Nurexus Logo

Recognizing knowledge gaps in biodiversity for the preservation of endangered flora

Review Article/ Systemic Review/ Meta-Analysis

Dr. shree R V

Paper ID : JMRP-01-2025-22

Published Date : January 31, 2025

DOI : 10.65188/nurexus.1010

Open AccessOpen Access
Peer ReviewedPeer Reviewed

Dr. shree R V . Recognizing knowledge gaps in biodiversity for the preservation of endangered flora. Nurexus; Journal of MedVerse Research & Practice. 2025;3(1):6-12. doi: 10.65188/nurexus.1010. Available from: https://nurexus.com/journals/published/JMRP-01-2025-22

Download PDF
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 1
Journal of MedVerse Research & Practice
Recognizing knowledge gaps in biodiversity for the preservation of
endangered flora
Dr. Shree R
1
Assistant Professor, Department of Chemistry and Biochemistry,
St. Joseph Arts & Science College (Autonomous), Cuddalore
Email ID: r.shree@gmail.com
Submission Date: 27.12.2024
Accepted Date: 23.01.2025
Published Date: 31.01.2025
DOI: 10.65188/nurexus.1010
Copyright © 2025. The author(s). Published by Journal of MedVerse Research and Practice. This is an open-access
article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits
unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Abstract
Background: Biodiversity data gaps can limit the identification and conservation of endangered plant
species. Incomplete geographic coverage, taxonomic uncertainty, and limited genetic information may
affect the assessment of species distribution and conservation priorities.
Objective: To assess spatial, taxonomic, genetic, and climate-related data gaps affecting the study's
selected endemic and endangered plant species.
Methods: This study integrated biodiversity occurrence records, taxonomic information, genetic sequence
records, and climatic variables. Species distribution models were developed using generalized linear
models, random forest, and gradient boosting algorithms. Model performance was assessed using the area
under the receiver operating characteristic curve (AUC), and spatial analyses were used to identify areas
with uneven sampling coverage and potential conservation priorities.
Results: The study dataset contained 10,965 species and 762,655 distribution records. Of these species,
8,295 were reported as having sufficient occurrence records for species distribution modelling, while 691
species were reported to have fewer than five occurrence records. These categories do not account for the
entire dataset and must be reconciled before the final results are reported. The principal spatial and
taxonomic findings should be presented using verified numerical results from the final analysis.
Conclusion: Integrating biodiversity, genetic, taxonomic, and climatic information may help identify gaps
in conservation research. Reliable conservation recommendations require transparent data sources, clearly
defined geographic coverage, validated model outputs, and reproducible analytical methods.
Keywords: Biodiversity, Endangered flora, Geographic distribution, Climate change
Introduction
The tropics harbour vast biodiversity, yet our knowledge remains fragmented. In recent decades,
scientific and conservation efforts have intensified to address these gaps, driven by the alarming decline
of species due to habitat destruction, overexploitation, pollution, invasive species, and climate change
[9]. Aquatic ecosystems, covering less than 1% of the Earth's surface, support over 50% of fish species
and 25% of vertebrates. Despite their ecological significance, policy measures often overlook freshwater
habitats [13].
The demand for botanical resources is global, particularly for medicinal, aesthetic, and commercial
purposes. Sub-Saharan Africa, rich in rare plant species, has become a prime target for botanical
extraction. Trees like sandalwood, valued for their essential oils, and rosewood, crucial for fuel, are
increasingly exploited [8]. Indigenous knowledge, passed down for generations, has played a crucial role
ORIGINAL ARTICLE
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 2
in ecological management. However, only recently has the scientific community begun to acknowledge
its value [5]. Important gaps in biodiversity data remain across many ecosystems, particularly in areas
with limited geographic sampling, incomplete taxonomic information, or insufficient genetic data. These
gaps can restrict the accurate assessment of species distributions and hinder the identification of priority
areas for conservation.
Protected areas (PAs) struggle to maintain rare and threatened species due to financial constraints.
Prioritization based on regional extinction risks can assist PA managers in species monitoring [14].
Despite their ecological significance, historical botanical collections are rarely recognized under global
conservation frameworks. Efforts are needed to integrate these collections into biodiversity management
strategies [11]. Birds, essential ecosystem contributors and environmental indicators, lack a coordinated
global conservation framework. A research and conservation priority index (RCPI) has been proposed to
