- Research
- Open access
- Published:
Fairy, tadpole, and clam shrimps (Branchiopoda) in seasonally inundated clay pans in the western Mojave Desert and effect on primary producers
Saline Systems volume 6, Article number: 11 (2010)
Abstract
Background
Fairy shrimps (Anostraca), tadpole shrimps (Notostraca), clam shrimps (Spinicaudata), algae (primarily filamentous blue-green algae [cyanobacteria]), and suspended organic particulates are dominant food web components of the seasonally inundated pans and playas of the western Mojave Desert in California. We examined the extent to which these branchiopods controlled algal abundance and species composition in clay pans between Rosamond and Rogers Dry Lakes. We surveyed branchiopods during the wet season to estimate abundances and then conducted a laboratory microcosm experiment, in which dried sediment containing cysts and the overlying algal crust were inundated and cultured. Microcosm trials were run with and without shrimps; each type of trial was run for two lengths of time: 30 and 60 days. We estimated the effect of shrimps on algae by measuring chlorophyll content and the relative abundance of algal species.
Results
We found two species of fairy shrimps (Branchinecta mackini and B. gigas), one tadpole shrimp (Lepidurus lemmoni), and a clam shrimp (Cyzicus setosa) in our wet-season field survey. We collected Branchinecta lindahli in a pilot study, but not subsequently. The dominant taxa were C. setosa and B. mackini, but abundances and species composition varied greatly among playas. The same species found in field surveys also occurred in the microcosm experiment. There were no significant differences as a function of experimental treatments for either chlorophyll content or algal species composition (Microcoleus vaginatus dominated all treatments).
Conclusions
The results suggest that there was no direct effect of shrimps on algae. Although the pans harbored an apparently high abundance of branchiopods, these animals had little role in regulating primary producers in this environment.
Background
Branchiopods and algae/cyanobacteria are often the dominant organisms inhabiting the flat, internally drained, and generally low-elevation playas [1] of arid basins in the desert U.S. Southwest, particularly the smaller playas referred to as pans [2–4]. This study investigated 1) branchiopod assemblage structure of flooded, low-salinity pans in the western Mojave Desert, California, USA, and 2) possible grazing effects of these shrimps on algae. The distribution and diversity of fairy, tadpole, and clam shrimps in ephemeral pools have been the focus of researchers and environmental managers in recent years in part because several species are listed as Threatened or Endangered Species in the United States [5]. The branchiopods of the playas and pans of the arid southwest U.S. have received less attention, perhaps because threatened or endangered species have not been reported [6].
Algae are often dominant and conspicuous as floating filamentous aggregations in inundated pans, on the moist edges of the pans, and on both the dry pan surface and adjacent upland areas where the algae form characteristic biotic crusts [7]. Brostoff et al. [3] estimated the photosynthesis of the constituent algae in biotic crusts on moist surfaces of the pans at 4 μmol C/m2/sec, a rate that is the same order of magnitude as nearby upland vegetation (no such data are available for algae during the inundated phase). The fate of such productivity is unclear, although fairy and clam shrimps ingest and digest planktonic and benthic algae, along with detritus and suspended organics, via non-selective filter feeding or scraping [8–13], and algal material can be the primary food resource of these shrimps [13–16]. Adult tadpole shrimps are opportunistic predators and scavengers, and the tadpole shrimp Lepidurus lemmoni Holmes consumes the fairy shrimp Branchinecta mackini Dexter in our Mojave assemblage [17]. One fairy shrimp species present in the Mojave assemblage, (Branchinecta gigas Lynch), is largely carnivorous, and B. mackini is a common prey item [18–20]. Branchinecta gigas may also consume filamentous algae [[20], but see [21]]. Fairy, clam, and tadpole shrimps (the latter only as juveniles) consume suspended detritus [17, 22] though neither carnivory nor detritivory were considered in the present study. These ephemeral desert waters also support insect (Hemiptera: Notonectidae; pers. obs.) and avian predators [17].
We characterize branchiopod species composition and abundance from field collections and explore the relationship between the shrimps and planktonic and benthic algae in intermittently flooded [sensu [23]] pans in the western Mojave Desert using laboratory microcosm experiments. This study is an initial effort towards better understanding of the trophic relationships in this ecosystem.
