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DIVERSITY AND DISTRIBUTION OF
HYMENOPTERA ACULEATA IN MIDWESTERN
BRAZILIAN DRY FORESTS
Rogerio Silvestre, Manoel F. Demétrio, Bhrenno M. Trad,
Felipe Varussa Lima, Tiago H. Auko and Paulo Robson de Souza
Laboratório de Ecologia de Hymenoptera HECOLAB
Faculdade de Ciências Biológicas e Ambientais- FCBA
Universidade Federal da Grande Dourados- UFGD
Cuzco Hymenoptera Congress 2014
We present here the first systematic inventory of Hymenoptera
Aculeata fauna made in the pristine dry forests of midwestern Brazil.
The goals: estimate species richness for each taxon and check which
model the distribution
Investigated groups
Formicidae
APOIDEA: Apidae (sensu latu), Sphecidae and Crabronidae
VESPOIDEA: Pompilidae, Mutillidae, Vespidae, Scoliidae,
Tiphiidae and Rhopalosomatidae
Introduction
Brian R. Johnson et. al. 2013- Current Biology 23
“Aculeata” clade
Methodology
The study was conducted over eight years, in two regions:
Bodoquena Mountain Range and Brazilian Chaco.
These locations are set in a large open area in a diagonal formation of
South America, the so-called "Pleistocenic Arc", extending from the
Caatinga in northeastern Brazil to the Chaco in Argentina, where the
contact areas occur between:
Pantanal, Cerrado, Chaco, and Atlantic Forest.
Eighteen wild expeditions were performed in this period with seven
days of collections in each, but not with all expert groups together.
Fig. 1-Map of Serra da Bodoquena, bordering the Pantanal province, State of Mato Grosso do Sul.
MATO GROSSO
DO SUL
BRASIL
Pantanal
Plain
Bodoquena
Mountain Range
Kadiwéu
Indians Land
Porto Murtinho
Bonito
Chaco
Sampled areas in midwestern Brazilian Dry Forest
Distribution analysis
• To compose the sample unit we combined the expeditions that have been made to
the same location, and those performed in nearby sites within a radius of 10 km
buffers were grouped. Nine sites emerged from this combination of collecting
expeditions.
• The frequencies of species based in presence/absence were analyzed in the range
of region and grouped into classes or octaves of abundance.
• The number of species in each octave varied as follows: 1 (0-2); 2 (2-4); 3 (4-8),
4 (8-16) and so on, allowing us to view the richness and quantitative distribution
of species per sample unit.
• The data set was analyzed using R software with the Vegan package.
Diversity analysis
• We built a table with the Shannon diversity index, Chao 1 richness estimator and
Second-order Jackknife richness estimator (Jack2).
• When comparing species similarity of nine localities, we calculate and use
Morisita-Horn sample similarity index, using also distance in km between
localities obtained with the software Google Earth 7.1.2., which was compared
with the similarity values obtained and distance using a Pearson correlation
computed on the software Statistica 8.0 (Statsoft Inc. 2007).
Sampling Protocol
• Entomological net: for qualitative samples.
• Moërick traps: For each sampling event we utilized 50 yellow pans arranged in transects of 500
m with 10 m distance between traps.
• Malaise traps: Four traps were set at ground level in each area, arranged for a period of five days
per locality.
• Mini-Winkler apparatus: The leaf-litter sampling was realized following Ants of the Leaf Litter
protocol. The sifted volume with up to 2 kg was transferred to a collector bag for 24h.
• Attractive baits: The bait, containing 1 cm3 of sardine, was dispersed in a piece of paper for 1 h.
A total of 100 baits were used in each of the sampled areas.
• Aromatic essences: Attractive with aromatic compounds for capturing Euglossine males contain
cineol, methyl salicylate, methyl benzoate, eugenol, and vanillin. Fifty traps were performed (ten
sets of five baits) dispersed at 200 meter intervals.
• The voucher specimens were deposited in the Biodiversity Museum of Universidade Federal da
Grande Dourados (UFGD), Mato Grosso do Sul State, Brazil.
Plate 2. Bodoquena mountain range in midwestern Brazil,
with predominance of deciduous and semi-deciduous plants
species in carbonate rocks formation and iron formation.
