Ecological Significance of floristic structure and Biological Spectrum of alpine floral biodiversity of Khunjerab National Park Gilgit-Baltistan Pakistan

Sujjad Haider1*, Nasiba Ibrahim2

1Department of Environmental Sciences Karakoram International University Gilgit-Baltistan Pakistan

2Govt girl’s high School Sikanderabad Nagar Gilgit-Baltistan Pakistan

*Correspondence: sajjadbotanist@gmail.com, Sujjad.Hyder@kiu.edu.pk

Citation |Haider. S, Ibrahim. N, “Ecological Significance of floristic structure and Biological Spectrum of alpine floral biodiversity of Khunjerab National Park Gilgit-Baltistan Pakistan”. International Journal of Innovations in Science and Technology. Vol 4, Issue 2, 2022, pp: 459-475

Received | March 25, 2022; Revised | April 28, 2022; Accepted | May 15, 2022; Published | May 18, 2022.

________________________________________________________________________

The current study was conducted in Khunjerab National Park which is situated in the subalpine zone. The study area was thoroughly surveyed to ensure the maximum collection of flowering plants diversity. The work aimed to investigate the ecological significance of floral structure and the biological spectrum of prevailing flowering plants' biodiversity in the study area. For this purpose, we recognized four ecological zones based on altitude in the park namely the subalpine zone (3000m to 3500m), alpine zone (3600m to 4000m), super alpine zone (4100-4500m), and sub naval zone was started from (4600-4800m) altitude. The collected specimens comprised (155) plant species that belong to 97 genera and 36 families. The life forms of the collected species were 72% Hemicryptophyte (H), 13% Therophytes, 10% Chaemephyte, and 5% Phanerophyte. While the habit categories of the flora were analyzed with the help of Theophrastus classification. The breakup of the habit categories shows that the herbs with 137 species held the highest percentage to contribute the flora of the study area was with 88%, followed by shrubs with 14 species which contributed to the flora of the area was 9.03%. Similarly, subshrubs and trees contained the same number of 2 spices. We observed the phenological status of each species, i.e., flowering and fruiting conditions, and of the species that were infrequent.

Keywords: biodiversity, flora, phenology, life-form, habit categories

Introduction

           The life form is an important physiognomic attributes that have been widely used in vegetation studies and also it indicates micro and macroclimate as well as human disturbance of a particular area [1]. The life forms of species point out the adjustment of perennating buds to environmental conditions [2]. Raunkiær described the biological spectrum in [3]. Climate determines the type of plants that can exist in each ecosystem and the general appearance of vegetation is referred to as physiognomy or structure. It constitutes the general structure, shape and life forms of the species comprising the vegetation and actually the classification of vegetation type has been done based on physiognomy [4].  Raunkiaer designed his life-form system to define what he called phytoclimates. The theoretical basis was familiar in plant geography [5] and may be expressed as follows: (1) Plants are limited in their capacity to endure different environmental complexes. (2) There is usually a correlation between the morphology (growth-form, life-form) of an organism and its environment, i.e., there is a morphological basis for adaptation in many if not all cases. (3) A plant, in its successful existence, represents what may be called an automatic physiological integration of all the factors of its environment. If these are general truths, it follows that the life-forms of the plants of an area are a measure of the environmental conditions, especially climate. It remains only to find the key to the plant-climate interrelations.

         Raunkiaer decided that the significant relationship was to be looked. for in the seasonal climates. When growth is slowed or dormancy forced upon a plant by cold or drought the most critical tissues are meristematic. Therefore, the amount of protection provided embryonic growing tissues and their success in enduring the unfavorable period represent a critical adaptation [1].

          The five principal classes of the life-form system of Raunkiaer (based, on the protection the perennating buds during the unfavorable season) are arranged according to increasing protection: Phanerophyte (trees and shrubs), chamaephytes (low perennials with buds close to the ground surface or semi-woody plant), Hemicryptophytes (buds at the soil surface), cryptophytes (buds beneath the soil or underwater), and Therophytes (annuals, herbaceous plant which produces seeds). These classes are subject to subdivision. The chamaephytes are so few in number that no breakdown was made. My information concerning the hemi cryptophytes is inadequate for the detailed treatment of subclasses. The geophytes (the major group 0 (cryptophytes) were c1assified according to whether the subterranean organs bearing the perennating buds are rhizomes, bulbs, stem tubers, root tubers, or roots, but the various groups seen to have little significance for present purposes. The Phanerophyte, however, were easily treated according to four Subclasses based 0n height. Megaphanerophytes exceed 30 meters; Mesophanerophytes are between 8 and 30 meters; Mesophanerophytes are between 2 and 8 meters; and Nanophytes are less tall than 2 meters and taller than chamaephytes (about 25 cm.) [1]. The geological and Ecological varieties zones of the world support various types of floristic composition [6].

Material and Methods

Investigation site

          The study area lies between latitude 36° 45.5’ N and 74° 49.7’ E longitude. The entire area comprises three vallies and constituting the national park falls in the former Hunza state, which, together with neighboring Nagar, is an independent district. The KNP comprises mostly difficult and terrain mountains snow-covered peaks which provide heterogeneous diversity to the ecosystem. The biodiversity pattern in mountains depends upon the physical environmental conditions such as solar radiation, precipitation, soil, wind, and biotic pressure. The physical complexity of the alpine environment encourages rapid speciation, especially because of flora and fauna [7]. Researches in alpine regions demonstrate enormous intra-specific variation even within a small area, for example, in flowering rhythms [8], [9].The alpine mountain system provides distinct altitudinal zones which enhance the local, regional and global biodiversity.  

Figure 1- Map of the study area

Collection of field data

         The reconnaissance study was conducted in the Khunjerab National Park (KNP), situated in the district of Hunza Nagar Gilgit-Baltistan. Field trips in different seasons thoroughly surveyed the study area. It provides an opportunity to make plant collection observations. During the field survey and the collection of plant specimens, we observed each species' phenological and ecological parameters. 

