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Research article · 2026 · Full text

International Journal of Geography Geology and Environment

Comparative assessment of hemipteran diversity across wet and dry seasons in a suburban-rural interface of Lagos, Nigeria

Adeyemi OTChidinma Nkechi OkaforBalogun SA

Volume 8(7) · Pages 141–147 · DOI: 10.22271/27067483.2026.v8.i7b.807 ↗

Research areasHemiptera Insect StudiesFreshwater macroinvertebrate diversity and ecologyInsect-Plant Interactions and Control

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Abstract

Author-written

Hemiptera, comprising both herbivorous and predatory lineages, constitute an ecologically significant but frequently overlooked insect order in tropical peri-urban biodiversity assessments. This research conducted a comparative evaluation of hemipteran diversity across wet (April-October) and dry (November-March) seasons at five habitat types along the suburban-rural interface of the Epe-Ibeju-Lekki corridor in eastern Lagos State, Nigeria, from April 2025 through March 2026. Sampling employed sweep nets, beat sheets, and visual searches across 25 sampling stations (five habitats × five replicates). A total of 4,678 hemipteran specimens representing 112 species from 23 families were documented. Cicadellidae was the most species-rich family (28 species), while Pentatomidae dominated numerically (1,234 individuals, 26.4%). Wet season collections exceeded dry season catches by a factor of 1.9, with the peak occurring in July-August coinciding with maximum rainfall intensity. Shannon-Wiener diversity was highest in riparian buffer habitats (H' = 3.41) and lowest in residential garden plots (H' = 2.12). Species accumulation curves indicated that sampling achieved approximately 84% estimated completeness for the overall assemblage. Beta diversity analysis revealed that habitat type explained more compositional variation (42.8%) than season (31.2%). The findings demonstrate that hemipteran assemblages in the Lagos suburban-rural interface are structured primarily by habitat heterogeneity, with seasonal rainfall modulating abundance and activity patterns within each habitat context. Conservation of riparian corridors and agricultural margins is recommended as a priority for maintaining hemipteran diversity in this rapidly developing region.

Summary

Source-checked

Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Rapid suburban expansion in the Epe and Ibeju-Lekki areas of Lagos, Nigeria, is transforming coastal wetlands, secondary forests, and agricultural lands into urban developments. View evidence ↗

      Why it matters

      Rapid suburban expansion in the Epe and Ibeju-Lekki areas of Lagos, Nigeria, is transforming coastal wetlands, secondary forests, and agricultural lands into urban developments.

      In the paper's own words

      “The eastern corridor of Lagos State, encompassing the Epe and Ibeju-Lekki Local Government Areas, has emerged as a primary zone of suburban expansion... This expansion is converting substantial areas of coastal wetland, secondary forest, and agricultural land into residential and commercial developments”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Lagos experiences a West African monsoon climate characterized by a long wet season from April to October and a shorter dry season from November to March. View evidence ↗

      Why it matters

      Lagos experiences a West African monsoon climate characterized by a long wet season from April to October and a shorter dry season from November to March.

      In the paper's own words

      “The seasonal climate of Lagos follows a West African monsoon pattern, with a prolonged wet season (April-October) and a shorter dry season (November-March)”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. The question

    • The study aimed to quantify hemipteran species richness and abundance across five habitat types during wet and dry seasons to determine how habitat and timing influence community composition. View evidence ↗

      The question

      The study aimed to quantify hemipteran species richness and abundance across five habitat types during wet and dry seasons to determine how habitat and timing influence community composition.

      In the paper's own words

      “This research addressed this gap by comparing hemipteran diversity and community composition across five habitat types during wet and dry seasons, with the objectives of quantifying species richness and abundance patterns, assessing the relative contributions of habitat type and seasonal timing to assemblage variation, and identifying conservation-priority habitats”

      Page 2

      Found in: Introduction

      Read it in the full textOpen PDF at page 2 ↗
  3. What they did

    • The researchers compared five distinct habitats: residential gardens, vacant lots, active agricultural smallholdings, riparian buffer strips, and mixed scrubland. View evidence ↗

      What they did

      The researchers compared five distinct habitats: residential gardens, vacant lots, active agricultural smallholdings, riparian buffer strips, and mixed scrubland.

