Intraspecific variation of radial symmetry number of a 535 million-year-old jellyfish

2020 ◽  
Vol 349 ◽  
pp. 105412 ◽  
Author(s):  
T.Q. Shao ◽  
B. Hu ◽  
Y. Shao ◽  
Y.N. Zhang ◽  
Y.H. Liu ◽  
...  
2016 ◽  
Vol 85 (4) ◽  
Author(s):  
Miho S. Kitazawa ◽  
Koichi Fujimoto

Merosity, indicating the basic number of floral organs such as sepals and petals, has been constrained to specific and stable numbers during the evolution of angiosperms. The ancestral flower is considered to have a spiral arrangement of perianth organs, as in phyllotaxis, the arrangement of leaves. How has the ancestral spiral evolved into flowers with specific merosities? To address this question, we studied perianth organ arrangement in the <em>Anemone</em> genus of the basal eudicot family Ranunculaceae, because various merosities are found in this genus. In three species, <em>A. flaccida</em>, <em>A. scabiosa</em>, and <em>A. nikoensis</em> that are normally pentamerous, we found positional arrangement of the excessive sixth perianth organ indicating the possibility of a transition from pentamerous to trimerous arrangement. Arrangement was intraspecifically stochastic, but constrained to three of five types, where trimerous arrangement was the most frequent in all species except for a form of <em>A. scabiosa</em>. The rank of frequency of the other two types was species-dependent. We connect these observations with classical theories of spiral phyllotaxis. The phyllotaxis model for initiation of the sixth organ showed that the three arrangements occur at a divergence angle &lt;144°, indicating the spiral nature of floral phyllotaxis rather than a perfect penta-radial symmetry of 144°. The model further showed that selective occurrence of trimerous arrangement is mainly regulated by the organ growth rate. Differential organ growth as well as divergence angle may regulate transitions between pentamerous and trimerous flowers in intraspecific variation as well as in species evolution.


2020 ◽  
Vol 64 (10) ◽  
pp. 9-19
Author(s):  
V. V. Volchkov ◽  
Vit. V. Volchkov

2019 ◽  
Vol 6 (1) ◽  
pp. 13 ◽  
Author(s):  
Denise M. D. S. Mouga ◽  
Gabriel R. Schroeder ◽  
Nilton P. Vieira Junior ◽  
Enderlei Dec

The pollen morphology of thirteen species of Cactaceae was studied: M. backebergiana F.G. Buchenau, M. decipiens Scheidw, M. elongata DC, M. gracilis Pfeiff., M. hahniana Werderm., M. marksiana Krainz, M. matudae Bravo, M. nejapensis R.T. Craig & E.Y. Dawson, M. nivosa Link ex Pfeiff., M. plumosa F.A.C. Weber, M. prolifera (Mill.) Haw, M. spinosissima var. “A Peak” Lem. and M. voburnensis Scheer. All analysed pollen grains are monads, with radial symmetry, medium size (M. gracilis, M. marksiana, M. prolifera, large), tricolpates (dimorphs in M. plumosa [3-6 colpus] and M. prolifera [3-6 colpus]), with circular-subcircular amb (quadrangular in M. prolifera and M. plumosa with six colpus). The pollen grains presented differences in relation to the shape and exine thickness. The exine was microechinate and microperforated. The pollen morphological data are unpublished and will aid in studies that use pollen samples. These pollen grains indicate ornamental cacti.


Forests ◽  
2020 ◽  
Vol 11 (8) ◽  
pp. 884
Author(s):  
Shufen Chen ◽  
Wataru Ishizuka ◽  
Toshihiko Hara ◽  
Susumu Goto

Research Highlights: The complete chloroplast genome for eight individuals of Japanese larch, including from the isolated population at the northern limit of the range (Manokami larch), revealed that Japanese larch forms a monophyletic group, within which Manokami larch can be phylogenetically placed in Japanese larch. We detected intraspecific variation for possible candidate cpDNA markers in Japanese larch. Background and Objectives: The natural distribution of Japanese larch is limited to the mountainous range in the central part of Honshu Island, Japan, with an isolated northern limit population (Manokami larch). In this study, we determined the phylogenetic position of Manokami larch within Japanese larch, characterized the chloroplast genome of Japanese larch, detected intraspecific variation, and determined candidate cpDNA markers. Materials and Methods: The complete genome sequence was determined for eight individuals, including Manokami larch, in this study. The genetic position of the northern limit population was evaluated using phylogenetic analysis. The chloroplast genome of Japanese larch was characterized by comparison with eight individuals. Furthermore, intraspecific variations were extracted to find candidate cpDNA markers. Results: The phylogenetic tree showed that Japanese larch forms a monophyletic group, within which Manokami larch can be phylogenetically placed, based on the complete chloroplast genome, with a bootstrap value of 100%. The value of nucleotide diversity (π) was calculated at 0.00004, based on SNP sites for Japanese larch, suggesting that sequences had low variation. However, we found three hyper-polymorphic regions within the cpDNA. Finally, we detected 31 intraspecific variations, including 19 single nucleotide polymorphisms, 8 simple sequence repeats, and 4 insertions or deletions. Conclusions: Using a distant genotype in a northern limit population (Manokami larch), we detected sufficient intraspecific variation for the possible candidates of cpDNA markers in Japanese larch.


2021 ◽  
Vol 763 ◽  
pp. 144591
Author(s):  
Run Liu ◽  
Yueting Pan ◽  
You Fang ◽  
Lu Pang ◽  
Jiachen Shen ◽  
...  

