More stories

  • in

    GPS-telemetry unveils the regular high-elevation crossing of the Himalayas by a migratory raptor: implications for definition of a “Central Asian Flyway”

    1.
    Webster, M. S., Marra, P. P., Haig, S. M., Bensch, S. & Holmes, R. T. Links between worlds: unraveling migratory connectivity. Trends Ecol. Evol. 17, 76–83 (2002).
    Google Scholar 
    2.
    Newton, I. The migration ecology of birds (Elsevier-Academic Press, London, 2008).
    Google Scholar 

    3.
    Schaub, M., Kania, W. & Köppen, U. Variation of primary production during winter induces synchrony in survival rates in migratory white storks Ciconia ciconia. J. Anim. Ecol. 74, 656–666 (2005).
    Google Scholar 

    4.
    Higuchi, H. et al. Migration of Honey-buzzards Pernis apivorus based on satellite tracking. Ornithol. Sci. 4, 109–115 (2005).
    Google Scholar 

    5.
    Takekawa, J. et al. Geographic variation in Bar-headed Geese Anser indicus: connectivity of wintering areas and breeding grounds across a broad front. Wildfowl 59, 100–123 (2009).
    Google Scholar 

    6.
    Batbayar, N. & Lee, H. Steppe eagle migration from Mongolia to India. In Bird migration across the Himalayas: wetland functioning amidst mountains and glaciers (eds Prins, H. H. T. & Namgali, T.) 117–127 (Cambridge University Press, Cambridge, 2017).
    Google Scholar 

    7.
    Dixon, A., Rahman, L., Sokolov, A. & Sokolov, V. A. Peregrine falcons crossing the ‘roof of the world.’ In Bird migration across the Himalayas: wetland functioning amidst mountains and glaciers (eds Prins, H. H. & Namgali, T.) 53–67 (Cambridge University Press, Cambridge, 2017).
    Google Scholar 

    8.
    Zalles, J. I. & Bildstein, K. L. Raptor watch: a global directory of raptor migration sites (Hawk Mountain Sanctuary, Kempton, 2000).
    Google Scholar 

    9.
    Den Besten, J. W. Migration of Steppe Eagles Aquila nipalensis and other raptors along the Himalayas past Dharamsala, India, in autumn 2001 and spring 2002. Forktail 20, 9–13 (2004).
    Google Scholar 

    10.
    Juhant, M. A. & Bildstein, K. L. Raptor migration across and around the Himalayas. In Bird migration across the Himalayas: wetland functioning amidst mountains and glaciers, pp 98–116 (eds Prins, H. H. & Namgali, T.) (Cambridge University Press, Cambridge, 2017).
    Google Scholar 

    11.
    Clark, N. E., Boakes, E. H., Mcgowan, P. J. K., Mace, G. M. & Fuller, R. A. Protected areas in South Asia have not prevented habitat loss: a study using historical models of land-use change. PLoS ONE 8, e65298 (2013).
    ADS  PubMed  PubMed Central  CAS  Google Scholar 

    12.
    Malakoff, D., Wigginton, N. S., Fahrenkamp-Uppenbrink, J. & Wible, B. Rise of the urban planet. Science 80, 272 (2016).
    Google Scholar 

    13.
    Yasue, M., Feare, C. J., Bennun, L. & Fiedler, W. The epidemiology of H5N1 Avian influenza in wild birds: why we need better ecological data. Bioscience 56, 923–929 (2006).
    Google Scholar 

    14.
    Yanjie, Xu., Gong, P., Wielstra, B. & Si, Y. Southward autumn migration of waterfowl facilitates cross-continental transmission of the highly pathogenic avian influenza H5N1 virus. Sci. Rep. 6, 30262 (2016).
    Google Scholar 

    15.
    Palm, E. C. et al. Mapping migratory flyways in Asia using dynamic Brownian bridge movement models. Mov. Ecol. 3, 3 (2015).
    PubMed  PubMed Central  Google Scholar 

    16.
    Parr, N. et al. High altitude flights by ruddy shelduck Tadorna ferruginea during trans-Himalayan migrations. J. Avian Biol. 48, 1310–1315 (2017).
    Google Scholar 

    17.
    Galushin, V. M. A huge urban population of birds of prey in Delhi India. Ibis (Lond. 1859) 113, 522 (1971).
    Google Scholar 

    18.
    Kumar, N., Jhala, Y. V., Qureshi, Q., Gosler, A. G. & Sergio, F. Human-attacks by an urban raptor are tied to human subsidies and religious practices. Sci. Rep. 9, 2545 (2019).
    ADS  PubMed  PubMed Central  Google Scholar 

    19.
    Kumar, N. et al. The population density of an urban raptor is inextricably tied to human cultural practices. Proc. R. Soc. B Biol. Sci. 286, 20182932 (2019).
    Google Scholar 

    20.
    Naoroji, R. Birds of prey of the Indian subcontinent (Christopher Helm, London, 2006).
    Google Scholar 

    21.
    Ferguson-Lees, J. & Christie, D. A. Raptors of the world. (2001).

    22.
    Choudhury, A. Migration of Black-eared Kite or Large Indian Kite Milvus migrans lineatus(Gray) from Mongolia to North-Eastern India. J. Bombay Nat. Hist. Soc. 102, 229–230 (2003).
    Google Scholar 

    23.
    Forsman, D. Identification of black-eared kite. Bird. World 16, 56–60 (2003).
    Google Scholar 

    24.
    DeCandido, R., Subedi, T., Siponen, M., Sutasha, K. & Pierce, A. Flight identification of Milvus migrans lineatus ‘Black-eared’Kite and Milvus migrans govinda ‘Pariah’Kite in Nepal and Thailand. Bird. ASIA 20, 32–36 (2013).
    Google Scholar 

    25.
    Scott, G. R. Elevated performance: the unique physiology of birds that fly at high altitudes. J. Exp. Biol. 214, 2455 (2011).
    PubMed  CAS  Google Scholar 

    26.
    Sergio, F. et al. Individual improvements and selective mortality shape lifelong migratory performance. Nature 515, 410–413 (2014).
    ADS  PubMed  CAS  Google Scholar 

    27.
    Sergio, F. et al. Migration by breeders and floaters of a long-lived raptor: implications for recruitment and territory quality. Anim. Behav. 131, 59–72 (2017).
    Google Scholar 

    28.
    Panuccio, M., Agostini, N., Mellone, U. & Bogliani, G. Circannual variation in movement patterns of the Black Kite (Milvus migrans migrans): a review. Ethol. Ecol. Evol. 26, 1–18 (2014).
    Google Scholar 

    29.
    Kokko, H. Competition for early arrival in migratory birds. J. Anim. Ecol. 68, 940–950 (1999).
    Google Scholar 

    30.
    Sergio, F., Blas, J., Forero, M. G., Donazar, J. A. & Hiraldo, F. Sequential settlement and site dependence in a migratory raptor. Behav. Ecol. 18, 811–821 (2007).
    Google Scholar 

    31.
    Bildstein, K. L. Migrating raptors of the world: their ecology & conservation (Cornell University Press, Cornell, 2006).
    Google Scholar 

    32.
    Flack, A. et al. Costs of migratory decisions: a comparison across eight white stork populations. Science Advances 2, e1500931 (2016).
    ADS  PubMed  PubMed Central  Google Scholar 

    33.
    Board, C. P. C. Solid waste management in slaughterhouses (Ministry of Environment and Forests, Government of India, 2004).
    Google Scholar 

    34.
    Kumar, N. et al. Habitat selection by an avian top predator in the tropical megacity of Delhi: human activities and socio-religious practices as prey-facilitating tools. Urban Ecosyst. 21, 339–349 (2018).
    Google Scholar 

    35.
    Meyburg, B.-U. & Meyburg, C. GPS-Satelliten-Telemetrie bei einem adulten Schwarzmilan (Milvus migrans): Aufenthaltsraum während der Brutzeit, Zug und Überwinterung. Popul. Greifvogel und Eulenarten 6, 311–352 (2009).
    Google Scholar 

    36.
    Blanco, G. et al. Integrating population connectivity into pollution assessment: overwintering mixing reveals flame retardant contamination in breeding areas in a migratory raptor. Environ. Res. 166, 553–561 (2018).
    PubMed  CAS  Google Scholar 

    37.
    Sergio, F. et al. No effect of satellite tagging on survival, recruitment, longevity, productivity and social dominance of a raptor, and the provisioning and condition of its offspring. J. Appl. Ecol. 52, 1665–1675 (2015).
    Google Scholar 

    38.
    Tanferna, A., López-Jiménez, L., Blas, J., Hiraldo, F. & Sergio, F. Different location sampling frequencies by satellite tags yield different estimates of migration performance: pooling data requires a common protocol (migration estimates by satellite tracking). PLoS ONE 7, e49659 (2012).
    ADS  PubMed  PubMed Central  CAS  Google Scholar 

    39.
    Seaman, D. E. & Powell, R. A. An evaluation of the accuracy of Kernel density estimators for home range analysis. Ecology 77, 2075–2085 (1996).
    Google Scholar 

    40.
    Terraube, J. et al. Broad wintering range and intercontinental migratory divide within a core population of the near-threatened pallid harrier. Divers. Distrib. 18, 401–409 (2012).
    Google Scholar 

    41.
    DeCandido, R., Gurung, S., Subedi, T. & Allen, D. The east–west migration of Steppe Eagle Aquila nipalensis and other raptors in Nepal and India. Bird ASIA 19, 18–25 (2013).
    Google Scholar 

    42.
    Subedi, T. R. et al. Population structure and annual migration pattern of Steppe Eagles at Thoolakharka Watch Site, Nepal, 2012–2014. J. Raptor Res. 51, 165–171 (2017).
    Google Scholar  More

  • in

    Identifying volatile organic compounds used for olfactory navigation by homing pigeons

    Regional observations of volatile organic compounds
    Measurements were conducted in summer 2017 and spring 2018 in the area of Pisa, Italy, as part of the HOMING project (Hunting Organic Molecules In NaviGation). Measurements consisted of: (i) a pilot study (summer 2017) to investigate the volatile organic compounds (VOCs) emitted by three representative local ecosystems surrounding the bird’s home aviary; (ii) a 2-month intensive field campaign (spring 2018) at the bird’s home aviary to monitor VOCs along with meteorological variables; (iii) three flights on board of a Cessna aircraft to sample at ca. 180 m, within the birds typical flight altitude (spring 2018). Specifically, (i) was conducted to identify the chemical composition of surrounding forest sites and test whether they can be smelled distinctly from the aviary. (ii) Was performed to derive the olfactory maps developed by birds based on the assumption that birds and our analytical equipment have comparable detection thresholds. (iii) Was needed to examine any regional scale gradient used by pigeons when flying. The home aviary is operated by the University of Pisa and is located at the rural site Arnino (43°39′25.7″N 10°18′14.7″E), outside the city of Pisa (11 km North–East), close to the Tyrrenian sea (1.8 km West) and the mouth of river Arno (3.2 km North) (Fig. 1).
    Figure 1

    Map of the sampling area. The point designated as “home” refers to the birds aviary of Arnino (43°39′25.7″N 10°18′14.7″E) located in Tuscany in the area of Pisa-Livorno. Points on the map show the three sites used for releasing birds during a navigational experiment and the main biogenic and anthropogenic sites in the area. Photos show an aerial view of the Arnino field site during the airborne sampling (left) and a homing pigeon equipped with a GPS-tag before being released for testing its homing performance (right). Figure drawn with Igor WaveMetrics.

    Full size image

    Arnino houses hundreds homing pigeons (Columba livia) used for navigational experiments. Volatile organic compound mixing ratios were determined with state-of-the-art on-line and off-line analytical techniques (PTR-MS and GC–MS) and speciated in their isomeric and enantiomeric forms.
    Navigational experiments entailed releasing 174 pigeons equipped with GPS loggers (N. 80/2013-A), who had never left their home before, from unfamiliar sites 50–70 km from their home (Fig. 1). For logistical reasons (power availability and shelter for technological equipment at release points), no simultaneous measurement of air composition and bird release was possible. Therefore, we used results from the most recent available flight experiments (summer 2016 and summer 2017) to determine general homing performance indicators and examined the latter in conjunction with available meteorological information, as modelled air masses trajectories.
    The daily variation of volatile organic compounds at the aviary site
    Meteorological parameters including, temperature, relative humidity, wind direction and wind speed were measured in May–June 2018 during the ground-based campaign at the home aviary (Supplementary Fig. 1). Air temperature and relative humidity ranged between 12–25 °C and 60–85%, respectively (Fig. 2 and Supplementary Fig. 1), showing the expected mirrored diel cycle, whereby temperature is highest and RH lowest by day. Wind direction and speed exhibited a repeating daily pattern during the 2 months of measurements (Fig. 2 and Supplementary Fig. 1).
    Figure 2

    Diel cycle of meteorological parameters (a,b) and measured VOCs (c–f). The volumetric mixing ratio (VMR) of the volatile organic compounds are reported as their measured mass fragment by PTR-MS: m/z 63 (c), m/z 69 (d), m/z 81 (e) and m/z 107 (f); identified respectively as dimethyl sulphide (c), isoprene (d), sum of monoterpenes (e) and sum of xylenes (f). Meteorological parameters are plotted as mean campaign values (marker), median (line) and interquartile range (shaded area). VOC box plots report mean campaign values (marker), median (line), interquartile range (box) and 10th and 90th percentiles (whiskers).