Identification and analysis

         The collected specimens were identified with the help of Flora of Pakistan [10], [11] using available literature and a comparison of specimens at Karachi University Herbarium.  The study area was thoroughly surveyed to collect the plant specimens with the help of a presser and ecological data was collected with the help of an altimeter and Raunkiaer classification system . Habit categories and life cycle was categorized with the help of the Theophrastus system of classification [12]. While for the data analysis simple statistics and tabulation format was used.

Results

         The Khunjerab National Park in the district Hunza Nagar of Gilgit-Baltistan comprises 2,269 square kilometers in the Hunza, Gojal on either side of the Karakoram Highway from Dih to the Pak- China border at the Khunjerab pass. Based on altitude and Phytoclimatic conditions, we recognized four ecological zones: subalpine zone, Alpine zone, super alpine zone, and sub naval zone detail is given in (Figure-2). The distribution of plant taxa (Subalpine zone) from 3000m to 3500m altitude was 55 belonging to 20 families with 42 genera, followed the next alpine zone from 3600m to 4000m altitude 54 species were belonging to 19 families with 39 genera. While the super-alpine zone was started from 4100-4500m altitudes where 26 genera followed 33 species with 13 families, the sub naval zone was started from 4600-4800m only 13 species with 8 genera belonging with 6 families. Here it was noticed that the number of species was decreased with the higher altitude.

Figure-2 Distribution of taxa in Ecological zone

         During the inventory of alpine vegetation survey, 155 plant species were recorded belonging to 97 genera and 36 families (Table-1). The taxonomic breakup of the inventorying shows that the Gymnosperms comprised 2 families followed by 2 genera and 2 species. Among gymnosperms, only one family and one species belonged to the subgroup conifers, while one family and three species belonged to the subgroup Gnetophyte. The Angiosperms were 29 families belonging to 80 genera followed with 128 species and monocots were 23 species followed by 2 families and 15 genera. Based on the highest number of species, the Compositae family was disproportionately higher than other families. The second-largest family Poaceae had less than half the number of species (about 40%) as compared to Compositae.

Figure 3 Larger families in the study area

Figure 4 Life-form of the study area

Figure 5 Raunkaeir’s Life forms normal spectrum

 

 

 

 

The collected data show that only 5species are rare, 7 species are common and 141 species are infrequent in the study area (Figure-6).

 

Figure 7 Breakup of the habit categories and their percentage.

         The breakup of the habit categories shows that the herbs were with 137 species holding the highest percentage to contribute to the flora of the study area was herbs with 88% followed by shrubs with 14 species which contributed to the flora of the area was 9.03%. Similarly, subshrubs and trees contained the same number of spices (Figure-7).

 

Table-1: Cumulative check list the of species with observed ecological parameters on the study area

S.No.

Family

Species

Habit

Life form

Altitude

Abun.

Phenological status

Flo.

Fruiting.

 

GYMNOSPERMS

 

CONIFERS

1.        

Cupressaceae

JuniperusturkestanicaKomarov

Tree

Ph

3500m

In

-

+

 

GNETOPHYTES

2.        

Ephedraceae

Ephedra gerardianaWall.exStapf

Shrub

Ph

3500m

In

+

-

3.        

Ephedraceae

Ephedra intermedia schrank& Mayer

Shrub

Ph

3600m

In

-

-

4.        

Ephedraceae

Ephedra regelianaFlorin

Shrub

Ph

4000m

In

-

-

 

ANGOSPERMS-DICOTS

5.        

Apocynaceae

Trachomitumvenetum(L.) Woodson

Perennial  herb

Ch

3000m

In

-

+

6.        

Berberidaceae

BerberisbrevissimaJafri

Shrub

Ph

3500m

In

-

+

7.        

Berberidaceae

BerberisulicinaHook,f&Thoms.

Shrub

Ph

3500m

C

-

+

8.        

Betulaceae

BetulautilisD.Don

Tree

Ph

3000m

In

+

-

9.        

Boraginaceae

ArnebiaguttataBunge

Perennial  herb

H

3300m

In

+

-

10.    

Boraginaceae

CynoglossumglochidiatumWall.exBenth.

Perennial  herb

H

3600m

In

-

+

11.    

Boraginaceae

Eritrichiumcanum (Benth. in Royle) KitamuraVar.canum

Perennial  herb

H

4000m

In

+

-

12.    

Boraginaceae

Lappulaconsanguinea(F. &C.A. Meyer)Gurke

Perennial  herb

H

4200m

In

+

-

13.    

Boraginaceae

Lindelofiaanchusoides(Lindl.)Lehm.

Perennial  herb

H

4000m

In

+

-

14.    

Boraginaceae

MyosotisalpestisF.W.Schmidt

var. asiaticaVest.exHulten

Perennial  herb

H

4300m

In

+

-

15.    

Boraginaceae

Myosotisarvensis(L.)Hill

Perennial  herb

H

4000m

In

+

-

16.    

Boraginaceae

OnosmahispidaWall. ex G.Don

Perennial  herb

H

3600m

R

-

+

17.    

Boraginaceae

Pseudomertensiaechioides(Benth.) Riedl

Perennial  herb

H

3600m

In

+

-

18.    

Brassicaceae

Brayarosea(Turcz.)Bunge

Perennial  herb

H

4300m

In

+

-

19.    

Brassicaceae

Capsella bursa-pastoris(L.) Medik.

Perennial  herb

H

3500m

In

+

-

20.    

Brassicaceae

ChristoleacrassifoliaCamb.

Perennial  herb

H

4400m

In

+

-

21.    

Brassicaceae

Christoleahimalayensis(Camb.)Jafri

Perennial  herb

H

4200m

In

+

-

22.    

Brassicaceae

Descurainiasophia(L.)Webb & Berth.

Perennial  herb

H

3500m

In

+

-

23.    