      In the paper's own words

      “Five habitat types were delineated for comparative assessment: (1) residential gardens within planned housing estates (managed lawns, ornamental plantings, fruit trees), (2) vacant lots in development areas (cleared land with ruderal vegetation), (3) active agricultural smallholdings (cassava, maize, vegetable plots with associated margins), (4) riparian buffer strips along seasonal and perennial streams (3-30 m width, retaining gallery forest elements), and (5) mixed scrubland on laterite uplands (secondary regrowth 5-15 years post-disturbance).”

      Page 2

      Found in: Material

      Read it in the full textOpen PDF at page 2 ↗
    • Sampling was conducted at 25 stations in total, with five replicates per habitat type spaced at least 600 meters apart. View evidence ↗

      What they did

      Sampling was conducted at 25 stations in total, with five replicates per habitat type spaced at least 600 meters apart.

      In the paper's own words

      “Five replicate sampling stations were established within each habitat type, totaling 25 stations, with minimum inter-station distance of 600 m.”

      Page 2

      Found in: Material

      Read it in the full textOpen PDF at page 2 ↗
    • Between April 2025 and March 2026, insects were collected biweekly using a combination of sweep nets, beat sheets, and 20-minute visual searches per station. View evidence ↗

      What they did

      Between April 2025 and March 2026, insects were collected biweekly using a combination of sweep nets, beat sheets, and 20-minute visual searches per station.

      In the paper's own words

      “Hemipteran sampling was conducted biweekly from April 2025 through March 2026, producing 26 sampling events per station. Three complementary sampling methods were employed: (1) Sweep net surveys along 100-m transects (100 standardized sweeps per transect per event)... (2) Beat sheet sampling (1 m² white cloth beneath selected woody plants, 10 branches beaten per station per event)... (3) Visual searching of microhabitats (ground litter, bark surfaces, wall surfaces, under stones) for 20 person-minutes per station per event.”

      Page 2

      Found in: Methods

      Read it in the full textOpen PDF at page 2 ↗
  4. What they found

    • The study documented 112 species from 23 families, with a total of 4,678 specimens collected over one year. View evidence ↗

      What they found

      The study documented 112 species from 23 families, with a total of 4,678 specimens collected over one year.

      In the paper's own words

      “Over the 12-month sampling period, 4,678 hemipteran specimens were collected, representing 112 species across 23 families.”

      Page 2

      Found in: Results

      Read it in the full textOpen PDF at page 2 ↗
    • Cicadellidae was the most species-rich family with 28 species, while Pentatomidae was the most numerous, accounting for 26.4% (1,234 individuals) of the total. View evidence ↗

      What they found

      Cicadellidae was the most species-rich family with 28 species, while Pentatomidae was the most numerous, accounting for 26.4% (1,234 individuals) of the total.

      In the paper's own words

      “Cicadellidae (leafhoppers) was the most species-rich family overall (28 species)... Numerically, Pentatomidae dominated (1,234 individuals, 26.4%)”

      Page 2

      Found in: Results

      Read it in the full textOpen PDF at page 2 ↗
    • Insect abundance was significantly higher in the wet season (3,012 individuals) than in the dry season (1,666 individuals), resulting in a ratio of 1.9:1. View evidence ↗

      What they found

      Insect abundance was significantly higher in the wet season (3,012 individuals) than in the dry season (1,666 individuals), resulting in a ratio of 1.9:1.

      In the paper's own words

      “Wet season collections (April-October) yielded 3,012 individuals (64.4%), while dry season catches totaled 1,666 individuals (35.6%), representing a wet:dry ratio of 1.9:1.”

      Page 2

      Found in: Introduction

      Read it in the full textOpen PDF at page 2 ↗
    • Riparian buffer habitats exhibited the highest Shannon-Wiener diversity (H' = 3.41), while residential gardens had the lowest (H' = 2.12). View evidence ↗

      What they found

      Riparian buffer habitats exhibited the highest Shannon-Wiener diversity (H' = 3.41), while residential gardens had the lowest (H' = 2.12).

