Abstract
Background
The data we present are part of the long-term project SLAM (Long Term Ecological Study of the Impacts of Climate Change in the natural forest of Azores) aiming to assess the impact of biodiversity erosion drivers on Azorean native biota, using long-term ecological data. Additionally to SLAM (Sea, Land and Air Malaise) traps, nocturnal Active Aerial Searching and nocturnal Foliage Beating methods were used to sample, between 2017 and 2018, the arthropod biodiversity on two historical urban gardens of Azores, the “Jardim Botânico” of Faial Island and “Jardim Duque da Terceira” of Terceira Island.
New information
We provided an inventory of arthropods collected between 2017 and 2018 in two urban gardens of Faial and Terceira Islands (Azores). A total of 8342 specimens were collected, in which 7493 specimens were identified to species/subspecies level (Faial n = 3296; Terceira n = 4197). The identified specimens belong to four classes, 15 orders, 80 families and 159 species and subspecies of arthropods. A total of 84 species and subspecies are considered introduced (n = 2454 specimens), 50 native non-endemic (n = 4444 specimens), eight endemic (n = 217) and 17 have an indeterminate origin (n = 378). This study also revises the arthropod inventory of these Azorean gardens, by adding/updating the taxonomic names of three orders, ten families and 22 species.
Keywords: arthropods, biodiversity, dataset, inventory, introduced species, native species, Oceanic Islands, urban gardens
Introduction
Habitat loss, associated with landscape transformation, is one of the major causes of biodiversity loss worldwide (Diamond et al. 1989, Ntshanga et al. 2021). Particularly, the urbanisation process radically modifies the ecology of natural landscapes (Tratalos et al. 2007, Goddard et al. 2010). In addition to habitat loss, urbanisation also facilitates the introduction and establishment of exotic species and can affect the ecological interactions between local species (McKinney 2006).
In this context, urban gardens may play an important role in biodiversity conservation by provisioning a refuge for native biota and mitigating the effects of landscape fragmentation (Smith et al. 2005, Fuller et al. 2007, Goddard et al. 2010, Arteaga et al. 2020). Although the design and planning of urban gardens can affect positively native biodiversity, many urban gardens include exotic plant species that could facilitate the establishment of generalist introduced species (Matteson et al. 2008, Kowarik 2011).
This study complements the publication of Arteaga et al. (2020), which provides an inventory of arthropod diversity in Azorean urban gardens and studies the effect of plant species composition in the colonisation status of arthropods. Arteaga et al. (2020) demonstrated that, in general, arthropod communities are related with the plant species composition of gardens. More endemic and native arthropod species are found in gardens dominated by native plants, in comparison with gardens dominated by ornamental exotic plant species, where the proportion of introduced arthropods (individuals and species) was higher.
General description
Purpose
The main objective of this publication is to provide a recent inventory of the arthropod diversity present in two historical gardens of Azores, the “Jardim Botânico” of Faial Island and “Jardim Duque da Terceira” of Terceira Island, complementing the work of Arteaga et al. (2020). This study also updates the taxonomic inventory of Arteaga et al. (2020) and contributes to the study of the urban garden’s role in the conservation of native biodiversity.
Additional information
The data we present are part of the long-term project SLAM (Long Term Ecological Study of the Impacts of Climate Change in the natural forest of Azores) aiming to assess the impact of biodiversity erosion drivers on Azorean native biota, using long-term ecological data.
This is the sixth dataset contribution for this project (previous ones in Costa and Borges (2021), Borges et al. (2022b), Borges et al. (2022a), Lhoumeau et al. (2022), Lhoumeau and Borges (2022)). Another publication dedicated to Lepidoptera contributed with information about some new exotic species for Azores (Pérez Santa-Rita et al. 2018). However, in the current study, additional sampling methods were also used, to include Active Aerial Searching and nocturnal Foliage Beating (see more details below).
Project description
Title
Inventory of Arthropods of Azorean Urban Gardens.
Personnel
The project was conceived and is being led by Paulo A.V. Borges.
Fieldwork:
Terceira Island: Paulo A.V. Borges, Rosalina Gabriel, Alejandra Ros-Prieto.
Faial Island: Paulo A.V. Borges, Rosalina Gabriel, Pedro Casimiro.
Parataxonomists: Alejandra Ros-Prieto, Alba Arteaga.
Taxonomists: Paulo A. V. Borges and Luís Carlos Crespo.
Curation: Voucher specimen management was mainly undertaken by Alejandra Ros-Prieto, Alba Arteaga, Lucas Lamelas-López and Paulo A. V. Borges.
Study area description
The study area comprises Terceira (total area: 400.2 km²; maximum elevation: 1021 m a.s.l.) and Faial (total area: 172 km2; maximum elevation 1043 m a.s.l.) Islands. They are located in the central group of the Azores Archipelago (North Atlantic), roughly at: 38°43′40″N, 27°12′48″W (Terceira Island), and 38°34′57″N, 28°42′17″W (Faial Island). The climate of the Archipelago is temperate oceanic, characterised by regular and abundant rainfall, high levels of relative humidity and persistent winds. The landscape of the Islands is mainly dominated by urban and agricultural areas at the lowest elevations; pasturelands and exotic tree plantations inland; and native forests located at highest elevations (Gaspar et al. 2010). The study was carried out on two botanical gardens, named “Jardim Botânico”, in Faial Island and “Jardim Duque da Terceira” in Terceira Island.
The Faial Island Botanical Garden (“Jardim Botânico”) was initially implemented in 1986 with the aim to promote the conservation of the flora of the Azores (Melo 2020). Initially occupying an area of 5,600 m², it is located in the parish of Flamengos, at an altitude of 118 m (Melo 2020). Additional terrain was added in the last decades and now it occupies 15,000 m² (1.5 ha) (Melo 2020). This is currently an iconic place in Faial Island visited by many tourists. In addition to a large collection of native and endemic plants, in 2003, this Boatnical Garden created the "Azores Seed Bank", whose purpose is to collect and maintain a collection of viable seeds of all Azorean species that are possible to conserve in a conventional seed bank (Melo 2020).
The “Jardim Duque da Terceira” in Terceira Island is located in the historic centre of the main town, Angra do Heroísmo, at an altitude of 34 m. Initially occupying an area of 16,000 m² in 1882, it now occupies a larger area that reaches 2 ha (Barcelos 2012). This Garden is dominated by exotic plants, transported to the Island since the period of the Portuguese discoveries and includes both tropical and subtropical species (Barcelos 2012).