Plate 3. Brazilian Chaco in Porto Murtinho Municipality. Aspects of diversified dry forest vegetation
Table 1. Richness estimated for Hymenoptera Aculeata in midwestern Brazilian dry forest, and diversity index
Taxon Species Jack-II Chao 1 Shannon
Observed Estimated Estimated Diversity Index
Ants 294 468.58 443.50 5.40
Bees 150 310.63 369.19 4.84
Spheciformes 94 182.05 186.42 4.34
Vespoidea 225 444.81 516.26 5.12
Total 763 1,406.09 1,476.77 6.36
Results
Results
Figure 1. Distribution models for Hymenoptera, based on abundance of octaves, sampled in
midwestern Brazilian dry forest, between the years 2005 and 2013, in 9 buffer localities from
Bodoquena mountain range to Brazilian Chaco.
truncated lognormal pattern
0
0,1
0,2
0,3
0,4
0,5
0 50 100 150 200
Similarity(Morisita-
Horn)
Distance Km
Figure 2. Correlation analysis between similarities, based on Morisita-Horn index, and
distance in km of the sampled points in midwestern Brazilian dry forest, between the
years 2005 and 2013, in 9 buffer localities from Bodoquena mountain range to
Brazilian Chaco (r= -0,397).
Results
Plate 4. Bombus sp. (Apidae).
Plate 7. Argogorytes umbratilis Bohart, 2000
Plate 5. Plebeia sp. (Apidae).
Apoidea group
Plate 6. Sceliphron asiaticum Linnaeus, 1758
Plate 8. Traumatomutilla sp. (Mutillidae).
Plate 10. Proctonectarina sp. (Vespidae).
Plate 9. Poecilopompilus sp. (Pompilidae).
Plate 11. Campsomeris sp. (Scoliidae)
Vespoidea group
Plate 12. Cephalotes clypeatus (Fabricius, 1804)
Plate 15. Cylindromyrmex brasiliensis Emery, 1901
Plate 13. Pseudomyrmex termitarius ((Smith F., 1855)
Plate 14. Dinoponera australis Emery, 1901
Formicidae
Discussion
Rasmussen and Asenjo (2009) reported species-group taxa of aculeate wasps of
Peru and presented the first checklist of the 225 genera and 1,169 species,
including Chrysidoidea wasps, not considered here.
Taxa Species in Peru Species in Bodoquena-BR
Crabronidae 262 74
Sphecidae 38 20
Ampulicidae 1 1
Vespidae 403 79
Pompilidae 158 103
Mutillidae 88 21
Scoliidae 8 6
Tiphiidae 32 15
Rhopalossomatidae 2 1
TOTAL 992 319
CONCLUSION
The species abundance distribution (SAD) is one of the most studied patterns in ecology due to its
potential insights into commonness and rarity, community assembly, and patterns of biodiversity.
The distribution pattern of species abundance found in this study revealed that the Hymenoptera
fauna on dry forests is strongly influenced by the rarity of the species, or else there are a great
number of species with low frequency of occurrence and a smaller number of species with high
frequency of occurrence in all Hymenoptera groups presented in this study.
Ecological
implications
Biogeographical
implications
Evolutionary
implications
We can not define the alpha diversity scale?
Is this region an area of ​​ecotone between biomes, or
the center of origin and dispersal of fauna?
The Natural Selection operating on the same
conditions produced the same results for
different taxa?
The same syndrome of niche overlap occurs in
all groups?
Some questions to answer
References
Agosti D. & Alonso L.E. 2000. The ALL Protocol: a standard protocol for the collection of ground-dwelling ants. In: Agosti
D.; Majer J.D.; Alonso L.E.; Schultz T.R. (Eds.). pp. 204–206. Ants: Standard Methods for Measuring and Monitoring
Biodiversity. Smithsonian Institution Press, Washington.
Carpenter J.M. & Marques O.M. 2001. Contribuição ao estudo dos vespídeos do Brasil. Série: Publicações Digitais-UFB. 2: 1-
147.