      In the paper's own words

      “Riparian buffer habitats supported the highest diversity (H' = 3.41±0.08), followed by mixed scrubland (H' = 3.12±0.10), agricultural margins (H' = 2.78±0.12), vacant lots (H' = 2.34±0.16), and residential gardens (H' = 2.12±0.19).”

      Page 2

      Found in: Material

      Read it in the full textOpen PDF at page 2 ↗
    • Habitat type was the primary driver of community composition, explaining 42.8% of the variation, compared to 31.2% explained by the season. View evidence ↗

      What they found

      Habitat type was the primary driver of community composition, explaining 42.8% of the variation, compared to 31.2% explained by the season.

      In the paper's own words

      “Variance partitioning revealed that habitat type explained 42.8% of total compositional variation, season accounted for 31.2%, and their interaction contributed 8.7%.”

      Page 3

      Found in: Results

      Read it in the full textOpen PDF at page 3 ↗
    • Beta diversity analysis showed that different habitats support distinct species (turnover = 0.64) rather than just smaller versions of the same species pool (nestedness = 0.18). View evidence ↗

      What they found

      Beta diversity analysis showed that different habitats support distinct species (turnover = 0.64) rather than just smaller versions of the same species pool (nestedness = 0.18).

      In the paper's own words

      “Beta diversity analysis showed that species turnover between habitat types (βturn = 0.64) exceeded nestedness (βnest = 0.18), indicating that habitats differ primarily in species identity rather than representing subsets of a common species pool.”

      Page 3

      Found in: Results

      Read it in the full textOpen PDF at page 3 ↗
  5. What it means

    • The authors recommend prioritizing the conservation of riparian corridors and maintaining a mosaic of various habitat types to maximize regional hemipteran diversity. View evidence ↗

      What it means

      The authors recommend prioritizing the conservation of riparian corridors and maintaining a mosaic of various habitat types to maximize regional hemipteran diversity.

      In the paper's own words

      “Conservation priorities should focus on maintaining riparian corridors and restricting development within buffer zones along waterways, while also preserving the mosaic of scrubland, agricultural, and vacant lot habitats that support complementary hemipteran communities.”

      Page 5

      Found in: Conclusion

      Read it in the full textOpen PDF at page 5 ↗
    • The study may have missed canopy-dwelling species because beat sheet sampling was restricted to branches below 3 meters. View evidence ↗

      What it means

      The study may have missed canopy-dwelling species because beat sheet sampling was restricted to branches below 3 meters.

      In the paper's own words

      “Beat sheet sampling was limited to accessible branches below 3 m height, potentially missing canopy-dwelling hemipteran species.”

      Page 5

      Found in: Limitations

      Read it in the full textOpen PDF at page 5 ↗
    • Species richness for Miridae and Tingidae may be underestimated because some specimens could not be identified to the species level. View evidence ↗

      What it means

      Species richness for Miridae and Tingidae may be underestimated because some specimens could not be identified to the species level.

      In the paper's own words

      “Some Miridae and Tingidae specimens could not be resolved to species level due to taxonomic uncertainty, resulting in potential underestimation of species richness within these families.”

      Page 5

      Found in: Limitations

      Read it in the full textOpen PDF at page 5 ↗

Visual summary

3 visuals

Illustrations explain the paper; charts are replotted from the paper's own table values.

AI-generated illustration
AI-generated conceptual illustration (Hemipteran insects (true bugs) in a Nigerian suburban-rural landscape). It explains the idea and does not show study data.↗ Enlarge
Drivers of Community Composition
AI-generated conceptual illustration (Hemipteran insects (true bugs) in a Nigerian suburban-rural landscape). It explains the idea and does not show study data.

AI-generated conceptual illustration (Hemipteran insects (true bugs) in a Nigerian suburban-rural landscape). It explains the idea and does not show study data.

