Red-leafed species for urban “greening” in the age of global climate change

Ermes Lo Piccolo , Marco Landi

Journal of Forestry Research ›› 2020, Vol. 32 ›› Issue (1) : 151 -159.

PDF
Journal of Forestry Research ›› 2020, Vol. 32 ›› Issue (1) : 151 -159. DOI: 10.1007/s11676-020-01154-2
Original Paper

Red-leafed species for urban “greening” in the age of global climate change

Author information +
History +
PDF

Abstract

Urban trees provide vital ecosystem services such as mitigating heat island, improving air quality by removing various air pollutants, capturing rainwater, and acting as topsoil carbon storage. The aesthetic value of urban trees is also another feature that has to be considered in the context of urban greening. Classical criteria for the selection of urban trees have to respond to new challenges imposed to the cities in a near future. Global climate change factors increase the harshness of our cities, and thereby the plant resilience to abiotic stresses has also to be seriously considered for planning the urban greening. Red-leafed species, characterized by the permanent presence of foliar anthocyanins, show a greater tolerance to different environmental cues than green-leafed species commonly used in our cities. In addition, red tree species own a great aesthetic value which has been underestimated in the context of urban areas, especially in the harsh Mediterranean cities. In this study, we emphasize the “privilege of being red” from different point of view, in order to drive the attention to the possibility to increase the use of red-leafed species for urban “greening”. Some possible negative aspects related to their use are rebutted and the direction of future researches are proposed.

Keywords

Abiotic stress / Anthocyanin / Ecosystem service / Photoprotection / Urban forestry

Cite this article

Download citation ▾
Ermes Lo Piccolo, Marco Landi. Red-leafed species for urban “greening” in the age of global climate change. Journal of Forestry Research, 2020, 32(1): 151-159 DOI:10.1007/s11676-020-01154-2

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Allen KS, Harper RW, Bayer A, Brazee NJ. A review of nursery production systems and their influence on urban tree survival. Urban For Urban Green, 2017, 21: 183-191.

[2]

Antal TK, Lo W, Armstrong WH, Tyystjärvi E. Illumination with ultraviolet or visible light induces chemical changes in the water-soluble manganese complex, [Mn4O6 (bpea)4]Br4. Photochem Photobiol, 2009, 85: 663-668.

[3]

Araminiene V, Sicard P, Anav A Trends and inter-relationships of ground-level ozone metrics and forest health in Lithuania. Sci Tot Environ, 2019, 658: 1265-1277.

[4]

Azeemi STY, Raza M. A Critical analysis of chromotherapy and its ccientific evolution. Evid Based Complement Alternat Med, 2005, 2: 481-488.

[5]

Berland A, Shiflett SA, Shuster WD The role of trees in urban stormwater management. Landsc Urban Plan, 2017, 162: 167-177.

[6]

Campanella JJ, Smalley JV, Dempsey ME. A phylogenetic examination of the primary anthocyanin production pathway of the Plantae. Bot Stud, 2014, 55: 10.

[7]

Cavender-Bares J, Apostol S, Moya I Chilling-Induced photoinhibition in two oak species: Are evergreen leaves inherently better protected than deciduous leaves?. Photosynthetica, 1999, 36: 587-596.

[8]

Chalker-Scott L. Environmental significance of anthocyanins in plant stress responses. Photochem Photobiol, 1999, 70: 1-9.

[9]

Churkina G, Grote R, Butler TM, Lawrence M. Natural selection? Picking the right trees for urban greening. Environ Sci Policy, 2015, 47: 12-17.

[10]

Cotrozzi L, Remorini D, Pellegrini E Plasticity of physiological and biochemical traits can assist oak species under drought and ozone in Mediterranean environment. Physiol Plantarum, 2016, 157: 69-84.

[11]

Cotrozzi L, Remorini D, Pellegrini E Cross-talk between physiological and metabolic adjustments adopted by Quercus cerris to mitigate the effects of severe drought and realistic future ozone concentrations. Forests, 2017, 8: 148.

[12]

Cotrozzi L, Remorini D, Pellegrini E Living in a Mediterranean city in 2050: broadleaf or evergreen ‘citizens’?. Environ Sci Pollut Res, 2018, 25: 8161-8173.

[13]

Das PK, Shin DH, Choi S-B, Park Y-I. Sugar-hormone cross-talk in anthocyanin biosynthesis. Mol Cells, 2012, 34: 501-507.

[14]

Ellestad GA. Structure and chiroptical properties of supramolecular flower pigments. Chirality, 2006, 18: 134-144.

[15]

Fedenko VS, Shemet SA, Landi M. UV–vis spectroscopy and colorimetric models for detecting anthocyanin-metal complexes in plants: an overview of in vitro and in vivo techniques. J Plant Physiol, 2017, 212: 13-28.

