Introduction

Altitudinal changes in the composition and biodiversity of fish fauna have been widely recorded1,2,3,4. Most of the studies covered a large scale of altitudinal gradient of fish assemblages, which are up to few thousand meters above sea level. For instance, the distinctiveness of the fish fauna had increased with elevation in streams of the central Andes of Colombia, where the greatest turnover was observed between 1000 and 1750 m above sea level, with nearly 90% of the species recorded between 250 and 1250 m above sea level1. Mercado-silva and Lyons investigated the fish assemblage patterns in a high gradient piedmont river in Mexico2. The authors demonstrated that sites with high altitude (> 1393 m) were dominated by non-native Onchorhynchus mykiss whereas higher species and guild diversity were found in sites with lower altitudes. However, a small scale of altitudinal gradient also exhibited effects on the patterns of fish assemblages. For instance, altitude was identified as one of the variables that had significant relationships with the fish assemblages in the North Tiaoxi River, China, located at an elevation ranging from 33 to 329 m5. Similarly, altitude was the main determinant of fish species richness and composition assemblages in streams of the Ivinhema River basin, Brazil, of which there were two zones of fish assemblages where species richness, size and composition in streams located above 430 m are different from streams below this altitude6.

Physical habitat and water quality variables are known as key components structuring fish assemblages7,8. Environmental conditions such as dissolved oxygen, water temperature, and water pH change with increasing elevation over short spatial distances in mountainous forest streams, thus affecting fish species distribution and biodiversity. Most fish communities experience losses of diversity with increasing altitude3,4,5,6, but not all respond to altitude in the same way where the trends could be peak at mid and high elevation or exhibited non-linear pattern9,10,11. The low diversity in high altitude sites is often attribute to the increasing harshness of environment conditions and to the decrease in the available habitat area. On the other hand, moderate environment condition and complex habitat diversity in the low altitude sites are among the factors contributing to higher diversity and richness in the downstream area3. However, other factors such as climate and anthropogenic activities in the local area could disrupt the altitudinal gradients as well10,12. For freshwater fishes, changes in environmental parameters could be deadly to them as they are flourish within specific optimum range and sensitive to the environmental changes13,14.

Knowledge of the fundamental aspects of ecology such as the patterns of fish species distribution and biodiversity in the forest streams is the first and basic step to develop effective conservation strategies. Yet, there is no known information on the composition and biodiversity of freshwater fish fauna and the factors affecting them within the altitudinal gradients of the Baleh River Basin in Sarawak, Borneo. The major activity in the vicinity is logging which could render the modification of water quality15 and subsequently alteration of fish distribution and biodiversity along the altitudinal gradients of the river16,17. Besides, a hydroelectric project has also been proposed at the Baleh River18 where dam construction could further alter water quality and environmental condition of the river when the project starts off19,20. Hence, the present study aimed to explore not only the composition and biodiversity of the fish fauna in the Baleh River Basin, but also to identify the altitudinal changes of fish abundance and biodiversity. We predicted that abundance and biodiversity of Bornean freshwater fish fauna varies along the altitudinal gradients of this mountainous forest streams in Sarawak. Lastly, we also investigated the relationship between fish species composition and selected environmental parameters within the altitudinal gradients of the Baleh River Basin. We predicted that there are key environmental factors that shape the fish community structure which would be useful for evaluating fish fauna with respect to their conservation management and for any potential mitigation measures if or where necessary, in the future.

Materials and methods

Study area

Borneo forests are among the most biologically diverse habitats and act as a hotspot for biodiversity conservation. The Baleh River Basin is one of the mountainous forest streams in Sarawak, Malaysia, on the island of Borneo (Fig. 1). The forests are mostly characterized as mixed dipterocarp forest (MDF) and secondary forest21. The area is sparsely populated where the major activity in the vicinity is logging where signs of sedimentation problems in the river have been demonstrated15. A hydroelectric project has been proposed to build at the mid-stream of Baleh River (Fig. 1). Field samplings were conducted at a total of 72 stations located along the Baleh River and its two representative tributaries namely Mengiong River and Gaat River (Fig. 1). Majority of the sampling stations have been logged-over which result in a certain degree of habitat alterations. Sampling was conducted between April and August which corresponded with the dry season of the study area.

Figure 1
figure 1

The location of the seven groups with a total of 72 sampling stations at the Baleh River Basin, Kapit, Sarawak.

