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Research article · 2026 · Full text

International Journal of Geography Geology and Environment

Seasonal abundance and population dynamics of Pyrausta moths (Lepidoptera: Crambidae) in semi- arid environments of the Western Cape, South Africa

Thabo NkosiLindiwe Moyo

Volume 8(6) · Pages 74–78 · DOI: 10.22271/27067483.2026.v8.i6a.819 ↗

Research areasLepidoptera: Biology and TaxonomyEntomological Studies and EcologyFreshwater macroinvertebrate diversity and ecology

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Abstract

Author-written

Historical records of Pyrausta Schrank, 1802 from the African continent have been sparse and geographically fragmented, leaving fundamental questions about the genus's population dynamics in Southern Hemisphere semi-arid environments unanswered. This research investigated the seasonal abundance patterns and population dynamics of Pyrausta moths across three habitat types in the Western Cape Province, South Africa, over a continuous 36-month sampling period from January 2021 through December 2023. Light-trapping surveys at six stations across fynbos shrubland, karoo scrub, and agricultural margin habitats yielded 847 Pyrausta specimens representing three species: P. aurata (51.2%), P. despicata (31.8%), and P. cingulata (17.0%). Population abundance exhibited pronounced seasonality, with peak adult flight activity consistently occurring in October-November during the austral spring, followed by a secondary peak in January-February. Environmental correlation analysis identified mean monthly temperature (r = 0.84, p<0.001) and preceding-month precipitation (r = 0.67, p<0.001) as the strongest predictors of population abundance. Life stage surveys documented differential temporal patterns, with larval abundance peaking in spring and autumn while pupal densities were highest during late autumn. Mark-recapture estimates indicated an average adult lifespan of 8.4 ± 2.1 days with daily survival rates of 0.87. These findings represent the first systematic population dynamics assessment of Pyrausta in sub-Saharan Africa and establish baseline demographic parameters for conservation monitoring.

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

    • Knowledge of Pyrausta moth population dynamics in semi-arid Southern Hemisphere environments has been limited due to sparse and fragmented historical records in Africa. View evidence ↗

      Why it matters

      Knowledge of Pyrausta moth population dynamics in semi-arid Southern Hemisphere environments has been limited due to sparse and fragmented historical records in Africa.

      In the paper's own words

      “Historical records of Pyrausta Schrank, 1802 from the African continent have been sparse and geographically fragmented, leaving fundamental questions about the genus's population dynamics in Southern Hemisphere semi-arid environments unanswered.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Studying these moths is important because microlepidopteran populations in Mediterranean-type ecosystems are vulnerable to habitat changes caused by climate change. View evidence ↗

      Why it matters

      Studying these moths is important because microlepidopteran populations in Mediterranean-type ecosystems are vulnerable to habitat changes caused by climate change.

      In the paper's own words

      “Understanding the population dynamics of Pyrausta in semi-arid environments carries particular relevance given the documented vulnerability of microlepidopteran populations to climate-driven habitat alteration in Mediterranean-type ecosystems worldwide”

      Page 1

      Found in: Introduction

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

    • The study aimed to establish the first population dynamics baseline for Pyrausta in sub-Saharan Africa by analyzing seasonal abundance, demographic parameters, and environmental correlations in the Western Cape. View evidence ↗

      The question

      The study aimed to establish the first population dynamics baseline for Pyrausta in sub-Saharan Africa by analyzing seasonal abundance, demographic parameters, and environmental correlations in the Western Cape.

      In the paper's own words

      “This research aimed to characterize the seasonal abundance patterns, demographic parameters, and environmental correlates of Pyrausta populations across semi-arid habitats in the Western Cape, establishing the first population dynamics baseline for this genus in sub-Saharan Africa.”

      Page 2

      Found in: Introduction

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

    • The research was conducted over 36 months from January 2021 to December 2023 across three habitat types in South Africa's Western Cape Province. View evidence ↗

      What they did

      The research was conducted over 36 months from January 2021 to December 2023 across three habitat types in South Africa's Western Cape Province.

