Skip to main content

Advertisement

Log in

The distribution of four Caragana species is related to their differential responses to drought stress

  • Published:
Plant Ecology Aims and scope Submit manuscript

Abstract

Caragana species are widespread in northwest China. However, species in semiarid areas of Inner Mongolia experience summer and autumn rainfall, whereas morphologically similar close relatives in arid areas in Xinjiang Province experience wet springs, but hot dry summers. We hypothesize that the differences among species in response to soil drought help to explain their distributions. A comparison of the closely related species C. intermedia and C. microphylla from Inner Mongolia (semiarid species) and C. pruinosa and C. spinosa from Xinjiang (arid species) was conducted to examine whether responses to a water deficit in a pot experiment were associated with the environments of their habitat. In the two semiarid species, the stomatal conductance was relatively insensitive to the decrease in predawn leaf water potential (Ψleaf), and leaves did not abscise or die even when the Ψleaf decreased below −6.0 MPa, while in seedlings of the two arid species the stomata closed at a relatively high Ψleaf, and the leaves abscised gradually when Ψleaf fell below about −3.0 MPa. Furthermore, major vein density, minor vein density and the cubed ratio of the conduit wall thickness to the conduit lumen breadth [(t/b)3] of minor veins increased by an average of 60, 150 and 220 %, respectively, in the semiarid species compared with the arid species. The results indicated that semiarid species have typical anisohydric properties, while arid species have typical isohydric properties. We suggest that the divergence in water-use strategies in the genus may be associated with variation in vein architecture, and may possibly play an important role in determining the distribution of these species in the different environments of northwest China.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • An ZS, Kutzbach JE, Prell WL, Porter SC (2001) Evolution of Asian monsoons and phased uplift of the Himalaya—Tibetan plateau since Late Miocene times. Nature 411:62–66

    Article  CAS  Google Scholar 

  • Baltzer JL, Davies SJ, Bunyavejchewin S, Noor NSM (2008) The role of desiccation tolerance in determining tree species distributions along the Malay–Thai Peninsula. Funct Ecol 22:221–231

    Article  Google Scholar 

  • Blackman CJ, Brodribb TJ, Jordan GJ (2010) Leaf hydraulic vulnerability is related to conduit dimensions and drought resistance across a diverse range of woody angiosperms. New Phytol 188:1113–1123

    Article  PubMed  Google Scholar 

  • Blackman CJ, Brodribb TJ, Jordan GJ (2009) Leaf hydraulics and drought stress: response, recovery and survivorship in four woody temperate plant species. Plant Cell Environ 32:1584–1595

    Article  PubMed  Google Scholar 

  • Brodribb TJ, Cochard H (2009) Hydraulic failure defines the recovery and point of death in water-stressed conifers. Plant Physiol 149:575–584

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Brodribb TJ, McAdam SAM (2013) Abscisic acid mediates a divergence in the drought response of two conifers. Plant Physiol 162:1370–1377

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Chabot BF, Hicks DJ (1982) The ecology of leaf life spans. Ann Rev Ecol Syst 13:229–259

    Article  Google Scholar 

  • Chen JW, Zhang Q, Li XS, Li XS, Cao KF (2009) Independence of stem and leaf hydraulic traits in six Euphorbiaceae tree species with contrasting leaf phenology. Planta 230:459–468

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Choat B, Sack L, Holbrook NM (2007) Diversity of hydraulic traits in nine Cordia species growing in tropical rainforests with contrasting precipitation. New Phytol 175:686–698

    Article  PubMed  Google Scholar 

  • Edwards EJ (2006) Correlated evolution of stem and leaf hydraulic traits in Pereskia (Cactaceae). New Phytol 172:479–489

    Article  PubMed  Google Scholar 

  • Engelbrecht BM, Comita LS, Condit R, Kursar TA, Tyree MT, Turner BL, Hubbell SP (2007) Drought sensitivity shapes species distribution patterns in tropical forests. Nature 447:80–82

