphology and phenology |
Flower diameter |
107 |
continuous |
NA |
mm |
|
The width of the corolla or group of corollas functioning as a
flower (distance between the tips of opposite
corolla lobes) |
| Core |
Reproductive morphology and phenology |
Floral symmetry |
108 |
nominal |
4 |
NA |
TJM2 |
|
| Core |
Reproductive morphology and phenology |
Flower color |
109 |
nominal |
12 |
NA |
|
Flower color or description of flower coloration. |
| Core |
Reproductive morphology and phenology |
Plant sex expression |
112 |
nominal |
6 |
NA |
|
|
| Core |
Reproductive morphology and phenology |
Begin of flowering |
113 |
circular continuous |
NA |
months |
|
month of first flower production |
| Core |
Reproductive morphology and phenology |
End of flowering |
114 |
circular continuous |
NA |
months |
|
month of last flower production |
| Core |
Reproductive morphology and phenology |
Begin of fruiting |
115 |
circular continuous |
NA |
months |
|
month of first fruit production |
| Core |
Reproductive morphology and phenology |
End of fruiting |
116 |
circular continuous |
NA |
months |
|
month of last fruit production |
| Core |
Habitat and distribution |
Typical habitat |
120 |
nominal |
29 |
NA |
Ornduff et al. |
Plant community types as defined by Munz (table I); data in
Baker database. |
| Core |
Habitat and distribution |
Fed Rarity status |
128 |
nominal |
3 |
NA |
|
Federal t/e status |
| Core |
Habitat and distribution |
CA Rarity status |
129 |
nominal |
3 |
NA |
|
CA state T/E status |
| Core |
Habitat and distribution |
CA nativity |
130 |
nominal |
2 |
NA |
|
native or alien to California |
| Core |
Habitat and distribution |
CA alien status |
131 |
nominal |
6 |
NA |
Pysek et al. 2004 |
alien status |
| Core |
Habitat and distribution |
CA endemicity |
135 |
nominal |
2 |
NA |
EFC: Rejmanek |
|
| Core |
Habitat and distribution |
CFP endemicity |
136 |
nominal |
2 |
NA |
EFC: Rejmanek |
|
| Core |
Habitat and distribution |
Endemic type |
137 |
nominal |
2 |
NA |
EFC: Rejmanek |
|
| Ext |
Vegetative: whole plant |
Flower height (d) |
7 |
ordered discrete |
8 |
NA |
Cornelissen et al. 2003; EFC |
Shortest distance between upper boundary of flowers on a plant
at reproductive maturity and the ground level |
| Ext |
Vegetative: whole plant |
Dead branch retention |
9 |
ordered discrete |
3 |
NA |
Keeley; Schwilk |
|
| Ext |
Vegetative: whole plant |
Degree of ramification (branching) |
10 |
nominal |
5 |
NA |
Cornelissen et al 2003 |
Number of ramification orders, as predictor
of canopy architectural complexity (= Cornelissen flammability 4) |
| Ext |
Vegetative: whole plant |
Standing fine litter in driest season |
11 |
nominal |
6 |
NA |
Cornelissen et al 2003 |
The relative amount of fine dead plant material (branches,
leaves, inflorescences, bark) still attached to
the plant during the dry season. ÔFineÕ litter means litter with diameter or
thickness less than 6 mm (= Cornelissen flammability 6) |
| Ext |
Vegetative: whole plant |
Volatile oils, waxes and/or resins |
12 |
nominal |
5 |
NA |
Cornelissen et al 2003 |
(= Cornelissen flammability 7) |
| Ext |
Vegetative: leaves |
Blade area (d) |
25 |
ordered discrete |
7 |
NA |
|
Blade is leaflet if compound leaf. |
| Ext |
Vegetative: leaves |
Stomatal distribution |
33 |
nominal |
5 |
NA |
|
