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Article

Bird Assemblages in Coffee Agroforestry Systems and Other Human Modified Habitats in Indonesia

1
Faculty of Forestry, Universitas Gajah Madah, Yogyakarta 55281, Indonesia
2
Sustainable and Resilient Futures Network, Oxford Brookes University, Oxford OX3 0BP, UK
3
ARuPA, Yogyakarta 55284, Indonesia
*
Author to whom correspondence should be addressed.
Biology 2022, 11(2), 310; https://doi.org/10.3390/biology11020310
Submission received: 18 January 2022 / Revised: 12 February 2022 / Accepted: 13 February 2022 / Published: 15 February 2022
(This article belongs to the Section Conservation Biology and Biodiversity)

Abstract

:

Simple Summary

Given the high degree of deforestation in the tropics due to shifting agriculture, it is a priority for conservation to find sustainable agriculture systems. We assessed bird communities over 1228 plots from 21 sites in the highly populated island of Java, Indonesia. We found that commercial coffee polycultures (i.e., fields comprised of coffee plants, other crops and/or fruit trees, and diverse shade trees) could sustain similar levels of bird abundance, diversity, and richness than coffee systems under natural forests and community managed forests. Commercial coffee polyculture fields host higher bird abundance, diversity, and richness than sun-exposed coffee fields, fields with other crops or fruit trees, and tree farms. We provide evidence that complex commercial agroforestry systems can host similar levels of biodiversity to agroforestry systems under natural forest.

Abstract

Deforestation in the tropics is mainly driven by the need to expand agriculture and forestry land. Tropical cropland has also undergone a process of intensification, particularly evident in regions that are the main exporters of deforestation-driven commodities. Around 25 million people in the world depend on coffee production, which has a profound contribution to global biodiversity loss through agricultural extensification and intensification. Nevertheless, coffee agroforestry systems have been postulated to serve as an alternative refuge for biodiversity across different regions. We aim to compare bird abundance, diversity, and richness in commercial polyculture coffee systems (i.e., the highest degree of habitat complexity that can be achieved in coffee fields after deforestation) with other coffee agroforestry systems and human modified habitats in Java, Indonesia. We collected data in 21 sites (1228 points) on Java from February to August 2021 using the point sampling method. Via generalised additive models, we tested whether the abundance, diversity, and richness of birds were different between different human modified habitats including other potential predictors such as elevation, distance to protected areas, shade tree richness, and plant diversity. Using the non-metric multidimensional scaling, we tested whether there was a difference in terms of the composition of foraging guilds between habitats. Commercial polyculture coffee fields can sustain levels of bird abundance, diversity, and richness comparable to agroforestry systems under natural forest, and higher than sun coffee and shaded monoculture coffee, and of other human modified habitats such as crop/fruit fields and tree farms. Coffee agroforestry systems have a higher proportion of nectarivores, insectivores, and frugivores than other systems that can sustain high diversity and richness of birds such as paddy fields that mainly have granivores and carnivores. Complex polycultures can represent an avenue for the future of sustainable agriculture in conditions where deforestation rates are high and in crops such as coffee, which maintain high yield in the presence of diverse shade.

1. Introduction

Deforestation in the tropics is mainly driven by the need to expand agriculture and forestry land, resulting in around 5–10 million hectares of natural forest lost every year [1,2]. This process is not likely to lessen in the near future given the increased demand of deforestation-driven commodities [3]. A series of other indirect risks related to this expansion of agriculture and forestry land use include the spread of diseases and pests, and the increase in the trade of protected species [4,5]. Tropical cropland has further encountered a process of intensification, particularly evident in regions that are the main exporters of deforestation-driven commodities [6].
Coffee (Coffea spp.) is among the main commodities produced in tropical regions form Latin America, Asia, and Africa, with more than 25 million people depending on its production for their livelihoods [7]. This global commodity has a profound contribution to global biodiversity loss through agricultural extensification and intensification [4]. Nevertheless, coffee agroforestry systems have been recognised as an alternative refuge for biodiversity across different regions [8,9,10,11,12,13,14]. This is because, traditionally, coffee plants are cultivated under the forest and can maintain high yield with intermediate levels of shade cover [15,16,17]; however, there are cases when coffee productivity has decreased with increased shade cover [18]. The quality of coffee also benefits from diverse shade cover since coffee berry borer (Hypothenemus hampei) infestation is higher in sun-exposed fields [19]. Despite these advantages of diverse shade, coffee fields have encountered a process of agricultural intensification (i.e., reduction in crop and shade diversity and increased use of agrochemicals) during the last 30 years, allegedly to gain more revenue [20,21].
Diverse shade systems have been known to play important roles in maintaining biodiversity and crop productivity [22]. Coffee agroforestry systems are potential refugia for various wildlife including butterflies [23], birds [24,25], and mammals [16,26,27]. Evidence on the effect of shade tree removal on wildlife diversity are, however, still unclear and evidence is biased towards the Neotropics and Africa [8,15,16,18,26,27]. This is a huge gap in knowledge since the response of these interventions are taxon-specific and depend on other local factors such as biogeographical regions and resource availability.
Indonesia is the fourth largest coffee producer in the world and a global biodiversity hotspot [28,29]. Despite its importance in this industry, the impact of agriculture intensification on biodiversity is still understudied [13]. Java is the most populated island in Indonesia, with a human population density of around 1000 individuals/km2. The island has experienced massive deforestation since the 16th century for fulfilling global demand on agricultural production, particularly coffee production [30]. This habitat loss, combined with poaching and agriculture intensification, has reduced bird diversity, particularly in the bird species of most conservation concern [31,32]. While protected areas on Java are small and scattered [30], wildlife related exploitation for wildlife trade has a profound negative effect on avian [33,34] and mammal [35] conservation. Agroforestry systems using shade grown coffee can serve an important role in the future of biodiversity conservation on Java [13,26,33,36,37,38].
We aimed to understand the responses of birds, one of the most important taxa given their wide ecological role, between different coffee agroforestry types and other human modified habitats. In particular, we investigated the possible role of shade tree removal on bird assemblages. Given the inevitable and irreversible transition towards more intensive farming practices, understanding how species react to shade tree removal is a conservation priority. We expect that shade tree removal will have a negative effect on bird abundance, diversity, and richness, with agriculture systems with low complexity having significantly less bird abundance, diversity, and richness than agriculture systems with high complexity and under a natural forest cover. We also expect commercial polyculture coffee systems to host higher bird abundance, diversity, and richness than coffee systems with low complexity (i.e., shade monoculture coffee) or no shade (i.e., sun coffee).

