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    Fungivorous mites enhance the survivorship and development of stingless bees even when exposed to pesticides

    Goulson, D., Nicholls, E., Botías, C. & Rotheray, E. L. Bee declines driven by combined stress from parasites, pesticides, and lack of flowers. Science 347, 1255957 (2015).Article 
    PubMed 

    Google Scholar 
    – Potts, S. G., et al. Summary for Policymakers of the Assessment Report of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services on pollinators, pollination, and food production (eds. Potts, S. G. et al.). 36 pages. (Bonn, Germany, 2016).Dolezal, A. G. et al. Interacting stressors matter: Diet quality and virus infection in honeybee health. R. Soc. Open Sci. 6, 181803 (2019).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Annoscia, D. et al. Neonicotinoid Clothianidin reduces honeybee immune response and contributes to Varroa mite proliferation. Nat. Commun. 11, 1–7 (2020).Article 

    Google Scholar 
    Macías-Macías, J. O. et al. Nosema ceranae causes cellular immunosuppression and interacts with thiamethoxam to increase mortality in the stingless bee Melipona colimana. Sci. Rep. 10, 1–8 (2020).Article 

    Google Scholar 
    Michener, C. D. Pot-honey. In Pot-Honey: A Legacy of Stingless Bees (eds Vit, P. et al.) 3–17 (Springer, 2013).Chapter 

    Google Scholar 
    Rosa, C. A. et al. Yeast communities associated with stingless bees. FEMS Yeast Res. 4, 271–275 (2003).Article 
    PubMed 

    Google Scholar 
    Menezes, C., Vollet-Neto, A. & Fonseca, V. L. I. An advance in the in vitro rearing of stingless bee queens. Apidologie 44, 491–500 (2013).Article 

    Google Scholar 
    Morais, P. B., Calaça, P. S. S. T. & Rosa, C. A. Microorganisms associated with stingless bees. In Pot-Honey Bees (eds Vit, P. et al.) 173–186 (Springer, 2013).Chapter 

    Google Scholar 
    Menegatti, C. et al. Paenibacillus polymyxa associated with the stingless bee Melipona scutellaris produces antimicrobial compounds against entomopathogens. J. Chem. Ecol. 44, 1158–1169 (2018).Article 
    PubMed 

    Google Scholar 
    Paludo, C. R. et al. Stingless bee larvae require fungal steroid to pupate. Sci. Rep. 8, 1122321 (2018).Article 

    Google Scholar 
    Paludo, C. R. et al. Microbial community modulates growth of symbiotic fungus required for stingless bee metamorphosis. PLoS ONE 14, e0219696 (2019).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Hamzah, S. A., Zawawi, N. & Sabri, S. A review on the association of bacteria with stingless bees. Sains Malays. 49, 1853–1863 (2020).Article 

    Google Scholar 
    de Paula, G. T., Menezes, C., Pupo, M. T. & Rosa, C. A. Stingless bees and microbial interactions. Curr. Opin. Insect Sci. 44, 41–47 (2020).Article 
    PubMed 

    Google Scholar 
    Menezes, C. et al. A Brazilian social bee must cultivate fungus to survive. Curr. Biol. 25, 2851–2855 (2015).Article 
    PubMed 

    Google Scholar 
    – Flechtmann, C. H. W. & de Camargo, C. A. Acari associated with stingless bees (Meliponidae, Hymenoptera) from Brazil. in Proceedings of the 4th International Congress of Acarology, Saalfelden (Austria)/edited by Edward Piffl (Budapest, Akademiai Kiado,1979).Dorigo, A. S. et al. In vitro larval rearing protocol for the stingless bee species Melipona scutellaris for toxicological studies. PLoS ONE 14, e0213109 (2019).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Rosa-Fontana, A., Dorigo, A. S., Galaschi-Teixeira, J. S., Nocelli, R. C. F. & Malaspina, O. What is the most suitable native bee species from the neotropical region to be proposed as model-organism for toxicity tests during the larval phase?. Environ. Pollut. 265, 114849 (2020).Article 
    PubMed 

    Google Scholar 
    Miotelo, L., Dos Reis, A. L. M., Malaquias, J. B., Malaspina, O. & Roat, T. C. Apis mellifera and Melipona scutellaris exhibit differential sensitivity to thiamethoxam. Environ. Pollut. 268, 115770 (2021).Article 
    PubMed 

    Google Scholar 
    Rosa, A. E., André, H. & Flechtmann, C. H. W. Acari domun meliponirarum brasiliensium habitantes. Proctotydaeus alvearii 45(1–2), 79–83 (1985).
    Google Scholar 
    Da-Costa, T., dos Santos, C. F., Rodighero, L. F., Ferla, N. J. & Blochtein, B. Mite diversity is determined by the stingless bee host species. Apidologie 52(5), 950–959. https://doi.org/10.1007/s13592-021-00878-2 (2021).Article 

    Google Scholar 
    de Rosa, A. S. et al. Consumption of the neonicotinoid thiamethoxam during the larval stage affects the survival and development of the stingless bee Scaptotrigona aff. depilis. Apidologie 47, 729–738 (2016).Article 

    Google Scholar 
    Wu, J. Y., Anelli, C. M. & Sheppard, W. S. Sub-lethal effects of pesticide residues in brood comb on worker honeybee (Apis mellifera) development and longevity. PLoS One 6, e14720 (2011).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Tavares, D. A., Roat, T. C., Carvalho, S. M., Silva-Zacarin, E. C. M. & Malaspina, O. In vitro effects of thiamethoxam on larvae of Africanized honeybee Apis mellifera (Hymenoptera: Apidae). Chemosphere 135, 370–378 (2015).Article 
    PubMed 

    Google Scholar 
    Biani, N. B., Mueller, U. G. & Wcislo, W. T. Cleaner mites: sanitary mutualism in the miniature ecosystem of neotropical bee nests. Am. Nat. 173, 841–847 (2009).Article 
    PubMed 

    Google Scholar 
    Gilliam, M., Roubik, D. W. & Lorenz, B. J. Microorganisms associated with pollen, honey, and brood provisions in the nest of a stingless bee Melipona fasciata. Apidologie 21, 89–97 (1990).Article 

    Google Scholar 
    Rebelo, K. S., Ferreira, A. G. & Carvalho-Zilse, G. A. Physicochemical characteristics of pollen collected by Amazonian stingless bees. Ciência Rural 46, 927–932 (2016).Article 

    Google Scholar 
    Mohammad, S. M., Mahmud-Ab-Rashid, N.-K. & Zawawi, N. Stingless bee-collected pollen (bee bread): Chemical and microbiology properties and health benefits. Molecules 26, 957 (2021).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    da Cruz Landim, C. (2009). Abelhas. Unesp.Rosa, A. S. et al. Quantification of larval food and its pollen content in the diet of stingless bees: Subsidies for toxicity bioassays studies. Braz. J. Biol. 75(3), 771–772. https://doi.org/10.1590/1519-6984.22314 (2015).Article 
    PubMed 

    Google Scholar 
    Vollet-Neto, A., Maia-Silva, C., Menezes, C. & Imperatriz-Fonseca, V. L. Newly emerged workers of the stingless bee Scaptotrigona aff. depilis prefer stored pollen to fresh pollen. Apidologie 48, 204–210 (2017).Article 

    Google Scholar 
    Hartfelder, K. & Engels, W. The composition of larval food in stingless bees: evaluating nutritional balance by chemosystematic methods. Insect. Soc. 36, 1–14 (1989).Article 

    Google Scholar 
    Costa, R. A. C. & da Cruz-Landim, C. Distribution of acid phosphatases in the hypopharyngeal glands from workers, queens, and males of a Brazilian stingless bee Scaptotrigona postica Latreille: An ultrastructural cytochemical study. Histochem. J. 33, 653–662 (2001).Article 
    PubMed 