Field protocols

Various fish sampling methods including electrofishing, cast net, three-layered nets, and monofilament gill nets of various mesh sizes were used. Electrofishing was done by using a portable electro-shocker (copper electrodes on wooden handles) that was powered by a portable AC generator. At each station, electrofishing was carried out from downstream to upstream at shallow, narrow, and fast flowing stretches for a distance of approximately 80 m for a duration of about 30 min. A scoop net (mesh size = 1 cm) was then used to collect the fishes. Cast net with a mesh size of 2.5 cm was thrown approximately 10 times at each station in the shallow water region of the stream. In addition, three-layered net (mesh size = 2.5, 7.6, and 12.7 cm) and monofilament gill net of different mesh sizes (mesh size, depth × length = 2.5 cm, 1.2 m × 6.0 m; 5.0 cm, 2.0 m × 10.0 m; 7.6 cm, 2.0 m × 10.0 m; 10.1 cm, 1.5 m × 12.0 m; and 12.7 cm, 2.0 m × 15.0 m) were placed at a deeper and wider part of the river and were left overnight. Nets were then checked at regular intervals of 5 h during the day. These methods were done at equal effort and distance at each station. The environmental parameters were measured concurrently with the sampling of fish. Elevation was taken using a Portable Global Positioning System (Garmin GPSmap 62sc). Temperature, dissolved oxygen (DO), turbidity, pH, and conductivity were measured from the surface water of streams at each station by using a multi-parameter Sonde (YSI 6920 V2-2). Fish were counted and identified in situ to the species level according to the taxonomic keys22,23,24,25,26 and confirmed with FishBase27 and Eschmeyer’s Catalog of Fishes28 for the latest taxonomic status. Samples that were unable to be identified in the field were fixed in 10% formalin and preserved in 70% ethanol for further identification in the laboratory.

Data analysis

The 72 sampling stations were restructured into seven groups for data and statistical analysis (Table 1). Stations located along the Baleh River were grouped into five groups from upstream to downstream directions. Group 1 and Group 2 were located at the upstream of Baleh River. Group 3 and Group 4 were formed based on the location of the proposed dam site where Group 3 was located upstream of the proposed dam site and Group 4 was located below the dam site. Group 5 was located downstream of the Baleh River. The spatial distance between the groups of stations were approximately 10 km except for Group 3 and Group 4. Stations located at the two main tributaries namely Mengiong River and Gaat River were grouped as Group 6 and Group 7, respectively. Metrics of diversity including Shannon’s diversity index (H)29, Margalef index of species richness (D)30 and Pielou’s evenness (J)31 of fish at each station, each group of river segment, and the Baleh River Basin were determined by using the PAleontological STatistics software package (PAST, Palaeontological Association, 2001).

Table 1 Details of sampling regime and environmental parameters in the Baleh River Basin.

A generalized linear mixed model (GLMM) analysis was performed to determine whether fish abundance and species richness were affected by elevation. In this analysis, data of fish abundance and species richness at each station was used as a response variable, whereas group type with a small scale of altitudinal gradients ranging from 53 to 269 m above sea level was treated as a fixed factor. To account statistically for the effects of differences in sampling time affecting the fish abundance and species richness at each station, sampling time was also included as a random factor in the model. Poisson was used as a family object and log link function was applied in the analysis. The Pearson correlation was conducted to identify environmental variables that affecting the abundance, species number, and metrics of diversity of freshwater fish along the altitudinal gradients of the Baleh River Basin by using data collected from the 72 sampling stations. The GLMM analysis and Pearson correlation were carried out by using the Statistical Software for Social Sciences (SPSS Version 26, SPSS Inc., 1995).

Finally, an ordination technique of Canonical Correspondence Analysis (CCA) was used in the direct analyses of the relationships between fish assemblages and environmental parameters32. Fifteen species that individually contributed more than 2% of the total fish caught and six environmental parameters were loaded in the CCA to study the relationships between fish assemblages and environmental parameters in the Baleh River Basin. The fish abundance data were standardized according to the number of stations at each group and Hellinger transformed prior for statistical analysis. The environmental parameters collected at each sampling station were pooled to determine the average value at each group. Table 1 summarizes the environmental parameters used in the analysis. Statistical significance (p value < 0.05) of the CCA relationships between the set of environmental factors and abundance of fish species was evaluated using a permutation test with 999 permutations33. CCA was carried out by using the PAleontological STatistics software package (PAST, Palaeontological Association, 2001).