Open full-size image ↗

Drivers of Community Composition

AI-generated conceptual illustration (Hemipteran insects (true bugs) in a Nigerian suburban-rural landscape). It explains the idea and does not show study data.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.↗ Enlarge
Riparian and Scrubland and more: Phytophagous sap vs Phytophagous seed vs Herbivorous piercing vs Predatory vs Aquatic/semi-aquatic
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

Riparian and Scrubland and more: Phytophagous sap vs Phytophagous seed vs Herbivorous piercing vs Predatory vs Aquatic/semi-aquatic

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

View source evidence ↗
Replotted from source data
Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.↗ Enlarge
Abundance (N): Pentatomidae vs Cicadellidae vs Miridae vs Reduviidae vs Lygaeidae
Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.

Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

Abundance (N): Pentatomidae vs Cicadellidae vs Miridae vs Reduviidae vs Lygaeidae

Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.

View source evidence ↗

Figures & tables

From the original paper
Classification of hemipteran functional groups and their representation across habitat typesTable 1Page 2Timeline of peak hemipteran activity for dominant families across the annual cycle in the Lagos suburban-rural interfaceTable 2Page 3Grouped bar chart comparing abundance of six major hemipteran families (Pentatomidae, Miridae, Cicadellidae, Reduviidae,Figure 1Page 3Heatmap depicting species counts across five habitat types and four quarterly periods, with darker shading indicating higher speciesFigure 2Page 4Box plot comparison of Simpson's diversity index (1-D) across five habitat types, showing median values and interquartile rangesFigure 3Page 4
FULL TEXT Original article · reflowed for reading

Introduction

The global surge in urban expansion has directed considerable research attention toward understanding how arthropod communities respond to habitat modification along urbanization gradients [1] . However, within this growing body of literature, certain insect orders have received disproportionate attention while others remain comparatively understudied. Hemiptera, the "true bugs" and their allies, represent one such relatively neglected group despite their ecological significance as herbivores, predators, disease vectors, and indicators of vegetation quality [2] . Lagos, Nigeria, stands as the most populous city in sub-Saharan Africa, with a metropolitan population exceeding 16 million and projected to reach 24 million by 2035 [3] . The eastern corridor of Lagos State, encompassing the Epe and Ibeju-Lekki Local Government Areas, has emerged as a primary zone of suburban expansion, driven by the Lekki Free Trade Zone development and associated infrastructure construction [4] . This expansion is converting substantial areas of coastal wetland, secondary forest, and agricultural land into residential and commercial developments, creating a dynamic suburban-rural interface along which habitat conditions change rapidly over short spatial distances. The seasonal climate of Lagos follows a West African monsoon pattern, with a prolonged wet season (April-October) and a shorter dry season (November-March), punctuated by a brief dry interlude (August break) within the wet season [5] . These seasonal oscillations drive pronounced changes in vegetation phenology, soil moisture, and microclimate conditions that are expected to influence hemipteran community dynamics through effects on host plant Availability, reproductive phenology, and predator-prey interactions. Despite the ecological importance and potential indicator value of Hemiptera, no previous research has systematically characterized hemipteran assemblages across the Lagos suburban-rural gradient. This research addressed this gap by comparing hemipteran diversity and community composition across five habitat types during wet and dry seasons, with the objectives of quantifying species richness and abundance patterns, assessing the relative contributions of habitat type and seasonal timing to assemblage variation, and identifying conservation-priority habitats for hemipteran diversity in this rapidly developing region.

Material and methods

Material and methods

Material

The research was conducted along the suburban-rural gradient of the Epe-Ibeju-Lekki corridor in eastern Lagos State, Nigeria (6°25'-6°35'N, 3°50'-4°05'E). The corridor extends approximately 40 km from the expanding Lekki suburban fringe through agricultural hinterland to the Epe Lagoon margins. The climate is equatorial monsoon (Am), with mean annual rainfall of 1,693 mm, mean temperature of 27.2°C, and relative humidity ranging from 65% (February) to 88% (July). Native vegetation comprises lowland rainforest (substantially modified), freshwater swamp forest, and mangrove formations along waterways. Five habitat types were delineated for comparative assessment: (1) residential gardens within planned housing estates (managed lawns, ornamental plantings, fruit trees), (2) vacant lots in development areas (cleared land with ruderal vegetation), (3) active agricultural smallholdings (cassava, maize, vegetable plots with associated margins), (4) riparian buffer strips along seasonal and perennial streams (3-30 m width, retaining gallery forest elements), and (5) mixed scrubland on laterite uplands (secondary regrowth 5-15 years post-disturbance). Five replicate sampling stations were established within each habitat type, totaling 25 stations, with minimum inter-station distance of 600 m.