2. Materials and Methods

2.1. Data Collection

We collected data in 21 sites on Java Island from February to August 2021 (Figure 1). Java contributes around 11–13% of the total coffee production in Indonesia [39]. Coffee is produced from large plantations as well as from the agroforestry systems of small holders. We used the point sampling method for collecting data at each site with 10 min duration and 50 m radius from the observer. Three teams with extensive field experience, headed by D.A.B., F.D.R., and F.E.N. and composed of 3–4 members each, conducted the surveys between 6:00–9:00 and 15:00–18:00. In total, we collected 1128 points (Table 1). We collected data on the number of individuals for each species recorded during the sampling period. We then calculated the abundance (total abundance), diversity (Shannon Index), and richness (total number of species) in each plot. We also considered the foraging guild of each species encountered and calculated the proportion of individuals encountered for each foraging guild. In addition, we collected vegetation data through the establishment of nested plots (20 × 20 m for shade trees, 10 × 10 m for poles, 5 × 5 m for saplings, and 2 × 2 m for seedlings) in each sample point. The stages of trees were defined as follows: (i) seedling: germinated seeds to <1.5 m in height; (ii) sapling: height > 1.5 m and diameter at breast height (dbh) < 10 cm; (iii) pole: 10 cm < dbh < 20 cm; (iv) shade tree: dbh > 20 cm. We defined the habitat around each point sampling (Table S1). For the coffee agroforestry systems, we used the classification by Philpott et al. [40]. In summary, sun coffee are fields with coffee plants often mixed with other crops but no shade trees; shade monoculture coffee are fields with coffee plants often mixed with other crops and fruit trees and with shade trees but total plant richness is equal or less than five species; commercial polyculture coffee are fields with coffee plants mixed with other crops, fruit trees, and shade trees and with a total plant richness of six species or higher; traditional polyculture coffee are complex agroforestry systems under a natural forest cover; and rustic coffee systems are similar to traditional polyculture coffee systems but with a lower density of crops and a higher plant diversity. In addition, we identified the following habitats: (1) community managed forest: crops and fruit trees managed under natural forest but not including coffee plants; (2) other commercial polyculture: polyculture (i.e., agriculture field with a plant richness of more than six species) including crops, fruit trees, and shade trees but not including coffee plants; (3) other crop/fruit field: fields including crops, fruits trees, and shade trees with a plant richness of five or less species and not including coffee plants; (4) paddy field: flooded fields dominated by rice or other semiaquatic crops; and (5) tree farm: a forest managed for timber production. We also included plots dominated by mangroves in this assessment since they were in cities and often mixed with fishponds and paddy fields. We calculated the Shannon diversity index of both plant (including seedlings, saplings, poles, and shade trees) and bird species for each plot.

2.2. Data Analysis

To test the differences between habitats around sample points, we ran generalised additive models (GAMs) with abundance, diversity, or richness of birds per plot as response variables. We included the coordinates of the plots in the models to account for spatial autocorrelation of data via Gaussian process smooths [41]. We further included the elevation, distance to protected areas, shade tree richness, and plant diversity in the plot as other potential predictors of bird abundance, diversity, and richness [42,43,44]. We used the “gam” command in the package “mgcv” to run the GAMs. We plotted the incident rate ratios comparing habitat types with the reference category commercial polyculture coffee.
For the non-metric multidimensional scaling (NMDS), we used the proportion of observed total number of birds by foraging guilds for each site. We considered the following foraging guilds: carnivore, granivore, frugivore, insectivore, nectarivore, and omnivore. We plotted the results in terms of the main habitat in the study sites to see whether there was a difference in terms of composition of foraging guilds between habitats. We used the “metaMDS” function in the package “vegan” to run the NMDS [45]. We used R v. 4.1.0.

3. Results

The abundance of birds in commercial polyculture coffee fields (i.e., fields comprised of coffee plants, other crops and/or fruit trees, and diverse shade trees) was significantly higher than the abundance in all the other habitats apart from rustic coffee, traditional polyculture coffee, and community managed forest (Table 2; Figure 2). The diversity and richness of birds in commercial polyculture coffee fields were higher than in other crop/fruit fields, sun coffee, tree farms, and shade monoculture coffee (Table 2; Figure 3 and Figure 4). The diversity and richness of birds in commercial polyculture coffee fields were similar to the diversity/richness in traditional polyculture coffee and rustic coffee systems as well as in community managed forests. Paddy fields, mangrove patches, and other commercial polyculture fields also had a similar diversity and richness to commercial polyculture coffee.
The composition of bird communities is also different depending on the habitat. Mangrove patches mainly had carnivores, and sites mixed with mixed mangroves, paddy fields, and/or other crops had mainly carnivores and granivores. Agroforestry systems mainly dominated by coffee had a higher proportion of nectarivores and frugivores (in the case of traditional polyculture coffee), omnivores (rustic coffee), or insectivores (mixed coffee gardens ranging from sun-exposed to commercial polyculture coffee) (NMDS: stress = 0.08; Figure 5).