Methods
Study site
The study site was in the western Mojave Desert between Rogers and Rosamond Playas ("Dry Lakes"), on Edwards Air Force Base (EAFB), about 90 km NE of Los Angeles, California, U.S.A. at 34° 50.68', 117° 55.54' [7]. The pan-dune complex includes 3000 pans ranging in size from 0.005 to 125 ha (mean size - 0.5 ha [24]). The pans are comprised of impermeable silt-clay. The 0.25 km2 site was established by resource managers and researchers because the habitat is representative of the larger dune pan environment at EAFB and has been used for ecological research and hydrologic modeling in support of resource management [3, 7, 25]. The area has restricted access, is at least 200 m from the nearest seldom-used unimproved road, and shows few signs of recent anthropogenic disturbance. The site, a complex of pans (small playas [2, 26]) and dunes between two large playas, included three medium-sized (ca. 2 ha) pans and many smaller pans ranging in size from 0.5 ha to <1 m2 [7]. Sodium accumulation ratio (SAR) of surface pan soil was 836, electrical conductivity was 12,620 μS/cm, sodium concentration was 418 meq/l, and pH was 9 (Soil Testing Laboratory Division of Agriculture and Natural Resources, University of California, Davis). The soil composition was 20% clay, 40% sand, and 40% silt. The pans were surrounded by dunes, ranging from 0.5 to 10 m in height; many dunes have a luxuriant biotic crust cover, particularly adjacent to frequently inundated areas [7]. The vegetation around the pans is characteristically halophytic occurring in narrow belts of strongly salt tolerant species. These communities are generally dominated by Atriplex spp., especially A. confertifolia. (Torr. & Frem.) S. Wats., Allenrolfea occidentalis (S. Wats.) Kuntze, Suaeda moquinii (Torr.) Greene, Sarcobatus vermicularis (Hook.) Torr., Kochia californica S. Wats., and Nitrophila occidentalis (Moq.) S. Wats., as well as grasses such as Distichlis spicata (L.) E. Greene. When flooded, the Edwards waters range from pH 8.8 to 9.2 [27], and salinity ranged from 0 to 10 g/L (refractometer measurements during study site reconnaissance). Turbidity appeared to be related to wind speed and was often > 3,000 NTU. The pans and playas contain water for at least two weeks in 51% of the years, but may remain dry for several years at a time [25], a typical "intermittent" flood regime [23]. When moist or inundated, filamentous and/or mat-forming algae were often conspicuous on the substrate or in the water column. When dry, the surfaces of many of the pans are covered with biotic crusts dominated by blue-green algae; the main constituents are Microcoleus vaginatus (Vauch.) Gom. and Scytonema sp. Agardh [7]. Branchiopods were surveyed at EAFB by Simovich et al. (unpublished) and Sassaman [28] who reported three species of fairy shrimps (Branchinecta gigas, B. lindahli Packard and B. mackini), two tadpole shrimps (Lepidurus lemmoni and Triops newberryi Packard), and a clam shrimp (Eocyzicus digueti Richard). Although waterbirds were present when the pans were inundated, fish were absent (pers. obs.).
Field collections
Shrimps were collected in April 2001 when many of the pans in and around the study site had been inundated for several weeks. Two pans (Pans 1 and 2) had been previously surveyed for algae in a study of biotic crusts and numerically correspond to site locations in that study [7]. We also studied two additional pans: Pan 3, for which a pilot study indicated the presence of Branchinecta gigas, and Pan 4 from a lightly disturbed area about 2 km south of the study site.
Shrimps were sampled with a throw trap using protocols derived from Sogard et al. [29, 30] and Holmquist et al. [31, 32]. Throw traps have been shown to be highly efficient, relative to other collecting devices, for quantitatively sampling demersal organisms [33–35]. This method yields densities, because the trap encloses a known area and virtually all fauna are removed. The trap, constructed of sheet aluminum, was a 0.75 m × 0.75 m box without a top or bottom. The clearing device was a 0.5 m-wide framed and handled net (bar seine) with 0.5 mm square mesh. We threw the trap downwind and then pressed it into the sediment. The bar seine was passed repeatedly through the trap for a minimum of ten passes, and until three successive passes produced no additional animals. Because of occasional high abundances, the numbers of B. mackini males and females were estimated from subsamples. We made 10 such throw trap collections from each of the four pans.