Fernández F. 2000. Sistemática y filogenia de los himenópteros de la región Neotropical: Estado del conocimiento
perspectivas. pp. 211-231. In: Martín-Piera F.; Morrone J.J.; Melic A. (Eds.). Monografias tercer Milenio, Sociedad
Entomológica Aragonesa (SEA), Zaragoza, España.
Johnson B.R.; Borowiec M.L.; Chiu J.C.; Lee E.K.; Atallah J.; Ward P.S. 2013. Phylogenomics resolves evolutionary
relationships among ants, bees, and wasps. Current Biology 23: 1–5.
Kimsey L.S. & Brothers D.J. 2006. Familia Tiphiidae. pp. 597-608. In: Fernández F.& Sharkey M.J. (Eds.). Introducción a los
Hymenoptera de la región Neotropical (Sociedad Colombiana de Entomologia y Universidad Nacional de Colombia,
Bogotá, Colombia.
Melo G.A.R. & Gonçalves R.B. 2005. Higher-level bee classifications (Hymenoptera, Apoidea, Apidae sensu lato). Revista
Brasileira de Zoologia 22(1):153–159.
Michener C.D. 2007. The Bees of the World. The Johns Hopkins University Press, Baltimore, Maryland.
MMA. 2002. Avaliação e identificação de áreas e ações prioritárias para a conservação, utilização sustentável e repartição
dos benefícios da biodiversidade nos biomas brasileiros. MMA/SBF, Brasília. 404 p
Pulawski W.J. 2014. Catalog of Sphecidae senso lato.
Rasmussen C. & Asenjo A. 2009. A check list to wasps of Peru (Hymenoptera: Aculeata). Zookeys 15: 1-78.
Santos E.F.; Noll F.B.; Brandão C.R. 2014. Functional and Taxonomic Diversity of Stinging Wasps in Brazilian Atlantic
Rainforest Areas. Neotropical Entomology 43: 97-105.
Silvestre R.; Demétrio M.F.; Delabie J.H.C. 2012. Community Structure of Leaf-Litter Ants in a Neotropical Dry Forest: A
Biogeographic Approach to Explain Betadiversity. Psyche 2012: 1-15.

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Silvestre Peru Cuzco Hymenoptera Congress 2014

  • 1. DIVERSITY AND DISTRIBUTION OF HYMENOPTERA ACULEATA IN MIDWESTERN BRAZILIAN DRY FORESTS Rogerio Silvestre, Manoel F. Demétrio, Bhrenno M. Trad, Felipe Varussa Lima, Tiago H. Auko and Paulo Robson de Souza Laboratório de Ecologia de Hymenoptera HECOLAB Faculdade de Ciências Biológicas e Ambientais- FCBA Universidade Federal da Grande Dourados- UFGD Cuzco Hymenoptera Congress 2014
  • 2.
  • 3. We present here the first systematic inventory of Hymenoptera Aculeata fauna made in the pristine dry forests of midwestern Brazil. The goals: estimate species richness for each taxon and check which model the distribution Investigated groups Formicidae APOIDEA: Apidae (sensu latu), Sphecidae and Crabronidae VESPOIDEA: Pompilidae, Mutillidae, Vespidae, Scoliidae, Tiphiidae and Rhopalosomatidae Introduction
  • 4. Brian R. Johnson et. al. 2013- Current Biology 23 “Aculeata” clade
  • 5. Methodology The study was conducted over eight years, in two regions: Bodoquena Mountain Range and Brazilian Chaco. These locations are set in a large open area in a diagonal formation of South America, the so-called "Pleistocenic Arc", extending from the Caatinga in northeastern Brazil to the Chaco in Argentina, where the contact areas occur between: Pantanal, Cerrado, Chaco, and Atlantic Forest. Eighteen wild expeditions were performed in this period with seven days of collections in each, but not with all expert groups together.