[16]

Feild TS, Lee DW, Holbrook NM. Why leaves turn red in autumn. The role of anthocyanins in senescing leaves of red-osier dogwood. Plant Physiol, 2001, 127: 566-574.

[17]

Foyer CH, Lelandais M, Kunert KJ. Photooxidative stress in plants. Physiol Plant, 1994, 92: 696-717.

[18]

Garala K, Basu B, Bhalodia R Alternative to drug delivery system: Chromotherapy. Drug Invent Today, 2009, 1: 130-134.

[19]

Gould KS, Jay-Allemand C, Logan BA When are foliar anthocyanins useful to plants? Re-evaluation of the photoprotection hypothesis using Arabidopsis thaliana mutants that differ in anthocyanin accumulation. Environ Exp Bot, 2018, 154: 11-22.

[20]

Grotewold E. The genetics and biochemistry of floral pigments. Annu Rev Plant Biol, 2006, 57: 761-780.

[21]

Gururani MA, Venkatesh J, Tran LSP. Regulation of photosynthesis during abiotic stress-induced photoinhibition. Mol Plant, 2015, 8: 1304-1320.

[22]

Gutteridge JMC, Halliwell B. The measurement and mechanism of lipid peroxidation in biological systems. Trends Biochem Sci, 1990, 15: 129-135.

[23]

Hale KL, McGrath SP, Lombi E Molybdenum sequestration in Brassica species. A role for anthocyanins?. Plant Physiol, 2001, 126: 1391-1402.

[24]

Hale KL, Tufan HA, Pickering IJ Anthocyanins facilitate tungsten accumulation in Brassica. Physiol Plant, 2002, 116: 351-358.

[25]

Hernández I, Alegre L, Van Breusegem F, Munné-Bosch S. How relevant are flavonoids as antioxidants in plants?. Trends Plant Sci, 2009, 14: 125-132.

[26]

Hoch WA, Singsaas EL, McCown BH. Resorption protection. anthocyanins facilitate nutrient recovery in autumn by shielding leaves from potentially damaging light levels. Plant Physiol, 2003, 133: 1296-1305.

[27]

Holland V, Fragner L, Jungcurt T Girdling interruption between source and sink in Quercus pubescens does not trigger leaf senescence. Photosynthetica, 2016, 54: 589-597.

[28]

Hughes NM, Burkey KO, Cavender-Bares J, Smith WK. Xanthophyll cycle pigment and antioxidant profiles of winter-red (anthocyanic) and winter-green (acyanic) angiosperm evergreen species. J Exp Bot, 2012, 63: 1895-1905.

[29]

Hughes NM, Carpenter KL, Keidel TS Photosynthetic costs and benefits of abaxial versus adaxial anthocyanins in Colocasia esculenta ‘Mojito’. Planta, 2014, 240: 971-981.

[30]

Hughes NM, Morley CB, Smith WK. Coordination of anthocyanin decline and photosynthetic maturation in juvenile leaves of three deciduous tree species. New Phytol, 2007, 175: 675-685.

[31]

Hughes NM, Smith WK. Attenuation of incident light in Galax urceolata (Diapensiaceae): concerted influence of adaxial and abaxial anthocyanic layers on photoprotection. Am J Bot, 2007, 94: 784-790.

[32]

Hughes NM, Vogelmann TC, Smith WK. Optical effects of abaxial anthocyanin on absorption of red wavelengths by understorey species: revisiting the back-scatter hypothesis. J Exp Bot, 2008, 59: 3435-3442.

[33]

Juadjur A, Mohn C, Schantz M Fractionation of an anthocyanin-rich bilberry extract and in vitro antioxidative activity testing. Food Chem, 2015, 167: 418-424.

[34]

Kaya N, Epps H. Relationship between color and emotion: a study of college students. Coll Stud, 2004, 38: 396.

[35]

Krapp A, Stitt M. An evaluation of direct and indirect mechanisms for the “sink-regulation” of photosynthesis in spinach: changes in gas exchange, carbohydrates, metabolites, enzyme activities and steady-state transcript levels after cold-girdling source leaves. Planta, 1995

[36]

Kumar PBAN, Dushenkov V, Motto H, Raskin I. Phytoextraction: the use of plants to remove heavy metals from soils. Environ Sci Technol, 1995, 29: 1232-1238.

[37]

Kyparissis A, Grammatikopoulos G, Manetas Y. Leaf morphological and physiological adjustments to the spectrally selective shade imposed by anthocyanins in Prunus cerasifera. Tree Physiol, 2007, 27: 849-857.

