|
| |
|
Año |
|
Tipo de Vegetación |
Superficie (hectáreas) |
Coeficiente Minimo (hectáreas/unidad animal) |
Coeficiente Máximo (hectáreas/unidad animal) |
2002 |
Pastizal |
Mediano abierto |
8,475,925.00 |
5.01 |
20.52 |
|
|
Mediano arbofrutescente |
4,523,758.00 |
8.05 |
23.00 |
|
|
Mediano arborescente |
643,740.00 |
11.00 |
18.24 |
|
|
Amacollado abierto |
2,571,793.00 |
7.59 |
24.34 |
|
|
Amacollado arborescente |
684,534.00 |
13.50 |
18.00 |
|
|
Amacollado arbofrutescente |
784,118.00 |
11.37 |
22.00 |
|
|
Inducido |
13,750.00 |
7.41 |
10.40 |
|
|
Halófito abierto |
2,218,583.00 |
7.00 |
20.37 |
|
|
Halófito arbofrutescente |
2,502,189.00 |
9.00 |
19.00 |
|
|
Vegetación halófita |
1,915,883.00 |
7.60 |
48.19 |
|
|
Subtotal Pastizal |
24,334,273.00 |
- |
- |
|
Matorral |
Alto subinerme |
2,290,002.00 |
10.30 |
28.73 |
|
|
Alto espinoso |
4,782,490.00 |
8.20 |
29.00 |
|
|
Mediano esclerófilo |
720,592.00 |
21.41 |
25.92 |
|
|
Mediano parvifolio |
13,429,218.00 |
14.70 |
77.10 |
|
|
Mediano subinerme |
7,426,774.00 |
12.30 |
43.00 |
|
|
Mediano subespinoso |
1,108,908.00 |
21.90 |
48.00 |
|
|
Mediano espinoso |
4,016,842.00 |
8.79 |
35.46 |
|
|
Mediano crasicaulescente espinoso |
24,689.00 |
23.00 |
23.00 |
|
|
Bajo subespinoso |
468,611.00 |
24.00 |
40.00 |
|
|
Bajo espinoso |
238,639.00 |
7.46 |
25.20 |
|
|
Bajo crasifolio |
3,134,709.00 |
50.00 |
80.00 |
|
|
Crasicaule |
613,186.00 |
9.16 |
24.63 |
|
|
Arbocrasicaulescente |
2,639,008.00 |
12.60 |
60.00 |
|
|
Arborescente |
2,319,540.00 |
9.80 |
44.00 |
|
|
Arbofrutescente |
4,516,542.00 |
17.00 |
60.00 |
|
|
Mediano parvifolio crasicaulescente |
3,698,710.00 |
23.00 |
46.00 |
|
|
Crasirosulifolio espinoso |
7,653,211.00 |
14.10 |
61.25 |
|
|
Sarcocaulescente |
921,566.00 |
25.20 |
50.00 |
|
|
Sarcocrasicaulescente subinerme |
911,086.00 |
34.00 |
60.00 |
|
|
Oligocilindrocaule afilo |
218,291.00 |
13.96 |
34.70 |
|
|
Vegetación de dunas |
1,024,723.00 |
54.00 |
60.00 |
|
|
Subtotal Matorral |
62,157,337.00 |
- |
- |
|
Selva |
Alta perennifolia |
7,876,474.00 |
0.80 |
3.44 |
|
|
Alta subperennifolia |
823,178.00 |
2.54 |
2.54 |
|
|
Alta subcaducifolia |
333,601.00 |
1.20 |
2.00 |
|
|
Mediana subperennifolia |
9,914,679.00 |
0.80 |
6.84 |
|
|
Mediana subcaducifolia |
7,675,304.00 |
0.90 |
8.58 |
|
|
Mediana caducifolia |
1,953,361.00 |
2.00 |
5.30 |
|
|
Mediana subcaducifolia subespinosa |
15,249.00 |
3.80 |
3.80 |
|
|
Mediana perennifolia subespinosa |
8,133.00 |
2.10 |
2.10 |
|
|
Baja caducifolia |
15,587,181.00 |
1.30 |
32.04 |
|
|
Baja caducifolia espinosa |
2,071,471.00 |
1.95 |
12.00 |
|
|
Baja subperennifolia espinosa |
789,861.00 |
7.00 |
7.80 |
|
|
Baja caducifolia subespinosa |
322,472.00 |
6.30 |
14.00 |
|
|
Baja subperennifolia |
231,353.00 |
3.60 |
4.36 |
|
|
Baja perennifolia |
95,000.00 |
2.30 |
2.30 |
|
|
Baja subcaducifolia |
92,254.00 |
4.30 |
4.90 |
|
|
Baja subperennifolia subespinosa |
17,816.00 |
2.00 |
2.50 |
|
|
Baja subcaducifolia espinosa |
11,323.00 |
13.66 |
13.66 |
|
|
Subtotal Selva |
47,818,710.00 |
- |
- |
|
Bosque |
Aciculifolio |
14,044,509.00 |
2.90 |
35.60 |
|
|
Aciculi-esclerófilo |
11,257,545.00 |
2.00 |
30.77 |
|
|
Aciculi-linerifolio |
444,188.00 |
2.00 |
32.80 |
|
|
Aciculi-escuamifolio |
370,845.00 |
18.90 |
21.40 |
|
|
Esclerófilo-caducifolio |
10,454,935.00 |
3.24 |
33.01 |
|
|
Esclero-aciculifolio |
2,639,362.00 |
8.18 |
33.20 |
|
|
Esclero-escuamifolio |
101,649.00 |
17.00 |
26.30 |
|
|
Esclerófilo-subcaducifolio |
25,218.00 |
10.40 |
10.40 |
|
|
Linearifolio |
432,724.00 |
10.25 |
18.55 |
|
|
Escuamifolio |
664,720.00 |
6.36 |
32.80 |
|
|
Caducifolio |
1,422,699.00 |
1.10 |
20.00 |
|
|
Caducifolio espinoso |
3,148,221.00 |
5.47 |
27.40 |
|
|
Esclerófilo perennifolio |
542,076.00 |
0.80 |
18.60 |
|
|
Oligocilindrocaule rosulifolio |
425,906.00 |
17.35 |
43.52 |
|
|
Páramos de altura |
18,764.00 |
24.60 |
24.60 |
|
|
Vegas arboladas |
39,309.00 |
4.50 |
4.50 |
|
|
Subtotal Bosque |
46,032,670.00 |
150.65 |
1,080.16 |
|
Otras superficies |
Otras Superficies |
16,374,310.00 |
- |
- |
|
Total |
Total |
196,717,300.00 |
- |
- |
|
|
|
|
| |
|