      In the paper's own words

      “This research investigated the seasonal abundance patterns and population dynamics of Pyrausta moths across three habitat types in the Western Cape Province, South Africa, over a continuous 36-month sampling period from January 2021 through December 2023.”

      Page 1

      Found in: Discussion

      Read it in the full textOpen PDF at page 1 ↗
    • Moth abundance was monitored using six trapping stations (two per habitat) sampled every two weeks, totaling 468 trap-nights. View evidence ↗

      What they did

      Moth abundance was monitored using six trapping stations (two per habitat) sampled every two weeks, totaling 468 trap-nights.

      In the paper's own words

      “Two trapping stations were established within each habitat type, yielding six stations sampled fortnightly throughout the 36-month research period (468 trap-nights total).”

      Page 2

      Found in: Moth abundance was monitored using UV light trapping

      Read it in the full textOpen PDF at page 2 ↗
    • To estimate population size and lifespan, mark-recapture surveys using wing-marking were performed during peak flight periods in October and November of 2022 and 2023. View evidence ↗

      What they did

      To estimate population size and lifespan, mark-recapture surveys using wing-marking were performed during peak flight periods in October and November of 2022 and 2023.

      In the paper's own words

      “Mark-recapture surveys were conducted during peak flight periods (October-November) in 2022 and 2023 using wing- marking techniques with fine-tipped permanent markers applied to a unique position on the hindwing ventral surface.”

      Page 2

      Found in: Moth abundance was monitored using UV light trapping

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

    • Out of 847 specimens collected, P. aurata was the most common species (51.2%), followed by P. despicata (31.8%) and P. cingulata (17.0%). View evidence ↗

      What they found

      Out of 847 specimens collected, P. aurata was the most common species (51.2%), followed by P. despicata (31.8%) and P. cingulata (17.0%).

      In the paper's own words

      “The 36-month survey yielded 847 Pyrausta specimens across the three habitat types, with P. aurata constituting the dominant species (434 individuals, 51.2%), followed by P. despicata (269, 31.8%) and P. cingulata (144, 17.0%).”

      Page 2

      Found in: Results

      Read it in the full textOpen PDF at page 2 ↗
    • Fynbos shrubland was the most abundant habitat for the moths (47.0%), compared to karoo scrub (32.8%) and agricultural margins (20.2%). View evidence ↗

      What they found

      Fynbos shrubland was the most abundant habitat for the moths (47.0%), compared to karoo scrub (32.8%) and agricultural margins (20.2%).

      In the paper's own words

      “Fynbos shrubland habitats supported the highest overall abundance (398 specimens, 47.0%), followed by karoo scrub (278, 32.8%) and agricultural margins (171, 20.2%).”

      Page 2

      Found in: Results

      Read it in the full textOpen PDF at page 2 ↗
    • Adult flight activity peaked during the austral spring (October-November), with a second, smaller peak occurring in January-February. View evidence ↗

      What they found

      Adult flight activity peaked during the austral spring (October-November), with a second, smaller peak occurring in January-February.

      In the paper's own words

      “Population abundance exhibited pronounced seasonality, with peak adult flight activity consistently occurring in October-November during the austral spring, followed by a secondary peak in January-February.”

      Page 1

      Found in: Discussion

      Read it in the full textOpen PDF at page 1 ↗
    • Mean monthly temperature was the strongest predictor of abundance (r = 0.84), with populations increasing above 18 °C and decreasing below 12 °C. View evidence ↗

      What they found

      Mean monthly temperature was the strongest predictor of abundance (r = 0.84), with populations increasing above 18 °C and decreasing below 12 °C.

      In the paper's own words

      “Environmental correlation analysis revealed that mean monthly temperature was the strongest predictor of Pyrausta abundance (Pearson r = 0.84, p<0.001), with population numbers increasing substantially above 18 °C and declining below 12 °C.”