Microcosm experiment
The experiment evaluated algal assemblages grown with (W/Shrimp) and without (W/O Shrimp) the naturally occurring crustacean assemblage after periods of 30 and 60 days. We collected 500 g samples of dried sediment (to a depth of 4 cm) in August 2001 from portions of pans that contained algal crusts using an 11 cm diameter hole saw affixed to a T-handle [17]. We gathered all sediment from Pan 3, where we found the highest abundances of shrimps, to maximize potential grazing effects. The experiment included 40 samples, 10 of which were randomly assigned to each of the four treatments (30 and 60 days, each with W/Shrimp and without W/O Shrimp), thus a 2 × 2 design. The cores were placed in 16 cm diameter plastic chambers and inundated with water to a depth of 10 cm (2 liters). The chambers were randomly interspersed on a laboratory bench 6 cm beneath a bank of General Electric, 40 w, "Plant and Aquarium" lights (GE F40PL/AQ) set to a 12 h photoperiod. Water levels were maintained at a depth of 10 cm throughout the experiment; each chamber was provided with an air stone. We measured pH, total dissolved solids, and conductivity with a Hanna model HI98129 combination meter. We used Hanna HI7031 conductivity calibration solution, Orion perpHect buffer, and Hanna HI70300 storage solution. The microcosms were relatively basic (mean pH = 9.10; SE = 0.0295). We recorded a mean conductivity of 3259 μS/cm (SE = 499) and mean total dissolved solids of 1713 ppm (SE = 293). Suspended particles were generally < 0.4 mm in size; the mode was 0.01 mm. Temperature ranged from 17.0 to 21.5°C ( = 18.6°). Like the field sites, microcosms had low salinity ( = 5.33 g/L, SE = 0.33; Fisher refractometer) and high turbidity ( = 3,089 NTU, SE = 591; Hanna HI 93703). Our pilot work indicated that shrimp hatch was equally good across a variety of initial and subsequent temperature regimes, a finding consistent with those of Maynard [36]. Thirty days was a sufficient time for hatched Branchinecta mackini to develop to sexual maturity [36].
We removed shrimps daily from the W/O Shrimp chambers using a 0.2 mm mesh dipnet. We made successive net passes until two passes failed to collect additional shrimps. Equivalent water column and substrate disturbance was simulated in the W/Shrimp chambers by stirring. Removed animals were counted with the aid of a dissecting microscope. Clam and tadpole shrimps were identifiable to species (Cyzicus setosa (Pearse) and Lepidurus lemmoni, respectively), whereas small fairy shrimps were identifiable only as Branchinecta spp. It was not possible to make these counts of shrimps in the W/Shrimp chambers because of the likelihood of damage to the animals from handling. Given that a) all W/and W/O shrimp chambers used substrate material from the same pan, which had abundant shrimps in each field sample, b) clam and fairy shrimps were counted in all W/O Shrimp chambers, c) abundant clam and fairy shrimps were observed in all W/Shrimp chambers (see Results), and d) all chambers had identical treatment, with the exception of shrimp removal from the W/O Shrimp chambers, there was a strong basis for the assumption that the hatch in the W/Shrimp chambers would be generally similar to that of the W/O shrimp chambers.
After 30 and 60 days, ten W/O Shrimp and ten W/Shrimp microcosms were removed from the experimental array for drying. Full chambers were moved into a plant dryer equipped with halogen bulbs, an exhaust fan, and small supplemental fans and were dried over a period of four days. This material was subsequently used for the analyses below.
Chlorophyll processing
Subsamples of the dried soil were analyzed using high performance liquid chromatography HPLC [37]. Algae in these dried soils were both planktonic and benthic in origin; we did not attempt to separate the two sources. Material was ground by mortar and pestle and subsamples (ca. 1 g) were extracted in 100% acetone at -4C for 8 hrs. Pigment samples were then filtered through 0.7 μm porosity filters (Whatman, NJ), ampulated, then analyzed using a HP1100 HPLC system (Agilent Technologies, Palo Alto, CA) equipped with diode array and fluorescence detectors. Pigments were identified using spectral libraries derived from standards, and linear regression relationships of pigment concentration and peak area were used to quantify pigments.
Relative abundance of algal species
The procedure was a modification of that used by Brostoff [7]. The dried material from each experimental chamber was ground in a mortar and pestle; 2.5 g of material was placed in a 10-cm plastic petri dish and saturated with 4 ml of distilled water. For each chamber, five such sub-samples were taken and analyzed. The material was cultured under greenhouse conditions for one month (parallel trials run under fluorescent plant growth lights with PFD [light intensity] of 600 μmol/m2/s1 yielded identical results). Plates were scanned at 50 × using a dissecting microscope and fiber optic light source; enumerating the species occurring in the center of the field of view at 100 points per plate. Identifications were confirmed using a compound microscope. The limited number of species, as determined from previous work [7], and the unambiguous appearance of the colonies formed by each species at this magnification, when properly corroborated, made this technique reliable and efficient. There are several inherent biases in these methods, because as desiccated, dormant individuals respond to moisture, both relative species abundance and biomass change. However, similar changes occur in natural populations, and previous work [7] showed no difference in the relative abundance or species reported between this and other methods.
Analysis
Although the chlorophyll data demonstrated homogenous variance (Fmax and Cochran's tests [38, 39]), the data from several treatments were shown to be nonnormal by Lilliefors tests [40]. Various transformations did not establish normality, so we performed a 2 × 2 ANOVA on ranked data making use of the Scheirer-Ray-Hare extension of the Kruskal-Wallis test [41–43]. Data were ranked, and df, SS, and MS were generated by a standard 2 × 2 ANOVA. These values were then used to calculate a correction factor for each source of variation that was ultimately tested as a X2 variable with a resulting alpha level.