Surfaces in which stomata are present |
| Ext |
Vegetative: leaves |
Leaf duration |
48 |
continuous |
NA |
months |
Cornelissen et al 2003 |
Leaf duration is the number of months per year that the leaf
canopy (or analogous main photosynthetic unit) is
green |
| Ext |
Vegetative: leaves |
Leaf flush begins |
50 |
circular continuous |
NA |
months |
Ackerly 2004 |
Month of first new leaf production |
| Ext |
Vegetative: leaves |
Leaf flush ends |
51 |
circular continuous |
NA |
months |
Ackerly 2004 |
Month of last new leaf production |
| Ext |
Vegetative: leaves |
Leaf drop begins |
52 |
circular continuous |
NA |
months |
Ackerly 2004 |
Month of first leaf drop |
| Ext |
Vegetative: leaves |
Leaf drop ends |
53 |
circular continuous |
NA |
months |
Ackerly 2004 |
Month of last leaf drop |
| Ext |
Vegetative: leaves |
Photosynthetic pathway |
55 |
nominal |
3 |
NA |
|
[Cornelissen et al 2003] |
| Ext |
Vegetative: stems/defenses |
Bark surface structure (texture) |
63 |
nominal |
5 |
NA |
Cornelissen et al 2003 |
|
| Ext |
Vegetative: stems/defenses |
Surface indumenta on leaves |
65 |
nominal |
9 |
NA |
TJM2 |
|
| Ext |
Vegetative: stems/defenses |
Surface indumenta on stems |
66 |
nominal |
9 |
NA |
TJM2 |
|
| Ext |
Vegetative: stems/defenses |
Surface indumenta on flowers |
67 |
nominal |
9 |
NA |
TJM2 |
|
| Ext |
Vegetative: stems/defenses |
Surface indumenta on fruits |
68 |
nominal |
9 |
NA |
TJM2 |
|
| Ext |
Vegetative: stems/defenses |
Surface indumenta on buds |
69 |
nominal |
9 |
NA |
TJM2 |
|
| Ext |
Vegetative: stems/defenses |
Aromatic/Chemical defences |
70 |
nominal |
5 |
NA |
Taiz & Zeiger 2002 |
A diverse array of organic compounds produced by plants that
appear to have no direct function in growth and
development |
| Ext |
Vegetative: roots |
Root depth: 1. type |
71 |
nominal |
2 |
NA |
EFBI |
With respect to height of stems |
| Ext |
Vegetative: roots |
Root depth: 2. depth |
72 |
ordered discrete |
7 |
NA |
Cornelissen et al 2003, Schenk and Jackson 2002 |
Depth above which 95% of the root biomass of a species is
located |
| Ext |
Vegetative: roots |
Root type |
74 |
nominal |
5 |
NA |
EFBI |
|
| Ext |
Vegetative: roots |
Mycorrhizal association |
75 |
nominal |
6 |
NA |
Cornelissen et al 2003 |
|
| Ext |
Vegetative: roots |
Strength of mycorrhizal association |
76 |
nominal |
4 |
NA |
|
|
| Ext |
Vegetative: roots |
N fixation |
77 |
nominal |
3 |
NA |
Cornelissen et al 2003 |
Symbiosis with N2-fixing bacteria |
| Ext |
Life history and regeneration |
Seed longevity |
79 |
ordered discrete |
3 |
NA |
Thompson 1992 |
Length of time that the species survive in the soil |
| Ext |
Life history and regeneration |
Annual seed production per plant |
83 |
ordered discrete |
5 |
NA |
EFCI |
|
| Ext |
Life history and regeneration |
Heterocarpy |
85 |
nominal |
2 |
NA |
|
Production of more than one kind of seed (morphology,
dispersal behavior, dormancy behavior, etc.) |
| Ext |
Life history and regeneration |
Seed structure |
88 |
nominal |
15 |
NA |
LEDA |
A coarse categorization of six morphological structures. Per
category subcategories allow the classification of
seed morphology into a finer scale |
| Ext |
Life history and regeneration |
Number of seeds per fruit |
93 |
ordered discrete |
11 |
NA |
|
|
| Ext |
Life history and regeneration |
