The Brazil Nut Research Atlas
Of 401 accepted Lecythidaceae species, 223 (55.6 percent) have no indexed paper; 3,588 indexed studies concentrate on 178 species.
We tagged 3,510 of the 3,588 studies of the Lecythidaceae indexed at the time of this atlas (October 2026), the family of the Brazil nut, the cannonball tree and the Amazon’s great canopy emergents, against 46 dimensions shared across domains plus domain-specific extensions. It is a family whose economy depends on the forest staying intact. The research covers a handful of species well and the rest very little.
Every species in the family
We load every accepted Lecythidaceae species from Kew's World Checklist of Vascular Plants (Version 16) and link each, together with its WCVP synonyms, to the indexed literature. A species with no linked papers is recorded as having no indexed research.
The family is a Neotropical giant with a paleotropical tail: Bertholletia excelsa, the Brazil nut; Couroupita, the cannonball tree; Eschweilera and the genera Kew has recently split from it, the subtly flowered “matchbox” trees that dominate Amazonian forests; the timber genera Couratari and Cariniana; and the Old World Barringtonia of tropical coasts. COMPASS links each of the 401 accepted species to OpenAlex, tags every study, and geocodes each to its study site. What emerges is a portrait of a family the world eats, trades and logs, and has barely begun to catalogue.
Research focus: products, trade and livelihoods
This is the rare family whose economic value depends on not converting the forest. Its most-studied use is wild harvest: production is overwhelmingly wild-harvested, and plantations exist but remain marginal because of slow growth, pollinator dependence and long juvenility.
About a third of studies (1,208 of 3,588) touch some economic dimension, and the pattern is unmistakably one of a standing-forest economy: edible product, commercial processing, non-timber forest-product harvest and trade, rural livelihoods, and sustainable-use management. The seed, the nut, is the single most-studied plant part. The Brazil nut is its emblem: a globally traded commodity gathered from wild trees that resist cultivation, depending on intact forest, its orchid-bee pollinators and the agoutis that crack and disperse it.
Species with no indexed paper
A resilient bioeconomy needs many species, products, and markets. The research so far covers only a few of them.
Research concentrates on a familiar few, and most of the family has little or no indexed research. The largest genus on the WCVP census is the Old World coastal genus Barringtonia, 73 species, 68% of them with no indexed paper. Eschweilera keeps 66 accepted species, 53% of them with no indexed paper, after Kew's recent revision moved many former Eschweilera names into Scottmoria, Chytroma, Imbiriba, Guaiania and Pachylecythis; together these matchbox trees remain a structural backbone of Amazonian forest, and the two largest segregates fare no better: Scottmoria 57% of 35 species, Chytroma 61% of 18. Gustavia is 55% without an indexed paper (26 of 47), Foetidia 72% (13 of 18). Many are trees with edible fruits, useful timbers and little-studied chemistry, potential products of a bioeconomy that still rests on a single nut.
Research effort by IUCN category
As in the other families we have mapped, research runs opposite to risk. Here that pattern meets the bioeconomy case directly: the species with the most untapped value are also among those most likely to disappear first.
Among least-concern species, 43% have no indexed research; among the vulnerable, 83%; among the data-deficient, 86%. Some of this is structural: a species is often listed as threatened because it is rare or narrowly ranged, the same traits that depress study, so it is an association rather than simple neglect. But the consequence is concrete: the very species a diversified forest economy might one day rest on are the ones being lost before they are documented. Conservation framing appears in just 6% of studies.
Study-site countries compared with range countries
The research is concentrated in one country, but the resource is regional. Where the work happens and where the gaps are do not line up.
For where research sits against species ranges, coverage cells and access distances, see section 6; for the same sites set against environmental change and split by decade, section 7.
The map above is fixed. The interactive version plots the same study sites and lets you filter them by this atlas’s own tags, country, year and citations, then read the papers behind any cluster.