    Google Scholar 
    de Moraes, R. L. M. S., Brochetto-Braga, M. R. & Azevedo, A. Electrophoretical studies of proteins of the hypopharyngeal glands and of the larval food of Melipona quadrifasciata anthidioides Lep. (Hymenoptera, Meliponinae). Insect. Soc. 43, 183–188 (1996).Article 

    Google Scholar 
    Fernandes-da-Silva, P. G., Muccillo, G. & Zucoloto, F. S. Determination of minimum quantity of pollen and nutritive value of different carbohydrates for Scaptotrigona depilis Moure (Hymenoptera, Apidae). Apidologie 24, 73–79 (1993).Article 

    Google Scholar 
    Fernandes-da-Silva, P. G. & Serrão, J. E. Nutritive value and apparent digestibility of bee-collected and bee-stored pollen in the stingless bee, Scaptotrigona postica Latr. (Hymenoptera, Apidae, Meliponini). Apidologie 31, 39–45 (2000).Article 

    Google Scholar 
    Crailsheim, K. & Stolberg, E. Influence of diet, age and colony condition upon intestinal proteolytic activity and size of the hypopharyngeal glands in the honeybee (Apis mellifera L.). J. Insect Physiol. 35, 595–602 (1989).Article 

    Google Scholar 
    Oliveira, R. A., Roat, T. C., Carvalho, S. M. & Malaspina, O. Side-effects of thiamethoxam on the brain and midgut of the africanized honeybee Apis mellifera (Hymenopptera: Apidae). Environ. Toxicol. 29, 1122–1133 (2014).Article 
    PubMed 

    Google Scholar 
    Christen, V., Schirrmann, M., Frey, J. E. & Fent, K. Global transcriptomic effects of environmentally relevant concentrations of the neonicotinoids clothianidin, imidacloprid, and thiamethoxam in the brain of honeybees (Apis mellifera). Environ. Sci. Technol. 52, 7534–7544 (2018).Article 
    PubMed 

    Google Scholar 
    Moreira, D. R. et al. Toxicity and effects of the neonicotinoid thiamethoxam on Scaptotrigona bipunctata Lepeletier, 1836 (Hymenoptera: Apidae). Environ. Toxicol. 33, 463–475 (2018).Article 
    PubMed 

    Google Scholar 
    Tavares, D. A., Roat, T. C., Silva-Zacarin, E. C. M., Nocelli, R. C. F. & Malaspina, O. Exposure to thiamethoxam during the larval phase affects synapsin levels in the brain of the honeybee. Ecotoxicol. Environ. Saf. 169, 523–528 (2019).Article 
    PubMed 

    Google Scholar 
    Roat, T. C. et al. Using a toxicoproteomic approach to investigate the effects of thiamethoxam into the brain of Apis mellifera. Chemosphere 258, 127362 (2020).Article 
    PubMed 

    Google Scholar 
    Caesar, L. et al. The virome of an endangered stingless bee suffering from annual mortality in southern Brazil. J. Gen. Virol. 100, 1153–1164 (2019).Article 
    PubMed 

    Google Scholar 
    Guimarães-Cestaro, L. et al. Occurrence of virus, microsporidia, and pesticide residues in three species of stingless bees (Apidae: Meliponini) in the field. Sci. Nat. 107, 1–14 (2020).Article 

    Google Scholar 
    Teixeira, É. W. et al. European Foulbrood in stingless bees (Apidae: Meliponini) in Brazil: Old disease, renewed threat. J. Invertebr. Pathol. 172, 107357 (2020).Article 
    PubMed 

    Google Scholar 
    Alberoni, D., Gaggìa, F., Baffoni, L. & Di Gioia, D. Beneficial microorganisms for honeybees: problems and progresses. Appl. Microbiol. Biotechnol. 100, 9469–9482 (2016).Article 
    PubMed 

    Google Scholar 
    Manley, R., Boots, M. & Wilfert, L. Emerging viral disease risk to pollinating insects: ecological, evolutionary, and anthropogenic factors. J. Appl. Ecol. 52, 331–340 (2015).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Manley, R. et al. Knock- on community impacts of a novel vector: spillover of emerging DWV- B from Varroa- infested honeybees to wild bumblebees. Ecol. Lett. 22, 1306–1315 (2019).PubMed 
    PubMed Central 

    Google Scholar 
    Graystock, P., Blane, E. J., McFrederick, Q. S., Goulson, D. & Hughes, W. O. H. Do managed bees drive parasite spread and emergence in wild bees?. Int. J. Parasitol. Parasit. Wildl. 5, 64–75 (2016).Article 

    Google Scholar 
    Requier, F. et al. The conservation of native honeybees is crucial. Trends Ecol. Evol. 34, 789–798 (2019).Article 
    PubMed 

    Google Scholar 
    Test No. 237: Honey Bee (Apis Mellifera) Larval Toxicity Test, Single Exposure. (2013). OECD. https://doi.org/10.1787/9789264203723-enMoral, R. A., Hinde, J. & Demétrio, C. G. Half-normal plots and overdispersed models in R: the hnp package. J. Stat. Softw. 81(1), 1–23 (2017).
    Google Scholar 
    – Kassambara, A. Survminer. GitHub repository. https://github.com/kassambara/survminer (2020).- Therneau, T., Crowson, C., & Atkinson, E. Multi-state models and competing risks. CRAN-R https://cran.r-project.org/web/packages/survival/vignettes/compete (2020). More

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    Revealing the global longline fleet with satellite radar

