COMPASS ID  ·  Research Evidence Atlas
LECYTHIDACEAE  /  THE BRAZIL-NUT FAMILY  /  v1.2 · OCTOBER 2026
A map of the science beneath a standing-forest economy

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.

Explore the interactive map →

401
accepted species in the family's checklist (Kew WCVP Version 16)
56%
have no indexed research: 223 of 401 species
3,588
studies, spread across only 178 of 401 species
4.6 : 1
wild-harvested over cultivated: production is overwhelmingly wild-harvested
83%
of Vulnerable species have no indexed research
01

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.

02

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.

Socio-economic use recorded · number of studies
Food & nutrition / edible product
348
Commercial product & processing
340
NTFP harvest & trade
292
Livelihoods & economic value
292
Timber & forestry
282
Sustainable-use management
224
4.6 : 1
Wild-harvested over cultivated. 336 studies concern wild-collected material against just 73 on cultivation. The value of this family is largely a property of the standing forest; plantations exist but remain marginal because of slow growth, pollinator dependence and long juvenility.
68%
A field science, not only a lab one. Unlike most plant families we read, this one is studied as much through field survey and ecology as through chemistry, because its worth is ecological before it is molecular.
An economy built on this family depends on the forest remaining standing.
03

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.

Largest genera on the WCVP census · accepted species (bar) and share with no indexed paper
Barringtonia
73 · 68%
Eschweilera
66 · 53%
Gustavia
47 · 55%
Scottmoria (split from Eschweilera)
35 · 57%
Couratari (timber)
19 · 47%
Chytroma (split from Eschweilera)
18 · 61%
Foetidia
18 · 72%
The Amazon bioeconomy has one well-studied product and hundreds of little-studied ones.
04

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.

Least Concern
43% no indexed research
Endangered
69%
Near Threatened
75%
Critically End.
77%
Vulnerable
83%
Data Deficient
86%
05

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.

Each dot is one geolocated study site, where the fieldwork was done, not where its authors sit. Denser, darker clusters mean more studies; grey land has no indexed study.
928 of 3,588 studies name a locatable study site (25.9 percent). The map draws those sites and lists up to six studies per site. Studies with no locatable field site (lab, national-scale or review work) are not drawn.
Each dot = a geolocated study site ·  smaller / fainter = fewer studies  →  larger / darker = a dense cluster ·  grey land = no indexed study

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.

Explore this map interactively

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.