Results

Freshwater fish composition and biodiversity in the Baleh River Basin

A total of 3565 specimens belonging to six orders, 14 families, and 76 species were captured in the Baleh River Basin (Table 2). Cyprinidae was the most dominant family (74.4%) in the Baleh River Basin. The most dominant species was Tor tambra (12.9%) and Lobocheilos ovalis (12.3%), followed by Rasbora volzii (7.1%), Crossocheilus cobitis (5.8%), and Rasbora borneensis (5.5%), all of which are from the family Cyprinidae. On the other hand, family Gastromyzontidae was the second most dominant family (16.2%) in the Baleh River Basin where Parhomaloptera microstoma (3.5%) was the most dominant fish species. The metrics of diversity including Shannon’s diversity index (H), Margalef index of species richness (D), and Pielou’s evenness (J) in the Baleh River Basin and each group of river segment were summarized in Table 2.

Table 2 Summary of the fish composition and metrics of diversity in the Baleh River Basin.

Altitudinal changes of freshwater fish in the Baleh River Basin

Generalized linear mixed model (GLMM) demonstrated that elevation significantly influences fish abundance (p value < 0.001) in the Baleh River basin after statistically controlling for differences in sampling time as random variable. Significantly higher fish abundance was found in Group 1 and Group 2 that located at upstream (positive coefficient values range: 0.621 to 1.037, p value < 0.05, Table 3) whereas significantly lower fish abundance was found in Groups 3, 4, and 5 that located at downstream (negative coefficient values range: − 1.011 to − 0.989, p value < 0.05, Table 3) as compared to Group 7 (as reference). On the other hand, species richness at Group 3 (negative coefficient value: − 2.188, p value = 0.032, Table 3) was significantly low in the Baleh River Basin. Fish abundance of the Baleh River Basin was also found to be significantly and positively correlated with elevation, water pH, and conductivity, and negatively correlated with turbidity (Table 4, p value < 0.05). In contrast to fish abundance, no significant correlations (p value ≥ 0.05) between environmental variables and species richness or metrics of diversity were found in the present study.

Table 3 Generalized linear mixed-effects model (GLMM) for the effect of elevation on fish abundance and species richness (n = 72).
Table 4 Pearson correlation analysis between fish biodiversity and environmental parameters (n = 72).

Fish assemblages of the Baleh River Basin associated with environmental parameters

The first CCA axis (CCA1) had an eigenvalue of 0.219 and explained 42.5% of the species-environment relation variance (Fig. 2). The CCA2 accounted for 37.5% of total variance with an eigenvalue of 0.193. These two axes were statistically significant (p value < 0.05) according to the Monte-Carlo permutation test. The CCA1 was positively correlated with DO but negatively correlated with conductivity. On the other hand, the elevation, water pH, and DO were found positively loaded on CCA2. Gastromyzonid fishes were highly loaded on CCA1 but exhibited different responses. Protomyzon sp., Gastromyzon sp 1, and G. punctulatus were negatively loaded on CCA1 whereas G. fasciatus was positively loaded on CCA1. One cyprinid, Barbonymus schwanenfeldii was positively loaded on CCA 1. Gastromyzon fasciatus was positively loaded on CCA2 whereas two cyprinids (Rasbora volzii and Rasbora hosii) had high negative loadings on CCA2. Figure 2 illustrates that fish assemblages of the Baleh River Basin varied according to groups. Groups 1, 2, and 6 were located at upper right portion of the CCA ordination triplot whereas Groups 3, 4, and 5 were located at lower right portion of the triplot. Group 7 was located at the lower left portion of the CCA ordination triplot.

Figure 2
figure 2

CCA ordination triplots of the abundance of the 15 species (> 2%) with six environmental parameters at seven groups in the Baleh River Basin. Bar_col = Barbonymus collingwoodii, Bar_sch = Barbonymus schwanenfeldii, Cro_cob = Crossocheilus cobitis, Lob_ova = Lobocheilos ovalis, Lob_fal = Lobocheilos cf. falcifer, Ost_vit = Osteochilus vittatus, Ras_bor = Rasbora borneensis, Ras_vol = Rasbora volzii, Ras_hos = Rasbora hosii, Tor_tam = Tor tambra, Gas_sp 1 = Gastromyzon sp 1, Gas_fas = Gastromyzon fasciatus, Gas_pun = Gastromyzon punctulatus, Par_mic = Parhomaloptera microstama, Pro_sp. = Protomyzon sp.