Design description
Passive Flight Interception traps (SLAM traps - Sea, Land and Air Malaise) (Fig. 1), nocturnal Active Aerial Searching (AAS) and nocturnal Foliage Beating (FBN) methods were used to sample the arthropod biodiversity on two historical urban gardens of Azores: the “Jardim Botânico”, located in the surroundings of Horta, in Faial Island and “Jardim Duque da Terceira” located in Angra do Heroísmo, in Terceira Island. AAS and FBN are reliable methods to collect samples of arthropods that are mainly active during the night (Borges et al. 2018). The collected specimens were preserved in ethanol 96%. SLAM traps were placed in both gardens in order to collect mainly diurnal flying and non-flying arthropods, through interception and conservation on a propylene-glycol recipient of the captured specimens (Borges et al. 2017). The SLAM traps were placed during six consecutive months and checked monthly.
Figure 1.
SLAM trap (Sea, Land and Air Malaise trap) located in a site on Terceira Island (Credit: Paulo A. V. Borges)
Funding
Fieldwork: FEDER in 85% and by Azorean Public funds by 15% through Operational Programme Azores 2020, under the project Green Garden Azores (ACORES-01-0145-FEDER-000070).
Taxomomic work: FEDER in 85% and by Azorean Public funds by 15% through Operational Programme Azores 2020, under the project AZORESBIOPORTAL (ACORES-01-0145-FEDER-000072) and also the project Portal da Biodiversidade dos Açores (2022-2023) - PO Azores Project - M1.1.A/INFRAEST CIENT/001/2022.
Data curation (Darwin Core): MACRISK-Trait-based prediction of extinction risk and invasiveness for Northern Macaronesian arthropods (FCT-PTDC/BIA-CBI/0625/2021).
Sampling methods
Study extent
The study was conducted on two urban gardens, the “Jardim Botânico”, located in the surroundings of Horta, in Faial Island and “Jardim Duque da Terceira” located in Angra do Heroísmo, in Terceira Island. The first is mainly composed of endemic and native plant species, but also includes some introduced species, common and widespread in the Azores. The second garden includes mainly collections of introduced trees, shrubs and palms from across the world (see for more details, Arteaga et al. (2020)).
Sampling description
Passive Flight Interception traps (SLAM traps - Sea, Land and Air Malaise trap) (Fig. 1), nocturnal Active Aerial Searching (AAS) and nocturnal Foliage Beating (FBN) methods were used to sample the arthropod biodiversity (Arachnida, Chilopoda, Diplopoda and Insecta Classes) on two historical urban gardens of the Azores, between 2017 and 2018: the “Jardim Botânico”, located in Horta, in Faial Island and “Jardim Duque da Terceira”, located in Angra do Heroísmo, in Terceira Island. AAS consists on collecting arthropods found above knee-level by hand, forceps, pooter or brush and immediately transferring them into vials containing ethanol 96%. FBN consists of beating tree and shrub branches with a wooden stick and collecting the fallen specimens on a beating tray, posteriorly transferred to vials containing ethanol 96%. AAS and FBN are reliable methods to collect samples of arthropods that are mainly active during the night (Borges et al. 2018). The SLAM trap consists on a structure of 110 × 110 × 110 cm (MegaView Science Co.) designed to intercept flying and non-flying arthropods. They were placed in the gardens during six consecutive months, checked monthly. For more details about sampling methods, see Arteaga et al. (2020).
Quality control
All collected specimens were sorted and posteriorly identified by an expert taxonomist (P.A.V.B) in the laboratory.
Geographic coverage
Description
Faial and Terceira Islands, Azores, Portugal
Coordinates
38.508 and 38.807 Latitude; -28.839 and -27.0389 Longitude.
Taxonomic coverage
Description
The following Classes and Orders are covered:
Arachnida: Araneae; Opiliones; Pseudoscorpiones.
Chilopoda: Scutigeromorpha.
Diplopoda: Julida.
Insecta: Archaeognatha; Blattodea; Coleoptera; Dermaptera; Hemiptera; Hymenoptera; Neuroptera; Phasmida; Psocodea; Thysanoptera.
Temporal coverage
Notes
The data were collected between April 2017 and 30 June 2018.
Collection data
Collection name
Entomoteca Dalberto Teixeira Pombo at University of the Azores.
Collection identifier
DTP
Specimen preservation method
Alcohol
Usage licence
Usage licence
Creative Commons Public Domain Waiver (CC-Zero)
Data resources
Data package title
Inventory of Arthropods of Azorean Urban Gardens
Resource link
http://ipt.gbif.pt/ipt/resource?r=arthropods_azorean_urban_gardens
Alternative identifiers
https://www.gbif.org/dataset/3c314464-509f-4971-80d7-cd9f02110ea7
Number of data sets
2
Data set 1.
Data set name
Event Table
Data format
Darwin Core Archive format
Character set
UTF-8
Download URL
http://ipt.gbif.pt/ipt/resource?r=arthropods_azorean_urban_gardens
Data format version
1.5
Description
The dataset was published in the Global Biodiversity Information Facility platform, GBIF (Borges and Lamelas-López 2022). The following data table includes all the records for which a taxonomic identification of the species was possible. The dataset submitted to GBIF is structured as a sample event dataset that has been published as a Darwin Core Archive (DwCA), which is a standardised format for sharing biodiversity data as a set of one or more data tables. The core data file contains 20 records (eventID). This GBIF IPT (Integrated Publishing Toolkit, Version 2.5.6) archives the data and, thus, serves as the data repository. The data and resource metadata are available for download in the Portuguese GBIF Portal IPT (Borges and Lamelas-López 2022).