    Article  CAS  PubMed  Google Scholar 

  • Fang XW, Wang XZ, Chen K, Li H, Wang G (2006) Responses of Caragana korshinskii to different aboveground partial shoot removal: combining defence and tolerance strategies. Ann Bot 98:203–211

    Article  PubMed  Google Scholar 

  • Fang XW, Turner NC, Li FM, Li WJ, Guo XS (2011) Caragana korshinskii seedlings maintain positive photosynthesis during short-term, severe drought stress. Photosynthetica 49:603–609

    Article  CAS  Google Scholar 

  • Fang XW, Turner NC, Xu DH, Jin Y, He J, Li FM (2013) Limits to the height growth of Caragana korshinskii resprouts. Tree Physiol 33:275–284

    Article  CAS  PubMed  Google Scholar 

  • Fu PL, Jiang YJ, Wang AY, Brodribb TJ, Zhang JL, Zhu SD, Cao KF (2012) Stem hydraulic traits and leaf water-stress tolerance are coordinated with the leaf phenology of angiosperm trees in an Asian tropical dry karst forest. Ann Bot 110:189–199

    Article  PubMed  Google Scholar 

  • Gomez-Cadenas A, Tadeo FR, Talon M, Primo-Millo E (1996) Leaf abscission induced by ethylene in water-stressed intact seedlings of Cleopatra Mandarin requires previous abscisic acid accumulation in roots. Plant Physiol 112:401–408

    CAS  PubMed Central  PubMed  Google Scholar 

  • Hacke UG, Sperry JS, Pockman WT, Davis SD, McCulloh KA (2001) Trends in wood density and structure are linked to prevention of xylem implosion by negative pressure. Oecologia 126:457–461

    Article  Google Scholar 

  • Hao GY, Hoffmann WA, Scholz FG, Bucci SJ, Meinzer FC, Franco AC, Cao KF, Goldstein G (2008) Stem and leaf hydraulics of congeneric tree species from adjacent tropical savanna and forest ecosystems. Oecologia 155:405–415

    Article  PubMed  Google Scholar 

  • Jacobsen AL, Ewers FW, Pratt RB, Paddock WA, Davis SD (2005) Do xylem fibers affect vessel cavitation resistance? Plant Physiol 139:546–556

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Kumagai T, Porporato A (2012) Strategies of a Bornean tropical rainforest water use as a function of rainfall regime: anisohydric or isohydric? Plant Cell Environ 35:61–71

    Article  PubMed  Google Scholar 

  • Kursar TA, Engelbrecht BMJ, Burke A, Tyree MT, EI Omari B, Giraldo JP (2009) Tolerance to low leaf water status of tropical tree seedlings is related to drought performance and distribution. Funct Ecol 23:93–102

    Article  Google Scholar 

  • Li JF (1981) Climate in Xinjiang. China Meteorological Press, Beijing

    Google Scholar 

  • McDowell N, Pockman WT, Allen CD, Breshears DD, Cobb N, Kolb T, Plaut J, Sperry J, West A, Williams DG, Yepez EA (2008) Mechanisms of plant survival and mortality during drought: why do some plants survive while others succumb to drought. New Phytol 178:719–739

    Article  PubMed  Google Scholar 

  • Perry GLW, Enright NJ, Miller BP, Lamont BB (2012) Do plant functional traits determine spatial pattern? A test on species-rich shrublands, Western Australia. J Veget Sci 24:441–452

    Article  Google Scholar 

  • Quiroga RE, Fernández RJ, Golluscio RA, Blanco LJ (2013) Differential water-use strategies and drought resistance in Trichloris crinita plants from contrasting aridity origins. Plant Ecol 214:1027–1035

