miércoles, 29 de julio de 2020
viernes, 24 de julio de 2020
Phylogenetic relatedness, co-occurrence, and rhizomes increase lateral gene transfer among grasses 
Hibdige, et al., 2020
https://www.biorxiv.org/content/10.1101/2020.02.17.952150v1
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Hibdige, et al., 2020
Background: Lateral gene transfer (LGT) has been documented in a broad 
range of eukaryotes, where it can promote adaptation. In plants, LGT of 
functional nuclear genes has been repeatedly reported in parasitic 
plants, ferns and grasses, but the exact extent of the phenomenon 
remains unknown. Systematic studies are now needed to identify the 
factors that govern the frequency of LGT among plants.
Results: Here we scan the genomes of a diverse set of grass species that
 span more than 50 million years of divergence and include major crops. 
We identify protein coding LGT in a majority of them (13 out of 17). 
There is variation among species in the amount of LGT received, with 
rhizomatous species receiving more genes. In addition, the amount of LGT
 increases with phylogenetic relatedness, which might reflect genomic 
compatibility among close relatives facilitating successful transfers. 
However, we also observe genetic exchanges among distantly related 
species that diverged shortly after the origin of the grass family when 
they co-occur in the wild, pointing to a role of biogeography. The 
dynamics of successful LGT in grasses therefore appear to be dependent 
on both opportunity (co-occurrence and rhizomes) and compatibility 
(phylogenetic distance).
Conclusion: Overall, we show that LGT is a widespread phenomenon in 
grasses, which is boosted by repeated contact among related lineages. 
The process has moved functional genes across the entire grass family 
into domesticated and wild species alike.
Time-calibrated phylogenetic tree of 17 model grass species used in this study (extracted from Christin et al. 2014; scale in million years - Myr). The direction of LGT between grass clades is shown with arrows whose size is proportional to the number of LGT. The black portion of pie charts on key nodes of the phylogeny indicates the quartet support for the observed topology based on a multigene coalescence analysis. The size of each pie chart is proportional to the number of species within the clade.
https://www.biorxiv.org/content/10.1101/2020.02.17.952150v1
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miércoles, 22 de julio de 2020
Integrating agroecological production in a robust post-2020 Global Biodiversity Framework   
Wanger et al., 2020
The 15th Conference of the Parties (COP) meeting to the Convention on 
Biological Diversity in China — now to be held in 2021 due to the 
coronavirus pandemic — will provide new opportunities for biodiversity 
conservation (https://go.nature.com/31YAVNF)
 through the decision on the post-2020 Global Biodiversity Framework 
(GBF). In short, the GBF is a global and solution-oriented framework 
aiming for transformative action by governments, civil society and 
businesses, to help biodiversity recover for the benefit of people and 
planet1.
 Agriculture is the most extensive form of land use, occupying more than
 one-third of the global landmass, and imperilling 62% of all threatened
 species globally2.
 Habitat conversion and conventional farming practices — including heavy
 use of agrochemicals — have negative effects on biodiversity3,
 even spilling into protected areas. However, if designed appropriately,
 agricultural landscapes can provide habitats for biodiversity, promote 
connectivity between protected areas, and increase the capacity of 
species to respond to environmental threats4,5.
 While halting the loss of protected and intact nature is essential to 
halt species loss, bending the curve on biodiversity will require 
sustainable agriculture. We argue that the GBF must include conservation
 actions in agricultural landscapes based on agroecological principles 
(sensu High Level Panel of Experts6)
 in the three ‘2030 Action Targets’ (hereafter ‘Targets’) to reach its 
goals of biodiversity recovery. Agroecology is widely recognized as a 
necessary transformation in order to achieve food system sustainability.
Agroecological principles in the post-2020 Global Biodiversity Framework
Agroecological principles in the post-2020 Global Biodiversity Framework
Below, we elaborate on how agroecological production can help to support the GBF targets.