    Full size image

    The proximity to the coast exposes the measurement site to influence by the local sea breeze system. Air masses reaching the aviary came from inland (mean wind angle 150°) every day until midday, and thereafter between 12:00 and 20:00–21:00 (local time) the air masses were advected from the sea (mean angle 270°). The wind speed, like the wind direction, also showed a diurnal profile. Figure 2 shows the diurnal profile of some compounds measured by proton transfer reaction mass spectrometry (PTR-MS). They have contrasting diel cycles and hereafter investigated further: dimethyl sulphide (DMS, m/z 63), isoprene (m/z 69), sum of monoterpenes (MT, m/z 81) and sum of xylenes (m/z 107). The full mass list and identities are reported in Supplementary Table 4 with other compound diel variations in Supplementary Fig. 2. We refer to the abbreviations included at the beginning of the manuscript for a reader not familiar with the terms used herein.
    Dimethyl sulphide is a biogenic compound emitted by phytoplankton activity in seawater21,22,23; it is insoluble in water, and so readily transfers to the air at a rate dependent on the temperature and wind speed. Our measurements show that DMS mixing ratios at the site remained low and constant until 12:00, possibly reflecting weak soil emissions from the land24, to increase to a maximum at 20:00 due to continued marine emission, until the reversal of the wind back to offshore. The maximum hourly averaged mixing ratio of DMS is 0.17 ± 0.8 ppbv, comparable to 0.12 ppbv measured by Derstroff et al.25 at a coastal site on Cyprus.
    Isoprene mixing ratios showed a bimodal distribution with two maxima at 11:00–12:00, and 18:00–20:00; similar to methyl ethyl ketone (MEK) and isoprene oxidation products methyl vinyl ketone, methacrolein and isoprene peroxides (MVK + MACR + ISOPOOH) and acetic acid (Supplementary Fig. 2). At both morning and afternoon maxima, the isoprene mixing ratio reached 0.7 ± 0.6 ppbv (maximum hourly average ± 1σ standard deviation). This is 10 times higher than the value observed during wintertime at a similar rural Mediterranean site in Spain26, but lower than the value measured in summertime by Steinbacher and coauthors27 at a rural site in the Po valley, Italy. Isoprene emission from terrestrial vegetation is mainly light dependent28, therefore near-source measurements typically exhibit a broad maximum around noon when irradiation is highest29,30. The two isoprene maxima observed here are the result of the sea breeze system, which brings isoprene poor marine influenced air to the site around midday.
    Monoterpenes (C10H16) are emitted from vegetation, and are to a large part responsible for the scent of forests. Their sum at the site reached 1.6 ± 1 ppbv as a maximum hourly average at 01:00. Despite monoterpene emissions being also a function of temperature they do not show the same profile as isoprene. Monoterpene mixing ratios were higher at night, decreasing slowly from 03:00 and then sharply at 08:00, and remaining low through the day before rising back to early morning levels in the late evening. While isoprene is formed in the plant and released directly, mainly in response to light, many plant species emit monoterpenes day and night from resin duct storage pools contained in the leaves or needles31. The rates of monoterpene emission therefore depend strongly on temperature, and although lower in the night, continued emission into a shallower boundary layer can generate significant mixing ratios, as has been observed elsewhere (for example in the boreal forest32). As expected, air advected from the more vegetated inland had higher monoterpene mixing ratios than air from the sea. Although, marine monoterpene and isoprene emissions have been observed previously33, in this region terrestrial vegetation emissions clearly dominate. A similar profile (higher nighttime daytime ambient mixing ratio) was reported by Davison et al.34 from the Mediterranean forest of Castelporziano, however, the average daytime and nighttime concentrations were 3 times lower than reported here.
    Xylenes (Fig. 2), benzene, toluene, and sum of trimethylbenzenes (Supplementary Fig. 2) are aromatic compounds predominantly emitted from anthropogenic sources, for example fossil fuel use. Mixing ratios increased in the morning at 8:00, probably due to traffic emissions, and decreased steadily between 9:00–12:00, as the wind direction changed. They remained low in the afternoon as the wind came from the sea, reflecting the expected absence of significant sources from this sector. The mixing ratios of all compounds increased again after 17:00, slowly for benzene and toluene and faster for xylenes and trimethylbenzene, suggesting different anthropogenic sources of such species (i.e. road traffic and industries). Although evidence for biogenic aromatic species has been documented35,36, here no evidence of natural sources of aromatic compounds was found. The maximum mixing ratios for benzene, toluene, sum of xylenes and trimethylbenzene, were 0.16 ± 0.08 ppbv, 0.32 ± 0.7 ppbv, 0.22 ± 0.09 ppbv and 0.11 ± 0.9 (hourly average maximum ± 1σ standard deviation), respectively. Similar results were found for benzene and toluene at a rural Mediterranean site in Spain (0.19 and 0.41 ppbv, respectively26).
    Chiral monoterpenes
    Many monoterpenes exist in two chiral forms, meaning they exist in nature as two non-superimposable mirror image forms (enantiomers), often with different biological activities. Insects can perceive each enantiomer differently and each may act as entirely distinct chemical signals37. We investigated the abundance of the prevalent chiral monoterpenes at the home aviary and at three ecosystems surrounding the aviary North (lake), East (mixed forest) and South (pine forest). This was to test whether unique mixtures could be ascertained at each site which is a condition of the mosaic hypothesis. At all sites, including the aviary, the (−) configuration dominated over the (+) for the monoterpene species α-pinene, β-pinene and limonene. This has been also observed in the tropical rainforest for α-pinene38. Relative ratios for the same monoterpene enantiomeric pair do not change significantly across the investigated sites, however, their absolute concentrations and relative abundance to the other terpene species do differ (see Fig. 3).
    Figure 3

    Volume mixing ratio (VMR) distribution of enantiomers from three ecosystems surrounding the birds’ aviary and at the birds’ aviary. Category plots show mean measured values with their standard deviation from three days of sampling during summer 2017. Box plots show mean campaign values (marker), median (line), interquartile range (box) and 10th and 90th percentiles (whiskers) from 2 months intensive field campaign at the birds’ aviary in spring 2018 (home) and from three flights conducted at 180 m altitude over the region during the airborne campaign. The x axes shows the retention time (min) of the chiral molecules in the gas chromatography mass spectrometer (GC–MS) and shows the good resolution achieved with the method. The left y axes indicate the volume mixing ratio of all molecules, except for (−)limonene measured at the aviary, whose VMR is indicated by the right y axes.

    Full size image

    At the aviary, (−)limonene was the most abundant species (0.89 ± 1.7 ppbv and 2.5 ± 2.7 ppbv), followed by (−)α-pinene (0.42 ± 0.57 ppbv and 1 ± 1 ppbv), (+)limonene (0.26 ± 0.29 ppbv and 0.37 ± 0.42 ppbv) and (−)β-pinene (0.17 ± 0.45 ppbv and 0.27 ± 0.49 ppbv, values indicate mean daytime and nighttime values ± 1σ standard deviation, respectively). The lake site emitted the least monoterpenes, followed by the pine forest and the mixed forest, the latter showing the highest concentration of measured terpenes. Since (−)limonene dominates the terpene blend measured at the aviary, we can surmise that the surrounding pine forest had a strong impact on the air chemical composition at the site (Fig. 3). A similar suite of biogenic molecules was found at all locations, albeit with differing ratios. In other words, there were no clear unique chemical markers for a particular area. Therefore, the source of biogenic molecules near to the aviary has the potential to interfere with or mask, odours from more distant sites. These findings are not consistent with the original “mosaic” hypothesis in which each location in the region has a unique chemical signature that can be determined from the aviary.
    Olfactory maps: spatial and temporal distribution of VOCs
    Soon after fledging, the young pigeons are housed in a loft with an associated aviary, and from the end of May are allowed to perform spontaneous flights around the loft typically until October, when the season of the experiments usually ends. During the first months after fledging39 young pigeons are exposed to the changing chemical conditions at the home site and according to the Papi olfactory hypothesis, they learn to associate wind-borne odours with wind directions thereby generating an olfactory map. It is thought that this olfactory map is continually updated throughout their life depending on conditions experienced40,41. A visual representation of this spatio-temporal information can be expressed in the form of a bivariate plot of the measured volatile organic compounds. Bivariate polar plots represent the mean campaign mixing ratio of a given compound as a function of the wind direction (angle) and wind speed (radius), similarly to a wind rose they can highlight spatial gradients in the surrounding of a measurement site. Figure 4 shows that methanol (a biogenic compound and biomass burning marker) mixing ratios were higher for higher wind speed and easterly winds (from inland). However, mixing ratios were elevated at both high and low wind speeds; indicating some methanol sources were also local. Dimethyl sulphide mixing ratios were larger for higher wind speeds originating from the North–West and South–West sectors, spanning from the mouth of the river Arno to the sea. The largest mixing ratios for isoprene came from inland, in particularly from the West–North–East for higher wind speeds and the South–East for lower ones. Smaller mixing ratios are found from the sea for large wind speed (North–West), suggestive of a weaker marine isoprene emission source. Small marine isoprene emissions have been measured previously, especially in chlorophyll rich waters12,33,42. Monoterpene mixing ratios are higher at lower wind speeds, mostly for winds coming from South–East but also East–North–East and South–West. The polar graph highlights the multiple sources of monoterpenes, and that the levels at the site are also locally influenced. The anthropogenic aromatic species xylenes and trimethylbenzene were larger when the air was transported from inland, in particular from the South-East, where heavy-traffic roads such as highway E80, the road FI-PI-LI and via AureliaSS1 are located. Additional sources of aromatics appear South of the aviary for high wind conditions, especially for trimethylbenzene. Trimethylbenzene (C6H3(CH3)3), is an aromatic hydrocarbon characterized by a strong odour, which is generally isolated from the C9 fraction of aromatics during petroleum distillation. South of the aviary, in the Stagno industrial area, there is a large petroleum refinery (Fig. 1).
    Figure 4

    Spatial distributions of measured VOCs reported as protonated masses and identified as: methanol (m/z 33), DMS (m/z 63), isoprene (m/z 69), sum of monoterpenes (m/z 81), sum of xylenes (m/z 107), trimethylbenzene (m/z 121). Mean campaign values of VOCs (colored scale) are showed as a function of wind direction (angle) and wind speed (radius). Figures drawn with R.

    Full size image

    This air composition measured at the aviary is the air breathed and smelled by the birds during their first months after fledging. The birds are therefore likely to be aware of, mixed biogenic and anthropogenic sources to the South-East, a more biogenic dominated source (with differing composition) to the West-North–East, and a marine source to the West. Thus, the ground based measurement campaign mapped several chemical compounds that vary distinctly at the site according to the wind direction and time of day. Which VOCs are useful for navigation will also depend on their respective atmospheric lifetimes. Following emission to the atmosphere VOCs are oxidized mainly by OH radicals, with small contributions by O3, NO3 and Cl radicals. Methanol, the most abundant species measured, has a lifetime of 12 days (based on OH reactivity only, assuming OH radical concentration of 2 × 106 molecules cm–343). The corresponding lifetime of isoprene is 1.4 h, therefore with a typical windspeed of 2.2 m/s the concentration of isoprene will be reduced to 1/e of the initial value in 11 km, while limonene in 2 km, xylenes in 33 km and DMS in 88 km. Therefore, over distances of ca. 50–100 km, VOCs with moderate lifetimes such as DMS and the aromatic species appear capable of creating regional gradients. The more reactive VOCs are usually photochemically transformed into less reactive products which themselves, or their combination, may create regional gradients. Significantly, the three regional gradients highlighted in Fig. 4, namely DMS, the aromatics and the monoterpenes are not aligned, rather they slope in different directions. Theoretically then, by comparing the level of these compounds to that experienced at the aviary the pigeon may, with reference to the wind-odour experience at the aviary, orient homeward. For example if the DMS level is lower at the release site than at the aviary, and the bird “knows” from the olfactory map learning phase that DMS comes from the West, then the birds homeward direction will have a westerly component. Having multiple gradients available would enable the pigeon to triangulate a homeward direction.
    Regional spatial gradients
    To verify that the spatial gradients observed from the olfactory maps exist at a larger regional scale we measured the air composition at the altitudes and over distances typically flown by homing pigeons (10–300 m, 100 km). Results from a flight campaign conducted on 26/05/2018 and 27/05/2018, in conjunction with the ground based campaign, are depicted in Figs. 3, 5 and Supplementary Fig. 3. Figure 3 shows the speciation of chiral molecules from ground measurements at four distinct sites (including the aviary) and above the sampled region considering all the airborne samples taken with the three flights. Interestingly, the regionally predominant compound at 180 m is α-pinene, rather than limonene observed at the ground. This is because α-pinene has a longer atmospheric lifetime (2.6 h), in comparison to β-pinene (1.8 h) and limonene (49 min)43. Figure 5 shows the mixing ratio of a biogenic precursor compound (−)α-pinene and the common terpene photochemical oxidation product nopinone44 sampled at different locations above the home aviary, and the release sites. The terpene airborne concentrations compare well with the ground-based ones (higher above the mixed Mediterranean forest, followed by the pine forest, followed by the lake site, as reported in Fig. 3). However, as expected, the terpene airborne concentrations are smaller compared to ground concentrations (40–50 pptv and 80–208 pptv, respectively) consistent with the ground based emissions being progressively oxidized by OH radicals and ozone as well as being mixed with the relatively clean air in the free troposphere above. This means that the birds will encounter strong vertical gradients of primary emitted species during flight with lower concentrations aloft. Furthermore oxidation chemistry will generate entirely different species, complicating the mixture, weakening the primary chemical signal and possibly obfuscating the originally emitted olfactory signals. In Fig. 5 we observe during the afternoon flights (with onshore winds) the nopinone mixing ratios generally increase to the East. This demonstrates that monoterpenes emitted at ground level during the day and in onshore winds are being oxidized to (among other species) nopinone on the time and space scales of the pigeon release experiments. Therefore, spatial gradients of reactive VOC do exist for the primary emitted species and their oxidation products, at a spatial scale compatible with the distances used for navigation experiments.
    Figure 5

    Spatial distributions of measured (−)α-pinene (a) and nopinone (b) from airborne sampling during three flights conducted on 26/05/2018 and 27/05/2018. Colored scales indicate respectively volume mixing ratio and counts of chromatograms peak area. Figures drawn with Igor WaveMetrics.