Open the interactive map →Brazil accounts for more of the located studies than every other country combined: 563 of the 928 studies with a locatable study site have one in Brazil, at 354 distinct sites, against 56 studies in Indonesia, 53 in Colombia and 35 in Peru. The Brazil-nut economy has made the family a Brazilian research subject. But the family, and its potential, are pan-Amazonian and pan-tropical.
Where the species with no indexed research are
Map instead the species with no indexed research, using each species' native range countries from the WCVP distribution table, and the frontier moves off Brazil. They concentrate across the northern Amazon and Guiana Shield, Colombia (43 species with no indexed research, against 42 in Brazil), Venezuela (21), Panama (21), Guyana (16), Ecuador (15) and French Guiana (15), and into the paleotropics: Malaysia (25), Indonesia (24), Gabon (19) and Cameroon (18). Colombia now holds more species with no indexed research than Brazil, on a fraction of the research. A species counts in every country of its native range.
Geographic distribution of study sites
Of the 400 species with known range countries, 286 (71.5%) have no locatable study site inside any of them; the sites that exist cluster in a few cells and close to cities.
1 · Species ranges against study sites
For each of the 401 species we compared two country lists: where it is known to occur, and where its indexed papers were carried out. Known range countries come from the Kew World Checklist of Vascular Plants distribution table (TDWG level-3 areas mapped to countries, native and introduced), so a country counts as range wherever the checklist records the species; in-range is a country-level test, generous within a large country and conservative for a species studied only just across a border. Of the 400 species with range data, 286 (71.5%) have no locatable study site inside any range country. That figure mixes two things that only a paper-level check can separate: species with no research (223 of 401 have no indexed research) and species whose papers name no place a geoparser can locate (63 of the 178 studied species). A further 1 species were studied only outside their known range countries.
Range shortfall by country
Each country is shaded by the share of its range species that have no locatable study site inside it: darker means a larger share of the species known to occur there have not been studied in the field there. Unshaded land has no census species in range. The four countries with the most range species lacking a site are labelled (Colombia, Brazil, Venezuela, Indonesia); they also head the table below.
| Country | Range species | With an in-country study site | Shortfall | Study sites in country |
|---|---|---|---|---|
| Colombia | 90 | 18 | 80% | 58 |
| Brazil | 119 | 49 | 59% | 354 |
| Venezuela | 56 | 10 | 82% | 9 |
| France | 42 | 0 | 100% | 0 |
| Indonesia | 48 | 8 | 83% | 60 |
| Guyana | 39 | 0 | 100% | 0 |
| Malaysia | 45 | 6 | 87% | 8 |
| Panama | 41 | 3 | 93% | 7 |
| Ecuador | 50 | 13 | 74% | 18 |
| Peru | 35 | 4 | 89% | 17 |
2 · Where the study sites are
Each cell is one hexagon of the H3 grid, drawn on its true boundary so that the cells tile without overlap; darker cells hold more distinct study sites. Most cells hold one site; the fieldwork of the whole corpus concentrates in a small number of them.
The densest window, enlarged
The dashed rectangle on the map above marks the window that holds the most study sites (86°W to 32°W, 24°S to 4°N). Here it is at a larger scale and at the grid's own resolution 3 (about 12,400 km2 per cell), with its own log ramp.
Many species, few studies
The ten range countries with the most census species and two or fewer locatable study sites from this corpus. Because the range lists include cultivated and museum records, a country can appear here through garden and herbarium holdings rather than wild populations; read the list as a prompt to check, not a verdict.
| Country | Species in range | Study sites in country |
|---|---|---|
| France | 42 | 0 |
| Guyana | 39 | 0 |
| Singapore | 31 | 1 |
| Suriname | 29 | 0 |
| Brunei | 26 | 0 |
| Gabon | 24 | 1 |
| Papua New Guinea | 24 | 2 |
| Madagascar | 16 | 0 |
| Congo (Brazzaville) | 15 | 1 |
| Myanmar | 13 | 1 |
3 · How far the sites are from a city
Distance from each study site to the nearest populated place of 100,000 people or more is a rough measure of how reachable the fieldwork was. The busiest access points, counted greedily so that no site is counted twice, are Castanhal (Brazil, 21 sites within 100 km), Rio Claro (Brazil, 19 sites within 100 km), Cabo de Santo Agostinho (Brazil, 18 sites within 100 km); 17.7% of all sites lie within 100 km of one of the ten busiest.