Target 1 — reduce the threats to biodiversity
Target 1 — reduce the threats to biodiversity
Comprehensive
 spatial planning for diversified agriculture benefits biodiversity 
conservation and nature’s contributions to people (NCP)7,8,
 when integrating multiple spatial scales from local to regional and 
multi-stakeholder participatory approaches. Diversified farmlands 
enhance biodiversity, biocontrol, pollination and reduce pathogen and 
pest impact7,
 thereby contributing to achieve conservation objectives in proximate 
protected areas, as more protected areas are seeing impact in intensive 
land use in surrounding areas9. Agroecological practices can considerably reduce the use of synthetic pesticides10, a major cause of biodiversity loss11.
 A more effective use of fertilizers can reduce nutrient pollution and 
mitigate climate impacts by maintaining healthier, carbon-sequestering 
soil microbiota12.
 Diversified cropping systems can further mitigate greenhouse gas 
emissions by, for example, non-crop tree diversification in agroforestry
 systems, thereby enhancing agrobiodiversity benefits13,14.
Target 2 — meeting people’s needs through sustainable use and benefit sharing
Target 2 — meeting people’s needs through sustainable use and benefit sharing
Agroecological
 production is a comprehensive framework for the sustainable use of 
biodiversity that also supports productivity and resilience15.
 Farmers benefit from diversified systems through increased economic 
resilience, reduced dependency on agrochemical inputs, and in 
subsistence systems more diverse and nutritious foods16,17,18.
 Moreover, agroecological production can reduce negative externalities 
and off-farm inputs, while increasing biodiversity and NCP19,20. Trade-offs between agroecological approaches and yield are often assumed, but not inherent21.
 New crop varieties, crop combinations and technological innovations 
will only further reduce yield gaps between conventional and 
agroecological production19,22, when the availability is fair and locally appropriate.
Target 3 — tools and solutions for implementation and mainstreaming
Eco-certification
 and agricultural policies — if well informed and implemented — provide 
important opportunities to encourage diversified farm and landscape 
measures for conservation23,24.
 Corporate and government commitments to zero-deforestation and 
eco-labelling could be enhanced by coupling production and protection 
goals within innovative investment models that emphasize natural assets.
 Investing in diversified systems can mitigate environmental 
vulnerability by embedding resilience into supply chains25.
 Promotion and equitable participation of indigenous peoples and local 
communities in decision-making processes is critical to incorporate 
their perspective on and knowledge about agroecological approaches. 
Lastly, an understanding of agroecological production, benefits for 
biodiversity conservation, food security, and overall better quality of 
life can help to shape new social norms for sustainability6.
A way forward for the post-2020 Global Biodiversity Framework and agroecology
A way forward for the post-2020 Global Biodiversity Framework and agroecology
A
 global transition from conventional to agroecological production will 
be critical to achieve the action targets and meet the GBF goals. 
Diversification at the field, farm and landscape scale holds large 
promises to make food systems more sustainable; however, farmers alone 
cannot achieve this major transformation. Action is required across the 
entire supply chain, from the processing industry to distributors to the
 consumers. Future research on agroecological production (Box 1)
 needs to (1) depart from traditional research approaches and 
increasingly engage in multi-stakeholder networks to define options that
 work in practice and across scales; (2) build on ‘theories of change’ 
and indicators to develop actionable strategies and quantify change; (3)
 support policy makers through easily accessible advisory services to 
promote change in the wider socioecological landscape, incentivize local
 innovation systems and increase budget allocations for agroecological 
transition; and (4) enable public and private funding for long-term 
research programmes more apt for the timescales that agroecological 
interventions operate on. By integrating agroecological principles and 
related future research, the GBF will be more robust in considering 
threats to biodiversity, people’s needs and identifying tools and 
solutions in support of its 2050 vision of ‘Living in harmony with 
nature’.
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lunes, 20 de julio de 2020
Intensive farming drives long-term shifts in avian community composition     
Hendershot et al., 2020
Hendershot et al., 2020
Agricultural practices constitute both the greatest cause of biodiversity loss and the greatest opportunity for conservation,
 given the shrinking scope of protected areas in many regions. Recent 
studies have documented the high levels of biodiversity—across many taxa
 and biomes—that agricultural landscapes can support over the short term. However, little is known about the long-term effects of alternative agricultural practices on ecological communities.