Fiji: 1 of 4 native species with no indexed paper Tanzania: 0 of 4 native species with no indexed paper Western Sahara: no census species recorded in the native range Canada: no census species recorded in the native range United States: no census species recorded in the native range Kazakhstan: no census species recorded in the native range Uzbekistan: no census species recorded in the native range Papua New Guinea: 11 of 24 native species with no indexed paper Indonesia: 24 of 48 native species with no indexed paper Argentina: no census species recorded in the native range Chile: no census species recorded in the native range Democratic Republic of the Congo: 10 of 12 native species with no indexed paper Somalia: no census species recorded in the native range Kenya: 0 of 1 native species with no indexed paper Sudan: no census species recorded in the native range Chad: no census species recorded in the native range Haiti: no census species recorded in the native range Dominican Republic: no census species recorded in the native range Russian Federation: no census species recorded in the native range Bahamas: no census species recorded in the native range Falkland Islands / Malvinas: no census species recorded in the native range Norway: no census species recorded in the native range Greenland: no census species recorded in the native range French Southern and Antarctic Lands: no census species recorded in the native range Timor-Leste: no census species recorded in the native range South Africa: 0 of 1 native species with no indexed paper Lesotho: no census species recorded in the native range Mexico: 0 of 1 native species with no indexed paper Uruguay: no census species recorded in the native range Brazil: 42 of 119 native species with no indexed paper Bolivia: 2 of 19 native species with no indexed paper Peru: 12 of 35 native species with no indexed paper Colombia: 43 of 90 native species with no indexed paper Panama: 21 of 41 native species with no indexed paper Costa Rica: 10 of 20 native species with no indexed paper Nicaragua: 2 of 5 native species with no indexed paper Honduras: 1 of 3 native species with no indexed paper El Salvador: 1 of 1 native species with no indexed paper Guatemala: 0 of 1 native species with no indexed paper Belize: 0 of 1 native species with no indexed paper Venezuela: 21 of 55 native species with no indexed paper Guyana: 16 of 39 native species with no indexed paper Suriname: 8 of 29 native species with no indexed paper France: no census species recorded in the native range Ecuador: 15 of 50 native species with no indexed paper Puerto Rico: no census species recorded in the native range Jamaica: 0 of 1 native species with no indexed paper Cuba: no census species recorded in the native range Zimbabwe: no census species recorded in the native range Botswana: no census species recorded in the native range Namibia: no census species recorded in the native range Senegal: no census species recorded in the native range Mali: no census species recorded in the native range Mauritania: no census species recorded in the native range Benin: 1 of 2 native species with no indexed paper Niger: no census species recorded in the native range Nigeria: 7 of 13 native species with no indexed paper Cameroon: 18 of 23 native species with no indexed paper Togo: 1 of 1 native species with no indexed paper Ghana: 3 of 5 native species with no indexed paper Côte d'Ivoire: 3 of 5 native species with no indexed paper Guinea: 1 of 5 native species with no indexed paper Guinea-Bissau: no census species recorded in the native range Liberia: 3 of 7 native species with no indexed paper Sierra Leone: 2 of 6 native species with no indexed paper Burkina Faso: 0 of 1 native species with no indexed paper Central African Republic: 4 of 6 native species with no indexed paper Republic of the Congo: 11 of 15 native species with no indexed paper Gabon: 19 of 24 native species with no indexed paper Equatorial Guinea: 7 of 10 native species with no indexed paper Zambia: 1 of 1 native species with no indexed paper Malawi: no census species recorded in the native range Mozambique: 0 of 1 native species with no indexed paper Kingdom of eSwatini: no census species recorded in the native range Angola: 4 of 5 native species with no indexed paper Burundi: no census species recorded in the native range Israel: no census species recorded in the native range Lebanon: no census species recorded in the native range Madagascar: 13 of 16 native species with no indexed paper Palestine: no census species recorded in the native range The Gambia: no census species recorded in the native range Tunisia: no census species recorded in the native range Algeria: no census species recorded in the native range Jordan: no census species recorded in the native range United Arab Emirates: no census species recorded in the native range Qatar: no census species recorded in the native range Kuwait: no census species recorded in the native range Iraq: no census species recorded in the native range Oman: no census species recorded in the native range Vanuatu: 0 of 5 native species with no indexed paper Cambodia: 1 of 7 native species with no indexed paper Thailand: 5 of 18 native species with no indexed paper Lao PDR: 0 of 5 native species with no indexed paper Myanmar: 2 of 13 native species with no indexed paper Vietnam: 4 of 11 native species with no indexed paper Dem. Rep. Korea: no census species recorded in the native range Republic of Korea: no census species recorded in the native range Mongolia: no census species recorded in the native range India: 1 of 10 native species with no indexed paper Bangladesh: 0 of 5 native species with no indexed paper Bhutan: 0 of 1 native species with no indexed paper Nepal: 0 of 2 native species with no indexed paper Pakistan: 0 of 1 native species with no indexed paper Afghanistan: 0 of 2 native species with no indexed paper Tajikistan: no census species recorded in the native range Kyrgyzstan: no census species recorded in the native range Turkmenistan: no census species recorded in the native range Iran: no census species recorded in the native range Syria: no census species recorded in the native range Armenia: no census species recorded in the native range Sweden: no census species recorded in the native range Belarus: no census species recorded in the native range Ukraine: no census species recorded in the native range Poland: no census species recorded in the native range Austria: no census species recorded in the native range Hungary: no census species recorded in the native range Moldova: no census species recorded in the native range Romania: no census species recorded in the native range Lithuania: no census species recorded in the native range Latvia: no census species recorded in the native range Estonia: no census species recorded in the native range Germany: no census species recorded in the native range Bulgaria: no census species recorded in the native range Greece: no census species recorded in the native range Turkey: no census species recorded in the native range Albania: no census species recorded in the native range Croatia: no census species recorded in the native range Switzerland: no census species recorded in the native range Luxembourg: no census species recorded in the native range Belgium: no census species recorded in the native range Netherlands: no census species recorded in the native range Portugal: no census species recorded in the native range Spain: no census species recorded in the native range Ireland: no census species recorded in the native range New Caledonia: 3 of 5 native species with no indexed paper Solomon Islands: 3 of 8 native species with no indexed paper New Zealand: no census species recorded in the native range Australia: 0 of 6 native species with no indexed paper Sri Lanka: 1 of 4 native species with no indexed paper China: 0 of 2 native species with no indexed paper Taiwan: 0 of 2 native species with no indexed paper Italy: no census species recorded in the native range Denmark: no census species recorded in the native range United Kingdom: no census species recorded in the native range Iceland: no census species recorded in the native range Azerbaijan: no census species recorded in the native range Georgia: no census species recorded in the native range Philippines: 5 of 11 native species with no indexed paper Malaysia: 25 of 45 native species with no indexed paper Brunei Darussalam: 11 of 26 native species with no indexed paper Slovenia: 0 of 1 native species with no indexed paper Finland: no census species recorded in the native range Slovakia: no census species recorded in the native range Czech Republic: no census species recorded in the native range Eritrea: no census species recorded in the native range Japan: 0 of 2 native species with no indexed paper Paraguay: 0 of 1 native species with no indexed paper Yemen: no census species recorded in the native range Saudi Arabia: no census species recorded in the native range Northern Cyprus: no census species recorded in the native range Cyprus: no census species recorded in the native range Morocco: no census species recorded in the native range Egypt: no census species recorded in the native range Libya: no census species recorded in the native range Ethiopia: no census species recorded in the native range Djibouti: no census species recorded in the native range Somaliland: no census species recorded in the native range Uganda: 1 of 1 native species with no indexed paper Rwanda: no census species recorded in the native range Bosnia and Herzegovina: no census species recorded in the native range North Macedonia: no census species recorded in the native range Serbia: no census species recorded in the native range Montenegro: no census species recorded in the native range Kosovo: no census species recorded in the native range Trinidad and Tobago: 1 of 3 native species with no indexed paper South Sudan: no census species recorded in the native range
Species with no indexed paper per native range country · log shading (darker green = more such species) · Colombia 43 · Brazil 42 · Malaysia 25 · Indonesia 24 · Venezuela 21 · Panama 21
FewerMore species with no indexed paper
Denominator: 100 native range countries with at least one census species (WCVP distribution table, TDWG level-3 areas mapped to countries); 51 of them hold at least one species with no indexed paper. A species counts in every country of its native range. Hover a country for its figures.
An economy that spans the whole Amazon is studied mostly in one country. Many of the species with no indexed research are in Colombia, the Guianas and forests on two other continents.
06