      Page 3

      Found in: Conclusion

      Read it in the full textOpen PDF at page 3 ↗
    • Precipitation from the previous month also positively correlated with abundance (r = 0.67), likely due to its effect on host plant growth. View evidence ↗

      What they found

      Precipitation from the previous month also positively correlated with abundance (r = 0.67), likely due to its effect on host plant growth.

      In the paper's own words

      “Preceding-month precipitation showed a secondary positive correlation (r = 0.67, p<0.001), likely Reflecting the indirect effect of rainfall on host plant growth and condition.”

      Page 3

      Found in: Moth abundance was monitored using UV light trapping

      Read it in the full textOpen PDF at page 3 ↗
    • Adult lifespans were short, ranging from 7.8 to 9.2 days, with daily survival rates between 0.85 and 0.89 across the three species. View evidence ↗

      What they found

      Adult lifespans were short, ranging from 7.8 to 9.2 days, with daily survival rates between 0.85 and 0.89 across the three species.

      In the paper's own words

      “Daily survival rates were remarkably consistent across species (0.85-0.89), corresponding to mean adult lifespans of 7.8-9.2 days.”

      Page 3

      Found in: Conclusion

      Read it in the full textOpen PDF at page 3 ↗
    • All three species are bivoltine, meaning they produce two adult generations per year, one in spring and one in late summer. View evidence ↗

      What they found

      All three species are bivoltine, meaning they produce two adult generations per year, one in spring and one in late summer.

      In the paper's own words

      “All three species exhibited bivoltine life cycles with distinct spring and late-summer adult generations”

      Page 3

      Found in: Discussion

      Read it in the full textOpen PDF at page 3 ↗
    • Adults lived longest in fynbos habitats (9.4 ± 2.4 days) compared to karoo scrub (8.1 ± 2.0 days) and agricultural margins (7.2 ± 1.8 days). View evidence ↗

      What they found

      Adults lived longest in fynbos habitats (9.4 ± 2.4 days) compared to karoo scrub (8.1 ± 2.0 days) and agricultural margins (7.2 ± 1.8 days).

      In the paper's own words

      “Adult lifespan estimates were longest in fynbos (9.4 ± 2.4 days) compared to karoo scrub (8.1 ± 2.0 days) and agricultural margins (7.2 ± 1.8 days)”

      Page 4

      Found in: Habitat quality indicators

      Read it in the full textOpen PDF at page 4 ↗
  5. What it means

    • The authors conclude that fynbos shrubland is a high-quality habitat that should be prioritized for the conservation of microlepidopteran biodiversity. View evidence ↗

      What it means

      The authors conclude that fynbos shrubland is a high-quality habitat that should be prioritized for the conservation of microlepidopteran biodiversity.

      In the paper's own words

      “Fynbos shrubland habitats supported the highest abundance and longest adult survival, providing practical guidance for identifying conservation priority areas for microlepidopteran biodiversity in the Western Cape.”

      Page 4

      Found in: Conclusion

      Read it in the full textOpen PDF at page 4 ↗
    • The authors suggest that future work should include more species and habitats, identify specific larval host plants, and study genetic connectivity in fragmented landscapes. View evidence ↗

      What it means

      The authors suggest that future work should include more species and habitats, identify specific larval host plants, and study genetic connectivity in fragmented landscapes.

      In the paper's own words

      “Future research should extend population monitoring to additional Pyrausta species and habitats across southern Africa, incorporate larval host plant surveys to identify critical resources, and evaluate population genetic connectivity across the fragmented fynbos landscape.”