    Full size image

    Pigeon flight tracks and air masses trajectories analysis
    To test whether the intensity of atmospheric odour signals could potentially aid in the homing of pigeons, we provide here a first preliminary analysis based on real pigeon tracks and simulated air masses trajectories. We hypothesize that overall stronger gradients of indicative aerial chemicals enable better navigational performance in pigeons18. To do this we examine the GPS logged tracks of homing birds in relation to the general gradients of atmospheric chemicals determined in the previous sections, and to the origin of air at the release sites. Bird release experiments were conducted over six days in summer 2016 and summer 2017 from three release sites simultaneously (Fig. 1). Those experiments were chosen for being the most recent results available for indices analysis, and for being conducted on sunny days, when air temperature, humidity and atmospheric pressure were comparable to those encountered during VOCs measurements (Supplementary Fig. 4). Each release experiment involved 9 or 10 individual birds, released singly every 5–10 min, over approximately 1 h and involved 27–30 individuals released on the same day from three sites (N = 174). The total number of tracks obtained was 143, due to either the loss of the device by some birds or the misfunctioning of the GSM GPS logger. Bird flight tracks were used to determine: the pigeon initial flight direction, the homing capabilities en route with the homing efficiency index (HEI45) and for the whole track with a mean aggregate azimuth penalty (MAAP); see Methods and supplementary information. Due to lack of power and shelter at the release sites, chemical information of atmospheric composition was not available during those experiments, therefore a meteorological approach, based on modelled air trajectories, was developed in order to examine how air mass transport was related to the birds’ homing performance. Specifically, we generated forward and backward trajectories of the air masses for each release day, for the site and time of release. Forward trajectories analysis showed that the prevalent wind direction during the days and time of pigeons’ flights was from west (supplementary information). We cannot yet test the bouquet of potential chemical information, but concentrate here on one traceable chemical gradient: DMS (Dimethyl sulphide) emanating from the Tyrrhenian sea. DMS, a chemical compound of marine origin (see Supplementary Fig. 5), is here identified to be a suitable candidate for homing by olfaction. Figures 2 and 4 show that it was among the most abundant compounds measured during daytime at the aviary, it follows a regular pattern of emission, is known to be detectable by birds, and it is atmospherically stable enough to survive transport over longer distances, likely decreasing along the West–East direction. Air masses reaching the aviary diurnally during the ground campaign were found to spend considerable time ( > 20 h in most cases) in the marine boundary layer in the past 24 h (see table 1 supplementary material). For these reasons, we tested if more marine-influenced air masses can influence the pigeon initial orientation (Fig. 6) and the homing path en route (homing efficiency index, supplementary material). We examined where each air mass was located (during 24 h prior to the release) reported in latitude and longitude coordinates and determined the time the air masses spent in the marine boundary layer, and the time the air masses spent over non-marine areas. As shown in Fig. 4, pigeons at the home loft are exposed to DMS associated with westerly winds; easterly winds are unlikely to carry DMS. According to the olfactory navigation hypothesis5 it is expected that a low atmospheric level of DMS at the release site is likely to produce a bias towards west in the orientation of the birds, regardless of their ultimate home direction. To test this hypothesis, the deviation from west of the individual mean vectors computed on the initial part of each track (within 10 km from the release site) is tested against the ratio of the time the air masses spent over sea versus over land (ratio sea/land) and the opposite (ratio land/sea). The Spearman ranking test highlighted that the deviation from west is positively correlated to the sea/land ratio of the air masses trajectories (n = 135, S = 0.163, p  More

  • in

    Vegetation traits of pre-Alpine grasslands in southern Germany

    Study area
    The study area is located in the TERENO Pre-Alpine Observatory28,29 in southern Bavaria, Germany (Fig. 2). The ten test plots are situated on three sites at different elevations: Fendt (FE), Rottenbuch (RB), and Eschenlohe (EL). Table 1 gives an overview about the main characteristics of these sites and the plots.
    Fig. 2

    Location of the study sites (pink stars). Background: Sentinel-2b (27/04/2018), true colour composite (contains modified Copernicus Sentinel data [2018], processed by ESA). Used coordinate reference system: EPSG: 25832. EL = Eschenlohe, FE = Fendt, RB = Rottenbuch.

    Full size image

    Table 1 Site and plot characteristics.
    Full size table

    Geologically, the plots in FE are located in the major structural unit of the molasse basin of the Bavarian Alpine foreland, while the other ones lie in the major structural unit of the Alps with the major tectonic units folded molasse (RB) and northern calcareous Alps (EL)33. Glacial erosion and Quaternary deposition processes influenced most of the molasse area. Therefore, alluvial structures and moraines largely effect soil parent material here28. The dominant soil types in the northern part of the study area are Cambisols, Luvisols, and Regosols, and in the southern part Rendzic Leptosols and Calcaric Cambisols. Gleysols and Histosols characterize areas along the course of rivers and areas of recent and paleo lakes28. According to the Köppen-Geiger climate classification the study area has a warm temperate climate without a dry season and warm summers (Cfb)34. Mean annual precipitation at the study sites varied between 1008 mm and 1419 mm35, and mean annual air temperature between 8.0 °C and 8.6 °C36 (see Table 1). The land cover around the study sites is characterized by a mix of pastures, natural grasslands, forests (needle-leaf, broad-leaf, mixed), discontinuous urban fabric, and in EL additionally peat bogs37. All ten plots are situated on managed grasslands, the dominant land use around the study sites. The management intensity of the plots range from very extensive management with only one cut and no fertilizer application per year to intensive management with five cuts and five slurry applications per year (Table 1).
    Sampling design
    The field campaign with UAS flights and vegetation sampling took place on 24–25 April 2018 at ten different grassland plots (FE1, FE2, FE3, FE4, RB1, RB2, RB3, EL1, EL2, EL3). Plots were selected by i) visual characterisation of standing biomass to select plots that differ in management as well as soil nutrient and water status (based on talks with local farmers and corresponding field visits; no specific method was applied), and that fulfil other criteria such as ii) homogeneous, flat area, iii) accessibility (including permission by farmers), and iv) proximity of the plots to ideally cover several plots with one UAS flight.
    When designing the sampling strategy, a perspective linkage of the sample data to Sentinel-2 images with a spatial resolution of 10 m × 10 m was taken into account. Therefore, we adapted the sampling strategy proposed by Baret et al.38 for the validation of medium spatial resolution land satellite products. The authors suggested relatively flat and homogeneous validation sites of 3 km × 3 km for validating data of sensors with a spatial resolution of up to 1 km × 1 km. Their validation sites were sampled at several so called elementary sampling units (ESUs, 20 m × 20 m). These ESUs were spread across the validation site using a division of the site in nine 1 km × 1 km squares (three to five ESUs per square) with a higher sampling density in the central square (five to seven ESUs)38.
    In our study, we used 30 m × 30 m plots that were ideally sampled at 12 subplots (corresponding to the ESUs of Baret et al.38) of 0.25 m × 0.25 m (Fig. 1). We divided each plot in nine equally sized squares of 10 m × 10 m, in which we randomly placed one subplot. Following the suggestions of Baret et al.38, we sampled the central square with a higher density (i.e. with four subplots). Compared to Baret et al.38 we targeted a smaller number of subplots per plot (12 instead of 30 to 50) as our plot size is notably smaller than their plot size and hence it is easier to select a homogenous area. During the sampling campaign, we needed to reduce the number of subplots in the central square for EL1 (11 subplots were sampled) and EL2 (9 subplots) due to time constraints. In all other plots, we sampled 12 subplots.
    Preparations in the field
    Some arrangements needed to be done in the field prior to sampling to prepare accompanying UAS flights. The resulting images of these UAS flights were used among others for retrieving the exact location of the subplots. After the localisation of the plots in the field (aiming for a north-orientation of one plot site), bright 0.5 m × 0.5 m flakeboards were distributed in the plots at the approximate locations of the subplots (Fig. 3). These flakeboards were used to identify the location of the subplots in the orthophotos that were generated from images of the UAS.
    Fig. 3

    Sampling design. (a) Scheme of a sampling plot with subplots. The location of subplots within a 10 m × 10 m square was chosen randomly; (b) Location of a subplot with respect to the flakeboard.

    Full size image

    Additionally, several ground control points (GCPs) were distributed in the overflight area of the UAS. The exact location of the GCPs’ centre was measured with a Global Navigation Satellite System (GNSS) receiver (Viva GNSS GS 10, Leica Geosystems AG, Switzerland) in static mode for 10 minutes. The data from the GNSS was reprocessed with Leica Geo Office 8.3 software (Leica Geosystems AG, Heerbrugg, Switzerland) utilising reference data from the satellite positioning service of the surveying administration of the federal states of Germany (SAPOS) for the real reference stations 0285-Garmisch, 0270-Bad Tölz, and 1271-Weilheim. The reference data were obtained via the SAPOS website of Bavaria (https://sapos.bayern.de/). The accuracy of the used GNSS in post-processing mode is 0.003 m in horizontal direction and 0.005 m in vertical direction39. The transformation of the corrected coordinates from ellipsoidal heights to physical (geoid-based) heights (height system: DHHN2016, EPSG 7837) was done with the online processing service “CRS-Transformation Bayern” from SAPOS (https://sapos.bayern.de/coord_tm.php). The transformation accuracy for this height transformation is 0.005 m40.
    The UAS flights were conducted after the preparation of the respective field site, followed by the field measurements and vegetation sampling. A RGB camera (Sony Cyber-shot WX 220, Sony Corp., Minato, Japan) mounted on a fixed-wing UAS (eBee, senseFly, Cheseaux-sur-Lausanne, Switzerland) was used to acquire high-resolution images of the study sites. In total, four UAS-flights were necessary to cover all ten plots – one in FE, one in RB and two in EL (EL-N, EL-S).
    Acquisition of field measurements and field samples
    The methods for acquiring in-situ data of canopy height, destructive vegetation sampling, and subsequent sample processing were adapted from the Integrated Carbon Observation System (ICOS) instructions for vegetation measurements in grasslands41,42.
    Canopy height measurements and sampling for biomass and element content measurements
    After the UAS flight, first the subplot area was identified (0.3 m south of the corresponding flakeboard, one site centred and parallel to the flakeboard, see Fig. 3b). Second, the bulk canopy height of the grassland canopy within the subplot was measured with a platemeter, which had the same area as the subplot for destructive sampling (0.25 m × 0.25 m) and was build according to the ICOS instructions41. The plate of the platemeter was constructed from acrylic glass and weighed 1680 g. Third, a metallic sampling frame (size: 0.25 m × 0.25 m × 0.03 m) was put on the subplot. After verifying that the sampling frame was not sliding on the vegetation, the vegetation within the sampling frame was clipped down to stubble height (0.03 m) with a manual grass cutter for later determination of biomass and element contents. Finally, the clipped vegetation was put in a labelled paper bag, then in an airtight plastic bag and afterwards in a cooling box until further processing in the laboratory.
    Sampling for leaf mass per area determination
    Additional samples were taken outside the subplots (within a radius of 2 m; one sample per subplot) to determine LMA. First, the area percentage of the PFTs legumes, other forbs and graminoids of the 30 m × 30 m plot was visually estimated (rough estimation based on field observations, no specific method applied). Then, the corresponding number of samples for each PFT was determined in relation to the number of subplots. That is, if the percentage of PFTs is e.g. 50% graminoids, 25% legumes, and 25% other forbs, and we have 12 subplots, there were six samples for graminoids, three for legumes and three for other forbs in this plot. At each subplot we took one LMA sample for just one specific PFT. One LMA sample consisted of fully expanded, undamaged leaves of the selected PFT originating from different individuals. The number of leaves per sample varied between one and seven depending on the leave size and the species composition of the PFT. However, the species composition could just be considered for dominant and easily distinguishable species, as the team was not specifically trained in grassland botany. Therefore, multiple species samples occurred mainly for forb samples. The clipped leaves were wrapped in humid paper. Then, the sample was put in a labelled plastic bag which was hermetically closed before it was placed in the cooling box.
    Sample processing in the laboratory
    After transportation, the samples were stored in the fridge and/or in a cooling room at 4 °C until further processing. Sample processing in the lab started within one to nine days after the sampling date.
    Samples for the determination of biomass, green area index, and element content
    The samples were removed from the plastic bags and weighed. The weight of the fresh material was multiplied by 16 to determine the fresh weight per 1 m² (Biom wm). Afterwards, the sample material was sorted into the PFT non-green vegetation (NG; representing photosynthetically inactive structures), legumes (L), non-leguminous forbs (F), and graminoids (G). Then, the fresh weight of each PFT was determined. The sorting was done either on the full sample or on a representative smaller subsample in case there was a lot of sample material. For taking a subsample, the vegetation material was thoroughly mixed and then a handful of material was taken out. The remaining material was dried and further processed/analysed for C and N content like the PFT specific samples.
    The total hemi-surface area of the green material (GA) needs to be obtained to determine the GAI of a sample. As we have flat vegetation structures, we used a planimeter (LI-3100A Area Meters, LI-COR, USA) to obtain the hemi-surface area. The hemi-surface area was measured separately for each PFT of a sample, but not for the non-green vegetation. The GAI of a certain PFT (GAIPFT) was then calculated by dividing the hemi-surface area of the PFT (GAPFT) by the area of the subplot (A; 0.25 m × 0.25 m) and in case a subsample was taken by multiplying with the ratio of the fresh weight of the sample (Biomass wmsample) to the subsample (Biomass wmsubsample):

    $$GA{I}_{PFT}=frac{G{A}_{PFT}}{A}frac{Biom,w{m}_{sample}}{Biom,w{m}_{subsample}}$$
    (1)

    The total GAI (GAItot) of the sample was calculated by summing the GAI of each PFT:

    $$GA{I}_{tot}=sum GA{I}_{PFT}=GA{I}_{L}+GA{I}_{F}+GA{I}_{G}$$
    (2)

    After the planimeter measurements the samples were dried in an oven at 65 °C until constant weight was achieved. Then, the dry weight of each PFT of each sample was measured (dmPFT). The total weight of dry biomass of a sample (Biomass dm) was obtained by summing up the dry weights of all PFTs and if applicable the dry weight of the remaining material (dmrest) of a sample and then scaled to 1 m²:

    $$Biomass,dm=16times sum d{m}_{PFT}=16times (d{m}_{NG}+d{m}_{L}+d{m}_{F}+d{m}_{G}+d{m}_{rest})$$
    (3)

    The percentage of each PFT (PPFT) with respect to the total dry biomass weight of the sorted material (either subsample or full sample) (ΣdmPFT) was calculated as follows:

    $${P}_{PFT}=frac{d{m}_{PFT}}{sum d{m}_{PFT}}times 100=frac{d{m}_{PFT}}{d{m}_{NG}+d{m}_{L}+d{m}_{F}+d{m}_{G}}times 100$$
    (4)

    The plant water content (PWC) was calculated from the weight of the fresh (Biom wm) and dry biomass (Biom dm) as follows:

    $$PWC=frac{Biom,wm-Biom,dm}{Biom,wm}times 100$$
    (5)

    Finally, the dried vegetation material was ground in a ball mill for elemental analysis of C and N.
    Samples for the determination of leaf mass per area
    After returning from the field work, the leaves for the LMA determination were rehydrated until full turgescence. When the leaves were fully expanded, the last mature leaf from each tiller (in case tillers were sampled) were separated and the petiole was recut at the base of the leave blade. Then, the hemi-surface area of each sample was determined with the planimeter. Afterwards, the samples were dried in an oven at 65 °C until constant weight was achieved, before the dry weight of the LMA samples was measured. The LMA of a sample i was calculated by the ratio of the leaf dry weight (Wi) to its fresh area (Ai):

    $$LM{A}_{i}=frac{{W}_{i}}{{A}_{i}}$$
    (6)