Brassicaceae

Hediniatibetica(Thoms.) Ostenf.

Perennial  herb

H

4500m

R

+

-

24.    

Brassicaceae

LepidiumapetalumWilld.

Annual herb

Th

3700m

In

+

-

25.    

Brassicaceae

LepidiumlatifoliumL.

Annual herb

Th

3600m

In

+

-

26.    

Brassicaceae

LepidiumsativumL.

Annual herb

Th

3800m

In

+

-

27.    

Brassicaceae

ParryaexscapaLedeb.

Perennial  herb

H

4300m

In

+

-

28.    

Brassicaceae

SisymbriumheteromallumC.A.Mey

Annual herb

Th

3300m

In

+

-

29.    

Brassicaceae

SisymbriumbrassiciformeC.A.Mey.

Annual herb

Th

3500m

In

-

+

30.    

Brassicaceae

Smelowskia alba (Pall) Regel

Perennial herb

H

4500m

R

-

+

31.    

Brassicaceae

Smelowskiacalycina(Steph. ex Willd.)C.AMey.

Perennial herb

H

4500m

R

-

+

32.    

Campanulaceae

Campanula pallidaWall.

var.tibetica(Hook.f.et Thoms.)Hara

Perennial herb

H

3800m

In

+

-

33.    

Capparidaceae

CapparishimalayensisJafri

Sub shrub

Ch

3700m

In

-

+

34.    

Caprifoliaceae

LoniceramicrophyllaWilld.exRoem. &Schultes

Shrub

Ph

3700m

In

+

-

35.    

Caprifoliaceae

LonicerasemenoviiRegel

Shrub

Ph

3600m

In

+

-

36.    

Caryophyllaceae

CerastiumpusillumSer

Perennial herb

H

3800m

In

+

-

37.    

Caryophyllaceae

Silenegonosperma(Rupr.)Bocquet

Perennial herb

H

4200m

In

+

-

38.    

Caryophyllaceae

SilenekunawarensisBenth.

Perennial herb

H

3700m

In

+

-

39.    

Chenopodiaceae

Chenopodium album L.

Annual  herb

Th

3500m

In

+

-

40.    

Chenopodiaceae

ChenopodiumbotrysL.

Annual  herb

Th

3500

In

+

-

41.    

Chenopodiaceae

ChenopodiumfoliosumAsch.

Annual  herb

Th

3600m

In

-

+

42.    

Chenopodiaceae

HalogetontibeticusBunge

Perennial  herb

H

3500m

In

-

+

43.    

Chenopodiaceae

Kochiaprostrata(L.)Schrad.

Perennial  herb

H

3000m

In

+

-

44.    

Chenopodiaceae

Krascheninnikoviaceratoides(L.) Guldenst.

Sub shrub

Ch

3300m

In

+

-

45.    

Compositae

Acroptilonrepens(L.) DC.

Perennial  herb

H

3600m

In

+

-

46.    

Compositae

Ajaniafruticulosa(Ledeb.)Poljakov

Perennial  herb

Ch

4000m

C

+

-

47.    

Compositae

Anaphalisnepalensis(Spreng.)Hand.-Mazz.

Perennial  herb

H

4200m

In

+

-

48.    

Compositae

Artemisia absinthiumL.

Perennial  herb

Ch

3600m

In

+

-

49.    

Compositae

Artemisia biennisWilld.

Perennial  herb

Ch

3500m

In

+

-

50.    

Compositae

Artemisia capillaris Thunb.

Perennial  herb

Ch

3600m

In

+

-

51.    

Compositae

Artemisia dracunculusL.

Perennial  herb

Ch

3500m

In

+

-

52.    

Compositae

Artemisia elegantissimaPamp.

Perennial  herb

Ch

3800m

In

+

-

53.    

Compositae

Artemisia macrocephalaJacquem. ex Besser

Perennial  herb

Ch

3300m

In

+

-

54.    

Compositae

Artemisia persicaBoiss.

Perennial  herb

Ch

3300m

In

-

+

55.    

Compositae

Artemisia rupestrisL.

Perennial  herb

Ch

4500m

In

+

-

56.    

Compositae

Artemisia rutifoliaSpreng.

Perennial  herb

Ch

3300m

In

+

-

57.    

Compositae

Artemisia roxburghianaWall.exBesser

Perennial  herb

Ch

3200m

In

+

-

58.    

Compositae

Artemisia santolinifoliaTurcz.exKrasch

Perennial  herb

Ch

3300m

In

+

-

59.    

Compositae

Artemisia vulgaris L.

Perennial  herb

Ch

3500m

C

+

-

60.    

Compositae

SeneciokraschenninikoviiSchischkin

Perennial  herb

H

3500m

In

+

-

61.    

Compositae

Crepisflexuosa(DC.) Bth.&Hk.f.

Perennial  herb

H

4000m

C

+

-

62.    

Compositae

EchinopscornigerusDC.

Annual herb

Th

3500m

In

+

-

63.    

Compositae

HieraciumumbellatumL.

Perennial  herb

H

3000m

In

+

-

64.    

Compositae

HieraciumvirosumPall.

Perennial  herb

H

3300m

In

+

-

65.    

Compositae

HieraciumvulgatumFries

Perennial  herb

H

3400m

In

+

-

66.    

Compositae

LeontopodiumbrachyactisGandoger

Perennial  herb

H

3600m

In

+

-

67.    

Compositae

Leontopodiumleontopodinum(DC.)Hand.-Mazz

Perennial  herb

H

4000m

In

+

-

68.    

Compositae

Leontopodiumnanum(Hook.f. & Thomson ex C. B. Clarke) Hand.-Mazz.

Perennial  herb

H

3800m

In

+

-

69.    

Compositae

Saussureagnaphalodes(Royle) Sch.-Bip.

Perennial  herb

H

4700m

R

+

-

70.    

Compositae

Saussureajacea(Klotzsch) Clarke

Perennial  herb

H

3000m

In

+

-

71.    