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.

400
of 401 species have known range countries (WCVP distribution countries)
114
of 400 species with range data have a study site inside a range country (28.5%)
63
of 178 species with indexed papers have no locatable study site anywhere (35.4%)
Species with a study site inside a range country, by IUCN class. Denominator per row = species in that class with range data.
Critically Endangered
2 of 26 (8%)
Endangered
6 of 39 (15%)
Vulnerable
4 of 36 (11%)
Near Threatened
3 of 16 (19%)
Least Concern
50 of 133 (38%)
Data Deficient
1 of 14 (7%)
Not evaluated
48 of 136 (35%)

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.

Colombia 80%Brazil 59%Venezuela 82%Indonesia 83%
Range species without an in-country study siteunder 50%50 to 74%75 to 89%90 to 99%100%no census species in rangefewer than 5 range species
Denominator: 120 range countries with at least one census species; shading = range species with no locatable study site in the country / range species in the country. 73 of the 120 have a polygon on this basemap (Natural Earth 1:110m, public domain); the rest are small islands and dependent territories, which Natural Earth draws with their sovereign state or not at all. Dashed outlines mark countries with fewer than 5 range species, where one species moves the share a long way.
Ten countries with the most range species lacking an in-country study site. Range species = census species whose WCVP distribution countries include the country; shortfall = share of those with no locatable study site in that country.
CountryRange speciesWith an in-country study siteShortfallStudy sites in country
Colombia901880%58
Brazil1194959%354
Venezuela561082%9
France420100%0
Indonesia48883%60
Guyana390100%0
Malaysia45687%8
Panama41393%7
Ecuador501374%18
Peru35489%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.

Study sites per resolution-2 cell (summed over child cells), log ramp from 1 to 241251024 (most)
660 precise study sites fall in 391 hexagonal cells (H3 resolution 3, about 12,400 km2 each); the ten fullest cells hold 12.7% of the sites and 262 cells hold a single site. At this scale a resolution-3 cell is a few pixels wide, so the main map aggregates them to H3 resolution 2 (about 86,800 km2 each): 223 cells, each holding the summed sites of its child cells. The inset below keeps resolution 3.
Equirectangular, the same basemap as the map above; every cell is drawn on its true H3 boundary, so the cells tile without overlap; no cell crosses the antimeridian.

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.