address these gaps [7].
Improved wildlife monitoring is crucial for effective conservation, particularly in developing nations
rich in biodiversity. Expanding ecological surveillance is essential to bridge critical knowledge gaps
[15]. Environmental DNA (eDNA) has emerged as a valuable tool for species identification, aiding
conservation efforts in ecologically significant yet understudied regions [1]. Addressing biodiversity
knowledge gaps requires prioritization, especially in vulnerable ecosystems. Large carnivore populations
have declined significantly, underscoring the need for systematic population monitoring [10]. Effective
management of invasive species must incorporate community engagement rather than relying solely on
government initiatives [3,4].
Materials and Methods
Study Design and Data Sources
This study used biodiversity records to examine gaps in the distributional, taxonomic, genetic, and climatic
information available for endemic plant species. Records associated with 123 wildlife conservation areas
were cross-referenced to compile information on plant species and their distribution. Taxonomic
information and species occurrence records were used to assess the availability and completeness of
biodiversity data. The compiled dataset was subsequently used for spatial analysis and species distribution
modelling to identify gaps in species occurrence records and areas requiring further investigation. The
identification of species, geographic coverage of the conservation areas, database sources, and criteria used
for selecting the conservation areas should be consistent with the original study records to ensure the
reproducibility of the analysis.
Georeferencing and Spatial Data
Species distribution records were georeferenced at a quarter-degree square (QDS) resolution, corresponding
to approximately 25 × 25 km. Spatial information was compiled from the National Vegetation Map, the
Custodians of Endangered Wildflowers initiative, and multiple biodiversity databases. These datasets were
supplemented with additional field-verified records to improve the spatial coverage and reliability of
occurrence information.
Genetic Data Analysis
Genetic data availability was assessed using records from GenBank. The database, containing DNA
sequence information for approximately 260,000 species, was queried for indigenous organisms to evaluate
the availability and potential taxonomic biases in genetic sequencing data. Analyses were performed using
R version 3.5.2. Genetic data availability was subsequently compared with species conservation status to
identify potentially underrepresented threatened species.
Species Distribution Modelling
Species distribution modelling was performed using occurrence records available for the plant species
included in the study dataset. Species with at least five recorded occurrences were considered for species
distribution modelling, while species with fewer than five occurrence records were assessed separately
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 3
because of the limited availability of distributional information. The manuscript reports that 8,295 species
had at least five occurrence records and that 691 species had fewer than five records. Spatial range
estimates for the latter group were derived using ArcGIS version 10.5, as reported in the original
manuscript. These two categories account for 8,986 species out of the reported total of 10,965 species. The
classification of the remaining 1,979 species is not explained in the available text and must be resolved
before the final species counts and modelling results can be considered complete.
Climate Suitability Analysis
SDM outputs were overlaid with climate suitability maps to identify regions predicted to be ecologically
favourable for endemic plant species. Spatial resolution was standardized across datasets to facilitate
comparison. Areas with high predicted species richness were identified based on the combined spatial
modelling outputs. Coastal grid cells containing 50% or less land area were excluded to minimize potential
underestimation of species richness.
Assessment of Spatial and Taxonomic Gaps
Spatial sampling coverage was evaluated by comparing observed species richness with species richness
predicted by the SDMs. Sampling effort was assessed using sampling-density metrics to identify areas with
inadequate or uneven collection coverage. Road-network data were overlaid on sampling records to assess
potential accessibility-related biases in species collection.
Taxonomic gaps were assessed by comparing the availability of genetic sequence data with species
conservation status, including IUCN Red List classifications. This analysis was used to identify threatened
species that were underrepresented in genetic databases. Spatial and taxonomic gaps were subsequently
integrated to identify priority areas and species requiring additional sampling, genetic characterization, and
conservation research.
Data Analysis
Data integration, statistical analysis, and species distribution modelling were performed using R, while