    Analysis of C and N content
    The C and N content of the milled vegetation samples was determined using an elemental analyser (varioMax CUBE, Elementar Analysesysteme GmbH, Germany) operated in CNS (carbon, nitrogen, sulphur) mode with the plant method and a weighted sample of 17 mg at the laboratory of the Technical University Munich, Chair of Soil Science, in Freising (Germany). The detection limits of the instrument were 0.020 wt.% for C and 0.015 wt.% for N.
    Due to the sorting of the sample in different PFTs, the C and N contents were obtained specific for each PFT. In cases where a subsample was taken for the sorting into PFT, C and N contents were additionally measured also for the mixed remaining sample material.
    Mean concentrations of C and N for each subplot (plant community C and N) were calculated as follows:

    $$bar{E}={P}_{NG}times {E}_{NG}+{P}_{L}times {E}_{L}+{P}_{F}times {E}_{F}+{P}_{G}times {E}_{G}$$
    (7)

    where (bar{E}) is the mean element content (C or N), PPFT is the percentage of the PFT (NG = non-green, L = legumes, F = non-leguminous forbs, G = graminoids), and EPFT is the element content (C or N) in the PFT.
    Retrieving the coordinates of the subplot centres
    The single images from each UAS flight were processed with the photogrammetric software PIX4D (Pix4Dmapper Pro, Pix4D S.A., Prilly, Switzerland) to obtain orthophotos. The GCPs in the orthophotos were used to georeference the orthophotos. The final spatial resolution of the orthophotos was 0.036 m (FE), 0.034 m (RB), 0.030 m (EL-N), and 0.043 m (EL-S).
    Afterwards, the coordinates of the subplots centres were manually extracted from the high-resolution georeferenced orthophotos utilizing QGIS (Version 3.0.0-Girona)43. The bright flakeboards were visually localised in the images. Then the subplots centres were identified (0.425 m perpendicular away from the middle of the southern flakeboards site) and their coordinates extracted.
    Characterisation of grassland type and plant community composition on the plot-level
    Vegetation relevés were carried out on 18–19 June 2020 for each of the ten 30 m × 30 m plots. Within each plot all vascular plant species were systematically determined and their cover was visually estimated to the nearest percentage as a proxy for abundance. Data is provided as percentage cover per plot. Plant species names were updated according to The Plant List, a working list of all known plant species, aiming to be comprehensive for all species of vascular plants, including flowering plants, conifers, ferns and their allies, and of bryophytes, including mosses and liverworts (theplantlist.org). The grassland type was classified sensu Oberdorfer (1977 and updated since)44. Please note that vegetation relevés from 2020 may slightly differ in relative coverage to actual species specific data from sampling in 2018. Nevertheless, most grassland species reach life spans of several decades and persist through time. More

  • in

    Mapping the bacterial metabolic niche space

    1.
    Hutchinson, G. E. Cold Spring Harbor symposium on quantitative biology. Concluding Remarks 22, 415–427 (1957).
    Google Scholar 
    2.
    MacArthur, R. H. In Challenging Biological Problems: Directions Toward Their Solution (ed. Behnke, J. A.) pp. 253–259 (Oxford University Press, 1972).

    3.
    Chase, J. M. & Leibold, M. A. Ecological Niches: Linking Classical and Contemporary Approaches (University of Chicago Press, 2003).

    4.
    Holt, R. D. Bringing the Hutchinsonian niche into the 21st century: ecological and evolutionary perspectives. Proc. Natl Acad. Sci. USA 106, 19659–19665 (2009).
    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

    5.
    Winemiller, K. O., Fitzgerald, D. B., Bower, L. M. & Pianka, E. R. Functional traits, convergent evolution, and periodic tables of niches. Ecol. Lett. 18, 737–751 (2015).
    PubMed  PubMed Central  Article  Google Scholar 

    6.
    Pianka, E. R., Vitt, L. J., Pelegrin, N., Fitzgerald, D. B. & Winemiller, K. O. Toward a periodic table of niches, or exploring the lizard niche hypervolume. Am. Naturalist 190, 601–616 (2017).
    Article  Google Scholar 

    7.
    Blonder, B., Lamanna, C., Violle, C. & Enquist, B. J. The n-dimensional hypervolume. Glob. Ecol. Biogeogr. 23, 595–609 (2014).
    Article  Google Scholar 

    8.
    Hoogenboom, M. O. & Connolly, S. R. Defining fundamental niche dimensions of corals: synergistic effects of colony size, light, and flow. Ecology 90, 767–780 (2009).
    PubMed  Article  PubMed Central  Google Scholar 

    9.
    Porter, W. P. & Kearney, M. Size, shape, and the thermal niche of endotherms. Proc. Natl Acad. Sci. USA 106, 19666–19672 (2009).
    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

    10.
    Kraft, N. J. B., Godoy, O. & Levine, J. M. Plant functional traits and the multidimensional nature of species coexistence. Proc. Natl Acad. Sci. USA 112, 797–802 (2015).
    ADS  CAS  PubMed  Article  Google Scholar 

    11.
    Benjamin, B. Hypervolume concepts in niche-and trait-based ecology. Ecography 41, 1441–1455 (2018).
    Article  Google Scholar 

    12.
    González, A. L., Dézerald, O., Marquet, P. A., Romero, G. Q. & Srivastava, D. S. The multidimensional stoichiometric niche. Front. Ecol. Evol. 5, 110 (2017).
    Article  Google Scholar 

    13.
    Stevenson, B. G. The Hutchinsonian niche: multivariate statistical analysis of dung beetle niches. Coleopter. Bull. 36, 246–249 (1982).

    14.
    Inward, D. J. G., Davies, R. G., Pergande, C., Denham, A. J. & Vogler, A. P. Local and regional ecological morphology of dung beetle assemblages across four biogeographic regions. J. Biogeogr. 38, 1668–1682 (2011).
    Article  Google Scholar 

    15.
    Díaz, S. et al. The global spectrum of plant form and function. Nature 529, 167–171 (2016).
    ADS  PubMed  Article  CAS  Google Scholar 

    16.
    Green, J. L., Bohannan, B. J. M. & Whitaker, R. J. Microbial biogeography: from taxonomy to traits. science 320, 1039–1043 (2008).
    ADS  CAS  PubMed  Article  Google Scholar 

    17.
    Noah, F., Bradford, M. A. & Jackson, R. B. Toward an ecological classification of soil bacteria. Ecology 88, 1354–1364 (2007).
    Article  Google Scholar 

    18.
    Claire Horner-Devine, M. & Bohannan, B. J. M. Phylogenetic clustering and overdispersion in bacterial communities. Ecology 87, S100–S108 (2006).
    PubMed  Article  Google Scholar 

    19.
    Lennon, J. T., Aanderud, Z. T., Lehmkuhl, B. K. & Schoolmaster Jr, D. R. Mapping the niche space of soil microorganisms using taxonomy and traits. Ecology 93, 1867–1879 (2012).
    PubMed  Article  Google Scholar 

    20.
    Fisher, C. K., Thierry, M. & Walczak, A. M. Variable habitat conditions drive species covariation in the human microbiota. PLoS Comput. Biol. 13, e1005435 (2017).

    21.
    Prosser, J. I. et al. The role of ecological theory in microbial ecology. Nat. Rev. Microbiol. 5, 384–392 (2007).
    CAS  PubMed  Article  Google Scholar 

    22.
    Elhanan, B., Martin, K., Feldman, M. W. & Ruppin, E. Large-scale reconstruction and phylogenetic analysis of metabolic environments. Proc. Natl Acad. Sci. USA 105, 14482–14487 (2008).
    ADS  Article  Google Scholar 

    23.
    Humphries, M. M. & McCann, K. S. Metabolic ecology. J. Anim. Ecol. 83, 7–19 (2014).
    PubMed  Article  Google Scholar 

    24.
    Chase, J. M. In The theory of ecology (eds Scheiner, S. M. and Willig, M. R.) pp. 93–107 (2011).

    25.
    D’Andrea, R. & Ostling, A. Challenges in linking trait patterns to niche differentiation. Oikos 125, 1369–1385 (2016).
    Article  Google Scholar 

    26.
    Barter, E. & Gross, T. Manifold cities: Social variables of urban areas in the uk. Proc. R. Soc. A 475, 20180615 (2019).
    ADS  PubMed  Article  PubMed Central  Google Scholar 

    27.
    Coifman, R. R. et al. Geometric diffusions as a tool for harmonic analysis and structure definition of data: diffusion maps. Proc. Natl Acad. Sci. USA 102, 7426–7431 (2005).
    ADS  CAS  PubMed  MATH  Article  PubMed Central  Google Scholar 

    28.
    Coifman, R. R. & Lafon, S. Diffusion maps. Appl. Comput. Harmonic Anal. 21, 5–30 (2006).
    MathSciNet  MATH  Article  Google Scholar 

    29.
    Kac, M. Can one hear the shape of a drum? Am. Math. Monthly 73, 1–23 (1966).
    MathSciNet  MATH  Article  Google Scholar 

    30.
    Boaz, N., Stephane, L., Ioannis, K. & Coifman, R. R. Diffusion maps, spectral clustering and eigenfunctions of fokker-planck operators. In Advances in Neural Information Processing Systems 955–962 (2006).

    31.
    Jones, P. W., Mauro, M. & Schul, R. Manifold parametrizations by eigenfunctions of the laplacian and heat kernels. Proc. Natl Acad. Sci. USA 105, 1803–1808 (2008).
    ADS  MathSciNet  CAS  PubMed  MATH  Article  PubMed Central  Google Scholar 

    32.
    Daniel, M., Sergej, A., Melanie, T. & Patil, K. R. Fast automated reconstruction of genome-scale metabolic models for microbial species and communities. Nucleic Acids Res. 46, 7542–7553 (2018).
    Article  CAS  Google Scholar 

    33.
    Pruitt, K. D., Tatiana, T. & Maglott, D. R. Ncbi reference sequences (refseq): a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res. 35, D61–D65 (2006).
    PubMed  PubMed Central  Article  Google Scholar 

    34.
    Mendes-Soares, H., Michael, M., Soares, L. M. & Chia, N. Mminte: an application for predicting metabolic interactions among the microbial species in a community. BMC Bioinforma. 17, 343 (2016).
    Article  Google Scholar 

    35.
    Boaz, N., Stephane, L., Ronald, C. & Kevrekidis, I. G. In Principal Manifolds For Data Visualization and Dimension Reduction pp. 238–260 (Springer, 2008).

    36.
    Moon, K. R. et al. Visualizing structure and transitions in high-dimensional biological data. Nat. Biotechnol. 37, 1482–1492 (2019).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    37.
    Marion, E. et al. The photorespiratory glycolate metabolism is essential for cyanobacteria and might have been conveyed endosymbiontically to plants. Proc. Natl Acad. Sci. USA 105, 17199–17204 (2008).
    Article  Google Scholar 

    38.
    Watzer, B. & Forchhammer, K. Cyanophycin synthesis optimizes nitrogen utilization in the unicellular cyanobacterium synechocystis sp. strain pcc 6803. Appl. Environ. Microbiol. 84, e01298–18 (2018).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    39.
    Sonia, F., Lunn, J. E., Franck, B. & Ferrer, J.-L. The structure of a cyanobacterial sucrose-phosphatase reveals the sugar tongs that release free sucrose in the cell. Plant Cell 17, 2049–2058 (2005).
    Article  CAS  Google Scholar 

    40.
    Amy, N., Thilo, G. & Bassler, K. E. Mesoscopic structures and the laplacian spectra of random geometric graphs. J. Complex Netw. 3, 543–551 (2015).
    MathSciNet  Article  Google Scholar 

    41.
    Komagata, K., Iino, T., Yamada, Y. The Family Acetobacteraceae. In The Prokaryotes (eds Rosenberg, E., DeLong, E. F., Lory, S., Stackebrandt, E., Thompson, F.) pp. 3–78 (Springer, Berlin, Heidelberg, 2014).

    42.
    Meadows, J. A. & Wargo, M. J. Carnitine in bacterial physiology and metabolism. Microbiology 161, 1161 (2015).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    43.
    Kämpfer, P., Svenja, M. & Müller, H. E. Characterization of buttiauxella and kluyvera species by analysis of whole cell fatty acid patterns. Syst. Appl. Microbiol. 20, 566–571 (1997).
    Article  Google Scholar 

    44.
    Parsons, J. B. & Rock, C. O. Bacterial lipids: metabolism and membrane homeostasis. Prog. Lipid Res. 52, 249–276 (2013).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    45.
    Foster, D. B. et al. Phosphatidylethanolamine recognition promotes enteropathogenic E. coli and enterohemorrhagic E. coli host cell attachment. Microb. Pathogenesis 27, 289–301 (1999).
    Article  CAS  Google Scholar 

    46.
    Mayer, C. & Boos, W. Hexose/pentose and hexitol/pentitol metabolism. EcoSal Plus 1 (2005).

    47.
    Reimer, L. C. et al. Bac dive in 2019: bacterial phenotypic data for high-throughput biodiversity analysis. Nucleic Acids Res. 47, D631–D636 (2019).
    CAS  PubMed  Article  PubMed Central  Google Scholar 

    48.
    Devinder, K., Brennan, P. J. & Crick, D. C. Decaprenyl diphosphate synthesis in mycobacterium tuberculosis. J. Bacteriol. 186, 7564–7570 (2004).
    Article  CAS  Google Scholar 

    49.
    Newton, G. L., Nancy, B. & Fahey, R. C. Biosynthesis and functions of mycothiol, the unique protective thiol of Actinobacteria. Microbiol. Mol. Biol. Rev. 72, 471–494 (2008).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    50.
    Yaozhu, W., Xiaofei, Z., Sixue, Z. & Tan, X. Structural and functional insights into corrinoid iron-sulfur protein from human pathogen Clostridium difficile. J. Inorg. Biochem. 170, 26–33 (2017).
    Article  CAS  Google Scholar 

    51.
    Charles, D., Plants-Paris, K., Dayna, B. & DuPont, H. L. Clostridium difficile modulates the gut microbiota by inducing the production of indole, an interkingdom signaling and antimicrobial molecule. mSystems 4, e00346–18 (2019).
    Google Scholar 

    52.
    Luo, H. & Moran, M. A. How do divergent ecological strategies emerge among marine bacterioplankton lineages? Trends Microbiol. 23, 577–584 (2015).
    CAS  PubMed  Article  PubMed Central  Google Scholar 

    53.
    Kanehisa, M. & Goto, S. Kegg: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 28, 27–30 (2000).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    54.
    Neshich, I. A. P., Eduardo, K. & Arruda, P. Genome-wide analysis of lysine catabolism in bacteria reveals new connections with osmotic stress resistance. ISME J. 7, 2400–2410 (2013).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    55.
    Chang, H.-H. et al. Complete genome sequence of ?candidatus sulcia muelleri? ml, an obligate nutritional symbiont of maize leafhopper (dalbulus maidis). Genome Announc. 3, e01483–14 (2015).
    PubMed  PubMed Central  Google Scholar 

    56.
    López-Madrigal, S., Amparo, L., Andres, M. & Gil, R. The link between independent acquisition of intracellular gamma-endosymbionts and concerted evolution in tremblaya princeps. Front. Microbiol. 6, 642 (2015).
    PubMed  PubMed Central  Article  Google Scholar 

    57.
    Dale, C. & Moran, N. A. Molecular interactions between bacterial symbionts and their hosts. Cell 126, 453–465 (2006).
    CAS  PubMed  Article  Google Scholar 

    58.
    Langille, M. G. I. et al. Predictive functional profiling of microbial communities using 16s rrna marker gene sequences. Nat. Biotechnol. 31, 814 (2013).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    59.
    Stilianos, L. et al. Function and functional redundancy in microbial systems. Nat. Ecol. Evol. 2, 936 (2018).
    Article  Google Scholar 

    60.
    Douglas, G. M. et al. Picrust2: an improved and extensible approach for metagenome inference. BioRxiv https://www.biorxiv.org/content/10.1101/672295v2 (2019).