    To estimate the total number of non-broadcasting vessels, including those that were not detected by SAR, we: (1) obtained SAR detections of vessels from RADARSAT-2 and the corresponding vessel lengths as estimated from the SAR image; (2) processed a global feed of AIS data to identify every broadcasting vessel that should have appeared in the SAR images at the moment the images were taken; (3) developed a novel technique to determine which vessels in AIS matched to detections in SAR, which AIS vessels were not detected by SAR, and which SAR detections represented non-broadcasting vessels; (4) after matching SAR to AIS, we could then (a) model the relationship between a vessel’s actual length and the length as estimated by the SAR image (Fig. 3b) and (b) model the relationship between the likelihood that a vessel is detected and its length (Fig. 3a); and (5) finally, we combined these relationships to develop an estimate of the number and lengths of non-broadcasting vessels in the region.SAR imagery and vessel detectionsWorking with the satellite company Kongsberg Satellite Services (KSAT), we tasked the Canadian Space Agency’s satellite RADARSAT-2 to acquire SAR images from its ship detection mode (DVWF mode, GRD product), with a pixel size of about 40 m and a swath width over 400 km (19). These images were processed following standard procedures for GRD products (e.g. applying radiometric calibration and geometric corrections)29,30. Vessel locations were extracted from the images with the widely used ship detection algorithms, which discriminates objects at sea based on the backscatter difference (pixel values) between the sea clutter and the targets31. Vessel lengths were estimated by measuring distances directly on the images with the aid of a graphical user interface tool31.Identifying Vessels using AISIn each region, AIS data, obtained from satellite providers ORBCOMM and Spire, were processed using Global Fishing Watch’s data pipeline1. The identities and lengths of all AIS devices that operated near the SAR scenes in both space and time were first obtained using Global Fishing Watch’s database1. To be sure vessels were identified correctly, two analysts reviewed the tracks of every AIS device in each region.In both regions, it is common practice for fishers to put AIS beacons on their longlines, likely to aid in retrieving them, meaning that many AIS devices were longline gear and not vessels. Because gear outnumbered vessels by several-fold, it was critical to differentiate gear and fishing vessels. In the Indian Ocean, 521 unique AIS devices associated with gear were detected that were likely within the SAR scenes, and 390 unique AIS devices associated with gear in the Pacific that were likely within the SAR scenes. Transponders were determined to be associated with gear by inspecting the name broadcast in the AIS messages (gear frequently broadcasts one of several standard names and/or a voltage reading) and classification using the Global Fishing Watch vessel classification algorithm1. Most gear also had an MMSI number (unique identifier number for AIS) that started with 1, 8, or 9 or broadcast names that signified gear. We eliminated all gear from the analysis because (1) these gear buoys have reflectors that are only ~ 1 m in size, and they should not be visible in ~ 40 m resolution SAR images, and (2) we found that gear matched to SAR detections only when traveling faster than 2 knots (and thus was on the deck of a boat); of 159 instances of gear in scenes where the gear was traveling slower than two knots, zero matched to a radar detection (Fig. S9).Generating probability rasters for matching AIS to SARMost AIS positions did not correspond to the exact time when the SAR images were taken. Hence, to determine the likelihood that a vessel broadcasting AIS corresponded to a specific SAR detection, we first developed probability rasters of where a vessel was likely to be minutes before or after a GPS position was recorded (Figs. S1,S2). We mined one year of global AIS data, including roughly 10 billion GPS positions, and computed these rasters for six different vessel classes (trawlers, purse seines, tug, cargo or tanker, drifting longlines, and others) and considered six different speeds (1, 3, 5, 7, 9, and 12.5 knots) and 36 time intervals (− 448, − 320, − 224, − 160, − 112, − 80, − 56, − 40, − 28, − 20, − 14, − 10, − 7, − 5, − 3.5, − 2.5, − 1.5, − 0.5, 0.5, 1.5, 2.5, 3.5, 5, 7, 10, 14, 20, 28, 40, 56, 80, 112, 160, 224, 320, and 448 min).For example, we queried a year of AIS data to find every example of where a tugboat had two positions that were 10 min apart from one another when the vessel had been traveling at 10 knots at the first position. We then recorded each of these locations relative to the location the vessel would have been if it traveled in a straight line, with x coordinates being in the direction of travel and the y coordinates being perpendicular to the direction of travel. When collected for hundreds of thousands of examples across the AIS dataset, the result is a heatmap of where tug boats are located 10 min after a position when it was traveling at 10 knots. The raster is centered on a point that is the extrapolated position of the vessel based on its speed. For instance, the purse seine raster that corresponds to a vessel traveling between 6 and 8 knots between 96 and 128 min after the most recent position is centered at a point that is 13.1 km (7 knots × 112 min) straight ahead of the direction the vessel was traveling. Figure S1 shows samples of these rasters for different vessels.We built rasters of 1000 by 1000 pixels for each vessel class and time interval, with the area covered by the raster dependent on the time interval (longer time intervals imply longer traveled distances, covering more area). The scale of each pixel was given by:$${text{pixel}};{text{width = max(1, }}Delta {text{m) / 1000}}$$
    (1)
    where Δm is the time interval in minutes, and pixel width is measured in km. Thus, if the Δm is under one minute, the entire raster is one kilometer wide with each pixel one meter by one meter. If the time is 10 min, then each pixel is 10 m wide, and the entire raster is 10 km by 10 km.Since the pixel width varies between rasters, the units of the rasters are probability per km2, thus summing the area of each pixel times its value equals one. Six vessel classes with 36 time intervals for each and six speeds led to 1296 different rasters. This probability raster approach could be seen as a utilization distribution32—for each vessel class, speed and time interval—where the space is relative to the position of the individual.Combining probability rasters to produce a matching scoreFor a few vessels (~ 4%) there was only one AIS position available before or after the scene. This resulted from a long gap in the AIS data due to poor reception, a weak AIS device, or cases where the vessels disabled their AIS. For these vessels, we used the raster values for a single position. For the vast majority of vessels, however, there was a GPS position right before and after the scene, and thus two probability rasters. We used two methods to combine these probability rasters to obtain information about the most likely location:Multiply and renormalize the rastersTo multiply the rasters, we interpolated the raster values, using bilinear interpolation, to a constant grid at the highest resolution between the before and after rasters. Then, we multiplied the values at each point and renormalized the resulting raster (Fig. S2):$$p_{i} = frac{{p_{ai} cdot p_{bi} }}{{mathop sum nolimits_{k = 0}^{N} p_{ak} cdot p_{bk} cdot da}}$$
    (2)
    where pi is the probability in vessel density per km2 at location i, pai is the value of the raster before the image, pbi is the value of the raster after the image. The denominator is the sum of all multiplied values across the raster, scaled by the area of each cell, da.Weight and average the rasters For this method, we weighted the raster by the squared value of the probabilities of that scene. This has the effect of giving the concentrated raster a higher weight, thus weighting higher the raster that is closer in time to the image:$${w}_{a}=sum_{k=0}^{N} {p}_{ak}^{2}cdot da$$
    (3)
    and the weighted average at location i is:$${p}_{i}=frac{{p}_{ai}cdot {w}_{a}+{p}_{bi}cdot {w}_{b}}{{w}_{a}+{w}_{b}}$$
    (4)
    where wa is the weight for raster a, wb the weight for raster b (calculation analogous to wa’s in Eq. 3), pi is the probability in vessel density per km2 at location i.To determine whether we should multiply (Eq. 2) or average (Eq. 4) the probabilities, we compared the performance of these two metrics against a direct inspection of the detections. We found that at short intervals, multiplying the rasters and renormalizing often made probability values extremely small ( {d}_{d}cdot {p}_{d} + {p}_{f}$$
    (5)
    where ({p}_{v}) is the probability density of the vessel presence at the location of the SAR detection (the score listed above), ({p}_{d}) is the probability that the vessel is detected by SAR, ({d}_{d}) is the density of non-broadcasting vessels in the region, and ({p}_{f}) is the density of false detections in the scene. The greater ({p}_{d}), the more dark vessels there are in a scene, and the more likely it is that any given detection is a dark vessel instead of a vessel broadcasting AIS. The right-hand side of the equation ({d}_{d}cdot {p}_{d} + {p}_{f}) should roughly equal the number of detections per unit area that do not match to AIS in the region. In other words, the probability of the vessel with AIS being at that specific location and detected by SAR (left side of the equation) should be greater than the probability of a dark vessel or a false detection at that location (right side of the equation).The total number of unmatched vessels in each studied region normalized by total area covered gives a density of non-broadcasting vessels of 2.6–2.8 × 10–5 vessels km-2 (Indian Ocean) and 6.8–7.2 × 10–6 vessels km−2 (Pacific Ocean), similar to the thresholds estimated by analysts. For the most likely number of matched vessels, we use a threshold that is halfway between the higher and lower bound of the analyst (5 × 10–5 to 1 × 10–4), 2.5 × 10–5 which is also roughly equal to the theoretical estimate of the Indian Ocean.This threshold approach performed significantly better than a metric based on the distance between the SAR detection and the most likely location of the vessel, where the likely location is based on extrapolating speed and course of the position closest in time to the image (Fig. S4).Determining whether a vessel with AIS was within a sceneVessel positions from AIS are usually available before and/or after the SAR images, and sometimes it is unclear if a vessel should have been within the scene footprint at the time of the image.To estimate the probability that a vessel (with AIS) was within a scene, we used the multiplied probability raster, summing the values inside the scene boundaries. This provides an estimate of the likelihood that the vessel was within the scene footprint at the time of the image. We applied this to every vessel that had at least one AIS position within 12 h and 200 nautical miles of the scene footprint. The vast majority of vessels were either very likely inside or outside the scene footprints, with 516 vessels having a probability of  > 95% and only 16 having a probability between 5 and 95%. We filtered out all vessels that were definitely outside of the image footprint before matching.Estimating the likelihood of detecting a vessel with SARThe AIS data show that not all vessels broadcasting AIS were captured by the RADARSAT-2 images (Fig. 3a). Using the known lengths of detected vessels with AIS, we estimated the likelihood of detecting a vessel with SAR as a function of vessel length (Fig. 3a). For vessels shorter than 60 m, we approximated the detection rate as a linear function. Treating each vessel as an individual detection, we fitted the 50th percentile using quantile regression to approximate the detection rate. For vessels above 60 m, we assumed a constant detection rate as very few vessels above this length did now show up in the SAR images. Of the 46 unique vessels larger than 62 m, 42 were detected, implying a detection rate of ~ 91%. Given that it is highly likely that large vessels will be captured by medium-resolution SAR imagery, we manually reviewed these cases to confirm that they were (almost surely) inside the scene footprints at the time the images were taken.We should note that the probability of detecting a vessel in SAR also depends on the sea state, incidence angle, polarization, material of the vessel, and orientation of the vessel. We are unable, however, to measure these effects directly so we cannot explicitly model these effects.With sufficient scenes, these effects should be randomly distributed across our scenes, so they likely account for some of the variability in detectability and the inaccuracy in our length estimates from SAR.Estimating the number and length of non-broadcasting vesselsBecause SAR does not detect all vessels, and because the length as estimated by SAR can be incorrect, there are many possible distributions of actual non-broadcasting vessels that could have produced the distribution of unmatched SAR detections that we found in the scenes. To estimate the most likely such distribution, we built a model to combine the two key relationships—between vessel length and likelihood of detection, and between vessel length and the length as estimated by SAR. This model allowed us to estimate, based on the number and distribution of SAR vessels, the likely number and distribution of actual vessels present (Fig. 3c,d).We binned the likelihood of vessel detection as a function of length into 1 m intervals, yielding a vector (alpha) of length 400. We also binned into 1 m intervals the population of lengths of all detected vessels ((ell_{D})) as reported by AIS (i.e. number of vessels at each length bin), the population of expected SAR lengths ((ell_{E})), and the population of lengths of all vessels ((ell_{A}), the quantity we wish to estimate). Thus, (ell_{D}) can be expressed as the product of (alpha) and (ell_{A}):$$ell_{D} = {upalpha } odot ell_{{text{A}}}$$
    (6)
    where (odot) is the element-wise product. We then estimated a matrix (L_{{}}) that relates (ell_{D}) to (ell_{E}).$$ell_{E} = Lell_{D}$$
    (7)
    where each element (L_{ij}) represents the probability that a vessel with length in bin j would be estimated by SAR to be of length in bin i. We calculated these probabilities as lognormal probability density functions, with one distribution per column. To estimate the scale and shape parameters of these distributions, we first fitted a quantile regression using the (non-binned) lengths from AIS of detected vessels as the predictor for the lengths reported by SAR. Assuming that the predicted 1/3 and 2/3 quantiles (as shown in Fig. 3a) represent the quantiles of a lognormal distribution, allow us to calculate the shape and scale parameters. We chose a lognormal distribution because: 1) the variable of interest, length, was always greater than zero, 2) the population of lengths was skewed towards larger values, and 3) there is an explicit and relatively simple relationship between the lognormal quantiles and the shape and scale parameters that simplified the calculations.Combining Eqs. (6) and (7) provides a relation between (ell_{A}) and (ell_{E}):$$ell_{E} = {text{L}}left( {alpha odot ell_{A} } right)$$
    (8)
    To estimate ({mathcal{l}}_{A}) we minimized an objective function (O({mathcal{l}}_{E},{mathcal{l}}_{o})) between the vector of expected counts binned by length (({mathcal{l}}_{E})) and the vector of counts observed in SAR binned by length (({mathcal{l}}_{o})). For this objective function, we chose the sum of the Kolmogorov –Smirnov distance between length distributions and the squared difference of the total numbers of detections. The first term controls the shape of the resulting distribution while the second one controls the magnitude. Specifically:$$Oleft( {ell_{E} ,ell_{o} } right) = max left( {left| {C_{E} – C_{O} } right|} right) + left( {T_{E} – T_{O} } right)^{2}$$
    (9)
    where:$$T_{x} = mathop sum limits_{ } ell_{x}$$$$D_{x} = ell_{x} /T_{x}$$$$C_{x} = cumsumleft( {D_{x} } right)$$Assessing the uncertainty in the estimationTo test how accurately our approach predicts the correct number of vessels, we performed a bootstrap simulation. We computed the vector (alpha) and the matrix L from a random subset of vessels with AIS that had a high confidence ( > 95%) of appearing within the scenes. We then used our method on the SAR detections that matched the remaining vessels to predict the number of vessels they corresponded to ((ell_{text{A}})). By running 10,000 experiments we found a mean absolute percent error of + − 9% (Figs. S5 and S6). This provides a rough estimate of the uncertainty in our prediction due to the estimation process itself. We used the distribution of these samples to estimate the 90% confidence interval that we report with our estimates. We note that this uncertainty refers to the parametrization of the model and there may be other sources of error, such as the possibility that vessels without AIS have different radar properties (e.g. made out of materials with different reflectiveness), that we did not account for in our model.Catch and effort data in the overlapping area between WCPFC and IATTCWe downloaded gridded effort and catch data from the WCPFC and IATTC websites, and compared the reported number of hooks and catch from September to December of 2019 for the area between − 140 to − 150 longitude and − 5 to − 15 latitude, a bounding box that contains our study region in the Pacific and which is entirely within both the WCPFC and IATTC convention zones. We found that the reported number of hooks for Korea is three times higher for the IATTC as it is for the WCPFC (Fig. S7), and the numbers of hooks also disagree by more than 10% for most other flag states. Catch is also 2.5 times higher for IATTC than for WCPFC for Korea as well, with catch also differing by more than 10% for most other flag states. This finding suggests that the different RFMOs may not be accounting for the same vessels in the overlap region between the two RFMOs. More