These are straight-line distances, not travel times; roads, terrain, sea ice and protected-area access are not modelled. Study-site coordinates are geoparsed from abstracts, and region-level places sit at their centroid.
4 · Method note
Sources. known range countries = Kew WCVP distribution table (TDWG level-3 areas mapped to countries, native and introduced; entity_places role=range, source wcvp / wcvp_introduced; no polygons); access points = Natural Earth ne_10m_populated_places_simple, GitHub master 5.2.0-pre (nvkelso/natural-earth-vector, downloaded 2026-09-29) (populated places with 100,000 people or more), public domain; grid = H3 resolution 3 (h3-js 4.5.0), drawn on the true cell boundaries from h3-js and aggregated one level (h3 cellToParent) on the main maps. A study site is a place a paper's abstract names as the location of the work, resolved to coordinates by a gazetteer and kept only when it came from one of the six trusted geocode sources; 928 of 3,588 studies (25.9%) have one. Density and distance use precise sites only (not a whole country, not a rounded centroid): 660 distinct places.
Caveat. Study-site coordinates come from automated geoparsing; a 40-site manual check found 31 plausible; a 100 to 200 pin human check is planned. Range coverage is a country-level test, so a study in the right country but far from the species' actual distribution still counts as in range.
Provenance. Generated 2026-10-14 from the published database. Figures in this section are recomputed by phase1/spatial_shortfall.js and checked by the figures audit.
5 · Explore these layers
The coverage cells are a layer on the interactive map, switched on when you open it from here, with the study sites and this atlas's tag filters underneath. A second layer, range shortfall by country, shades each country as the map above does. Any country, ecoregion, administrative region or drawn area can be queried against the whole database in the place explorer, which lists the papers inside it and the topics that are thin there.
Research against change
Three questions of the same study sites: where the environment is changing fastest with the least located research, whether research effort tracks change at all (it does not: the correlation is near zero), and when the located research was published. 97 of 431 ecoregions sit in the high-change, low-research quadrant for forest loss.
In this corpus the rate of environmental change and the density of located research are essentially unrelated: Spearman's rank correlation between the two, unit by unit, is near zero. For forest loss it is 0.074 across 431 ecoregions and 0.059 across 1,143 admin1 regions; for drying it is −0.262 across 167 ecoregions and −0.149 across 215 admin1 regions. These are descriptive figures: they do not show that change causes or deters research, and the units differ in area, accessibility and richness. What they do show is where fast change and little located research coincide, which is the list each block below ranks.
1 · Forest loss 2001 to 2024
Change here is the share of the area that was forest in 2000 (tree cover of 30 percent or more) with a loss event between 2001 and 2024, from Hansen Global Forest Change v1.12 at 30 m. Each ecoregion and each first-level administrative region is placed in one of four quadrants: the top third of the universe by forest loss is high change, the bottom third by located research density (papers of this corpus with a precise study site inside the unit, per 10,000 km2) is low research. The high-change, low-research quadrant is the candidate gap list.
Loss is any stand-replacing event, including fire and the rotational harvest of plantations, and regrowth is not subtracted, so a high value can be a working plantation landscape as easily as a cleared forest; the 30 percent canopy threshold makes open woodland "not forest".
