» Articles » PMID: 28309220

The Distribution of C and C Grasses and Carbon Isotope Discrimination Along an Altitudinal and Moisture Gradient in Kenya

Overview
Journal Oecologia
Date 2017 Mar 18
PMID 28309220
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

More than 500 species of the Poaceae are found in Kenya, East Africa. Eighteen of twenty-seven tribes are exclusively (except the Paniceae and Danthonieae) of the C photosynthetic type. A floristic analysis of low altitude grasslands suggests that nearly all species at these low altitudes are of the C photosynthetic type. At high altitudes, however, nearly all grasses are of the C photosynthetic type. Open grassland vegetation was sampled along a transect from arid low altitude sites to the top of Mt. Kenya in an attempt to document the general distributions of the photosynthetic types.The major tribes illustrated three general patterns of distribution. The C tribes Chlorideae, Eragrosteae, Sporoboleae, and Aristideae were abundant at low altitudes (or low indices of available soil moisture). The Paniceae and Andropogoneae were also exclusively C but were more common at intermediate altitudes. The C tribes Aveneae, Festuceae, and Agrostideae were found only at high altitudes. In these open grasslands there were no C species below 2,000 m and no C species above 3,000 m. The variation in δC of the live grass vegetation with altitude confirms these distributional patterns and suggests a sharp transition zone between these two photosynthetic types. The photosynthetic type accounts for broad distributions within the Poaceae but these distributions are further modified by characteristics which may be inherent in the tribal groups. Ecological and paleoecological significance of these patterns of distribution are discussed.

Citing Articles

Intra-tooth stable isotope analysis reveals seasonal dietary variability and niche partitioning among bushpigs/red river hogs and warthogs.

Yang D, Uno K, Cerling T, Mwebi O, Leakey L, Grine F Curr Zool. 2024; 70(6):739-751.

PMID: 39678826 PMC: 11634686. DOI: 10.1093/cz/zoae007.


Linking African herbivore community enamel isotopes and environments: challenges, opportunities, and paleoecological implications.

Norwood A, Wang B, Kingston J Oecologia. 2024; 204(3):467-489.

PMID: 38517529 DOI: 10.1007/s00442-024-05532-z.


The Pleistocene high-elevation environments between 2.02 and 0.6 Ma at Melka Kunture (Upper Awash Valley, Ethiopia) based upon stable isotope analysis.

Briatico G, Bocherens H, Geraads D, Melis R, Mussi M Sci Rep. 2024; 14(1):6619.

PMID: 38503829 PMC: 10950861. DOI: 10.1038/s41598-024-56768-x.


Intrataxonomic trends in herbivore enamel δC are decoupled from ecosystem woody cover.

Robinson J, Rowan J, Barr W, Sponheimer M Nat Ecol Evol. 2021; 5(7):995-1002.

PMID: 33941906 DOI: 10.1038/s41559-021-01455-7.


Russ Monson and the evolution of C photosynthesis.

Sage R Oecologia. 2021; 197(4):823-840.

PMID: 33661402 DOI: 10.1007/s00442-021-04883-1.


References
1.
Troughton J, Card K . Temperature effects on the carbon-isotope ratio of C3, C 4 and crassulacean-acid-metabolism (CAM) plants. Planta. 2014; 123(2):185-90. DOI: 10.1007/BF00383867. View

2.
Tieszen L, Hein D, Qvortrup S, Troughton J, Imbamba S . Use of δC values to determine vegetation selectivity in East African herbivores. Oecologia. 2017; 37(3):351-359. DOI: 10.1007/BF00347911. View

3.
Breman H, Cisse A . Dynamics of sahelian pastures in relation to drought and grazing. Oecologia. 2017; 28(4):301-315. DOI: 10.1007/BF00345986. View

4.
Ehleringer J . Implications of quantum yield differences on the distributions of C and C grasses. Oecologia. 2017; 31(3):255-267. DOI: 10.1007/BF00346246. View

5.
Williams G . Photosynthetic adaptation to temperature in c(3) and c(4) grasses: a possible ecological role in the shortgrass prairie. Plant Physiol. 1974; 54(5):709-11. PMC: 366587. DOI: 10.1104/pp.54.5.709. View