4. Discussion

Given the high rate of deforestation in the tropics, our finding that commercial polyculture coffee can sustain good levels of bird abundance, diversity, and richness that are comparable to coffee agroforestry systems under natural forest is of crucial importance. Commercial polycultures, in fact, represent the highest degree of habitat complexity that can be achieved in croplands after deforestation. Coffee polycultures hosted a higher abundance of birds than polycultures with other crops, and this is not surprising given the predisposition of coffee plants to maintain high yields and good quality coffee under a diverse shade cover [15,16,17]. We note that Indonesia offers a unique case, since, of the 1.2 million ha of coffee fields present, 96% belongs to smallholder farmers [46]. There is thus a possibility to work together with farmers and integrate wildlife-friendly practices that can be beneficial for both farmers, by producing other commodities and guaranteeing high coffee yields, and wildlife and by offering a diverse system of shade trees and crops that promote ecosystem services. Additionally, most of the commercial polyculture coffee fields considered in this study are currently included in programs where organic farming and other wildlife-friendly practices are encouraged [47].
The ecosystem services provided by coffee agroforestry systems were also increased compared to other habitats that had a similar diversity and richness of birds such as paddy fields. This is because coffee agroforestry systems have a higher proportion of insectivores, nectarivores, and frugivores, meaning that ecosystem services such as pollination, natural pest control, and seed dispersal are favoured [48]. The complexity of the agroforestry system also promotes an increase in ecosystem services, for example, the number of pollinators can also increase in coffee fields with higher complexity in terms of shade tree richness [13]. A diverse shade also provides key services such as increasing soil quality by nitrogen fixation and increasing litter biomass, protecting from direct sun, attracting pollinators, and increasing habitat connectivity [47,49].
Our study adds to the current literature that supports that coffee agroforestry systems can sustain good levels of animal diversity in Indonesia. For example, a study on Sunda leopard cat Prionailurus bengalensis javanensis showed that non-protected areas, particularly coffee agroforestry, outcompeted small and scattered protected areas in supporting this carnivore [33]. Another study compared the detection rates on wildlife via camera traps in a coffee agroforestry system and a protected forest and found that at least ten mammal species used the agroforestry system [50]. Only Javan leopard Panthera pardus melas, Sunda porcupine Hystrix javanica, and grizzled langur Presbytis comata were not detected in the agroforestry system, but the authors recognized that the matrix could bring benefits to these species by acting as a buffer zone to reduce the human pressure on the forest, reduce human–wildlife conflicts, and help maintain ecosystem services.
Our findings highlight the importance of polyculture practices that are used in various agroforestry schemes in Indonesia as alternatives in supporting wildlife conservation in the future land use change scenarios. However, such incentive mechanisms to provide biodiversity refuges in human-modified land use that can have also agricultural benefits still need to be implemented [51]. The Indonesian government promotes organic farming and provides incentives for farmers willing to convert to organic practices via the Go Organic program and the Indonesian Food Law (18/2012) [52]. The process to obtain organic certification, however, is complex and requires a long-term commitment by farmers and monetary incentives for farmers such as premium prices and payments for ecosystem services are difficult to achieve [47,53,54]. Still, promoting wildlife-friendly agroforestry systems is a promising solution to ensure the long-term sustainability of both biodiversity and the livelihoods of local farmers in Indonesia [47]. This is particularly urgent given the current predictions that there would be a production decline in Arabica coffee due to climate change and that this will result in an expansion of coffee cultivated areas of around 30% by 2050 [55]. It is important to work on persuading farmers in joining wildlife-friendly initiatives and empower farmers that wish to join such programs [47]. This solution may work better with some crops such as coffee, which allow for good yields in complex agroforestry systems and not with other crops such as oil palm, where wildlife-friendly farming is often unsuccessful due to low yields [56].

5. Conclusions

We presented evidence that commercial polyculture coffee can sustain similar bird abundance, diversity, and richness than traditional coffee systems under natural forest cover. We discussed the implications of this finding, suggesting a certain optimism that sustainable and complex farming systems can help deal with the likely agricultural intensification and extensification in the near future. We recognise that the implications of our findings can be applied to our context (coffee agroforestry systems in Java) and regional variations should be considered when extending our findings to other regions or crops. We suggest similar multi-site studies in other regions, especially in Southeast Asia and Africa, where coffee agroforestry systems are relatively understudied compared to the Neotropics [13,57].

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/biology11020310/s1, Table S1: Dataset used for the analysis.

Author Contributions

Conceptualisation, M.A.I., M.C., and K.A.I.N.; Methodology, M.A.I., M.C., B.B., K.F.W. and E.S.; Software, M.C.; Validation, M.A.I. and M.C.; Formal analysis, M.A.I. and M.C.; Investigation, M.C., F.D.R., F.E.N. and D.A.B.; Resources, M.A.I., E.S., V.N. and K.A.I.N.; Data curation, M.A.I. and M.C.; Writing—original draft preparation, M.A.I. and M.C.; Writing—review and editing, V.N. and K.A.I.N.; Visualisation, M.C. and D.A.B.; Supervision, M.A.I., M.C., B.B. and K.A.I.N.; Project administration, M.A.I. and K.A.I.N.; Funding acquisition, M.A.I., E.S. and K.A.I.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Ministry of Education and Culture grant through PDUPT program, USAID Indonesia program, and ARuPa provided grants for surveys in East Java, and the Global Challenges Fund, People Trust for Endangered Species, Disney Worldwide Conservation Fund, and Cleveland Zoo provided funds for survey in West Java. The APC was funded by UGM with postdoctoral program under the grant number 6144/UN1.P.III/DITLIT/PT/2021.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in Table S1. Additional raw data are available on request from the corresponding author.