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    Dominant phytoplankton groups as the major source of polyunsaturated fatty acids for hilsa (Tenualosa ilisha) in the Meghna estuary Bangladesh

    Valle-Levinson, A. Contemporary Issues in Estuarine Physics (Cambridge University Press, 2010).Book 

    Google Scholar 
    Singh, S. Analysis of plankton diversity and density with physico-chemical parameters of open pond in town Deeg (Bhratpur) Rajasthan, India. Int. Res. J. Biol. Sci 4, 61–69 (2015).
    Google Scholar 
    Roussel, M., Pontier, D., Cohen, J.-M., Lina, B. & Fouchet, D. Quantifying the role of weather on seasonal influenza. BMC Public Health 16, 1–14 (2016).Article 

    Google Scholar 
    Davies, O., Abowei, J. & Tawari, C. Phytoplankton community of Elechi creek, Niger Delta, Nigeria-a nutrient-polluted tropical creek. Am. J. Appl. Sci. 6, 1143–1152 (2009).Article 
    CAS 

    Google Scholar 
    Choudhury, S. & Panigrahy, R. Seasonal distribution and behavior of nutrients in the Greek and coastal waters of Gopalpur, East coast of India: Mahasagar. Bull. Natl. Inst. Oeanogr 24, 91–88 (1991).
    Google Scholar 
    Ratheesh, K., Krishnan, A., Das, R. & Vimexen, V. Seasonal phytoplankton succession in Netravathi-Gurupura estuary, Karnataka, India: Study on a three tier hydrographic platform. Estuar. Coast. Shelf Sci. 242, 106830 (2020).Article 

    Google Scholar 
    Deng, Y., Tang, X., Huang, B. & Ding, L. Effect of temperature and irradiance on the growth and reproduction of the green macroalga, Chaetomorpha valida (Cladophoraceae, Chlorophyta). J. Appl. Phycol. 24, 927–933 (2012).Article 
    CAS 

    Google Scholar 
    Gamier, J., Billen, G. & Coste, M. Seasonal succession of diatoms and Chlorophyceae in the drainage network of the Seine River: Observation and modeling. Limnol. Oceanogr. 40, 750–765 (1995).Article 