Compositae

Saussureaobvellata (DC.) Sch.

Perennial  herb

H

4400m

R

+

-

72.    

Compositae

Saussureasimpsoniana (Field &Garden)Lipschitz

Perennial  herb

H

4800m

R

+

-

73.    

Compositae

Seriphidiumbrevifolium(Wall. ex DC.) Ling & Y.R. Ling

Perennial  herb

Ch

4000m

C

+

-

74.    

Compositae

TanacetumartemisioidesSchultz-Bip.exHook.f.

Perennial  herb

H

4000m

In

+

-

75.    

Compositae

TanacetumbaltistanicumPodlech

Perennial  herb

Ch

3600m

In

+

-

76.    

Compositae

TaraxacumafficinaleL.

Perennial  herb

H

3500m

In

+

-

77.    

Compositae

Taraxacumlati-base v.S.

Perennial  herb

H

4300m

In

+

-

78.    

Compositae

Taraxacumnasiriv. S.

Perennial  herb

H

4700m

In

+

-

79.    

Compositae

TricholepistibeticaHook.f.& Thomson

Perennial  herb

H

3100m

In

+

-

80.    

Crassulaceae

Hylotelephiumewersii (Ledeb.) H.Ohba

Perennial  herb

H

3300m

In

+

-

81.    

Crassulaceae

Orostachysthyrsiflora(Fisch.)D.C.

Perennial  herb

H

4200m

In

+

-

82.    

Crassulaceae

Rhodiolawallichiana(Hook) S.H.Fu

Perennial  herb

H

4000m

In

+

-

83.    

Elaeagnaceae

HippophaerhamnoidesL.

subsp.turkestanicaRousi

Shrub

Ph

3500m

In

+

-

84.    

Fumariaceae

Corydalis adiantifoliaHook f. &Thoms.

Perennial  herb

H

3600m

In

+

-

85.    

Gentianaceae

Aloitismoorcroftiana (wall.ex G Don) Omer, Qaiser& Ali.

Perennial  herb

H

4200m

In

+

-

86.    

Gentianaceae

Ciminalisaquatica(L.)Zuyev

Perennial  herb

H

4300m

In

+

-

87.    

Gentianaceae

Ciminaliskarelinii(Griseb.) Omer

Perennial  herb

H

4000m

In

+

-

88.    

Gentianaceae

Comastomafalcatum(Turcz.exKar. &Kir) T

Perennial  herb

H

4100m

In

+

-

89.    

Gentianaceae

Comastomapulmonarium(Turcz) Toyok.

Perennial  herb

H

4400m

In

+

-

90.    

Gentianaceae

GentianopsisPaludosa(Munro ex Hook.f.) Ma

Perennial  herb

H

3300m

In

+

-

91.    

Labiatae

DracocephalumstamineumKar. &Kir.

Perennial  herb

H

4000m

In

+

-

92.    

Labiatae

MentharoyleanaBenth.

Perennial  herb

H

3500m

F

+

-

93.    

Labiatae

NepetalongibracteataBenth.

Perennial  herb

H

3700m

In

+

-

94.    

Labiatae

PerovskiaabrotanoidesKarel.

Perennial  herb

H

4000m

C

+

-

 

95.    

Papaveraceae

PapavernudicauleL.

Perennial  herb

H

4500m

In

+

-

 

96.    

Papilionaceae

AstragalusfalconeriBunge

Perennial  herb

H

4600m

In

+

-

 

97.    

Papilionaceae

Oxytropismicrophylla(Pallas) DC.

Perennial  herb

H

4000m

In

+

-

 

98.    

Papilionaceae

OxytropissavellanicaBunge ex Boiss.

Perennial  herb

H

4600m

In

+

-

 

99.    

Papilionaceae

OxytropisstaintonianaAli

Perennial  herb

H

3300m

In

+

-

 

100.                        

Plantaginaceae

PlantagogentianoidesSibth.& Sm. subsp.gentianoides

Perennial  herb

H

3900m

In

+

-

 

101.                        

Polygonaceae

Rheum tibeticumMaxim. ex Hook. f.

Perennial  herb

H

4200m

In

+

-

 

102.                        

Primulaceae

PrimulanutansJ.G.Georgi

Perennial  herb

H

4300m

In

+

-

 

103.                        

Ranunculaceae

Delphinium pyramidaleRoyle

Perennial  herb

H

4200m

In

+

-

 

104.                        

Ranunculaceae

Pulsatillawallichiana(Royle) Ulbr.

Perennial  herb

H

4100m

In

+

-

 

105.                        

Ranunculaceae

Delphinium vestitumWall.exRoyle

Perennial  herb

H

4300m

In

+

-

 

106.                        

Ranunculaceae

Ranunculus pulchellusC.A.Mey.

Perennial  herb

H

4700m

In

+

-

 

107.                        

Rosaceae

Potentilladryadanthoides(Juz.) Viroshilov

Shrub

Ph

4000m

In

+

-

 

108.                        

Rosaceae

PotentillapamiricaTh. Wolf var.pamirica

Perennial  herb

H

3600m

In

+

-

 

109.                        

Rosaceae

PotentillasalesovianaSteph.

Shrub

Ph

4000m

In

+

-

 

110.                        

Rosaceae

Rosa microphyllaLindl.

Shrub

Ph

3500m

In

+

-

 

111.                        

Rosaceae

SibbaldiapurpureaRoyle

Perennial  herb

H

4200m

In

+

-

 

112.                        

Rubiaceae

GaliumceratophylloidesHook.f.

Perennial  herb

H

3900m

In

+

-

 

113.                        

Rubiaceae

GaliumverumL.

Perennial  herb

H

4000m

In

+

-

 

114.                        

Rubiaceae

RubiatibeticaHook.f.Rubia

Perennial  herb

H

3100m

In

+

-

 

115.                        

Saxifragaceae

SaxifragaflagellarisWilld ex Sternb.