Results
Field collection
We collected Branchinecta gigas, B. mackini, Lepidurus lemmoni, and Cyzicus setosa, but there was considerable variability among pans (Table 1). Cyzicus setosa, the numerical dominant in two of the three pans that had shrimps, showed a difference of two orders of magnitude among pans. Branchinecta gigas was the least abundant branchiopod and was found in only two pans. Although we did not encounter B. lindahli Packard in the quantitative field collections, this species was collected in our pilot sampling. Algal material and other organic and inorganic particles were apparent in the anterior portions of clam and fairy shrimp digestive tracts; these materials generally ranged from 0.001 to 0.4 mm in size.
Microcosm experiment
A total of 4778 clam shrimps, 1091 fairy shrimps, and three tadpole shrimps hatched from the ten 30 d W/O Shrimp chambers and the ten 60 d W/O Shrimp chambers (900 chamber-days) and were subsequently removed. Fairy shrimps were the first to hatch (day 4; Figure 1). There was a large hatch on the first day (mean hatch per chamber = 27.0; SE = 3.8). Fairy shrimp hatch decreased rapidly after the initial pulse, and was close to nil after day 12; there were no secondary pulses. In contrast, clam shrimps began hatching on day 9, and mean hatch slowly increased to an apex on day 22 ( = 28.5; SE = 7.7). Mean hatch per chamber decreased to about two clam shrimps/chamber/day by day 30, but this minimal hatch activity continued for the duration of the experiment. Single tadpole shrimps hatched on days 13, 16, and 22. All W/Shrimp and W/O Shrimp chambers yielded both clam and fairy shrimps. The shrimps in the W/Shrimp microcosms were not removed and counted as was the case in the W/O Shrimp microcosms, but clam and fairy shrimps were observed to be abundantly present in all W/Shrimp chambers throughout the experiment (~10-40 fairy shrimp and >100 clam shrimp per chamber). Algal cells and cell fragments were present, along with clay and organic particles, in dissected shrimp digestive tracts from both W/and W/O Shrimp chambers. Particle sizes were similar to those observed in field-collected shrimps.
All microcosms developed a distinct layer of algae associated with the substrate surface, and algae were also apparent on the sides of the chambers. Mean Chlorophyll a ranged from 12.3 to 16.6 mg/m2 for various treatments and Chlorophyll b ranged from 1.78 to 2.63 mg/m2 . There were several replicates for each treatment with Chlorophyll b values of 0.0 mg/m2. We did not find significant differences in Chlorophyll a or Chlorophyll b for any of the planned comparisons (Table 2). The samples were dominated by Microcoleus with the exception of two Nostoc colonies, one each in the 60 day W/and the W/O Shrimp trials.
Discussion
We collected four of the six shrimp species previously reported at Edwards Air Force Base (Branchinecta gigas, B. mackini, B. lindahli, and Lepidurus lemmoni; Simovich et al., unpublished) as well as Cyzicus setosa, which had not been previously reported. Neither Eocyzicus digueti, a clam shrimp, nor Triops newberryi, a tadpole shrimp, both previously reported as infrequent on the site (Simovich et al., unpublished), were found. Although we collected B. lindahli and B. mackini together in early 2001 pilot studies, B. lindahli was absent from our quantitative collections in April. The two species are similar in physiology, so their distributions would be expected to be similar [17]; but B. lindahli matures more rapidly and has lower fecundity than B. mackini [36]. As a result, Maynard [36] suggests that B. mackini outcompetes B. lindahli in longer lasting pools during wet years. We did our quantitative field sampling late in the season of a particularly wet year, and B. lindahli may have thus been excluded by the time that we took our quantitative samples. In contrast, B. mackini populations can persist up to four months [18].
Branchinecta gigas preys upon B. mackini, and the two species often occur together [17–19]. We found far fewer B. gigas than B. mackini (Table 1). Brown and Carpelan [18] found the ratio of B. gigas to B. mackini to approximate 1:40,000, whereas Daborn [19] found a ratio of about 1:35. We found a ratio of 1:1487 in Pan 3 and 1:75 in Pan 4, i.e., towards the more abundant end of the B. gigas spectrum seen in previous reports. We cannot explain the absence of shrimps from Pan 1 during our Spring 2001 sampling; we observed shrimps in this pan during some previous and subsequent years. Although the pans had similar areas, substrata, and algal assemblages, variability as a function of hatch timing, spatial and temporal extent of inundation, and unknown predation intensities may have led to the differing pan assemblages. Ecological processes in desert wetlands may have relatively high levels of stochasticity as a function of isolation [44–46] in a xeric matrix [47–49].