    Google Scholar 
    Meng, F. et al. Phytoplankton alpha diversity indices response the trophic state variation in hydrologically connected aquatic habitats in the Harbin Section of the Songhua River. Sci. Rep. 10, 1–13 (2020).Article 

    Google Scholar 
    Köhler, J. Growth, production and losses of phytoplankton in the lowland River Spree. I. Population dynamics. J. Plankton Res. 15, 335–349 (1993).Article 

    Google Scholar 
    Murrell, M. C. & Caffrey, J. M. High cyanobacterial abundance in three northeastern Gulf of Mexico estuaries. Gulf Caribbean Res. 17, 95–106 (2005).Article 

    Google Scholar 
    Haldar, G., Rahman, M. & Haroon, A. Hilsa, Tenualosa ilisha (Ham.) fishery of the Feni River with reference to the impacts of the flood control structure. J. Zool. 7, 51–56 (1992).
    Google Scholar 
    Hossain, M. S., Sarker, S., Chowdhury, S. R. & Sharifuzzaman, S. Discovering spawning ground of Hilsa shad (Tenualosa ilisha) in the coastal waters of Bangladesh. Ecol. Model. 282, 59–68 (2014).Article 

    Google Scholar 
    Bhaumik, U. & Sharma, A. The fishery of Indian Shad (Tenualosa ilisha) in the Bhagirathi-Hooghly river system. Fishing Chimes 31, 21–27 (2011).
    Google Scholar 
    Mitra, G. & Devsundaram, M. P. On the hilsa of Chilka Lake with note on the Hilsa in Orissa. J. Asiatic Soc. Sci. 20, 33–40 (1954).
    Google Scholar 
    Abdul, W., Phillips, M. & Beveridge, M. (WorldFish (WF), 2020).Hasan, K. M. M., Wahab, M. A., Ahmed, Z. F. & Mohammed, E. Y. The biophysical assessments of the hilsa fish (Tenualosa ilisha) habitat in the lower Meghna, Bangladesh (International Institute for Environment and Development, 2015).Begum, M. et al. Fatty acid composition of Hilsa (Tenualosa ilisha) fish muscle from different locations in Bangladesh. Thai J. Agric. Sci. 52, 172–179 (2019).
    Google Scholar 
    Jónasdóttir, S. H. Fatty acid profiles and production in marine phytoplankton. Mar. Drugs 17, 151 (2019).Article 

    Google Scholar 
    Otero, P., Ruiz-Villarreal, M., Peliz, Á. & Cabanas, J. M. Climatology and reconstruction of runoff time series in northwest Iberia: Influence in the shelf buoyancy budget off Ría de Vigo. Sci. Mar. 74, 247–266 (2010).Article 

    Google Scholar 
    Grasshoff, K., Kremling, K. & Ehrhardt, M. Methods of Seawater Analysis (Wiley, 2009).
    Google Scholar 
    Parsons, T., Maita, Y. & Lalli, C. A manual of chemical and biological methods for seawater analysis. Pergamon, Oxford sized algae and natural seston size fractions. Mar. Ecol. Prog. Ser. 199, 43–53 (1984).
    Google Scholar 
    Scor-Unesco, W. Determination of photosynthetic pigments. Determination of Photosynthetic Pigments in Sea-water, 9–18 (1966).Snow, G., Bate, G. & Adams, J. The effects of a single freshwater release into the Kromme Estuary. 2: Microalgal response. Water SA-Pretoria 26, 301–310 (2000).CAS 

    Google Scholar 
    Ward, H. B. & Whipple, G. C. Freshwater Biology Vol. 2, 12–48 (Willey, London, 1959).
    Google Scholar 
    Prescott, G. W. Algae of the western Great Lakes area. (1962).Bellinger, E. G. A Key to Common Algae: Freshwater, Estuarine and Some Coastal Species (Institution of Water and Environmental Management London, 1992).
    Google Scholar 
    Kimmerer, W. J. & Slaughter, A. M. A new electivity index for diet studies that use count data. Limnol. Oceanogr. Methods 19, 552–565 (2021).Article 

    Google Scholar 
    Pinheiro, J., Bates, D., DebRoy, S. & Sarkar, D. R Development Core Team. nlme: Linear and nonlinear mixed effects models, 2012. http://CRAN.R-project.org/package=nlme. R package version, 3.1–103 (2020).Lê, S., Josse, J. & Husson, F. FactoMineR: an R package for multivariate analysis. J. Stat. Softw. 25, 1–18 (2008).Article 

    Google Scholar 
    Galili, T., O’Callaghan, A., Sidi, J. & Sievert, C. heatmaply: an R package for creating interactive cluster heatmaps for online publishing. Bioinformatics 34, 1600–1602 (2018).Article 
    CAS 

    Google Scholar 
    Wickham, H., Chang, W. & Wickham, M. H. Package ‘ggplot2’. Create Elegant Data Visualisations Using the Grammar of Graphics. Version 2, 1–189 (2016).Peterson, B. G. et al. Package ‘PerformanceAnalytics’. R Team Cooperation (2018).Lewis, R. E. & Uncles, R. J. Factors affecting longitudinal dispersion in estuaries of different scale. Ocean Dyn. 53, 197–207 (2003).Article 

    Google Scholar 
    Shaha, D., Cho, Y.-K., Seo, G.-H., Kim, C.-S. & Jung, K. Using flushing rate to investigate spring-neap and spatial variations of gravitational circulation and tidal exchanges in an estuary. Hydrol. Earth Syst. Sci. 14, 1465–1476 (2010).Article 

    Google Scholar 
    Shaha, D. C., Cho, Y.-K., Kim, T.-W. & Valle-Levinson, A. Spatio-temporal variation of flushing time in the Sumjin River Estuary. Terrestr. Atmos. Ocean. Sci. 23, 119 (2012).Article 

    Google Scholar 
    Shivaprasad, A. et al. Seasonal stratification and property distributions in a tropical estuary (Cochin estuary, west coast, India). Hydrol. Earth Syst. Sci. 17, 187–199 (2013).Article 

    Google Scholar 
    Haralambidou, K., Sylaios, G. & Tsihrintzis, V. A. Salt-wedge propagation in a Mediterranean micro-tidal river mouth. Estuar. Coast. Shelf Sci. 90, 174–184 (2010).Article 
    CAS 

    Google Scholar 
    Dyer, K. R. Estuaries: A physical introduction (1973).Rahman, M. et al. Impact assessment of twenty-two days fishing ban in the major spawning grounds of Tenualosa ilisha (Hamilton, 1822) on its spawning success in Bangladesh. J. Aquac. Res. Dev. 8, 489 (2017).Article 

    Google Scholar 
    Alves, A. S. et al. Spatial distribution of subtidal meiobenthos along estuarine gradients in two southern European estuaries (Portugal). J. Mar. Biol. Assoc. U.K. 89, 1529–1540 (2009).Article 
    CAS 

    Google Scholar 
    Teixeira, H., Salas, F., Borja, A., Neto, J. & Marques, J. A benthic perspective in assessing the ecological status of estuaries: The case of the Mondego estuary (Portugal). Ecol. Ind. 8, 404–416 (2008).Article 

    Google Scholar 
    Garmendia, M. et al. Eutrophication assessment in Basque estuaries: Comparing a North American and a European method. Estuar. Coasts 35, 991–1006 (2012).Article 

    Google Scholar 
    Istvánovics, V. Eutrophication of Lakes and Reservoirs. Lake Ecosystem Ecology 47–55 (Elsevier, 2010).
    Google Scholar 
    Dodds, W. K. Eutrophication and trophic state in rivers and streams. Limnol. Oceanogr. 51, 671–680 (2006).Article 
    CAS 