Discussion

The present study demonstrated that the most dominant family in the Baleh River Basin, Sarawak was Cyprinidae followed by Gastromyzontidae. Dominance by the family Cyprinidae (74.4%) in this tropical forest stream is common due to their highly morphological adaptations34 and is corroborated by previous studies35,36,37,38. The family Gastromyzontidae that was resurrected by Kottelat39 in his revision of the loaches was the second most dominant family (16.2%) in the Baleh River Basin. Gastromyzontidae (sucker loaches), Balitoridae (hill stream loaches), and Nemacheilidae (stone loaches) are families of loaches which are small and elongated bottom-dwelling freshwater fishes with several barbels near the mouth. Most species are rheophilic, living in the headwater and hill streams, typically in fast-flowing water over a rocky substratum and high elevation mountainous areas40. They are found mostly at high altitude mountainous areas38,41. Hence, it is not surprising that these families contribute up to 28.3% and 33.8% at the upstream segment of the Baleh River (Group 1) and upstream of the Gaat River (Group 7), respectively (Table 2). Similarly, the Balitoridae contributed 36% to the fish fauna composition in the headwater of Ulu Tungud Forest Reserve, Meliau, Sabah, and ranked as the second most dominant family in the study area42. The loaches family (Balitoridae and Nemacheilidae) also contributed 20.59% of fish composition in the Upper Pelus River, Perak17. Overall, the fish diversity in the Baleh River Basin was observed to be moderate with a Shannon’s diversity index of 3.443 while the species richness with an index value of 9.2 was high44. The fish assemblages were evenly spread in the Baleh River Basin with an evenness index of 0.831.

The fish abundance in the Baleh River Basin was significantly influenced by elevation (p value < 0.05) where fish abundance steadily increased as altitude increased except for Mengiong River (Group 6). The high fish abundance in upstream river of the Baleh River and Gaat River is attributable to a better water quality in upstream as indicated by the positive correlation of fish abundance with elevation, pH, and conductivity, and negative correlation of fish abundance with turbidity. On the other hand, water quality of the Mengiong River is comparatively poorer with lower water pH and conductivity, and higher turbidity than those rivers at similar elevation. The present study areas are subjected to logging activities that leads to the low water pH and high turbidity15. Turbid condition in water can influence freshwater fishes in many ways, such as causing physical damage to gill structure of fish and clogging which leads to respiratory failure, and decreasing anti predator behavior, foraging efficiency, and hatching rate of fish45,46,47. In addition, sedimentation and degradation of stream substrates can diminish the food base for benthic fish species such as loaches48. Quality of the environment affects fish abundance and reproductive rate49,50,51 thus it might not be linearly correlated with elevation. A unimodal response of total fish abundance was also observed in the European part of Russia where the highest fish numbers were found at elevations between 250 and 500 m50.

Fish species richness in the present study did not follow the well documented trend of species richness decrease with altitude, instead significantly low fish species richness (p value < 0.05) was observed at Group 3. Group 3 was located at the midstream segment of the Baleh River that follows a sinuous trail through the basin. It was consistently possessing lowest values in fish abundance and metrics of diversity between the five groups located in the Baleh River, despite the spatial structure of the fish assemblages along the Baleh River demonstrating noticeable upstream–downstream gradient. The discontinuity of the upstream–downstream gradient at the midstream segment is most probably due to the influence of the inflow water from the Mengiong River coupled with the meandering feature of the segment. The midstream segment is receiving the inflow water of the Mengiong River which contains high organic matter and suspended solids. The meandering feature of the midstream segment decreases water velocity at the segment contributing to the lower turbidity at the area. However, it also increases accumulation of organic matter which is evidenced by the low conductivity value and acidic pH value at the midstream segment (Table 1). Low water pH has been shown to have detrimental effects on fish growth and physiological responses52,53. Hence, the low abundance and metrics of diversity in the midstream segment are most probably attributable to the acidic water in the river. Previous literature also showed that species richness can respond to altitude in many other ways. Fish species richness could be peaked at mid-elevation as seen in the Tibetan Plateau and its adjacent regions10. Higher species richness was observed in upstream rivers of the Tayabas River in Philippines where the authors attributed the phenomenon to the effect of anthropogenic disturbances at the downstream area54.