Data set 1.
| Column label | Column description |
|---|---|
| eventID | Identifier of the events, unique for the dataset. |
| stateProvince | Name of the region of the sampling site. |
| islandGroup | Name of the archipelago. |
| island | Name of the island. |
| country | Country of the sampling site. |
| countryCode | ISO code of the country of the sampling site. |
| municipality | Municipality of the sampling site. |
| locality | Locality of the sampling site. |
| locationID | Identifier of the location. |
| habitat | The habitat of the sampling site. |
| decimalLongitude | The geographic longitude (in decimal degrees, using the spatial reference system given in geodeticDatum) of the geographic centre of a Location. |
| decimalLatitude | The geographic latitude (in decimal degrees, using the spatial reference system given in geodeticDatum) of the geographic centre of a Location. |
| geodeticDatum | The ellipsoid, geodetic datum or spatial reference system (SRS) upon which the geographic coordinates given in decimalLatitude and decimalLongitude are based. |
| coordinateUncertaintyInMetres | Uncertainty of the coordinates of the centre of the sampling plot in metres. |
| coordinatePrecision | A decimal representation of the precision of the coordinates given in the decimalLatitude and decimalLongitude. |
| georeferenceSources | A list (concatenated and separated) of maps, gazetteers or other resources used to georeference the Location, described specifically enough to allow anyone in the future to use the same resources. |
| minimumElevationInMetres | The lower limit of the range of elevation (altitude, above sea level), in metres. |
| samplingProtocol | The sampling protocol used to capture the species. |
| sampleSizeValue | The numeric amount of time spent in each sampling. |
| sampleSizeUnit | The unit of the sample size value. |
| eventDate | Date or date range the record was collected. |
| year | Year of the event. |
| month | Month of the event. |
| day | Day of the event. |
Data set 2.
Data set name
Occurrence_Table
Data format
Darwin Core Archive format
Character set
UTF-8
Download URL
http://ipt.gbif.pt/ipt/resource?r=arthropods_azorean_urban_gardens
Data format version
1.5
Description
The dataset was published in the Global Biodiversity Information Facility platform, GBIF (Borges and Lamelas-López 2022), structured as an occurrence table that has been published as a Darwin Core Archive (DwCA), which is a standardised format for sharing biodiversity data as a set of one or more data tables. The core data file contains 762 records (occurrenceID). This GBIF IPT (Integrated Publishing Toolkit, Version 2.5.6) archives the data and, thus, serves as the data repository. The data and resource metadata are available for download in the Portuguese GBIF Portal IPT (Borges and Lamelas-López 2022).
Data set 2.
| Column label | Column description |
|---|---|
| eventID | Identifier of the events, unique for the dataset. |
| type | Type of the record, as defined by the Public Core standard. |
| licence | Reference to the licence under which the record is published. |
| institutionID | The identity of the institution publishing the data. |
| institutionCode | The code of the institution publishing the data. |
| collectionID | The identity of the collection publishing the data. |
| collectionCode | The code of the collection where the specimens are conserved. |
| datasetName | Name of the dataset |
| basisOfRecord | The nature of the data record. |
| occurrenceID | Identifier of the record, coded as a global unique identifier. |
| recordedBy | A list (concatenated and separated) of names of people, groups or organisations who performed the sampling in the field. |
| identifiedBy | A list (concatenated and separated) of names of people, groups or organisations who performed the sampling in the field. |
| dateIdentified | The date on which the subject was determined as representing the Taxon. |
| organismQuantity | A number or enumeration value for the quantity of organisms. |
| organismQuantityType | The type of quantification system used for the quantity of organisms. |
| sex | The sex and quantity of the individuals captured. |
| lifeStage | The life stage of the organisms captured. |
| identificationRemarks | Information about morphospecies identification (code in Dalberto Teixeira Pombo Collection). |
| scientificName | Complete scientific name including author and year. |
| kingdom | Kingdom name. |
| phylum | Phylum name. |
| class | Class name. |
| order | Order name. |
| family | Family name. |
| genus | Genus name. |
| specificEpithet | Specific epithet. |
| infraspecificEpithet | Infraspecific epithet. |
| scientificNameAuthorship | Name of the author of the lowest taxon rank included in the record. |
| taxonRank | Lowest taxonomic rank of the record. |
| establishmentMeans | The process of establishment of the species in the location, using a controlled vocabulary: 'native', 'introduced', 'endemic', 'indeterminate'. |
Additional information