Study sites per resolution-3 cell, log ramp from 1 to 12123612 (most)
Inset denominator: 204 resolution-3 cells inside the window with 400 of the 660 precise study sites (60.6%). Most of those sites are in Brazil, Ecuador and Peru. The window is chosen by the sum of sites, not by area or country.

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.

CountrySpecies in rangeStudy sites in country
France420
Guyana390
Singapore311
Suriname290
Brunei260
Gabon241
Papua New Guinea242
Madagascar160
Congo (Brazzaville)151
Myanmar131
Denominator: 120 range countries with at least one census species; species in range counts the census species whose WCVP distribution countries include the country.

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.

76.6 km
median straight-line distance from a study site to the nearest city of 100,000 or more (660 sites)
37.4%
of study sites lie within 50 km of such a city
78.3%
of study sites lie within 200 km of such a city
Denominator: 660 precise study sites (distinct places with coordinates, not paper-weighted). Quartiles 27.7 and 179.0 km; the farthest site is 2,917 km from any such city.

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.

07

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.

97 eco
321 adm1
high change, low research: ecoregions of 431, admin1 regions of 1,143
47 eco
60 adm1
high change, more research: ecoregions of 431, admin1 regions of 1,143
214 eco
676 adm1
less change, low research: ecoregions of 431, admin1 regions of 1,143
73 eco
86 adm1
less change, more research: ecoregions of 431, admin1 regions of 1,143
Thresholds. Ecoregions: high change = 21.41% of the 2000 forest lost or more (67th percentile of 431 units); low research = no located paper at all (a third or more of the units have none, so the bottom tercile is zero) (33rd percentile). Admin1: high change = 21.44% of the 2000 forest lost or more (67th percentile of 1,143 units); low research = no located paper at all (a third or more of the units have none, so the bottom tercile is zero) (33rd percentile). Spearman rho between forest loss and research density across the universe: ecoregions: rho 0.074 (n 431); admin1: rho 0.059 (n 1,143). Descriptive only.

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".

Ten ecoregions with the most forest loss and bottom-tercile located research, of 97 in that quadrant. Denominator: 431 ecoregions in the universe.
EcoregionCountryForest lostPapers with a sitePer 10,000 km2Range species without a site
Piney WoodsTemperate Conifer ForestsUnited States75.4%90% forested in 200000.001
Sumatran freshwater swamp forestsTropical & Subtropical Moist Broadleaf ForestsIndonesia72.3%76% forested in 200000.0048
Southeast US conifer savannasTemperate Grasslands, Savannas & ShrublandsUnited States70.9%85% forested in 200000.001
Esperance malleeMediterranean Forests, Woodlands & ScrubAustralia69.3%21% forested in 200000.006
Drakensberg grasslandsTropical & Subtropical Grasslands, Savannas & ShrublandsSouth Africa, Lesotho68.8%7% forested in 200000.001
Madagascar humid forestsTropical & Subtropical Moist Broadleaf ForestsMadagascar67.7%88% forested in 200000.0016
California montane chaparral and woodlandsMediterranean Forests, Woodlands & ScrubUnited States, México65.7%30% forested in 200000.002
Western Guinean lowland forestsTropical & Subtropical Moist Broadleaf ForestsLiberia, Sierra Leone, Côte d'Ivoire, Guinea62.0%95% forested in 200000.009
Northern Khorat Plateau moist deciduous forestsTropical & Subtropical Moist Broadleaf ForestsThailand, Laos61.3%25% forested in 200000.0018
Naracoorte woodlandsMediterranean Forests, Woodlands & ScrubAustralia59.3%18% forested in 200000.006
Ten administrative regions (admin1) with the most forest loss and bottom-tercile located research, of 321 in that quadrant. Denominator: 1,143 administrative regions (admin1) in the universe.
RegionCountryForest lostPapers with a sitePer 10,000 km2Range species without a site
Bình DươngVietnam96.3%37% forested in 200000.0011
BongLiberia95.5%100% forested in 200000.007
MontserradoLiberia90.4%88% forested in 200000.007
BomiLiberia89.3%99% forested in 200000.007
MelakaMalaysia88.7%83% forested in 200000.0045
MargibiLiberia87.3%95% forested in 200000.007
Otdar Mean CheyCambodia84.7%45% forested in 200000.007
SouthernSierra Leone83.8%90% forested in 200000.006
Bangka BelitungIndonesia83.5%91% forested in 200000.0048
Grand BassaLiberia80.4%100% forested in 200000.007