    61.
    Cooley, S. M., Timothy, H., Deeds, E. J. & Ray, J. C. J. A novel metric reveals previously unrecognized distortion in dimensionality reduction of scRNA-seq data. BioRxiv https://www.biorxiv.org/content/10.1101/689851v3 (2019).

    62.
    Thompson, L. R. et al. A communal catalogue reveals earth’s multiscale microbial diversity. Nature 551, 457 (2017).
    ADS  CAS  PubMed  PubMed Central  Article  Google Scholar 

    63.
    Lozupone, C. & Knight, R. UniFrac: a new phylogenetic method for comparing microbial communities. Appl. Environ. Microbiol. 71, 8228–8235 (2005).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    64.
    Franzosa, E. A. et al. Species-level functional profiling of metagenomes and metatranscriptomes. Nat. Methods 15, 962–968 (2018).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    65.
    King, Z. A. et al. Bigg models: a platform for integrating, standardizing and sharing genome-scale models. Nucleic Acids Res. 44, D515–D522 (2015).
    PubMed  PubMed Central  Article  CAS  Google Scholar 

    66.
    Lee, M. D. GtoTree: a user-friendly workflow for phylogenomics. Bioinformatics 1, 3 (2019).
    Google Scholar 

    67.
    Hug, L. A. et al. A new view of the tree of life. Nat. Microbiol. 1, 16048 (2016).
    CAS  PubMed  Article  Google Scholar 

    68.
    Eddy, S. R. Accelerated profile hmm searches. PLoS Comput. Biol. 7, e1002195 (2011).
    ADS  MathSciNet  CAS  PubMed  PubMed Central  Article  Google Scholar 

    69.
    Edgar, R. C. Muscle: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 32, 1792–1797 (2004).
    CAS  PubMed  PubMed Central  Article  Google Scholar 

    70.
    Capella-Gutiérrez, S., Silla-Martínez, J. M. & Gabaldón, T. trimal: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics 25, 1972–1973 (2009).
    PubMed  PubMed Central  Article  CAS  Google Scholar 

    71.
    Price, M. N., Dehal, P. S. & Arkin, A. P. Fasttree 2–approximately maximum-likelihood trees for large alignments. PloS ONE 5, e9490 (2010).
    ADS  PubMed  PubMed Central  Article  CAS  Google Scholar 

    72.
    Letunic, I. & Bork, P. Interactive tree of life (iTol) v4: recent updates and new developments. Nucleic Acids Res. 47, 256–259 (2019).

    73.
    Aravind, S. et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl Acad. Sci. USA 102, 15545–15550 (2005).
    Article  CAS  Google Scholar 

    74.
    R Core Team. R: A Language and Environment for Statistical Computing (R Foundation for Statistical Computing, Vienna, 2019).

    75.
    Benjamini, Y. & Hochberg, Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J. R. Stat. Soc. Ser. B 57, 289–300 (1995).
    MathSciNet  MATH  Google Scholar 

    76.
    Altschul, S. F., Warren, G., Webb, M., Myers, E. W. & Lipman, D. J. Basic local alignment search tool. J. Mol. Biol. 215, 403–410 (1990).
    CAS  PubMed  Article  PubMed Central  Google Scholar 

    77.
    Wright, E. S. Using DECIPHER v2.0 to analyze big biological sequence data in R. R. J. 8, 352–359 (2016).

    78.
    Ward Jr, J. H. Hierarchical grouping to optimize an objective function. J. Am. Stat. Assoc. 58, 236–244 (1963).
    MathSciNet  Article  Google Scholar  More

  • in

    Winter in a warming Arctic

    1.
    Cooper, E. J. Annu. Rev. Ecol. Evol. S. 45, 271–295 (2014).
    Article  Google Scholar 
    2.
    Rapacz, M. et al. Plant Sci. 225, 34–44 (2014).
    CAS  Article  Google Scholar 

    3.
    Bokhorst, S., Bjerke, J. W., Tømmervik, H., Preece, C. & Phoenix, G. K. Ambio 41, 246–255 (2012).
    Article  Google Scholar 

    4.
    Niitynen, P. et al. Nat. Clim. Change https://doi.org/10.1038/s41558-020-00916-4 (2020).

    5.
    Blok, D. et al. Environ. Res. Lett. 6, 035502 (2011).
    Article  Google Scholar 

    6.
    Elmendorf, S. C. et al. Nat. Clim. Change 2, 453–457 (2012).
    Article  Google Scholar 

    7.
    Myers-Smith, I. H. et al. Nat. Clim. Change 5, 887–891 (2015).
    Article  Google Scholar 

    8.
    Snow, Water, Ice and Permafrost in the Arctic (SWIPA) (Arctic Monitoring and Assessment Programme (AMAP), 2017).

    9.
    Zhu, L. K., Ives, A. R., Zhang, C., Guo, Y. Y. & Radeloff, V. C. Nat. Clim. Change 9, 886–893 (2019).
    Article  Google Scholar  More

  • in

    Revealing soil legacy phosphorus to promote sustainable agriculture in Brazil

    1.
    Godfray, H. C. J. et al. Food security: the challenge of feeding 9 billion people. Science 327, 812–818. https://doi.org/10.1126/science.1185383 (2010).
    ADS  CAS  Article  PubMed  Google Scholar 
    2.
    OECD/FAO. Agricultural Outlook 2018–2027, OECD Publishing, Paris/Food and Agriculture Organization of the United Nations, Rome. https://doi.org/10.1787/agr_outlook-2018-en (2018).

    3.
    FAO. The future of food and agriculture – Trends and challenges. Rome. (2017).

    4.
    Strassburg, B. B. N. et al. When enough should be enough: improving the use of current agricultural lands could meet production demands and spare natural habitats in Brazil. Glob. Environ. Chang. 28, 84–97 (2014).
    Article  Google Scholar 

    5.
    Bowman, M. S. et al. Persistence of cattle ranching in the Brazilian Amazon: a spatial analysis of the rationale for beef production. Land Use Policy 29, 558–568 (2012).
    Article  Google Scholar 

    6.
    Bustamante, M. M. C. et al. Estimating greenhouse gas emissions from cattle raising in Brazil. Clim. Chang. 115, 559–577 (2012).
    ADS  CAS  Article  Google Scholar 

    7.
    Oliveira, D. M. S. et al. Is the expansion of sugarcane over pasturelands a sustainable strategy for Brazil’s bioenergy industry?. Renew. Sust. Energy Rev. 102, 346–355 (2019).
    Article  Google Scholar 

    8.
    Roy, E. D. et al. Soil phosphorus sorption capacity after three decades of intensive fertilization in Mato Grosso, Brazil. Agric. Ecos. Environ. 249, 206–214 (2017).
    CAS  Article  Google Scholar 

    9.
    Jarvie, H. P. et al. The pivotal role of phosphorus in a resilient water–energy–food security nexus. J. Environ. Qual. 44, 1049–1062 (2015).
    CAS  Article  Google Scholar 

    10.
    ANDA – Associação Nacional para Difusão de Adubos. Indicadores – Fertilizantes entregues ao mercado. https://anda.org.br/index.php?mpg=03.00.00 (2017).

    11.
    U.S. Geological Survey. Mineral commodity summaries 2016. https://doi.org/10.3133/70140094 (2016).

    12.
    MacDonald, G. K., Bennett, E. M., Potter, P. A. & Ramankutty, N. Agronomic phosphorus imbalances across the world’s croplands. Proc. Nat. Acad. Sci. 108(7), 3086–3091. https://doi.org/10.1073/pnas.1010808108 (2011).
    ADS  Article  PubMed  Google Scholar 

    13.
    Lun, F. et al. Global and regional phosphorus budgets in agricultural systems and their implications for phosphorus-use efficiency. Earth Syst. Sci. Data 10, 1–18. https://doi.org/10.5194/essd-10-1-2018 (2018).
    ADS  Article  Google Scholar 

    14.
    Rodrigues, M., Pavinato, P. S., Withers, P. J. A., Teles, A. P. B. & Herrera, W. F. B. Legacy phosphorus and no tillage agriculture in tropical oxisols of the Brazilian savanna. Sci. Total Environ. 542, 1050–1061 (2016).
    ADS  CAS  Article  Google Scholar 

    15.
    Sattari, S. Z., Bouwman, A. F., Giller, K. E. & van Ittersum, M. K. Residual soil phosphorus as the missing piece in the global phosphorus crisis puzzle. Proc. Nat. Acad. Sci. 109, 6348–6353 (2012).
    ADS  CAS  Article  Google Scholar 

    16.
    Rowe, H. et al. Integrating legacy soil phosphorus into sustainable nutrient management practices on farms. Nutr. Cycl. Agroec. 104, 393–412 (2016).
    CAS  Article  Google Scholar 

    17.
    Shen, J. et al. Phosphorus dynamics: from soil to plant. Plant Phys. 156, 997–1005 (2011).
    CAS  Article  Google Scholar 

    18.
    IBGE – Instituto Brasileiro de Geografia e Estatística. Sistema IBGE de Recuperação Automática – SIDRA. Brasil. https://sidra.ibge.gov.br (2018).

    19.
    Projeto MapBiomas. Coleção 4.0 da Série Anual de Mapas de Cobertura e Uso de Solo do Brasil. https://mapbiomas.org (2019).

    20.
    Dias, L. C. P., Pimenta, F. M., Santos, A. B., Costa, M. H. & Ladle, R. J. Patterns of land use, extensification, and intensification of Brazilian agriculture. Glob. Chang. Biol. 22, 2887–2903 (2016).
    ADS  Article  Google Scholar 

    21.
    Du, E. et al. Global patterns of terrestrial nitrogen and phosphorus limitation. Nat. Geosci. 13, 221–226. https://doi.org/10.1038/s41561-019-0530-4 (2020).
    ADS  CAS  Article  Google Scholar 

    22.
    Withers, P. J. A. et al. Transitions to sustainable management of phosphorus in Brazilian agriculture. Sci. Rep. 8, 2537. https://doi.org/10.1038/s41598-018-20887-z (2018).
    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

    23.
    FAO. World fertiliser trends and outlook to 2018. Rome. 53p. (2015).

    24.
    Kassam, A., Friedrich, T. & Derpsch, R. Global spread of conservation agriculture. Int. J. Environ. Studies. 76, 29–51. https://doi.org/10.1080/00207233.2018.1494927 (2018).
    CAS  Article  Google Scholar 

    25.
    Franchini, J. C. et al. Evolution of crop yields in different tillage and cropping systems over two decades in southern Brazil. Field Crops Res. 137, 178–185 (2012).
    Article  Google Scholar 

    26.
    Roy, E. D. et al. The phosphorus cost of agricultural intensification in the tropics. Nat. Plants 2, 16043. https://doi.org/10.1038/nplants.2016.43 (2016).
    CAS  Article  PubMed  Google Scholar 

    27.
    Schoumans, O. F., Bouraoui, F., Kabbe, C., Oenema, O. & van Dijk, K. C. Phosphorus management in Europe in a changing world. Ambio 44(Suppl. 2), S180–S192. https://doi.org/10.1007/s13280-014-0613-9 (2015).
    CAS  Article  PubMed  Google Scholar 

    28.
    Antoniadis, V., Hatzis, F., Bachtsevanidis, D. & Koutroubas, S. D. Phosphorus availability in low-P and acidic soils as affected by liming and P addition. Commun. Soil Sci. Plant Anal. 46, 1288–1298. https://doi.org/10.1080/00103624.2015.1033539 (2015).
    CAS  Article  Google Scholar 

    29.
    Bouwman, A. F., Beusen, A. H. W. & Billen, G. Human alteration of the global nitrogen and phosphorus soil balances for the period 1970–2050, Global Biogeoc. Cyc. 23, GB0A04. https://doi.org/10.1029/2009GB003576 (2009).

    30.
    Withers, P. J. A. et al. Stewardship to tackle global phosphorus inefficiency: the case of Europe. Ambio 44(2), 193–206 (2015).
    CAS  Article  Google Scholar 

    31.
    Soltangheisi, A. et al. Improving phosphorus sustainability of sugarcane production in Brazil. GCB Bioenergy 11, 1444–1455. https://doi.org/10.1111/gcbb.12650 (2019).
    CAS  Article  PubMed  Google Scholar 

    32.
    MacDonald, G. K. et al. Guiding phosphorus stewardship for multiple ecosystem services. Ecos. Health Sust. 2(12), e01251. https://doi.org/10.1002/ehs2.1251 (2016).
    Article  Google Scholar 

    33.
    Schipanski, M. E. et al. Realizing resilient food systems. Bioscience 66(7), 600–610. https://doi.org/10.1093/biosci/biw052 (2016).
    Article  Google Scholar 

    34.
    MAPA – Ministério da Agricultura, Pecuária e Abastecimento. Projeções do Agronegócio. Brasil 2015/16 a 2025/26. Projeções de Longo Prazo. 138p. (2016).

    35.
    Forest Act. Federal Law # 12,651. https://www.planalto.gov.br/ccivil_03/Ato2011-2014/2012/Lei/L12651compilado.htm (2012).

    36.
    Dias-Filho, M. B. Diagnóstico das Pastagens no Brasil. Embrapa Amazônia Oriental. Série Documentos 402. Belém-PA, 36p. (2014).

    37.
    Bouwman, A. F. et al. Lessons from temporal and spatial patterns in global use of N and P fertiliser on cropland. Sci. Rep. 7, 40366. https://doi.org/10.1038/srep40366 (2017).
    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

    38.
    MacDonald, G. K., Bennett, E. M. & Carpenter, S. R. Embodied phosphorus and the global connections of United States agriculture. Environ. Res. Letters 7, 044024. https://doi.org/10.1088/1748-9326/7/4/044024 (2012).
    ADS  CAS  Article  Google Scholar 

    39.
    Novais, R.F., Smyth, T.J. & Nunes, F.N. Fósforo. In: Novais, R.F. et al. Fertilidade do solo. Viçosa, MG, Sociedade Brasileira de Ciência do Solo, p. 471–537 (2007).