    Google Scholar 
    Bricker, S., Ferreira, J. & Simas, T. An integrated methodology for assessment of estuarine trophic status. Ecol. Model. 169, 39–60 (2003).Article 
    CAS 

    Google Scholar 
    Vega, M., Pardo, R., Barrado, E. & Debán, L. Assessment of seasonal and polluting effects on the quality of river water by exploratory data analysis. Water Res. 32, 3581–3592 (1998).Article 
    CAS 

    Google Scholar 
    Huang, Y., Yang, C., Wen, C. & Wen, G. S-type dissolved oxygen distribution along water depth in a canyon-shaped and algae blooming water source reservoir: Reasons and control. Int. J. Environ. Res. Public Health 16, 987 (2019).Article 
    CAS 

    Google Scholar 
    Rahman, M. & Cowx, I. Lunar periodicity in growth increment formation in otoliths of hilsa shad (Tenualosa ilisha, Clupeidae) in Bangladesh waters. Fish. Res. 81, 342–344 (2006).Article 

    Google Scholar 
    Rahman, M. J. Population Biology and Management of hilsa shad (Tenualosa ilisha) in Bangladesh (University of Hull, 2001).Milton, D. A. & Chenery, S. R. Movement patterns of the tropical shad hilsa (Tenualosa ilisha) inferred from transects of 87Sr/86Sr isotope ratios in their otoliths. Can. J. Fish. Aquat. Sci. 60, 1376–1385 (2003).Article 

    Google Scholar 
    Rahman, S., Sarker, M. R. H. & Mia, M. Y. Spatial and temporal variation of soil and water salinity in the South-Western and South-Central Coastal Region of Bangladesh. Irrig. Drain. 66, 854–871 (2017).Article 

    Google Scholar 
    Kida, S. & Yamazaki, D. The mechanism of the freshwater outflow through the Ganges–Brahmaputra–Meghna delta. Water Resour. Res. 56, e2019WR026412 (2020).Article 

    Google Scholar 
    Sarma, V. et al. Intra-annual variability in nutrients in the Godavari estuary, India. Contin. Shelf Res. 30, 2005–2014 (2010).Article 

    Google Scholar 
    Burford, M. et al. Controls on phytoplankton productivity in a wet–dry tropical estuary. Estuar. Coast. Shelf Sci. 113, 141–151 (2012).Article 
    CAS 

    Google Scholar 
    Vitousek, P. M. et al. Towards an ecological understanding of biological nitrogen fixation. Biogeochemistry 57, 1–45 (2002).Article 

    Google Scholar 
    Galloway, J. N. & Cowling, E. B. Reactive nitrogen and the world: 200 years of change. Ambio 31, 64–71 (2002).Article 

    Google Scholar 
    Kennish, M. & De Jonge, V. in Human-Induced Problems (Uses and Abuses) 113–148 (Elsevier Inc., 2012).Alongi, D., Boto, K. & Robertson, A. Nitrogen and phosphorus cycles. Coastal and Estuarine Studies, 251–251 (1993).Wolanski, E., McLusky, D., Laane, R. & Middleburg, J. (Academic Press, 2011).Suthers, I., Rissik, D. & Richardson, A. Plankton: A Guide to Their Ecology and Monitoring for Water Quality (CSIRO Publishing, 2019).Book 

    Google Scholar 
    Mackay, D. W. & Fleming, G. Correlation of dissolved oxygen levels, fresh-water flows and temperatures in a polluted estuary. Water Res. 3, 121–128 (1969).Article 

    Google Scholar 
    Lomas, M. W. & Glibert, P. M. Temperature regulation of nitrate uptake: A novel hypothesis about nitrate uptake and reduction in cool-water diatoms. Limnol. Oceanogr. 44, 556–572 (1999).Article 
    CAS 

    Google Scholar 
    Dortch, Q. The interaction between ammonium and nitrate uptake in phytoplankton. Mar. Ecol. Prog. Ser. Oldendorf 61, 183–201 (1990).Article 
    CAS 

    Google Scholar 
    Admiraal, W., Riaux-Gobin, C. & Laane, R. W. Interactions of ammonium, nitrate, and D-and L-amino acids in the nitrogen assimilation of two species of estuarine benthic diatoms. Mar. Ecol. Prog. Ser. 40, 267–273 (1987).Article 
    CAS 

    Google Scholar 
    Rabalais, N., Turner, R., Dortch, Q., Wiseman, W. Jr. & Sen Gupta, B. Nutrient changes in the Mississippi River and system responses on the adjacent continental shelf. Estuaries 19, 386 (1996).Article 
    CAS 

    Google Scholar 
    Gholizadeh, M. H., Melesse, A. M. & Reddi, L. Water quality assessment and apportionment of pollution sources using APCS-MLR and PMF receptor modeling techniques in three major rivers of South Florida. Sci. Total Environ. 566, 1552–1567 (2016).Article 

    Google Scholar 
    Elser, J. J. et al. Global analysis of nitrogen and phosphorus limitation of primary producers in freshwater, marine and terrestrial ecosystems. Ecol. Lett. 10, 1135–1142 (2007).Article 

    Google Scholar 
    Teichberg, M. et al. Eutrophication and macroalgal blooms in temperate and tropical coastal waters: Nutrient enrichment experiments with Ulva spp. Glob. Change Biol. 16, 2624–2637 (2010).Article 

    Google Scholar 
    Valiela, I. & Bowen, J. Nitrogen sources to watersheds and estuaries: Role of land cover mosaics and losses within watersheds. Environ. Pollut. 118, 239–248 (2002).Article 
    CAS 

    Google Scholar 
    Woodland, R. J. et al. Nitrogen loads explain primary productivity in estuaries at the ecosystem scale. Limnol. Oceanogr. 60, 1751–1762 (2015).Article 

    Google Scholar 
    Howarth, R. et al. Coupled biogeochemical cycles: Eutrophication and hypoxia in temperate estuaries and coastal marine ecosystems. Front. Ecol. Environ. 9, 18–26 (2011).Article 

    Google Scholar 
    Winder, J. A. & Cheng, D. M. Quantification of Factors Controlling the Development of Anabaena Circinalis Blooms (Urban Water Research Association of Australia, 1995).
    Google Scholar 
    Descy, J.-P. Phytoplankton composition and dynamics in the River Meuse (Belgium). Arch. Hydrobiol. Supplementband. Monographische Beiträge 78, 225–245 (1987).
    Google Scholar 
    Robarts, R. D. & Zohary, T. Temperature effects on photosynthetic capacity, respiration, and growth rates of bloom-forming cyanobacteria. NZ J. Mar. Freshw. Res. 21, 391–399 (1987).Article 
    CAS 

    Google Scholar 
    Visser, P. M., Ibelings, B. W., Bormans, M. & Huisman, J. Artificial mixing to control cyanobacterial blooms: A review. Aquat. Ecol. 50, 423–441 (2016).Article 
    CAS 

    Google Scholar 
    Krishnan, A., Das, R. & Vimexen, V. Seasonal phytoplankton succession in Netravathi-Gurupura estuary, Karnataka, India: Study on a three tier hydrographic platform. Estuar. Coast. Shelf Sci. 242, 106830 (2020).Article 

    Google Scholar 
    Srinivas, L., Seeta, Y. & Reddy, M. Bacillariophyceae as ecological indicators of water quality in Manair Dam, Karimnagar, India. Int. J. Sci. Res. Sci. Tech 4, 468–474 (2018).
    Google Scholar 
    Mohanty, B. P. et al. Fatty acid profile of Indian shad Tenualosa ilisha oil and its dietary significance. Natl. Acad. Sci. Lett. 35, 263–269 (2012).Article 
    CAS 