Forest loss 2001 to 2024, cell by cell

Share of the 2000 forest lost 2001 to 20240 to 5%5 to 10%10 to 20%20 to 35%35 to 50%50% or morenot applicable
Dots: papers with a site in the cell (summed over child cells), log ramp from 1 to 104131030104 (most)
Denominator: 391 resolution-3 cells with at least one precise study site from this corpus (853 of 3,588 papers); 317 have an applicable forest loss value and 74 do not. They are drawn on their true H3 boundaries and aggregated to 223 cells at H3 resolution 2 (about 86,800 km2 each): a drawn cell takes the valid-area-weighted mean of its child cells' values and the sum of their papers; 183 of the 223 drawn cells carry a value and 40 carry none (dashed outline). Cells with no located research are not on this map; the unit tables above include them.

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.

56 eco
70 adm1
high change, low research: ecoregions of 167, admin1 regions of 215
0 eco
2 adm1
high change, more research: ecoregions of 167, admin1 regions of 215
98 eco
129 adm1
less change, low research: ecoregions of 167, admin1 regions of 215
13 eco
14 adm1
less change, more research: ecoregions of 167, admin1 regions of 215
Thresholds. Ecoregions: high change = drying of 3.77% of the 1990s index per decade or more (67th percentile of 167 units); low research = no located paper at all (a third or more of the units have none, so the bottom tercile is zero) (33rd percentile). Admin1: high change = drying of 2.51% of the 1990s index per decade or more (67th percentile of 215 units); low research = no located paper at all (a third or more of the units have none, so the bottom tercile is zero) (33rd percentile). Spearman rho between drying and research density across the universe: ecoregions: rho −0.262 (n 167); admin1: rho −0.149 (n 215). Descriptive only.

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.

Ten ecoregions with the most drying and bottom-tercile located research, of 56 in that quadrant. Denominator: 167 ecoregions in the universe.
EcoregionCountryAridity trendPapers with a sitePer 10,000 km2Range species without a site
Dry ChacoTropical & Subtropical Grasslands, Savannas & ShrublandsArgentina, Paraguay, Bolivia−10.3%semi-arid00.0019
Western Australian Mulga shrublandsDeserts & Xeric ShrublandsAustralia−9.5%arid00.004
Knysna-Amatole montane forestsTropical & Subtropical Moist Broadleaf ForestsSouth Africa−9.2%dry sub-humid00.001
Namaqualand-Richtersveld steppeDeserts & Xeric ShrublandsSouth Africa, Namibia−8.6%arid00.001
Succulent Karoo xeric shrublandsDeserts & Xeric ShrublandsSouth Africa−8.6%arid00.001
Southern Andean YungasTropical & Subtropical Moist Broadleaf ForestsArgentina, Bolivia−8.5%dry sub-humid00.0019
Edwards Plateau savannaTemperate Grasslands, Savannas & ShrublandsUnited States−8.2%semi-arid00.001
Fynbos shrublandMediterranean Forests, Woodlands & ScrubSouth Africa−7.8%semi-arid00.001
Galápagos Islands xeric scrubDeserts & Xeric ShrublandsEcuador−7.8%semi-arid00.0050
Chihuahuan desertDeserts & Xeric ShrublandsMéxico, United States−7.8%arid00.002
Ten administrative regions (admin1) with the most drying and bottom-tercile located research, of 70 in that quadrant. Denominator: 215 administrative regions (admin1) in the universe.
RegionCountryAridity trendPapers with a sitePer 10,000 km2Range species without a site
HilmandAfghanistan−10.8%arid00.002
XizangChina−10.5%semi-arid00.002
FarahAfghanistan−10.3%arid00.002
Bamingui-BangoranCentral African Republic−9.3%dry sub-humid00.006
Alto ParaguayParaguay−8.7%semi-arid00.001
KandaharAfghanistan−8.4%arid00.002
VakagaCentral African Republic−8.4%semi-arid00.006
New MexicoUnited States−8.2%semi-arid00.001
GalápagosEcuador−7.8%semi-arid00.0050
Western CapeSouth Africa−7.7%semi-arid00.001

Aridity trend 1990 to 2024, cell by cell

Trend of the aridity index P/PET, percent of the 1990s mean per decadedrier by 10% or more per decade5 to 10% drier1 to 5% drierwithin 1% (no trend)1 to 5% wetter5 to 10% wetterwetter by 10% or morenot applicable
Dots: papers with a site in the cell (summed over child cells), log ramp from 1 to 104131030104 (most)
Denominator: 391 resolution-3 cells with at least one precise study site from this corpus (853 of 3,588 papers); 309 have an applicable drying value and 82 do not. They are drawn on their true H3 boundaries and aggregated to 223 cells at H3 resolution 2 (about 86,800 km2 each): a drawn cell takes the valid-area-weighted mean of its child cells' values and the sum of their papers; 182 of the 223 drawn cells carry a value and 41 carry none (dashed outline). Cells with no located research are not on this map; the unit tables above include them.