    40.
    Negassa, W. & Leinweber, P. How does the Hedley sequential phosphorus fractionation reflect impacts of land use and management on soil phosphorus: a review. J. Plant Nutr. Soil Sci. 172, 305–325 (2009).
    CAS  Article  Google Scholar 

    41.
    CONAB – Companhia Nacional de Abastecimento. Acompanhamento da safra brasileira de grãos. Brasília. https://www.conab.gov.br/info-agro/safras/graos (2018).

    42.
    Dong, W. Y. et al. Responses of soil microbial communities and enzyme activities to nitrogen and phosphorus additions in Chinese fir plantations of subtropical China. Biogeosci. 12, 5537–5546. https://doi.org/10.5194/bg-12-5537-2015 (2015).
    ADS  Article  Google Scholar 

    43.
    Cherubin, M. R. et al. Sugarcane straw removal: Implications to soil fertility and fertiliser demand in Brazil. Bioeng. Res. 12, 888–900. https://doi.org/10.1007/s12155-019-10021-w (2019).
    CAS  Article  Google Scholar 

    44.
    Balemi, T. & Negisho, K. Management of soil phosphorus and plant adaptation mechanisms to phosphorus stress for sustainable crop production: a review. J. Soil Sci. Plant Nutr. 12(3), 547–562. https://doi.org/10.4067/S0718-95162012005000015 (2012).
    Article  Google Scholar 

    45.
    Khan, M. S., Zaidi, A. & Wani, P. A. Role of phosphate-solubilizing microorganisms in sustainable agriculture – a review. Agron. Sust. Develop. 27, 29–43. https://doi.org/10.1051/agro:2006011 (2007).
    Article  Google Scholar 

    46.
    Kalayu, G. Phosphate solubilizing microorganisms: promising approach as biofertilisers. Int. J. Agron. 2019, 4917256. https://doi.org/10.1155/2019/4917256 (2019).
    CAS  Article  Google Scholar 

    47.
    Simpson, R. J. et al. Strategies and agronomic interventions to improve the phosphorus-use efficiency of farming systems. Plant Soil 349, 89–120. https://doi.org/10.1007/s11104-011-0880-1 (2011).
    CAS  Article  Google Scholar 

    48.
    Almeida, D. S., Penn, C. J. & Rosolem, C. A. Assessment of phosphorus availability in soil cultivated with ruzigrass. Geoderma 312, 64–73 (2018).
    ADS  CAS  Article  Google Scholar 

    49.
    Bindraban, P. S., Dimkpa, C., Nagarajan, L., Roy, A. & Rabbinge, R. Revisiting fertilisers and fertilisation strategies for improved nutrient uptake by plants. Biol. Fert. Soils 51, 897–911. https://doi.org/10.1007/s00374-015-1039-7 (2015).
    CAS  Article  Google Scholar 

    50.
    Johnston, A. M. & Bruulsema, T. W. 4R nutrient stewardship for improved nutrient use efficiency. Procedia Eng. 83, 365–370. https://doi.org/10.1016/j.proeng.2014.09.029 (2014).
    Article  Google Scholar 

    51.
    Shigaki, F., Sharpley, A. & Prochnow, L. I. Animal-based agriculture, phosphorus management and water quality in Brazil: options for the future. Sci. Agric. 63(2), 194–209. https://doi.org/10.1590/S0103-90162006000200013 (2006).
    CAS  Article  Google Scholar 

    52.
    Almagro, A., Oliveira, P. T. S., Nearing, M. A. & Hagemann, S. Projected climate change impacts in rainfall erosivity over Brazil. Sci. Rep. 7, 8130. https://doi.org/10.1038/s41598-017-08298-y (2017).
    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

    53.
    FAO – Food and agriculture organization. The world agricultural production. https://faostat.fao.org/site/339/default.aspx (2006).

    54.
    Nunes, S. P. O campo político da agricultura familiar e a idéia de “Projeto alternativo de desenvolvimento”. Master dissertation. Federal University of Paraná – UFPR. Curitiba. 152p. (2007).

    55.
    Alves, E., Teixeira Filho, A. & Tolloni, H. Demographic aspects of agricultural development: Brazil, 1950–74. In: Yeganiantz, L. (Ed.). Brazilian agriculture and agricultural research. Brasília: Embrapa, p. 9–60 (1984).

    56.
    IFA – International Fertiliser Association. Ifadata. https://ifadata.fertiliser.org/ucResult.aspx?temp=20160502093015 (2016).

    57.
    Marin, F. R., Pilau, F. G., Spolador, H. F. S., Otto, O. & Pedreira, C. G. S. Intensificação sustentável da agricultura brasileira, cenários para 2050. Rev. Pol. Agríc. XXV(3), 108–124 (2016).
    Google Scholar 

    58.
    Nicolella, A. C., Dragone, D. S. & Bacha, C. J. C. Determinantes da demanda de fertilizantes no Brasil no período de 1970 a 2002. Rev. Econ. Sociol. Rural 43(1), 81–100. https://doi.org/10.1590/S0103-20032005000100005 (2005).
    Article  Google Scholar 

    59.
    QGIS Development Team. QGIS Geographic Information System. Open Source Geospatial Foundation Project. https://qgis.osgeo.org (2018).

    60.
    CNA Brasil – Confederação Nacional da Agricultura. https://www.cnabrasil.org.br/noticias/assocon-divulga-crescimento-de-5-no-numero-de-bovinos-confinados-em-2017 (2017).

    61.
    Costa-Junior, C., Cerri, C. E., Pires, A. V. & Cerri, C. C. Net greenhouse gas emissions from manure management using anaerobic digestion technology in a beef cattle feedlot in Brazil. Sci. Total Environ. 505, 1018–1025 (2015).
    ADS  CAS  Article  Google Scholar 

    62.
    Prado, R. M., Caione, G. & Campos, C. N. S. Filter Cake and Vinasse as fertilisers contributing to conservation agriculture. Appl. Environ. Soil Sci. https://doi.org/10.1155/2013/581984 (2013).
    Article  Google Scholar 

    63.
    Francisco, E. A. B., Câmara, G. M. S. & Segatelli, C. R. Estado nutricional e produção do capim-pé-de-galinha e da soja cultivada em sucessão em sistema antecipado de adubação. Bragantia 66(2), 259–266 (2007).
    Article  Google Scholar 

    64.
    Pauletti, V. Nutrientes: teor e interpretação. Campinas: Fundação ABC/Fundação Cargill, 59p. (1998).

    65.
    Broch, D. L. & Ranno, S. K. Fertilidade do solo, Adubação e Nutrição da Cultura da Soja. In: Fundação MS, Tecnologia de Produção: Soja e Milho 2012/2013. Maracaju: Fundação MS, p. 2–38 (2012).

    66.
    Corrêa, J. C., Nicoloso, R. S., Menezes, J. F. S. & Benites, V. M. Critérios Técnicos para Recomendação de Biofertilizante de Origem Animal em Sistemas de Produção Agrícolas e Florestais. https://pt.engormix.com/suinocultura/artigos/biofertilizante-producao-agricolas-florestais-t37769.htm (2012).

    67.
    Rosseto, R., Dias, F. L. F., Vitti, A. C., Cantarella, H. & Landell, M. G. A. Manejo conservacionista e reciclagem de nutrientes em cana-de-açúcar tendo em vista a colheita mecânica. Inf. Agron. 124, 8–13 (2008).
    Google Scholar 

    68.
    Malavolta, E. Manual de Nutrição Mineral de Plantas (Agronômica Ceres, São Paulo, 2006).
    Google Scholar  More

  • in

    Coupled changes in soil organic carbon fractions and microbial community composition in urban and suburban forests

    1.
    Hui, D., Deng, Q., Tian, H. & Luo, Y. Climate Change and Carbon Sequestration in Forest Ecosystems 555–594 (Springer, New York, 2017).
    Google Scholar 
    2.
    Lal, R. & Augustin, B. Carbon Sequestration in Urban Ecosystems (Springer, Dordrecht, 2012).
    Google Scholar 

    3.
    Zhang, J. & Sta, P. Effects of urbanization on forest vegetation, soil and landscape. Acta Ecol. Sin. 19, 654–658 (1999).
    Google Scholar 

    4.
    George, K., Ziska, L. H., Bunce, J. A. & Quebedeaux, B. Elevated atmospheric CO2 concentration and temperature across an urban–rural transect. Atmos. Environ. 41, 7654–7665. https://doi.org/10.1016/j.atmosenv.2007.08.018 (2007).
    ADS  CAS  Article  Google Scholar 

    5.
    Pouyat, R. V. et al. Soil Carbon in Urban Forest Ecosystems (CRC Press, Cambridge, 2003).
    Google Scholar 

    6.
    Zhang, W. et al. Methane uptake in forest soils along an urban-to-rural gradient in Pearl River Delta, South China. Sci. Rep. 4, 5120. https://doi.org/10.1038/srep05120 (2014).
    CAS  Article  PubMed  PubMed Central  Google Scholar 

    7.
    Zhou, D. et al. Spatiotemporal trends of urban heat island effect along the urban development intensity gradient in China. Sci. Total Environ. 544, 617–626. https://doi.org/10.1016/j.scitotenv.2015.11.168 (2016).
    ADS  CAS  Article  PubMed  Google Scholar 

    8.
    Norman, J., MacLean, H. L. & Kennedy, C. A. Comparing high and low residential density: Life-cycle analysis of energy use and greenhouse gas emissions. J. Urban Plan. Dev. 132, 10–21. https://doi.org/10.1061//ASCE/0733-9488/2006/132:1/10 (2006).
    Article  Google Scholar 

    9.
    Carreiro, M. M. & Tripler, C. E. Forest remnants along urban-rural gradients: Examining their potential for global change research. Ecosystems 8, 568–582. https://doi.org/10.1007/s10021-003-0172-6 (2005).
    Article  Google Scholar 

    10.
    Meng, L. et al. Responses of ecosystem carbon cycle to experimental warming: A meta-analysis. Ecology 94, 726. https://doi.org/10.1890/12-0279.1 (2013).
    Article  Google Scholar 

    11.
    Lukac, M. et al. Forest soil carbon cycle under elevated CO2—A case of increased throughput?. Forestry 82, 75–86. https://doi.org/10.1093/forestry/cpn041 (2009).
    Article  Google Scholar 

    12.
    Luo, Y. & Weng, E. Dynamic disequilibrium of the terrestrial carbon cycle under global change. Trends Ecol. Evol. 26, 96–104. https://doi.org/10.1016/j.tree.2010.11.003 (2011).
    Article  PubMed  Google Scholar 

    13.
    Deng, Q. et al. Effects of CO2 enrichment, high nitrogen deposition and high precipitation on a model forest ecosystem in southern China. Chin. J. Plant Ecol. 33, 1023–1033 (2009).
    Google Scholar 

    14.
    De Graaff, M., Van Groenigen, K., Six, J. & Hungate, B. K. C. Interactions between plant growth and soil nutrient cycling under elevated CO2: A meta-analysis. Glob. Change Biol. 12, 2077–2091. https://doi.org/10.1111/j.1365-2486.2006.01240.x (2010).
    Article  Google Scholar 

    15.
    Chen, X., Deng, Q., Lin, G., Lin, M. & Wei, H. Changing rainfall frequency affects soil organic carbon concentrations by altering non-labile soil organic carbon concentrations in a tropical monsoon forest. Sci. Total Environ. 644, 762–769. https://doi.org/10.1016/j.scitotenv.2018.07.035 (2018).
    ADS  CAS  Article  PubMed  Google Scholar 

    16.
    Stockmann, U. et al. The knowns, known unknowns and unknowns of sequestration of soil organic carbon. Agric. Ecosyst. Environ. 164, 80–99. https://doi.org/10.1016/j.agee.2012.10.001 (2013).
    CAS  Article  Google Scholar 

    17.
    von Lützow, M. et al. SOM fractionation methods: Relevance to functional pools and to stabilization mechanisms. Soil Biol. Biochem. 39, 2183–2207. https://doi.org/10.1016/j.soilbio.2007.03.007 (2007).
    CAS  Article  Google Scholar 

    18.
    Garten, C. T. Comparison of forest soil carbon dynamics at five sites along a latitudinal gradient. Geoderma 167–168, 30–40. https://doi.org/10.1016/j.geoderma.2011.08.007 (2011).
    ADS  CAS  Article  Google Scholar 

    19.
    Mclauchlan, K. K. & Hobbie, S. E. Comparison of labile soil organic matter fractionation techniques. Soil Sci. Soc. Am. J. 68, S34–S34. https://doi.org/10.2136/sssaj2004.1616 (2004).
    Article  Google Scholar 

    20.
    von Lützow, M. et al. Stabilization of organic matter in temperate soils: Mechanisms and their relevance under different soil conditions—A review. Eur. J. Soil Sci. 57, 426–445. https://doi.org/10.1111/j.1365-2389.2006.00809.x (2006).
    CAS  Article  Google Scholar 

    21.
    Schmidt, M. W. et al. Persistence of soil organic matter as an ecosystem property. Nature 478, 49–56. https://doi.org/10.1038/nature10386 (2011).
    ADS  CAS  Article  PubMed  Google Scholar 

    22.
    Pan, G. et al. Soil carbon sequestration with bioactivity: A new emerging frontier for sustainable soil management. Adv. Earth Sci. 30, 940–951 (2015).
    CAS  Google Scholar 

    23.
    You, Y. et al. Relating microbial community structure to functioning in forest soil organic carbon transformation and turnover. Ecol. Evol. 4, 633–647. https://doi.org/10.1002/ece3.969 (2014).
    Article  PubMed  PubMed Central  Google Scholar 

    24.
    Shao, S. et al. Linkage of microbial residue dynamics with soil organic carbon accumulation during subtropical forest succession. Soil Biol. Biochem. 114, 114–120. https://doi.org/10.1016/j.soilbio.2017.07.007 (2017).
    CAS  Article  Google Scholar 

    25.
    Cotrufo, M. F., Wallenstein, M. D., Boot, C. M., Denef, K. & Paul, E. The Microbial Efficiency-Matrix Stabilization (MEMS) framework integrates plant litter decomposition with soil organic matter stabilization: Do labile plant inputs form stable soil organic matter?. Glob. Change Biol. 19, 988–995. https://doi.org/10.1111/gcb.12113 (2013).
    ADS  Article  Google Scholar 

    26.
    Newbound, M., Bennett, L. T., Tibbits, J. & Kasel, S. Soil chemical properties, rather than landscape context, influence woodland fungal communities along an urban-rural gradient. Austral. Ecol. 37, 236–247. https://doi.org/10.1111/j.1442-9993.2011.02269.x (2012).
    Article  Google Scholar 

