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’.
.
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.
.
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
.
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
.
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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