    Google Scholar 
    De, D. et al. Nutritional profiling of hilsa (Tenualosa ilisha) of different size groups and sensory evaluation of their adults from different riverine systems. Sci. Rep. 9, 1–11 (2019).Article 
    CAS 

    Google Scholar 
    Hasan, K. M. M., Ahmed, Z. F., Wahab, M. A. & Mohammed, E. Y. Food and Feeding Ecology of hilsa (Tenualosa ilisha) in Bangladesh’s Meghna River Basin. (International Institute for Environment and Development, 2016). More

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    10 startling images of nature in crisis — and the struggle to save it

    Global statistics on declining biodiversity can give the impression that every population of every species is in a downward spiral. In fact, many populations are stable or growing, while a small number of species faces truly existential challenges. These photos capture some specific crises. They are images of threats unfolding, of desperate attempts at species defence and of the beautiful living world that is at stake.
    The 15th United Nations Biodiversity Conference, COP15, opens in Montreal, Canada, on 7 December. At the meeting, delegates will attempt to agree on goals for stabilizing species’ declines by 2030 and reverse them by mid-century. The current draft framework agreement promises nothing less than a “transformation in society’s relationship with biodiversity”.
    Help for the kelp. Tasmania’s forests of giant kelp (Macrocystis pyrifera) are dying as climate change shifts ocean currents, bringing warm water to the east coast of the temperate Australian island. The kelp forests host an entire ecosystem, including abalone and crayfish — both economically important species and part of local food culture. Now, researchers at the Institute for Marine and Antarctic Studies in Hobart are breeding kelp plants that can tolerate warmer conditions, and replanting them along the coast — a trial for what they hope will become a landscape-scale restoration. More

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    Sewage surveillance of antibiotic resistance holds both opportunities and challenges

    Huijbers, P. M. C., Flach, C.-F. & Larsson, D. G. J. A conceptual framework for the environmental surveillance of antibiotics and antibiotic resistance. Environ. Int. 130, 104880 (2019).Article 

    Google Scholar 
    Aarestrup, F. M. & Woolhouse, M. E. J. Using sewage for surveillance of antimicrobial resistance. Science 367, 630–632 (2020).Article 

    Google Scholar 
    European Commission. Proposal for a revised Urban Wastewater Treatment Directive. European Commission https://environment.ec.europa.eu/publications/proposal-revised-urban-wastewater-treatment-directive_en (2022).US Centres for Disease Control and Prevention. COVID-19 impacts on environment (e.g., water, soil) and sanitation: addressing antimicrobials and antimicrobial resistant threats in the environment. US Centres for Disease Control and Prevention https://www.cdc.gov/drugresistance/pdf/covid19/COVID19-Impacts-AR-Environment-Sanitation-508.pdf (2021).Flach, C.-F., Hutinel, M., Razavi, M., Åhrén, C. & Larsson, D. G. J. Monitoring of hospital sewage shows both promise and limitations as an early-warning system for carbapenemase-producing Enterobacterales in a low-prevalence setting. Water Res. 200, 117261 (2021).Article 

    Google Scholar 
    Larsson, D. G. J. & Flach, C.-F. Antibiotic resistance in the environment. Nat. Rev. Microbiol. 20, 257–269 (2022).Article 

    Google Scholar 
    Newton, R. J. et al. Sewage reflects the microbiomes of human populations. mBio 6, e02574 (2015).Article 

    Google Scholar 
    Huijbers, P. M. C., Larsson, D. G. J. & Flach, C. F. Surveillance of antibiotic resistant Escherichia coli in human populations through urban wastewater in ten European countries. Environ. Pollut. 261, 114200 (2020).Article 

    Google Scholar 
    Laxminarayan, R. & Macauley, M. K. The Value of Infromation: Methodological Frontiers and New Applications in Environment and Health 1st edn (Springer Dordrecht, 2012).Munk, P. et al. Genomic analysis of sewage from 101 countries reveals global landscape of antimicrobial resistance. Nat. Commun. 13, 7251 (2022).Article 

    Google Scholar  More

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    Reply to: Erroneous predictions of auxotrophies by CarveMe

    Machado, D. et al. Polarization of microbial communities between competitive and cooperative metabolism. Nat. Ecol. Evol. 5, 195–203 (2021).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Thompson, L. R. et al. A communal catalogue reveals Earth’s multiscale microbial diversity. Nature 551, 457–463 (2017).Article 
    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 
    Price, M. Erroneous predictions of auxotrophies by CarveMe. https://doi.org/10.1038/s41559-022-01936-3 (2022).Machado, D., Andrejev, S., Tramontano, M. & 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 
    PubMed 
    PubMed Central 

    Google Scholar 
    Price, M. N., Deutschbauer, A. M. & Arkin, A. P. GapMind: automated annotation of amino acid biosynthesis. mSystems 5, e00291-20 (2020).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Mee, M. T., Collins, J. J., Church, G. M. & Wang, H. H. Syntrophic exchange in synthetic microbial communities. Proc. Natl. Acad. Sci. USA 111, E2149–E2156 (2014).Article 
    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 
    Ponomarova, O. et al. Yeast creates a niche for symbiotic lactic acid bacteria through nitrogen overflow. Cell Syst. 5, 345–357.e6 (2017).Article 
    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 
    Zengler, K. & Zaramela, L. S. The social network of microorganisms—how auxotrophies shape complex communities. Nat. Rev. Microbiol. 16, 383–390 (2018).Article 
    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 
    Giri, S. et al. Metabolic dissimilarity determines the establishment of cross-feeding interactions in bacteria. Curr. Biol. 31, 5547–5557.e6 (2021).Article 
    CAS 
    PubMed 

    Google Scholar 
    Morris, J. J., Lenski, R. E. & Zinser, E. R. The black queen hypothesis: evolution of dependencies through adaptive gene loss. mBio 3, e00036-12 (2012).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Campbell, K. et al. Self-establishing communities enable cooperative metabolite exchange in a eukaryote. eLife 4, e09943 (2015).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    D’Souza, G. & Kost, C. Experimental evolution of metabolic dependency in bacteria. PLOS Genet. 12, e1006364 (2016).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Ziesack, M. et al. Engineered interspecies amino acid cross-feeding increases population evenness in a synthetic bacterial consortium. mSystems 4, e00352-19 (2019).Article 
    PubMed 
    PubMed Central 

    Google Scholar 
    Ryback, B., Bortfeld-Miller, M. & Vorholt, J. A. Metabolic adaptation to vitamin auxotrophy by leaf-associated bacteria. ISME J. https://doi.org/10.1038/s41396-022-01303-x (2022). More

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    Carbon turnover gets wet

    Whether land acts as a carbon sink or source depends largely on two opposite fluxes: carbon uptake through photosynthesis and carbon release through turnover. Turnover occurs through multiple processes, including but not limited to, leaf senescence, tree mortality, and respiration by plants, microbes, and animals. Each of these processes is sensitive to climate, and ecologists and climatologists have been working to figure out how temperature regulates biological activities and to what extent the carbon cycle responds to global warming. Previous theoretical and experimental studies have yielded conflicting relationships between temperature and carbon turnover, with large variations across ecosystems, climate and time-scale1,2,3,4. Writing in Nature Geoscience, Fan et al.5 find that hydrometeorological factors have an important influence on how the turnover time of land carbon responds to changes in temperature. More

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    Analysis of influencing factors of phenanthrene adsorption by different soils in Guanzhong basin based on response surface method