The composition of the branchiopod assemblage that hatched in the course of the microcosm experiment was similar to that observed in the field collection, with the exception of tadpole shrimps. Notostracans represented about 20% of the field collection, but accounted for only three of the roughly 6,000 shrimps that hatched from the microcosms. The very early hatch of Branchinecta mackini paralleled field observations [18].
Control of algae by both selective and non-selective grazers has been demonstrated in a variety of aquatic habitats, although such control does not always occur [50, 51]. Shifts in species composition and/or biomass have been observed in both microcosm and field experiments in which herbivorous or omnivorous marine crustaceans (e.g., amphipods) have been eliminated [52, 53]. Similarly in freshwater environments, elimination of Trichoptera from stream systems has been shown to increase periphyton by at least a factor of five [54, 55], and elimination of grazing decapod shrimps can result in a nine-fold increase in algal biomass in tropical streams [56].
Although algae were apparent in shrimp digestive tracts, we found no effect of shrimps on algal biomass. This lack of grazing influence is particularly striking, because sediment for the experiment was intentionally chosen from the pan with the highest shrimp abundance, presumably providing the greatest grazing intensity; experiments conducted with sediments from the pans with fewer shrimps would not be expected to show greater grazing effects. The grazing effect may have been below the level detectable by the experiment; suspended organics are an additional important food resource that were also available to shrimps, and consumption of this suspended material may have lessened the detectable grazing effect. Branchiopods can increase turbidity in both microcosms [57] and natural waters [58]; our microcosms were turbid, and turbidity can limit algal abundance [59]. The lack of grazing effect, however, was not due to lack of algae because algae were visually apparent in the microcosms, detected in the assays, and observed in shrimp digestive tracts.
The source of Chlorophyll b, which was present in about half the samples, is unknown as we did not find algae known to contain Chlorophyll b (e.g., euglenoids, coccoid greens) previously collected from the site. Brostoff [7] found no relation between measured Chlorophyll b and the presence of organisms known to contain Chlorophyll b. Possibly sources for this pigment would include terrestrial debris or cells not culturable in the media used.
Conversely, algal production may have been sufficiently high so as to prevent regulation by grazing in the microcosms. Hansson [50], building on the classic Hairston, Smith, and Slobodkin [60] model, provided evidence that planktonic algae in highly productive lake systems without a second level of predators can "grow away" from grazing pressure. Predatory tadpole shrimps were almost absent from the chambers, and Branchinecta gigas was not observed. Thus even though these secondary consumers were lacking, the productive microcosms may have functioned without significant regulation by grazing pressure. Further, assemblages in temporary waters with unpredictable flooding that may not occur in a given year [23], such as our Mojave pans, are more likely to be controlled by physical, rather than biological factors [[23], see also [61]].
The lack of detectable effect on algal species composition was not completely unexpected, although there is some evidence of algal control by anostracans offered by other microcosm [11] and field [13] studies. In a survey of algal species on the same site, Microcoleus dominated the flora [7]; only small amounts of other algal species were present. Nostoc was only found in trace quantities and has not been reported before for pan-surface habitats. Nostoc's colonial structure may break down when inundated [62], suggesting that this alga either proliferated during the dry-down period or was a contaminant from nearby dunes where Nostoc may constitute up to 3% of the algal biomass [7].
Conclusions
Field sampling revealed an abundant shrimp assemblage dominated by putative grazers. The assemblage that developed in the microcosm experiment was similar to that observed in the field, but with a somewhat higher proportion of fauna hypothesized to exert a negative influence on the algae in this system. The microcosm results nonetheless indicate that there was neither a direct nor indirect effect of shrimps on either algal biomass or species composition. Our microcosm results suggest that the abundant shrimps have little role in regulating primary producers in this environment.
References
Neal JT: Playas and dried lakes. 1975, Stroudsberg, PA: Dowden, Hutchinson & Ross
Shaw PA, Thomas DSG: Playas, pans and salt lakes. Arid Zone Geomorphology. Edited by: Thomas DSG. 1989, London: Belhaven Press, 184-208.
Brostoff WN, Sharifi MR, Rundel PW: Photosynthesis of cryptobiotic crusts of a seasonally inundated system of pans and dunes at Edwards Air Force Base, western Mojave Desert, California: laboratory studies. Flora. 2002, 197: 143-151.
Lichvar R, Brostoff W, Sprecher S: Surficial features associated with ponded water on playas of the arid southwestern United States: indicators for delineating regulated areas under the Clean Water Act. Wetlands. 2006, 26: 385-399. 10.1672/0277-5212(2006)26[385:SFAWPW]2.0.CO;2.
Eng LL, Belk D, Eriksen CH: California Anostraca: distribution, habitat, and status. J Crust Biol. 1990, 1: 247-277. 10.2307/1548485.
