1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28.
Abrahamson, W.G. Reproductive strategies in dewberries. Ecology 1975, 56, 721–726. [CrossRef]
Alpert, P.; Stuefer, J.F. Division of labour in clonal plants. In The Ecology and Evolution of Clonal Plants; de Kroon, H.,
van Groenendael, J., Eds.; Backhuys: Leiden, Netherlands, 1997; pp. 137–154.
Radosavljevi´c, I.; Antoni´c, O.; Hruševar, D.; Križan, J.; Satovic, Z.; Turkovi´c, D.; Liber, Z. The influence of a seedling recruitment
strategy and a clonal architecture on a spatial genetic structure of a Salvia brachyodon (Lamiaceae) population. Plants 2020, 9, 828.
[CrossRef] [PubMed]
De Kroon, H.; Huber, H.; Stuefer, J.F.; Van Groenendael, J.M. A modular concept of phenotypic plasticity in plants. New Phytol.
2005, 166, 73–82. [CrossRef] [PubMed]
Guo, J.; Li, H.; Yang, Y. Physiological integration increases sexual reproductive performance of the rhizomatous grass Hierochloe
glabra. Plants 2020, 9, 1608. [CrossRef]
Vallejo-Marín, M.; Dorken, M.E.; Barrett, S.C.H. The ecological and evolutionary consequences of clonality for plant mating.
Annu. Rev. Ecol. Evol. Syst. 2010, 41, 193–213. [CrossRef]
Slade, A.J.; Hutchings, M.J. The effects of light intensity on foraging in the clonal herb Glechoma hederacea. J. Ecol. 1987, 75, 639–650.
[CrossRef]
Slade, A.J.; Hutchings, M.J. The effects of nutrient availability on foraging in the clonal herb Glechoma hederacea. J. Ecol. 1987, 75, 95–112.
[CrossRef]
Evans, J.P.; Cain, M.L. A spatially explicit test of foraging behavior in a clonal plant. Ecology 1995, 76, 1147–1155. [CrossRef]
Dong, M. Morphological responses to local light conditions in clonal herbs from contrasting habitats, and their modification due
to physiological integration. Oecologia 1995, 101, 282–288. [CrossRef]
Roiloa, S.R.; Retuerto, R. Small-scale heterogeneity in soil quality influences photosynthetic efficiency and habitat selection in a
clonal plant. Ann. Bot. 2006, 98, 1043–1052. [CrossRef]
Xie, K.; Zhao, X.; Zhang, Y.; Dong, K.; Fenghe, L.; LI, X. Growth characteristics of Potentilla anserina determined by analyzing
small-scale patchy habitats. Pak. J. Bot. 2015, 47, 967–978.
Tomimatsu, H.; Matsuo, A.; Kaneko, Y.; Kudo, E.; Taniguchi, R.; Saitoh, T.; Suyama, Y.; Makita, A. Spatial genet dynamics of a
dwarf bamboo: Clonal expansion into shaded forest understory contributes to regeneration after an episodic die-off. Plant Spec.
Biol. 2020, 35, 185–196. [CrossRef]
Wang, J.; Xu, T.; Wang, Y.; Li, G.; Abdullah, I.; Zhong, Z.; Liu, J.; Zhu, W.; Wang, L.; Wang, D.; et al. A meta-analysis of effects of
physiological integration in clonal plants under homogeneous vs. heterogeneous environments. Funct. Ecol. 2021, 35, 578–589.