spatial analyses and range estimation were conducted using ArcGIS version 10.5. Model outputs were
evaluated using AUC-based performance measures. Species richness, sampling density, genetic data
availability, conservation status, and predicted climatic suitability were integrated to identify biodiversity
hotspots and potential gaps in current conservation and research coverage.
Results
The spatial distribution of biodiversity data gaps
By combining Species Distribution Models (SDMs) and existing biodiversity frequency reports, we
mapped the regional characteristics of actual and predicted native species diversity across 1790 grid cells.
Our findings indicate that 4% of the country's indigenous organisms remain untested, despite our SDMs
showing that every grid cell contains an area with a temperature within a seasonal range of at least 69.
While SDMs and reported records display similar overall patterns of relative diversity, the predicted
established biodiversity from SDMs aligns well with current knowledge, even in grid cells with complete
ecosystems. The spatial analysis identified variation in predicted plant species richness across the study
region. Areas with higher predicted richness were identified from the species distribution model outputs.
The geographic units, grid-cell definitions, and species-richness estimates are reported according to the
verified spatial analysis. The names of the regions and ecological zones used in the analysis should
correspond to established geographic classifications and be supported by appropriate sources.
Distribution of biodiversity data gaps
This collection encompasses species from 175 families and 1061 genera, exhibiting diverse biological data
organization across taxonomic and chronological scales. The leading 10 families, in terms of native species
count, account for 61% of the indigenous plants in the database. Forty family groups are represented by just
one native species each. The Proteaceae, Asteraceae, and Fabaceae families boast the highest number of
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 4
unique species location occurrence records. The top 10 families by sample constitute 69% of all occurrence
records in the database. In this study, three groups are represented by a single record. As expected, if all
species had equal sampling probability, generally, more species-rich groups were sampled more
extensively than less species-rich ones. However, sampling intensity varies significantly among families.
For example, the Anemiaceae family, despite having only one endemic species, has 508 entries.
Conversely, numerous underrepresented groups may warrant additional conservation attention.
Distribution of Threatened Plant Taxa
Regarding the family-wise distribution of endangered species, the IHR's Fab plants (84 threatened species),
Cyperaceae (65 species), and Poaceae (36 species) families were the most prevalent (Figure 1). Threatened
plant taxa were classified into the life-form categories used in the original analysis. The number of taxa in
each category is presented in Figure 2. The category labels, number of categories, and corresponding
counts should be checked against the underlying dataset to ensure that all groups are correctly defined and
that the reported totals are consistent. The vulnerable species exhibit significant disparities in their
distribution across states, influenced by forest cover and geographical location (Table 1).
Figure 1: Distribution of Threatened Plant Taxa
Table 1: Outcomes of IHR
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 5
The Eastern Himalayan region, comprising states such as SK, MN, ML, TR, MZ, NL, and AR, along with
two constituent areas (AS hills and WB hills), harbors a greater number of endangered species compared to
the Western Himalayan states (UK, JK, and HP). Despite this, the Eastern Himalayan territories have been
subject to less scientific investigation, leaving much of their wildlife largely unexplored. Among the Indian
Himalayan Region (IHR) sectors, SK (203 species), HP (190 species), and JK (189 species) boast the
highest counts of threatened groups (refer to table 2).
Table 2: Life of threatened taxa
States of IHR
Number of taxa
H
S
T
C
Br
Pt
MZ
80
32
25
7
0
1
NL
75
35
33
10
1
5
SK
125
40
45
8
1
4
TR
60
25
60
10
0
1
UK
78
20
48
4
1
3
WB
30
0
15
0
0
1
AR
75
30
40
20
0
3
AS
60
10
35
2
0
2
HP
120
40
55
5
3
5
JK
130
40
45
5
1
7
MN
100
25
33
5
0
2
ML
110
38
45
10
0
2
The table summarizes the distribution of different plant taxa across 12 states of the Indian Himalayan
Region (IHR). Trees (T) and herbaceous plants (H) are the most abundant groups, with JK (Jammu &
Kashmir) and SK (Sikkim) having the highest numbers of taxa. Shrubs (S) and climbers (C) show moderate
representation, while bryophytes (Br) and pteridophytes (Pt) are comparatively rare across all states. This
indicates that the IHR harbors rich diversity in higher plants, particularly herbs and trees, whereas lower
plants are less widespread.
Population trends of threatened taxa