Belk D, Brtek J: Checklist of the Anostraca. Hydrobiologia. 1995, 298: 315-353. 10.1007/BF00033826.
Brostoff WN: Algae of a cryptobiotic crust dominated dune/pan system in the Western Mojave Desert. J Arid Environ. 2002, 51: 339-361. 10.1006/jare.2001.0965.
Lowndes AG: The feeding mechanism of Chirocephalus diaphanus Prevost, the fairy shrimp. Proc Zool Soc London. 1933, 103: 1093-1118. 10.1111/j.1096-3642.1933.tb01641.x.
Martin JW: Morphology of feeding structures in the Conchostraca with special reference to Lynceus. Functional Morphology of Feeding and Grooming in Crustacea. Edited by: Felgenhauer BE, Watling L, Thistle AB. 1989, Rotterdam, Netherlands: A.A. Balkema, 123-136.
Brendonck L: Feeding in the fairy shrimp Streptocephalus proboscideus (Frauenfeld) (Branchiopoda: Anostraca). I. Aspects of the feeding biology. J Crust Biol. 1993, 13: 235-244. 10.2307/1548971.
Beladjal L, Peiren N, Dierckens KR, Mertens J: Feeding strategy of two sympatric anostracan species (Crustacea). Hydrobiologia. 1997, 359: 207-212. 10.1023/A:1003177828859.
Olesen J, Timms B: Caenestheriella mariae sp. nov. (Crustacea: Branchiopoda: Spinicaudata: Cyzicidae): a new clam shrimp from Western Australia. Zootaxa. 2005, 824: 1-8.
Mai MG, Silva TAS, Almeida VLS, Serafini RL: First record of the invasion of Dendrocephalus brasiliensis Pesta, 1921 (Crustacea: Anostraca: Thamnocephalidae) in São Paulo State, Brazil. Pan-Am J Aquat Sci. 2008, 3: 269-274.
Bernice R: Food, feeding and digestion in Streptocephalus dichotomus Baird (Crustacea: Anostraca). Hydrobiologia. 1971, 38: 507-520.
Royan JP: Studies on the gut contents of Leptestheriella maduraiensis (Conchostraca: Branchiopoda) Nayar and Nair. Hydrobiologia. 1976, 51: 209-212. 10.1007/BF00005745.
Anaya-Soto A, Sarma SSS, Nandini S: Longevity of the freshwater anostracan Streptocephalus mackini (Crustacean: Anostraca) in relation to food (Chlorella vulgaris) concentration. Freshwater Biol. 2003, 48: 432-439. 10.1046/j.1365-2427.2003.01015.x.
Erikson CH, Belk D: Fairy shrimps of California's puddles, pools, and playas. 1999, Eureka, CA: Mad River Press
Brown LR, Carpelan LH: Egg hatching and life history of a fairy shrimp Branchinecta mackini Dexter (Crustacea: Anostraca) in a Mojave Desert Playa (Rabbit Dry Lake). Ecology. 1971, 52: 41-54. 10.2307/1934736.
Daborn GR: Life history and energy relations of the giant fairy shrimp Branchinecta gigas Lynch 1937 (Crustacea: Anostraca). Ecology. 1975, 56: 1025-1039. 10.2307/1936144.
Belk D, Ballantyne R: Filamentous algae an additional food for the predatory anostracan Branchinecta gigas. J Crust Biol. 1996, 16: 552-555. 10.2307/1548746.
Ampe F, Thiéry A: Microflora associated with the digestive tract of the fairy shrimp Branchinella spinosa (H. Milne Edwards, 1840) (Crustacea, Branchiopoda). FEMS Microbiol Lett. 1998, 158: 201-205. 10.1111/j.1574-6968.1998.tb12821.x.
Dierckens KR, Beladjal L, Vandenberghe , Swings J, Mertens J: Filter-feeding shrimps (Anostraca) grazing on bacteria. J Crust Biol. 1997, 17: 264-268. 10.2307/1549276.
Williams DD: The Biology of temporary waters. 2006, Oxford: Oxford University Press
Lichvar R, Sprecher S: Delineation and characterization of "Waters of the United States" at Edwards Air Force Base, California. 1996, Vicksburg, MS: U.S. Army Waterways Experiment Station
Lichvar R, Gustina G, Bolus R: Ponding duration, ponding frequency, and field indicators: a case study on three California playas. Wetlands. 2004, 24: 115-126. 10.1672/0277-5212(2004)024[0406:PDPFAF]2.0.CO;2.