 Here we document changes in bird communities in intensive-agriculture, 
diversified-agriculture and natural-forest habitats in 4 regions of 
Costa Rica over a period of 18 years. Long-term directional shifts in 
bird communities were evident in intensive- and diversified-agricultural
 habitats, but were strongest in intensive-agricultural habitats, where 
the number of endemic and International Union for Conservation of Nature
 (IUCN) Red List species fell over time. All major guilds, including 
those involved in pest control, pollination and seed dispersal, were 
affected. Bird communities in intensive-agricultural habitats proved 
more susceptible to changes in climate, with hotter and drier periods 
associated with greater changes in community composition in these 
settings. These findings demonstrate that diversified agriculture can 
help to alleviate the long-term loss of biodiversity outside natural 
protected areas.
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sábado, 18 de julio de 2020
Farmer seed networks make a limited contribution to agriculture? Four common misconceptions 
Coomes et al., 2015.
Coomes et al., 2015.
Highlights
- •
- Food and agricultural policy undervalues farmer seed networks.
- •
- These networks are important globally in circulating planting material among farmers.
- •
- We challenge four common misconceptions in policy and practice about seed networks.
- •
- Farmer seed networks are efficient and open but also selective in seed provisioning.
- •
- Commercialization and regulation are unlikely to eradicate farmer seed networks.
Abstract
The
 importance of seed provisioning in food security and nutrition, 
agricultural development and rural livelihoods, and agrobiodiversity and
 germplasm conservation is well accepted by policy makers, practitioners
 and researchers. The role of farmer seed networks is less well 
understood and yet is central to debates on current issues ranging from 
seed sovereignty and rights for farmers to GMOs and the conservation of 
crop germplasm. In this paper we identify four common misconceptions 
regarding the nature and importance of farmer seed networks today. (1) 
Farmer seed networks are inefficient for seed dissemination. (2) Farmer 
seed networks are closed, conservative systems. (3) Farmer seed networks
 provide ready, egalitarian access to seed. (4) Farmer seed networks are
 destined to weaken and disappear. We challenge these misconceptions by 
drawing upon recent research findings and the authors’ collective field 
experience in studying farmer seed systems in Africa, Europe, Latin 
America and Oceania. Priorities for future research are suggested that 
would advance our understanding of seed networks and better inform 
agricultural and food policy.
. 
viernes, 17 de julio de 2020
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The wisest and noblest teacher is nature itself.
Leonardo da Vinci
.
The wisest and noblest teacher is nature itself.
Leonardo da Vinci
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lunes, 13 de julio de 2020
 Increasing growth temperature alters the within-host competition of viral strains and influences virus genetic variation 
Alcaide et al., 2020
Alcaide et al., 2020
The emergence 
of viral diseases in plant crops hamper the sustainability of food 
production, and this may be boosted by global warming.  Concurrently, 
mixed viral infections are becoming common in plants, of which 
epidemiology are unpredictable due to within-host virus-virus 
interactions.  However, the extent in which the combined effect of 
variations in the abiotic components of the plant ecological niche 
(e.g., temperature) and the prevalence of mixed infections (i.e., 
within-host interactions among viruses) affect the evolutionary dynamics
 of viral populations is not well understood.  Here, we explore the 
interplay between ecological and evolutionary factors during viral 
infections, and show that two individual strains of pepino mosaic virus 
(PepMV) coexisted in a temperature-dependent continuum between neutral 
and antagonistic interactions in tomato plants.  After a long-term 
infection, the mutational analysis of the evolved viral genomes revealed
 strain-specific single-nucleotide polymorphisms that were modulated by 
the interaction between the type of infection and temperature.  
Mathematical modeling allowed us to asses a thermal reaction norm for 
both strains, which indicated that viral replication rates were 
increased along with increasing temperature in mixed infections, with a 
remarkable strain-dependent effect.  These results suggest that the 
growth temperature is an ecological driver of virus-virus interactions, 
with an effect on the genetic diversity of individual viruses 
co-infecting a host.  This research provides insights into the effect 
that climate change will have on the evolutionary dynamics of viral 
populations.