| Ecoregion | Country | Forest lost | Papers with a site | Per 10,000 km2 | Range species without a site |
|---|---|---|---|---|---|
| Piney WoodsTemperate Conifer Forests | United States | 75.4%90% forested in 2000 | 0 | 0.00 | 1 |
| Sumatran freshwater swamp forestsTropical & Subtropical Moist Broadleaf Forests | Indonesia | 72.3%76% forested in 2000 | 0 | 0.00 | 48 |
| Southeast US conifer savannasTemperate Grasslands, Savannas & Shrublands | United States | 70.9%85% forested in 2000 | 0 | 0.00 | 1 |
| Esperance malleeMediterranean Forests, Woodlands & Scrub | Australia | 69.3%21% forested in 2000 | 0 | 0.00 | 6 |
| Drakensberg grasslandsTropical & Subtropical Grasslands, Savannas & Shrublands | South Africa, Lesotho | 68.8%7% forested in 2000 | 0 | 0.00 | 1 |
| Madagascar humid forestsTropical & Subtropical Moist Broadleaf Forests | Madagascar | 67.7%88% forested in 2000 | 0 | 0.00 | 16 |
| California montane chaparral and woodlandsMediterranean Forests, Woodlands & Scrub | United States, México | 65.7%30% forested in 2000 | 0 | 0.00 | 2 |
| Western Guinean lowland forestsTropical & Subtropical Moist Broadleaf Forests | Liberia, Sierra Leone, Côte d'Ivoire, Guinea | 62.0%95% forested in 2000 | 0 | 0.00 | 9 |
| Northern Khorat Plateau moist deciduous forestsTropical & Subtropical Moist Broadleaf Forests | Thailand, Laos | 61.3%25% forested in 2000 | 0 | 0.00 | 18 |
| Naracoorte woodlandsMediterranean Forests, Woodlands & Scrub | Australia | 59.3%18% forested in 2000 | 0 | 0.00 | 6 |
| Region | Country | Forest lost | Papers with a site | Per 10,000 km2 | Range species without a site |
|---|---|---|---|---|---|
| Bình Dương | Vietnam | 96.3%37% forested in 2000 | 0 | 0.00 | 11 |
| Bong | Liberia | 95.5%100% forested in 2000 | 0 | 0.00 | 7 |
| Montserrado | Liberia | 90.4%88% forested in 2000 | 0 | 0.00 | 7 |
| Bomi | Liberia | 89.3%99% forested in 2000 | 0 | 0.00 | 7 |
| Melaka | Malaysia | 88.7%83% forested in 2000 | 0 | 0.00 | 45 |
| Margibi | Liberia | 87.3%95% forested in 2000 | 0 | 0.00 | 7 |
| Otdar Mean Chey | Cambodia | 84.7%45% forested in 2000 | 0 | 0.00 | 7 |
| Southern | Sierra Leone | 83.8%90% forested in 2000 | 0 | 0.00 | 6 |
| Bangka Belitung | Indonesia | 83.5%91% forested in 2000 | 0 | 0.00 | 48 |
| Grand Bassa | Liberia | 80.4%100% forested in 2000 | 0 | 0.00 | 7 |
Forest loss 2001 to 2024, cell by cell
2 · Aridity trend 1990 to 2024
Change here is the linear trend of the annual aridity index (precipitation over potential evapotranspiration, P/PET) from 1990 to 2024, as percent change per decade of the 1990 to 1999 mean, from TerraClimate at about 4.6 km; a negative number means drying. Each ecoregion and each first-level administrative region is placed in one of four quadrants: the top third of the universe by drying is high change, the bottom third by located research density (papers of this corpus with a precise study site inside the unit, per 10,000 km2) is low research. The high-change, low-research quadrant is the candidate gap list.
TerraClimate is an interpolated climate surface, so a 35-year trend at 4 km carries station-density and interpolation error, and a relative trend is unstable where the baseline is near zero; the ranking is restricted to drylands (mean P/PET under 0.65) and excludes hyper-arid units (mean under 0.05) for that reason.