Germination (seed type) |
94 |
nominal |
4 |
NA |
Baskin and Baskin 2001 |
|
| Ext |
Life history and regeneration |
Germination requirements |
95 |
nominal |
14 |
NA |
Baskin and Baskin 2001 |
Environmental factors breaking dormancy (physiological,
physical, or both) |
| Ext |
Reproductive morphology and phenology |
Mating system |
103 |
ordered discrete |
4 |
NA |
BiolFlor |
Presence and strength of self-incompatibility of
self-sterility |
| Ext |
Reproductive morphology and phenology |
Heterostyly |
110 |
nominal |
4 |
NA |
TJM2 |
Pertaining to a taxon in which individual plants produce only
one of two or more flower types, each differing in
style (and generally stamen) length |
| Ext |
Reproductive morphology and phenology |
Breeding system |
111 |
nominal |
6 |
NA |
BiolFlor |
Origin of gametes that unite to form offspring |
| Ext |
Habitat and distribution |
Jepson (TJM2) geographic units |
117 |
nominal |
29 |
NA |
TJM2 |
A four-tiered hierarchical system of geographic units that
will be used in TJM2 to convey distributional
information. In this system California is divided into three provinces. Each
province is divided into regions all but one of which are further divided
into subregions; some subregions are even further divided into districts |
| Ext |
Habitat and distribution |
Low elevation |
118 |
continuous |
NA |
m |
TJM2 |
Range from minimum to maximum altitude recorded for the
species. |
| Ext |
Habitat and distribution |
High elevation |
119 |
continuous |
NA |
m |
TJM2 |
Range from minimum to maximum altitude recorded for the
species. |
| Ext |
Habitat and distribution |
Rabinowitz rarity: geographic |
125 |
nominal |
2 |
NA |
Rabinowitz 1981 |
Rabinowitz (1981) classified species based on three criteria:
geographic range (wide or narrow), habitat
specificity (broad or restricted), and local abundance (somewhere large or
everywhere small). Only one of the eight possible combinations (wide range,
broad habitat specificity, and somewhere large local abundance) is classified
as common. The other seven each include some form of rarity. |
| Ext |
Habitat and distribution |
Rabinowitz rarity: habitat specificity |
126 |
nominal |
2 |
NA |
|
|
| Ext |
Habitat and distribution |
Rabinowitz rarity: local abundance |
127 |
nominal |
2 |
NA |
|
|
| Ext |
Habitat and distribution |
Native range |
132 |
nominal |
16 |
NA |
EFC: Rejmanek |
|
| Ext |
Habitat and distribution |
Native latitude-equatorial limit |
133 |
continuous |
NA |
deg |
EFC: Rejmanek |
|
| Ext |
Habitat and distribution |
Native latitude-polar limit |
134 |
continuous |
NA |
deg |
EFC: Rejmanek |
|
| Ext |
Vegetative: whole plant |
Stem density |
3 |
continuous |
NA |
- |
Ackerly 2004 |
Number of stems at 1/10 of plant height |
| Ext |
Vegetative: whole plant |
Maximum height (c) |
6 |
continuous |
NA |
m |
|
|
| Ext |
Vegetative: whole plant |
Flower height (c) |
8 |
continuous |
NA |
m |
|
|
| Ext |
Vegetative: leaves |
Blade length (c) |
18 |
continuous |
NA |
cm |
|
Blade is leaflet if compound leaf |
| Ext |
Vegetative: leaves |
Blade width (c) |
19 |
continuous |
NA |
cm |
|
Blade is leaflet if compound leaf |
| Ext |
Vegetative: leaves |
Compound leaf length (c) |
22 |
continuous |
NA |
cm |
|
Only for compound leaves |
| Ext |
Vegetative: leaves |
Compound leaf width (c) |