Brostoff WN, Lichvar R, Sprecher S: Delineating playas in the arid southwest: a literature review. 2001, Hanover, NH: U.S. Army Engineer Research and Development Laboratory Technical Report ERDC TR-01-4
Gonzalez RJ, Drazen J, Hathaway S, Bauer B, Simovich M: Physiological correlates of water chemistry requirements in fairy shrimps (Anostraca) from southern California. J Crust Biol. 1996, 16: 315-322. 10.2307/1548889.
Sassaman C: Bioenergetics of branchiopod crustaceans in clay pan pools at Edwards Air Force Base. Ecosystem Model For The Dune/Pan System at Edwards Air Force Base: Phase I. Edited by: Brostoff WN, Rundel PW. 1998, Vicksburg, MS: USAE Waterways Experiment Station, 59-73.
Sogard SM, Powell GVN, Holmquist JG: Epibenthic fish communities on Florida Bay banks: relations with physical parameters and seagrass cover. Mar Ecol Prog Ser. 1987, 40: 25-39. 10.3354/meps040025.
Sogard SM, Powell GVN, Holmquist JG: Spatial distribution and trends in abundance of fishes residing in seagrass meadows on Florida Bay mudbanks. Bull Mar Sci. 1989, 44: 179-199.
Holmquist JG, Powell GVN, Sogard SM: Decapod and stomatopod assemblages on a system of seagrass-covered mud banks in Florida Bay. Mar Biol. 1989, 100: 473-483. 10.1007/BF00394824.
Holmquist JG, Powell GVN, Sogard SM: Decapod and stomatopod communities of seagrass-covered mud banks in Florida Bay: inter- and intra-bank heterogeneity with special reference to isolated subenvironments. Bull Mar Sci. 1989, 44: 251-262.
Kushlan JA: Sampling characteristics of enclosure fish traps. Trans Am Fish Soc. 1981, 110: 557-562. 10.1577/1548-8659(1981)110<557:SCOEFT>2.0.CO;2.
Jacobsen T, Kushlan JA: Sources of sampling bias in enclosure fish trapping: effects on estimates of density and diversity. Fish Res. 1987, 5: 401-412. 10.1016/0165-7836(87)90055-5.
Rozas LR, Minello TJ: Estimating densities of small fishes and decapod crustaceans in shallow estuarine habitats: a review of sampling design with focus on gear selection. Estuaries. 1997, 20: 199-213. 10.2307/1352731.
Maynard SDS: Life history strategies of fairy shrimps (Crustacea: Anostraca) as a function of environmental predictability. PhD Thesis, University of Utah, Department of Biology. 1977
Zimba PV, Dionigi CP, Millie DF: Evaluating the relationship between photopigment synthesis and 2-methylisoborneol accumulation in cyanobacteria. J Phycol. 1999, 35: 1422-1429. 10.1046/j.1529-8817.1999.3561422.x.
Cochran WG: The distribution of the largest of a set of estimated variances as a fraction of their total. Ann Eugenics. 1941, 11: 47-52.
Kirk RE: Experimental Design: Procedures for the Behavioral Sciences. 1995, Pacific Grove, CA: Brooks/Cole Publishing Co, 3
Lilliefors HW: On the Kolmogorov-Smirnov test for normality with mean and variance unknown. J Am Stat Assoc. 1967, 64: 399-402. 10.2307/2283970.
Scheirer CJ, Roy WS, Hare N: The analysis of ranked data derived from completely randomized factorial designs. Biometrics. 1976, 32: 429-434. 10.2307/2529511.
Zar JH: Biostatistical Analysis. 2009, Englewood Cliffs, NJ: Prentice Hall, 5
Sokal RR, Rohlf FJ: Biometry. 1995, New York: W. H. Freeman and Co, 3
Myers MJ, Sperling FAH, Resh VH: Dispersal of two species of Trichoptera from desert springs: Conservation implications for isolated vs connected populations. J Insect Conserv. 2001, 5: 207-215. 10.1023/A:1017998513721.
Leibowitz SG: Isolated wetlands and their functions: An ecological perspective. Wetlands. 2003, 23: 517-531. 10.1672/0277-5212(2003)023[0517:IWATFA]2.0.CO;2.
Holmquist JG, Schmidt-Gengenbach J, Slaton MR: Influence of invasive palms on terrestrial arthropod assemblages in desert spring habitat. Biol Conserv.
Shepard WD: Desert springs - both rare and endangered. Aquat Conserv. 1993, 3: 351-359. 10.1002/aqc.3270030409.
Tiner RW: Geographically isolated wetlands of the United States. Wetlands. 2003, 23: 494-516. 10.1672/0277-5212(2003)023[0494:GIWOTU]2.0.CO;2.
Perla BS, Stevens LE: Biodiversity and productivity at an undisturbed spring in comparison with adjacent grazed riparian and upland habitats. Aridland Springs in North America: Ecology and Conservation. Edited by: Stevens LE, Meretsky VJ. 2008, Tucson, Arizona: University of Arizona Press, 230-243.