| Ecoregion | Country | Aridity trend | Papers with a site | Per 10,000 km2 | Range species without a site |
|---|---|---|---|---|---|
| Dry ChacoTropical & Subtropical Grasslands, Savannas & Shrublands | Argentina, Paraguay, Bolivia | −10.3%semi-arid | 0 | 0.00 | 19 |
| Western Australian Mulga shrublandsDeserts & Xeric Shrublands | Australia | −9.5%arid | 0 | 0.00 | 4 |
| Knysna-Amatole montane forestsTropical & Subtropical Moist Broadleaf Forests | South Africa | −9.2%dry sub-humid | 0 | 0.00 | 1 |
| Namaqualand-Richtersveld steppeDeserts & Xeric Shrublands | South Africa, Namibia | −8.6%arid | 0 | 0.00 | 1 |
| Succulent Karoo xeric shrublandsDeserts & Xeric Shrublands | South Africa | −8.6%arid | 0 | 0.00 | 1 |
| Southern Andean YungasTropical & Subtropical Moist Broadleaf Forests | Argentina, Bolivia | −8.5%dry sub-humid | 0 | 0.00 | 19 |
| Edwards Plateau savannaTemperate Grasslands, Savannas & Shrublands | United States | −8.2%semi-arid | 0 | 0.00 | 1 |
| Fynbos shrublandMediterranean Forests, Woodlands & Scrub | South Africa | −7.8%semi-arid | 0 | 0.00 | 1 |
| Galápagos Islands xeric scrubDeserts & Xeric Shrublands | Ecuador | −7.8%semi-arid | 0 | 0.00 | 50 |
| Chihuahuan desertDeserts & Xeric Shrublands | México, United States | −7.8%arid | 0 | 0.00 | 2 |
| Region | Country | Aridity trend | Papers with a site | Per 10,000 km2 | Range species without a site |
|---|---|---|---|---|---|
| Hilmand | Afghanistan | −10.8%arid | 0 | 0.00 | 2 |
| Xizang | China | −10.5%semi-arid | 0 | 0.00 | 2 |
| Farah | Afghanistan | −10.3%arid | 0 | 0.00 | 2 |
| Bamingui-Bangoran | Central African Republic | −9.3%dry sub-humid | 0 | 0.00 | 6 |
| Alto Paraguay | Paraguay | −8.7%semi-arid | 0 | 0.00 | 1 |
| Kandahar | Afghanistan | −8.4%arid | 0 | 0.00 | 2 |
| Vakaga | Central African Republic | −8.4%semi-arid | 0 | 0.00 | 6 |
| New Mexico | United States | −8.2%semi-arid | 0 | 0.00 | 1 |
| Galápagos | Ecuador | −7.8%semi-arid | 0 | 0.00 | 50 |
| Western Cape | South Africa | −7.7%semi-arid | 0 | 0.00 | 1 |
Aridity trend 1990 to 2024, cell by cell
3 · When the research happened
The same study sites split by decade of publication. Of the 853 located papers, 75.7% were published in the 2010s or 2020s and 50.5% since 2016. The whole corpus of 3,588 papers, located or not, is 76.1% from those two decades, so located research is about as recent as the corpus. Of the 140 ecoregions with a located paper, 16 have none published since 2010; of the 165 admin1 regions, 26. 2 located papers have no publication year.
The decade with the most located papers, cell by cell
4 · Method note
Change layers. Forest loss 2001 to 2024 = UMD/hansen/global_forest_change_2024_v1_12 (v1.12 (2024 update)), 2001-2024, sampled at 1,000 m (native 30 m), CC BY 4.0; Aridity trend 1990 to 2024 = IDAHO_EPSCOR/TERRACLIMATE (TerraClimate monthly, EE catalogue copy (1958-01 to 2024-12 at run time)), 1990-2024, sampled at 4,638 m (native 4,638 m), TerraClimate: CC0 1.0 (public domain). MODIS: NASA, no restrictions; dryland classes after UNEP 1992. Values are area means of a systematic sample over each H3 cell of the grid (the maps above draw them one resolution coarser, as valid-area-weighted means of the child cells) and each unit outline (RESOLVE Ecoregions 2017 and GADM 4.1, simplified for display), computed in Google Earth Engine; boundary pixels are weighted fractionally. Layers are remote-sensing and reanalysis products, not field measurements.