We collected a total of 8342 individuals in both urban gardens, in which 7493 specimens were identified to species/subspecies level (Faial n = 3296; Terceira n = 4197). The identified specimens belong to four classes, 15 orders, 80 families and 159 species and subspecies of arthropods. A total of 84 species and subspecies are considered introduced (n = 2454 specimens), 50 native non-endemic (n = 4444 specimens), eight endemic (n = 217) and 17 have an indeterminate origin (n = 378) (Table 1).
Table 1.
Inventory of arthropods recorded in Azorean urban gardens of “Jardim Botânico” of Faial Island (FAI) and “Jardim Duque da Terceira” of Terceira Island (TER), between 2017 and 2018. The colonisation status (C.S.: End – Endemic; Nat – Native non-endemic; Int – Introduced; Ind – Indeterminate) and abundance values per island and total are provided.
| Class | Order | Family | Scientific name | C.S. | FAI | TER | Total |
| Arachnida | Araneae | Agelenidae | Textrixcaudata L. Koch, 1872 | Int | 10 | 0 | 10 |
| Arachnida | Araneae | Araneidae | Agalenatearedii (Scopoli, 1763) | Int | 0 | 11 | 11 |
| Arachnida | Araneae | Araneidae | Argiopebruennichi (Scopoli, 1772) | Nat | 0 | 2 | 2 |
| Arachnida | Araneae | Araneidae | Mangoraacalypha (Walckenaer, 1802) | Int | 1 | 0 | 1 |
| Arachnida | Araneae | Araneidae | Neosconacrucifera (Lucas, 1838) | Int | 287 | 44 | 331 |
| Arachnida | Araneae | Araneidae | Zygiellax-notata (Clerck, 1757) | Int | 8 | 2 | 10 |
| Arachnida | Araneae | Cheiracanthiidae | Cheiracanthiummildei L. Koch, 1864 | Int | 2 | 0 | 2 |
| Arachnida | Araneae | Clubionidae | Clubionaterrestris Westring, 1851 | Int | 2 | 0 | 2 |
| Arachnida | Araneae | Clubionidae | Porrhoclubionadecora (Blackwall, 1859) | Nat | 172 | 292 | 464 |
| Arachnida | Araneae | Clubionidae | Porrhoclubionagenevensis (L. Koch, 1866) | Int | 3 | 2 | 5 |
| Arachnida | Araneae | Dictynidae | Emblynaacoreensis Wunderlich, 1992 | End | 50 | 7 | 57 |
| Arachnida | Araneae | Dictynidae | Nigmapuella (Simon, 1870) | Int | 13 | 15 | 28 |
| Arachnida | Araneae | Linyphiidae | Agynetafuscipalpa (C. L. Koch, 1836) | Int | 0 | 8 | 8 |
| Arachnida | Araneae | Linyphiidae | Entelecaraschmitzi Kulczynski, 1905 | Nat | 71 | 4 | 75 |
| Arachnida | Araneae | Linyphiidae | Erigoneatra Blackwall, 1833 | Int | 1 | 1 | 2 |
| Arachnida | Araneae | Linyphiidae | Erigoneautumnalis Emerton, 1882 | Int | 0 | 1 | 1 |
| Arachnida | Araneae | Linyphiidae | Mermessusbryantae (Ivie & Barrows, 1935) | Int | 1 | 0 | 1 |
| Arachnida | Araneae | Linyphiidae | Mermessusfradeorum (Berland, 1932) | Int | 2 | 0 | 2 |
| Arachnida | Araneae | Linyphiidae | Microlinyphiajohnsoni (Blackwall, 1859) | Nat | 0 | 1 | 1 |
| Arachnida | Araneae | Linyphiidae | Nerieneclathrata (Sundevall, 1830) | Int | 1 | 1 | 2 |
| Arachnida | Araneae | Linyphiidae | Pelecopsisparallela (Wider, 1834) | Int | 1 | 1 | 2 |
| Arachnida | Araneae | Linyphiidae | Tenuiphantestenuis (Blackwall, 1852) | Int | 23 | 14 | 37 |
| Arachnida | Araneae | Mimetidae | Eroaphana (Walckenaer, 1802) | Int | 0 | 5 | 5 |
| Arachnida | Araneae | Oecobiidae | Oecobiusnavus Blackwall, 1859 | Int | 0 | 1 | 1 |
| Arachnida | Araneae | Pholcidae | Pholcusphalangioides (Fuesslin, 1775) | Int | 0 | 2 | 2 |
| Arachnida | Araneae | Salticidae | Chalcoscirtusinfimus (Simon, 1868) | Int | 0 | 2 | 2 |
| Arachnida | Araneae | Salticidae | Macaroerisdiligens (Blackwall, 1867) | Nat | 0 | 17 | 17 |
| Arachnida | Araneae | Salticidae | Pseudeuophrysvafra (Blackwall, 1867) | Int | 0 | 10 | 10 |
| Arachnida | Araneae | Salticidae | Salticusmutabilis Lucas, 1846 | Int | 0 | 3 | 3 |
| Arachnida | Araneae | Tetragnathidae | Metellinamerianae (Scopoli, 1763) | Int | 2 | 1 | 3 |
| Arachnida | Araneae | Theridiidae | Cryptachaeablattea (Urquhart, 1886) | Int | 15 | 4 | 19 |
| Arachnida | Araneae | Theridiidae | Dipoenaumbratilis (Simon, 1873) | Int | 23 | 0 | 23 |
| Arachnida | Araneae | Theridiidae | Paidiscuraorotavensis (Schmidt, 1968) | Nat | 0 | 15 | 15 |
| Arachnida | Araneae | Theridiidae | Parasteatodatepidariorum (C. L. Koch, 1841) | Int | 0 | 4 | 4 |
| Arachnida | Araneae | Theridiidae | Steatodagrossa (C. L. Koch, 1838) | Int | 43 | 0 | 43 |
| Arachnida | Araneae | Theridiidae | Steatodanobilis (Thorell, 1875) | Nat | 8 | 10 | 18 |
| Arachnida | Araneae | Theridiidae | Theridionhannoniae Denis, 1945 | Int | 0 | 1 | 1 |
| Arachnida | Araneae | Theridiidae | Theridionmusivivum Schmidt, 1956 | Nat | 2 | 0 | 2 |
| Arachnida | Opiliones | Leiobunidae | Leiobunumblackwalli Meade, 1861 | Nat | 142 | 0 | 142 |
| Arachnida | Pseudoscorpiones | Chthoniidae | Chthoniusischnocheles (Hermann, 1804) | Int | 2 | 0 | 2 |
| Arachnida | Pseudoscorpiones | Chthoniidae | Ephippiochthoniustetrachelatus (Preyssler, 1790) | Int | 0 | 2 | 2 |
| Chilopoda | Scutigeromorpha | Scutigeridae | Scutigeracoleoptrata (Linnaeus, 1758) | Int | 0 | 71 | 71 |
| Diplopoda | Julida | Julidae | Ommatoiulusmoreleti (Lucas, 1860) | Int | 29 | 44 | 73 |
| Insecta | Archaeognatha | Machilidae | Diltasaxicola (Womersley, 1930) | Nat | 0 | 3 | 3 |