Methods

Hemipteran sampling was conducted biweekly from April 2025 through March 2026, producing 26 sampling events per station. Three complementary sampling methods were employed: (1) Sweep net surveys along 100-m transects (100 standardized sweeps per transect per event) targeting vegetation-dwelling species; (2) Beat sheet sampling (1 m² white cloth beneath selected woody plants, 10 branches beaten per station per event) targeting arboreal and shrubassociated species; (3) Visual searching of microhabitats (ground litter, bark surfaces, wall surfaces, under stones) for 20 person-minutes per station per event. All hemipteran specimens were preserved in 70% ethanol and identified at the Entomology Research Laboratory of the University of Lagos. Identification utilized regional taxonomic keys including Schuh and Slater's True Bugs of the World, Linnavuori's keys to West African Heteroptera, and Hamilton's keys for Auchenorrhyncha. Difficult specimens were verified through comparison with reference material at the Nigerian Institute for Oceanography and Marine Research. Environmental measurements at each sampling event included ambient temperature and relative humidity (digital psychrometer), vegetation height (3 random measurements), herbaceous ground cover percentage, canopy cover (densiometer), and the number of flowering plant species within 10 m of each station. Monthly rainfall data were obtained from the Nigerian Meteorological Agency Ibeju-Lekki recording station. Alpha diversity was quantified using species richness (S), Shannon-Wiener (H'), and Simpson's (1-D) indices. Beta diversity was partitioned into turnover and nestedness components using the betapart R package. Species accumulation curves were generated using EstimateS v9.1 with Chao 2 estimator. PERMANOVA with 999 permutations tested effects of habitat type and season on community composition. Indicator species analysis identified taxon-habitat and taxon-season associations using the indicspecies package. Variance partitioning was used to decompose the contributions of spatial, temporal, and environmental factors to assemblage variation.

Results

Over the 12-month sampling period, 4,678 hemipteran specimens were collected, representing 112 species across 23 families. The order was partitioned into Heteroptera (78 species, 16 families) and Auchenorrhyncha (34 species, 7 families). Cicadellidae (leafhoppers) was the most speciesrich family overall (28 species), followed by Pentatomidae (15 species), Miridae (14 species), and Reduviidae (12 species). Numerically, Pentatomidae dominated (1,234 individuals, 26.4%), followed by Cicadellidae (978 individuals, 20.9%), Miridae (612 individuals, 13.1%), and Lygaeidae (445 individuals, 9.5%). S pecies accumulation curves for the overall assemblage indicated that the Chao 2 estimated total richness was 133 species, suggesting that sampling achieved approximately 84.2% completeness. Habitat-specific completeness ranged from 78.4% (residential) to 89.7% (riparian), indicating that more intensively vegetated habitats were more thoroughly sampled. Variance partitioning revealed that habitat type explained 42.8% of total compositional variation, season accounted for 31.2%, and their interaction contributed 8.7%. The remaining 17.3% was attributable to unexplained spatial and temporal variation. PERMANOVA confirmed significant effects of both habitat (pseudo-F = 7.23, p = 0.001) and season (pseudo-F = 5.18, p = 0.001). Beta diversity analysis showed that species turnover between habitat types (βturn = 0.64) exceeded nestedness (βnest = 0.18), indicating that habitats differ primarily in species identity rather than representing subsets of a common species pool. Seasonal beta diversity was lower (βturn = 0.41, βnest = 0.12), reflecting greater temporal continuity within habitats than spatial similarity between them. Indicator species analysis identified 14 species with significant habitat associations and 9 with significant seasonal associations (p<0.05). Notable indicators included the predatory reduviid Platymeris biguttatus, strongly associated with scrubland during the wet season (indicator value = 0.79), and the agricultural pest Nezara viridula, abundant in farmland during both seasons (indicator value = 0.84).