Research. 853 of 3,588 papers in this corpus have a precise trusted study site (the same selection as the density map above); a paper counts once per cell and once per unit it has a site in, and a unit's density is papers per 10,000 km2 of its area. Only units of 1,000 km2 or more are ranked, and only units in a country where a census species is known to occur, so that a city-state's density is not set against a province's. 5 precise places (open sea, Southern Ocean, atoll centroids) fall in no ecoregion and 1 in no admin1 region; they are in the cell maps but not in the unit tables. Range species without a site is a country-level test (every unit in a country is credited with the country's whole range list), so it is an upper bound.
Reading it. A near-zero correlation says that, across these units, more change does not go with more or with less located research. It does not say that change deters research or that research prevents change, and units differ in area, accessibility, richness and national research capacity. A unit in the high-change, low-research quadrant is a candidate gap, not a proven one: papers whose text names no locatable site are invisible here, and the geoparsing caveat of the section above applies.
Provenance. Generated 2026-10-14 from the published database and the Earth Engine cache. Figures in this section are recomputed by phase1/research_vs_change.js, drawn by phase1/gen_atlas_change_section.js and checked by the figures audit.
5 · Explore these layers
These layers are on the interactive map as forest loss 2001 to 2024 and aridity trend 1990 to 2024, cell by cell with the value and the located papers on hover, and a decade selector that limits the study-site dots to one decade of publication.
Expected research Beta
How much located research would each place be expected to carry, given its size, species richness, access, environmental change, biome and national research effort, and where the record falls short of that expectation. Cross-validated pseudo-R2 0.67 for ecoregions and 0.44 for administrative regions. Beta: a first model, stated with its interval and its limits.
Beta This section fits a model of research attention: the number of papers of this corpus with a precise study site inside each ecoregion and each first-level administrative region, predicted from the unit's area, the number of census species whose known range countries include the unit (country level, so it separates countries rather than places within one), its distance to the nearest city of 100,000 people, forest loss and the aridity trend, its biome, realm and latitude band, and how much located research the rest of its country carries. The model predicts where research tends to go. It does not predict ecological importance, threat or need, and a unit with less research than expected is a candidate gap: a place where the record is thinner than in comparable places. It is never proof of neglect. Fit quality is measured out of sample by 5-fold spatial cross-validation (whole realms or whole countries held out): pseudo-R2 0.67 for ecoregions and 0.44 for administrative regions (admin1). Each unit carries a 90 percent prediction interval from the negative-binomial count spread about its expectation. Because located research is strongly clustered (theta under 1), that interval is wide: a unit with no located paper falls below it only when the model expects more than 190.8 papers there (ecoregions) or 1786.9 papers there (administrative regions (admin1)), and in this run no unit of either type does. The rankings therefore order units by the tail probability, the chance of a count at or under the observed one given the expectation, and carry the interval label alongside.
1 · Ecoregions: expected against observed Beta
Fit. 578 ecoregions in the universe, 135 with a located paper; negative binomial, dispersion theta 0.50, mean by Poisson quasi-likelihood, ridge lambda 30. 5-fold spatial cross-validation blocked by realm: pseudo-R2 0.67 (0.59 without the national-effort covariate), Spearman rho 0.55 out of fold. Labels against the 90 percent interval: 0 below, 560 within, 18 above.