Acknowledgments

We thank Ryan for help in coordinating the field work in Central Java, the Little Fireface Project for help in coordinating the field work in West Java, and all team members of the survey in East Java.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Hansen, M.C.; Potapov, P.V.; Moore, R.; Hancher, M.; Turubanova, S.A.; Tyukavina, A.; Thau, D.; Stehman, S.V.; Goetz, S.J.; Loveland, T.R.; et al. High-resolution global maps of 21st-century forest cover change. Science 2013, 342, 850–853. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Curtis, P.G.; Slay, C.M.; Harris, N.L.; Tyukavina, A.; Hansen, M.C. Classifying drivers of global forest loss. Science 2018, 361, 1108–1111. [Google Scholar] [CrossRef] [PubMed]
  3. Wiedmann, T.O.; Schandl, H.; Lenzen, M.; Moran, D.; Suh, S.; West, J.; Kanemoto, K. The material footprint of nations. Proc. Natl. Acad. Sci. USA 2015, 112, 6271–6276. [Google Scholar] [CrossRef] [Green Version]
  4. Lenzen, M.; Moran, D.; Kanemoto, K.; Foran, B.; Lobefaro, L.; Geschke, A. International trade drives biodiversity threats in developing nations. Nature 2012, 486, 109–112. [Google Scholar] [CrossRef] [PubMed]
  5. Chaves, L.S.M.; Fry, J.; Malik, A.; Geschke, A.; Sallum, M.A.M.; Lenzen, M. Global consumption and international trade in deforestation-associated commodities could influence malaria risk. Nat. Commun. 2020, 11, 1–10. [Google Scholar] [CrossRef] [Green Version]
  6. Hu, Q.; Xiang, M.; Chen, D.; Zhou, J.; Wu, W.; Song, Q. Global cropland intensification surpassed expansion between 2000 and 2010: A spatio-temporal analysis based on GlobeLand30. Sci. Total Environ. 2020, 746, 141035. [Google Scholar] [CrossRef]
  7. Bunn, C.; Läderach, P.; Ovalle Rivera, O.; Kirschke, D. A bitter cup: Climate change profile of global production of Arabica and Robusta coffee. Clim. Change 2015, 129, 89–101. [Google Scholar] [CrossRef] [Green Version]
  8. Schroth, G.; da Fonseca, G.A.B.; Harvey, C.A.; Gascon, C.; Vasconcelos, H.L.; Izac, A.M.N. The role of agroforestry in biodiversity conservation in tropical landscapes. In Agroforestry and Biodiversity Conservation in Tropical Landscapes; Schroth, G., da Fonseca, G.A.B., Harvey, C.A., Gascon, C., Vasconcelos, H.L., Izac, A.M.N., Eds.; Island Press: Washington, DC, USA, 2004; pp. 1–12. [Google Scholar]
  9. De Beenhouwer, M.; Aerts, R.; Honnay, O. A global meta-analysis of the biodiversity and ecosystem service benefits of coffee and cacao agroforestry. Agric. Ecosyst. Environ. 2013, 175, 1–7. [Google Scholar] [CrossRef]
  10. Bhagwat, S.A.; Willis, K.J.; Birks, H.J.N.; Whittaker, R.J. Agroforestry: A refuge for tropical biodiversity? Trends Ecol. Evol. 2008, 23, 261–267. [Google Scholar] [CrossRef]
  11. Estrada, A.; Raboy, B.E.; Oliveira, L.C. Agroecosystems and primate conservation in the tropics: A review. Am. J. Primatol. 2012, 74, 696–711. [Google Scholar] [CrossRef]
  12. Guzman, A.; Link, A.; Castillo, J.A.; Botero, J.E. Agroecosystems and primate conservation: Shade coffee as potential habitat for the conservation of Andean night monkeys in the northern Andes. Agric. Ecosyst. Environ. 2016, 215, 57–67. [Google Scholar] [CrossRef]
  13. Campera, M.; Balestri, M.; Manson, S.; Hedger, K.; Ahmad, N.; Adinda, E.; Nijman, V.; Budiadi, B.; Imron, M.A.; Nekaris, K.A.I. Shade trees and agrochemical use affect butterfly assemblages in coffee home gardens. Agric. Ecosyst. Environ. 2021, 319, 107547. [Google Scholar] [CrossRef]
  14. Meyfroidt, P.; Rudel, T.K.; Lambin, E.F. Forest transitions, trade, and the global displacement of land use. Proc. Natl. Acad. Sci. USA 2010, 107, 20917–20922. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Soto-Pinto, L.; Perfecto, I.; Castillo-Hernandez, J.; Caballero-Nieto, J. Shade effect on coffee production at the northern Tzeltal zone of the state of Chiapas, Mexico. Agric. Ecosyst. Environ. 2000, 80, 61–69. [Google Scholar] [CrossRef]
  16. Perfecto, I.; Mas, A.; Dietsch, T.; Vandermeer, J. Conservation of biodiversity in coffee agroecosystems: A tri-taxa comparison in southern Mexico. Biodivers. Conserv. 2003, 12, 1239–1252. [Google Scholar] [CrossRef]
  17. Meylan, L.; Gary, C.; Allinne, C.; Ortiz, J.; Jackson, L.; Rapidel, B. Evaluating the effect of shade trees on provision of ecosystem services in intensively managed coffee plantations. Agric. Ecosyst. Environ. 2017, 245, 32–42. [Google Scholar] [CrossRef]
  18. Sarmiento-Soler, A.; Vast, P.; Hoffmann, M.P.; Jassogne, L.; van Asten, P.; Graefe, S.; Rotter, R.P. Effect of cropping system, shade cover and altitudinal gradient on coffee yield components at Mt. Elgon, Uganda. Agric. Ecosyst. Environ. 2020, 295, 12. [Google Scholar] [CrossRef]