(A) What is the effect of mixed viral infections on the fitness and genetic diversity of viral populations within a host? (B and C) Barplots exhibiting the viral load (RNA molecules / ng RNA total) of each PepMV (CH2 and EU) strain in tomato plants grown at 20 ºC and 30 ºC under single (black) and mixed infection (grey) condition. Viral accumulation was inferred by absolute quantification using RT-qPCR after 7 dpi (B) and60 dpi (C). 
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domingo, 12 de julio de 2020
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I went to the woods because I wished to live deliberately, to front only the essential facts of life.
 Henry David Thoreau 
. 
sábado, 11 de julio de 2020
Native American gene flow into Polynesia predating Easter Island settlement      
Ioannidis et al., 2020
https://www.nature.com/articles/s41586-020-2487-2
.
Ioannidis et al., 2020
The possibility of voyaging contact between prehistoric Polynesian and 
Native American populations has long intrigued researchers. Proponents 
have pointed to the existence of New World crops, such as the sweet 
potato and bottle gourd, in the Polynesian archaeological record, but 
nowhere else outside the pre-Columbian Americas, while critics have argued that these botanical dispersals need not have been human mediated.
 The Norwegian explorer Thor Heyerdahl controversially suggested that 
prehistoric South American populations had an important role in the 
settlement of east Polynesia and particularly of Easter Island (Rapa 
Nui).
 Several limited molecular genetic studies have reached opposing 
conclusions, and the possibility continues to be as hotly contested 
today as it was when first suggested. Here we analyse genome-wide variation in individuals from islands 
across Polynesia for signs of Native American admixture, analysing 807 
individuals from 17 island populations and 15 Pacific coast Native 
American groups. We find conclusive evidence for prehistoric contact of 
Polynesian individuals with Native American individuals (around ad 1200) contemporaneous with the settlement of remote Oceania.
 Our analyses suggest strongly that a single contact event occurred in 
eastern Polynesia, before the settlement of Rapa Nui, between 
Polynesian individuals and a Native American group most closely related 
to the indigenous inhabitants of present-day Colombia.
https://www.nature.com/articles/s41586-020-2487-2
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miércoles, 8 de julio de 2020
Core microbiomes for sustainable agroecosystems      
Toju et al., 2018
https://www.nature.com/articles/s41477-018-0139-4
.
Toju et al., 2018
In an era of ecosystem degradation and climate change, maximizing 
microbial functions in agroecosystems has become a prerequisite for the 
future of global agriculture. However, managing species-rich communities
 of plant-associated microbiomes remains a major challenge. Here, we 
propose interdisciplinary research strategies to optimize microbiome 
functions in agroecosystems. Informatics now allows us to identify 
members and characteristics of ‘core microbiomes’, which may be deployed
 to organize otherwise uncontrollable dynamics of resident microbiomes. 
Integration of microfluidics, robotics and machine learning provides 
novel ways to capitalize on core microbiomes for increasing 
resource-efficiency and stress-resistance of agroecosystems.
https://www.nature.com/articles/s41477-018-0139-4
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lunes, 6 de julio de 2020
The role of modularity in self-organisation dynamics in biological networks 
Siebert et al., 2020
https://arxiv.org/abs/2003.12311
.
Siebert et al., 2020
Interconnected ensembles of biological entities are perhaps some of the most
complex systems that modern science has encountered so far. In particular,
scientists have concentrated on understanding how the complexity of the
interacting structure between different neurons, proteins or species influences
the functioning of their respective systems. It is well-established that many
biological networks are constructed in a highly hierarchical way with two main
properties: short average paths that join two apparently distant nodes
(neuronal, species, or protein patches) and a high proportion of nodes in
modular aggregations. Although several hypotheses have been proposed so far,
still little is known about the relation of the modules with the dynamical
activity in such biological systems. Here we show that network modularity is a
key ingredient for the formation of self-organising patterns of functional
activity, independently of the topological peculiarities of the structure of
the modules. In particular, we show that macroscopic spatial patterns at the
modular scale can develop in this case, which may explain how spontaneous order
in biological networks follows their modular structural organisation. Our
results also show that Turing patterns on biological complex networks can be a
signature of the presence of modular structure and consequently a possible
protocol for community detection. We test our results on real-world networks to
confirm the important role of modularity in creating macro-scale patterns. 
