Season and plant life history stage in revegetation influence competition of foundation species, subordinate species, and weeds in a reclaimed grassland

2021 ◽  
Vol 162 ◽  
pp. 106178 ◽  
Author(s):  
Susumu Yamada ◽  
Masayuki Nemoto ◽  
Toshiya Okuro
2010 ◽  
Vol 23 (10) ◽  
pp. 2185-2196 ◽  
Author(s):  
A. MUOLA ◽  
P. MUTIKAINEN ◽  
L. LAUKKANEN ◽  
M. LILLEY ◽  
R. LEIMU

Oikos ◽  
2018 ◽  
Vol 127 (9) ◽  
pp. 1390-1397 ◽  
Author(s):  
Gianalberto Losapio ◽  
Francisco I. Pugnaire ◽  
Michael J. O'Brien ◽  
Christian Schöb

2015 ◽  
Vol 103 (5) ◽  
pp. 1141-1152 ◽  
Author(s):  
Maren Meyer-Grünefeldt ◽  
Leonor Calvo ◽  
Elena Marcos ◽  
Goddert von Oheimb ◽  
Werner Härdtle

2020 ◽  
Vol 639 ◽  
pp. 185-197 ◽  
Author(s):  
MJ Malick ◽  
ME Hunsicker ◽  
MA Haltuch ◽  
SL Parker-Stetter ◽  
AM Berger ◽  
...  

Environmental conditions can have spatially complex effects on the dynamics of marine fish stocks that change across life-history stages. Yet the potential for non-stationary environmental effects across multiple dimensions, e.g. space and ontogeny, are rarely considered. In this study, we examined the evidence for spatial and ontogenetic non-stationary temperature effects on Pacific hake Merluccius productus biomass along the west coast of North America. Specifically, we used Bayesian additive models to estimate the effects of temperature on Pacific hake biomass distribution and whether the effects change across space or life-history stage. We found latitudinal differences in the effects of temperature on mature Pacific hake distribution (i.e. age 3 and older); warmer than average subsurface temperatures were associated with higher biomass north of Vancouver Island, but lower biomass offshore of Washington and southern Vancouver Island. In contrast, immature Pacific hake distribution (i.e. age 2) was better explained by a nonlinear temperature effect; cooler than average temperatures were associated with higher biomass coastwide. Together, our results suggest that Pacific hake distribution is driven by interactions between age composition and environmental conditions and highlight the importance of accounting for varying environmental effects across multiple dimensions.


2021 ◽  
Author(s):  
Lynette Morgan

Abstract Seeds are effective and efficient plant reproductive and dispersal structures consisting of an embryo, food supply and protected covering. As the start of the next generation, seeds occupy a critical position in plant life history and in the survival of the species (Black et al., 2000). Seed husbandry formed the basis for early agriculture and eventual civilization. People learned to plant, harvest, and preserve the seeds of certain grasses for winter and they abandoned nomadic life to build permanent settlements (Copeland and McDonald, 2001). Long viability has allowed seeds to be passed from generation to generation, with some, e.g. the Indian lotus (Nelumbo nucifera) remaining viable for as long as 1000 years (Janick, 1986). Seeds are remarkably varied and diverse. The orchid species boasts the smallest known seed, a dust-like particle hardly visible to the naked eye (Copeland and McDonald, 2001). Large perennial plants typically have the heaviest seed size, e.g. coconut.. Shape ranges from round or oval in many seed species, to triangular, elliptic, elongated, spiked, thorned, and hairy or winged, depending on the natural method of disposal. Together with differences in size and shape, seeds are highly diverse in a number of other aspects, many of which are relevant to horticultural production and seed technology which has developed to address such issues as seed dormancy, viability and storage life.


Botany ◽  
2014 ◽  
Vol 92 (1) ◽  
pp. 77-81 ◽  
Author(s):  
Christopher R. Webster ◽  
Michael A. Jenkins

We investigated the influence of chronic herbivory by white-tailed deer (Odocoileus virginianus (Zimmermann, 1780)) on the age structure and morphology of Trillium catesbaei Elliott. At sites with contrasting histories of deer abundance (Cades Cove, high; Whiteoak Sink, low), we measured morphological characteristics and determined minimum plant age for 60 plants (30 per site) in the single-leaf life-history stage. We chose this stage because its presence is considered an indication of successful reproduction by the previous generation, but its value could be inflated if plants regress or remain in this stage for extended periods. Our results suggest that T. catesbaei may spend upwards of a decade in this stage. Cades Cove single leaves were significantly older (p = 0.011) than those at Whiteoak Sink. Rhizome recession (decay of the oldest portion) was more common at Cades Cove, suggesting greater regression to this stage from three-leaf stages. Although minimum plant age was significantly associated with vegetative attributes (p < 0.002) at Whiteoak Sink, these attributes were decoupled at Cades Cove (p ≥ 0.642). Collectively, our results suggest that chronic herbivory may lead to a long and regressive residency period in the single-leaf stage. Consequently, in Trillium populations heavily impacted by deer, the number of single-leaf plants may be a poor indicator of reproductive success and population viability.


2007 ◽  
Vol 104 (40) ◽  
pp. 15777-15780 ◽  
Author(s):  
N. Marba ◽  
C. M. Duarte ◽  
S. Agusti

2018 ◽  
Vol 221 (8) ◽  
pp. jeb171629 ◽  
Author(s):  
Manuela Truebano ◽  
Phillip Fenner ◽  
Oliver Tills ◽  
Simon D. Rundle ◽  
Enrico L. Rezende

2020 ◽  
Vol 119 (10) ◽  
pp. 3401-3413
Author(s):  
Peter A. Seeber ◽  
Tetiana A. Kuzmina ◽  
Alex D. Greenwood ◽  
Marion L. East

Abstract In wildlife, endoparasite burden can be affected by host life history stage, environmental conditions, host abundance, and parasite co-infections. We tested the effects of these factors on gastrointestinal parasite infection in plains zebras (Equus quagga) in the Serengeti ecosystem, Tanzania, using fecal egg counts of two nematode families (Strongylidae and Ascarididae) and the presence/absence of cestode (Anoplocephalidae) eggs. We predicted higher egg counts of Strongylidae and Ascarididae, and increased likelihood of Anoplocephalidae infection in individuals (1) during energetically costly life history stages when resource allocation to immune processes may decrease and in young zebras after weaning because of increased uptake of infective stages with forage, (2) when climatic conditions facilitate survival of infective stages, (3) when large zebra aggregations increase forage contamination with infective stages, and (4) in individuals co-infected with more than one parasite group as this may indicate reduced immune competence. Strongylidae egg counts were higher, and the occurrence of Anoplocephalidae eggs was more likely in bachelors than in band stallions, whereas Ascarididae egg counts were higher in band stallions. Strongylidae and Ascarididae egg counts were not increased in lactating females. Strongylidae egg counts were higher in subadults than in foals. Regardless of sex and age, Ascarididae infections were more likely under wet conditions. Co-infections did not affect Strongylidae egg counts. Ascarididae egg counts in adult females were higher when individuals were co-infected with Anoplocephalidae. We present evidence that parasite burdens in plains zebras are affected by life history stage, environmental conditions, and co-infection.


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