[38]

Landi M, Cotrozzi L, Pellegrini E When “thirsty” means “less able to activate the signalling wave trigged by a pulse of ozone”: a case of study in two Mediterranean deciduous oak species with different drought sensitivity. Sci Tot Environ, 2019, 657: 379-390.

[39]

Landi M, Shemet S, Fedenko V. Metal toxicity in higher plants, 2020, New York: Nova Science Publishers Inc..

[40]

Landi M, Guidi L, Pardossi A Photoprotection by foliar anthocyanins mitigates effects of boron toxicity in sweet basil (Ocimum basilicum). Planta, 2014, 240: 941-953.

[41]

Landi M, Pardossi A, Remorini D, Guidi L. Antioxidant and photosynthetic response of a purple-leaved and a green-leaved cultivar of sweet basil (Ocimum basilicum) to boron excess. Environ Exp Bot, 2013, 85: 64-75.

[42]

Landi M, Remorini D, Pardossi A Sweet basil (Ocimum basilicum) with green or purple leaves: which differences occur in photosynthesis under boron toxicity?. J Plant Nutr Soil Sci, 2013, 176: 942-951.

[43]

Landi M, Tattini M, Gould KS. Multiple functional roles of anthocyanins in plant-environment interactions. Environ Exp Bot, 2015, 119: 4-17.

[44]

Lee DW, Lowry JB, Stone BC. Abaxial anthocyanin layer in leaves of tropical rain forest plants: Enhancer of light capture in deep shade. Biotropica, 1979, 11: 70-77.

[45]

Lo Piccolo E, Landi M, Giordani T et al (2020a) Can anthocyanin presence help Prunus saplings to alleviate water stress effects in an urban environment? Photosynthetica (in press)

[46]

Lo Piccolo E, Landi M, Massai R Girled-induced anthocyanin accumulation in red-leafed Prunus cerasifera: Effect on photosynthesis, photoprotection and sugar metabolism. Plant Sci, 2020, 294: 110456.

[47]

Lo Piccolo E, Landi M, Pellegrini E Multiple consequences induced by epidermally-located anthocyanins in young, mature and senescent leaves of Prunus. Front Plant Sci, 2018, 9: 917.

[48]

Logan BA, Stafstrom WC, Walsh MJL Examining the photoprotection hypothesis for adaxial foliar anthocyanin accumulation by revisiting comparisons of green- and red-leafed varieties of coleus (Solenostemon scutellarioides). Photosynth Res, 2015, 124: 267-274.

[49]

McDonnell MJ, MacGregor-Fors I. The ecological future of cities. Science, 2016, 352: 936-938.

[50]

Mittler R, Vanderauwera S, Gollery M, Van Breusegem F. Reactive oxygen gene network of plants. Trends Plant Sci, 2004, 9: 490-498.

[51]

Miyao M, Ikeuchi M, Yamamoto N, Ono T. Specific degradation of the D1 protein of photosystem II by treatment with hydrogen peroxide in darkness: Implications for the mechanism of degradation of the D1 protein under illumination. Biochemistry, 1995, 34: 10019-10026.

[52]

Murata N, Takahashi S, Nishiyama Y, Allakhverdiev SI. Photoinhibition of photosystem II under environmental stress. Biochim Biophys Acta BBA - Bioenerg, 2007, 1767: 414-421.

[53]

Neill SO, Gould KS. Anthocyanins in leaves: light attenuators or antioxidants?. Funct Plant Biol, 2003, 30: 865.

[54]

Ordóñez C, Duinker PN. Climate change vulnerability assessment of the urban forest in three Canadian cities. Clim Change, 2015, 131: 531-543.

[55]

Paul MJ, Foyer CH. Sink regulation of photosynthesis. J Exp Bot, 2001, 52: 1383-1400.

[56]

Pietrini F, Iannelli MA, Massacci A. Anthocyanin accumulation in the illuminated surface of maize leaves enhances protection from photo-inhibitory risks at low temperature, without further limitation to photosynthesis. Plant, Cell Environ, 2002, 25: 1251-1259.

[57]

Pretzsch H, Biber P, Uhl E Climate change accelerates growth of urban trees in metropolises worldwide. Sci Rep, 2017, 7: 15403.

[58]

Pringsheim N (1879) Ueber lichtwirkung und chlorophyll function in der pflanze. Ahrbücher Für Wiss Bot

[59]

Renner SS, Zohner CM. The occurrence of red and yellow autumn leaves explained by regional differences in insolation and temperature. New Phytol, 2019, 224: 1464-1471.

[60]

Sæbø A, Benedikz T, Randrup TB. Selection of trees for urban forestry in the Nordic countries. Urban For Urban Green, 2003, 2: 101-114.