| Ecoregion | Country | Observed | Expected, 90% interval | Tail probability | Label |
|---|---|---|---|---|---|
| Guianan piedmont moist forestsTropical & Subtropical Moist Broadleaf Forests | Venezuela, Brazil | 0 | 12.5690%: 0 to 49 | 0.194 | within |
| Cordillera Oriental montane forestsTropical & Subtropical Moist Broadleaf Forests | Colombia, Venezuela | 0 | 6.9090%: 0 to 27 | 0.258 | within |
| Peruvian YungasTropical & Subtropical Moist Broadleaf Forests | Peru | 0 | 6.2790%: 0 to 25 | 0.270 | within |
| Borneo montane rain forestsTropical & Subtropical Moist Broadleaf Forests | Indonesia, Malaysia | 0 | 5.8090%: 0 to 23 | 0.280 | within |
| Uruguayan savannaTropical & Subtropical Grasslands, Savannas & Shrublands | Uruguay, Brazil | 1 | 12.4690%: 0 to 48 | 0.289 | within |
| Rio Negro campinaranaTropical & Subtropical Moist Broadleaf Forests | Brazil, Venezuela, Colombia | 1 | 12.3290%: 0 to 48 | 0.290 | within |
| Guianan lowland moist forestsTropical & Subtropical Moist Broadleaf Forests | Guyana, Suriname, French Guiana | 1 | 10.9090%: 0 to 42 | 0.307 | within |
| Negro-Branco moist forestsTropical & Subtropical Moist Broadleaf Forests | Colombia, Venezuela, Brazil | 2 | 16.1990%: 0 to 63 | 0.316 | within |
| PantanalFlooded Grasslands & Savannas | Brazil, Bolivia, Paraguay | 1 | 10.2390%: 0 to 40 | 0.317 | within |
| Taiwan subtropical evergreen forestsTropical & Subtropical Moist Broadleaf Forests | Taiwan | 0 | 4.1290%: 0 to 16 | 0.327 | within |
| Ecoregion | Country | Observed | Expected, 90% interval | Tail probability | Label |
|---|---|---|---|---|---|
| Nansei Islands subtropical evergreen forestsTropical & Subtropical Moist Broadleaf Forests | Japan | 3 | 0.0190%: 0 to 0 | under 0.001 | above |
| Mascarene forestsTropical & Subtropical Moist Broadleaf Forests | Réunion, Mauritius | 3 | 0.0290%: 0 to 0 | under 0.001 | above |
| Arnhem Land tropical savannaTropical & Subtropical Grasslands, Savannas & Shrublands | Australia | 7 | 0.1790%: 0 to 1 | under 0.001 | above |
| Kimberly tropical savannaTropical & Subtropical Grasslands, Savannas & Shrublands | Australia | 6 | 0.3090%: 0 to 2 | 0.001 | above |
| Eastern Guinean forestsTropical & Subtropical Moist Broadleaf Forests | Côte d’Ivoire, Ghana, Togo | 5 | 0.2690%: 0 to 2 | 0.001 | above |
The "more than expected" list doubles as a geocoding audit: a small unit with tens of papers against an expectation under one is as likely a place-name collision, a herbarium or a field station as a genuine concentration of fieldwork.
2 · Administrative regions (admin1): expected against observed Beta
Fit. 1,356 administrative regions (admin1) in the universe, 159 with a located paper; negative binomial, dispersion theta 0.35, mean by Poisson quasi-likelihood, ridge lambda 30. 5-fold spatial cross-validation blocked by country: pseudo-R2 0.44 (0.44 without the national-effort covariate), Spearman rho 0.40 out of fold. Labels against the 90 percent interval: 0 below, 1,315 within, 41 above.
| Region | Country | Observed | Expected, 90% interval | Tail probability | Label |
|---|---|---|---|---|---|
| Goiás | Brazil | 0 | 15.3890%: 0 to 67 | 0.263 | within |
| Maranhão | Brazil | 0 | 8.1790%: 0 to 36 | 0.327 | within |
| Papua | Indonesia | 0 | 7.9390%: 0 to 35 | 0.330 | within |
| Tocantins | Brazil | 1 | 12.0990%: 0 to 53 | 0.383 | within |
| Mato Grosso do Sul | Brazil | 2 | 17.2090%: 0 to 75 | 0.398 | within |
| Rio Grande do Sul | Brazil | 1 | 9.7590%: 0 to 43 | 0.412 | within |
| Cusco | Peru | 0 | 4.0090%: 0 to 18 | 0.413 | within |
| Guaviare | Colombia | 0 | 3.7490%: 0 to 17 | 0.422 | within |
| Sumatera Selatan | Indonesia | 0 | 3.6490%: 0 to 16 | 0.426 | within |
| Ucayali | Peru | 0 | 3.5490%: 0 to 16 | 0.430 | within |
| Region | Country | Observed | Expected, 90% interval | Tail probability | Label |
|---|---|---|---|---|---|
| Okinawa | Japan | 3 | 0.0090%: 0 to 0 | under 0.001 | above |
| Panamá Oeste | Panama | 7 | 0.1690%: 0 to 1 | under 0.001 | above |
| Abidjan | Côte d'Ivoire | 2 | 0.0190%: 0 to 0 | under 0.001 | above |
| Taiwan | Taiwan | 3 | 0.0590%: 0 to 0 | under 0.001 | above |
| Madre de Dios | Peru | 31 | 1.9490%: 0 to 9 | 0.001 | above |
The "more than expected" list doubles as a geocoding audit: a small unit with tens of papers against an expectation under one is as likely a place-name collision, a herbarium or a field station as a genuine concentration of fieldwork.