[CrossRef]
Jing, X.; Cai, C.; Fan, S.; Liu, G.; Wu, C.; Chen, B. Effects of rhizome integration on the water physiology of Phyllostachys edulis
clones under heterogeneous water stress. Plants 2020, 9, 373. [CrossRef] [PubMed]
Eilts, J.A.; Mittelbach, G.G.; Reynolds, H.L.; Gross, K.L. Resource heterogeneity, soil fertility, and species diversity: Effects of
clonal species on plant communities. Am. Nat. 2011, 177, 574–588. [CrossRef]
Portela, R.; Barreiro, R.; Roiloa, S.R. Biomass partitioning in response to resources availability: A comparison between native and
invaded ranges in the clonal invader Carpobrotus edulis. Plant Spec. Biol. 2019, 34, 11–18. [CrossRef]
Martin, F.-M. Clonal growth strategies of Reynoutria japonica in response to light, shade, and mowing, and perspectives for
management. NeoBiota 2020, 56, 89–110. [CrossRef]
Roiloa, S.R.; Rodriguez-Echeverria, S.; Lopez-Otero, A.; Retuerto, R.; Freitas, H. Adaptive plasticity to heterogeneous environments increases capacity for division of labor in the clonal invader Carpobrotus edulis (Aizoaceae). Am. J. Bot. 2014, 101, 1301–1308.
[CrossRef]
Cole, P.G.; Weltzin, J.F. Light limitation creates patchy distribution of an invasive grass in eastern deciduous forests. Biol Invasions
2005, 7, 477–488. [CrossRef]
Klimešová, J.; Martínková, J.; Herben, T. Horizontal growth: An overlooked dimension in plant trait space. Perspect. Plant Ecol.
Evol. Syst. 2018, 32, 18–21. [CrossRef]
Ning, Y.; Zhang, Z.X.; Cui, L.J.; Zou, C.L. Adaptive significance of and factors affecting plasticity of biomass allocation and
rhizome morphology: A case study of the clonal plant Scirpus planiculmis (Cyperaceae). Pol. J. Ecol. 2014, 62, 77–88. [CrossRef]
Ruiz-Reynés, D.; Martín, L.; Hernández-García, E.; Knobloch, E.; Gomila, D. Patterns, localized structures and fronts in a reduced
model of clonal plant growth. Physica D 2020, 414, 132723. [CrossRef]
Van Kleunen, M.; Fischer, M.; Schmid, B. Effects of intraspecific competition on size variation and reproductive allocation in a
clonal plant. Oikos 2001, 94, 515–524. [CrossRef]
Bakacsy, L.; Bagi, I. Survival and regeneration ability of clonal common milkweed (Asclepias syriaca L.) after a single herbicide
treatment in natural open sand grasslands. Sci. Rep. 2020, 10, 14222. [CrossRef] [PubMed]
Wang, Y.-J.; Chen, D.; Yan, R.; Yu, F.-H.; van Kleunen, M. Invasive alien clonal plants are competitively superior over co-occurring
native clonal plants. Perspect. Plant Ecol. Evol. Syst. 2019, 40, 125484. [CrossRef]
O’Connor, R.C.; Taylor, J.H.; Nippert, J.B. Browsing and fire decreases dominance of a resprouting shrub in woody encroached
grassland. Ecology 2020, 101, e02935. [CrossRef] [PubMed]
Keser, L.H.; Dawson, W.; Song, Y.B.; Yu, F.H.; Fischer, M.; Dong, M.; van Kleunen, M. Invasive clonal plant species have a greater
root-foraging plasticity than non-invasive ones. Oecologia 2014, 174, 1055–1064. [CrossRef] [PubMed]
Plants 2021, 10, 809
29.
30.
31.
32.
33.
34.
35.
36.
37.
38.
39.
40.
41.
42.
43.
44.
45.
46.
47.
48.
49.
50.
51.
52.
53.
54.
55.
56.
57.
10 of 12
Zheng, Y.; Jiao, P.; Zhao, Z.; Li, Z. Clonal growth of Populus pruinosa Schrenk and its role in the regeneration of riparian forests.