| Insecta | Blattodea | Kalotermitidae | Cryptotermesbrevis (Walker, 1853) | Int | 0 | 1 | 1 |
| Insecta | Coleoptera | Apionidae | Aspidapionradiolus (Marsham, 1802) | Int | 6 | 8 | 14 |
| Insecta | Coleoptera | Apionidae | Kalcapionsemivittatumsemivittatum (Gyllenhal, 1833) | Ind | 4 | 85 | 89 |
| Insecta | Coleoptera | Carabidae | Dromiusmeridionalis Dejean, 1825 | Int | 3 | 0 | 3 |
| Insecta | Coleoptera | Chrysomelidae | Chaetocnemahortensis (Fourcroy, 1785) | Int | 0 | 62 | 62 |
| Insecta | Coleoptera | Chrysomelidae | Epitrixcucumeris (Harris, 1851) | Int | 0 | 172 | 172 |
| Insecta | Coleoptera | Chrysomelidae | Epitrixhirtipennis (Melsheimer, 1847) | Int | 0 | 4 | 4 |
| Insecta | Coleoptera | Chrysomelidae | Longitarsuskutscherai (Rye, 1872) | Int | 25 | 0 | 25 |
| Insecta | Coleoptera | Chrysomelidae | Psylliodesmarcida (Illiger, 1807) | Nat | 0 | 2 | 2 |
| Insecta | Coleoptera | Coccinellidae | Clitostethusarcuatus (Rossi, 1794) | Int | 0 | 7 | 7 |
| Insecta | Coleoptera | Coccinellidae | Scymniscushelgae (Fürsch, 1965) | Int | 0 | 13 | 13 |
| Insecta | Coleoptera | Coccinellidae | Scymnusinterruptus (Goeze, 1777) | Nat | 0 | 162 | 162 |
| Insecta | Coleoptera | Coccinellidae | Stethoruspusillus (Herbst, 1797) | Nat | 0 | 20 | 20 |
| Insecta | Coleoptera | Corylophidae | Sericoderuslateralis (Gyllenhal, 1827) | Int | 9 | 263 | 272 |
| Insecta | Coleoptera | Cryptophagidae | Cryptophaguscellaris (Scopoli, 1763) | Int | 0 | 2 | 2 |
| Insecta | Coleoptera | Curculionidae | Calacallessubcarinatus (Israelson, 1984) | End | 1 | 0 | 1 |
| Insecta | Coleoptera | Curculionidae | Coccotrypescarpophagus (Hornung, 1842) | Int | 0 | 69 | 69 |
| Insecta | Coleoptera | Curculionidae | Derelomuspiriformis (Hoffmann, 1938) | Int | 0 | 1 | 1 |
| Insecta | Coleoptera | Curculionidae | Lixuspulverulentus (Scopoli, 1763) | Int | 0 | 4 | 4 |
| Insecta | Coleoptera | Curculionidae | Mecinuspascuorum (Gyllenhal, 1813) | Int | 0 | 125 | 125 |
| Insecta | Coleoptera | Curculionidae | Naupactuscervinus (Boheman, 1840) | Int | 0 | 3 | 3 |
| Insecta | Coleoptera | Curculionidae | Naupactusleucoloma Boheman, 1840 | Int | 0 | 11 | 11 |
| Insecta | Coleoptera | Curculionidae | Otiorhynchuscribricollis Gyllenhal, 1834 | Int | 1 | 0 | 1 |
| Insecta | Coleoptera | Curculionidae | Sirocalodesmixtus (Mulsant & Rey, 1859) | Int | 0 | 3 | 3 |
| Insecta | Coleoptera | Curculionidae | Sitonacinnamomeus Allard, 1863 | Int | 0 | 1 | 1 |
| Insecta | Coleoptera | Dryophthoridae | Sitophilusoryzae (Linnaeus, 1763) | Int | 0 | 1 | 1 |
| Insecta | Coleoptera | Elateridae | Heteroderesazoricus (Tarnier, 1860) | End | 2 | 1 | 3 |
| Insecta | Coleoptera | Elateridae | Heteroderesvagus Candèze, 1893 | Int | 0 | 1 | 1 |
| Insecta | Coleoptera | Latridiidae | Cartoderebifasciata (Reitter, 1877) | Int | 1 | 28 | 29 |
| Insecta | Coleoptera | Latridiidae | Cartoderenodifer (Westwood, 1839) | Int | 0 | 4 | 4 |
| Insecta | Coleoptera | Mycetophagidae | Litargusbalteatus LeConte, 1856 | Int | 0 | 12 | 12 |
| Insecta | Coleoptera | Mycetophagidae | Typhaeastercorea (Linnaeus, 1758) | Int | 0 | 7 | 7 |
| Insecta | Coleoptera | Nitidulidae | Phenolialimbatatibialis (Boheman, 1851) | Int | 0 | 2 | 2 |
| Insecta | Coleoptera | Phalacridae | Stilbustestaceus (Panzer, 1797) | Nat | 0 | 68 | 68 |
| Insecta | Coleoptera | Ptiliidae | Ptenidiumpusillum (Gyllenhal, 1808) | Int | 0 | 2 | 2 |
| Insecta | Coleoptera | Ptinidae | Anobiumpunctatum (De Geer, 1774) | Int | 0 | 6 | 6 |
| Insecta | Coleoptera | Scraptiidae | Anaspisproteus Wollaston, 1854 | Nat | 1 | 0 | 1 |
| Insecta | Coleoptera | Silvanidae | Cryptamorphadesjardinsii (Guérin-Méneville, 1844) | Int | 0 | 2 | 2 |
| Insecta | Coleoptera | Staphylinidae | Athetafungi (Gravenhorst, 1806) | Ind | 0 | 62 | 62 |
| Insecta | Coleoptera | Staphylinidae | Carpelimuscorticinus (Gravenhorst, 1806) | Ind | 0 | 5 | 5 |
| Insecta | Coleoptera | Staphylinidae | Carpelimuszealandicus (Sharp, 1900) | Int | 0 | 1 | 1 |
| Insecta | Coleoptera | Staphylinidae | Coproporuspulchellus (Erichson, 1839) | Ind | 0 | 6 | 6 |
| Insecta | Coleoptera | Staphylinidae | Cordaliaobscura (Gravenhorst, 1802) | Ind | 0 | 3 | 3 |
| Insecta | Coleoptera | Staphylinidae | Hypomedondebilicornis (Wollaston, 1857) | Ind | 0 | 11 | 11 |
| Insecta | Coleoptera | Staphylinidae | Myrmecocephalusconcinnus (Erichson, 1839) | Ind | 0 | 1 | 1 |
| Insecta | Coleoptera | Staphylinidae | Oligotapumilio Kiesenwetter, 1858 | Ind | 0 | 14 | 14 |
| Insecta | Coleoptera | Staphylinidae | Oxypodalurida Wollaston, 1857 | Ind | 0 | 1 | 1 |
| Insecta | Coleoptera | Staphylinidae | Proteinusatomarius Erichson, 1840 | Ind | 0 | 53 | 53 |
| Insecta | Coleoptera | Staphylinidae | Rugilusorbiculatus (Paykull, 1789) | Ind | 0 | 3 | 3 |
| Insecta | Coleoptera | Staphylinidae | Scopaeusportai Luze, 1910 | Ind | 0 | 1 | 1 |
| Insecta | Coleoptera | Staphylinidae | Stenomastaxmadeirae Assing, 2003 | Ind | 0 | 1 | 1 |
| Insecta | Coleoptera | Staphylinidae | Suniuspropinquus (Brisout de Barneville, 1867) | Ind | 1 | 0 | 1 |