  19. Mariño, Y.A.; Pérez, M.E.; Gallardo, F.; Trifilio, M.; Cruz, M.; Bayman, P. Sun vs. shade affects infestation, total population and sex ratio of the coffee berry borer (Hypothenemus hampei) in Puerto Rico. Agric. Ecosyst. Environ. 2016, 222, 258–266. [Google Scholar] [CrossRef] [Green Version]
  20. Borkhataria, R.; Collazo, J.A.; Groom, M.J.; Jordan-Garcia, A. Shade-grown coffee in Puerto Rico: Opportunities to preserve biodiversity while reinvigorating a struggling agricultural commodity. Agric. Ecosyst. Environ. 2012, 149, 164–170. [Google Scholar] [CrossRef]
  21. Perfecto, I.; Vandermeer, J.; Mas, A.; Soto, L. Biodiversity, yield, and shade coffee certification. Ecol. Econ. 2005, 54, 435–446. [Google Scholar] [CrossRef]
  22. Pywell, R.F.; Heard, M.S.; Woodcock, B.A.; Hinsley, S.; Ridding, L.; Nowakowski, M.; Bullock, J.M. Wildlife-friendly farming increases crop yield: Evidence for ecological intensification. Proc. R. Soc. B Biol. Sci. 2015, 282, 12–19. [Google Scholar] [CrossRef] [Green Version]
  23. Richter, A.; Klein, A.M.; Tscharntke, T.; Tylianakis, J.M. Abandonement of coffee agroforests increases insect abundance and diversity. Agrofor. Syst. 2007, 69, 175–182. [Google Scholar] [CrossRef]
  24. Tejeda-Cruz, C.; Sutherland, W.J. Bird responses to shade coffee production. Anim. Conserv. 2004, 7, 169–179. [Google Scholar] [CrossRef]
  25. Buechley, E.R.; Sekercioglu, C.H.; Atickem, A.; Gebremichael, G.; Ndungu, J.K.; Mahamued, B.A.; Beyene, T.; Mekonnen, T.; Lens, L. Importance of Ethiopian shade coffee farms for forest bird conservation. Biol. Conserv. 2015, 188, 50–60. [Google Scholar] [CrossRef]
  26. Sari, D.F.; Budiadi, B.; Imron, M.A. The utilization of trees by endangered primate species Javan slow loris (Nycticebus javanicus) in shade-grown coffee agroforestry of Central Java. IOP Conf. Ser. Earth Environ. Sci. 2020, 449, 1. [Google Scholar] [CrossRef] [Green Version]
  27. Bali, A.; Kumar, A.; Krishnaswamy, J. The mammalian communities in coffee plantations around a protected area in the Western Ghats, India. Biol. Conserv. 2007, 139, 93–102. [Google Scholar] [CrossRef]
  28. Top Coffee Producing Countries. WorldAtlas. Available online: www.worldatlas.com/articles/top-coffee-producing-coun-tries.html (accessed on 10 January 2022).
  29. von Rintelen, K.; Arida, E.; Häuser, C. A review of biodiversity-related issues and challenges in megadiverse Indonesia and other Southeast Asian countries. Res. Ideas Outcomes. 2017, 3, e20860. [Google Scholar] [CrossRef] [Green Version]
  30. Breman, J. Keuntungan Kolonial Dari Kerja Paksa: Sistem Priangan Dari Tanam Paksa Kopi di Jawa, 1720–1870, 1st ed.; Yayasan Pustaka Obor Indonesia, KITLV Jakarta: Jakarta, Indonesia, 2014. [Google Scholar]
  31. Van Balen, S. Birds on Fragmented Islands: Persistence in the Forests of Java and Bali. Ph.D. Thesis, Wageningen University, Wageningen, The Netherlands, 1999. [Google Scholar]
  32. Eaton, J.A.; Shepherd, C.R.; Rheindt, F.E.; Harris, J.B.C.; van Balen, S.B.; Wilcove, D.S.; Collar, N.J. Trade-driven extinctions and near-extinctions of avian taxa in Sundaic Indonesia. Forktail 2015, 31, 1–12. [Google Scholar]
  33. Irawan, N.; Pudyatmoko, S.; Yuwono, P.S.H.; Tafrichan, M.; Giordano, A.J.; Imron, M.A. The Importance of unprotected areas as habitat for the leopard cat (Prionailurus bengalensis javanensis Desmarest, 1816) on Java, Indonesia. J. Ilmu Kehutan. 2020, 14, 198–212. [Google Scholar]
  34. Leupen, B.T.C.; Gomez, L.; Shepherd, C.R.; Nekaris, K.A.I.; Imron, M.A.; Nijman, V. Thirty years of trade data suggests population declines in a once common songbird in Indonesia. Eur. J. Wildl. Res. 2020, 66, 2020. [Google Scholar] [CrossRef]
  35. Condro, A.A.; Prasetyo, L.B.; Rushayati, S.B.; Santikayasa, I.P.; Iskandar, E. Predicting hotspots and prioritizing protected areas for endangered primate species in Indonesia under changing climate. Biology 2021, 10, 154. [Google Scholar] [CrossRef] [PubMed]
  36. Campera, M.; Brown, E.; Imron, M.A.; Nekaris, K.A.I. Unmonitored releases of small animals? The importance of considering natural dispersal, health, and human habituation when releasing a territorial mammal threatened by wildlife trade. Biol. Conserv. 2020, 242, 108404. [Google Scholar] [CrossRef]
  37. Birot, H.; Campera, M.; Imron, M.A.; Nekaris, K.A.I. Artificial canopy bridges improve connectivity in fragmented landscapes: The case of Javan slow lorises in an agroforest environment. Am. J. Primatol. 2020, 82, e23076. [Google Scholar] [CrossRef] [PubMed]
  38. Nekaris, K.A.I.; Handby, V.; Campera, M.; Birot, H.; Hedger, K.; Eaton, J.; Imron, M.A. Implementing and monitoring the use of artificial canopy bridges by mammals and birds in an Indonesian agroforestry environment. Diversity 2020, 12, 399. [Google Scholar] [CrossRef]