Ecol. Eng. 2016, 94, 380–392. [CrossRef]
Colleran, B.; Lacy, S.N.; Retamal, M.R. Invasive Japanese knotweed (Reynoutria japonica Houtt.) and related knotweeds as catalysts
for streambank erosion. River Res. Appl. 2020, 36, 1962–1969. [CrossRef]
Martin, F.-M.; Dommanget, F.; Evette, A. Improving the management of Japanese knotweed s.l.: A response to Jones and
colleagues. NeoBiota 2020, 63, 147–153. [CrossRef]
Deguchi, R.; Koyama, K. Photosynthetic and morphological acclimation to high and low light environments in Petasites japonicus
subsp. giganteus. Forests 2020, 11, 1365. [CrossRef]
Chazdon, R.L. Sunflecks and their importance to forest understorey plants. In Advances in Ecological Research; Begon, M., Fitter,
A.H., Ford, E.D., Macfadyen, A., Eds.; Academic Press: London, UK, 1988; Volume 18, pp. 1–63.
Morales, A.; Kaiser, E. Photosynthetic acclimation to fluctuating irradiance in plants. Front. Plant Sci. 2020, 11, 268. [CrossRef]
Parker, G.G.; Fitzjarrald, D.R.; Gonçalves Sampaio, I.C. Consequences of environmental heterogeneity for the photosynthetic
light environment of a tropical forest. Agr. Forest Meteorol. 2019, 278, 107661. [CrossRef]
Hartikainen, S.M.; Pieristè, M.; Lassila, J.; Robson, T.M. Seasonal patterns in spectral irradiance and leaf UV-A absorbance under
forest canopies. Front. Plant Sci. 2020, 10. [CrossRef]
Miyashita, A.; Sugiura, D.; Sawakami, K.; Ichihashi, R.; Tani, T.; Tateno, M. Long-term, short-interval measurements of the
frequency distributions of the photosynthetically active photon flux density and net assimilation rate of leaves in a cool-temperate
forest. Agr. For. Meteorol. 2012, 152, 1–10. [CrossRef]
Huber, H.; Wiggerman, L. Shade avoidance in the clonal herb Trifolium fragiferum: A field study with experimentally manipulated
vegetation height. Plant Ecol. 1997, 130, 53–62. [CrossRef]
Min, B.-M. Changes in resource allocation among vegetative organs during the clonal growth of Polygonatum humile (Liliaceae)
grown in a temperate forest gap. J. Ecol. Environ. 2017, 41, 30. [CrossRef]
Birch, C.P.D.; Hutchings, M.J. Exploitation of patchily distributed soil resources by the clonal herb Glechoma hederacea. J. Ecol.
1994, 82, 653–664. [CrossRef]
Waite, S. Field evidence of plastic growth responses to habitat heterogeneity in the clonal herb Ranunculus repens. Ecol. Res.
1994, 9, 311–316. [CrossRef]
Huber, H.; Fijan, A.; During, H.J. A comparative study of spacer plasticity in erect and stoloniferous herbs. Oikos 1998, 81, 576–586.
[CrossRef]
Takenaka, A. Effects of leaf blade narrowness and petiole length on the light capture efficiency of a shoot. Ecol. Res. 1994, 9, 109–114.
[CrossRef]
Huber, H.; de Brouwer, J.; de Caluwe, H.; Wijschede, J.; Anten, N.P.R. Shade induced changes in biomechanical petiole properties
in the stoloniferous herb Trifolium repens. Evol. Ecol. 2008, 22, 399–417. [CrossRef]
Huber, H.; Stuefer, J.F. Shade-induced changes in the branching pattern of a stoloniferous herb: Functional response or allometric
effect? Oecologia 1997, 110, 478–486. [CrossRef]
Huber, H. Plasticity of internodes and petioles in postrate and erect Potentilla species. Funct. Ecol. 1996, 10, 401–409. [CrossRef]
Wijesinghe, D.K.; Hutchings, M.J. Consequences of patchy distribution of light for the growth of the clonal herb Glechoma hederacea.
Oikos 1996, 77, 137–145. [CrossRef]
Poorter, H.; Fiorani, F.; Pieruschka, R.; Wojciechowski, T.; van der Putten, W.H.; Kleyer, M.; Schurr, U.; Postma, J. Pampered
inside, pestered outside? Differences and similarities between plants growing in controlled conditions and in the field. New
Phytol. 2016, 212, 838–855. [CrossRef] [PubMed]
Tammaru, K.; Košnar, J.; Abbas, A.F.; Barta, K.A.; de Bello, F.; Harrison, S.; Degli, E.I.; Kiss, R.; Lukács, K.; Neumann, S.M.; et al.