Discussion

The hemipteran assemblage documented across the Lagos suburban-rural interface demonstrates a community structured primarily by habitat heterogeneity, with seasonal rainfall serving as a secondary modulator of abundance and activity patterns. The finding that habitat type explains more compositional variation (42.8%) than season (31.2%) underscores the importance of spatial habitat management for conserving hemipteran diversity in this rapidly developing landscape [6] .

The exceptional diversity of riparian buffer habitats (H' = 3.41) reflects the combined effects of moisture availability, structural vegetation complexity, and the microhabitat heterogeneity provided by gallery forest elements along waterways [7] . Riparian zones in tropical landscapes serve as corridors facilitating insect movement between habitat patches and as refugia during unfavorable conditions, functions that are particularly important in fragmented suburban landscapes [8] . The high diversity documented in these narrow linear habitats argues strongly for their protection within urban planning frameworks. The dominance of Pentatomidae in overall abundance is consistent with the global pattern of stink bug numerical predominance in tropical hemipteran assemblages [9] . Several of the most abundant pentatomid species, including Nezara viridula and Acrosternum acutum, are recognized agricultural pests whose populations may be augmented by suburban gardening and farming activities that provide extended periods of host plant availability [2] . The beta diversity pattern, dominated by species turnover rather than nestedness, indicates that different habitats support distinct hemipteran communities rather than impoverished subsets of a regional species pool [10] . This finding has conservation implications: protecting only the most diverse habitat type (riparian buffers) would fail to capture the unique species associated with scrubland, agricultural margins, and other habitat types. A landscapelevel conservation strategy that maintains a mosaic of habitat types is therefore essential for maximizing regional hemipteran diversity. Kumari and Priya [11] reported comparable patterns of habitat-mediated insect diversity variation in transitioning suburban areas, with the finding that less intensively managed habitats consistently supported richer assemblages. The present research extends this understanding to Hemiptera specifically, demonstrating that this taxonomically diverse order responds to suburban habitat gradients in ways broadly consistent with patterns documented for other insect orders [12] . The seasonal wet:dry abundance ratio of 1.9:1 is somewhat lower than the ratios reported for Coleoptera and Lepidoptera in comparable West African settings, suggesting that certain hemipteran lineages (particularly sap-feeding Auchenorrhyncha associated with perennial woody plants) maintain more stable populations across seasonal transitions than herbivorous beetles or nectardependent butterflies [13] . This relative seasonal stability enhances the potential of hemipteran assemblages as yearround indicators of habitat quality, complementing the seasonally variable signals provided by other insect orders.

Conclusion

This research demonstrates that hemipteran diversity in the Lagos suburban-rural interface is governed primarily by habitat heterogeneity, with each of the five habitat types supporting distinct assemblage components that collectively contribute to landscape-level species richness. The 112 documented species, representing 84% of estimated total richness, provide a comprehensive baseline for monitoring future biodiversity responses to continued urban expansion. Conservation priorities should focus on maintaining riparian corridors and restricting development within buffer zones along waterways, while also preserving the mosaic of scrubland, agricultural, and vacant lot habitats that support complementary hemipteran communities. The integration of hemipteran monitoring into urban biodiversity assessment frameworks is recommended, given their ecological significance and relative ease of sampling.

Ethical considerations

All sampling was conducted under permit issued by the Federal Ministry of Environment, National Biodiversity Registry. No collections were made within the Lekki Conservation Centre or any designated protected area.

Sampling protocols avoided the use of chemical attractants or insecticides. The research was approved by the University of Lagos Research Ethics Committee.

Limitations

Beat sheet sampling was limited to accessible branches below 3 m height, potentially missing canopy-dwelling hemipteran species. The August break within the wet season created a brief interruption in the expected seasonal trend that may not be captured as a distinct seasonal phase in the biweekly sampling design. Some Miridae and Tingidae specimens could not be resolved to species level due to taxonomic uncertainty, resulting in potential underestimation of species richness within these families. The unequal area of riparian buffer habitats compared to other habitat types may have introduced confounding area effects.