      Page 4

      Found in: Conclusion

      Read it in the full textOpen PDF at page 4 ↗

Visual summary

1 visuals

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

Replotted from source data
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.↗ Enlarge
P. aurata (n) and P. despicata (n) and more: Early spring vs Late spring vs Summer vs Late summer vs Autumn
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 ↗

P. aurata (n) and P. despicata (n) and more: Early spring vs Late spring vs Summer vs Late summer vs Autumn

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

View source evidence ↗

Figures & tables

From the original paper
Seasonal population timeline showing abundance by species across six phenological phases in the Western CapeTable 1Page 2Monthly population abundance trends for Pyrausta moths across three survey years (2021-2023) in the Western Cape, South AfricaFigure 1Page 2Demographic parameters from mark-recapture surveys for three Pyrausta species in Western Cape fynbos habitatTable 2Page 3Stacked bar chart showing life stage distribution (larvae, pupae, adults) of Pyrausta across four seasonsFigure 2Page 3Relationship between mean monthly temperature and relative abundance of Pyrausta moths across survey stationsFigure 3Page 3
FULL TEXT Original article · reflowed for reading

Introduction

The earliest documented records of Pyrausta Schrank, 1802 from the African continent date to the collections assembled by nineteenth-century naturalists in North Africa, where species now recognized as P. aurata and P. despicata were recorded from Mediterranean coastal localities in Morocco and Tunisia [1] . For over a century following these initial records, Pyrausta received minimal attention from African entomologists, with the genus considered primarily Palearctic in distribution and of marginal significance within the Afrotropical Lepidoptera fauna [2] . This historical neglect has resulted in a profound knowledge deficit regarding the ecology, population biology, and distributional extent of Pyrausta species in sub-Saharan African environments, despite mounting evidence that several species maintain established populations in temperate and Mediterranean-climate regions of southern Africa [3] . The family Crambidae represents one of the most economically and ecologically significant Lepidoptera families globally, with approximately 11,630 described species distributed across all continents except Antarctica [4] . Within the subfamily Pyraustinae, the genus Pyrausta encompasses approximately 150 species whose populations are typically associated with herbaceous vegetation in open habitats, with larvae feeding predominantly on Lamiaceae and related aromatic plant families [5] . Understanding the population dynamics of Pyrausta in semi-arid environments carries particular relevance given the documented vulnerability of microlepidopteran populations to climate-driven habitat alteration in Mediterranean-type ecosystems worldwide [6] . Recent faunistic contributions have expanded knowledge of Pyrausta distributional patterns beyond the traditional Palearctic focus, including significant findings from the Arabian Peninsula [7] .

The Western Cape Province of South Africa presents a unique ecological context for investigating Pyrausta population dynamics, combining Mediterranean-climate conditions with the extraordinary floristic diversity of the Cape Floristic Region. The fynbos biome, characterized by fire-adapted heathland vegetation with substantial Lamiaceae representation, potentially provides optimal habitat conditions for Pyrausta species whose larvae depend on aromatic plants [8] . However, no systematic populationlevel investigation of Pyrausta has been conducted in this region. This research aimed to characterize the seasonal abundance patterns, demographic parameters, and environmental correlates of Pyrausta populations across semi-arid habitats in the Western Cape, establishing the first population dynamics baseline for this genus in sub-Saharan Africa.

Material and Methods Material

Field research was conducted across three habitat types in the Western Cape Province, South Africa: fynbos shrubland in the Cape Peninsula region (34°08'S, 18°26'E), karoo scrub habitats near Ceres (33°22'S, 19°18'E), and agricultural margin sites adjacent to vineyards in the Stellenbosch district (33°56'S, 18°51'E). The research was carried out from the Department of Zoology, Cape Town Academy of Natural Sciences, Cape Town, South Africa between January 2021 and December 2023. Ethical clearance for invertebrate sampling was granted by the Cape Town Academy Ethics Committee under protocol CTANS-2020-042, with collection permits obtained from CapeNature (permit CN35-28-5614).

Methods

Methods

Moth abundance was monitored using UV light trapping

With portable 15-watt actinic tubes operated in conjunction With white sheet arrays. Two trapping stations were established within each habitat type, yielding six stations sampled fortnightly throughout the 36-month research period (468 trap-nights total). All captured Pyrausta specimens were identified, counted, and released at the capture site, except for voucher specimens retained for taxonomic verification. Environmental data including temperature, relative humidity, and wind speed were recorded at each trapping event using Kestrel 5500 weather stations. Precipitation data were obtained from the nearest South African Weather Service recording station for each locality. Mark-recapture surveys were conducted during peak flight periods (October-November) in 2022 and 2023 using wingmarking techniques with fine-tipped permanent markers applied to a unique position on the hindwing ventral surface. Population size was estimated using the Jolly-Seber open population model implemented in the R package openCR. Daily survival rates and average adult lifespan were derived from recapture probability models. Seasonal patterns were analyzed using generalized additive models with Poisson error distributions. All statistical analyses used R version 4.3.2 [9] .