Ecological differentiation of Carex species coexisting in a wet meadow: Comparison of pot and field experiments. Acta Oecol.
2021, 110, 103692. [CrossRef]
Kitajima, K. Relative importance of photosynthetic traits and allocation patterns as correlates of seedling shade tolerance of 13
tropical trees. Oecologia 1994, 98, 419–428. [CrossRef]
Onoda, Y.; Schieving, F.; Anten, N.P. Effects of light and nutrient availability on leaf mechanical properties of Plantago major:
A conceptual approach. Ann. Bot. 2008, 101, 727–736. [CrossRef]
Wan, Y.; Zhang, Y.; Zhang, M.; Hong, A.; Yang, H.; Liu, Y. Shade effects on growth, photosynthesis and chlorophyll fluorescence
parameters of three Paeonia species. PeerJ 2020, 8, e9316. [CrossRef]
Jeong, H.H.; Kim, K.S. Effects of shading on the growth of Hedera rhombea Bean and Pachysandra terminalis Sieb. et Zucc. Korea J.
Hort. Sci. Tech. 1999, 17, 29–32.
Lee, J.S.; Jeong, S.J.; Heo, J.A.; Kang, H.J.; Hwang, S.Y.; Kim, Y.-K. Light intensity levels and growth inhibitors on growth of shade
tolerant Japanese spurge (Pachysandra terminalis). J. Korea Soc. Hort. Sci. 2002, 43, 137–142.
Lovett Doust, J.; Lovett Doust, L. Modules of production and reproduction in a dioecious clonal shrub, Rhus typhina. Ecology
1988, 69, 741–750. [CrossRef]
Yakimowski, S.B.; Eckert, C.G. Threatened peripheral populations in context: Geographical variation in population frequency
and size and sexual reproduction in a clonal woody shrub. Conserv. Biol. 2007, 21, 811–822. [CrossRef] [PubMed]
Würth, D.G.; Eusemann, P.; Trouillier, M.; Buras, A.; Burger, A.; Wilmking, M.; Roland, C.A.; Juday, G.P.; Schnittler, M. Environment
drives spatiotemporal patterns of clonality in white spruce (Picea glauca) in Alaska. Can. J. For. Res. 2018, 48, 1577–1586. [CrossRef]
Plants 2021, 10, 809
58.
59.
60.
61.
62.
63.
64.
65.
66.
67.
68.
69.
70.
71.
72.
73.
74.
75.
76.
77.
78.
79.
80.
81.
82.
83.
84.
85.
86.
87.
88.
89.
11 of 12
Isogimi, T.; Matsushita, M.; Nakagawa, M. Species-specific sprouting pattern in two dioecious Lindera shrubs: The role of
physiological integration. Flora 2014, 209, 718–724. [CrossRef]
Hosaka, N.; Kachi, N.; Kudoh, H.; Stuefer, J.F.; Whigham, D.F. Compensatory growth of the clonal understory tree, Asimina
triloba, in response to small-scale disturbances. Plant Ecol. 2016, 217, 471–480. [CrossRef]
Kimura, M.K.; Nagashima, T.; Kamitani, T.; Sakio, H.; Tsumura, Y. Recent clonal reproduction of Cryptomeria japonica in a snowy
region revealed by a survey of small-sized ramets. Silv. Gen. 2020, 69, 152–157. [CrossRef]
Yaegashi, S.; Omura, T.; Watanabe, K. Spatial genetic structure of the invasive tree Robinia pseudoacacia to determine migration
patterns to inform best practices for riparian restoration. AoB Plants 2020, 12, plaa043. [CrossRef]
Nakamura, M.; Nanami, S.; Okuno, S.; Hirota, S.K.; Matsuo, A.; Suyama, Y.; Tokumoto, H.; Yoshihara, S.; Itoh, A. Genetic diversity
and structure of apomictic and sexually reproducing Lindera species (Lauraceae) in Japan. Forests 2021, 12, 227. [CrossRef]
Ohashi, H.; Kadota, Y.; Murata, J.; Yonekura, K.; Kihara, H. Wild flowers of Japan; Heibonsha: Tokyo, Japan, 2015.