    27.
    Chai, L. et al. Urbanization altered regional soil organic matter quantity and quality: Insight from excitation emission matrix (EEM) and parallel factor analysis (PARAFAC). Chemosphere 220, 249–258. https://doi.org/10.1016/j.chemosphere.2018.12.132 (2019).
    ADS  CAS  Article  PubMed  Google Scholar 

    28.
    Wang, Y. D., Wang, H. M., Xu, M. J., Ma, Z. Q. & Wang, Z. L. Soil organic carbon stocks and CO2 effluxes of native and exotic pine plantations in subtropical China. CATENA 128, 167–173. https://doi.org/10.1016/j.catena.2015.02.003 (2015).
    CAS  Article  Google Scholar 

    29.
    Zhou, G. et al. Old-growth forests can accumulate carbon in soils. Science 314, 1417. https://doi.org/10.1126/science.1130168 (2006).
    ADS  CAS  Article  PubMed  Google Scholar 

    30.
    Chen, H. et al. Changes in soil carbon sequestration in Pinus massoniana forests along an urban-to-rural gradient of southern China. Biogeosciences 10, 6609–6616. https://doi.org/10.5194/bg-10-6609-2013 (2013).
    ADS  CAS  Article  Google Scholar 

    31.
    Fang, Y. T., Gundersen, P., Mo, J. M. & Zhu, W. X. Input and output of dissolved organic and inorganic nitrogen in subtropical forests of South China under high air pollution. Biogeosciences 5, 339–352 (2008).
    ADS  CAS  Article  Google Scholar 

    32.
    Hou, E., Xiang, H., Li, J., Li, J. & Wen, D. Heavy metal contamination in soils of remnant natural and plantation forests in an urbanized region of the Pearl River Delta, China. Forests 5, 885–900. https://doi.org/10.3390/f5050885 (2014).
    Article  Google Scholar 

    33.
    Huang, L. The Characteristics of Remnant Lower Subtropical Evergreen Broad-Leaved Forests and Their Relationships with Environmental Factors in Urbanized Areas (South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, 2012).
    Google Scholar 

    34.
    Song, P. et al. Effects of historical logging on soil microbial communities in a subtropical forest in southern China. Plant Soil 397, 115–126. https://doi.org/10.1007/s11104-015-2553-y (2015).
    CAS  Article  Google Scholar 

    35.
    Sun, F. F., da Wen, Z., Kuang, Y. W., Li, J. & Zhang, J. G. Concentrations of sulphur and heavy metals in needles and rooting soils of Masson pine (Pinus massoniana L.) trees growing along an urban-rural gradient in Guangzhou, China. Environ. Monit. Assess. 154, 263–274. https://doi.org/10.1007/s10661-008-0394-3 (2009).
    CAS  Article  PubMed  Google Scholar 

    36.
    Groffman, P. M., Pouyat, R. V., McDonnell, M. J., Pickett, S. T. & Zipperer, W. C. Carbon pools and trace gas fluxes in urban forest soils. In Soil Management and Greenhouse Effect: Advances in Soil Science (eds Kimble, J. M. et al.) 147–158 (CRC Press, Amsterdam, 1995).
    Google Scholar 

    37.
    Koerner, B. A. & Klopatek, J. M. Carbon fluxes and nitrogen availability along an urban–rural gradient in a desert landscape. Urban Ecosyst. 13, 1–21. https://doi.org/10.1007/s11252-009-0105-z (2009).
    Article  Google Scholar 

    38.
    Dungait, J. A. J., Hopkins, D. W., Gregory, A. S. & Whitmore, A. P. Soil organic matter turnover is governed by accessibility not recalcitrance. Glob. Change Biol. 18, 1781–1796. https://doi.org/10.1111/j.1365-2486.2012.02665.x (2012).
    ADS  Article  Google Scholar 

    39.
    Leifeld, J. & Kögel-Knabner, I. Soil organic matter fractions as early indicators for carbon stock changes under different land-use?. Geoderma 124, 143–155. https://doi.org/10.1016/j.geoderma.2004.04.009 (2005).
    ADS  CAS  Article  Google Scholar 

    40.
    Pouyat, R., Groffman, P., Yesilonis, I. & Hernandez, L. Soil carbon pools and fluxes in urban ecosystems. Environ. Pollut. 116, S107–S118. https://doi.org/10.1016/s0269-7491(01)00263-9 (2002).
    CAS  Article  PubMed  Google Scholar 

    41.
    Nadelhoffer, K. J. & Raich, J. W. Fine root production estimates and belowground carbon allocation in forest ecosystems. Ecology 73, 1139–1147. https://doi.org/10.2307/1940664 (1992).
    Article  Google Scholar 

    42.
    Luo, Z., Feng, W., Luo, Y., Baldock, J. & Wang, E. Soil organic carbon dynamics jointly controlled by climate, carbon inputs, soil properties and soil carbon fractions. Glob. Change Biol. 23, 4430–4439. https://doi.org/10.1111/gcb.13767 (2017).
    ADS  Article  Google Scholar 

    43.
    Urbanová, M., Šnajdr, J. & Baldrian, P. Composition of fungal and bacterial communities in forest litter and soil is largely determined by dominant trees. Soil Biol. Biochem. 84, 53–64. https://doi.org/10.1016/j.soilbio.2015.02.011 (2015).
    CAS  Article  Google Scholar 

    44.
    Bowden, R. D. et al. litter input controls on soil carbon in a temperate deciduous forest. Soil Sci. Soc. Am. J. 78, S66–S75. https://doi.org/10.2136/sssaj2013.09.0413nafsc (2014).
    Article  Google Scholar 

    45.
    Carreiro, M. M., Howe, K., Parkhurst, D. F. & Pouyat, R. V. Variation in quality and decomposability of red oak leaf litter along an urban-rural gradient. Biol. Fertil. Soils 30, 258–268. https://doi.org/10.1007/s003740050617 (1999).
    Article  Google Scholar 

    46.
    Xu, X. & Hirata, E. Decomposition patterns of leaf litter of seven common canopy species in a subtropical forest: N and P dynamics. Plant Soil 273, 279–289. https://doi.org/10.1007/s11104-004-8069-5 (2005).
    CAS  Article  Google Scholar 

    47.
    Wang, Q., Wang, S., Feng, Z. & Huang, Y. Active soil organic matter and its relationship with soil quality. Acta Ecol. Sin. 25, 513–519 (2005).
    CAS  Google Scholar 

    48.
    Hu, S., Coleman, D. C., Carroll, C. R., Hendrix, P. F. & Beare, M. H. Labile soil carbon pools in subtropical forest and agricultural ecosystems as influenced by management practices and vegetation types. Agric. Ecosyst. Environ. 65, 69–78. https://doi.org/10.1016/s0167-8809(97)00049-2 (1997).
    CAS  Article  Google Scholar 

    49.
    Blair, G. J., Lefroy, R. & Lisle, L. Soil carbon fractions based on their degree of oxidation, and the development of a carbon management index for agricultural systems. Aust. J. Agric. Res. 46, 393–406. https://doi.org/10.1071/AR9951459 (1995).
    Article  Google Scholar 

    50.
    Chen, X. et al. Effects of precipitation on soil organic carbon fractions in three subtropical forests in southern China. J. Plant Ecol. 9(1), 10–19. https://doi.org/10.1093/jpe/rtv027 (2015).
    Article  Google Scholar 

    51.
    Culman, S. W. et al. Permanganate oxidizable carbon reflects a processed soil fraction that is sensitive to management. Soil Sci. Soc. Am. J. 76, 494. https://doi.org/10.2136/sssaj2011.0286 (2012).
    ADS  CAS  Article  Google Scholar 

    52.
    Chen, S., Wang, X. & Lu, F. Research on forest microbial community function variations in urban and suburban forests. Chin. J. Soil Sci. 1, 614–620. https://doi.org/10.1001/archophthalmol.2012.1393 (2012).
    Article  Google Scholar 

    53.
    Zhao, Z. & Guo, H. Effects of urbanization on the quantity changes of microbes in urban-to-rural gradient forest soil. J. Anhui Agric. Sci. 38, 5188–5190 (2010).
    Google Scholar 

    54.
    Hackl, E., Pfeffer, M., Donat, C., Bachmann, G. & Zechmeister-Boltenstern, S. Composition of the microbial communities in the mineral soil under different types of natural forest. Soil Biol. Biochem. 37, 661–671. https://doi.org/10.1016/j.soilbio.2004.08.023 (2005).
    CAS  Article  Google Scholar 

    55.
    Brant, J. B., Myrold, D. D. & Sulzman, E. W. Root controls on soil microbial community structure in forest soils. Oecologia 148, 650–659. https://doi.org/10.1007/s00442-006-0402-7 (2006).
    ADS  Article  PubMed  Google Scholar 

    56.
    Wang, H. et al. Stable soil organic carbon is positively linked to microbial-derived compounds in four plantations of subtropical China. Biogeosci. Discuss. 10, 18093–18119. https://doi.org/10.5194/bgd-10-18093-2013 (2013).
    ADS  Article  Google Scholar 

    57.
    Six, J., Frey, S. D., Thiet, R. K. & Batten, K. M. Bacterial and fungal contributions to carbon sequestration in agroecosystems. Soil Sci. Soc. Am. J. 70, 555–569. https://doi.org/10.2136/sssaj2004.0347 (2006).
    ADS  CAS  Article  Google Scholar 

    58.
    Ziegler, S. E., Billings, S. A., Lane, C. S., Li, J. & Fogel, M. L. Warming alters routing of labile and slower-turnover carbon through distinct microbial groups in boreal forest organic soils. Soil Biol. Biochem. 60, 23–32. https://doi.org/10.1016/j.soilbio.2013.01.001 (2013).
    CAS  Article  Google Scholar 

    59.
    Baum, C., Fienemann, M., Glatzel, S. & Gleixner, G. Overstory-specific effects of litter fall on the microbial carbon turnover in a mature deciduous forest. For. Ecol. Manage. 258, 109–114. https://doi.org/10.1016/j.foreco.2009.03.047 (2009).
    Article  Google Scholar 

    60.
    Creamer, C. A. et al. Microbial community structure mediates response of soil C decomposition to litter addition and warming. Soil Biol. Biochem. 80, 175–188. https://doi.org/10.1016/j.soilbio.2014.10.008 (2015).
    CAS  Article  Google Scholar 

    61.
    Kramer, C. & Gleixner, G. Variable use of plant- and soil-derived carbon by microorganisms in agricultural soils. Soil Biol. Biochem. 38, 3267–3278. https://doi.org/10.1016/j.soilbio.2006.04.006 (2006).
    CAS  Article  Google Scholar 

    62.
    Brabcová, V., Štursová, M. & Baldrian, P. Nutrient content affects the turnover of fungal biomass in forest topsoil and the composition of associated microbial communities. Soil Biol. Biochem. 118, 187–198. https://doi.org/10.1016/j.soilbio.2017.12.012 (2018).
    CAS  Article  Google Scholar 

    63.
    Kaur, A., Chaudhary, A., Kaur, A., Choudhary, R. & Kaushik, R. Phospholipid fatty acid—A bioindicator of environment monitoring and assessment in soil ecosystem. Curr. Sci. 89, 1103–1112 (2005).
    CAS  Google Scholar 

    64.
    Hanson, C. A., Allison, S. D., Bradford, M. A., Wallenstein, M. D. & Treseder, K. K. Fungal taxa target different carbon sources in forest soil. Ecosystems 11, 1157–1167. https://doi.org/10.1007/s10021-008-9186-4 (2008).
    CAS  Article  Google Scholar 

    65.
    Liu, M., Hu, F. & Chen, X. A review on mechanisms of soil organic carbon stabilization. Acta Ecol. Sin. 27, 2642–2650 (2007).
    CAS  Article  Google Scholar 

    66.
    Fang, Y. et al. Nitrogen deposition and forest nitrogen cycling along an urban-rural transect in southern China. Glob. Change Biol. 17, 872–885. https://doi.org/10.1111/j.1365-2486.2010.02283.x (2011).
    ADS  Article  Google Scholar 

    67.
    Huang, L., Zhu, W., Ren, H., Chen, H. & Wang, J. Impact of atmospheric nitrogen deposition on soil properties and herb-layer diversity in remnant forests along an urban–rural gradient in Guangzhou, southern China. Plant Ecol. 213, 1187–1202. https://doi.org/10.1007/s11258-012-0080-y (2012).
    Article  Google Scholar 

    68.
    He, J. et al. Stoichiometric characteristics of soil C, N and P in subtropical forests along an urban-to-suburb gradient. Chin. J. Ecol. 35, 591–596 (2016).
    Google Scholar 

    69.
    Wu, J. et al. Prolonged acid rain facilitates soil organic carbon accumulation in a mature forest in Southern China. Sci. Total Environ. 544, 94–102. https://doi.org/10.1016/j.scitotenv.2015.11.025 (2016).
    ADS  CAS  Article  PubMed  Google Scholar 

    70.
    Duan, H., Liu, J., Deng, Q., Chen, X. & Zhang, D. Effects of elevated CO2 and N deposition on plant biomass accumulation and allocation in subtropical forest ecosystems: A mesocosm study. Chin. J. Plant Ecol. 33, 570–579. https://doi.org/10.1080/01443610410001685646 (2009).
    CAS  Article  Google Scholar 

    71.
    Chen, X., Liu, J., Deng, Q., Yan, J. & Zhang, D. Effects of elevated CO2 and nitrogen addition on soil organic carbon fractions in a subtropical forest. Plant Soil 357, 25–34. https://doi.org/10.1007/s11104-012-1145-3 (2012).
    CAS  Article  Google Scholar 

    72.
    Bird, J. A., Herman, D. J. & Firestone, M. K. Rhizosphere priming of soil organic matter by bacterial groups in a grassland soil. Soil Biol. Biochem. 43, 718–725. https://doi.org/10.1016/j.soilbio.2010.08.010 (2011).
    CAS  Article  Google Scholar 

    73.
    Hopkins, F. M. et al. Increased belowground carbon inputs and warming promote loss of soil organic carbon through complementary microbial responses. Soil Biol. Biochem. 76, 57–69. https://doi.org/10.1016/j.soilbio.2014.04.028 (2014).
    CAS  Article  Google Scholar 

    74.
    Curlevski, N. J. A., Drigo, B., Cairney, J. W. G. & Anderson, I. C. Influence of elevated atmospheric CO2 and water availability on soil fungal communities under Eucalyptus saligna. Soil Biol. Biochem. 70, 263–271. https://doi.org/10.1016/j.soilbio.2013.12.010 (2014).
    CAS  Article  Google Scholar 

    75.
    Crow, S. E. et al. Sources of plant-derived carbon and stability of organic matter in soil: Implications for global change. Glob. Change Biol. 15, 2003–2019. https://doi.org/10.1111/j.1365-2486.2009.01850.x (2009).
    ADS  Article  Google Scholar 

