NATIONAL COLLECTION OF ARACNIDA
(non-ACARI)
The National Collection of
Arachnida (non-Acari) (NCA), is the most comprehensive and fastest growing
collection of arachnids in South Africa. It contains 43,000 accessions
represented by approximately 180,000 alcohol preserved specimens sampled mainly
in South Africa. It serves as an invaluable scientific reference source and
research tool as well as an archive of South Africa’s arachnid biodiversity.
The collection was
established in 1976. A large part of the collection contains specimens collected
within agro-ecosystems through surveys that span periods of a year or more, as
well as surveys undertaken during the South African National Survey of Arachnida
(SANSA)
Six orders of
arachnida are housed in the collection:
Araneae
(Spiders)
40 525 accessions representing 75
families, 484 genera and 1 363 species
562 accessions are type specimens
representing 217 species
Amblypygi
(Whipspiders)
40 accessions representing 1
family, 2 genera and 4 species
Opiliones
(Harvestman)
248 accessions representing 10
families, 14 genera and 44 species
Pseudoscorpiones
295 accessions representing 15
families, 11 genera and 10 species
Scorpiones
859 accessions representing 4
families, 9 genera and 68 species
Solifugae
(Sunspiders)
505 accessions representing 6
families, 15 genera and 30 species.
NCA DATABASE:
Computerization of the NCA
(non-Acari) started in 1991 using a relational database for collected specimens,
article library and loan registry.
In 2000 the database was
migrated to a Microsoft Access database and a new module, the African Arachnida
Database (AFRAD) was added. AFRAD consists of a taxon dataset (including
descriptive and behavioural data, distribution per country, photographs and line
drawings) for all 6000 spider species of the Afrotropical Region. Synonym and
taxonomic name changes could now also be accommodated.
In 2005 all the modules were
migrated to a MySQL database written in PHP, housed on a special server at
ARC-Central Office. During this migration extensive data cleaning and
geo-referencing of all locality data were done.
In 2006 the South African National Survey of Arachnida (SANSA)
module was added. This module focuses only on published records of South
African species and incorporates information on species records from both
taxonomic and ecological papers from more than 17 institutions
world-wide.
Activities:
During 2009 the entire collection was inspected and
upgraded
On average 6,000 bottles containing approximately 20,000
specimens are newly accessioned annually. The specimens come from surveys
undertaken by teams under the auspices of the South African National Survey of
Arachnida (SANSA) as well as conservation agents, student and other projects and
citizen scientists
From 2010 a new dimension was added to the collection when
the DNA barcoding of new specimens through the International Barcode of Life
Project (iBOL) started
Contact:
Petro Marais (Collection Manager) at MaraisP@arc.agric.za
DNA BARCODING
BACKGROUND
In 2003 Paul Herbert and his
research group at the University of Guelph in Canada published a paper
“Biological identifications through DNA barcodes”. The paper proposed a new
system for identifying and discovering species using a very short sequence from
a standard part of the genome. This new molecular identification system is
called “DNA barcoding”.
In June 2007 delegates from
25 countries came together in Guelph, Canada to discuss a proposed global
collaboration of biodiversity scientists that would create a DNA barcode
reference library for all multi-cellular life.
Positive response and rapid
progress led to work beginning on establishing the administrative structures and
finalizing the research plans of the International Barcode of Life project
(iBOL) in July 2009. Formal activation of iBOL will take place in October
2010.
WHAT IS DNA
BARCODING?
DNA barcoding is similar to
the way a supermarket scanner distinguishes products using the black stripes of
the Universal Product Code (UPC).
A standard 648 base-pair gene
region (“CO1”) is being used for almost all animal groups. Using CO1 has the
advantage that it is short enough to be sequenced quickly and cheaply yet long
enough to identify variations among species.
THE BARCODE
PRODUCTION PIPELINE
DNA barcoding starts with a
specimen. The specimen may come from the field, a collection, zoo, botanical
garden, seed bank, etc.
In the laboratory a tiny
piece of tissue from the specimen is used by technicians to extract its DNA.
They isolate the barcode region, replicate it using PCR amplification and then
sequence the barcode. The sequence is represented by a series of the letters
CATG.
After obtaining the barcode
sequence, it is placed in the Barcode of Life Data Systems (BOLD)
database.
BOLD is a sophisticated
bioinformatics platform that incorporates a repository for DNA barcode records
made up out of stored specimen data and images as well as sequences and trace
files. It serves as a reference library of DNA barcodes used to assign
identities to unknown species, and monitors the number of barcode sequence
records and species coverage.
PURPOSE OF
iBOL
Hundreds of scientists and
technicians from 26 countries involved in this largest biodiversity genomics
initiative ever is using DNA barcode technology to create and extend the
geographic and taxonomic coverage of the barcode reference library, BOLD, for
all multi-cellular life. Over the next five years, iBOL collaborators will
gather DNA barcodes from five million specimens representing 500,000
species.
Once implemented, this DNA
based identification system will have wide-ranging impacts in areas such as pest
and disease control, food production and safety, resource management,
conservation, research, education and recreation. These impacts will translate
into economic benefits.
A number of DNA barcoding
campaigns have already started collecting and registering DNA barcodes focusing
on species endangered by human activity, species that are of particular
socio-economic importance or species that are used in environmental
assessment.