| Insecta | Coleoptera | Staphylinidae | Tachyporuschrysomelinus (Linnaeus, 1758) | Ind | 18 | 37 | 55 |
| Insecta | Coleoptera | Staphylinidae | Tachyporusnitidulus (Fabricius, 1781) | Ind | 48 | 24 | 72 |
| Insecta | Dermaptera | Anisolabididae | Euborelliaannulipes (Lucas, 1847) | Int | 4 | 0 | 4 |
| Insecta | Dermaptera | Forficulidae | Forficulaauricularia Linnaeus, 1758 | Int | 2 | 0 | 2 |
| Insecta | Dermaptera | Labiduridae | Labidurariparia (Pallas, 1773) | Nat | 4 | 0 | 4 |
| Insecta | Dermaptera | Spongiphoridae | Labiaminor (Linnaeus, 1758) | Int | 0 | 2 | 2 |
| Insecta | Hemiptera | Anthocoridae | Anthocorisnemoralis (Fabricius, 1794) | Nat | 0 | 11 | 11 |
| Insecta | Hemiptera | Anthocoridae | Buchananiellacontinua (White, 1880) | Int | 0 | 4 | 4 |
| Insecta | Hemiptera | Anthocoridae | Oriuslaevigatuslaevigatus (Fieber, 1860) | Nat | 2 | 14 | 16 |
| Insecta | Hemiptera | Aphididae | Cinarajuniperi (De Geer, 1773) | Nat | 374 | 0 | 374 |
| Insecta | Hemiptera | Cicadellidae | Eupteryxfilicum (Newman, 1853) | Nat | 5 | 15 | 20 |
| Insecta | Hemiptera | Cicadellidae | Euscelidiusvariegatus (Kirschbaum, 1858) | Nat | 0 | 40 | 40 |
| Insecta | Hemiptera | Cicadellidae | Sophoniaorientalis (Matsumura, 1912) | Int | 0 | 10 | 10 |
| Insecta | Hemiptera | Cixiidae | Cixiusazopifajoazofa Remane & Asche, 1979 | End | 1 | 0 | 1 |
| Insecta | Hemiptera | Delphacidae | Kelisiaribauti Wagner, 1938 | Nat | 0 | 5 | 5 |
| Insecta | Hemiptera | Flatidae | Cyphopterumadcendens (Herrich-Schäffer, 1835) | Nat | 725 | 0 | 725 |
| Insecta | Hemiptera | Flatidae | Siphantaacuta (Walker, 1851) | Int | 0 | 163 | 163 |
| Insecta | Hemiptera | Liviidae | Strophingiaharteni Hodkinson, 1981 | End | 39 | 0 | 39 |
| Insecta | Hemiptera | Lyctocoridae | Lyctocoriscampestris (Fabricius, 1794) | Int | 0 | 2 | 2 |
| Insecta | Hemiptera | Lygaeidae | Kleidocerysericae (Horváth, 1909) | Nat | 20 | 2 | 22 |
| Insecta | Hemiptera | Microphysidae | Loriculacoleoptrata (Fallén, 1807) | Nat | 57 | 0 | 57 |
| Insecta | Hemiptera | Miridae | Campyloneuravirgula (Herrich-Schaeffer, 1835) | Nat | 37 | 0 | 37 |
| Insecta | Hemiptera | Miridae | Heterotomaplanicornis (Pallas, 1772) | Nat | 1 | 0 | 1 |
| Insecta | Hemiptera | Miridae | Monalocorisfilicis (Linnaeus, 1758) | Nat | 0 | 6 | 6 |
| Insecta | Hemiptera | Miridae | Pilophorusconfusus (Kirschbaum, 1856) | Nat | 37 | 19 | 56 |
| Insecta | Hemiptera | Miridae | Taylorilygusapicalis (Fieber, 1861) | Int | 0 | 2 | 2 |
| Insecta | Hemiptera | Miridae | Trigonotyluscaelestialium (Kirkaldy, 1902) | Nat | 0 | 7 | 7 |
| Insecta | Hemiptera | Nabidae | Nabispseudoferusibericus Remane, 1962 | Nat | 0 | 1 | 1 |
| Insecta | Hemiptera | Oxycarenidae | Oxycarenuslavaterae (Fabricius, 1787) | Int | 0 | 281 | 281 |
| Insecta | Hemiptera | Pentatomidae | Nezaraviridula (Linnaeus, 1758) | Int | 0 | 1 | 1 |
| Insecta | Hemiptera | Reduviidae | Empicorisrubromaculatus (Blackburn, 1889) | Int | 14 | 7 | 21 |
| Insecta | Hemiptera | Rhyparochromidae | Aphanusrolandri (Linnaeus, 1758) | Nat | 0 | 4 | 4 |
| Insecta | Hemiptera | Rhyparochromidae | Beosusmaritimus (Scopoli, 1763) | Nat | 0 | 1 | 1 |
| Insecta | Hemiptera | Rhyparochromidae | Emblethisdenticollis Horváth, 1878 | Nat | 0 | 1 | 1 |
| Insecta | Hemiptera | Rhyparochromidae | Scolopostethusdecoratus (Hahn, 1833) | Nat | 0 | 6 | 6 |
| Insecta | Hemiptera | Triozidae | Triozalaurisilvae Hodkinson, 1990 | Nat | 21 | 0 | 21 |
| Insecta | Hymenoptera | Formicidae | Hypoponeraeduardi (Forel, 1894) | Nat | 4 | 0 | 4 |
| Insecta | Hymenoptera | Formicidae | Lasiusgrandis Forel, 1909 | Nat | 101 | 454 | 555 |
| Insecta | Hymenoptera | Formicidae | Linepithemahumile (Mayr, 1868) | Int | 0 | 30 | 30 |
| Insecta | Hymenoptera | Formicidae | Monomoriumcarbonarium (Smith, 1858) | Nat | 0 | 5 | 5 |
| Insecta | Hymenoptera | Formicidae | Tetramoriumcaespitum (Linnaeus, 1758) | Nat | 0 | 18 | 18 |
| Insecta | Hymenoptera | Formicidae | Tetramoriumcaldarium (Roger, 1857) | Int | 0 | 14 | 14 |
| Insecta | Neuroptera | Hemerobiidae | Hemerobiusazoricus Tjeder, 1948 | End | 87 | 5 | 92 |
| Insecta | Phasmida | Phasmatidae | Carausiusmorosus (Sinéty, 1901) | Int | 4 | 0 | 4 |
| Insecta | Psocodea | Caeciliusidae | Valenzuelaburmeisteri (Brauer, 1876) | Nat | 5 | 1 | 6 |
| Insecta | Psocodea | Caeciliusidae | Valenzuelaflavidus (Stephens, 1836) | Nat | 8 | 6 | 14 |
| Insecta | Psocodea | Ectopsocidae | Ectopsocusbriggsi McLachlan, 1899 | Int | 16 | 50 | 66 |
| Insecta | Psocodea | Ectopsocidae | Ectopsocusstrauchi Enderlein, 1906 | Nat | 1 | 90 | 91 |
| Insecta | Psocodea | Elipsocidae | Elipsocusazoricus Meinander, 1975 | End | 18 | 5 | 23 |
| Insecta | Psocodea | Elipsocidae | Elipsocusbrincki Badonnel, 1963 | End | 0 | 1 | 1 |
| Insecta | Psocodea | Epipsocidae | Bertkauialucifuga (Rambur, 1842) | Nat | 21 | 1 | 22 |
| Insecta | Psocodea | Peripsocidae | Peripsocusphaeopterus (Stephens, 1836) | Nat | 0 | 4 | 4 |
| Insecta | Psocodea | Psocidae | Atlantopsocusadustus (Hagen, 1865) | Nat | 98 | 5 | 103 |