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.

Located papers by decade of publication. Denominator = 853 papers with a precise study site; the tick marks the whole corpus's share of the same decade (3,588 papers).
before 1990
15 (1.8%) · corpus 4.5%
1990s
31 (3.6%) · corpus 3.9%
2000s
159 (18.6%) · corpus 15.2%
2010s
395 (46.3%) · corpus 44.2%
2020s
251 (29.4%) · corpus 31.9%

The decade with the most located papers, cell by cell

Peak decade of publicationbefore 1990 (2)1990s (9)2000s (22)2010s (109)2020s (81)
Denominator: 391 resolution-3 cells with at least one located paper of known year, drawn on their true H3 boundaries and aggregated to 223 cells at H3 resolution 2 (about 86,800 km2 each; decade counts summed over child cells); a cell is shaded by the decade in which most of its located papers were published (853 located papers in all; a tie goes to the later decade). Darker is more recent. Decades are publication years, not fieldwork years.

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.

08

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.

Tail probability of the observed count under the fitted expectationless than expected, tail probability under 0.05 (below the 90 percent interval) (0)less, 0.05 to 0.15 (0)less, 0.15 to 0.30 (6)near expectation (0.30 or more either way) (464)more, 0.15 to 0.30 (23)more, 0.05 to 0.15 (22)more than expected, under 0.05 (above the interval) (16)not in the model universe
Denominator: 578 ecoregions in the model universe, 135 with a located paper of this corpus; 531 are drawn on their outlines (RESOLVE Ecoregions 2017 and GADM 4.1, 5,000 m simplification, rounded to the canvas); 47 are too small to draw at this scale (one canvas unit is about 40 km at the equator). Shading is the tail probability of the observed count under NB(expected, theta): the two darkest classes are the interval labels below and above; a unit with no located paper and an expectation under 0.5 sits in the neutral class by construction (the zero rule). No unit reaches the "below the interval" class; 16 reach "above the interval". Unshaded land is outside the universe (under 1,000 km2, polar, or no census species in range). A shaded unit is a candidate gap or a candidate artefact, not a finding.
Ten ecoregions with the least located research relative to the model's expectation, ordered by the tail probability P(count at or under the observed). Denominator: 578 ecoregions in the model universe, 135 with a located paper.
EcoregionCountryObservedExpected, 90% intervalTail probabilityLabel
Guianan piedmont moist forestsTropical & Subtropical Moist Broadleaf ForestsVenezuela, Brazil012.5690%: 0 to 490.194within
Cordillera Oriental montane forestsTropical & Subtropical Moist Broadleaf ForestsColombia, Venezuela06.9090%: 0 to 270.258within
Peruvian YungasTropical & Subtropical Moist Broadleaf ForestsPeru06.2790%: 0 to 250.270within
Borneo montane rain forestsTropical & Subtropical Moist Broadleaf ForestsIndonesia, Malaysia05.8090%: 0 to 230.280within
Uruguayan savannaTropical & Subtropical Grasslands, Savannas & ShrublandsUruguay, Brazil112.4690%: 0 to 480.289within
Rio Negro campinaranaTropical & Subtropical Moist Broadleaf ForestsBrazil, Venezuela, Colombia112.3290%: 0 to 480.290within
Guianan lowland moist forestsTropical & Subtropical Moist Broadleaf ForestsGuyana, Suriname, French Guiana110.9090%: 0 to 420.307within
Negro-Branco moist forestsTropical & Subtropical Moist Broadleaf ForestsColombia, Venezuela, Brazil216.1990%: 0 to 630.316within
PantanalFlooded Grasslands & SavannasBrazil, Bolivia, Paraguay110.2390%: 0 to 400.317within
Taiwan subtropical evergreen forestsTropical & Subtropical Moist Broadleaf ForestsTaiwan04.1290%: 0 to 160.327within
Five ecoregions with the most located research relative to the model's expectation, ordered by the tail probability P(count at or over the observed). Denominator: 578 ecoregions in the model universe, 135 with a located paper.
EcoregionCountryObservedExpected, 90% intervalTail probabilityLabel
Nansei Islands subtropical evergreen forestsTropical & Subtropical Moist Broadleaf ForestsJapan30.0190%: 0 to 0under 0.001above
Mascarene forestsTropical & Subtropical Moist Broadleaf ForestsRéunion, Mauritius30.0290%: 0 to 0under 0.001above
Arnhem Land tropical savannaTropical & Subtropical Grasslands, Savannas & ShrublandsAustralia70.1790%: 0 to 1under 0.001above
Kimberly tropical savannaTropical & Subtropical Grasslands, Savannas & ShrublandsAustralia60.3090%: 0 to 20.001above
Eastern Guinean forestsTropical & Subtropical Moist Broadleaf ForestsCôte d’Ivoire, Ghana, Togo50.2690%: 0 to 20.001above