  39. Badan Pusat Statistik Indonesia, “Statistik Indonesia Tahun 2011–2020”. Available online: https://www.bps.go.id/indicator/54/132/3/produksi-tanaman-perkebunan.html (accessed on 19 October 2021).
  40. Philpott, S.M.; Arendt, W.J.; Armbrecht, I.; Bichier, P.; Diestch, T.V.; Gordon, C.; Greenberg, R.; Perfecto, I.; Reynoso-Santos, R.; Soto-Pinto, L.; et al. Biodiversity loss in Latin American coffee landscapes: Review of the evidence on ants, birds, and trees. Conserv. Biol. 2008, 22, 1093–1105. [Google Scholar] [CrossRef]
  41. Wood, S.N. Generalized Additive Models: An Introduction with R, 2nd ed.; Chapman and Hall/CRC: Boca Raton, FL, USA, 2017. [Google Scholar]
  42. Campera, M.; Santini, L.; Balestri, M.; Nekaris, K.A.I.; Donati, G. Elevation gradients of lemur abundance emphasise the importance of Madagascar’s lowland rainforest for the conservation of endemic taxa. Mamm. Rev. 2020, 1, 25–37. [Google Scholar] [CrossRef]
  43. Coetzee, B.W.T.; Gaston, K.J.; Chown, S.L. Local scale comparisons of biodiversity as a test for global protected area ecological performance: A meta-analysis. PLoS ONE 2014, 9, e105824. [Google Scholar] [CrossRef]
  44. Bąk-Badowska, J.; Wojciechowska, A.; Czerwik-Marcinkowska, J. Effects of open and forest habitats on distribution and diversity of Bumblebees (Bombus) in the Małopolska upland (Southern Poland): Case study. Biology 2021, 10, 1266. [Google Scholar] [CrossRef]
  45. Dixon, P. VEGAN, a package of R functions for community ecology. J. Veg. Sci. 2003, 6, 927–930. [Google Scholar] [CrossRef]
  46. Ibrahim, H.W.; Zailani, S. A review on the competitiveness of global supply chain in a coffee Industry in Indonesia. Int. Bus. Manag. 2010, 4, 105–115. [Google Scholar]
  47. Campera, M.; Budiadi, B.; Adinda, E.; Ahmad, N.; Balestri, M.; Hedger, K.; Imron, M.A.; Manson, S.; Nijman, V.; Nekaris, K.A.I. Fostering a wildlife-friendly program for sustainable coffee farming: The case of small-holder farmers in Indonesia. Land 2021, 10, 121. [Google Scholar] [CrossRef]
  48. Whelan, C.J.; Sekercioglu, C.H.; Wenny, D.G. Why birds matter: From economic ornithology to ecosystem services. J. Ornithol. 2015, 156, 227–238. [Google Scholar] [CrossRef]
  49. Perfecto, I.; Rice, R.A.; Greenberg, R.; VanderVoort, M.E. Shade coffee: A disappearing refuge for biodiversity. Bioscience 1996, 46, 598–608. [Google Scholar] [CrossRef] [Green Version]
  50. Campera, M.; Hedger, K.; Birot, H.; Manson, S.; Balestri, M.; Budiadi, B.; Imron, M.A.; Nijman, V.; Nekaris, K.A.I. Does the presence of shade trees and distance to the forest affect detection rates of terrestrial vertebrates in coffee home gardens? Sustainability 2021, 13, 8540. [Google Scholar] [CrossRef]
  51. Ricketts, T.H.; Daily, G.C.; Ehrlich, P.R.; Michener, C.D. Economic value of tropical forest to coffee production. Proc. Natl. Acad. Sci. USA 2004, 101, 12579–12582. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Schreer, V.; Padmanabhan, M. The many meanings of organic farming: Framing food security and food sovereignty in Indonesia. Org. Agric. 2020, 10, 327–338. [Google Scholar] [CrossRef] [Green Version]
  53. Ibanez, M.; Blackman, A. Is eco-certification a win–win for developing country agriculture? Organic coffee certification in Colombia. World Dev. 2016, 82, 14–27. [Google Scholar] [CrossRef]
  54. Chapman, M.; Satterfield, T.; Chan, K.M.A. When value conflicts are barriers: Can relational values help explain farmer participation in conservation incentive programs? Land Use Policy 2019, 82, 464–475. [Google Scholar] [CrossRef] [Green Version]
  55. Schroth, G.; Läderach, P.; Blackburn Cuero, D.S.; Neilson, J.; Bunn, C. Winner or loser of climate change? A modelling study of current and future climatic suitability of Arabica coffee in Indonesia. Reg. Environ. Change 2015, 15, 1473–1482. [Google Scholar] [CrossRef] [Green Version]
  56. Edwards, D.P.; Hodgson, J.A.; Hamer, K.C.; Mitchell, S.L.; Ahmad, A.H.; Cornell, S.J.; Wilcove, D.S. Wildlife-friendly oil palm plantations fail to protect biodiversity effectively. Conserv. Lett. 2010, 3, 236–242. [Google Scholar] [CrossRef]
  57. Smith, C.; Barton, D.; Johnson, M.D.; Wendt, C.; Milligan, M.C.; Njoroge, P.; Gichuki, P. Bird communities in sun and shade coffee farms in Kenya. Glob. Ecol. Conserv. 2015, 4, 479–490. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Map of 21 study areas across Java. (1) Cipaganti; (2) Kemuning; (3) Kepuharjo; (4) Jatimulyo; (5) Tuban; (6) Madiun-Kediri (7) Trenggalek; (8) Gunung Kelud; (9) Malang-Batu; (10) Surabaya-Gresik; (11) Sidoarjo; (12) Pasuruan; (13) Probolinggo; (14) Lumajang; (15) Jember; (16) Dataran Tinggi Hyang; (17) Situbondo; (18) Ijen-Baluran; (19) Banyuwangi Utara; (20) Alas-Purwo Merubetiri; (21) Sampang.