| Insecta | Psocodea | Trichopsocidae | Trichopsocusclarus (Banks, 1908) | Nat | 502 | 667 | 1169 |
| Insecta | Thysanoptera | Aeolothripidae | Aeolothripsgloriosus Bagnall, 1914 | Nat | 1 | 1 | 2 |
| Insecta | Thysanoptera | Phlaeothripidae | Hoplothripscorticis (De Geer, 1773) | Nat | 2 | 0 | 2 |
| Insecta | Thysanoptera | Thripidae | Ceratothripsericae (Haliday, 1836) | Nat | 42 | 0 | 42 |
| Insecta | Thysanoptera | Thripidae | Heliothripshaemorrhoidalis (Bouché, 1833) | Int | 8 | 3 | 11 |
| Insecta | Thysanoptera | Thripidae | Hercinothripsbicinctus (Bagnall, 1919) | Int | 1 | 245 | 246 |
| Insecta | Thysanoptera | Thripidae | Parthenothripsdracaenae (Heeger, 1854) | Int | 0 | 12 | 12 |
In general, the most abundant species were the barklice Trichopsocusclarus (Banks, 1908) (Psocodea, Trichopsocidae) (n = 1169), which were captured in both urban gardens (Faial n = 502; Terceira n = 667), the fulgoroid planthopper Cyphopterumadcendens (Herrich-Schäffer, 1835) (Hemiptera, Flatidae), recorded only in Faial urban garden (n = 725) and the ant Lasiusgrandis Forel, 1909 (Hymenoptera, Formicidae) (n = 555) being recorded in both Islands (Faial n = 101; Terceira n = 454; Table 2). These three species are considered native non-endemic in the Archipelago. The most common endemic species were the lacewing Hemerobiusazoricus Tjeder, 1948 (Neuroptera, Hemerobiidae) (n = 92) and the spider Emblynaacoreensis Wunderlich, 1992 (Araneae, Dictynidae) (n = 57), being more abundant in the Faial urban garden (n = 87 and n = 50, respectively), than in the Terceira urban garden (n = 5 and n = 7, respectively). The most abundant introduced species were the spider Neosconacrucifera (Lucas, 1838) (Araneae, Araneidae) (n = 331) and the true bug Oxycarenuslavaterae (Fabricius, 1787) (Hemiptera, Oxycarenidae) (n = 281), the first species being more abundant in Faial (n = 287) than in Terceira (n = 44) and the second one absent in Faial urban garden (Table 1). The most common recorded arthropod families were Flatidae (Hemiptera; n = 888) and Trichopsocidae (Psocodea; n = 1169), being relatively abundant in both urban gardens (Table 2).
Table 2.
Ranking of the ten most abundant species per urban garden. The colonisation statuses (C.S.: End – Endemic; Nat – Native non-endemic; Int – Introduced) and abundance values (N) are provided.
| Class | Order | Family | Scientific name | C.S. | N |
| Faial Urban Garden | |||||
| Insecta | Hemiptera | Flatidae | Cyphopterumadcendens (Herrich-Schäffer, 1835) | Nat | 725 |
| Insecta | Psocodea | Trichopsocidae | Trichopsocusclarus (Banks, 1908) | Nat | 502 |
| Insecta | Hemiptera | Aphididae | Cinarajuniperi (De Geer, 1773) | Nat | 374 |
| Arachnida | Araneae | Araneidae | Neosconacrucifera (Lucas, 1838) | Int | 287 |
| Arachnida | Araneae | Clubionidae | Porrhoclubionadecora (Blackwall, 1859) | Nat | 172 |
| Arachnida | Opiliones | Leiobunidae | Leiobunumblackwalli Meade, 1861 | Nat | 142 |
| Insecta | Hymenoptera | Formicidae | Lasiusgrandis Forel, 1909 | Nat | 101 |
| Insecta | Psocodea | Psocidae | Atlantopsocusadustus (Hagen, 1865) | Nat | 98 |
| Insecta | Neuroptera | Hemerobiidae | Hemerobiusazoricus Tjeder, 1948 | End | 87 |
| Arachnida | Araneae | Linyphiidae | Entelecaraschmitzi Kulczynski, 1905 | Nat | 71 |
| Terceira Urban Garden | |||||
| Insecta | Psocodea | Trichopsocidae | Trichopsocusclarus (Banks, 1908) | Nat | 667 |
| Insecta | Hymenoptera | Formicidae | Lasiusgrandis Forel, 1909 | Nat | 454 |
| Arachnida | Araneae | Clubionidae | Porrhoclubionadecora (Blackwall, 1859) | Nat | 292 |
| Insecta | Hemiptera | Oxycarenidae | Oxycarenuslavaterae (Fabricius, 1787) | Int | 281 |
| Insecta | Coleoptera | Corylophidae | Sericoderuslateralis (Gyllenhal, 1827) | Int | 263 |
| Insecta | Thysanoptera | Thripidae | Hercinothripsbicinctus (Bagnall, 1919) | Int | 245 |
| Insecta | Coleoptera | Chrysomelidae | Epitrixcucumeris (Harris, 1851) | Int | 172 |
| Insecta | Hemiptera | Flatidae | Siphantaacuta (Walker, 1851) | Int | 163 |
| Insecta | Coleoptera | Coccinellidae | Scymnusinterruptus (Goeze, 1777) | Nat | 162 |
| Insecta | Coleoptera | Curculionidae | Mecinuspascuorum (Gyllenhal, 1813) | Int | 125 |
Considering the identified taxa (Table 1), we recorded 72 species and subspecies in Faial, with 28 being considered native non-endemic, seven endemic, 33 introduced and four of indeterminate origin. On the other hand, in Terceira, a total of 124 species and subspecies were recorded, 37 being considered native non-endemic, five endemic, 67 introduced and 15 of indeterminate origin (Table 1). The proportion of native endemic and non-endemic species in Terceira urban garden (33.87%) is lower than in Faial (48.61%) and the proportion of introduced species is higher in Terceira urban garden (54.03%) in comparison with Faial (45.83%).
This study also updates the taxonomy of the arthropods of the Azorean urban gardens. A total of three orders, ten families and 22 species were taxonomically updated (Table 3).