    Article  Google Scholar 

  • Sack L, Scoffoni C, McKown AD, Frole K, Rawls M, Havran JC, Tran H, Tran T (2012) Developmentally based scaling of leaf venation architecture explains global patterns. Nat Commun 3:837

    Article  PubMed  Google Scholar 

  • Schulze ED, Turner NC, Nicolle D, Schumacher J (2006a) Leaf and wood carbon isotope ratios, specific leaf areas and tree ring growth of Eucalyptus species across a rainfall gradient in Australia. Tree Physiol 26:479–492

    Article  CAS  PubMed  Google Scholar 

  • Schulze ED, Turner NC, Nicolle D, Schumacher J (2006b) Species differences in carbon isotope ratios, specific leaf area and nitrogen concentrations in leaves of Eucalyptus growing in a common garden compared with along an aridity gradient. Physiol Plant 127:434–444

    Article  CAS  Google Scholar 

  • Scoffoni C, Rawls M, McKown A, Cochard H, Sack L (2011) Decline of leaf hydraulic conductance with dehydration: relationship to leaf size and venation architecture. Plant Physiol 156:832–843

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Stewart GR, Turnbull MH, Schmidt S, Erskine PD (1995) 13C natural abundance in plant communities along a rainfall gradient: a biological integrator of water availability. Aust J Plant Physiol 22:51–55

    Article  Google Scholar 

  • Turner NC (1988) Measurement of plant water status by the pressure chamber technique. Irrig Sci 9:289–308

    Article  Google Scholar 

  • Turner NC, Kramer PJ (1980) Introduction. In: Turner NC, Kramer PJ (eds) Adaptation of plants to water and high temperature stress. Wiley, New York

    Google Scholar 

  • Turner NC, Schulze ED, Nicolle D, Schumacher J, Kuhlmann I (2008) Annual rainfall does not directly determine the carbon isotope ratio of leaves of Eucalyptus species. Physiol Plant 132:440–445

    Article  CAS  PubMed  Google Scholar 

  • Yuan S, Tang H (2010) Patterns of ephemeral plant communities and their adaptations to temperature and precipitation regimes in Dzungaria Desert, Xinjiang. Biodiversity Sci 18:346–354

    Google Scholar 

  • Zhang LY (1985) A preliminary study the ephemerals in Mosowan district Xinjiang. Acta Phytoeologica et Geobotanica Sinica 9:213–224

    Google Scholar 

  • Zhang ML, Fritsch PW (2010) Evolutionary response of Caragana (Fabaceae) to Qinghai–Tibetan Plateau uplift and Asian interior aridification. Plant Syst Evol 288:191–199

    Article  Google Scholar 

  • Zhang ML, Fritsch PW, Cruz BC (2009) Phylogeny of Caragana (Fabaceae) based on DNA sequence data from rbcL, trnS–trnG, and ITS. Mol Phylogenet Evol 50:547–559

    Article  CAS  PubMed  Google Scholar 

  • Zhou D, Liu ZL, Ma YQ (2005) The study on phytogeographical distribution and differentiation of Caragana Fabr., Leguminosae. Bull Bot Res 25:471–487

    Google Scholar 

Download references

Acknowledgments

The authors thank S Z Zhang and Y M Li for their assistance with measurements at the experimental station. The research was partially supported by the NSFC (Nos. 31070354, 31370423, 30960060, 31160118), the Program for New Century Excellent Talents in University (NCET 11 0207), the Fundamental Research Funds for the Central Universities (860995), the Program of Introducing Talents of Discipline to Universities (‘111 Project’), and the UWA Institute of Agriculture and Centre for Legumes in Mediterranean Agriculture at the University of Western Australia.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Xiang-Wen Fang.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fang, XW., Turner, N.C., Palta, J.A. et al. The distribution of four Caragana species is related to their differential responses to drought stress. Plant Ecol 215, 133–142 (2014). https://doi.org/10.1007/s11258-013-0285-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11258-013-0285-8

Keywords

Navigation