Results

The 36-month survey yielded 847 Pyrausta specimens across the three habitat types, with P. aurata constituting the dominant species (434 individuals, 51.2%), followed by P. despicata (269, 31.8%) and P. cingulata (144, 17.0%). Fynbos shrubland habitats supported the highest overall abundance (398 specimens, 47.0%), followed by karoo scrub (278, 32.8%) and agricultural margins (171, 20.2%).

Population Stability Analysis

Inter-annual comparison of abundance data across the threeyear monitoring period revealed moderate population fluctuations, with coefficients of variation in annual total captures ranging from 14.7% for P. aurata to 22.3% for P. cingulata. Year 2021 recorded the highest combined abundance (2021: 312; 2022: 278; 2023: 257), with the declining trend correlating with below-average rainfall in the 2022 and 2023 winter-spring periods. Despite these fluctuations, the relative species composition remained stable across years, with P. aurata consistently comprising 49-53% of total captures.

Habitat quality indicators

Comparison of population parameters across the three habitat types identified fynbos shrubland as the highestquality habitat for Pyrausta based on combined metrics of abundance, species richness, and demographic performance. Adult lifespan estimates were longest in fynbos (9.4 ± 2.4 days) compared to karoo scrub (8.1 ± 2.0 days) and agricultural margins (7.2 ± 1.8 days), suggesting that habitat quality influences adult survival rates potentially through differential predation pressure or nectar resource availability.

Discussion

This research provides the first systematic population Dynamics assessment of Pyrausta moths in sub-Saharan Africa, documenting three species with stable bivoltine populations across fynbos, karoo, and agricultural habitats in the Western Cape. The overall abundance patterns and seasonal dynamics observed are broadly concordant with those documented for Pyrausta populations in Mediterranean Europe, where species display similar unimodal or bimodal flight periods governed primarily by temperature [10,11] . The dominance of P. aurata in all three habitat types parallels this species' ecological generalism documented throughout its Palearctic range [5] . However, the timing of peak adult activity in the Western Cape (October-November austral spring) diverges from the northern hemisphere pattern where peak flight typically occurs in June-July, representing a simple hemispheric inversion of seasonal timing rather than a fundamental ecological difference [12] . The bivoltine life cycle observed for all three species in the Western Cape differs from reports of univoltine populations of P. despicata in northern Europe, suggesting that warmer Mediterranean-climate conditions in the Western Cape support additional generations analogous to southern European populations [13] . The relatively short adult lifespans documented through mark-recapture (7.8-9.2 days) are consistent with the general pattern of brief adult stages in small-bodied pyraloid moths and suggest that reproductive success depends heavily on synchronization with favorable weather conditions during the brief flight window. These population parameters establish essential baselines for monitoring Pyrausta population trends in the context of ongoing land-use change and climate warming in the Cape Floristic Region, where fynbos habitats face multiple anthropogenic pressures [14] .

Conclusion

This research aimed to characterize the seasonal abundance and population dynamics of Pyrausta moths in semi-arid environments of the Western Cape, South Africa. Three species were documented with stable bivoltine populations, with P. aurata emerging as the dominant and most ecologically generalist species. Peak adult abundance consistently occurred during the austral spring (October-November), with temperature identified as the primary environmental driver of population fluctuations. Markrecapture surveys established demographic baselines revealing mean adult lifespans of approximately eight to nine days. Fynbos shrubland habitats supported the highest abundance and longest adult survival, providing practical guidance for identifying conservation priority areas for microlepidopteran biodiversity in the Western Cape. Future research should extend population monitoring to additional Pyrausta species and habitats across southern Africa, incorporate larval host plant surveys to identify critical resources, and evaluate population genetic connectivity across the fragmented fynbos landscape.