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.

Tail probability of the observed count under the fitted expectationless than expected, tail probability under 0.05 (below the 90 percent interval) (0)less, 0.05 to 0.15 (0)less, 0.15 to 0.30 (1)near expectation (0.30 or more either way) (1,042)more, 0.15 to 0.30 (40)more, 0.05 to 0.15 (26)more than expected, under 0.05 (above the interval) (32)not in the model universe
Denominator: 1,356 administrative regions (admin1) in the model universe, 159 with a located paper of this corpus; 1,141 are drawn on their outlines (RESOLVE Ecoregions 2017 and GADM 4.1, 5,000 m simplification, rounded to the canvas); 215 are too small to draw at this scale (one canvas unit is about 40 km at the equator). Shading is the tail probability of the observed count under NB(expected, theta): the two darkest classes are the interval labels below and above; a unit with no located paper and an expectation under 0.5 sits in the neutral class by construction (the zero rule). No unit reaches the "below the interval" class; 32 reach "above the interval". Unshaded land is outside the universe (under 1,000 km2, polar, or no census species in range). A shaded unit is a candidate gap or a candidate artefact, not a finding.
Ten administrative regions (admin1) with the least located research relative to the model's expectation, ordered by the tail probability P(count at or under the observed). Denominator: 1,356 administrative regions (admin1) in the model universe, 159 with a located paper.
RegionCountryObservedExpected, 90% intervalTail probabilityLabel
GoiásBrazil015.3890%: 0 to 670.263within
MaranhãoBrazil08.1790%: 0 to 360.327within
PapuaIndonesia07.9390%: 0 to 350.330within
TocantinsBrazil112.0990%: 0 to 530.383within
Mato Grosso do SulBrazil217.2090%: 0 to 750.398within
Rio Grande do SulBrazil19.7590%: 0 to 430.412within
CuscoPeru04.0090%: 0 to 180.413within
GuaviareColombia03.7490%: 0 to 170.422within
Sumatera SelatanIndonesia03.6490%: 0 to 160.426within
UcayaliPeru03.5490%: 0 to 160.430within
Five administrative regions (admin1) with the most located research relative to the model's expectation, ordered by the tail probability P(count at or over the observed). Denominator: 1,356 administrative regions (admin1) in the model universe, 159 with a located paper.
RegionCountryObservedExpected, 90% intervalTail probabilityLabel
OkinawaJapan30.0090%: 0 to 0under 0.001above
Panamá OestePanama70.1690%: 0 to 1under 0.001above
AbidjanCôte d'Ivoire20.0190%: 0 to 0under 0.001above
TaiwanTaiwan30.0590%: 0 to 0under 0.001above
Madre de DiosPeru311.9490%: 0 to 90.001above

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.

09

Summary of the record

Three moves, each turning a measured gap into an opportunity for a bioeconomy that keeps the Amazon standing.

Diversify beyond the nut. A one-product economy is a fragile one. More than two hundred species with no indexed research, among them edible Gustavia fruits, Lecythis monkey-pot nuts and Eschweilera timbers and chemistry, are candidate products no one has evaluated. This is where a resilient portfolio comes from.
Document before you lose. The species most likely to hold new value are the rarest, and 83% of the vulnerable have no indexed research. A survey programme targeting threatened Lecythidaceae with no indexed research is both a conservation and an economic investment.
Follow the resource, not the border. Research sits in Brazil; the species with no indexed research sit in Colombia, the Guianas and the paleotropics. A pan-Amazonian evidence effort would close a gap the national one structurally cannot.

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.

Granular case studies

Two country case studies

A standing-forest economy is local. Zoom into a single country and the research resolves into its use, its setting and its gaps. Two countries, read up close: Brazil, the country with the most located Lecythidaceae research, and Peru, a second range country of the Brazil nut with a far smaller located record.