Table 3.
Update of the taxonomy of the species recorded in the Azorean urban gardens of Faial and Terceira Islands. *Some species of Anthocoridae family change to Lyctocoridae; **Some species of Lygaeidae family change to Oxycarenidae and Rhyparochromidae; MF Morphospecies; *** - Not recorded in Arteaga et al. 2020.
| Level | Artega et al. (2020) | New Taxonomy |
| Order | Psocoptera | Psocodea |
| Order | Microcoryphia | Archaeognatha |
| Order | Phasmatodea | Phasmida |
| Family | Eutichuridae | Cheiracanthiidae |
| Family | Phalangiidae | Leiobunidae |
| Family | Anobiidae | Ptinidae |
| Family | Brentidae | Apionidae |
| Family | Lathridiidae | Latridiidae |
| Family | Lachnidae | Aphididae |
| Family | Anthocoridae* | Lyctocoridae |
| Family | Lygaeidae** | Oxycarenidae |
| Family | Lygaeidae** | Rhyparochromidae |
| Family | Psyllidae | Liviidae |
| Species | Meionetafuscipalpa (C. L. Koch, 1836) | Agynetafuscipalpa (C. L. Koch, 1836) |
| Species | Carpelimus sp. | Carpelimuszealandicus (Sharp, 1900) |
| Species | MF 1376 | Derelomuspiriformis (Hoffmann, 1938) |
| Species | Genus (?), species (?) *** | Dipoenaumbratilis (Simon, 1873) |
| Species | Chthoniustetrachelatus (Preyssler, 1790) | Ephippiochthoniustetrachelatus (Preyssler, 1790) |
| Species | Kleidocerysericae (Horváth, 1908) | Kleidocerysericae (Horváth, 1909) |
| Species | Loriculaelegantula (Bärensprung, 1858) | Loriculacoleoptrata (Fallén, 1807) |
| Species | Gymnetronpascuorum (Gyllenhal, 1813) | Mecinuspascuorum (Gyllenhal, 1813) |
| Species | Monomoriumcarbonarium (F. Smith, 1858) | Monomoriumcarbonarium (Smith, 1858) |
| Species | Myrmecocephalusconcinnus (Erichson, 1840) | Myrmecocephalusconcinnus (Erichson, 1839) |
| Species | Pantomoruscervinus (Boheman, 1849) | Naupactuscervinus (Boheman, 1840) |
| Species | MF 1385 | Oxypodalurida Wollaston, 1857 |
| Species | Psylliodesmarcidus (Illiger, 1807) | Psylliodesmarcida (Illiger, 1807) |
| Species | MF 551 | Scopaeusportai Luze, 1910 |
| Species | Nephushelgae Fürsch, 1965 | Scymniscushelgae (Fürsch, 1965) |
| Species | Sirocalodesmixtus (Mulsant & Rey, 1858) | Sirocalodesmixtus (Mulsant & Rey, 1859) |
| Species | MF 1398 | Sitonacinnamomeus Allard, 1863 |
| Species | MF 1274 | Sophoniaorientalis (Matsumura, 1912) |
| Species | Stethoruspusillus (Herbst, 1979) | Stethoruspusillus (Herbst, 1797) |
| Species | MF Formicidae F6 | Tetramoriumcaespitum (Linnaeus, 1758) |
| Species | MF Formicidae F6 | Tetramoriumcaldarium (Roger, 1857) |
| Species | Theridionhannoniae Denis, 1944 | Theridionhannoniae Denis, 1945 |
This publication includes a recent inventory and updates the knowledge about the arthropod diversity and taxonomy of Arteaga et al. (2020). In general, the Terceira garden is mainly dominated by exotic plant species and, consequently, the proportion of introduced arthropods species is higher than in Faial, which is mainly composed by native plant species. Contrarily, the proportion of native species (endemic and non-endemic) is higher in Faial than in Terceira. These results are according to the findings of Arteaga et al. (2020).
Public and botanical gardens are important green infrastructures that promote the conservation of plants species, support science dissemination activities and people's health. Additional positive functions may include microclimatic regulation and water retention (Macháč et al. 2022). However, there is an ongoing debate on the role of gardens dominated by exotic plants and their role as a source for the spread of exotic potentially invasive species (Dawson et al. 2008). Concerning arthropods, our study generated several interesting patterns:
i) no introduced species had a dominant role in any garden, despite several being part of the 50% most abundant species in Terceira;
iii) in Faial Botanical Garden, the 50% most abundant species are either endemic or native non-endemic, with only one introduced species;
iii) most introduced and species of indeterminate status are particularly rare.
In conclusion, in general, the origin of the plant composition of the urban gardens can have an effect on the arthropod biodiversity origin (native vs. introduced species) present in the gardens, but the two studied settings also constitute a repository of indigenous fauna playing an important role in the conservation of native biota of the Archipelago. In particular, the Faial Island Botanical Garden, which holds a large community of native species, can be part of a future corridor of native plants across the agricultural landscape in this Island.
Acknowledgements
We acknowledge the Municipality of Angra do Heroísmo (Terceira, Azores) and the Botanic Garden of Horta (Faial) for providing the necessary authorisation for conducting the study. We are grateful to FEDER that financed project Green Garden Azores (ACORES-01-0145-FEDER-000070 - 85% through Azorean Public funds and 15% through Operational Programme Azores 2020) for supporting the fieldwork and the projects AZORESBIOPORTAL (ACORES-01-0145-FEDER-000072) and Portal da Biodiversidade dos Açores (2022-2023) - PO Azores Project - M1.1.A/INFRAEST CIENT/001/2022, for supporting the taxonomic research.
Lucas Lamelas-Lopez was supported by the Project FCT-UIDP/00329/2020-2023 and Paulo A. V. Borges and Rosalina Gabriel performed research under the project MACRISK-Trait-based prediction of extinction risk and invasiveness for Northern Macaronesian arthropods (FCT-PTDC/BIA-CBI/0625/2021) that financed also the Open Access of this publication.
Author contributions
LLL: Data Curation; Darwin Core dataset preparation; Formal analysis and interpretation; manuscript writing.
RG: Research (fieldwork); Resources; Project leading; data interpretation and manuscript revision.
ARP: Research (field and laboratory work); Resources; Data Curation.
PAVB: Conceptualisation; Methodology; Research (field and laboratory work); Resources; Data Curation; Darwin Core dataset preparation; Formal analysis and interpretation; manuscript writing.
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