Hansson LA: The role of food chain composition and nutrient availability in shaping algal biomass development. Ecology. 1992, 73: 241-247. 10.2307/1938735.
Reynolds CS: The ecological basis for the successful biomanipulation of aquatic communities. Arch Hydrobiol. 1994, 130: 1-33.
Brawley SH, Adey WH: The effect of micrograzers on algal community structure in a coral reef microcosm. Mar Biol. 1981, 61: 167-177. 10.1007/BF00386656.
Brostoff WN: Seaweed community structure and productivity: the role of mesograzers. Proceedings of the Sixth International Coral Reef Symposium:8-12 August, 1988; Townsville, Australia. Edited by: Choat JH, Barnes D, Borowitzka MA, Coll JC, Davies PJ, Flood P, Hatcher BG, Hopley D, Hutchings PA, Kinsey D, Orme GR, Pichon M, Sale PF, Sammarco P, Wallace CC, Wilkinson C, Wolanski E, Bellwood O. 1988, Townsville, Australia: Sixth International Coral Reef Symposium Executive Committee, 2: 1-6.
Lamberti GA, Resh VH: Stream periphyton and insect herbivores: an experimental study of grazing by a caddisfly population. Ecology. 1983, 64: 1124-1135. 10.2307/1937823.
McAuliffe JR: Resource depression by a stream herbivore: effects on distributions and abundances of other grazers. Oikos. 1984, 42: 327-333. 10.2307/3544401.
Greathouse EA, Pringle CM, McDowell WH, Holmquist JG: Indirect upstream effects of dams: consequences of migratory consumer extirpation in Puerto Rico. Ecol Appl. 2006, 16: 339-352. 10.1890/05-0243.
Luzier JM, Summerfelt RC: Experimental demonstration of the effects of clam shrimp on turbidity of microcosms. Prog Fish-Cult. 1997, 59: 68-70. 10.1577/1548-8640(1997)059<0068:EDOTEO>2.3.CO;2.
Frank PW: Conchostraca. Palaeogeogr Palaeoclimatol Palaeoecol. 1988, 62: 399-403. 10.1016/0031-0182(88)90064-8.
Hutchinson GE: A treatise on limnology. Vol. 2. Introduction to the lake biology and the limnoplankton. 1967, New York: John Wiley & Sons
Hairston NG, Smith FE, Slobodkin LB: Community structure, population control, and competition. Am Nat. 1960, 94: 421-425. 10.1086/282146.
McLachlan AJ, Cantrell MA: Survival strategies in tropical rain pools. Oecologia. 1980, 47: 344-351. 10.1007/BF00398528.
Gao K, Ye C: Culture of the terrestrial cyanobacterium Nostoc flagelliforme (Cyanophyceae), under aquatic conditions. J Phycol. 2003, 39: 617-623. 10.1046/j.1529-8817.2003.02013.x.
Acknowledgements
This work was performed in part under contract from Edwards Air Force Base to the U.S. Army Engineer Research and Development Center. Mark Hagen and Wanda Deal, Edwards Air Force Base, were project sponsors and greatly facilitated logistics. Laboratory work was performed at the U.S. Army Engineer Research and Development Center, Sierra Nevada Aquatic Research Laboratory, USDA Thad Cochran National Warmwater Aquaculture Center, and Center for Coastal Studies, Texas A&M University. Stimulating discussions with Bob Lichvar, Wade Berry, Phil Rundel, Denton Belk, Marie Simovich, and others greatly contributed to the success of this project. Steve Parmenter, Wayne Urbonas, and John Wehausen kindly loaned equipment. We thank Christopher Rogers for confirming shrimp identifications and Dan Dawson for assistance at the Sierra Nevada Aquatic Research Laboratory.
Author information
Authors and Affiliations
Corresponding author
Additional information
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
WNB: Basic concept; acquisition of funding, collaboration in experimental design, algal (cyanobacterial) culture and identification, collaboration in field work, collaborated in drafting manuscript. JH: Collaboration in experimental design, collaboration in field work, shrimp culture and identification, collaborated in drafting manuscript. JS: Collaborated in field work, shrimp culture and identification, collaborated in drafting manuscript. PZ: Chlorophyll extraction, collaborated in drafting manuscript. All authors read and approved the final manuscript.
WN Brostoff, JG Holmquist contributed equally to this work.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Brostoff, W., Holmquist, J., Schmidt-Gengenbach, J. et al. Fairy, tadpole, and clam shrimps (Branchiopoda) in seasonally inundated clay pans in the western Mojave Desert and effect on primary producers. Aquat. Biosyst. 6, 11 (2010). https://doi.org/10.1186/1746-1448-6-11
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/1746-1448-6-11