[61]

Sami F, Yusuf M, Faizan M Role of sugars under abiotic stress. Plant Physiol Biochem, 2016, 109: 54-61.

[62]

Schaberg PG, van den Berg AK, Murakami PF Factors influencing red expression in autumn foliage of sugar maple trees. Tree Physiol, 2003, 23: 325-333.

[63]

Shi C, Watanabe T, Koike T. Leaf stoichiometry of deciduous tree species in different soils exposed to free-air O3 enrichment over two growing seasons. Environ Exp Bot, 2017, 138: 148-163.

[64]

Sicard P, Agathokleous E, Araminiene A Should we see urban trees as effective solutions to reduce increasing ozone levels in cities?. Environ Pollut, 2018, 243: 163-176.

[65]

Silva VO, Freitas AA, Maçanita AL, Quina FH. Chemistry and photochemistry of natural plant pigments: The anthocyanins. J Phys Org Chem, 2016, 29: 594-599.

[66]

Sjöman H, Hirons AD, Bassuk NL. Improving confidence in tree species selection for challenging urban sites: a role for leaf turgor loss. Urban Ecosyst, 2018, 21: 1171-1188.

[67]

Sjöman H (2012) Trees for tough urban sites-learning from nature. Doctoral thesis. Dept. of Landscape Management, Design and Construction, Swedish University of Agricultural Sciences, Alnarp

[68]

Solfanelli C, Poggi A, Loreti E Sucrose-specific induction of the anthocyanin biosynthetic pathway in Arabidopsis. Plant Physiol, 2006, 140: 637-646.

[69]

Song XP, Tan PY, Edwards P, Richards D. The economic benefits and costs of trees in urban forest stewardship: a systematic review. Urban For Urban Green, 2018, 29: 162-170.

[70]

Takahashi S, Badger MR. Photoprotection in plants: a new light on photosystem II damage. Trends Plant Sci, 2011, 16: 53-60.

[71]

Tattini M, Landi M, Brunetti C Epidermal coumaroyl anthocyanins protect sweet basil against excess light stress: multiple consequences of light attenuation. Physiol Plant, 2014, 152: 585-598.

[72]

Tattini M, Sebastiani F, Brunetti C Dissecting molecular and physiological response mechanisms to high solar radiation in cyanic and acyanic leaves: a case study on red and green basil. J Exp Bot, 2017, 68: 2425-2437.

[73]

Tyrväinen L, Pauleit S, Seeland K, de Vries S. Konijnendijk C, Nilsson K, Randrup T, Schipperijn J. Benefits and uses of urban forests and trees. urban forests and trees, 2005, Berlin: Springer 81 114

[74]

Vangelisti A, Guidi L, Cavallini A Red versus green leaves: transcriptomic comparison of foliar senescence between two Prunus cerasifera genotypes. Sci Rep, 2020, 10: 1959.

[75]

Verhoeven AS, Swanberg A, Thao M, Whiteman J. Seasonal changes in leaf antioxidant systems and xanthophyll cycle characteristics in Taxus x media growing in sun and shade environments. Physiol Plant, 2005, 123: 428-434.

[76]

Vogt J, Gillner S, Hofmann M Citree: A database supporting tree selection for urban areas in temperate climate. Landsc Urban Plan, 2017, 157: 14-25.

[77]

Watson GW, Hewitt AM, Custic M, Lo M. The management of tree root systems in urban and suburban settings: a review of soil influence on root growth. Arboric Urban For, 2014, 40: 193-217.

[78]

Winefield C, Davies K, Gould K. Anthocyanins, 2009, New York: Springer.

[79]

Xing Y, Brimblecombe P. Trees and parks as “the lungs of cities”. Urban For Urban Green, 2020, 48: 126552.

[80]

Yamasaki H, Sakihama Y, Ikehara N. Flavonoid-peroxidase reaction as a detoxification mechanism of plant cells against H2O2. Plant Physiol, 1997, 115: 1405-1412.

[81]

Yamasaki H, Uefuji H, Sakihama Y. Bleaching of the red anthocyanin induced by superoxide radical. Arch Biochem Biophys, 1996, 332: 183-186.

[82]

Yang J. Assessing the impact of climate change on urban tree species selection: a case study in Philadelphia. J For, 2009, 107: 364-372.

[83]

Yoshida K, Mori M, Kondo T. Blue flower color development by anthocyanins: from chemical structure to cell physiology. Nat Prod Rep, 2009, 26: 884.

[84]

Zuo J, Zhao Z-Y. Green building research–current status and future agenda: a review. Renew Sustain Energy Rev, 2014, 30: 271-281.

AI Summary AI Mindmap
PDF

201

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/