Perennial  herb

H

4500m

In

+

-

 

116.                        

Saxifragaceae

SaxifragapulvinariaH.Smith

Perennial  herb

H

4000m

In

+

-

 

117.                        

Saxifragaceae

Saxifragaflagellariswilld ex stermb.subsp.komarovii(A.Los.) Hulten

Perennial  herb

H

4000m

In

+

-

 

118.                        

Saxifragaceae

SaxifragaflagellarisWilld ex Sternb. subspcrassiflagellataHulten

Perennial  herb

H

4200m

In

+

-

 

119.                        

Saxifragaceae

SaxifragaflagellarisWilld ex Sternb. subsp.sentophylla(Royle) Hulten

Perennial  herb

H

4300m

In

+

-

 

120.                        

Saxifragaceae

SaxifragahirculusL.

Perennial  herb

H

4800m

In

+

-

 

121.                        

Scrophulariaceae

PedicularisalbidaPenn.

Perennial  herb

H

4000m

In

+

-

 

122.                        

Scrophulariaceae

PedicularisoederiVahl

Perennial  herb

H

3800m

In

+

-

 

123.                        

Scrophulariaceae

PedicularispurpureaPennell

Perennial  herb

H

4700m

In

+

-

 

124.                        

Scrophulariaceae

PedicularisrhinanthoidesSchrenk ex Fisch. &Mey.

Perennial  herb

H

4600m

In

+

-

 

125.                        

Scrophulariaceae

Pedicularisroylei Maxim.

Perennial  herb

H

4600m

In

+

-

 

126.                        

Tamaricaceae

MyricariasquamosaDesv.

Shrub

Ph

4000m

In

+

-

 

127.                        

Tamaricaceae

TamarixgallicaL.

Shrub

Ph

3000m

In

+

-

 

128.                        

Tamaricaceae

MuricariaelegansRoyle

Shrub

Ph

3500m

In

+

-

 

129.                        

Umbelliferae

TrachydiumroyleiLindl.

Perennial  herb

H

3300m

In

+

-

 

130.                        

Umbelliferae

VicatiawolffianaWolff.exFedde

Perennial  herb

H

3500

In

+

-

 

131.                        

Violaceae

Viola rupestrisF.W.Schm

Perennial  herb

H

4000m

In

+

-

 

132.                        

Zygophyllaceae

PeganumharmalaL.

Perennial  herb

H

3500m

In

 

+

 

 

ANGOSPERMS- MONOCOTS

 

133.                        

Cyperaceae

CarexpsychrophilaNees

Perennial  herb

H

4600m

In

-

+

 

134.                        

Cyperaceae

CarexdilutaM.Bieb.

Perennial  herb

H

4300m

In

-

+

 

135.                        

Cyperaceae

CarexdivisaHudson

Perennial  herb

H

4500m

In

-

+

 

136.                        

Cyperaceae

CarexpseudobicolorBoeck

Perennial  herb

H

4600m

In

-

-

 

137.                        

Cyperaceae

CarexstenophyllaWahlenb subsp. stenophylloides(V.Krecz.) Egor.

Perennial  herb

H

4700m

In

-

-

 

138.                        

Cyperaceae

Kobresiacapillifolia(Decne.) C.B.Clarke

Perennial  herb

H

4200m

In

 

-

 

139.                        

Cyperaceae

KobresianitensC.B.Clarke

Perennial  herb

H

4200m

In

-

+

 

140.                        

Cyperaceae

Kobresiaschoenoides(C.A.Mey.) Steud.

Perennial  herb

H

3500m

In

+

-

 

141.                        

Poaceae

SaccharumfilifoliumNees ex Steud.

Perennial  herb

H

3500m

In

+

-

 

142.                        

Poaceae

Agrostis stoloniferaL.

Perennial  herb

H

3700m

In

+

-

 

143.                        

Poaceae

Agrostis vinealisSchreb.

Perennial  herb

H

4000m

In

+

-

 

144.                        

Poaceae

AristidacyanthaNees ex Steud.

Perennial  herb

H

3700m

In

+

-

 

145.                        

Poaceae

Bothriochloabladhii(Retz.) S.T. blake

Perennial  herb

H

3600m

In

+

-

 

146.                        

Poaceae

Calamagrostispseudophragmites(Hall.f.) Koel.

Perennial  herb

H

3200m

In

+

-

 

147.                        

Poaceae

Cymbopogonpospischilii(K.Schum.) C.E. Hubb.

Perennial  herb

H

3000m

In

+

-

 

148.                        

Poaceae

Elymuscaninus(L.) L.

Perennial  herb

H

3500m

In

+

-

 

149.                        

Poaceae

Elymuslongearistatus(Boiss.) Tzvelev

Perennial  herb

H

3300m

In

+

-

 

150.                        

Poaceae

PennisetumlanatumKlotzsch

Perennial  herb

H

3300m

In

+

-

 

151.                        

Poaceae

Phragmiteskarka(Retz.) Trin. ex Steud.

Perennial  herb

H

3000m

In

+

-

 

152.                        

Poaceae

PoaalpinaL.

Perennial  herb

H

3700m

In

+

-

 

153.                        

Poaceae

PolypogonfugaxNees ex Steud.

Perennial  herb

H

3000m

In

+

--

 

154.                        

Poaceae

SaccharumspontaneumL.

Perennial  herb

H

3200m

In

+

-

 

155.                        

Poaceae

Sorghum halepense(L.) Pers.

Perennial  herb

H

3500m

In

+

-

 

                         

 

 

 

 

 

 

 

 

 

 Discussion

         The families ranging from 1st to 5th position were: Compositae (35), Poaceae (15), Brassicaceae (14), Boraginaceae (9), and Cyperaceous with (8) species (Figure-3), results of the current study are quite similar to [13], [14], [15].The Asteraceae family is the largest and most widespread family of flowering plants globally [16], [17].The wide ecological range of Asteraceae and Poaceae can be attributed to their adaptation to harsh conditions and effective wind dispersal strategies of their diasporas [18]. Besides inventory, we observed the phenological condition of each species; only 18 species were collected in fruiting conditions most of them belonging to the family Brassicaceae (Table-1).