23 |
continuous |
NA |
cm |
|
Only for compound leaves |
| Ext |
Vegetative: leaves |
Perimeter to Area Ratio |
24 |
continuous |
NA |
NA |
Weiher |
|
| Ext |
Vegetative: leaves |
Blade area (c) |
26 |
continuous |
NA |
cm2 |
|
Blade is leaflet if compound leaf. |
| Ext |
Vegetative: leaves |
Specific leaf area |
29 |
continuous |
NA |
mm2 mg-1 |
Cornelissen et al 2003 |
(Area/dry mass) |
| Ext |
Vegetative: leaves |
Specific leaf area (+petiole) |
30 |
continuous |
NA |
mm2 mg-1 |
Westoby 2000? |
(Area/dry mass) |
| Ext |
Vegetative: leaves |
Leaf dry matter content |
31 |
continuous |
NA |
mg g-1 |
Cornelissen et al 2003, Garnier et al 2001 |
Oven-dry mass (mg) of a leaf divided by its water-saturated
fresh mass (g). (It is 1 – leaf water
content expressed on a fresh mass basis) (= Cornelissen flammability 3) |
| Ext |
Vegetative: leaves |
Leaf thickness |
32 |
continuous |
NA |
micron |
|
Lamina thickness |
| Ext |
Vegetative: leaves |
Stomatal density in lower surface |
34 |
continuous |
NA |
mm-2 |
|
Number mm-2 |
| Ext |
Vegetative: leaves |
Stomatal density in upper surface |
35 |
continuous |
NA |
mm-2 |
|
Number mm-2 |
| Ext |
Vegetative: leaves |
Leaf toughness: 1. Tensile strength |
36 |
continuous |
NA |
N mm-1 |
Cornelissen et al 2003 |
Leaf tensile strength is the force needed to tear a leaf
(fragment) divided by its width (e.g. Cornelissen
and Thompson 1997) |
| Ext |
Vegetative: leaves |
Leaf toughness: 2. Resistance to fracture |
37 |
continuous |
NA |
N |
Cornelissen et al 2003 |
Leaf resistance to fracture (also called 'force of fracture'
or 'work to shear') as the mean force needed to
cut a leaf or leaf fragment at a constant angle (20) and speed (e.g. Wright
and Cannon 2001) |
| Ext |
Vegetative: leaves |
Leaf toughness: 3. Puncturability |
38 |
continuous |
NA |
unknown |
Cornelissen et al 2003, Aranwela et al. 1999 |
Leaf puncturability provides data for the resistance of the
actual leaf tissues (particularly the epidermis)
to rupture, excluding toughness provided by midribs and main veins. It is
measured with a punch test that involves punching a hole through the leaf
lamina |
| Ext |
Vegetative: leaves |
Leaf Nmass |
40 |
continuous |
NA |
% |
Cornelissen et al 2003, Glopnet |
Leaf nitrogen concentration (LNC) is the total amounts of N
per unit of dry leaf mass |
| Ext |
Vegetative: leaves |
Leaf Narea |
41 |
continuous |
NA |
g m-2 |
Cornelissen et al 2003, Glopnet |
Leaf nitrogen concentration (LNC) in an area basis is the
total amounts of N per unit of dry leaf area |
| Ext |
Vegetative: leaves |
Leaf Pmass |
42 |
continuous |
NA |
% |
Cornelissen et al 2003, Glopnet |
Leaf phosphorus concentration (LNC) is the total amounts of N
per unit of dry leaf mass |
| Ext |
Vegetative: leaves |
Leaf Parea |
43 |
continuous |
NA |
g m-2 |
Cornelissen et al 2003, Glopnet |
Leaf phosphorus concentration (LNC) in an area basis is the
total amounts of N per unit of dry leaf area |
| Ext |
Vegetative: leaves |
Leaf C:N |
44 |
continuous |
NA |
- |
|
Carbon:nitrogen ratio of the blade |
| Ext |
Vegetative: leaves |
Litter Nmass |
45 |
continuous |
NA |
% |
EFC: Suding |
Litter nitrogen concentration |
| Ext |
Vegetative: leaves |
Litter Pmass |
46 |
continuous |
NA |
% |
EFC: Suding |
Litter phosphorus concentration |
| Ext |