Figure 1. Map of 21 study areas across Java. (1) Cipaganti; (2) Kemuning; (3) Kepuharjo; (4) Jatimulyo; (5) Tuban; (6) Madiun-Kediri (7) Trenggalek; (8) Gunung Kelud; (9) Malang-Batu; (10) Surabaya-Gresik; (11) Sidoarjo; (12) Pasuruan; (13) Probolinggo; (14) Lumajang; (15) Jember; (16) Dataran Tinggi Hyang; (17) Situbondo; (18) Ijen-Baluran; (19) Banyuwangi Utara; (20) Alas-Purwo Merubetiri; (21) Sampang.
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Figure 2. Incidence rate ratios between the abundance of birds in commercial polyculture coffee (reference category) and other habitats considered during the survey on 1228 plots in Java, Indonesia. Data are standardised beta values and 95% confidence intervals from a generalised additive model. A description of the habitats can be found in the methods. Other predictors included in the model can be found in Table 2. ** p < 0.01; *** p < 0.001.
Figure 2. Incidence rate ratios between the abundance of birds in commercial polyculture coffee (reference category) and other habitats considered during the survey on 1228 plots in Java, Indonesia. Data are standardised beta values and 95% confidence intervals from a generalised additive model. A description of the habitats can be found in the methods. Other predictors included in the model can be found in Table 2. ** p < 0.01; *** p < 0.001.
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Figure 3. Incidence rate ratios between the diversity of birds (Shannon Index) in commercial polyculture coffee (reference category) and other habitats considered during the survey on 1228 plots in Java, Indonesia. Data are standardised beta values and 95% confidence intervals from a generalised additive model. A description of the habitats can be found in the methods. Other predictors included in the model can be found in Table 2. * p < 0.05; ** p < 0.01.
Figure 3. Incidence rate ratios between the diversity of birds (Shannon Index) in commercial polyculture coffee (reference category) and other habitats considered during the survey on 1228 plots in Java, Indonesia. Data are standardised beta values and 95% confidence intervals from a generalised additive model. A description of the habitats can be found in the methods. Other predictors included in the model can be found in Table 2. * p < 0.05; ** p < 0.01.
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Figure 4. Incidence rate ratios between the richness of birds in commercial polyculture coffee (reference category) and other habitats considered during the survey on 1228 plots in Java, Indonesia. Data are standardised beta values and 95% confidence intervals from a generalised additive model. A description of the habitats can be found in the methods. Other predictors included in the model can be found in Table 2. * p < 0.05; ** p < 0.01.
Figure 4. Incidence rate ratios between the richness of birds in commercial polyculture coffee (reference category) and other habitats considered during the survey on 1228 plots in Java, Indonesia. Data are standardised beta values and 95% confidence intervals from a generalised additive model. A description of the habitats can be found in the methods. Other predictors included in the model can be found in Table 2. * p < 0.05; ** p < 0.01.
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Figure 5. Non-metric multidimensional scaling representing the composition of foraging guilds at the 21 sites. Different colours indicate the main habitat in the study sites (or two main habitats if they were equally important).
Figure 5. Non-metric multidimensional scaling representing the composition of foraging guilds at the 21 sites. Different colours indicate the main habitat in the study sites (or two main habitats if they were equally important).
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Table 1. Number of sampling points, elevation range, mean (±SE) plant diversity per plot, and mean (±SE) bird diversity per plot in the 21 study sites on Java.
Table 1. Number of sampling points, elevation range, mean (±SE) plant diversity per plot, and mean (±SE) bird diversity per plot in the 21 study sites on Java.
SitesRegencyElevation Range (m above Sea Level)Plant DiversityBird DiversityNumber of Observation PointsMain Habitat Types
CipagantiGarut1300–16500.97 ± 0.060.65 ± 0.0457Mixed coffee systems: sun, shade monoculture, commercial polyculture
KemuningTemanggung459–6491.63 ± 0.031.83 ± 0.0489Rustic coffee
KepuhharjoSleman616–9851.36 ± 0.071.34 ± 0.1230Traditional polyculture coffee
JatimulyoKulon Progo514–7651.35 ± 0.071.10 ± 0.1230Traditional polyculture coffee
Ijen-BaluranBanyuwangi70–15950.20 ± 0.040.88 ± 0.0746Tree farms and other crops *