        The biological spectrum is developed when all the species of higher plants of a community are classified into life-forms and the ratio is expressed in several percentages [19]. The life forms of the collected species were 72% Hemicryptophytes (H), 13% Therophytes, 10% Chamaephytes, and 5% Phanerophyte. The life form and distribution of the flora interlinks with the altitude and soil characteristics of the area (Figure-4). The life forms of the current study were compared with the Raunkiaer normal spectrum,1918 (Figure-5). The normal spectrum showed that Phanerophyte (46%), Chamaephytes (9%), Hemicryptophytes were (26%) and Therophytes were (13%).

Interestingly our life-form spectrum is closely similar to Rainier’s normal spectrum with Therophytes and Chaemephyte, while the remaining values were quite different. The life form of the community composition is the aspect of adaptations of its constituent species to the climatic condition [20]. Therefore, the climates and the major linked soil types can be reflected by life forms [5]. Raunchier [3] acknowledged that the necessary patterns of climates are characterized by the fact that one or few life forms are, relatively or absolutely, dominant. A high percentage of Hemicryptophytes in any specific region indicate that the mid-latitude includes needle-leaved forest and moisture Steppes (moist temperate region) [21]. Cain Castro and Shimwell [22], [23] reported that hemicryptophyte indicates the temperate zone.

On the other hand, the second-largest life form was chamaephytes, indicating temperate phytoclimates [24]. It shows that the Khunjerab National park is laying in different Phytoclimatic zones due to its topography and altitude. The biological spectrum is also regarded as an indicator of the prevailing environment and the occurrence of a similar biological spectrum in different regions indicates similar environmental conditions [19].

The collected data show that only 5species are rare, 7 species are common and 141 species are infrequent in the study area (Figure-6). A significant number is considered globally threatened because of habitat decline and over [1] exploitation. In this study, we recorded only 7 species as being threatened [25].

         The habit categories of the flora were analyzed with the help of the Theophrastus (250-370 B.C) system of classification. Habit in woody plants – lianas, shrubs, and trees – is typically an intrinsic trait [26], [27], and [28]. The breakup of the habit categories shows that the herbs were with 137 species holding the highest percentage to contribute the flora of the study area was herbs with 88% followed by shrubs with 14 species which contributed the flora of the area was 9.03%. Similarly, sub shrubs and trees contained the same number of species (Figure-5). According to Hazrat et al.,[29], [6] they recorded (11%) shrubs, (16%) grasses,(01%) climbers, and 70% herbs, our current results are closely similar to their results. I will enclose my observations on the ecological significance of the herbaceous layer in ecosystems by highlighting five aspects of herb-layer ecology: (1) the contributions of the herb layer to forest biodiversity; (2) the importance of the herb layer as the site of initial competitive interactions for the regeneration phases of dominant canopy species; (3) the ability of the herb layer to form linkages with the overstory; (4) the influence of the herb layer on ecosystem functions, such as energy flow and nutrient cycling; and (5) the multifaceted responses of the herb layer to various disturbances of both natural and anthropogenic origin [30]. Rare plants of the herbaceous layer can be used as indicators of biodiversity [31].Most of the plant biodiversity in ecosystems are found in the herbaceous layer [32], [33], and [34]. This is ironic because herbaceous species have higher natural extinction rates than plant species in other strata [30]. Levin and Wilson [35] estimated that extinction rates in herbs are more than three times that of hardwood tree species and approximately five times that of gymnosperms. Therefore, threats to the floral biodiversity are most often a function of threats to herbaceous-layer species [36].One of the most important ecological benefits of woody plants (Shrubs and trees) for human health is the interception and reduction of air pollution [37].Trees can mitigate temperatures in built environments.  Not  only do  trees  provide shade  through  intercepting and  absorbing  light, but  through  evapotranspiration  trees actively cool the air of cities [38], [39], [40]. An analysis of 94 urban areas around the world indicates that trees have a significant impact on the temperature and are responsible for, on average, 1.9°C (SD 2.3) of cooling in a city, one of the key ways to limit the impacts of climate change is to reduce the amount of carbon released into the atmosphere [33]. Trees are beneficial to storing carbon, which is a major contributor to climate change [41]. Trees, specifically mature ones, perform a keystone role in terrestrial ecosystems [42].Trees are critically important, especially in urban areas, as they provide food and habitat for birds, invertebrates, mammals, and plants [43], [40], and [44]. Trees provide economic benefits; they can also provide resources, such as food, to a community. Tree cover is strongly linked to student academic performance, [45], [46], and [47]. Trees and shrubs at schools, as opposed to grass, were strongly related to future education plans and graduation rates [47]. The authors of this study classify  the  benefits of  trees  into five categories:  (a) health  and  social well‐being;  (b)  cognitive development  and  education; (c)  economy  and resources;  (d)  climate change mitigation and habitat; and (e) green infrastructure [37].

The increasing biotic pressure in the park is creating a threat to all-natural resources; therefore, it needs to explore thoroughly before losing any natural resources and document the data for the future. Intensive animal grazing alters vegetation patterns. Additionally, grazing people digging valuable medicinal herbs at Pak-China border area and abrupt cutting of shrubs by people increase variation within vegetation. As a result, the habitats of species are being changed.

CONCLUSION The Khunjerab National Park (research area) is rich floristically.  This area contains most important medicinal plants which are growing on high altitudes, one of the most important factor is that it is dire need to thorough study of ecological significance of these flora in the fergile ecosystem.  