Brazil

563 studies · 354 geolocated study sites

1 further geolocated site in Brazil, carrying 4 studies, falls outside this frame and is not drawn.

In Brazil, located Lecythidaceae research leans to ecology & population (213 studies). The use most often recorded is NTFP Harvest & Trade (115) and the setting most often named is Tropical Moist Forest & Rainforest (183). 42 of 119 native Lecythidaceae species have no indexed paper.

Cross-section · what the tags reveal
Research focus
Ecology213
Cultivation101
Conservation67
Phytochemistry32
Socio-economic use
NTFP Harvest & Trade115
Sustainable-Use Management109
Livelihoods & Economic Value108
Timber & Forestry91
Ecosystem
Tropical Moist Forest & Rainforest183
Agricultural & Anthropogenic73
Secondary & Disturbed Forest71
Wetland & Peatland20
Evidence gap matrix
focus × use
NTFP Harvest & TradeSustainable-Use ManagementLivelihoods & Economic ValueTimber & ForestryFood & Nutrition / Edible Product
Ecology344724353
Cultivation284228435
Conservation22172152
Phytochemistry1·4·18
Policy23132013
Rows × columns among this country's located studies · darker = more studies join the two · an empty cell (·) is a gap no study here connects.
use × ecosystem
Tropical Moist Forest & RainforestAgricultural & AnthropogenicSecondary & Disturbed ForestWetland & PeatlandTropical Dry & Seasonal Forest
NTFP Harvest & Trade47684·
Sustainable-Use Management5813172·
Livelihoods & Economic Value401073·
Timber & Forestry3815175·
Food & Nutrition / Edible Product5113·
Rows × columns among this country's located studies · darker = more studies join the two · an empty cell (·) is a gap no study here connects.
focus × method
Field SurveyPhytochemicalQuestionnairePopulation/Statistical ModelingMolecular
Ecology18414154
Cultivation451104·
Conservation371914
Phytochemistry·27··1
Policy7·16··
Rows × columns among this country's located studies · darker = more studies join the two · an empty cell (·) is a gap no study here connects.
Counts are studies of this atlas with a geolocated study site in Brazil; rows and columns are the five most frequent values of each dimension among those studies. Recomputed by compassid-api/scripts/gen_atlas_casestudy.cjs and checked independently by verify_atlas_casestudy.cjs.

Peru

35 studies · 17 geolocated study sites

In Peru, located Lecythidaceae research leans to conservation & threats (7 studies). The use most often recorded is NTFP Harvest & Trade (18) and the setting most often named is Tropical Moist Forest & Rainforest (10). 12 of 35 native Lecythidaceae species have no indexed paper.

Cross-section · what the tags reveal
Research focus
Conservation7
Ecology7
Cultivation5
Propagation4
Socio-economic use
NTFP Harvest & Trade18
Livelihoods & Economic Value14
Sustainable-Use Management11
Timber & Forestry5
Ecosystem
Tropical Moist Forest & Rainforest10
Agricultural & Anthropogenic5
Secondary & Disturbed Forest3
Wetland & Peatland1
Evidence gap matrix
focus × use
NTFP Harvest & TradeLivelihoods & Economic ValueSustainable-Use ManagementTimber & ForestryCommercial Product & Processing
Conservation7531·
Ecology533··
Cultivation3233·
Propagation341··
Genetics·····
Rows × columns among this country's located studies · darker = more studies join the two · an empty cell (·) is a gap no study here connects.
use × ecosystem
Tropical Moist Forest & RainforestAgricultural & AnthropogenicSecondary & Disturbed ForestWetland & Peatland
NTFP Harvest & Trade823·
Livelihoods & Economic Value422·
Sustainable-Use Management7·2·
Timber & Forestry3·1·
Commercial Product & Processing····
Rows × columns among this country's located studies · darker = more studies join the two · an empty cell (·) is a gap no study here connects.
focus × method
Field SurveyGerminationBioassayMolecularPhytochemical
Conservation61···
Ecology6····
Cultivation21···
Propagation24···
Genetics···2·
Rows × columns among this country's located studies · darker = more studies join the two · an empty cell (·) is a gap no study here connects.
Counts are studies of this atlas with a geolocated study site in Peru; rows and columns are the five most frequent values of each dimension among those studies. Recomputed by compassid-api/scripts/gen_atlas_casestudy.cjs and checked independently by verify_atlas_casestudy.cjs.