Modular vs. Small-world topology in Turing pattern formation. a) A Newman{Watts (NW) network with N = 125 nodes, and 660 edges, where patterns are absent. The colour of the nodes represents the concentration of the activator, ui(t), at long time. b) The dispersion relation of the NW network (red stars) overlain on the dispersion relation of the continuous case (blue curve), i.e. if the system was on a continuous domain and not on a network. Notice the absence of the unstable eigenvalues (inset) and the gap between the zero eigenvalue and the second smallest  2, known as the spectral gap. c) A modular network of the same size (same number of nodes and edges) as in a) where indeed Turing patterns are present. The  ve modules are of the Erdos-R enyi (ER) family. The colour of the nodes again represents the concentration of the activator, ui(t), at long time. d) The dispersion relation of the modular network (red stars) overlain on the dispersion relation of the continuous domain (blue curve). Notice here the presence of unstable eigenvalues (inset) and that the eigenvalues are separated in two sets by an important gap, between the  rst and second set of eigenvalues. The  rst four non-zero one are denoted as the modular eigenvalues and the rest non-negative ones as the non-modular eigenvalues. The parameters of the Fitzhugh-Nagumo model are in both cases Du = 1,   = 5:5, a = 0:7, b = 0:05; c = 1:7. Finally, note the di erent colormaps used between panels a) and c) to highlight the lack of patterns in the former.
https://arxiv.org/abs/2003.12311
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sábado, 4 de julio de 2020
miércoles, 1 de julio de 2020
Agri‐environment schemes enhance pollinator richness and abundance but bumblebee reproduction depends on field size 
Geppert et al., 2020
- Pollinators have experienced a dramatic decrease world‐wide due to agricultural intensification. In many countries, agri‐environment schemes (AES) have been introduced to counteract this current trend. However, until now, the relative importance of each AES for biodiversity and ecosystem services is still little understood and might change depending on landscape context. Complex landscape‐experiments are required to fill this knowledge gap, enabling the implementation of sustainable intensification of food production.
- In our study, we compared the effectiveness of the two most popular AES in Germany, organic farming and flower strips, in supporting pollinators and flower resources. We selected nine landscapes along a gradient of increasing field size, (configurational heterogeneity), each with a triplet of winter wheat fields: one organic, one conventional with flower strip and one conventional without flower strip as a control. We surveyed insect‐pollinated plants and pollinators (bumblebees, solitary bees and hoverflies). Additionally, we placed bumblebee colonies in the field edges to monitor their growth (colony weight gain) and reproduction (queen production).
- Flower strips stood out with the highest abundance and richness of pollinators. In contrast, bumblebee colony growth and plant richness benefited equally from organic and flower strip schemes. At the landscape scale, smaller fields had a positive effect on plant richness and bumblebee reproduction in flower strips. By contrast, bumblebee colonies in organic agriculture benefited most from large fields, as large organic fields provided much more flower resources than the narrow flower strips.
- Synthesis and applications . Our results showed that both local and landscape management shaped pollinator communities and their reproduction. Overall, organic farming and flower strips appeared to be effective tools to mitigate flower shortage in conventional cereal fields, with organic farming supporting the highest flowering plant cover per field. Flower strips enhanced local pollinator richness most, but increased bumblebee reproduction only when the surrounding landscapes had small fields with long field borders. Therefore, our results reveal that European Union policies need to take into account that the effectiveness of agri‐environment schemes depends on the structure of the surrounding landscape.
The effect of the interaction between management and mean field size in a 1,000‐m radius on colony queen brood cells (n  = 50).
 Different colours depict the management types, as indicated in the 
legend: CFS, conventional field edge with flower strip; CON, 
conventional field edge; ORG, organic field edge. The regression lines 
are based on the full model (link function: log). 
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