  • 6. Fig. 1-Map of Serra da Bodoquena, bordering the Pantanal province, State of Mato Grosso do Sul. MATO GROSSO DO SUL BRASIL Pantanal Plain Bodoquena Mountain Range Kadiwéu Indians Land Porto Murtinho Bonito Chaco Sampled areas in midwestern Brazilian Dry Forest
  • 7. Distribution analysis • To compose the sample unit we combined the expeditions that have been made to the same location, and those performed in nearby sites within a radius of 10 km buffers were grouped. Nine sites emerged from this combination of collecting expeditions. • The frequencies of species based in presence/absence were analyzed in the range of region and grouped into classes or octaves of abundance. • The number of species in each octave varied as follows: 1 (0-2); 2 (2-4); 3 (4-8), 4 (8-16) and so on, allowing us to view the richness and quantitative distribution of species per sample unit. • The data set was analyzed using R software with the Vegan package.
  • 8. Diversity analysis • We built a table with the Shannon diversity index, Chao 1 richness estimator and Second-order Jackknife richness estimator (Jack2). • When comparing species similarity of nine localities, we calculate and use Morisita-Horn sample similarity index, using also distance in km between localities obtained with the software Google Earth 7.1.2., which was compared with the similarity values obtained and distance using a Pearson correlation computed on the software Statistica 8.0 (Statsoft Inc. 2007).
  • 9. Sampling Protocol • Entomological net: for qualitative samples. • Moërick traps: For each sampling event we utilized 50 yellow pans arranged in transects of 500 m with 10 m distance between traps. • Malaise traps: Four traps were set at ground level in each area, arranged for a period of five days per locality. • Mini-Winkler apparatus: The leaf-litter sampling was realized following Ants of the Leaf Litter protocol. The sifted volume with up to 2 kg was transferred to a collector bag for 24h. • Attractive baits: The bait, containing 1 cm3 of sardine, was dispersed in a piece of paper for 1 h. A total of 100 baits were used in each of the sampled areas. • Aromatic essences: Attractive with aromatic compounds for capturing Euglossine males contain cineol, methyl salicylate, methyl benzoate, eugenol, and vanillin. Fifty traps were performed (ten sets of five baits) dispersed at 200 meter intervals. • The voucher specimens were deposited in the Biodiversity Museum of Universidade Federal da Grande Dourados (UFGD), Mato Grosso do Sul State, Brazil.
  • 10. Plate 2. Bodoquena mountain range in midwestern Brazil, with predominance of deciduous and semi-deciduous plants species in carbonate rocks formation and iron formation.
  • 11. Plate 3. Brazilian Chaco in Porto Murtinho Municipality. Aspects of diversified dry forest vegetation
  • 12. Table 1. Richness estimated for Hymenoptera Aculeata in midwestern Brazilian dry forest, and diversity index Taxon Species Jack-II Chao 1 Shannon Observed Estimated Estimated Diversity Index Ants 294 468.58 443.50 5.40 Bees 150 310.63 369.19 4.84 Spheciformes 94 182.05 186.42 4.34 Vespoidea 225 444.81 516.26 5.12 Total 763 1,406.09 1,476.77 6.36 Results
  • 13. Results Figure 1. Distribution models for Hymenoptera, based on abundance of octaves, sampled in midwestern Brazilian dry forest, between the years 2005 and 2013, in 9 buffer localities from Bodoquena mountain range to Brazilian Chaco. truncated lognormal pattern
  • 14. 0 0,1 0,2 0,3 0,4 0,5 0 50 100 150 200 Similarity(Morisita- Horn) Distance Km Figure 2. Correlation analysis between similarities, based on Morisita-Horn index, and distance in km of the sampled points in midwestern Brazilian dry forest, between the years 2005 and 2013, in 9 buffer localities from Bodoquena mountain range to Brazilian Chaco (r= -0,397). Results
  • 15. Plate 4. Bombus sp. (Apidae). Plate 7. Argogorytes umbratilis Bohart, 2000 Plate 5. Plebeia sp. (Apidae). Apoidea group Plate 6. Sceliphron asiaticum Linnaeus, 1758
  • 16. Plate 8. Traumatomutilla sp. (Mutillidae). Plate 10. Proctonectarina sp. (Vespidae). Plate 9. Poecilopompilus sp. (Pompilidae). Plate 11. Campsomeris sp. (Scoliidae) Vespoidea group
  • 17. Plate 12. Cephalotes clypeatus (Fabricius, 1804) Plate 15. Cylindromyrmex brasiliensis Emery, 1901 Plate 13. Pseudomyrmex termitarius ((Smith F., 1855) Plate 14. Dinoponera australis Emery, 1901 Formicidae
  • 18. Discussion Rasmussen and Asenjo (2009) reported species-group taxa of aculeate wasps of Peru and presented the first checklist of the 225 genera and 1,169 species, including Chrysidoidea wasps, not considered here. Taxa Species in Peru Species in Bodoquena-BR Crabronidae 262 74 Sphecidae 38 20 Ampulicidae 1 1 Vespidae 403 79 Pompilidae 158 103 Mutillidae 88 21 Scoliidae 8 6 Tiphiidae 32 15 Rhopalossomatidae 2 1 TOTAL 992 319
  • 19. CONCLUSION The species abundance distribution (SAD) is one of the most studied patterns in ecology due to its potential insights into commonness and rarity, community assembly, and patterns of biodiversity. The distribution pattern of species abundance found in this study revealed that the Hymenoptera fauna on dry forests is strongly influenced by the rarity of the species, or else there are a great number of species with low frequency of occurrence and a smaller number of species with high frequency of occurrence in all Hymenoptera groups presented in this study.