Author(s):  
Riccardo Molle ◽  
Donato Passaseo

AbstractThe paper deals with the equation $$-\Delta u+a(x) u =|u|^{p-1}u $$ - Δ u + a ( x ) u = | u | p - 1 u , $$u \in H^1({\mathbb {R}}^N)$$ u ∈ H 1 ( R N ) , with $$N\ge 2$$ N ≥ 2 , $$p> 1,\ p< {N+2\over N-2}$$ p > 1 , p < N + 2 N - 2 if $$N\ge 3$$ N ≥ 3 , $$a\in L^{N/2}_{loc}({\mathbb {R}}^N)$$ a ∈ L loc N / 2 ( R N ) , $$\inf a> 0$$ inf a > 0 , $$\lim _{|x| \rightarrow \infty } a(x)= a_\infty $$ lim | x | → ∞ a ( x ) = a ∞ . Assuming that the potential a(x) satisfies $$\lim _{|x| \rightarrow \infty }[a(x)-a_\infty ] e^{\eta |x|}= \infty \ \ \forall \eta > 0$$ lim | x | → ∞ [ a ( x ) - a ∞ ] e η | x | = ∞ ∀ η > 0 , $$ \lim _{\rho \rightarrow \infty } \sup \left\{ a(\rho \theta _1) - a(\rho \theta _2) \ :\ \theta _1, \theta _2 \in {\mathbb {R}}^N,\ |\theta _1|= |\theta _2|=1 \right\} e^{\tilde{\eta }\rho } = 0 \quad \text{ for } \text{ some } \ \tilde{\eta }> 0$$ lim ρ → ∞ sup a ( ρ θ 1 ) - a ( ρ θ 2 ) : θ 1 , θ 2 ∈ R N , | θ 1 | = | θ 2 | = 1 e η ~ ρ = 0 for some η ~ > 0 and other technical conditions, but not requiring any symmetry, the existence of infinitely many positive multi-bump solutions is proved. This result considerably improves those of previous papers because we do not require that a(x) has radial symmetry, or that $$N=2$$ N = 2 , or that $$|a(x)-a_\infty |$$ | a ( x ) - a ∞ | is uniformly small in $${\mathbb {R}}^N$$ R N , etc. ....


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Michel Schmidt ◽  
Yu Liu ◽  
Xianguang Hou ◽  
Joachim T. Haug ◽  
Carolin Haug ◽  
...  

Abstract Background The Chengjiang biota from southwest China (518-million-years old, early Cambrian) has yielded nearly 300 species, of which more than 80 species represent early chelicerates, crustaceans and relatives. The application of µCT-techniques combined with 3D software (e.g., Drishti), has been shown to be a powerful tool in revealing and analyzing 3D features of the Chengjiang euarthropods. In order to address several open questions that remained from previous studies on the morphology of the xandarellid euarthropod Sinoburius lunaris, we reinvestigated the µCT data with Amira to obtain a different approach of visualization and to generate new volume-rendered models. Furthermore, we used Blender to design 3D models showing aspects of intraspecific variation. Results New findings are: (1) antennulae consist of additional proximal articles that have not been detected before; (2) compared to other appendages, the second post-antennular appendage has a unique shape, and its endopod is comprised of only five articles (instead of seven); (3) the pygidium bears four pairs of appendages which are observed in all specimens. On the other hand, differences between specimens also have been detected. These include the presence/absence of diplotergites resulting in different numbers of post-antennular appendages and tergites and different distances between the tip of the hypostome and the anterior margin of the head shield. Conclusions Those new observations reveal intraspecific variation among Chengjiang euarthropods not observed before and encourage considerations about possible sexual dimorphic pairs or ontogenetic stages. Sinoburius lunaris is a variable species with respect to its morphological characters, cautioning that taxon-specific variabilities need to be considered when exploring new species.


2021 ◽  
Vol 155 ◽  
pp. 102982
Author(s):  
Marta Pina ◽  
Yasuhiro Kikuchi ◽  
Masato Nakatsukasa ◽  
Yoshihiko Nakano ◽  
Yutaka Kunimatsu ◽  
...  

2020 ◽  
Vol 8 (1) ◽  
Author(s):  
Louise C Archer ◽  
Stephen A Hutton ◽  
Luke Harman ◽  
W Russell Poole ◽  
Patrick Gargan ◽  
...  

Abstract Metabolic rates vary hugely within and between populations, yet we know relatively little about factors causing intraspecific variation. Since metabolic rate determines the energetic cost of life, uncovering these sources of variation is important to understand and forecast responses to environmental change. Moreover, few studies have examined factors causing intraspecific variation in metabolic flexibility. We explore how extrinsic environmental conditions and intrinsic factors contribute to variation in metabolic traits in brown trout, an iconic and polymorphic species that is threatened across much of its native range. We measured metabolic traits in offspring from two wild populations that naturally show life-history variation in migratory tactics (one anadromous, i.e. sea-migratory, one non-anadromous) that we reared under either optimal food or experimental conditions of long-term food restriction (lasting between 7 and 17 months). Both populations showed decreased standard metabolic rates (SMR—baseline energy requirements) under low food conditions. The anadromous population had higher maximum metabolic rate (MMR) than the non-anadromous population, and marginally higher SMR. The MMR difference was greater than SMR and consequently aerobic scope (AS) was higher in the anadromous population. MMR and AS were both higher in males than females. The anadromous population also had higher AS under low food compared to optimal food conditions, consistent with population-specific effects of food restriction on AS. Our results suggest different components of metabolic rate can vary in their response to environmental conditions, and according to intrinsic (population-background/sex) effects. Populations might further differ in their flexibility of metabolic traits, potentially due to intrinsic factors related to life history (e.g. migratory tactics). More comparisons of populations/individuals with divergent life histories will help to reveal this. Overall, our study suggests that incorporating an understanding of metabolic trait variation and flexibility and linking this to life history and demography will improve our ability to conserve populations experiencing global change.


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