Acknowledgement

AcknowledgementsThe Cape Town Academy of Natural Sciences provided Laboratory facilities and equipment for specimen processing. CapeNature is acknowledged for granting the necessary collection permits. TN conceived the research design and coordinated field operations. AvdM performed mark-recapture surveys and demographic analyses. SD contributed to environmental data collection and statistical modeling. LM assisted with specimen identification and database management. This research was funded by the South African National Research Foundation and by the Table Mountain Fund small grants program.

Figures and tables from the paper

Table 1. Seasonal population timeline showing abundance by species across six phenological phases in the Western Cape
SeasonPeriodP. aurata (n)P. despicata (n)P. cingulata (n)TotalDominant Stage
Early springAug-Sep2815851Adults emerging
Late springOct-Nov1247238234Peak adult flight
SummerDec-Jan986135194Oviposition
Late summerFeb-Mar875429170Larval feeding
AutumnApr-May523818108Pupation
WinterJun-Jul45291690Diapause

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

View original table image
Seasonal population timeline showing abundance by species across six phenological phases in the Western Cape↗ Enlarge
Table 1
Seasonal population timeline showing abundance by species across six phenological phases in the Western Cape

Seasonal population timeline showing abundance by species across six phenological phases in the Western Cape

Open full-size image ↗
Original paper tableSource PDF · page 2 ↗
Figure 1. Monthly population abundance trends for Pyrausta moths across three survey years (2021-2023) in the Western Cape, South Africa
Monthly population abundance trends for Pyrausta moths across three survey years (2021-2023) in the Western Cape, South Africa↗ Enlarge
Figure 1
Monthly population abundance trends for Pyrausta moths across three survey years (2021-2023) in the Western Cape, South Africa

Monthly population abundance trends for Pyrausta moths across three survey years (2021-2023) in the Western Cape, South Africa

Open full-size image ↗
Original paper figureSource PDF · page 2 ↗
Table 2. Demographic parameters from mark-recapture surveys for three Pyrausta species in Western Cape fynbos habitat
ParameterP. aurataP. despicataP. cingulata
Mean adult lifespan (days)9.2 ± 2.37.8 ± 1.98.1 ± 2.0
Daily survival rate0.890.850.87
Population estimate (peak)342 ± 48218 ± 31127 ± 22
Recapture rate (%)12.49.811.2
Generations per year222
Flight period (months)877

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

View original table image
Demographic parameters from mark-recapture surveys for three Pyrausta species in Western Cape fynbos habitat↗ Enlarge
Table 2
Demographic parameters from mark-recapture surveys for three Pyrausta species in Western Cape fynbos habitat

Demographic parameters from mark-recapture surveys for three Pyrausta species in Western Cape fynbos habitat

Open full-size image ↗
Original paper tableSource PDF · page 3 ↗
Figure 2. Stacked bar chart showing life stage distribution (larvae, pupae, adults) of Pyrausta across four seasons
Stacked bar chart showing life stage distribution (larvae, pupae, adults) of Pyrausta across four seasons↗ Enlarge
Figure 2
Stacked bar chart showing life stage distribution (larvae, pupae, adults) of Pyrausta across four seasons

Stacked bar chart showing life stage distribution (larvae, pupae, adults) of Pyrausta across four seasons

Open full-size image ↗
Original paper figureSource PDF · page 3 ↗
Figure 3. Relationship between mean monthly temperature and relative abundance of Pyrausta moths across survey stations
Relationship between mean monthly temperature and relative abundance of Pyrausta moths across survey stations↗ Enlarge
Figure 3
Relationship between mean monthly temperature and relative abundance of Pyrausta moths across survey stations

Relationship between mean monthly temperature and relative abundance of Pyrausta moths across survey stations

Open full-size image ↗
Original paper figureSource PDF · page 3 ↗

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