Acknowledgement

AcknowledgementsThis research was supported by the Tertiary Education Trust Fund (TETFund) Institution-Based Research Grant (TETF/DR&D/CE/UNI/UNILAG/IBR/2024/VOL.1/038). The Nigerian Institute for Oceanography and Marine Research provided access to reference insect collections. The authors gratefully acknowledge Dr. Adewale Ogunwale for assistance with Cicadellidae taxonomy and Mr. Chukwuemeka Nwosu for tireless field assistance throughout the sampling period. Community development committees in Epe and Ibeju-Lekki facilitated access to private lands for sampling.

Figures and tables from the paper

Table 1. Classification of hemipteran functional groups and their representation across habitat types
Functional GroupFamiliesTotal spp.RiparianScrublandAgri-margin
Phytophagous sapCicadellidae, Cercopidae, Delphacidae38141218
Phytophagous seedLygaeidae, Pyrrhocoridae12579
Herbivorous piercingPentatomidae, Miridae, Tingidae29181421
PredatoryReduviidae, Nabidae, Anthocoridae1815128
Aquatic/semi-aquaticGerridae, Veliidae, Corixidae9923
Mixed/omnivorousCoreidae, Alydidae6454

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Classification of hemipteran functional groups and their representation across habitat types↗ Enlarge
Table 1
Classification of hemipteran functional groups and their representation across habitat types

Classification of hemipteran functional groups and their representation across habitat types

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Original paper tableSource PDF · page 2 ↗
Table 2. Timeline of peak hemipteran activity for dominant families across the annual cycle in the Lagos suburban-rural interface
FamilyPeak PeriodPeak MonthAbundance (N)Trigger Factor
PentatomidaeEarly wetMay-Jun478Crop flush
CicadellidaeMid-wetJul-Aug412Grass growth
MiridaeLate wetSep-Oct234Flowering peak
ReduviidaeWet-dry transitionOct-Nov189Prey abundance
LygaeidaeEarly dryNov-Dec167Seed maturation
CoreidaeMid-wetJun-Jul156Legume fruiting

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Timeline of peak hemipteran activity for dominant families across the annual cycle in the Lagos suburban-rural interface↗ Enlarge
Table 2
Timeline of peak hemipteran activity for dominant families across the annual cycle in the Lagos suburban-rural interface

Timeline of peak hemipteran activity for dominant families across the annual cycle in the Lagos suburban-rural interface

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Original paper tableSource PDF · page 3 ↗
Figure 1. Grouped bar chart comparing abundance of six major hemipteran families (Pentatomidae, Miridae, Cicadellidae, Reduviidae,
Grouped bar chart comparing abundance of six major hemipteran families (Pentatomidae, Miridae, Cicadellidae, Reduviidae,↗ Enlarge
Figure 1
Grouped bar chart comparing abundance of six major hemipteran families (Pentatomidae, Miridae, Cicadellidae, Reduviidae,

Grouped bar chart comparing abundance of six major hemipteran families (Pentatomidae, Miridae, Cicadellidae, Reduviidae,

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Original paper figureSource PDF · page 3 ↗
Figure 2. Heatmap depicting species counts across five habitat types and four quarterly periods, with darker shading indicating higher species
Heatmap depicting species counts across five habitat types and four quarterly periods, with darker shading indicating higher species↗ Enlarge
Figure 2
Heatmap depicting species counts across five habitat types and four quarterly periods, with darker shading indicating higher species

Heatmap depicting species counts across five habitat types and four quarterly periods, with darker shading indicating higher species

Open full-size image ↗
Original paper figureSource PDF · page 4 ↗
Figure 3. Box plot comparison of Simpson's diversity index (1-D) across five habitat types, showing median values and interquartile ranges
Box plot comparison of Simpson's diversity index (1-D) across five habitat types, showing median values and interquartile ranges↗ Enlarge
Figure 3
Box plot comparison of Simpson's diversity index (1-D) across five habitat types, showing median values and interquartile ranges

Box plot comparison of Simpson's diversity index (1-D) across five habitat types, showing median values and interquartile ranges

Open full-size image ↗
Original paper figureSource PDF · page 4 ↗

References

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