  • 20. Ecological implications Biogeographical implications Evolutionary implications We can not define the alpha diversity scale? Is this region an area of ​​ecotone between biomes, or the center of origin and dispersal of fauna? The Natural Selection operating on the same conditions produced the same results for different taxa? The same syndrome of niche overlap occurs in all groups? Some questions to answer
  • 21. References Agosti D. & Alonso L.E. 2000. The ALL Protocol: a standard protocol for the collection of ground-dwelling ants. In: Agosti D.; Majer J.D.; Alonso L.E.; Schultz T.R. (Eds.). pp. 204–206. Ants: Standard Methods for Measuring and Monitoring Biodiversity. Smithsonian Institution Press, Washington. Carpenter J.M. & Marques O.M. 2001. Contribuição ao estudo dos vespídeos do Brasil. Série: Publicações Digitais-UFB. 2: 1- 147. Fernández F. 2000. Sistemática y filogenia de los himenópteros de la región Neotropical: Estado del conocimiento perspectivas. pp. 211-231. In: Martín-Piera F.; Morrone J.J.; Melic A. (Eds.). Monografias tercer Milenio, Sociedad Entomológica Aragonesa (SEA), Zaragoza, España. Johnson B.R.; Borowiec M.L.; Chiu J.C.; Lee E.K.; Atallah J.; Ward P.S. 2013. Phylogenomics resolves evolutionary relationships among ants, bees, and wasps. Current Biology 23: 1–5. Kimsey L.S. & Brothers D.J. 2006. Familia Tiphiidae. pp. 597-608. In: Fernández F.& Sharkey M.J. (Eds.). Introducción a los Hymenoptera de la región Neotropical (Sociedad Colombiana de Entomologia y Universidad Nacional de Colombia, Bogotá, Colombia. Melo G.A.R. & Gonçalves R.B. 2005. Higher-level bee classifications (Hymenoptera, Apoidea, Apidae sensu lato). Revista Brasileira de Zoologia 22(1):153–159. Michener C.D. 2007. The Bees of the World. The Johns Hopkins University Press, Baltimore, Maryland. MMA. 2002. Avaliação e identificação de áreas e ações prioritárias para a conservação, utilização sustentável e repartição dos benefícios da biodiversidade nos biomas brasileiros. MMA/SBF, Brasília. 404 p Pulawski W.J. 2014. Catalog of Sphecidae senso lato. Rasmussen C. & Asenjo A. 2009. A check list to wasps of Peru (Hymenoptera: Aculeata). Zookeys 15: 1-78. Santos E.F.; Noll F.B.; Brandão C.R. 2014. Functional and Taxonomic Diversity of Stinging Wasps in Brazilian Atlantic Rainforest Areas. Neotropical Entomology 43: 97-105. Silvestre R.; Demétrio M.F.; Delabie J.H.C. 2012. Community Structure of Leaf-Litter Ants in a Neotropical Dry Forest: A Biogeographic Approach to Explain Betadiversity. Psyche 2012: 1-15.