Madiun-KediriKediri780–12650.31 ± 0.051.08 ± 0.0660Tree farms and other crops *
Batu-MalangMalang881–14840.21 ± 0.040.92 ± 0.0760Tree farms and other crops
PasuruanPasuruan595–17930.50 ± 0.061.49 ± 0.0860Tree farms *
TrenggalekTrenggalek4–3720.47 ± 0.061.19 ± 0.0560Tree farms and other crops *
Gunung KeludKediri, Malang, Blitar712–10310.29 ± 0.051.33 ± 0.0660Tree farms and other crops
SampangSampang0–80.22 ± 0.051.89 ± 0.0560Mangrove and paddy fields
Kota SurabayaSurabaya0–470.43 ± 0.061.94 ± 0.0460Mangrove and other crops
Probolinggo (BTS)Probolinggo607–14120.25 ± 0.060.99 ± 0.0860Tree farms
DT HyangProbolinggo498–9680.83 ± 0.061.14 ± 0.0760Community managed forest
SitubondoSitubondo0–320.11 ± 0.040.87 ± 0.0660Paddy fields and other crops
TubanTuban3–320.10 ± 0.041.49 ± 0.0760Paddy fields and other crops
BanyuwangiBanyuwangi5–1820.44 ± 0.060.91 ± 0.0760Tree farms and other crops
JemberJember1–170.03 ± 0.021.19 ± 0.0660Paddy fields
LumajangLumajang1–260.12 ± 0.051.12 ± 0.0660Tree farms and other crops
SidoarjoSidoarjo0–40.25 ± 0.052.03 ± 0.0660Mangrove and other crops
Alas Purwo-Meru BetiriBanyuwangi0–1120.43 ± 0.060.86 ± 0.0860Tree farms
* Commercial coffee fields are present but do not represent the main habitat.
Table 2. Results of generalised additive models to understand the influence of habitat type and other environmental predictors on the abundance, diversity, and richness of birds in 21 sites, 1226 plots, in Java, Indonesia.
Table 2. Results of generalised additive models to understand the influence of habitat type and other environmental predictors on the abundance, diversity, and richness of birds in 21 sites, 1226 plots, in Java, Indonesia.
Response Variable aPredictorCategoryEstimate ± Std. ErrorZ-ValuepSmooth Termp
Edfχ2
Bird abundanceIntercept 4.06 ± 0.408.24 **<0.001
Habitat bCommunity managed forest−0.19 ± 0.41−0.480.634
Mangrove−1.19 ± 0.22−5.32 **<0.001
Other commercial polyculture−0.95 ± 0.25−3.83 **<0.001
Other crop/fruit field−0.82 ± 0.20−4.08 *<0.001
Paddy field−0.64 ± 0.21−3.02 **0.003
Rustic coffee0.05 ± 0.390.330.741
Shade monoculture coffee−0.93 ± 0.19−5.02 **<0.001
Sun coffee−0.99 ± 0.23−4.31 **<0.001
Traditional polyculture coffee−0.23 ± 0.26−0.880.378
Tree farm−1.18 ± 0.20−5.94 **<0.001
Shade tree richness 0.04 ± 0.022.030.043 *
s(plant diversity) 8.4253.22 **<0.001
s(elevation) 2.584.540.177
s(longitude, latitude) 31.681724.84 **<0.001
s(distance to protected areas) 8.07109.00 **<0.001
Bird diversityIntercept 0.55 ± 0.192.91 *0.004
Habitat bCommunity managed forest
Mangrove
Other commercial polyculture
Other crop/fruit field
Paddy field
Rustic coffee
Shade monoculture coffee
Sun coffee
Traditional polyculture coffee
Tree farm
Shade tree richness
s(plant diversity)
s(elevation)
s(longitude, latitude)
s(distance to protected areas)
Bird richnessIntercept 1.75 ± 0.237.74 **<0.001
HabitatbCommunity managed forest−0.05 ± 0.27−0.190.853
Mangrove−0.29 ± 0.19−1.570.117
Other commercial polyculture−0.20 ± 0.21−0.960.336
Other crop/fruit field−0.41 ± 0.17−2.37 *0.018
Paddy field−0.21 ± 0.18−1.200.23
Rustic coffee0.11 ± 0.310.670.502
Shade monoculture coffee−0.54 ± 0.17−3.19 **0.001
Sun coffee−0.56 ± 0.24−2.40 *0.016
Traditional polyculture coffee0.08 ± 0.280.290.769
Tree farm−0.48 ± 0.17−2.76 **0.006
Shade tree richness 0.01 ± 0.020.840.387
s(plant diversity) 1.000.150.699
s(elevation) 1.000.530.468
s(longitude, latitude) 25.45457.90 **<0.001
s(distance to protected areas) 2.673.400.484
a fit family for bird abundance: Poisson (link = “sqrt”); bird diversity: Tweedie; bird richness: Poisson (link = “log”); b reference category: commercial polyculture coffee; * p < 0.05; ** p < 0.01.
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Imron, M.A.; Campera, M.; Al Bihad, D.; Rachmawati, F.D.; Nugroho, F.E.; Budiadi, B.; Wianti, K.F.; Suprapto, E.; Nijman, V.; Nekaris, K.A.I. Bird Assemblages in Coffee Agroforestry Systems and Other Human Modified Habitats in Indonesia. Biology 2022, 11, 310. https://doi.org/10.3390/biology11020310

AMA Style

Imron MA, Campera M, Al Bihad D, Rachmawati FD, Nugroho FE, Budiadi B, Wianti KF, Suprapto E, Nijman V, Nekaris KAI. Bird Assemblages in Coffee Agroforestry Systems and Other Human Modified Habitats in Indonesia. Biology. 2022; 11(2):310. https://doi.org/10.3390/biology11020310

Chicago/Turabian Style

Imron, Muhammad Ali, Marco Campera, Dennis Al Bihad, Farah Dini Rachmawati, Febrian Edi Nugroho, Budiadi Budiadi, K. Fajar Wianti, Edi Suprapto, Vincent Nijman, and K.A.I. Nekaris. 2022. "Bird Assemblages in Coffee Agroforestry Systems and Other Human Modified Habitats in Indonesia" Biology 11, no. 2: 310. https://doi.org/10.3390/biology11020310

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