Over the past few generations, the composition of plant species has changed in response to various
ecological and social disturbances. Population trends among the assessed threatened plant taxa were
classified according to the criteria and data sources used in the study. The proportions of taxa with stable,
declining, increasing, and other or undetermined trends are reported in Figure 3 and Table 3. The
denominator used to calculate each percentage, the source of the population-trend information, and the
treatment of taxa with unavailable trend data are specified to ensure that all reported categories are
interpretable and internally consistent.
IUCN data indicate that merely 12% of species are currently experiencing population declines.
Furthermore, 35% of vulnerable plant species remain unassessed due to inaccessible locations or
insufficient published research.
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 6
Table 3: Number of threatened plant taxa recorded by state in the Indian Himalayan Region
Number of Texas
States
UK
124
WB
25
SK
203
TR
103
MZ
121
NL
110
MN
147
ML
170
HP
190
JK
189
AR
147
AS
101
The table shows the total number of taxa recorded in different states of the Indian Himalayan Region (IHR).
Himachal Pradesh (HP) and Jammu & Kashmir (JK) have the highest species richness, with 190 and 189
taxa respectively, indicating high biodiversity. In contrast, West Bengal (WB) has the lowest, with only 25
taxa. Other states like ML, MN, SK, and AR also show relatively high diversity, highlighting regional
variation in plant species richness across the IHR.
Discussion
Recent research has increasingly emphasized that endangered plant species do not exist in isolation but are
embedded within complex ecological networks. Isbell et al. and Achieng et al. have highlighted that plant
survival is closely linked to interactions with pollinators, seed dispersers, soil microbiota, and symbiotic
partners, and that biodiversity loss disrupts these interconnected systems [5,1]. Similarly, studies focusing
on biodiversity hotspots have demonstrated that disruptions to associated insect and animal communities
can indirectly accelerate plant population declines, reinforcing the need to consider ecosystem-level
processes rather than single-species conservation [9,10]. Consequently, conservation strategies that focus
solely on individual species without accounting for these ecological interactions risk failure, as the
fundamental processes supporting growth, reproduction, and resilience remain unaddressed.
A holistic conservation approach is therefore essential to safeguard vulnerable plant populations.
Hernandez et al. emphasized that effective conservation planning must integrate ecological research, threat
assessment, and prioritization frameworks to address both species-level and ecosystem-level needs [4].
Innovative conservation techniques such as ex situ propagation, seed banking, and in vitro technologies
have been widely recommended by Kulak et al. and Ye et al., who demonstrated their importance in
preserving genetic diversity and preventing irreversible losses, particularly for narrowly distributed or
critically endangered plant taxa [7,15]. In addition, large-scale collaborative initiatives, such as those
described by Pirie et al., illustrate how coordinated global networks can successfully reduce extinction risk
when conservation actions are informed by rigorous science and shared expertise [11,12].
Community engagement and traditional ecological knowledge also play a critical role in holistic
conservation strategies. Sinthumule underscored that incorporating indigenous and local knowledge
systems enhances conservation effectiveness by aligning scientific interventions with long-standing
sustainable practices [13]. Furthermore, Kor and Diazgranados demonstrated that identifying important
plant areas based on ecological, cultural, and utilitarian values can help prioritize habitats that are vital for
both biodiversity conservation and human well-being [6]. Monitoring and evaluation remain equally
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 7
important, as emphasized by Stephenson et al., who noted that systematic assessment of flora, fauna, and
funga is essential for measuring conservation impact and adapting management strategies over time [14].
Strengths of the Study
The study integrates multiple biodiversity, taxonomic, genetic, climatic, and spatial datasets to provide a
comprehensive assessment of endemic and endangered flora. The use of multiple SDM algorithms with
AUC-based ensemble weighting strengthens the prediction of species distributions. Incorporation of field-
verified records, genetic database information, and sampling-effort assessment provides a multidimensional
approach to identifying conservation priorities and data gaps.
Limitations of the Study
The absence of reliable true-absence records required the use of pseudo-absences, which may influence
SDM predictions. Species with fewer than five occurrence records could not be modelled using the same
approach and therefore required alternative spatial range estimation. Predicted climatic suitability and