    76.
    Fontaine, S., Mariotti, A. & Abbadie, L. The priming effect of organic matter: A question of microbial competition?. Soil Biol. Biochem. 35, 837–843. https://doi.org/10.1016/s0038-0717(03)00123-8 (2003).
    CAS  Article  Google Scholar 

    77.
    Zhou, D., Zhao, S., Liu, S. & Zhang, L. Spatiotemporal trends of terrestrial vegetation activity along the urban development intensity gradient in China’s 32 major cities. Sci. Total Environ. 488–489, 136–145. https://doi.org/10.1016/j.scitotenv.2014.04.080 (2014).
    ADS  CAS  Article  PubMed  Google Scholar 

    78.
    Liu, L. et al. Interactive effects of nitrogen and phosphorus on soil microbial communities in a tropical forest. PLoS ONE 8, e61188. https://doi.org/10.1371/journal.pone.0061188 (2013).
    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

    79.
    Saetre, P. & Bååth, E. Spatial variation and patterns of soil microbial community structure in a mixed spruce–birch stand. Soil Biol. Biochem. 32, 909–917. https://doi.org/10.1016/s0038-0717(99)00215-1 (2000).
    CAS  Article  Google Scholar 

    80.
    Bossio, D. A., Scow, K. M., Gunapala, N. & Graham, K. J. Determinants of soil microbial communities: Effects of agricultural management, season, and soil type on phospholipid fatty acid profiles. Microb. Ecol. 36, 1–12. https://doi.org/10.1007/s002489900087 (1998).
    CAS  Article  PubMed  Google Scholar 

    81.
    Wei, H., Chen, X., He, J., Zhang, J. & Shen, W. Exogenous nitrogen addition reduced the temperature sensitivity of microbial respiration without altering the microbial community composition. Front. Microbiol. 8, 2382. https://doi.org/10.3389/fmicb.2017.02382 (2017).
    Article  PubMed  PubMed Central  Google Scholar  More

  • in

    Fine-scale tundra vegetation patterns are strongly related to winter thermal conditions

    1.
    Natali, S. M. et al. Large loss of CO2 in winter observed across the northern permafrost region. Nat. Clim. Change 9, 852–857 (2019).
    CAS  Google Scholar 
    2.
    Myers-Smith, I. H. et al. Shrub expansion in tundra ecosystems: dynamics, impacts and research priorities. Environ. Res. Lett. 6, 15 (2011).
    Google Scholar 

    3.
    Elmendorf, S. C. et al. Plot-scale evidence of tundra vegetation change and links to recent summer warming. Nat. Clim. Change 2, 453–457 (2012).
    Google Scholar 

    4.
    Bjorkman, A. D. et al. Plant functional trait change across a warming tundra biome. Nature 562, 57–62 (2018).
    CAS  Google Scholar 

    5.
    Niittynen, P., Heikkinen, R. K. & Luoto, M. Snow cover is a neglected driver of Arctic biodiversity loss. Nat. Clim. Change 8, 997–1001 (2018).
    Google Scholar 

    6.
    Snow, Water, Ice and Permafrost in the Arctic (SWIPA) 2017 (Arctic Monitoring and Assessment Programme (AMAP), 2017).

    7.
    Box, J. E. et al. Key indicators of Arctic climate change: 1971–2017. Environ. Res. Lett. 14, 045010 (2019).
    CAS  Google Scholar 

    8.
    Bintanja, R. & Andry, O. Towards a rain-dominated Arctic. Nat. Clim. Change 7, 263–267 (2017).
    Google Scholar 

    9.
    Post, E. et al. Ecological dynamics across the Arctic associated with recent climate change. Science 325, 1355–1358 (2009).
    CAS  Google Scholar 

    10.
    Blok, D. et al. The response of Arctic vegetation to the summer climate: relation between shrub cover, NDVI, surface albedo and temperature. Environ. Res. Lett. 6, 9 (2011).
    Google Scholar 

    11.
    Cooper, E. J. Warmer shorter winters disrupt Arctic terrestrial ecosystems. Annu. Rev. Ecol. Evol. Syst. 45, 271–295 (2014).
    Google Scholar 

    12.
    Sanders-DeMott, R. & Templer, P. H. What about winter? Integrating the missing season into climate change experiments in seasonally snow covered ecosystems. Methods Ecol. Evol. 8, 1183–1191 (2017).
    Google Scholar 

    13.
    Bokhorst, S., Bjerke, J. W., Tommervik, H., Preece, C. & Phoenix, G. K. Ecosystem response to climatic change: the importance of the cold season. Ambio 41, 246–255 (2012).
    Google Scholar 

    14.
    Williams, C. M., Henry, H. A. L. & Sinclair, B. J. Cold truths: how winter drives responses of terrestrial organisms to climate change. Biol. Rev. 90, 214–235 (2015).
    Google Scholar 

    15.
    Wipf, S., Stoeckli, V. & Bebi, P. Winter climate change in alpine tundra: plant responses to changes in snow depth and snowmelt timing. Climatic Change 94, 105–121 (2009).
    Google Scholar 

    16.
    Bokhorst, S. F., Bjerke, J. W., Tommervik, H., Callaghan, T. V. & Phoenix, G. K. Winter warming events damage sub-Arctic vegetation: consistent evidence from an experimental manipulation and a natural event. J. Ecol. 97, 1408–1415 (2009).
    Google Scholar 

    17.
    Rapacz, M. et al. Overwintering of herbaceous plants in a changing climate: still more questions than answers. Plant Sci. 225, 34–44 (2014).
    CAS  Google Scholar 

    18.
    Loffler, J. & Pape, R. Thermal niche predictors of alpine plant species. Ecology 101, e02891 (2020).
    Google Scholar 

    19.
    Choler, P. Winter soil temperature dependence of alpine plant distribution: implications for anticipating vegetation changes under a warming climate. Perspect. Plant Ecol. Evol. Syst. 30, 6–15 (2018).
    Google Scholar 

    20.
    Billings, W. D. & Mooney, H. A. Ecology of Arctic and alpine plants. Biol. Rev. Camb. Phil. Soc. 43, 481–529 (1968).
    Google Scholar 

    21.
    Cornelissen, J. H. C. & Makoto, K. Winter climate change, plant traits and nutrient and carbon cycling in cold biomes. Ecol. Res. 29, 517–527 (2014).
    CAS  Google Scholar 

    22.
    Groffman, P. M. et al. Colder soils in a warmer world: a snow manipulation study in a northern hardwood forest ecosystem. Biogeochemistry 56, 135–150 (2001).
    CAS  Google Scholar 

    23.
    Deems, J. S., Fassnacht, S. R. & Elder, K. J. Interannual consistency in fractal snow depth patterns at two Colorado mountain sites. J. Hydrometeorol. 9, 977–988 (2008).
    Google Scholar 

    24.
    Wahren, C. H. A., Walker, M. D. & Bret-Harte, M. S. Vegetation responses in Alaskan Arctic tundra after 8 years of a summer warming and winter snow manipulation experiment. Glob. Change Biol. 11, 537–552 (2005).
    Google Scholar 

    25.
    Darrouzet-Nardi, A. et al. Limited effects of early snowmelt on plants, decomposers, and soil nutrients in Arctic tundra soils. Ecol. Evol. 9, 1820–1844 (2019).
    Google Scholar 

    26.
    Nobrega, S. & Grogan, P. Deeper snow enhances winter respiration from both plant-associated and bulk soil carbon pools in birch hummock tundra. Ecosystems 10, 419–431 (2007).
    CAS  Google Scholar 

    27.
    Niittynen, P. & Luoto, M. The importance of snow in species distribution models of Arctic vegetation. Ecography 41, 1024–1037 (2018).
    Google Scholar 

    28.
    Blankinship, J. C., Meadows, M. W., Lucas, R. G. & Hart, S. C. Snowmelt timing alters shallow but not deep soil moisture in the Sierra Nevada. Water Resour. Res. 50, 1448–1456 (2014).
    Google Scholar 

    29.
    Kranner, I., Beckett, R., Hochman, A. & Nash, T. H. Desiccation-tolerance in lichens: a review. Bryologist 111, 576–593 (2008).
    Google Scholar 

    30.
    Cornelissen, J. H. C., Lang, S. I., Soudzilovskaia, N. A. & During, H. J. Comparative cryptogam ecology: a review of bryophyte and lichen traits that drive biogeochemistry. Ann. Bot. 99, 987–1001 (2007).
    CAS  Google Scholar 

    31.
    Sonesson, M. & Callaghan, T. V. Strategies of survival in plants of the Fennoscandian tundra. Arctic 44, 95–105 (1991).
    Google Scholar 

    32.
    Bjerke, J. W. et al. Contrasting sensitivity to extreme winter warming events of dominant sub-Arctic heathland bryophyte and lichen species. J. Ecol. 99, 1481–1488 (2011).
    Google Scholar 

    33.
    Pannewitz, S., Schlensog, M., Green, T. G. A., Sancho, L. G. & Schroeter, B. Are lichens active under snow in continental Antarctica? Oecologia 135, 30–38 (2003).
    Google Scholar 

    34.
    Natali, S. M., Schuur, E. A. G. & Rubin, R. L. Increased plant productivity in Alaskan tundra as a result of experimental warming of soil and permafrost. J. Ecol. 100, 488–498 (2012).
    Google Scholar 

    35.
    Weijers, S., Buchwal, A., Blok, D., Loffler, J. & Elberling, B. High Arctic summer warming tracked by increased Cassiope tetragona growth in the world’s northernmost polar desert. Glob. Change Biol. 23, 5006–5020 (2017).
    Google Scholar 

    36.
    Morris, W. F. et al. Longevity can buffer plant and animal populations against changing climatic variability. Ecology 89, 19–25 (2008).
    Google Scholar 

    37.
    Strimbeck, G. R., Schaberg, P. G., Fossdal, C. G., Schroder, W. P. & Kjellsen, T. D. Extreme low temperature tolerance in woody plants. Front. Plant Sci. 6, 15 (2015).
    Google Scholar 

    38.
    Gonzalez, V. T. et al. High resistance to climatic variability in a dominant tundra shrub species. PeerJ 7, e6967 (2019).
    Google Scholar 

    39.
    Thomas, H. J. D. et al. Traditional plant functional groups explain variation in economic but not size-related traits across the tundra biome. Glob. Ecol. Biogeogr. 28, 78–95 (2019).
    CAS  Google Scholar 

    40.
    Shipley, B., Lechowicz, M. J., Wright, I. & Reich, P. B. Fundamental trade-offs generating the worldwide leaf economics spectrum. Ecology 87, 535–541 (2006).
    Google Scholar 

    41.
    Good, M., Morgan, J. W., Venn, S. & Green, P. Timing of snowmelt affects species composition via plant strategy filtering. Basic Appl. Ecol. 35, 54–62 (2019).
    Google Scholar 

    42.
    Cornelissen, J. H. C. et al. Global change and Arctic ecosystems: is lichen decline a function of increases in vascular plant biomass? J. Ecol. 89, 984–994 (2001).
    Google Scholar 

    43.
    Zhu, L. K., Ives, A. R., Zhang, C., Guo, Y. Y. & Radeloff, V. C. Climate change causes functionally colder winters for snow cover-dependent organisms. Nat. Clim. Change 9, 886–893 (2019).
    Google Scholar 

    44.
    Williams, J. W. & Jackson, S. T. Novel climates, no-analog communities, and ecological surprises. Front. Ecol. Environ. 5, 475–482 (2007).
    Google Scholar 

    45.
    Medlyn, B. E. et al. Using ecosystem experiments to improve vegetation models. Nat. Clim. Change 5, 528–534 (2015).
    Google Scholar 

    46.
    Myers-Smith, I. H. et al. Climate sensitivity of shrub growth across the tundra biome. Nat. Clim. Change 5, 887–891 (2015).
    Google Scholar 

    47.
    Potter, K. A., Woods, H. A. & Pincebourde, S. Microclimatic challenges in global change biology. Glob. Change Biol. 19, 2932–2939 (2013).
    Google Scholar 

    48.
    Alsos, I. G. et al. Frequent long-distance plant colonization in the changing Arctic. Science 316, 1606–1609 (2007).
    CAS  Google Scholar 

    49.
    Kemppinen, J., Niittynen, P., Aalto, J., le Roux, P. C. & Luoto, M. Water as a resource, stress and disturbance shaping tundra vegetation. Oikos 128, 811–822 (2019).
    Google Scholar 

    50.
    Robinson, S. A. et al. Rapid change in east Antarctic terrestrial vegetation in response to regional drying. Nat. Clim. Change 8, 879–884 (2018).
    CAS  Google Scholar 

    51.
    Chamberlain, S. A. & Szocs, E. taxize: taxonomic search and retrieval in R. F1000Res 2, 191 (2013).
    Google Scholar 

    52.
    McCune, B. & Keon, D. Equations for potential annual direct incident radiation and heat load. J. Veg. Sci. 13, 603–606 (2002).
    Google Scholar 

    53.
    R Core Team R: A language and environment for statistical computing (R Foundation for Statistical Computing, 2019); https://www.r-project.org/

    54.
    Minchin, P. R. An evaluation of the relative robustness of techniques for ecological ordination. Vegetatio 69, 89–107 (1987).
    Google Scholar 

    55.
    Oksanen, J. et al. vegan: community ecology package. R package version 2.3-3 (2016).

    56.
    Franklin, J. Mapping Species Distributions: Spatial Inference and Prediction (Cambridge Univ. Press, 2009).

    57.
    Elith, J., Leathwick, J. R. & Hastie, T. A working guide to boosted regression trees. J. Anim. Ecol. 77, 802–813 (2008).
    CAS  Google Scholar 

    58.
    Thuiller, W., Georges, D., Engler, R. & Breiner, F. biomod2: ensemble platform for species distribution modeling. R package version 3.3-7 (2016).

    59.
    Pedersen, E. J., Miller, D. L., Simpson, G. L. & Ross, N. Hierarchical generalized additive models in ecology: an introduction with mgcv. PeerJ 7, e6876 (2019).
    Google Scholar 

    60.
    Wood, S. N. Fast stable restricted maximum likelihood and marginal likelihood estimation of semiparametric generalized linear models. J. R. Stat. Soc. B 73, 3–36 (2011).
    Google Scholar 

    61.
    Ridgeway, G. gbm: generalized boosted regression models. R package version 2.1.1 (2015).

    62.
    Thuiller, W., Lafourcade, B., Engler, R. & Araujo, M. B. BIOMOD—a platform for ensemble forecasting of species distributions. Ecography 32, 369–373 (2009).
    Google Scholar  More