Ishioka, R.; Muller, O.; Hiura, T.; Kudo, G. Responses of leafing phenology and photosynthesis to soil warming in forest-floor
plants. Acta Oecologica 2013, 51, 34–41. [CrossRef]
Yoshie, F.; Arai, H.; Nakashima, H.; Kawano, S. Seasonal changes in nitrogen fractions of Pachysandra terminalis, a forest evergreen
chamaephyte. Physiol. Plant. 1990, 79, 7–14. [CrossRef]
Zhou, S.; Sauvé, R.J.; Mmbaga, M.T. Adaptation of Pachysandra terminalis Sieb. & Zucc. to freezing temperatures by the
accumulation of mRNA and cold-induced proteins. HortScience 2005, 40, 346. [CrossRef]
Jiao, Z.; Li, J. Phylogenetics and biogeography of eastern Asian–North American disjunct genus Pachysandra (Buxaceae) inferred
from nucleotide sequences. J. Syst. Evol. 2009, 47, 191–201. [CrossRef]
Jeong, M.I.; Jeong, N.R.; Han, S.W.; Kim, J.S. Analyzing growth reactions of herbaceous plants for irrigation management. J. People
Plants Environ. 2020, 23, 255–265. [CrossRef]
Ntawuhiganayo, E.B.; Uwizeye, F.K.; Zibera, E.; Dusenge, M.E.; Ziegler, C.; Ntirugulirwa, B.; Nsabimana, D.; Wallin, G.;
Uddling, J. Traits controlling shade tolerance in tropical montane trees. Tree Physiol. 2020, 40, 183–197. [CrossRef]
Dos Santos, V.A.H.F.; Ferreira, M.J. Are photosynthetic leaf traits related to the first-year growth of tropical tree seedlings?
A light-induced plasticity test in a secondary forest enrichment planting. For. Ecol. Manage. 2020, 460, 117900. [CrossRef]
Poorter, H.; Niinemets, U.; Ntagkas, N.; Siebenkas, A.; Maenpaa, M.; Matsubara, S.; Pons, T. A meta-analysis of plant responses to
light intensity for 70 traits ranging from molecules to whole plant performance. New Phytol. 2019, 223, 1073–1105. [CrossRef]
[PubMed]
Miyashita, A.; Tateno, M. A novel index of leaf RGR predicts tree shade tolerance. Funct. Ecol. 2014, 28, 1321–1329. [CrossRef]
Pons, T.L.; Poorter, H. The effect of irradiance on the carbon balance and tissue characteristics of five herbaceous species differing
in shade-tolerance. Front. Plant Sci. 2014, 5, 12. [CrossRef] [PubMed]
Niinemets, U.; Portsmuth, A.; Tena, D.; Tobias, M.; Matesanz, S.; Valladares, F. Do we underestimate the importance of leaf size in
plant economics? Disproportional scaling of support costs within the spectrum of leaf physiognomy. Ann. Bot. 2007, 100, 283–303.