3 · Calibration
Out of fold, by decile of expected count (observed / expected): ecoregions: deciles 3 to 8 between 0.44 and 1.70, top decile 2.39; administrative regions (admin1): deciles 3 to 8 between 0.52 and 1.88, top decile 1.50. The middle deciles are the best calibrated; the top decile is under-predicted in every model, because the busiest places (long-term field stations, provinces with a herbarium or a university) exceed what any smooth covariate model gives. That is one more reason the residuals are candidate gaps and candidate artefacts rather than findings.
4 · Method note Beta
Response and exposure. 853 of 3,588 papers in this corpus have a precise trusted study site (23.8 percent); the response per unit is the number of those papers with a site inside it (point in polygon, or the nearest unit within 25 km, as the place explorer counts), so a paper with sites in two units counts once in each: 1,010 unit-papers over 578 ecoregions and 936 over 1,356 administrative regions (of 847 and 3,686 units in all). The exposure is log(area), with log(area) also entering as a slope so the data set the area elasticity.
Covariates. log_area_km2, log_richness, log_access_km, forest_loss_pct, forest_loss_missing, aridity_trend_pct_per_decade, aridity_trend_missing, log_national_loo_density, national_loo_undefined, biome, realm, lat_band; continuous covariates standardised, categorical levels with fewer than 10 units pooled. Protected-area share is not available (no protected-area table in the database) and is stated as the natural next covariate. Richness is a country-level proxy: every unit of a country is credited with the national list.
Model and validation. Negative binomial (NB2) GLM with a log link and a ridge penalty on the standardised slopes (ecoregions lambda 30, administrative regions (admin1) lambda 30); the mean estimator and lambda are chosen on out-of-fold Poisson deviance over the same spatial folds; the dispersion is estimated by maximum likelihood. 5-fold spatial cross-validation blocked by realm (ecoregions) or country (admin1), never random rows; a held-out realm's own dummy is unseen in training. The 90 percent interval is the 5th and 95th percentile of NB(expected, theta) and carries no parameter uncertainty, so it is if anything too narrow. Zero rule: a unit with no located paper and an expectation under 0.5 is never labelled below and never ranked.
Limits. Located papers only: papers whose text names no locatable site are invisible here, and the geoparsing error rate of the sections above applies. The national-effort covariate carries most of the between-country signal; the fit without it is printed above. Terrestrial units only. This is a Beta layer: the numbers are honest as stated, and they will move when the geocoding, the corpus or the covariates change.
Provenance. Generated 2026-10-14 from the published database (SELECT only) and the change layers' cache. Refresh with node phase1/expected_research.js brazil-nut, redraw with phase1/gen_atlas_expected_section.js; every figure in this section is checked by the figures audit.
5 · Explore this layer
The same units are on the interactive map as the beta layer "Expected vs observed", ecoregions or administrative regions, with observed, expected, interval and label on hover, and a link from each unit to the place explorer. The place explorer shows the same figures for a selected unit under "Beta: expected research".
Summary of the record
Three moves, each turning a measured gap into an opportunity for a bioeconomy that keeps the Amazon standing.
This atlas is one view of a larger queryable corpus. A single genus’s evidence profile, the wild-harvest-versus-cultivation split for any species, or a shortlist of economically promising trees with no indexed research, ready for survey are each a query away, on the same reproducible foundation.