References

[1]       D. G. Jadhav, M. G. V’s, S. P. Hiray, and M. Mahavidyalaya, “International Journal of Advanced Research in Biological Sciences Biological spectrum with some other ecological attributes of the flora and vegetation of the Salher fort of Maharashtra, India,” Int. J. Adv. Res. Biol. Sci, vol. 7, no. 4, pp. 146–155, 2020, doi: 10.22192/ijarbs.

[2]       “Phenology and growth form distribution in an alpine pasture at Tungnath, Garhwal, Himalaya | HimalDoc.” https://lib.icimod.org/record/2482 (accessed Feb. 26, 2022).

[3]       C. Raunkiær, The life forms of plants and statistical plant geography; Oxford: The Clarendon Press, 1934.

[4]       S. Benzer, A. Gül, and M. Yilmaz, “Biological spectrum with some other ecological attributes of the flora and vegetation of the Asir Mountain of South West, Saudi Arabia,” African J. Biotechnol., vol. 9, no. 34, pp. 5560–5565, Aug. 2013, doi: 10.4314/ajb.v9i34.

[5]       S. A. Cain, “Life-forms and phytoclimate,” Bot. Rev. 1950 161, vol. 16, no. 1, pp. 1–32, Jan. 1950, doi: 10.1007/BF02879783.

[6]       “(PDF) Floristic diversity and ecological characteristics of flora of.” https://www.researchgate.net/publication/342144835_Floristic_diversity_and_ecological_characteristics_of_flora_of (accessed Feb. 26, 2022).

[7]       L. W. Price, “Mountains & man : a study of process and environment,” p. 506, 1981.

[8]       C. Körner, “Alpine Plant Diversity: A Global Survey and Functional Interpretations,” pp. 45–62, 1995, doi: 10.1007/978-3-642-78966-3_4.

[9]       B. Messerli and J. D. Ives, Mountains of the world: a global priority. New York: Parthenon Pub. Group, 1997.

[10]     “E. Nasir and S. I. Ali, ‘Flora of Pakistan,’ National Herbarium, NARC, Islamabad, Department of Botany, University of Karachi, Karachi, (Fascicles), 1972-1994. - References - Scientific Research Publishing.” https://www.scirp.org/(S(i43dyn45teexjx455qlt3d2q))/reference/ReferencesPapers.aspx?ReferenceID=708665 (accessed Feb. 26, 2022).

[11].    “the plant Families of Pakistan in the Department of Botany, University of Karachi and National Herbarium Islamabad, 1989-1991,Vol.Nos.190-210. - Google Search.” https://www.google.com/search?q=.+the+plant+Families+of+Pakistan+in+the+Department+of+Botany%2C+University+of+Karachi+and+National+Herbarium+Islamabad%2C+1989-1991%2CVol.Nos.190- (accessed Feb. 26, 2022).

[12]     “Theophrastus, Enquiry into Plants, Volume II: Books 6-9. On Odours. Weather Signs | Loeb Classical Library.” https://www.loebclassics.com/view/LCL079/1916/volume.xml (accessed Feb. 26, 2022).

[13]     W. Khan, S. M. Khan, H. Ahmad, Z. Ahmad, and S. Page, “Vegetation mapping and multivariate approach to indicator species of a forest ecosystem: A case study from the Thandiani sub Forests Division (TsFD) in the Western Himalayas,” Ecol. Indic., vol. 71, pp. 336–351, Dec. 2016, doi: 10.1016/J.ECOLIND.2016.06.059.

[14]     A. K. E. Osman and M. A. E.-H. Abdein, “Floristic diversity of Wadi Ar’ar, Saudi Arabia,” https://doi.org/10.1080/16583655.2019.1634177, vol. 13, no. 1, pp. 772–789, Dec. 2019, doi: 10.1080/16583655.2019.1634177.

[15]     “(PDF) Floristic and ecological studies on the plant cover of Wadi Al Rummah, Qassim Region, Saudi Arabia.” https://www.researchgate.net/publication/342534160_Floristic_and_ecological_studies_on_the_plant_cover_of_Wadi_Al_Rummah_Qassim_Region_Saudi_Arabia (accessed Feb. 26, 2022).

[16]     N. A. Al Shaye, Y. S. Masrahi, and J. Thomas, “Ecological significance of floristic composition and life forms of Riyadh region, Central Saudi Arabia,” Saudi J. Biol. Sci., vol. 27, no. 1, pp. 35–40, Jan. 2020, doi: 10.1016/J.SJBS.2019.04.009.

[17]     V. H. (Vernon H. Heywood, “Flowering plants of the world,” p. 335, 1979.

[18]     K. van R. van Oudtshoorn and M. W. van Rooyen, “Dispersal biology of desert plants,” p. 266, 1999, Accessed: Feb. 26, 2022. [Online]. Available: http://books.google.es/books?id=bdTfBfsl-DcC.

[19]     “(PDF) Biological spectrum of the grasslands at Canchipur, Manipur GEOBIOS.” https://www.researchgate.net/publication/343626986_Biological_spectrum_of_the_grasslands_at_Canchipur_Manipur_GEOBIOS (accessed Feb. 26, 2022).

[20]     S. A. Jamir and H. N. Pandey, “Vascular plant diversity in the sacred groves of Jaintia Hills in northeast India,” Biodivers. Conserv., vol. 12, no. 7, pp. 1497–1510, Jul. 2003, doi: 10.1023/A:1023682228549.

[21]     M. Ahmed, N. Khan, M. Wahab, U. Zafar, and J. Palmer, “Climate/growth correlations of tree species in the indus basin of the karakorum range, North Pakistan,” IAWA J., vol. 33, no. 1, pp. 51–61, 2012, doi: 10.1163/22941932-90000079.

[22]     S. Cain, Manual of vegetation analysis. New York: Harper, 1959.

[23]     “The Description and Classification of Vegetation, 1971, 322 pages with illustrations.: Shimwell, D. W.: Amazon.com: Books.” https://www.amazon.com/Description-Classification-Vegetation-pages-illustrations/dp/B01M9AV7SF (accessed Feb. 26, 2022).