[CrossRef]
Niinemets, Ü.; Portsmuth, A.; Tobias, M. Leaf size modifies support biomass distribution among stems, petioles and mid-ribs in
temperate plants. New Phytol. 2006, 171, 91–104. [CrossRef]
Schmid, B.; Harper, J.L. Clonal growth in grassland perennials: I. Density and pattern-dependent competition between plants
with different growth forms. J. Ecol. 1985, 73, 793–808. [CrossRef]
Doust, L.L. Population dynamics and local specialization in a clonal perennial (Ranunculus repens): I. The dynamics of ramets in
contrasting habitats. J. Ecol. 1981, 69, 743–755. [CrossRef]
Komamura, R.; Koyama, K.; Yamauchi, T.; Konno, Y.; Gu, L. Pollination contribution differs among insects visiting Cardiocrinum
cordatum flowers. Forests 2021, 12, 452. [CrossRef]
Rostás, M.; Bollmann, F.; Saville, D.; Riedel, M. Ants contribute to pollination but not to reproduction in a rare calcareous
grassland forb. PeerJ 2018, 6, e4369. [CrossRef] [PubMed]
Al-Qthanin, R.N.; Alharbi, S.A. Spatial structure and genetic variation of a mangrove species (Avicennia marina (Forssk.) Vierh) in
the Farasan Archipelago. Forests 2020, 11. [CrossRef]
Japan Meteorological Agency. Available online: https://www.jma.go.jp (accessed on 14 September 2020).
Anderson, M.C. Studies of the woodland light climate: I. The photographic computation of light conditions. J. Ecol. 1964, 52, 27–41.
[CrossRef]
Takenaka, A. CanopOn 2 ver. 2.03c. Available online: http://takenaka-akio.org/etc/canopon2/ (accessed on 26 September 2020).
Takenaka, A.; Inui, Y.; Osawa, A. Measurement of three-dimensional structure of plants with a simple device and estimation of
light capture of individual leaves. Funct. Ecol. 1998, 12, 159–165. [CrossRef]
Yoshie, F.; Kawano, S. Seasonal changes in photosynthetic characteristics of Pachysandra terminalis (Buxaceae), an evergreen
woodland chamaephyte, in the cool temperate regions of Japan. Oecologia 1986, 71, 6–11. [CrossRef]
Schneider, C.A.; Rasband, W.S.; Eliceiri, K.W. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 2012, 9, 671.
[CrossRef]
R Core Team. R: A Language and Environment for Statistical Computing; R Foundation for Statistical Computing: Vienna, Austria, 2021.
Wilke, C.O. Cowplot: Streamlined Plot Theme and Plot Annotations for ‘ggplot2’. CRAN Repos 2016, 2, R2.
Wickham, H. ggplot2: Elegant Graphics for Data Analysis; Springer International Publishing: Cham, Switzerland, 2016.
Plants 2021, 10, 809
90.
91.
92.
93.
94.
95.
96.
12 of 12
Bates, D.; Mächler, M.; Bolker, B.; Walker, S. Fitting linear mixed-effects models using lme4. J. Stat. Softw. 2015, 67, 48. [CrossRef]
Alcántara, J.M.; Rey, P.J. Conflicting selection pressures on seed size: Evolutionary ecology of fruit size in a bird-dispersed tree,
Olea europaea. J. Evol. Biol. 2003, 16, 1168–1176. [CrossRef] [PubMed]
Koyama, K.; Shirakawa, H.; Kikuzawa, K. Redeployment of shoots into better-lit positions within the crowns of saplings of five
species with different growth patterns. Forests 2020, 11, 1301. [CrossRef]
Staab, M.; Pereira-Peixoto, M.H.; Klein, A.-M. Exotic garden plants partly substitute for native plants as resources for pollinators
when native plants become seasonally scarce. Oecologia 2020, 194, 465–480. [CrossRef]
Koyama, K.; Tashiro, M. No effect of selective maturation on fruit traits for a bird-dispersed species, Sambucus racemosa. Plants
2021, 10, 376. [CrossRef] [PubMed]
Case, S.B.; Tarwater, C.E. Functional traits of avian frugivores have shifted following species extinction and introduction in the
Hawaiian Islands. Funct. Ecol. 2020, 34, 2467–2476. [CrossRef]
Barr, D.J.; Levy, R.; Scheepers, C.; Tily, H.J. Random effects structure for confirmatory hypothesis testing: Keep it maximal. J. Mem.
Lang. 2013, 68, 255–278. [CrossRef] [PubMed]
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