Vegetative: leaves |
Litter C:N |
47 |
continuous |
NA |
- |
EFC: Suding |
Litter C:N ratio |
| Ext |
Vegetative: leaves |
Leaf longevity |
49 |
continuous |
NA |
months |
Cornelissen et al 2003 |
Leaf lifespan (longevity) is defined as the number of months
during which an individual leaf (or leaf analogue)
or part of a leaf is alive and physiologically active |
| Ext |
Vegetative: stems/defenses |
Wood density |
56 |
continuous |
NA |
g cm-3 |
Cornelissen et al. 2003 |
Dry weight per fresh volume. |
| Ext |
Vegetative: stems/defenses |
Twig dry matter content |
57 |
ordered discrete |
5 |
NA |
Cornelissen et al 2003, Garnier et al 2001 |
Oven-dry mass (mg) of a twig divided by its water-saturated
fresh mass (g). (It is 1 – twig water
content expressed on a fresh mass basis) (= Cornelissen flammability 1) |
| Ext |
Vegetative: stems/defenses |
Twig drying time |
58 |
ordered discrete |
5 |
NA |
Cornelissen et al 2003 |
(= Cornelissen flammability 2) |
| Ext |
Vegetative: stems/defenses |
Bark thickness |
61 |
continuous |
NA |
mm |
Cornelissen et al 2003 |
The thickness of the bark, defined as the part of the stem
that is external to the wood or xylem—hence
it includes the vascular cambium |
| Ext |
Vegetative: stems/defenses |
Bark thickness |
62 |
ordered discrete |
3 |
NA |
Cornelissen et al 2003 |
The thickness of the bark, defined as the part of the stem
that is external to the wood or xylem—hence
it includes the vascular cambium |
| Ext |
Vegetative: roots |
Root depth: 2. depth |
73 |
continuous |
NA |
m |
Cornelissen et al 2003, Schenk and Jackson 2002 |
Depth above which 95% of the root biomass of a species is
located |
| Ext |
Life history and regeneration |
Seed mass |
78 |
continuous |
NA |
mg |
Cornelissen et al 2003 |
Oven-dry mass of average seed |
| Ext |
Life history and regeneration |
Dispersule shape |
82 |
continuous |
NA |
- |
LEDA |
Dispersule shape is the variance of its three dimensions, i.e.
the length, the width, and the thickness (breadth)
of the dispersule, after each of these values has been divided by the largest
of the three values (Thompson et al. 1993). The seed shape (Vs) is captured
by dividing length, width, and height of a seed separately by length and then
calculating the variance of the three values with the formula: Vs= S (xi
– mean (x))2/n, with n=3 and x1=length/length, x2=height/length,
x3=width/length. The unit for all of the three measured dimensions is
millimeters |
| Ext |
Life history and regeneration |
Annual seed production per plant (c) |
84 |
continuous |
NA |
- |
BSH |
seeds per plant |
| Ext |
Habitat and distribution |
Climate envelope: total annual precip |
121 |
continuous |
NA |
mm |
Loarie et al. |
Multivariate trait from Ackerly et al. |
| Ext |
Habitat and distribution |
Climate envelope: seasonality precip |
122 |
continuous |
NA |
mm |
Loarie et al. |
|
| Ext |
Habitat and distribution |
Climate envelope: mean annual temp |
123 |
continuous |
NA |
deg |
Loarie et al. |
|
| Ext |
Habitat and distribution |
Climate envelope: seasonality temp |
124 |
continuous |
NA |
deg |
Loarie et al. |
|
| Dbase |
Vegetative: stems/defenses |
Leaf area to sapwood area |
138 |
continuous |
NA |
mm2 mm-2 |
Preston et al. 2006 New Phyt |
ratio of leaf area to subtending sapwood area (inverse of
huber value) |