[24]     B. V. M. M. Eher-Homji, “LIFE-FORMS AND BIOLOGICAL SPECTRA AS EPHARMONIC CRITERIA OF ARIDITY AND HUMIDITY IN THE TROPICS.”

[25]     D. Cicuzza, A. Newton, and S. Oldfield, “The Red List of Magnoliaceae.”

[26]     A. Cronquist, The evolution and classification of flowering plants. Boston: Houghton Mifflin, 1968.

[27]     I. M. Sussex and N. M. Kerk, “The evolution of plant architecture,” Curr. Opin. Plant Biol., vol. 4, no. 1, pp. 33–37, 2001, doi: 10.1016/S1369-5266(00)00132-1.

[28]     D. Barthélémy and Y. Caraglio, “Plant Architecture: A Dynamic, Multilevel and Comprehensive Approach to Plant Form, Structure and Ontogeny,” Ann. Bot., vol. 99, no. 3, pp. 375–407, Mar. 2007, doi: 10.1093/AOB/MCL260.

[29]     A. Hazrat, J. Shah, and M. Nisar, “Medicinal plants of Sheringal Valley, Dir Upper, KPK, Pakistan,” J. Biol, vol. 1, no. 2, pp. 131–133, 2011, [Online]. Available: http://www.fuuastjb.org/index.php/fuuastjb/article/view/371.

[30]     F. S. Gilliam, “The Ecological Significance of the Herbaceous Layer in Temperate Forest Ecosystems,” Bioscience, vol. 57, no. 10, pp. 845–858, Nov. 2007, doi: 10.1641/B571007.

[31]     “Floristic Conservation Value, Nested Understory Floras, and the Development of Second-Growth Forest on JSTOR.” https://www.jstor.org/stable/40062007 (accessed Feb. 26, 2022).

[32]     “TThe Herbaceous Layer in Forests of Eastern North America - Frank Gilliam - Oxford University Press. (n.d.). Retrieved February 26, 2022, from https://global.oup.com/academic/product/the-herbaceous-layer-in-forests-of-eastern-north-america-9780199837656?c.” https://global.oup.com/academic/product/the-herbaceous-layer-in-forests-of-eastern-north-america-9780199837656?cc=ae&lang=en& (accessed Feb. 26, 2022).

[33]     M. R. Roberts, “Response of the herbaceous layer to natural disturbance in North American forests,” Can. J. Bot., vol. 82, no. 9, pp. 1273–1283, Sep. 2004, doi: 10.1139/B04-091.

[34]     D. F. Whigham, “Ecology of Woodland Herbs in Temperate Deciduous Forests*,” http://dx.doi.org/10.1146/annurev.ecolsys.35.021103.105708, vol. 35, pp. 583–621, Nov. 2004, doi: 10.1146/ANNUREV.ECOLSYS.35.021103.105708.

[35]     D. A. Levin and A. C. Wilson, “Rates of evolution in seed plants: Net increase in diversity of chromosome numbers and species numbers through time,” Proc. Natl. Acad. Sci. U. S. A., vol. 73, no. 6, p. 2086, Jun. 1976, doi: 10.1073/PNAS.73.6.2086.

[36]     C. L. Jolls and D. F. Whigham, “Populations of and Threats to Rare Plants of the Herb Layer: Still More Challenges and Opportunities for Conservation Biologists,” Herbaceous Layer For. East. North Am., Apr. 2014, doi: 10.1093/ACPROF:OSOBL/9780199837656.003.0006.

[37]     J. B. Turner-Skoff and N. Cavender, “The benefits of trees for livable and sustainable communities,” Plants, People, Planet, vol. 1, no. 4, pp. 323–335, Oct. 2019, doi: 10.1002/PPP3.39.

[38]     “Heat Island Compendium | US EPA.” https://www.epa.gov/heatislands/heat-island-compendium (accessed Feb. 26, 2022).

[39]     A. D. Hirons and P. Thomas, “Applied tree biology.”

[40]     “Planning the Urban Forest: Ecology, Economy, and Community Development.” https://www.planning.org/publications/report/9026879/ (accessed Feb. 26, 2022).

[41]     “Atmospheric carbon reduction by urban trees | Treesearch.” https://www.fs.usda.gov/treesearch/pubs/18803 (accessed Feb. 26, 2022).

[42]     A. D. Manning, J. Fischer, and D. B. Lindenmayer, “Scattered trees are keystone structures - Implications for conservation,” Biol. Conserv., vol. 132, no. 3, pp. 311–321, Oct. 2006, doi: 10.1016/J.BIOCON.2006.04.023.

[43]     “Oak Ecosystems Recovery Plan.”

[44]     “(PDF) Benefits and uses of urban forests and trees | Sjerp de Vries and Stephan Pauleit - Academia.edu.” https://www.academia.edu/3064108/Benefits_and_uses_of_urban_forests_and_trees (accessed Feb. 26, 2022).

[45]     M. Kuo, M. H. E. M. Browning, S. Sachdeva, K. Lee, and L. Westphal, “Might school performance grow on trees? Examining the link between ‘Greenness’ and academic achievement in Urban, high-poverty schools,” Front. Psychol., vol. 9, no. SEP, p. 1669, Sep. 2018, doi: 10.3389/FPSYG.2018.01669/BIBTEX.

[46]     B. S. Kweon, C. D. Ellis, J. Lee, and K. Jacobs, “The link between school environments and student academic performance,” Urban For. Urban Green., vol. 23, pp. 35–43, Apr. 2017, doi: 10.1016/J.UFUG.2017.02.002.

[47]     R. H. Matsuoka, “Student performance and high school landscapes: Examining the links,” Landsc. Urban Plan., vol. 97, no. 4, pp. 273–282, Sep. 2010, doi: 10.1016/J.LANDURBPLAN.2010.06.011.

.

 

Copyright © by authors and 50Sea. This work is licensed under Creative Commons Attribution 4.0 International License.