Fish species can prefer aquatic habitats with specific requirements, such as Gastromyzon fasciatus and Barbonymus schwanenfeldii that were found to be highly associated with elevated values of dissolved oxygen in the present study. In fact, the most important environmental parameters structuring the fish assemblage in the Baleh River Basin were dissolved oxygen and conductivity as indicated by their high loadings on CCA1. Dissolved oxygen in water is one of the most important factors in water quality where hypoxia is a common cause of fish kills around the world55. Fish abundance and diversity are highly associated with dissolved oxygen in river water7. Besides, conductivity has also been shown to be an important factor associated with fish composition and assemblages in aquatic ecosystem7,56. Stream conductivity is commonly associated with dissolved ions which are primarily affected by the geology of the area where the water flows through. In addition, conductivity could reflect anthropogenic interactions as it had been demonstrated that compositional differences between clear-felled, buffered (100 m width) and unlogged streams were related to the abundance of fine and coarse particulate organic matter and conductivity16. Also, the conductivity value decreased after the surrounding trees were harvested in wetlands of Georgia57. The lowest fish abundance at Mengiong River coincided with the lowest conductivity and the highest turbidity suggesting that high organic matter and suspended solids in the river due to logging activities have reduced fish abundance in the river. Organic compounds do not conduct electrical current well, hence the low conductivity value when organic matter is high in the stream. On the other hand, higher fish abundance is associated with higher values of conductivity at the upstream segments of the Baleh River and the Gaat River. The high conductivity value at those segments is probably attributable to its unique geological characteristic and marginally anthropogenic impact. Similarly, Cheimonopoulou et al.58 attributed the higher values of conductivity, hardness, and pH at the minimally impacted station from a small Mediterranean river to its unique geology and/or to low discharge values.

It has no doubt that elevation was one of the variables that had significant relationship with the fish assemblages in the Baleh River Basin despite the exception in the Mengiong River. The present study demonstrates that fishes from Gastromyzontidae family are common in upper stretches of river with higher elevation, which in this case are the upper segment of Baleh River. Fishes from Gastromyzontidae family were previously grouped as Balitoridae family which are often known as hill stream loaches due to their ability to cope with fast flowing water59. Previous study demonstrated that Gastromyzon spp. has morphologically adapted to live in torrential waters by clinging tightly to solid surfaces60 and were found restricted to headwater61. Hence, it is not surprising that those fishes were found proliferating in the hilly area at the Baleh River Basin. Nevertheless, Gastromyzon fasciatus is separated from other gastromyzonid species by its specific requirement of well-oxygenated waters and elevated water pH. The fish was found abundantly at the upstream segments of Baleh River (Group 1 and Group 2) and Mengiong River (Group 6) that positively loaded on CCA1 as those groups are high in DO values (≈ 7.73 mg/L). On the other hand, Protomyzon sp., Gastromyzon sp 1, and G. punctulatus have no specific requirement on high DO value. This is most apparent when they were found most abundantly or restricted at the Gaat River where the DO content (≈ 7.0 ± 0.9) was the lowest among the stream segments. The distinctive habitat associations among gastromyzonids are not uncommon. Some balitorid species in Thailand are also geographically separated, while others share similar distributions41. In contrast to gastromyzonids, two cyprinids from genus Rasbora were found mostly inhabiting in streams with lower elevation and water pH.

Conclusions

A total of 3565 specimens belonging to six orders, 14 families, and 76 species were collected at different altitudes at the Baleh River Basin. Cyprinidae was the most dominant family (74.4%) in the Baleh River Basin, followed by Gastromyzontidae (16.2%). Overall, the fish composition in the Baleh River Basin is rich in species, moderately diverse, and spread evenly along the river. The fish abundance increased significantly with increased altitude although the altitudinal gradient was disrupted at the midstream segment most probably due to the meandering feature of the midstream segment and the inflow from the Mengiong tributary. Elevation plays an important role in structuring fish assemblages in the Baleh River Basin that located at an elevation ranging from 53 to 269 m above sea level. However, anthropogenic activities had altered the environmental variables in the area. Thus, fish assemblages in the Baleh River Basin were found highly associated with DO and conductivity. Gastromyzonids which are characteristically present in more turbulent habitats are common in upper stretches of the river with higher elevation. The present study demonstrates that gastromyzonids could have similar habitat associations or be geographically separated in the Baleh River Basin. In contrast to gastromyzonids, cyprinids like Rasbora volzii and R. hosii were found inhabiting streams with lower elevation.