species richness may not fully represent actual distributions because habitat fragmentation, species
interactions, and other ecological factors were not completely incorporated. Sampling records may also be
affected by accessibility and road-network-related biases, potentially resulting in uneven representation of
some geographic regions or taxa.
Conclusion
Conserving endangered plant species is essential for maintaining ecological balance, preserving
biodiversity, and sustaining resources vital to human well-being. Identifying and addressing gaps in
biodiversity research, including incomplete species distribution records, taxonomic uncertainties, limited
genetic information, and inadequate assessment of climatic suitability, can strengthen conservation
planning. Integrating reliable biodiversity data, genetic tools, and traditional ecological knowledge may
improve species identification and help prioritize conservation efforts. Furthermore, systematic threat
assessment and long-term monitoring are necessary to evaluate the impacts of habitat loss,
overexploitation, invasive species, and climate change on threatened plant populations. Strengthening data
availability, improving research methods, and implementing targeted, environmentally sustainable
conservation strategies are therefore important for protecting endangered flora, enhancing ecosystem
resilience, and supporting biodiversity conservation for future generations.
Declaration
Conflict of Interest: The authors declare that they have no competing interests or conflicts of interest
related to this work.
Funding Source: Nil
References
1. Achieng, A.O., Arhonditsis, G.B., Mandrak, N., Febria, C., Opaa, B., Coffey, T.J., Masese, F.O., Irvine, K.,
Ajode, Z.M., Obiero, K. and Barasa, J.E., (2023). Monitoring biodiversity loss in rapidly changing
Afrotropical ecosystems: an emerging imperative for governance and research. Philosophical Transactions of
the Royal Society B, 378(1881), p.20220271.
2. Buechley, E.R., Santangeli, A., Girardello, M., Neate‐Clegg, M.H., Oleyar, D., McClure, C.J. and
Şekercioğlu, Ç.H., (2019). Global raptor research and conservation priorities: Tropical raptors fall prey to
knowledge gaps. Diversity and Distributions, 25(6), pp.856-869.
3. Fleischmann, A., München, B.S. and GeoBio-Center, L.M.U., (2018). Carnivorous plants and conservation–
the role of carnivorous plant enthusiasts.
4. Hernandez, J.O., Buot Jr, I.E. and Park, B.B., (2022). Prioritizing choices in the conservation of flora and
fauna: Research trends and methodological approaches. Land, 11(10), p.1645.
5. Isbell, F., Balvanera, P., Mori, A.S., He, J.S., Bullock, J.M., Regmi, G.R., Seabloom, E.W., Ferrier, S., Sala,
O.E., Guerrero‐Ramírez, N.R. and Tavella, J., (2023). Expert perspectives on global biodiversity loss and its
R S et al | Nurexus | Journal of MedVerse Research and Practice | Volume 3 | Issue – 01 | January 2025
Page 8
drivers and impacts on people. Frontiers in Ecology and the Environment, 21(2), pp.94-103.
6. Kor, L. and Diazgranados, M., (2023). Identifying important plant areas for useful plant species in
Colombia. Biological Conservation, 284, p.110187.
7. Kulak, V., Longboat, S., Brunet, N.D., Shukla, M. and Saxena, P., (2022). In vitro technology in plant
conservation: Relevance to biocultural diversity. Plants, 11(4), p.503.
8. Lannuzel, G., Pouget, L., Bruy, D., Hequet, V., Meyer, S., Munzinger, J. and Gâteblé, G., (2022). Mining
rare Earth elements: Identifying the plant species most threatened by ore extraction in an insular hotspot.
Frontiers in Ecology and Evolution, 10, p.740.
9. León-Cortés, J.L., Haaland, C., Pryke, J.S. and Maes, D., (2023). Special issue on insect conservation in
biodiversity hotspots. Journal of insect conservation, 27(1), pp.1-2.
10. Moir, M.L. and Young, D.A., (2023). Insects from the southwest Australia biodiversity hotspot: a barometer
of diversity and threat status of nine host-dependent families across three orders. Journal of Insect
Conservation, 27(1), pp.3-18.
11. AuBuchon-Elder T, et al. Plant conservation assessment at scale: Rapid triage of extinction risks.
Plants People Planet. 2023;5(3):386-397.
12. Pirie MD, Blackhall-Miles R, Bourke G, Crowley D, Ebrahim I, Forest F, et al. Preventing species
extinctions: a global conservation consortium for Erica. Plants People Planet. 2022;4(4):335-344.
13. Sinthumule, N.I., (2023). Traditional ecological knowledge and its role in biodiversity conservation: a
systematic review. Frontiers in Environmental Science, 11, p.1164900.
14. Stephenson, P.J., Londoño-Murcia, M.C., Borges, P.A., Claassens, L., Frisch-Nwakanma, H., Ling, N.,
McMullan-Fisher, S., Meeuwig, J.J., Unter, K.M.M., Walls, J.L. and Burfield, I.J., (2022). Measuring the
impact of conservation: the growing importance of monitoring fauna, flora and funga. Diversity, 14(10),
p.824.
15. Ye, J., Shan, Z., Peng, D., Sun, M., Niu, Y., Liu, Y., Zhang, Q., Yang, Y., Lin, Q., Chen, J. and Zhu, R.,
(2023). Identifying gaps in the ex situ conservation of native plant diversity in China. Biological
Conservation, 282, p.110044.