    Surface morphology analysisSEM images were shown in Fig. 1. It showed that the contour of three soils were fairly clear before adsorption. But it became fuzzier and the degree of cementation was increased when phenanthrene was adsorbed on the soils. According to the surface morphology, the silty sand (A) had furrows on the surface before adsorption compared with the fairly smooth without any furrows after adsorption (B). The silts (C) were flaky and the lamellar accumulation decreased (D). The loess (E) had a smooth surface with some flaky and rod like structure, after adsorption (F), the surface of loess increased in clay-like structure.Figure 1SEM micrographs of the three soil samples. (A) Silty sand; (B) Adsorbing 5 h of Silty sand; (C) Silts; (D) Adsorbing 5 h of Silts; (E) Loess; (F) Adsorbing 5 h of Loess.Full size imageAdsorption and desorption experimentsAdsorption and desorption kineticsAdsorption kinetics is one of the most important characteristics governing solute uptake rate and represents adsorption efficiency33. The sorption and desorption kinetics of phenanthrene in three soils were shown in Fig. 2. The results showed that the adsorption processes among all soils were similar. The kinetics of phenanthrene in soils was completed in two steps: a “fast” adsorption and a “slow” adsorption. The adsorption amount increased during 0-18h. It was a rapid reaction from 0 to 200 minutes. From 200 to 600 minutes, the adsorption amount increased slightly into balance. This phenomenon was due to the adsorption of phenanthrene occurred on the surface of soil organic matter. With the increase of time, soil surface adsorption sites were gradually saturated, causing the decrease of adsorption rate until reaching the equilibrium. Phenanthrene was a hydrophobic substance. It was easy to reach the soil surface and adhere to the grain surface. The results were consistent with the study of had also found that the balance time was approximately 18h and the adsorption amount increased with the adsorption reaction time34. Under the same conditions, loess had the highest adsorption capacity, which was mainly due to the highest organic content 18. The maximum phenanthrene sorption capacities ranked as follows: loess > silty sand > silts. As shown in Fig. 2, phenanthrene desorption in soils was relatively quick and its desorption equilibrium time was 3h. To reach an adequate desorption balance while remaining consistent with the adsorption reaction time, the balance time of the adsorption–desorption experiment was set at 18h. Generally, PAHs below 4 cycles could reach the adsorption equilibrium for about 16~24h.Figure 2(a)Adsorption equilibration curves of phenanthrene sorption in soils. (b) Desorption equilibration curves of phenanthrene sorption in soils.Full size imagePseudo-second-order and Elovich models were used to study the phenanthrene adsorption mechanism (Table 3). Phenanthrene sorption kinetics were satisfactorily described by a pseudo-second-order model with coefficients of determination (R2) ranging from 0.99875 to 0.99847, compared with R2 values of 0.26508–0.73901 for the Elovich model. This well-fitting pseudo-second-order model indicated that the rate-limiting step was chemical adsorption, including electronic forces through sharing or exchange of electrons35,36. Moreover, it suggested that sorption was governed by the availability of sorption sites on the soil surfaces instead of by the phenanthrene concentration in solution.Table 3 Constants and coeffients of determination of Pseudo-second-order kinetics and Elovich models of sorption.Full size tableAdsorption and desorption isothermsThe isotherm was used for quantitative analysis of phenanthrene transport from liquid to solid phase and for understanding the nature of interactions between phenanthrene and the soil matrix. The sorption and desorption isotherms of phenanthrene in soils were shown in Fig. 3. The data showed that phenanthrene adsorption and desorption capacities of three soils varied markedly due to their different physicochemical properties. With the increase of phenanthrene concentration, the adsorbed amount increased. At the same temperature, the adsorption capacity of silty sand was minimum while loess was maximum. This is mainly related to the soil physicochemical properties. At the same initial concentration, the temperature increase from 20 °C to 40 °C showed that the adsorption and desorption capacity decreased with temperature increase. On the one hand, the rise of temperature can increase the phenanthrene solubility in the liquid phase. On the other hand, it could reduce various forces between the soil surface and phenanthrene37.Figure 3(a)20 °C adsorption isotherms for phenanthrene in soils. (b)30 °C adsorption isotherms for phenanthrene in soils. (c)40 °C adsorption isotherms for phenanthrene in soils. (d) 20 °C desorption isotherms for phenanthrene in soils. (e) 30 °C desorption isotherms for phenanthrene in soils. (f) 40 °C desorption isotherms for phenanthrene in soils.Full size imageThe Freundlich isotherm was used mainly for adsorption surfaces with nonuniform energy distribution, and the Langmuir isotherm was used for monolayer adsorption on perfectly smooth and homogeneous surfaces38. The experimental data were fitted with the Langmuir and Freundlich adsorption models, and the isotherm parameters logKF, 1/n, KL, qmax and the coefficient of determination (R2) of phenanthrene in soils were listed in Table 4.Table 4 Isotherm parameters for Phenanthrene sorption in soils.Full size tableAs shown in Table 4, according to the coefficients of determination (R2), all soils were better fitted with the Freundlich model, which assumes that phenanthrene sorption and desorption occurs on a heterogeneous surface with the possibility of sorption being multi-layered39. This phenomenon has also been observed in humic acid and nanometer clay mineral40. It showed that the soil adsorption of organic matter was not only surface adsorption but also the process of soil organic matter distribution41,42,43 reached the equilibrium isotherm fitted well with the Freundlich equation when studying the adsorption behavior of aromatic compounds by solids.Adsorption and desorption thermodynamicsTo clarify the adsorption mechanisms, the thermodynamic parameters mentioned earlier were calculated and presented in Table 5. Generally, the value of Gibbs free energy changeΔG0 indicated the spontaneity of a chemical reaction. Therefore, it could evaluate whether sorption was relate to spontaneous interaction44. Negative values of ΔG0 indicated that the feasibility and spontaneous nature. The research was under the temperature range about 293–313 K. For adsorption process, all soils ΔG0 was  0 and desorption ΔH  1, P  temperature  > phenanthrene concentration  > pH. In the interaction, the phenanthrene concentration and organic matter have a significant effect on the silt adsorption rate. The coefficient of determination of the silt complex correlation is R2 = 0.9464, indicating that the response model has a good fit, and the experimental error is within the acceptable range. Adjusting the complex correlation coefficient R2 = 0.8982 indicates that the regression relationship can explain 89.82% of the change in the dependent variable. Therefore, this The model can be used to analyze and predict the effect of different factors on the adsorption rate of phenanthrene.3D response surface analysisIn response surface optimization, the three-dimensional response surface graph reflects the influence of the interaction of the other two variables on the response value, and the slope of the response surface reflects the significance of the interaction of the two variables on the response value. The more significant the interaction effect is on the response value, when the slope is gentle, the effect is not significant. If the contour map is elliptical, it indicates that the interaction between the two variables is significant, and if the contour map is circular, it is not significant46. In addition, the slope and density of the contour line also reflect the influence of the variable on the response value. The steeper the contour line and the greater the density, the greater the influence of the variable on the response value47.

    (1) Loess Fig. 5 is a three-dimensional response surface diagram of the interaction between initial phenanthrene concentration and pH to phenanthrene adsorption on loess. It can be seen from the figure that the slope of the response surface graph is steep, and the contour line is an approximate circle, indicating that the interaction between phenanthrene concentration and pH is not significant for the response value. With the increase of pH, the adsorption rate of phenanthrene on loess showed a slow decline at first to the lowest point at 6, and then gradually increased. When the soil pH was close to 6, with the increase of the initial phenanthrene concentration, the adsorption rate of loess also showed a trend of first decreasing and then increasing. According to the F value, F = 0.337, P = 0.5532  > 0.05, it can be concluded that soil pH and initial phenanthrene concentration of the solution have no significant interaction on the adsorption rate of loess.

    Figure 6 shows the effects of initial phenanthrene concentration and organic matter on phenanthrene adsorption on Loess under the condition that pH value and temperature are at the central point. It can be seen from the figure that the initial phenanthrene concentration and soil organic matter contour are steep, indicating that their interaction is significant. The range of phenanthrene adsorption rate is 70 ~ 95, and the change of surface is steep. From the Loess error analysis, it can be seen that if f value is 6.05 and P value is 0.0275  More